A literature review of the healthcare resource use and productivity burden of X-linked hypophosphataemia.

IF 1.6 Q3 HEALTH CARE SCIENCES & SERVICES
Frontiers in health services Pub Date : 2025-04-09 eCollection Date: 2025-01-01 DOI:10.3389/frhs.2025.1285246
Rafael Pinedo-Villanueva, Muhammad K Javaid, Angela Williams, Isabelle Whittle, Matilde Franceschini, Ben Johnson
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Abstract

Introduction: X-linked hypophosphataemia (XLH) is a rare, genetic, renal phosphate wasting disorder that causes a lifelong rapid progression of morbidities, which are associated with substantial humanistic and economic burden. A structured literature review was carried out to identify publications reporting healthcare resource use and productivity impact of XLH to provide a comprehensive description of the burden.

Methods: Literature searches of the Embase®, Medline®, and EconLit electronic databases were carried out in August 2022 using free-text and subject heading search terms regarding XLH-related clinical morbidities and associated healthcare resource use, limited to English language records from 1992 onwards.

Results: After screening by pre-specified inclusion/exclusion criteria, 22 publications were selected for inclusion in the review. Use of conventional pharmacological therapy with oral phosphate and/or active vitamin D was reported in 15 publications, in up to 100% of paediatric patients and 75% of adults. Findings indicated that a high proportion of patients with XLH undergo orthopaedic procedures/surgeries, including a history of osteotomy in up to 25% of paediatric patients and 61% of adults, and a history of growth plate stapling in up to 63% of paediatric patients and 20% of adults. A high prevalence of fractures (in up to 61% of adults) and use of assistive mobility devices was also reported. The findings highlighted a substantial prevalence of morbidities, either due to persistently low phosphate levels or complications of conventional therapy, that had directly associated healthcare resource use, including dental problems, hearing problems, hyperparathyroidism, and nephrocalcinosis. Healthcare resource use and associated clinical events were generally found to be higher in adults compared with paediatric patients, which is consistent with the natural history of XLH as a progressive lifelong condition. Studies also highlighted the negative impact of XLH on school attendance and the ability to work.

Discussion: The results of this structured literature review emphasise the lifelong impact of XLH, showing that it is associated with a substantial economic burden, across many healthcare resource use categories including pharmacological therapy, management of pain and mobility, orthopaedic procedures, morbidities due to XLH or conventional therapy, and work/school productivity.

关于x连锁低磷血症的医疗资源使用和生产力负担的文献综述
简介:x连锁低磷血症(XLH)是一种罕见的遗传性肾性磷酸盐消耗疾病,可导致终生快速进展的疾病,并带来巨大的人文和经济负担。进行了结构化的文献综述,以确定报告XLH的医疗资源使用和生产力影响的出版物,以提供对负担的全面描述。方法:于2022年8月对Embase®、Medline®和EconLit电子数据库进行文献检索,使用自由文本和主题标题检索词检索与xlm相关的临床发病率和相关医疗资源的使用,仅限于1992年以来的英文记录。结果:通过预先设定的纳入/排除标准筛选后,22篇出版物被纳入综述。15篇出版物报道了使用口服磷酸盐和/或活性维生素D的常规药物治疗,高达100%的儿科患者和75%的成人。研究结果表明,很大比例的XLH患者接受了骨科手术,包括高达25%的儿科患者和61%的成人患者有截骨史,以及高达63%的儿科患者和20%的成人患者有生长钢板装订史。骨折的高患病率(高达61%的成年人)和辅助行动装置的使用也有报道。研究结果强调了大量的发病率,无论是由于持续的低磷酸盐水平还是常规治疗的并发症,都与医疗资源的使用直接相关,包括牙齿问题、听力问题、甲状旁腺功能亢进和肾钙质沉着症。与儿科患者相比,成人的医疗资源使用和相关临床事件通常更高,这与XLH作为进行性终身疾病的自然史是一致的。研究还强调了XLH对出勤率和工作能力的负面影响。讨论:这篇结构化文献综述的结果强调了XLH的终身影响,表明它与大量的经济负担有关,涉及许多医疗资源使用类别,包括药物治疗、疼痛和活动管理、骨科手术、XLH或传统治疗引起的发病率,以及工作/学校生产力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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