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Anything you want to know about Anesthesia-- definition, doctor description, symptoms, types, labor condition, pregnancy, spinals, nausea and vomiting, pain management, operative assessment, growth and development, ultrasound guided blocks, neuromuscular relaxants and many other topics are includes in my more than 100 lectures here. Specifically, this lecture teaches you Anesthesia, History, Principles, Agents, Nitrous, Oxide, Effects, Halothane
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Ether synthesized in 1540 by Cordus Ether used as anesthetic in 1842 by Dr. Crawford W. Long Ether publicized as anesthetic in 1846 by Dr. William Morton Chloroform used as anesthetic in 1853 by Dr. John Snow
Endotracheal tube discovered in 1878 Local anesthesia with cocaine in 1885 Thiopental first used in 1934 Curare first used in 1942 - opened the “Age of Anesthesia”
Anesthesia defined as the abolition of sensation
Analgesia defined as the abolition of pain
“Triad of General Anesthesia” need for unconsciousness need for analgesia need for muscle relaxation
Nitrous Oxide
Prepared by Priestly in 1776 Anesthetic properties described by Davy in 1799 Characterized by inert nature with minimal metabolism Colorless, odorless, tasteless, and does not burn
Nitrous Oxide
Simple linear compound Not metabolized Only anesthetic agent that is inorganic
Nitrous Oxide Systemic Effects
Minimal effects on heart rate and blood pressure May cause myocardial depression in sick patients Little effect on respiration Safe, efficacious agent
Nitrous Oxide Side Effects
Manufacturing impurities toxic Hypoxic mixtures can be used Large volumes of gases can be used Beginning of case: second gas effect End of case: diffusion hypoxia
Nitrous Oxide Side Effects
Inhibits methionine synthetase (precursor to DNA synthesis) Inhibits vitamin B-12 metabolism Dentists, OR personnel, abusers at risk
Halothane
Synthesized in 1956 by Suckling Halogen substituted ethane Volatile liquid easily vaporized, stable, and nonflammable
Halothane Systemic Effects
Inhibits sympathetic response to painful stimuli Inhibits sympathetic driven baroreflex response (hypovolemia) Sensitizes myocardium to effects of exogenous catecholamines-- ventricular arrhythmias Johnson found median effective dose 2.1 ug/kg Limit of 100 ug or 10 mL over 10 minutes Limit dose to 300 ug over one hour Other medications
Halothane Systemic Effects
Decreases respiratory drive-- central response to CO 2 and peripheral to O 2 Respirations shallow-- atelectasis Depresses protective airway reflexes Depresses myocardium-- lowers BP and slows conduction Mild peripheral vasodilation
Halothane Side Effects
Malignant Hyperthermia-- 1/60,000 with succinylcholine to 1/260,000 without halothane in 60%, succinylcholine in 77% Classic-- rapid rise in body temperature, muscle rigidity, tachycardia, rhabdomyolysis, acidosis, hyperkalemia, DIC most common masseter rigidity family history
Halothane Side Effects
Malignant Hyperthermia (continued) high association with muscle disorders autosomal dominant inheritance diagnosis--previous symptoms, increase CO2, rise in CPK levels, myoglobinuria, muscle biopsy physiology--hypermetabolic state by inhibition of calcium reuptake in sarcoplasmic reticulum