This prospective randomized clinical trial was performed between October 2013 and July 2014 in Fatemieh Hospital, Hamadan, Iran, after obtaining ethical clearance from the institutional ethics committee (3209/9/35/16/P/D).
A written informed consent was obtained from all patients prior to the study. A total of 100 parturients aged 19 - 49 years with the American society of anesthesiologists (ASA) physical status I-II were enrolled in this study. The patients were randomly allocated to either the sitting or the left lateral decubitus position group. The randomization scheme for the two groups was generated using the randomization.com website (http://www.randomization.com). Our exclusion criteria were parturients with contraindication for spinal anesthesia, history of migraine headaches, more than one puncture, any obstetric complications, and chronic use of analgesics.
After pre-anesthetic evaluation, routine monitoring, i.e., non-invasive blood pressure, pulse oximetry, and electrocardiography, was instituted in for all patients in the operation room. No sedative was prescribed for the patients to provide successful lactation.
All parturients received 10 mL/kg crystalloid solution before spinal anesthesia as prehydration.
Spinal anesthesia was administered with 2 mL of 0.5% hyperbaric bupivacaine (AstraZeneca; 10 mg) plus 1 mL sufentanil (5 µg) by a 24-gauge Quincke spinal needle either in the sitting or in the left lateral decubitus position. The needle was introduced with the bevel parallel to the sagittal plane. The technique was lumbar puncture in the midline approach at the L3-L4 interspinal space using a standard precaution and procedure.
In the left lateral decubitous position, parturients lay on their left side parallel to the rim of the operating table, their thighs were bent on their belly, and their neck was flexed to enable the forehead to be as close as possible to the knees. Data were collected by an unaware nurse.
The intensity of PDPH was assessed postoperatively using a numeric rating scale (NRS-11) immediately on either postoperative day (POD) one, two, or three as described to the parturients during the preoperative visit. NRS-11 is an 11-point numeric scale for patient self-reporting of pain intensity. On the scale, 0 is the absence of headache, 1 - 3 mild pain (nagging, annoying, and interfering slightly with activities of daily living [ADL]), 4 - 6 is moderate pain (interferes significantly with ADL), and 7 - 10 is severe pain (disabling; unable to perform ADL).
During follow-up in the ward, an unaware nurse charted the pain intensity using the NRS-11 scale.
The following factors were evaluated: age, weight, height, body mass index (BMI), PDPH and PONV.
Student’s independent sample t test was used to compare age, weight, BMI, and height between the two groups, and the chi-square test was used to assess the relationship between position and complications (PDPH and PONV).
The Mann–Whitney U test was used to determine the significant differences in the values of quantity variables without normal distribution, such as the day of onset of headache, head severity score, mean sensory block duration, and sensory block level between the two groups. P value less than 0.05 was considered statistically significant. All statistical calculations were performed using the SPSS version 16 software.