Factors Associated with Severe Impact of Lipodystrophy on the Quality of Life of Patients Infected with HIV-1
Author(s) -
Jordi Blanch,
Araceli Rousaud,
Estebán Martínez,
Elisa de Lazzari,
Ana Milinkovic,
JosepMaria Peri,
José L. Blanco,
Juan Javier,
Vı́ctor Navarro,
Guillem Massana,
Josep M. Gatell
Publication year - 2004
Publication title -
clinical infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.44
H-Index - 336
eISSN - 1537-6591
pISSN - 1058-4838
DOI - 10.1086/383573
Subject(s) - medicine , lipodystrophy , quality of life (healthcare) , dermatology life quality index , psychosocial , asymptomatic , body mass index , shame , sida , viral disease , human immunodeficiency virus (hiv) , immunology , psychiatry , viral load , disease , antiretroviral therapy , nursing , political science , law
A standardized questionnaire was used to assess the impact of lipodystrophy (LD) on quality of life (QoL). Eighty-four consecutive asymptomatic human immunodeficiency virus type 1 (HIV-1)-infected outpatients with clinical LD completed a modified version of the Dermatology Life Quality Index (DLQI) survey to measure the impact of body fat changes on their QoL. Body changes influenced dressing for 55 patients (65%), produced feelings of shame for 41 (49%), and disrupted sexual life for 23 (27%). There was a greater impact on the DLQI due to body changes among women, injection drug users, patients with abdominal or breast lipoaccumulation, and patients with a high number of non-LD side effects. Multivariate proportional odds model analysis showed that the severity of non-LD-associated side effects and the presence of breast lipoaccumulation were associated with impaired psychosocial functioning. Specific characteristics of patients, antiretroviral-based side effects, and breast lipoaccumulation exert a greater impact on QoL in HIV-1-infected patients with LD.
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