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

Androgens hereditary angioedema on-demand therapy plasma derived C1-estrase inhibitor prophylaxis tranexamic acid

Journal

Asia Pacific allergy
ISSN: 2233-8276
Titre abrégé: Asia Pac Allergy
Pays: Netherlands
ID NLM: 101561954

Informations de publication

Date de publication:
Jun 2023
Historique:
received: 18 04 2023
accepted: 25 04 2023
medline: 30 6 2023
pubmed: 30 6 2023
entrez: 30 6 2023
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 37388810
doi: 10.5415/apallergy.0000000000000100
pmc: PMC10287105
doi:

Types de publication

Journal Article

Langues

eng

Pagination

60-65

Informations de copyright

Copyright © 2023. Asia Pacific Association of Allergy, Asthma and Clinical Immunology.

Déclaration de conflit d'intérêts

The authors have no financial conflicts of interest.

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Auteurs

Ankur Kumar Jindal (AK)

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

Archan Sil (A)

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

Ridhima Aggarwal (R)

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

Keshavamurthy Vinay (K)

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

Anuradha Bishnoi (A)

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

Deepti Suri (D)

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

Amit Rawat (A)

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

Muthu Sendhil Kumaran (MS)

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

Biman Saikia (B)

Department of Immunopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

Rashmi Sarkar (R)

Department of Dermatology, Lady Hardinge Medical College and Associated Hospitals, New Delhi, India.

Lalit Gupta (L)

Department of Dermatology, RNT Medical College, Udaipur, India.

D Dinesh Kumar (DD)

Dr. Dinesh's Skin & Hair Clinic, Chennai, India.

Rashmi Jindal (R)

Department of Dermatology, Himalayan Institute of Medical Sciences, Dehradun, India.

T U Sukumaran (TU)

Caritas Hospital, Kottayam, Kerala, India.

Jose Ouseph (J)

Government Medical College, Alappuzha, Kerala, India.

Hilary Longhurst (H)

Department of Immunology, Auckland City Hospital, Te Toka Tumai.
Department of Medicine, University of Auckland, Auckland, New Zealand.

Ruby Pawankar (R)

Department of Pediatrics, Nippon Medical School, Tokyo, Japan.

Surjit Singh (S)

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

Sunil Dogra (S)

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

Classifications MeSH