Gaida B J, Gervais H W, Mauer D, Leyser K H, Eberle B
Klinik für Anaesthesiologie, Johannes Gutenberg-Universität Mainz.
Anaesthesist. 1991 Jan;40(1):1-6.
Takayasu's disease is a rare form of nonspecific obliterative panarteritis of unknown origin, mainly located at supraaortic, renal, and pulmonary arteries and resulting in multiple stenoses and occlusion of major arteries. Predominantly young women in the first three decades of life are affected. Absence of arm pulses, vascular bruits, and retinopathy are classic symptoms. Another symptom is hypertension of the lower extremities and hypotension of the upper extremities, thus potentially impairing cerebral perfusion. A 25-year-old female patient with a 2-year history of Takayasu's disease presented for therapeutic abortion on the grounds of her medical condition. There were significant stenoses of the left common carotid artery and the internal carotid artery. The left subclavian artery was totally obliterated. The arterial blood supply to the left arm was accomplished by the left vertebral artery via a subclavian steal syndrome. Brachial and radial pulses were absent in both arms. General, spinal or epidural anesthesia can produce arterial hypotension. Blood pressure assessment at the lower extremities does not allow conclusions about perfusion of supraaortic arteries and cerebral perfusion pressure. Thus, a paracervical block was performed; sedation and analgesia were achieved with small doses of midazolam and alfentanil. We planned that if general anesthesia became necessary we would induce anesthesia with etomidate and alfentanil and maintain anesthesia by mask ventilation with nitrous oxide in oxygen and supplementary doses of alfentanil. Invasive monitoring such as arterial or Swan Ganz catheterization, was contraindicated because of the possibility that inflamed vessels would become irritated. Therefore, we only monitored ECG, blood pressure at the leg, ventilation parameters, and oxygen saturation at the ear lobe by pulse oximetry.(ABSTRACT TRUNCATED AT 250 WORDS)
高安氏病是一种罕见的不明原因的非特异性闭塞性全动脉炎,主要累及主动脉弓、肾动脉和肺动脉,导致主要动脉多处狭窄和闭塞。主要影响20至30岁的年轻女性。无臂脉搏、血管杂音和视网膜病变是典型症状。另一个症状是下肢高血压和上肢低血压,从而可能损害脑灌注。一名患有高安氏病2年的25岁女性患者因自身病情前来进行治疗性流产。左颈总动脉和颈内动脉有明显狭窄。左锁骨下动脉完全闭塞。通过锁骨下动脉窃血综合征,左臂的动脉血供由左椎动脉完成。双臂均无肱动脉和桡动脉搏动。全身麻醉、脊髓麻醉或硬膜外麻醉可导致动脉低血压。下肢血压评估无法得出关于主动脉弓动脉灌注和脑灌注压的结论。因此,实施了宫颈旁阻滞;使用小剂量咪达唑仑和阿芬太尼实现镇静和镇痛。我们计划,如果需要全身麻醉,将使用依托咪酯和阿芬太尼诱导麻醉,并通过面罩通气吸入氧化亚氮和补充剂量的阿芬太尼维持麻醉。由于发炎的血管可能会受到刺激,因此禁忌进行动脉或 Swan Ganz 导管插入术等有创监测。因此,我们仅通过脉搏血氧饱和度仪监测心电图、腿部血压、通气参数和耳垂血氧饱和度。(摘要截短于250字)