评估初级保健为基础的阿片类药物和疼痛审查服务:在英国两个全科医生实践的混合方法评估

L. Scott, J. Kesten, K. Bache, M. Hickman, R. Campbell, A. Pickering, S. Redwood, K. Thomas
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引用次数: 13

摘要

尽管缺乏长期安全性和有效性的证据,但用于治疗慢性非癌性疼痛的阿片类药物处方已迅速增加。开发了疼痛审查服务,与长期服用阿片类药物的患者一起探索阿片类药物的使用,鼓励非药物替代品,并在适当情况下支持减少剂量。目的评估该服务及其对阿片类药物使用、健康和福祉结果以及生活质量(QoL)的潜在影响。2016年9月至2017年12月,在英国南格洛斯特郡的两个全科医生实践中,设计和设置了基于一对一服务的混合方法评估。方法收集基线人口统计学定量资料;在基线和随访时收集有关阿片类药物使用、滥用和剂量、健康、福祉、生活质量、疼痛和干扰生活措施的数据。25个半结构化访谈(n = 18个服务使用者,n = 7个服务提供者)探讨了服务的体验,包括感知到的影响和好处。结果入选的59例患者中,34例(57.6%)入选。处方阿片类药物的中位数剂量从90毫克(平均每日吗啡当量;基线时的四分位数间距[IQR] 60 ~ 240)至随访时的72 mg (IQR 30 ~ 160) (P<0.001);三名服务使用者完全停止使用阿片类药物。平均而言,服务用户在大多数健康、福祉和生活质量结果上都有所改善。感知到的益处与健康有关,例如,增强了信心和自尊,使用了疼痛管理策略,改变了药物使用,减少了剂量。这项服务受到了好评,健康和福祉结果表明它有潜在的好处。随着服务的进一步发展,有必要进行随机对照试验来检验这种护理途径。
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Evaluation of a primary care-based opioid and pain review service: a mixed-methods evaluation in two GP practices in England
Background Opioid prescribing to treat chronic non-cancer pain has rapidly increased, despite a lack of evidence for long-term safety and effectiveness. A pain review service was developed to work with patients taking opioids long-term to explore opioid use, encourage non-drug-based alternatives, and, where appropriate, support dose reduction. Aim To evaluate the service and its potential impact on opioid use, health and wellbeing outcomes, and quality of life (QoL). Design and setting Mixed-methods evaluation of a one-to-one service based in two GP practices in South Gloucestershire, England, which took place from September 2016 to December 2017. Method Quantitative data were collected on baseline demographics; data on opioid use, misuse, and dose, health, wellbeing, QoL, and pain and interference with life measures were collected at baseline and follow-up. Twenty-five semi-structured interviews (n = 18 service users, n = 7 service providers) explored experiences of the service including perceived impacts and benefits. Results Of 59 patients who were invited, 34 (57.6%) enrolled in the service. The median prescribed opioid dose reduced from 90 mg (average daily morphine equivalent; interquartile range [IQR] 60 to 240) at baseline to 72 mg (IQR 30 to 160) at follow-up (P<0.001); three service users stopped using opioids altogether. On average, service users showed improvement on most health, wellbeing, and QoL outcomes. Perceived benefits were related to wellbeing, for example, improved confidence and self-esteem, use of pain management strategies, changes in medication use, and reductions in dose. Conclusion The service was well received, and health and wellbeing outcomes suggest a potential benefit. Following further service development, a randomised controlled trial to test this type of care pathway is warranted.
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