Evidence map›Paper›PMID 41026487›Full record

Trial reportJAMA network open2025

Good Outcome Following Attempted Resuscitation Score and Clinical Frailty Scale for Estimating Long-Term Mortality: An Ancillary Study of the CLEAR Randomized Clinical Trial.

Samuel Kaspar Zumbrunn, Benjamin Bissmann, Sebastian Gross, Christoph Becker, Armon Arpagaus, Flavio Gössi, Philipp Schuetz, Jörg D Leuppi, Drahomir Aujesky, Balthasar L Hug and 4 more

Abstract readRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in JAMA network open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Samuel Kaspar ZumbrunnMedical Communication and Psychosomatic Medicine, University Hospital Basel, Basel, Switzerland.
Benjamin BissmannMedical Communication and Psychosomatic Medicine, University Hospital Basel, Basel, Switzerland.
Sebastian GrossMedical Communication and Psychosomatic Medicine, University Hospital Basel, Basel, Switzerland.
Christoph BeckerMedical Communication and Psychosomatic Medicine, University Hospital Basel, Basel, Switzerland.
Armon ArpagausMedical Communication and Psychosomatic Medicine, University Hospital Basel, Basel, Switzerland.
Flavio GössiMedical Communication and Psychosomatic Medicine, University Hospital Basel, Basel, Switzerland.
Philipp SchuetzFaculty of Medicine, University of Basel, Basel, Switzerland.
Jörg D LeuppiFaculty of Medicine, University of Basel, Basel, Switzerland.
Drahomir AujeskyDepartment of General Internal Medicine, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Balthasar L HugDivision of Internal Medicine, Cantonal Hospital Lucerne, Lucerne, Switzerland.
Thomas PetersDivision of Internal Medicine, St Claraspital, Basel, Switzerland.
Arnoud J TempletonFaculty of Medicine, University of Basel, Basel, Switzerland.
Stefano BassettiFaculty of Medicine, University of Basel, Basel, Switzerland.
Sabina HunzikerMedical Communication and Psychosomatic Medicine, University Hospital Basel, Basel, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: In an aging and increasingly complex patient population, risk estimation tools are critical for optimizing clinical decision-making. The Clinical Frailty Scale (CFS) evaluates frailty and mortality risk, whereas the Good Outcome Following Attempted Resuscitation (GO-FAR) score aims to estimate survival after potential in-hospital cardiac arrest. However, their ability to estimate all-cause mortality in medical inpatients across all ages remains unclear. Objective: To assess the accuracy of the CFS and GO-FAR score in estimating long-term all-cause mortality among medical inpatients. Design, Setting, and Participants: This ancillary analysis of the CLEAR trial, a cluster randomized trial, included 2840 medical inpatients from 6 Swiss teaching hospitals. Intervention: At admission from June 1, 2019, to April 30, 2023, the CFS, GO-FAR, and Charlson Comorbidity Index (CCI) scores were recorded. Regardless of randomization group, long-term follow-up of vital status occurred between June and October 2024. Main Outcomes and Measures: The outcome was long-term all-cause mortality. Results: Among 2840 patients (mean [SD] age, 68.5 [15.8] years; 1552 [54.6%] male), 969 (34.1%) died during a mean (SD) follow-up of 3.3 (0.91) years. The GO-FAR and CFS showed good discriminatory performance for all-cause mortality with time-dependent areas under the receiver operating characteristic curve (AUROC) of 0.78 and 0.74, respectively. Combining both scores with the CCI in a combined regression model improved the overall AUROC to 0.87. Patients in the highest-risk categories had significantly increased all-cause mortality risk (GO-FAR: adjusted hazard ratio, 20.31; 95% CI, 14.71-28.06; P < .001; and CFS: adjusted hazard ratio, 8.69; 95% CI, 6.83-11.07; P < .001). Both scores demonstrated high specificity in their highest-risk categories (GO-FAR: 98.2%; CFS: 99.1%) but low sensitivity (GO-FAR: 7.8%; CFS: 9.4%). Results indicated that of 100 hospitalized patients in the highest GO-FAR category (≥14 points), approximately 69 are expected to die, whereas among those in the lower categories, approximately 67 are expected to survive (positive and negative predictive value of 69.1% and 67.3%, respectively). Conclusions and Relevance: In this ancillary study of the CLEAR trial, the GO-FAR score and CFS effectively estimated long-term all-cause mortality, particularly when combined with the CCI. These tools may help clinical decision-making, resource allocation, and advanced care planning in aging, multimorbid patient populations.

Indexed as

Cardiopulmonary ResuscitationFrailtyHeart ArrestAgedAged, 80 and overFemaleHumansMaleMiddle AgedRisk AssessmentSwitzerland

Identifiers

PMID41026487
PMCPMC12485637

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Registered trials

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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.