Pediatric ALL Clinical Trial
Official title:
Peri-operative Hypothermia in Children: Improving Outcomes With Risk Prediction
This study aims to determine the incidence of hypothermia in the local paediatric population in the peri-operative period, identify the risk factors involved, and thereafter develop and implement clinical practice guidelines to reduce IPH such that temperature monitoring and heat conservation measures can be implemented in a cost-effective way. The secondary objectives are to determine the adverse outcomes of hypothermia and warming measures
Background Hypothermia, defined as core body temperature less than 36 degrees Celsius, occurs
frequently during the course of surgery in patients across all ages, especially in the young.
It causes significant medical consequences including cardiac events, bleeding, surgical site
infection, increased shivering and patient discomfort, as well as longer hospital stays.
Although guidelines exist for health care providers in terms of temperature management during
surgery, these guidelines are not always followed as the warming measures can be costly, for
example, single-use temperature probes and disposable blankets, with potential risks of the
equipment overheating causing burns and contamination during surgery
Methodology The investigators aim to include up to 6,000 children presenting for either
scheduled or emergency surgeries. Core temperature before, during and after surgery using
routine temperature monitoring devices such as tympanic, axillary, oral, rectal and SPOTON (a
non-invasive method using a sticker placed on the forehead) will be measured. Other outcomes
collected will include cardiac arrhythmias, blood loss, hyperthermia, burn injuries,
shivering, discomfort, length of PACU and length of hospitalization, wound infection rates, .
Patients will receive the usual heat-loss prevention and warming measures.
Interim analysis of the first 2000 patients using the SPOTON method of continuous core
temperature monitoring will be done to determine incidence and duration of peri-operative
hypothermia. This monitoring modality will be compared for agreement with the conventional
tympanic and forehead infra-red thermoscan methods. Patient and perioperative risk factors
predisposing to hypothermia will be identified to guide in the formulation of clinical
practice guidelines tailored to the local population. Guidelines will be implemented, and
post-implementation incidence of IPH will be determined A pre- versus post-implementation
cost analysis will be carried out.
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