About this trial
This research project is a descriptive, longitudinal prospective observational study in the HUMV neurosurgery operating rooms. The patients included will be adults 18 years old or older, who will be scheduled for surgery by the Neurosurgery service. Those who meet the selection criteria determined for this study will be chosen consecutively and will be followed from the immediate preoperative moment until 72 hours after the end of the surgery. Data collection shall be carried out by direct observation and immersion in clinical records of patients who have signed the informed consent. The study will be carried out in 4 phases: immediate preoperative, intraoperative, immediate postoperative and late postoperative, recording the data using various measuring instruments, and a record sheet. Finally, the cumulative incidence of LPPs developed in the perioperative environment will be calculated and a statistical analysis will be performed.
Eligibility criteria
Qualifiers
Patients who understand and sign the informed consent.
Adult patients of both sexes who will undergo a schedule surgery of more than 3 hours, by the service of neurosurgery of the University Hospital Marqués of Valdecilla (HUMV), between 2023 and 2024.
Patients positioned in prone, supine, lateral and beach chair/sitting.
Surgeries susceptible to bladder catheterisation with body temperature measurement.
Disqualifiers
Patients who do not sign informed consent.
Patients with visible pressure injurie present before surgery.
Patients with cognitive disorder or written and oral knowledge difficulty.
Patients who reject the operation.
Trial design
Treatments tested in this trial
- Neurosurgery