Turbelin Caroline, Mallat Jihad
Department of Anesthesiology and Critical Care Medicine, CH Lens, Lens, France.
Department of Critical Care Medicine, Critical Care Institute, Cleveland Clinic Abu Dhabi, Abu Dhabi, UAE.
Medicine (Baltimore). 2020 Jan;99(5):e18862. doi: 10.1097/MD.0000000000018862.
Horner's syndrome is an unusual side effect of epidural analgesia. We report an unusual symptom after epineural axis analgesia for labor, which happened three times in the same patient. Horner's syndrome occurrence following epidural catheterization should lead the anesthetic team to search for a subdural position of the catheter because of its potentially threatening complications.
PATIENT'S CONCERN: Our patient, a 38 years old pregnant woman, was managed by the anesthetic team for the analgesia of her second labor. Anesthetic consultation pointed out that she had a history of Horner's syndrome after epidural analgesia attempt during her first pregnancy.During our anesthetic management of her second labor, she presented, on the left side of the body, with the same symptom as she had during her first labor a few years ago, associated with high unilateral sensory block after epidural catheterization. After the total regression of neurological signs, a second catheterization attempt was followed by a contralateral isolated Horner's syndrome with no sensory block.
A few minutes after the induction of analgesia, our patient presented left ptosis, meiosis, and enophthalmos associated with a high homolateral sensory block. The subdural catheter position was suspected, and the catheter was removed.
Because of this repeated unusual complication and because we would not have used the catheter for an emergency C section, we chose to remove it definitively.
Our patient had a total regression of the symptoms 1 h after the catheter withdrawal. Delivery was rapid, with no complications, and she was discharged from the hospital 3 days after.
Our observations suggest the possibility of a potential anatomical particularity of the dural canal in this patient and question the safety of performing an epidural catheterization for further procedures.
霍纳综合征是硬膜外镇痛一种不常见的副作用。我们报告了一例分娩时进行神经轴镇痛后出现的不寻常症状,该症状在同一患者身上发生了三次。硬膜外导管插入术后发生霍纳综合征应促使麻醉团队寻找导管的硬膜下位置,因为其可能会引发危及生命的并发症。
我们的患者是一名38岁的孕妇,麻醉团队为其第二次分娩实施镇痛。麻醉会诊指出,她在第一次怀孕时尝试硬膜外镇痛后曾出现过霍纳综合征病史。在我们对她第二次分娩进行麻醉管理期间,她身体左侧出现了与几年前第一次分娩时相同的症状,同时伴有硬膜外导管插入术后的高平面单侧感觉阻滞。神经体征完全消退后,再次尝试插入导管,结果对侧出现孤立性霍纳综合征,无感觉阻滞。
镇痛诱导几分钟后,我们的患者出现左侧上睑下垂、瞳孔缩小和眼球内陷,并伴有高平面同侧感觉阻滞。怀疑导管处于硬膜下位置,遂将导管拔除。
鉴于这种反复出现的不寻常并发症,且我们不会在紧急剖宫产时使用该导管,因此我们选择将其彻底拔除。
拔除导管1小时后,患者症状完全消退。分娩过程迅速,无并发症,患者于3天后出院。
我们的观察结果提示该患者的硬脊膜管可能存在潜在的解剖学特殊性,并对进一步操作时进行硬膜外导管插入术的安全性提出了质疑。