4.1 Article

Abacavir and risk of myocardial infarction in HIV-infected patients on highly active antiretroviral therapy: a population-based nationwide cohort study

期刊

HIV MEDICINE
卷 11, 期 2, 页码 130-136

出版社

WILEY-BLACKWELL PUBLISHING, INC
DOI: 10.1111/j.1468-1293.2009.00751.x

关键词

highly active antiretroviral therapy; HIV; ischemic heart disease; myocardial infarction; nucleotide analogues

资金

  1. Preben and Anna Simonsen's Foundation
  2. Clinical Institute of Copenhagen University
  3. Roche, Bristol-Myers Squibb, Merck Sharp & Dohme, GlaxoSmithKline, Abbott, Boehringer Ingelheim, Janssen-Cilag and Swedish Orphan
  4. Abbott, Roche, Bristol-Myers Squibb, Merck Sharp & Dohme, GlaxoSmithKline, Swedish Orphan and Boehringer Ingelheim
  5. Abbott, Roche, Bristol-Myers Squibb, Merck Sharp & Dohme, PharmAsia, GlaxoSmithKline, Swedish Orphan and Boehringer Ingelheim
  6. Aarhus University

向作者/读者索取更多资源

Objective The aim of the study was to examine whether exposure to abacavir increases the risk for myocardial infarction (MI). Design, setting and subjects This was a prospective nationwide cohort study which included all Danish HIV-infected patients on highly active antiretroviral therapy (HAART) from 1995 to 2005 (N=2952). Data on hospitalization for MI and comorbidity were obtained from Danish medical databases. Hospitalization rates for MI after HAART initiation were calculated for patients who used abacavir and those who did not. We used Cox's regression to compute incidence rate ratios (IRR) as a measure of relative risk for MI, while controlling for potential confounders (as separate variables and via propensity score) including comorbidity. Main outcome Relative risk of hospitalization with MI in abacavir users compared with abacavir nonusers. Results Hospitalization rates for MI were 2.4/1000 person-years (PYR) [95% confidence interval (CI) 1.7-3.4] for abacavir nonusers and 5.7/1000 PYR (95% CI 4.1-7.9) for abacavir users. The risk of MI increased after initiation of abacavir [unadjusted IRR=2.22 (95% CI 1.31-3.76); IRR adjusted for confounders=2.00 (95% CI 1.10-3.64); IRR adjusted for propensity score=2.00 (95% CI 1.07-3.76)]. This effect was also observed among patients initiating abacavir within 2 years after the start of HAART and among patients who started abacavir as part of a triple nucleoside reverse transcriptase inhibitor (NRTI) regimen. Conclusions We confirmed the association between abacavir use and increased risk of MI. Further studies are needed to control for potential confounding not measured in research to date.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.1
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据