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Oral anticoagulants and relative risk of acute kidney injury in patients with atrial fibrillation: A systematic review and network meta-analysis.
Luo, Shengyuan; Derbas, Laith A; Wen, Yumeng; Arif, Sally; Tracy, Melissa; Wasserlauf, Jeremiah; Huang, Henry D; Reiser, Jochen; Williams, Kim A; Volgman, Annabelle Santos.
Affiliation
  • Luo S; Department of Internal Medicine, Rush University Medical Center, Chicago, IL, USA.
  • Derbas LA; Department of Internal Medicine, Rush University Medical Center, Chicago, IL, USA.
  • Wen Y; Division of Nephrology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Arif S; Department of Internal Medicine, Rush University Medical Center, Chicago, IL, USA.
  • Tracy M; Department of Internal Medicine, Rush University Medical Center, Chicago, IL, USA.
  • Wasserlauf J; Department of Internal Medicine, Rush University Medical Center, Chicago, IL, USA.
  • Huang HD; Department of Internal Medicine, Rush University Medical Center, Chicago, IL, USA.
  • Reiser J; Department of Internal Medicine, Rush University Medical Center, Chicago, IL, USA.
  • Williams KA; Department of Internal Medicine, Rush University Medical Center, Chicago, IL, USA.
  • Volgman AS; Department of Internal Medicine, Rush University Medical Center, Chicago, IL, USA.
Am Heart J Plus ; 15: 100132, 2022 Mar.
Article in En | MEDLINE | ID: mdl-38558757
ABSTRACT
Study

objective:

Oral anticoagulants (direct oral anticoagulants [DOACs] or warfarin) prevent stroke in patients with atrial fibrillation (AF), but their use may be associated with acute kidney injury (AKI). We aimed to compare AKI risk across individual oral anticoagulants in patients with AF.

Design:

Systematic review and network meta-analysis.

Setting:

Randomized trials and population-based studies.

Participants:

Patients with AF.

Interventions:

Oral anticoagulants. Main outcome

measures:

AKI.

Results:

A systematic literature search in Medline and Embase databases performed on December 17, 2021 identified ten randomized trials and eight population-based longitudinal studies based on prespecified inclusion criteria for systematic review. Clinical trials had short follow-ups and reported only low event rates of serious AKI. Retrospective longitudinal studies were assessed to be at higher risk for bias from confounding and outcome ascertainment, but follow-up was longer (1.5 to 8 years), with AKI incidence ranging from 2 to 29/100 person-years. Eight longitudinal studies that met transitivity assumption were included in a random-effects network meta-analysis within a Bayesian framework. All DOACs were associated with significantly lower risk of AKI compared to warfarin. Dabigatran was associated with lower risk of AKI compared to apixaban (hazard ratio [HR] = 0.82; 95% confidence interval [CI] 0.68-0.99), rivaroxaban (HR = 0.84; 95%CI 0.72-0.98), and warfarin (HR = 0.68; 95%CI 0.59-0.77). Effect size estimates varied by chronic kidney disease status and study geographic locations.

Conclusion:

Apixaban, rivaroxaban, and dabigatran were associated with lower long-term risk of AKI compared to warfarin among patients with AF, with dabigatran potentially associated with the lowest risk.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Am Heart J Plus Year: 2022 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Am Heart J Plus Year: 2022 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos