cLFM-Qol: A specific quality of life measurement tool for children from 11 to 15 years with low-flow malformations.


Journal

Journal of the European Academy of Dermatology and Venereology : JEADV
ISSN: 1468-3083
Titre abrégé: J Eur Acad Dermatol Venereol
Pays: England
ID NLM: 9216037

Informations de publication

Date de publication:
Jul 2023
Historique:
received: 18 10 2022
accepted: 08 03 2023
medline: 14 6 2023
pubmed: 28 3 2023
entrez: 27 3 2023
Statut: ppublish

Résumé

Low-flow malformations (LFMs) are rare diseases with a significant impact on health-related quality of life (HRQoL), especially in children. No disease-specific questionnaire is available for children with LFMs. To develop and validate a specific HRQoL questionnaire for children from 11 to 15 years old suffering from LFMs. A preliminary questionnaire based on a verbatim from focus groups was created and sent to children from 11 to 15 years old suffering from LFMs, together with a dermatology-specific and a generic HRQoL questionnaire (cDLQI and EQ-5D-Y). A total of 75 from 201 included children responded to the questionnaires. The final version of the questionnaire (cLFM-QoL) included 15 questions and was not divisible into subscales. It demonstrated excellent internal consistency (cronbach 0.89), convergent validity and readability (SMOG 6.04). cLFM-QoL mean score (± SD) was 12.9/45 (8.03) for all grades of severity, for mild 8.22/45 (7.5), moderate 14.03/45 (8.35), severe 12.35/45 (6.59) or very severe patients 20.7/45 (3.39) (p 0.006). cLFM-QoL is a validated short and easy to use specific questionnaire with excellent psychometric capacities. It will be suitable for any children aged 11-15 with LFMs, in daily practice or clinical trials.

Sections du résumé

BACKGROUND BACKGROUND
Low-flow malformations (LFMs) are rare diseases with a significant impact on health-related quality of life (HRQoL), especially in children. No disease-specific questionnaire is available for children with LFMs.
OBJECTIVE OBJECTIVE
To develop and validate a specific HRQoL questionnaire for children from 11 to 15 years old suffering from LFMs.
METHODS METHODS
A preliminary questionnaire based on a verbatim from focus groups was created and sent to children from 11 to 15 years old suffering from LFMs, together with a dermatology-specific and a generic HRQoL questionnaire (cDLQI and EQ-5D-Y).
RESULTS RESULTS
A total of 75 from 201 included children responded to the questionnaires. The final version of the questionnaire (cLFM-QoL) included 15 questions and was not divisible into subscales. It demonstrated excellent internal consistency (cronbach 0.89), convergent validity and readability (SMOG 6.04). cLFM-QoL mean score (± SD) was 12.9/45 (8.03) for all grades of severity, for mild 8.22/45 (7.5), moderate 14.03/45 (8.35), severe 12.35/45 (6.59) or very severe patients 20.7/45 (3.39) (p 0.006).
CONCLUSION CONCLUSIONS
cLFM-QoL is a validated short and easy to use specific questionnaire with excellent psychometric capacities. It will be suitable for any children aged 11-15 with LFMs, in daily practice or clinical trials.

Identifiants

pubmed: 36972023
doi: 10.1111/jdv.19061
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1435-1442

Informations de copyright

© 2023 The Authors. Journal of the European Academy of Dermatology and Venereology published by John Wiley & Sons Ltd on behalf of European Academy of Dermatology and Venereology.

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Auteurs

Marion Godeau (M)

Reference Center for Rare Skin Diseases, Dermatology Department, CHU toulouse, Paul Sabatier University, Occitanie, Toulouse, France.

Jason Shourick (J)

Pôle santé publique et médecine sociale, Epidemiology Department, CHU Toulouse, Faculté de médecine de Purpan, Occitanie, Toulouse, France.

Isabelle Dreyfus (I)

Reference Center for Rare Skin Diseases, Dermatology Department, CHU toulouse, Paul Sabatier University, Occitanie, Toulouse, France.

Éline Casassa (É)

Reference Center for Rare Skin Diseases, Dermatology Department, CHU toulouse, Paul Sabatier University, Occitanie, Toulouse, France.

Anaïs Bergeron (A)

Centre d'Etudes et de Recherches en Psychopathologie et psychologie de la Santé, Psychopathology Department, Toulouse II Jean Jaurès University, Occitanie, Toulouse, France.

Maella Severino-Freire (M)

Reference Center for Rare Skin Diseases, Dermatology Department, CHU toulouse, Paul Sabatier University, Occitanie, Toulouse, France.

Céline Granier Tournier (C)

Reference Center for Rare Skin Diseases, Dermatology Department, CHU toulouse, Paul Sabatier University, Occitanie, Toulouse, France.

Julie Malloizel-Delaunay (J)

Vascular Disease Department, CHU toulouse, Occitanie, Toulouse, France.

Olivia Boccara (O)

Reference Center for Genodermatoses and Rare Skin Diseases (MAGEC), Dermatology Department, Necker-Enfants Malades Hospitals, Île-de-France, Paris, France.

Hélène Aubert (H)

Dermatology Derpartment, CHU Nantes, Nantes, Pays de la Loire, France.

Annabel Maruani (A)

Dermatology Department, CHRU Tours, François Rabelais University, Centre, Tours, France.

Christine Chiaverini (C)

Dermatology Department, CHU Nice, Archet 2 Hospital, Provence-Alpes-Côte d'Azu, Nice, France.

Christine Labrèze (C)

Pediatric Dermatology Unit, CHU Bordeaux, Pellegrin children's Hospital, Aquitaine, Bordeaux, France.

Juliette Mazereeuw-Hautier (J)

Reference Center for Rare Skin Diseases, Dermatology Department, CHU toulouse, Paul Sabatier University, Occitanie, Toulouse, France.

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