TY - JOUR
T1 - Therapeutic hypothermia can be induced and maintained using either commercial water bottles or a "phase changing material" mattress in a newborn piglet model
AU - Iwata, S.
AU - Iwata, O.
AU - Olson, L.
AU - Kapetanakis, A.
AU - Kato, T.
AU - Evans, S.
AU - Araki, Y.
AU - Kakuma, T.
AU - Matsuishi, T.
AU - Setterwall, F.
AU - Lagercrantz, H.
AU - Robertson, N. J.
PY - 2009/5
Y1 - 2009/5
N2 - Background: Therapeutic hypothermia, a safe and effective treatment for neonatal encephalopathy in an intensive care setting, is not available in low-resource settings. Aims/Methods: To assess two low-tech, low-cost cooling devices for use in low-resource settings: (i) commercially available water bottles filled with tepid water (25̊C); (ii) a mattress made of phase changing material (PCM) with a melting point of 32̊C (PCM works as a heat buffer at this temperature). Eleven anaesthetised newborn piglets were studied following transient hypoxia-ischaemia. The cooling device was applied 226 h after hypoxia-ischaemia with a target rectal temperature (Trectal) of 33-34̊C. Trectal undershoot was adjusted using cotton blankets; the cooling device was renewed when Trectal rose above 35̊C. Trectal data during cooling were dichotomised (within or without target) to assess: (a) the total period within the target Trectal range; (b) the stability and fluctuation of Trectal during cooling. Results: Therapeutic hypothermia was achieved with both water bottles (n = 5) and the PCM mattress (n = 6). The mean (SD) time to reach target T rectal was 1.8 (0.5) h with water bottles and 1.9 (0.3) h with PCM. PCM cooling led to a longer period within the target Trecta| range (p<0.01) and more stable cooling (p<0.05). Water bottle cooling required device renewal (in four out of five piglets). Conclusion: Simple, low-tech cooling devices can induce and maintain therapeutic hypothermia effectively in a porcine model of neonatal encephalopathy, although frequent fine tuning by adjusting the number of blankets insulating the piglet was required to maintain a stable temperature. PCM may induce more stable cooling compared with water bottles.
AB - Background: Therapeutic hypothermia, a safe and effective treatment for neonatal encephalopathy in an intensive care setting, is not available in low-resource settings. Aims/Methods: To assess two low-tech, low-cost cooling devices for use in low-resource settings: (i) commercially available water bottles filled with tepid water (25̊C); (ii) a mattress made of phase changing material (PCM) with a melting point of 32̊C (PCM works as a heat buffer at this temperature). Eleven anaesthetised newborn piglets were studied following transient hypoxia-ischaemia. The cooling device was applied 226 h after hypoxia-ischaemia with a target rectal temperature (Trectal) of 33-34̊C. Trectal undershoot was adjusted using cotton blankets; the cooling device was renewed when Trectal rose above 35̊C. Trectal data during cooling were dichotomised (within or without target) to assess: (a) the total period within the target Trectal range; (b) the stability and fluctuation of Trectal during cooling. Results: Therapeutic hypothermia was achieved with both water bottles (n = 5) and the PCM mattress (n = 6). The mean (SD) time to reach target T rectal was 1.8 (0.5) h with water bottles and 1.9 (0.3) h with PCM. PCM cooling led to a longer period within the target Trecta| range (p<0.01) and more stable cooling (p<0.05). Water bottle cooling required device renewal (in four out of five piglets). Conclusion: Simple, low-tech cooling devices can induce and maintain therapeutic hypothermia effectively in a porcine model of neonatal encephalopathy, although frequent fine tuning by adjusting the number of blankets insulating the piglet was required to maintain a stable temperature. PCM may induce more stable cooling compared with water bottles.
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U2 - 10.1136/adc.2008.143602
DO - 10.1136/adc.2008.143602
M3 - Article
C2 - 19155230
AN - SCOPUS:65649138385
SN - 0003-9888
VL - 94
SP - 387
EP - 391
JO - Archives of Disease in Childhood
JF - Archives of Disease in Childhood
IS - 5
ER -