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Endoscopy, in full.

All 4 Endoscopy 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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Endoscopy guideline · Jul 21, 2026 · Endoscopy · IF 11.8

Sedation for gastrointestinal endoscopy: European Society of Gastrointestinal Endoscopy (ESGE) and European Society of Gastroenterology and Endoscopy Nurses and Associates (ESGENA) Guideline.

Guideline / reviewguidelinesedationhealth services
Clinical takeawayIn your endoscopy practice: (1) adopt propofol as your first-line procedural sedation unless contraindicated or unavailable; (2) use midazolam with opiates as alternative if propofol not accessible; (3) consider remimazolam specifically for elderly patients or those with significant cardiac or pulmonary disease, but exercise caution when combining with other sedatives or analgesics; if analgesia is required, carefully coordinate drug selection with your sedation team; (4) ensure a dedicated, specifically trained staff member (not dual-tasking) administers all sedation; (5) perform pre-procedure risk assessment for each patient and calibrate your sedation regimen and monitoring based on both procedure complexity and patient risk factors; include capnography monitoring for high-risk patients; (6) individualize sedation decisions for patients taking GLP-1 receptor agonists rather than using a standard approach; (7) routinely offer unsedated diagnostic colonoscopy and gastroscopy as a patient option.
What it foundESGE/ESGENA guideline specifies propofol as first-line procedural sedation (where permissible), midazolam with opiates as alternative, and remimazolam for elderly patients or those with cardiovascular/respiratory comorbidities; mandates sedation delivery by dedicated trained professionals and tailors pre-assessment and periprocedural monitoring to both procedure complexity and patient risk profile.
ContextThis European guideline formalizes and standardizes endoscopy sedation practice. Propofol is already used first-line in many centers but is now officially endorsed across Europe where resources and law permit. Remimazolam is newly highlighted as a dedicated option for high-risk patients (elderly, cardiovascular/pulmonary comorbidities), reflecting evidence on ultrashort-acting agents in medically complex populations. The emphasis on dedicated trained sedation staff and explicit risk stratification strengthens safety protocols.
Reinforcessuggested applicable standard· ESGE/ESGENA 2026 (PMID 42480549); ESGE/ESGENA/ESA NAAP 2015; ASGE 2018; ASA 2018 moderate sedation; multisociety GLP-1 perioperative guidance 2024

Decision at stakesedation regimen and monitoring should be scaled to patient risk and procedure complexity, using propofol first-line or midazolam with opiates, with dedicated staffing and trained recovery

Scale pre-sedation assessment, regimen and monitoring to patient risk and procedure complexity. Propofol AND midazolam-with-opiate are both strongly recommended; propofol as first line is conditioned on national legislation and staffing, not on demonstrated superiority.

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

Scale pre-sedation assessment, regimen and monitoring to patient risk and procedure complexity. Assess ASA class, Mallampati, BMI, OSA risk and fasting status before every sedated procedure. Propofol AND midazolam-with-opiate are both strongly recommended; propofol as first line is conditioned on national legislation and staffing, not on demonstrated superiority. Consider remimazolam in the elderly and in cardiorespiratory comorbidity. Whoever administers sedation must be able to rescue a patient one level deeper than intended. Involve an anesthesiology specialist for emergency endoscopy with increased aspiration risk, hemodynamic instability, OR significant comorbidities, and electively for ASA >=3, Mallampati >=3, severe OSA or anticipated difficult airway. Individualize GLP-1 receptor agonist management rather than withholding blindly. Discharge against a scoring system with an accompanying adult and 24-hour restrictions.

ESGE/ESGENA 2026 (PMID 42480549); ESGE/ESGENA/ESA NAAP 2015; ASGE 2018; ASA 2018 moderate sedation; multisociety GLP-1 perioperative guidance 2024 ↗
Triantafyllou K … Sidhu R · Endoscopy · IF 11.8 · PubMed ↗Permalink
Endoscopy rct · n=827 · Jul 22, 2026 · Endoscopy · IF 11.8

Computer-assisted versus standard colonoscopy for adenoma detection in a population-based colorectal cancer screening program: a randomized clinical trial.

New evidencecolorectal cancer screeningadenomacomputer-aided detection
Clinical takeawayCADe systems should not be expected to improve adenoma detection rates in screening practice. This trial found no benefit across all tested subgroups, including endoscopists with lower baseline adenoma detection and those with suboptimal bowel preparation.
What it foundComputer-aided detection (CADe) did not significantly improve adenoma detection rate compared to standard colonoscopy in a CRC screening program (60.8% vs 57.7%; adjusted risk ratio 1.05, 95% CI 0.94-1.17), with similar rates for serrated lesions, advanced adenomas, and polyp detection overall.
ContextThis RCT contradicts prior optimism that CADe would enhance detection in screening settings. In a diverse population-based program (mean age 62, two-thirds positive FIT cases, mixed endoscopist experience), standard colonoscopy without computer assistance remains the evidence-supported baseline.
Reinforcessuggested applicable standard· U.S. Multi-Society Task Force on Colorectal Cancer (Rex DK, Boland CR, Dominitz JA, et al.), "Colorectal Cancer Screening: Recommendations for Physicians and Patients From the U.S. Multi-Society Task Force on Colorectal Cancer," Gastroenterology, 2017

Decision at stakestandard colonoscopy without computer-assisted detection is appropriate for colorectal cancer screening

Begin average-risk colorectal cancer screening at age 45 using a patient-centered shared-decision modality choice, colonoscopy every 10 years (preferred) or annual FIT as Tier 1 options, with multi-target stool DNA every 3 years, CT colonography every 5 years, or flexible sigmoidoscopy every 5 to 10 years as Tier 2 alternatives. A positive stool-based test requires diagnostic colonoscopy, and stool tests should not be ordered for patients who would decline follow-up colonoscopy. Generally stop at age 75 with individualized decisions for ages 76-85 and no screening beyond 85.

U.S. Multi-Society Task Force on Colorectal Cancer (Rex DK, Boland CR, Dominitz JA, et al.), "Colorectal Cancer Screening: Recommendations for Physicians and Patients From the U.S. Multi-Society Task Force on Colorectal Cancer," Gastroenterology, 2017 · reviewed 2026-07-23 ↗
Davila-Piñón P … Cubiella J · Endoscopy · IF 11.8 · PubMed ↗Permalink
Endoscopy meta analysis · n=1,939 · Jul 22, 2026 · Eur J Gastro Hep · IF 2.2

Ferric carboxymaltose for iron-deficiency anemia secondary to gastrointestinal bleeding: a systematic review and meta-analysis.

New evidencemeta-analysismicronutrient deficiencyhemostasissystematic review
Clinical takeawayFCM is more effective than other iron formulations for treating anemia from gastrointestinal bleeding. This evidence applies to patients requiring IV iron due to intolerance or inadequate response to oral iron therapy. Monitor serum phosphate during therapy; hypophosphatemia occurs substantially more often and requires active surveillance and supplementation if depleted.
What it foundFCM increased hemoglobin response rate 24% over other iron formulations (RR 1.24, 95% CI 1.14-1.34) and raised serum ferritin by 294 units (95% CI 169-418), but increased hypophosphatemia risk 21-fold (RR 21.00, 95% CI 8.90-49.56).
ContextConfirms FCM superiority to alternative iron therapies in the GI bleeding setting; establishes hypophosphatemia as a significant, quantified safety consideration requiring management in patients receiving FCM.
Refinessuggested applicable standard· American Gastroenterological Association, "AGA Clinical Practice Update on Management of Iron Deficiency Anemia: Expert Review," 2024

Decision at stakechoice of IV iron formulation for patients with inadequate response to optimized oral iron

Judge response objectively: in an adherent anemic patient, hemoglobin should increase by about 1 g/dL within 2 weeks and ferritin should show improvement within about 1 month, expected responses that serve to confirm adherence and adequate absorption during the oral trial, not fixed cutoffs whose miss by itself mandates IV iron; a shortfall should prompt reassessment of adherence and absorption, and escalation to IV iron rests on an inadequate response to an adequate trial of oral iron.

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

Per the AGA 2024 management update (Best Practice Advice statements): Start oral iron; no single oral formulation is superior and ferrous sulfate is preferred as the least expensive (BPA1). Dose oral iron once daily at most, with every-other-day dosing an accepted alternative that may be better tolerated at similar or equal absorption (BPA2). Add vitamin C to improve absorption (BPA3). Judge response objectively: in an adherent anemic patient, hemoglobin should increase by about 1 g/dL within 2 weeks and ferritin should show improvement within about 1 month, expected responses that serve to confirm adherence and adequate absorption during the oral trial, not fixed cutoffs whose miss by itself mandates IV iron; a shortfall should prompt reassessment of adherence and absorption, and escalation to IV iron rests on an inadequate response to an adequate trial of oral iron. Use IV iron if the patient cannot tolerate oral iron, if ferritin/blood counts do not improve with a trial of oral iron, or in a condition where oral iron is unlikely to be absorbed, the update names active inflammatory bowel disease and the post-bariatric state (particularly procedures disrupting duodenal absorption, in a patient with no identifiable source of chronic GI blood loss) (BPA4, BPA7). Prefer IV formulations that replace the deficit in 1-2 infusions over those needing more than 2; all IV formulations carry similar risk and true anaphylaxis is very rare (BPA5, BPA6). Condition-specific qualifiers the update keeps separate: in IBD, first determine whether the anemia reflects inadequate intake/absorption versus GI blood loss and treat active inflammation to improve absorption/reduce loss; in celiac disease, ensure gluten-free-diet adherence to restore absorption rather than defaulting straight to IV; for gastric antral vascular ectasia with an inadequate response to iron replacement, use endoscopic therapy (band ligation or argon plasma coagulation) rather than treating it as an absorption problem. The update also suggests that in uncomplicated asymptomatic patients with negative bidirectional endoscopy, a trial of iron is preferred over routine video capsule endoscopy.

American Gastroenterological Association, "AGA Clinical Practice Update on Management of Iron Deficiency Anemia: Expert Review," 2024 · reviewed 2026-07-23 ↗
Yang Y … Tan Y · European Journal of Gastroenterology & Hepatology · IF 2.2 · PubMed ↗Permalink
Endoscopy prospective cohort · Jul 23, 2026 · Endoscopy · IF 11.8

Prophylaxis of esophageal stricture after endoscopic submucosal dissection with autologous adipose-derived stromal cells.

New therapyESD
Clinical takeawayevaluate autologous stromal cell injection as a stricture prophylaxis option for high-risk esophageal ESD if efficacy is established
What it foundautologous adipose-derived stromal cell injection as a regenerative medicine approach to stricture prophylaxis after ESD
ContextThe available literature comprises one Tier-2 report of autologous adipose-derived stromal cells as a prophylactic intervention for preventing esophageal stricture following endoscopic submucosal dissection.
Emergingsuggested applicable standard· British Society of Gastroenterology, 'UK guidelines on oesophageal dilatation in clinical practice' (Sami SS et al., Gut 2018;67(6):1000-1023). DOI 10.1136/gutjnl-2017-315414, PMID 29478034. Achalasia-specific dilation is governed by ASGE, 'ASGE guideline on the management of achalasia' (Khashab MA et al., Gastrointest Endosc 2020;91(2):213-227.e6, DOI 10.1016/j.gie.2019.04.231, PMID 31839408).

Decision at stakeprophylactic strategies to prevent esophageal stricture formation after endoscopic submucosal dissection

Balloon (TTS/hydrostatic) dilation is governed instead by matching the balloon to the stricture and dilating to a pre-selected target diameter under direct endoscopic vision, with fluoroscopy added for tortuous, long or high-risk strictures; limit the first session to 10-12 mm when the stricture will not admit an adult gastroscope (9 mm or less if filiform) and repeat sessions weekly to fortnightly until easy passage of a 15 mm or larger dilator is achieved along with symptomatic improvement.

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

Widen symptomatic GI luminal strictures with mechanical bougie (Savary-Gilliard) or through-the-scope hydrostatic balloon dilation. For achalasia, use a pneumatic balloon (Rigiflex, starting at 30 mm) with graded dilation over multiple sessions to minimize perforation risk, and always biopsy to rule out malignancy at the index procedure. For non-achalasia strictures, keep the two techniques distinct rather than applying one rule to both. The 'rule of 3' is a BOUGIE (wire-guided push-dilator) rule and its trigger is tactile: once moderate resistance is felt, pass no more than 3 progressively larger dilators in roughly 1 mm (3-Fr) steps in that session. A balloon transmits no such resistance, so the rule does not transfer to it. Balloon (TTS/hydrostatic) dilation is governed instead by matching the balloon to the stricture and dilating to a pre-selected target diameter under direct endoscopic vision, with fluoroscopy added for tortuous, long or high-risk strictures; limit the first session to 10-12 mm when the stricture will not admit an adult gastroscope (9 mm or less if filiform) and repeat sessions weekly to fortnightly until easy passage of a 15 mm or larger dilator is achieved along with symptomatic improvement. BSG 2018 does advise using no more than three successively larger diameter increments in a single session for BOTH bougie and balloon dilators, but grades that advice low quality / low strength and states explicitly that the precise 3x1 mm restriction is not evidence based, 2x1 mm may be safer in very tight or long strictures and 4x1 mm or 3x2 mm may be used safely in looser strictures or ones that have completely recurred. Treat it as a ceiling to be justified, not as a technique-independent law, and do not carry the bougie resistance trigger over to balloon dilation. Treat the underlying condition first, topical steroid optimization for EoE strictures and biologic optimization for inflammatory Crohn's strictures, before or alongside dilation. For refractory benign strictures, inject intralesional triamcinolone (40 mg in 4 quadrants) and escalate to POEM/surgery or SEMS for malignant strictures as indicated.

British Society of Gastroenterology, 'UK guidelines on oesophageal dilatation in clinical practice' (Sami SS et al., Gut 2018;67(6):1000-1023). DOI 10.1136/gutjnl-2017-315414, PMID 29478034. Achalasia-specific dilation is governed by ASGE, 'ASGE guideline on the management of achalasia' (Khashab MA et al., Gastrointest Endosc 2020;91(2):213-227.e6, DOI 10.1016/j.gie.2019.04.231, PMID 31839408). · reviewed 2026-07-21 ↗
Fortes Y … Maluf-Filho F · Endoscopy · IF 11.8 · PubMed ↗Permalink
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