TY - JOUR
T1 - Clinical practice guidelines
T2 - Oral health care for children and adults living with epidermolysis bullosa
AU - Krämer, Susanne
AU - Lucas, James
AU - Gamboa, Francisca
AU - Peñarrocha Diago, Miguel
AU - Peñarrocha Oltra, David
AU - Guzmán-Letelier, Marcelo
AU - Paul, Sanchit
AU - Molina, Gustavo
AU - Sepúlveda, Lorena
AU - Araya, Ignacio
AU - Soto, Rubén
AU - Arriagada, Carolina
AU - Lucky, Anne W.
AU - Mellerio, Jemima E.
AU - Cornwall, Roger
AU - Alsayer, Fatimah
AU - Schilke, Reinhard
AU - Antal, Mark Adam
AU - Castrillón, Fernanda
AU - Paredes, Camila
AU - Serrano, Maria Concepción
AU - Clark, Victoria
N1 - Publisher Copyright:
© 2020 The Authors. Special Care in Dentistry published by Special Care Dentistry Association and Wiley Periodicals LLC
PY - 2020/11
Y1 - 2020/11
N2 - 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.
AB - 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.
KW - clinical practice guideline
KW - dental implants
KW - dental treatment
KW - dystrophic epidermolysis bullosa
KW - epidermolysis bullosa
KW - epidermolysis bullosa simplex
KW - general anesthesia
KW - junctional epidermolysis bullosa
KW - kindler epidermolysis bullosa
KW - oral care
KW - oral rehabilitation
KW - recessive dystrophic epidermolysis bullosa
KW - sedation
UR - http://www.scopus.com/inward/record.url?scp=85096321330&partnerID=8YFLogxK
U2 - 10.1111/scd.12511
DO - 10.1111/scd.12511
M3 - Article
C2 - 33202040
AN - SCOPUS:85096321330
SN - 0275-1879
VL - 40
SP - 3
EP - 81
JO - Special Care in Dentistry
JF - Special Care in Dentistry
IS - S1
ER -