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Pharmacovigilance study of anti-infective-related acute kidney injury using the Japanese adverse drug event report database

BACKGROUND: Acute kidney injury (AKI) is associated with significant increases in short- and long-term morbidity and mortality. Drug-induced AKI is a major concern in the present healthcare system. Our spontaneous reporting system (SRS) analysis assessed links between AKI, along with patients’ age,...

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Autores principales: Nakao, Satoshi, Hasegawa, Shiori, Umetsu, Ryogo, Shimada, Kazuyo, Mukai, Ririka, Tanaka, Mizuki, Matsumoto, Kiyoka, Yoshida, Yu, Inoue, Misaki, Satake, Riko, Nishibata, Yuri, Liao, Jun, Nakamura, Mitsuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8404262/
https://www.ncbi.nlm.nih.gov/pubmed/34462002
http://dx.doi.org/10.1186/s40360-021-00513-x
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author Nakao, Satoshi
Hasegawa, Shiori
Umetsu, Ryogo
Shimada, Kazuyo
Mukai, Ririka
Tanaka, Mizuki
Matsumoto, Kiyoka
Yoshida, Yu
Inoue, Misaki
Satake, Riko
Nishibata, Yuri
Liao, Jun
Nakamura, Mitsuhiro
author_facet Nakao, Satoshi
Hasegawa, Shiori
Umetsu, Ryogo
Shimada, Kazuyo
Mukai, Ririka
Tanaka, Mizuki
Matsumoto, Kiyoka
Yoshida, Yu
Inoue, Misaki
Satake, Riko
Nishibata, Yuri
Liao, Jun
Nakamura, Mitsuhiro
author_sort Nakao, Satoshi
collection PubMed
description BACKGROUND: Acute kidney injury (AKI) is associated with significant increases in short- and long-term morbidity and mortality. Drug-induced AKI is a major concern in the present healthcare system. Our spontaneous reporting system (SRS) analysis assessed links between AKI, along with patients’ age, as healthcare-associated risks and administered anti-infectives. We also generated anti-infective-related AKI-onset profiles. METHOD: We calculated reporting odds ratios (RORs) for reports of anti-infective-related AKI (per Medical Dictionary for Regulatory Activities) in the Japanese Adverse Drug Event Report database and evaluated the effect of anti-infective combination therapy. The background factors of cases with anti-infective monotherapy and combination therapy (≥ 2 anti-infectives) were matched using propensity score. We evaluated time-to-onset data and hazard types using the Weibull parameter. RESULTS: Among 534,688 reports (submission period: April 2004–June 2018), there were 21,727 AKI events. The reported number of AKI associated with glycopeptide antibacterials, fluoroquinolones, third-generation cephalosporins, triazole derivatives, and carbapenems were 596, 494, 341, 315, and 313, respectively. Crude RORs of anti-infective-related AKI increased among older patients and were higher in anti-infective combination therapies [anti-infectives, ≥ 2; ROR, 1.94 (1.80–2.09)] than in monotherapies [ROR, 1.29 (1.22–1.36)]. After propensity score matching, the adjusted RORs of anti-infective monotherapy and combination therapy (≥ 2 anti-infectives) were 0.67 (0.58–0.77) and 1.49 (1.29–1.71), respectively. Moreover, 48.1% of AKI occurred within 5 days (median, 5.0 days) of anti-infective therapy initiation. CONCLUSION: RORs derived from our new SRS analysis indicate potential AKI risks and number of administered anti-infectives. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40360-021-00513-x.
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spelling pubmed-84042622021-08-30 Pharmacovigilance study of anti-infective-related acute kidney injury using the Japanese adverse drug event report database Nakao, Satoshi Hasegawa, Shiori Umetsu, Ryogo Shimada, Kazuyo Mukai, Ririka Tanaka, Mizuki Matsumoto, Kiyoka Yoshida, Yu Inoue, Misaki Satake, Riko Nishibata, Yuri Liao, Jun Nakamura, Mitsuhiro BMC Pharmacol Toxicol Research Article BACKGROUND: Acute kidney injury (AKI) is associated with significant increases in short- and long-term morbidity and mortality. Drug-induced AKI is a major concern in the present healthcare system. Our spontaneous reporting system (SRS) analysis assessed links between AKI, along with patients’ age, as healthcare-associated risks and administered anti-infectives. We also generated anti-infective-related AKI-onset profiles. METHOD: We calculated reporting odds ratios (RORs) for reports of anti-infective-related AKI (per Medical Dictionary for Regulatory Activities) in the Japanese Adverse Drug Event Report database and evaluated the effect of anti-infective combination therapy. The background factors of cases with anti-infective monotherapy and combination therapy (≥ 2 anti-infectives) were matched using propensity score. We evaluated time-to-onset data and hazard types using the Weibull parameter. RESULTS: Among 534,688 reports (submission period: April 2004–June 2018), there were 21,727 AKI events. The reported number of AKI associated with glycopeptide antibacterials, fluoroquinolones, third-generation cephalosporins, triazole derivatives, and carbapenems were 596, 494, 341, 315, and 313, respectively. Crude RORs of anti-infective-related AKI increased among older patients and were higher in anti-infective combination therapies [anti-infectives, ≥ 2; ROR, 1.94 (1.80–2.09)] than in monotherapies [ROR, 1.29 (1.22–1.36)]. After propensity score matching, the adjusted RORs of anti-infective monotherapy and combination therapy (≥ 2 anti-infectives) were 0.67 (0.58–0.77) and 1.49 (1.29–1.71), respectively. Moreover, 48.1% of AKI occurred within 5 days (median, 5.0 days) of anti-infective therapy initiation. CONCLUSION: RORs derived from our new SRS analysis indicate potential AKI risks and number of administered anti-infectives. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40360-021-00513-x. BioMed Central 2021-08-30 /pmc/articles/PMC8404262/ /pubmed/34462002 http://dx.doi.org/10.1186/s40360-021-00513-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Nakao, Satoshi
Hasegawa, Shiori
Umetsu, Ryogo
Shimada, Kazuyo
Mukai, Ririka
Tanaka, Mizuki
Matsumoto, Kiyoka
Yoshida, Yu
Inoue, Misaki
Satake, Riko
Nishibata, Yuri
Liao, Jun
Nakamura, Mitsuhiro
Pharmacovigilance study of anti-infective-related acute kidney injury using the Japanese adverse drug event report database
title Pharmacovigilance study of anti-infective-related acute kidney injury using the Japanese adverse drug event report database
title_full Pharmacovigilance study of anti-infective-related acute kidney injury using the Japanese adverse drug event report database
title_fullStr Pharmacovigilance study of anti-infective-related acute kidney injury using the Japanese adverse drug event report database
title_full_unstemmed Pharmacovigilance study of anti-infective-related acute kidney injury using the Japanese adverse drug event report database
title_short Pharmacovigilance study of anti-infective-related acute kidney injury using the Japanese adverse drug event report database
title_sort pharmacovigilance study of anti-infective-related acute kidney injury using the japanese adverse drug event report database
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8404262/
https://www.ncbi.nlm.nih.gov/pubmed/34462002
http://dx.doi.org/10.1186/s40360-021-00513-x
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