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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Comparative study of patients with and without SARS WHO fulfilled the WHO SARS case definition</title><author><name sortKey="Chang, Shang Miao" sort="Chang, Shang Miao" uniqKey="Chang S" first="Shang-Miao" last="Chang">Shang-Miao Chang</name><affiliation><nlm:aff id="aff1">Division of Chest Medicine, Department of Medicine, Mackay Memorial Hospital, Taipei, Taiwan</nlm:aff></affiliation></author><author><name sortKey="Liu, Ching Lung" sort="Liu, Ching Lung" uniqKey="Liu C" first="Ching-Lung" last="Liu">Ching-Lung Liu</name><affiliation><nlm:aff id="aff1">Division of Chest Medicine, Department of Medicine, Mackay Memorial Hospital, Taipei, Taiwan</nlm:aff></affiliation></author><author><name sortKey="Kuo, Hsu Tah" sort="Kuo, Hsu Tah" uniqKey="Kuo H" first="Hsu-Tah" last="Kuo">Hsu-Tah Kuo</name><affiliation><nlm:aff id="aff1">Division of Chest Medicine, Department of Medicine, Mackay Memorial Hospital, Taipei, Taiwan</nlm:aff></affiliation></author><author><name sortKey="Chen, Pei Jan" sort="Chen, Pei Jan" uniqKey="Chen P" first="Pei-Jan" last="Chen">Pei-Jan Chen</name><affiliation><nlm:aff id="aff1">Division of Chest Medicine, Department of Medicine, Mackay Memorial Hospital, Taipei, Taiwan</nlm:aff></affiliation></author><author><name sortKey="Lee, Chun Ming" sort="Lee, Chun Ming" uniqKey="Lee C" first="Chun Ming" last="Lee">Chun Ming Lee</name><affiliation><nlm:aff id="aff1">Division of Chest Medicine, Department of Medicine, Mackay Memorial Hospital, Taipei, Taiwan</nlm:aff></affiliation></author><author><name sortKey="Lin, Fung J" sort="Lin, Fung J" uniqKey="Lin F" first="Fung-J." last="Lin">Fung-J. Lin</name><affiliation><nlm:aff id="aff1">Division of Chest Medicine, Department of Medicine, Mackay Memorial Hospital, Taipei, Taiwan</nlm:aff></affiliation></author><author><name sortKey="Lin, Ching Chi" sort="Lin, Ching Chi" uniqKey="Lin C" first="Ching-Chi" last="Lin">Ching-Chi Lin</name><affiliation><nlm:aff id="aff1">Division of Chest Medicine, Department of Medicine, Mackay Memorial Hospital, Taipei, Taiwan</nlm:aff></affiliation></author><author><name sortKey="Lee, Chao Hsien" sort="Lee, Chao Hsien" uniqKey="Lee C" first="Chao-Hsien" last="Lee">Chao-Hsien Lee</name><affiliation><nlm:aff id="aff1">Division of Chest Medicine, Department of Medicine, Mackay Memorial Hospital, Taipei, Taiwan</nlm:aff></affiliation></author><author><name sortKey="Lu, Yen Ta" sort="Lu, Yen Ta" uniqKey="Lu Y" first="Yen-Ta" last="Lu">Yen-Ta Lu</name><affiliation><nlm:aff id="aff2">Department of Medical Research, Mackay Memorial Hospital, Taipei, Taiwan</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">15837019</idno><idno type="pmc">7135563</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7135563</idno><idno type="RBID">PMC:7135563</idno><idno type="doi">10.1016/j.jemermed.2004.11.022</idno><date when="2005">2005</date><idno type="wicri:Area/Pmc/Corpus">001129</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">001129</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Comparative study of patients with and without SARS WHO fulfilled the WHO SARS case definition</title><author><name sortKey="Chang, Shang Miao" sort="Chang, Shang Miao" uniqKey="Chang S" first="Shang-Miao" last="Chang">Shang-Miao Chang</name><affiliation><nlm:aff id="aff1">Division of Chest Medicine, Department of Medicine, Mackay Memorial Hospital, Taipei, Taiwan</nlm:aff></affiliation></author><author><name sortKey="Liu, Ching Lung" sort="Liu, Ching Lung" uniqKey="Liu C" first="Ching-Lung" last="Liu">Ching-Lung Liu</name><affiliation><nlm:aff id="aff1">Division of Chest Medicine, Department of Medicine, Mackay Memorial Hospital, Taipei, Taiwan</nlm:aff></affiliation></author><author><name sortKey="Kuo, Hsu Tah" sort="Kuo, Hsu Tah" uniqKey="Kuo H" first="Hsu-Tah" last="Kuo">Hsu-Tah Kuo</name><affiliation><nlm:aff id="aff1">Division of Chest Medicine, Department of Medicine, Mackay Memorial Hospital, Taipei, Taiwan</nlm:aff></affiliation></author><author><name sortKey="Chen, Pei Jan" sort="Chen, Pei Jan" uniqKey="Chen P" first="Pei-Jan" last="Chen">Pei-Jan Chen</name><affiliation><nlm:aff id="aff1">Division of Chest Medicine, Department of Medicine, Mackay Memorial Hospital, Taipei, Taiwan</nlm:aff></affiliation></author><author><name sortKey="Lee, Chun Ming" sort="Lee, Chun Ming" uniqKey="Lee C" first="Chun Ming" last="Lee">Chun Ming Lee</name><affiliation><nlm:aff id="aff1">Division of Chest Medicine, Department of Medicine, Mackay Memorial Hospital, Taipei, Taiwan</nlm:aff></affiliation></author><author><name sortKey="Lin, Fung J" sort="Lin, Fung J" uniqKey="Lin F" first="Fung-J." last="Lin">Fung-J. Lin</name><affiliation><nlm:aff id="aff1">Division of Chest Medicine, Department of Medicine, Mackay Memorial Hospital, Taipei, Taiwan</nlm:aff></affiliation></author><author><name sortKey="Lin, Ching Chi" sort="Lin, Ching Chi" uniqKey="Lin C" first="Ching-Chi" last="Lin">Ching-Chi Lin</name><affiliation><nlm:aff id="aff1">Division of Chest Medicine, Department of Medicine, Mackay Memorial Hospital, Taipei, Taiwan</nlm:aff></affiliation></author><author><name sortKey="Lee, Chao Hsien" sort="Lee, Chao Hsien" uniqKey="Lee C" first="Chao-Hsien" last="Lee">Chao-Hsien Lee</name><affiliation><nlm:aff id="aff1">Division of Chest Medicine, Department of Medicine, Mackay Memorial Hospital, Taipei, Taiwan</nlm:aff></affiliation></author><author><name sortKey="Lu, Yen Ta" sort="Lu, Yen Ta" uniqKey="Lu Y" first="Yen-Ta" last="Lu">Yen-Ta Lu</name><affiliation><nlm:aff id="aff2">Department of Medical Research, Mackay Memorial Hospital, Taipei, Taiwan</nlm:aff></affiliation></author></analytic><series><title level="j">The Journal of Emergency Medicine</title><idno type="ISSN">0736-4679</idno><idno type="eISSN">0736-4679</idno><imprint><date when="2005">2005</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>To differentiate severe acute respiratory syndrome (SARS) from non-SARS illness, we retrospectively compared 53 patients with probable SARS and 31 patients with non-SARS who were admitted to Mackay Memorial Hospital from April 27 to June 16, 2003. Fever (> 38°C) was the earliest symptom (50/53 SARS vs. 5/31 non-SARS, <italic>p</italic> < 0.0001), preceding cough by a mean of 4.5 days. The initial chest X-ray study was normal in 22/53 SARS cases versus 5/31 non-SARS cases. SARS patients with an initially normal chest X-ray study developed infiltrates at a mean of 5 ± 3.44 days after onset of fever (21/22 SARS vs. 0/5 non-SARS). Rapid radiographic progression of unifocal involvement to multifocal infiltrates was seen in 22 of 24 SARS vs. 0 of 26 non-SARS patients (<italic>p</italic> < 0.0001). Pleural effusion was not present in any SARS patients but was seen in 6 of 26 non-SARS cases (<italic>p</italic> < 0.0001). Initial lymphopenia, thrombocytopenia, and elevated lactate dehydrogenase were all more common in SARS than non-SARS (<italic>p</italic> < 0.0001). They may help differentiate SARS from non-SARS if a reliable and rapid diagnostic test is not available.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Ksiazek, T G" uniqKey="Ksiazek T">T.G. Ksiazek</name></author><author><name sortKey="Erdman, D" uniqKey="Erdman D">D. Erdman</name></author><author><name sortKey="Goldsmith, C" uniqKey="Goldsmith C">C. Goldsmith</name></author></analytic></biblStruct><biblStruct></biblStruct><biblStruct><analytic><author><name sortKey="Peiris, J S M" uniqKey="Peiris J">J.S.M. Peiris</name></author><author><name sortKey="Lai, S T" uniqKey="Lai S">S.T. Lai</name></author><author><name sortKey="Poon, L L M" uniqKey="Poon L">L.L.M. Poon</name></author></analytic></biblStruct><biblStruct></biblStruct><biblStruct><analytic><author><name sortKey="Drosten, C" uniqKey="Drosten C">C. Drosten</name></author><author><name sortKey="Gunther, S" uniqKey="Gunther S">S. Gunther</name></author><author><name sortKey="Preiser, W" uniqKey="Preiser W">W. Preiser</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Hon, K L E" uniqKey="Hon K">K.L.E. Hon</name></author><author><name sortKey="Li, A M" uniqKey="Li A">A.M. Li</name></author><author><name sortKey="Cheng, F W T" uniqKey="Cheng F">F.W.T. Cheng</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Dolin, R" uniqKey="Dolin R">R. Dolin</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Lee, N" uniqKey="Lee N">N. Lee</name></author><author><name sortKey="Hui, D" uniqKey="Hui D">D. Hui</name></author><author><name sortKey="Wu, A" uniqKey="Wu A">A. Wu</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Poutanen, S M" uniqKey="Poutanen S">S.M. Poutanen</name></author><author><name sortKey="Low, D E" uniqKey="Low D">D.E. Low</name></author><author><name sortKey="Henry, B" uniqKey="Henry B">B. Henry</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Tomlinson, B" uniqKey="Tomlinson B">B. Tomlinson</name></author><author><name sortKey="Cockram, C" uniqKey="Cockram C">C. Cockram</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Hon, K L E" uniqKey="Hon K">K.L.E. Hon</name></author><author><name sortKey="Leung, C W" uniqKey="Leung C">C.W. Leung</name></author><author><name sortKey="Cheng, W T F" uniqKey="Cheng W">W.T.F. Cheng</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Booth, C M" uniqKey="Booth C">C.M. Booth</name></author><author><name sortKey="Matukas, L M" uniqKey="Matukas L">L.M. Matukas</name></author><author><name sortKey="Tomlinson, G A" uniqKey="Tomlinson G">G.A. Tomlinson</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Avendano, M" uniqKey="Avendano M">M. Avendano</name></author><author><name sortKey="Derkach, P" uniqKey="Derkach P">P. Derkach</name></author><author><name sortKey="Swan, S" uniqKey="Swan S">S. Swan</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Siddell, S G" uniqKey="Siddell S">S.G. Siddell</name></author><author><name sortKey="Snijder, E J" uniqKey="Snijder E">E.J. Snijder</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Wege, H" uniqKey="Wege H">H. Wege</name></author><author><name sortKey="Siddell, S" uniqKey="Siddell S">S. Siddell</name></author><author><name sortKey="Ter Meulen, V" uniqKey="Ter Meulen V">V. ter Meulen</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Wong, K T" uniqKey="Wong K">K.T. Wong</name></author><author><name sortKey="Antonio, G E" uniqKey="Antonio G">G.E. Antonio</name></author><author><name sortKey="Hui, D S C" uniqKey="Hui D">D.S.C. Hui</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Wong, G W K" uniqKey="Wong G">G.W.K. Wong</name></author><author><name sortKey="Hui, D S C" uniqKey="Hui D">D.S.C. Hui</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Antonio, G E" uniqKey="Antonio G">G.E. Antonio</name></author><author><name sortKey="Wong, K T" uniqKey="Wong K">K.T. Wong</name></author><author><name sortKey="Hui, D S" uniqKey="Hui D">D.S. Hui</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="O Onnell, D R O" uniqKey="O Onnell D">D.R.O. O’Donnell</name></author><author><name sortKey="Tasker, R C" uniqKey="Tasker R">R.C. Tasker</name></author><author><name sortKey="Roe, M F E" uniqKey="Roe M">M.F.E. Roe</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Panesar, N S" uniqKey="Panesar N">N.S. Panesar</name></author></analytic></biblStruct></listBibl></div1></back></TEI><pmc article-type="research-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">J Emerg Med</journal-id><journal-id journal-id-type="iso-abbrev">J Emerg Med</journal-id><journal-title-group><journal-title>The Journal of Emergency Medicine</journal-title></journal-title-group><issn pub-type="ppub">0736-4679</issn><issn pub-type="epub">0736-4679</issn><publisher><publisher-name>Elsevier Inc.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">15837019</article-id><article-id pub-id-type="pmc">7135563</article-id><article-id pub-id-type="publisher-id">S0736-4679(05)00024-7</article-id><article-id pub-id-type="doi">10.1016/j.jemermed.2004.11.022</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title-group><article-title>Comparative study of patients with and without SARS WHO fulfilled the WHO SARS case definition</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Chang</surname><given-names>Shang-Miao</given-names></name><degrees>MD</degrees><xref rid="aff1" ref-type="aff">⁎</xref></contrib><contrib contrib-type="author"><name><surname>Liu</surname><given-names>Ching-Lung</given-names></name><degrees>MD</degrees><xref rid="aff1" ref-type="aff">⁎</xref></contrib><contrib contrib-type="author"><name><surname>Kuo</surname><given-names>Hsu-Tah</given-names></name><degrees>MD</degrees><xref rid="aff1" ref-type="aff">⁎</xref></contrib><contrib contrib-type="author"><name><surname>Chen</surname><given-names>Pei-Jan</given-names></name><degrees>MD</degrees><xref rid="aff1" ref-type="aff">⁎</xref></contrib><contrib contrib-type="author"><name><surname>Lee</surname><given-names>Chun Ming</given-names></name><degrees>MD</degrees><xref rid="aff1" ref-type="aff">⁎</xref></contrib><contrib contrib-type="author"><name><surname>Lin</surname><given-names>Fung-J.</given-names></name><degrees>MD</degrees><xref rid="aff1" ref-type="aff">⁎</xref></contrib><contrib contrib-type="author"><name><surname>Lin</surname><given-names>Ching-Chi</given-names></name><degrees>MD</degrees><xref rid="aff1" ref-type="aff">⁎</xref></contrib><contrib contrib-type="author"><name><surname>Lee</surname><given-names>Chao-Hsien</given-names></name><degrees>MD</degrees><xref rid="aff1" ref-type="aff">⁎</xref></contrib><contrib contrib-type="author"><name><surname>Lu</surname><given-names>Yen-Ta</given-names></name><degrees>MD, PhD</degrees><xref rid="aff2" ref-type="aff">†</xref><xref rid="cor1" ref-type="corresp">⁎</xref></contrib></contrib-group><aff id="aff1"><label>⁎</label>Division of Chest Medicine, Department of Medicine, Mackay Memorial Hospital, Taipei, Taiwan</aff><aff id="aff2"><label>†</label>Department of Medical Research, Mackay Memorial Hospital, Taipei, Taiwan</aff><author-notes><corresp id="cor1"><label>⁎</label><italic>Reprint Address</italic>: Yen-Ta Lu, <sc>md</sc>, <sc>p</sc>h<sc>d</sc>, Department of Medical Research, Mackay Memorial Hospital, 92, Sec 2, Chung-Shan North Road, Taipei, Taiwan</corresp></author-notes><pub-date pub-type="pmc-release"><day>14</day><month>4</month><year>2005</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"><month>5</month><year>2005</year></pub-date><pub-date pub-type="epub"><day>14</day><month>4</month><year>2005</year></pub-date><volume>28</volume><issue>4</issue><fpage>395</fpage><lpage>402</lpage><history><date date-type="received"><day>16</day><month>12</month><year>2003</year></date><date date-type="rev-recd"><day>13</day><month>10</month><year>2004</year></date><date date-type="accepted"><day>29</day><month>11</month><year>2004</year></date></history><permissions><copyright-statement>Copyright © 2005 Elsevier Inc. All rights reserved.</copyright-statement><copyright-year>2005</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><abstract><p>To differentiate severe acute respiratory syndrome (SARS) from non-SARS illness, we retrospectively compared 53 patients with probable SARS and 31 patients with non-SARS who were admitted to Mackay Memorial Hospital from April 27 to June 16, 2003. Fever (> 38°C) was the earliest symptom (50/53 SARS vs. 5/31 non-SARS, <italic>p</italic> < 0.0001), preceding cough by a mean of 4.5 days. The initial chest X-ray study was normal in 22/53 SARS cases versus 5/31 non-SARS cases. SARS patients with an initially normal chest X-ray study developed infiltrates at a mean of 5 ± 3.44 days after onset of fever (21/22 SARS vs. 0/5 non-SARS). Rapid radiographic progression of unifocal involvement to multifocal infiltrates was seen in 22 of 24 SARS vs. 0 of 26 non-SARS patients (<italic>p</italic> < 0.0001). Pleural effusion was not present in any SARS patients but was seen in 6 of 26 non-SARS cases (<italic>p</italic> < 0.0001). Initial lymphopenia, thrombocytopenia, and elevated lactate dehydrogenase were all more common in SARS than non-SARS (<italic>p</italic> < 0.0001). They may help differentiate SARS from non-SARS if a reliable and rapid diagnostic test is not available.</p></abstract><kwd-group><title>Keywords</title><kwd>coronavirus</kwd><kwd>non-severe acute respiratory syndrome</kwd><kwd>nasopharyngeal swab</kwd><kwd>reverse-transcriptase polymerase chain reaction</kwd><kwd>severe acute respiratory syndrome</kwd></kwd-group></article-meta></front><body><sec><title>Introduction</title><p>Severe acute respiratory syndrome (SARS) is a rapidly progressive disease caused by a novel coronavirus. It spread to several continents in a very short time (<xref rid="bib1" ref-type="bibr">1</xref>, <xref rid="bib2" ref-type="bibr">2</xref>, <xref rid="bib3" ref-type="bibr">3</xref>). Due to the apparent contagiousness and severity of the infection, prevention of further spread depended on isolation of patients and quarantine of contacts. A rapid, reliable diagnostic test was not widely available, so that early diagnosis had to be based on a clinical case definition established by the World Health Organization (WHO), resulting in many misdiagnoses (<xref rid="bib4" ref-type="bibr">4</xref>).</p><p>At the end of April 2003, a major outbreak of SARS emerged in Taipei City. Any suspected patient was immediately isolated, using negative pressure rooms when available. The strain on health care facilities was tremendous. Suspected cases had to be reported promptly to the Health Department. Contacts of the index patient were quarantined by government order, resulting in widespread disruption of society and the economy. Had we been better able to distinguish SARS from non-SARS during the epidemic, this disruption could have been reduced. Should the infection reappear, we must be prepared with more precise diagnostic criteria to avoid a repeat of the serious health and societal consequences experienced in the recent outbreak.</p><p>We reported to the Health Department a total of 167 patients at our hospital who had either suspected or probable SARS according to the WHO case definition. In retrospect, a number of these patients did not have SARS. We retrospectively reviewed that experience to see if there were aspects of the presentation that would help differentiate between SARS and non-SARS illness.</p></sec><sec><title>Methods</title><sec><title>Patients</title><p>From 27 April to 16 June, 2003, 167 patients with probable (71) or suspected (96) SARS according to the modified WHO case definition (revised 1 May 2003) were seen at Mackay Memorial Hospital and reported to the Taipei City Health Department (<xref rid="bib4" ref-type="bibr">4</xref>). We excluded 83 patients from the study because they were not admitted to our hospital. These included 9 who died in the emergency department (ED), 31 who were transferred to other hospitals, 1 who left, and 42 who were discharged from the ED and isolated at home due to resolution of symptoms within a few days in the ED. Of the remaining 84 patients who were admitted, 53 had convincing evidence of severe acute respiratory syndrome coronavirus (SARS-CoV) infection and 31 patients had no evidence of SARS-CoV infection. These 31 patients had an alternative diagnosis that fully explained their symptoms (<xref rid="tbl1" ref-type="table">Table 1</xref>) and all except one who died during hospitalization had two negative anti-SARS CoV. The evidence confirming SARS consisted of either a positive polymerase chain reaction (PCR) and a typical clinical course or, in the absence of a positive PCR, a typical clinical course with a definite contact history or evidence that the patient transmitted the infection to someone else. On subsequent serologic testing for anti-SARS-CoV antibody, all 53 patients had positive results.<table-wrap position="float" id="tbl1"><label>Table 1</label><caption><p>Alternative Diagnoses that Fully Explained the Symptoms in Non-SARS Group</p></caption><table frame="hsides" rules="groups"><thead><tr><th align="center">Illness</th><th align="center">Number of patients</th></tr></thead><tbody><tr><td>Mycoplasma pneumonia</td><td>7</td></tr><tr><td>Chlamydia pneumonia</td><td>4</td></tr><tr><td>Legionella pneumonia</td><td>1</td></tr><tr><td>Pneumocystis carinii pneumonia</td><td>1</td></tr><tr><td>Pulmonary tuberculosis</td><td>1</td></tr><tr><td>Nosocomial Staphylococcal pneumonia</td><td>1</td></tr><tr><td>Community-acquired pneumonia</td><td>2<xref rid="tblfn1" ref-type="table-fn">⁎</xref></td></tr><tr><td>Acute myocardial infarction with pulmonary edema</td><td>1</td></tr><tr><td>Uremia with pulmonary edema</td><td>1</td></tr><tr><td>Alpha hemolytic streptococcal infective endocarditis with acute respiratory and heart failure</td><td>1</td></tr><tr><td>COPD with secondary infection</td><td>3<xref rid="tblfn1" ref-type="table-fn">⁎</xref></td></tr><tr><td>COPD with acute respiratory failure</td><td>2</td></tr><tr><td>Acute bronchitis</td><td>2</td></tr><tr><td>Acute tonsillitis</td><td>1</td></tr><tr><td>Acute upper respiratory tract infection</td><td>2</td></tr><tr><td>Lower extremity cellulitis</td><td>1</td></tr></tbody></table><table-wrap-foot><fn id="tblfn1"><label>⁎</label><p>Responded to intravenous broad-spectrum antibiotics (ceftriaxone 500 mg q 12 h, or cefepime 500 mg q 12 h) and oral fluoroquinolones (levofloxacin 500 mg once daily, or moxifloxacin 400 mg once daily) and negative to RT-PCR test.</p></fn></table-wrap-foot></table-wrap></p></sec><sec><title>Clinical data</title><p>Data collected from the medical records included symptoms, underlying diseases, physical findings, and radiologic and laboratory data. As a clear reference point for defining chronological progression, the first day of fever > 38°C was designated as fever day (FD) 1.</p></sec><sec><title>Radiological data</title><p>Serial chest radiographs were obtained once the patient was isolated, on presentation to the ED and then throughout the hospital course.</p></sec><sec><title>Laboratory data</title><p>Results of consecutive hematologic examinations including absolute lymphocyte and platelet counts and serum biochemistry assays including lactate dehydrogenase (LDH), creatine kinase (CK), aspartate aminotransferase (AST), and alanine aminotransferase (ALT) performed during observation in the ED and during hospitalization were also recorded for all patients in whom they were done.</p></sec><sec><title>Microbiological studies</title><p>To look for other possible infections, patients had blood cultures for bacteria and serologic tests for <italic>Mycoplasma pneumoniae</italic> IgM antibodies, Chlamydial IgA, IgM, and IgG antibodies, Widal test for S<italic>almonella typhosa</italic> O and H antigen, <italic>Salmonella paratyphosa</italic> type A and B antigen, <italic>Streptococcus pneumoniae</italic> antigen, <italic>Haemophilus influenzae</italic> antigen, hepatitis B surface antigen (HBsAg), and antibody to hepatitis C (Anti-HCV).</p></sec><sec><title>Reverse-transcriptase PCR specific for SARS-CoV</title><p>Early in the course of the outbreak, there were no specific diagnostic tests available. Once we had the reverse-transcriptase polymerase chain reaction (RT-PCR) test, either a throat or nasopharyngeal swab was obtained for detection of SARS-CoV RNA in patients with suspected or probable SARS in the ED or the isolation ward after admission (<xref rid="bib2" ref-type="bibr">2</xref>, <xref rid="bib5" ref-type="bibr">5</xref>).</p></sec><sec><title>Detection of SARS Co-V antibodies</title><p>Both indirect immunofluorescent test (IIFT) and enzyme immunoassay (EIA) were used for all samples to detect anti-SARS CoV antibodies.</p></sec><sec><title>Statistical analysis</title><p>Categorical variables were analyzed by using Fisher’s exact test or a chi-square test. Significance was defined as a <italic>p</italic> value of < 0.05.</p></sec></sec><sec><title>Results</title><sec><title>Clinical presentation and confirmation of diagnosis</title><p><xref rid="tbl2" ref-type="table">Table 2</xref>shows patients’ demographic features. Forty SARS patients had a positive PCR and were accompanied by a typical clinical course. The remaining 13 had a typical clinical course and were clearly linked in a chain of transmission by a history of close contact with a SARS patient or evidence of transmission to other(s) subsequently diagnosed with SARS. These 13 included 7 with a negative PCR and 6 others in whom PCR was not done. The latter included both staff and patients from the hospital in which significant local transmission initially occurred in Taiwan (no PCR test was available at that time). On subsequent serologic testing for anti-SARS-CoV antibodies, all 53 patients had positive results, whereas non-SARS patients had negative results. There were 7 family clusters involving 17 patients.<table-wrap position="float" id="tbl2"><label>Table 2</label><caption><p>Demographic Features in Patients with SARS and Non-SARS</p></caption><table frame="hsides" rules="groups"><thead><tr><th align="center">Demographic Features</th><th align="center">SARS (n = 53)</th><th align="center">Non-SARS (n = 31)</th></tr></thead><tbody><tr><td>Mean (SD) age (yr)</td><td align="center">39.3 ± 18.1</td><td align="center">42.8 ± 24.73</td></tr><tr><td>Sex (M/F ratio)</td><td align="center">18/35<xref rid="tblfn4" ref-type="table-fn">†</xref></td><td align="center">16/15</td></tr><tr><td>Underlying diseases</td><td align="center">12<xref rid="tblfn2" ref-type="table-fn">⁎</xref></td><td align="center">15<xref rid="tblfn3" ref-type="table-fn">⁎⁎</xref></td></tr><tr><td>Contact history</td><td></td><td></td></tr><tr><td> Health care worker</td><td>13 (25)</td><td>3 (10)</td></tr><tr><td> Hospital visit</td><td>21 (42)</td><td>8 (26)</td></tr><tr><td> Community contact</td><td>11 (21)</td><td>6 (20)</td></tr><tr><td> Travel to SARS area</td><td>1 (2)</td><td>2 (6)</td></tr><tr><td> Unclear contact</td><td>7 (13)</td><td>12 (39)</td></tr></tbody></table><table-wrap-foot><fn><p>Note: Number in parentheses is percentage.</p></fn></table-wrap-foot><table-wrap-foot><fn id="tblfn2"><label>⁎</label><p>Diabetes mellitus (4 patients), essential hypertension (3), congestive heart failure (1), chronic obstructive pulmonary disease (1), rheumatoid arthritis (1), chronic hepatitis B (1), and end-stage renal disease with regular hemodialysis (1).</p></fn></table-wrap-foot><table-wrap-foot><fn id="tblfn3"><label>⁎⁎</label><p>Chronic obstructive pulmonary disease (5 patients), diabetes mellitus (3), essential hypertension (3), hepatoma (1), old pulmonary TB (1), schizophrenia (1) and end stage renal disease (1).</p></fn></table-wrap-foot><table-wrap-foot><fn id="tblfn4"><label>†</label><p>Pregnancy (4).</p></fn></table-wrap-foot></table-wrap></p><p>Being a health care worker and visiting a hospital where SARS patients had been treated were risk factors for SARS. Lack of a clear contact history was more common in non-SARS patients than SARS patients. All of the latter had a typical clinical course and most had a positive PCR (<xref rid="tbl2" ref-type="table">Table 2</xref>).</p><p><xref rid="tbl3" ref-type="table">Table 3</xref>shows clinical features. SARS patients sought medical care at a mean of FD 3.1 ± 2.8, whereas non-SARS patients came at a mean of 4.2 ± 5.5 days after onset of their symptoms. In the SARS patients, fever (> 38°C) was both the most common (52/53, 98%) and the earliest symptom (50/53, 94%). The one patient without a fever initially was a 10-year-old girl who was part of a family cluster and had a positive PCR on throat swab. All of the patients presented with fever as their first symptom except for 2, of whom one had chronic obstructive pulmonary disease and the other congestive heart failure. Both had pre-existing respiratory symptoms related to these underlying chronic diseases, including productive cough and dyspnea on exertion. Of the non-SARS patients, only 5 of 31 (16%) presented with fever as the first symptom (<italic>p</italic> < 0.0001). The mean (SD) duration of fever was 10 ± 3.69 days in the SARS group and 3 ± 2.57 days in the non-SARS group (<italic>p</italic> < 0.0001).<table-wrap position="float" id="tbl3"><label>Table 3</label><caption><p>Clinical Features of SARS and Non-SARS</p></caption><table frame="hsides" rules="groups"><thead><tr><th align="center">Clinical Features</th><th align="center">SARS (n = 53)</th><th align="center">Non-SARS (n = 31)</th><th align="center"><italic>p</italic> Value</th></tr></thead><tbody><tr><td>First symptom</td><td></td><td></td><td></td></tr><tr><td> Fever</td><td>50 (94)</td><td>5 (16)</td><td>< 0.0001</td></tr><tr><td> Cough/dyspnea</td><td>2 (4)</td><td>26 (84)</td><td>< 0.0001</td></tr><tr><td>Associated symptom</td><td></td><td></td><td></td></tr><tr><td> Myalgia</td><td>30 (57)</td><td>6 (19)</td><td></td></tr><tr><td> Headache</td><td>24 (45)</td><td>3 (10)</td><td></td></tr><tr><td> Sore throat</td><td>13 (25)</td><td>4 (13)</td><td></td></tr><tr><td> Diarrhea</td><td>35 (66)</td><td>4 (13)</td><td>< 0.0001</td></tr><tr><td> Abdominal pain</td><td>5 (9)</td><td>4 (13)</td><td></td></tr><tr><td>Mean (SD) duration from symptom to admission (day)</td><td align="char">3.1 ± 2.8</td><td align="char">4.2 ± 5.5</td><td></td></tr><tr><td>Mean (SD) admission temperature (C)</td><td align="char">38.4 ± 0.96</td><td align="char">37.9 ± 1.07</td><td></td></tr><tr><td>Mean (SD) duration of fever (day)</td><td align="char">10 ± 3.69</td><td align="char">3 ± 2.57</td><td>< 0.0001</td></tr></tbody></table><table-wrap-foot><fn><p>Note: Number in parentheses is the percentage.</p></fn></table-wrap-foot></table-wrap></p><p>As noted above, only two SARS patients (4%) with underlying illnesses had cough on the first day of fever. However, 75% (40/53) of patients with SARS eventually developed cough at a mean of FD 4.5 ± 1.9. By a mean of FD 9.3 ± 2.7, 35% (19/53) developed desaturation and dyspnea, and 8 (15%) needed mechanical ventilation. In non-SARS, 26 of 31 (84%) patients had cough or dyspnea preceding their fever (<italic>p</italic> < 0.0001).</p><p>Diarrhea was more common in SARS than in non-SARS patients (66% vs. 13%, respectively, <italic>p</italic> < 0.0001). Only 4 patients (8%) with SARS had diarrhea on FD 1. The onset of diarrhea varied considerably, at a mean (SD) of FD 6.0 ± 3.3. It lasted for a mean (SD) of 6.8 ± 5.1 days. In non-SARS, only 1 patient (3%) had diarrhea, developing 2 days before fever. Three other patients (10%) had diarrhea during their hospitalization.</p></sec><sec><title>Radiologic changes</title><p>Initial chest X-ray studies were normal in 22 of 53 SARS patients (41%) and 5 of 31 non-SARS patients (16%) (<xref rid="tbl4" ref-type="table">Table 4</xref>). Conversely, 31 SARS patients (59%) and 26 non-SARS patients (84%) had abnormal films on presentation (<italic>p</italic> = 0.0001). At initial presentation, air-space opacity was commonly found in SARS patients (25/31, 80% in SARS vs. 13/26, 50% in non-SARS, <italic>p</italic> < 0.0001). No pleural effusion was found in SARS (0 vs. 6/26, 23% in non-SARS, <italic>p</italic> < 0.0001). No patient in either group had hilar lymphadenopathy or cavitation.<table-wrap position="float" id="tbl4"><label>Table 4</label><caption><p>Radiographic Findings in SARS and Non-SARS</p></caption><table frame="hsides" rules="groups"><thead><tr><th align="center">Radiographic findings</th><th align="center">SARS (n = 53)</th><th align="center">Non-SARS (n = 31)</th><th align="center"><italic>p</italic> Value</th></tr></thead><tbody><tr><td>Initial CXR</td><td></td><td></td><td></td></tr><tr><td> Negative</td><td>22 (41)</td><td>5 (16)</td><td>0.0001</td></tr><tr><td> Positive</td><td>31 (59)</td><td>26 (84)</td><td></td></tr><tr><td> Air-space opacity</td><td>25/31 (80)</td><td>13/26 (50)</td><td>< 0.0001</td></tr><tr><td> Interstitial infiltrate</td><td>6/31 (20)</td><td>13/26 (50)</td><td></td></tr><tr><td> Pleural effusion</td><td align="center">0</td><td>6/26 (23)</td><td>< 0.0001</td></tr><tr><td> Hilar lymphadenopathy</td><td align="center">0</td><td align="center">0</td><td></td></tr><tr><td> Cavitation</td><td align="center">0</td><td align="center">0</td><td></td></tr><tr><td>Serial CXR</td><td></td><td></td><td></td></tr><tr><td> Pneumothorax or pneumomediastinum</td><td>5/53 (9)</td><td align="center">0</td><td>0.0016</td></tr><tr><td>No. of lesions</td><td></td><td></td><td></td></tr><tr><td> Static unifocal</td><td>2/52 (4)</td><td>11/26 (42)</td><td></td></tr><tr><td> Uni- to multifocal</td><td>22/52 (42)</td><td align="center">0</td><td>< 0.0001</td></tr><tr><td> Static multifocal</td><td>28/52 (54)</td><td>15/26 (58)</td><td></td></tr><tr><td>Location</td><td></td><td></td><td></td></tr><tr><td> Unilateral infiltrate</td><td>13/52 (25)</td><td>14/26 (54)</td><td></td></tr><tr><td> Bilateral infiltrates</td><td>39/52 (75)</td><td>12/26 (46)</td><td></td></tr><tr><td>Mean (SD) duration in days</td><td></td><td></td><td></td></tr><tr><td>From negative to abnormal CXR</td><td align="center">5 ± 3.44</td><td align="center">0</td><td></td></tr><tr><td>From first symptom to progression of CXR</td><td align="char">6.55 ± 2.95</td><td align="char">2.88 ± 2.3</td><td>< 0.0001</td></tr><tr><td>From first symptom to resolution of CXR</td><td align="char">19.25 ± 9.03</td><td align="char">11.09 ± 8.04</td><td>0.0001</td></tr></tbody></table><table-wrap-foot><fn><p>Note: Number in parentheses is the percentage.</p></fn></table-wrap-foot></table-wrap></p><p>All but 1 (52/53, 98%) SARS patient eventually had an abnormal chest X-ray. On presentation, 14 patients already had multifocal involvement. Of the remaining 38, two-thirds (24/38, 63%) initially (either on admission or once the chest X-ray became abnormal) had a unifocal lesion. All but 2 of these patients progressed to multifocal involvement. The remaining one-third (14/38, 37%) had multifocal infiltrates as the first chest X-ray abnormality observed after admission. The infiltrates remained unilateral (either uni- or multifocal) in 13 patients (25%) and were bilateral (either initially or on progression) in 39 patients (75%). Pneumothorax or pneumomediastinum developed in 5 of the 53 SARS patients (9%), 3 of whom were mechanically ventilated and eventually died.</p><p>In the non-SARS patients, 26 of 31 had X-ray abnormalities on admission. The lesions were unifocal in 11 (42%) and multifocal in 15 (58%). Among the latter 15, 3 had unilateral and 12 bilateral lung involvement. In contrast to the SARS patients, the non-SARS patients’ serial X-ray studies did not have progression of unifocal to multifocal infiltrates. No non-SARS patient had a pneumothorax or pneumomediastinum.</p><p>All except 1 of the 22 SARS patients with an initially normal chest X-ray study eventually developed abnormalities (mean FD 5 ± 3.44). No non-SARS patient with an initially negative chest X-ray developed abnormalities on follow-up films.</p></sec><sec><title>Laboratory findings (<xref rid="tbl5" ref-type="table">Table 5</xref>)</title><p>Two-thirds of the SARS patients for whom we had data (30/43, 70%) had lymphopenia on the first day of hospitalization. The absolute lymphocyte count decreased, as the disease progressed, to less than 1.0 × 10<sup>9</sup>/L after FD 4. Ninety-five percent of hospitalized SARS patients were initially or became lymphopenic during hospitalization. Nearly one-third of the non-SARS patients (9/31, 29%) had lymphopenia initially and (6/25, 24%) developed lymphopenia during hospitalization (<italic>p</italic> < 0.0001 comparing SARS with non-SARS initially and during the hospital course).</p><p>One-third of the SARS patients for whom data were available (12/43, 28%) had thrombocytopenia on presentation, and a total of 16 of 40 had thrombocytopenia during hospitalization. In most cases, the low platelet counts were near the lower limit of normal and usually returned to normal during the course of the disease. None of the non-SARS patients had thrombocytopenia either initially or during their hospital course (<italic>p</italic> < 0.0001 comparing SARS with non-SARS initially and during the hospital course).</p><p>LDH elevation was found in half of the SARS patients tested (23/40, 58%) on presentation and in most (35/40, 88%) at some point in the hospital course. It increased to a mean (SD) highest value of 445 ± 184 IU/L as the disease progressed at an average of FD 5. Among non-SARS patients, about one-third of patients (8/27, 30%) tested initially and half eventually (10/24, 43%) had LDH elevation (<italic>p</italic> < 0.0001 comparing SARS with non-SARS initially and during the hospital course).</p><p>In the SARS group, 40 of 47 patients tested (85%) had a positive SARS-CoV RT-PCR and Q-PCR compared with none of the non-SARS patients (29 negative of 29 tested) (<italic>p</italic> < 0.0001).</p></sec><sec><title>Feasibility analysis of additional parameters</title><p>In our series, the WHO case definition had a positive predictive value (PPV) for SARS of only 63% (<xref rid="bib4" ref-type="bibr">4</xref>). <xref rid="tbl6" ref-type="table">Table 6</xref>, <xref rid="tbl7" ref-type="table">Table 7</xref>show how the PPV changes with exclusion of various other factors.<table-wrap position="float" id="tbl6"><label>Table 6</label><caption><p>Positive Predictive Values and False Negative Changes with Exclusions of Various Factors</p></caption><table frame="hsides" rules="groups"><thead><tr><th rowspan="2" align="center">Exclusion factors</th><th colspan="3" align="center">Positive Predictive Value<hr></hr></th><th colspan="3" align="center">False Negative<hr></hr></th></tr><tr><th align="center">Before (%)</th><th align="center">After (%)</th><th align="center"><italic>p</italic></th><th align="center">Before (%)</th><th align="center">After (%)</th><th align="center"><italic>p</italic></th></tr></thead><tbody><tr><td>No fever on the first day of symptoms.</td><td>63</td><td>91</td><td>< 0.0001</td><td>0</td><td>1</td><td>0.5000</td></tr><tr><td>Cough/dyspnea on the first day of symptoms.</td><td>63</td><td>91</td><td>< 0.0001</td><td>0</td><td>2</td><td>0.2487</td></tr><tr><td>Patients with preexisting cardiopulmonary disease who had cough/dyspnoea on the first day of symptoms.</td><td>63</td><td>80</td><td>0.0082</td><td>0</td><td>2</td><td>0.2487</td></tr><tr><td>Patients without preexisting cardiopulmonary disease who had cough/dyspnoea on the first day of symptoms.</td><td>63</td><td>83</td><td>0.0015</td><td>0</td><td>0</td><td>1</td></tr><tr><td>Initial leukocytosis</td><td>63</td><td>71</td><td>0.2341</td><td>0</td><td>7</td><td>0.0070</td></tr><tr><td>Initial leukopenia</td><td>63</td><td>60</td><td>0.6663</td><td>0</td><td>12</td><td>0.0002</td></tr><tr><td>Initial lymphopenia</td><td>63</td><td>42</td><td>0.0031</td><td>0</td><td>44</td><td>< 0.0001</td></tr><tr><td>Initial thrombocytopenia</td><td>63</td><td>55</td><td>0.2549</td><td>0</td><td>18</td><td>< 0.0001</td></tr><tr><td>Initial elevated LDH</td><td>63</td><td>50</td><td>0.0661</td><td>0</td><td>37</td><td>< 0.0001</td></tr><tr><td>Initial elevated CK</td><td>63</td><td>60</td><td>0.6663</td><td>0</td><td>12</td><td>0.0002</td></tr><tr><td>Initial elevated AST</td><td>63</td><td>61</td><td>0.7732</td><td>0</td><td>17</td><td>< 0.0001</td></tr><tr><td>Initial negative CXR</td><td>63</td><td>54</td><td>0.2010</td><td>0</td><td>26</td><td>< 0.0001</td></tr><tr><td>Airspace opacity on initial CXR</td><td>63</td><td>42</td><td>0.0031</td><td>0</td><td>50</td><td>< 0.0001</td></tr><tr><td>Pleural effusion on initial CXR</td><td>63</td><td>68</td><td>0.4621</td><td>0</td><td>0</td><td>1</td></tr></tbody></table></table-wrap><table-wrap position="float" id="tbl7"><label>Table 7</label><caption><p>Positive Predictive Values and False Negative Rates for SARS with Exclusion of Various Factors</p></caption><table frame="hsides" rules="groups"><thead><tr><th align="left">Increased PPV</th><th align="left">Decreased PPV</th><th align="left">No significant change in PPV</th></tr><tr><th align="left">Decreased FN</th><th align="left">Increased FN</th><th align="left">No FN</th></tr></thead><tbody><tr><td>No fever on first day of symptoms.</td><td>Initial lymphopenia</td><td>Pleural effusion (initial CXR)</td></tr><tr><td></td><td>Initial leukopenia<xref rid="tblfn12" ref-type="table-fn">⁎</xref></td><td></td></tr><tr><td>Cough/dyspnea on first day of symptoms.</td><td>Initial leukocytosis <xref rid="tblfn13" ref-type="table-fn">⁎⁎</xref></td><td></td></tr><tr><td></td><td>Initial thrombocytopenia</td><td></td></tr><tr><td>Patients with pre-existing cardiopulmonary disease</td><td>Initial elevated LDH</td><td></td></tr><tr><td></td><td>Initial elevated CK who had cough/dyspnea</td><td></td></tr><tr><td></td><td>Initial elevated GOT on first day of symptoms.</td><td></td></tr><tr><td></td><td>Airspace opacity (initial CXR)<xref rid="tblfn13" ref-type="table-fn">⁎⁎</xref></td><td></td></tr><tr><td>Patients without pre-existing cardiopulmonary disease</td><td>Negative initial CXR</td><td></td></tr><tr><td></td><td></td><td></td></tr><tr><td>who had cough/dyspnea on the first day of Symptoms.<xref rid="tblfn14" ref-type="table-fn">†</xref></td><td></td><td></td></tr><tr><td></td><td></td><td></td></tr></tbody></table><table-wrap-foot><fn><p>PPV = Positive Predictive Value; FN = False Negative.</p></fn></table-wrap-foot><table-wrap-foot><fn id="tblfn12"><label>⁎</label><p>No significantly increase in PPV but significantly increased FN for SARS.</p></fn></table-wrap-foot><table-wrap-foot><fn id="tblfn13"><label>⁎⁎</label><p>Very significantly decreased PPV and increased FN for SARS.</p></fn></table-wrap-foot><table-wrap-foot><fn id="tblfn14"><label>†</label><p>Increased PPV but no false positives.</p></fn></table-wrap-foot></table-wrap></p></sec></sec><sec><title>Discussion</title><p>We have described the clinical course and findings in a set of patients in whom the diagnosis of SARS is fairly certain and a group of non-SARS patients who had other diagnoses sufficient to account for their symptoms. Case series published during the outbreak most likely included some patients with diseases other than SARS, but it was difficult to separate the diagnoses at that point in the epidemic (<xref rid="bib6" ref-type="bibr">6</xref>). The disease pattern we have delineated for SARS and non-SARS should be useful for comparison with other series of patients with confirmed diagnoses.</p><p>Other respiratory viral infections (such as influenza) are known to manifest with the abrupt onset of systemic symptoms including fever, chills, myalgia, headache or malaise. Respiratory complaints often become more prominent as systemic symptoms subside (<xref rid="bib7" ref-type="bibr">7</xref>). In our series, fever was the sole initial symptom in SARS patients with 3 exceptions. Two patients also had cough and dyspnea at fever onset, but they both had already had those symptoms for years, related to underlying disease. The other exception was the 10-year-old girl who was part of a family cluster. It will be important to look at the course of the disease in other children to see if fever is less prominent in that age group than we found it to be in our adults with SARS. Others have also reported fever as an early sign in almost all patients with SARS (<xref rid="bib8" ref-type="bibr">8</xref>, <xref rid="bib9" ref-type="bibr">9</xref>, <xref rid="bib10" ref-type="bibr">10</xref>, <xref rid="bib11" ref-type="bibr">11</xref>, <xref rid="bib12" ref-type="bibr">12</xref>, <xref rid="bib13" ref-type="bibr">13</xref>). Although it has been noted that fever may be absent in elderly patients, we did not observe this in any of our patients (<xref rid="bib10" ref-type="bibr">10</xref>). Among the non-SARS patients, only 5 (16%) complained of fever as the earliest symptom.</p><p>Although cough and dyspnea were very common in SARS patients, they did not appear as early as did the high fever, with the exception of the 2 patients noted above. By contrast, 84% of non-SARS patients had cough or dyspnea preceding their fever. This suggests that, in the absence of an underlying cardiopulmonary disease, patients presenting with a cough that precedes or is concurrent with a high fever are less likely to have SARS.</p><p>Diarrhea was more common in SARS patients than in those with non-SARS illnesses, and it started in the former only after the onset of high fever. Fever to this degree is less common in other viral infections that cause similar abdominal symptoms. Coronaviruses are known to cause both respiratory and enteric diseases of humans and domestic animals (<xref rid="bib14" ref-type="bibr">14</xref>, <xref rid="bib15" ref-type="bibr">15</xref>). However, abdominal symptoms alone do not seem to be sufficient to discriminate between SARS and non-SARS.</p><p>In a series reported from Hong Kong, 20% of patients with SARS had normal chest X-ray studies on initial presentation, compared with 41% in our series (<xref rid="bib16" ref-type="bibr">16</xref>, <xref rid="bib17" ref-type="bibr">17</xref>). This discrepancy may be because in most cases we did not perform conventional or high-resolution computed tomography (HRCT) imaging. However, all but 1 patient eventually had abnormal X-rays. (This patient contracted the disease from her husband who died of SARS. Serial X-rays and an HRCT of the thorax were all negative.) An initially negative chest radiograph thus cannot exclude SARS. Serial films should be done if SARS is suspected. We found that abnormalities appeared by a mean of FD 5, with a range of 2 to 8 days.</p><p>Overall, SARS patients were more likely than non-SARS patients to have air-space opacities (80% vs. 50%, respectively, <italic>p</italic> < 0.0001) on the initial chest X-ray study. A series in Hong Kong also reported airspace infiltrates in 78% of SARS patients (<xref rid="bib15" ref-type="bibr">15</xref>). However, the appearance of the initial film alone cannot differentiate SARS from non-SARS. None of our SARS patients had pleural effusion, cavitation or hilar lymphadenopathy, in agreement with other series (<xref rid="bib8" ref-type="bibr">8</xref>, <xref rid="bib16" ref-type="bibr">16</xref>, <xref rid="bib17" ref-type="bibr">17</xref>). In contrast, 23% of our non-SARS patients did have pleural effusion, a statistically significant difference.</p><p>Of perhaps greater use as a discriminatory feature is the relatively common pattern in SARS of progression of air-space opacities from unifocal to multifocal, found in our series as well as others (<xref rid="bib8" ref-type="bibr">8</xref>, <xref rid="bib16" ref-type="bibr">16</xref>). This contrasted with a lack of such progression in non-SARS (<italic>p</italic> < 0.0001). This particular factor will not help to discriminate between SARS and non-SARS on admission, but rapid progression of the radiographic abnormalities over several days may help confirm the diagnosis of SARS. Although pneumothorax or pneumomediastinum occurred in 5 of 53 SARS patients, none of the non-SARS patients had these complications (<italic>p</italic> = 0.0016). A possible explanation for this is that SARS-affected lungs may be less compliant and therefore more subject to barotrauma.</p><p>Many SARS patients had prominent pulmonary function impairment and residual pulmonary fibrosis at discharge from hospital. However, after 2 months of follow-up, their pulmonary function and pulmonary fibrosis had improved (data not shown). This implies that SARS-induced radiographic features suggested by early publication as fibrosis could in fact be viral pneumonitis and may resolve completely without leaving permanent damage (<xref rid="bib18" ref-type="bibr">18</xref>).</p><p>Leukopenia (34%), lymphopenia (70%), and thrombocytopenia (45%) are non-specific but may suggest SARS (<xref rid="bib8" ref-type="bibr">8</xref>). In our series, we found that SARS patients were more likely to have a normal or decreased leukocyte count on presentation, along with lymphocytopenia and thrombocytopenia, whereas those with non-SARS generally had normal or elevated white cell counts and normal lymphocyte and platelet counts (<xref rid="tbl5" ref-type="table">Table 5</xref>). There is quite a bit of overlap in these findings, but results at one end of the extreme or the other may add to the evidence for or against SARS.<table-wrap position="float" id="tbl5"><label>Table 5</label><caption><p>Laboratory Changes in SARS and Non-SARS</p></caption><table frame="hsides" rules="groups"><thead><tr><th rowspan="2" align="center">Laboratory findings</th><th colspan="3" align="center">Initial Laboratory Findings<hr></hr></th><th colspan="3" align="center">During Hospitalization<hr></hr></th></tr><tr><th align="center">SARS (n = 53)</th><th align="center">Non-SARS (n = 31)</th><th align="center"><italic>p</italic> Value</th><th align="center">SARS (n = 53)</th><th align="center">Non-SARS (n = 31)</th><th align="center"><italic>p</italic> Value</th></tr></thead><tbody><tr><td>Hematology</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><td> Mean (SD) total Leukocyte count (× 10<sup>9</sup>/L)</td><td align="char">6.68 ± 3.26</td><td align="char">10.16 ± 4.59</td><td>0.0008</td><td></td><td></td><td></td></tr><tr><td> Leukopenia<xref rid="tblfn5" ref-type="table-fn">⁎</xref></td><td>10/53 (19)</td><td>2/31 (6)</td><td>0.0057</td><td></td><td></td><td></td></tr><tr><td> Leukocytosis<xref rid="tblfn6" ref-type="table-fn">⁎⁎</xref></td><td>6/53 (11)</td><td>12/31 (39)</td><td>< 0.0001</td><td></td><td></td><td></td></tr><tr><td> Normal leukocyte Counts<xref rid="tblfn7" ref-type="table-fn">†</xref></td><td>37/53 (70)</td><td>17/31 (55)</td><td>0.0298</td><td></td><td></td><td></td></tr><tr><td> Mean (SD) Lymphocyte count (× 10<sup>9</sup>/L)</td><td align="char">0.8 ± 0.47</td><td align="char">1.82 ± 1.69</td><td>0.0026</td><td></td><td></td><td></td></tr><tr><td> Lymphopenia<xref rid="tblfn11a" ref-type="table-fn">‡</xref></td><td>30/43 (70)</td><td>9/31(29)</td><td>< 0.0001</td><td>38/40 (95)</td><td>6/25 (24)</td><td>< 0.0001</td></tr><tr><td> Thrombocytopenia<xref rid="tblfn8" ref-type="table-fn">§</xref></td><td>12/43 (28)</td><td align="center">0</td><td>< 0.0001</td><td>16/40 (40)</td><td align="center">0</td><td>< 0.0001</td></tr><tr><td>Biochemistry</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><td> Elevated LDH<xref rid="tblfn9" ref-type="table-fn">∥</xref></td><td>23/40 (58)</td><td>8/27(30)</td><td>< 0.0001</td><td>35/40 (88)</td><td>10/24 (43)</td><td>< 0.0001</td></tr><tr><td> Elevated CK <xref rid="tblfn10" ref-type="table-fn">¶</xref></td><td>7/39 (18)</td><td>2/30 (7)</td><td>< 0.02</td><td>12/37 (32)</td><td>4/27 (15)</td><td>0.0072</td></tr><tr><td> Elevated AST<xref rid="tblfn11" ref-type="table-fn">#</xref></td><td>11/41 (27)</td><td>6/30 (20)</td><td>< 0.3170</td><td>19/39 (49)</td><td>9/27 (33)</td><td>0.0308</td></tr></tbody></table><table-wrap-foot><fn><p>Note: Number in parentheses is the percentage.</p></fn></table-wrap-foot><table-wrap-foot><fn id="tblfn5"><label>⁎</label><p>Total leukocyte count is < 4 × 10<sup>9</sup>/L.</p></fn></table-wrap-foot><table-wrap-foot><fn id="tblfn6"><label>⁎⁎</label><p>Total leukocyte count is > 10 × 10<sup>9</sup>/L.</p></fn></table-wrap-foot><table-wrap-foot><fn id="tblfn7"><label>†</label><p>Total leukocyte count is 4–10 × 10<sup>9</sup>/L.</p></fn></table-wrap-foot><table-wrap-foot><fn id="tblfn8"><label>§</label><p>Platelet count is less than 130 × 10<sup>9</sup>/L.</p></fn></table-wrap-foot><table-wrap-foot><fn id="tblfn9"><label>∥</label><p>LDH (Lactase dehydrogenase) level is > 200 U/L.</p></fn></table-wrap-foot><table-wrap-foot><fn id="tblfn10"><label>¶</label><p>CK (Creatine Kinase) level is > 232 U/L.</p></fn></table-wrap-foot><table-wrap-foot><fn id="tblfn11"><label>#</label><p>AST (Aspartase aminotransferase) level is > 45 U/L.</p></fn></table-wrap-foot><table-wrap-foot><fn id="tblfn11a"><label>‡</label><p>Lymphocyte count is less than 1.0 × 10<sup>9</sup>/L.</p></fn></table-wrap-foot></table-wrap></p><p>Lymphopenia in SARS may be due to apoptosis or the use of glucocorticoids or stimulation of the hypothalamic-pituitary-adrenal axis (<xref rid="bib19" ref-type="bibr">19</xref>, <xref rid="bib20" ref-type="bibr">20</xref>). In our series, on admission, 70% of SARS patients tested had lymphopenia, at a time when they had not yet received any steroid therapy. At some point in their illness, 95% of our patients who were tested were lymphopenic, but a number had received glucocorticoids. It is therefore unclear if the development or persistence of lymphopenia in our patients was a result of the disease or of the treatment.</p><p>Although elevations of LDH and CK were statistically more common in SARS than non-SARS, these are unlikely by themselves to provide adequate discrimination, given the degree of overlap. However, they may be helpful in combination with other findings.</p><p>In our series, RT-PCR for SARS-CoV was positive in 85% of the patients tested. We believe the 7 negative results were false negatives. However, the possibility of false positives and negatives with the tests used in the recent epidemic implies that we still need better means for differentiating SARS from non-SARS.</p></sec><sec><title>Conclusion</title><p>According to our findings in SARS and non-SARS, a high fever (> 38°C) that precedes the onset of cough by several days; an initially normal or decreased leukocyte count; lymphopenia and thrombocytopenia; elevated LDH; and air space opacities on initial chest X-rays are suggestive of SARS. If these features are present along with a positive PCR for SARS-CoV, we can be fairly confident of the diagnosis of SARS. For patients whose initial presentation is not so clear, rapid progression of chest X-ray abnormalities, particularly with changes from uni- to multifocal or uni- to bilateral infiltrates is also strong evidence of SARS. These clinical patterns are particularly important if PCR testing is not available. However, further comparison with other series of patients with confirmed SARS and non-SARS is necessary to ascertain important discriminatory features.</p></sec></body><back><ref-list><title>References</title><ref id="bib1"><label>1</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Ksiazek</surname><given-names>T.G.</given-names></name><name><surname>Erdman</surname><given-names>D.</given-names></name><name><surname>Goldsmith</surname><given-names>C.</given-names></name></person-group><article-title>A novel coronavirus associated with severe acute respiratory syndrome</article-title><source>N Engl J Med</source><volume>348</volume><year>2003</year><fpage>1953</fpage><lpage>1966</lpage><pub-id pub-id-type="pmid">12690092</pub-id></element-citation></ref><ref id="bib2"><label>2</label><mixed-citation publication-type="other">Centers for Diseases Control and Prevention. SARS coronavirus sequencing. Available at: <ext-link ext-link-type="uri" xlink:href="http://www.cdc.gov/ncidod/sars/sequence.htm">http://www.cdc.gov/ncidod/sars/sequence.htm</ext-link> Accessed July 13, 2004.</mixed-citation></ref><ref id="bib3"><label>3</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Peiris</surname><given-names>J.S.M.</given-names></name><name><surname>Lai</surname><given-names>S.T.</given-names></name><name><surname>Poon</surname><given-names>L.L.M.</given-names></name></person-group><article-title>Coronavirus as a possible cause of severe acute respiratory syndrome</article-title><source>Lancet</source><volume>361</volume><year>2003</year><fpage>1319</fpage><lpage>1325</lpage><pub-id pub-id-type="pmid">12711465</pub-id></element-citation></ref><ref id="bib4"><label>4</label><element-citation publication-type="book"><person-group person-group-type="author"><collab>World Health Organization</collab></person-group><source>Case definitions for surveillance of severe acute respiratory syndrome (SARS)</source><year>2003</year><publisher-name>WHO</publisher-name><publisher-loc>Geneva</publisher-loc><comment>revised 1 May, Available at: <ext-link ext-link-type="uri" xlink:href="http://www.who.int/crs/sars/casedefinition">http://www.who.int/crs/sars/casedefinition</ext-link>Accessed July 12, 2004.</comment></element-citation></ref><ref id="bib5"><label>5</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Drosten</surname><given-names>C.</given-names></name><name><surname>Gunther</surname><given-names>S.</given-names></name><name><surname>Preiser</surname><given-names>W.</given-names></name></person-group><article-title>Identification of a novel coronavirus in patients with severe acute respiratory syndrome</article-title><source>N Engl J Med</source><volume>348</volume><year>2003</year><fpage>1967</fpage><lpage>1976</lpage><pub-id pub-id-type="pmid">12690091</pub-id></element-citation></ref><ref id="bib6"><label>6</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Hon</surname><given-names>K.L.E.</given-names></name><name><surname>Li</surname><given-names>A.M.</given-names></name><name><surname>Cheng</surname><given-names>F.W.T.</given-names></name></person-group><article-title>Personal view of SARS: confusing definition, confusing diagnoses</article-title><source>Lancet</source><volume>361</volume><year>2003</year><fpage>1984</fpage><lpage>1985</lpage><pub-id pub-id-type="pmid">12801758</pub-id></element-citation></ref><ref id="bib7"><label>7</label><element-citation publication-type="book"><person-group person-group-type="author"><name><surname>Dolin</surname><given-names>R.</given-names></name></person-group><chapter-title>Influenza</chapter-title><person-group person-group-type="editor"><name><surname>Braunwald</surname><given-names>E.</given-names></name><name><surname>Fauci</surname><given-names>A.S.</given-names></name><name><surname>Kasper</surname><given-names>D.L.</given-names></name></person-group><source>Harrison’s principles of internal medicine</source><edition>15<sup>th</sup> edn</edition><year>2001</year><publisher-name>McGraw-Hill</publisher-name><publisher-loc>New York, NY</publisher-loc><fpage>1125</fpage><lpage>1130</lpage></element-citation></ref><ref id="bib8"><label>8</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Lee</surname><given-names>N.</given-names></name><name><surname>Hui</surname><given-names>D.</given-names></name><name><surname>Wu</surname><given-names>A.</given-names></name></person-group><article-title>A major out-break of severe acute respiratory syndrome in Hong Kong</article-title><source>N Engl J Med</source><volume>348</volume><year>2003</year><fpage>1986</fpage><lpage>1994</lpage><pub-id pub-id-type="pmid">12682352</pub-id></element-citation></ref><ref id="bib9"><label>9</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Poutanen</surname><given-names>S.M.</given-names></name><name><surname>Low</surname><given-names>D.E.</given-names></name><name><surname>Henry</surname><given-names>B.</given-names></name></person-group><article-title>Identification of severe acute respiratory syndrome in Canada</article-title><source>N Engl J Med</source><volume>348</volume><year>2003</year><fpage>1995</fpage><lpage>2005</lpage><pub-id pub-id-type="pmid">12671061</pub-id></element-citation></ref><ref id="bib10"><label>10</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Tomlinson</surname><given-names>B.</given-names></name><name><surname>Cockram</surname><given-names>C.</given-names></name></person-group><article-title>SARS: experience at Prince of Wales Hospital, Hong Kong</article-title><source>Lancet</source><volume>361</volume><year>2003</year><fpage>1486</fpage><lpage>1487</lpage><pub-id pub-id-type="pmid">12737853</pub-id></element-citation></ref><ref id="bib11"><label>11</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Hon</surname><given-names>K.L.E.</given-names></name><name><surname>Leung</surname><given-names>C.W.</given-names></name><name><surname>Cheng</surname><given-names>W.T.F.</given-names></name></person-group><article-title>Clinical presentations and outcome of severe acute respiratory syndrome in children</article-title><source>Lancet</source><volume>361</volume><year>2003</year><fpage>1701</fpage><lpage>1703</lpage><pub-id pub-id-type="pmid">12767737</pub-id></element-citation></ref><ref id="bib12"><label>12</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Booth</surname><given-names>C.M.</given-names></name><name><surname>Matukas</surname><given-names>L.M.</given-names></name><name><surname>Tomlinson</surname><given-names>G.A.</given-names></name></person-group><article-title>Clinical features and short-term outcomes of 144 patients with SARS in the greater Toronto area</article-title><source>JAMA</source><volume>289</volume><year>2003</year><fpage>2801</fpage><lpage>2809</lpage><pub-id pub-id-type="pmid">12734147</pub-id></element-citation></ref><ref id="bib13"><label>13</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Avendano</surname><given-names>M.</given-names></name><name><surname>Derkach</surname><given-names>P.</given-names></name><name><surname>Swan</surname><given-names>S.</given-names></name></person-group><article-title>Clinical course and management of SARS in health care workers in Toronto: a case series</article-title><source>CMAJ</source><volume>168</volume><year>2003</year><fpage>1649</fpage><lpage>1660</lpage><pub-id pub-id-type="pmid">12821618</pub-id></element-citation></ref><ref id="bib14"><label>14</label><element-citation publication-type="book"><person-group person-group-type="author"><name><surname>Siddell</surname><given-names>S.G.</given-names></name><name><surname>Snijder</surname><given-names>E.J.</given-names></name></person-group><chapter-title>Coronaviruses, toroviruses, and arteriviruses</chapter-title><person-group person-group-type="editor"><name><surname>Mahy</surname><given-names>B.W.J.</given-names></name><name><surname>Collier</surname><given-names>L.</given-names></name></person-group><source>Tropley and Wilson’s microbiology and microbial infections</source><year>1998</year><publisher-name>Edward Arnold</publisher-name><publisher-loc>London</publisher-loc><fpage>463</fpage><lpage>484</lpage></element-citation></ref><ref id="bib15"><label>15</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Wege</surname><given-names>H.</given-names></name><name><surname>Siddell</surname><given-names>S.</given-names></name><name><surname>ter Meulen</surname><given-names>V.</given-names></name></person-group><article-title>The biology and pathogenesis of coronaviruses</article-title><source>Curr Top Microbiol Immunol</source><volume>99</volume><year>1982</year><fpage>165</fpage><lpage>200</lpage><pub-id pub-id-type="pmid">6178564</pub-id></element-citation></ref><ref id="bib16"><label>16</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Wong</surname><given-names>K.T.</given-names></name><name><surname>Antonio</surname><given-names>G.E.</given-names></name><name><surname>Hui</surname><given-names>D.S.C.</given-names></name></person-group><article-title>Severe acute respiratory syndrome: radiographic appearances and pattern of progression in 138 patients</article-title><source>Radiology</source><volume>228</volume><year>2003</year><fpage>401</fpage><lpage>406</lpage><pub-id pub-id-type="pmid">12759474</pub-id></element-citation></ref><ref id="bib17"><label>17</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Wong</surname><given-names>G.W.K.</given-names></name><name><surname>Hui</surname><given-names>D.S.C.</given-names></name></person-group><article-title>Severe acute respiratory syndrome (SARS): epidemiology, diagnosis and management</article-title><source>Thorax</source><volume>58</volume><year>2003</year><fpage>558</fpage><lpage>560</lpage><pub-id pub-id-type="pmid">12832664</pub-id></element-citation></ref><ref id="bib18"><label>18</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Antonio</surname><given-names>G.E.</given-names></name><name><surname>Wong</surname><given-names>K.T.</given-names></name><name><surname>Hui</surname><given-names>D.S.</given-names></name></person-group><article-title>Thin-section CT in patients with severe acute respiratory syndrome following hospital discharge</article-title><source>Radiology</source><volume>228</volume><year>2003</year><fpage>810</fpage><lpage>815</lpage><pub-id pub-id-type="pmid">12805557</pub-id></element-citation></ref><ref id="bib19"><label>19</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>O’Donnell</surname><given-names>D.R.O.</given-names></name><name><surname>Tasker</surname><given-names>R.C.</given-names></name><name><surname>Roe</surname><given-names>M.F.E.</given-names></name></person-group><article-title>SARS: understanding the coronavirus: apoptosis may explain lymphopenia of SARS</article-title><source>BMJ</source><volume>327</volume><year>2003</year><fpage>620</fpage></element-citation></ref><ref id="bib20"><label>20</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Panesar</surname><given-names>N.S.</given-names></name></person-group><article-title>Lymphopenia in SARS</article-title><source>Lancet</source><volume>361</volume><year>2003</year><fpage>1985</fpage></element-citation></ref></ref-list><ack><title>Acknowledgments</title><p>We thank Dr. Chin-Yin Sheu, Chairman of the Radiology Department, Mackay Memorial Hospital, for reviewing the X-rays and Dr. Mary Jeanne Buttrey, Consulting Physician, Department of Internal Medicine, Mackay Memorial Hospital, for critical review and revision of the manuscript. This study was partly supported by the Taiwan National Science Council (Grant No. NSC92-2751-B-195-001-Y) and National SARS Research Program (SCLI01).</p></ack></back></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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