Improved Renal Function After Percutaneous Coronary Intervention in Non-Dialysis Patients With Acute Coronary Syndrome and Advanced Renal Dysfunction.


Journal

Cardiovascular revascularization medicine : including molecular interventions
ISSN: 1878-0938
Titre abrégé: Cardiovasc Revasc Med
Pays: United States
ID NLM: 101238551

Informations de publication

Date de publication:
03 2021
Historique:
received: 12 07 2020
revised: 01 09 2020
accepted: 03 09 2020
pubmed: 22 9 2020
medline: 14 9 2021
entrez: 21 9 2020
Statut: ppublish

Résumé

The deterioration of renal function is a strong prognostic predictor in patients with coronary artery disease. Although percutaneous coronary intervention (PCI) has sometimes resulted in improved renal function (IRF) in acute coronary syndrome (ACS) patients, its clinical implications have not been fully elucidated. This study aimed to investigate the prevalence and predictors of IRF after PCI and its relationship with long-term renal outcomes. In this retrospective observational cohort study, we examined data from 177 ACS patients with non-dialysis advanced renal dysfunction (estimated glomerular filtration rate [eGFR] < 30 mL/min/1.73 m IRF was observed in 66 (37.3%) patients. ST-elevation myocardial infarction and shock during PCI were independent predictors of IRF. Patients were followed up for a median of 695 days. Kaplan-Meier analyses demonstrated that patients with IRF had the lower incidence of initiation of permanent dialysis than those without IRF (Log-rank P = 0.015). IRF was relatively common in non-dialysis patients with ACS and advanced renal dysfunction who underwent PCI. ST-elevation myocardial infarction and shock, which may be indicative of hemodynamic instability during PCI, were independent predictors of IRF. Further, IRF was associated with favorable renal outcomes. Hemodynamic stabilization may be important for improving the short-term and long-term renal outcomes of high-risk patients.

Sections du résumé

BACKGROUND
The deterioration of renal function is a strong prognostic predictor in patients with coronary artery disease. Although percutaneous coronary intervention (PCI) has sometimes resulted in improved renal function (IRF) in acute coronary syndrome (ACS) patients, its clinical implications have not been fully elucidated. This study aimed to investigate the prevalence and predictors of IRF after PCI and its relationship with long-term renal outcomes.
METHODS
In this retrospective observational cohort study, we examined data from 177 ACS patients with non-dialysis advanced renal dysfunction (estimated glomerular filtration rate [eGFR] < 30 mL/min/1.73 m
RESULTS
IRF was observed in 66 (37.3%) patients. ST-elevation myocardial infarction and shock during PCI were independent predictors of IRF. Patients were followed up for a median of 695 days. Kaplan-Meier analyses demonstrated that patients with IRF had the lower incidence of initiation of permanent dialysis than those without IRF (Log-rank P = 0.015).
CONCLUSIONS
IRF was relatively common in non-dialysis patients with ACS and advanced renal dysfunction who underwent PCI. ST-elevation myocardial infarction and shock, which may be indicative of hemodynamic instability during PCI, were independent predictors of IRF. Further, IRF was associated with favorable renal outcomes. Hemodynamic stabilization may be important for improving the short-term and long-term renal outcomes of high-risk patients.

Identifiants

pubmed: 32952075
pii: S1553-8389(20)30560-1
doi: 10.1016/j.carrev.2020.09.011
pii:
doi:

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

26-30

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest H.I. received lecture fees from Astellas Pharma Inc., Astrazeneca Inc., Daiichi-Sankyo Pharma Inc., and MSD K. K. T.M. received lecture fees from Bayel Pharmaceutical Co., Ltd., Daiichi-Sankyo Co., Ltd., Dainippon Sumitomo Pharma Co., Ltd., Kowa Co., Ltd., MSD K. K., Mitsubishi Tanabe Pharma Co., Nippon Boehringer Ingelheim Co., Ltd., Novartis Pharma K. K., Pfizer Japan Inc., Sanofi-Aventis K. K., and Takeda Pharmaceutical Co., Ltd. T.M. received an unrestricted research grant for the Department of Cardiology, Nagoya University Graduate School of Medicine from Astellas Pharma Inc., Daiichi-Sankyo Co., Ltd., Dainippon Sumitomo Pharma Co., Ltd., Kowa Co., Ltd., MSD K. K., Mitsubishi Tanabe Pharma Co., Nippon Boehringer Ingelheim Co., Ltd., Novartis Pharma K. K., Otsuka Pharma Ltd., Pfizer Japan Inc., Sanofi-Aventis K. K., Takeda Pharmaceutical Co., Ltd., and Teijin Pharma Ltd.

Auteurs

Yusuke Uemura (Y)

Department of Cardiology, Cardiovascular Center, Anjo Kosei Hospital, Anjo, Japan. Electronic address: yusuke0307@kosei.anjo.aichi.jp.

Shinji Ishikawa (S)

Department of Cardiology, Cardiovascular Center, Anjo Kosei Hospital, Anjo, Japan.

Kenji Takemoto (K)

Department of Cardiology, Cardiovascular Center, Anjo Kosei Hospital, Anjo, Japan.

Yosuke Negishi (Y)

Department of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Akihito Tanaka (A)

Department of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Kensuke Takagi (K)

Department of Cardiology, Ogaki Municipal Hospital, Ogaki, Japan.

Naoki Yoshioka (N)

Department of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Hiroshi Tashiro (H)

Department of Cardiology, Ichinomiya Municipal Hospital, Ichinomiya, Japan.

Norio Umemoto (N)

Department of Cardiology, Ichinomiya Municipal Hospital, Ichinomiya, Japan.

Yosuke Inoue (Y)

Department of Cardiology, Tosei General Hospital, Seto, Japan.

Itsuro Morishima (I)

Department of Cardiology, Ogaki Municipal Hospital, Ogaki, Japan.

Kiyokazu Shimizu (K)

Department of Cardiology, Ichinomiya Municipal Hospital, Ichinomiya, Japan.

Naoki Shibata (N)

Department of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Hiroshi Asano (H)

Department of Cardiology, Tosei General Hospital, Seto, Japan.

Hideki Ishii (H)

Department of Cardiology, Fujita Health University Bantane Hospital, Nagoya, Japan.

Masato Watarai (M)

Department of Cardiology, Cardiovascular Center, Anjo Kosei Hospital, Anjo, Japan.

Toyoaki Murohara (T)

Department of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

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