Sah Neera, Vallejo Manuel C, Ramanathan Sivam, Golebiewski Kristy
Department of Anesthesia, Magee-Womens Hospital, Pittsburgh, PA 15213, USA.
J Clin Anesth. 2005 Mar;17(2):91-5. doi: 10.1016/j.jclinane.2004.05.004.
To compare the intensity and duration of motor block and the duration of sensory block with racemic bupivacaine and l-bupivacaine for combined spinal-epidural analgesia, as previous studies have shown contradictory results.
A prospective, randomized, double-blinded study.
Birth Center at Magee-Womens Hospital, Pittsburgh, Pa.
Multiparous American Society of Anesthesiologists physical status I and II patients requesting labor analgesia. There were 2 groups: group A with 34 patients and group B with 33.
Group A received a mixture of 2.5 mg of racemic bupivacaine and 25 microg of fentanyl into the subarachnoid space. Group B received 2.5 mg of intrathecal L-bupivacaine and 25 microg of fentanyl. Pain verbal analog score (VAS, 0-10) scores and Bromage scores were recorded at 5, 15, 30, and every 30 minutes thereafter until the VAS increased to 3 or higher, at which time the epidural block was activated with 0.125% bupivacaine and fentanyl. Patients' vital signs and fetal heart rate were monitored for 30 minutes after the block.
None of the patients in both groups had any demonstrable motor block. The median VAS decreased from 7 to 0 in 5 minutes in group A and from 7.5 to 0 in group B. The average durations of sensory block in groups A and B were 114.85 +/- 26.27 and 101.9 +/- 35.20 minutes (P = NS), respectively.
Contrary to earlier studies, we did not find any difference in the intensity and duration of sensory or motor blocks between racemic bupivacaine and l-bupivacaine. Based on our findings in the parturient population studied, we conclude that l-bupivacaine does not offer any advantages over racemic bupivacaine when used for combined spinal-epidural for labor analgesia.
由于既往研究结果相互矛盾,本研究旨在比较消旋布比卡因和左旋布比卡因用于腰麻-硬膜外联合镇痛时运动阻滞的强度和持续时间以及感觉阻滞的持续时间。
一项前瞻性、随机、双盲研究。
宾夕法尼亚州匹兹堡市梅杰妇女医院分娩中心。
要求分娩镇痛的美国麻醉医师协会身体状况I级和II级经产妇。分为两组:A组34例患者,B组33例患者