Evidence map›Paper›PMID 39285338›Full record

ArticleBMC medical research methodology2024

Conducting two evidence syntheses in six weeks - experiences with and evaluation of a pilot project.

Heather Melanie R Ames, Hege Kornør, Line Holtet Evensen, Ingeborg Beate Lidal, Elisabet Hafstad, Christine Hillestad Hestevik, Patricia Sofia Jacobsen Jardim, Gyri Hval

Abstract read
In one paragraph

Article in BMC medical research methodology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Heather Melanie R AmesThe Norwegian Institute of Public Health (NIPH), PO Box 222, Oslo, Skøyen, 0213, Norway. heather.ames@fhi.no.
Hege KornørThe Norwegian Institute of Public Health (NIPH), PO Box 222, Oslo, Skøyen, 0213, Norway.
Line Holtet EvensenThe Norwegian Institute of Public Health (NIPH), PO Box 222, Oslo, Skøyen, 0213, Norway.
Ingeborg Beate LidalThe Norwegian Institute of Public Health (NIPH), PO Box 222, Oslo, Skøyen, 0213, Norway.
Elisabet HafstadThe Norwegian Institute of Public Health (NIPH), PO Box 222, Oslo, Skøyen, 0213, Norway.
Christine Hillestad HestevikThe Norwegian Institute of Public Health (NIPH), PO Box 222, Oslo, Skøyen, 0213, Norway.
Patricia Sofia Jacobsen JardimThe Norwegian Institute of Public Health (NIPH), PO Box 222, Oslo, Skøyen, 0213, Norway.
Gyri HvalThe Norwegian Institute of Public Health (NIPH), PO Box 222, Oslo, Skøyen, 0213, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEvidence synthesis organisations are trying to meet commissioners' needs for rapid responses to their evidence synthesis commissions. In this project we piloted an intensive process, working to complete evidence syntheses within six-weeks, rather than the standard lead time of 4-6 months. Our objective was to explore how researchers experience working intensively, identify barriers and facilitators, and determine how a more intensive approach to evidence synthesis could be more systematically introduced in the future.

methodsIn a pre-planning phase, an intensive work group was established, and two commissions were selected for this pilot project. The evidence synthesis process was divided into two phases: planning and intensive. The planning phase, involved scheduling the intensive phase, exploring new digital tools, and identifying peer reviewers. The intensive phase encompassed the entire evidence synthesis process. Two review teams were formed, each with a team lead supported by a process lead and leadership contact point. Throughout the project, teams engaged in reflective meetings to evaluate and adjust processes as needed.

resultsDuring the planning phase, teams identified significant uncertainties regarding scopes, research questions, and inclusion criteria. To address this, they engaged with commissioners earlier than originally planned, clarified these aspects, and prepared protocols. Despite some minor deviations from the original plan, both reviews were completed on schedule, with one team expanding their scope due to the absence of eligible studies. Teams operated flexibly, held regular meetings, and found the process seamless due to fewer interruptions. Machine learning tools facilitated rapid study selection. The process lead role, created to guide and evaluate the project, proved beneficial, providing structure and support, although clearer role delineation with the leadership contact point could have improved efficiency.

conclusionsOverall, the intensive process fostered focus and productivity, allowing teams to manage short-term deliverables effectively. The researchers preferred working intensively with one evidence synthesis over being involved with many projects at the same time. They felt that time use was more effective, and they were able to complete the tasks in a focused way. However, there are several implications that should be considered before implementing an intensive approach in future evidence syntheses.

Indexed as

Evidence-Based MedicineHumansPilot ProjectsResearch DesignEvidence synthesisLeanSystematic reviewWorkflow

Identifiers

PMID39285338
PMCPMC11403876

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.