Key result
Mild hypothermia attenuates cardiopulmonary dysfunction, raising SaO2 ~8 percentage points vs normothermia in experimental endotoxemia.
Why the study?
The impact of mild hypothermia on circulatory and respiratory dysfunction during experimental endotoxemia was not well understood.
Does mild hypothermia attenuate circulatory and respiratory dysfunction in a pig model of experimental endotoxemia?
RCT (n=13)
Randomized
No
Does mild hypothermia attenuate circulatory and respiratory dysfunction in a pig model of experimental endotoxemia?
Absolute Event Rate: 100% vs 92%
p-value: p=<0.05
In a porcine model of endotoxemia, mild hypothermia attenuated cardiac and respiratory dysfunction and reduced sympathetic activation despite higher cytokine levels.
Hypothesis-generating in porcine endotoxemia; human trials needed before any clinical consideration.
Objective We tested whether mild hypothermia impacts on circulatory and respiratory dysfunction during experimental endotoxemia. Design Randomized controlled prospective experimental study. Setting Large animal facility, Medical University of Graz, Austria. Subjects Thirteen anesthetized and mechanically ventilated pigs. Interventions Lipopolysaccharide was administered for 4 hours. With the beginning of lipopolysaccharide infusion, animals were assigned to either normothermia (38°C, n = 7) or mild hypothermia (33°C, n = 6, intravascular cooling) and followed for 8 hours in total. Measurements and main results At the end of the protocol, cardiac output was lower in mild hypothermia than in normothermia (4.5 ± 0.4 L/min vs 6.6 ± 0.4 L/min, p < 0.05), but systemic vascular resistance (885 ± 77 dyn·s/cm vs 531 ± 29 dyn·s/cm, p < 0.05) and (Equation is included in full-text article.)(77% ± 6% vs 54% ± 3%, p < 0.05) were higher. Indices of left ventricular contractility in vivo were not different between groups. The high-frequency band in spectral analysis of heart rate variability indicated a better preserved vagal autonomic modulation of sinuatrial node activity in mild hypothermia versus normothermia (87 ± 5 vs 47 ± 5, normalized units, p < 0.05). Plasma norepinephrine levels were elevated compared with baseline in normothermia (2.13 ± 0.27 log pg/mL vs 0.27 ± 0.17 log pg/mL, p < 0.05) but not in mild hypothermia (1.02 ± 0.31 vs 0.55 ± 0.26, p = not significant). At 38°C in vitro, left ventricular muscle strips isolated from the mild hypothermia group had a higher force response to isoproterenol. SaO2 (100% ± 0% vs 92% ± 3%, p < 0.05) and the oxygenation index (PO2/FIO2, 386 ± 52 mm Hg vs 132 ± 32 mm Hg, p < 0.05) were substantially higher in mild hypothermia versus normothermia. Plasma cytokine levels were not consistently different between groups (interleukin 10) or higher (tumor necrosis factor-α and interleukin 6 and 8) during mild hypothermia versus normothermia. Conclusion The induction of mild hypothermia attenuates cardiac and respiratory dysfunction and counteracts sympathetic activation during experimental endotoxemia. This was not associated with lower plasma cytokine levels, indicating a reduction of cytokine responsiveness by mild hypothermia.
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Schwarzl et al. (2013) conducted an RCT in Experimental endotoxemia (n=13). Mild hypothermia vs. Normothermia (38°C) was evaluated on SaO2 at the end of the protocol (%) (p=<0.05). Mild hypothermia attenuated cardiac and respiratory dysfunction during experimental endotoxemia, yielding a higher SaO2 (100% vs 92%, p<0.05) and oxygenation index compared with normothermia.
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