Finding studies
Finding studies
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Lead
Trabzon Karadeniz Teknik Universitesi
This prospective, randomized clinical study was conducted at Karadeniz Technical University Faculty of Medicine after receiving ethics committee approval (Protocol No: 2021/268) * The study included 60 patients aged 65-80, classified as ASA II-III, who had been diagnosed with hypertension and on stable medication for at least 6 months Randomization and Blinding: Participants were randomized into two groups (n=30 each) using computer-based random number generation * Allocation was concealed using sequentially numbered envelopes * Researchers involved in data recording and statistical analysis were blinded to the group assignments Anesthesia Protocol: All patients received standard monitoring (ECG, SpO₂, and non-invasive blood pressure) and were sedated with intravenous midazolam (0.05 mg/kg) and fentanyl (1 µg/kg) * Following a 3-minute rest in the supine position, Group L patients were moved to the lithotomy position for 120 seconds before induction, while Group S remained in the supine position * Anesthesia was induced with 3-5 mg/kg thiopental administered over 120 seconds * A laryngeal mask airway (LMA) was inserted at the 60th second post-induction * Maintenance of anesthesia was achieved with desflurane (BIS target: 40-60) and remifentanil infusion Hemodynamic Monitoring and Intervention: Non-invasive blood pressure (NIBP) was measured immediately after induction (Minute 0) and every minute thereafter for the first 5 minutes * Post-induction hypotension (PIH) was defined as a Mean Arterial Pressure (MAP) falling below 65 mmHg or a decrease of more than 20% from the baseline value * In the event of hypotension, 5 mg of intravenous ephedrine was administered as a rescue medication Statistical Analysis: Sample size was calculated based on a 20% expected difference in PIH incidence, requiring 27 patients per group for 95% power . Statistical analyses were performed using IBM SPSS v23.0, including t-tests, Mann-Whitney U tests, and Kaplan-Meier analysis for time-to-event (onset of hypotension)
Age
65–80
Sex
ALL
Healthy volunteers
Not accepted
