Ikegami Hiromi, Hotta Kunihisa, Toba Yoshie
Department of Anesthesiology, Seirei Hamamatsu General Hospital, 2-12-12 Sumiyoshi, Naka-ku, Hamamatsu city, Shizuoka, 430-8558, Japan.
Department of Anesthesiology and Critical Care Medicine, Jichi Medical University, Tochigi, Japan.
JA Clin Rep. 2020 Oct 2;6(1):75. doi: 10.1186/s40981-020-00383-y.
In single-space combined spinal-epidural anesthesia (CSEA), it is important to correctly determine if the fluid coming out of the spinal needle is cerebrospinal fluid (CSF) or the liquid used in the loss of resistance (LOR) technique. In this study, we used mepivacaine for LOR and measured the pH values of CSF and mepivacaine to determine whether the pH test is a reliable method to confirm CSF when performing single-space CSEA.
This clinical trial included 47 full-term pregnant women who underwent cesarean section. Single-space CSEA was administered at the lumbar intervertebral space using a small amount of mepivacaine for LOR. The pH values of CSF and mepivacaine were determined by the color of the test strip immediately after dropping. The area under the curve (AUC) for the pH values was calculated to determine the cutoff value for distinguishing between CSF and mepivacaine.
The median pH values were 7.7 (7.1-8.0) and 6.2 (5.9-6.8) for CSF and mepivacaine, respectively. When the cutoff value of pH for distinguishing CSF from mepivacaine was 7.1 or greater, the AUC was 1.0 (100% sensitivity and specificity). Our result demonstrated that CSF can be correctly distinguished from mepivacaine in patients undergoing cesarean section under single-space CSEA using a cutoff value of pH 7.1.
The pH test is a simple and reliable method to confirm CSF when performing single-space CSEA with mepivacaine for LOR.
Accuracy of pH test paper for cerebrospinal fluid during spinal anesthesia: prospective study in healthy pregnant women under scheduled caesarean section; University Hospital Medical Information Network, UMIN000036454 . Registered 1 May 2019.
在单间隙腰麻-硬膜外联合麻醉(CSEA)中,正确判断从腰麻针流出的液体是脑脊液(CSF)还是阻力消失(LOR)技术中使用的液体非常重要。在本研究中,我们使用甲哌卡因进行LOR,并测量CSF和甲哌卡因的pH值,以确定pH测试是否是在进行单间隙CSEA时确认CSF的可靠方法。
本临床试验纳入了47例行剖宫产的足月孕妇。在腰椎间隙进行单间隙CSEA,使用少量甲哌卡因进行LOR。滴液后立即通过试纸颜色测定CSF和甲哌卡因的pH值。计算pH值的曲线下面积(AUC)以确定区分CSF和甲哌卡因的临界值。
CSF和甲哌卡因的pH值中位数分别为7.7(7.1-8.0)和6.2(5.9-6.8)。当区分CSF和甲哌卡因的pH临界值为7.1或更高时,AUC为1.0(敏感性和特异性均为100%)。我们的结果表明,在单间隙CSEA下行剖宫产的患者中,使用pH值7.1的临界值可以正确区分CSF和甲哌卡因。
在使用甲哌卡因进行LOR的单间隙CSEA中,pH测试是确认CSF的简单可靠方法。
脊髓麻醉期间脑脊液pH试纸的准确性:择期剖宫产健康孕妇的前瞻性研究;大学医院医学信息网络,UMIN000036454。2019年5月1日注册。