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青少年特发性脊柱侧弯的经济和社会负担:一项疾病负担研究方案

The economic and societal burden associated with adolescent idiopathic scoliosis: A burden-of-disease study protocol.

作者信息

Hoelen Thomáy-Claire Ayala, Willems Paul C, Arts Jacobus J, van Mastrigt Ghislaine, Evers Silvia

机构信息

Department of Orthopedic Surgery and CAPHRI Research School, Maastricht University Medical Center (MUMC+), P.Debyelaan 25, Maastricht, 6202AZ, The Netherlands.

Department of Health Services Research, Faculty of Health, Medicine and Life Sciences, CAPHRI, Maastricht University, , Universiteitssingel 40, Maastricht, 6229 ER, The Netherlands.

出版信息

N Am Spine Soc J. 2023 May 18;14:100231. doi: 10.1016/j.xnsj.2023.100231. eCollection 2023 Jun.

Abstract

BACKGROUND

Adolescent idiopathic scoliosis (AIS) has an estimated general population prevalence of 2% to 3%. The impact of adolescent idiopathic scoliosis (AIS) on the patients' experienced quality of life and psychological well-being and the resulting societal burden are increasingly recognized. However, there is limited knowledge on the economic burden of AIS. This cross-sectional, prevalence-based, bottom-up approach burden of disease study aims to determine the impact associated with adolescent idiopathic scoliosis in terms of the cost-of-illness and health-related quality of life from a societal perspective in the Netherlands.

METHODS

Persons diagnosed with AIS or parents of a child with AIS that are willing and able to answer the questionnaires will be eligible to participate. Patients will be included consecutively between June until January 2023. Costs and self-perceived health-related quality of life will be estimated using 3 steps: identification, measurement and valuation. To assess the costs associated with AIS the institute for Medical Technology Assessment - Medical Consumption Questionnaire and the institute for Medical Technology Assessment - Productivity Cost Questionnaire will be used. To assess the HRQoL of adult AIS patients the EuroQol 5-dimensions or EuroQol 5-dimensions Youth questionnaire for children under the age of 12 and the Scoliosis Research Society-22 revised questionnaire will be considered.

DISCUSSION

This is the first study in this field. It will help raise awareness for AIS and wider support for both the patient community and informal care takers among healthcare professionals and policymakers. Major strengths of this study will be the use of mostly validated, standardized questionnaires. Limitations include the cross-sectional and retrospective nature of the study design.

摘要

背景

青少年特发性脊柱侧凸(AIS)在一般人群中的患病率估计为2%至3%。青少年特发性脊柱侧凸(AIS)对患者生活质量和心理健康的影响以及由此产生的社会负担日益受到关注。然而,关于AIS经济负担的了解有限。这项基于患病率的横断面、自下而上的疾病负担研究旨在从荷兰社会角度确定青少年特发性脊柱侧凸在疾病成本和健康相关生活质量方面的影响。

方法

被诊断为AIS的患者或患有AIS儿童的父母,愿意且能够回答问卷的将有资格参与。患者将在2023年6月至1月期间连续纳入。成本和自我感知的健康相关生活质量将通过三个步骤进行估计:识别、测量和估值。为评估与AIS相关的成本,将使用医疗技术评估研究所的医疗消费问卷和医疗技术评估研究所的生产力成本问卷。为评估成年AIS患者的健康相关生活质量,将考虑使用欧洲五维度健康量表或针对12岁以下儿童的欧洲五维度青少年问卷以及脊柱侧凸研究学会22项修订问卷。

讨论

这是该领域的第一项研究。它将有助于提高对AIS的认识,并在医疗专业人员和政策制定者中为患者群体和非正式护理人员提供更广泛的支持。本研究的主要优势将是大多使用经过验证的标准化问卷。局限性包括研究设计的横断面性质和回顾性性质。

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