Study Protocol for a Pilot, Open-Label, Prospective, and Observational Study to Evaluate the Pharmacokinetics of Drugs Administered to Patients during Extracorporeal Circulation; Potential of In Vivo Cytochrome P450 Phenotyping to Optimise Pharmacotherapy.

cardiopulmonary bypass cytochrome P450 (CYP), CYP phenotyping extracorporeal circulation extracorporeal membrane oxygenation

Journal

Methods and protocols
ISSN: 2409-9279
Titre abrégé: Methods Protoc
Pays: Switzerland
ID NLM: 101720073

Informations de publication

Date de publication:
13 May 2019
Historique:
received: 25 02 2019
revised: 05 05 2019
accepted: 07 05 2019
entrez: 6 6 2019
pubmed: 6 6 2019
medline: 6 6 2019
Statut: epublish

Résumé

Pharmacokinetic alterations of medications administered during surgeries involving cardiopulmonary bypass (CPB) and extracorporeal membrane oxygenation (ECMO) have been reported. The impact of CPB on the cytochrome P450 (CYP) enzymes' activity is the key factor. The metabolic rates of caffeine, dextromethorphan, midazolam, omeprazole, and Losartan to the CYP-specific metabolites are validated measures of in vivo CYP 1A2, 2D6, 3A4, 2C19, and 2C9 activities, respectively. The study aim is to assess the activities of major CYPs in patients on extracorporeal circulation (EC). This is a pilot, prospective, open-label, observational study in patients undergoing surgery using EC and patients undergoing laparoscopic cholecystectomy as a control group. CYP activities will be measured on the day, and 1-2 days pre-surgery/3-4 days post-surgery (cardiac surgery and Laparoscopic cholecystectomy) and 1-2 days after starting ECMO, 1-2 weeks after starting ECMO, and 1-2 days after discontinuation from ECMO. Aforementioned CYP substrates will be administered to the patient and blood samples will be collected at 0, 1, 2, 4, and 6 h post-dose. Major CYP enzymes' activities will be compared in each participant on the day, and before/after surgery. The CYP activities will be compared in three study groups to investigate the impact of CYPs on EC.

Identifiants

pubmed: 31164617
pii: mps2020038
doi: 10.3390/mps2020038
pmc: PMC6632166
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Santosh Kumar Sreevatsav Adiraju (SKS)

Centre for Integrated Preclinical Drug Development, School of Biomedical Sciences, Faculty of Medicine, University of Queensland, 4072 Brisbane, Australia. s.adiraju@uq.edu.au.

Kiran Shekar (K)

Adult Intensive Care Services, The Prince Charles Hospital, 4032 Chermside, Australia. shekarkiran@yahoo.com.
Critical Care Research Group, The Prince Charles Hospital, 4032 Chermside, Australia. shekarkiran@yahoo.com.

Peter Tesar (P)

Department of Cardiothoracic Surgery, The Prince Charles Hospital, 4032 Chermside, Australia. peter.tesar@health.qld.gov.au.

Rishendran Naidoo (R)

Critical Care Research Group, The Prince Charles Hospital, 4032 Chermside, Australia. rishendran.naidoo@health.qld.gov.au.

Ivan Rapchuk (I)

Department of Anesthesia, The Prince Charles Hospital, 4032 Chermside, Australia. ivan.rapchuk@health.qld.gov.au.

Stephen Belz (S)

Adult Intensive Care Services, The Prince Charles Hospital, 4032 Chermside, Australia. stephen.belz@health.qld.gov.au.

John F Fraser (JF)

Adult Intensive Care Services, The Prince Charles Hospital, 4032 Chermside, Australia. john.fraser@health.qld.gov.au.

Maree T Smith (MT)

Centre for Integrated Preclinical Drug Development, School of Biomedical Sciences, Faculty of Medicine, University of Queensland, 4072 Brisbane, Australia. maree.smith@uq.edu.au.
School of Pharmacy, Faculty of Health and Behavioral Sciences, The University of Queensland, 4072 Brisbane, Australia. maree.smith@uq.edu.au.

Sussan Ghassabian (S)

Centre for Integrated Preclinical Drug Development, School of Biomedical Sciences, Faculty of Medicine, University of Queensland, 4072 Brisbane, Australia. Susan.ghassabian@gmail.com.

Classifications MeSH