This study was designed to evaluate how vital organ and skin-surface t
emperatures correlate with other clinical signs of a malignant hyperth
ermia (MH) episode. Six susceptible swine were anesthetized with thiop
ental and nitrous oxide and kept normothermic (approximate to 38 degre
es C). After a 30-min control period, halothane (1 minimum alveolar an
esthetic concentration) was administered, followed in 5 min by a bolus
of succinylcholine (2 mg/kg intravenously). Monitoring included: 1) E
Tco(2); 2) Pao(2), Paco(2), pH(a); 3) cardiovascular function; 4) core
temperatures (esophagus, pulmonary artery, and rectum); 5) organ temp
eratures (brain, kidney, liver, and four skeletal muscles); and 6) ski
n temperatures (forehead, neck, and axilla). Within 10 min after expos
ure to halothane and succinylcholine, all animals developed fulminant
MH. Kidney, liver, and brain temperatures increased more rapidly than
pulmonary artery temperature with the onset of MH. Temperatures signif
icantly increased in the visceral organs prior to the detection of con
tractures within skeletal muscles. The masseter, longissimus dorsi, qu
adriceps, deltoid, and extensor digiti II intramuscular temperatures w
ere 1-2 degrees C less than pulmonary artery and esophageal temperatur
es during the episodes, whereas those of the kidney, liver, and brain
were the same or slightly greater. When it occurs, core hyperthermia d
uring acute MI-I results largely from heat produced in central organs,
not in skeletal muscle per se. In these swine, changes in axilla skin
surface temperatures correlated well with core temperature trends, wh
ereas those of the neck and forehead did not. Unless a skin-surface pr
obe can be placed in close proximity to a major vessel, cutaneous temp
eratures should not be substituted for measurements at an appropriate
core site.