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العنوان
Malignant Hyperthermia “updating”
المؤلف
fahmy,Hussam hamdy Mohamed
هيئة الاعداد
باحث / Hussam hamdy Mohamed fahmy
مشرف / Ahmed Abd El-Aala ElShawarby
مشرف / Reem Hamdy El-Kabarity
الموضوع
Aetiology and pathophysiology of Malignant <br>-<br>Hyperthermia
تاريخ النشر
2009
عدد الصفحات
120.p:
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
التخدير و علاج الألم
تاريخ الإجازة
1/1/2009
مكان الإجازة
جامعة عين شمس - كلية الطب - anesthesiology
الفهرس
Only 14 pages are availabe for public view

from 120

from 120

Abstract

Malignant hyperthermia, which is called the nightmare syndrome of anesthesiologists, is an acute life-threatening syndrome. It is a subclinical myopathy that is unmasked upon exposure to the potent inhalational anesthetic agents and succinylcholine. Skeletal muscle acutely and unexpectedly increases its oxygen consumption and lactase production resulting in greater heat production, respiratory and metabolic acidosis, muscle rigidity, sympathetic stimulation, and increased cellular permeability.
Its exact mechanism is still being debated. The most accepted theory is that MH is caused by an inability to control calcium concentrations within the muscle fiber and that it may involve a generalized alteration in cellular or subcellular membrane permeability.
Close monitoring of patients especially in susceptible individuals should be carried on in order to detect MH as early as possible and to perform rapid interference to stop the process.
Diagnosis is based on the basis of extraordinary temperature and acid-base and muscle aberration. Specific treatment is the action of dantrolene on muscle calcium movements. Symptomatic treatment is by reversal of acid-base and temperature changes.
Evaluation of affected families is guided by movements of circulating creatine phosphokinase and by analysis of drug-induced contractures in muscle biopsy specimens. Either general or regional anesthesia is safe for patients susceptible to MH, provided that if a general technique is chosen, care is taken to specially prepare the anesthesia machine and to avoid all anesthetic trigger agents.
Challenges for the future include identification of the gene or genes responsible for MH and eludication of the mechanism that links exposure to the subsequent loss of calcium control. We hope that continuing research will reveal the answers to many of these mysteries, so that the next generation of anesthesiologists will consider the description and conquest of MH an interesting aspect of anesthesia history.