Abstract

BackgroundThe relative risk of acute kidney injury (AKI) following different infections, and whether angiotensin-converting enzyme inhibitors (ACEIs)/angiotensin receptor blockers (ARBs) modify the risk, is unclear. We aimed to determine the risks of hospital admission with AKI following infections (urinary tract infection [UTI], lower respiratory tract infection [LRTI], and gastroenteritis) among users of antihypertensive drugs.MethodsWe used UK electronic health records from practices contributing to the Clinical Practice Research Datalink linked to the Hospital Episode Statistics database. We identified adults initiating ACEIs/ARBs or alternative antihypertensive therapy (β-blockers, calcium channel blockers, or thiazide diuretics) between April 1997 and March 2014 with at least 1 year of primary care registration prior to first prescription, who had a hospital admission for AKI, and who had a primary care record for incident UTI, LRTI, or gastroenteritis. We used a self-controlled case series design to calculate age-adjusted incidence rate ratios (IRRs) for AKI during risk periods following acute infection relative to noninfected periods (baseline).ResultsWe identified 10,219 eligible new users of ACEIs/ARBs or other antihypertensives with an AKI record. Among these, 2,012 had at least one record for a UTI during follow-up, 2,831 had a record for LRTI, and 651 had a record for gastroenteritis. AKI risk was higher following infection than in baseline noninfectious periods. The rate ratio was highest following gastroenteritis: for the period 1–7 days postinfection, the IRR for AKI following gastroenteritis was 43.4 (95% CI=34.0–55.5), compared with 6.0 following LRTI (95% CI=5.0–7.3), and 9.3 following UTI (95% CI=7.8–11.2). Increased risks were similar for different antihypertensives.ConclusionAcute infections are associated with substantially increased transient AKI risk among antihypertensive users, with the highest risk after gastroenteritis. The increase in relative risk is not greater among users of ACEIs/ARBs compared with users of other antihypertensives.

Highlights

  • Acute kidney injury (AKI) is a rapid deterioration in kidney function, associated with increased mortality,[1,2] prolonged hospital stay,[3,4] and the risk of chronic kidney disease.[5]

  • We investigated how the relative risk of AKI associated with acute infection differed in angiotensin-converting enzyme inhibitors (ACEIs)/angiotensin receptor blockers (ARBs) users compared with the risk in users of other antihypertensives, which are prescribed for similar indications and not considered substantial risk factors for AKI.[8]

  • AKI rate ratio was highest following gastroenteritis; for the period 1–7 days postinfection, incidence rate ratios (IRRs) for gastroenteritis was 43.3, compared with 6.0 in lower respiratory tract infection (LRTI) and 9.3 in urinary tract infection (UTI)

Read more

Summary

Introduction

Acute kidney injury (AKI) is a rapid (within hours or days) deterioration in kidney function, associated with increased mortality,[1,2] prolonged hospital stay,[3,4] and the risk of chronic kidney disease.[5]. The extent to which this risk is increased among patients prescribed ACEIs/ARBs compared with users of other antihypertensive drugs is unclear This information is needed to allow health care professionals to identify patients at a high risk of AKI. The relative risk of acute kidney injury (AKI) following different infections, and whether angiotensin-converting enzyme inhibitors (ACEIs)/angiotensin receptor blockers (ARBs) modify the risk, is unclear. We aimed to determine the risks of hospital admission with AKI following infections (urinary tract infection [UTI], lower respiratory tract infection [LRTI], and gastroenteritis) among users of antihypertensive drugs. We used a self-controlled case series design to calculate age-adjusted incidence rate ratios (IRRs) for AKI during risk periods following acute infection relative to noninfected periods (baseline).

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call