Potential Cytochrome P450 Drug-Drug Interaction Among Adult and Adolescent Patients Undergoing Tonsillectomy.

adenotonsillectomy adult cytochrome P450 medication interaction obstructive sleep apnea opioid patient safety tonsillectomy

Journal

OTO open
ISSN: 2473-974X
Titre abrégé: OTO Open
Pays: United States
ID NLM: 101717942

Informations de publication

Date de publication:
Historique:
received: 27 01 2020
accepted: 09 05 2020
entrez: 30 6 2020
pubmed: 1 7 2020
medline: 1 7 2020
Statut: epublish

Résumé

To assess the frequency of potential drug-drug interactions affecting cytochrome P450 (CYP)-mediated metabolism of opioids among adult and adolescent patients who underwent adenotonsillectomy. Retrospective chart review. Tertiary care university hospital. A retrospective review was conducted of 279 patients who underwent adenotonsillectomy at the University of Rochester. The discharge medication list was reviewed for all patients, and their postoperative medications were compared with a reference list published by the Food and Drug Administration and the University of Indiana's Department of Clinical Pharmacology (Flockhart Table) to determine whether CYP-inducing or CYP-inhibiting medication was present. Out of 279 patients, 197 different medications were taken postoperatively. Approximately 70% of patients were taking 2 medications in addition to the standard postoperative analgesics (acetaminophen, hydrocodone, oxycodone, morphine, and/or ibuprofen). The 5 most commonly prescribed medications excluding the posttonsillectomy medications were oral contraceptives, ondansetron, amoxicillin, albuterol, and methylprednisolone. Four percent of patients were taking a medication that inhibits CYP3A4; <1% were taking a medication that induces CYP3A4; and 15% were taking a medication that inhibits CYP2D6. Nearly 20% of the patients in this cohort were taking a medication that may alter opioid metabolism through induction or inhibition of CYP3A4 or CYP2D6. Some of these interactions have the potential to be more clinically relevant than others, particularly interactions that can lead to enhanced toxicity of opioids due to accumulation of active metabolites.

Identifiants

pubmed: 32596625
doi: 10.1177/2473974X20932503
pii: 10.1177_2473974X20932503
pmc: PMC7303781
doi:

Types de publication

Journal Article

Langues

eng

Pagination

2473974X20932503

Informations de copyright

© The Authors 2020.

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Auteurs

Sai Nimmagadda (S)

University of Rochester, Rochester, New York, USA.

Stephanie Jung-Ying Wong (SJ)

University of Rochester, Rochester, New York, USA.

Madlin Faria (M)

Independent, Rochester, New York, USA.

Paul Allen (P)

University of Rochester, Rochester, New York, USA.

John Faria (J)

University of Rochester, Rochester, New York, USA.

Classifications MeSH