Evidence map›Paper›PMID 34238247›Full record

ArticleBMC medical research methodology2021

Evaluating the relationship between citation set size, team size and screening methods used in systematic reviews: a cross-sectional study.

Katie O'Hearn, Cameron MacDonald, Anne Tsampalieros, Leo Kadota, Ryan Sandarage, Supun Kotteduwa Jayawarden, Michele Datko, John M Reynolds, Thanh Bui, Shagufta Sultan and 6 more

Open access · goldAbstract read
In one paragraph

Article in BMC medical research methodology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 21% of its field
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

5 citing papers in PubMed, 13 citations in OpenAlex.

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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

16 authors at 10 institutions in 3 countries.

Katie O'HearnCHEO Research Institute, Ottawa, ON, Canada.
Cameron MacDonaldSchool of Engineering and Applied Sciences, McMaster University, Hamilton, ON, Canada.
Anne TsampalierosCHEO Research Institute, Ottawa, ON, Canada.
Leo KadotaDepartment of Pediatrics, Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada.
Ryan SandarageFaculty of Medicine, University of British Columbia, Vancouver, BC, Canada.
Supun Kotteduwa JayawardenFaculty of Medicine, University of British Columbia, Vancouver, BC, Canada.
Michele DatkoECRI Information Center, ECRI, Plymouth Meeting, PA, USA.
John M ReynoldsCalder Memorial Library, University of Miami Miller School of Medicine, MLIS, Miami, FL, USA.
Thanh BuiFaculty of Arts & Science, University of Toronto, Toronto, ON, Canada.
Shagufta SultanTherapeutic Products Directorate, Health Canada, Ottawa, ON, Canada.
Margaret SampsonLibrary Services, CHEO, Ottawa, ON, Canada.
Misty PrattCHEO Research Institute, Ottawa, ON, Canada.
Nick BarrowmanCHEO Research Institute, Ottawa, ON, Canada.
Nassr NamaDepartment of Pediatrics, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada.
Matthew PageSchool of Public Health and Preventive Medicine, Monash University, Melbourne, Australia.
James Dayre McNallyCHEO Research Institute, Ottawa, ON, Canada. dmcnally@cheo.on.ca.
Agricultural Research Institute of Ontario · CAUniversity of British Columbia · CAECRI Institute · USHealth Canada · CALibrary and Archives Canada · CAMcMaster University · CAMonash University · AUUniversity of Miami · USUniversity of Ottawa · CAUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStandard practice for conducting systematic reviews (SRs) is time consuming and involves the study team screening hundreds or thousands of citations. As the volume of medical literature grows, the citation set sizes and corresponding screening efforts increase. While larger team size and alternate screening methods have the potential to reduce workload and decrease SR completion times, it is unknown whether investigators adapt team size or methods in response to citation set sizes. Using a cross-sectional design, we sought to understand how citation set size impacts (1) the total number of authors or individuals contributing to screening and (2) screening methods.

methodsMEDLINE was searched in April 2019 for SRs on any health topic. A total of 1880 unique publications were identified and sorted into five citation set size categories (after deduplication): < 1,000, 1,001-2,500, 2,501-5,000, 5,001-10,000, and > 10,000. A random sample of 259 SRs were selected (~ 50 per category) for data extraction and analysis.

resultsWith the exception of the pairwise t test comparing the under 1000 and over 10,000 categories (median 5 vs. 6, p = 0.049) no statistically significant relationship was evident between author number and citation set size. While visual inspection was suggestive, statistical testing did not consistently identify a relationship between citation set size and number of screeners (title-abstract, full text) or data extractors. However, logistic regression identified investigators were significantly more likely to deviate from gold-standard screening methods (i.e. independent duplicate screening) with larger citation sets. For every doubling of citation size, the odds of using gold-standard screening decreased by 15 and 20% at title-abstract and full text review, respectively. Finally, few SRs reported using crowdsourcing (n = 2) or computer-assisted screening (n = 1).

conclusionsLarge citation set sizes present a challenge to SR teams, especially when faced with time-sensitive health policy questions. Our study suggests that with increasing citation set size, authors are less likely to adhere to gold-standard screening methods. It is possible that adjunct screening methods, such as crowdsourcing (large team) and computer-assisted technologies, may provide a viable solution for authors to complete their SRs in a timely manner.

Indexed as

CrowdsourcingCross-Sectional StudiesHumansMass ScreeningResearch DesignSystematic Reviews as TopicCrowdsourcingMachine learningScoping reviewsSystematic reviews

Identifiers

PMID34238247
PMCPMC8264476
OpenAlexW3179388700

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.