Evidence map›Paper›PMID 35741305›Full record

ArticleDiagnostics (Basel, Switzerland)2022

Diagnostic Coding Intensity among a Pneumonia Inpatient Cohort Using a Risk-Adjustment Model and Claims Data: A U.S. Population-Based Study.

Ruchi Mishra, Himadri Verma, Venkata Bhargavi Aynala, Paul R Arredondo, John Martin, Michael Korvink, Laura H Gunn

Abstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

7 authors.

Ruchi MishraSchool of Data Science, University of North Carolina at Charlotte, Charlotte, NC 28223, USA.
Himadri VermaSchool of Data Science, University of North Carolina at Charlotte, Charlotte, NC 28223, USA.
Venkata Bhargavi AynalaSchool of Data Science, University of North Carolina at Charlotte, Charlotte, NC 28223, USA.
Paul R ArredondoSchool of Data Science, University of North Carolina at Charlotte, Charlotte, NC 28223, USA.
John MartinITS Data Science, Premier, Inc., Charlotte, NC 28277, USA.
Michael KorvinkITS Data Science, Premier, Inc., Charlotte, NC 28277, USA.ORCID 0000-0002-4802-4293
Laura H GunnSchool of Data Science, University of North Carolina at Charlotte, Charlotte, NC 28223, USA.ORCID 0000-0003-3962-4526

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hospital payments depend on the Medicare Severity Diagnosis-Related Group's estimated cost and the set of diagnoses identified during inpatient stays. However, over-coding and under-coding diagnoses can occur for different reasons, leading to financial and clinical consequences. We provide a novel approach to measure diagnostic coding intensity, built on commonly available administrative claims data, and demonstrated through a 2019 pneumonia acute inpatient cohort (N = 182,666). A Poisson additive model (PAM) is proposed to model risk-adjusted additional coded diagnoses. Excess coding intensity per patient visit was estimated as the difference between the observed and PAM-based expected counts of secondary diagnoses upon risk adjustment by patient-level characteristics. Incidence rate ratios were extracted for patient-level characteristics and further adjustments were explored by facility-level characteristics to account for facility and geographical differences. Facility-level factors contribute substantially to explain the remaining variability in excess diagnostic coding, even upon adjusting for patient-level risk factors. This approach can provide hospitals and stakeholders with a tool to identify outlying facilities that may experience substantial differences in processes and procedures compared to peers or general industry standards. The approach does not rely on the availability of clinical information or disease-specific markers, is generalizable to other patient cohorts, and can be expanded to use other sources of information, when available.

Indexed as

coding intensityICD-10-CM diagnosispneumoniaPoisson additive modelrisk adjustment

Identifiers

PMID35741305
PMCPMC9221672

What OpenQuestion holds

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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.