Around the world, theophylline (1,3-dimethylxanthine) is primarily used as a bronchodilator for patients with asthma and chronic obstructive pulmonary disease (COPD). However, in the United States, asthma and COPD are mainly treated with other agents, and theophylline is largely used to treat bradycardia and apnea in premature newborns. Theophylline causes endogenous release catecholamines through indirect stimulation of beta-1 and beta-2 receptors, which at therapeutic levels cause desired bronchodilation. Unfortunately, theophylline has a narrow therapeutic window, and even levels slightly above this therapeutic window can have many adverse effects in the setting of acute and chronic toxicity. The excess circulating catecholamines cause the serious clinical effects that are associated with theophylline toxicity. Depending on the dose and route of administration, theophylline can have a wide range of cardiovascular, neurologic, metabolic, musculoskeletal and gastrointestinal manifestations. Emergency department providers should become familiar with how to manage patients with theophylline toxicity since arrhythmias, seizures, hyperglycemia, and rhabdomyolysis are several of the complications that can arise.
Theophylline has an extremely narrow therapeutic window. Theophylline toxicity occurs when serum theophylline levels surpass the levels in the therapeutic range. This can occur by intentional overdose or unintentionally when metabolism and/or clearance of theophylline is altered due to certain physiological stressors.
Toxic exposures to theophylline have decreased significantly since its management for asthma and COPD has declined. From 1985 to 1995 in the United States, theophylline poisoning requiring hemodialysis or hemoperfusion accounted for 49 cases per one million poison center calls, compared to the 6 cases per one million poison center calls from 1996 to 2005. According to the American Association of Poison Control Centers, there were 133 exposures to theophylline in 2014. Of these, 14 were in children younger than 6 years old, and 107 were in patients older than 19 years old. There were 2 deaths out of 81 patients treated for theophylline exposure treated at healthcare facilities.
Theophylline has 2 primary mechanisms. One mechanism is that theophylline blocks adenosine receptors, which has both therapeutic and toxic effects such as bronchodilation, tachycardia, cardiac arrhythmias, seizures, and cerebral vasoconstriction. At larger doses, theophylline inhibits phosphodiesterase causing increased cyclic adenosine monophosphate resulting in increased levels of adrenergic activation and catecholamine release. In theophylline toxicity, epinephrine levels can be 4- to 8-times higher than normal, and norepinephrine concentrations can be 4- to 10-times higher than normal. Increased catecholamine concentrations have a variety of adverse effects such as cardiac arrhythmias, metabolic acidosis, hyperglycemia, and hypokalemia. Chronic theophylline toxicity can occur when there is an accumulation of the drug due to metabolism being overwhelmed or inhibited. It can also occur when clearance is decreased.
Toxic doses of theophylline can be as low as 7.5 mg/kg. When taken orally, 80% to 100% of theophylline is absorbed in the gastrointestinal tract. Peak serum levels can occur from 30 to 120 minutes for immediate release formulations. Sustained release formulations have peak levels between 6 and 10 hours. Intravenously, theophylline takes 30 minutes to reach peak levels. Therapeutic serum levels range from 10 to 20 mcg/mL. Toxic levels are considered to be 20 mcg/mL or higher. However, toxic effects can be seen within therapeutic levels as well. Cardiac dysrhythmias, seizures, and death can be seen with levels of 80 to 100 mcg/mL. Chronic toxicity can be seen at levels of 40 to 60 mcg/mL. Fifty percent to 65% of theophylline is protein-bound in the circulation. Volume distribution is small, at 0.45 L/kg. The half-life varies with age. A half-life of 4 to 8 hours is seen in young adults. A shorter half-life is seen in newborns. Theophylline is metabolized in the liver by the cytochrome P450 system and excreted by the kidneys. Therefore, any agents or pathology that alters the cytochrome P450 system or renal function can have a substantial effect on theophylline levels.
Depending on the dose, route of administration, and coingestants, there is a wide spectrum of clinical effects of theophylline toxicity, ranging from abdominal pain to cardiac arrhythmias to seizures. Many times, patients cannot give a clear history, so it is imperative to obtain a history from EMS personnel, family, friends, and witnesses.
Workup should include the following:
Most patients with theophylline toxicity are successfully managed with supportive care. Airway, breathing, circulation, and hemodynamic monitoring are essential to the care of patients with theophylline toxicity. Intubation with ventilator support may be required for airway protection.
GI decontamination: Activated charcoal (1 g/kg) by mouth or nasogastric tube is recommended in patients that present to the emergency department within if there are no contraindications to activated charcoal. Gastric lavage or induced emesis is not recommended in theophylline toxicity. Whole bowel irrigation is controversial as animal models do not demonstrate that it is a beneficial therapy. Multiple-dose activated charcoal is recommended for acute theophylline toxicity if there are no contraindications.
Hypotension-isotonic saline (20 mL/kg): Hypotension refractory to IV fluid administration, an alpha agonist such as phenylephrine is recommended. Primarily alpha agonists such as norepinephrine can be used as well. Treatment of hypotension with a beta antagonist should only be used in consultation with a toxicologist.
Nausea and vomiting: Ondansetron is recommended. Metoclopramide can be used in cases that are refractory to ondansetron.
Cardiac arrhythmias: Treatment of cardiac arrhythmias should be managed according to advanced cardiac life support and pediatric advanced life support protocols.
Seizures: In adults benzodiazepines (lorazepam, midazolam, diazepam) are the first-line treatment for theophylline-induced seizures. Phenobarbital and continuous infusion of propofol or midazolam can be used for seizures refractory to benzodiazepines. In pediatrics, benzodiazepines are the first-line treatment for seizures. Phenobarbital or continuous infusion of midazolam or pentobarbital or propofol can be used refractory seizures.
Hemodialysis: In acute overdose, hemodialysis is indicated for life-threatening arrhythmias and seizures, theophylline levels greater than 100 mcg/mL, clinical instability, or increased theophylline levels despite appropriate care. In chronic theophylline toxicity, hemodialysis is indicated with severe symptoms, such as life-threatening arrhythmias, seizures, and theophylline levels greater than 60 mcg/mL in patients between the ages of 6 months to 60 years, or levels greater than 50 mcg/mL in patients of age less than 6 months or greater than 60 years. Hemodialysis is preferred as opposed to hemoperfusion. However, if hemodialysis is not available, hemoperfusion may be used instead. Decisions to initiate hemodialysis or hemoperfusion should always be made in consultation with a medical toxicologist.
Theophylline toxicity is best managed in a multidisciplinary fashion. The drug can affect many organ systems including the heart, lung, central nervous system (CNS), and GI tract. The key to theophylline toxicity is prevention. First, healthcare providers should avoid prescribing this agent for asthma when other safer drugs are available. All patients should be educated about the dangers of theophylline. Parents should be told to store theophylline in a safe place away from the reach of children. For those who intentionally overdose on the drug, a mental health consult is recommended before discharge. (Level V)
Only anecdotal reports and small case series exist on short-term outcomes after theophylline toxicity. However, despite the few cases being reported, the drug is associated with high morbidity and mortality. Several deaths have been reported both in the United States and abroad following theophylline toxicity. But overall, the number of cases of theophylline toxicity are subsiding as healthcare providers are no longer prescribing this agent for asthma. (Level V)
|||Greene SC,Halmer T,Carey JM,Rissmiller BJ,Musick MA, Theophylline toxicity: An old poisoning for a new generation of physicians. Turkish journal of emergency medicine. 2018 Mar [PubMed PMID: 29942882]|
|||Sharma S,Chakraborty RK, Asthma Medications null. 2018 Jan [PubMed PMID: 30285350]|
|||Aggelopoulou E,Tzortzis S,Tsiourantani F,Agrios I,Lazaridis K, Atrial Fibrillation and Shock: Unmasking Theophylline Toxicity. Medical principles and practice : international journal of the Kuwait University, Health Science Centre. 2018 [PubMed PMID: 29936503]|
|||Khan Z,Khan MS, Rare Case of Theophylline Toxicity due to Influenza A Infection in an Adult With Asthma. American journal of therapeutics. 2018 Jul 10 [PubMed PMID: 30048245]|
|||Monteiro J,Alves MG,Oliveira PF,Silva BM, Pharmacological potential of methylxanthines: Retrospective analysis and future expectations. Critical reviews in food science and nutrition. 2018 Apr 6 [PubMed PMID: 29624433]|
|||Blix HS,Viktil KK,Moger TA,Reikvam A, Drugs with narrow therapeutic index as indicators in the risk management of hospitalised patients. Pharmacy practice. 2010 Jan [PubMed PMID: 25152793]|
|||Mohamad N,Abd Halim NN,Ahmad R,Baharuddin KA, Theophylline toxicity: A case report of the survival of an undiagnosed patient who presented to the emergency department. The Malaysian journal of medical sciences : MJMS. 2009 Apr [PubMed PMID: 22589656]|
|||Shannon MW, Comparative efficacy of hemodialysis and hemoperfusion in severe theophylline intoxication. Academic emergency medicine : official journal of the Society for Academic Emergency Medicine. 1997 Jul [PubMed PMID: 9223689]|