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Clinical Malaria Diagnosis in Pregnancy in Relation to Early Perinatal Mother-to-Child-Transmission of HIV: A Prospective Cohort Study

Identifieur interne : 001960 ( Pmc/Corpus ); précédent : 001959; suivant : 001961

Clinical Malaria Diagnosis in Pregnancy in Relation to Early Perinatal Mother-to-Child-Transmission of HIV: A Prospective Cohort Study

Auteurs : Ae Ezeamama ; C. Duggan ; Kp Manji ; D. Spiegelman ; E. Hertzmark ; Rj Bosch ; R. Kupka ; Jo Okuma ; R. Kisenge ; S. Aboud ; Ww Fawzi

Source :

RBID : PMC:4299572

Abstract

Objectives

We prospectively investigated fever symptoms and maternal diagnosis of malaria in pregnancy (MIP) in relation to child HIV infection among 2,368 pregnant HIV-positive women and their infants, followed-up from pregnancy until birth and 6 weeks post-delivery in Tanzania.

Methods

Doctors clinically diagnosed and treated MIP and fever symptoms during prenatal healthcare. Child HIV status was determined via DNA-PCR. Multivariable logistic regression models estimated relative risks (RR) and 95% confidence intervals (CI) for HIV mother-to-child-transmission (MTCT) by 6th week of life.

Results

Mean gestational age at enrollment was 22.2 weeks. During follow-up, 16.6% had ≥1 MIP diagnosis, 15.9% reported fever symptoms and 8.7% had both fever and MIP diagnosis. Eleven percent of HIV-exposed infants were HIV-positive by 6 weeks. The RR of HIV MTCT was statistically similar for infants whose mothers were ever vs. never clinical MIP diagnosed (RR=1.24, 95%CI:0.94–1.64), were diagnosed with 1 vs. 0 clinical MIP episode (RR=1.07;95%CI:0.77–1.48) and had ever vs. never reported fever symptoms (RR=1.04, 95%CI:0.78,1.38) in pregnancy. However, HIV MTCT risk increased by 29% (95%CI:4–58%) per MIP episode. Infants of women with ≥2 vs. 0 MIP diagnoses were 2.1 times more likely to be HIV infected by 6weeks old (95%CI:1.31–3.45).

Conclusions

Clinical MIP diagnosis, but not fevers, in HIV-positive pregnant women was associated with elevated risk of early HIV MTCT suggesting that malaria prevention and treatment in pregnant HIV-positive women may enhance the effectiveness of HIV prevention in MTCT programs in this setting. Future studies using laboratory confirmed malaria is needed to confirm this association.


Url:
DOI: 10.1111/hiv.12111
PubMed: 24215465
PubMed Central: 4299572

Links to Exploration step

PMC:4299572

Le document en format XML

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<nlm:aff id="A5">Department of Epidemiology, HSPH, Boston, MA</nlm:aff>
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<title level="j">HIV medicine</title>
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<div type="abstract" xml:lang="en">
<sec id="S1">
<title>Objectives</title>
<p id="P1">We prospectively investigated fever symptoms and maternal diagnosis of malaria in pregnancy (MIP) in relation to child HIV infection among 2,368 pregnant HIV-positive women and their infants, followed-up from pregnancy until birth and 6 weeks post-delivery in Tanzania.</p>
</sec>
<sec id="S2">
<title>Methods</title>
<p id="P2">Doctors clinically diagnosed and treated MIP and fever symptoms during prenatal healthcare. Child HIV status was determined via DNA-PCR. Multivariable logistic regression models estimated relative risks (RR) and 95% confidence intervals (CI) for HIV mother-to-child-transmission (MTCT) by 6
<sup>th</sup>
week of life.</p>
</sec>
<sec id="S3">
<title>Results</title>
<p id="P3">Mean gestational age at enrollment was 22.2 weeks. During follow-up, 16.6% had ≥1 MIP diagnosis, 15.9% reported fever symptoms and 8.7% had both fever and MIP diagnosis. Eleven percent of HIV-exposed infants were HIV-positive by 6 weeks. The RR of HIV MTCT was statistically similar for infants whose mothers were ever vs. never clinical MIP diagnosed (RR=1.24, 95%CI:0.94–1.64), were diagnosed with 1 vs. 0 clinical MIP episode (RR=1.07;95%CI:0.77–1.48) and had ever vs. never reported fever symptoms (RR=1.04, 95%CI:0.78,1.38) in pregnancy. However, HIV MTCT risk increased by 29% (95%CI:4–58%) per MIP episode. Infants of women with ≥2 vs. 0 MIP diagnoses were 2.1 times more likely to be HIV infected by 6weeks old (95%CI:1.31–3.45).</p>
</sec>
<sec id="S4">
<title>Conclusions</title>
<p id="P4">Clinical MIP diagnosis, but not fevers, in HIV-positive pregnant women was associated with elevated risk of early HIV MTCT suggesting that malaria prevention and treatment in pregnant HIV-positive women may enhance the effectiveness of HIV prevention in MTCT programs in this setting. Future studies using laboratory confirmed malaria is needed to confirm this association.</p>
</sec>
</div>
</front>
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<pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<pmc-dir>properties manuscript</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-journal-id">100897392</journal-id>
<journal-id journal-id-type="pubmed-jr-id">26808</journal-id>
<journal-id journal-id-type="nlm-ta">HIV Med</journal-id>
<journal-id journal-id-type="iso-abbrev">HIV Med.</journal-id>
<journal-title-group>
<journal-title>HIV medicine</journal-title>
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<issn pub-type="ppub">1464-2662</issn>
<issn pub-type="epub">1468-1293</issn>
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<article-id pub-id-type="pmid">24215465</article-id>
<article-id pub-id-type="pmc">4299572</article-id>
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<article-id pub-id-type="manuscript">NIHMS532759</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Article</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Clinical Malaria Diagnosis in Pregnancy in Relation to Early Perinatal Mother-to-Child-Transmission of HIV: A Prospective Cohort Study</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Ezeamama</surname>
<given-names>AE</given-names>
</name>
<degrees>PhD</degrees>
<xref ref-type="aff" rid="A1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Duggan</surname>
<given-names>C</given-names>
</name>
<degrees>MD, MPH</degrees>
<xref ref-type="aff" rid="A2">2</xref>
<xref ref-type="aff" rid="A3">3</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Manji</surname>
<given-names>KP</given-names>
</name>
<degrees>MBBS,MMED, MPH</degrees>
<xref ref-type="aff" rid="A4">4</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Spiegelman</surname>
<given-names>D</given-names>
</name>
<degrees>ScD</degrees>
<xref ref-type="aff" rid="A5">5</xref>
<xref ref-type="aff" rid="A6">6</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Hertzmark</surname>
<given-names>E</given-names>
</name>
<degrees>MS</degrees>
<xref ref-type="aff" rid="A5">5</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Bosch</surname>
<given-names>RJ</given-names>
</name>
<degrees>PhD</degrees>
<xref ref-type="aff" rid="A6">6</xref>
<xref ref-type="aff" rid="A7">7</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Kupka</surname>
<given-names>R</given-names>
</name>
<degrees>ScD</degrees>
<xref ref-type="aff" rid="A2">2</xref>
<xref ref-type="aff" rid="A8">8</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Okuma</surname>
<given-names>JO</given-names>
</name>
<degrees>MS</degrees>
<xref ref-type="aff" rid="A2">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Kisenge</surname>
<given-names>R</given-names>
</name>
<xref ref-type="aff" rid="A9">9</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Aboud</surname>
<given-names>S</given-names>
</name>
<degrees>MD, MMED</degrees>
<xref ref-type="aff" rid="A9">9</xref>
<xref ref-type="aff" rid="A10">10</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Fawzi</surname>
<given-names>WW</given-names>
</name>
<degrees>MD, DrPH</degrees>
<xref ref-type="aff" rid="A2">2</xref>
<xref ref-type="aff" rid="A5">5</xref>
<xref ref-type="aff" rid="A11">11</xref>
</contrib>
</contrib-group>
<aff id="A1">
<label>1</label>
Department of Epidemiology & Biostatistics, The University of Georgia, B.S. Miller Hall, Room 125, 101 Buck Rd, Athens, GA 30602, USA</aff>
<aff id="A2">
<label>2</label>
Department of Nutrition, Harvard School of Public Health (HSPH), Boston, MA</aff>
<aff id="A3">
<label>3</label>
Division of Gastroenterology and Nutrition, Children's Hospital, Boston, MA</aff>
<aff id="A4">
<label>4</label>
Department of Pediatrics and Child Health, School of Medicine, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania</aff>
<aff id="A5">
<label>5</label>
Department of Epidemiology, HSPH, Boston, MA</aff>
<aff id="A6">
<label>6</label>
Department of Biostatistics, HSPH, Boston, MA</aff>
<aff id="A7">
<label>7</label>
Center for Biostatistics in AIDS Research, HSPH, Boston, MA</aff>
<aff id="A8">
<label>8</label>
United Nations Children’s Fund, Regional Office for West and Central Africa, Dakar, Senegal</aff>
<aff id="A9">
<label>9</label>
Department of Pediatrics and Child Health, School of Medicine, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania</aff>
<aff id="A10">
<label>10</label>
Department of Microbiology and Immunology, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania</aff>
<aff id="A11">
<label>11</label>
Department of Global Health and Population, HSPH, Boston, MA</aff>
<author-notes>
<corresp id="cor1">
<bold>Corresponding Author:</bold>
Amara E. Ezeamama, PhD. Department of Epidemiology & Biostatistics, The University of Georgia, B.S. Miller Hall, Room 125, 101 Buck Rd, Athens, GA 30602, USA;
<email>aezeamam@uga.edu</email>
</corresp>
</author-notes>
<pub-date pub-type="nihms-submitted">
<day>13</day>
<month>1</month>
<year>2015</year>
</pub-date>
<pub-date pub-type="epub">
<day>11</day>
<month>11</month>
<year>2013</year>
</pub-date>
<pub-date pub-type="ppub">
<month>5</month>
<year>2014</year>
</pub-date>
<pub-date pub-type="pmc-release">
<day>01</day>
<month>5</month>
<year>2015</year>
</pub-date>
<volume>15</volume>
<issue>5</issue>
<fpage>276</fpage>
<lpage>285</lpage>
<pmc-comment>elocation-id from pubmed: 10.1111/hiv.12111</pmc-comment>
<abstract>
<sec id="S1">
<title>Objectives</title>
<p id="P1">We prospectively investigated fever symptoms and maternal diagnosis of malaria in pregnancy (MIP) in relation to child HIV infection among 2,368 pregnant HIV-positive women and their infants, followed-up from pregnancy until birth and 6 weeks post-delivery in Tanzania.</p>
</sec>
<sec id="S2">
<title>Methods</title>
<p id="P2">Doctors clinically diagnosed and treated MIP and fever symptoms during prenatal healthcare. Child HIV status was determined via DNA-PCR. Multivariable logistic regression models estimated relative risks (RR) and 95% confidence intervals (CI) for HIV mother-to-child-transmission (MTCT) by 6
<sup>th</sup>
week of life.</p>
</sec>
<sec id="S3">
<title>Results</title>
<p id="P3">Mean gestational age at enrollment was 22.2 weeks. During follow-up, 16.6% had ≥1 MIP diagnosis, 15.9% reported fever symptoms and 8.7% had both fever and MIP diagnosis. Eleven percent of HIV-exposed infants were HIV-positive by 6 weeks. The RR of HIV MTCT was statistically similar for infants whose mothers were ever vs. never clinical MIP diagnosed (RR=1.24, 95%CI:0.94–1.64), were diagnosed with 1 vs. 0 clinical MIP episode (RR=1.07;95%CI:0.77–1.48) and had ever vs. never reported fever symptoms (RR=1.04, 95%CI:0.78,1.38) in pregnancy. However, HIV MTCT risk increased by 29% (95%CI:4–58%) per MIP episode. Infants of women with ≥2 vs. 0 MIP diagnoses were 2.1 times more likely to be HIV infected by 6weeks old (95%CI:1.31–3.45).</p>
</sec>
<sec id="S4">
<title>Conclusions</title>
<p id="P4">Clinical MIP diagnosis, but not fevers, in HIV-positive pregnant women was associated with elevated risk of early HIV MTCT suggesting that malaria prevention and treatment in pregnant HIV-positive women may enhance the effectiveness of HIV prevention in MTCT programs in this setting. Future studies using laboratory confirmed malaria is needed to confirm this association.</p>
</sec>
</abstract>
<kwd-group>
<kwd>Co-infection</kwd>
<kwd>Malaria</kwd>
<kwd>AIDS</kwd>
<kwd>HIV mother-to-child-transmission</kwd>
<kwd>HIV-exposed Infant</kwd>
</kwd-group>
</article-meta>
</front>
</pmc>
</record>

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}}

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HfdIndexSelect -h $EXPLOR_AREA/Data/Pmc/Corpus/RBID.i   -Sk "pubmed:24215465" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/Pmc/Corpus/biblio.hfd   \
       | NlmPubMed2Wicri -a SidaSubSaharaV1 

Wicri

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