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Non-steroidal anti-inflammatory drugs and risk of acute adverse renal outcomes in diabetes and diabetic kidney disease.
Lim, Cynthia Ciwei; Kadir, Hanis Bte Abdul; Tan, Ngiap Chuan; Ang, Andrew Teck Wee; Bee, Yong Mong; Lee, Puay Hoon; Goh, Bandy Qiuling; Ang, Alcey Li Chang; Xin, Xiaohui; Kwek, Jia Liang; Lam, Amanda Yun Rui; Choo, Jason Chon Jun.
Afiliação
  • Lim CC; Department of Renal Medicine, Singapore General Hospital, Singapore.
  • Kadir HBA; Health Services Research Unit, Singapore General Hospital, Singapore.
  • Tan NC; SingHealth Polyclinics, Singapore.
  • Ang ATW; SingHealth Polyclinics, Singapore.
  • Bee YM; Department of Endocrinology, Singapore General Hospital, Singapore.
  • Lee PH; Pharmacy, Singapore General Hospital, Singapore.
  • Goh BQ; SingHealth Polyclinics, Singapore.
  • Ang ALC; Research Efficiency Enhancement Program, Division of Medicine, Singapore General Hospital, Singapore.
  • Xin X; Health Services Research Unit, Singapore General Hospital, Singapore.
  • Kwek JL; Department of Renal Medicine, Singapore General Hospital, Singapore.
  • Lam AYR; Department of Endocrinology, Singapore General Hospital, Singapore.
  • Choo JCJ; Department of Renal Medicine, Singapore General Hospital, Singapore.
Int J Risk Saf Med ; 33(1): 27-36, 2022.
Article em En | MEDLINE | ID: mdl-34397422
ABSTRACT

BACKGROUND:

Individuals with diabetes mellitus (DM) may be susceptible to non-steroidal anti-inflammatory drug (NSAID)-induced acute kidney injury (AKI) but data on NSAID-related adverse renal events is sparse.

OBJECTIVE:

We aimed to evaluate the risk of acute kidney injury and/or hyperkalemia after systemic NSAID among individuals with DM and diabetic chronic kidney disease (CKD).

METHODS:

Retrospective cohort study of 3896 adults with DM with incident prescriptions between July 2015 and December 2017 from Singapore General Hospital and SingHealth Polyclinics. Laboratory, hospitalization and medication data were retrieved from electronic medical records. The primary outcome was the incidence of AKI and/ or hyperkalemia within 30 days after prescription.

RESULTS:

AKI and/or hyperkalemia occurred in 13.5% of all DM and 15.8% of diabetic CKD. The association between systemic NSAID >14 days and 30-day risk of AKI and/or hyperkalemia failed to reach statistical significance in unselected DM (adjusted OR 1.62, 95% CI 0.99-2.65, p = 0.05) and diabetic CKD (adjusted OR 0.64, 95% CI 0.15-2.82, p = 0.64), but the odds of AKI and/or hyperkalemia were markedly and significantly increased when NSAID was prescribed with renin-angiotensin-aldosterone system (RAAS) blocker (adjusted OR 4.17, 95% CI 1.74-9.98, p = 0.001) or diuretic (adjusted OR 3.31, 95% CI 1.09-10.08, p = 0.04) and in the absence of diabetic CKD (adjusted OR 1.98, 95% CI 1.16-3.36, p = 0.01).

CONCLUSION:

NSAID prescription >14 days in individuals with DM with concurrent RAAS blockers or diuretics was associated with higher 30-day risk of AKI and/or hyperkalemia.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diabetes Mellitus / Nefropatias Diabéticas / Insuficiência Renal Crônica / Injúria Renal Aguda / Hiperpotassemia Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diabetes Mellitus / Nefropatias Diabéticas / Insuficiência Renal Crônica / Injúria Renal Aguda / Hiperpotassemia Idioma: En Ano de publicação: 2022 Tipo de documento: Article