Non-specific symptoms and post-treatment Lyme disease syndrome in patients with Lyme borreliosis : a prospective cohort study in Belgium (2016–2020)

Background Patients with Lyme borreliosis (LB) may report persisting non-specific symptoms such as fatigue, widespread musculoskeletal pain or cognitive difficulties. When present for more than 6 months and causing a reduction in daily activities, this is often referred to as post-treatment Lyme disease syndrome (PTLDS). This study aimed to compare the occurrence of symptoms between LB patients and controls, to estimate the proportion of LB patients developing PTLDS and to identify risk factors. Methods A prospective cohort study was set up including three subpopulations: patients with an eryt... Mehr ...

Verfasser: Geebelen, Laurence
Lernout, Tinne
Devleesschauwer, Brecht
Kabamba-Mukadi, Benoît
Saegeman, Veroniek
Belkhir, Leïla
De Munter, Paul
Dubois, Bénédicte
Westhovens, Rene
Van Oyen, Herman
Speybroeck, Niko
Tersago, Katrien
Giot, Jean-Baptiste
Léonard, Philippe
Vangheluwe, Riet
Wieërs, Grégoire
Marot, Jean-Christophe
Evrard, Frédéric
Delaere, Bénédicte
Noirhomme, Séverine
Binnemans, Els
Vanhoof, Johan
Humtick Hospital Group, missing
Dokumenttyp: journalarticle
Erscheinungsdatum: 2022
Schlagwörter: Medicine and Health Sciences / Lyme borreliosis / Erythema migrans / Disseminated Lyme borreliosis / Post-treatment Lyme disease syndrome / Persisting non-specific symptoms / TERM-FOLLOW-UP / ANTIBIOTIC-TREATMENT / HEALTH SURVEY / NEUROBORRELIOSIS / DIAGNOSIS / THERAPY / TRIALS / F-36
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-28959494
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : https://biblio.ugent.be/publication/8768493

Background Patients with Lyme borreliosis (LB) may report persisting non-specific symptoms such as fatigue, widespread musculoskeletal pain or cognitive difficulties. When present for more than 6 months and causing a reduction in daily activities, this is often referred to as post-treatment Lyme disease syndrome (PTLDS). This study aimed to compare the occurrence of symptoms between LB patients and controls, to estimate the proportion of LB patients developing PTLDS and to identify risk factors. Methods A prospective cohort study was set up including three subpopulations: patients with an erythema migrans (EM) (i) or disseminated/late LB (ii) and a non-LB control group (iii). At 6- and 12-months follow-up, the occurrence of several symptoms, including six symptoms used to define PTLDS, i.e. muscle pain, joint pain, fatigue, memory problems, difficulties concentrating and problems finding words, and impact on daily activities, was compared between LB patients and controls. Finally, the proportion of LB patients developing PTLDS as defined by the Infectious Disease Society of America was estimated, including a time frame for symptoms to be present. Results Although the risk of presenting PTLDS-related symptoms was significantly higher in EM patients (n = 120) compared to controls (n = 128) at 6 months follow-up, the risk of presenting at least one of these symptoms combined with impact on daily activities was not significantly higher in EM patients, at either 6- or 12-months follow-up. A significant association was found between disseminated/late LB (n = 15) and the occurrence of any PTLDS-symptom with an impact on daily activities at both time points. The proportion of patients with PTLDS was estimated at 5.9% (95% CI 2.7-12.9) in EM patients and 20.9% (95% CI 6.8-64.4) in patients with disseminated/late LB (RR = 3.53, 95% CI 0.98-12.68, p = 0.053). No significant risk factors were identified, which may be explained by small sample sizes. Conclusions In our study, PTLDS was present in both LB cohorts, yet with a ...