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ERNICA guidelines for the management of rectosigmoid Hirschsprung's disease.
Kyrklund, Kristiina; Sloots, Cornelius E J; de Blaauw, Ivo; Bjørnland, Kristin; Rolle, Udo; Cavalieri, Duccio; Francalanci, Paola; Fusaro, Fabio; Lemli, Annette; Schwarzer, Nicole; Fascetti-Leon, Francesco; Thapar, Nikhil; Johansen, Lars Søndergaard; Berrebi, Dominique; Hugot, Jean-Pierre; Crétolle, Célia; Brooks, Alice S; Hofstra, Robert M; Wester, Tomas; Pakarinen, Mikko P.
Afiliación
  • Kyrklund K; Department of Pediatric Surgery, Children's Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, Finland. kristiina.kyrklund@hus.fi.
  • Sloots CEJ; Department of Pediatric Surgery, Erasmus MC - Sophia Children's Hospital, Rotterdam, The Netherlands.
  • de Blaauw I; Department of Surgery, Division of Pediatric Surgery, Radboudumc-Amalia Children's Hospital, Nijmegen, The Netherlands.
  • Bjørnland K; Department of Pediatric Surgery, Oslo University Hospital and University of Oslo, Oslo, Norway.
  • Rolle U; Department of Pediatric Surgery and Pediatric Urology, University Hospital Frankfurt, Frankfurt/M, Germany.
  • Cavalieri D; Department of Biology, University of Florence, A.Mor.Hi, The Italian Association for Hirschsprung's disease, Florence, Italy.
  • Francalanci P; Pathology Unit, Bambino Gesù Children's Hospital, IRCSS, Rome, Italy.
  • Fusaro F; Neonatal Surgery Unit - Department of Medical and Surgical Neonatology, Bambino Gesù Children's Hospital, IRCSS, Rome, Italy.
  • Lemli A; SoMA, The German patient support organization for anorectal malformations and Hirschsprung Disease, Munich, Germany.
  • Schwarzer N; SoMA, The German patient support organization for anorectal malformations and Hirschsprung Disease, Munich, Germany.
  • Fascetti-Leon F; Pediatric Surgery, Department of Women's and Children's Health, University Hospital of Padua, Padua, Italy.
  • Thapar N; UCL Great Ormond Street Institute of Child Health; Department of Pediatric Gastroenterology, Great Ormond Street Hospital for Children, London, UK.
  • Johansen LS; Department of Surgery and Transplantation, Abdominal Centre, Rigshospitalet, Copenhagen, Denmark.
  • Berrebi D; Department of Pediatric Pathology, Hôpital Universitaire Robert Debré, Paris Diderot University, Paris, France.
  • Hugot JP; Department of Pediatric Gastroenterology, Hôpital Universitaire Robert Debré, Assistance Publique Hôpitaux de Paris, Université de Paris, Paris, France.
  • Crétolle C; Department of Pediatric Surgery, University Hospital Necker-Enfants Malades, APHP centre, Paris University, Paris, France.
  • Brooks AS; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Hofstra RM; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Wester T; Department of Pediatric Surgery, Karolinska University Hospital, Stockholm, Sweden.
  • Pakarinen MP; Department of Pediatric Surgery, Children's Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Orphanet J Rare Dis ; 15(1): 164, 2020 06 25.
Article en En | MEDLINE | ID: mdl-32586397
ABSTRACT

BACKGROUND:

Hirschsprung's disease (HSCR) is a serious congenital bowel disorder with a prevalence of 1/5000. Currently, there is a lack of systematically developed guidelines to assist clinical decision-making regarding diagnostics and management.

AIMS:

This guideline aims to cover the diagnostics and management of rectosigmoid HSCR up to adulthood. It aims to describe the preferred approach of ERNICA, the European Reference Network for rare inherited and congenital digestive disorders.

METHODS:

Recommendations within key topics covering the care pathway for rectosigmoid HSCR were developed by an international workgroup of experts from 8 European countries within ERNICA European Reference Network from the disciplines of surgery, medicine, histopathology, microbiology, genetics, and patient organization representatives. Recommendation statements were based on a comprehensive review of the available literature and expert consensus. AGREE II and GRADE approaches were used during development. Evidence levels and levels of agreement are noted.

RESULTS:

Thirty-three statements within 9 key areas were generated. Most recommendations were based on expert opinion.

CONCLUSION:

In rare or low-prevalence diseases such as HSCR, there remains limited availability of high-quality clinical evidence. Consensus-based guidelines for care are presented.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedad de Hirschsprung Tipo de estudio: Diagnostic_studies / Guideline / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Humans País/Región como asunto: Europa Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2020 Tipo del documento: Article País de afiliación: Finlandia

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedad de Hirschsprung Tipo de estudio: Diagnostic_studies / Guideline / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Humans País/Región como asunto: Europa Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2020 Tipo del documento: Article País de afiliación: Finlandia