What is the appropriate management and treatment for a patient who has ingested rat cake (rodenticide bait)?

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Rat Cake (Rodenticide) Poisoning Management

Immediate Actions

Contact poison control immediately (1-800-222-1222 in the US) and prioritize supportive care over identifying the specific rodenticide type—focus on airway management, hemodynamic support, and correcting critical vital signs before confirmation of the toxin. 1, 2

Life-Threatening Presentations

  • Activate EMS immediately if the patient exhibits sleepiness, seizures, difficulty breathing, or vomiting after rodenticide exposure 3, 2
  • Secure the airway early if there is CNS depression, loss of protective reflexes, or respiratory compromise 2, 4
  • Establish IV access and correct hemodynamic instability before pursuing specific antidote therapy 2

What NOT to Do

Critical Pitfalls to Avoid

  • Do NOT delay supportive care while awaiting rodenticide identification—treatment must begin immediately based on clinical presentation 1, 2
  • Do NOT administer activated charcoal, ipecac, or perform gastric lavage in presentations beyond 1-2 hours post-ingestion, as these are ineffective once absorption has occurred and only delay definitive care 3, 1, 2, 5
  • Do NOT give milk or water for dilution unless specifically advised by poison control—there is insufficient evidence of benefit and it may cause emesis and aspiration 3, 2
  • Do NOT administer vitamin K prophylactically before coagulopathy is documented in asymptomatic patients without significant exposure 1, 5

Risk Stratification and Monitoring

Low-Risk Patients (Can Be Observed at Home)

  • Unintentional ingestion of <1 mg active ingredient (includes practically all unintentional pediatric ingestions in children <6 years) can be safely observed at home without laboratory monitoring 5
  • No routine INR measurement is necessary for young children with typical unintentional exposures 6

Moderate-Risk Patients (Require Outpatient Monitoring)

  • Unintentional ingestion of ≥1 mg active ingredient in asymptomatic patients should have coagulopathy evaluation at 48-72 hours post-exposure 5
  • Patients on therapeutic anticoagulants who ingest any dose should have baseline prothrombin time measured, then repeated at 48-72 hours 5
  • If INR is normal at 36-48 hours post-exposure, even with long-acting formulations, no further action is required 6

High-Risk Patients (Require Emergency Department Evaluation)

  • Any suspected self-harm, abuse, misuse, or malicious administration—refer immediately regardless of reported dose 5
  • Any symptoms of bleeding or bruising—refer immediately regardless of reported dose 5
  • Chronic ingestion—refer immediately for evaluation of intent and potential coagulopathy 5

Management of Established Coagulopathy

For Active Bleeding

Administer prothrombin complex concentrate 50 units/kg (preferred), OR recombinant activated factor VII 1.2-4.8 mg, OR fresh frozen plasma 15 mL/kg if concentrate unavailable, PLUS phytomenadione (vitamin K1) 10 mg IV (100 mcg/kg for children). 6, 7

For Elevated INR Without Active Bleeding

  • INR <4.0: No treatment required 6
  • INR ≥4.0: Administer phytomenadione 10 mg IV 6

Long-Term Management of Anticoagulant Rodenticide Poisoning

  • Acute hemorrhagic symptoms often require IV vitamin K1 in excess of 50-100 mg 2, 8
  • Chronic maintenance typically requires 100 mg PO vitamin K1 daily to suppress coagulopathy 8
  • Treatment courses average 168 days for long-acting anticoagulant rodenticides 8
  • Monitor for metabolic derangements requiring immediate correction 1, 2

Important caveat: Normalization of INR alone is insufficient to discontinue vitamin K1 treatment—over half of patients may have serum rodenticide concentrations above safe levels (>10 ng/mL) despite normal INR, risking symptom recurrence 9

Management of Specific Complications

Intracranial Hemorrhage

  • Administer benzodiazepines for seizures or agitation 1, 2
  • Perform EEG monitoring for non-convulsive seizures in patients with altered mental status 1, 2

Rebound Coagulopathy

  • Long-acting anticoagulant rodenticides have extremely high affinity for vitamin K epoxide reductase compared to warfarin, characterized by rebound coagulopathy after initial treatment 8
  • Phenobarbital has been used to expedite rodenticide metabolism in severe cases 8

When to Consult Medical Toxicology

  • Complex presentations with multiorgan bleeding 1, 2
  • Late presentations with established coagulopathy and bleeding 1, 2
  • Prolonged coagulopathy requiring extended treatment courses 1

Decontamination

  • Remove all contaminated clothing and avoid self-contamination when handling the patient 4
  • For dermal exposures, wash skin with mild soap and water 5
  • For chemical powder exposure, brush off with gloved hand before washing 3

References

Guideline

Management of Late Presentation Rodenticide Poisoning

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Treatment of Rodenticide Ingestion

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Management of Rodenticide Poisoning

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Anticoagulant rodenticides.

Toxicological reviews, 2005

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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