TY - JOUR
T1 - Population-based study of statins, angiotensin II receptor blockers, and angiotensin-converting enzyme inhibitors on pneumonia-related outcomes
AU - Mortensen, Eric M.
AU - Nakashima, Brandy
AU - Cornell, John
AU - Copeland, Laurel A.
AU - Pugh, Mary Jo
AU - Anzueto, Antonio
AU - Good, Chester
AU - Restrepo, Marcos
AU - Downs, John R
AU - Frei, Chris
AU - Fine, Michael J.
N1 - Funding Information:
Financial support. This work was supported by the National Institute of Nursing Research (grant number R01NR010828). This material is the result of work supported with resources and the use of facilities at the South Texas Veterans Health Care System.
PY - 2012/12/1
Y1 - 2012/12/1
N2 - Background.Studies suggest that statins and angiotensin-converting enzyme (ACE) inhibitors might be beneficial for the treatment of infections. Our purpose was to examine the association of statin, ACE inhibitor, and angiotensin II receptor blocker (ARB) use with pneumonia-related outcomes.Methods.We conducted a retrospective cohort study using Department of Veterans Affairs data of patients aged ≥65 years hospitalized with pneumonia. We performed propensity-score matching for 3 medication classes simultaneously.Results.Of 50 119 potentially eligible patients, we matched 11 498 cases with 11 498 controls. Mortality at 30 days was 13; 34 used statins, 30 ACE inhibitors, and 4 ARBs. In adjusted models, prior statin use was associated with decreased mortality (odds ratio [OR], 0.74; 95 confidence interval [CI],. 68-.82) and mechanical ventilation (OR, 0.81; 95 CI,. 70-.94), and inpatient use with decreased mortality (OR, 0.68; 95 CI,. 59-.78) and mechanical ventilation (OR, 0.68; 95 CI,. 60-.90). Prior (OR, 0.88; 95 CI,. 80-.97) and inpatient (OR, 0.58; 95 CI,. 48-.69) ACE inhibitor use was associated with decreased mortality. Prior (OR, 0.73; 95 CI,. 58-.92) and inpatient ARB use (OR, 0.47; 95 CI,. 30-.72) was only associated with decreased mortality. Use of all 3 medications was associated with reduced length of stay.Conclusions.Statins, and to a lesser extent ACE inhibitors and ARBs, are associated with improved pneumonia-related outcomes. Prospective cohort and randomized controlled trials are needed to examine potential mechanisms of action and whether acute initiation at the time of presentation with these infections is beneficial.
AB - Background.Studies suggest that statins and angiotensin-converting enzyme (ACE) inhibitors might be beneficial for the treatment of infections. Our purpose was to examine the association of statin, ACE inhibitor, and angiotensin II receptor blocker (ARB) use with pneumonia-related outcomes.Methods.We conducted a retrospective cohort study using Department of Veterans Affairs data of patients aged ≥65 years hospitalized with pneumonia. We performed propensity-score matching for 3 medication classes simultaneously.Results.Of 50 119 potentially eligible patients, we matched 11 498 cases with 11 498 controls. Mortality at 30 days was 13; 34 used statins, 30 ACE inhibitors, and 4 ARBs. In adjusted models, prior statin use was associated with decreased mortality (odds ratio [OR], 0.74; 95 confidence interval [CI],. 68-.82) and mechanical ventilation (OR, 0.81; 95 CI,. 70-.94), and inpatient use with decreased mortality (OR, 0.68; 95 CI,. 59-.78) and mechanical ventilation (OR, 0.68; 95 CI,. 60-.90). Prior (OR, 0.88; 95 CI,. 80-.97) and inpatient (OR, 0.58; 95 CI,. 48-.69) ACE inhibitor use was associated with decreased mortality. Prior (OR, 0.73; 95 CI,. 58-.92) and inpatient ARB use (OR, 0.47; 95 CI,. 30-.72) was only associated with decreased mortality. Use of all 3 medications was associated with reduced length of stay.Conclusions.Statins, and to a lesser extent ACE inhibitors and ARBs, are associated with improved pneumonia-related outcomes. Prospective cohort and randomized controlled trials are needed to examine potential mechanisms of action and whether acute initiation at the time of presentation with these infections is beneficial.
UR - http://www.scopus.com/inward/record.url?scp=84869020353&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84869020353&partnerID=8YFLogxK
U2 - 10.1093/cid/cis733
DO - 10.1093/cid/cis733
M3 - Article
C2 - 22918991
AN - SCOPUS:84869020353
SN - 1058-4838
VL - 55
SP - 1466
EP - 1473
JO - Clinical Infectious Diseases
JF - Clinical Infectious Diseases
IS - 11
ER -