TY - JOUR
T1 - Non-recovery of vancomycin-associated nephrotoxicity is related to worsening survival outcomes
T2 - Combined retrospective analyses of two real-world databases
AU - Chuma, Masayuki
AU - Hamano, Hirofumi
AU - Bando, Takashi
AU - Kondo, Masateru
AU - Okada, Naoto
AU - Izumi, Yuki
AU - Ishida, Shunsuke
AU - Yoshioka, Toshihiko
AU - Asada, Mizuho
AU - Niimura, Takahiro
AU - Zamami, Yoshito
AU - Takechi, Kenshi
AU - Goda, Mitsuhiro
AU - Miyata, Koji
AU - Yagi, Kenta
AU - Kasamo, Sachiko
AU - Izawa-Ishizawa, Yuki
AU - Azuma, Momoyo
AU - Yanagawa, Hiroaki
AU - Tasaki, Yoshikazu
AU - Ishizawa, Keisuke
N1 - Funding Information:
This work was supported by JSPS KAKENHI (Grant 19K16448 and 20H05798) from the Ministry of Education, Culture, Sports, Science, and Technology of Japan. We thank Editage (Tokyo, Japan) for the English language editing.
Publisher Copyright:
© 2022 Nordic Association for the Publication of BCPT (former Nordic Pharmacological Society). Published by John Wiley & Sons Ltd.
PY - 2022
Y1 - 2022
N2 - There has been growing concern in worsening survival and renal outcomes following vancomycin-associated nephrotoxicity (VAN) onset, but the factors associated with these phenomena remain unclear. To examine these factors, we performed a retrospective study combining the analysis of two real-world databases. Initially, the FDA Adverse Event Reporting System (FAERS) was used to evaluate the relationship between VAN and mortality using odds ratios (ORs) and 95% confidence intervals (CIs). Next, electronic medical records (EMRs) were examined in a more robust cohort for evaluation of the association between renal outcomes and worsening survival using Cox proportional hazards regression models. FAERS analysis revealed a significant correlation between VAN occurrence and increased mortality (OR: 1.30; 95% CI: 1.17–1.46). EMR analysis showed that non-recovery of VAN was associated with increased hospital mortality (hazard ratio [HR]: 4.05; 95% CI: 2.42–6.77) and 1-year mortality (HR: 3.03, 95% CI: 1.98–4.64). The HR for VAN recovery was lower for patients with acute kidney injury (AKI) stage ≥2 (HR: 0.09; 95% CI: 0.02–0.40). Thus, worsening survival outcomes were associated with non-recovery of VAN, whereby AKI stage ≥2 was a significant risk factor. Progression to severe VAN should be prevented for better survival outcomes.
AB - There has been growing concern in worsening survival and renal outcomes following vancomycin-associated nephrotoxicity (VAN) onset, but the factors associated with these phenomena remain unclear. To examine these factors, we performed a retrospective study combining the analysis of two real-world databases. Initially, the FDA Adverse Event Reporting System (FAERS) was used to evaluate the relationship between VAN and mortality using odds ratios (ORs) and 95% confidence intervals (CIs). Next, electronic medical records (EMRs) were examined in a more robust cohort for evaluation of the association between renal outcomes and worsening survival using Cox proportional hazards regression models. FAERS analysis revealed a significant correlation between VAN occurrence and increased mortality (OR: 1.30; 95% CI: 1.17–1.46). EMR analysis showed that non-recovery of VAN was associated with increased hospital mortality (hazard ratio [HR]: 4.05; 95% CI: 2.42–6.77) and 1-year mortality (HR: 3.03, 95% CI: 1.98–4.64). The HR for VAN recovery was lower for patients with acute kidney injury (AKI) stage ≥2 (HR: 0.09; 95% CI: 0.02–0.40). Thus, worsening survival outcomes were associated with non-recovery of VAN, whereby AKI stage ≥2 was a significant risk factor. Progression to severe VAN should be prevented for better survival outcomes.
KW - electronic medical records (EMRs)
KW - renal outcome
KW - spontaneous adverse event reporting database
KW - survival outcome
KW - vancomycin-associated nephrotoxicity (VAN)
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U2 - 10.1111/bcpt.13799
DO - 10.1111/bcpt.13799
M3 - Article
C2 - 36169161
AN - SCOPUS:85139393974
SN - 1742-7835
JO - Basic and Clinical Pharmacology and Toxicology
JF - Basic and Clinical Pharmacology and Toxicology
ER -