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Improvement Initiative to Develop and Implement a Tool for Detecting Drug-Drug Interactions During Oncology Clinical Trial Enrollment Eligibility Screening.
Marcath, Lauren A; Coe, Taylor D; Shakeel, Faisal; Reynolds, Edward; Bayuk, Mike; Haas, Steven; Redman, Bruce G; Wong, Siu-Fun; Hertz, Daniel L.
Affiliation
  • Marcath LA; From the Department of Pharmacotherapy, College of Pharmacy and Pharmaceutical Sciences, Washington State University, Spokane, Washington.
  • Coe TD; Department of Clinical Pharmacy, College of Pharmacy, University of Michigan, Ann Arbor, Michigan.
  • Shakeel F; Department of Clinical Pharmacy, College of Pharmacy, University of Michigan, Ann Arbor, Michigan.
  • Reynolds E; ©PEPID, LLC, Phoenix, Arizona.
  • Bayuk M; ©PEPID, LLC, Phoenix, Arizona.
  • Haas S; ©PEPID, LLC, Phoenix, Arizona.
  • Redman BG; Department of Internal Medicine-Hematology/Oncology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan.
  • Wong SF; Chapman University School of Pharmacy, Irvine, California.
  • Hertz DL; Department of Clinical Pharmacy, College of Pharmacy, University of Michigan, Ann Arbor, Michigan.
J Patient Saf ; 17(1): e28-e34, 2021 01 01.
Article de En | MEDLINE | ID: mdl-33003175
ABSTRACT

OBJECTIVES:

Screening subjects for drug-drug interactions (DDIs) before enrollment in oncology clinical trials is integral to ensuring safety, but standard procedures or tools are not readily available to screen DDI in this setting. Our objectives were to develop a DDI screening tool for use during oncology clinical trial enrollment and to test usability in single-center and multicenter pilot studies.

METHODS:

A multistage approach was used for this quality improvement intervention. Semistructured interviews with individuals responsible for DDI screening were conducted to develop a prototype tool. The tool was used for screening DDI in subjects enrolling in National Clinical Trials Network trials of commercially available agents during a single-center 3-month pilot. Improvements were made, and a 3-month multicenter pilot was conducted at volunteer SWOG Cancer Research Network sites. Participants were surveyed to determine tool usability and efficiency.

RESULTS:

A tool was developed from semistructured interviews. A critical feature was reporting which medications had specific pharmacokinetic and pharmacodynamic characteristics including transporter and cytochrome P450 substrates, inhibitors, or inducers and QT prolongation. In the 12-site study, average (SD) DDI screening time for each patient decreased by 15.7 (10.2) minutes (range, 3-35 minutes; P < 0.001). Users reported the tool highly usable, with >90% agreeing with all positive usability characterizations and disagreeing with all negative complexity characterizations.

CONCLUSIONS:

A DDI screening tool for oncology clinical trial enrollment was created and its usability confirmed. Further testing with more diverse investigator sites and study drugs during eligibility screening is warranted to improve safety and data accuracy within clinical trials.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Interactions médicamenteuses / Détermination de l&apos;admissibilité / Tumeurs Type d'étude: Clinical_trials / Diagnostic_studies / Prognostic_studies / Qualitative_research / Screening_studies Limites: Female / Humans / Male Langue: En Journal: J Patient Saf Sujet du journal: SERVICOS DE SAUDE Année: 2021 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Interactions médicamenteuses / Détermination de l&apos;admissibilité / Tumeurs Type d'étude: Clinical_trials / Diagnostic_studies / Prognostic_studies / Qualitative_research / Screening_studies Limites: Female / Humans / Male Langue: En Journal: J Patient Saf Sujet du journal: SERVICOS DE SAUDE Année: 2021 Type de document: Article