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

被引:6
作者
Geerts, Laura [1 ,2 ]
Fantini-Hauwel, Carole [1 ,2 ]
Brugalle, Elodie [2 ]
Boute, Odile [3 ]
Frenois, Frederic [3 ]
Defrance, Lydie [2 ]
Manouvrier-Hanu, Sylvie [3 ]
Petit, Florence [3 ]
Antoine, Pascal [2 ]
机构
[1] Univ Libre Bruxelles, Campus Solbosch,CP 122,Ave Franklin Roosevelt 50, B-1050 Brussels, Belgium
[2] Univ Lille, CNRS, SCALab Sci Cognit & Sci Affect, UMR 9193, F-59000 Lille, France
[3] Univ Lille, CHU Lille, RADEME Malad RAres Dev Embryonnaire & Metab Pheno, EA 7364, F-59000 Lille, France
关键词
Hereditary hemorrhagic telangiectasia; Hereditary disease; Genetic diagnosis; Diagnosis delay; Psychological consequences; Children transmission; OF-LIFE; POPULATION; GENOTYPE; DISEASE; HHT;
D O I
10.1007/s10897-016-0033-z
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
收藏
页码:612 / 619
页数:8
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