Clemens K E, Quednau I, Heller A R, Klaschik E
Department of Anesthesiology, Intensive Care Medicine, Palliative Medicine and Pain Therapy, Malteser Hospital Bonn/Rhein-SiegUniversity of Bonn, Bonn, Germany.
Minerva Ginecol. 2010 Dec;62(6):515-24.
Maternal hypotension is the most frequent complication in spinal anesthesia for Cesarean delivery. Malperfusion of the foetus and nausea and vomiting of the mother are hallmarks of maternal hypotension. In this retrospective data analysis and anesthesia protocols we have investigated to explore the effects of therapeutic interventions for hypotension with cafedrine/theodrenaline (Akrinor® ) during spinal anesthesia for elective Cesarean section.
In a retrospective study anesthesia charts of 173 parturients undergoing spinal anesthesia for Cesarean delivery with 10mg hyperbaric bupivacaine + 5 µg sufentanil were reviewed for 30 min after onset of hypotension with respect to blood pressure, heart rate, respiration rate, as well as APGAR scores and umbilical arterial pH. Maternal data were compared to baseline values recorded and documented immediately before placing the spinal anesthesia in the operating room. The cohort was divided into two groups according to their hemodynamic response to spinal anesthesia: 117 parturients had a drop of systolic blood pressure to <120 mmHg or <80% of baseline blood pressure and were therefore treated with Akrinor® (cafedrine/theodrenaline; treatment group); 56 patients remained within the specified limits (non-treatment group). Maternal cardiovascular parameters and newborn outcome between the groups were compared.
Both groups were comparable with regard to baseline characteristics. In the treatment group one minute after the first application of cafedrine (43 mg)/theodrenaline (2.2 mg) mean systolic blood pressure raised from 108.6 mmHg to 117.2 mmHg (P=0.0004), mean of maximal changes of systolic blood pressure after the first application of Akrinor® was 21.3 mmHg. Blood pressure levels of the non-treatment group were regained in the treatment group 8 min after hypotension onset and remained at that level until the end of 30 min observation. No clinically relevant changes of heart rate were detectable. While mean APGAR score one minute post partum was significantly higher in the treatment group (8.9±1.2 vs. 8.4±1.1 P=0.043), mean umbilical arterial cord pH was 7.3±0.1 and APGAR scores 5 and 10 minutes postpartum did not differ significantly.
The results of this study confirm a rapid and sustained increase in blood pressure after application of Akrinor® for treatment of sympathicolysis induced hypotension. No negative impact of Akrinor® on umbilical arterial cord pH and APGAR scores was observed.
产妇低血压是剖宫产脊髓麻醉中最常见的并发症。胎儿灌注不足以及产妇恶心呕吐是产妇低血压的特征。在这项回顾性数据分析和麻醉方案中,我们进行研究以探索在择期剖宫产脊髓麻醉期间使用卡非君/茶丙胺(阿立诺®)治疗低血压的干预效果。
在一项回顾性研究中,对173例接受脊髓麻醉剖宫产的产妇麻醉记录进行审查,这些产妇使用10mg重比重布比卡因 + 5μg舒芬太尼,在低血压发作后30分钟内观察其血压、心率、呼吸频率,以及阿氏评分和脐动脉pH值。将产妇数据与在手术室进行脊髓麻醉前立即记录和存档的基线值进行比较。根据对脊髓麻醉的血流动力学反应,该队列分为两组:117例产妇收缩压降至<120 mmHg或低于基线血压的80%,因此接受阿立诺®(卡非君/茶丙胺)治疗(治疗组);56例患者血压保持在规定范围内(非治疗组)。比较两组之间的产妇心血管参数和新生儿结局。
两组在基线特征方面具有可比性。在治疗组首次应用卡非君(43mg)/茶丙胺(2.2mg)后1分钟,平均收缩压从108.6 mmHg升至117.2 mmHg(P = 0.0004),首次应用阿立诺®后收缩压的最大平均变化为21.3 mmHg。低血压发作后8分钟,治疗组恢复到非治疗组的血压水平,并在30分钟观察期结束时保持该水平。未检测到心率有临床相关变化。虽然产后1分钟治疗组的平均阿氏评分显著更高(8.9±1.2对8.4±1.1,P = 0.043),但平均脐动脉血pH值为7.3±0.1,产后5分钟和10分钟的阿氏评分无显著差异。
本研究结果证实,应用阿立诺®治疗交感神经阻滞引起的低血压后,血压迅速且持续升高。未观察到阿立诺®对脐动脉血pH值和阿氏评分有负面影响。