Adrenergic storm

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An adrenergic storm is a sudden and dramatic increase in serum levels of the catecholamines adrenalin and noradrenalin (also known as epinephrine and norepinephrine respectively), with a less significant increase in dopamine transmission. It is a life-threatening condition because of extreme tachycardia and hypertension, and is especially dire for those with prior heart problems. If treatment is prompt, prognosis is good; typically large amounts of diazepam or other benzodiazepines are administered alongside beta blockers. Beta blockers are contraindicated in some patients, so other anti-hypertensive medication such as clonidine may be used. It is usually caused by overdose of stimulants, especially cocaine, but can also arise from improper eating habits while taking monoamine oxidase inhibitors. A subarachnoid hemorrhage can also cause an adrenergic storm, and catecholamine storm is part of the normal course of Rabies infection, and is responsible for the severe feelings of agitation, terror, and dysautonomia present in the pre-coma stage of the disease.

Symptoms[edit]

The symptoms are similar to those of an amphetamine, cocaine or caffeine overdose; massive overstimulation of the central nervous system results in a state of hyperkinetic movement and unpredictable mental status; the patient may become easily enraged, or alternatively suicidal, but mania is the typical reaction.

Physical symptoms are more serious and include heart arrhythmias as well as outright heart attack or stroke in people who are at risk of coronary disease. Breathing is rapid and shallow while both pulse and blood pressure are dangerously elevated.[1]

Causes[edit]

There are several known causes of adrenergic storms; in the United States, cocaine overdose is the leading cause.[2] Any stimulant drug has the capacity to cause this syndrome if taken in excess, but even non-psychotropic drugs can very rarely provoke a reaction.

MAOIs, i.e. monoamineoxidase inhibitors, are a class of drugs that inhibit the enzyme monoamine oxidase. This enzyme is responsible for breaking down many compounds; basically, anything with a primary amine moiety is likely to be oxidized by monoamine oxidase. Important substrates of the enzyme MAO include tyrosine and tyramine, which are precursors to dopamine. MAOIs inhibit the enzyme either reversibly, in which MAO is inhibited only until the drug is cleared from the system, or irreversibly, in which the substrate binds permanently to the enzyme, rendering it inactive and effectively destroying it. These types of MAOIs are more dangerous, because the body takes about two weeks to regenerate its MAO enzymes to functional levels.[3] There are also two subtypes of MAO: MAO-A and MAO-B; this is not relevant to adrenergic storms in any known way, but there are significant differences between the two types, such as their differential expression throughout the body and brain.

Harmine and moclobemide are two examples of reversible inhibitors; the first is a mild psychedelic used by recreational or spiritual drug users to greatly increase the bioavailability of DMT, normally entirely broken down by MAO in the stomach. The latter is an antidepressant and anxiolytic which works by reversibly inhibiting MAO-A and MAO-B, with a greater effect on MAO-A (80% inhibition) than MAO-B (30% inhibition).[4]

With this in mind, the importance of MAOIs to adrenergic storms is that these enzymes break down substances in food that are either precursors to stimulatory drugs, or that are themselves excitatory chemicals. Aged cheese; beer; red wine; some mushrooms; fermented products such as pickles; and many other seemingly innocuous foods can provoke a hypertensive crisis. The main culprit is tyramine, a derivative of the amino acid tyrosine that is a direct precursor to dopamine. However, other substances in food can also modulate or change the effects. Hypertension will always result, however, so patients on MAOIs must be careful what they eat.

Adrenergic storms are not provoked often from MAOI-tyramine interactions; hypertensive crisis alone does not diagnose adrenergic storm, although there will always be hypertension in an adrenergic storm, along with tachycardia and rapid, shallow breathing. However, if a patient on MAOIs uses recreational quantities of any drug with stimulant effects on the CNS, it can provoke an adrenergic crisis (along with the inevitable hypertensive crisis). Deaths have occurred from individuals attempting to combine MAOIs with various entheogens to attain a stronger psychedelic experience, both from adrenergic storms and serotonin syndrome. Combining drugs like MDMA, 2C-B, mescaline, 2C-T-7, etc. with even small quantities of MAOIs - small quantities of both drugs - is still extremely risky. Nevertheless, some users claim to use certain combinations successfully.

Subarachnoid hemorrhage is an extremely serious condition in which a neural membrane is breached and the brain itself is compromised. The onset is sudden, described as "the worst headache of one's life," and many grave symptoms follow. Adrenergic storm is often present among these symptoms, and is responsible for some of the dangers, both long-term and short, of subarachnoid hemhorrhage adrenergic storm, through a complex cascade of processes starting with the movement of subarachnoid blood into the brain. Apparently, as the intracranial pressure increases, the brain is squeezed and catecholamines are forced out of their vesicles into the synapses and extracellular space.[5] An alternative explanation that has been proposed is that this increased in intracranial pressure transduces through the brain parenchyma through to the blood vessels producing a loss in effective cerebral perfusion. This triggers the sympathetic nervous system to secrete more norepinepherine and epinepherine increasing blood pressure and heart rate to dangerous levels in order to maintain cerebral perfusion.

Rarely, a pheochromocytoma (tumor of the medullar tissue of the adrenal glands, which are located anterior to the kidney), may result in an adrenergic storm. This type of tumor is not common to begin with, and furthermore, the subtype that can cause massive adrenaline release is rarer still. Patients with pheochromocytoma can unexpectedly fly into a rage or sink into trembling fear, possibly dangerous to themselves and others as their judgment is impaired, their senses and pain threshold are heightened, and the level of the adrenalin in their bloodstream is more than most people ever experience; pheochromocytoma can, very rarely, kill by internal adrenaline overdose.[6] But overall, adrenergic storm is an uncommon but certainly not rare phenomenon associated with the unfortunate but also uncommon condition of pheochromocytoma.

Differential diagnosis[edit]

Because the adrenergic storm overlaps with so many other similar conditions, such as hypertensive crises, stimulant intoxication or overdose, or even panic attack, and because the treatments for these overlapping conditions are largely alike, it is not necessary to obtain a differential and definitive diagnosis before initiating treatment. However, analysis of the patient's medical history, checked against the possible causes of the adrenergic storm such as those above, should be done, because some adrenergic storms can be caused by serious underlying conditions. If a patient has an adrenergic storm and all or most of the other factors are ruled out, the adrenergic storm could lead to the discovery of a pheochromocytoma, which can become malignant. However, not all cases of adrenergic storm have an identifiable cause. Like a seizure, sometimes a patient has a single one, or perhaps a few, and then does not for the rest of their life. The mechanisms of idiopathic adrenergic storm are very poorly understood.

Serotonin syndrome, in which an excess of serotonin in the synapses causes a similar crisis of hypertension and mental confusion, could be confused with an adrenergic storm. The difference is that serotonin, being a tryptamine (non-catecholamine) involved in higher brain functions, can cause dangerous hypertension and tachycardia from its effects on the sympathetic nervous system, but as there are no serotonin receptors in the heart or blood vessels there are no direct effects on the heart. Thus, the presence of arrythmia, abnormal echocardiograms, or chest pain indicates an adrenergic crisis and rules out serotonin syndrome.

Treatment[edit]

If an overdose by ingestion is suspected, the patient should be given gastric lavage, activated charcoal, or both; this could make the difference between life and death in a close situation, but it should be avoided unless there is evidence of overdose as it can aggravate the patient.

The first line treatments are diazepam and a non-selective beta blocker; other antihypertensive drugs may also be used. Not all benzodiazepines and beta blockers are safe to use in an adrenergic storm; for instance, alprazolam and propranolol; alprazolam weakly agonizes dopamine receptors and causes catecholamine release while propranolol mildly promotes some catecholamine release.

After bringing the heart rate and blood pressure down, treatment is supportive; if there is an underlying condition causing the adrenergic storm, then that must be addressed. However, many cases of adrenergic storms are completely idiopathic in nature; indeed, they are a poorly understood phenomena.

References[edit]

  1. ^ Mayersohn, M., Guentert, T.W. "Clinical pharmacokinetics of the monoamine oxidase-A inhibitor moclobemide." 1995. Clinical Pharmacokinetics 29(5):292-332
  2. ^ Jones, C., Owens D., "The recreational drug user in the intensive care unit: a review." 1996. Intensive and Critical Care Nursing 12(3):126-130
  3. ^ Yamada, M., Yasuhara, H. "Clinical pharmacology of MAO inhibitors: safety and future." Neurotoxicology 25(1-2):215-21
  4. ^ Physician's Desk Reference, 2005. 59th edition.
  5. ^ Rodman, K., and Issam, A.A. 1993. "Clinical Presentation: Subarachnoid Hemorrhage." From Current Management of Cerebral Aneurysms, ed. Issam, A.A. AANS Publications Committee. pgs. 21-43
  6. ^ Whalen, R.K., et al. "Extra-adrenal pheochromocytoma." 1992. Journal of Urology 147(1):1-10.