Overview

Remifentanil on Hemodynamic Response to Anesthesia Induction

Status:
Completed
Trial end date:
2015-12-01
Target enrollment:
0
Participant gender:
All
Summary
Effects of different doses of remifentanil on hemodynamic response to anesthesia induction in elderly patients ABSTRACT OBJECTİVE: The investigators compared the effects of three different doses of remifentanil infusion, which have been performed for the induction of anesthesia in elder patients, on cardiovascular response. PATIENTS AND METHODS: The present study was designed as a randomized, prospective and double-blind study. A total of 90 ASA I-II patients over the age of 65 years were enrolled and each group consisted of 30 subjects. The patients were randomly (by lot) assigned to receive one of the three doses of remifentanil infusion (0.1, 0.2 or 0.3 µg/kg/min) for two minutes. Subsequently, 0.5 mg/kg propofol was administered via IV route and, 0.5 mg/kg rocuronium was administered via IV route at the time eyelash reflex disappeared. Intubation was performed after two minutes. After recording baseline values of heart rate (HR), systolic arterial pressure (SBP), diastolic arterial pressure (DBP) and mean arterial pressure (MAP), these values were recorded at the 1st, 2nd, 3rd, 4th and 5th minutes of induction.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Dokuz Eylul University
Treatments:
Atropine
Remifentanil
Criteria
Inclusion Criteria:

- Normotensive patients

- ASA I-II

- Patients over the age of 65 years

- Undergoing elective non-cardiac surgery

Exclusion Criteria:

- Patients who had allergy against opioids

- Chronic benzodiazepine, opioid, alcohol or substance users

- Obese (body mass index > 30)

- Expected to have difficult airway

- Patients had hypertension

- Patients have been receiving any drug influencing the cardiovascular system (beta
-adrenergic blocker, calcium channel blocker, etc.)