Evidence map›Paper›PMID 30470563›Full record

ArticleAcademic pediatrics2019

Potential Impact of Initial Clinical Data on Adjustment of Pediatric Readmission Rates.

Mari M Nakamura, Sara L Toomey, Alan M Zaslavsky, Carter R Petty, Chen Lin, Guergana K Savova, Sherri Rose, Mark S Brittan, Jody L Lin, Maria C Bryant and 2 more

Abstract read
In one paragraph

Article in Academic pediatrics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Prediction of Prednisolone Dose Correction Using Machine Learning.Journal of healthcare informatics research · 2023
    Article
  3. Article
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

12 authors.

Mari M NakamuraDivision of General Pediatrics (MM Nakamura, SL Toomey, MC Bryant, S Ashrafzadeh, and MA Schuster); Division of Infectious Diseases (MM Nakamura), Institutional Centers for Clinical and Translational Research (CR Petty); Informatics Program (C Lin and GK Savova), Boston Children's Hospital. Electronic address: mari.nakamura@childrens.harvard.edu.
Sara L ToomeyDivision of General Pediatrics (MM Nakamura, SL Toomey, MC Bryant, S Ashrafzadeh, and MA Schuster); Informatics Program (C Lin and GK Savova), Boston Children's Hospital.
Alan M ZaslavskyDepartment of Pediatrics (MM Nakamura, SL Toomey, GK Savova, and MA Schuster).
Carter R PettyDepartment of Health Care Policy (AM Zaslavsky and S Rose).
Chen LinHarvard Medical School, Boston, Mass; Department of Pediatrics (MS Brittan).
Guergana K SavovaInformatics Program (C Lin and GK Savova), Boston Children's Hospital; Harvard Medical School, Boston, Mass; Department of Pediatrics (MS Brittan).
Sherri RoseDepartment of Pediatrics (MM Nakamura, SL Toomey, GK Savova, and MA Schuster).
Mark S BrittanChildren's Hospital Colorado, Aurora; Department of Pediatrics (JL Lin).
Jody L LinStanford School of Medicine, Stanford, Calif.
Maria C BryantDivision of General Pediatrics (MM Nakamura, SL Toomey, MC Bryant, S Ashrafzadeh, and MA Schuster).
Sepideh AshrafzadehDivision of General Pediatrics (MM Nakamura, SL Toomey, MC Bryant, S Ashrafzadeh, and MA Schuster).
Mark A SchusterDivision of General Pediatrics (MM Nakamura, SL Toomey, MC Bryant, S Ashrafzadeh, and MA Schuster); Informatics Program (C Lin and GK Savova), Boston Children's Hospital; Kaiser Permanente School of Medicine (MA Schuster), Pasadena, Calif.

Funding

Children's Hospital Boston Center of Excellence for Quality MeasurementU18HS020513 · AHRQ · BOSTON CHILDREN'S HOSPITAL · PI SCHUSTER, MARK A. · 2011 to 2014
$7.9M
Improving Child Health and Healthcare through Dissemination and Implementation of Pediatric Quality Measures: Adapting the Child Clinician and Group CAHPS Survey for Pediatric Telemedicine VisitsU18HS025299 · AHRQ · BOSTON CHILDREN'S HOSPITAL · PI TOOMEY, SARA LOUISE · 2016 to 2021
$3.4M
AHRQ HHS U18 HS020513AHRQ HHS U18 HS025299
6 · The paper itself

Abstract

objectiveComparison of readmission rates requires adjustment for case-mix (ie, differences in patient populations), but previously only claims data were available for this purpose. We examined whether incorporation of relatively readily available clinical data improves prediction of pediatric readmissions and thus might enhance case-mix adjustment.

methodsWe examined 30-day readmissions using claims and electronic health record data for patients ≤18 years and 29 days of age who were admitted to 3 children's hospitals from February 2011 to February 2014. Using the Pediatric All-Condition Readmission Measure and starting with a model including age, gender, chronic conditions, and primary diagnosis, we examined whether the addition of initial vital sign and laboratory data improved model performance. We employed machine learning to evaluate the same variables, using the L2-regularized logistic regression with cost-sensitive learning and convolutional neural network.

resultsControlling for the core model variables, low red blood cell count and mean corpuscular hemoglobin concentration and high red cell distribution width were associated with greater readmission risk, as were certain interactions between laboratory and chronic condition variables. However, the C-statistic (0.722 vs 0.713) and McFadden's pseudo R

conclusionsReadily available clinical variables do not meaningfully improve the prediction of pediatric readmissions and would be unlikely to enhance case-mix adjustment unless their distributions varied widely across hospitals.

Indexed as

Patient ReadmissionQuality Indicators, Health CareAdolescentChildChild, PreschoolFemaleHumansMaleRisk AdjustmentRisk AssessmentRisk FactorsSocioeconomic FactorsTime Factorspatient readmissionquality improvementrisk adjustment

Identifiers

PMID30470563
PMCPMC6788282

What OpenQuestion holds

Textmetadata
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.