Quality of life and use of health care among people with genital herpes inFrance

Citation
F. Taboulet et al., Quality of life and use of health care among people with genital herpes inFrance, ACT DER-VEN, 79(5), 1999, pp. 380-384
Citations number
22
Categorie Soggetti
Dermatology,"da verificare
Journal title
ACTA DERMATO-VENEREOLOGICA
ISSN journal
00015555 → ACNP
Volume
79
Issue
5
Year of publication
1999
Pages
380 - 384
Database
ISI
SICI code
0001-5555(199909)79:5<380:QOLAUO>2.0.ZU;2-P
Abstract
In order to assess psychological morbidity in France related to genital her pes infection, me carried out a transversal study comparing infected patien ts with a control group. A total of 236 patients with genital herpes mere f irst identified by means of a postal survey, then matched against a witness group of 236 noninfected persons. Detailed questionnaires were sent out to each person in the 2 groups. A total of 150 herpes patients and 200 non-in fected persons answered the questionnaire, which enabled us to measure the incidence of the disease by means of 2 indicators: a herpes-specific scale and the SF-36 quality of life questionnaire. Emotional trauma due to genita l herpes was reported amongst 23% of the participants. Of the participants, 57% indicated that herpes interfered with their sexual relationships; 50% felt it difficult to live with genital herpes; and 37% felt that herpes rui ns their lives. An analysis assessing health-related quality of life indica ted significant differences between the scores of the 2 groups and showed t hat quality of life is lower amongst herpes patients. Respondents with geni tal herpes required more frequent consultations with GPs (81% vs. 73%), and significantly more frequent consultations with specialists (59% vs. 45%). Our study confirms that substantial psychological morbidity exists in patie nts with genital herpes.