Evidence map›Paper›PMID 39913541›Full record

SynthesisPLoS medicine2025

Accuracy and clinical effectiveness of risk prediction tools for pressure injury occurrence: An umbrella review.

Bethany Hillier, Katie Scandrett, April Coombe, Tina Hernandez-Boussard, Ewout Steyerberg, Yemisi Takwoingi, Vladica M Veličković, Jacqueline Dinnes

Abstract readSystematic Review
In one paragraph

Synthesis in PLoS medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
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  8. 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

8 authors.

Bethany HillierDepartment of Applied Health Sciences, College of Medicine and Health, University of Birmingham, Edgbaston, Birmingham, United Kingdom.ORCID https://orcid.org/0000-0002-2072-1601
Katie ScandrettDepartment of Applied Health Sciences, College of Medicine and Health, University of Birmingham, Edgbaston, Birmingham, United Kingdom.ORCID https://orcid.org/0000-0001-6111-2805
April CoombeDepartment of Applied Health Sciences, College of Medicine and Health, University of Birmingham, Edgbaston, Birmingham, United Kingdom.
Tina Hernandez-BoussardDepartment of Medicine, Stanford University, Stanford, California, United States of America.ORCID https://orcid.org/0000-0001-6553-3455
Ewout SteyerbergDepartment of Biomedical Data Sciences, Leiden University Medical Center, Leiden, the Netherlands.
Yemisi TakwoingiDepartment of Applied Health Sciences, College of Medicine and Health, University of Birmingham, Edgbaston, Birmingham, United Kingdom.ORCID https://orcid.org/0000-0002-5828-9746
Vladica M VeličkovićEvidence Generation Department, HARTMANN GROUP, Heidenheim, Germany.ORCID https://orcid.org/0000-0001-7146-1267
Jacqueline DinnesDepartment of Applied Health Sciences, College of Medicine and Health, University of Birmingham, Edgbaston, Birmingham, United Kingdom.ORCID https://orcid.org/0000-0003-1343-7335

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPressure injuries (PIs) pose a substantial healthcare burden and incur significant costs worldwide. Several risk prediction tools to allow timely implementation of preventive measures and a subsequent reduction in healthcare system burden are available and in use. The ability of risk prediction tools to correctly identify those at high risk of PI (prognostic accuracy) and to have a clinically significant impact on patient management and outcomes (effectiveness) is not clear. We aimed to evaluate the prognostic accuracy and clinical effectiveness of risk prediction tools for PI and to identify gaps in the literature. METHODS AND

findingsThe umbrella review was conducted according to Cochrane guidance. Systematic reviews (SRs) evaluating the accuracy or clinical effectiveness of adult PI risk prediction tools in any clinical settings were eligible. Studies on paediatric tools, sensor-only tools, or staging/diagnosis of existing PIs were excluded. MEDLINE, Embase, CINAHL, and EPISTEMONIKOS were searched (inception to June 2024) to identify relevant SRs, as well as Google Scholar (2013 to 2024) and reference lists. Methodological quality was assessed using adapted AMSTAR-2 criteria. Results were described narratively. We identified 26 SRs meeting all eligibility criteria with 19 SRs assessing prognostic accuracy and 11 assessing clinical effectiveness of risk prediction tools for PI (4 SRs assessed both aspects). The 19 SRs of prognostic accuracy evaluated 70 tools (39 scales and 31 machine learning (ML) models), with the Braden, Norton, Waterlow, Cubbin-Jackson scales (and modifications thereof) the most evaluated tools. Meta-analyses from a focused set of included SRs showed that the scales had sensitivities and specificities ranging from 53% to 97% and 46% to 84%, respectively. Only 2/19 (11%) SRs performed appropriate statistical synthesis and quality assessment. Two SRs assessing machine learning-based algorithms reported high prognostic accuracy estimates, but some of which were sourced from the same data within which the models were developed, leading to potentially overoptimistic results. Two randomised trials assessing the effect of PI risk assessment tools (within the full test-intervention-outcome pathway) on the incidence of PIs were identified from the 11 SRs of clinical effectiveness; both were included in a Cochrane SR and assessed as high risk of bias. Both trials found no evidence of an effect on PI incidence. Limitations included the use of the AMSTAR-2 criteria, which may have overly focused on reporting quality rather than methodological quality, compounded by the poor reporting quality of included SRs and that SRs were not excluded based on low AMSTAR-2 ratings (in order to provide a comprehensive overview). Additionally, diagnostic test accuracy principles, rather than prognostic modelling approaches were heavily relied upon, which do not account for the temporal nature of prediction.

conclusionsAvailable systematic reviews suggest a lack of high-quality evidence for the accuracy of risk prediction tools for PI and limited reliable evidence for their use leading to a reduction in incidence of PI. Further research is needed to establish the clinical effectiveness of appropriately developed and validated risk prediction tools for PI.

Indexed as

Pressure UlcerHumansPrognosisRisk AssessmentRisk Factors

Identifiers

PMID39913541
PMCPMC11844857

What OpenQuestion holds

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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.