Prolonged QT interval, syncope, and delirium with galantamine
Alexander A Fisher1, Michael W Davis
1Australian National University Medical School, Australia. alex.fisher@act.gov.au
The Annals of Pharmacotherapy
|January 10, 2008
Summary
Acetylcholinesterase inhibitors (AChIs) like galantamine can cause serious side effects including QT interval prolongation, syncope, and delirium. Careful patient monitoring is essential when prescribing these dementia medications.
Area of Science:
- Geriatric Medicine
- Clinical Pharmacology
- Neuroscience
Background:
- Acetylcholinesterase inhibitors (AChIs) are commonly prescribed for dementia.
- Galantamine is an AChI used to treat mild to moderate Alzheimer's disease.
Observation:
- An 85-year-old man experienced syncope, bradycardia, and hypotension while on galantamine.
- Discontinuation of galantamine led to cognitive and functional decline, prompting its reintroduction.
- Upon re-initiation, the patient developed syncope, delirium, hypotension, and QT interval prolongation with cardiac arrhythmias.
Findings:
- The patient's delirium resolved, and QT interval normalized after discontinuing galantamine.
- Analysis of Australian Adverse Drug Reaction Advisory Committee (ADRAC) reports revealed associations between galantamine, donepezil, and rivastigmine with delirium, syncope, bradycardia, hypotension, and arrhythmias.
- Galantamine was identified as the probable cause of the patient's adverse events.
Implications:
- AChIs, including galantamine, can precipitate serious adverse events such as QT prolongation, syncope, and delirium.
- Vigilance and risk factor assessment are crucial during galantamine and other AChI administration.
- Healthcare providers should carefully weigh the benefits and risks of AChIs in elderly patients.
Related Concept Videos
Antiepileptic Drugs: Potassium Channel Activators
Ezocgabine or retigabine, an antiepileptic drug of remarkable efficacy, has revolutionized the management of seizures. It is a potassium channel activator, explicitly targeting the family of Q subtype potassium channels. It enhances the transmembrane potassium currents, regulating neuronal excitability. This action stabilizes the resting membrane potential, a pivotal factor in mitigating the hyperexcitability that characterizes epilepsy.
Ezogabine has gained approval as an adjunctive treatment...
Ezogabine has gained approval as an adjunctive treatment...
Sedatives and Hypnotics Drugs: Miscellaneous Agents
Sedatives and hypnotics encompass a wide range of substances, each with its unique mechanism of action, uses, and potential adverse effects.
Melatonin congeners like ramelteon (Rozerem) and tasimelteon (Hetlioz) selectively bind to melatonin receptors (MT1 and MT2) and thus mimic the actions of melatonin, a hormone that regulates sleep-wake cycles. Tasimelteon is primarily used for non-24-hour sleep-wake disorder, common in blind patients. They are also used to treat conditions like insomnia...
Melatonin congeners like ramelteon (Rozerem) and tasimelteon (Hetlioz) selectively bind to melatonin receptors (MT1 and MT2) and thus mimic the actions of melatonin, a hormone that regulates sleep-wake cycles. Tasimelteon is primarily used for non-24-hour sleep-wake disorder, common in blind patients. They are also used to treat conditions like insomnia...
Parkinson's Disease: Treatment
Neurodegenerative disorders, such as Parkinson's Disease (PD), involve the gradual and irreversible destruction of neurons in particular brain areas. These disorders exhibit standard features like proteinopathies, selective vulnerability of some neurons, and an interaction of intrinsic properties, genetics, and environmental influences in neural injury.
Parkinson's Disease is primarily a result of the loss of dopaminergic neurons in the substantia nigra pars compacta. The cornerstone of its...
Parkinson's Disease is primarily a result of the loss of dopaminergic neurons in the substantia nigra pars compacta. The cornerstone of its...
Alzheimer's Disease: Treatment
Alzheimer's Disease (AD), a neurodegenerative disorder, is pathologically identified by amyloid plaques and neurofibrillary tangles composed of tau protein. AD pharmacotherapy aims to manage cognitive symptoms, delay disease progression, and treat behavioral symptoms. The treatment is primarily symptomatic and palliative, with no definitive disease-modifying therapy available. Cholinesterase inhibitors, including donepezil (Aricept), rivastigmine (Exelon), and galantamine (Razadyne), are...
Hepatic Encephalopathy
DefinitionHepatic encephalopathy is a reversible neurologic syndrome that results from advanced liver dysfunction or portosystemic shunting. It leads to disturbances in cognition, behavior, and motor function due to the brain’s exposure to gut-derived toxins that the liver fails to detoxify.EtiologyThis condition develops either in the setting of acute fulminant hepatitis or progressively during chronic liver disease, such as cirrhosis and portal hypertension. Portosystemic shunting—including...
Antiarrhythmic Drugs: Class III Agents as Potassium Channel Blockers
Class III antiarrhythmic drugs are a group of medications that can prolong action potentials in the heart. They achieve this by blocking potassium channels or enhancing inward currents from sodium channels. However, these drugs have a unique property of "reverse use-dependence," which is most pronounced at slower heart rates and can lead to torsades de pointes—a specific type of arrhythmia. However, it is essential to note that excessive QT interval prolongation—a measure of the heart's...

