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Related Concept Videos

Antiarrhythmic Drugs: Class III Agents as Potassium Channel Blockers01:12

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...
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Sulfonylureas are oral hypoglycemic agents utilized in treating type 2 diabetes. They are characterized by their unique sulfonylurea chemical structure. The family of sulfonylureas is divided into generations. First-generation sulfonylureas, including tolbutamide (Orinase), chlorpropamide (Diabinese), and tolazamide (Tolinase), trigger insulin release from pancreatic β cells and enhance peripheral tissues' insulin sensitivity. The second-generation members, such as glipizide (Glucotrol),...
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Depolarizing Blockers: Pharmocokinetics

Depolarizing blockers are administered through intravenous injection. Succinylcholine is the most common choice of depolarizing blockers in emergency clinical practices. Although they have a rapid onset, they readily diffuse away from the motor end plate into the extracellular fluid. They are metabolized by enzymes such as liver butyrylcholinesterase and plasma pseudocholinesterases. This produces a short duration of action, typically 5-10 minutes long, unlike nondepolarizing blockers, which...
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Dysrhythmias VI: Management of Dysrhythmias

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Antiarrhythmic Drugs: Class I Agents as Sodium Channel Blockers01:22

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Class I antiarrhythmic drugs are used to treat various types of arrhythmias or irregular heart rhythms. These drugs block the sodium (Na+) channels in the cardiac cells, thereby affecting the movement of electrical impulses across the heart. Class I antiarrhythmic drugs are divided into three subgroups: Class IA, Class IB, and Class IC, each with distinct mechanisms of action and effects on the heart.
Class 1A Antiarrhythmic Drugs: These drugs work by moderately blocking sodium channels,...

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Sulpiride induced torsade de pointes.

Bien-Hsien Huang, Chih-Ping Hsia, Chung-Yin Chen

    International Journal of Cardiology
    |April 6, 2007
    PubMed
    Summary

    Antipsychotic medications can prolong the QT interval, increasing torsade de pointes risk. Sulpiride caused this dangerous heart rhythm in a patient, highlighting the need for close monitoring.

    Area of Science:

    • Cardiology
    • Psychiatry
    • Clinical Pharmacology

    Background:

    • Antipsychotic medications are frequently associated with cardiac adverse events, including QT interval prolongation and potentially fatal torsade de pointes.
    • Identifying specific agents and risk factors is crucial for patient safety in psychiatric care.

    Observation:

    • A 69-year-old female presented with syncope, revealing torsade de pointes and a significantly prolonged QT interval (QTc=680 ms) on electrocardiogram.
    • Detailed drug history identified sulpiride as the causative agent responsible for the observed cardiac event.

    Findings:

    • Discontinuation of sulpiride led to a rapid normalization of the QT interval (QTc=420 ms), confirming its role in the torsade de pointes episode.
    • This case underscores the proarrhythmic potential of sulpiride, particularly concerning its effects on cardiac repolarization.

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    Implications:

    • Clinicians must exercise vigilance when prescribing sulpiride, closely monitoring patients for signs of QT prolongation and cardiac arrhythmias.
    • Concurrent use of sulpiride with other medications known to affect the QT interval, such as certain antidepressants, warrants heightened caution and careful risk-benefit assessment.