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Timing of maternal HIV testing and uptake of Prevention of Mother-to-Child Transmission interventions among women and their infected infants in Johannesburg, South Africa

Identifieur interne : 001927 ( Pmc/Corpus ); précédent : 001926; suivant : 001928

Timing of maternal HIV testing and uptake of Prevention of Mother-to-Child Transmission interventions among women and their infected infants in Johannesburg, South Africa

Auteurs : Karl-Günter Technau ; Emma Kalk ; Ashraf Coovadia ; Vivian Black ; Sam Pickerill ; Claude A. Mellins ; Elaine J. Abrams ; Renate Strehlau ; Louise Kuhn

Source :

RBID : PMC:3999509

Abstract

Background

By 2011, South African prevention of mother-to-child transmission of HIV (PMTCT) programmes had reduced perinatal HIV transmission at 6-weeks of age to 2.7%. We investigated the profile of newly-diagnosed vertically-infected children and their mothers to identify short-falls in the PMTCT programme.

Methods

In this operational follow-up study, fieldworkers enrolled mothers of newly-diagnosed HIV-infected children up to 2 years of age at 5 major healthcare facilities in Johannesburg. Structured questionnaires and clinical record reviews were conducted and analysed to describe the population and assess factors associated with PMTCT uptake.

Results

289 mother-child pairs were enrolled. Timing of maternal HIV diagnosis influenced PMTCT access and feeding choices, and was associated with infants’ age at HIV diagnosis (7 weeks vs. 11 weeks vs. 31 weeks where mothers tested before, during or after the pregnancy respectively; p <0.0001). Women diagnosed before pregnancy (12%) were older (median 31 years) than those diagnosed during the index pregnancy (53% - median 27 years). Women diagnosed after delivery (35%) were younger (median 25 years, p<0.0001), of lower parity, and less likely to be South African citizens. In 81 cases (29%) late maternal diagnosis precluded any PMTCT access. Where women were diagnosed during or before pregnancy, the recommended PMTCT guidelines for mother and infant were followed in 86 (61%) pairs.

Conclusion

Failure to diagnose maternal HIV infection before delivery was the main reason for missing PMTCT prophylaxis and early infant testing. Timely maternal diagnosis enables PMTCT uptake, but implementation and follow-up gaps require attention to improve infant outcomes.


Url:
DOI: 10.1097/QAI.0000000000000068
PubMed: 24759066
PubMed Central: 3999509

Links to Exploration step

PMC:3999509

Le document en format XML

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<name sortKey="Kuhn, Louise" sort="Kuhn, Louise" uniqKey="Kuhn L" first="Louise" last="Kuhn">Louise Kuhn</name>
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<title>Background</title>
<p id="P1">By 2011, South African prevention of mother-to-child transmission of HIV (PMTCT) programmes had reduced perinatal HIV transmission at 6-weeks of age to 2.7%. We investigated the profile of newly-diagnosed vertically-infected children and their mothers to identify short-falls in the PMTCT programme.</p>
</sec>
<sec id="S2">
<title>Methods</title>
<p id="P2">In this operational follow-up study, fieldworkers enrolled mothers of newly-diagnosed HIV-infected children up to 2 years of age at 5 major healthcare facilities in Johannesburg. Structured questionnaires and clinical record reviews were conducted and analysed to describe the population and assess factors associated with PMTCT uptake.</p>
</sec>
<sec id="S3">
<title>Results</title>
<p id="P3">289 mother-child pairs were enrolled. Timing of maternal HIV diagnosis influenced PMTCT access and feeding choices, and was associated with infants’ age at HIV diagnosis (7 weeks vs. 11 weeks vs. 31 weeks where mothers tested before, during or after the pregnancy respectively; p <0.0001). Women diagnosed before pregnancy (12%) were older (median 31 years) than those diagnosed during the index pregnancy (53% - median 27 years). Women diagnosed after delivery (35%) were younger (median 25 years, p<0.0001), of lower parity, and less likely to be South African citizens. In 81 cases (29%) late maternal diagnosis precluded any PMTCT access. Where women were diagnosed during or before pregnancy, the recommended PMTCT guidelines for mother and infant were followed in 86 (61%) pairs.</p>
</sec>
<sec id="S4">
<title>Conclusion</title>
<p id="P4">Failure to diagnose maternal HIV infection before delivery was the main reason for missing PMTCT prophylaxis and early infant testing. Timely maternal diagnosis enables PMTCT uptake, but implementation and follow-up gaps require attention to improve infant outcomes.</p>
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</front>
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<journal-id journal-id-type="nlm-journal-id">100892005</journal-id>
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<journal-id journal-id-type="nlm-ta">J Acquir Immune Defic Syndr</journal-id>
<journal-id journal-id-type="iso-abbrev">J. Acquir. Immune Defic. Syndr.</journal-id>
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<journal-title>Journal of acquired immune deficiency syndromes (1999)</journal-title>
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<article-id pub-id-type="manuscript">NIHMS542888</article-id>
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<subject>Article</subject>
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<title-group>
<article-title>Timing of maternal HIV testing and uptake of Prevention of Mother-to-Child Transmission interventions among women and their infected infants in Johannesburg, South Africa</article-title>
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<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Technau</surname>
<given-names>Karl-Günter</given-names>
</name>
<degrees>MBBCh, MSc</degrees>
<xref ref-type="aff" rid="A1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Kalk</surname>
<given-names>Emma</given-names>
</name>
<degrees>MBBCh, PhD</degrees>
<xref ref-type="aff" rid="A2">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Coovadia</surname>
<given-names>Ashraf</given-names>
</name>
<degrees>MBBCh, FCPaed</degrees>
<xref ref-type="aff" rid="A1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Black</surname>
<given-names>Vivian</given-names>
</name>
<degrees>MBBCh, MSc</degrees>
<xref ref-type="aff" rid="A3">3</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Pickerill</surname>
<given-names>Sam</given-names>
</name>
<degrees>MSc</degrees>
<xref ref-type="aff" rid="A1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Mellins</surname>
<given-names>Claude A.</given-names>
</name>
<degrees>Ph.D.</degrees>
<xref ref-type="aff" rid="A4">4</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Abrams</surname>
<given-names>Elaine J.</given-names>
</name>
<degrees>MD</degrees>
<xref ref-type="aff" rid="A5">5</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Strehlau</surname>
<given-names>Renate</given-names>
</name>
<degrees>MBBCh MSc</degrees>
<xref ref-type="aff" rid="A1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Kuhn</surname>
<given-names>Louise</given-names>
</name>
<degrees>PhD</degrees>
<xref ref-type="aff" rid="A6">6</xref>
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<aff id="A1">
<label>1</label>
Empilweni Services and Research Unit, Department of Paediatrics & Child Health, Rahima Moosa Mother and Child Hospital, Faculty of Health Sciences, University of the Witwatersrand, South Africa</aff>
<aff id="A2">
<label>2</label>
Centre for Infectious Disease Epidemiology and Research, School of Public Health and Family Medicine, Faculty of Health Sciences, University of Cape Town, South Africa</aff>
<aff id="A3">
<label>3</label>
Wits Reproductive Health and HIV Institute, Faculty of Health Sciences, University of Witwatersrand, Johannesburg, South Africa</aff>
<aff id="A4">
<label>4</label>
HIV Center for Clinical and Behavioral Studies in the Division of Gender Sexuality and Health, Department of Psychiatry, Columbia University and the New York State Psychiatric Institute, New York, NY</aff>
<aff id="A5">
<label>5</label>
ICAP, Mailman School of Public Health, and Department of Pediatrics, College of Physicians & Surgeons, Columbia University, New York, NY</aff>
<aff id="A6">
<label>6</label>
Gertrude H. Sergievsky Center, College of Physicians and Surgeons, and Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, NY</aff>
<author-notes>
<corresp id="cor1">
<bold>Corresponding Author:</bold>
Dr Karl-Günter Technau, Tel: +27 82 6873633; Fax: +27 11 673 4905;
<email>karltechnau@gmail.com</email>
</corresp>
</author-notes>
<pub-date pub-type="nihms-submitted">
<day>30</day>
<month>11</month>
<year>2013</year>
</pub-date>
<pub-date pub-type="ppub">
<day>15</day>
<month>4</month>
<year>2014</year>
</pub-date>
<pub-date pub-type="pmc-release">
<day>15</day>
<month>4</month>
<year>2015</year>
</pub-date>
<volume>65</volume>
<issue>5</issue>
<fpage>e170</fpage>
<lpage>e178</lpage>
<pmc-comment>elocation-id from pubmed: 10.1097/QAI.0000000000000068</pmc-comment>
<abstract>
<sec id="S1">
<title>Background</title>
<p id="P1">By 2011, South African prevention of mother-to-child transmission of HIV (PMTCT) programmes had reduced perinatal HIV transmission at 6-weeks of age to 2.7%. We investigated the profile of newly-diagnosed vertically-infected children and their mothers to identify short-falls in the PMTCT programme.</p>
</sec>
<sec id="S2">
<title>Methods</title>
<p id="P2">In this operational follow-up study, fieldworkers enrolled mothers of newly-diagnosed HIV-infected children up to 2 years of age at 5 major healthcare facilities in Johannesburg. Structured questionnaires and clinical record reviews were conducted and analysed to describe the population and assess factors associated with PMTCT uptake.</p>
</sec>
<sec id="S3">
<title>Results</title>
<p id="P3">289 mother-child pairs were enrolled. Timing of maternal HIV diagnosis influenced PMTCT access and feeding choices, and was associated with infants’ age at HIV diagnosis (7 weeks vs. 11 weeks vs. 31 weeks where mothers tested before, during or after the pregnancy respectively; p <0.0001). Women diagnosed before pregnancy (12%) were older (median 31 years) than those diagnosed during the index pregnancy (53% - median 27 years). Women diagnosed after delivery (35%) were younger (median 25 years, p<0.0001), of lower parity, and less likely to be South African citizens. In 81 cases (29%) late maternal diagnosis precluded any PMTCT access. Where women were diagnosed during or before pregnancy, the recommended PMTCT guidelines for mother and infant were followed in 86 (61%) pairs.</p>
</sec>
<sec id="S4">
<title>Conclusion</title>
<p id="P4">Failure to diagnose maternal HIV infection before delivery was the main reason for missing PMTCT prophylaxis and early infant testing. Timely maternal diagnosis enables PMTCT uptake, but implementation and follow-up gaps require attention to improve infant outcomes.</p>
</sec>
</abstract>
<kwd-group>
<kwd>HIV infection</kwd>
<kwd>pregnancy</kwd>
<kwd>vertical transmission</kwd>
<kwd>children</kwd>
<kwd>maternal diagnosis</kwd>
</kwd-group>
</article-meta>
</front>
</pmc>
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