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Veterans Health Administration response to 2021 recall of Philips Respironics devices: A case study.
Belkora, Jeffrey K; Fields, Barry; Shamim-Uzzaman, Q Afifa; Stratford, Donna; Alfandre, David; Hollingshaus, Scott; Yackel, Edward; Geppert, Cynthia; Nechanicky, Penny; Nichols, Ardene; Williams, Katherine; Reichert, Jill; Whooley, Mary A; Francis, Joe; Sarmiento, Kathleen F.
Afiliação
  • Belkora JK; Institute for Health Policy Studies, University of California, San Francisco, San Francisco, CA, United States.
  • Fields B; San Francisco Veterans Affairs Health Care System, San Francisco, CA, United States.
  • Shamim-Uzzaman QA; Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine, Emory University, Atlanta, GA, United States.
  • Stratford D; Atlanta Veterans Affairs Medical Center, Decatur, GA, United States.
  • Alfandre D; Department of Internal Medicine and Neurology, Veterans Affairs Ann Arbor Healthcare System, University of Michigan, Ann Arbor, MI, United States.
  • Hollingshaus S; Office of Quality and Patient Safety, Veterans Health Administration, Washington, DC, United States.
  • Yackel E; Department of Medicine and Population Health, New York University School of Medicine, New York, NY, United States.
  • Geppert C; National Center for Ethics in Health Care, Veterans Health Administration, Washington, DC, United States.
  • Nechanicky P; Division of Pulmonary Medicine, Department of Medicine, Salt Lake City Veterans Affairs Medical Center, University of Utah, Salt Lake City, UT, United States.
  • Nichols A; National Center for Patient Safety, Veterans Health Administration, Ann Arbor, MI, United States.
  • Williams K; National Center for Ethics in Health Care, Veterans Health Administration, Washington, DC, United States.
  • Reichert J; Department of Psychiatry and Internal Medicine, Ethics Education, University of New Mexico School of Medicine, Albuquerque, NM, United States.
  • Whooley MA; Prosthetic and Sensory Aids Services, Veterans Health Administration, Washington, DC, United States.
  • Francis J; Prosthetic and Sensory Aids Services, Veterans Health Administration, Washington, DC, United States.
  • Sarmiento KF; San Francisco Veterans Affairs Health Care System, San Francisco, CA, United States.
Front Sleep ; 22023 Apr 12.
Article em En | MEDLINE | ID: mdl-38585370
ABSTRACT
This case study describes, for the time frame of June 2021 through August 2022, the U.S. Veterans Health Administration (VHA) organizational response to a manufacturer's recall of positive airway pressure devices used in the treatment of sleep disordered breathing. VHA estimated it could take over a year for Veterans to receive replacement devices. Veterans awaiting a replacement faced a dilemma. They could continue using the recalled devices and bear the product safety risks that led to the recall, or they could stop using them and bear the risks of untreated sleep disordered breathing. Using a program monitoring approach, we report on the processes VHA put in place to respond to the recall. Specifically, we report on the strategic, service, and operational plans associated with VHA's response to the recall for Veterans needing replacement devices. In program monitoring, the strategic plan reflects the internal process objectives for the program. The service plan articulates how the delivery of services will intersect the customer journey. The operational plan describes how the program's resources and actions must support the service delivery plan. VHA's strategic plan featured a clinician-led, as opposed to primarily legal or administrative response to the recall. The recall response team also engaged with VHA's medical ethics service to articulate an ethical framework guiding the allocation of replacement devices under conditions of scarcity. This framework proposed allocating scarce devices to Veterans according to their clinical need. The service plan invited Veterans to schedule visits with sleep providers who could assess their clinical need and counsel them accordingly. The operational plan distributed devices according to clinical need as they became available. Monitoring our program processes in real time helped VHA launch and adapt its response to a recall affecting more than 700,000 Veterans.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Sleep Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Sleep Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Suíça