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Clinical practice guidelines: Oral health care for children and adults living with epidermolysis bullosa
Author(s) -
Krämer Susanne,
Lucas James,
Gamboa Francisca,
Peñarrocha Diago Miguel,
Peñarrocha Oltra David,
GuzmánLetelier Marcelo,
Paul Sanchit,
Molina Gustavo,
Sepúlveda Lorena,
Araya Ignacio,
Soto Rubén,
Arriagada Carolina,
Lucky Anne W,
Mellerio Jemima E,
Cornwall Roger,
Alsayer Fatimah,
Schilke Reinhard,
Antal Mark Adam,
Castrillón Fernanda,
Paredes Camila,
Serrano Maria Concepción,
Clark Victoria
Publication year - 2020
Publication title -
special care in dentistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.328
H-Index - 41
eISSN - 1754-4505
pISSN - 0275-1879
DOI - 10.1111/scd.12511
Subject(s) - medicine , epidermolysis bullosa , guideline , clinical practice , health care , quality of life (healthcare) , sedation , dentistry , family medicine , intensive care medicine , dermatology , nursing , surgery , pathology , economics , economic growth
Background Inherited epidermolysis bullosa (EB) is a genetic disorder characterized by skin fragility and unique oral features. Aims To provide (a) a complete review of the oral manifestations in those living with each type of inherited EB, (b) the current best practices for managing oral health care of people living with EB, (c) the current best practices on dental implant‐based oral rehabilitation for patients with recessive dystrophic EB (RDEB), and (d) the current best practice for managing local anesthesia, principles of sedation, and general anesthesia for children and adults with EB undergoing dental treatment. Methods Systematic literature search, panel discussion including clinical experts and patient representatives from different centers around the world, external review, and guideline piloting. Results This article has been divided into five chapters: (i) general information on EB for the oral health care professional, (ii) systematic literature review on the oral manifestations of EB, (iii) oral health care and dental treatment for children and adults living with EB—clinical practice guidelines, (iv) dental implants in patients with RDEB—clinical practice guidelines, and (v) sedation and anesthesia for adults and children with EB undergoing dental treatment—clinical practice guidelines. Each chapter provides recommendations on the management of the different clinical procedures within dental practice, highlighting the importance of patient‐clinician partnership, impact on quality of life, and the importance of follow‐up appointments. Guidance on the use on nonadhesive wound care products and emollients to reduce friction during patient care is provided. Conclusions Oral soft and hard tissue manifestations of inherited EB have unique patterns of involvement associated with each subtype of the condition. Understanding each subtype individually will help the professionals plan long‐term treatment approaches.