Delay in diagnosis is the most important proximate reason for mortality in hereditary angio-oedema: our experience at Chandigarh, India

Author:

Kumar Jindal Ankur1ORCID,Basu Suprit1ORCID,Tyagi Reva1,Barman Prabal1,Sil Archan1ORCID,Chawla Sanchi1,Kaur Anit1,Tyagi Rahul1,Jangra Isheeta1,Machhua Sanghamitra1,Sendhil Kumaran Muthu2,Dogra Sunil2ORCID,Vinay Keshavamurthy2,Bishnoi Anuradha2,Sharma Rajni1,Garg Ravinder1,Saka Ruchi1,Suri Deepti1,Pandiarajan Vignesh1ORCID,Pilania Rakesh1,Dhaliwal Manpreet1,Sharma Saniya1,Rawat Amit1ORCID,Singh Surjit1

Affiliation:

1. Pediatric Allergy Immunology Unit, Department of Pediatrics, Postgraduate Institute of Medical Education and Research , Chandigarh , India

2. Department of Dermatology, Venereology and Leprology, Postgraduate Institute of Medical Education and Research , Chandigarh , India

Abstract

Abstract Background Hereditary angio-oedema (HAE) is a rare autosomal dominant disorder characterized clinically by recurrent episodes of nonpruritic subcutaneous and/or submucosal oedema. Laryngeal oedema is the commonest cause of mortality in patients with HAE. Prior to the availability of first-line treatment options for the management of HAE, mortality was as high as 30%. Mortality has significantly declined in countries where first-line treatment options are available and patients can access these therapies. There is a paucity of literature on the outcomes of patients with HAE in developing countries where availability of and access to first-line treatment options are still a challenge. Objectives To report our experience on mortality in patients with HAE and to report factors associated with the death of these patients. Methods We carried out a record review of all patients diagnosed with HAE between January 1996 and August 2022. Families with HAE who had reported the death of at least one family member/relative from laryngeal oedema were studied in detail. Results Of the 65 families (170 patients) registered in the clinic, 16 families reported the death of at least one family member/relative from laryngeal oedema (total of 36 deaths). Of these 16 families, 14 reported that 1 or more family members had experienced at least 1 attack of laryngeal oedema. One patient died during follow-up when she was taking long-term prophylaxis with stanozolol and tranexamic acid, while the remaining 35 patients were not diagnosed with HAE at the time of their death. At the time of death of all 36 patients, at least 1 other family member had symptoms suggestive of HAE, but the diagnosis was not established for the family. Conclusions To our knowledge, this is the largest single-centre cohort of patients with HAE in India reporting mortality data and factors associated with death in these families. The delay in diagnosis is the most important reason for mortality.

Publisher

Oxford University Press (OUP)

Subject

Dermatology

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