McEntire Caleb R S, Chung Sun Young, Chang Brian, Barrera Keisha Judith, Zhao Yan, Joseph Joshua W, Wormser Gary P, Jowett Nate, Chwalisz Bart K
Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA.
Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA.
Neurol Clin Pract. 2025 Jun;15(3):e200476. doi: 10.1212/CPJ.0000000000200476. Epub 2025 Apr 18.
Facial palsy is a common manifestation of Lyme disease, accounting for up to 5% of acute facial palsies in endemic regions. Lyme disease-associated facial palsy (LDFP) warrants prompt antibiotic therapy while corticosteroid therapy is indicated for Bell palsy. The role of adjuvant corticosteroids in the treatment of acute LDFP is unclear. Current limitations of diagnostic laboratory tests for Lyme disease render acute differentiation of LDFP and BP challenging in many cases.
We reviewed records from 285 patients with LDFP (N = 76) and BP (N = 209) referred to a specialized facial nerve center from 2005 to 2021 to determine clinical characteristics at time of presentation to medical care. We developed and internally validated a clinical risk assessment tool ("FACE DROPS") based on pertinent differences between signs and symptoms of LDFP and BP at presentation.
The risk assessment tool distinguishes LDFP from BP using 7 clinical criteria: fever (+8 to FACE DROPS score), aches (arthralgia/myalgia; +6), cephalalgia (headache; +3), exhaustion (unusual fatigue; +4), dermatomal or radicular pattern (transverse myelitis or radiculitis; +4), otalgia or postauricular pain (-1), and stiff neck (nuchal rigidity; +3). FACE DROPS scores ≤4 predicted BP with ≥93.5% accuracy while scores of ≥7 predicted LDFP with ≥96.0% accuracy.
A novel risk assessment tool to distinguish LDFP from BP was developed. This tool may help guide the prescribing of antimicrobials for Lyme disease in the setting of acute facial palsy pending confirmatory laboratory evidence in the absence of an erythema migrans skin lesion.
面神经麻痹是莱姆病的常见表现,在流行地区占急性面神经麻痹的比例高达5%。莱姆病相关性面神经麻痹(LDFP)需要及时进行抗生素治疗,而贝尔麻痹则需使用皮质类固醇治疗。辅助性皮质类固醇在急性LDFP治疗中的作用尚不清楚。目前莱姆病诊断实验室检查的局限性使得在许多情况下急性区分LDFP和BP具有挑战性。
我们回顾了2005年至2021年转诊至一家专业面神经中心的285例LDFP患者(n = 76)和BP患者(n = 209)的记录,以确定就诊时的临床特征。我们基于LDFP和BP就诊时体征和症状的相关差异,开发并在内部验证了一种临床风险评估工具(“FACE DROPS”)。
该风险评估工具使用7项临床标准区分LDFP和BP:发热(FACE DROPS评分加8)、疼痛(关节痛/肌痛;加6)、头痛(加3)、疲惫(异常疲劳;加4)、皮节或神经根模式(横贯性脊髓炎或神经根炎;加4)、耳痛或耳后疼痛(减1)以及颈部僵硬(颈项强直;加3)。FACE DROPS评分≤4预测BP的准确率≥93.5%,而评分≥7预测LDFP的准确率≥96.0%。
开发了一种区分LDFP和BP的新型风险评估工具。在没有游走性红斑皮肤病变且缺乏确诊实验室证据的情况下,该工具可能有助于指导急性面神经麻痹患者莱姆病抗菌药物的处方。