Design, implementation and evaluation of a model of care for patients with germline predisposition to haematological malignancy and bone marrow failure syndromes

The EMBRACE study has established a stakeholder-informed, multidisciplinary care framework for patients with BMFS. This care programme continues to undergo evaluation and audit consistent with principles of an implementation-effectiveness study to determine both patient and physician satisfaction, and iterative refinement to provide optimum care.

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Publication Details

Journal
Internal Medicine Journal
Published
2025-07-01
DOI
https://doi.org/10.1111/imj.70125
Primary Topic
Genomics and Rare Diseases
Type
article
Field-Weighted Citation Impact
0.00
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article

Design, implementation and evaluation of a model of care for patients with germline predisposition to haematological malignancy and bone marrow failure syndromes

Anna Jarmolowicz, Paul A. James, Ashish Bajel, Nicole den Elzen et al.
Internal Medicine Journal
Genomics and Rare Diseases
article

Design, implementation and evaluation of a model of care for patients with germline predisposition to haematological malignancy and bone marrow failure syndromes

Anna Jarmolowicz, Paul A. James, Ashish Bajel, Nicole den Elzen, Mary Panjari, Piers A. Blombery, Lucy C. Fox, Karin Thursky, David Ritchie, Stephanie Best, Lin Cheng, Kelsey Man, Erin Goode, Laura Barth
article en

Abstract

The EMBRACE study has established a stakeholder-informed, multidisciplinary care framework for patients with BMFS. This care programme continues to undergo evaluation and audit consistent with principles of an implementation-effectiveness study to determine both patient and physician satisfaction, and iterative refinement to provide optimum care.

Internal Medicine JournalVol. 55(8)
The Royal Melbourne Hospital (AU), The University of Melbourne (AU), Peter MacCallum Cancer Centre (AU), Government of Western Australia Department of Health (AU), Monash Health (AU), Monash University (AU), RMIT University (AU)
Openalex Percentile: Top 82%
Genomics and Rare Diseases
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