Journal
CLINICAL INFECTIOUS DISEASES
Volume 53, Issue 10, Pages 1008-1014Publisher
OXFORD UNIV PRESS INC
DOI: 10.1093/cid/cir608
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Funding
- National Institutes of Health [K23 AI084544, RR 024369, MH 088341, R24 A067039]
- Agency for Health Research and Quality [R18 HS17784]
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Background. Although early initiation of antiretroviral therapy in HIV-infected patients after a diagnosis of Pneumocystis pneumonia increased after ACTG 5164 (7.4%-50.0%), a subsequent implementation and dissemination initiative optimized uptake of early antiretroviral therapy as clinically routine (50.0%-80.3%). Methods. We evaluated patients who received a diagnosis of Pneumocystis jirovecii pneumonia (PCP) from 1 January 2001 through 30 March 2011. Survival analyses were used to assess changes in the time to initiation of ART after PCP, and logistic regression was used to evaluate changes in the odds of early ART (ie, within 14 days) because of ACTG 5164 and SFGH 5164 Initiative. Results. Among 162 patients, the adjusted hazard of ART initiation increased by 3.05 (95% confidence interval [CI], 1.86-5.02) after ACTG 5164 and by 4.89 (95% CI, 2.76-8.67) after the SFGH Initiative, compared with before ACTG 5164. When compared with before ACTG 5164, the proportion of patients who received ART within the 14 days after PCP diagnosis increased from 7.4% to 50.0% (P < .001) after ACTG 5164 and from 50.0% to 83.0% (P = .02) after the SFGH 5164 Initiative. Conclusions. Diffusion of findings from of a randomized trial changed practice at an academic medical center, but dissemination and implementation efforts were required to establish early ART at acceptable levels. Early ART initiation can be achieved in real-world patient populations.
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