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导致遗传性血管性水肿按需治疗指南依从性不佳的因素。

Factors contributing to non-compliance with on-demand treatment guidelines in hereditary angioedema.

作者信息

Betschel Stephen D, Peter Jonny, Lumry William, Longhurst Hilary, Katelaris Constance H, van Kooten Sally, Heckmann Markus, Malloy Neil, Ulloa Julie, Danese Sherry, Magerl Markus

机构信息

Department Division Director Clinical Immunology and Allergy, Staff Clinical Immunologist and Allergist, University of Toronto, St. Michael's Hospital, 36 Toronto St, Suite 700, Toronto, ON, M5C 2C5, Canada.

University of Cape Town, Cape Town, South Africa.

出版信息

Allergy Asthma Clin Immunol. 2025 May 21;21(1):25. doi: 10.1186/s13223-025-00969-0.

Abstract

BACKGROUND

Hereditary angioedema (HAE) is a rare genetic disorder characterized by painful and potentially life-threatening tissue swelling due to a deficiency or dysfunction of the C1 esterase inhibitor protein. Despite the availability of comprehensive on-demand treatment guidelines, compliance to guideline recommendations remains suboptimal, resulting in persisting unmet need.

METHODS

This observational, online survey was conducted between September 6, 2022, and October 19, 2022 to understand the behaviors and perspectives of individuals in the US with hereditary angioedema (HAE). Participants were recruited by the US Hereditary Angioedema Association and were eligible if they were US residents with clinician-diagnosed HAE type I or II and had experienced at least one HAE attack. The survey included multiple-choice, rank-order, and scale-based responses using a 5-point Likert scale for agreement and an 11-point Likert scale for anxiety. Statistical analysis was performed using Microsoft Excel, summarizing continuous variables as means, medians, and ranges, and categorical variables as frequency distributions and percentages.

RESULTS

A total of 107 out of 155 participants completed the survey (mean age = 41 years; 80.4% female). Half of the respondents used both prophylaxis and on-demand therapy, while the other half used on-demand therapy only. Icatibant was the most commonly used on-demand treatment (78.5%). The survey revealed that 57% of respondents did not treat all HAE attacks, and only 14% treated attacks immediately. Delays in treatment were common, with a mean time to treatment of 2.4 h, and younger patients were less likely to carry on-demand treatment. Reasons for delaying treatment included the perceived severity of the attack, lack of on-demand treatment availability, and pain associated with treatment. Additionally, 32.7% of respondents experienced the return of an HAE attack after initial treatment, with those delaying treatment more likely to experience recurrence. The survey also found that delayed treatment led to more severe attacks and longer recovery times, impacting work, social activities, and overall quality of life.

CONCLUSIONS

Although guidelines recommend early treatment of HAE attacks, many respondents do not treat immediately. This finding underscores the importance of incorporating open patient-physician communication to improve guideline compliance and the management of HAE.

摘要

背景

遗传性血管性水肿(HAE)是一种罕见的遗传性疾病,其特征是由于C1酯酶抑制蛋白缺乏或功能障碍导致疼痛且可能危及生命的组织肿胀。尽管有全面的按需治疗指南,但对指南建议的依从性仍然不理想,导致需求未得到满足的情况持续存在。

方法

这项观察性在线调查于2022年9月6日至2022年10月19日进行,旨在了解美国遗传性血管性水肿(HAE)患者的行为和观点。参与者由美国遗传性血管性水肿协会招募,符合条件的为临床诊断为I型或II型HAE的美国居民且经历过至少一次HAE发作。调查包括多项选择、排序以及基于量表的回答,使用5点李克特量表表示同意程度,11点李克特量表表示焦虑程度。使用Microsoft Excel进行统计分析,将连续变量总结为均值、中位数和范围,将分类变量总结为频率分布和百分比。

结果

155名参与者中有107名完成了调查(平均年龄 = 41岁;80.4%为女性)。一半的受访者同时使用预防治疗和按需治疗,另一半仅使用按需治疗。依库珠单抗是最常用的按需治疗药物(78.5%)。调查显示,57%的受访者并未治疗所有的HAE发作,只有14%的人立即治疗发作。治疗延迟很常见,平均治疗时间为2.4小时,年轻患者携带按需治疗药物的可能性较小。延迟治疗的原因包括对发作严重程度的认知、按需治疗药物不可用以及治疗相关的疼痛。此外,32.7%的受访者在初始治疗后经历了HAE发作复发,延迟治疗的人更有可能经历复发。调查还发现,延迟治疗导致发作更严重、恢复时间更长,影响工作、社交活动和总体生活质量。

结论

尽管指南建议对HAE发作进行早期治疗,但许多受访者并未立即治疗。这一发现强调了纳入开放的医患沟通以提高指南依从性和HAE管理的重要性。

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