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Increased mortality among publicly insured participants in the HIV Outpatient Study despite HAART treatment.

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posted on 2012-11-06, 00:00 authored by FJ Jr Palella, RK Baker, K Buchacz, JS Chmiel, EM Tedaldi, RM Novak, MD Durham, JT Brooks
Objective: Understanding mortality differences among HIV-infected patients can focus efforts to improve survival. Design: We evaluated death rates, causes and associated factors among treated patients in the HOPS, a large, prospective, multicenter observational cohort of HIV-infected persons seen at diverse U.S. sites of care. Methods: Among 3754 HOPS participants seen during 1996-2007 with > 6 months of follow-up after initiating HAART and ≥ 75% of time under observation receiving HAART (“substantially treated”), we calculated hazard ratios for death using proportional hazards regression models, death causes and comorbidities. Results: Substantially treated participants, followed a median 4.7 years (IQR, 2.2-8.5), experienced 331 deaths. In multivariable analyses, higher mortality was associated with index CD4 < 200 counts/mm3 (adjusted hazard ratio [aHR], 2.86; 95% CI, 1.95-4.21), older age (aHR, 1.50 per 10 years; 95% CI, 1.33-1.70), log10HIV RNA (aHR, 1.67 per log10; 95% CI, 1.51-1.85), but not race/ethnicity (aHR, 0.99 for blacks vs whites, p=0.92). Mortality was increased among publicly insured (PUB) vs privately insured participants (PRV ) when index CD4 >200 (aHR, 2.03; 95% CI, 1.32-3.14) but not when index CD4 < 200 cells/mm3 (aHR, 1.3, p=0.13). By death cause, PUB had significantly more cardiovascular events and hepatic disorders than PRV. Comorbidities more frequent among PUB vs PRV decedents included cardiovascular disease, renal impairment and chronic hepatitis. Conclusions: Among HAART treated participants with CD4 ≥ 200 cells/mm3, PUB experienced higher death rates than PRV. Non-AIDS death and disease causes predominated among publicly insured decedents, suggesting that treatable comorbidities contributed to survival disparities.

Funding

The HOPS is funded by the Centers for Disease Control and Prevention (CDC, contract no. 200-2006-18797).

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Publisher Statement

Post print version of article may differ from published version. The definitive version is available through Lippincott, Williams & Wilkins at DOI:10.1097/QAD.0b013e32834b3537

Publisher

Lippincott, Williams & Wilkins

Language

  • en_US

issn

0269-9370

Issue date

2011-09-24

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