TY - JOUR
T1 - The effect of AIDS clinical trials group protocol 5164 on the time from pneumocystis jirovecii pneumonia diagnosis to antiretroviral initiation in routine clinical practice
T2 - A case study of diffusion, dissemination, and implementationa
AU - Geng, Elvin H.
AU - Kahn, James S.
AU - Chang, Olivia C.
AU - Hare, C. Bradley
AU - Christopoulos, Katerina A.
AU - Jones, Diane
AU - Petersen, Maya L.
AU - Deeks, Steven G.
AU - Havlir, Diane V.
AU - Gandhi, Monica
N1 - Funding Information:
Financial support. This work was supported by National Institutes of Health (K23 AI084544, RR 024369, MH 088341, R24 A067039) and the Agency for Health Research and Quality (R18 HS17784). Potential conflicts of interest. All authors: No reported conflicts. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.
PY - 2011/11/15
Y1 - 2011/11/15
N2 - Background. Diffusion, dissemination, and implementation of scientific evidence into routine clinical practice is not well understood. The Adult AIDS Clinical Trials Group (ACTG) Protocol 5164 showed that early antiretroviral therapy (ART; ie, within 14 days) after diagnosis of an opportunistic infection improved clinical outcomes, compared with later initiation. Subsequently, the San Francisco General Hospital (SFGH) HIV/AIDS Service performed the SFGH 5164 Initiative to disseminate and implement the findings of ACTG 5164. 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.
AB - Background. Diffusion, dissemination, and implementation of scientific evidence into routine clinical practice is not well understood. The Adult AIDS Clinical Trials Group (ACTG) Protocol 5164 showed that early antiretroviral therapy (ART; ie, within 14 days) after diagnosis of an opportunistic infection improved clinical outcomes, compared with later initiation. Subsequently, the San Francisco General Hospital (SFGH) HIV/AIDS Service performed the SFGH 5164 Initiative to disseminate and implement the findings of ACTG 5164. 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.
UR - http://www.scopus.com/inward/record.url?scp=80054751098&partnerID=8YFLogxK
U2 - 10.1093/cid/cir608
DO - 10.1093/cid/cir608
M3 - Article
C2 - 21960715
AN - SCOPUS:80054751098
SN - 1058-4838
VL - 53
SP - 1008
EP - 1014
JO - Clinical Infectious Diseases
JF - Clinical Infectious Diseases
IS - 10
ER -