This randomized controlled trial looked at adults scheduled for elective video-assisted thoracoscopic surgery under general anesthesia. The researchers tested whether transcutaneous electrical acupoint stimulation could prevent perioperative hypothermia. Participants received stimulation at predefined acupoints starting 30 minutes before anesthesia induction and continuing until the end of surgery. The control group received sham stimulation. The primary outcome measured was the incidence of perioperative hypothermia, defined as a core temperature drop. The study followed patients until the end of surgery to see if the treatment made a difference. No adverse events, serious adverse events, discontinuations, or tolerability issues were reported in the available data. The main reason to be careful is that evidence from randomized controlled trials on this specific topic remains limited. Readers should understand that while the results are promising, more research is needed before this becomes a standard recommendation for all patients undergoing this type of surgery.
Transcutaneous electrical acupoint stimulation may reduce perioperative hypothermia in adults undergoing elective VATSTEAS May Reduce Hypothermia Risk During Elective Thoracic Surgery
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This randomized controlled trial investigated the effect of transcutaneous electrical acupoint stimulation (TEAS) on perioperative hypothermia. The study population consisted of adults scheduled for elective video-assisted thoracoscopic surgery (VATS) under general anesthesia. The sample size was not reported. The setting was not reported. Funding or conflicts of interest were not reported.
The intervention involved TEAS applied at predefined acupoints starting 30 min before anesthesia induction and continuing until the end of surgery. The comparator was sham stimulation. The primary outcome was the incidence of perioperative hypothermia, defined as a core temperature. The follow-up period extended until the end of surgery. Specific results for the primary outcome were not reported in the provided data.
Safety and tolerability data were not reported. Discontinuations were not reported. Serious adverse events were not reported. Adverse events were not reported. The study limitations include that evidence from randomized controlled trials remains limited. Practice relevance was not reported. The certainty note was not reported.