Evidence map›Paper›PMID 40604646›Full record

ArticleBMC pediatrics2025

Long-term clinical outcomes after Lyme neuroborreliosis in children.

R A Bruinsma, B H Skogman, M Boele van Hensbroek, Y M Vermeeren, J W Hovius, T P Zomer

Abstract read
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Article in BMC pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

R A BruinsmaDepartment of Pediatrics, Gelre Hospital, Apeldoorn, PO Box 9014, 7300 DS, The Netherlands. r.bruinsma@gelre.nl.
B H SkogmanCenter for Clinical Research Dalarna, Uppsala University, Falun, Sweden.
M Boele van HensbroekDepartment of Pediatrics, Amsterdam Medical Center, University of Amsterdam, Amsterdam, the Netherlands.
Y M VermeerenDepartment of Internal Medicine, Gelre Hospital, Apeldoorn, the Netherlands.
J W HoviusAmsterdam UMC Multidisciplinary Lyme borreliosis Center, Amsterdam UMC Medical Centers, location AMC, University of Amsterdam, Amsterdam, the Netherlands.
T P ZomerDepartment of Internal Medicine, Gelre Hospital, Apeldoorn, the Netherlands.

Funding

Science Fund of Gelre Hospitals, The Netherlands 2023.01
6 · The paper itself

Abstract

backgroundLyme neuroborreliosis (LNB) is a tick-borne infection caused by spirochetes of the Borrelia burgdorferi sensu lato complex. Facial nerve palsy and subacute meningitis are the most prevalent neurological manifestations. Long-term prognosis is a major concern of many parents. These concerns relate to persisting neurological deficiencies as well as long-term non-specific symptoms such as fatigue. The aim of this study is to determine long-term outcome in pediatric LNB by using patient-reported outcome measures (PROMs) of facial impairment and self-reported fatigue and to compare these outcomes between children with LNB and idiopathic facial nerve palsy (IFP).

methodsA long-term follow-up study was performed including all children (< 18 years) who visited the departments of pediatrics, neurology, or otorhinolaryngology of Gelre hospitals Apeldoorn and Zutphen between 1 January 2010 and 31 December 2023 with the diagnosis LNB or IFP. After consent, children and/or parents (or guardians) were invited to complete an electronic questionnaire, including the Facial Clinimetric Evaluation (FaCE) scale and the Checklist Individual Strength (CIS).

resultsDuring the study period, 105 children were identified with facial nerve palsy and 4 with LNB with only headache. These 4 patients with meningitis but without facial nerve palsy were not included in further analyses. Seven children were lost to follow up. In total, 102 children were invited to complete the questionnaires, of which 84 responded (82%) after a median follow-up period of 93.5 months after the acute facial nerve palsy. The median total score of the FaCE scale was 99.2 (IQR 89.2-100) in children with LNB and 98.3 (IQR 93.3-100) in children with IFP and results did not differ between groups (p = 0.787). There were no significant differences between patients with LNB and IFP in the CIS total score (median (IQR), respectively 42.0 (26.3-69.5) versus 48.0 (40.3-60.5) (p = 0.301)).

conclusionsThis long-term follow-up study adds new data on self/parent reported disease specific outcomes in children with facial nerve palsy from two important patient groups (LNB and IFP). Both facial impairment and fatigue were uncommon and did not differ between LNB and IFP patients at long-term follow-up.

Indexed as

Bell PalsyFacial ParalysisLyme NeuroborreliosisAdolescentChildChild, PreschoolFatigueFemaleFollow-Up StudiesHumansMalePatient Reported Outcome MeasuresBorreliaChildrenFacial nerve palsyFollow-upIdiopathic facial nerve palsyLyme neuroborreliosis

Identifiers

PMID40604646
PMCPMC12219135

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