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Screening trials of spinal cord stimulation for neuropathic pain in England-A budget impact analysis.
Duarte, Rui V; Houten, Rachel; Nevitt, Sarah; Brookes, Morag; Bell, Jill; Earle, Jenny; Gulve, Ashish; Thomson, Simon; Baranidharan, Ganesan; North, Richard B; Taylor, Rod S; Eldabe, Sam.
Afiliação
  • Duarte RV; Liverpool Reviews and Implementation Group, University of Liverpool, Liverpool, United Kingdom.
  • Houten R; Saluda Medical Pty Ltd., Artarmon, NSW, Australia.
  • Nevitt S; Liverpool Reviews and Implementation Group, University of Liverpool, Liverpool, United Kingdom.
  • Brookes M; Liverpool Reviews and Implementation Group, University of Liverpool, Liverpool, United Kingdom.
  • Bell J; The James Cook University Hospital, Middlesbrough, United Kingdom.
  • Earle J; Patient and Public Involvement Representatives, Middlesbrough, United Kingdom.
  • Gulve A; Patient and Public Involvement Representatives, Middlesbrough, United Kingdom.
  • Thomson S; The James Cook University Hospital, Middlesbrough, United Kingdom.
  • Baranidharan G; Department of Pain Medicine and Neuromodulation, Mid and South Essex University Hospitals, Essex, United Kingdom.
  • North RB; Leeds Neuromodulation Centre, Leeds Teaching Hospitals, Leeds, United Kingdom.
  • Taylor RS; Neurosurgery, Anesthesiology and Critical Care Medicine (ret.), Johns Hopkins University School of Medicine, Baltimore, MD, United States.
  • Eldabe S; College of Medicine and Health, University of Exeter, Exeter, United Kingdom.
Front Pain Res (Lausanne) ; 3: 974904, 2022.
Article em En | MEDLINE | ID: mdl-36147037
ABSTRACT
Screening trials of spinal cord stimulation (SCS) prior to full implantation of a device are recommended by expert guidelines and international regulators. The current study sought to estimate the budget impact of a screening trial of SCS and the costs or savings of discontinuing the use of a screening trial. A budget impact analysis was performed considering a study population that reflects the size and characteristics of a patient population with neuropathic pain in England eligible for SCS. The perspective adopted was that of the NHS with a 5-year time horizon. The base case analysis indicate that a no screening trial strategy would result in cost-savings to the NHS England of £400,000-£500,000 per year. Sensitivity analyses were conducted to evaluate different scenarios. If ≥5% of the eligible neuropathic pain population received a SCS device, cost-savings would be >£2.5 million/year. In contrast, at the lowest assumed cost of a screening trial (£1,950/patient), a screening trial prior to SCS implantation would be cost-saving. The proportion of patients having an unsuccessful screening trial would have to be ≥14.4% for current practice of a screening trial to be cost-saving. The findings from this budget impact analysis support the results of a recent UK multicenter randomized controlled trial (TRIAL-STIM) of a policy for the discontinuation of compulsory SCS screening trials, namely that such a policy would result in considerable cost-savings to healthcare systems.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido