Upper Gastrointestinal Bleed (UGIB)

Not normally difficult to spot, but look for it in unexplained anaemia, or collapse.

Questions

  • Is it VARICEAL? Mortality 35%, so is an emergency whatever the GBS is.
  • Non-Variceal what’s the GBS? will help guide treatment

Anyone being admitted should be brought to HRI

Emergency Endoscopy is arranged by Med Reg

Causes

Variceal – 10% of Upper GI Bleeds (35% mort.) Hx indicating liver failure
Ulcers – Epigastric pains, reflux, dysphagia
Mallory-Wiess – Retching/coughing/vomiting prior to bleed
Malignancy – Often painless, weight loss, dysphagia

Actions

Full Observations
Cannula – large (x2)
Bloods: FBC/U&E/LFT/Coag/G&S
Record GBS score


Consider for ALL

  • Reverse Anticoagulants: Discuss with Haematologist
  • Massive Transfusion Pathway: Refer to MTP guide

Consider for Variceal

  • Terlipressin 2mg IV Bolus – Mortality Risk Reduction(RR) 34%
  • IV Antibiotics (Antibiotic Page) – Mort RR 27%, Sepsis RR 60%

Glasgow-Blatchford Score (GBS)

Urea levelHaemoglobin [Male]Haemoglobin [Female]Systolic BPOther
≥6·5 <8·02≥120 <130 1≥100 <1201100–1091Pulse ≥100 bpm1
≥8·0 <10·03≥100 <1203<100690–99 2Melaena1
≥10·0 <25·04<1006<903Syncope 2
≥256Hepatic disease2
Cardiac failure2

GBS Actions

0 – Suitable for Discharge (NICE)
1-2 – Suitable for medical review potential discharge
>5 High risk – >50% will need intervention (Med Reg must be informed)


Significant UGIB


Ensure Senior involved
Aggressive Resuscitation
Transferred to HRI (ED/AMU)
Urgent assessment by Med Reg
> Med Reg to liaise with Emergency Endoscopy + Surgical teams
Senior discussion with Emergency Endoscopist: if unable to resuscitate and early endoscopy to be considered.


Sengstaken tube


Consider if endoscopy required but not possible
Only buys time – stops 90%, but will re-bleed within 24hr
Require intubation prior to insertion
> Insert to 60cm
> Inflate gastric balloon ONLY – 250ml/Resistance
> Traction attach 1000ml bag and hang over drip stand


ESGE guidance – learning points for ED

1. Resuscitation before endoscopy

ESGE makes a strong recommendation for immediate haemodynamic assessment and prompt intravascular volume replacement in unstable patients, initially using crystalloid.

This does not mean indiscriminate aggressive fluid loading. The aim is effective resuscitation, haemorrhage control and restoration of perfusion, with blood products as indicated.

What is the evidence on very early endoscopy?

TimingESGE position
≤6 hoursNot routinely recommended
≤12 hoursNot routinely recommended
Within 24 hoursRecommended after haemodynamic resuscitation
Persistent instability despite resuscitationConsider emergency endoscopy

The guideline reviews evidence associating very early endoscopy with higher mortality in some observational studies. However, confounding by severity and incomplete resuscitation may explain this association.

Importantly, a randomised trial comparing endoscopy within 6 hours against 6–24 hours found no improvement in 30-day mortality, rebleeding, transfusion requirements or hospital length of stay.

2. Prokinetics before endoscopy

The purpose is to empty blood and clots from the stomach, improving visualisation and potentially reducing repeat procedures. (Only shortly before endoscopy and would be directed by endoscopist)

DrugRecommendationEvidence
IV erythromycinPreferred in selected patients with severe or ongoing bleedingStrong recommendation, high-quality evidence
IV metoclopramideAlternative when erythromycin is unavailableConditional recommendation, low-quality evidence

The guideline’s evidence review includes erythromycin 250 mg IV, typically 30–60 minutes before endoscopy, and metoclopramide 10 mg IV, administered 10–30 minutes before endoscopy in one major trial.

The pooled metoclopramide evidence showed improved endoscopic visualisation (mean difference 0.37, 95% CI 0.12–0.62; p=0.004), but no significant improvement in transfusion requirements or length of stay. The reduction in repeat endoscopy was not statistically significant (RR 0.60, 95% CI 0.32–1.11).

3. Antiplatelets and anticoagulants

The guideline also reinforces several practical decisions:

  • Aspirin for secondary prevention: generally continue; if interrupted, restart promptly, preferably within 3–5 days.
  • Aspirin for primary prevention: temporarily interrupt and reassess the indication.
  • Dual antiplatelet therapy: generally continue aspirin, temporarily withhold the second agent and seek cardiology advice.
  • Warfarin and DOACs: withhold during acute bleeding; consider reversal for severe bleeding or instability as appropriate.
  • Platelet transfusion: not routinely indicated solely because the patient is taking antiplatelet medication.

These antithrombotic recommendations are largely carried forward from 2021 rather than newly reassessed in 2026. esge.com

4. Consideration of PPI

There is no convincing evidence that routine IV PPI administration before endoscopy in suspected upper gastrointestinal bleeding reduces mortality, rebleeding or the need for surgery. Although it may reduce the requirement for endoscopic haemostatic intervention, this has not translated into demonstrated improvements in major clinical outcomes.

The ESGE 2026 guideline therefore makes only a conditional recommendation to consider pre-endoscopy IV PPI therapy, supported by low-quality evidence. Routine IV PPI administration in the ED is not required; treatment may be considered selectively and must not delay definitive endoscopic assessment.

High-dose PPI treatment following endoscopic haemostasis of high-risk peptic ulcers remains strongly recommended.

The guideline cites a Cochrane meta-analysis of six randomised trials examining PPI treatment before endoscopy.

OutcomeOdds ratio (95% CI)Interpretation
Mortality1.14 (0.76–1.70)No demonstrated benefit
Rebleeding0.81 (0.62–1.06)Possible benefit, not statistically significant
Surgery0.91 (0.65–1.26)No demonstrated benefit
Endoscopic haemostasis required0.68 (0.50–0.93)Statistically significant reduction
High-risk endoscopic stigmata0.80 (0.52–1.21)No clear reduction

A further observational study involving 2,566 patients found no significant difference in high-risk endoscopic appearances between patients receiving pre-endoscopy PPIs and those not receiving them (51.8% versus 53.4%; p=0.58)

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