Emergency management in epidermolysis bullosa: consensus clinical recommendations from the European reference network for rare skin diseases.

Airway obstruction Blister Corneal erosion ERN-skin Epidermolysis bullosa Esophageal obstruction Pain Sepsis Urinary retention

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:
06 06 2020
Historique:
received: 08 02 2020
accepted: 07 05 2020
entrez: 8 6 2020
pubmed: 9 6 2020
medline: 22 6 2021
Statut: epublish

Résumé

Epidermolysis bullosa (EB) comprises a group of genetic disorders with the hallmark of fragility of the skin and mucosal surfaces. The severity of different types of EB varies markedly as does the occurrence of extra-cutaneous involvement and complications. A number of emergency situations may occur in the context of EB including obstruction to oral intake from oral or esophageal blisters or scarring, acute airway obstruction, acute urinary retention, sepsis and corneal erosions. Whilst general management principles apply in each of these settings, specific considerations are essential in managing EB to avoid undue trauma or damage to delicate tissues. These recommendations have been developed from a literature review and consensus from experts of the European Network for Rare Skin Disorders (ERN-Skin) to aid decision-making and optimize clinical care by non-EB expert health professionals encountering emergency situations in babies, children and adults with EB.

Identifiants

pubmed: 32505191
doi: 10.1186/s13023-020-01403-x
pii: 10.1186/s13023-020-01403-x
pmc: PMC7276067
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

142

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Auteurs

Jemima E Mellerio (JE)

St John's Institute of Dermatology, Guy's and St Thomas' NHS Foundation Trust, London, UK.

Maya El Hachem (M)

Dermatology Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.

Nathalia Bellon (N)

Dermatology Department, reference Centre MAGEC, Necker- Enfants Malades Hospital, Paris-Centre University, Paris, France.

Giovanna Zambruno (G)

Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.

Hana Buckova (H)

Dermatology Department, Children's Hospital, University Hospital Brno, Brno, Czech Republic.

Rudolf Autrata (R)

Pediatric Ophthalmology Department, Children's Hospital, University Hospital Brno, Brno, Czech Republic.

Carmen Salavastru (C)

Paediatric Dermatology Department, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.

Tamara Caldaro (T)

Endoscopy and Digestive Surgery Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.

Celine Greco (C)

Department of Pain and Palliative Medicine, reference Centre MAGEC, Necker- Enfants Malades Hospital, Paris-Centre University, Paris, France.

Cristina Has (C)

Department of Dermatology, Medical Center, University of Freiburg, Faculty of Medicine, University of Freiburg, Breisgau, Germany.

Christine Bodemer (C)

Dermatology Department, reference Centre MAGEC, Necker- Enfants Malades Hospital, Paris-Centre University, Paris, France. ChristineBodemer@aphp.fr.
Service de Dermatologie, Hôpital Necker Enfants Malades, 149 rue de Sèvres, 75015, Paris, France. ChristineBodemer@aphp.fr.

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