Respiratory Syncytial Virus (RSV)
Identifieur interne : 000255 ( Pmc/Corpus ); précédent : 000254; suivant : 000256Respiratory Syncytial Virus (RSV)
Auteurs : Edward E. Walsh ; Caroline Breese HallSource :
- Mandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases ; 2014.
Url:
DOI: 10.1016/B978-1-4557-4801-3.00160-0
PubMed: NONE
PubMed Central: 7173590
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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Respiratory Syncytial Virus (RSV)</title><author><name sortKey="Walsh, Edward E" sort="Walsh, Edward E" uniqKey="Walsh E" first="Edward E." last="Walsh">Edward E. Walsh</name></author><author><name sortKey="Hall, Caroline Breese" sort="Hall, Caroline Breese" uniqKey="Hall C" first="Caroline Breese" last="Hall">Caroline Breese Hall</name></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmc">7173590</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7173590</idno><idno type="RBID">PMC:7173590</idno><idno type="doi">10.1016/B978-1-4557-4801-3.00160-0</idno><idno type="pmid">NONE</idno><date when="2014">2014</date><idno type="wicri:Area/Pmc/Corpus">000255</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000255</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Respiratory Syncytial Virus (RSV)</title><author><name sortKey="Walsh, Edward E" sort="Walsh, Edward E" uniqKey="Walsh E" first="Edward E." last="Walsh">Edward E. Walsh</name></author><author><name sortKey="Hall, Caroline Breese" sort="Hall, Caroline Breese" uniqKey="Hall C" first="Caroline Breese" last="Hall">Caroline Breese Hall</name></author></analytic><series><title level="j">Mandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases</title><imprint><date when="2014">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Hall, C" uniqKey="Hall C">C Hall</name></author><author><name sortKey="Weinberg, G" uniqKey="Weinberg G">G Weinberg</name></author><author><name sortKey="Iwane, M" uniqKey="Iwane M">M Iwane</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Zhou, H" uniqKey="Zhou H">H Zhou</name></author><author><name sortKey="Thompson, Ww" uniqKey="Thompson W">WW Thompson</name></author><author><name sortKey="Viboud, Cg" 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<front><journal-meta><journal-id journal-id-type="nlm-ta">Mandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases</journal-id><journal-title-group><journal-title>Mandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases</journal-title></journal-title-group></journal-meta><article-meta><article-id pub-id-type="pmc">7173590</article-id><article-id pub-id-type="publisher-id">B978-1-4557-4801-3.00160-0</article-id><article-id pub-id-type="doi">10.1016/B978-1-4557-4801-3.00160-0</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title-group><article-title>Respiratory Syncytial Virus (RSV)</article-title></title-group><contrib-group><contrib contrib-type="author" id="au0010"><name><surname>Walsh</surname><given-names>Edward E.</given-names></name></contrib><contrib contrib-type="author" id="au0015"><name><surname>Hall</surname><given-names>Caroline Breese</given-names></name><xref rid="fn0010" ref-type="fn">*</xref></contrib></contrib-group><contrib-group><contrib contrib-type="editor"><name><surname>Bennett</surname><given-names>John E.</given-names></name><degrees>MD, MACP</degrees></contrib><aff>Adjunct Professor of Medicine, Uniformed Services University of the Health Sciences, F. Edward Hebert School of Medicine, Bethesda, Maryland</aff></contrib-group><contrib-group><contrib contrib-type="editor"><name><surname>Dolin</surname><given-names>Raphael</given-names></name><degrees>MD</degrees></contrib><aff>Maxwell Finland Professor of Medicine (Microbiology and Molecular Genetics), Harvard Medical School, Boston, Massachusetts</aff><aff>Attending Physician, Beth Israel Deaconess Medical Center, Boston, Massachusetts</aff><aff>Brigham and Women' s Hospital, Boston, Massachusetts</aff></contrib-group><contrib-group><contrib contrib-type="editor"><name><surname>Blaser</surname><given-names>Martin J.</given-names></name><degrees>MD</degrees></contrib><aff>Muriel G. and George W. Singer Professor of Translational Medicine, Professor of Microbiology, Director, Human Microbiome Program, Departments of Medicine and Microbiology, New York University School of Medicine, Langone Medical Center, New York, New York</aff></contrib-group><pub-date pub-type="pmc-release"><day>31</day><month>10</month><year>2014</year></pub-date><pmc-comment> PMC Release delay is 0 months and 0 days and was based on .</pmc-comment>
<pub-date pub-type="ppub"><year>2015</year></pub-date><pub-date pub-type="epub"><day>31</day><month>10</month><year>2014</year></pub-date><fpage>1948</fpage><lpage>1960.e3</lpage><permissions><copyright-statement>Copyright © 2015 Elsevier Inc. All rights reserved.</copyright-statement><copyright-year>2015</copyright-year><copyright-holder>Elsevier Inc.</copyright-holder><license><license-p>Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.</license-p></license></permissions><kwd-group id="kwd0010"><title>Keywords</title><kwd>acute bronchitis</kwd><kwd>apnea</kwd><kwd>bronchiolitis</kwd><kwd>chronic obstructive lung disease (COPD)</kwd><kwd>croup</kwd><kwd>otitis media</kwd><kwd>palivizumab</kwd><kwd>pneumonia</kwd><kwd>respiratory syncytial virus</kwd><kwd>ribavirin</kwd></kwd-group></article-meta></front><body><p id="p0105"><disp-quote><p><italic>Were we but able to explain</italic></p><p><italic>The fiefdom of the microbe—</italic></p><p><italic>Why one man is his serf,</italic></p><p><italic>Another is his lord</italic></p><p><italic>When all are his domain.</italic></p><p><bold>C.B.H.</bold></p></disp-quote></p><p id="p0110">Respiratory syncytial virus (RSV) is the major cause of lower respiratory tract illness in young children.<xref rid="bib1" ref-type="bibr">1</xref>, <xref rid="bib2" ref-type="bibr">2</xref>, <xref rid="bib3" ref-type="bibr">3</xref>, <xref rid="bib4" ref-type="bibr">4</xref> So effectively does RSV spread that essentially all persons have experienced RSV infection within the first few years of life. Immunity, however, is not complete, and reinfection is common. Although life-threatening infections most commonly occur during the first couple of years of life, RSV infections contribute an appreciable share of the morbidity caused by acute upper and lower respiratory tract infections among older children and adults. The health care costs associated with outpatient infections add appreciably to the estimated cost of $300 to $600 million for hospitalized infants with RSV infection.<xref rid="bib2" ref-type="bibr">2</xref>, <xref rid="bib5" ref-type="bibr">5</xref>, <xref rid="bib6" ref-type="bibr">6</xref> Of concern and increasing recognition are the growing morbidity and costs associated with RSV infections in older adults.<xref rid="bib7" ref-type="bibr">7</xref>, <xref rid="bib8" ref-type="bibr">8</xref>, <xref rid="bib9" ref-type="bibr">9</xref></p><sec id="s0010"><title>History</title><p id="p0115">RSV was discovered in 1956 but was not initially associated with respiratory illness among infants. Indeed, when a group of 14 chimpanzees were noted to be suffering from colds and coryza, Morris and co-workers<xref rid="bib10" ref-type="bibr"><sup>10</sup></xref> isolated a new virus originally named <italic>chimpanzee coryza agent</italic> (CCA).<xref rid="bib1" ref-type="bibr"><sup>1</sup></xref> Subsequently, Chanock and co-workers<xref rid="bib11" ref-type="bibr"><sup>11</sup></xref>confirmed that the agent caused respiratory illness in humans when they obtained isolates from two children, one with laryngotracheobronchitis and the other with bronchopneumonia, that were indistinguishable from CCA. When specific neutralizing antibody to CCA was found to be present in most school-aged children, “chimpanzee coryza agent” was more appropriately renamed <italic>respiratory syncytial virus</italic> to denote its clinical and laboratory manifestations.</p></sec><sec id="s0015"><title>Description</title><sec id="s0020"><title>Classification</title><p id="p0120">RSV belongs to the order Mononegavirales, family Paramyxoviridae, and the subfamily Pneumovirinae.<xref rid="bib12" ref-type="bibr"><sup>12</sup></xref> The two genera within the Pneumovirinae subfamily are <italic>Metapneumovirus</italic>, containing human metapneumovirus (hMPV), and <italic>Pneumovirus</italic>, which contains human RSV and the morphologically and biologically similar murine pneumovirus and canine pneumovirus, bovine RSV, ovine RSV, and caprine RSV.<xref rid="bib13" ref-type="bibr"><sup>13</sup></xref> Distinctive features of RSV include the number and order of genes and the lack of hemagglutinin and neuraminidase activity.</p></sec><sec id="s0025"><title>Viral Structure and Characteristics</title><p id="p0125">RSV is an enveloped, medium-sized (120 to 300 nm) RNA virus with a nonsegmented, single-stranded, negative-sense genome that is associated with viral proteins throughout its length, which form the nucleocapsid (<xref rid="f0010" ref-type="fig">Figs. 160-1</xref>and <xref rid="f0015" ref-type="fig">160-2</xref>).<xref rid="bib6" ref-type="bibr">6</xref>, <xref rid="bib12" ref-type="bibr">12</xref> The viral envelope has a bilipid layer derived from the plasma membrane of the host cells. Its surface has transmembrane surface glycoprotein spikes 11 to 12 nm in length and 6 to 10 nm apart, which on electron microscopy give it a thistle-like appearance (<xref rid="f0020" ref-type="fig">Fig. 160-3</xref>).<xref rid="bib12" ref-type="bibr"><sup>12</sup></xref><fig id="f0010"><label>FIGURE 160-1</label><caption><p>Structure of respiratory syncytial virus.</p></caption><graphic xlink:href="f160-001-9781455748013"></graphic><attrib>(Modified from Hall CB. Respiratory syncytial virus and parainfluenza virus. <italic>N Engl J Med</italic>. 2001;344:1917-1928.)</attrib></fig><fig id="f0015"><label>FIGURE 160-2</label><caption><p>Simplified representation of the negative-sense RNA genome of respiratory syncytial virus (RSV) and the encoded proteins.</p><p>The genome is shown 3′ with the leader extragenic region (ler) and with the 5′ trailer extragenic region (ter). The viral genes are depicted by the divided bars. Each viral gene transcribes a single messenger RNA (mRNA) encoding a single protein, with the exception of M2 mRNA, which transcribes two proteins, M2-1 and M2-2.</p></caption><graphic xlink:href="f160-002-9781455748013"></graphic></fig><fig id="f0020"><label>FIGURE 160-3</label><caption><p>Negative contrast electron micrograph of respiratory syncytial virus.</p></caption><graphic xlink:href="f160-003-9781455748013"></graphic></fig></p><p id="p0130">The complete genome of RSV (A2 strain) has been sequenced (see <xref rid="f0015" ref-type="fig">Fig. 160-2</xref>).<xref rid="bib12" ref-type="bibr">12</xref>, <xref rid="bib14" ref-type="bibr">14</xref> The viral RNA consists of 15,222 nucleotides containing 10 genes. Each gene encodes for a single protein, except for the <italic>M2</italic> gene, which possesses two overlapping open reading frames that encode for two separate proteins (M2-1 and M2-2, the transcription processivity factor and a transcriptional regulatory protein, respectively). Four proteins—N (nucleoprotein), P (phosphoprotein), L (polymerase), and M2-1—are associated with the RNA-containing nucleocapsid complex. Associated with the envelope are three transmembrane surface proteins, F (fusion), G (attachment), and SH (proposed viroporin protein), that are important for viral infectivity.<xref rid="bib15" ref-type="bibr"><sup>15</sup></xref> In addition, a truncated secreted form of G (Gs) is transcribed from a second start codon. The M (matrix) protein accumulates at the inner surface of the envelope and is important in viral morphogenesis. Two proteins, NS1 and NS2, are nonstructural proteins that inhibit cellular type I interferon activity and subsequently effect the adaptive immune response to RSV.<xref rid="bib12" ref-type="bibr">12</xref>, <xref rid="bib16" ref-type="bibr">16</xref></p><p id="p0135">The two major glycosylated surface proteins, F and G, are the major immunoprotective antigens and are targets for antibody-mediated neutralization. The G protein is the primary mediator of attachment of the virus to host cells, although the F protein also can facilitate viral attachment.<xref rid="bib17" ref-type="bibr"><sup>17</sup></xref> After attachment in the pretriggered form, F undergoes structural changes into a post-triggered form that initiates viral penetration by fusing viral and host cellular membranes and promotes fusion of infected cells to adjacent uninfected cells, thereby resulting in the characteristic RSV syncytia.<xref rid="bib18" ref-type="bibr"><sup>18</sup></xref> Maximally efficient fusion requires participation of all three of the surface glycoproteins, F, G, and SH.</p></sec><sec id="s0030"><title>Laboratory Properties</title><p id="p0140">RSV poorly withstands slow freezing and thawing and changes in pH. At 55° C, infectivity is rapidly diminished, and at room temperature (25° C), only 10% infectivity remains at 48 hours, and even at 4° C only 1% remains after 7 days.<xref rid="bib19" ref-type="bibr"><sup>19</sup></xref> The optimal pH for RSV is 7.5. Inactivation occurs quickly with acidic media (pH < 5), ether, and chloroform and with detergents such as sodium dodecyl sulfate and Triton X-100.</p><p id="p0145">The survival of RSV in the environment appears to depend in part on the drying time and dew point. At room temperature, RSV in the secretions of patients may survive on nonporous surfaces, such as countertops, for 3 to 30 hours.<xref rid="bib20" ref-type="bibr"><sup>20</sup></xref> On porous surfaces, such as cloth and paper tissue, survival is generally shorter, usually less than 1 hour. The infectivity of RSV on the hands is variable from person to person but is usually less than 1 hour.</p><p id="p0150">Human heteroploid cell lines are usually preferred for primary isolation. Most commonly used are HEp-2, HeLa, and A549 cell lines. RSV may also be recovered in human kidney, amnion, diploid fibroblastic cells, and monkey kidney cells. With primary isolation in sensitive cell cultures, characteristic cytopathic effect may be first detected after an average of 3 to 5 days. The typical syncytia develop about 10 to 24 hours later and progress until the cell sheet is completely destroyed, which is usually within 4 days. Cell-free virus may be demonstrated in the culture medium, but up to 90% of the virus remains cell-associated.<xref rid="bib12" ref-type="bibr"><sup>12</sup></xref></p></sec><sec id="s0035"><title>Infection in Animals</title><p id="p0155">Humans and chimpanzees are the only known natural hosts for human RSV, although a variety of small animal species may be experimentally infected with RSV.<xref rid="bib21" ref-type="bibr"><sup>21</sup></xref> Cows are the natural hosts of bovine RSV (BRSV), which is antigenically and genetically closely related to human RSV, and some antibodies directed against the F, N, P, and M proteins of either virus recognize the heterologous virus. Ovine and caprine strains of RSV also have been recovered, and genetic analysis suggests that caprine RSV is more closely related than ovine RSV to BRSV and human RSV.<xref rid="bib12" ref-type="bibr"><sup>12</sup></xref></p><p id="p0160">Although many animal models develop upper respiratory tract infection, their lack of symptomatic lower respiratory tract disease comparable to that observed with infants limits their utility. Closest is disease in chimpanzees because they readily acquire infection from infected contacts and shed moderate levels of RSV in respiratory secretions.<xref rid="bib12" ref-type="bibr"><sup>12</sup></xref> Nevertheless, their disease is generally mild and without the degree of lower respiratory tract involvement observed in infants. Rodents are the most commonly used models, particularly cotton rats and mice, but replication of RSV is only semipermissive and highly variable.<xref rid="bib22" ref-type="bibr"><sup>22</sup></xref></p></sec></sec><sec id="s0040"><title>Epidemiology</title><sec id="s0045"><title>Distribution</title><p id="p0165">In every geographic area studied, RSV infections are ubiquitous and clinically similar in causing the most severe disease during infancy and repetitive infections throughout life.<xref rid="bib6" ref-type="bibr">6</xref>, <xref rid="bib23" ref-type="bibr">23</xref>, <xref rid="bib24" ref-type="bibr">24</xref> The seasonal occurrence, however, varies according to geography and climate.<xref rid="bib25" ref-type="bibr"><sup>25</sup></xref></p></sec><sec id="s0050"><title>Seasonal Occurrence</title><p id="p0170">RSV is singular in its ability to produce reliably a major burden of infections every year.<xref rid="bib3" ref-type="bibr">3</xref>, <xref rid="bib26" ref-type="bibr">26</xref> In temperate climates, the outbreaks occur primarily in the late fall through early spring and spread across the United States over a period of 20 or more weeks, generally from October to May. In warmer climates, RSV activity may be more prolonged or even present throughout the year.<xref rid="bib24" ref-type="bibr">24</xref>, <xref rid="bib25" ref-type="bibr">25</xref>, <xref rid="bib27" ref-type="bibr">27</xref>, <xref rid="bib28" ref-type="bibr">28</xref>, <xref rid="bib29" ref-type="bibr">29</xref> What factors initiate and terminate the recurring patterns of RSV activity has been a subject of ongoing curiosity and investigation but remains a conundrum.<xref rid="bib29" ref-type="bibr">29</xref>, <xref rid="bib30" ref-type="bibr">30</xref>, <xref rid="bib31" ref-type="bibr">31</xref> A complex, and currently incompletely understood, interaction of local meteorologic conditions may explain part of the geographically variable epidemiologic patterns.<xref rid="bib32" ref-type="bibr"><sup>32</sup></xref> Among these are the ambient temperature, humidity, and sunlight, and their effects on RSV's stability and infectivity. However, because the only source of RSV infection is an infected individual, human behavior is an indefinable factor integral to its transmission.<xref rid="bib29" ref-type="bibr">29</xref>, <xref rid="bib33" ref-type="bibr">33</xref></p></sec><sec id="s0055"><title>Antigenic Variation</title><p id="p0175">Strain differences among RSV isolates may also affect the intensity, severity, and diversity of RSV outbreaks.<xref rid="bib34" ref-type="bibr">34</xref>, <xref rid="bib35" ref-type="bibr">35</xref>, <xref rid="bib36" ref-type="bibr">36</xref> RSV isolates are divided into two major antigenic groups, A and B, each of which can be further divided into multiple subgroups containing separate genotypes.<xref rid="bib12" ref-type="bibr">12</xref>, <xref rid="bib14" ref-type="bibr">14</xref>, <xref rid="bib37" ref-type="bibr">37</xref> The two major groups have 81% nucleotide identity, but some of the proteins between the A and B strains vary appreciably. The major genetic diversity between groups A and B resides with the G protein, followed by M2-2 and SH proteins. This is reflected in the relative low antigenic relatedness between the two groups of only 1% to 7% for the G proteins, compared with 50% for the F proteins. Nucleotide and amino acid sequence analysis within both A and B strain groups has further revealed subtypes of distinctive lineage, or clades.<xref rid="bib12" ref-type="bibr">12</xref>, <xref rid="bib14" ref-type="bibr">14</xref></p><p id="p0180">Strains of both groups circulate simultaneously during outbreaks, but the proportions that are A and B vary, as do the subtypes.<xref rid="bib34" ref-type="bibr">34</xref>, <xref rid="bib35" ref-type="bibr">35</xref>, <xref rid="bib36" ref-type="bibr">36</xref>, <xref rid="bib37" ref-type="bibr">37</xref>, <xref rid="bib38" ref-type="bibr">38</xref> Even in widely separated geographic areas, the cocirculating strains may have similar genotypes and parallel evolutionary lineages. Analyses of the proteins of strains collected over decades and from diverse areas suggest that the pressure of the population's immunity may result in a selective advantage for the dominance of strains that are most divergent from those that have recently circulated in the area. Evidence indicates that a recently emerged RSV B strain containing a unique 20-amino-acid duplication in the G protein has spread throughout the world and currently is the dominant variant among group B viruses, suggesting an evolutionary advantage over prior strains.<xref rid="bib39" ref-type="bibr"><sup>39</sup></xref> However, the relationship of the circulating strain groups and subtypes to the clinical severity and manifestations of the RSV infections among young children has been inconsistent and thus inconclusive.<xref rid="bib35" ref-type="bibr">35</xref>, <xref rid="bib36" ref-type="bibr">36</xref>, <xref rid="bib38" ref-type="bibr">38</xref>, <xref rid="bib40" ref-type="bibr">40</xref>, <xref rid="bib41" ref-type="bibr">41</xref> The relationship between the substantial antigenic diversity of the G protein to reinfection with RSV has not been established.</p></sec><sec id="s0060"><title>Epidemiologic Manifestations</title><p id="p0185">The characteristic epidemiologic ramifications of RSV's presence within a community are notable rises in the number of cases of bronchiolitis, pneumonia, and hospital admissions of young children, especially infants with acute lower respiratory tract disease.<xref rid="bib2" ref-type="bibr">2</xref>, <xref rid="bib42" ref-type="bibr">42</xref>, <xref rid="bib43" ref-type="bibr">43</xref> RSV outbreaks may vary year to year in size and intensity. Severe lower respiratory tract illness from RSV in previously healthy children occurs most frequently in the first year of life and is almost always associated with primary infection. Essentially all children have experienced RSV infection within the first several years of life one or more times. Repeated infections are common not only among young children but throughout life.<xref rid="bib7" ref-type="bibr">7</xref>, <xref rid="bib44" ref-type="bibr">44</xref>, <xref rid="bib45" ref-type="bibr">45</xref>, <xref rid="bib46" ref-type="bibr">46</xref></p></sec><sec id="s0065"><title>Prevalence and Incidence</title><p id="p0190">RSV is the most frequent cause of bronchiolitis and is estimated to cause 40% to 90% of bronchiolitis hospitalizations and up to 50% of pneumonia admissions among infants.<xref rid="bib2" ref-type="bibr">2</xref>, <xref rid="bib3" ref-type="bibr">3</xref>, <xref rid="bib5" ref-type="bibr">5</xref>, <xref rid="bib43" ref-type="bibr">43</xref> Ten to 30% of tracheobronchitis cases have been associated with RSV infection, but only 2% to 10% of croup cases. Bronchiolitis is the leading cause of all hospitalizations among infants in the United States. Overall, as many as 172,000 children younger than 5 years are reported to be hospitalized annually with RSV infection in the United States.<xref rid="bib3" ref-type="bibr">3</xref>, <xref rid="bib4" ref-type="bibr">4</xref>, <xref rid="bib47" ref-type="bibr">47</xref> The yearly rates of RSV hospitalizations estimated from national databases have been variable, ranging from about 2 to 44 per 1000 children within the first 2 to 5 years of life.<xref rid="bib42" ref-type="bibr">42</xref>, <xref rid="bib48" ref-type="bibr">48</xref>, <xref rid="bib49" ref-type="bibr">49</xref> Children within the first year of life consistently had the highest rates of hospitalization for bronchiolitis and other RSV-associated illnesses, and the preponderance of admissions were among infants younger than 6 months.<xref rid="bib4" ref-type="bibr"><sup>4</sup></xref> Recent population-based studies in the United States have indicated the current hospitalization rates are 17 per 1000 children younger than 6 months and 3 per 1000 children younger than 5 years.<xref rid="bib2" ref-type="bibr">2</xref>, <xref rid="bib43" ref-type="bibr">43</xref> These rates, which are similar to those derived from RSV-coded hospitalization data, were more than three times the rates from parainfluenza or influenza viral infections over 4 years of surveillance among the same population of children.<xref rid="bib50" ref-type="bibr">50</xref>, <xref rid="bib51" ref-type="bibr">51</xref> The reported RSV hospitalization rates from European countries have been generally similar, ranging from 2.5 to 11 per 1000 children within the first 4 years of life and highest among those younger than 12 months of age—19 to 22 per 1000 children.<xref rid="bib5" ref-type="bibr">5</xref>, <xref rid="bib52" ref-type="bibr">52</xref>, <xref rid="bib53" ref-type="bibr">53</xref>, <xref rid="bib54" ref-type="bibr">54</xref> Estimates of lower respiratory tract infection from RSV in developing countries are estimated to be twice that of developed countries.<xref rid="bib27" ref-type="bibr"><sup>27</sup></xref></p><p id="p0195">The rates of hospitalization among children, however, vary according to the presence of risk factors. Many host, socioeconomic, and environmental factors have been associated with a greater likelihood of young children developing more severe RSV infection and requiring hospitalization (see “<xref rid="s0120" ref-type="sec">Patients at High Risk for Severe Infection</xref>”).</p><p id="p0200">Population-based surveillance during 2000 to 2004, examining laboratory-proven RSV hospitalizations and emergency department and outpatient visits in the counties surrounding Rochester, New York; Nashville, Tennessee; and Cincinnati, Ohio, indicated that outpatient visits constituted a major proportion of the health care burden attributable to RSV infection.<xref rid="bib2" ref-type="bibr"><sup>2</sup></xref> Of all visits for acute respiratory illnesses (ARI) among children within the first 5 years of life, RSV infection was documented among 20% of ARI hospitalizations, 18% of emergency department ARI visits, and 15% of office ARI visits. The estimated rates of ARI visits from RSV among children younger than 5 years in pediatric practices (80 per 1000 children) was about 3 times higher than that observed among emergency department patients and 26 times the rates among hospitalized children.</p><p id="p0205">Less information exists on the health care burden imposed by RSV infection among older children and adults. Recurrent RSV infections are common among school-aged children and adults who are exposed to RSV at school, home, work, or during military training.<xref rid="bib49" ref-type="bibr">49</xref>, <xref rid="bib55" ref-type="bibr">55</xref> In urban Rochester, 44% of the families with young children who were followed became infected with RSV during the winter months, when RSV was prevalent in the community.<xref rid="bib46" ref-type="bibr"><sup>46</sup></xref> Of the exposed family members, 46% acquired RSV infection. Although the attack rate was highest among infants, 38% to 47% of older children and adults developed RSV infection. In the Houston family study, in which children were followed from birth, the infection rate was 68.8 per 100 children in the first year of life, and during the second year, at least half were reinfected.<xref rid="bib44" ref-type="bibr"><sup>44</sup></xref></p><p id="p0210">More recently recognized is the frequency of RSV infections among older adults and the resulting appreciable clinical and economic impact.<xref rid="bib7" ref-type="bibr">7</xref>, <xref rid="bib9" ref-type="bibr">9</xref>, <xref rid="bib56" ref-type="bibr">56</xref> In one study spanning 4 years, rates of RSV infection ranged from 2% to 10% per year in persons 65 years of age or older and in high-risk persons with underlying cardiopulmonary disease.<xref rid="bib7" ref-type="bibr"><sup>7</sup></xref> RSV infection among older individuals is remarkably similar to influenza with respect to clinical manifestations and as a cause of hospitalization. In London, the rate of hospitalization attributable to RSV infection among the elderly has been estimated at 0.7 per 1000 adults 65 years of age or older, compared with 1.1 per 1000 estimated for influenza.<xref rid="bib57" ref-type="bibr"><sup>57</sup></xref></p></sec></sec><sec id="s0070"><title>Pathogenesis</title><p id="p0215">Infection with RSV is primarily acquired through close contact with an infected individual or direct inoculation into the eyes and nose of infectious secretions.<xref rid="bib33" ref-type="bibr">33</xref>, <xref rid="bib58" ref-type="bibr">58</xref> Large-particle aerosols engendered by coughs and sneezes of an ill person may transmit RSV to others within a radius of about 3 feet. Longer-distance spread by small-particle (droplet nuclei) aerosols appears to be much less likely.<xref rid="bib33" ref-type="bibr"><sup>33</sup></xref> However, infection occurring from touching objects that have been contaminated with infectious secretions, followed by self-inoculation into the eyes or nose, is an important mode of transmission.</p><p id="p0220">Experimental infection occurs in adult volunteers after an average incubation period of 3 to 5 days.<xref rid="bib59" ref-type="bibr">59</xref>, <xref rid="bib60" ref-type="bibr">60</xref>, <xref rid="bib61" ref-type="bibr">61</xref>, <xref rid="bib62" ref-type="bibr">62</xref>, <xref rid="bib63" ref-type="bibr">63</xref> In naturally acquired infection, the average incubation period appears similar, with a range of 2 to 8 days. The mucosa of the nose and eye appears to be equally sensitive portals of entry, in contrast to the mouth.<xref rid="bib61" ref-type="bibr"><sup>61</sup></xref> In hospitalized infants with primary RSV infection, peak viral titers range from 10<sup>1</sup> to 10<sup>7</sup> plaque-forming units (pfu)/mL of nasal secretions (mean of 10<sup>5</sup>) and fall slowly.<xref rid="bib64" ref-type="bibr">64</xref>, <xref rid="bib65" ref-type="bibr">65</xref> Shedding duration is typically 7 to 10 days, but virus can occasionally be detected as long as 30 days later. Increased viral load has variably been associated with greater disease severity.<xref rid="bib64" ref-type="bibr">64</xref>, <xref rid="bib65" ref-type="bibr">65</xref>, <xref rid="bib66" ref-type="bibr">66</xref></p><p id="p0225">RSV replicates in respiratory epithelium, primarily involving the ciliated columnar cells, but additional cells, such as type I and II pneumocytes, may be involved.<xref rid="bib67" ref-type="bibr"><sup>67</sup></xref> During primary infection, lower respiratory tract infection usually is manifest by bronchiolitis, and the initial pathologic findings are a lymphocytic peribronchiolar infiltration, predominantly CD69<sup>+</sup> monocytes, with edema of the walls and surrounding tissue.<xref rid="bib67" ref-type="bibr">67</xref>, <xref rid="bib68" ref-type="bibr">68</xref>, <xref rid="bib69" ref-type="bibr">69</xref> Subsequently, the characteristic proliferation and necrosis of the epithelium of the bronchioles develop. The lumina of these small airways become obstructed from the sloughed epithelium and from the increased mucus secretion. The airway of the young infant is particularly vulnerable to any degree of inflammation and obstruction because resistance to the flow of air is related inversely to the cube of the radius. Impedance to the flow of air occurs during both inspiration and expiration but is greater in the latter when the lumen is narrowed further by the positive expiratory pressure. Hyperinflation, therefore, results from air trapping peripheral to the sites of partial occlusion. With complete obstruction, the trapped air eventually becomes absorbed, producing the characteristic multiple areas of atelectasis. Young infants are at increased risk for developing such areas of atelectasis because the collateral channels that maintain alveolar expansion in the presence of airway obstruction are not yet well developed. These changes result in an increase in lung volume and expiratory resistance.</p><p id="p0230">Infants with lower respiratory tract disease from RSV often have pathologic evidence of both pneumonia and bronchiolitis. Patients with pneumonia demonstrate an interstitial infiltration of mononuclear cells that may be accompanied by edema and necrotic areas that lead to alveolar filling.<xref rid="bib67" ref-type="bibr">67</xref>, <xref rid="bib68" ref-type="bibr">68</xref> Some histologic evidence of recovery is present in most children with bronchiolitis within the first week of illness and is marked by the beginning regeneration of the bronchiolar epithelium. However, ciliated cells may not be present for weeks.</p><sec id="s0075"><title>Immunity and Pathogenesis of Disease</title><p id="p0235">Diverse theories and supporting data have been offered to explain how RSV engenders these pathogenic findings. Much of our current knowledge regarding the immunologic responses to RSV is from studies in vitro and in animal models. In humans, the immune response cannot be separated from the confounding and poorly understood influence of genetics, environment, age, and antigenic experience.<xref rid="bib70" ref-type="bibr">70</xref>, <xref rid="bib71" ref-type="bibr">71</xref>, <xref rid="bib72" ref-type="bibr">72</xref>, <xref rid="bib73" ref-type="bibr">73</xref> Consensus exists that during primary infection, disease is both virally and immunologically mediated. RSV produces its most devastating illness when specific, maternally derived antibody is present at variable amounts. The severity of RSV infection in the young infant with high levels of specific antibody and the augmented disease induced by the inactivated RSV vaccine developed in the 1960s first suggested the putative singular role of the immune response in RSV's pathogenesis in infants.<xref rid="bib73" ref-type="bibr">73</xref>, <xref rid="bib74" ref-type="bibr">74</xref>, <xref rid="bib75" ref-type="bibr">75</xref>, <xref rid="bib76" ref-type="bibr">76</xref>, <xref rid="bib77" ref-type="bibr">77</xref></p><p id="p0240">The potential importance of the host's immune response to the development of disease and the subsequent rowen of long-term complications has been further supported by the observation that RSV is not very invasive or cytopathogenic.<xref rid="bib73" ref-type="bibr"><sup>73</sup></xref> Although viral loads correlate with disease severity in humans, reducing viral replication with the administration of neutralizing antibody to the F protein has not ameliorated clinical disease in infants.<xref rid="bib78" ref-type="bibr">78</xref>, <xref rid="bib79" ref-type="bibr">79</xref> However, recent data in murine models of RSV indicate that administration of non-neutralizing antibodies to the centrally conserved CX3C chemokine motif of the G protein can reduce inflammatory responses and illness even after infection is established.<xref rid="bib80" ref-type="bibr">80</xref>, <xref rid="bib81" ref-type="bibr">81</xref></p><p id="p0245">The relative contribution of the immune response to disease in infants, however, has been questioned by the observation that among children with bronchiolitis, those with RSV bronchiolitis produced a more robust response of proinflammatory cytokines in their nasal washes than did children with non-RSV bronchiolitis, but it was not associated with more severe disease and, indeed, appeared protective against hypoxia.<xref rid="bib82" ref-type="bibr"><sup>82</sup></xref> Furthermore, examination of fatal RSV cases has shown that RSV antigen was extensively present in the pulmonary tissue, indicating abundant viral replication.<xref rid="bib83" ref-type="bibr"><sup>83</sup></xref> Cytokine production, on the other hand, was nearly absent, and the expression of apoptosis was increased, with the conclusion that the patients had an inadequate immune response and unchecked viral replication. Whether the innate or adaptive immune responses, or both, are enhanced or suppressed in association with more severe disease remains controversial, but most likely the pathogenicity of RSV infection results from varying and currently ill-defined combinations of the contributions of the virus and host.</p><sec id="s0080"><title>Innate Immunity</title><p id="p0250">The first barrier of defense against RSV infection in infants is the innate immune response, which is initiated by infection of the respiratory epithelium.<xref rid="bib73" ref-type="bibr">73</xref>, <xref rid="bib77" ref-type="bibr">77</xref>, <xref rid="bib84" ref-type="bibr">84</xref>, <xref rid="bib85" ref-type="bibr">85</xref> RSV is a potent inhibitor of cellular antiviral type I interferons (α, β, and λ) via the production of the NS1 and NS2 proteins.<xref rid="bib16" ref-type="bibr"><sup>16</sup></xref> In addition, RSV interacts with the Toll-like receptor (TLR)2, 3, 4, and 7, which triggers secretion of inflammatory cytokines.<xref rid="bib77" ref-type="bibr"><sup>77</sup></xref> Infection of the respiratory epithelium, antigen-processing cells (dendrites), and macrophages produces multiple alterations in gene expression, which result in the production of cell surface markers and the release of cytokines and chemokines (<xref rid="f0025" ref-type="fig">Fig. 160-4</xref>). Inflammatory cells are recruited to the respiratory tract and consist of neutrophils as well as macrophages, mononuclear cells, T cells, natural killer (NK) cells, and eosinophils. Intubated infants with severe primary RSV infection have an early and robust neutrophilic infiltration into the airway, as determined by bronchoalveoloar lavage, and this correlated with a decline in viral load before the development of T-cell responses.<xref rid="bib86" ref-type="bibr"><sup>86</sup></xref> The variability in the endowed innate defense and susceptibility of the host are also being increasingly correlated with polymorphisms in genes that are integral to various components of innate immunity.<xref rid="bib72" ref-type="bibr">72</xref>, <xref rid="bib87" ref-type="bibr">87</xref><fig id="f0025"><label>FIGURE 160-4</label><caption><p>Early innate and adaptive immunity response to respiratory syncytial virus (RSV).</p><p>RSV's envelope glycoprotein G attaches to the respiratory tract epithelial cells by glucosamine glycans expressed on the cell surface, and F interacts with antigen-presenting cells (macrophages, dendritic cells) through Toll-like receptor 4 (TLR4) protein. This triggers the production and release of antiviral interferons (IFN-α, IFN-β, IFN-γ) and a cascade of proinflammatory cytokines and chemokines. Two early nonstructural RSV gene products (NS1, NS2) antagonize interferon production. The chemokines recruit polymorphonuclear neutrophils (PMN cells), natural killer (NK) cells, and CD4<sup>+</sup> and CD8<sup>+</sup> T cells. A Th1-type cellular response becomes dominant under the influence of IFN-γ and interleukin-12 (IL-12), whereas under the influence of IL-4 and IL-13, the cellular response is skewed toward Th2, with the production of immunoglobulin E (IgE) and eosinophils. CTL, cytotoxic lymphocyte; CXC, cysteine X cysteine; MCP, monocyte chemotactic protein; MIP, macrophage inhibitory protein; RANTES, regulated on activation, normal T-cell expressed and secreted.</p></caption><graphic xlink:href="f160-004-9781455748013"></graphic><attrib>(Modified from Hall CB, Walsh EE. Respiratory syncytial virus. In: Feigin R, Cherry J, Demmler G, Kaplan S, eds. <italic>Textbook of Pediatric Infectious Diseases</italic>. 6th ed. Philadelphia: Saunders; 2009:2462-2487.)</attrib></fig></p></sec><sec id="s0085"><title>Adaptive Immunity</title><p id="p0255">The relative contributions and interactions of different arms of the immune response to either a primary or recurrent exposure to RSV or after immunization with experimental vaccines are complex and unclear. Considerable evidence suggests that an effective, nondetrimental immune response to RSV infection requires a fine balance of the multiple components of immunity, and that balance is determined by both host and viral factors.<xref rid="bib70" ref-type="bibr">70</xref>, <xref rid="bib73" ref-type="bibr">73</xref></p><p id="p0260">Serum neutralizing antibody provides some, but not complete, protection against RSV infection. Higher titers of antibody generally correlate with better resistance to infection, but no defined level of neutralizing antibody is predictive of the risk for infection, the severity of illness, or recovery in children or adults.<xref rid="bib8" ref-type="bibr">8</xref>, <xref rid="bib88" ref-type="bibr">88</xref>, <xref rid="bib89" ref-type="bibr">89</xref>, <xref rid="bib90" ref-type="bibr">90</xref> Higher levels of maternal antibody have been correlated with lower infection rates and with less severe illness in some studies, but not in others.<xref rid="bib91" ref-type="bibr">91</xref>, <xref rid="bib92" ref-type="bibr">92</xref> More recently, the trials of administration of RSV monoclonal antibody to high-risk infants have demonstrated protection against more severe RSV disease.<xref rid="bib93" ref-type="bibr"><sup>93</sup></xref></p><p id="p0265">Passively derived maternal antibody usually declines to undetectable levels by 6 months of age, but occasionally, it may remain up to 9 to 12 months of age. During primary infection, serum immunoglobulin M (IgM) antibody appears within several days, but it is transient and detectable usually only for a few weeks.<xref rid="bib73" ref-type="bibr"><sup>73</sup></xref> During the second week, IgG antibody appears, usually peaks in the fourth week, and begins to decline after 1 to 2 months. The IgA serum antibody response is more variable in infants. An anamnestic response involving all three immunoglobulin classes occurs after reinfection, and after about three infections, the titers reach levels similar to those in adults.</p><p id="p0270">Primary and subsequent infection produce antibody to many of the RSV proteins. However, the major immunoprotective antigens are two large surface glycoproteins, F and G.<xref rid="bib12" ref-type="bibr"><sup>12</sup></xref> Both contain neutralizing epitopes, but those on the F protein are conserved between the two strain groups, resulting in antibody to the F protein being cross-reactive between group A and B strains. In contrast, the response to the variable G protein is group and genotype specific.<xref rid="bib94" ref-type="bibr"><sup>94</sup></xref> Most adults with RSV infection develop IgG responses to the centrally conserved chemokine motif of G, although their role in recovery or protection from infection or illness is not clear.<xref rid="bib95" ref-type="bibr"><sup>95</sup></xref></p><p id="p0275">Although young children are able to produce neutralizing antibodies directed against both the F and G proteins, the neutralizing antibody responses are blunted in infants younger than 6 months because of a dampening effect of maternal antibody.<xref rid="bib96" ref-type="bibr"><sup>96</sup></xref> In infants, the antibody response to the F and G proteins mainly involves the subclasses IgG1 and IgG3. However, adults respond to the G protein with antibodies in both the IgG1 and the IgG2 subclasses, and the adult response to the F protein is predominantly IgG1. Antibodies after primary and recurrent infection usually decline substantially within months. Subsequent to natural infection, 75% of adults demonstrate a fourfold or greater drop in titer, returning to preinfection titers within 2 years in most.<xref rid="bib97" ref-type="bibr"><sup>97</sup></xref> A protective role for local antibody in RSV infection has been suggested because animal studies indicate that circulating IgG does not prevent viral replication in the nasal passages.<xref rid="bib90" ref-type="bibr">90</xref>, <xref rid="bib98" ref-type="bibr">98</xref> RSV-specific IgA antibody, which is produced in nasal secretions during primary and subsequent infection, has been associated with protecting the upper respiratory tract from infection in adults and has been correlated with clearance of viral shedding in infants.<xref rid="bib88" ref-type="bibr">88</xref>, <xref rid="bib90" ref-type="bibr">90</xref>, <xref rid="bib99" ref-type="bibr">99</xref> Children with RSV infection may also produce transient specific IgE antibody responses in the respiratory tract. Levels in the nasal secretions of both RSV-specific IgE antibodies and of cysteinyl leukotrienes have been correlated with increased risk for more severe acute infection, with wheezing and with later episodes of recurrent wheezing.<xref rid="bib100" ref-type="bibr">100</xref>, <xref rid="bib101" ref-type="bibr">101</xref></p><p id="p0280">Cell-mediated immunity is likely to be pivotal in the clearance of virus and in recovery, but has not been definitively shown to protect against reinfection and illness in humans. Adults and children with deficiencies of cellular immunity, as well as experimentally immunosuppressed animals, have more severe disease and prolonged virus shedding.<xref rid="bib102" ref-type="bibr">102</xref>, <xref rid="bib103" ref-type="bibr">103</xref> Most information delineating the specific components of the cellular response induced by RSV are derived from rodent models and, to a much lesser extent, from humans.<xref rid="bib70" ref-type="bibr">70</xref>, <xref rid="bib73" ref-type="bibr">73</xref></p><p id="p0285">RSV infection has multiple suppressive effects on the cellular immune response. Diminished in vitro lymphoproliferative responses during initial and repeated infections suggest impaired RSV-specific helper T-cell responses. Furthermore, RSV-infected dendritic cells have diminished ability to activate CD4<sup>+</sup> T cells, and enhanced apoptosis of CD4<sup>+</sup> and CD8<sup>+</sup> lymphocytes is observed among infants with RSV bronchiolitis.<xref rid="bib104" ref-type="bibr">104</xref>, <xref rid="bib105" ref-type="bibr">105</xref></p><p id="p0290">RSV infection in both animals and humans engenders a spectrum of both Th1- and Th2-dominant responses (see <xref rid="f0025" ref-type="fig">Fig. 160-4</xref>). Th1-dominant responses, characterized by the production of CD8<sup>+</sup> cytotoxic lymphocyte and Th1 CD4<sup>+</sup> cells secreting interleukin-2 (IL-2), interferon-γ (IFN-γ), and tumor necrosis factor-α (TNF-α) are associated with viral clearance and minimal pulmonary cytopathology. In contrast, Th2-dominant responses induce Th2 CD4<sup>+</sup> cells, which stimulate IL-4, IL-5, IL-10, and IL-13 secretion. These Th2 cytokines affect CD8<sup>+</sup> T-cell function and impair viral clearance.<xref rid="bib22" ref-type="bibr"><sup>22</sup></xref> IL-4 and IL-13 also augment isotype switching to IgE, and a Th2-biased response has been correlated with wheezing, more severe disease, and greater cellular inflammation and eosinophilia in the lung.<xref rid="bib100" ref-type="bibr"><sup>100</sup></xref></p><p id="p0295">Whether RSV evokes predominantly a Th1- or Th2-biased response has been shown to be influenced by the individual's genetic background, age, and previous RSV experience and the specific antigen. Infants, within the first several months of life, have been observed to have higher levels of Th2-type cytokines in nasal secretions than older infants.<xref rid="bib106" ref-type="bibr"><sup>106</sup></xref> Inactivated virus, as used in the initial formalin-inactivated vaccine and even in subunit vaccines, is more likely to induce a Th2-like response in experiments with unprimed animals than is live virus.<xref rid="bib22" ref-type="bibr"><sup>22</sup></xref> Antigenic stimulation with the F protein is associated with a predominantly Th1 response, whereas the G protein produces a Th2-biased response, possibly because its CX3C motif adversely affects the CD8<sup>+</sup> T-cell response.<xref rid="bib107" ref-type="bibr"><sup>107</sup></xref></p></sec></sec></sec><sec id="s0090"><title>Clinical Manifestations</title><p id="p0300">Clinical observations over the half century of RSV's recognition have confirmed the important immunologic correlates that naturally acquired immunity to RSV infection is incomplete, variable, and not durable. Repeated infections are common, but severe disease rarely occurs after the primary encounter in normal healthy children. Lower respiratory tract involvement and severe disease may occur during repeat infections, but it is generally confined to those at either end of the age spectrum.<xref rid="bib7" ref-type="bibr">7</xref>, <xref rid="bib44" ref-type="bibr">44</xref>, <xref rid="bib45" ref-type="bibr">45</xref></p><sec id="s0095"><title>Infection among Young Children</title><p id="p0305">Primary infections with RSV frequently involve the lower respiratory tract, particularly among infants within the first several months of life. Most commonly, these present as bronchiolitis, followed by pneumonia and tracheobronchitis.<xref rid="bib2" ref-type="bibr">2</xref>, <xref rid="bib44" ref-type="bibr">44</xref>, <xref rid="bib45" ref-type="bibr">45</xref> Croup is the least common form of clinical illness and usually accounts for less than 2% to 10% of cases. Upper respiratory tract signs almost always accompany lower respiratory tract disease, or the infection may be confined to the upper respiratory tract, which in young children is commonly associated with fever and otitis media (<xref rid="f0030" ref-type="fig">Fig. 160-5</xref>). Rarely is the first infection asymptomatic.<xref rid="bib44" ref-type="bibr">44</xref>, <xref rid="bib45" ref-type="bibr">45</xref>, <xref rid="bib46" ref-type="bibr">46</xref> The risk for lower respiratory tract involvement occurring with the first infection is high. Pneumonia or bronchiolitis has been estimated to occur in 30% to 71%, depending on the age and population.<xref rid="bib2" ref-type="bibr">2</xref>, <xref rid="bib44" ref-type="bibr">44</xref>, <xref rid="bib45" ref-type="bibr">45</xref>, <xref rid="bib108" ref-type="bibr">108</xref> Among infants younger than 6 months, those with underlying cardiopulmonary disease, and those in close contact with other young children, such as those attending daycare, the proportion developing lower respiratory tract disease may be even higher.<xref rid="bib45" ref-type="bibr"><sup>45</sup></xref> Furthermore, the severity of illness among outpatient preschool-aged children is considerable, with two thirds manifesting wheezing and three fourths developing labored breathing (see <xref rid="f0030" ref-type="fig">Fig. 160-5</xref>).<fig id="f0030"><label>FIGURE 160-5</label><caption><p>Clinical characteristics of children younger than 5 years with respiratory syncytial virus (RSV) who were outpatients, compared with those who were hospitalized.</p><p>RSV infection was laboratory confirmed during population-based surveillance of acute respiratory illnesses conducted in counties surrounding Nashville, Tennessee; Rochester, New York; and Cincinnati, Ohio, during 2000 to 2004.</p></caption><graphic xlink:href="f160-005-9781455748013"></graphic><attrib>(Data from Hall CB, Weinberg GA, Iwane MK, et al. The burden of respiratory syncytial virus infection in young children. <italic>N Engl J Med</italic>. 2009;360:588-598.)</attrib></fig></p><p id="p0310">RSV infection among young children and older individuals usually starts with an upper respiratory tract illness with nasal congestion and a cough. Hoarseness and laryngitis are not prominent features. A low-grade fever, lasting for 2 to 4 days, occurs in most young children early in the course of the illness. The height or duration of the fever does not correlate with the severity of the disease and is frequently absent in the presence of lower respiratory tract involvement and at the time of hospitalization. With progression of disease to the lower respiratory tract, the cough may become more prominent and productive, followed by an increased respiratory rate, dyspnea, and retractions of the intercostal muscles. With bronchiolitis, both expiratory and inspiratory obstruction may be evident. On auscultation, the infant may have crackles and wheezing. The rapid variability in the presence and intensity of these physical findings is characteristic of bronchiolitis, with marked transient swings in oxygen saturation often noted. Repeated observations of the infant, therefore, are required for adequate assessment of clinical severity.<xref rid="bib109" ref-type="bibr"><sup>109</sup></xref></p><p id="p0315">Infants hospitalized with RSV lower respiratory tract infection commonly have some impairment of oxygenation.<xref rid="bib109" ref-type="bibr"><sup>109</sup></xref> This reflects diffuse viral involvement of the lung parenchyma, which causes an abnormally low ratio of ventilation to perfusion. Usually, this is not clinically apparent, and mild degrees of desaturation may persist despite clinical improvement. Approximately 10% of hospitalized infants will develop alveolar hypoventilation and progressive hypercarbia and may require assisted ventilation. Hospitalization, if required, averages 3 days, but prolonged hospitalization is not uncommon.<xref rid="bib2" ref-type="bibr"><sup>2</sup></xref> For most infants, however, the duration of the acute illness is 3 to 10 days, but respiratory signs, especially cough, may be present for 4 or more weeks.</p><p id="p0320">The abnormalities observed on chest radiograph may be minimal, irrespective of the severity of the child's illness. Hyperaeration has been shown to be especially indicative of RSV infection and may be associated with peribronchial thickening.<xref rid="bib110" ref-type="bibr">110</xref>, <xref rid="bib111" ref-type="bibr">111</xref> Most children exhibit only airway disease. Less than 10% of bronchiolitis cases have evidence of both airway and airspace disease, and only about 1% have parenchymal consolidation.<xref rid="bib110" ref-type="bibr"><sup>110</sup></xref> However, about 20% to 35% of children with RSV lower respiratory tract disease have opacities, which are commonly misdiagnosed as bacterial pneumonia. These most commonly are subsegmental in the right upper or middle lobe and result from atelectasis. Pleural fluid is rarely demonstrated.</p></sec><sec id="s0100"><title>Otitis Media</title><p id="p0325">Acute otitis media is a common complication of RSV infection among young children.<xref rid="bib112" ref-type="bibr">112</xref>, <xref rid="bib113" ref-type="bibr">113</xref>, <xref rid="bib114" ref-type="bibr">114</xref> Among children within the first 3 years of life who developed acute otitis media, as many as 74% have had RSV detected in their middle ear fluid. Acute otitis media usually develops about 5 days after the onset of the respiratory illness and is more common among children older than 1 year than in infants. Even among older children and previously healthy adults with RSV infection, otitis and earache are common complications, noted in approximately half of hospitalized infants in one study.<xref rid="bib46" ref-type="bibr">46</xref>, <xref rid="bib55" ref-type="bibr">55</xref>, <xref rid="bib114" ref-type="bibr">114</xref> RSV has been recovered from the middle ear fluid as the sole pathogen, with bacteria, or with another virus in up 2% to 22% of cases.<xref rid="bib112" ref-type="bibr">112</xref>, <xref rid="bib114" ref-type="bibr">114</xref> RSV increases adherence of bacteria to respiratory epithelial cells, and the most frequent concurrent bacterial pathogens are those commonly found in the respiratory tract, especially <italic>Streptococcus pneumoniae, Haemophilus influenzae</italic>, and <italic>Moraxella catarrhalis.</italic><xref rid="bib114" ref-type="bibr"><sup>114</sup></xref> Clinical and experimental evidence suggests that coinfection of RSV with a bacterial pathogen may prolong the duration and worsen the outcome of otitis media, resulting in a greater chance of treatment failure with antibiotics and persistent effusion.</p></sec><sec id="s0105"><title>Infections among Older Children</title><p id="p0330">The frequency of RSV infections at all ages is well illustrated among families with young children and among those in contact with young children, as in schools and daycare facilities.<xref rid="bib44" ref-type="bibr">44</xref>, <xref rid="bib45" ref-type="bibr">45</xref>, <xref rid="bib46" ref-type="bibr">46</xref> Among longitudinally followed children attending daycare facilities who have had primary RSV infection in their first winter, 75% and 65% develop infection during their second and third years, respectively.<xref rid="bib45" ref-type="bibr"><sup>45</sup></xref> Recurrent infections commonly are upper respiratory tract illnesses, but 20% to 50% of recurrent infections among preschool-aged children involve the lower respiratory tract.<xref rid="bib44" ref-type="bibr"><sup>44</sup></xref> Although second episodes of lower respiratory tract illness among children are rarely as severe as the initial episode, many are associated with wheezing. The overall burden of repeated infection in children younger than 5 years is substantial.<xref rid="bib2" ref-type="bibr"><sup>2</sup></xref></p></sec><sec id="s0110"><title>Infections among Adults</title><p id="p0335">Adults also may have repetitive RSV infection occurring within sequential years, especially those living or working with children or in confined military and university settings.<xref rid="bib46" ref-type="bibr">46</xref>, <xref rid="bib55" ref-type="bibr">55</xref>, <xref rid="bib58" ref-type="bibr">58</xref>, <xref rid="bib115" ref-type="bibr">115</xref>, <xref rid="bib116" ref-type="bibr">116</xref> The lack of durable immunity evoked by natural infection is illustrated by a study of 15 healthy adults who became ill with a community-acquired RSV A strain and were subsequently challenged with an RSV A strain at repetitive intervals over 2 to 26 months.<xref rid="bib88" ref-type="bibr"><sup>88</sup></xref> Within 2 months of their natural infection, 47% became reinfected, and by 8 months, two thirds had been reinfected. However, successive infections, especially those occurring within close intervals, were associated with decreasing symptoms and shedding. Nevertheless, observational studies have noted that both infection and severity of RSV infection in adults are reduced by higher titers of serum and mucosal antibody.<xref rid="bib8" ref-type="bibr">8</xref>, <xref rid="bib90" ref-type="bibr">90</xref></p><p id="p0340">The extent of the burden RSV places on the health care of this growing population has only recently been appreciated fully.<xref rid="bib3" ref-type="bibr">3</xref>, <xref rid="bib7" ref-type="bibr">7</xref>, <xref rid="bib9" ref-type="bibr">9</xref>, <xref rid="bib56" ref-type="bibr">56</xref>, <xref rid="bib117" ref-type="bibr">117</xref>, <xref rid="bib118" ref-type="bibr">118</xref>, <xref rid="bib119" ref-type="bibr">119</xref> Those at greatest risk of severe illness include the frail elderly; those with underlying cardiopulmonary disease, especially chronic obstructive pulmonary disease (COPD); and the severely immunocompromised. Adults, even those with severe disease, shed RSV at titers considerably lower than infants, and thus estimates of the incidence of RSV infection in this population have been hampered until recently by the lack of sensitive diagnostic tests. The incidence of RSV hospitalization, found by using a regression model incorporating viral culture data from infants and hospital coding data from adults, has been estimated at 86 per 100,000, or 28% of the incidence of influenza hospitalizations.<xref rid="bib3" ref-type="bibr"><sup>3</sup></xref> Using similar methods from the Netherlands to model data, RSV mortality was 64% of that attributable to influenza.<xref rid="bib9" ref-type="bibr"><sup>9</sup></xref> Others have noted similar hospitalization and mortality rates in comparison to influenza.<xref rid="bib120" ref-type="bibr">120</xref>, <xref rid="bib121" ref-type="bibr">121</xref>, <xref rid="bib122" ref-type="bibr">122</xref></p><p id="p0345">In long-term care facilities, 5% to 27% of respiratory infections have been reported to be caused by RSV. The attack rate generally has been estimated as 1% to 15%, the rate of pneumonia as 10% to 20%, and the mortality as 2% to 5%.<xref rid="bib117" ref-type="bibr"><sup>117</sup></xref> A retrospective cohort analysis estimated that among Tennessee nursing home patients, RSV was associated with 15 hospitalizations, 17 deaths, and 76 antibiotic courses per 1000 people, and 7% of hospitalizations and 9% of deaths from cardiopulmonary disease.<xref rid="bib122" ref-type="bibr"><sup>122</sup></xref> In a study of older adults admitted with cardiopulmonary conditions, 10% had RSV infection, compared with 13% with influenza.<xref rid="bib119" ref-type="bibr"><sup>119</sup></xref> Illness was equally severe among the two groups: 18% required intensive care, and 10% of the RSV patients died, compared with 6% of the influenza patients. Similarly, among a prospectively studied population of older adults living in the community, RSV was identified as the cause of 7% and influenza as the cause of 9% of respiratory illnesses with identifiable pathogens.<xref rid="bib123" ref-type="bibr"><sup>123</sup></xref> The morbidity associated with the two viruses was also comparable, with 82% of the RSV patients and 79% of the influenza patients developing lower respiratory tract disease. Among adults attending daycare facilities, 10% of acute respiratory infections were found to be caused by RSV, a rate similar to the rates for influenza and coronaviruses.<xref rid="bib124" ref-type="bibr"><sup>124</sup></xref></p><p id="p0350">The highest risk for severe RSV infection is in persons with underlying cardiopulmonary disease, especially COPD and congestive heart failure.<xref rid="bib7" ref-type="bibr">7</xref>, <xref rid="bib56" ref-type="bibr">56</xref>, <xref rid="bib119" ref-type="bibr">119</xref>, <xref rid="bib125" ref-type="bibr">125</xref>, <xref rid="bib126" ref-type="bibr">126</xref>, <xref rid="bib127" ref-type="bibr">127</xref> A 4-year study of respiratory illnesses among prospectively followed elderly and high-risk adults living in the community emphasizes the epidemiologic and clinical impact of RSV infection among these populations (<xref rid="t0010" ref-type="table">Table 160-1</xref>).<xref rid="bib7" ref-type="bibr"><sup>7</sup></xref> In this study, 608 healthy persons age 65 and older and 504 high-risk people with cardiopulmonary conditions were evaluated for RSV infection by culture, reverse-transcriptase polymerase chain reaction (RT-PCR), and serology. A third group of 1388 adults hospitalized with acute cardiopulmonary conditions was also evaluated. During 4 years, RSV infection was identified in 3% to 7% of the elderly cohort, 4% to 10% of the high-risk cohort, and 10% of the hospitalized group. In comparison, influenza infection was identified among 4% of the individuals in the prospectively followed cohorts and among 11% of the hospitalized patients. Clinically, the illnesses from RSV and influenza were remarkably similar. Among the healthy elderly outpatients, those with RSV infection and those with influenza were ill for an average of 16 days. Of those with RSV infection, 39% were unable to perform their activities of daily living, only slightly less than with influenza. Among the hospitalized RSV patients, intensive care was required for 15%, and the mortality rate was 8%, compared with 12% and 7%, respectively, among influenza patients. RSV was identified in 5.4% of admissions for congestive heart failure, 11.4% of COPD exacerbations, and 10.6% of pneumonia diagnoses. Among the prospective cohorts, almost all RSV infections were symptomatic and frequently associated with appreciable functional impairment and use of health care services. The clinical illness caused by RSV in elderly persons is nonspecific and not readily distinguishable from other common respiratory viruses.<xref rid="bib118" ref-type="bibr"><sup>118</sup></xref> Typical upper respiratory symptoms are more frequent than with influenza and precede lower respiratory symptoms by several days. Wheezing is more common with RSV infection, especially in patients with COPD, and chest radiographic findings are often minimal.<table-wrap position="float" id="t0010"><label>TABLE 160-1</label><caption><p>Respiratory Syncytial Virus (RSV) Compared with Influenza among Hospitalized Adults<xref rid="tn0010" ref-type="table-fn">*</xref></p></caption><table frame="hsides" rules="groups"><thead><tr><th align="left">CHARACTERISTICS</th><th align="left">RSV (<italic>N</italic> = 132)</th><th align="left">Influenza A (<italic>N</italic> = 144)</th></tr></thead><tbody><tr><td align="left">Age (yr)</td><td align="left">76 ± 13</td><td align="left">76 ± 12</td></tr><tr><td align="left">Female sex—<italic>N</italic> (%)</td><td align="char">84 (64)</td><td align="char">81 (56)</td></tr><tr><td align="left">Chronic illness—<italic>N</italic> (%)</td><td align="left"></td><td align="left"></td></tr><tr><td align="left"> Any cardiac disease</td><td align="char">71 (54)</td><td align="char">71 (49)</td></tr><tr><td align="left"> Congestive heart failure</td><td align="char">39 (30)</td><td align="char">33 (23)</td></tr><tr><td align="left"> Any lung disease</td><td align="char">77 (58)</td><td align="char">79 (55)</td></tr><tr><td align="left"> Any heart or lung disease</td><td align="char">106 (80)</td><td align="char">113 (78)</td></tr><tr><td align="left"> Diabetes mellitus</td><td align="char">35 (27)</td><td align="char">28 (19)</td></tr><tr><td align="left">Residence in a long-term care facility—<italic>N</italic> (%)</td><td align="char">16 (12)</td><td align="char">15 (10)</td></tr><tr><td align="left">Smoking (current or past)—<italic>N</italic> (%)</td><td align="char">88 (67)</td><td align="char">98 (68)</td></tr><tr><td align="left">Influenza vaccination—<italic>N</italic> (%)</td><td align="char">99 (75)</td><td align="char">98 (68)</td></tr><tr><td align="left">Katz ADL score—mean ± SD</td><td align="left">1.2 ± 2.4</td><td align="left">1.3 ± 3.0</td></tr><tr><td align="left">IADL score—mean ± SD</td><td align="left">4.1 ± 4.1</td><td align="left">3.3 ± 4.0</td></tr><tr><td align="left">Length of hospital stay—days</td><td align="left">14 ± 41</td><td align="left">8 ± 5</td></tr><tr><td align="left">Findings on chest radiography—<italic>N</italic> (%)</td><td align="left"></td><td align="left"></td></tr><tr><td align="left"> Infiltrate found</td><td align="char">41 (31)</td><td align="char">43 (30)</td></tr><tr><td align="left"> Congestive heart failure</td><td align="char">17 (13)</td><td align="char">15 (10)</td></tr><tr><td align="left"> Other</td><td align="char">24 (18)</td><td align="char">27 (19)</td></tr><tr><td align="left">Admission to intensive care unit—<italic>N</italic> (%)</td><td align="char">20 (15)</td><td align="char">17 (12)</td></tr><tr><td align="left">Use of mechanical ventilation—<italic>N</italic> (%)</td><td align="char">17 (13)</td><td align="char">15 (10)</td></tr><tr><td align="left">Higher level of care at discharge than at admission—<italic>N</italic> (%)</td><td align="char">7 (5)</td><td align="char">8 (6)</td></tr><tr><td align="left">Death—<italic>N</italic> (%)</td><td align="char">10 (8)</td><td align="char">10 (7)</td></tr></tbody></table><table-wrap-foot><fn><p>SD, standard deviation.</p></fn></table-wrap-foot><table-wrap-foot><fn id="tn0010"><label>*</label><p id="np0015">Plus-minus values are means plus or minus standard deviation. The Katz Activities of Daily Living (ADL) score and the Instrumental Activities of Daily Living (IADL) score are functional assessments based on a 12-point scale, with 0 representing total independence and 12 representing total dependence. Percentage may not sum to 100 because of rounding.</p></fn></table-wrap-foot><attrib>Modified from Falsey A, Hennessey PA, Formica MA, et al. Respiratory syncytial virus infection in elderly and high-risk adults. <italic>N Engl J Med.</italic> 2005;352:1749-1759.</attrib></table-wrap></p><p id="p0355">Peak viral titers in nasal secretions in nonhospitalized adults with RSV infection are substantially lower than in infants, ranging from 1 to 10<sup>5</sup> pfu/mL of nasal secretions (mean, 10<sup>2.3</sup>), and slightly higher among hospitalized persons and those older than 65 years.<xref rid="bib128" ref-type="bibr"><sup>128</sup></xref> When simultaneously measured, virus titers in sputum are generally higher than those found in nasal secretions. The duration of virus shedding in adults averages about 10 days but can be detected for as long as 20 to 30 days in some patients. In individual patients, RSV cannot be distinguished from other viral infections in this population. However, as in infants, wheezing is more common with RSV infection than influenza but similar to that caused by human metapneumovirus. Bacterial coinfection can occur during RSV infection, although the precise incidence is unknown. There are no controlled data on antiviral treatment for RSV in adults, and thus treatment is rarely considered except in immunocompromised patients (see later).</p><p id="p0360">The increased morbidity associated with RSV infection observed among older adults is only partly explained by the presence of comorbid conditions and age-associated decline in pulmonary function.<xref rid="bib129" ref-type="bibr"><sup>129</sup></xref> Evidence is accumulating that among healthy older adults, age adversely affects the immune response to RSV infection. Humoral immunity to RSV among elderly people, however, is equal to or greater than that produced by young adults.<xref rid="bib56" ref-type="bibr">56</xref>, <xref rid="bib89" ref-type="bibr">89</xref> Age may have its greatest effect on the cellular adaptive response, which demonstrates diminished RSV-specific CD8<sup>+</sup> T-cell function in elderly persons.<xref rid="bib130" ref-type="bibr">130</xref>, <xref rid="bib131" ref-type="bibr">131</xref>, <xref rid="bib132" ref-type="bibr">132</xref> Experiments with rodents have shown specific defects in the cellular response to RSV infection related to senescence, including the timing and type of the pulmonary cytokine response.<xref rid="bib133" ref-type="bibr"><sup>133</sup></xref></p><p id="p0365">The burden of RSV among young healthy adults may be considerable and comparable to that from influenza.<xref rid="bib46" ref-type="bibr">46</xref>, <xref rid="bib55" ref-type="bibr">55</xref>, <xref rid="bib115" ref-type="bibr">115</xref> Among working, healthy adults, RSV infection was symptomatic in 84%, and 22% had lower respiratory tract manifestations (<xref rid="t0015" ref-type="table">Table 160-2</xref>). Compared with influenza infection occurring in these same individuals, fever was less frequent, but earache and sinus pain and a persistent productive cough were significantly more common with RSV infection (<xref rid="t0020" ref-type="table">Table 160-3</xref>). Thirty-eight percent of those with RSV infection missed work, and the average duration of illness was 9.5 days, which was significantly longer than that produced by influenza.<xref rid="bib115" ref-type="bibr">115</xref>, <xref rid="bib116" ref-type="bibr">116</xref> Wheezing was more frequently associated with RSV infection, and the proportion of military recruits with RSV infection requiring ward confinement was the same as for influenza. Among university students with cough persisting for 6 or more days, RSV was identified more often than the parainfluenza viruses, adenoviruses, pertussis, <italic>Mycoplasma pneumoniae</italic>, or <italic>Chlamydia pneumoniae.</italic> In more than half of those with RSV infection, the clinical manifestations were indistinguishable from those of pertussis, and most were treated with a macrolide.<xref rid="bib116" ref-type="bibr"><sup>116</sup></xref><table-wrap position="float" id="t0015"><label>TABLE 160-2</label><caption><p>Types of Acute Respiratory Infection in Adults Who Are Infected with Respiratory Syncytial Virus (RSV)</p></caption><table frame="hsides" rules="groups"><thead><tr><th align="left">TYPE OF ACUTE RESPIRATORY ILLNESS</th><th align="left">NO. OF PATIENTS</th><th align="left">PERCENTAGE OF PATIENTS WITH SYMPTOMATIC RSV INFECTION (<italic>n</italic> = 177)</th><th align="left">PERCENTAGE OF ALL PATIENTS WITH RSV INFECTION (<italic>n</italic> = 211)</th></tr></thead><tbody><tr><td align="left">Asymptomatic</td><td align="left">34</td><td align="left">—</td><td align="left">16</td></tr><tr><td align="left">Symptomatic</td><td align="left">177</td><td align="left">—</td><td align="left">84</td></tr><tr><td align="left"> Upper respiratory tract</td><td align="left">131</td><td align="left">74</td><td align="left">62</td></tr><tr><td align="left"> With fever</td><td align="left">52</td><td align="left">29</td><td align="left">25</td></tr><tr><td align="left"> Without fever</td><td align="left">79</td><td align="left">45</td><td align="left">37</td></tr><tr><td align="left"> Lower respiratory tract</td><td align="left">46</td><td align="left">26</td><td align="left">22</td></tr><tr><td align="left"> Tracheobronchitis</td><td align="left">36</td><td align="left">20</td><td align="left">17</td></tr><tr><td align="left"> Wheezing</td><td align="left">10</td><td align="left">6</td><td align="left">5</td></tr></tbody></table><attrib>From Hall CB, Long CE, Schnabel KC. Respiratory syncytial virus infections in previously healthy working adults. <italic>Clin Infect Dis.</italic> 2001;33:792-796. Copyright 2001 with permission from the Infectious Diseases Society of America.</attrib><permissions><copyright-statement>© 2015 </copyright-statement><copyright-year>2015</copyright-year><license><license-p>Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.</license-p></license></permissions></table-wrap><table-wrap position="float" id="t0020"><label>TABLE 160-3</label><caption><p>Clinical Characteristics of Illness Caused by Influenza or Respiratory Syncytial Virus (RSV) among 211 Previously Healthy Adults</p></caption><table frame="hsides" rules="groups"><thead><tr><th align="left"></th><th colspan="2" align="center">NO. (%) OF ADULTS WITH ILLNESS CAUSED BY:<hr></hr></th><th align="left"></th></tr><tr><th align="left">CHARACTERISTIC</th><th align="left">RSV (<italic>n</italic> = 177)</th><th align="left">Influenza (<italic>n</italic> = 59)</th><th align="center"><italic>P</italic></th></tr></thead><tbody><tr><td align="left">Sign or symptom</td><td align="left"></td><td align="left"></td><td align="left"></td></tr><tr><td align="left"> Fever (temperature, >37.8° C)</td><td align="char">50 (58)</td><td align="char">43 (73)</td><td align="char"><.001</td></tr><tr><td align="left"> Nasal congestion, rhinorrhea</td><td align="char">157 (89)</td><td align="char">46 (78)</td><td align="char"><.04</td></tr><tr><td align="left"> Sore throat</td><td align="char">102 (58)</td><td align="char">32 (54)</td><td align="char">.65</td></tr><tr><td align="left"> Ear pain</td><td align="char">35 (20)</td><td align="char">3 (5)</td><td align="char"><.01</td></tr><tr><td align="left"> Headache</td><td align="char">70 (40)</td><td align="char">48 (81)</td><td align="char"><.001</td></tr><tr><td align="left"> Sinus pain</td><td align="char">55 (31)</td><td align="char">8 (14)</td><td align="char"><.01</td></tr><tr><td align="left"> Cough</td><td align="left"></td><td align="left"></td><td align="left"></td></tr><tr><td align="left"> Nonproductive</td><td align="char">150 (85)</td><td align="char">47 (80)</td><td align="char">.36</td></tr><tr><td align="left"> Productive</td><td align="char">92 (52)</td><td align="char">14 (24)</td><td align="char"><.001</td></tr><tr><td align="left"> Lower respiratory tract signs, wheezing</td><td align="char">28 (16)</td><td align="char">5 (9)</td><td align="char">.16</td></tr><tr><td align="left"> Work absence</td><td align="char">67 (38)</td><td align="char">39 (66)</td><td align="char"><.001</td></tr><tr><td align="left">Duration of illness, mean days (range)</td><td align="char">9.5 (1-20)</td><td align="char">6.8 (39-66)</td><td align="char"><.001</td></tr></tbody></table><attrib>From Hall CB, Long CE, Schnabel KC. Respiratory syncytial virus infections in previously healthy working adults. <italic>Clin Infect Dis.</italic> 2001;33:792-796. Copyright<sup>©</sup> Infectious Diseases Society of America.</attrib><permissions><copyright-statement>© 2015 </copyright-statement><copyright-year>2015</copyright-year><license><license-p>Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.</license-p></license></permissions></table-wrap></p></sec></sec><sec id="s0115"><title>Complications</title><sec id="s0120"><title>Patients at High Risk for Severe Infection</title><p id="p0370">Children with underlying conditions affecting cardiopulmonary function or immunity are most likely to increase the risk for developing complicated RSV infection among individuals of any age. Among young children, those most likely to require hospitalization are those who are premature and those with underlying chronic lung disease, cyanotic or complicated congenital heart disease, immunosuppressive conditions, or other chronic diseases that affect the handling of respiratory secretions, such as neuromuscular disease.<xref rid="bib2" ref-type="bibr">2</xref>, <xref rid="bib93" ref-type="bibr">93</xref>, <xref rid="bib134" ref-type="bibr">134</xref>, <xref rid="bib135" ref-type="bibr">135</xref> About one third of children who are hospitalized with RSV infection within the first 5 years of life have one or more of these underlying conditions, and the proportion is greater among those older than 2 years.<xref rid="bib2" ref-type="bibr"><sup>2</sup></xref> Among children with RSV infection evaluated in pediatric practices and emergency departments, about one fourth have a preexisting chronic condition.</p><p id="p0375">Preterm gestation, with or without associated chronic lung disease, is clearly a major risk factor for more severe RSV disease.<xref rid="bib2" ref-type="bibr">2</xref>, <xref rid="bib93" ref-type="bibr">93</xref>, <xref rid="bib135" ref-type="bibr">135</xref> Hospitalization rates among infants with gestational ages of less than 36 weeks are three or more times higher than the rate for full-term infants. As the gestational age decreases below 32 weeks, the chance of admission with RSV infections rises, and the need for intensive care significantly increases. Recently recognized, however, is the disproportionate economic and clinical burden contributed by late preterm infants—those with gestational ages of 33 to 35 weeks—with RSV infections who represent about three fourths of all preterm infants.<xref rid="bib93" ref-type="bibr">93</xref>, <xref rid="bib136" ref-type="bibr">136</xref> These late preterm infants, compared with full-term infants, not only have significantly increased costs and risk for hospitalization but also have a significantly greater need for medical resources for at least the subsequent year.</p><p id="p0380">Congenital heart conditions, especially cyanotic heart conditions and those accompanied by pulmonary hypertension, have ranked among the top three major conditions among infants hospitalized with RSV infection, and about one fourth to one third require intensive care, and one fifth require mechanical ventilation.<xref rid="bib137" ref-type="bibr">137</xref>, <xref rid="bib138" ref-type="bibr">138</xref>, <xref rid="bib139" ref-type="bibr">139</xref> Infants hospitalized in the first few months of life with uncorrected cyanotic congenital heart disease are at particular peril. However, the increased rate of hospitalization for RSV among children with congenital heart disease remains beyond infancy and appears greatest during the second year of life.<xref rid="bib137" ref-type="bibr">137</xref>, <xref rid="bib139" ref-type="bibr">139</xref> Early surgical correction of cardiac defects have appreciably reduced the mortality from RSV infection among infants with congenital heart disease from 30% in the 1970s to less than 2% currently.</p><p id="p0385">Multiple demographic and environmental factors also have been evaluated for augmenting the risk for more severe RSV infection.<xref rid="bib2" ref-type="bibr">2</xref>, <xref rid="bib140" ref-type="bibr">140</xref>, <xref rid="bib141" ref-type="bibr">141</xref> Those most frequently associated with RSV disease requiring hospitalization among young children are male gender, crowded living conditions, lower socioeconomic status, exposure to other young children in the home or daycare, exposure to tobacco smoke, and lack of breast-feeding. However, the degree of risk these factors play in the expression of RSV disease in children has been difficult to quantify, and the reported data have been inconsistent and conflicting. The two independent risk factors that appear to be most important for hospitalization with RSV infection are prematurity and young age, especially within the first 3 months of life.<xref rid="bib2" ref-type="bibr">2</xref>, <xref rid="bib93" ref-type="bibr">93</xref></p><p id="p0390">The genetic background of an individual has important, but mostly undefined, effects on the susceptibility to RSV infection and more severe disease. Groups of children with certain racial and ethnic backgrounds have notably increased rates of hospitalization and severe RSV infection, including Native American Indian and Alaskan Native infants, especially those living in the Yukon-Kuskokwim Delta region who have RSV hospitalization rates three to four times that observed for other U.S. infants.<xref rid="bib93" ref-type="bibr">93</xref>, <xref rid="bib142" ref-type="bibr">142</xref> Severe disease with primary RSV infection has been correlated with specific polymorphisms in certain genetic loci affecting the immune response, including expression of cytokines and inflammatory chemokines.<xref rid="bib70" ref-type="bibr">70</xref>, <xref rid="bib72" ref-type="bibr">72</xref>, <xref rid="bib87" ref-type="bibr">87</xref></p><sec id="s0125"><title>Immunocompromised Patients</title><p id="p0395">Greater awareness of RSV as a cause of morbidity and mortality among immunocompromised patients has resulted from the increasing numbers of patients receiving solid-organ and hematopoietic cell transplantation (HCT) with more intensive chemotherapy regimens and also from the greater availability of sensitive techniques for identification of RSV infection, such as PCR assays.<xref rid="bib143" ref-type="bibr">143</xref>, <xref rid="bib144" ref-type="bibr">144</xref> The reported frequency of RSV infection among immunocompromised patients varies widely from about 2% to 50%, depending on the population and type of immunosuppression.<xref rid="bib103" ref-type="bibr">103</xref>, <xref rid="bib143" ref-type="bibr">143</xref>, <xref rid="bib144" ref-type="bibr">144</xref>, <xref rid="bib145" ref-type="bibr">145</xref>, <xref rid="bib146" ref-type="bibr">146</xref>, <xref rid="bib147" ref-type="bibr">147</xref>, <xref rid="bib148" ref-type="bibr">148</xref>, <xref rid="bib149" ref-type="bibr">149</xref>, <xref rid="bib150" ref-type="bibr">150</xref> Retrospective case series suggest a mortality rate of about 9% to 18%.</p><p id="p0400">RSV is often introduced onto wards that house immunocompromised patients by medical staff or visitors, and spread may be rapid and difficult to control and accompanied by appreciable morbidity and mortality.<xref rid="bib103" ref-type="bibr">103</xref>, <xref rid="bib145" ref-type="bibr">145</xref>, <xref rid="bib147" ref-type="bibr">147</xref>, <xref rid="bib148" ref-type="bibr">148</xref>, <xref rid="bib149" ref-type="bibr">149</xref> The severity of the RSV infection among these patients is primarily related to the degree of immunosuppression<xref rid="bib103" ref-type="bibr">103</xref>, <xref rid="bib148" ref-type="bibr">148</xref>, <xref rid="bib149" ref-type="bibr">149</xref>, <xref rid="bib151" ref-type="bibr">151</xref>; severe combined immunodeficiency states and HCT recipients are particularly at risk for a poor outcome. Among transplant recipients, factors associated with poor outcomes include use of bone marrow cells (in contrast to peripheral stem cells), occurrence of RSV infection before engraftment, the presence of acute or chronic graft-versus-host disease, and lymphopenia. Among children, young age also is associated with a poorer prognosis.</p><p id="p0405">RSV infection in these patients may clinically mimic other opportunistic agents, and the correct etiology may not be suspected. Sinusitis and wheezing may be more indicative of RSV infection than other pathogens. Concurrent infections by other infectious agents, including community-acquired infections, may further confound or delay the diagnosis of RSV infection.<xref rid="bib149" ref-type="bibr"><sup>149</sup></xref> In adult HCT recipients with RSV, upper respiratory tract signs precede pneumonia in 80% to 90% of patients, with progression to pneumonia in 30% to 40% after a median of 7 days.<xref rid="bib143" ref-type="bibr">143</xref>, <xref rid="bib144" ref-type="bibr">144</xref> The need for oxygen supplementation at the time of presentation is associated with significantly higher rates of respiratory failure and mortality.<xref rid="bib152" ref-type="bibr"><sup>152</sup></xref> With lower respiratory tract involvement, radiographic findings range from focal interstitial infiltrates, sometimes with hyperinflation or with lobar consolidation, to generalized alveolar and interstitial infiltrates, or even to a picture of acute respiratory distress syndrome.<xref rid="bib147" ref-type="bibr"><sup>147</sup></xref> With high-resolution computed tomography, the characteristic findings are airspace consolidation, small centrilobular nodules, ground-glass opacities, and thickening of the bronchial walls. These manifestations tend to have an asymmetrical but bilateral distribution.<xref rid="bib153" ref-type="bibr"><sup>153</sup></xref> Long-term complications include bronchiolitis obliterans syndrome (BOS) in nearly 10%, although rates as high as 50% can be seen in lung transplant recipients with RSV lower respiratory infection.<xref rid="bib154" ref-type="bibr"><sup>154</sup></xref> Overall mortality with RSV pneumonia is as high as 45%, although treatment with ribavirin, with or without immunoglobulin (intravenous immune globulin [IVIG] or monoclonal antibody), has been thought by some observers to reduce morbidity and mortality (see “<xref rid="s0145" ref-type="sec">Therapy</xref>”).</p><p id="p0410">Among children with human immunodeficiency virus (HIV) infection, RSV has been the most frequently identified cause of viral respiratory disease, either acquired in the community or nosocomially.<xref rid="bib145" ref-type="bibr"><sup>145</sup></xref> The manifestations of RSV infection vary according to the stage and severity of the HIV infection, and although most develop lower respiratory tract disease, it generally is not as severe as that occurring among the more highly immunosuppressed transplant recipients.<xref rid="bib155" ref-type="bibr"><sup>155</sup></xref> HIV patients may shed RSV for prolonged periods. Confounding this, however, is the observation that children with HIV infection and concurrent viral respiratory infections also have a higher rate of bacterial coinfections.<xref rid="bib155" ref-type="bibr"><sup>155</sup></xref> Of importance, the clinical outcome of respiratory viral infections has not been consistently different between children with and those without HIV infection.</p><p id="p0415">Although many authorities generally recommend treatment of severely immunocompromised adults with ribavirin and antibody therapy, definitive guidelines are not available because of the lack of prospective controlled trials (see “<xref rid="s0145" ref-type="sec">Therapy</xref>”). Most important in the management of immunocompromised patients is prevention of RSV infection by strict adherence to infection control policies. The Centers for Disease Control and Prevention guidelines for preventing opportunistic infections in hematopoietic stem cell transplant recipients provides evidence-based recommendations for control of RSV infection and transmission. These guidelines emphasize preventing the introduction of community respiratory viruses, including RSV, onto units with compromised patients and stress the importance of early diagnosis.<xref rid="bib143" ref-type="bibr">143</xref>, <xref rid="bib156" ref-type="bibr">156</xref>, <xref rid="bib157" ref-type="bibr">157</xref></p></sec></sec><sec id="s0130"><title>Acute Complications in Infants</title><p id="p0420">Apnea is one of the most frightening and striking of acute complications among young infants with RSV infection. Up to 20% of infants hospitalized with RSV infection have been admitted with apnea.<xref rid="bib157" ref-type="bibr">157</xref>, <xref rid="bib158" ref-type="bibr">158</xref> Among infants evaluated in the emergency department with unspecified bronchiolitis, 3% had a diagnosis of apnea. Most at risk for developing apnea are preterm infants with a gestational age of 32 weeks or less, those with a history of apnea of prematurity, and infants of young postnatal age of less than 44 weeks after conception. Characteristically, the apnea occurs at the onset of the RSV infection and may be the initial sign before respiratory symptoms are noted. The pathophysiology of apnea associated with RSV is not clear, although it is nonobstructive. The prognosis is generally good after the acute RSV infection with no subsequent episodes, even with later-acquired respiratory infections.</p><p id="p0425">Infants admitted with RSV lower respiratory tract disease may be at increased risk for aspiration, which can appear clinically similar to bronchiolitis with airway hyperreactivity.<xref rid="bib159" ref-type="bibr"><sup>159</sup></xref> In one study of infants hospitalized with the diagnosis of RSV bronchiolitis and followed over a 12-month period, 83% developed reactive airway disease if they received neither ribavirin nor therapy for aspiration. However, the development of hyperreactive airways was reduced to 45% in infants who were given thickened feedings along with early ribavirin therapy. Furthermore, the decrease in episodes of reactive airway disease was greater in infants who received both ribavirin and thickened feedings than in infants who received either therapy alone.</p><p id="p0430">Coexistent bacterial infection is a frequent concern in infants hospitalized with RSV lower respiratory tract disease, and many children receive unnecessary antibiotic treatment. In part, this is because of their young age, the presence of fever, and, particularly, the relatively common appearance on the chest radiograph of opacities from viral infiltrates and atelectasis, which are commonly mistaken for consolidation of bacterial pneumonia. However, multiple studies in the United States have shown that a secondary bacterial infection is an unusual complication of RSV infection.<xref rid="bib160" ref-type="bibr">160</xref>, <xref rid="bib161" ref-type="bibr">161</xref>, <xref rid="bib162" ref-type="bibr">162</xref> A 9-year prospective study of infants hospitalized with RSV lower respiratory tract disease identified secondary bacterial pneumonia in less than 1%.<xref rid="bib160" ref-type="bibr"><sup>160</sup></xref> Furthermore, antibiotic therapy has not been shown to improve the rate of recovery among infants with RSV lower respiratory tract disease.<xref rid="bib163" ref-type="bibr"><sup>163</sup></xref> More frequent is coinfection with another viral or bacterial agent. Most common of these coinfections are other respiratory viruses, such as adenoviruses, influenza, parainfluenza viruses, human metapneumovirus, and bocavirus.<xref rid="bib164" ref-type="bibr"><sup>164</sup></xref> However, there is no definitive evidence that viral coinfection carries a worse outcome. Urinary tract infections are the most frequently identified concurrent bacterial infections.<xref rid="bib165" ref-type="bibr"><sup>165</sup></xref> In developing countries, however, complicating bacterial infections are more common and may contribute appreciably to the high mortality rate from RSV.</p></sec><sec id="s0135"><title>Long-term Complications</title><p id="p0435">Recurrent wheezing after RSV lower respiratory tract disease and bronchiolitis in infancy has long been recognized as a frequent sequela, but a causal link between the two remains unclear. About 30% to 50% of children hospitalized with RSV infection later develop repeated occurrences of wheezing.<xref rid="bib164" ref-type="bibr">164</xref>, <xref rid="bib166" ref-type="bibr">166</xref>, <xref rid="bib167" ref-type="bibr">167</xref> For many children, the severity of the recurrent wheezing episodes decreases with age, although in some, pulmonary function abnormalities may persist without clinical manifestations.<xref rid="bib168" ref-type="bibr">168</xref>, <xref rid="bib169" ref-type="bibr">169</xref> Others may have persistent wheezing into adolescence, or have wheezing cease during childhood, but recur as adults. The frequency of this long-term sequela in the general population is confounded by most studies having focused on children with more severe illness.<xref rid="bib170" ref-type="bibr"><sup>170</sup></xref> Similarities between the immune responses after RSV infection and the responses observed with reactive airway disease have been offered as a possible explanation for the immunopathogenesis of the putative link between RSV bronchiolitis reactive airways in adolescence and adulthood.</p><p id="p0440">Epidemiologic evidence indicates that atopy in the child or family is not a major cause of this link. However, in a murine model of allergen-induced airway inflammation and remodeling, previous RSV infection could induce airway abnormalities in mice exposed to allergen through the airway, even though these mice had not been previously sensitized to the allergens.<xref rid="bib171" ref-type="bibr"><sup>171</sup></xref> This suggests that even without an atopic family background, RSV infection may provoke an allergic phenotype. In addition, RSV infection has been shown both in vitro and in children infected with RSV to produce an immunologic response similar to that observed with allergic sensitization, one with a predominantly Th2 T-cell profile and release of proinflammatory mediators, IgE, and neuropeptides<xref rid="bib70" ref-type="bibr">70</xref>, <xref rid="bib170" ref-type="bibr">170</xref>, <xref rid="bib172" ref-type="bibr">172</xref> (see “<xref rid="s0075" ref-type="sec">Immunity and Pathogenesis of Disease</xref>”). A similar response, however, may be produced by viruses other than RSV.<xref rid="bib170" ref-type="bibr"><sup>170</sup></xref> The direct correlation between RSV lower respiratory tract disease and pulmonary sequelae likely remains elusive because the clinical syndrome of hyperreactive airways results from many different genetic, developmental, and environmental disorders.<xref rid="bib173" ref-type="bibr"><sup>173</sup></xref></p></sec></sec><sec id="s0140"><title>Diagnosis</title><p id="p0445">RSV infection among young children is most often diagnosed clinically in the setting of the community's RSV season. Among adults, however, the findings are less specific, and RSV is commonly not suspected. Laboratory diagnosis may be made by viral isolation, by one of the rapid diagnostic tests, by RT-PCR, or by serology.</p><p id="p0450">Viral isolation, once the standard technique, has been supplanted by one of the rapid antigen assays or by nucleic acid amplification, RT-PCR. The sensitivity of each of these tests is dependent on the viral load, and thus the choice of test must take into consideration the population under study. The sensitivity of viral isolation is highly dependent on the sensitivity of the cell lines, the specific laboratory's expertise, and the quality and handling of the specimen. RSV is a relatively labile virus and requires prompt inoculation without subjecting the specimen to major temperature changes during transportation. Nasopharyngeal washes or tracheal secretions are generally better than nasal swabs, although combined throat swab and swabs of both nares improve the rate of recovery over a single nasal swab.<xref rid="bib174" ref-type="bibr">174</xref>, <xref rid="bib175" ref-type="bibr">175</xref> Specific cytopathic changes usually appear within 2 to 5 days, but the range is 2 to 10 days. Shell vial culture assays allow diagnosis within 48 hours.</p><p id="p0455">Multiple rapid direct antigen detection tests are widely available and are used by most laboratories.<xref rid="bib174" ref-type="bibr"><sup>174</sup></xref> In hospitalized infants, direct and indirect immunofluorescent assays are both sensitive (93% to 98%) and specific (92% to 97%) but require several hours and skilled laboratory personnel. Most frequently used for infants are the commercially available rapid detection tests using an enzyme immunoassay (EIA) method and, to a lesser extent, the optical immunoassay (OIA), which has a sensitivity of 88% to 95% and specificity of 97% to 100% when compared with culture.<xref rid="bib174" ref-type="bibr"><sup>174</sup></xref> The accuracy of these tests may vary according to the manufacturer and the viral strain but are highly dependent on the adequacy of the specimen and whether it was obtained during the peak of RSV activity in the community. The positive predictive value of these assays falls precipitously when the prevalence of RSV is low in the community. These tests perform poorly in adults, including the immunocompromised and elderly populations, because of the low viral titers in secretions.<xref rid="bib117" ref-type="bibr">117</xref>, <xref rid="bib174" ref-type="bibr">174</xref>, <xref rid="bib176" ref-type="bibr">176</xref></p><p id="p0460">RT-PCR assay for the diagnosis of RSV infections has consistently demonstrated much higher rates of specificity and sensitivity than the rapid antigen diagnostic assays.<xref rid="bib174" ref-type="bibr"><sup>174</sup></xref> Among 496 specimens obtained from children with RSV infection determined by viral isolation or duplicate positive RT-PCR assays, about 50% were positive by both RT-PCR and culture, and 50% by RT-PCR alone. Less than 1% were positive only by viral isolation. The RT-PCR assays also allow the strain group of RSV to be concurrently determined. The rapidly expanding microassay technology allows the simultaneous highly sensitive detection of potentially innumerable agents.<xref rid="bib175" ref-type="bibr">175</xref>, <xref rid="bib177" ref-type="bibr">177</xref></p><p id="p0465">Serologic diagnosis of RSV infection is primarily useful for epidemiologic studies rather than for patient management because of the delay required to obtain convalescent sera and because young infants and immunocompromised patients may not produce a significant rise in antibody titer. Serologic diagnosis is most useful in elderly adults, who curiously have the most vigorous antibody responses to RSV.<xref rid="bib178" ref-type="bibr"><sup>178</sup></xref></p></sec><sec id="s0145"><title>Therapy</title><p id="p0470">Most children and adults with RSV infection require no more than the usual care given to ensure comfort, fever control, and adequate fluid intake. For bronchiolitis, the most commonly administered medications are those used for exacerbations of hyperreactive airway disease, primarily bronchodilators and corticosteroids, and also antibiotics.<xref rid="bib109" ref-type="bibr">109</xref>, <xref rid="bib179" ref-type="bibr">179</xref>, <xref rid="bib180" ref-type="bibr">180</xref> Multiple studies and meta-analyses have shown these agents are not consistently effective for RSV disease or bronchiolitis of unspecified cause among previously healthy young children and thus are not routinely recommended (see Chapter 68).</p><p id="p0475">Antibiotic therapy for children with RSV lower respiratory tract disease should be reserved for those with specific evidence of a coexisting bacterial infection.<xref rid="bib109" ref-type="bibr"><sup>109</sup></xref> Preemptive administration of antibiotics to children with RSV infection or bronchiolitis has not been associated with an improved outcome. Furthermore, complicating or secondary bacterial infections, other than otitis media among children with RSV infection in developed countries, is unusual.<xref rid="bib160" ref-type="bibr">160</xref>, <xref rid="bib161" ref-type="bibr">161</xref></p><p id="p0480">Ribavirin (1-β-<sc>d</sc>-ribofuranosyl-1,2,4-triazole-3-carboxamide), a synthetic nucleoside, is the only currently approved specific treatment for RSV lower respiratory tract disease in hospitalized infants (see Chapter 44). The drug, administered as a small-particle aerosol, has shown modest clinical benefit and improved levels of oxygenation in some studies, but an improvement in the duration of hospitalization or short-term outcome has not been consistently demonstrated. An analysis of the studies examining the effect of ribavirin therapy among children with RSV lower respiratory tract disease included 11 relatively small, randomized controlled trials. Of these, 7 showed clinical benefit, and 4 did not.<xref rid="bib109" ref-type="bibr"><sup>109</sup></xref> A Cochrane Review analysis of randomized placebo-controlled trials evaluating ribavirin for the therapy of children hospitalized with RSV lower respiratory tract disease found that ribavirin reduced the duration of mechanical ventilation and length of hospitalization.<xref rid="bib181" ref-type="bibr"><sup>181</sup></xref> Significant reduction in respiratory failure or deaths was not shown, but few children progressed to either. Ribavirin has teratogenic properties, and precautions must be taken to guard against exposing women of potential childbearing capacity.</p><p id="p0485">In view of the unclear degree of benefit relative to the considerable cost of aerosolized ribavirin, the American Academy of Pediatrics recommends that ribavirin should not be used routinely in the management of RSV lower respiratory tract infections.<xref rid="bib93" ref-type="bibr">93</xref>, <xref rid="bib109" ref-type="bibr">109</xref> Ribavirin therapy should be considered on an individual basis for children who have severe disease or who are at high risk for developing complicated or severe disease.</p><p id="p0490">The data supporting ribavirin treatment of RSV infection in severely immunocompromised persons with RSV infection is primarily drawn from retrospective case series.<xref rid="bib103" ref-type="bibr">103</xref>, <xref rid="bib143" ref-type="bibr">143</xref>, <xref rid="bib182" ref-type="bibr">182</xref>, <xref rid="bib183" ref-type="bibr">183</xref> In a large retrospective single-center analysis of 280 HCT patients with RSV infection, progression to lower respiratory disease and mortality was reduced significantly in patients in whom administration of inhaled ribavirin was started when symptoms were limited to the upper respiratory tract.<xref rid="bib182" ref-type="bibr"><sup>182</sup></xref> The only prospective placebo-controlled study was performed in 14 HCT patients with RSV upper respiratory tract infection. Although ribavirin was safe and showed a trend of decreasing viral load during therapy, the number of subjects was too small to make firm conclusions.<xref rid="bib184" ref-type="bibr"><sup>184</sup></xref> Inhaled ribavirin has been given either continuously (6 g over 18 hours) or intermittently (2 g over 2 to 3 hours three times per day). In a prospective randomized trial comparing these two dosing schedules in immunocompromised patients with RSV infection, the intermittent schedule appeared more effective in preventing development of lower respiratory disease.<xref rid="bib185" ref-type="bibr"><sup>185</sup></xref></p><p id="p0495">The efficacy of systemic ribavirin, administered either by the oral or the intravenous route, is unknown in the immunocompromised patient with RSV infection, although retrospective case studies suggest they may provide some benefit.<xref rid="bib186" ref-type="bibr">186</xref>, <xref rid="bib187" ref-type="bibr">187</xref>, <xref rid="bib188" ref-type="bibr">188</xref> Experimental therapies, such as one described in a recent report of inhaled RNA interference therapy in lung transplant patients, or newer inhibitors of the RSV fusion protein, may offer possible future therapy.<xref rid="bib154" ref-type="bibr"><sup>154</sup></xref></p><p id="p0500">The benefit of immunoglobulin therapy for RSV infection among highly immunocompromised patients is based primarily on retrospective observational studies. The results with either polyclonal IVIG or the anti-F monoclonal antibody (palivizumab) alone or in combination with ribavirin have been mixed, with some studies suggesting a trend toward diminished morbidity and progression to lower respiratory tract disease when used therapeutically.<xref rid="fn0015" ref-type="fn">*</xref> However, consensus exists that these monoclonals appear safe and well tolerated by highly immunosuppressed patients. Prophylactic administration of palivizumab to immunocompromised patients has not been adequately evaluated and is not recommended.<xref rid="bib93" ref-type="bibr"><sup>93</sup></xref> The American Academy of Pediatrics, nevertheless, states that children with severe immunodeficiencies may benefit from prophylaxis. Using a decision analysis model to evaluate the effect of palivizumab prophylaxis to prevent RSV mortality after bone marrow transplantation in children, the survival rate was estimated to increase by 10%, and it was calculated that 12 children would need to be treated to prevent one fatal RSV infection.<xref rid="bib191" ref-type="bibr"><sup>191</sup></xref> Palivizumab is extraordinarily expensive in dosages administered to adults and is approved only for intramuscular use.</p><p id="p0505">New approaches are being investigated to develop therapies specific for RSV disease.<xref rid="bib12" ref-type="bibr">12</xref>, <xref rid="bib192" ref-type="bibr">192</xref> Among these include the development of inhibitors of attachment and fusion, including small peptide fusion inhibitors, N protein inhibitors, and RNA-dependent RNA polymerase inhibitors.<xref rid="bib193" ref-type="bibr"><sup>193</sup></xref> Much interest and effort recently has been focused on developing oligonucleotides that interfere with viral RNA, antisense/small interfering RNA (siRNA) inhibitors.<xref rid="bib154" ref-type="bibr"><sup>154</sup></xref> Some of these have shown promise in clinical trials.</p></sec><sec id="s0150"><title>Prevention</title><p id="p0510"><disp-quote><p><italic>The viper's venom,</italic></p><p><italic>the serpent's spell</italic></p><p><italic>daunts not the tortoise</italic></p><p><italic>beneath his shell.</italic></p><p><bold>C.B.H.</bold></p></disp-quote></p><sec id="s0155"><title>Infection Control</title><p id="p0515">Prevention rather than treatment is the preferable, but yet unattained, goal for the control of RSV infection. Avoiding infection at home through interruption of the transmission of the virus is difficult and unlikely to be effective. However, general precautions may be useful against the spread of infectious secretions on hands and fomites. These include good hand hygiene, use of hand-rub antiseptic products, and care of contaminated tissues, toys, and other objects likely to be contaminated with secretions.<xref rid="bib194" ref-type="bibr"><sup>194</sup></xref></p><p id="p0520">On hospital wards, however, RSV poses a particular hazard for nosocomial spread.<xref rid="bib58" ref-type="bibr">58</xref>, <xref rid="bib147" ref-type="bibr">147</xref>, <xref rid="bib195" ref-type="bibr">195</xref>, <xref rid="bib196" ref-type="bibr">196</xref>, <xref rid="bib197" ref-type="bibr">197</xref> Yearly outbreaks occur with widespread infection among both children and adults, including medical personnel who may continue to work despite upper respiratory tract signs. Considerable morbidity and mortality have been associated with nosocomial RSV infection among those with underlying conditions, especially prematurity, and cardiopulmonary and immunocompromised conditions. Strict adherence to recommended guidelines, therefore, is essential and cost-effective.</p><p id="p0525">RSV may be spread by close contact and by direct inoculation of large droplets from the secretions of an infected person, as well as by indirect spread from hands that touch infectious secretions in the environment.<xref rid="bib58" ref-type="bibr">58</xref>, <xref rid="bib196" ref-type="bibr">196</xref> Careful hand hygiene by all personnel, therefore, is integral to preventing nosocomial transmission (<xref rid="t0025" ref-type="table">Table 160-4</xref>). Additional procedures aimed at preventing self-inoculation include the wearing of eye-nose goggles and gloves. Procedures aimed at reducing the risk for the introduction and spread of RSV to other personnel and patients include the wearing gowns for close contact with infected patients, isolation or cohorting of infected patients, and use of rapid diagnostic techniques. In addition, during the RSV season, staff with signs of respiratory illness should not care for high-risk patients, and visitors should be screened for respiratory illness.<xref rid="bib58" ref-type="bibr"><sup>58</sup></xref><table-wrap position="float" id="t0025"><label>TABLE 160-4</label><caption><p>Infection Control Procedures, Both Standard Precautions and Contact Precautions, for Prevention of Respiratory Syncytial Virus (RSV) Infection Recommended by Centers for Disease Control and Prevention</p></caption><table frame="hsides" rules="groups"><thead><tr><th align="left">RECOMMENDATION CATEGORY, PROCEDURE</th><th align="left">COMMENTS</th></tr></thead><tbody><tr><td colspan="2" align="left"><bold>Category 1-B Recommendations</bold><xref rid="tn0015" ref-type="table-fn">*</xref></td></tr><tr><td align="left">Hand washing</td><td align="left">Water with soap or antibacterial agent or waterless antiseptic hand rub</td></tr><tr><td align="left">Wearing gloves</td><td align="left">Combined with hand washing before and after each glove change; may diminish self-inoculation</td></tr><tr><td align="left">Wearing gowns</td><td align="left">When direct contact with patient or patient secretions is likely</td></tr><tr><td align="left">Wearing masks plus eye protection</td><td align="left">Eyes and nose are major sites for inoculation</td></tr><tr><td align="left">Housing patient in private room or in a cohort isolated from other patients</td><td align="left">Patients with documented infection can be grouped and isolated from other patients; beds should be separated by >0.9 m</td></tr><tr><td align="left">Use of dedicated patient care equipment</td><td align="left">Equipment, including toys, assigned to specific patients</td></tr><tr><td colspan="2" align="left"><bold>Sometimes Recommended with Less or No Supporting Evidence</bold></td></tr><tr><td align="left">Staff assigned according to patient's RSV status</td><td align="left">Specific staff care only for patients with RSV infection</td></tr><tr><td align="left">Visitor restrictions during RSV season</td><td align="left">Some qualify by restricting young children only</td></tr><tr><td align="left">Screening visitors for illness during RSV season</td><td align="left">Visitor assessed by trained personnel or advised by use of an educational patient information list</td></tr></tbody></table><table-wrap-foot><fn id="tn0015"><label>*</label><p id="np0025">From Garner JS. Guidelines for isolation precautions in hospitals. <italic>Infect Control Hosp Epidemiol.</italic> 1996;17:53-80.</p></fn></table-wrap-foot><attrib>From Hall CB. Nosocomial respiratory syncytial virus infections: the “Cold War” has not ended. <italic>Clin Infect Dis.</italic> 2000;360:588-598.</attrib></table-wrap></p></sec><sec id="s0160"><title>Prophylaxis</title><p id="p0530">Prophylaxis using the passive administration of RSV-specific antibody currently is available primarily for those groups most at risk for developing severe or complicated RSV disease. High-risk children administered monthly doses of intravenous immune globulin containing high levels of RSV neutralizing antibody (RSV-IVIG) or intramuscular monoclonal antibody have shown reduced rates of hospitalization from RSV infection.<xref rid="bib93" ref-type="bibr"><sup>93</sup></xref> RSV-IVIG is no longer available and has been replaced by palivizumab, a humanized monoclonal antibody. Palivizumab was developed from a mouse monoclonal antibody directed against a protective epitope of the RSV fusion (F) protein. Immunoprophylaxis of five monthly intramuscular doses of 15 mg/kg initiated a month before the RSV season has been shown to reduce hospitalization rates by 34% to 82% among selected groups of high-risk infants.<xref rid="bib93" ref-type="bibr"><sup>93</sup></xref> Palivizumab administration does not prevent infection with RSV but is associated with diminished clinical severity, the risk for developing lower respiratory tract disease, and need for hospitalization.</p><p id="p0535">Currently, palivizumab is recommended for selected children who are younger than 2 years and are considered to have a high risk for developing severe RSV disease. Included are those with prematurity (<32 weeks' gestation), chronic lung disease, functionally important cardiac disease, and chronic conditions that interfere with the handling of respiratory secretions.<xref rid="bib93" ref-type="bibr"><sup>93</sup></xref> Infants born between 32 and 35 weeks' gestation also have significantly greater risk for hospitalization and use of medical services for RSV disease than full-term infants.<xref rid="bib93" ref-type="bibr"><sup>93</sup></xref> However, considering that most premature infants are between 32 and 35 weeks' gestation and that palivizumab prophylaxis is very expensive, the American Academy of Pediatrics recommends that infants born from 32 to 35 weeks' gestation be considered for prophylaxis if they are younger than 3 months at the start of the RSV season and have additional risk factors.<xref rid="bib93" ref-type="bibr"><sup>93</sup></xref></p><p id="p0540">Controversy exists concerning the extent of the use of palivizumab prophylaxis based primarily on the concern of its considerable cost relative to its benefit. Economic analyses in general have not shown an overall savings in health care costs for prophylaxis of all infants less than 32 weeks' gestation and with underlying high-risk conditions, but the benefit relative to the cost among those at highest risk increases.<xref rid="bib198" ref-type="bibr">198</xref>, <xref rid="bib199" ref-type="bibr">199</xref> Palivizumab prophylaxis has not been shown to reduce the mortality from RSV, but currently in the United States, the mortality from RSV infection, even among high-risk infants, is very low. The effect of palivizumab on the long-term sequelae of RSV infection has not been adequately evaluated.<xref rid="bib200" ref-type="bibr"><sup>200</sup></xref></p><p id="p0545">Additional products are being evaluated for the prevention of RSV disease in high-risk individuals, including a newer humanized monoclonal antibody, motavizumab.<xref rid="bib201" ref-type="bibr"><sup>201</sup></xref> Motavizumab is derived from palivizumab and is also directed against the F protein. In vitro, it exhibits a 20-fold improvement in RSV neutralization. A recent multicenter study of more than 6000 high-risk infants showed that infants receiving motavizumab, compared with those receiving palivizumab, had a 26% relative reduction in RSV hospitalization, and motavizumab was superior to palivizumab in reducing RSV-related outpatient visits for lower respiratory tract disease.<xref rid="bib202" ref-type="bibr"><sup>202</sup></xref> However, the U.S. Food and Drug Administration panel raised questions regarding motavizumab's safety (primarily allergic reactions), and it has not been approved for prophylaxis or treatment of RSV infection in high-risk infants currently.</p></sec><sec id="s0165"><title>Immunization</title><p id="p0550">Currently, an effective vaccine for prevention of RSV for use in infants or in adults is not available. Ideally, a vaccine should provide better protection than natural disease, which does not confer durable immunity. This is compounded by the lack of identifiable correlates of solid immunity to infection. Also, concern still exists that an unpredictable abnormal immune-mediated response could occur in some vaccinees during their first RSV infection, such as was observed during the trials with the initial formalin-inactivated RSV vaccine.<xref rid="bib74" ref-type="bibr"><sup>74</sup></xref> Furthermore, immunization would have to be initiated within the first weeks of life because most hospitalization for RSV occurs in the first several months of life. Even the response to a vaccine administered to adults and healthy older children may not predict the vaccine's safety or protection among very young infants.</p><p id="p0555">Experimental live-attenuated vaccines, produced by chemical mutagenesis and reverse-genetic techniques, have thus far proven to be poorly immunogenic or underattenuated, resulting in upper airway obstruction from increased production of mucus and secretions. Among infants administered a candidate live-attenuated RSV vaccine, all seronegative children older than 6 months developed at least a fourfold antibody response after a dose of vaccine, whereas only 44% of infants 2 to 4 months of age were able to do so after two doses.<xref rid="bib203" ref-type="bibr"><sup>203</sup></xref> In addition, the induction of a cytotoxic cellular response from RSV immunization appears variable.<xref rid="bib203" ref-type="bibr"><sup>203</sup></xref> Of the children given a live candidate RSV vaccine, less than 40% of those younger than 5 months produced a detectable, but transient, cytotoxic T-cell response to RSV, compared with 65% of those 6 to 24 months of age. RSV immunization in early life is further complicated by the apparent bias toward a Th2-type immunologic response to RSV that exists during the first 3 months of life.<xref rid="bib106" ref-type="bibr"><sup>106</sup></xref></p><p id="p0560">The efficacy of a candidate RSV vaccine may also relate to its ability to stimulate an adequate local antibody response in the respiratory tract, which may be the first line of defense.<xref rid="bib12" ref-type="bibr"><sup>12</sup></xref> Despite high levels of RSV antibodies in the serum, little reaches the respiratory secretions. Transudation of serum antibodies is poor, resulting in RSV antibody levels being 80 to 160 times less in the respiratory tract secretions or even less in the nasal secretions, compared with the antibody levels in the serum. Nevertheless, a major potential advantage of a live-attenuated intranasal vaccine in comparison to a subunit vaccine is that it is more apt to mimic naturally evoked immunity and induce local respiratory tract antibodies.</p><p id="p0565">Subunit candidate vaccines have focused on F and G proteins, primarily using the F protein because of its considerable cross-reactivity between group A and B RSV strains. These purified F protein vaccines have been safe and immunogenic among individuals who are seropositive from previous natural RSV infection and should theoretically boost neutralizing serum antibodies, especially in adults.<xref rid="bib204" ref-type="bibr">204</xref>, <xref rid="bib205" ref-type="bibr">205</xref>, <xref rid="bib206" ref-type="bibr">206</xref> They may offer the possibility of boosting the immunity among some groups of older children and adults who have an increased risk for developing more severe RSV infection and among pregnant women as a means of augmenting maternal antibody levels in the infant.<xref rid="bib207" ref-type="bibr"><sup>207</sup></xref> However, because of the aforementioned concerns about the initial experience with RSV as elicited by nonreplicating virus, live-attenuated vaccines have been judged a more appropriate approach for RSV-naïve infants.</p><p id="p0570">The use of reverse genetics has resulted in generations of newly designed candidate strains that contain mutations specifically chosen for their attenuating, immunogenic, and other advantageous characteristics.<xref rid="bib208" ref-type="bibr"><sup>208</sup></xref> These candidate “designer gene” vaccines are potentially safer, have increased breadth of antigenic expression, and allow combination vaccines with parainfluenza and other respiratory pathogens.<xref rid="bib209" ref-type="bibr"><sup>209</sup></xref></p></sec></sec></body><back><ref-list id="fr0010"><title>Key References</title><p id="p0575"><italic>The complete reference list is available online at Expert Consult.</italic></p><ref id="bib210"><label>2</label><element-citation publication-type="journal" id="sr0010"><person-group person-group-type="author"><name><surname>Hall</surname><given-names>C</given-names></name><name><surname>Weinberg</surname><given-names>G</given-names></name><name><surname>Iwane</surname><given-names>M</given-names></name></person-group><article-title>The burden of respiratory syncytial virus infection among healthy children</article-title><source>N Engl J Med</source><volume>360</volume><year>2009</year><fpage>588</fpage><lpage>598</lpage><pub-id pub-id-type="pmid">19196675</pub-id></element-citation></ref><ref id="bib211"><label>3</label><element-citation publication-type="journal" id="sr0015"><person-group person-group-type="author"><name><surname>Zhou</surname><given-names>H</given-names></name><name><surname>Thompson</surname><given-names>WW</given-names></name><name><surname>Viboud</surname><given-names>CG</given-names></name></person-group><article-title>Hospitalizations associated with influenza and respiratory syncytial virus in the United States, 1993-2008</article-title><source>Clin Infect Dis</source><volume>54</volume><year>2012</year><fpage>1427</fpage><lpage>1436</lpage><pub-id pub-id-type="pmid">22495079</pub-id></element-citation></ref><ref id="bib212"><label>7</label><element-citation publication-type="journal" id="sr0020"><person-group person-group-type="author"><name><surname>Falsey</surname><given-names>A</given-names></name><name><surname>Hennessey</surname><given-names>P</given-names></name><name><surname>Formica</surname><given-names>M</given-names></name></person-group><article-title>Respiratory syncytial virus infection in elderly and high-risk adults</article-title><source>N Engl J Med</source><volume>352</volume><year>2005</year><fpage>1749</fpage><lpage>1759</lpage><pub-id pub-id-type="pmid">15858184</pub-id></element-citation></ref><ref id="bib213"><label>9</label><element-citation publication-type="journal" id="sr0025"><person-group person-group-type="author"><name><surname>van Asten</surname><given-names>L</given-names></name><name><surname>van den Wijngaard</surname><given-names>C</given-names></name><name><surname>van Pelt</surname><given-names>W</given-names></name></person-group><article-title>Mortality attributable to 9 common infections: significant effect of influenza A, respiratory syncytial virus, influenza B, norovirus, and parainfluenza in elderly persons</article-title><source>J Infect Dis</source><volume>206</volume><year>2012</year><fpage>628</fpage><lpage>639</lpage><pub-id pub-id-type="pmid">22723641</pub-id></element-citation></ref><ref id="bib214"><label>11</label><element-citation publication-type="journal" id="sr0030"><person-group person-group-type="author"><name><surname>Chanock</surname><given-names>R</given-names></name><name><surname>Roizman</surname><given-names>B</given-names></name><name><surname>Myers</surname><given-names>R</given-names></name></person-group><article-title>Recovery from infants with respiratory illness of a virus related to chimpanzee coryza agent (CCA), I. 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She was the author for this and other chapters for previous editions of this book. This chapter is dedicated to her memory.</p></fn><fn id="fn0015"><label>*</label><p id="np0020">References <xref rid="bib147" ref-type="bibr">147</xref>, <xref rid="bib148" ref-type="bibr">148</xref>, <xref rid="bib151" ref-type="bibr">151</xref>, <xref rid="bib184" ref-type="bibr">184</xref>, <xref rid="bib189" ref-type="bibr">189</xref>, <xref rid="bib190" ref-type="bibr">190</xref>.</p></fn></fn-group></back></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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