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Consensus guidelines for diagnosis and management of anemia in epidermolysis bullosa.
Liy-Wong, Carmen; Tarango, Cristina; Pope, Elena; Coates, Thomas; Bruckner, Anna L; Feinstein, James A; Schwieger-Briel, Agnes; Hubbard, Lynne D; Jane, Clapham; Torres-Pradilla, Mauricio; Zmazek, Matija; Lara-Corrales, Irene.
Afiliação
  • Liy-Wong C; Division of Dermatology and Rheumatology, Children's Hospital of Eastern Ontario, University of Ottawa, Ottawa, ON, Canada. cliywong@cheo.on.ca.
  • Tarango C; Division of Hematology, Cancer and Blood Diseases Institute, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
  • Pope E; Division of Dermatology, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
  • Coates T; Keck School of Medicine, Division of Hematology/Oncology, Department of Pediatrics, Children's Hospital Los Angeles, University of Southern California, Los Angeles, CA, USA.
  • Bruckner AL; Epidermolysis Bullosa Clinic, Children's Hospital Colorado, University of Colorado School of Medicine, Aurora, CO, USA.
  • Feinstein JA; Epidermolysis Bullosa Clinic, Children's Hospital Colorado, University of Colorado School of Medicine, Aurora, CO, USA.
  • Schwieger-Briel A; Pediatric Skin Center, Department of Dermatology, University Children's Hospital Zurich, Zurich, Switzerland.
  • Hubbard LD; Department of Nutrition and Dietetics, Rare Diseases Centre at St Thomas' Hospital, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Jane C; Lead EB CNS, Rare Diseases Centre, St John's Institute of Dermatology, St Thomas' Hospital, Guy's and St Thomas' NHS Foundation Trust and DEBRA UK, London, UK.
  • Torres-Pradilla M; Fundación Universitaria de Ciencias de la Salud and Hospital de San José, Bogotá, Colombia.
  • Zmazek M; DEBRA, Zagreb, Croatia.
  • Lara-Corrales I; Division of Dermatology, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
Orphanet J Rare Dis ; 18(1): 38, 2023 02 23.
Article em En | MEDLINE | ID: mdl-36823529
BACKGROUND: Anemia is a common complication of severe forms of epidermolysis bullosa (EB). To date, there are no guidelines outlining best clinical practices to manage anemia in the EB population. The objective of this manuscript is to present the first consensus guidelines for the diagnosis and management of anemia in EB. RESULTS: Due to the lack of high-quality evidence, a consensus methodology was followed. An initial survey exploring patient preferences, concerns and symptoms related to anemia was sent to EB patients and their family members. A second survey was distributed to EB experts and focused on screening, diagnosis, monitoring and management of anemia in the different types of EB. Information from these surveys was collated and used by the panel to generate 26 consensus statements. Consensus statements were sent to healthcare providers that care for EB patients through EB-Clinet. Statements that received more than 70% approval (completely agree/agree) were adopted. CONCLUSIONS: The end result was a series of 6 recommendations which include 20 statements that will help guide management of anemia in EB patients. In patients with moderate to severe forms of EB, the minimum desirable level of Hb is 100 g/L. Treatment should be individualized. Dietary measures should be offered as part of management of anemia in all EB patients, oral iron supplementation should be used for mild anemia; while iron infusion is reserved for moderate to severe anemia, if Hb levels of > 80-100 g/L (8-10 g/dL) and symptomatic; and transfusion should be administered if Hb is < 80 g/L (8 g/dL) in adults and < 60 g/L (6 g/dL) in children.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Epidermólise Bolhosa Distrófica / Epidermólise Bolhosa / Anemia Tipo de estudo: Diagnostic_studies / Etiology_studies / Guideline / Qualitative_research Limite: Adult / Child / Humans Idioma: En Revista: Orphanet J Rare Dis Assunto da revista: MEDICINA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Epidermólise Bolhosa Distrófica / Epidermólise Bolhosa / Anemia Tipo de estudo: Diagnostic_studies / Etiology_studies / Guideline / Qualitative_research Limite: Adult / Child / Humans Idioma: En Revista: Orphanet J Rare Dis Assunto da revista: MEDICINA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Canadá
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