Evidence map›Paper›PMID 27993905›Full record

ArticleBMJ open2016

Enhancing risk stratification for use in integrated care: a cluster analysis of high-risk patients in a retrospective cohort study.

Sabine I Vuik, Erik Mayer, Ara Darzi

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In one paragraph

Article in BMJ open, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

3 authors.

Sabine I VuikInstitute of Global Health Innovation, Imperial College, St Mary's Hospital, London, UK.
Erik MayerDepartment of Surgery, Imperial College, St Mary's Hospital, London, UK.
Ara DarziInstitute of Global Health Innovation, Imperial College, St Mary's Hospital, London, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo show how segmentation can enhance risk stratification tools for integrated care, by providing insight into different care usage patterns within the high-risk population.

designA retrospective cohort study. A risk score was calculated for each person using a logistic regression, which was then used to select the top 5% high-risk individuals. This population was segmented based on the usage of different care settings using a k-means cluster analysis. Data from 2008 to 2011 were used to create the risk score and segments, while 2012 data were used to understand the predictive abilities of the models. SETTING AND

participantsData were collected from administrative data sets covering primary and secondary care for a random sample of 300 000 English patients. MAIN MEASURES: The high-risk population was segmented based on their usage of 4 different care settings: emergency acute care, elective acute care, outpatient care and GP care.

resultsWhile the risk strata predicted care usage at a high level, within the high-risk population, usage varied significantly. 4 different groups of high-risk patients could be identified. These 4 segments had distinct usage patterns across care settings, reflecting different levels and types of care needs. The 2008-2011 usage patterns of the 4 segments were consistent with the 2012 patterns. DISCUSSION: Cluster analyses revealed that the high-risk population is not homogeneous, as there exist 4 groups of patients with different needs across the care continuum. Since the patterns were predictive of future care use, they can be used to develop integrated care programmes tailored to these different groups.

conclusionsUsage-based segmentation augments risk stratification by identifying patient groups with different care needs, around which integrated care programmes can be designed.

Indexed as

Cluster AnalysisDatabases, FactualDelivery of Health Care, IntegratedHumansLogistic ModelsPatient CareRetrospective StudiesRisk AssessmentSoftwareSTATISTICS & RESEARCH METHODS

Identifiers

PMID27993905
PMCPMC5168666

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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.