Evidence map›Paper›PMID 29766019›Full record

ArticleOpen forum infectious diseases2018

Abacavir Use and Risk for Myocardial Infarction and Cardiovascular Events: Pooled Analysis of Data From Clinical Trials.

Cassandra Nan, Mark Shaefer, Rimgaile Urbaityte, James Oyee, Judy Hopking, Leigh Ragone, Teodora Perger, Beta Win, Harald Vangerow, Cynthia McCoig and 1 more

Open access · goldAbstract read
In one paragraph

Article in Open forum infectious diseases, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 3 pooled it
5.8field-weighted citation impact, top 3% 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.

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

20 citing papers in PubMed, 3 syntheses or guidelines pooled it, 40 citations in OpenAlex.

  1. Pooled it
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  7. Cardiometabolic health in people with HIV: expert consensus review.The Journal of antimicrobial chemotherapy · 2024
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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 at 3 institutions in 2 countries.

Cassandra NanReal World Evidence & Epidemiology, GlaxoSmithKline, Stevenage, Hertfordshire, United Kingdom.
Mark ShaeferGlobal Medical Sciences, ViiV Healthcare, Research Triangle Park, North Carolina.
Rimgaile UrbaityteClinical Statistics, Stockley Park, United Kingdom.
James OyeeClinical Statistics, Stockley Park, United Kingdom.
Judy HopkingClinical Statistics, Stockley Park, United Kingdom.
Leigh RagoneEpidemiology & Real World Evidence, ViiV Healthcare, Research Triangle Park, North Carolina.
Teodora PergerSafety & Pharmacovigilance, ViiV Healthcare, GSK House, United Kingdom.
Beta WinGlobal Clinical Safety & Pharmacovigilance, Stockley Park, United Kingdom.
Harald VangerowSafety Evaluation & Risk Management, GlaxoSmithKline, Stockley Park, United Kingdom.
Cynthia McCoigClinical Development, ViiV Healthcare, Tres Cantos, Spain.
Vani VannappagariEpidemiology & Real World Evidence, ViiV Healthcare, Research Triangle Park, North Carolina.
GlaxoSmithKline (United Kingdom) · GBViiV Healthcare (Spain) · ESViiV Healthcare (United Kingdom) · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSome observational studies and randomized controlled trials (RCTs) have suggested an association between abacavir (ABC) use and myocardial infarction (MI), whereas others have not.

methodsThis pooled analysis of 66 phase II-IV RCTs estimates exposure-adjusted incidence rates (IRs) and relative rates (RRs) of MI and cardiovascular events (CVEs) in participants receiving ABC- and non-ABC-containing combination antiretroviral therapy (cART). The primary analysis of MI included ABC-randomized trials with ≥48-week follow-up. Sensitivity analyses of MI and CVEs included non-ABC-randomized and <48-week follow-up trials.

resultsIn 66 clinical trials, 13 119 adults (75% male, aged 18-85 years) were on ABC-containing cART and 7350 were not. Exposure-adjusted IR for MI was 1.5 per 1000 person-years (PY; 95% confidence interval [CI], 0.67-3.34) in the ABC-exposed group and 2.18 per 1000 PY (95% CI, 1.09-4.40) in the unexposed group. The IR for CVEs was 2.9 per 1000 PY (95% CI, 2.09-4.02) in the exposed group and 4.69 per 1000 PY (95% CI, 3.40-6.47) in the unexposed group with studies of ≥48 weeks of follow-up, with an RR of 0.62 (95% CI, 0.39-0.98). The inclusion of nonrandomized and shorter-duration trials did not significantly change the RR for MI or coronary artery disease.

conclusionsThis pooled analysis found comparable IRs for MI and CVEs among ABC-exposed and -unexposed participants, suggesting no increased risk for MI or CVEs following ABC exposure in a clinical trial population. Modifiable risk factors for MI and CVEs should be addressed when prescribing ART.

Indexed as

abacaviracute myocardial infarctionanginacardiovascular eventcoronary artery diseaseHIVpooled analysissafety

Identifiers

PMID29766019
PMCPMC5946856
OpenAlexW2800811989

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.