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在巴西公共卫生系统中,对因C1抑制剂缺乏而接受达那唑治疗的遗传性血管性水肿患者进行的一项真实世界研究。

A real-world study of hereditary angioedema patients due to C1 inhibitor deficiency treated with danazol in the Brazilian Public Health System.

作者信息

Ritter Alessandra Mileni Versuti, Silva Suelen, de Paula Robson, Senra Juliana, Carvalho Fabio, Ribeiro Tatiane, Valle Solange Oliveira Rodrigues

机构信息

IQVIA, São Paulo, Brazil.

Takeda Distribuidora Ltd., São Paulo, Brazil.

出版信息

Front Med (Lausanne). 2024 Sep 6;11:1343547. doi: 10.3389/fmed.2024.1343547. eCollection 2024.

Abstract

INTRODUCTION

Hereditary angioedema (HAE) due to C1 inhibitor (C1-INH) deficiency is an ultra-rare autosomal dominant inherited disease that affects 1 in 67,000 people in the world. The attacks are based on subcutaneous and submucosal edema that can lead to death if not properly managed. Considering the lack of information on the clinical management of Brazilian patients with HAE, this study aimed to identify and characterize patients with HAE-C1-INH that used danazol prophylactic treatment in the Brazilian Public Health System (SUS) and the healthcare resource utilization (HCRU).

METHODS

This was an observational retrospective database study with patients treated with danazol from January 2011 until December 2021 within the SUS. The HAE cohort included patients with 12 years or older with at least one record for ICD-10 D84.1, one claim for danazol record, and at least 6 months of available history in the database.

RESULTS

Our study included 799 patients treated in the SUS, with a mean (SD) age at danazol initiation of 40 years (16). The number of patients with HAE showed a similar distribution over this 10-year period analyzed with the highest number of patients in 2015 ( = 509) and 2016 ( = 480). A total of 253 (32%) patients had a record of at least one attack. Of those, 45 (17.8%) had at least one procedure HAE-related hospital admission, and 128 (50.6%) had at least one HAE-related hospital admission. The mean (SD) hospitalization length of stay was 5 (8) days. Over 14% ( = 36) of HAE patients with attack ( = 253) had at least one HAE-related ICU admission.

CONCLUSION

This database study is the strategy used to allow us to find and describe the characteristics of patients with HAE who use danazol for long-term prophylaxis in the SUS and identify HCRU outcomes of interest such as hospitalizations, inpatient, and outpatient settings. The high rate of attacks, hospitalizations, and general resource uses highlights the necessity to increase awareness of new strategies and accurate approaches to treat HAE patients. Therefore, our findings are important indicators that our health system and guidelines need to be revised and improved to properly diagnose, treat, and assist patients with HAE.

摘要

引言

由于C1抑制剂(C1-INH)缺乏引起的遗传性血管性水肿(HAE)是一种极为罕见的常染色体显性遗传病,全球每67000人中就有1人受其影响。发病表现为皮下和粘膜下水肿,若处理不当可导致死亡。鉴于巴西HAE患者临床管理方面的信息匮乏,本研究旨在识别和描述在巴西公共卫生系统(SUS)中使用达那唑进行预防性治疗的HAE-C1-INH患者及其医疗资源利用情况(HCRU)。

方法

这是一项观察性回顾性数据库研究,研究对象为2011年1月至2021年12月期间在SUS接受达那唑治疗的患者。HAE队列包括年龄在12岁及以上、至少有一条ICD-10 D84.1记录、一条达那唑记录且数据库中有至少6个月可用病史的患者。

结果

我们的研究纳入了799例在SUS接受治疗的患者,开始使用达那唑时的平均(标准差)年龄为40岁(16岁)。在这10年的分析期内,HAE患者数量呈现相似的分布,2015年患者数量最多(n = 509),2016年(n = 480)次之。共有253例(32%)患者有至少一次发病记录。其中,45例(17.8%)有至少一次与HAE相关的住院治疗,128例(50.6%)有至少一次与HAE相关的住院。平均(标准差)住院天数为5天(8天)。超过14%(n = 36)有发病记录的HAE患者(n = 253)有至少一次与HAE相关的重症监护病房(ICU)住院。

结论

这项数据库研究是一种策略,使我们能够找到并描述在SUS中使用达那唑进行长期预防的HAE患者的特征,并识别如住院、住院和门诊等相关的HCRU结果。高发病率、住院率和总体资源使用率凸显了提高对治疗HAE患者新策略和准确方法的认识的必要性。因此,我们的研究结果是重要指标,表明我们的卫生系统和指南需要修订和改进,以正确诊断、治疗和帮助HAE患者。

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