Kratom toxicity: Difference between revisions

No edit summary
Line 8: Line 8:
*Effects are dose dependent and may mimic those of both opioid and stimulant toxicity
*Effects are dose dependent and may mimic those of both opioid and stimulant toxicity
*Stimulant effects typically predominate at low doses (<5 g) with sedating effects more prevalent at higher doses
*Stimulant effects typically predominate at low doses (<5 g) with sedating effects more prevalent at higher doses


==Differential Diagnosis==
==Differential Diagnosis==
Line 19: Line 18:
*Clinical diagnosis
*Clinical diagnosis
*Labs not routinely required unless severe vomiting, seizure, or unclear diagnosis
*Labs not routinely required unless severe vomiting, seizure, or unclear diagnosis


==Management==
==Management==
Line 27: Line 25:
**NSAIDs, antiemetics, fluids, etc. for opioid withdrawal symptoms
**NSAIDs, antiemetics, fluids, etc. for opioid withdrawal symptoms
***Medication-assisted treatment with buprenorphine or methadone
***Medication-assisted treatment with buprenorphine or methadone


==Disposition==
==Disposition==
*Discharge unless presenting with severe/intractable symptoms
*Discharge unless presenting with severe/intractable symptoms


==See Also==
==See Also==


==External Links==
==External Links==


==References==
==References==

Revision as of 19:32, 27 June 2019

Background

  • Derived from Mitragyna speciosa, a plant native to Southeast Asia
  • Contains numerous chemicals acting on mu opioid, adrenergic, serotonin, and GABA receptors
  • Increasingly popular in US for attempted self-treatment of pain, opioid addiction/withdrawal, and depression
    • Patients often perceive incorrectly as a "safe" alternative to opioids

Clinical Features

  • Effects are dose dependent and may mimic those of both opioid and stimulant toxicity
  • Stimulant effects typically predominate at low doses (<5 g) with sedating effects more prevalent at higher doses

Differential Diagnosis

Evaluation

  • Clinical diagnosis
  • Labs not routinely required unless severe vomiting, seizure, or unclear diagnosis

Management

  • Management should be tailored to primary symptoms
    • Naloxone for respiratory depression
    • Benzodiazepines for hyperarousal, tachycardia, hypertension, and seizures
    • NSAIDs, antiemetics, fluids, etc. for opioid withdrawal symptoms
      • Medication-assisted treatment with buprenorphine or methadone

Disposition

  • Discharge unless presenting with severe/intractable symptoms

See Also

External Links

References

  • Swogger M, Walsh D. Kratom use and mental health: A systematic review. Drug and Alcohol Dependence. 2017;183:134-140.
  • Vestal C. Kratom Concerns. State Legislatures Magazine. 2018; 44(4)
  • Killelea E. Kratom: Why Did the FDA Declare the Herbal Supplement an Opiate? Rolling Stone Magazine. March 2018.
  • Gottlieb, S. Statement from FDA Commissioner Scott Gottlieb, M.D., on new warning letters FDA is issuing to companies marketing kratom with unproven medical claims; and the agency’s ongoing concerns about kratom [press release]. Sep 11, 2018.