Prise en charge anesthésique d'un accouchement chez une patiente atteinte d'un déficit en inhibiteur de C1 estérase

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

Résultats de recherche: Contribution à un journalArticleRevue par des pairs

3 Citations (Scopus)

Résumé

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.

Titre traduit de la contributionAnaesthesic management of vaginal delivery in a parturient with C1 esterase deficiency
langue originaleFrançais
Pages (de - à)375-380
Nombre de pages6
journalAnnales Francaises d'Anesthesie et de Reanimation
Volume28
Numéro de publication4
Les DOIs
étatPublié - 1 avr. 2009
Modification externeOui

mots-clés

  • Anaesthesia
  • C1 inhibitor deficiency
  • Hereditary angio-oedema
  • Labour
  • Treatment

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