南澳大利亚州的遗传性血管性水肿发病率和预防满意度

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Alexander Troelnikov MBBS , Karen Milburn RN , Pravin Hissaria MBBS, MD , Thanh Thao (Adriana) Le MBBS , William Smith MBBS, PhD
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引用次数: 0

摘要

背景由于缺乏 C1 抑制剂(C1INH-HAE)而导致的遗传性血管性水肿(HAE)是一种罕见、不可预测且可能致命的遗传性疾病。系统性的人群发病率研究相对较少,各国的报告显示,发病率在二万分之一到十五万分之一之间,澳大利亚没有相关数据。近年来,HAE的治疗方法发生了巨大变化,重点是高效预防,目的是完全抑制血管性水肿,实现正常生活。方法在2021年1月至2022年7月的18个月内,采用一系列方法进行病例确认,目的是确定南澳大利亚州所有C1INH-HAE患者。结果我们在南澳大利亚州发现了35名HAE患者,人口患病率为52,400人中有1人,与国际平均患病率一致。在 4 名澳大利亚土著患者中发现了 HAE。31 名成年患者中有 17 人完成了一项额外的多问卷调查,结果显示总体疾病控制情况令人满意。最常见的预防性疗法是达那唑、拉那度单抗和皮下注射 C1 抑制剂。许多病情较轻的患者(多为男性)对小剂量达那唑反应良好,耐受性良好,并继续使用该疗法,而病情较重的患者目前正在使用更新的疗法,对当前预防疗法的总体满意度很高。我们的人群调查显示,考虑到疾病活动性、药物风险和耐受性,对合适的患者使用目前的长期预防疗法(包括达那唑、拉那度单抗和 C1 抑制剂)可有效预防 HAE 发作,且满意度较高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hereditary angioedema prevalence and satisfaction with prophylaxis in South Australia

Background

Hereditary angioedema (HAE) due to deficiency of C1 Inhibitor (C1INH-HAE) is a rare, unpredictable and potentially fatal genetic disorder. There are relatively few systematic population prevalence studies, with reports from various countries of between 1 in 20,000 and 1 in 150,000. and no Australian data. The therapeutic landscape for HAE has changed dramatically in recent years with a focus on highly effective prophylaxis, with the aim of total suppression of angioedema and achievement of a normal life.

Objectives

Epidemiological survey of HAE in South Australia, with description of patient characteristics, quality of life and treatment, with a focus on prophylaxis.

Methods

Case ascertainment was conducted over 18 months from January 2021 to July 2022, using a range of approaches with the aim of identifying all people with C1INH-HAE in South Australia. Questionnaires were administered to consenting patients utilising established HAE-specific and general survey instruments.

Results

We identified 35 people with HAE in South Australia, yielding a population prevalence of 1 in 52,400, in line with average established international prevalence. HAE was identified in 4 patients of Indigenous Australian heritage. Seventeen of 31 adult patients completed an additional multi-questionnaire survey, revealing overall satisfactory disease control. Most common prophylactic therapies were danazol, lanadelumab, and subcutaneous C1 inhibitor. Many patients (mostly male) with milder disease had responded well to low-dose danazol with good tolerance and have continued to use it, whereas patients with higher disease burden are now using newer therapies, and overall satisfaction with current prophylaxis is high.

Conclusions

Prevalence of HAE in South Australia aligns with international reports. Our population survey indicates that current long-term prophylaxis therapies including danazol, lanadelumab and C1-inhibitor, applied to appropriate patients taking into account disease activity and drug risks and tolerance, are effective for HAE attack prevention and produce high levels of satisfaction.

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CiteScore
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