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DOI 10.1186/s13023-025-03753-w

Медицинская библиотека · Orphanet journal of rare diseases · 2025

The health-related quality of life of Brazilians with epidermolysis bullosa.

Togo Camille Cristine Gomes, Zidório Ana Paula Caio, Gonçalves Vivian Siqueira Santos, Dutra Eliane Said

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Аннотация

BACKGROUND

Epidermolysis bullosa (EB) presents various complications that can affect an individual's health-related quality of life (HRQoL) and nutritional status. This cross-sectional study evaluates HRQoL and its association with the socio-demographic, nutritional, and clinical profiles of Brazilians with EB.

RESULTS

The sample consisted of 129 individuals (median age: 15 years), approximately 57% female, mostly composed of the EB simplex clinical type, followed by the dystrophic EB type (DEB). The mean score on the Children's Dermatology Life Quality Index questionnaire was 11.01 [standard deviation (SD) = 7.31], with a moderate impact on HRQoL. The median and interquartile range (IQR) of the score obtained in the Quality of Life Evaluation in Epidermolysis Bullosa- Brazilian Portuguese questionnaire was 13 (IQR: 8-19), which also indicated a moderate impact on HRQoL. In the subgroup aged ≥ 17 years, schooling positively influenced HRQoL, and decreased HRQoL was directly associated with underweight nutritional status. Family income promoted HRQoL in both subgroups.

CONCLUSIONS

HRQoL assessment showed that the DEB type was associated with the most severe effect. Additionally, the large impact, in < 17 years, was associated with family income, but did not present an association with nutritional status. While the severe impact on HRQoL, in ≥ 17 years, presented an association with nutritional status, family income, and education. Future research is important, to understand this population's needs, provide adequate care, and promote the best HRQoL.

Для цитирования: Togo Camille Cristine Gomes, Zidório Ana Paula Caio, Gonçalves Vivian Siqueira Santos, Dutra Eliane Said. The health-related quality of life of Brazilians with epidermolysis bullosa.. Orphanet journal of rare diseases. 2025. DOI: 10.1186/s13023-025-03753-w.

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