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Risk Factors for Teicoplanin-Associated Acute Kidney Injury in Patients with Hematological Malignancies: Focusing on Concomitant Use of Tazobactam/Piperacillin.
Morinaga, Yuko; Tanaka, Ryota; Tatsuta, Ryosuke; Takano, Kuniko; Hashimoto, Takehiro; Ogata, Masao; Hiramatsu, Kazufumi; Itoh, Hiroki.
Affiliation
  • Morinaga Y; Department of Clinical Pharmacy, Oita University Hospital.
  • Tanaka R; Department of Clinical Pharmacy, Oita University Hospital.
  • Tatsuta R; Department of Clinical Pharmacy, Oita University Hospital.
  • Takano K; Department of Hematology, Oita University Hospital.
  • Hashimoto T; Hospital Infection Control Center, Oita University Hospital.
  • Ogata M; Department of Hematology, Oita University Hospital.
  • Hiramatsu K; Hospital Infection Control Center, Oita University Hospital.
  • Itoh H; Department of Clinical Pharmacy, Oita University Hospital.
Biol Pharm Bull ; 47(5): 988-996, 2024.
Article in En | MEDLINE | ID: mdl-38763761
ABSTRACT
Patients with hematological malignancies (HM) often receive tazobactam/piperacillin (TAZ/PIPC) and glycopeptide antibiotics for febrile neutropenia. The effect of concomitant use of TAZ/PIPC on risk of teicoplanin (TEIC)-associated acute kidney injury (AKI) remains unclear. We investigated the impact of concomitant TAZ/PIPC use on TEIC-associated AKI in HM patients and identified the risk factors. In this retrospective, single-center, observational cohort study, 203 patients received TEIC, 176 of whom satisfied the selection criteria and were divided into TEIC cohort (no TAZ/PIPC; n = 118) and TEIC + TAZ/PIPC cohort (n = 58). AKI was defined as serum creatinine increase ≥0.3 mg/dL within 48 h or ≥50% from baseline. Incidence of AKI in TEIC cohort before and after propensity score matching was 9.3 and 5.9%, respectively, and that in TEIC + TAZ/PIPC cohort was 10.3 and 11.8%. AKI incidence and risk were not significantly different between two cohorts before (p = 0.829; odds ratio (OR) 1.122, 95% confidence interval (CI) 0.393-3.202) and after matching (p = 0.244; OR 2.133, 95% CI 0.503-9.043). Logistic regression analysis with factors clinically or mechanistically potentially related to TEIC-associated AKI, including concomitant TAZ/PIPC use, as independent variables identified baseline hemoglobin level as the only significant risk factor for TEIC-associated AKI (p = 0.011; OR 0.484, 95% CI 0.276-0.848). In HM patients treated with TEIC, concomitant TAZ/PIPC use did not increase AKI risk whereas lower hemoglobin levels had higher risk for TEIC-associated AKI development, suggesting the necessity to monitor serum creatinine when using TEIC in patients with anemia.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Teicoplanin / Hematologic Neoplasms / Acute Kidney Injury / Piperacillin, Tazobactam Drug Combination / Anti-Bacterial Agents Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Biol Pharm Bull Journal subject: BIOQUIMICA / FARMACOLOGIA Year: 2024 Document type: Article Country of publication: Japón

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Teicoplanin / Hematologic Neoplasms / Acute Kidney Injury / Piperacillin, Tazobactam Drug Combination / Anti-Bacterial Agents Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Biol Pharm Bull Journal subject: BIOQUIMICA / FARMACOLOGIA Year: 2024 Document type: Article Country of publication: Japón