Evidence map›Paper›PMID 40835852›Full record

ArticleScientific reports2025

Successful implementation of a risk assessment and mitigation program to control bovine digital dermatitis at the herd-level.

Jim Weber, Marina Hillen, Torsten Seuberlich, Andreas Fürmann, Corinne Gurtner, Jens Becker, Claudia Syring, Maria Welham Ruiters, Maher Alsaaod, Lina Mazurek and 2 more

Abstract readClinical Trial, VeterinaryMulticenter Study
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Frontiers in cellular and infection microbiology · 2026
    Review
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

12 authors.

Jim WeberClinic for Ruminants, Department of Clinical Veterinary Medicine, Vetsuisse Faculty, University of Bern, Bern, 3012, Switzerland. jim.weber@unibe.ch.
Marina HillenClinic for Ruminants, Department of Clinical Veterinary Medicine, Vetsuisse Faculty, University of Bern, Bern, 3012, Switzerland.
Torsten SeuberlichDivision of Neurological Sciences, Vetsuisse Faculty, University of Bern, Bern, 3012, Switzerland.
Andreas FürmannClinic for Ruminants, Department of Clinical Veterinary Medicine, Vetsuisse Faculty, University of Bern, Bern, 3012, Switzerland.
Corinne GurtnerInstitute of Animal Pathology, Department of Infectious Diseases and Pathobiology, Vetsuisse Faculty, University of Bern, Bern, 3012, Switzerland.
Jens BeckerClinic for Ruminants, Department of Clinical Veterinary Medicine, Vetsuisse Faculty, University of Bern, Bern, 3012, Switzerland.
Claudia SyringClinic for Ruminants, Department of Clinical Veterinary Medicine, Vetsuisse Faculty, University of Bern, Bern, 3012, Switzerland.
Maria Welham RuitersClinic for Ruminants, Department of Clinical Veterinary Medicine, Vetsuisse Faculty, University of Bern, Bern, 3012, Switzerland.
Maher AlsaaodClinic for Ruminants, Department of Clinical Veterinary Medicine, Vetsuisse Faculty, University of Bern, Bern, 3012, Switzerland.
Lina MazurekClinic for Ruminants, Department of Clinical Veterinary Medicine, Vetsuisse Faculty, University of Bern, Bern, 3012, Switzerland.
Gertraud SchüpbachVetsuisse Faculty, Veterinary Public Health Institute, University of Bern, Bern, 3097, Switzerland.
Adrian SteinerClinic for Ruminants, Department of Clinical Veterinary Medicine, Vetsuisse Faculty, University of Bern, Bern, 3012, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This nonrandomized clinical intervention study was designed as a prospective, multicenter group comparison to evaluate the efficacy of a risk assessment and mitigation program to control bovine digital dermatitis (BDD). The program was implemented over a 1-year period on 9 intervention (INT) farms and 10 control (CTR) farms. Mainstays of the program derived from results of a previous BDD risk factor analysis. All farms were visited monthly to assess within-herd BDD prevalences to perform risk assessments and to treat BDD lesions with salicylic acid paste. Bulk milk samples were collected every 4 months. Diagnosis of BDD was based on visual inspection (clinical scoring) of the feet. Risk-associated management practices were identified on each farm, and management changes expected to prevent further introduction or spread of BDD within INT farms were suggested and agreed upon with farmers of the INT farms. Lesional biopsies were taken from a subset of cows of the INT group before and 2 months after treatment for histopathological and molecular biological examination to confirm histological and bacteriological cure in addition to clinical cure. The initial BDD prevalences for the INT and CTR farms averaged 39.8% (IQR 16.2) and 41.0% (IQR 12.4) for overall BDD lesions, 25.9% (IQR 10.8) and 26.2% (IQR 14.5) for active BDD lesions, and 22.1% (IQR 6.9) and 23.7% (IQR 22.3) for chronic BDD lesions, respectively. After 1 year of implementation, overall BDD prevalences were reduced to 14.1% (IQR 8.2) on INT farms but remained at 41.6% (IQR 10.8) on CTR farms. A significant decline in bulk milk anti-Treponema antibodies over the 1-year period was found in INT as compared to CTR farms. Considering the results of the histopathological examination, of 16S metagenomic sequencing and of the Fluorescence in situ hybridization as indicators for healing, 6/7 (85.7%) selected lesions were cured 2 months post completion of treatment. The results of this study show that the described BDD control measures can markedly reduce the within-herd prevalence of BDD. The proposed procedure might provide the basis for a nationwide BDD mitigation program that could be of importance also beyond national borders.

Indexed as

Cattle DiseasesDigital DermatitisAnimalsCattleFemaleMilkPrevalenceProspective StudiesRisk AssessmentCattleDisease controlLamenessSurveillanceTreponemes

Identifiers

PMID40835852
PMCPMC12368109

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.