Evidence map›Paper›PMID 42654748›Full record

ArticlePathogens (Basel, Switzerland)2026

Post-Treatment Lyme Disease Syndrome in Six European Countries Using Data from the Burden of Lyme Disease (BOLD) Study.

Holly Yu, Amanda R Mercadante, Kate Halsby, Alexandra Loew-Baselli, Ye Tan, Frederick J Angulo, Elizabeth Begier, Mendwas Dzingina, Johan S Berglund, Anna Moniuszko-Malinowska and 5 more

Abstract read
In one paragraph

Article in Pathogens (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Holly YuHTA Value and Evidence, Pfizer, Inc., Collegeville, PA 19426, USA.ORCID 0000-0001-8625-4201
Amanda R MercadanteHTA Value and Evidence, Pfizer, Inc., New York, NY 10001, USA.ORCID 0000-0002-4576-4405
Kate HalsbyPfizer Research & Development, Tadworth, Surrey KT20 7NS, UK.
Alexandra Loew-BaselliPfizer Corporation Austria GmbH, Floridsdorfer Hauptstraße 1, 1210 Vienna, Austria.ORCID 0000-0003-2924-0836
Ye TanEvidence Generation Statistics, Pfizer Inc., Cambridge, MA 02139, USA.
Frederick J AnguloHTA Value and Evidence, Pfizer, Inc., Collegeville, PA 19426, USA.
Elizabeth BegierPfizer Healthcare Ireland Unlimited Company, The Watermarque Building, Ringsend Road, Dublin 4, D04 K7N3 Dublin, Ireland.ORCID 0000-0002-1287-5416
Mendwas DzinginaPfizer Research & Development, Tadworth, Surrey KT20 7NS, UK.ORCID 0000-0002-6237-9250
Johan S BerglundDepartment of Health, Blekinge Institute of Technology, Valhallavägen 1, 371 79 Karlskrona, Sweden.ORCID 0000-0003-4312-2246
Anna Moniuszko-MalinowskaDepartment of Infectious Diseases and Neuroinfections, Medical University of Białystok, ul. Zurawia 14, Blok D, 15-540 Bialystok, Poland.ORCID 0000-0002-3994-8785
Viliam CibikVseobecna Ambulancia pre Dospelych, Pruské 293, 018 52 Pruské, Slovakia.
Dagmar ZakovaAmbulancia Vnutorneho Lekarstva, 911 01 Trencin, Slovakia.
Franc StrleDepartment of Infectious Diseases, University Medical Centre Ljubljana, Japljeva 2, 1525 Ljubljana, Slovenia.ORCID 0000-0003-4163-0503
James H StarkEvidence Generation Statistics, Pfizer Inc., Cambridge, MA 02139, USA.
On Behalf Of The Bold Study Group

Funding

Pfizer (USA) N/AValneva (Austria) N/A
6 · The paper itself

Abstract

Up to 10% of patients with Lyme borreliosis (LB) will experience symptoms that fulfill the Infectious Disease Society of America (IDSA) criteria of post-treatment Lyme disease syndrome (PTLDS). This study assesses PTLDS in the Burden of Lyme Disease (BOLD) study through clinical assessment ("PTLDS Assessed by Clinicians") and by post hoc evaluation of patient-reported outcomes, including the 36-Item Short Form Health Survey, Fatigue Severity Scale, and Cognitive Failures Questionnaire ("PTLDS Assessed by Questionnaire"). Among 242 LB cases who completed antibiotic treatment and had objective manifestations stabilized or resolved, 99 (40.9%) reported ≥1 symptom of fatigue, musculoskeletal pain, or cognitive impairment 10 months after diagnosis. Fifteen (6.2%) cases met the PTLDS criteria assessed by either clinicians or predefined questionnaire severity thresholds; four (1.7%) met both. PTLDS cases assessed by questionnaires and LB cases with persistent symptoms both reported greater symptom severity and poorer physical functioning than PTLDS cases assessed by clinicians. These exploratory findings suggest that clinician- and questionnaire-based assessments may identify partially different subsets of patients with PTLDS and either method could underestimate the proportion of patients with PTLDS.

Indexed as

Anti-Bacterial AgentsLyme DiseasePost-Lyme Disease SyndromeAdultAgedEuropeFemaleHumansMaleMiddle AgedSeverity of Illness IndexSurveys and QuestionnairesSymptom BurdenAnti-Bacterial AgentsLyme borreliosisLyme diseasepatient reported outcomespost-treatment Lyme disease syndromepreventionquality of life

Identifiers

PMID42654748
PMCPMC13516344

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.