Evidence map›Paper›PMID 21914062›Full record

Trial reportJournal of viral hepatitis2011

HBV lamivudine resistance among hepatitis B and HIV coinfected patients starting lamivudine, stavudine and nevirapine in Kenya.

H N Kim, J Scott, A Cent, L Cook, R A Morrow, B Richardson, K Tapia, K R Jerome, G Lule, G John-Stewart and 1 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of viral hepatitis, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 3 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

12 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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  7. Slow CD4Open forum infectious diseases · 2016
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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

11 authors.

H N KimDepartment of Medicine, University of Washington, Seattle, WA 98104, USA. hyangkim@uw.edu
J Scott
A Cent
L Cook
R A Morrow
B Richardson
K Tapia
K R Jerome
G Lule
G John-Stewart
M H Chung

Funding

University of Washington/Fred Hutch Center for AIDS ResearchP30AI027757 · NIAID · UNIVERSITY OF WASHINGTON · PI Judith Tsui · 1988 to 2026
$104.9M
HAART Adherence Interventions in Africa: an RCTK23AI065222 · NIAID · UNIVERSITY OF WASHINGTON · PI CHUNG, MICHAEL HOONBAE · 2005 to 2009
$639k
NIAID NIH HHS 5K23AI065222NIAID NIH HHS K23 AI065222NIAID NIH HHS P30 AI027757NIAID NIH HHS P30AI027757
6 · The paper itself

Abstract

Widespread use of lamivudine in antiretroviral therapy may lead to hepatitis B virus resistance in HIV-HBV coinfected patients from endemic settings where tenofovir is not readily available. We evaluated 389 Kenyan HIV-infected adults before and for 18 months after starting highly active antiretroviral therapy with stavudine, lamivudine and nevirapine. Twenty-seven (6.9%) were HBsAg positive and anti-HBs negative, 24 were HBeAg negative, and 18 had HBV DNA levels ≤ 10,000 IU/mL. Sustained HBV suppression to <100 IU/mL occurred in 89% of 19 evaluable patients. Resistance occurred in only two subjects, both with high baseline HBV DNA levels. Lamivudine resistance can emerge in the setting of incomplete HBV suppression but was infrequently observed among HIV-HBV coinfected patients with low baseline HBV DNA levels.

Indexed as

Drug Resistance, ViralAdultAnti-HIV AgentsAntiretroviral Therapy, Highly ActiveDNA, ViralFemaleHepatitis BHepatitis B AntibodiesHepatitis B Surface AntigensHepatitis B virusHIV InfectionsHumansKenyaLamivudineMaleNevirapineAnti-HIV AgentsDNA, ViralHepatitis B AntibodiesHepatitis B Surface AntigensLamivudineNevirapineStavudine

Identifiers

PMID21914062
PMCPMC3177102

What OpenQuestion holds

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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.