[QTc prolongation induced by intravenous sedation with Haloperidol, Prothipendyl and Lorazepam]

Joachim Scharfetter1, Peter Fischer

  • 1Abteilung für Psychiatrie, Sozialmedizinisches Zentrum Ost - Donauspital, Wiener Krankenanstaltenverbund, Langobardenstraße 122, 1220, Wien, Österreich, joachim.scharfetter@wienkav.at.

Insights

Intravenous Haloperidol and Prothipendyl can prolong QTc intervals, with Prothipendyl showing more pronounced effects. Combination therapy significantly increases QTc prolongation, necessitating cardiac monitoring for both drugs.

Area of Science:

  • Cardiology
  • Psychopharmacology
  • Clinical Pharmacology

Background:

  • Intravenous Haloperidol is frequently used for acute psychosis sedation despite cardiac risks (QTc prolongation).
  • IV administration offers crucial advantages, yet its use is restricted due to safety concerns.
  • Prothipendyl is a low-potency neuroleptic for unspecific sedation.

Purpose of the Study:

  • To objectively assess QTc prolongation caused by intravenous Haloperidol and Prothipendyl.
  • To compare the QTc prolonging effects of Haloperidol monotherapy, Prothipendyl monotherapy, and their combination.

Main Methods:

  • ECG monitoring of patients receiving IV Haloperidol, Prothipendyl, or Lorazepam (control) over 3 years.
  • Analysis of QTc prolongation in different treatment subgroups.
  • Non-parametric statistical tests were used due to non-normal data distribution.

Main Results:

  • Haloperidol/Prothipendyl combination and Prothipendyl monotherapy showed significant QTc prolongation compared to Lorazepam.
  • Haloperidol monotherapy did not result in significant QTc prolongation.
  • Combination therapy exhibited a greater QTc prolongation than Haloperidol monotherapy.

Conclusions:

  • IV Haloperidol causes significant QTc prolongation, but IV Prothipendyl's effect is more pronounced.
  • Combined Haloperidol and Prothipendyl therapy leads to the most significant QTc prolongation, likely a dose-dependent effect.
  • ECG monitoring is recommended for both Haloperidol and Prothipendyl IV administration due to ongoing clinical need and lack of alternatives.
Abstract

Related Concept Videos

Parenteral Anesthetics: Overview01:24

Parenteral Anesthetics: Overview

Intravenous anesthetics are drugs administered parenterally to induce anesthesia or sedation. Propofol is a widely used agent formulated as a 1% emulsion in soybean oil, glycerol, and egg phosphatide. It induces rapid anesthesia primarily due to its rapid distribution from the bloodstream to target tissues and is metabolized in the liver. However, it can cause significant pain on injection and hypertriglyceridemia. Fospropofol, a water-based prodrug of propofol, lacks these adverse effects.
1.0K
Sedatives and Hypnotics Drugs: Miscellaneous Agents01:17

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...
981
Sedatives and Hypnotics Drugs: Benzodiazepines01:19

Sedatives and Hypnotics Drugs: Benzodiazepines

Benzodiazepines have both sedative and hypnotic properties. They include compounds such as diazepam (Valium) and alprazolam (Xanax). Structurally, their cores are similar, consisting of the fusion of a benzene ring and a diazepine ring, but they share a common mechanism of action in the central nervous system (CNS).
Benzodiazepines work by enhancing the effects of the inhibitory neurotransmitter GABA. They bind to the GABAA receptor, increasing its affinity for GABA, which opens chloride...
1.5K
Sedatives and Hypnotics Drugs: Barbiturates01:20

Sedatives and Hypnotics Drugs: Barbiturates

Sedatives and hypnotics encompass a drug class that acts on the central nervous system (CNS) to alleviate anxiety, promote relaxation and induce sleep.These drugs function by amplifying the actions of the neurotransmitter γ-aminobutyric acid (GABA), resulting in reduced neuronal activity. Barbiturates, a subset of sedatives and hypnotics first synthesized in the late 1800s, are categorized into ultra-short, short, intermediate, and long-acting groups based on their duration of effect. A...
1.5K
Depolarizing Blockers: Pharmocokinetics01:19

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...
784
CNS Depressants: Barbiturates and Benzodiazepines01:14

CNS Depressants: Barbiturates and Benzodiazepines

CNS depressants include drugs from the category of barbiturates and benzodiazepines. They are valuable medications for managing anxiety disorders and insomnia. Barbiturates, once used to induce and maintain sleep, have been replaced mainly by benzodiazepines due to barbiturate's toxicity, tolerance, and overdose risks. They interact with GABAA receptors, leading to sedation at low doses and potentially coma and death at higher doses. Phenobarbital, a long-acting barbiturate, possesses...
1.9K