Upper Gastrointestinal Bleeding (UGIB)
Definition
Upper GI bleeding refers to hemorrhage originating proximal to the ligament of Treitz (esophagus, stomach, duodenum).
Anatomical Classification
|
Site |
Examples |
|
Esophagus |
Varices, Mallory–Weiss tear, esophagitis |
|
Stomach |
Peptic ulcer, erosive gastritis, malignancy |
|
Duodenum |
Peptic ulcer, Dieulafoy lesion |
Table of Contents
ToggleEtiology
1. Non-Variceal UGIB (≈ 80–85%)
Peptic Ulcer Disease (most common)
- Duodenal ulcer > Gastric ulcer
- Causes:H. pylori,NSAIDs,Stress ulcers
Other causes
- Erosive gastritis / duodenitis
- Esophagitis (reflux, pill-induced)
- Mallory–Weiss tear
- Dieulafoy lesion
- Upper GI malignancy
- Iatrogenic (post-ERCP, biopsy)
- Aortoenteric fistula(present with melena as a sentinel bleed before the development of brisk, hemodynamically significant bleeding. Patients typically have a history of endovascular intervention of the aorta, where graft material erodes through the gastrointestinal lumen.)
- Hemosuccus pancreaticus
- Hemobilia
2. Variceal UGIB (≈ 15–20%)
- Esophageal > gastric varices
History
|
History Component |
Reason / Clinical Significance |
|
Duration and frequency of bleeding episodes |
Helps estimate severity and ongoing blood loss. |
|
Volume of blood vomited/passed |
Assesses magnitude of hemorrhage and transfusion needs. |
|
Symptoms of hypovolemia (dizziness, syncope, presyncope, weakness, palpitations) |
Suggest significant blood loss and hemodynamic compromise. |
|
Dyspnea or chest pain |
May indicate severe anemia, myocardial ischemia, or shock. |
|
Epigastric pain |
Suggests peptic ulcer disease, gastritis, or duodenitis. |
|
Sudden severe abdominal pain |
Raises suspicion for perforated peptic ulcer. |
|
Retching or repeated vomiting before hematemesis |
Suggests Mallory-Weiss tear. |
|
Dysphagia or odynophagia |
May indicate esophageal malignancy, esophagitis, or stricture. |
|
Heartburn / GERD symptoms |
Associated with erosive esophagitis. |
|
Early satiety, weight loss, anorexia |
Suggest gastric or esophageal malignancy. |
|
Previous episodes of GI bleeding |
Identifies recurrent disease and predicts future bleeding risk. |
|
History of peptic ulcer disease |
Major risk factor for non-variceal UGIB. |
|
History of cirrhosis |
Strong predictor of variceal bleeding. |
|
History of portal hypertension |
Suggests esophageal or gastric varices. |
|
Previous endoscopy findings |
Identifies known ulcers, varices, malignancy, or angiodysplasia. |
|
NSAID use |
Major cause of peptic ulcer disease and UGIB. |
|
Aspirin use |
Increases risk of ulcer formation and bleeding. |
|
P2Y12 inhibitors (clopidogrel, prasugrel, ticagrelor) |
Increase bleeding risk and influence management. |
|
Anticoagulants (warfarin, heparin, DOACs) |
Predispose to severe bleeding and may require reversal. |
|
Corticosteroid use |
Increases ulcer risk, especially with NSAIDs. |
|
SSRI use |
Associated with increased GI bleeding risk. |
|
Herbal medications (ginkgo, garlic, ginseng, etc.) |
Can impair coagulation and platelet function. |
|
Alcohol use |
Associated with cirrhosis, portal hypertension, gastritis, and varices. |
|
Illicit drug use (especially cocaine) |
May contribute to ischemia or liver disease. |
|
Chronic liver disease history |
Supports variceal or portal hypertensive bleeding. |
|
Viral hepatitis history |
Risk factor for cirrhosis and varices. |
|
History of malignancy |
Gastric, esophageal, pancreatic, or metastatic lesions may bleed. |
|
Family history of GI malignancy |
Increases suspicion for gastrointestinal cancers. |
|
Family history of bleeding disorders |
Suggests inherited coagulopathy. |
|
Known bleeding disorder |
Hemophilia, von Willebrand disease, thrombocytopenia increase bleeding risk. |
|
ICU admission / critical illness |
Risk factor for stress-related mucosal disease. |
|
Cardiovascular disease |
Influences transfusion targets and antithrombotic management. |
Physical Examination
|
Physical Examination Finding |
Reason / Clinical Significance |
|
Cool extremities, delayed capillary refill |
Peripheral hypoperfusion. |
|
Pallor |
Suggests significant anemia. |
|
Abdominal tenderness |
May indicate ulcer disease, gastritis, pancreatitis, or other pathology. |
|
Rebound tenderness / guarding |
Suggests perforation or peritonitis. |
|
Hepatomegaly |
Suggests chronic liver disease. |
|
Splenomegaly |
Indicates portal hypertension. |
|
Ascites |
Suggests decompensated cirrhosis and portal hypertension. |
|
Jaundice |
Evidence of chronic liver disease. |
|
Palmar erythema |
Stigmata of chronic liver disease. |
|
Spider angiomas |
Suggest cirrhosis/portal hypertension. |
|
Gynecomastia |
Chronic liver disease. |
|
Caput medusae |
Portal hypertension. |
|
Asterixis |
Hepatic encephalopathy. |
|
Digital rectal examination |
Confirms melena or hematochezia and excludes anorectal source. |
Clinical Presentation
Symptoms
- Hematemesis
- Fresh blood → active bleed
- Coffee-ground → old bleed
- Melena
- Hematochezia (if massive UGIB with rapid transit of blood through the GI tract)
- Syncope, dizziness
Initial Investigations
Laboratory
- CBC (Hb may be normal initially)
- blood urea nitrogen to creatinine ratio >30 suggests an upper GI source of bleeding.
- Blood group & cross-match
- PT/INR, aPTT
- LFTs
- TEG if cirrhosis or complex coagulopathy (e.g., DIC).
- RFTs(Hepatorenal syndrome)
- Serum lactate
- ABG (shock)
Urea rises disproportionately in UGIB due to digestion and absorption of blood proteins.
Risk Stratification Scores
|
Score |
Variables |
Interpretation |
|
Glasgow-Blatchford Score (GBS) |
Blood Urea Nitrogen (BUN), Hemoglobin, Systolic BP, Pulse Rate, Melena, Syncope, Hepatic Disease, Cardiac Failure |
Pre-endoscopy score. Predicts need for intervention (transfusion, endoscopy, surgery). GBS 0–1: Very low risk; outpatient management possible. GBS ≥6: High likelihood of intervention. Preferred initial risk stratification tool. |
|
AIMS65 Score |
A = Albumin <3.0 g/dL, I = INR >1.5, M = Altered Mental Status (GCS <14), S = Systolic BP ≤90 mmHg, 65 = Age ≥65 years |
Predicts in-hospital mortality, ICU admission, and length of stay. One point for each variable (0–5). Score ≥2: Increased mortality risk. Score ≥3: High-risk patient requiring intensive monitoring. |
|
Rockall Score |
Pre-endoscopy: Age, Shock (BP/Pulse), Comorbidities. Post-endoscopy: Diagnosis and Stigmata of Recent Hemorrhage (active bleeding, visible vessel, adherent clot). |
Predicts rebleeding and mortality. Can be calculated before and after endoscopy. Score <3: Low risk. Score 3–4:Moderate risk. Score ≥8: High mortality risk. Less commonly used than GBS for initial triage. |
|
Forrest classification |
describes peptic ulcer appearance and guides endoscopic Management. |
|
Initial Resuscitation
Fluids
- Balanced crystalloids
- Avoid over-resuscitation in cirrhotics
- Variceal hemorrhage originates from the portal venous circulation; therefore, excessive fluid administration can increase central venous and portal pressures, potentially worsening bleeding. Patients with portal hypertension and cirrhosis often have a lower baseline blood pressure (typically systolic 80–90 mmHg) and may tolerate mild hypotension. Consequently, a restrictive resuscitation strategy is preferred, as aggressive volume replacement may exacerbate ongoing hemorrhage and increase the risk of rebleeding.
Blood Transfusion
- Restrictive strategy preferred
- Target Hb >7g/dL
- Exceptions:—-CAD,Ongoing massive bleeding(target hemoglobin >8 g/dL).
Correction of Coagulopathy
if Patient is actively bleeding and
- INR > 1.5 → FFP / PCC
- Platelets < 50,000 → transfuse
- DOACs → specific reversal if life-threatening
if Patient is Not bleeding actively and prepping For Endoscopy
|
Parameter |
Suggested Target |
|
Platelets |
>50,000/µL |
|
INR (warfarin-associated bleed) |
Reverse with PCC + vitamin K |
|
INR in cirrhosis |
Do not routinely correct |
|
Fibrinogen |
>100–120 mg/dL (consider cryoprecipitate if lower) |
Pharmacological Therapy
1. Non-variceal Bleed
- IV Pantoprazole:Reduces high-risk stigmata
- Intermittent IV PPI(40 mg IV B.D or Q.I.D) ≈ continuous infusion (recent meta-analysis)
- Still infusion preferred in high-risk ulcers
|
Drug |
Dose |
|
Pantoprazole |
80 mg IV bolus → 8 mg/hr infusion |
|
Omeprazole |
80 mg IV bolus → 8 mg/hr infusion |
|
Esomeprazole |
80 mg bolus → 8 mg/hr infusion |
- High-risk for rebleeding Peptic lesion → 72 hr IV infusion
- peptic ulcers with low-risk features, then an oral daily dose can be continued for ulcer treatment.
Preferred Vasopressor: Norepinephrine
Norepinephrine
Why?
- Recommended first-line vasopressor in hemorrhagic shock.
- Potent vasoconstriction with less tachycardia than dopamine.
- Maintains MAP while definitive bleeding control is achieved.
Target—MAP ≥65 mmHg
Dose—0.05–1 mcg/kg/min (titrate to MAP)
If refractory shock—Add:Vasopressin (0.03 units/min)
2. Variceal Bleeding Suspected
Terlipressin or Octreotide(These are not being used primarily as vasopressors but as Splanchnic Vasoconstrictors)
A. TERLIPRESSIN
selective V1 receptor action-Potent splanchnic vasoconstriction
- 2 mg IV every 4-6 hours until bleeding is controlled ,upto 48 hours
- After bleeding control 1 mg IV every 4–6 hr upto 48-72 hr
Contraindication
- Myocardial ischemia,heart failure, prolonged Qtc
- Peripheral ischemia
- Hyponatremia
- Only drug shown to reduce mortality in variceal bleed??
B. OCTREOTIDE(First Choice)
- Analogue of Somatostatin
- Dose-50 mcg IV bolus → 50 mcg/hr infusion
- Duration-2–5 days
Side Effects
- Bradycardia
- Hyperglycemia / hypoglycemia
- GI upset
If Variceal Bleeding Patient Remains in Shock
Use both:
- Portal pressure reducing agent—Octreotide or Terlipressin
- Systemic vasopressor—Norepinephrine (preferred)
C. SOMATOSTATIN
intravenous bolus of 250 µg, followed by a continuous infusion of 250 to 500 µg/hour.
D.Role of Noradrenaline in Variceal Bleeding
Noradrenaline (norepinephrine) does NOT treat variceal bleeding itself. It is used to treat hemorrhagic shock and maintain organ perfusion while definitive hemostatic therapy is provided.If Variceal Bleeding Patient Remains in Shock
Use both:
- Portal pressure reducing agent—Octreotide or Terlipressin
- Systemic vasopressor—Norepinephrine (preferred)
E. Role of Vasopressin in Upper GI Bleeding
1. Not a Routine First-Line Vasopressor
In UGIB with hemorrhagic shock, the preferred vasopressor is:
- Norepinephrine
Vasopressin is not routinely used as first-line therapy because:
- May cause excessive vasoconstriction
- Risk of myocardial ischemia
- Risk of mesenteric ischemia
- Risk of digital ischemia
2. Role in Refractory Hemorrhagic Shock
When hypotension persists despite:
- Adequate blood product resuscitation
- Control of bleeding
- Moderate/high-dose norepinephrine
Add:Vasopressin 0.03 units/min
Antibiotic Prophylaxis(Controversial)
- No role(one thought)
- (Second thought)Antibiotic prophylaxis for 2 to 5 days is advised in patients with cirrhosis presenting with acute GI bleeding due to the risks of bacterial translocation, aspiration pneumonia, and spontaneous bacterial peritonitis. Antibiotics can be discontinued once bleeding is controlled and no active infection is evident.
- Empiric antibiotics, if initiated, should be reassessed within 48–72 hours and discontinued if microbiological studies remain negative and there is no clinical evidence of infection.
|
Drug |
Dose |
Duration |
|
Ceftriaxone |
1 g IV OD |
5 days |
|
Norfloxacin(Used only if:
|
400 mg PO BD |
5 days |
TRANEXAMIC ACID (TXA)
Evidence
- HALT-IT trial → NO mortality benefit
- ↑ thromboembolic events
PROKINETICS
Role-Improve endoscopic visualization
Erythromycin
- 250 mg IV over 30 min
- Given 30–90 min before endoscopy
Side Effects
- QT prolongation(contraindication)
- Arrhythmia
Review Medication
- Discontinue anticoagulants (e.g., DVT prophylaxis).
- Discontinue antihypertensives.
- Aspirin for Primary Prevention (No Prior Cardiovascular Event) Stop aspirin during acute UGIB and do not routinely restart it.
- Aspirin for Secondary Prevention (Prior MI, Stroke, PCI, CABG)—Temporarily hold aspirin if bleeding is ongoing or endoscopic hemostasis has not yet been achieved.After Hemostasis Restart aspirin early, usually within 1–3 days, and certainly within 3–5 days after successful endoscopic control.
Endoscopy
- Within 24 hours (all UGIB)
- Within 12 hours (suspected variceal bleed).
- In patients who achieve hemostasis after initial endoscopy, high-risk patients should undergo evaluation for preemptive or “early” TIPS.
Failure of Endoscopic Control
If endoscopy doesn’t show any source of bleeding, consider CT angiography to evaluate for a lower GI bleed.
Non-Variceal
- Angioembolization(interventional radiology)
- Surgery (last resort)
Variceal
- Balloon tamponade (temporary)
- Salvage TIPS(interventional radiology)
Intubation
- Indication-Poor GCS,unable tolerate procedure, severe hemetmesis
- High risk of aspiration-Consider NG suction to reduce the risk of aspiration (varices aren’t a contraindication to NG tube placement)
- High risk of Collapse—Resuscitate and start vasopressor before intubation.
Secondary Prevention
Non-Variceal
- H. pylori eradication
- Stop NSAIDs
- Long-term PPI if needed
Variceal
- Non-selective beta blockers (propranolol / carvedilol)—During Acute GI Bleeding Hold initially.Restart before discharge or within several days after successful hemostasis.
- Repeat EVL sessions
Drugs & Dose
|
Drug |
Starting Dose |
Target |
|
Propranolol |
20 mg BD |
HR 55–60 |
|
Carvedilol |
6.25 mg OD → BD |
↓ portal pressure |
Titration-Adjust to HR 55–60 bpm
Side Effects
- Hypotension
- Bradycardia
- Bronchospasm
Management of Rebleeding
- This will depend on the lesion seen initially. However, the usual sequence of events is as follows:
- 1st line: Repeat endoscopy.
- 2nd line: Interventional radiology.
- 3rd line: Surgery.
Balloon Tamponade
Indications
- Massive variceal bleed
- Failure or unavailability of endoscopic control
- Hemodynamic instability despite resuscitation
- As a bridge to early TIPS or repeat endoscopy
Not definitive therapy
Contraindications (Relative/Absolute)
- Unprotected airway (must intubate first)
- Esophageal rupture or stricture
- Recent esophageal surgery
- Uncontrolled coagulopathy (relative)
Types of Balloon Tamponade Devices
1. Sengstaken–Blakemore (SB) Tube
- 3 lumens
- Gastric balloon
- Esophageal balloon
- Gastric aspiration
Used for esophageal varices
2. Minnesota Tube
- 4 lumens
- Gastric balloon
- Esophageal balloon
- Gastric aspiration
- Esophageal aspiration
Allows better suction above esophageal balloon
3. Linton–Nachlas Tube
- Large gastric balloon
- Used mainly for gastric varices
- Less commonly used now
Mechanism of Action
- Gastric balloon compresses:
- Gastroesophageal junction
- Gastric varices
- Esophageal balloon directly compresses:
- Esophageal varices
Insertion Technique
Mandatory endotracheal intubation Prevents aspiration
- Insert orally (preferred) or nasally
- Advance to 50–55 cm
- Inflate with 250–300 mL air
- Confirm position:
- Auscultation over epigastrium
- Chest X-ray (best)
Apply Traction
- Pull tube gently until resistance felt
- Fix with:
- Helmet
- 500 mL IV fluid bottle as counterweight
Assess Bleeding
- Aspirate gastric contents
- If bleeding stops → do NOT inflate esophageal balloon
Esophageal Balloon (If Needed)
- Inflate to 30–45 mmHg
- Use manometer
- Clamp lumen
Duration of Use
Maximum: 12–24 hours
- Esophageal balloon:
- Deflate every 6 hours (5–10 min) to prevent ischemia
- Remove as soon as definitive therapy available
Efficacy
- Controls bleeding in 80–90% initially
- High rebleeding rate once deflated
- Does NOT improve mortality
Complications
Common & Dangerous
- Aspiration pneumonia
- Esophageal ulceration
- Esophageal necrosis
- Esophageal perforation
- Airway obstruction
- Pressure necrosis
- Rebleeding after deflation
Risk increases with
- Prolonged use (>24 h)
- High balloon pressure
- Improper positioning
Monitoring in ICU
- Continuous vitals
- Hourly suction output
- Balloon pressure checks
- Chest X-ray
- Watch for:
- Chest pain
- Subcutaneous emphysema
- Sudden deterioration
Role in Current Guidelines
- Baveno VII / AASLD / ESGE
- Balloon tamponade = salvage bridge therapy
- Prefer early TIPS over prolonged tamponade
- Self-expanding esophageal metal stents (SEMS)
- Emerging alternative
- Fewer complications
- Can remain for up to 7 days
