Literature DB >> 23839260

Quality of life in family members of vitiligo patients: a questionnaire study in Saudi Arabia.

Ghada A Bin Saif1, Amal O Al-Balbeesi, Rawan Binshabaib, Deema Alsaad, Shawn G Kwatra, Abdullateef A Alzolibani, Gil Yosipovitch.   

Abstract

BACKGROUND: Many dermatologic disorders are known to adversely affect quality of life (QoL) in close relatives or partners of patients; however, it is unknown whether vitiligo impacts the QoL of family members.
OBJECTIVE: The aim of this study was to identify the level and domains in which the QoL of partners/relatives of patients with vitiligo are affected by the disease.
METHODS: A total of 141 patients with vitiligo, along with their family members, were recruited to complete validated QoL questionnaires, including the Dermatology Life Quality Index (DLQI) and the Family Dermatology Life Quality Index (FDLQI).
RESULTS: Family member QoL was affected in 129 (91.5 %) of subjects. Mean FDLQI score was 10.3 ± 6.4 standard deviation. Higher FDLQI score (greater impairment in QoL) was significantly associated with male patients, a shorter duration of disease, and higher educational levels in family members. The most affected FDLQI items in order of decreasing incidence were emotional impact, burden of care, impact on the physical well-being of the family member, problems due to the reaction of others in response to the patient's skin appearance and effect on social life. Overall FDLQI score and the number of items affected correlated with overall patient DLQI score (p < 0.001, r = 0.56 and p < 0.001, r = 0.53, respectively).
CONCLUSIONS: Vitiligo has a major impact on the QoL of family members of patients and often significantly impairs many aspects of their lives. Educational and supportive programs are recommended for family members of vitiligo patients who are at an increased risk for QoL impairments.

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Year:  2013        PMID: 23839260     DOI: 10.1007/s40257-013-0037-5

Source DB:  PubMed          Journal:  Am J Clin Dermatol        ISSN: 1175-0561            Impact factor:   7.403


  9 in total

1.  Vitiligo: Patient stories, self-esteem, and the psychological burden of disease.

Authors:  P E Grimes; M M Miller
Journal:  Int J Womens Dermatol       Date:  2018-01-08

2.  Relationship Between Depression and Quality of Life Among Vitiligo Patients: A Self-assessment Questionnaire-based Study.

Authors:  Narumol Silpa-Archa; Chutipon Pruksaeakanan; Nattha Angkoolpakdeekul; Chayada Chaiyabutr; Kanokvalai Kulthanan; Woraphat Ratta-Apha; Chanisada Wongpraparut
Journal:  Clin Cosmet Investig Dermatol       Date:  2020-08-04

3.  Worsening Quality of Life in Young Adult, Highly Educated, and Married Female Patients with Vitiligo: A Hospital-Based Case Control Study in Taiwan.

Authors:  Yuan-Ting Yang; Chung-Hao Hsu; Yu-Fen Wang; Yu-Jun Chang; Hui-Ju Yang; Jiunn-Liang Ko; Kuo-Chia Yang
Journal:  Int J Environ Res Public Health       Date:  2022-05-31       Impact factor: 4.614

4.  Chronic diseases among vitiligo patients. A case control study.

Authors:  Abdullah O Al Houssien; Rana O Al Houssien; Waleed Al Ajroush; Hassan S Al Kahtani
Journal:  Saudi Med J       Date:  2017-04       Impact factor: 1.484

5.  Quality of life of adult vitiligo patients using camouflage: A survey in a Chinese vitiligo community.

Authors:  Dian Chen; HsiaoHan Tuan; Eray Yihui Zhou; DeHua Liu; Yi Zhao
Journal:  PLoS One       Date:  2019-01-24       Impact factor: 3.240

6.  Family impact of pemphigus disease in an Iranian population using the Family Dermatology Life Quality Index.

Authors:  S Zahra Ghodsi; Arefeh Asadi; Narges Ghandi; Kamran Balighi; Hamidreza Mahmoudi; Robabeh Abedini; Maryam Ghiasi; Vahideh Lajevardi; Cheyda Chams-Davatchi; Maryam Daneshpazhooh
Journal:  Int J Womens Dermatol       Date:  2020-09-12

7.  Impact of narrow-band ultraviolet B radiation therapy on the quality of life of patients with vitiligo.

Authors:  Hani M J Khojah; Assaf G Alharbi; Abdulrahman A Alshaeri; Yaser M Alahmadi; Hossein M Elbadawy
Journal:  J Taibah Univ Med Sci       Date:  2021-06-12

8.  Psychosocial Effects of Vitiligo: A Systematic Literature Review.

Authors:  Khaled Ezzedine; Viktoria Eleftheriadou; Heather Jones; Kristen Bibeau; Fiona I Kuo; Daniel Sturm; Amit G Pandya
Journal:  Am J Clin Dermatol       Date:  2021-09-23       Impact factor: 7.403

9.  Quality of life in vitiligo patients in central Saudi Arabia.

Authors:  Sulaiman A Al-Shammari; Hatim M Alotaibi; Mohammed A Assiri; Moataz I Altokhais; Mazyad S Alotaibi; Mohammad S Alkhowailed
Journal:  Saudi Med J       Date:  2021-06       Impact factor: 1.422

  9 in total

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