Survival from a malignant hyperthermia (MH) crisis is highly dependent on early recognition and prompt action. MH crises are very rare and an increasing use of total i.v. anaesthesia is likely to make it even rarer, leading to the potential risk of reduced awareness of MH. In addition, dantrolene, the cornerstone of successful MH treatment, is unavailable in large areas around the world thereby increasing the risk of MH fatalities in these areas. The European Malignant Hyperthermia Group collected and reviewed all guidelines available from the various MH centres in order to provide a consensus document. The guidelines consist of two textboxes: Box 1 on recognizing MH and Box 2 on the treatment of an MH crisi
AbstractA 33year old lady with no obvious reason to suspect susceptibility to malignant hyperpyrexia...
Abstract Malignant Hyperthermia (MH) is a rare inherited disorder in which exposure to triggering ag...
Background Malignant hyperthermia (MH) is a rare, hereditary disease with a hypermetabolic response ...
It is 30 yr since the British Journal of Anaesthesia published the first consensus protocol for the ...
Background: The autosomal dominant inherited trait of malignant hyperthermia (MH) may result in a fa...
Malignant Hyperthermia is a rare but fatal disorder usually triggered using succinylcholine, a depol...
It is 30 yr since the British Journal of Anaesthesia published the first consensus protocol for the ...
Rethinking Malignant Hyperthermia Protocols In person poster Undergraduate Student: Currie, Kelsey R...
Purpose: Malignant hyperthermia (MH) is a critical and potentially life-threatening emergency associ...
The EMHG first published its protocol for an in vitro contracture test (IVCT) in 19841 and this has ...
Malignant hyperthermia, though uncommon, is a serious and life threatening condition. Malignant hype...
Purpose: Malignant hyperthermia is a rare crisis associated with anesthesia that boasts an 80%fatali...
Malignant hyperthermia (MH) is a potentially fatal, inherited disorder of muscle hypermetabolism tha...
Cognitive aids help the stressed practitioner in an emergency setting carry out complex tasks. Ideal...
Background Malignant hyperthermia (MH), a metabolic myopathy triggered by volatile anesthetics an...
AbstractA 33year old lady with no obvious reason to suspect susceptibility to malignant hyperpyrexia...
Abstract Malignant Hyperthermia (MH) is a rare inherited disorder in which exposure to triggering ag...
Background Malignant hyperthermia (MH) is a rare, hereditary disease with a hypermetabolic response ...
It is 30 yr since the British Journal of Anaesthesia published the first consensus protocol for the ...
Background: The autosomal dominant inherited trait of malignant hyperthermia (MH) may result in a fa...
Malignant Hyperthermia is a rare but fatal disorder usually triggered using succinylcholine, a depol...
It is 30 yr since the British Journal of Anaesthesia published the first consensus protocol for the ...
Rethinking Malignant Hyperthermia Protocols In person poster Undergraduate Student: Currie, Kelsey R...
Purpose: Malignant hyperthermia (MH) is a critical and potentially life-threatening emergency associ...
The EMHG first published its protocol for an in vitro contracture test (IVCT) in 19841 and this has ...
Malignant hyperthermia, though uncommon, is a serious and life threatening condition. Malignant hype...
Purpose: Malignant hyperthermia is a rare crisis associated with anesthesia that boasts an 80%fatali...
Malignant hyperthermia (MH) is a potentially fatal, inherited disorder of muscle hypermetabolism tha...
Cognitive aids help the stressed practitioner in an emergency setting carry out complex tasks. Ideal...
Background Malignant hyperthermia (MH), a metabolic myopathy triggered by volatile anesthetics an...
AbstractA 33year old lady with no obvious reason to suspect susceptibility to malignant hyperpyrexia...
Abstract Malignant Hyperthermia (MH) is a rare inherited disorder in which exposure to triggering ag...
Background Malignant hyperthermia (MH) is a rare, hereditary disease with a hypermetabolic response ...