Evidence map›Paper›PMID 30431493›Full record

ArticleCritical care medicine2019

Variation in Identifying Sepsis and Organ Dysfunction Using Administrative Versus Electronic Clinical Data and Impact on Hospital Outcome Comparisons.

Chanu Rhee, Maximilian S Jentzsch, Sameer S Kadri, Christopher W Seymour, Derek C Angus, David J Murphy, Greg S Martin, Raymund B Dantes, Lauren Epstein, Anthony E Fiore and 12 more

Open access · greenAbstract read
In one paragraph

Article in Critical care medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
4.9field-weighted citation impact, top 4% 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

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 75 citations in OpenAlex.

  1. Electronic health record data quality assessment and tools: a systematic review.Journal of the American Medical Informatics Association : JAMIA · 2023
    Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Observational
  13. Observational
  14. SepsisJournal of medical microbiology · 2025
    Review
  15. Article
  16. Article
  17. Improving Sepsis Outcomes in the Era of Pay-for-Performance and Electronic Quality Measures: A Joint IDSA/ACEP/PIDS/SHEA/SHM/SIDP Position Paper.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2024
    Article
  18. Article
  19. Article
  20. Patterns, Predictors, and Intercenter Variability in Empiric Gram-Negative Antibiotic Use Across 928 United States Hospitals.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2023
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 7 institutions in 1 country.

Chanu RheeDepartment of Population Medicine, Harvard Medical School/Harvard Pilgrim Health Care Institute, Boston, MA.
Maximilian S JentzschDepartment of Population Medicine, Harvard Medical School/Harvard Pilgrim Health Care Institute, Boston, MA.
Sameer S KadriCritical Care Medicine Department, Clinical Center, National Institutes of Health, Bethesda, MD.
Christopher W SeymourThe Clinical Research, Investigation and Systems Modeling of Acute illness (CRISMA) Center, Department of Critical Care and Emergency Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Derek C AngusThe Clinical Research, Investigation and Systems Modeling of Acute illness (CRISMA) Center, Department of Critical Care and Emergency Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA.
David J MurphyDivision of Pulmonary, Allergy, Critical Care and Sleep Medicine, Department of Medicine, Emory University School of Medicine, Emory Critical Care Center, Atlanta, GA.
Greg S MartinDivision of Pulmonary, Allergy, Critical Care and Sleep Medicine, Department of Medicine, Emory University School of Medicine, Emory Critical Care Center, Atlanta, GA.
Raymund B DantesDivision of Healthcare Quality Promotion, Centers for Disease Control and Prevention, Atlanta, GA.
Lauren EpsteinDivision of Healthcare Quality Promotion, Centers for Disease Control and Prevention, Atlanta, GA.
Anthony E FioreDivision of Healthcare Quality Promotion, Centers for Disease Control and Prevention, Atlanta, GA.
John A JerniganDivision of Healthcare Quality Promotion, Centers for Disease Control and Prevention, Atlanta, GA.
Robert L DannerCritical Care Medicine Department, Clinical Center, National Institutes of Health, Bethesda, MD.
David K WarrenDepartment of Medicine, Washington University School of Medicine, St. Louis, MO.
Edward J SeptimusDepartment of Population Medicine, Harvard Medical School/Harvard Pilgrim Health Care Institute, Boston, MA.
Jason HickokClinical Services Group, HCA Healthcare, Nashville, TN.
Russell E PolandDepartment of Population Medicine, Harvard Medical School/Harvard Pilgrim Health Care Institute, Boston, MA.
Robert JinDepartment of Population Medicine, Harvard Medical School/Harvard Pilgrim Health Care Institute, Boston, MA.
David FramCommonwealth Informatics, Waltham, MA.
Richard SchaafCommonwealth Informatics, Waltham, MA.
Rui WangDepartment of Population Medicine, Harvard Medical School/Harvard Pilgrim Health Care Institute, Boston, MA.
Michael KlompasDepartment of Population Medicine, Harvard Medical School/Harvard Pilgrim Health Care Institute, Boston, MA.
Centers for Disease Control and Prevention (CDC) Prevention Epicenters Program
Centers for Disease Control and Prevention · USHarvard Pilgrim Health Care · USHarvard University · USNational Institutes of Health Clinical Center · USBrigham and Women's Hospital · USTexas A&M Health Science Center · USWashington University in St. Louis · US

Funding

Sepsis subtypes: biology, treatment, and bedside applicationR35GM119519 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Christopher W. Seymour · 2016 to 2026
$4.9M
Objective Evaluation of Variation in Sepsis Incidence, Mortality, and CareK08HS025008 · AHRQ · HARVARD PILGRIM HEALTH CARE, INC. · PI RHEE, CHANU · 2017 to 2019
$450k
Preclinical and Clinical Investigations of Severe Infection and Critical Illness ZIACL008060 · CLC · CLINICAL CENTER · PI DANNER, ROBERT L · 2009 to 2025
$0k
Big Data - Epidemiology of Critical Illness and SepsisZIACL090045 · CLC · CLINICAL CENTER · PI KADRI, SAMEER · 2017 to 2025
$0k
AHRQ HHS K08 HS025008NCEZID CDC HHS U54 CK000172NIGMS NIH HHS R35 GM119519
6 · The paper itself

Abstract

objectivesAdministrative claims data are commonly used for sepsis surveillance, research, and quality improvement. However, variations in diagnosis, documentation, and coding practices for sepsis and organ dysfunction may confound efforts to estimate sepsis rates, compare outcomes, and perform risk adjustment. We evaluated hospital variation in the sensitivity of claims data relative to clinical data from electronic health records and its impact on outcome comparisons. DESIGN, SETTING, AND PATIENTS: Retrospective cohort study of 4.3 million adult encounters at 193 U.S. hospitals in 2013-2014.

interventionsNone. MEASUREMENTS AND MAIN

resultsSepsis was defined using electronic health record-derived clinical indicators of presumed infection (blood culture draws and antibiotic administrations) and concurrent organ dysfunction (vasopressors, mechanical ventilation, doubling in creatinine, doubling in bilirubin to ≥ 2.0 mg/dL, decrease in platelets to < 100 cells/µL, or lactate ≥ 2.0 mmol/L). We compared claims for sepsis prevalence and mortality rates between both methods. All estimates were reliability adjusted to account for random variation using hierarchical logistic regression modeling. The sensitivity of hospitals' claims data was low and variable: median 30% (range, 5-54%) for sepsis, 66% (range, 26-84%) for acute kidney injury, 39% (range, 16-60%) for thrombocytopenia, 36% (range, 29-44%) for hepatic injury, and 66% (range, 29-84%) for shock. Correlation between claims and clinical data was moderate for sepsis prevalence (Pearson coefficient, 0.64) and mortality (0.61). Among hospitals in the lowest sepsis mortality quartile by claims, 46% shifted to higher mortality quartiles using clinical data. Using implicit sepsis criteria based on infection and organ dysfunction codes also yielded major differences versus clinical data.

conclusionsVariation in the accuracy of claims data for identifying sepsis and organ dysfunction limits their use for comparing hospitals' sepsis rates and outcomes. Using objective clinical data may facilitate more meaningful hospital comparisons.

Indexed as

AdultElectronic Health RecordsFemaleHospital MortalityHumansMaleMiddle AgedMultiple Organ FailureQuality Indicators, Health CareRetrospective StudiesSepsisUnited States

Identifiers

PMID30431493
PMCPMC7970408
OpenAlexW2901221479

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.