Theophylline toxicity: Difference between revisions

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==Evaluation==
==Evaluation==
*Theophylline level
*Theophylline level<ref name="Aggelopoulou">Aggelopoulou, E., Tzortzis, S., Tsiourantani, F., Agrios, I., & Lazaridis, K. (2018). Atrial Fibrillation and Shock: Unmasking Theophylline Toxicity. Medical principles and practice : international journal of the Kuwait University, Health Science Centre, 27(4), 387-391.</ref>
**10–20 μg/mL - Therapeutic
**20-80 μg/mL - Toxic level
**80-100 μg/mL - Severe toxicity or death
*[[ECG]]
*[[ECG]]
*Metabolic panel
*Metabolic panel
*Lactic acid level
*Lactic acid level
*CK
*CK
*Evaluate for co-ingestion


==Management==
==Management==
*Supportive care is the mainstay of treatment
*Supportive care is the mainstay of treatment
*Cardiovascular
*Cardiovascular
**Consider norepinephrine (alpha-agonist) for hypotension
**Norepinephrine (alpha-agonist) for hypotension resistant to IVF
**Refractory hypotension may respond to non-selective beta-blockers<ref name="Fisher" />
**Refractory hypotension may respond to non-selective beta-blockers<ref name="Fisher" />
**Beta-blockers (esmolol preferred due to short half-life) for tachydysrhythmias
*GI decontamination ([[Multidose Activated Charcoal]], [[Whole Bowel Irrigation]])
*GI decontamination ([[Multidose Activated Charcoal]], [[Whole Bowel Irrigation]])
**Consider in recent severe overdose
**Consider in recent severe overdose
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**Phenobarbital if [[lorazepam]] ineffective
**Phenobarbital if [[lorazepam]] ineffective
**Phenytoin (Dilantin) contraindicated as increases seizure in animal studies
**Phenytoin (Dilantin) contraindicated as increases seizure in animal studies
*Dialysis
*Dialysis or plasmapheresis
**Indicated in [[seizures]], severe [[arrhythmias]]
**Indicated in [[seizures]], severe [[arrhythmias]], hypotension, serum level >90 μg/mL (>40 μg/mL in chronic ingestion)
**Theophylline level >90mcg/ml in acute ingestion
**Theophylline level >40mcg/ml in chronic ingestion


==Disposition==
==Disposition==
===Immediate release===
*Almost all patients will require admission
*Home after 6 hours if:
*Can consider discharge with close followup (in conjunction with toxicology) if unintentional overdose, asymptomatic, and normal vital signs
**nontoxic
**asymptomatic
**and, normal vital sign
 
===Sustained release===
*Home after 12 hours if:
**nontoxic
**asymptomatic
**and, normal vital sign


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

Latest revision as of 23:51, 15 November 2018

See theophylline for general drug information.

Background

  • Primarily used as a bronchodilator, however rarely used now due to better available options
  • Also studied for treatment of Acute Mountain Sickness and Contrast-Induced Nephropathy
  • PO available as elixer and capsule (12 or 24-hour extended release)
  • IV as aminophylline (shorter acting than PO)
  • Mechanism of action[1]:
    • Release of endogenous catecholamines → β2 agonism → bronchodilation
    • PDE inhibition → increases cAMP
    • Adenosine antagonist

Clinical Features

Differential Diagnosis

Evaluation

  • Theophylline level[2]
    • 10–20 μg/mL - Therapeutic
    • 20-80 μg/mL - Toxic level
    • 80-100 μg/mL - Severe toxicity or death
  • ECG
  • Metabolic panel
  • Lactic acid level
  • CK
  • Evaluate for co-ingestion

Management

  • Supportive care is the mainstay of treatment
  • Cardiovascular
    • Norepinephrine (alpha-agonist) for hypotension resistant to IVF
    • Refractory hypotension may respond to non-selective beta-blockers[1]
    • Beta-blockers (esmolol preferred due to short half-life) for tachydysrhythmias
  • GI decontamination (Multidose Activated Charcoal, Whole Bowel Irrigation)
  • Seizures
    • Lorazepam (Ativan) 1st line
    • Phenobarbital if lorazepam ineffective
    • Phenytoin (Dilantin) contraindicated as increases seizure in animal studies
  • Dialysis or plasmapheresis
    • Indicated in seizures, severe arrhythmias, hypotension, serum level >90 μg/mL (>40 μg/mL in chronic ingestion)

Disposition

  • Almost all patients will require admission
  • Can consider discharge with close followup (in conjunction with toxicology) if unintentional overdose, asymptomatic, and normal vital signs

See Also

External Links

References

  1. 1.0 1.1 Fisher, J., & Graudins, A. (2015). Intermittent haemodialysis and sustained low-efficiency dialysis (SLED) for acute theophylline toxicity. Journal of medical toxicology : official journal of the American College of Medical Toxicology, 11(3), 359-63.
  2. Aggelopoulou, E., Tzortzis, S., Tsiourantani, F., Agrios, I., & Lazaridis, K. (2018). Atrial Fibrillation and Shock: Unmasking Theophylline Toxicity. Medical principles and practice : international journal of the Kuwait University, Health Science Centre, 27(4), 387-391.