Evidence map›Paper›PMID 38786394›Full record

ArticleHealthcare (Basel, Switzerland)2024

A Data-Driven Approach to Defining Risk-Adjusted Coding Specificity Metrics for a Large U.S. Dementia Patient Cohort.

Kaylla Richardson, Sankari Penumaka, Jaleesa Smoot, Mansi Reddy Panaganti, Indu Radha Chinta, Devi Priya Guduri, Sucharitha Reddy Tiyyagura, John Martin, Michael Korvink, Laura H Gunn

Abstract read
In one paragraph

Article in Healthcare (Basel, Switzerland), 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

10 authors.

Kaylla RichardsonDepartment of Public Health Sciences, University of North Carolina at Charlotte (UNC Charlotte), Charlotte, NC 28223, USA.
Sankari PenumakaSchool of Data Science, University of North Carolina at Charlotte (UNC Charlotte), Charlotte, NC 28223, USA.ORCID 0009-0009-1050-0248
Jaleesa SmootDepartment of Public Health Sciences, University of North Carolina at Charlotte (UNC Charlotte), Charlotte, NC 28223, USA.
Mansi Reddy PanagantiSchool of Data Science, University of North Carolina at Charlotte (UNC Charlotte), Charlotte, NC 28223, USA.
Indu Radha ChintaSchool of Data Science, University of North Carolina at Charlotte (UNC Charlotte), Charlotte, NC 28223, USA.
Devi Priya GuduriSchool of Data Science, University of North Carolina at Charlotte (UNC Charlotte), Charlotte, NC 28223, USA.
Sucharitha Reddy TiyyaguraSchool of Data Science, University of North Carolina at Charlotte (UNC Charlotte), Charlotte, NC 28223, USA.
John MartinITS Data Science, Premier, Inc., Charlotte, NC 28277, USA.ORCID 0000-0002-5217-4980
Michael KorvinkITS Data Science, Premier, Inc., Charlotte, NC 28277, USA.ORCID 0000-0002-4802-4293
Laura H GunnDepartment of Public Health Sciences, University of North Carolina at Charlotte (UNC Charlotte), Charlotte, NC 28223, USA.ORCID 0000-0003-3962-4526

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Medical coding impacts patient care quality, payor reimbursement, and system reliability through the precision of patient information documentation. Inadequate coding specificity can have significant consequences at administrative and patient levels. Models to identify and/or enhance coding specificity practices are needed. Clinical records are not always available, complete, or homogeneous, and clinically driven metrics to assess medical practices are not logistically feasible at the population level, particularly in non-centralized healthcare delivery systems and/or for those who only have access to claims data. Data-driven approaches that incorporate all available information are needed to explore coding specificity practices. Using N = 487,775 hospitalization records of individuals diagnosed with dementia and discharged in 2022 from a large all-payor administrative claims dataset, we fitted logistic regression models using patient and facility characteristics to explain the coding specificity of principal and secondary diagnoses of dementia. A two-step approach was produced to allow for the flexible clustering of patient-level outcomes. Model outcomes were then used within a Poisson binomial model to identify facilities that over- or under-specify dementia diagnoses against healthcare industry standards across hospitalizations. The results indicate that multiple factors are significantly associated with dementia coding specificity, especially for principal diagnoses of dementia (AUC = 0.727). The practical use of this novel risk-adjusted metric is demonstrated for a sample of facilities and geospatially via a U.S. map. This study's findings provide healthcare facilities with a benchmark for assessing coding specificity practices and developing quality enhancements to align with healthcare industry standards, ultimately contributing to better patient care and healthcare system reliability.

Indexed as

coding specificitydementiaICD-10

Identifiers

PMID38786394
PMCPMC11120868

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.