Best-worst scaling methodology to evaluate constructs of the Consolidated Framework for Implementation Research: application to the implementation of pharmacogenetic testing for antidepressant therapy.

Best–worst scaling Consolidated Framework for Implementation Research Pharmacogenetic testing

Journal

Implementation science communications
ISSN: 2662-2211
Titre abrégé: Implement Sci Commun
Pays: England
ID NLM: 101764360

Informations de publication

Date de publication:
14 May 2022
Historique:
received: 23 02 2022
accepted: 25 04 2022
entrez: 15 5 2022
pubmed: 16 5 2022
medline: 16 5 2022
Statut: epublish

Résumé

Despite the increased demand for pharmacogenetic (PGx) testing to guide antidepressant use, little is known about how to implement testing in clinical practice. Best-worst scaling (BWS) is a stated preferences technique for determining the relative importance of alternative scenarios and is increasingly being used as a healthcare assessment tool, with potential applications in implementation research. We conducted a BWS experiment to evaluate the relative importance of implementation factors for PGx testing to guide antidepressant use. We surveyed 17 healthcare organizations that either had implemented or were in the process of implementing PGx testing for antidepressants. The survey included a BWS experiment to evaluate the relative importance of Consolidated Framework for Implementation Research (CFIR) constructs from the perspective of implementing sites. Participating sites varied on their PGx testing platform and methods for returning recommendations to providers and patients, but they were consistent in ranking several CFIR constructs as most important for implementation: patient needs/resources, leadership engagement, intervention knowledge/beliefs, evidence strength and quality, and identification of champions. This study demonstrates the feasibility of using choice experiments to systematically evaluate the relative importance of implementation determinants from the perspective of implementing organizations. BWS findings can inform other organizations interested in implementing PGx testing for mental health. Further, this study demonstrates the application of BWS to PGx, the findings of which may be used by other organizations to inform implementation of PGx testing for mental health disorders.

Sections du résumé

BACKGROUND BACKGROUND
Despite the increased demand for pharmacogenetic (PGx) testing to guide antidepressant use, little is known about how to implement testing in clinical practice. Best-worst scaling (BWS) is a stated preferences technique for determining the relative importance of alternative scenarios and is increasingly being used as a healthcare assessment tool, with potential applications in implementation research. We conducted a BWS experiment to evaluate the relative importance of implementation factors for PGx testing to guide antidepressant use.
METHODS METHODS
We surveyed 17 healthcare organizations that either had implemented or were in the process of implementing PGx testing for antidepressants. The survey included a BWS experiment to evaluate the relative importance of Consolidated Framework for Implementation Research (CFIR) constructs from the perspective of implementing sites.
RESULTS RESULTS
Participating sites varied on their PGx testing platform and methods for returning recommendations to providers and patients, but they were consistent in ranking several CFIR constructs as most important for implementation: patient needs/resources, leadership engagement, intervention knowledge/beliefs, evidence strength and quality, and identification of champions.
CONCLUSIONS CONCLUSIONS
This study demonstrates the feasibility of using choice experiments to systematically evaluate the relative importance of implementation determinants from the perspective of implementing organizations. BWS findings can inform other organizations interested in implementing PGx testing for mental health. Further, this study demonstrates the application of BWS to PGx, the findings of which may be used by other organizations to inform implementation of PGx testing for mental health disorders.

Identifiants

pubmed: 35568931
doi: 10.1186/s43058-022-00300-7
pii: 10.1186/s43058-022-00300-7
pmc: PMC9107643
doi:

Types de publication

Journal Article

Langues

eng

Pagination

52

Subventions

Organisme : NHLBI NIH HHS
ID : K23 HL143161
Pays : United States
Organisme : Agency for Healthcare Research and Quality
ID : K12HS026379
Organisme : NHLBI NIH HHS
ID : K24HL133373
Pays : United States
Organisme : AHRQ HHS
ID : K12 HS026379
Pays : United States
Organisme : NHGRI NIH HHS
ID : U01 HG010245
Pays : United States
Organisme : NHGRI NIH HHS
ID : U01HG007269
Pays : United States
Organisme : NCATS NIH HHS
ID : KL2 TR002492
Pays : United States
Organisme : NCATS NIH HHS
ID : U54TR001857
Pays : United States
Organisme : NCATS NIH HHS
ID : KL2TR002492
Pays : United States
Organisme : NHGRI NIH HHS
ID : U01HG007775
Pays : United States
Organisme : NHGRI NIH HHS
ID : U01 HG010232
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1TR001427
Pays : United States
Organisme : NHLBI NIH HHS
ID : K24 HL133373
Pays : United States
Organisme : NHGRI NIH HHS
ID : U01 HG007775
Pays : United States

Informations de copyright

© 2022. The Author(s).

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Auteurs

Ramzi G Salloum (RG)

University of Florida Clinical and Translational Science Institute, Gainesville, FL, USA.
University of Florida College of Medicine, Gainesville, FL, USA.

Jeffrey R Bishop (JR)

University of Minnesota Medical School, Minneapolis, MN, USA.
University of Minnesota College of Pharmacy, Minneapolis, MN, USA.

Amanda L Elchynski (AL)

University of Florida College of Pharmacy, Gainesville, FL, USA.

D Max Smith (DM)

MedStar Health, Georgetown University Medical Center, Washington, DC, USA.

Elizabeth Rowe (E)

Indiana University School of Medicine, Indianapolis, IN, USA.

Kathryn V Blake (KV)

Nemours Children's Health, Jacksonville, FL, USA.

Nita A Limdi (NA)

University of Alabama Heersink School of Medicine, Birmingham, AL, USA.

Christina L Aquilante (CL)

School of Medicine and Pharmacy, University of Colorado, Aurora, CO, USA.

Jill Bates (J)

Durham VA Healthcare System, Durham, NC, USA.

Amber L Beitelshees (AL)

University of Maryland School of Medicine, Baltimore, MD, USA.

Amber Cipriani (A)

University of North Carolina Medical Center, Chapel Hill, NC, USA.

Benjamin Q Duong (BQ)

Nemours Children's Health, Wilmington, DE, USA.

Philip E Empey (PE)

University of Pittsburgh School of Pharmacy, Pittsburgh, PA, USA.

Christine M Formea (CM)

Intermountain Healthcare, Salt Lake City, UT, USA.

J Kevin Hicks (JK)

Moffitt Cancer Center, Tampa, FL, USA.

Pawel Mroz (P)

University of Minnesota Medical School, Minneapolis, MN, USA.

David Oslin (D)

Corporal Michael J. Cresenz VA Medical Center, Philadelphia, PA, USA.

Amy L Pasternak (AL)

University of Michigan College of Pharmacy, Ann Arbor, MI, USA.

Natasha Petry (N)

North Dakota State University/Sanford Health, Fargo, ND, USA.

Laura B Ramsey (LB)

Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.

Allyson Schlichte (A)

Fairview Pharmacy Services, Minneapolis, MN, USA.

Sandra M Swain (SM)

MedStar Health, Georgetown University Medical Center, Washington, DC, USA.

Kristen M Ward (KM)

University of Michigan College of Pharmacy, Ann Arbor, MI, USA.

Kristin Wiisanen (K)

University of Florida College of Pharmacy, Gainesville, FL, USA.

Todd C Skaar (TC)

Indiana University School of Medicine, Indianapolis, IN, USA.

Sara L Van Driest (SL)

Vanderbilt University Medical Center, Nashville, TN, USA.

Larisa H Cavallari (LH)

University of Florida Clinical and Translational Science Institute, Gainesville, FL, USA.
University of Florida College of Pharmacy, Gainesville, FL, USA.

Sony Tuteja (S)

University of Pennsylvania Perelman School of Medicine, Smilow Center for Translational Research, 3400 Civic Center Boulevard, Bldg. 421 11th Floor, Room 143, Philadelphia, PA, 19104-5158, USA. sonyt@pennmedicine.upenn.edu.

Classifications MeSH