Shared decision‐making related to treatment of haemophilia: A scoping review of influential factors and available support tools

Author:

Sun Haowei (Linda)1ORCID,Klaassen Robert J.2ORCID,Anger Dana L.3ORCID,Mendell Ari L.4,Olatunde Shade5

Affiliation:

1. Division of Hematology Department of Medicine University of Alberta Edmonton Alberta Canada

2. Division of Pediatric Hematology/Oncology Department of Pediatrics University of Ottawa Children's Hospital of Eastern Ontario Ottawa Ontario Canada

3. WRITRIX Medical Communications Inc. Burlington Ontario Canada

4. Compass Leaf Medical Communications Inc. Guelph Ontario Canada

5. Hoffmann‐La Roche Limited Mississauga Ontario Canada

Abstract

AbstractIntroductionTreatment selection in haemophilia is increasingly challenging given evolving therapeutic options and the need for individualization. Shared decision‐making (SDM) approaches have recently gained interest, though a synthesis of available studies is lacking.AimA scoping review was conducted to summarize literature reporting on factors impacting treatment SDM in haemophilia and tools or models available to support such decisions.MethodsPubMed, Embase, the Cochrane Library, Web of Science and grey literature were searched for studies published through August 2023. Original studies reporting on facilitators and barriers to haemophilia SDM and SDM tools were included and analyzed for themes, characteristics and gaps.ResultsA total of 625 records were identified and 14 unique studies were selected (factors influencing treatment SDM, n = 7; SDM tools, n = 7). The studies typically included input from persons with haemophilia, caregivers and healthcare practitioners (HCPs). Thematic organization of factors influencing SDM revealed three main categories: knowledge, patient characteristics and HCP‐patient interactions. Availability of information was a commonly reported facilitator of SDM, while poor HCP‐patient engagement was a commonly reported barrier. Tools varied in focus, with some facilitating general treatment SDM while others supported selection of certain therapy types. The studies underscored additional factors critical for SDM, such as alignment of HCP‐patient perceptions, shared language and tailoring of tools to specific subpopulations.ConclusionFew studies report on treatment SDM factors and tools in haemophilia; available tools vary considerably. It remains unclear whether published tools have been successfully implemented into clinical practice. Additional research is warranted.

Publisher

Wiley

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