This double-blind clinical trial study was conducted in 2015 at 15 Khordad Hospital in Gonabad City after receiving the ethical code IR.GMU.REC.1394 and IRCT code IRCT2015120712312N3, on 80 patients aged 25 to 75 who were candidates for surgery and underwent spinal anesthesia. The aim was to compare the effect of propofol sedative drug dose with midazolam on PDPH.
The inclusion criteria were patient consent, no coagulation problem, no history of headaches, no skin infection at the site of spinal anesthesia, ASA class one and two patients, and no history of seizures. In addition, more than 2 punctures in the dura for spinal anesthesia drug injection, the need for narcotic drugs during surgery, and the need for general anesthesia after spinal anesthesia were the exclusion criteria from this study.
After obtaining informed consent and if they met the inclusion criteria, the patients were divided into 2 groups, A and B, using the permutation block randomization technique.
In both groups, 6 mL/kg of Ringer's fluid was given as a compensatory volume. Then, the patient was placed in a sitting position; the skin was prepared with 10% betadine, and under sterile conditions, Quincke No. 25 spinal needles were used to enter the subcutaneous tissue parallel to the spinal cord fibers. After entering the dura and removing the cerebrospinal fluid, 2 cc of spinal marcaine was injected. The needle was removed, and after dressing the patient's skin, he was placed in a supine position. After obtaining anesthesia and maintaining the anesthesia level, in group A, propofol was infused slowly at a dose of 30 µg/min. In group B, midazolam was injected intravenously at 1 mg. Also, in both groups, in case of blood pressure dropping more than 30% of the initial amount, 5 mg of ephedrine was used intravenously.
The main variable investigated in this study was the headache of the patient after spinal anesthesia and the severity of the headache of the patient after the operation was recorded by a trained nurse immediately after entering the recovery room and in the ward for up to 24 hours based on the VAS pain criterion in the checklist that was prepared for this purpose. In the case of headaches in patients, the usual treatments include complete rest, hydration, and the use of analgesics, which in this research included acetaminophen, codeine 300 mg every 6 hours, and the use of an abdominal binder.
3.1. Statistical Analysis
The data analysis was performed using the statistical analysis software SPSS version 20. Descriptive statistics (determining the indices of central tendency and dispersion and drawing frequency tables) were used to determine pain intensity and examine demographic variables. The non-parametric Mann-Whitney test was used to compare pain intensity in two groups. The difference between the groups in terms of other demographic variables according to their type was investigated with t-test and chi-square tests. Data analysis was considered at a 5% significance level and 80% statistical power.