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Development of a palliative paramedicine framework to standardise best practice: A Delphi study. Palliative Medicine.

Development of a palliative paramedicine framework to standardise best practice

A Delphi study

Paper

Juhrmann, M. L., Clayton, J. M., Butow, P. N., Simpson, P., Boughey, M., & Makeham, M. (2024). Development of a palliative paramedicine framework to standardise best practice: A Delphi study. Palliative Medicine.
PMID: 38483052 PMCID: PMC11457439 DOI: 10.1177/02692163241234004

Modified 3-round Delphi

Eliciting Expert Opinions

The modified Delphi process comprised 3 rounds: (1) completion of a web-based questionnaire; (2) participation in an online discussion forum; and (3) submission of final responses to the questionnaire from round 1.

Marlon Graf, PhD; Rifat Tuly, MPH; Carolyn Harley, PhD; Priti Pednekar, PhD; and Katharine Batt, MD, MSc

Authors

August, 2021

Published Online

Abstract

The landscape for hemophilia A prophylaxis is rapidly expanding from factor VIII replacement therapy to include novel treatments such as nonfactor replacement therapies that may enhance coagulation (e.g., emicizumab) or inhibit anticoagulant pathways (e.g., fitusiran and concizumab). For payers, this expansion presents challenges in balancing well-established treatments with new options that cost more and have lesser known real-world safety and efficacy.
Payers prefer treatments with well-understood efficacy, safety, and cost over newer treatments with uncertain long-term effects. Relatively unrestricted access to legacy and new hemophilia A prophylaxis will likely continue unless additional real-world safety concerns or major cost differences emerge.

  • Marlon Graf
  • Rifat Tuly
  • Carolyn Harley
  • Priti Pednekar
  • Katharine Batt

Volume 27. N. 8 . 2021

Published Online: August, 2021
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