This study aims to evaluate the effectiveness of prewarming methods in preventing intraoperative hypothermia in patients undergoing HoLEP surgery. Designed as a randomized controlled study, patients who receive prewarming will be compared with those in the control group.
Male patients aged 18 years and older
Patients undergoing HoLEP surgery under general anesthesia
Patients who consent to participate in the study
Patients who refuse to participate in the study.
Patients unable to read, understand, or sign the informed consent form.
Hemodynamically unstable patients.
Patients with a preoperative or intraoperative body temperature >37°C.