TY - JOUR
T1 - Bacterial pneumonia, HIV therapy, and disease progression among HIV-infected women in the HIV epidemiologic research (HER) study
AU - Kohli, Rakhi
AU - Lo, Yungtai
AU - Homel, Peter
AU - Flanigan, Timothy P.
AU - Gardner, Lytt I.
AU - Howard, Andrea A.
AU - Rompalo, Anne M.
AU - Moskaleva, Galina
AU - Schuman, Paula
AU - Schoenbaum, Ellie E.
N1 - Funding Information:
Financial support. The HER Study was funded by the Division of HIV/ AIDS and Prevention and Division of Reproductive Health, Centers for Disease Control and Prevention and National Institute on Drug Abuse. R.K. was supported by National Institute of Allergy and Infectious Diseases institutional training grant (T32-AI07501). The statistical analysis was supported by the Einstein/Montefiore Center for AIDS Research (AI-051519). Potential conflicts of interest. All authors: no conflicts.
PY - 2006/7/1
Y1 - 2006/7/1
N2 - Background. To determine the rate and predictors of community-acquired bacterial pneumonia and its effect on human immunodeficiency virus (HIV) disease progression in HIV-infected women, we performed a multiple-site, prospective study of HIV-infected women in 4 cities in the United States. Methods. During the period of 1993-2000, we observed 885 HIV-infected and 425 HIV-uninfected women with a history of injection drug use or high-risk sexual behavior. Participants underwent semiannual interviews, and CD4+ lymphocyte count and viral load were assessed in HIV-infected subjects. Data regarding episodes of bacterial pneumonia were ascertained from medical record reviews. Results. The rate of bacterial pneumonia among 885 HIV-infected women was 8.5 cases per 100 person-years, compared with 0.7 cases per 100 person-years in 425 HIV-uninfected women (P < .001). In analyses limited to follow-up after 1 January 1996, highly active antiretroviral therapy (HAART) and trimethoprim-sulfamethoxazole (TMP-SMX) use were associated with a decreased risk of bacterial pneumonia. Among women who had used TMP-SMX for 12 months, each month of HAART decreased bacterial pneumonia risk by 8% (adjusted hazard ratio [HRadj], 0.92; 95% confidence interval [CI], 0.89-0.95). Increments of 50 CD4+ cells/mm3 decreased the risk (HRadj, 0.88; 95% CI, 0.84-0.93), and smoking doubled the risk (HRadj, 2.12; 95% CI, 1.26-3.55). Bacterial pneumonia increased mortality risk (HRadj, 5.02; 95% CI, 2.12-11.87), with adjustment for CD4+ lymphocyte count and duration of HAART and TMP-SMX use. Conclusions. High rates of bacterial pneumonia persist among HIV-infected women. Although HAART and TMP-SMX treatment decreased the risk, bacterial pneumonia was associated with an accelerated progression to death. Interventions that improve HAART utilization and promote smoking cessation among HIV-infected women are warranted.
AB - Background. To determine the rate and predictors of community-acquired bacterial pneumonia and its effect on human immunodeficiency virus (HIV) disease progression in HIV-infected women, we performed a multiple-site, prospective study of HIV-infected women in 4 cities in the United States. Methods. During the period of 1993-2000, we observed 885 HIV-infected and 425 HIV-uninfected women with a history of injection drug use or high-risk sexual behavior. Participants underwent semiannual interviews, and CD4+ lymphocyte count and viral load were assessed in HIV-infected subjects. Data regarding episodes of bacterial pneumonia were ascertained from medical record reviews. Results. The rate of bacterial pneumonia among 885 HIV-infected women was 8.5 cases per 100 person-years, compared with 0.7 cases per 100 person-years in 425 HIV-uninfected women (P < .001). In analyses limited to follow-up after 1 January 1996, highly active antiretroviral therapy (HAART) and trimethoprim-sulfamethoxazole (TMP-SMX) use were associated with a decreased risk of bacterial pneumonia. Among women who had used TMP-SMX for 12 months, each month of HAART decreased bacterial pneumonia risk by 8% (adjusted hazard ratio [HRadj], 0.92; 95% confidence interval [CI], 0.89-0.95). Increments of 50 CD4+ cells/mm3 decreased the risk (HRadj, 0.88; 95% CI, 0.84-0.93), and smoking doubled the risk (HRadj, 2.12; 95% CI, 1.26-3.55). Bacterial pneumonia increased mortality risk (HRadj, 5.02; 95% CI, 2.12-11.87), with adjustment for CD4+ lymphocyte count and duration of HAART and TMP-SMX use. Conclusions. High rates of bacterial pneumonia persist among HIV-infected women. Although HAART and TMP-SMX treatment decreased the risk, bacterial pneumonia was associated with an accelerated progression to death. Interventions that improve HAART utilization and promote smoking cessation among HIV-infected women are warranted.
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U2 - 10.1086/504871
DO - 10.1086/504871
M3 - Article
C2 - 16758423
AN - SCOPUS:33745299968
SN - 1058-4838
VL - 43
SP - 90
EP - 98
JO - Clinical Infectious Diseases
JF - Clinical Infectious Diseases
IS - 1
ER -