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Review paper

A comparison of different doses of fentanyl for patients undergoing elective colonoscopy: a randomized double-blind clinical trial

By
Mirza Kovačević Orcid logo ,
Mirza Kovačević
Contact Mirza Kovačević

Department of Anaesthesiology and Intensive Care Unit, Cantonal Hospital Zenica, Zenica, Bosnia and Herzegovina

Adisa Šabanović Adilović ,
Adisa Šabanović Adilović

Department of Anaesthesiology and Intensive Care Unit, Cantonal Hospital Zenica, Zenica, Bosnia and Herzegovina

Nermina Rizvanović ,
Nermina Rizvanović

Department of Anaesthesiology and Intensive Care Unit, Cantonal Hospital Zenica, Zenica, Bosnia and Herzegovina

Harun Adilović ,
Harun Adilović

Department of Internal Medicine, Cantonal Hospital Zenica, Zenica, Bosnia and Herzegovina

Malik Ejubović ,
Malik Ejubović

Department of Internal Medicine, Cantonal Hospital Zenica, Zenica, Bosnia and Herzegovina

Alma Jahić Čampara
Alma Jahić Čampara

Clinic for Anaesthesiology and Reanimatology, University Clinical Centre Tuzla, Tuzla, Bosnia and Herzegovina

Abstract

Aim
To investigate analgesic and side effects of different doses of fentanyl in combination with propofol for colonoscopy.
Methods
This prospective randomized double-blind study conducted between 2019 and 2020 included 64 patients. Patients were randomized: Group 1 (fentanyl 0.5 μg/kg) and Group 2 (fentanyl 1.0 μg/kg) both in combination with propofol. Ramsay sedation score (RSS) was obtained at 5 with an additional dose of propofol. The primary outcome was the patient’s postprocedural pain and adverse events during and after the procedure.
Results
The RSS means were statistically lower for Group 2 at the beginning and every 5 minutes of the procedure. Mean arterial pressure (MAP) for Group 2 (first, 5, 25 and 30 min) was significantly lower (p=0.000, and heart rate (HR) was significantly higher for Group 1 (during the entire procedure) (p=0.000) than in another group; peripheral oxygen saturation (SpO2
) was significantly lower for measurements within both groups (Group 1, 5, 10, 15 min; Group 2, 5, 10,15 min) (p=0.000 and p=0.000, respectively). Anxiety (p=0.010), weakness (p=0.000) and confusion (p=0.023)
proved to be significantly higher for Group 1, and hypotension (p=0.001) for Group 2 than in another group. No statistical significance of Visual Analogue Pain Scale (VAS) (p=0.501) and Aldrete recovery score (ARS) (p=0.845) was found.
Conclusion
There was no significance in postprocedural abdominal pain between the group of patients administered fentanyl at a
dose of 0.5 μg/kg and the group of patients administered fentanyl at a dose of 1.0 μg/kg; however, prevalence of complications was more significant in the group with a fentanyl at a dose of 0.5 μg/kg.

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