Infection Prevention Bundle in Brain Tumor Surgery
Surgical Site Infection, Brain Tumor
About this trial
This is an interventional prevention trial for Surgical Site Infection focused on measuring Care Bundles,, Surgical Wound Infection,, craniyal surgery, nursing care
Eligibility Criteria
Inclusion Criteria:
- Patients with American Society of Anesthesiologists score I-II-III
- Surgical intervention planned with the diagnosis of brain tumor
- No systemic infection such as sepsis, pneumonia, blood infections, or intracranial infection such as meningitis, abscess or local infection.
- Not having a mental illness
Exclusion Criteria:
- Being morbidly obese (BMI> 40kg / m2)
- Immune deficiency
- Using immunosuppressive drugs
- Being addicted to alcohol and substances
- Having received radiotherapy and / or chemotherapy before surgery
- Having the disease that requires infective endocarditis prophylaxis (Rheumatic valve diseases, prosthetic heart valves, previous endocarditis, etc.)
- Corruption of cranium integrity and emergency surgery planned
- Having systemic or intracranial infections
- Transfenoidal surgery intervention planned
- Using implants during surgical intervention
- Using external ventricular drainage / lumbar drainage during and after surgical intervention
Sites / Locations
- Department of Neurosurgery, Bakirkoy Research and Training Hospital for Neurology, Neurosurgery, and Psychiatry, İstanbul, Turkey
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
group 1
group 2 control
During the outpatient clinic visit, an information leaflet will be given about the subjects that should be considered for prevention of SSI before surgery. 2% mupirocin ointment will be applied to the nostrils with the swab twice-daily before surgery and once on the morning of surgery. Body cleaning will be done with 4% chlorhexidine gluconate shower the night before the surgery. Prophylactic antibiotics by weight will be administered within 60 minutes of anesthesia induction. The planned aseptic technique will be applied and a strict draping will be used in the incision site. Body temperature, blood pressure, respiratory rate, heart rate and O2 saturation of the patients will be monitored every 1 hour during the operation and data will be recorded on the data collection form. Before the skin closes, the surgical site will be washed with warm Isotonic NaCl solution. Wound care education will be provided to the patient and family before discharge.
The pre-operative service sociodemographic characteristics form, preoperative, intra and postoperative evaluation forms will be completed. Body temperature, blood pressure, respiratory rate, heart rate and O2 saturation of the patients will be monitored every 1 hour during the operation and data will be recorded on the data collection form.