Evidence map›Paper›PMID 38629944›Full record

Trial reportActa orthopaedica2024

A simplified, 2-question grading system for evaluating abstracts in orthopedic scientific meetings: a serial randomization study.

Walter Van der Weegen, Jeroen C Van Egmond, Ruth E Geuze, Taco Gosens, Barbara Snoeker, Rudolf W Poolman, Dutch Orthopedic Association Scientific Committee Abstract Group

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Acta orthopaedica, 2024. 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

7 authors.

Walter Van der WeegenDepartment of Orthopedics, Sint Anna Ziekenhuis, Eindhoven.
Jeroen C Van EgmondDepartment of Orthopedics, Bravis Ziekenhuis, Roosendaal. j.vanegmond@bravis.nl.
Ruth E GeuzeDepartment of Orthopedics, Elisabeth-Tweesteden Ziekenhuis, Tilburg.
Taco GosensDepartment of Orthopedics, Elisabeth-Tweesteden Ziekenhuis, Tilburg.
Barbara SnoekerDepartment of Clinical Epidemiology, Biostatistics and Bioinformatics, Amsterdam Medical Center, University of Amsterdam.
Rudolf W PoolmanDepartment of Orthopedics, Leiden University Medical Center, Leiden; Department of Orthopedics, Joint Research, OLVG, Amsterdam, the Netherlands.
Dutch Orthopedic Association Scientific Committee Abstract Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeEfficient abstract scoring for congress presentation is important. Given the emergence of new study methodologies, a scoring system that accommodates all study designs is warranted. We aimed to assess the equivalence of a simplified, 2-question abstract grading system with a more complex currently used system in assessing abstracts submitted for orthopedic scientific meetings in a serial randomized study.

methodsDutch Orthopedic Association Scientific Committee (DOASC) members were randomized to grade abstracts using either the current grading system, which includes up to 7 scoring categories, or the new grading system, which consists of only 2 questions. Pearson correlation coefficient and mean abstract score with 95% confidence intervals (CI) were calculated.

resultsAnalysis included the scoring of 195 abstracts by 12-14 DOASC members. The average score for an abstract using the current system was 60 points (CI 58-62), compared with 63 points (CI 62-64) using the new system. By using the new system, abstracts were scored higher by 3.3 points (CI 1.7-5.0). Pearson correlation was poor with coefficient 0.38 (P < 0.001).

conclusionThe simplified abstract grading system exhibited a poor correlation with the current scoring system, while the new system offers a more inclusive evaluation of varying study designs and is preferred by almost all DOASC members.

Indexed as

OrthopedicsCorrelation of DataHumansRandom AllocationResearch Design

Identifiers

PMID38629944
PMCPMC11022873

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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.