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Does the use of patient decision aids lead to cost savings? a systematic review.
Scalia, Peter; Barr, Paul J; O'Neill, Ciaran; Crealey, Grainne E; Bagley, Pamela J; Blunt, Heather B; Elwyn, Glyn.
Afiliação
  • Scalia P; The Dartmouth Institute for Health Policy and Clinical Practice, Dartmouth College, Lebanon, New Hampshire, USA.
  • Barr PJ; The Dartmouth Institute for Health Policy and Clinical Practice, Dartmouth College, Lebanon, New Hampshire, USA.
  • O'Neill C; Centre for Public Health, Queen's University Belfast, Belfast, Belfast, UK.
  • Crealey GE; Clinical Costing Solutions, Belfast, UK.
  • Bagley PJ; Dartmouth College Biomedical Libraries, Hanover, New Hampshire, USA.
  • Blunt HB; Dartmouth College Biomedical Libraries, Hanover, New Hampshire, USA.
  • Elwyn G; The Dartmouth Institute for Health Policy and Clinical Practice, Dartmouth College, Lebanon, New Hampshire, USA glynelwyn@gmail.com.
BMJ Open ; 10(11): e036834, 2020 11 16.
Article em En | MEDLINE | ID: mdl-33199416
ABSTRACT

OBJECTIVES:

To update a previous systematic review to determine if patient decision aid (PDA) interventions generate savings in healthcare settings, and if so, from which perspective (ie, patient, organisation providing care, society).

DESIGN:

Systematic review. DATA SOURCES MEDLINE, CINAHL, PsycINFO, Web of Science, Cochrane Library, Embase, Campbell Collaboration Library, EconLit, Business Source Complete, Centre for Reviews and Dissemination NHS Economic Evaluations Database (NHS EED), Database of Abstracts of Reviews of Effects (DARE) and Health Technology Assessment (HTA) from 15 March 2013 to 25 January 2019. The references of studies that met the eligibility criteria and any publications related to conference abstracts or registered clinical trials were reviewed to increase the sensitivity of the search. ELIGIBILITY CRITERIA Full and partial economic evaluations with an experimental, quasi-experimental or randomised controlled design were included. The intervention had to satisfy the pre-determined minimum conditions necessary to be defined as a PDA, and (for full evaluations) provide details on the comparator used. DATA EXTRACTION AND

SYNTHESIS:

All study outcomes and economic data were extracted. The reporting and quality of the economic analyses were independently assessed by two health economists.

RESULTS:

Of 5066 studies, 22 studies were included, including the 8 studies from the previous review. Twelve studies reported cost-savings (range=US$10 to US$81 156; US dollars in 2020), primarily from the organisational or health system perspective, and 10 studies did not. However, due to the quality of the economic analyses, and the related issues with the interpretative validity of results it would be inappropriate to say that PDAs will generate savings, from any perspective.

CONCLUSIONS:

It is unclear whether PDAs will generate savings. Greater consensus on what constitutes a PDA and the need to compare them against usual care over a sufficient time horizon to allow valid assessment of costs and outcomes is required. PROSPERO REGISTRATION NUMBER CRD42019118457.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Avaliação da Tecnologia Biomédica / Técnicas de Apoio para a Decisão Tipo de estudo: Clinical_trials / Health_economic_evaluation / Health_technology_assessment / Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Avaliação da Tecnologia Biomédica / Técnicas de Apoio para a Decisão Tipo de estudo: Clinical_trials / Health_economic_evaluation / Health_technology_assessment / Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article