Evidence map›Paper›PMID 26265222›Full record

ArticleBMC infectious diseases2015

Supporting Option B+ scale up and strengthening the prevention of mother-to-child transmission cascade in central Malawi: results from a serial cross-sectional study.

Michael E Herce, Tiwonge Mtande, Frank Chimbwandira, Innocent Mofolo, Christine K Chingondole, Nora E Rosenberg, Kathy E Lancaster, Esmie Kamanga, Jacqueline Chinkonde, Wiza Kumwenda and 6 more

Abstract read
In one paragraph

Article in BMC infectious diseases, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 2 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

28 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  10. Level of quality of option BBMC health services research · 2020
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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

16 authors.

Michael E HerceTidziwe Centre, UNC Project-Malawi, Private Bag A-104, Lilongwe, Malawi. michael_herce@med.unc.edu.
Tiwonge MtandeTidziwe Centre, UNC Project-Malawi, Private Bag A-104, Lilongwe, Malawi. tiwongemtande@gmail.com.
Frank ChimbwandiraHIV Unit, Ministry of Health, Government of the Republic of Malawi, P.O. Box 30377, Lilongwe 3, Malawi. frankchimbwandira@gmail.com.
Innocent MofoloTidziwe Centre, UNC Project-Malawi, Private Bag A-104, Lilongwe, Malawi. imofolo@unclilongwe.org.
Christine K ChingondoleTidziwe Centre, UNC Project-Malawi, Private Bag A-104, Lilongwe, Malawi. 33711623@mylife.unisa.ac.za.
Nora E RosenbergTidziwe Centre, UNC Project-Malawi, Private Bag A-104, Lilongwe, Malawi. nrosenbe@email.unc.edu.
Kathy E LancasterUniversity of North Carolina at Chapel Hill, 130 Mason Farm Rd. (Bioinformatics), CB# 7030, Chapel Hill, NC, 27599-7030, USA. klanc@live.unc.edu.
Esmie KamangaTidziwe Centre, UNC Project-Malawi, Private Bag A-104, Lilongwe, Malawi. ekamanga@unclilongwe.org.
Jacqueline ChinkondeUNICEF Malawi, P.O. Box 30375, Lilongwe 3, Malawi. jnkhoma@unicef.org.
Wiza KumwendaTidziwe Centre, UNC Project-Malawi, Private Bag A-104, Lilongwe, Malawi. wkumwenda@unclilongwe.org.
Gerald TeghaTidziwe Centre, UNC Project-Malawi, Private Bag A-104, Lilongwe, Malawi. gtegha@unclilongwe.org.
Mina C HosseinipourTidziwe Centre, UNC Project-Malawi, Private Bag A-104, Lilongwe, Malawi. mina_hosseinipour@med.unc.edu.
Irving F HoffmanTidziwe Centre, UNC Project-Malawi, Private Bag A-104, Lilongwe, Malawi. irving_hoffman@med.unc.edu.
Francis E MartinsonTidziwe Centre, UNC Project-Malawi, Private Bag A-104, Lilongwe, Malawi. fmartinson@unclilongwe.org.
Eva SteinUniversity of North Carolina at Chapel Hill, 130 Mason Farm Rd. (Bioinformatics), CB# 7030, Chapel Hill, NC, 27599-7030, USA. estein@email.unc.edu.
Charles M van der HorstTidziwe Centre, UNC Project-Malawi, Private Bag A-104, Lilongwe, Malawi. charles_vanderhorst@med.unc.edu.

Funding

Virology, Immunology, and Microbiology CoreP30AI050410 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DAVID M. MARGOLIS · 2001 to 2026
$76.9M
North Carolina Translational & Clinical Sciences Institute (NC TraCS)UL1TR001111 · NCATS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BUSE, JOHN BERNARD, CAREY, TIMOTHY S · 2013 to 2017
$43.9M
Training in Sexually Transmitted Infections and HIVT32AI007001 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SENA-SOBERANO, ARLENE C. · 1985 to 2025
$10.9M
Fogarty Global Health Fellows Coordinating CenterR25TW009340 · FIC · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CHI, BENJAMIN H. · 2012 to 2016
$6.9M
Developing and Assessing a Male Engagement Intervention for Option B+ in MalawiK99MH104154 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ROSENBERG, NORA · 2015 to 2016
$168k
FIC NIH HHS 5R25TW009340-03FIC NIH HHS R25 TW009340NCATS NIH HHS 5UL1TR001111-03NCATS NIH HHS UL1 TR001111NIAID NIH HHS 5P30AI50410-15NIAID NIH HHS 5T32AI007001-36NIAID NIH HHS P30 AI050410NIAID NIH HHS T32 AI007001NIMH NIH HHS K99 MH104154
6 · The paper itself

Abstract

backgroundWe established Safeguard the Family (STF) to support Ministry of Health (MoH) scale-up of universal antiretroviral therapy (ART) for HIV-infected pregnant and breastfeeding women (Option B+) and to strengthen the prevention of mother-to-child transmission (PMTCT) cascade from HIV testing and counseling (HTC) through maternal ART provision and post-delivery early infant HIV diagnosis (EID). To these ends, we implemented the following interventions in 5 districts: 1) health worker training and mentorship; 2) couples' HTC and male partner involvement; 3) women's psychosocial support groups; and 4) health and laboratory system strengthening for EID.

methodsWe conducted a serial cross-sectional study using facility-level quarterly (Q) program data and individual-level infant HIV-1 DNA PCR data to evaluate STF performance on PMTCT indicators for project years (Y) 1 (April-December 2011) through 3 (January-December 2013), and compared these results to national averages.

resultsFacility-level uptake of HTC, ART, infant nevirapine prophylaxis, and infant DNA PCR testing increased significantly from quarterly baselines of 66 % (n/N = 32,433/48,804), 23 % (n/N = 442/1,958), 1 % (n/N = 10/1,958), and 52 % (n/N = 1,385/2,644) to 87 % (n/N = 39,458/45,324), 96 % (n/N = 2,046/2,121), 100 % (n/N = 2,121/2,121), and 62 % (n/N = 1,462/2,340), respectively, by project end (all p < 0.001). Quarterly HTC, ART, and infant nevirapine prophylaxis uptake outperformed national averages over years 2-3. While transitioning EID laboratory services to MoH, STF provided first-time HIV-1 DNA PCR testing for 2,226 of 11,261 HIV-exposed infants (20 %) tested in the MoH EID program in STF districts from program inception (Y2) through Y3. Of these, 78 (3.5 %) tested HIV-positive. Among infants with complete documentation (n = 608), median age at first testing decreased from 112 days (interquartile range, IQR: 57-198) in Y2 to 76 days (IQR: 46-152) in Y3 (p < 0.001). During Y3 (only year with national data for comparison), non-significantly fewer exposed infants tested HIV-positive (3.6 %) at first testing in STF districts than nationally (4.1 %) (p = 0.4).

conclusionsSTF interventions, integrated within the MoH Option B+ program, achieved favorable HTC, maternal ART, infant prophylaxis, and EID services uptake, and a low proportion of infants found HIV-infected at first DNA PCR testing. Continued investments are needed to strengthen the PMTCT cascade, particularly around EID.

Indexed as

Antiretroviral Therapy, Highly ActiveAdultBreast FeedingCross-Sectional StudiesEarly DiagnosisFemaleHIV InfectionsHumansInfantInfant, NewbornInfectious Disease Transmission, VerticalMalawiMalePost-Exposure ProphylaxisPostpartum PeriodPregnancy

Identifiers

PMID26265222
PMCPMC4533797

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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.