Evidence map›Paper›PMID 25585302›Full record

ArticleJournal of acquired immune deficiency syndromes (1999)2015

Implementation and operational research: the impact of option B+ on the antenatal PMTCT cascade in Lilongwe, Malawi.

Maria H Kim, Saeed Ahmed, Mina C Hosseinipour, Thomas P Giordano, Elizabeth Y Chiao, Xiaoying Yu, Chi Nguyen, Frank Chimbwandira, Peter N Kazembe, Elaine J Abrams

Abstract read
In one paragraph

Article in Journal of acquired immune deficiency syndromes (1999), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed, 4 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

69 citing papers in PubMed, 4 syntheses or guidelines pooled it.

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9 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Maria H Kim*Baylor International Pediatric AIDS Initiative at Texas Children's Hospital, Houston, TX; †Baylor College of Medicine-Abbott Fund Children's Clinical Center of Excellence, Lilongwe, Malawi; ‡University of North Carolina School of Medicine, Chapel Hill, NC; §UNC Project, Lilongwe, Malawi; ‖Department of Medicine, Baylor College of Medicine, Houston, TX; ¶Department of Pediatrics, Epidemiology Center, Baylor College of Medicine, Houston, TX; #Department of HIV and AIDS, Ministry of Health, Lilongwe, Malawi; **ICAP-Columbia University, Mailman School of Public Health, New York, NY; and ††College of Physicians and Surgeons, Columbia University, New York, NY.
Saeed Ahmed
Mina C Hosseinipour
Thomas P Giordano
Elizabeth Y Chiao
Xiaoying Yu
Chi Nguyen
Frank Chimbwandira
Peter N Kazembe
Elaine J Abrams

Funding

Virology, Immunology, and Microbiology CoreP30AI050410 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DAVID M. MARGOLIS · 2001 to 2026
$76.9M
Virology CoreP30AI036211 · NIAID · BAYLOR COLLEGE OF MEDICINE · PI KOZINETZ, CLAUDIA A. · 1994 to 2015
$21.7M
Improving prevention of mother-to-child HIV transmission outcomes in MalawiK01TW009644 · FIC · BAYLOR COLLEGE OF MEDICINE · PI KIM, MARIA HYOUN · 2013 to 2017
$663k
FIC NIH HHS K01 TW009644NIAID NIH HHS P30 AI036211NIAID NIH HHS P30 AI050410NIAID NIH HHS P30-AI36211
6 · The paper itself

Abstract

objectiveIn 2011, Malawi implemented Option B+ (B+), lifelong antiretroviral therapy (ART) for pregnant and breastfeeding women. We aimed to describe changes in service uptake and outcomes along the antenatal prevention of mother-to-child transmission (PMTCT) cascade post-B+ implementation.

designPre/post study using routinely collected program data from 2 large Lilongwe-based health centers.

methodsWe compared the testing of HIV-infected pregnant women at antenatal care, enrollment into PMTCT services, receipt of ART, and 6-month ART outcomes pre-B+ (October 2009-March 2011) and post-B+ (October 2011-March 2013).

resultsA total of 13,926 (pre) and 14,532 (post) women presented to antenatal care. Post-B+, a smaller proportion were HIV-tested (99.3% vs. 87.7% post-B+; P < 0.0001). There were 1654 (pre) and 1535 (post) HIV-infected women identified, with a larger proportion already known to be HIV-infected (18.1% vs. 41.2% post-B+; P < 0.0001) and on ART post-B+ (18.7% vs. 30.2% post-B+; P < 0.0001). A significantly greater proportion enrolled into the PMTCT program (68.3% vs. 92.6% post-B+; P < 0.0001) and was retained through delivery post-B+ (51.1% vs. 65% post-B+; P < 0.0001). Among those not on ART at enrollment, there was no change in the proportion newly initiating ART/antiretrovirals (79% vs. 81.9% post-B+; P = 0.11), although median days to initiation of ART decreased [48 days (19, 130) vs. 0 days (0, 15.5) post-B+; P < 0.0001]. Among those newly initiating ART, a smaller proportion was alive on ART 6 months after initiation (89.3% vs. 78.8% post-B+; P = 0.0004).

conclusionsAlthough several improvements in PMTCT program performance were noted with implementation of B+, challenges remain at several critical steps along the cascade requiring innovative solutions to ensure an AIDS-free generation.

Indexed as

AdultAnti-Retroviral AgentsAntiretroviral Therapy, Highly ActiveDrug UtilizationFemaleHIV InfectionsHumansInfectious Disease Transmission, VerticalMalawiPregnancyPregnancy Complications, InfectiousAnti-Retroviral Agents

Identifiers

PMID25585302
PMCPMC4359035

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.