Management of hereditary angioedema in resource-constrained settings: A consensus statement from Indian subcontinent.

IF 1.6 Q3 ALLERGY Asia Pacific Allergy Pub Date : 2023-06-01 DOI:10.5415/apallergy.0000000000000100
Ankur Kumar Jindal, Archan Sil, Ridhima Aggarwal, Keshavamurthy Vinay, Anuradha Bishnoi, Deepti Suri, Amit Rawat, Muthu Sendhil Kumaran, Biman Saikia, Rashmi Sarkar, Lalit Gupta, D Dinesh Kumar, Rashmi Jindal, T U Sukumaran, Jose Ouseph, Hilary Longhurst, Ruby Pawankar, Surjit Singh, Sunil Dogra
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Abstract

Hereditary angioedema (HAE) is an uncommon disorder characterized clinically by recurrent episodes of nonitchy subcutaneous and/or submucosal swellings. The estimated prevalence of HAE is ~ 1: 10,000 to 1: 50,000. There are no prevalence data from India, however, estimates suggest that there are 27,000 to 135,000 patients with HAE in India at present. The majority of these, however, remain undiagnosed. Replacement of plasma-derived or recombinant C1-esterase inhibitor (C1-INH) protein, administered intravenously, is the treatment of choice during the management of acute episodes of angioedema (i.e., "on-demand treatment") and is also useful for short-term prophylaxis (STP) and long-term prophylaxis (LTP). This has been found to be effective and safe even in young children and during pregnancy. Until recently, none of the first-line treatment options were available for "on-demand treatment," STP or LTP in India. As a result, physicians had to use fresh frozen plasma for both "on-demand treatment" and STP. For LTP, attenuated androgens (danazol or stanozolol) and/or tranexamic acid were commonly used. These drugs have been reported to be useful for LTP but are associated with a significant risk of adverse effects. Intravenous pd-C1-INH, the first-line treatment option, is now available in India. However, because there is no universal health insurance, access to pd-C1-INH is a significant challenge. HAE Society of India has developed these consensus guidelines for India and other resource-constrained settings where plasma-derived C1-INH therapy is the only available first-line treatment option for the management of HAE and diagnostic facilities are limited. These guidelines have been developed because it may not be possible for all patients to access the recommended therapy and at the recommended doses as suggested by the international guidelines. Moreover, it may not be feasible to follow the evaluation algorithm suggested by the international guidelines.

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资源受限环境下遗传性血管性水肿的管理:来自印度次大陆的共识声明。
遗传性血管性水肿(HAE)是一种罕见的疾病,临床表现为反复发作的非瘙痒性皮下和/或粘膜下肿胀。HAE的估计患病率为1∶1万至1∶5万。没有来自印度的流行数据,然而,估计目前印度有27,000至135,000例HAE患者。然而,其中大多数仍未得到诊断。静脉给药替代血浆源性或重组c1 -酯酶抑制剂(C1-INH)蛋白是急性血管性水肿发作(即“按需治疗”)的首选治疗方法,也可用于短期预防(STP)和长期预防(LTP)。这已被发现是有效和安全的,即使在幼儿和怀孕期间。直到最近,印度还没有一线治疗方案可用于“按需治疗”,即STP或LTP。因此,医生不得不使用新鲜的冷冻血浆进行“按需治疗”和STP。对于LTP,通常使用减效雄激素(达那唑或斯坦诺唑)和/或氨甲环酸。据报道,这些药物对LTP有用,但有显著的不良反应风险。静脉注射pd-C1-INH是一线治疗选择,目前已在印度提供。然而,由于没有全民健康保险,获得pd-C1-INH是一个重大挑战。印度HAE协会为印度和其他资源受限的地区制定了这些共识指南,在这些地区,血浆源性C1-INH治疗是HAE管理的唯一可用一线治疗选择,诊断设施有限。制定这些指南的原因是,可能并非所有患者都能获得国际指南建议的推荐治疗和推荐剂量。此外,按照国际准则建议的评价算法可能并不可行。
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来源期刊
CiteScore
2.50
自引率
5.90%
发文量
33
期刊介绍: Asia Pacific Allergy (AP Allergy) is the official journal of the Asia Pacific Association of Allergy, Asthma and Clinical Immunology (APAAACI). Although the primary aim of the journal is to promote communication between Asia Pacific scientists who are interested in allergy, asthma, and clinical immunology including immunodeficiency, the journal is intended to be available worldwide. To enable scientists and clinicians from emerging societies appreciate the scope and intent of the journal, early issues will contain more educational review material. For better communication and understanding, it will include rational concepts related to the diagnosis and management of asthma and other immunological conditions. Over time, the journal will increase the number of original research papers to become the foremost citation journal for allergy and clinical immunology information of the Asia Pacific in the future.
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