医学
触诊
脊髓麻醉
麻醉
随机对照试验
剖宫产
外科
超声科
局部麻醉
怀孕
生物
遗传学
作者
Mohamed Mohamed Tawfik,Mohamed Ahmed Tolba,Olfat Mostafa Ismail,Medhat Mikhail Messeha
出处
期刊:Regional Anesthesia and Pain Medicine
[BMJ]
日期:2023-05-15
卷期号:49 (1): 41-48
被引量:6
标识
DOI:10.1136/rapm-2022-104272
摘要
Introduction Ultrasonography may facilitate neuraxial blocks in obstetrics. This randomized controlled trial aimed to compare preprocedural ultrasonography with landmark palpation for spinal anesthesia in obese parturients undergoing cesarean delivery. Methods 280 American Society of Anesthesiologists (ASA) physical status II–III parturients with body mass index ≥35 kg/m 2 , full-term singleton pregnancy, undergoing elective cesarean delivery under spinal anesthesia, were randomly assigned to two equal groups (ultrasonography and palpation); preprocedural systematic ultrasound approach and conventional landmark palpation were performed, respectively. Patients and outcome assessors were blinded to the study group. All ultrasound and spinal anesthetic procedures were performed by a single experienced anesthesiologist. The primary outcome was the number of needle passes required to obtain free cerebrospinal fluid (CSF) flow. Secondary outcomes were the number of skin punctures required to obtain free CSF flow, success rate at the first needle pass, success rate at the first skin puncture, duration of the spinal procedure, patient satisfaction and incidence of vascular puncture, paresthesia, failure to obtain CSF flow and failed spinal block. Results There were no significant differences in primary or secondary outcomes between the two groups. The median (IQR) of the number of needle passes required to obtain free CSF flow was 3 (1–7) in ultrasonography group and 3 (1–7) in palpation group; p=0.62. Conclusions Preprocedural ultrasonography did not decrease the number of needle passes required to obtain free CSF flow or improve other outcomes compared with landmark palpation during spinal anesthesia performed by a single experienced anesthesiologist in obese parturients undergoing cesarean delivery. Trial registration number NCT03792191; https://clinicaltrials.gov/ct2/show/NCT03792191
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