Host Brian D, Sloan Walker
Baptist Health Lexington, KY, USA.
Ann Pharmacother. 2014 Jan;48(1):142-4. doi: 10.1177/1060028013507050. Epub 2013 Oct 15.
To describe a case of orofacial dyskinesia in a patient treated with levofloxacin for acute diverticulitis.
A 77-year-old woman with mild renal insufficiency was admitted with acute diverticulitis. She was initiated on levofloxacin 500 mg IV daily and metronidazole 500 mg IV every 8 hours. On day 4 of treatment, she experienced involuntary, rhythmic facial grimacing accompanied by periodic cervical muscular contractures. Her speech became dysarthric, interrupted by uncontrolled facial and tongue movements, all findings consistent with orofacial dyskinesia. Antibiotics were discontinued, and symptoms resolved after administration of diphenhydramine and lorazepam IV.
Fluoroquinolone-associated central nervous system (CNS) toxicities are infrequently observed. They are most commonly associated with ciprofloxacin and are thought to be related to inhibition of γ-aminobutyric acid receptors and activation of N-methyl-d-aspartate receptors. Orofacial dyskinesia has previously been reported primarily with second-generation fluoroquinolones, with only a single case report implicating a third-generation fluoroquinolone. To our knowledge, we report the second case of orofacial dyskinesia with a third-generation fluoroquinolone, the first such case associated with levofloxacin. The orofacial dyskinesia experienced in this case was categorized as probably related to levofloxacin, as assessed by the Naranjo adverse drug reaction probability assessment tool. Contributing factors likely included age and renal function.
Although rare, CNS toxicities such as orofacial dyskinesia have been reported with levofloxacin. Patients on fluoroquinolones of advanced age and with renal insufficiency should be monitored closely for such toxicities.
描述1例因急性憩室炎接受左氧氟沙星治疗的患者出现口面部运动障碍的病例。
一名77岁轻度肾功能不全女性因急性憩室炎入院。开始每日静脉注射500mg左氧氟沙星及每8小时静脉注射500mg甲硝唑治疗。治疗第4天,她出现不自主、有节律的面部抽搐,伴有周期性颈部肌肉痉挛。她的言语变得构音障碍,被不受控制的面部和舌部运动打断,所有表现均符合口面部运动障碍。停用抗生素,静脉注射苯海拉明和劳拉西泮后症状缓解。
氟喹诺酮类药物相关的中枢神经系统(CNS)毒性很少见。它们最常与环丙沙星相关,被认为与γ-氨基丁酸受体抑制和N-甲基-D-天冬氨酸受体激活有关。口面部运动障碍此前主要报道与第二代氟喹诺酮类药物有关,仅有1例病例报告涉及第三代氟喹诺酮类药物。据我们所知,我们报告了第2例与第三代氟喹诺酮类药物相关的口面部运动障碍病例,首例与左氧氟沙星相关。根据Naranjo药物不良反应概率评估工具评估,该病例出现的口面部运动障碍可能与左氧氟沙星有关。促成因素可能包括年龄和肾功能。
尽管罕见,但左氧氟沙星已报告有口面部运动障碍等中枢神经系统毒性。老年和肾功能不全的氟喹诺酮类药物使用者应密切监测此类毒性。