Lorazepam metabolism is done by glucuronidation in order to form pharmacologically inactive metabolites that are excreted by the kidneys. Lorazepam IV is a long-acting benzodiazepine which is more potent sedative and amnesic than midazolam and diazepam. The effects on ventilation, the cardiovascular system, and skeletal muscles resemble those of other benzodiazepines. The elimination half-time is […]
Pain with propofol injection occurs in majority of patients. Propofol injection pain can be reduced by the following methods explained here. Propofol causes pain or discomfort on injection in 28% to 90% of awake patients. A number of techniques have been tried for minimizing propofol injection pain with variable results. The propofol injection pain decreases
Clonidine is an alpha-2 receptor agonist that down regulates the sympathetic nervous system. By stimulating alpha-2 adrenergic receptors in the brain stem, clonidine activates inhibitory pathways in the central nervous system (CNS), which results in reduced catecholamine release and reduced sympathetic outflow from the CNS. This effectively causes a decrease in blood pressure, heart rate,
Benzodiazepines effects appear to produce all their pharmacologic effects by facilitating the actions of gamma-amino butyric acid (GABA). The area where it causes it effect is the principal inhibitory neurotransmitter in the CNS by enhancing their affinity towards GABA receptors leading to increased chloride conductance and hyperpolarization of the postsynaptic cell membrane, and thereby rendering
Physiotherapy management electrotherapy is the application of electrical current to the area of generation of nociception. Physiotherapeutic methods are based on use of mainly two different modalities: 1. Electrotherapy 2. Exercise therapy This can be achieved with following methods of electrical current: • Low frequency • Medium frequency • High frequency Low frequency: i) The
Barbiturates list is explained in detail in this article. Thiopentone is prepared commercially from highly alkaline solutions as sodium salt that is readily soluble in water or saline. It is supplied as a yellowish, hygroscopic powder. The pH of a 2.5% solution of thiopental is 10.5. The following is a list of Barbiturates in common
Drugs like sufentanil, alfentanil, fentanyl and other opiates although belong to phenyl piperidine group like pethidine (meperidine), their spectrum of action is more morphine-mimicking, more like mediated through β endorphin and t receptors. Actually there are some very striking differences between the two: Fentanyl and other opiates unlike, morphine, is very highly lipid soluble, so
Ketamine is metabolized extensively by hepatic microsornal enzymes. Ketamine metabolism is demethylated to the corresponding N-desmethyl compound to form norketamine (about 60%) the main metabolite. Norketamine rapidly appears (approximately within 5 minutes) in plasma following ketamine administration and had a terminal half-life of 63.6 +1- 23.9 minutes. In animals, norketamine is one-fifth to one-third as
What are Barbiturates drugs? Barbiturates are the derivatives of barbituric acid which is a condensation product of urea with malonic acid. Barbituric acid itself is devoid of any hypnotic activity. Barbiturates drugs are hardly soluble in water; however, their sodium salts form alkaline solutions in water. Conventionally, they are divided according to their duration of
Diethyl ether (C2H5-O-C2H5) is one of the metabolically safe non-halogenated anesthetics . About 6% is metabolized in the liver to ethanol and acetaldehyde, thereafter to acetic acid and onto carbon dioxide and water. Examples of non-halogenated anesthetics Divinyl ether Cyclopropane Trichloroethylene Non-halogenated anesthetics are all anesthetic agents mostly inhalation agents that do not contain a hologen in their structure. Divinyl
