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Comparison of the effects of different PEEP (positive end-expiratory pressure) levels on cerebral oxygen saturation in patients undergoing laparoscopic cholecystectomy

Comparison of the effects of different PEEP levels on cerebral oxygen saturation with near infrared spectroscopy during laparoscopic cholecystectomy

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12615000581561
Enrollment
105
Registered
2015-06-03
Start date
2015-07-01
Completion date
2016-02-01
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Laparoscopic surgeries have increased in frequency as replacements for a variety of surgical procedures. However, they require pneumoperitoneum, which raises concerns about the adverse effects on respiratory mechanics. It is demonstrated that application of positive end-expiratory pressure improved respiratory mechanics during pneumoperitoneum. Carbon dioxide (CO2) pneumoperitoneum also affects cerebral hemodynamics. We aimed to investigate changes in rSO2, as assessed by nearinfrared spectroscopy, associated with different PEEP levels during laparoscopic cholecystectomy.

Interventions

One hundred and five patients between the ages of 18-60 yr, ASA physical status I and II, scheduled to undergo routine laparoscopic cholecystectomy under general anesthesia, were studied. The patients were randomized, by using a computer-generated block randomisation, into 3 groups: Group I (n=35) with no external PEEP, Group II (n=35) with external PEEP of 5 cmH2O, Group III (n=35) with external PEEP of 10 cmH2O. Routine monitors (consisting of a pulse oximeter, 3-lead ECG and a non-invasive bl

One hundred and five patients between the ages of 18-60 yr, ASA physical status I and II, scheduled to undergo routine laparoscopic cholecystectomy under general anesthesia, were studied. The patients were randomized, by using a computer-generated block randomisation, into 3 groups: Group I (n=35) with no external PEEP, Group II (n=35) with external PEEP of 5 cmH2O, Group III (n=35) with external PEEP of 10 cmH2O. Routine monitors (consisting of a pulse oximeter, 3-lead ECG and a non-invasive blood pressure cuff ) and BIS monitoring were applied. In addition to this monitoring cerebral oximeter sensors were attached to frontotemporal areas (both right and left). Fasting periods were in accordance with ASA guidelines, and no one premedicated. Anesthesia was induced with propofol (2 mg/kg) and fentanyl (1-2 microg/kg), and endotracheal intubation was facilitated using rocuronium. After induction, volume- controlled mechanical ventilation (tidal volume adjusted to 8 mL/kg with no application of PEEP in Group I, 5 cmH2O in Group II, 10 cmH2O in Group III and respiratory rates were adjusted to achieve an end-tidal carbon dioxide of 30 to 35 mmHg) was initiated. All patients were ventilated with the same anesthetic machine. Anaesthesia was maintained using sevoflurane 1–2% in an oxygen / air mixture and remifentanil (0,25 microg/kg/min) accompanied by BIS monitoring. The CO2 pneumoperitoneum (PP) was introduced with a closed Veress needle technique, and the intraa-bdominal insufflation pressure was limited to 10-12 mmHg. After introduction of the four trocars and insufflation of CO2, the patient was placed in the reverse Trendelenburg position, using up to 30 degree of head-up tilt. HR, MBP, oxygen saturation (SpO2) and rSO2 values were continuously recorded from awake status to tracheal extubation (basal, after induction, after intubation, immediately after pneumoperitoneum, every 5 minutes during pneumoperitoneum, immediately after desufflation of CO2, at the end of surgery, after). ETCO2, peak inspiratory pressure (PIP) (after intubation, immediately after pneumoperitoneum, every 5 minutes during pneumoperitoneum, immediately after desufflation of CO2, at the end of surgery, after), operation time, PP time and intraoperative fluid administration were also recorded.

Sponsors

Konya Training and Research Hospital
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Primary purpose
Prevention

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

Scheduled for elective laparoscopic cholecystectomy. ASA physical status I and II.

Exclusion criteria

Patients with morbid obessity (body mass index > 30 kg/m2), Patients with cerebrovascular disease, Patients with respiratory disease, Patients with cardiovascular disease, Patients with metabolic disease patients with acute cholecystitis.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026