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首页> 外文期刊>Canadian journal of anesthesia: Journal canadien d'anesthesie >Obstetrical anaesthesia for a parturient with preeclampsia, HELLP syndrome and acute cortical blindness.
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Obstetrical anaesthesia for a parturient with preeclampsia, HELLP syndrome and acute cortical blindness.

机译:产前先兆子痫,HELLP综合征和急性皮质盲的产科麻醉。

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PURPOSE: To report the management of a multigravida presenting with preeclampsia, HELLP syndrome and acute cortical blindness for Caesarean section. CLINICAL FEATURES: A 39-yr-old woman, with three past uncomplicated pregnancies presented at 33 wk with acute cortical blindness. Based on clinical and laboratory assessment, a diagnosis of preeclampsia with HELLP syndrome was made. A CT scan of her head demonstrated ischaemic lesions of her basal ganglia, extending superiorly to involve both posterior parietal and occipital regions. Infusions of magnesium sulphate and hydralazine were started and an urgent Caesarean section was performed under subarachnoid anaesthesia after insertion of an arterial line and intravenous hydration. The course of anaesthesia and surgery was uneventful and she delivered a live 1540 g female infant. By the following morning, she had recovered some vision and visual recovery was complete by 72 hr postpartum. She underwent an MRI with angiography on the first postpartum day. Ischaemic lesions were confirmed in the same sites identified on CT scan but all major cerebral vessels were patent and no significant vascular abnormality was noted. Her postoperative course was uneventful and she was discharged home seven days postpartum after being prescribed labetalol for continued hypertension. CONCLUSION: The anaesthetic management of a parturient with acute cortical blindness and HELLP syndrome is modeled on the underlying preeclamptic condition. Invasive monitoring is not routinely indicated but is specifically indicated in some cases. Provided that it is not contraindicated because of prohibitive risk to the mother, regional anaesthesia has particular advantage in these patients. In particular, the use of spinal anaesthesia, which has been discouraged by some for this patient population, should be re-evaluated.
机译:目的:报告剖宫产时先兆子痫,HELLP综合征和急性皮质盲的多胎症的处理。临床特征:一名39岁的妇女,在33 wk时出现了3例过去无并发症的妊娠,并伴有急性皮层失明。根据临床和实验室评估,对先兆子痫合并HELLP综合征进行了诊断。头部的CT扫描显示出其基底神经节的缺血性病变,向上延伸至累及后顶叶区和枕叶区。开始输注硫酸镁和肼屈嗪,并在插入动脉管路和静脉水化后在蛛网膜下麻醉下进行紧急剖腹产。麻醉和手术过程顺利进行,她分娩了1540 g的活婴。第二天早上,她恢复了一些视力,并且在产后72小时完成了视力恢复。产后第一天,她接受了血管造影的MRI检查。在CT扫描确定的相同部位证实了缺血性病变,但所有主要脑血管均已开放,未发现明显的血管异常。术后病情平稳,产后7天因持续性高血压被处方使用拉贝洛尔后出院回家。结论:以潜在的先兆子痫状态为模型,对急性皮质盲和HELLP综合征的产妇进行麻醉管理。侵入性监视不是常规指示,而是在某些情况下特别指示。如果不因母亲的高风险而禁忌使用局部麻醉,则在这些患者中具有特殊优势。尤其应重新评估这种患者人群不鼓励使用的麻醉方法。

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