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 level | Haemoglobin [Male] | Haemoglobin [Female] | Systolic BP | Other | |||||
|---|---|---|---|---|---|---|---|---|---|
| ≥6·5 <8·0 | 2 | ≥120 <130 | 1 | ≥100 <120 | 1 | 100–109 | 1 | Pulse ≥100 bpm | 1 |
| ≥8·0 <10·0 | 3 | ≥100 <120 | 3 | <100 | 6 | 90–99 | 2 | Melaena | 1 |
| ≥10·0 <25·0 | 4 | <100 | 6 | <90 | 3 | Syncope | 2 | ||
| ≥25 | 6 | Hepatic disease | 2 | ||||||
| Cardiac failure | 2 | ||||||||
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?
| Timing | ESGE position |
|---|---|
| ≤6 hours | Not routinely recommended |
| ≤12 hours | Not routinely recommended |
| Within 24 hours | Recommended after haemodynamic resuscitation |
| Persistent instability despite resuscitation | Consider 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)
| Drug | Recommendation | Evidence |
|---|---|---|
| IV erythromycin | Preferred in selected patients with severe or ongoing bleeding | Strong recommendation, high-quality evidence |
| IV metoclopramide | Alternative when erythromycin is unavailable | Conditional 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.
| Outcome | Odds ratio (95% CI) | Interpretation |
|---|---|---|
| Mortality | 1.14 (0.76–1.70) | No demonstrated benefit |
| Rebleeding | 0.81 (0.62–1.06) | Possible benefit, not statistically significant |
| Surgery | 0.91 (0.65–1.26) | No demonstrated benefit |
| Endoscopic haemostasis required | 0.68 (0.50–0.93) | Statistically significant reduction |
| High-risk endoscopic stigmata | 0.80 (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)