QT Changes in Geriatric Patients: a Comparison of Spinal and General Anesthesia

Investigators designed a prospective, randomized trial to compare spinal and general anesthesia in elderly patients on the effects of QT interval changes. The study protocol was approved by the Health Science University Haseki Training and Research Hospital Ethics Committee, Istanbul, Turkey (date: 03/29/2023 and number: 44-2023). This study was conducted according to the Declaration of Helsinki, and written informed consent was obtained from all patients. The study was performed at a tertiary referral hospital with 700 beds in Istanbul, Turkey between 03/29/2023-05/29/2023.

The patients who will undergo lower abdominal or extremity surgery and urological surgery older than 65 years will be included in this study. The exclusion criteria are as follows: any preoperative ECG abnormalities, QTc interval > 440 ms, family history of long QT syndome, use of any medications known to affect the QTc interval, serum electrolyte abnormalities, any contraindications for spinal anesthesia (e.g. coagulation disorders), unstable angina pektoris, chronic obstructive pulmonary disease, hepatic or renal failure, American Society of Anesthesiologists (ASA) physical classification status > III, pregnancy and obesity (BMI > 30).

Participants will be divided into two groups: the spinal anesthesia (group S) and general anesthesia (group G). Randomization and group allocations will be performed by a researcher who did not participate the collection of data.

In the preoperative care unit all patients will receive 10 ml/kg Ringer's lactate solution via a peripheral vein over 30 minutes. In the operating room premedication will be obtained with 0.015 mg/kg of midazolam and 1 µg/kg fentanyl intravenously.

In group G, a 2.0 mg/kg propofol injection will be used for the induction of anesthesia and facilitating of endotracheal intubation was provided with 0.6 mg/kg rocuronium. After the intubation the patients will be ventilated with a 6-8 ml/kg of tidal volume in volume control ventilation (VCV) mode with an anesthesia machine (Dräger Primus, Dräger Medical Systems, Inc. Danvers, MA, USA). Frequency of respiration will be adjusted to maintain PET CO2 at 32-36 mm Hg. Maintenance of anesthesia will be provided with sevoflurane (1.5-2%) in an oxygen-air mixture (FiO2 = 0.4) and 0.015 mg/kg rocuronium as needed. At the end of the surgery residual neuromuscular block will be antagonized with 4 mg/kg sugammedex.

In group S, spinal anesthesia will be performed in the sitting position at the level of L3-4 or L4-5 using a 25-gauge Whitacre (pencil point) spinal needle after the obtaining strict sterile conditions and local anesthesia with intradermal lidocaine hydrochloride 1%. Hyperbaric bupivacaine (Marcaine Spinal 0.5% Heavy; AstraZeneca, Turkey) 3-4 mL of 0.5% will be injected to the subarachnoid space with the observation of cerebrospinal fluid outflow. The patient was placed in the supine position immediately after drug injection. Dermatomal level of sensorial block will be evaluated with pinprick test and modified Bormage scale was used to assess motor blockade. Surgery will be allowed after the achievement of sensorial block at the T10 level.

Monitoring and data collection Non-invasive blood pressure, heart rate (HR), peripheral oxygen saturation (SpO2) and continuous ECG monitorization will be obtained for all patients throughout the study via Mindray Bene View T8 (Shenzhen Mindray Bio-Medical Electronics Co., LTD, PR China. The QT interval will be measured automatically in lead II and calculation of the QTc interval was also achieved automatically with using Bazett's formula (QTc=QT/radqRR(sec)) from ECG monitorization. QT and QTc intervals will be measured and recorded in the following manner: before the anesthesia induction or subarachnoid injection (in group S), 1, 5, 10 minute after after endotracheal intubation or subarachnoid injection (in group S), and immediately after surgery. Presence of arrhythmia will also be recorded.

Patient characteristics including age, gender, height, weight, body mass index (BMI), comorbidity, ASA physical status classification and duration of surgery will be recorded. Moreover maximum sensory block level and motor block recovery time will be investigated in the group S. Also all cardiopulmonary adverse events will be evaluated including hypotension (decrease in mean blood pressure > 20%), bradycardia (HR < 50 beats/min) and hypoxemia (SpO2 < 90%).

Statistical analysis SPSS software package for Windows (Statistical Package for Social Sciences, version 22.0, SPSS Inc., Chicago, Illinois, USA) will be used for statistical analysis of study data. Quantitative variables were emitted as mean ± standard deviation (SD), whereas categorical variables as number of patients and percentage. Quantitative variables will be evaluated for distribution normality using the Kolmogorov-Smirnov/Shapiro-Wilk's test and independent student's t-test will be used to compare normally distributed variables between groups. To compare categorical variables chi-square or Fisher's exact test will be used. QT and QTc intervals within groups will be investigated with repeated measures analysis of variance and post hoc multiple comparisons will be performed by Bonferroni test. Sample size calculation was based on QTc interval. Based on a previous study, QTc interval was found 397.3±27.4 msec after spinal anesthesia in non-geriatric patients. Power analysis with α = 0.05 and β = 0.2 to detect an increase of at least 20 msec in QTc interval revealed that a min of 28 patients should be included in each group. A p value < 0.05 was considered to show a statistically significant result.