Occupational therapy for epidermolysis bullosa: clinical practice guidelines.


Journal

Orphanet journal of rare diseases
ISSN: 1750-1172
Titre abrégé: Orphanet J Rare Dis
Pays: England
ID NLM: 101266602

Informations de publication

Date de publication:
07 06 2019
Historique:
received: 23 11 2018
accepted: 08 04 2019
entrez: 9 6 2019
pubmed: 9 6 2019
medline: 31 3 2020
Statut: epublish

Résumé

The purpose of this article is to summarize the Dystrophic Epidermolysis Bullosa Research Association (DEBRA) International evidence-based Clinical Practice Guidelines (CPGs) for the provision of occupational therapy (OT) for children and adults living with inherited epidermolysis bullosa (EB). This is a rare genetic disorder characterized by skin fragility leading to blister formation occurring spontaneously or following minor trauma. Current OT practice for persons with EB is based on anecdotal care, clinical expertise and trial and error with collaboration between caregiver and patient. Intervention based on research is needed to establish a foundation of knowledge to guide international practitioners to create and improve standards of care and to be able to work effectively with those living with the rare diagnosis of this condition.This CPG was created by an international panel with expertise working with persons with EB. The panel was made up of 11 members including OT's, a physiotherapist, a medical doctor, social worker, person with EB and a carer of a person with EB. It describes the development of recommendations for 5 outcomes determined by survey of persons with EB, caregivers, and experienced healthcare professionals. The outcomes include independence in activities of daily living (ADL), independence in instrumental ADL, maximization of hand function (non-surgical), fine motor development and retention, and oral feeding skills. The recommendations are supplemented with additional files that include photos and specific examples to further guide occupational therapists or, in situations where an OT is not available, other members of the healthcare team.As the disorder of EB is rare, evidence-based CPGs are needed to provide a base of knowledge and practice for OTs throughout the world with the goal of providing quality care to patients, while improving their functional independence and quality of life. In addition, this information is valuable as a basis for further research.

Identifiants

pubmed: 31174559
doi: 10.1186/s13023-019-1059-8
pii: 10.1186/s13023-019-1059-8
pmc: PMC6556021
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

129

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Auteurs

Jennifer M Chan (JM)

Department of Rehabilitation, Lucile Packard Children's Hospital Stanford, 321 Middlefield Road, Menlo Park, CA, 94025, USA. Jennifer.chan@sbcglobal.net.

Amy Weisman (A)

Department of Rehabilitation, Lucile Packard Children's Hospital Stanford, 321 Middlefield Road, Menlo Park, CA, 94025, USA.

Alex King (A)

Phoenix Children's Hospital, Phoenix, USA.

Susan Maksomski (S)

Brooklyn Methodist Hospital, Brooklyn, USA.

Carrissa Shotwell (C)

Cincinnati Children's Hospital Medical Centre, Cincinnati, USA.

Claire Bailie (C)

Sydney Children's Hospital, Sydney, Australia.

Helen Weaver (H)

Community Project Lead DEBRA UK, Crowthorne, UK.

Rebecca Bodan (R)

School of Nursing, California State University Fullerton, Fullerton, USA.

Estrella Guerrero (E)

Community Social worker DEBRA Spain, Marbella, Spain.

Matija Zmazek (M)

DEBRA Croatia, Zagreb, Croatia.

Phuong Khuu (P)

Department of Rehabilitation, Lucile Packard Children's Hospital Stanford, 321 Middlefield Road, Menlo Park, CA, 94025, USA.

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