What is the management of barbiturate poisoning?

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Management of Barbiturate Poisoning

Optimal supportive care with airway protection is mandatory in all cases of barbiturate poisoning, with multiple-dose activated charcoal (MDAC) as first-line enhanced elimination therapy, and extracorporeal treatment (ECTR) reserved for severe cases with prolonged coma, shock, or respiratory failure. 1, 2

Initial Stabilization and Assessment

Immediate Interventions

  • Secure the airway and provide respiratory support, including intubation and mechanical ventilation for patients exhibiting respiratory depression, as barbiturates suppress the medullary respiratory center 1, 2
  • Hemodynamic stabilization with aggressive fluid resuscitation is critical for hypotension and shock, since cardiovascular depression occurs when medullary vasomotor centers are depressed 1, 2
  • Administer oxygen, naloxone (if co-ingestion suspected), glucose, and thiamine in patients with altered mental status 3

Clinical Assessment Parameters

  • Monitor for the barbiturate toxidrome: CNS depression (sedation, sluggishness, lack of coordination, slow speech, drowsiness progressing to coma), respiratory depression with shallow breathing, and cardiovascular depression with hypotension 1
  • Obtain serum barbiturate concentration, particularly for phenobarbital (therapeutic range 10-25 mg/L; >50 mg/L may induce coma; >80 mg/L may be fatal), though serum levels confirm diagnosis but do not reliably predict duration or severity of toxicity 1, 2
  • Perform urine drug screen and blood ethanol concentration to identify co-ingested drugs, as combinations with other CNS depressants (alcohol, opiates, benzodiazepines) create additive life-threatening effects 1, 2

Enhanced Elimination: Multiple-Dose Activated Charcoal

MDAC (15-20 g orally every 6 hours) is the first-line enhanced elimination therapy and should be used in all significant barbiturate poisoning cases, particularly for phenobarbital and primidone 1, 2, 4

Critical Precautions for MDAC

  • Only administer MDAC after the airway is secured and hemodynamic stabilization has been addressed 1, 2
  • Gastric emptying decreases in barbiturate toxicity, increasing risks of impaction, gut perforation, and aspiration 1
  • MDAC decreases phenobarbital elimination half-life from approximately 80 hours to 40 hours, though clinical benefit data are limited 4

Interventions NOT Recommended

  • Urinary alkalinization is no longer recommended as first-line treatment because it does not significantly increase renal clearance and MDAC is considered superior 1, 2
  • Gastric lavage and induced emesis have not consistently reduced mortality and are rarely indicated 5, 3

Extracorporeal Treatment (ECTR): Indications for Severe Cases

ECTR is indicated for long-acting barbiturate poisoning when ANY of the following conditions are met:

Strong Indications (Level 1D)

  • Prolonged coma is present or expected 1, 2
  • Shock persists after fluid resuscitation 1, 2
  • Despite MDAC treatment, toxicity persists 1, 2

Moderate Indications (Level 2D)

  • Despite MDAC treatment, serum barbiturate concentration rises or remains elevated 1
  • Respiratory depression necessitating mechanical ventilation is present 1, 2

ECTR Implementation

  • Initiate ECTR as soon as technically possible, ideally within 24 hours of barbiturate exposure 1, 2
  • Continue MDAC concurrently with ECTR for maximal barbiturate removal, as the combination provides greater removal than either alone 1, 2
  • Continue ECTR until clinical improvement is apparent 2
  • The primary goal is to reduce duration of coma and incidence of complications (pneumonia, cardiorespiratory compromise, kidney failure) 1

Rationale for ECTR

The EXTRIP Workgroup consensus supports ECTR because: (1) death after severe barbiturate poisoning is commonly reported despite full supportive care; (2) no highly effective antidote exists; (3) ECTR significantly enhances barbiturate removal compared to endogenous elimination; (4) complications are infrequent; and (5) cost may be balanced by reduced ICU duration 1

High-Risk Populations Requiring Closer Monitoring

  • Patients with chronic obstructive pulmonary disease are more susceptible to respiratory depression even at therapeutic doses 1, 2
  • Patients with congestive heart failure are more vulnerable to cardiovascular effects and hypotension 1, 2
  • Long-term barbiturate users tolerate higher doses but not higher serum concentrations before lethal toxicity, and are at greater risk of withdrawal if concentrations are reduced rapidly with ECTR 1

Common Pitfalls to Avoid

  • Do not rely solely on ingested dose or serum concentrations to guide ECTR decisions—clinical status is paramount, as estimates are often inaccurate and interpatient variability is significant 1
  • Do not delay airway protection—death from barbiturate overdose is often due to aspiration pneumonia caused by respiratory depression 1
  • Do not use MDAC without first securing the airway—aspiration risk is significantly elevated 1, 2
  • Recognize that patients can have rapid decline in mental or hemodynamic status even when initially appearing to compensate 6

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Treatment of Phenobarbital Overdose

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Approach to the poisoned patient.

Disease-a-month : DM, 1996

Research

Enhanced elimination in acute barbiturate poisoning - a systematic review.

Clinical toxicology (Philadelphia, Pa.), 2011

Research

Clinical toxicology: part I. Diagnosis and management of common drug overdosage.

Critical care and resuscitation : journal of the Australasian Academy of Critical Care Medicine, 2002

Research

Recognition and management of acute medication poisoning.

American family physician, 2010

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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