← Issue №9/ week of Aug 30, 2026/ the whole section, in full

Esophagus/Reflux, in full.

All 6 Esophagus/Reflux papers in this issue, as full cards, ranked by clinical utility. The issue page carries the strongest few; this is the section, whole.

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most clinically useful first · the 1 the issue led with is ruled in green
Esophagus/Reflux guideline · Aug 24, 2026 · J Gastroenterology · IF 5.7

Evidence-based clinical practice guidelines for peptic ulcer disease 2026.

Guideline / reviewguidelineepidemiologybasic sciencebiomarker
Clinical takeawayConsider vonoprazan as first-line therapy for peptic ulcers and NSAID- or LDA-induced ulcers, replacing PPIs where available, particularly in Japan where insurance coverage supports its use.
What it foundVonoprazan is now recommended as first-line treatment for peptic ulcers and NSAID- and LDA-induced ulcers due to superior acid-inhibition and evidence of efficacy and safety compared to proton pump inhibitors (PPIs), per the 2026 JSGE guidelines.
ContextUpdates the 2026 JSGE guidelines, confirming existing therapeutic algorithms but upgrading vonoprazan to first-line based on new evidence. Note that this recommendation is specific to the Japanese healthcare context.
Refinessuggested applicable standard· European Society of Gastrointestinal Endoscopy (ESGE), "Endoscopic diagnosis and management of nonvariceal upper gastrointestinal hemorrhage (NVUGIH): European Society of Gastrointestinal Endoscopy (ESGE) Guideline, Update 2021", 2021

Decision at stakethe acid suppression used to heal peptic ulcers, and PPI or PCAB co-therapy when NSAIDs or low-dose aspirin must continue

… Heal ulcers with PPI (duodenal ulcer 4 weeks, gastric ulcer 8 weeks, with repeat EGD at 8-12 weeks to confirm healing and exclude malignancy), discontinue or mitigate NSAIDs with long-term PPI or PCAB co-therapy if NSAIDs must continue, maintain long-term acid suppression in idiopathic (H. pylori-negative, NSAID-negative) ulcers, and pursue gastrinoma/ZES or refractory-ulcer workup in H. pylori-negative/NSAID-negative or non-healing cases.

From our summary of this standard, unedited — the part the paper bears on. … marks omitted text. Our wording, not the guideline's; read the source for its own text.

Our full summary of this standard

Confirm peptic ulcer disease with EGD, biopsy all gastric ulcers to exclude malignancy, and test every PUD patient for H. pylori. In ulcer bleeding, risk-stratify pre-endoscopy with the Glasgow-Blatchford score (GBS ≤1 may be managed as an outpatient), resuscitate with crystalloid, and transfuse restrictively in hemodynamically stable patients with no history of cardiovascular disease (transfusion threshold hemoglobin ≤7 g/dL, post-transfusion target 7-9 g/dL); in hemodynamically stable patients with a history of acute or chronic cardiovascular disease use a more liberal strategy (transfusion threshold ≤8 g/dL, post-transfusion target ≥10 g/dL); the restrictive strategy applies only to non-massive bleeding, so in exsanguinating or hemodynamically unstable hemorrhage transfuse based on hemodynamics and ongoing blood loss rather than waiting for a hemoglobin threshold. Perform endoscopy within 24 hours of presentation; emergent (≤6 h) or urgent (≤12 h) endoscopy is NOT recommended unless the patient remains hemodynamically unstable despite adequate resuscitation. Give pre-endoscopy IV erythromycin (IV metoclopramide if erythromycin is unavailable, in clinically severe or ongoing active bleeding); pre-endoscopy high-dose IV PPI may be considered but must not delay endoscopy. Treat by Forrest class: Ia/Ib get combination therapy (dilute epinephrine injection plus a second modality, contact/noncontact thermal or mechanical TTS/OTS clip), with over-the-scope clip monotherapy now an accepted first-line alternative to combination therapy given its lower rate of further bleeding, and hemostatic forceps with soft coagulation a further alternative; IIa (nonbleeding visible vessel) gets thermal, mechanical (TTS or OTS clip), or sclerosant injection as monotherapy or combined with epinephrine; IIb (adherent clot) gets clot removal with treatment of underlying stigmata where the endoscopist is technically competent to manage conversion to a higher-risk lesion; IIc/III (flat spot, clean base) get no endoscopic therapy and may be discharged early on oral PPI. Epinephrine injection must never be used as monotherapy, and topical hemostatic agents must not be used as first-line monotherapy (they are reserved, with OTS clips, for bleeding refractory to standard modalities). After hemostasis, give high-dose PPI as 80 mg IV bolus then 8 mg/h infusion for 72 hours (twice-daily IV bolus or twice-daily oral high-dose PPI are acceptable alternatives); the same applies to untreated FIIb clot. Routine second-look endoscopy is not recommended. For recurrent bleeding, repeat endoscopy and consider an OTS clip if not already used; if the second attempt fails, proceed to transcatheter angiographic embolization (TAE), with surgery when TAE is unavailable or unsuccessful. Prophylactic TAE may be considered in selected high-risk cases (hemodynamic instability at presentation, posterior duodenal wall ulcer, ulcer >2 cm, or uncertain durability of hemostasis). Start clear liquids/early oral nutrition within 24 hours of durable hemostasis, and initiate iron therapy before discharge for iron deficiency and/or anemia. Resume anticoagulation as soon as clinically indicated based on thromboembolic risk, resume aspirin for secondary prevention within 24 hours, and give PPI co-therapy to patients continuing DAPT or anticoagulation after a bleed. Test for H. pylori at the index endoscopy and treat if positive; retest patients testing negative acutely (a false-negative is common in the bleeding setting), holding PPI at least 2 weeks before retesting, and document successful eradication in every treated patient. For eradication, first-line therapy in treatment-naive patients with unknown susceptibility is optimized bismuth quadruple therapy for 14 days (PPI twice daily, tetracycline 500 mg four times daily, metronidazole 500 mg three to four times daily, bismuth four times daily); rifabutin triple therapy or vonoprazan-amoxicillin dual therapy for 14 days are acceptable empiric alternatives in patients without penicillin allergy. PPI-clarithromycin triple therapy and levofloxacin-based regimens are recommended against unless susceptibility testing proves the organism is sensitive. Salvage therapy in treatment-experienced patients is optimized bismuth quadruple therapy for 14 days if not previously used, otherwise a susceptibility-guided or non-cross-resistant regimen. Test of cure is required in ALL treated patients by urea breath test, fecal antigen, or biopsy-based test at least 4 weeks after completing antibiotics and at least 2 weeks off PPI. Heal ulcers with PPI (duodenal ulcer 4 weeks, gastric ulcer 8 weeks, with repeat EGD at 8-12 weeks to confirm healing and exclude malignancy), discontinue or mitigate NSAIDs with long-term PPI or PCAB co-therapy if NSAIDs must continue, maintain long-term acid suppression in idiopathic (H. pylori-negative, NSAID-negative) ulcers, and pursue gastrinoma/ZES or refractory-ulcer workup in H. pylori-negative/NSAID-negative or non-healing cases.

European Society of Gastrointestinal Endoscopy (ESGE), "Endoscopic diagnosis and management of nonvariceal upper gastrointestinal hemorrhage (NVUGIH): European Society of Gastrointestinal Endoscopy (ESGE) Guideline, Update 2021", 2021 · reviewed 2026-07-23 ↗
Sugimoto M … Mochida S · Journal of Gastroenterology · IF 5.7 · PubMed ↗Permalink
Esophagus/Reflux prospective cohort · n=5,499 · Aug 28, 2026 · J Neurogastro Motil · IF 3.4

Effectiveness and Patient Satisfaction With Zastaprazan in Real-world Practice: A Large-Scale Prospective Observational Study.

New evidenceGERDproton pump inhibitorshealth services
Clinical takeawayConsider zastaprazan as an alternative P-CAB for adults with GERD, including those previously treated with PPIs or other P-CABs, given its symptom relief, high satisfaction rates, and low need for additional medications.
What it foundZastaprazan 20 mg daily reduced mean GERD symptom score from 2.07 to 0.44 at 4 weeks (change -1.63, P < 0.0001) in adults with GERD, with 90% patient satisfaction, 0.05% mild adverse events, and only 2.25% requiring concomitant medications. Symptom improvement was consistent regardless of prior treatment with H2RAs, PPIs, or other P-CABs.
ContextConfirms and extends prior evidence on P-CAB efficacy to real-world practice, showing consistent benefit across treatment-naïve and previously treated GERD patients.
Reinforcessuggested applicable standard· British Society of Gastroenterology-endorsed international consensus, "Updates to the modern diagnosis of GERD: Lyon consensus 2.0" (Gyawali CP, Yadlapati R, Fass R, et al.), Gut, 2024

Decision at stakethe recommendation to reserve P-CABs for PPI failure with confirmatory GERD evidence

… Empiric escalation to vonoprazan/P-CAB is NOT a routine pre-testing step: the AGA 2024 P-CAB clinical practice update advises against P-CABs as first-line therapy and reserves them for PPI failure with confirmatory GERD evidence (LA grade B or worse erosive esophagitis, biopsy-proven Barrett's, peptic stricture, or acid exposure time >6%). …

From our summary of this standard, unedited — the part the paper bears on. … marks omitted text. Our wording, not the guideline's; read the source for its own text.

Our full summary of this standard

For heartburn or regurgitation persisting despite PPI therapy, current practice (ACG 2022 GERD guideline, still the operative ACG guideline, plus the AGA 2022 personalized-GERD CPU) is to first optimize the PPI: confirm adherence, dose 30-60 minutes before meals, escalate to twice-daily dosing or switch agents for an 8-week trial. Empiric escalation to vonoprazan/P-CAB is NOT a routine pre-testing step: the AGA 2024 P-CAB clinical practice update advises against P-CABs as first-line therapy and reserves them for PPI failure with confirmatory GERD evidence (LA grade B or worse erosive esophagitis, biopsy-proven Barrett's, peptic stricture, or acid exposure time >6%). If symptoms persist after optimization, perform EGD (ideally 2-4 weeks off PPI when GERD is unproven) with esophageal biopsies to exclude EoE (>=15 eos/hpf; the ACG 2025 EoE guideline has removed the PPI trial from the diagnostic pathway) and then physiologic testing per Lyon Consensus 2.0: in unproven GERD, ambulatory reflux monitoring OFF therapy, applying Lyon 2.0's modality-specific thresholds -- on catheter-based single-day (24-hour) pH or pH-impedance, AET >6% is conclusive for GERD, 4-6% is inconclusive, and <4% argues against GERD; on prolonged wireless (Bravo, up to 96-hour) monitoring, AET >6% on >=2 days is conclusive for GERD while AET <4% on all days excludes it, and a study meeting neither threshold is inconclusive (the number of days with AET <4% carries prognostic weight for PPI discontinuation) -- and, in either modality, a normal-AET (<4%) study with positive symptom association indicates reflux hypersensitivity or, without it, functional heartburn; in previously proven GERD, pH-impedance ON optimized therapy, where AET >4% plus >80 reflux episodes defines actionable refractory GERD (MNBI <1500 ohms supportive, >2300 ohms against). High-resolution manometry per Chicago Classification 4.0 (still current) excludes achalasia and major motility disorders and is required before anti-reflux surgery. Therapy is phenotype-directed: surgical or endoscopic anti-reflux intervention for confirmed refractory pathologic reflux, and neuromodulators with or without brain-gut behavioral therapy for reflux hypersensitivity and functional heartburn.

British Society of Gastroenterology-endorsed international consensus, "Updates to the modern diagnosis of GERD: Lyon consensus 2.0" (Gyawali CP, Yadlapati R, Fass R, et al.), Gut, 2024 · reviewed 2026-07-23 ↗
Seo SI … Kim YS · Journal of Neurogastroenterology and Motility · IF 3.4 · PubMed ↗Permalink
Esophagus/Reflux prospective cohort · n=52 · Aug 27, 2026 · Aliment Pharm Ther · IF 6.7

Treatment Patterns in Patients With Eosinophilic Oesophagitis Referred for Expert Consultation.

New evidenceeosinophilic esophagitishealth services
Clinical takeawayBefore referring EoE patients as refractory, ensure optimal dosing and administration of PPIs, topical steroids, and elimination diets as per guideline recommendations, and assess adherence. Consider dupilumab in eligible patients. Re-evaluate for functional/behavioral contributors (e.g., esophageal hypersensitivity, ARFID) if refractory symptoms persist.
What it foundExperts estimated true refractoriness to medical therapy at 15% (IQR 10-25) and to diet therapy at 31% (IQR 20-50); most referred patients had suboptimal prior treatment compared to guideline-recommended therapies (PPIs 80%, topical steroids 55%, elimination diets 45%, dupilumab 10%).
ContextChallenges current referral patterns by showing most 'refractory' EoE cases in adults are due to suboptimal treatment or adherence, not true refractoriness. Confirms guideline-recommended therapies are underutilized prior to referral.
Measured against the standard of care· ACG 2025 (Dellon et al., Am J Gastroenterol 120(1):31-59) / ASGE 2026 consensus Part 2 (Dellon et al., Gastrointest Endosc 103(3):396-417)

Decision at stakethe choice among initial anti-inflammatory therapies for EoE should be individualized within a shared decision-making framework

… Choose a single initial therapy by shared decision-making. …

From our summary of this standard, unedited — the part the paper bears on. … marks omitted text. Our wording, not the guideline's; read the source for its own text. The rest of this standard includes DIAGNOSIS, DILATION, MAINTENANCE and 2 more.

Our full summary of this standard

ACG 2025 (GRADE) is still the governing guideline. The ASGE 2026 consensus Part 2 (modified Delphi, 28 statements at ≥80% agreement; not GRADE) adds endoscopic and pediatric detail without contradicting it. DIAGNOSIS: symptoms of esophageal dysfunction plus ≥15 eos/hpf after excluding other causes of esophageal eosinophilia. A PPI trial is not a diagnostic criterion (PPI-REE abandoned). Do the initial diagnostic EGD off PPI, topical steroid and dietary therapy (ACG key concept; ASGE consensus, which gives no washout duration). Initial assessment is a standard EGD, not a less-invasive modality, so that full biopsies and dilation are possible (ASGE). Take ≥6 esophageal biopsies from ≥2 levels in anyone with symptoms or endoscopic findings consistent with EoE, targeting visible lesions. In CHILDREN with suspected EoE, also biopsy the stomach and duodenum (ASGE). Use EREFS at every endoscopy and report a quantified peak eosinophil count (ACG strong/low; ASGE). TREATMENT (ACG): swallowed topical steroids STRONG/moderate; high-dose PPI CONDITIONAL/low; empiric elimination diet CONDITIONAL/low. Choose a single initial therapy by shared decision-making. Fluticasone or budesonide are both reasonable. Adult doses: PPI double the reflux dose (e.g., omeprazole 20 mg BID or 40 mg daily); budesonide 2-4 mg/day (BOS 2 mg BID); fluticasone 1,760 mcg/day divided. Pediatric doses: PPI 2 mg/kg/day; budesonide 1-2 mg/day; fluticasone 110-880 mcg/day. Allergy testing is not used to direct diets. A 1FED/2FED step-up diet with a dietitian is acceptable, with endoscopic and biopsy confirmation after each reintroduced food. Dupilumab is CONDITIONAL for PPI-nonresponsive patients aged ≥12 (moderate) and for ages 1-11 at ≥15 kg (low). Weight-band dosing: 15-<30 kg 200 mg q2w; 30-<40 kg 300 mg q2w; ≥40 kg 300 mg weekly. Recommendations AGAINST: omalizumab, cromolyn, montelukast. No recommendation for cendakimab, benralizumab, lirentelimab, mepolizumab or reslizumab. DILATION: an adjunct to anti-inflammatory therapy for strictures causing dysphagia (ACG conditional/low). Start low and go slow; target ≥16 mm in adults and adolescents over ≥1 session. In children, ASGE supports dilation of symptomatic strictures or a narrow-caliber esophagus regardless of disease activity, using the same start-low/go-slow approach. MAINTENANCE: continue effective therapy (ACG STRONG despite low evidence) at the lowest effective dose. MONITORING: judge response on symptoms, endoscopy and histology together, never symptoms alone. Assess response endoscopically at 8-12 weeks after starting a PPI or topical steroid. For diet, ACG says 8-12 weeks and ASGE says 6-8 weeks. For dupilumab or biologics, assess at 12-24 weeks (ASGE: up to 24 weeks). Allow appropriate washout or timing after any treatment change before the follow-up EGD (ASGE). Take monitoring biopsies from the most severe-appearing lesions (rings, furrows, exudates) (ASGE). Monitoring biopsies may be limited to the esophagus when prior gastric and duodenal biopsies were normal and nothing new suggests other pathology (ASGE). The histologic response threshold of <15 eos/hpf is a 'may consider' target, read alongside endoscopic and symptom findings. Shorten follow-up after complications. Care gaps of ≥2 years are associated with fibrostenosis. PEDIATRIC (ACG): esophagram for children with dysphagia to assess fibrostenotic disease; feeding therapy and dietitian for feeding dysfunction; growth, development and nutrition are treatment goals.

ACG 2025 (Dellon et al., Am J Gastroenterol 120(1):31-59) / ASGE 2026 consensus Part 2 (Dellon et al., Gastrointest Endosc 103(3):396-417) · reviewed 2026-10-11 ↗
Pomenti SF … Katzka DA · Alimentary Pharmacology & Therapeutics · IF 6.7 · PubMed ↗Permalink
Esophagus/Reflux rct · n=156 · Aug 27, 2026 · Clin Transl Gastro · IF 3.4

Dupilumab Improves Endoscopic Features in Adult and Adolescent Patients With Eosinophilic Esophagitis: Post Hoc Analysis of LIBERTY EoE TREET Study.

New evidenceeosinophilic esophagitispediatric
Clinical takeawayConsider dupilumab 300 mg weekly for adult and adolescent EoE patients with active endoscopic inflammation or fibrostenosis, as it significantly improves endoscopic features over 24 weeks, though long-term efficacy beyond 52 weeks remains unstudied.
What it foundDupilumab improved EREFS WOR total score by -2.17 (95% CI -2.59, -1.75) vs placebo at 24 weeks, with greater endoscopic remission (≤2) and normalization (0) rates, and improved fibrostenotic subscore by -0.50 (95% CI -0.71, -0.29).
ContextConfirms dupilumab's efficacy in EoE, extending prior evidence to endoscopic outcomes and supporting its use in clinical practice for up to 52 weeks.
Measured against the standard of care· ACG 2025 (Dellon et al., Am J Gastroenterol 120(1):31-59) / ASGE 2026 consensus Part 2 (Dellon et al., Gastrointest Endosc 103(3):396-417)

Decision at stakeusing dupilumab for EoE in individuals 12 years or older who are nonresponsive to PPI therapy

… MONITORING: judge response on symptoms, endoscopy and histology together, never symptoms alone. Assess response endoscopically at 8-12 weeks after starting a PPI or topical steroid. For diet, ACG says 8-12 weeks and ASGE says 6-8 weeks. For dupilumab or biologics, assess at 12-24 weeks (ASGE: up to 24 weeks). Allow appropriate washout or timing after any treatment change before the follow-up EGD (ASGE). Take monitoring biopsies from the most severe-appearing lesions (rings, furrows, exudates) (ASGE). Monitoring biopsies may be limited to the esophagus when prior gastric and duodenal biopsies were normal and nothing new suggests other pathology (ASGE). The histologic response threshold of <15 eos/hpf is a 'may consider' target, read alongside endoscopic and symptom findings. Shorten follow-up after complications. Care gaps of ≥2 years are associated with fibrostenosis. …

From our summary of this standard, unedited — the part the paper bears on. … marks omitted text. Our wording, not the guideline's; read the source for its own text. The rest of this standard includes DIAGNOSIS, TREATMENT (ACG), DILATION and 2 more.

Our full summary of this standard

ACG 2025 (GRADE) is still the governing guideline. The ASGE 2026 consensus Part 2 (modified Delphi, 28 statements at ≥80% agreement; not GRADE) adds endoscopic and pediatric detail without contradicting it. DIAGNOSIS: symptoms of esophageal dysfunction plus ≥15 eos/hpf after excluding other causes of esophageal eosinophilia. A PPI trial is not a diagnostic criterion (PPI-REE abandoned). Do the initial diagnostic EGD off PPI, topical steroid and dietary therapy (ACG key concept; ASGE consensus, which gives no washout duration). Initial assessment is a standard EGD, not a less-invasive modality, so that full biopsies and dilation are possible (ASGE). Take ≥6 esophageal biopsies from ≥2 levels in anyone with symptoms or endoscopic findings consistent with EoE, targeting visible lesions. In CHILDREN with suspected EoE, also biopsy the stomach and duodenum (ASGE). Use EREFS at every endoscopy and report a quantified peak eosinophil count (ACG strong/low; ASGE). TREATMENT (ACG): swallowed topical steroids STRONG/moderate; high-dose PPI CONDITIONAL/low; empiric elimination diet CONDITIONAL/low. Choose a single initial therapy by shared decision-making. Fluticasone or budesonide are both reasonable. Adult doses: PPI double the reflux dose (e.g., omeprazole 20 mg BID or 40 mg daily); budesonide 2-4 mg/day (BOS 2 mg BID); fluticasone 1,760 mcg/day divided. Pediatric doses: PPI 2 mg/kg/day; budesonide 1-2 mg/day; fluticasone 110-880 mcg/day. Allergy testing is not used to direct diets. A 1FED/2FED step-up diet with a dietitian is acceptable, with endoscopic and biopsy confirmation after each reintroduced food. Dupilumab is CONDITIONAL for PPI-nonresponsive patients aged ≥12 (moderate) and for ages 1-11 at ≥15 kg (low). Weight-band dosing: 15-<30 kg 200 mg q2w; 30-<40 kg 300 mg q2w; ≥40 kg 300 mg weekly. Recommendations AGAINST: omalizumab, cromolyn, montelukast. No recommendation for cendakimab, benralizumab, lirentelimab, mepolizumab or reslizumab. DILATION: an adjunct to anti-inflammatory therapy for strictures causing dysphagia (ACG conditional/low). Start low and go slow; target ≥16 mm in adults and adolescents over ≥1 session. In children, ASGE supports dilation of symptomatic strictures or a narrow-caliber esophagus regardless of disease activity, using the same start-low/go-slow approach. MAINTENANCE: continue effective therapy (ACG STRONG despite low evidence) at the lowest effective dose. MONITORING: judge response on symptoms, endoscopy and histology together, never symptoms alone. Assess response endoscopically at 8-12 weeks after starting a PPI or topical steroid. For diet, ACG says 8-12 weeks and ASGE says 6-8 weeks. For dupilumab or biologics, assess at 12-24 weeks (ASGE: up to 24 weeks). Allow appropriate washout or timing after any treatment change before the follow-up EGD (ASGE). Take monitoring biopsies from the most severe-appearing lesions (rings, furrows, exudates) (ASGE). Monitoring biopsies may be limited to the esophagus when prior gastric and duodenal biopsies were normal and nothing new suggests other pathology (ASGE). The histologic response threshold of <15 eos/hpf is a 'may consider' target, read alongside endoscopic and symptom findings. Shorten follow-up after complications. Care gaps of ≥2 years are associated with fibrostenosis. PEDIATRIC (ACG): esophagram for children with dysphagia to assess fibrostenotic disease; feeding therapy and dietitian for feeding dysfunction; growth, development and nutrition are treatment goals.

ACG 2025 (Dellon et al., Am J Gastroenterol 120(1):31-59) / ASGE 2026 consensus Part 2 (Dellon et al., Gastrointest Endosc 103(3):396-417) · reviewed 2026-10-11 ↗
Dellon ES … Radin A · Clinical and Translational Gastroenterology · IF 3.4 · PubMed ↗Permalink
Esophagus/Reflux retrospective · n=8,231 · Aug 24, 2026 · Clin Gastro Hep · IF 16.2

The Incidence of Esophageal Food Impactions and Risk Factors for Recurrence in a Large, Community-Based Healthcare System in Northern California.

New evidenceepidemiologydysphagiahealth services
Clinical takeawayCounsel patients with malignancy, EoE, or stricture on their recurrence risk (33.7%, 24.0%, and 23.4% respectively within 5 years) and optimize disease-specific management (e.g., dilation, steroids).
What it found5-year recurrence rates for esophageal food impaction were highest in malignancy (33.7%), eosinophilic esophagitis (24.0%), and stricture (23.4%) compared to other etiologies.
ContextAdults with endoscopy-confirmed EFBI show high recurrence risk in malignancy, EoE, and stricture, with malignancy highest but EoE and stricture more prevalent.
Measured against the standard of care· ACG 2025 (Dellon et al., Am J Gastroenterol 120(1):31-59) / ASGE 2026 consensus Part 2 (Dellon et al., Gastrointest Endosc 103(3):396-417)

Decision at stakethe need to optimize diagnosis and treatment of EoE in patients with esophageal food impactions

… DIAGNOSIS: symptoms of esophageal dysfunction plus ≥15 eos/hpf after excluding other causes of esophageal eosinophilia. A PPI trial is not a diagnostic criterion (PPI-REE abandoned). Do the initial diagnostic EGD off PPI, topical steroid and dietary therapy (ACG key concept; ASGE consensus, which gives no washout duration). Initial assessment is a standard EGD, not a less-invasive modality, so that full biopsies and dilation are possible (ASGE). Take ≥6 esophageal biopsies from ≥2 levels in anyone with symptoms or endoscopic findings consistent with EoE, targeting visible lesions. In CHILDREN with suspected EoE, also biopsy the stomach and duodenum (ASGE). Use EREFS at every endoscopy and report a quantified peak eosinophil count (ACG strong/low; ASGE). …

From our summary of this standard, unedited — the part the paper bears on. … marks omitted text. Our wording, not the guideline's; read the source for its own text. The rest of this standard includes TREATMENT (ACG), DILATION, MAINTENANCE and 2 more.

Our full summary of this standard

ACG 2025 (GRADE) is still the governing guideline. The ASGE 2026 consensus Part 2 (modified Delphi, 28 statements at ≥80% agreement; not GRADE) adds endoscopic and pediatric detail without contradicting it. DIAGNOSIS: symptoms of esophageal dysfunction plus ≥15 eos/hpf after excluding other causes of esophageal eosinophilia. A PPI trial is not a diagnostic criterion (PPI-REE abandoned). Do the initial diagnostic EGD off PPI, topical steroid and dietary therapy (ACG key concept; ASGE consensus, which gives no washout duration). Initial assessment is a standard EGD, not a less-invasive modality, so that full biopsies and dilation are possible (ASGE). Take ≥6 esophageal biopsies from ≥2 levels in anyone with symptoms or endoscopic findings consistent with EoE, targeting visible lesions. In CHILDREN with suspected EoE, also biopsy the stomach and duodenum (ASGE). Use EREFS at every endoscopy and report a quantified peak eosinophil count (ACG strong/low; ASGE). TREATMENT (ACG): swallowed topical steroids STRONG/moderate; high-dose PPI CONDITIONAL/low; empiric elimination diet CONDITIONAL/low. Choose a single initial therapy by shared decision-making. Fluticasone or budesonide are both reasonable. Adult doses: PPI double the reflux dose (e.g., omeprazole 20 mg BID or 40 mg daily); budesonide 2-4 mg/day (BOS 2 mg BID); fluticasone 1,760 mcg/day divided. Pediatric doses: PPI 2 mg/kg/day; budesonide 1-2 mg/day; fluticasone 110-880 mcg/day. Allergy testing is not used to direct diets. A 1FED/2FED step-up diet with a dietitian is acceptable, with endoscopic and biopsy confirmation after each reintroduced food. Dupilumab is CONDITIONAL for PPI-nonresponsive patients aged ≥12 (moderate) and for ages 1-11 at ≥15 kg (low). Weight-band dosing: 15-<30 kg 200 mg q2w; 30-<40 kg 300 mg q2w; ≥40 kg 300 mg weekly. Recommendations AGAINST: omalizumab, cromolyn, montelukast. No recommendation for cendakimab, benralizumab, lirentelimab, mepolizumab or reslizumab. DILATION: an adjunct to anti-inflammatory therapy for strictures causing dysphagia (ACG conditional/low). Start low and go slow; target ≥16 mm in adults and adolescents over ≥1 session. In children, ASGE supports dilation of symptomatic strictures or a narrow-caliber esophagus regardless of disease activity, using the same start-low/go-slow approach. MAINTENANCE: continue effective therapy (ACG STRONG despite low evidence) at the lowest effective dose. MONITORING: judge response on symptoms, endoscopy and histology together, never symptoms alone. Assess response endoscopically at 8-12 weeks after starting a PPI or topical steroid. For diet, ACG says 8-12 weeks and ASGE says 6-8 weeks. For dupilumab or biologics, assess at 12-24 weeks (ASGE: up to 24 weeks). Allow appropriate washout or timing after any treatment change before the follow-up EGD (ASGE). Take monitoring biopsies from the most severe-appearing lesions (rings, furrows, exudates) (ASGE). Monitoring biopsies may be limited to the esophagus when prior gastric and duodenal biopsies were normal and nothing new suggests other pathology (ASGE). The histologic response threshold of <15 eos/hpf is a 'may consider' target, read alongside endoscopic and symptom findings. Shorten follow-up after complications. Care gaps of ≥2 years are associated with fibrostenosis. PEDIATRIC (ACG): esophagram for children with dysphagia to assess fibrostenotic disease; feeding therapy and dietitian for feeding dysfunction; growth, development and nutrition are treatment goals.

ACG 2025 (Dellon et al., Am J Gastroenterol 120(1):31-59) / ASGE 2026 consensus Part 2 (Dellon et al., Gastrointest Endosc 103(3):396-417) · reviewed 2026-10-11 ↗
Lam AY … Lee JK · Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association · IF 16.2 · PubMed ↗Permalink
Esophagus/Reflux review · Aug 27, 2026 · Am J Gastro · IF 9.8

Can Early Control of Inflammation Change the Trajectory of Pediatric Eosinophilic Esophagitis?

New evidencepediatriceosinophilic esophagitisbiomarkertranslational
Clinical takeawayNo clinical action yet: a hypothesis-generating finding in pediatric EoE, suggesting potential long-term benefits of early inflammation control but requiring prospective validation.
What it foundDupilumab improved inflammatory endoscopic features in pediatric EoE, with fibrostenotic lesions remaining absent or unchanged over short-term follow-up.
ContextChallenges the traditional focus on symptom control in pediatric EoE by proposing that early, sustained suppression of type 2 inflammation may prevent long-term fibrostenotic complications.
Measured against the standard of care· ACG 2025 (Dellon et al., Am J Gastroenterol 120(1):31-59) / ASGE 2026 consensus Part 2 (Dellon et al., Gastrointest Endosc 103(3):396-417)

Decision at stakethe use of biologics like dupilumab in pediatric EoE

… MONITORING: judge response on symptoms, endoscopy and histology together, never symptoms alone. Assess response endoscopically at 8-12 weeks after starting a PPI or topical steroid. For diet, ACG says 8-12 weeks and ASGE says 6-8 weeks. For dupilumab or biologics, assess at 12-24 weeks (ASGE: up to 24 weeks). Allow appropriate washout or timing after any treatment change before the follow-up EGD (ASGE). Take monitoring biopsies from the most severe-appearing lesions (rings, furrows, exudates) (ASGE). Monitoring biopsies may be limited to the esophagus when prior gastric and duodenal biopsies were normal and nothing new suggests other pathology (ASGE). The histologic response threshold of <15 eos/hpf is a 'may consider' target, read alongside endoscopic and symptom findings. Shorten follow-up after complications. Care gaps of ≥2 years are associated with fibrostenosis. …

From our summary of this standard, unedited — the part the paper bears on. … marks omitted text. Our wording, not the guideline's; read the source for its own text. The rest of this standard includes DIAGNOSIS, TREATMENT (ACG), DILATION and 2 more.

Our full summary of this standard

ACG 2025 (GRADE) is still the governing guideline. The ASGE 2026 consensus Part 2 (modified Delphi, 28 statements at ≥80% agreement; not GRADE) adds endoscopic and pediatric detail without contradicting it. DIAGNOSIS: symptoms of esophageal dysfunction plus ≥15 eos/hpf after excluding other causes of esophageal eosinophilia. A PPI trial is not a diagnostic criterion (PPI-REE abandoned). Do the initial diagnostic EGD off PPI, topical steroid and dietary therapy (ACG key concept; ASGE consensus, which gives no washout duration). Initial assessment is a standard EGD, not a less-invasive modality, so that full biopsies and dilation are possible (ASGE). Take ≥6 esophageal biopsies from ≥2 levels in anyone with symptoms or endoscopic findings consistent with EoE, targeting visible lesions. In CHILDREN with suspected EoE, also biopsy the stomach and duodenum (ASGE). Use EREFS at every endoscopy and report a quantified peak eosinophil count (ACG strong/low; ASGE). TREATMENT (ACG): swallowed topical steroids STRONG/moderate; high-dose PPI CONDITIONAL/low; empiric elimination diet CONDITIONAL/low. Choose a single initial therapy by shared decision-making. Fluticasone or budesonide are both reasonable. Adult doses: PPI double the reflux dose (e.g., omeprazole 20 mg BID or 40 mg daily); budesonide 2-4 mg/day (BOS 2 mg BID); fluticasone 1,760 mcg/day divided. Pediatric doses: PPI 2 mg/kg/day; budesonide 1-2 mg/day; fluticasone 110-880 mcg/day. Allergy testing is not used to direct diets. A 1FED/2FED step-up diet with a dietitian is acceptable, with endoscopic and biopsy confirmation after each reintroduced food. Dupilumab is CONDITIONAL for PPI-nonresponsive patients aged ≥12 (moderate) and for ages 1-11 at ≥15 kg (low). Weight-band dosing: 15-<30 kg 200 mg q2w; 30-<40 kg 300 mg q2w; ≥40 kg 300 mg weekly. Recommendations AGAINST: omalizumab, cromolyn, montelukast. No recommendation for cendakimab, benralizumab, lirentelimab, mepolizumab or reslizumab. DILATION: an adjunct to anti-inflammatory therapy for strictures causing dysphagia (ACG conditional/low). Start low and go slow; target ≥16 mm in adults and adolescents over ≥1 session. In children, ASGE supports dilation of symptomatic strictures or a narrow-caliber esophagus regardless of disease activity, using the same start-low/go-slow approach. MAINTENANCE: continue effective therapy (ACG STRONG despite low evidence) at the lowest effective dose. MONITORING: judge response on symptoms, endoscopy and histology together, never symptoms alone. Assess response endoscopically at 8-12 weeks after starting a PPI or topical steroid. For diet, ACG says 8-12 weeks and ASGE says 6-8 weeks. For dupilumab or biologics, assess at 12-24 weeks (ASGE: up to 24 weeks). Allow appropriate washout or timing after any treatment change before the follow-up EGD (ASGE). Take monitoring biopsies from the most severe-appearing lesions (rings, furrows, exudates) (ASGE). Monitoring biopsies may be limited to the esophagus when prior gastric and duodenal biopsies were normal and nothing new suggests other pathology (ASGE). The histologic response threshold of <15 eos/hpf is a 'may consider' target, read alongside endoscopic and symptom findings. Shorten follow-up after complications. Care gaps of ≥2 years are associated with fibrostenosis. PEDIATRIC (ACG): esophagram for children with dysphagia to assess fibrostenotic disease; feeding therapy and dietitian for feeding dysfunction; growth, development and nutrition are treatment goals.

ACG 2025 (Dellon et al., Am J Gastroenterol 120(1):31-59) / ASGE 2026 consensus Part 2 (Dellon et al., Gastrointest Endosc 103(3):396-417) · reviewed 2026-10-11 ↗
Francavilla R, Cristofori F · American Journal of Gastroenterology · IF 9.8 · PubMed ↗Permalink
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