新生儿高铁血红蛋白的发展是否会影响丙洛卡因用于阴部麻醉的适宜性?围生期临床研究[j]。

IF 1.9 Q2 POLITICAL SCIENCE
Regional-Anaesthesie Pub Date : 1989-05-01
J Biscoping, B Bachmann-M, M Kirschbaum, G Hempelmann
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引用次数: 0

摘要

阴部阻滞是在分娩第二阶段实现镇痛的一种行之有效的方法。当需要在血管化良好的组织中注射大量的局麻药时,应使用全身性毒性低的局麻药,以尽量减少副作用。这意味着丙胺卡因是首选药物。众所周知,丙胺卡因的代谢物诱发高铁血红蛋白血症,因此高铁血红蛋白血症是否影响胎儿的问题就产生了。患者和方法。在17名母亲中,每名母亲使用2 × 10ml 1%的丙胺卡因实现阴部阻滞。用气相色谱法测定分娩时母亲和新生儿的血液样本中第二产程局麻药的血浆浓度。此外,通过新生儿6 h前的毛细血管血标本测定高铁血红蛋白血症的时间过程。为了评估新生儿的高铁血红蛋白血症,125微升肝素化毛细血管血用200微升0.9%氯化钠稀释;采用吸光度法检测高铁血红蛋白。结果。阴部阻滞前母体高铁血红蛋白浓度约为总血红蛋白浓度的0.2%,在生理范围内。在分娩的那一刻,它只增加了很小的程度,没有统计学意义。新生儿的平均高铁血红蛋白浓度在分娩后立即约为总血红蛋白的1%,在接下来的2小时内上升至1.8%,然后持续下降。分娩时,产妇平均浓度为0.57微克/毫升,新生儿平均浓度为0.29微克/毫升。讨论。关于全身毒性,当局部麻醉不需要长时间麻醉时,丙胺卡因是首选药物;它保证短潜伏期和充分缓解疼痛。其代谢物引起的高铁血红蛋白血症不是人类使用的禁忌症。以前,由于胎儿红细胞氧化还原能力小,丙胺卡因被认为是孕妇分娩时的禁忌症。然而,我们的研究表明,用于阴部阻滞的200毫克丙洛卡因不会在任何显著程度上诱导新生儿高铁血红蛋白血症。一种解释可能是新生儿局部麻醉剂的肾脏消除增加和低胎母比。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Does the development of methemoglobin in the newborn infant affect the suitability of prilocaine for pudendal anesthesia? A clinical study in the peripartum phase].

Pudendal block is a well established method of achieving analgesia during the second stage of labor. Whenever a large amount of a local anesthetic has to be injected in well vascularized tissue, local anesthetic drugs with low systemic toxicity should be used, to minimize side effects. This means that prilocaine is the drug of choice. It is well known that the metabolites of prilocaine induce methemoglobinemia, and thus the question arises as to whether the methemoglobinemia affects the fetus. PATIENTS AND METHODS. Pudendal block was achieved with 2 x 10 ml prilocaine 1% in each of 17 mothers. Plasma concentrations of the local anesthetic in the second stage of labor were determined by gas chromatography in blood samples drawn from the mother and the newborn at the moment of childbirth. In addition, the time course of methemoglobinemia was determined by capillary blood samples from the neonate up to 6 h. To evaluate methemoglobinemia in the newborn, 125 microliters heparinized capillary blood was diluted with 200 microliters 0.9% sodium chloride; methemoglobin was detected by absorbance spectrometry. RESULTS. Before the pudendal block maternal methemoglobin concentrations were about 0.2% of the total hemoglobin concentration and within the physiological range. At the moment of delivery it was increased only to a small extent, without statistical significance. In the neonates mean methemoglobin concentrations were about 1% of total hemoglobin immediately after delivery, increasing up to 1.8% in the next 2 h and then decreasing continuously in all. At the moment of childbirth maternal mean prilocaine concentrations were 0.57 micrograms/ml on an average and 0.29 micrograms/ml in the newborn. DISCUSSION. With respect to systemic toxicity, prilocaine is the drug of choice in local anesthetic procedures when a long duration of anesthesia is not required; it guarantees short latency and adequate relief of pain. Methemoglobinemia induced by its metabolites is not a contraindication for its use in humans. Formerly prilocaine was judged to be contraindicated in pregnant women during delivery because of the small redox capacity of fetal erythrocytes. Our study, however, demonstrates that 200 mg prilocaine for pudendal block does not induce methemoglobinemia in newborns to any significant extent. One explanation for this may be the increased renal elimination of local anesthetics in newborns and the low fetomaternal ratio.

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