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In susceptible individuals, malignant hyperthermia (MH) can be
triggered by various anesthetics during surgery. First described in
1960, research since then has concentrated on reducing the very
high mortality rate associated with MH. Although significant
progress in treatment has been made with the introduction of
dantrolene sodium in 1979, many questions remain unanswered.
Following on the results of more than 30 years of investigative
efforts, the Third International Symposium on MH was held in
Hiroshima, Japan, in 1994, immediately before the Seventh
International Workshop on MH. Specialists in the field discussed
the most up-to-date findings from the point of view of clinical
classification, history, and incidence based on the evidence of
epidemiology, diagnostic muscle testing, genetics, and
biochemistry. These proceedings of the symposium present important
keys to understanding the mechanism of MH and related syndromes at
the genetic level and include procedures for the monitoring and
care of patients. This volume will be invaluable not only for
surgeons and anesthesiologists but also for physiologists and
researchers.
In susceptible individuals, malignant hyperthermia (MH) can be
triggered by various anesthetics during surgery. First described in
1960, research since then has concentrated on reducing the very
high mortality rate associated with MH. Although significant
progress in treatment has been made with the introduction of
dantrolene sodium in 1979, many questions remain unanswered.
Following on the results of more than 30 years of investigative
efforts, the Third International Symposium on MH was held in
Hiroshima, Japan, in 1994, immediately before the Seventh
International Workshop on MH. Specialists in the field discussed
the most up-to-date findings from the point of view of clinical
classification, history, and incidence based on the evidence of
epidemiology, diagnostic muscle testing, genetics, and
biochemistry. These proceedings of the symposium present important
keys to understanding the mechanism of MH and related syndromes at
the genetic level and include procedures for the monitoring and
care of patients. This volume will be invaluable not only for
surgeons and anesthesiologists but also for physiologists and
researchers.
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