Pregnancy loss and role of infant HIV status on perinatal mortality among HIV-infected women
Identifieur interne : 001289 ( Pmc/Curation ); précédent : 001288; suivant : 001290Pregnancy loss and role of infant HIV status on perinatal mortality among HIV-infected women
Auteurs : Hae-Young Kim [États-Unis] ; Prisca Kasonde [Zambie] ; Mwiya Mwiya [Zambie] ; Donald M. Thea [États-Unis] ; Chipepo Kankasa [Zambie] ; Moses Sinkala [Zambie] ; Grace Aldrovandi [États-Unis] ; Louise Kuhn [États-Unis]Source :
- BMC Pediatrics [ 1471-2431 ] ; 2012.
Abstract
HIV-infected women, particularly those with advanced disease, may have higher rates of pregnancy loss (miscarriage and stillbirth) and neonatal mortality than uninfected women. Here we examine risk factors for these adverse pregnancy outcomes in a cohort of HIV-infected women in Zambia considering the impact of infant HIV status.
A total of 1229 HIV-infected pregnant women were enrolled (2001–2004) in Lusaka, Zambia and followed to pregnancy outcome. Live-born infants were tested for HIV by PCR at birth, 1 week and 5 weeks. Obstetric and neonatal data were collected after delivery and the rates of neonatal (<28 days) and early mortality (<70 days) were described using Kaplan-Meier methods.
The ratio of miscarriage and stillbirth per 100 live-births were 3.1 and 2.6, respectively. Higher maternal plasma viral load (adjusted odds ratio [AOR] for each log10 increase in HIV RNA copies/ml = 1.90; 95% confidence interval [CI] 1.10–3.27) and being symptomatic were associated with an increased risk of stillbirth (AOR = 3.19; 95% CI 1.46–6.97), and decreasing maternal CD4 count by 100 cells/mm3 with an increased risk of miscarriage (OR = 1.25; 95% CI 1.02–1.54). The neonatal mortality rate was 4.3 per 100 increasing to 6.3 by 70 days. Intrauterine HIV infection was not associated with neonatal morality but became associated with mortality through 70 days (adjusted hazard ratio = 2.76; 95% CI 1.25–6.08). Low birth weight and cessation of breastfeeding were significant risk factors for both neonatal and early mortality independent of infant HIV infection.
More advanced maternal HIV disease was associated with adverse pregnancy outcomes. Excess neonatal mortality in HIV-infected women was not primarily explained by infant HIV infection but was strongly associated with low birth weight and prematurity. Intrauterine HIV infection contributed to mortality as early as 70 days of infant age. Interventions to improve pregnancy outcomes for HIV-infected women are needed to complement necessary therapeutic and prophylactic antiretroviral interventions.
Url:
DOI: 10.1186/1471-2431-12-138
PubMed: 22937874
PubMed Central: 3480840
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<front><div type="abstract" xml:lang="en"><sec><title>Background</title>
<p>HIV-infected women, particularly those with advanced disease, may have higher rates of pregnancy loss (miscarriage and stillbirth) and neonatal mortality than uninfected women. Here we examine risk factors for these adverse pregnancy outcomes in a cohort of HIV-infected women in Zambia considering the impact of infant HIV status.</p>
</sec>
<sec><title>Methods</title>
<p>A total of 1229 HIV-infected pregnant women were enrolled (2001–2004) in Lusaka, Zambia and followed to pregnancy outcome. Live-born infants were tested for HIV by PCR at birth, 1 week and 5 weeks. Obstetric and neonatal data were collected after delivery and the rates of neonatal (<28 days) and early mortality (<70 days) were described using Kaplan-Meier methods.</p>
</sec>
<sec><title>Results</title>
<p>The ratio of miscarriage and stillbirth per 100 live-births were 3.1 and 2.6, respectively. Higher maternal plasma viral load (adjusted odds ratio [AOR] for each log10 increase in HIV RNA copies/ml = 1.90; 95% confidence interval [CI] 1.10–3.27) and being symptomatic were associated with an increased risk of stillbirth (AOR = 3.19; 95% CI 1.46–6.97), and decreasing maternal CD4 count by 100 cells/mm<sup>3</sup>
with an increased risk of miscarriage (OR = 1.25; 95% CI 1.02–1.54). The neonatal mortality rate was 4.3 per 100 increasing to 6.3 by 70 days. Intrauterine HIV infection was not associated with neonatal morality but became associated with mortality through 70 days (adjusted hazard ratio = 2.76; 95% CI 1.25–6.08). Low birth weight and cessation of breastfeeding were significant risk factors for both neonatal and early mortality independent of infant HIV infection.</p>
</sec>
<sec><title>Conclusions</title>
<p>More advanced maternal HIV disease was associated with adverse pregnancy outcomes. Excess neonatal mortality in HIV-infected women was not primarily explained by infant HIV infection but was strongly associated with low birth weight and prematurity. Intrauterine HIV infection contributed to mortality as early as 70 days of infant age. Interventions to improve pregnancy outcomes for HIV-infected women are needed to complement necessary therapeutic and prophylactic antiretroviral interventions.</p>
</sec>
</div>
</front>
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<pmc article-type="research-article" xml:lang="en"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">BMC Pediatr</journal-id>
<journal-id journal-id-type="iso-abbrev">BMC Pediatr</journal-id>
<journal-title-group><journal-title>BMC Pediatrics</journal-title>
</journal-title-group>
<issn pub-type="epub">1471-2431</issn>
<publisher><publisher-name>BioMed Central</publisher-name>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">22937874</article-id>
<article-id pub-id-type="pmc">3480840</article-id>
<article-id pub-id-type="publisher-id">1471-2431-12-138</article-id>
<article-id pub-id-type="doi">10.1186/1471-2431-12-138</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject>
</subj-group>
</article-categories>
<title-group><article-title>Pregnancy loss and role of infant HIV status on perinatal mortality among HIV-infected women</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" id="A1"><name><surname>Kim</surname>
<given-names>Hae-Young</given-names>
</name>
<xref ref-type="aff" rid="I1">1</xref>
<xref ref-type="aff" rid="I2">2</xref>
<email>hk2553@columbia.edu</email>
</contrib>
<contrib contrib-type="author" id="A2"><name><surname>Kasonde</surname>
<given-names>Prisca</given-names>
</name>
<xref ref-type="aff" rid="I3">3</xref>
<email>pkasonde@fhi.org</email>
</contrib>
<contrib contrib-type="author" id="A3"><name><surname>Mwiya</surname>
<given-names>Mwiya</given-names>
</name>
<xref ref-type="aff" rid="I3">3</xref>
<email>mwiya2002@yahoo.com</email>
</contrib>
<contrib contrib-type="author" id="A4"><name><surname>Thea</surname>
<given-names>Donald M</given-names>
</name>
<xref ref-type="aff" rid="I4">4</xref>
<email>dthea@bu.edu</email>
</contrib>
<contrib contrib-type="author" id="A5"><name><surname>Kankasa</surname>
<given-names>Chipepo</given-names>
</name>
<xref ref-type="aff" rid="I3">3</xref>
<email>ckankasa@zamnet.zm</email>
</contrib>
<contrib contrib-type="author" id="A6"><name><surname>Sinkala</surname>
<given-names>Moses</given-names>
</name>
<xref ref-type="aff" rid="I5">5</xref>
<email>mosessinkala81@msn.com</email>
</contrib>
<contrib contrib-type="author" id="A7"><name><surname>Aldrovandi</surname>
<given-names>Grace</given-names>
</name>
<xref ref-type="aff" rid="I6">6</xref>
<email>galdrovandi@chla.usc.edu</email>
</contrib>
<contrib contrib-type="author" corresp="yes" id="A8"><name><surname>Kuhn</surname>
<given-names>Louise</given-names>
</name>
<xref ref-type="aff" rid="I1">1</xref>
<xref ref-type="aff" rid="I2">2</xref>
<email>lk24@columbia.edu</email>
</contrib>
</contrib-group>
<aff id="I1"><label>1</label>
Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, NY, USA</aff>
<aff id="I2"><label>2</label>
Gertrude H. Sergievsky Center, College of Physicians and Surgeons, Columbia University, 630 W 168th St, New York, NY, USA</aff>
<aff id="I3"><label>3</label>
University Teaching Hospital, University of Zambia, Lusaka, Zambia</aff>
<aff id="I4"><label>4</label>
Center for International Health and Development, Boston University of School of Public Health, Boston, USA</aff>
<aff id="I5"><label>5</label>
Lusaka District Health Management Team, Lusaka, Zambia</aff>
<aff id="I6"><label>6</label>
Department of Pediatrics, Children's Hospital Los Angeles, University of Southern California, Los Angeles, USA</aff>
<pub-date pub-type="collection"><year>2012</year>
</pub-date>
<pub-date pub-type="epub"><day>31</day>
<month>8</month>
<year>2012</year>
</pub-date>
<volume>12</volume>
<fpage>138</fpage>
<lpage>138</lpage>
<history><date date-type="received"><day>7</day>
<month>5</month>
<year>2012</year>
</date>
<date date-type="accepted"><day>17</day>
<month>8</month>
<year>2012</year>
</date>
</history>
<permissions><copyright-statement>Copyright ©2012 Kim et al.; licensee BioMed Central Ltd.</copyright-statement>
<copyright-year>2012</copyright-year>
<copyright-holder>Kim et al.; licensee BioMed Central Ltd.</copyright-holder>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/2.0"><license-p>This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/2.0">http://creativecommons.org/licenses/by/2.0</ext-link>
), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
</license>
</permissions>
<self-uri xlink:href="http://www.biomedcentral.com/1471-2431/12/138"></self-uri>
<abstract><sec><title>Background</title>
<p>HIV-infected women, particularly those with advanced disease, may have higher rates of pregnancy loss (miscarriage and stillbirth) and neonatal mortality than uninfected women. Here we examine risk factors for these adverse pregnancy outcomes in a cohort of HIV-infected women in Zambia considering the impact of infant HIV status.</p>
</sec>
<sec><title>Methods</title>
<p>A total of 1229 HIV-infected pregnant women were enrolled (2001–2004) in Lusaka, Zambia and followed to pregnancy outcome. Live-born infants were tested for HIV by PCR at birth, 1 week and 5 weeks. Obstetric and neonatal data were collected after delivery and the rates of neonatal (<28 days) and early mortality (<70 days) were described using Kaplan-Meier methods.</p>
</sec>
<sec><title>Results</title>
<p>The ratio of miscarriage and stillbirth per 100 live-births were 3.1 and 2.6, respectively. Higher maternal plasma viral load (adjusted odds ratio [AOR] for each log10 increase in HIV RNA copies/ml = 1.90; 95% confidence interval [CI] 1.10–3.27) and being symptomatic were associated with an increased risk of stillbirth (AOR = 3.19; 95% CI 1.46–6.97), and decreasing maternal CD4 count by 100 cells/mm<sup>3</sup>
with an increased risk of miscarriage (OR = 1.25; 95% CI 1.02–1.54). The neonatal mortality rate was 4.3 per 100 increasing to 6.3 by 70 days. Intrauterine HIV infection was not associated with neonatal morality but became associated with mortality through 70 days (adjusted hazard ratio = 2.76; 95% CI 1.25–6.08). Low birth weight and cessation of breastfeeding were significant risk factors for both neonatal and early mortality independent of infant HIV infection.</p>
</sec>
<sec><title>Conclusions</title>
<p>More advanced maternal HIV disease was associated with adverse pregnancy outcomes. Excess neonatal mortality in HIV-infected women was not primarily explained by infant HIV infection but was strongly associated with low birth weight and prematurity. Intrauterine HIV infection contributed to mortality as early as 70 days of infant age. Interventions to improve pregnancy outcomes for HIV-infected women are needed to complement necessary therapeutic and prophylactic antiretroviral interventions.</p>
</sec>
</abstract>
<kwd-group><kwd>Perinatal mortality</kwd>
<kwd>Infant mortality</kwd>
<kwd>Risk factors</kwd>
<kwd>Adverse pregnancy outcome</kwd>
<kwd>HIV infection</kwd>
<kwd>Vertical transmission</kwd>
</kwd-group>
</article-meta>
</front>
</pmc>
</record>
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