Development of an Arterial Pressure Monitoring Set Fixation Apparatus

This study aims to develop an arterial pressure monitoring set fixation device and evaluate its effectiveness in clinical settings. The device is designed to increase the stability and comfort of arterial pressure monitoring during patient care. An experimental study will be conducted with patients requiring arterial pressure monitoring. The device's effectiveness will be evaluated by measuring fixation stability and postoperative arterial blood pressure-CVP parameters over 48 hours. The study aims to demonstrate that the new fixation device can improve patient safety and monitoring accuracy compared to the standard method using adhesive tape, thereby contributing to better clinical outcomes.

Inclusion Criteria: * Adult patients aged 18-80 years * Patients undergoing arterial catheterization for invasive blood pressure and CVP monitoring * Patients able to provide informed consent * Hemodynamically stable patients undergoing Coronary Artery Bypass Grafting (CABG) Exclusion Criteria: * Patients younger than 18 or older than 80 years * Patients with coagulopathy or bleeding disorders * Patients with local infection or skin lesions at the catheter insertion site * Patients unable to provide informed consent * Hemodynamically unstable patients * Patients with known allergy to device materials or adhesive tapes