Serviço de Anestesiologia, Hospital Santo António, Porto, Portugal.
Eur J Anaesthesiol. 2010 Nov;27(11):985-90. doi: 10.1097/EJA.0b013e32833e263f.
Myasthenia gravis is an autoimmune neuromuscular disease, usually affecting women in the second and third decades. The course is unpredictable during pregnancy and puerperium. Myasthenia gravis can cause major interference in labour and partum and exacerbations of the disease frequently occur. The aim of this series of cases is to analyse retrospectively the anaesthetic management of myasthenia gravis patients and complications during the peripartum period.
Retrospective, single centre study from clinical files of female myasthenia gravis patients who delivered between 1985 and 2007 at Hospital de Santo António, Porto, Portugal.
Seventeen myasthenia gravis patients delivered between 1985 and 2007 in Hospital Santo António. Two women were not included in the study as they had a spontaneous abortion in the first trimester. Four patients presented exacerbations of the disease during pregnancy, no exacerbation occurred in eight patients and three patients presented their first symptoms of myasthenia gravis during pregnancy (without diagnosis at time of delivery). Concerning the eight patients without exacerbations of the disease during pregnancy, pregnancy was brought to term in 87.5% of the cases; five women were submitted to nonurgent caesarean section (62.5%); and epidural block was performed in six patients (75%). No complications related to anaesthesia occurred in the peripartum period. Concerning the four patients with exacerbations of the disease, pregnancy was brought to term in three cases (75%); three women were submitted to nonurgent caesarean section (75%); and epidural block was performed in three patients (75%). One patient underwent an uncomplicated thymectomy under general anaesthesia during pregnancy and, in the postpartum period, there was a myasthenic crisis in another patient. Concerning the three patients without a myasthenia gravis diagnosis at partum, one woman already being followed for presenting muscular weakness had a vaginal delivery under epidural block, without complications; another patient, presenting discrete supine dyspnoea, was submitted to elective caesarean section under spinal block and developed severe dyspnoea that required mechanical ventilation and ICU admission; and in the remaining case, a woman presenting mild blurred vision was submitted to general anaesthesia, which resulted in delayed emergence, muscular weakness and respiratory failure. Pregnancy went full term in all cases (100%). No newborn had a myasthenic crisis.
Myasthenia gravis can interfere slightly with pregnancy and partum, although exacerbations of the disease occur frequently. Strict surveillance and therapeutic optimisation are crucial. In women with controlled disease, caesarean section should be carried out only if there are obstetric reasons. Locoregional anaesthesia is preferred, mainly epidural block. A good multidisciplinary cooperation, specific precautions and surveillance can certainly contribute to an improved outcome in myasthenia gravis patients during the peripartum period.
重症肌无力是一种自身免疫性神经肌肉疾病,通常影响 20 至 30 岁的女性。妊娠和产褥期的病程不可预测。重症肌无力可导致分娩和产程出现严重干扰,并经常导致疾病恶化。本系列病例旨在回顾性分析重症肌无力患者围产期的麻醉管理和并发症。
对葡萄牙波尔图圣安东尼医院 1985 年至 2007 年间分娩的重症肌无力女性患者的临床病历进行回顾性单中心研究。
1985 年至 2007 年间,圣安东尼医院共有 17 名重症肌无力患者分娩。由于 2 名女性在妊娠早期自然流产,因此未将她们纳入研究。4 名患者在妊娠期间出现疾病恶化,8 名患者无恶化,3 名患者在妊娠期间首次出现重症肌无力症状(分娩时未确诊)。对于妊娠期间无疾病恶化的 8 名患者,87.5%的患者足月分娩;5 名女性接受非紧急剖宫产(62.5%);6 名患者接受硬膜外阻滞(75%)。围产期无麻醉相关并发症。对于 4 名疾病恶化的患者,3 名患者足月分娩(75%);3 名女性接受非紧急剖宫产(75%);3 名患者接受硬膜外阻滞(75%)。1 名患者在妊娠期间接受全身麻醉下的胸腺切除术,产后另 1 名患者出现肌无力危象。对于分娩时未确诊重症肌无力的 3 名患者,1 名已因肌肉无力而接受治疗的女性接受硬膜外阻滞下的阴道分娩,无并发症;1 名患者表现为轻微的仰卧位呼吸困难,接受选择性剖宫产和脊髓阻滞,发展为严重呼吸困难,需要机械通气和 ICU 入院;另 1 名患者表现为轻度视力模糊,接受全身麻醉,导致苏醒延迟、肌无力和呼吸衰竭。所有病例均足月分娩(100%)。无新生儿出现肌无力危象。
重症肌无力可轻度影响妊娠和产褥期,尽管疾病常恶化。严格的监测和治疗优化至关重要。对于病情控制良好的女性,只有在存在产科原因时才应进行剖宫产。局部麻醉是首选,主要是硬膜外阻滞。良好的多学科合作、具体预防措施和监测肯定有助于改善围产期重症肌无力患者的结局。