Literature DB >> 27796677

The Subjective Experience of Patients Diagnosed with Hereditary Hemorrhagic Telangiectasia: a Qualitative Study.

Laura Geerts1,2, Carole Fantini-Hauwel3,4, Elodie Brugallé4, Odile Boute5, Frédéric Frénois5, Lydie Defrance4, Sylvie Manouvrier-Hanu5, Florence Petit5, Pascal Antoine4.   

Abstract

The aim of the present study was to understand the context and psychological impact for patients diagnosed with hereditary hemorrhagic telangiectasia (HHT). Semi-structured interviews were conducted with 9 patients affected by HHT, and the transcripts were analyzed using interpretative phenomenological analysis. The results of this study allowed us to propose a new hypothesis to explain the delay in diagnosis: the trivialization of symptoms associated with HHT. Moreover, the results showed that a genetic diagnosis of HHT results in emotional shock, uncertainty about the future, and worry about one's children in parents who are confronted with the dilemma of facing the reality of the diagnosis or delaying dealing with the diagnosis until disease onset. Family and personal perceptions of the disease influenced not only the delay in diagnosis but also the emotional and behavioral reactions of patients following a genetic diagnosis.

Entities:  

Keywords:  Children transmission; Diagnosis delay; Genetic diagnosis; Hereditary disease; Hereditary hemorrhagic telangiectasia; Psychological consequences

Mesh:

Year:  2016        PMID: 27796677     DOI: 10.1007/s10897-016-0033-z

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  17 in total

1.  Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype.

Authors:  Aaron D Bossler; Jennifer Richards; Cicily George; Lynn Godmilow; Arupa Ganguly
Journal:  Hum Mutat       Date:  2006-07       Impact factor: 4.878

2.  Chronic illness -- a disruption in life: identity-transformation among women with chronic fatigue syndrome and fibromyalgia.

Authors:  P Asbring
Journal:  J Adv Nurs       Date:  2001-05       Impact factor: 3.187

3.  The natural history of epistaxis in patients with hereditary hemorrhagic telangiectasia in the Norwegian population: a cross-sectional study.

Authors:  Sinan Dheyauldeen; Michael Abdelnoor; Gregor Bachmann-Harildstad
Journal:  Am J Rhinol Allergy       Date:  2011 Jul-Aug       Impact factor: 2.467

4.  Altered quality of life in Rendu-Osler-Weber disease related to recurrent epistaxis.

Authors:  I Ingrand; P Ingrand; B Gilbert-Dussardier; G Defossez; V Jouhet; V Migeot; X Dufour; J M Klossek
Journal:  Rhinology       Date:  2011-06       Impact factor: 3.681

5.  Health-related quality of life in a rare disease: hereditary hemorrhagic telangiectasia (HHT) or Rendu-Osler-Weber disease.

Authors:  Giovanna Pasculli; Francesco Resta; Edoardo Guastamacchia; Leonardo Di Gennaro; Patrizia Suppressa; Carlo Sabbà
Journal:  Qual Life Res       Date:  2004-12       Impact factor: 4.147

6.  Long-term outcome of patients with hereditary hemorrhagic telangiectasia and severe hepatic involvement after orthotopic liver transplantation: a single-center study.

Authors:  Sophie Dupuis-Girod; Anne-Laure Chesnais; Isabelle Ginon; Jérôme Dumortier; Jean-Christophe Saurin; Gérard Finet; Evelyne Decullier; Denis Marion; Henri Plauchu; Olivier Boillot
Journal:  Liver Transpl       Date:  2010-03       Impact factor: 5.799

7.  Life expectancy in patients with hereditary haemorrhagic telangiectasia.

Authors:  C Sabbà; G Pasculli; P Suppressa; F D'Ovidio; G Mariano Lenato; F Resta; G Assennato; G Guanti
Journal:  QJM       Date:  2006-04-04

8.  Constructing sexual health: gay men and 'risk' in the context of a public sex environment.

Authors:  P Flowers; G Hart; C Marriott
Journal:  J Health Psychol       Date:  1999-07

9.  Impact of genotype and mutation type on health-related quality of life in patients with hereditary hemorrhagic telangiectasia.

Authors:  Markus Pfister; Ilse M Zalaman; Gunnar Blumenstock; Paul-Stefan Mauz; Ingo Baumann
Journal:  Acta Otolaryngol       Date:  2009-08       Impact factor: 1.494

10.  A long diagnostic delay in patients with Hereditary Haemorrhagic Telangiectasia: a questionnaire-based retrospective study.

Authors:  Paola Pierucci; Gennaro M Lenato; Patrizia Suppressa; Patrizia Lastella; Vincenzo Triggiani; Raffaella Valerio; Mario Comelli; Daniela Salvante; Alessandro Stella; Nicoletta Resta; Giancarlo Logroscino; Francesco Resta; Carlo Sabbà
Journal:  Orphanet J Rare Dis       Date:  2012-06-07       Impact factor: 4.123

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  1 in total

1.  Thalidomide for the Management of Bleeding Episodes in Patients with Hereditary Hemorrhagic Telangiectasia: Effects on Epistaxis Severity Score and Quality of Life

Authors:  Mehmet Baysal; Elif G. Ümit; Hakkı Onur Kırkızlar; Ali Caner Özdöver; Ahmet Muzaffer Demir
Journal:  Turk J Haematol       Date:  2018-06-08       Impact factor: 1.831

  1 in total

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