Evidence map›Paper›PMID 23114104›Full record

Trial reportBMC infectious diseases2012

Growth patterns among HIV-exposed infants receiving nevirapine prophylaxis in Pune, India.

Malathi Ram, Nikhil Gupte, Uma Nayak, Aarti A Kinikar, Mangesh Khandave, Anita V Shankar, Jayagowri Sastry, Robert C Bollinger, Amita Gupta, SWEN India and BJMC-JHU Clinical Trials Study Team

Registry-linked trialOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in BMC infectious diseases, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00061321 (Prevention of Maternal to Infant HIV Transmission in India), which is not on this map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 22% of its field
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.

NCT00061321 phase3completednot on this map

Prevention of Maternal to Infant HIV Transmission in India

TypeinterventionalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2002 to 2007Enrolled770ConditionsHIV InfectionsArmsNevirapine and mulitvitamins
3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 19 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Child Growth According to Maternal and Child HIV Status in Zimbabwe.The Pediatric infectious disease journal · 2017
    Article
  6. Article
  7. Article
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 at 5 institutions in 2 countries.

Malathi RamJohns Hopkins Bloomberg School of Public Health, Dept, of International Health/GDEC, Suite W5506, 615 N, Wolfe Street, Baltimore, MD 21205, USA. mram@jhsph.edu
Nikhil Gupte
Uma Nayak
Aarti A Kinikar
Mangesh Khandave
Anita V Shankar
Jayagowri Sastry
Robert C Bollinger
Amita Gupta
SWEN India and BJMC-JHU Clinical Trials Study Team
B. J. Medical College & Sassoon Hospital · INJohns Hopkins University · USJohns Hopkins Medicine · USSmt. Kashibai Navale Medical College and General hospital · INUniversity of Virginia · US

Funding

TUBERCULOSIS INTERNATIONAL TRAINING AND RESEARCH PROGRAMD43TW000010 · FIC · JOHNS HOPKINS UNIVERSITY · PI BEYRER, CHRISTOPHER C. · 1988 to 2012
$19.8M
FIC NIH HHS D43-TW000010-22PHS HHS R01A145462PHS HHS U01A1069497
6 · The paper itself

Abstract

backgroundIndia has among the highest rates of infant malnutrition. Few studies investigating the growth patterns of HIV-exposed infants in India or the impact of timing of HIV infection on growth in settings such as India exist.

methodsWe used data from the Six Week Extended Nevirapine (SWEN) trial to compare the growth patterns of HIV-infected and HIV-exposed but uninfected infants accounting for timing of HIV infection, and to identify risk factors for stunting, underweight and wasting. Growth and timing of HIV infection were assessed at weeks 1, 2, 4, 6, 10, 14 weeks and 6, 9, 12 months of life. Random effects multivariable logistic regression method was used to assess factors associated with stunting, underweight and wasting.

resultsAmong 737 HIV-exposed infants, 93 (13%) were HIV-infected by 12 months of age. Among HIV-infected and uninfected infants, baseline prevalence of stunting (48% vs. 46%), underweight (27% vs. 26%) and wasting (7% vs. 11%) was similar (p>0.29), but by 12 months stunting and underweight, but not wasting, were significantly higher in HIV-infected infants (80% vs. 56%, 52% vs. 29%, p< 0.0001; 5% vs. 6%, p=0.65, respectively). These differences rapidly manifested within 4-6 weeks of birth. Infants infected in utero had the worst growth outcomes during the follow-up period. SWEN was associated with non-significant reductions in stunting and underweight among HIV-infected infants and significantly less wasting in HIV-uninfected infants. In multivariate analysis, maternal CD4 < 250, infant HIV status, less breastfeeding, low birth weight, non-vaginal delivery, and infant gestational age were significant risk factors for underweight and stunting.

conclusionBaseline stunting and underweight was high in both HIV-infected and uninfected infants; growth indices diverged early and were impacted by timing of infection and SWEN prophylaxis. Early growth monitoring of all HIV-exposed infants is an important low-cost strategy for improving health and survival outcomes of these infants.

trial registrationNCT00061321.

Indexed as

AdultAnthropometryFemaleHIV InfectionsHIV SeropositivityHumansIndiaInfantInfant, NewbornInfectious Disease Transmission, VerticalMaleNevirapinePregnancyProspective StudiesRisk FactorsThinnessNevirapine

Identifiers

PMID23114104
PMCPMC3556061
OpenAlexW2065037718

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.