Applicability and Validity of an e-Health Tool for the Appropriate Referral and Selection of Patients With Chronic Pain for Spinal Cord Stimulation: Results From a European Retrospective Study

被引:12
|
作者
Thomson, Simon [1 ]
Huygen, Frank [2 ]
Prangnell, Simon [3 ]
Baranidharan, Ganesan [4 ]
Belaid, Hayat [5 ]
Billet, Bart [6 ]
Eldabe, Sam [7 ]
De Carolis, Giuliano [8 ]
Demartini, Laura [9 ]
Gatzinsky, Kliment [10 ]
Kallewaard, Jan Willem [11 ,12 ]
Paroli, Mery [8 ]
Winkelmueller, Matthias
Helsen, Nicky [13 ]
Stoevelaar, Herman [13 ,14 ]
机构
[1] Mid & South Essex Univ Hosp, Pain & Neuromodulat Ctr, Basildon, Essex, England
[2] Erasmus Univ, Dept Anaesthesiol, Med Ctr, Rotterdam, Netherlands
[3] Oxford Univ Hosp NHS Fdn Trust, Clin Neuropsychol Serv, Oxford, Oxfordshire, England
[4] Leeds Teaching Hosp, Leeds Pain & Neuromodulat Ctr, Leeds, England
[5] Fdn Ophtalmol Adolphe Rothschild, Dept Neurosurg, Paris, France
[6] AZ Delta, Dept Anaesthesiol, Roeselare, Belgium
[7] James Cook Univ Hosp, Dept Pain Med, Middlesbrough, North Yorkshire, England
[8] Santa Chiara Univ Hosp, Anaesthesiol & Pain Therapy Unit, Pisa, Italy
[9] Clin Sci Inst Maugeri, Pain Unit, Pavia, Italy
[10] Sahlgrens Univ Hosp, Dept Neurosurg, Gothenburg, Sweden
[11] Rijnstate Hosp, Dept Anaesthesiol & Pain Management, Velp, Netherlands
[12] Univ Amsterdam, Dept Anaesthesiol & Pain Treatment, Med Ctr, Amsterdam, Netherlands
[13] Ismar Healthcare, Ctr Decis Anal & Support, Lier, Belgium
[14] Ismar Healthcare, Ctr Decis Anal & Support, Leopoldpl 39, B-2500 Lier, Belgium
来源
NEUROMODULATION | 2023年 / 26卷 / 01期
关键词
Chronic pain; e-health tool; patient selection; RAND; UCLA Appropriateness Method; spinal cord stimulation; OUTCOMES; CRITERIA;
D O I
10.1016/j.neurom.2021.12.006
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Objectives: To support rational decision-making on spinal cord stimulation (SCS), a European expert panel developed an educational e-health tool using the RAND/University of California at Los Angeles Appropriateness Method. This retrospective study aimed to determine the applicability and validity of the tool using data from patients for whom SCS had been considered. Materials and Methods: A total of 12 European implant centers retrieved data from 25 to 50 consecutive patients for whom SCS was considered in 2018-2019. For each patient, data were captured on the clinical and psychosocial variables included in the e-health tool, center decisions on SCS, and patient outcomes. Patient outcomes included global perception of effect by the patient and observer, and pain reduction (numeric pain rating scale) at six-month follow-up. Results: In total, 483 patients were included, of whom 133 received a direct implant, 258 received an implant after a positive trial, 32 had a negative trial, and 60 did not receive SCS for reasons other than a negative trial. The most frequent indication was persistent spinal pain syndrome type 1 and type 2 (74%), followed by neuropathic pain syndromes (13%), complex regional pain syndrome (12%), and ischemic pain syndromes (0.8%). Data on the clinical and psychosocial variables were complete for 95% and 93% of patients, respectively, and missing data did not have a significant impact on the study outcomes. In patients who had received SCS, panel recommendations were significantly associated with patient outcomes (p < 0.001 for all measures). Substantial improvement ranged from 25% if the e-health tool outcome was "not recommended" to 83% if SCS was "strongly recommended". In patients who underwent a trial (N = 290), there was 3% of trial failure when SCS was "strongly recommended" vs 46% when SCS was "not recommended". Conclusions: Retrospective application of the e-health tool on patient data showed a strong relationship between the panel recommendations and both SCS trial results and treatment outcomes.
引用
收藏
页码:164 / 171
页数:8
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