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Clinical practice guidelines: Oral health care for children and adults living with epidermolysis bullosa

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 c...

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Autores principales: Krämer, Susanne, Lucas, James, Gamboa, Francisca, Peñarrocha Diago, Miguel, Peñarrocha Oltra, David, Guzmán‐Letelier, 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756753/
https://www.ncbi.nlm.nih.gov/pubmed/33202040
http://dx.doi.org/10.1111/scd.12511
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author Krämer, Susanne
Lucas, James
Gamboa, Francisca
Peñarrocha Diago, Miguel
Peñarrocha Oltra, David
Guzmán‐Letelier, 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
author_facet Krämer, Susanne
Lucas, James
Gamboa, Francisca
Peñarrocha Diago, Miguel
Peñarrocha Oltra, David
Guzmán‐Letelier, 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
author_sort Krämer, Susanne
collection PubMed
description 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.
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spelling pubmed-77567532020-12-28 Clinical practice guidelines: Oral health care for children and adults living with epidermolysis bullosa Krämer, Susanne Lucas, James Gamboa, Francisca Peñarrocha Diago, Miguel Peñarrocha Oltra, David Guzmán‐Letelier, 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 Spec Care Dentist Special Issue Articles 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. John Wiley and Sons Inc. 2020-11-17 2020-11 /pmc/articles/PMC7756753/ /pubmed/33202040 http://dx.doi.org/10.1111/scd.12511 Text en © 2020 The Authors. Special Care in Dentistry published by Special Care Dentistry Association and Wiley Periodicals LLC This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Special Issue Articles
Krämer, Susanne
Lucas, James
Gamboa, Francisca
Peñarrocha Diago, Miguel
Peñarrocha Oltra, David
Guzmán‐Letelier, 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
Clinical practice guidelines: Oral health care for children and adults living with epidermolysis bullosa
title Clinical practice guidelines: Oral health care for children and adults living with epidermolysis bullosa
title_full Clinical practice guidelines: Oral health care for children and adults living with epidermolysis bullosa
title_fullStr Clinical practice guidelines: Oral health care for children and adults living with epidermolysis bullosa
title_full_unstemmed Clinical practice guidelines: Oral health care for children and adults living with epidermolysis bullosa
title_short Clinical practice guidelines: Oral health care for children and adults living with epidermolysis bullosa
title_sort clinical practice guidelines: oral health care for children and adults living with epidermolysis bullosa
topic Special Issue Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756753/
https://www.ncbi.nlm.nih.gov/pubmed/33202040
http://dx.doi.org/10.1111/scd.12511
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