What could be the cause of throwing up blood clots?

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Vomiting Blood Clots: Emergency Evaluation and Management

Vomiting blood clots (hematemesis) indicates acute upper gastrointestinal bleeding that requires immediate medical evaluation, as this carries a mortality risk exceeding 10% and demands urgent endoscopy within 24 hours to identify and treat the bleeding source. 1, 2

Immediate Life-Threatening Causes to Consider

The most critical bleeding sources include:

  • Peptic ulcer disease (most common cause) - particularly ulcers with exposed blood vessels that have a 43% rebleeding rate within 72 hours without intervention 3, 2
  • Esophageal or gastric varices - carries up to 30% mortality and requires immediate vasoactive therapy (terlipressin) if cirrhosis is suspected 1, 4
  • Mallory-Weiss tears - typically self-limited but can cause severe hemorrhage 1
  • Gastric malignancy - particularly in older patients with weight loss 1
  • Vascular malformations including Dieulafoy lesions 1

Critical Initial Assessment

Hemodynamic Stability Markers

Calculate the shock index (heart rate ÷ systolic blood pressure) - if >1, this indicates hemodynamic instability requiring ICU admission 5. Look for:

  • Tachycardia, hypotension, altered mental status 5
  • Signs requiring >1,000 mL blood/plasma within one hour or >2,000 mL within 24 hours define massive bleeding 3
  • Hemoglobin ≤8.0 g/dL with shock indicates life-threatening hemorrhage 3

High-Risk Features Requiring Aggressive Intervention

  • Active hematemesis with cardiovascular instability - proceed directly to resuscitation and urgent endoscopy 1, 2
  • Peritoneal signs or abdominal distension - suggests perforation or bowel ischemia requiring emergency surgery 5
  • Known cirrhosis or suspected varices - mortality approaches 30% 4
  • Anticoagulant use (warfarin, DOACs) - increases bleeding risk substantially 6

Immediate Management Protocol

Resuscitation (First Priority)

  • Transfusion threshold: hemoglobin <70 g/L (target 70-100 g/L), but use <90 g/L threshold if cardiovascular disease is present 1
  • Initiate large-bore IV access and aggressive crystalloid resuscitation 5
  • Correct coagulopathy: fresh frozen plasma if INR >1.5, prothrombin complex concentrate for warfarin reversal 1, 6
  • Target fibrinogen >1.5 g/L and platelets >75 × 10⁹/L in active bleeding 1

Pharmacological Therapy

Administer high-dose intravenous proton pump inhibitor (omeprazole 80 mg bolus, then 8 mg/hour infusion) immediately before endoscopy - this reduces rebleeding rates, transfusion requirements, and hospital stay 1, 2.

If cirrhosis/varices suspected, give terlipressin immediately 1.

Urgent Endoscopy Timing

  • Within 24 hours for all patients - success rate is highest within first 36 hours 4, 2
  • Immediate endoscopy (<12 hours) if hemodynamically unstable, ongoing hematemesis, or suspected variceal bleeding 1, 2

Endoscopic Treatment Options

For peptic ulcers with high-risk stigmata (active bleeding, visible vessel, adherent clot):

  • Combination therapy is superior: dilute adrenaline injection PLUS thermal coagulation (heater probe/BICAP) or mechanical clips 1, 2
  • Adrenaline injection alone is insufficient for high-risk ulcers 1
  • Avoid sclerosants (can cause life-threatening necrosis) and absolute alcohol (perforation risk) 1

For varices: endoscopic band ligation preferred over sclerotherapy 2

Anticoagulant Considerations

Warfarin Reversal

Patients on warfarin have significantly increased bleeding risk, particularly with INR >4.0, age ≥65, history of GI bleeding, or concomitant NSAIDs 6.

Reverse immediately with prothrombin complex concentrate (dose based on INR: 25 units/kg for INR 2-3.9,35 units/kg for INR 4-5.9,50 units/kg for INR >6) plus intravenous vitamin K 5-10 mg 1.

Direct Oral Anticoagulants (DOACs)

Critical limitation: dabigatran, rivaroxaban, apixaban, and edoxaban cannot be reversed with standard agents 1. Supportive care with transfusion and prothrombin complex concentrate may provide partial benefit.

When Surgery is Required

Immediate surgical consultation if:

  • Hemodynamic instability despite aggressive resuscitation 5
  • Failed endoscopic therapy or rebleeding after repeat endoscopy 2
  • Peritoneal signs, pneumoperitoneum, or suspected perforation 5
  • Persistent bleeding requiring >6 units packed red blood cells 1

Common Pitfalls to Avoid

  • Do not delay endoscopy - mortality increases significantly after 36 hours 4
  • Do not use H2-receptor antagonists - they do not reliably raise gastric pH above 6 and are ineffective 1
  • Avoid vasopressors if possible in suspected mesenteric ischemia - they worsen bowel perfusion 5
  • Do not perform routine phlebotomy in cyanotic patients unless severe hyperviscosity symptoms with hematocrit >65% 1
  • Never assume bleeding has stopped - 25% rebleed after initial cessation, mostly within 48 hours 4

Post-Stabilization Monitoring

Admit to critical care for:

  • Continuous hemodynamic monitoring 1
  • Serial hemoglobin, coagulation studies, and blood gases 1
  • Venous thromboprophylaxis once bleeding controlled (patients rapidly develop prothrombotic state) 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Management of haematemesis and melaena.

Postgraduate medical journal, 2004

Research

[Hematemesis. Extramural emergency].

Schweizerische medizinische Wochenschrift, 1993

Guideline

Ischemic Colitis Secondary to Metoclopramide-Induced Mesenteric Vasoconstriction

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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