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[Anaesthesic management of vaginal delivery in a parturient with C1 esterase deficiency].

作者信息

Libert N, Schérier S, Dubost C, Franck L, Rouquette I, Tortosa J-C, Rousseau J-M

机构信息

Département d'anesthésie et de réanimation, hôpital d'instruction des armées Bégin, 69, avenue de Paris, 94160 Saint-Mandé, France.

出版信息

Ann Fr Anesth Reanim. 2009 Apr;28(4):375-80. doi: 10.1016/j.annfar.2009.02.035. Epub 2009 Apr 8.

DOI:10.1016/j.annfar.2009.02.035
PMID:19359129
Abstract

Hereditary and acquired angioedema (HAE/AAE) are the clinical translation of a qualitative or a quantitative deficit of C1 esterase inhibitor (C1 INH). The frequency and severity of clinical manifestations vary greatly, ranging from a moderate swelling of the extremities to obstruction of upper airway. Anaesthesiologists and intensivists must be prepared to manage acute manifestations of this disease in case of life-threatening laryngeal edema. Surgery, physical trauma and labour are classical triggers of the disease. The anaesthesiologists should be aware of the drugs used as prophylaxis and treatment of acute attacks when considering labour and caesarean section. Androgens are contraindicated during pregnancy. If prophylaxis is required, tranexamic acid may be used with caution. The safest obstetric approach appears to be to administer a predelivery infusion of C1 INH concentrate. It is important to avoid manipulation of the airway as much as possible by relying on regional techniques. We report the case of a patient suffering from an HAE discovered during pregnancy. The management included administration of C1 INH during labor and early epidural analgesia for pain relief. A short review of the pathophysiology and therapeutic options follows.

摘要

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