Effect of Renin-Angiotensin-Aldosterone System Inhibitors on Short-Term Mortality After Sepsis

Author:

Hsu Wan-Ting1,Galm Brandon Patrick23,Schrank Gregory24,Hsu Tzu-Chun56,Lee Shih-Hao7,Park James Yeongjun8,Lee Chien-Chang56

Affiliation:

1. From the Department of Epidemiology (W.-T.H.), Harvard T.H. Chan School of Public Health, Boston, MA

2. Harvard Medical School, Boston, MA (B.P.G., G.S.)

3. Neuroendocrine Unit, Massachusetts General Hospital, Boston, MA (B.P.G.)

4. Division of Infectious Diseases, Beth Israel Deaconess Medical Center, Boston, MA (G.S.)

5. Department of Emergency Medicine (T.-C.H., C.-C.L.), National Taiwan University Hospital, Taipei

6. College of Medicine (T.-C.H., C.-C.L.), National Taiwan University Hospital, Taipei

7. Medical Wizdom, LLC, Spring, Texas (S.-H.L.).

8. Department of Biostatistics (J.Y.P.), Harvard T.H. Chan School of Public Health, Boston, MA

Abstract

Antagonists of the renin-angiotensin-aldosterone system (RAAS), including ACEIs (angiotensin-converting enzyme inhibitors) and ARBs (angiotensin II receptor blockers), may prevent organ failure. We, therefore, investigated whether specific RAAS inhibitors are associated with reduced mortality in patients with sepsis.We conducted a population-based retrospective cohort study using multivariable propensity score–based regression to control for differences among patients using different RAAS inhibitors. A multivariable-adjusted Cox proportional-hazards regression model was used to determine the association between RAAS inhibitors and sepsis outcomes. To directly compare ACEI users, ARB users, and nonusers, a 3-way propensity score matching approach was performed. Results were pooled with previous evidence via a random-effects meta-analysis. A total of 52 727 patients were hospitalized with sepsis, of whom 7642 were prescribed an ACEI and 4237 were prescribed an ARB. Using propensity score–matched analyses, prior ACEI use was associated with decreased 30-day mortality (hazard ratio, 0.84 [95% CI, 0.75–0.94]) and 90-day mortality (hazard ratio, 0.83 [95% CI, 0.75–0.92]) compared with nonuse. Prior ARB use was associated with an improved 90-day survival (hazard ratio, 0.88 [95% CI, 0.83–0.94]). These results persisted in sensitivity analyses focusing on patients without cancer and patients with hypertension. By contrast, no beneficial effect was found for antecedent β-blockers exposure (hazard ratio, 0.99 [95% CI, 0.94–1.05]). The pooled estimates obtained from the meta-analysis was 0.71 (95% CI, 0.58–0.87) for prior use of ACEI/ARB.The short-term mortality after sepsis was substantially lower among those who were already established on RAAS inhibitor treatment when sepsis occurred.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Internal Medicine

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