The Management of Peutz-Jeghers Syndrome : European Hereditary Tumour Group (EHTG) Guideline

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Wagner , A , Aretz , S , Auranen , A , Bruno , M J , Cavestro , G M , Crosbie , E J , Goverde , A , Jelsig , A M , Latchford , A R , van Leerdam , M E , Lepisto , A H , Puzzono , M , Winship , I , Zuber , V & Moslein , G 2021 , ' The Management of Peutz-Jeghers Syndrome : European Hereditary Tumour Group (EHTG) Guideline ' , Journal of clinical medicine , vol. 10 , no. 3 , 473 . https://doi.org/10.3390/jcm10030473

Title: The Management of Peutz-Jeghers Syndrome : European Hereditary Tumour Group (EHTG) Guideline
Author: Wagner, Anja; Aretz, Stefan; Auranen, Annika; Bruno, Marco J.; Cavestro, Giulia M.; Crosbie, Emma J.; Goverde, Anne; Jelsig, Anne Marie; Latchford, Andrew R.; van Leerdam, Monique E.; Lepisto, Anna H.; Puzzono, Marta; Winship, Ingrid; Zuber, Veronica; Moslein, Gabriela
Contributor organization: HUS Abdominal Center
II kirurgian klinikka
Clinicum
Helsinki University Hospital Area
Date: 2021-02
Language: eng
Number of pages: 18
Belongs to series: Journal of clinical medicine
ISSN: 2077-0383
DOI: https://doi.org/10.3390/jcm10030473
URI: http://hdl.handle.net/10138/328260
Abstract: The scientific data to guide the management of Peutz-Jeghers syndrome (PJS) are sparse. The available evidence has been reviewed and discussed by diverse medical specialists in the field of PJS to update the previous guideline from 2010 and formulate a revised practical guideline for colleagues managing PJS patients. Methods: Literature searches were performed using MEDLINE, Embase, and Cochrane. Evidence levels and recommendation strengths were assessed using the Grading of Recommendations Assessment, Development and Evaluation (GRADE). A Delphi process was followed, with consensus being reached when >= 80% of the voting guideline committee members agreed. Recommendations and statements: The only recent guidelines available were for gastrointestinal and pancreatic management. These were reviewed and endorsed after confirming that no more recent relevant papers had been published. Literature searches were performed for additional questions and yielded a variable number of relevant papers depending on the subject addressed. Additional recommendations and statements were formulated. Conclusions: A decade on, the evidence base for recommendations remains poor, and collaborative studies are required to provide better data about this rare condition. Within these restrictions, multisystem, clinical management recommendations for PJS have been formulated.
Subject: Peutz&#8211
Jeghers syndrome
STK11
guideline
3121 General medicine, internal medicine and other clinical medicine
Peer reviewed: Yes
Rights: cc_by
Usage restriction: openAccess
Self-archived version: publishedVersion


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