Cardiovascular Critical Care II
| (e) | Axillary or oral temperature monitoring is inadequate for temperature control (Acta |
|---|
Anaesthesiol Scand 1998;42:1222-6; J Cardiothorac Vasc Anesth 1996;10:336-41), which
requires central/core temperatures by esophageal, bladder (avoid in anuric patients), or
pulmonary artery temperature monitoring. Ideally, the monitoring modality chosen will
be used for other indications as well.
The major complications of temperature control are related to the physiologic and adaptive
responses to the temperature-changing process of temperature control (Table 4). The adverse
events of sepsis, myoclonus, seizures, and hypoglycemia within 72 hours of temperature control
Musculoskeletal
N Engl J Med 2013;369:2197-206;
Anesthesiology 2009;111:110-5; Br
J Anaesth 2005;94:756-62; N Engl
J Med 2002;346:549-56; N Engl
1960;198:481-6)
Shivering:
Bodyβs natural response to hypothermia, preceded by arteriovenous
vasoconstriction; most common complication of hypothermia; can increase
metabolic heat production by 600%, thereby slowing the induction of
hypothermia. Typically slows or stops at core temperatures < 33.5Β°C
1.β Agents that decrease the shivering threshold (i.e., decreases the
temperature at which shivering will occur):
a)β Scheduled acetaminophen 650 mg q4β6 hr or buspirone 30 mg
q12 hr reduces the shivering threshold by 0.2ΒΊCβ0.4ΒΊC
b)β Magnesium sulfate reduces the shivering threshold by ~0.3Β°C
c)β Meperidine decreases the shivering threshold by up to 2Β°C but
should be avoided because of decreased effective glomerular
filtration rate (GFR) during hypothermia and increased risk of
seizures when meperidine is used in patients with decreased GFR
d)β Dexmedetomidine and clonidine decrease the shivering threshold
by ~0.8Β°C, but extreme caution should be used because of the
hypotensive and bradycardic effects of both agents
e)β Propofol decreases the shivering threshold by ~0.6Β°C and has a
linear relationship between serum concentrations and reduction in
body temperature; caution should be used, given the hypotensive
and bradycardic effects
2.β Options to stop shivering include:
a)β Continuous or as-needed paralytics can be used for prevention
and treatment of shivering (see the chapter on management of
paralytics for appropriate selection and dosing of agent[s])
βHypothermia decreases clearance and prolongs the duration of
neuromuscular blockade (see Table 5 for examples)
βTrain of four is not a reliable method of monitoring
during hypothermia; clinical monitoring or continuous EEG
(electroencephalography) may be warranted
b)β Surface warming if using internal cooling devices
c)β Chilled fluids to promote faster core temperature reduction