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Association of sociodemographic and clinical factors with the quality of life of Brazilian individuals with Neurofibromatosis type 1: a cross-sectional study.
Bicudo, Natália Parenti; Germano, Carla Maria Ramos; de Moraes, Roberta Teixeira; de Avó, Lucimar Retto da Silva; Ferner, Rosalie E; Melo, Débora Gusmão.
Afiliação
  • Bicudo NP; Department of Medicine, Universidade Federal de São Carlos, São Carlos, SP, Brazil.
  • Germano CMR; Department of Medicine, Universidade Federal de São Carlos, São Carlos, SP, Brazil.
  • de Moraes RT; Department of Medicine, Universidade Federal de São Carlos, São Carlos, SP, Brazil.
  • de Avó LRDS; Department of Medicine, Universidade Federal de São Carlos, São Carlos, SP, Brazil.
  • Ferner RE; National Neurofibromatosis Service, Department of Neurology, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Melo DG; Department of Medicine, Universidade Federal de São Carlos, São Carlos, SP, Brazil. Electronic address: dgmelo@ufscar.br.
An Bras Dermatol ; 99(4): 520-526, 2024.
Article em En | MEDLINE | ID: mdl-38493052
ABSTRACT

BACKGROUND:

Neurofibromatosis type 1 (NF1) is a rare genetic disorder with a wide range of clinical manifestations, notably neurocutaneous features, that can lead to emotional and physical consequences.

OBJECTIVES:

This study assessed the influence of sociodemographic factors and clinical features of the disease on the quality of life of Brazilian individuals with NF1.

METHODS:

This is a descriptive cross-sectional study. Data were collected from 101 individuals with NF1 using the Brazilian version of the Impact of NF1 on Quality of Life Questionnaire (INF1-QoL), a form with information on sociodemographic characteristics, and an NF1 visibility self-evaluation scale. The relationship between variables was evaluated through statistical testing, and the significance level was defined as 0.05.

RESULTS:

The study included 101 adults with NF1 aged 18 to 59 years, with a mean age of 35.54 years (±9.63) and a female predominance (n = 84, 83.17%). The mean total INF1-QoL score was 10.62 (±5.63), with a median of 10, minimum value of 0, and maximum of 31 points. Two characteristics of the participants were significantly associated with the quality of life educational level (p = 0.003) and familial history of NF1 (p = 0.019). There was a statistically significant correlation between the INF1-QoL score and the degree of disease visibility (rho = 0.218; p = 0.028). STUDY

LIMITATIONS:

Cross-sectional study, conducted with a convenience sample and using self-reported measures.

CONCLUSIONS:

The findings support the significant impact of NF1 on quality of life. The authors recommend multidisciplinary follow-up for patients, with adherence to anticipatory clinical care measures, adequate pain control, psychological assistance, and genetic counseling.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Fatores Socioeconômicos / Neurofibromatose 1 Limite: Adolescent / Adult / Female / Humans / Male / Middle aged País/Região como assunto: America do sul / Brasil Idioma: En Revista: An Bras Dermatol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Brasil

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Fatores Socioeconômicos / Neurofibromatose 1 Limite: Adolescent / Adult / Female / Humans / Male / Middle aged País/Região como assunto: America do sul / Brasil Idioma: En Revista: An Bras Dermatol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Brasil