Literature DB >> 26304015

Efficacy of on-demand treatment in reducing morbidity in patients with hereditary angioedema due to C1 inhibitor deficiency.

A Zanichelli1, M Mansi1, G M Azin1, M A Wu1, G Periti1, G Casazza1, R Vacchini1, C Suffritti1, M Cicardi1.   

Abstract

BACKGROUND: Angioedema due to hereditary deficiency of C1 inhibitor causes temporarily disability. Guidelines recommend early on-demand treatment of attacks to reduce morbidity. In this prospective observational study, we evaluated the efficacy of on-demand approach.
METHODS: From January 2009 to August 2014, data on attacks and treatments were collected from 227 patients from our centre in Milan.
RESULTS: A total of 4244 attacks were reported; 50% were treated with approved therapies (pdC1-INH or icatibant), 15% were with tranexamic acid, and 35% were not treated. Attack locations were peripheral cutaneous (46%), abdominal (34%), multiple (12%), facial (5%) and laryngeal (3%). Attack severities were moderate (48%), mild (28%) and severe (24%). Median attack duration (data available for 2393 attacks) with approved therapies was 10 h, significantly shorter than without treatment (45 h) or with tranexamic acid (38 h). Most of the treatments were self-administered: 93% with icatibant and 59% with pd-C1-INH. Median attack duration with icatibant was 8 and 11.5 h with pd-C1 INH. Median time from onset of symptoms to drug administration was 1 h with icatibant and 2 h with pd-C1INH and median time from drug administration to complete resolution was 5.5 and 8 h, respectively. Second treatment was required in 12.7% of icatibant-treated attacks and in 1.9% of pdC1-INH-treated attacks.
CONCLUSION: This study provides evidence that on-demand treatment is effective in reducing disease-related morbidity. The use of on-demand treatment in Italy has increased up to 50% of attacks in the last years, reflecting a better adherence to international guidelines.
© 2015 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  C1 inhibitor; hereditary angioedema; icatibant; plasma-derived C1 Inhibitor; tranexamic acid

Mesh:

Substances:

Year:  2015        PMID: 26304015     DOI: 10.1111/all.12731

Source DB:  PubMed          Journal:  Allergy        ISSN: 0105-4538            Impact factor:   13.146


  8 in total

1.  The international WAO/EAACI guideline for the management of hereditary angioedema - The 2021 revision and update.

Authors:  Marcus Maurer; Markus Magerl; Stephen Betschel; Werner Aberer; Ignacio J Ansotegui; Emel Aygören-Pürsün; Aleena Banerji; Noémi-Anna Bara; Isabelle Boccon-Gibod; Konrad Bork; Laurence Bouillet; Henrik Balle Boysen; Nicholas Brodszki; Paula J Busse; Anette Bygum; Teresa Caballero; Mauro Cancian; Anthony J Castaldo; Danny M Cohn; Dorottya Csuka; Henriette Farkas; Mark Gompels; Richard Gower; Anete S Grumach; Guillermo Guidos-Fogelbach; Michihiro Hide; Hye-Ryun Kang; Allen P Kaplan; Constance H Katelaris; Sorena Kiani-Alikhan; Wei-Te Lei; Richard F Lockey; Hilary Longhurst; William Lumry; Andrew MacGinnitie; Alejandro Malbran; Inmaculada Martinez Saguer; Juan José Matta Campos; Alexander Nast; Dinh Nguyen; Sandra A Nieto-Martinez; Ruby Pawankar; Jonathan Peter; Grzegorz Porebski; Nieves Prior; Avner Reshef; Marc Riedl; Bruce Ritchie; Farrukh Rafique Sheikh; William B Smith; Peter J Spaeth; Marcin Stobiecki; Elias Toubi; Lilian Agnes Varga; Karsten Weller; Andrea Zanichelli; Yuxiang Zhi; Bruce Zuraw; Timothy Craig
Journal:  World Allergy Organ J       Date:  2022-04-07       Impact factor: 5.516

2.  Breakthrough attacks in patients with hereditary angioedema receiving long-term prophylaxis are responsive to icatibant: findings from the Icatibant Outcome Survey.

Authors:  Werner Aberer; Marcus Maurer; Laurence Bouillet; Andrea Zanichelli; Teresa Caballero; Hilary J Longhurst; Amandine Perrin; Irmgard Andresen
Journal:  Allergy Asthma Clin Immunol       Date:  2017-07-05       Impact factor: 3.406

Review 3.  Optimum Use of Acute Treatments for Hereditary Angioedema: Evidence-Based Expert Consensus.

Authors:  Hilary Longhurst
Journal:  Front Med (Lausanne)       Date:  2018-03-12

4.  The physician and hereditary angioedema friend or foe: 62-year diagnostic delay and iatrogenic procedures.

Authors:  Anna Valerieva; Marco Cicardi; James Baraniuk; Maria Staevska
Journal:  Allergy Asthma Clin Immunol       Date:  2018-10-25       Impact factor: 3.406

5.  Costs and effects of on-demand treatment of hereditary angioedema in Italy: a prospective cohort study of 167 patients.

Authors:  Carlo Federici; Francesca Perego; Ludovica Borsoi; Valentina Crosta; Andrea Zanichelli; Antonio Gidaro; Rosanna Tarricone; Marco Cicardi
Journal:  BMJ Open       Date:  2018-07-30       Impact factor: 2.692

Review 6.  Mitigating Disparity in Health-care Resources Between Countries for Management of Hereditary Angioedema.

Authors:  Ankur Kumar Jindal; Avner Reshef; Hilary Longhurst
Journal:  Clin Rev Allergy Immunol       Date:  2021-05-18       Impact factor: 8.667

7.  Safety, effectiveness, and impact on quality of life of self-administration with plasma-derived nanofiltered C1 inhibitor (Berinert®) in patients with hereditary angioedema: the SABHA study.

Authors:  Andrea Zanichelli; Giulia Maria Azin; Federico Cristina; Romualdo Vacchini; Teresa Caballero
Journal:  Orphanet J Rare Dis       Date:  2018-04-10       Impact factor: 4.123

8.  Therapeutic management of hereditary angioedema: past, present, and future.

Authors:  Anna Valerieva; Denislava Nedeva; Vania Yordanova; Elena Petkova; Maria Staevska
Journal:  Balkan Med J       Date:  2021-03       Impact factor: 2.021

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.