Evidence map›Paper›PMID 38964673›Full record

ArticleChest2024

Development and Validation of the Hospital Medicine Safety Sepsis Initiative Mortality Model.

Hallie C Prescott, Megan Heath, Elizabeth S Munroe, John Blamoun, Paul Bozyk, Rachel K Hechtman, Jennifer K Horowitz, Namita Jayaprakash, Keith E Kocher, Mariam Younas and 4 more

Abstract readValidation Study
In one paragraph

Article in Chest, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Observational
  3. Article
  4. Article
  5. Article
  6. 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

14 authors.

Hallie C PrescottDepartment of Internal Medicine, University of Michigan, Ann Arbor, MI; VA Center for Clinical Management Research, Ann Arbor, MI. Electronic address: hprescot@med.umich.edu.
Megan HeathDepartment of Internal Medicine, University of Michigan, Ann Arbor, MI.
Elizabeth S MunroeDepartment of Internal Medicine, University of Michigan, Ann Arbor, MI.
John BlamounMyMichigan Health, Midland, MI.
Paul BozykCorewell Health, Royal Oak, MI.
Rachel K HechtmanDepartment of Internal Medicine, University of Michigan, Ann Arbor, MI.
Jennifer K HorowitzDepartment of Internal Medicine, University of Michigan, Ann Arbor, MI.
Namita JayaprakashHenry Ford Health, Detroit, MI.
Keith E KocherVA Center for Clinical Management Research, Ann Arbor, MI; Department of Emergency Medicine, University of Michigan, Ann Arbor, MI.
Mariam YounasHurley Medical Center, Flint, MI.
Stephanie P TaylorDepartment of Internal Medicine, University of Michigan, Ann Arbor, MI.
Patricia J PosaDepartment of Internal Medicine, University of Michigan, Ann Arbor, MI.
Elizabeth McLaughlinDepartment of Internal Medicine, University of Michigan, Ann Arbor, MI.
Scott A FlandersDepartment of Internal Medicine, University of Michigan, Ann Arbor, MI.

Funding

PULMONARY CELLULAR AND MOLECULAR BIOLOGY TRAININGT32HL007749 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Robert Pickett Dickson · 1993 to 2026
$19.9M
Optimizing Vasopressor Delivery in Early SepsisF32HL172463 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MUNROE, ELIZABETH · 2024 to 2025
$108k
NHLBI NIH HHS F32 HL172463NHLBI NIH HHS L30 HL170379NHLBI NIH HHS T32 HL007749
6 · The paper itself

Abstract

backgroundWhen comparing outcomes after sepsis, it is essential to account for patient case mix to make fair comparisons. We developed a model to assess risk-adjusted 30-day mortality in the Michigan Hospital Medicine Safety sepsis initiative (HMS-Sepsis). RESEARCH QUESTION: Can HMS-Sepsis registry data adequately predict risk of 30-day mortality? Do performance assessments using adjusted vs unadjusted data differ? STUDY DESIGN AND

methodsRetrospective cohort of community-onset sepsis hospitalizations in the HMS-Sepsis registry (April 2022-September 2023), with split derivation (70%) and validation (30%) cohorts. We fit a risk-adjustment model (HMS-Sepsis mortality model) incorporating acute physiologic, demographic, and baseline health data and assessed model performance using concordance (C) statistics, Brier scores, and comparisons of predicted vs observed mortality by deciles of risk. We compared hospital performance (first quintile, middle quintiles, fifth quintile) using observed vs adjusted mortality to understand the extent to which risk adjustment impacted hospital performance assessment.

resultsAmong 17,514 hospitalizations from 66 hospitals during the study period, 12,260 hospitalizations (70%) were used for model derivation and 5,254 hospitalizations (30%) were used for model validation. Thirty-day mortality for the total cohort was 19.4%. The final model included 13 physiologic variables, two physiologic interactions, and 16 demographic and chronic health variables. The most significant variables were age, metastatic solid tumor, temperature, altered mental status, and platelet count. The model C statistic was 0.82 for the derivation cohort, 0.81 for the validation cohort, and ≥ 0.78 for all subgroups assessed. Overall calibration error was 0.0%, and mean calibration error across deciles of risk was 1.5%. Standardized mortality ratios yielded different assessments than observed mortality for 33.9% of hospitals.

interpretationThe HMS-Sepsis mortality model showed strong discrimination and adequate calibration and reclassified one-third of hospitals to a different performance category from unadjusted mortality. Based on its strong performance, the HMS-Sepsis mortality model may aid in fair hospital benchmarking, assessment of temporal changes, and observational causal inference analysis.

Indexed as

Hospital MortalityRegistriesSepsisAgedFemaleHospitalizationHumansMaleMichiganMiddle AgedRetrospective StudiesRisk AdjustmentRisk Assessmentbenchmarkinghealth care quality indicatorhospitalizationrisk adjustment

Identifiers

PMID38964673
PMCPMC11638544

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.