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Practice Guideline
. 2025 Aug;57(8):1550-1577.
doi: 10.1016/j.dld.2025.04.020. Epub 2025 May 30.

Italian guidelines for the diagnosis and management of gastro-esophageal reflux disease: Joint consensus from the Italian Societies of: Gastroenterology and Endoscopy (SIGE), Neurogastroenterology and Motility (SINGEM), Hospital Gastroenterologists and Endoscopists (AIGO), Digestive Endoscopy (SIED), and General Medicine (SIMG)

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Practice Guideline

Italian guidelines for the diagnosis and management of gastro-esophageal reflux disease: Joint consensus from the Italian Societies of: Gastroenterology and Endoscopy (SIGE), Neurogastroenterology and Motility (SINGEM), Hospital Gastroenterologists and Endoscopists (AIGO), Digestive Endoscopy (SIED), and General Medicine (SIMG)

Edoardo Vincenzo Savarino et al. Dig Liver Dis. 2025 Aug.

Abstract

Gastroesophageal reflux disease (GERD) is one of the most common conditions encountered in outpatient general medicine and gastroenterology clinics. However, uncertainties remain, particularly concerning the optimal diagnostic work-up and the most effective management. To address this issue, experts from 5 Italian Societies conducted a Delphi consensus process, which included a review of the current literature and voting process on 27 key statements. Recommendations and quality of evidence were evaluated using the Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) criteria. Consensus for each statement was defined as ≥ 80 % agreement. Diagnostic Approach: The consensus supports a symptom-based diagnostic strategy for GERD, focusing on the exclusion of alarm symptoms and/or multiple risk factors for Barrett's esophagus or eosinophilic esophagitis (EoE) as well as non-GERD causes in cases of extra-esophageal symptoms. Esophago-gastro-duodenoscopy (EGD) is recommended in patients with alarm features or in patients unresponsive to proton pump inhibitors (PPIs). In addition, the consensus recommends esophageal pH-metry or impedance-pH recording in patients with reflux-like symptoms not responding to medical treatments, in those with extra-oesophageal symptoms, prior to anti-reflux endoscopic or surgical procedures, in patients with belching disorders and to diagnose functional heartburn (FH) and reflux hypersensitivity (RH) in PPI-refractory patients. Treatment Approach: The consensus strongly supports a standard 4-8 weeks course of PPIs for patients with heartburn and regurgitation but without alarm symptoms and an 8 weeks treatment for those with erosive oesophagitis. Twice daily dose PPIs is recommended only if a concomitant Barrett oesophagus is present, in patients with laryngopharyngeal reflux disease (LPRD) or when there is no response or an incomplete response to once daily dose. Bedtime histamine-2 receptor antagonists (H2RAs) as add-on therapy is suggested in patients with persistent nocturnal symptoms and in those with objective evidence of nocturnal acid reflux on pH monitoring despite PPI treatment, while prokinetic agents are advocated as add-on therapy in patients with concomitant symptoms suggestive of delayed gastric emptying. Moreover, the consensus voted for the use of potassium competitive acid blockers (P-CABs), antacids, alginate-containing formulations, neuromodulators in treating visceral hypersensitivity, complementary and alternative medicine and anti-reflux surgery in patients with refractory GERD. Finally, the consensus voted against surgical anti-reflux therapy in patients with extra-esophageal symptoms of GERD, who do not respond to PPI therapy and against the use of ensoscopic procedures [i.e., Medigus ultrasonic surgical endostapler (MUSE), radiofrequency energy application (Stretta), anti-reflux mucosectomy (ARMS)] outside clinical trials.

Keywords: Alginate; GERD; Guidelines; PPI; Reflux disease; Vonoprazan.

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Conflict of interest statement

Conflict of interest Edoardo Vincenzo Savarino: Edoardo Vincenzo Savarino has served as speaker for Abbvie, Abivax, Agave, AGPharma, Alfasigma, Apoteca, Biosline, CaDiGroup, Celltrion, Dr Falk, EG Stada Group, Fenix Pharma, Galapagos, Johnson&Johnson, JB Pharmaceuticals, Innovamedica/Adacyte, Eli Lilly, Malesci, Mayoly Biohealth, Montefarco, Novartis, Omega Pharma, Pfizer, Rafa, Reckitt Benckiser, Sandoz, Sanofi/Regeneron, SILA, Sofar, Takeda, Tillots, Unifarco; has served as consultant for Abbvie, Agave, Alfasigma, Biogen, Bristol-Myers Squibb, Celltrion, Dr. Falk, Eli Lilly, Fenix Pharma, Ferring, Giuliani, Grunenthal, Johnson&Johnson, JB Pharmaceuticals, Merck & Co, Nestlè, Pfizer, Reckitt Benckiser, Sanofi/Regeneron, SILA, Sofar, Takeda, Unifarco; he received research support from Bonollo, Difass, Pfizer, Reckitt Benckiser, Sanofi/Regeneron, SILA, Sofar, Unifarco, Zeta Farmaceutici. Brigida Barberio: has served as speaker for Abbvie, Agave, Alfasigma, AGpharma, Janssen, Eli Lilly, MSD, Pfizer, Sofar, Takeda, Unifarco; has served as consultant for Abbvie and Janssen. Giovanni Barbara: Consultancies, business interests or sources of honoraria payments from Aboca, AB Biotics, Agave, Alfa Sigma, AGPharma, Bayer, Biocodex, Boeringer, Bromatech, Cadigroup, Danone, Diadema, Falk Pharma, GE Healthcare, Giuliani, Mayoly, Malesci, Monteresearch, Sanofy, Sofar, Yakult Nicola de Bortoli: none Giuseppe Esposito: none Marzio Frazzoni: none Giuseppe Galloro: none Luigi Gatta: none Matteo Ghisa: none Claudio Londoni: none Elisa Marabotto: none Alberto Meggio: none Antonio Pisani: none Mentore Ribolsi: none Paolo Usai Satta: none Vincenzo Savarino: has served as speaker for Malesci, Grunenthal, Takeda and Alfasigma Carmelo Scarpignato: has served as a speaker, consultant, and/or advisory board member for Alfasigma, Pfizer, Takeda, Reckitt Benckiser, and Shionogi, and has in the past received funding from Giuliani Pharmaceuticals and Pfizer. Vincenzo Stanghellini: none. Cesare Tosetti: has served as consultant for NAMED, SILA. Pierfrancesco Visaggi: none. Fabiana Zingone: none. Marcella Pesce: none. Giovanni Sarnelli: none.

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