FACE DROPS: A Clinical Risk Assessment Tool for Differentiation of Acute Lyme Disease-Associated Facial Palsy From Bell Palsy.

IF 2.3 Q3 CLINICAL NEUROLOGY
Neurology. Clinical practice Pub Date : 2025-06-01 Epub Date: 2025-04-18 DOI:10.1212/CPJ.0000000000200476
Caleb R S McEntire, Sun Young Chung, Brian Chang, Keisha Judith Barrera, Yan Zhao, Joshua W Joseph, Gary P Wormser, Nate Jowett, Bart K Chwalisz
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Abstract

Background and objectives: 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.

Methods: 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.

Results: 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.

Discussion: 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.

面部滴液:区分急性莱姆病相关面瘫与贝尔麻痹的临床风险评估工具
背景和目的:面瘫是莱姆病的常见表现,在流行地区占急性面瘫的5%。莱姆病相关面瘫(LDFP)需要及时的抗生素治疗,而贝尔麻痹则需要皮质类固醇治疗。辅助皮质类固醇在急性LDFP治疗中的作用尚不清楚。目前莱姆病诊断实验室检测的局限性使得LDFP和BP的急性分化在许多病例中具有挑战性。方法:我们回顾了285例LDFP (N = 76)和BP (N = 209)患者的记录,这些患者于2005年至2021年在专门的面神经中心就诊,以确定就诊时的临床特征。我们开发并内部验证了一种临床风险评估工具(“FACE DROPS”),该工具基于LDFP和BP在发病时体征和症状之间的相关差异。结果:风险评估工具通过7个临床标准将LDFP与BP区分开来:发烧(+8到FACE DROPS评分),疼痛(关节痛/肌痛;+6)、头痛(头痛;+3),疲劳(异常疲劳;+4),皮结节型或神经根型(横切性脊髓炎或神经根炎;+4),耳痛或耳后疼痛(-1)和颈部僵硬(颈部僵硬;+ 3)。FACE DROPS评分≤4分预测BP准确率≥93.5%,评分≥7分预测LDFP准确率≥96.0%。讨论:开发了一种新的风险评估工具来区分LDFP和BP。该工具可能有助于指导莱姆病抗菌剂的处方设置在急性面瘫待确认的实验室证据,在没有迁移性红斑皮肤损害。
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来源期刊
Neurology. Clinical practice
Neurology. Clinical practice CLINICAL NEUROLOGY-
CiteScore
4.00
自引率
0.00%
发文量
77
期刊介绍: Neurology® Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. The journal publishes original articles in all areas of neurogenetics including rare and common genetic variations, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease genes, and genetic variations with a putative link to diseases. Articles include studies reporting on genetic disease risk, pharmacogenomics, and results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology® Genetics, but studies using model systems for treatment trials, including well-powered studies reporting negative results, are welcome.
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