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The 2018 ISDE achalasia guidelines

Authors :
Giovanni Sarnelli
Tim Vanuytsel
Blair A. Jobe
Cathy Bennett
David I. Watson
Piero M. Fisichella
Ivan Cecconello
Ulysses Ribeiro
Richard H. Holloway
D. Liu
M. Y. A. van Herwaarden-Lindeboom
Edoardo Savarino
Rubens Antonio Aissar Sallum
Daniel Sifrim
David A. Katzka
Eric S. Hungness
John E. Pandolfino
Fernando A. M. Herbella
Silvana Perretta
Roger P. Tatum
Lee L. Swanstrom
Guy E. Boeckxstaens
Chandra Prakash Gyawali
Richard Ricachenevsky Gurski
Marco G. Patti
L. Faccio
George Triadafilopoulos
Nathaniel J. Soper
D. Inama
M. F. Vaezi
Frank Zerbib
Sheraz R. Markar
Joel E. Richter
An Moonen
S. Vermigli
Pankaj J. Pasricha
Ines Gockel
Nelson Adami Andreollo
Guido Costamagna
Peter J. Kahrilas
Francisco Schlottmann
Giovanni Zaninotto
Mark K. Ferguson
M. F. Vela
Stuart Gittens
Karl-Hermann Fuchs
Renato Salvador
Donald E. Low
C. Pontillo
J. R. M. Da Rocha
Jan Tack
Mario Costantini
Roberto Penagini
Kulwinder S. Dua
Michio Hongo
Ary Nasi
Zaninotto, G
Bennett, C
Boeckxstaens, G
Costantini, M
Ferguson, M K
Pandolfino, J E
Patti, M G
Ribeiro, U
Richter, J
Swanstrom, L
Tack, J
Triadafilopoulos, G
Markar, S R
Salvador, R
Faccio, L
Andreollo, N A
Cecconello, I
Costamagna, G
da Rocha, J R M
Hungness, E S
Fisichella, P M
Fuchs, K H
Gockel, I
Gurski, R
Gyawali, C P
Herbella, F A M
Holloway, R H
Hongo, M
Jobe, B A
Kahrilas, P J
Katzka, D A
Dua, K S
Liu, D
Moonen, A
Nasi, A
Pasricha, P J
Penagini, R
Perretta, S
Sallum, R A A
Sarnelli, G
Savarino, E
Schlottmann, F
Sifrim, D
Soper, N
Tatum, R P
Vaezi, M F
van Herwaarden-Lindeboom, M
Vanuytsel, T
Vela, M F
Watson, D I
Zerbib, F
Gittens, S
Pontillo, C
Vermigli, S
Inama, D
Low, D E
Source :
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual), Universidade de São Paulo (USP), instacron:USP
Publication Year :
2018
Publisher :
Oxford University Press (OUP), 2018.

Abstract

Achalasia is a relatively rare primary motor esophageal disorder, characterized by absence of relaxations of the lower esophageal sphincter and of peristalsis along the esophageal body. As a result, patients typically present with dysphagia, regurgitation and occasionally chest pain, pulmonary complication and malnutrition. New diagnostic methodologies and therapeutic techniques have been recently added to the armamentarium for treating achalasia. With the aim to offer clinicians and patients an up-to-date framework for making informed decisions on the management of this disease, the International Society for Diseases of the Esophagus Guidelines proposed and endorsed the Esophageal Achalasia Guidelines (I-GOAL). The guidelines were prepared according the Appraisal of Guidelines for Research and Evaluation (AGREE-REX) tool, accredited for guideline production by NICE UK. A systematic literature search was performed and the quality of evidence and the strength of recommendations were graded according to the Grading of Recommendations Assessment, Development and Evaluation (GRADE). Given the relative rarity of this disease and the paucity of high-level evidence in the literature, this process was integrated with a three-step process of anonymous voting on each statement (DELPHI). Only statements with an approval rate >80% were accepted in the guidelines. Fifty-one experts from 11 countries and 3 representatives from patient support associations participated to the preparations of the guidelines. These guidelines deal specifically with the following achalasia issues: Diagnostic workup, Definition of the disease, Severity of presentation, Medical treatment, Botulinum Toxin injection, Pneumatic dilatation, POEM, Other endoscopic treatments, Laparoscopic myotomy, Definition of recurrence, Follow up and risk of cancer, Management of end stage achalasia, Treatment options for failure, Achalasia in children, Achalasia secondary to Chagas' disease.

Details

ISSN :
14422050 and 11208694
Volume :
31
Database :
OpenAIRE
Journal :
Diseases of the Esophagus
Accession number :
edsair.doi.dedup.....180bfc1363c14bc558b11397af4f1ad1