Effects of Different Routes of Local Anesthetic Administration in Epidural Anesthesia for Transurethral Resection of The Prostate
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 60
- 试验地点
- 2
- 主要终点
- Time to Reach Sensory Block at T10
研究概览
简要总结
The aim of this study is to assess the effects of different routes of local anesthetic administration in epidural anesthesia applied to patients undergoing transurethral resection of the prostate (TUR-P). ASA I-III 60 patients were enrolled in the study. Patients were randomized into the following three groups: in Group N (needle), total dose of local anesthetic was administered through the Tuohy needle (n=20), in Group C (catheter), local anesthetic was administered through the epidural catheter (n=20) and in Group N/C (needle/catheter), local anestetic was administered half volume through the needle and half through the catheter (n=20). Hemodynamics, times to reach sensory block T10 (block levels), side effects, patient and surgeon satisfaction were evaluated.
详细描述
In urological procedures, the preferred anaesthetic modalities may be topical, regional or general. The decision is made by the anaesthesiologists based on patient age, sex, general condition and the surgical procedure to be performed. Transurethral procedures are frequently applied to geriatric patients, who are more likely to have comorbidities. In such cases, epidural anaesthesia may be preferred for geriatric patients.
In this study, we utilised various routes for the administration of local anaesthetics to induce epidural anaesthesia in patients scheduled for transurethral resection of the prostate (TUR-P) due to benign prostatic hyperplasia. The study encompassed the evaluation of haemodynamic stability, the time to reach sensory block T10, the occurrence of side effects, and the levels of patient and surgeon satisfaction.
Following the approval of the hospital ethics committee, 60 male patients aged 40-75, ASA class I-III, scheduled for elective TUR-P surgery were enrolled in the study.According to the method of local anaesthetic administration, patients were randomly divided into three groups:
Group N (needle); total local anaesthetic administered through the Tuohy needle,Group C (catheter); local anaesthetic administered through the epidural catheter,Group NC (needle/catheter); 50% of local anaesthetic administered through the needle and 50% through the catheter.Patients underwent standard monitorisation in the operating theatre. Each patient received 0.03 mg/kg of midazolam intravenously following catheterisation with a 20-gauge intravenous cannula.Prior to the commencement of epidural block, patients were preloaded with 10 ml/kg of 0.9% isotonic saline infused over a 30-minute period. The hemodynamic parameters were then recorded before and after the premedication, following the epidural block, and every 5 minutes until the patient's sensory block level regressed to L1 dermatome.The epidural anaesthesia was then attempted with an 18-gauge Tuohy needle at the L3-4 interspinal level using the loss of resistance technique following infiltration with 2% lidocaine. Patients in Group N received a mixture of 8ml 2% prilocaine, 7ml 0.5% levobupivacaine and 50μg fentanyl through the epidural space using a Tuohy needle. Patients in Group C received the same drug combination through the epidural catheter. Patients in Group NC received half of the same drug combination through the needle and half through the epidural catheter. Patients were positioned in the right lateral decubitus position with thighs flexed up and neck flexed forward (fetal position), and then placed supine following drug administration.In all groups, time "0" was considered as the time that drug administration was started.
The sensory and motor block levels, heart rates and mean arterial blood pressure values, times to reach sensory block level T10, and side effects were recorded for all patients. Patient and surgeon satisfaction levels were evaluated using a 3-point satisfaction scale by an observer unaware of the study's objectives.Surgeon satisfaction was evaluated during the operation, and patient satisfaction was assessed in the recovery room before patients were transferred to their service bed.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 40 Years 至 75 Years(Adult, Older Adult)
- 性别
- Male
- 接受健康志愿者
- 否
入选标准
- •Male undergoing transurethral prostatic resection,
- •40 to 75 years old,
- •ASA-I-III
- •Not using anticoagulants or antiaggregants,
- •No peripheral neuropathy or muscle disease,
- •Can be orientated and co-operated,
- •No vertebral deformity,
- •Body Mass Index <30,
- •Patients consenting to epidural anaesthesia.
排除标准
- •TUR-P operation will not be male,
- •Female patients,
- •Not in the appropriate age range (40-75),
- •Taking anticoagulants or antiaggregants, Previous lumbar surgery or skeletal deformity in the lumbar region,
- •Peripheral neuropathy, neuromuscular or neuropsychiatric disease,
- •Alcohol or drug addiction,
- •Obese with a body mass index >30,
- •History of frequent analgesic use,
- •Patients shorter than 155 cm and taller than 180 cm,
- •Who refused epidural anaesthesia,
- •Patients without orientation and co-operation.
结局指标
主要结局
Time to Reach Sensory Block at T10
时间窗: Within 20 minutes after anesthetic administration
Times to reach sensory block T10 (block levels)
Time to Reach Sensory Block at T10
时间窗: Within 20 minutes after anesthetic administration
Times to reach sensory block T10 (block levels)
次要结局
- Motor Block Intensity Based on Bromage Score at 20 Minutes(20 minutes after epidural block administration)
- Degree of Sensory Block Regression at 60 Minutes Post-Epidural Block(60 minutes after epidural block administration)
- Change in Systolic Blood Pressure (SBP)(From 5 minutes after sedation to 20 minutes after epidural block)
- Maximum Sensory Block Level at the 20th Minute Post-Epidural Block(20 minutes after epidural administration)
- Change in Systolic Blood Pressure (SBP)(From 5 minutes after sedation to 20 minutes after epidural block)
- Maximum Sensory Block Level at the 20th Minute Post-Epidural Block(20 minutes after epidural administration)
- Motor Block Intensity Based on Bromage Score at 20 Minutes(20 minutes after epidural block administration)
- Degree of Sensory Block Regression at 60 Minutes Post-Epidural Block(60 minutes after epidural block administration)
研究者
Emine OZCAN
Principal Investigator
Başakşehir Çam & Sakura City Hospital
