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美国 X 连锁肌小管肌病(XLMTM)患者的医疗资源利用真实世界分析。

Real-world analysis of healthcare resource utilization by patients with X-linked myotubular myopathy (XLMTM) in the United States.

机构信息

Division of Critical Care Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.

Department of Neurology, Neuromuscular Program, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.

出版信息

Orphanet J Rare Dis. 2023 Jun 6;18(1):138. doi: 10.1186/s13023-023-02733-2.

Abstract

BACKGROUND

X-linked myotubular myopathy (XLMTM) is a rare, life-threatening congenital myopathy with multisystem involvement, often requiring invasive ventilator support, gastrostomy tube feeding, and wheelchair use. Understanding healthcare resource utilization in patients with XLMTM is important for development of targeted therapies but data are limited.

METHODS

We analyzed individual medical codes as governed by Healthcare Common Procedure Coding System, Current Procedural Terminology, and International Classification of Diseases, 10th Revision (ICD-10) for a defined cohort of XLMTM patients within a US medical claims database. Using third-party tokenization software, we defined a cohort of XLMTM patient tokens from a de-identified dataset in a research registry of diagnostically confirmed XLMTM patients and de-identified data from a genetic testing company. After approval of an ICD-10 diagnosis code for XLMTM (G71.220) in October 2020, we identified additional patients.

RESULTS

A total of 192 males with a diagnosis of XLMTM were included: 80 patient tokens and 112 patients with the new ICD-10 code. From 2016 to 2020, the annual number of patients with claims increased from 120 to 154 and the average number of claims per patient per year increased from 93 to 134. Of 146 patients coded with hospitalization claims, 80 patients (55%) were first hospitalized between 0 and 4 years of age. Across all patients, 31% were hospitalized 1-2 times, 32% 3-9 times, and 14% ≥ 10 times. Patients received care from multiple specialty practices: pulmonology (53%), pediatrics (47%), neurology (34%), and critical care medicine (31%). The most common conditions and procedures related to XLMTM were respiratory events (82%), ventilation management (82%), feeding difficulties (81%), feeding support (72%), gastrostomy (69%), and tracheostomy (64%). Nearly all patients with respiratory events had chronic respiratory claims (96%). The most frequent diagnostic codes were those investigating hepatobiliary abnormalities.

CONCLUSIONS

This innovative medical claims analysis shows substantial healthcare resource use in XLMTM patients that increased over the last 5 years. Most patients required respiratory and feeding support and experienced multiple hospitalizations throughout childhood and beyond for those that survived. This pattern delineation will inform outcome assessments with the emergence of novel therapies and supportive care measures.

摘要

背景

X 连锁肌小管肌病(XLMTM)是一种罕见的、危及生命的先天性肌病,多系统受累,常需呼吸机支持、胃造口管喂养和轮椅使用。了解 XLMTM 患者的医疗资源利用情况对于开发靶向治疗至关重要,但数据有限。

方法

我们根据医疗保健通用程序编码系统、当前程序术语和国际疾病分类第 10 版(ICD-10)对美国医疗索赔数据库中的一组 XLMTM 患者的个人医疗代码进行了分析。使用第三方标记化软件,我们从 XLMTM 患者诊断确认研究注册中心的去识别数据集和基因检测公司的去识别数据中定义了一组 XLMTM 患者标记。在 2020 年 10 月批准 XLMTM(G71.220)的 ICD-10 诊断代码后,我们确定了更多的患者。

结果

共纳入 192 名男性 XLMTM 患者:80 名患者标记和 112 名新 ICD-10 编码患者。2016 年至 2020 年,有索赔的患者人数从 120 人增加到 154 人,每位患者每年的平均索赔次数从 93 次增加到 134 次。在 146 名编码为住院索赔的患者中,80 名患者(55%)在 0 至 4 岁之间首次住院。在所有患者中,31%住院 1-2 次,32%住院 3-9 次,14%住院 10 次以上。患者接受了多个专业实践的治疗:肺病学(53%)、儿科学(47%)、神经病学(34%)和重症监护医学(31%)。与 XLMTM 相关的最常见病症和程序是呼吸事件(82%)、通气管理(82%)、喂养困难(81%)、喂养支持(72%)、胃造口术(69%)和气管切开术(64%)。几乎所有有呼吸事件的患者都有慢性呼吸系统的索赔(96%)。最常见的诊断代码是那些调查肝胆异常的代码。

结论

这项创新的医疗索赔分析显示,XLMTM 患者的医疗资源使用量在过去 5 年中大幅增加。大多数患者需要呼吸和喂养支持,并且在儿童时期和之后多次住院治疗。这种模式的描述将为新型治疗方法和支持性护理措施的出现提供信息,以评估结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4407/10242920/a6216c02b220/13023_2023_2733_Fig1_HTML.jpg

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