Evidence map›Paper›PMID 28747298›Full record

ArticleJMIR medical informatics2017

Estimating One-Year Risk of Incident Chronic Kidney Disease: Retrospective Development and Validation Study Using Electronic Medical Record Data From the State of Maine.

Shiying Hao, Tianyun Fu, Qian Wu, Bo Jin, Chunqing Zhu, Zhongkai Hu, Yanting Guo, Yan Zhang, Yunxian Yu, Terry Fouts and 8 more

Open access · goldAbstract read
In one paragraph

Article in JMIR medical informatics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 11% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 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

18 authors at 7 institutions in 2 countries.

Shiying HaoDepartment of Epidemiology and Health Statistics, School of Public Health, School of Medicine, Zhejiang University, Hangzhou, China.ORCID http://orcid.org/0000-0002-7527-2460
Tianyun FuHBI Solutions Inc, Palo Alto, CA, United States.ORCID http://orcid.org/0000-0001-8103-8841
Qian WuDepartment of Surgery, Stanford University, Stanford, CA, United States.ORCID http://orcid.org/0000-0002-9253-5322
Bo JinHBI Solutions Inc, Palo Alto, CA, United States.ORCID http://orcid.org/0000-0001-9268-7134
Chunqing ZhuHBI Solutions Inc, Palo Alto, CA, United States.ORCID http://orcid.org/0000-0003-0649-4403
Zhongkai HuDepartment of Cardiothoracic Surgery, Stanford University, Stanford, CA, United States.ORCID http://orcid.org/0000-0003-2541-6187
Yanting GuoDepartment of Surgery, Stanford University, Stanford, CA, United States.ORCID http://orcid.org/0000-0002-4972-4427
Yan ZhangDepartment of Surgery, Stanford University, Stanford, CA, United States.ORCID http://orcid.org/0000-0002-2198-5393
Yunxian YuDepartment of Epidemiology and Health Statistics, School of Public Health, School of Medicine, Zhejiang University, Hangzhou, China.ORCID http://orcid.org/0000-0002-3394-9832
Terry FoutsEmpactful Capital, San Francisco, CA, United States.ORCID http://orcid.org/0000-0001-6866-6499
Phillip NgSequoia Hospital, Redwood City, CA, United States.ORCID http://orcid.org/0000-0001-8502-9328
Devore S CulverHealthInfoNet, Portland, ME, United States.ORCID http://orcid.org/0000-0001-5826-2079
Shaun T AlfredsHealthInfoNet, Portland, ME, United States.ORCID http://orcid.org/0000-0003-1752-4823
Frank StearnsHBI Solutions Inc, Palo Alto, CA, United States.ORCID http://orcid.org/0000-0003-2049-9163
Karl G SylvesterDepartment of Surgery, Stanford University, Stanford, CA, United States.ORCID http://orcid.org/0000-0002-8559-0155
Eric WidenHBI Solutions Inc, Palo Alto, CA, United States.ORCID http://orcid.org/0000-0002-8999-4659
Doff B McElhinneyDepartment of Cardiothoracic Surgery, Stanford University, Stanford, CA, United States.ORCID http://orcid.org/0000-0001-7242-0934
Xuefeng B LingDepartment of Epidemiology and Health Statistics, School of Public Health, School of Medicine, Zhejiang University, Hangzhou, China.ORCID http://orcid.org/0000-0002-5386-3884
Lucile Packard Children's Hospital · USLifenet Health · USStanford University · USFirst Hospital of Shijiazhuang · CNNorth China Electric Power University · CNSequoia Hospital · USZhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChronic kidney disease (CKD) is a major public health concern in the United States with high prevalence, growing incidence, and serious adverse outcomes.

objectiveWe aimed to develop and validate a model to identify patients at risk of receiving a new diagnosis of CKD (incident CKD) during the next 1 year in a general population.

methodsThe study population consisted of patients who had visited any care facility in the Maine Health Information Exchange network any time between January 1, 2013, and December 31, 2015, and had no history of CKD diagnosis. Two retrospective cohorts of electronic medical records (EMRs) were constructed for model derivation (N=1,310,363) and validation (N=1,430,772). The model was derived using a gradient tree-based boost algorithm to assign a score to each individual that measured the probability of receiving a new diagnosis of CKD from January 1, 2014, to December 31, 2014, based on the preceding 1-year clinical profile. A feature selection process was conducted to reduce the dimension of the data from 14,680 EMR features to 146 as predictors in the final model. Relative risk was calculated by the model to gauge the risk ratio of the individual to population mean of receiving a CKD diagnosis in next 1 year. The model was tested on the validation cohort to predict risk of CKD diagnosis in the period from January 1, 2015, to December 31, 2015, using the preceding 1-year clinical profile.

resultsThe final model had a c-statistic of 0.871 in the validation cohort. It stratified patients into low-risk (score 0-0.005), intermediate-risk (score 0.005-0.05), and high-risk (score ≥ 0.05) levels. The incidence of CKD in the high-risk patient group was 7.94%, 13.7 times higher than the incidence in the overall cohort (0.58%). Survival analysis showed that patients in the 3 risk categories had significantly different CKD outcomes as a function of time (P<.001), indicating an effective classification of patients by the model.

conclusionsWe developed and validated a model that is able to identify patients at high risk of having CKD in the next 1 year by statistically learning from the EMR-based clinical history in the preceding 1 year. Identification of these patients indicates care opportunities such as monitoring and adopting intervention plans that may benefit the quality of care and outcomes in the long term.

Indexed as

chronic kidney diseaseelectronic medical recordretrospective studyrisk model

Identifiers

PMID28747298
PMCPMC5550735
OpenAlexW2737873903

What OpenQuestion holds

Textmetadata
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.