Influence of venovenous extracorporeal membrane oxygenation on pharmacokinetics of vancomycin in lung transplant recipients.

What is known and objective: The influence of venovenous extracorporeal membrane oxygenation (VV‐ECMO) on the population pharmacokinetics (PPK) of vancomycin in recipients after lung transplantation (LTx) is unknown. We investigated whether VV‐ECMO influences vancomycin PPK and determined optimal re...

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Publicado en:Journal of Clinical Pharmacy & Therapeutics Vol. 45; no. 5; pp. 1066 - 1076
Autores principales: Liu, Donglin, Chen, Wenqian, Wang, Qianlin, Li, Min, Zhang, Zhu, Cui, Gang, Li, Pengmei, Zhang, Xianglin, Ma, Yi, Zhan, Qingyuan, Wang, Chen
Formato: research tables/charts Journal Article
Publicado: Wiley-Blackwell Oct2020
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Oct2020
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        atl: Influence of venovenous extracorporeal membrane oxygenation on pharmacokinetics of vancomycin in lung transplant recipients.
      aug:
        au:
          Liu, Donglin
          Chen, Wenqian
          Wang, Qianlin
          Li, Min
          Zhang, Zhu
          Cui, Gang
          Li, Pengmei
          Zhang, Xianglin
          Ma, Yi
          Zhan, Qingyuan
          Wang, Chen
        affil: Department of Pulmonary and Critical Care Medicine, Center of Respiratory Medicine, China‐Japan Friendship Hospital, Capital Medical University, Beijing, China
      sug:
        subj:
          Extracorporeal Membrane Oxygenation
          Vancomycin Pharmacokinetics
          Lung Transplantation
          Transplant Recipients
          Human
          Vancomycin Blood
          Systems Analysis
          Simulations
          Methicillin-Resistant Staphylococcus Aureus
          Vancomycin
      ab: What is known and objective: The influence of venovenous extracorporeal membrane oxygenation (VV‐ECMO) on the population pharmacokinetics (PPK) of vancomycin in recipients after lung transplantation (LTx) is unknown. We investigated whether VV‐ECMO influences vancomycin PPK and determined optimal recommended dosage for patients after LTx. Methods: We tested vancomycin serum concentration and calculated PPK parameters using NONMEM. To check for any potential influence of ECMO on vancomycin PK, we compared ECMO patients with a non‐ECMO patient control group, and patients before and after ECMO weaning as self‐control to analysed changes in vancomycin PK. Monte Carlo dosing simulation was conducted to explore vancomycin dosing regimens. Results: Nineteen ECMO and 6 non‐ECMO lung transplant recipients were enrolled. Vancomycin serum concentrations did not significantly differ between patients with and without ECMO support. Comparison of separate vancomycin population pharmacokinetic models showed that ECMO patients had smaller peripheral compartment volume of distribution (V2) [Estimate (relative standard error, RSE, %) 19.7 (12) vs. 22 (17) L, P =.003] than non‐ECMO patients. For treatment of methicillin‐resistant Staphylococcus aureus (MRSA) infections with MIC ≤ 0.5 µg/mL, venous infusion of 400 mg vancomycin every 8 hours was recommended. For MRSA infection with MIC ≤ 1 µg/mL, the proposed dosage was 600 mg every 8 hours. What is new and conclusion: Venovenous extracorporeal membrane oxygenation slightly alters vancomycin PK but does not significantly impact vancomycin serum concentration in patients after LTx. Dose adjustment is not necessary for VV‐ECMO support. Specific vancomycin dosing regimens with lower nephrotoxicity may benefit LTx recipients with VV‐ECMO.
      pubtype: Academic Journal
      doctype:
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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