Evidence map›Paper›PMID 31393900›Full record

ArticlePloS one2019

Personalized prediction of adverse heart and kidney events using baseline and longitudinal data from SPRINT and ACCORD.

Gal Dinstag, David Amar, Erik Ingelsson, Euan Ashley, Ron Shamir

Abstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Can Machine Learning from Real-World Data Support Drug Treatment Decisions? A Prediction Modeling Case for Direct Oral Anticoagulants.Medical decision making : an international journal of the Society for Medical Decision Making · 2022
    Article
  3. Article
  4. 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

5 authors.

Gal DinstagBlavatnik School of Computer Science, Tel-Aviv University, Tel Aviv, Israel.
David AmarDivision of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, California, United States of America.
Erik IngelssonDivision of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, California, United States of America.ORCID 0000-0003-2256-6972
Euan AshleyDivision of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, California, United States of America.
Ron ShamirBlavatnik School of Computer Science, Tel-Aviv University, Tel Aviv, Israel.ORCID 0000-0003-1889-9870

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe 2017 guidelines of the American College of Cardiology and the American Heart Association propose substantial changes to hypertension management. The guidelines lower the blood pressure threshold defining hypertension and promote more aggressive treatments. Thus, more individuals are now classified as hypertensive and as a result, medication usage may become more extensive. An inevitable byproduct of greater medication use is higher incidence of adverse effects. Here, we examined these issues by developing models that predict both cardiovascular events and other adverse events based on the treatment chosen and other patient's data. METHODS AND

resultsWe used data from the SPRINT trial to produce patient-specific predictions of the risks for adverse cardiovascular or kidney outcomes. Unlike prior models, we used both the baseline characteristics collected upon recruitment and the longitudinal data during the follow-up. Importantly, our cardiovascular predictor outperformed extant models on SPRINT participants, achieving AUC = 0.765, and was validated with good performance in an independent cohort of the ACCORD trial.

conclusionsOur study illustrates the importance of including longitudinal data for assessing personalized risk and provides means for recommending personalized treatment decisions.

Indexed as

AdultAmerican Heart AssociationAntihypertensive AgentsBlood PressureCardiovascular DiseasesCardiovascular SystemFemaleForecastingHeartHumansHypertensionIncidenceKidneyLongitudinal StudiesMaleMiddle AgedAntihypertensive Agents

Identifiers

PMID31393900
PMCPMC6687091

What OpenQuestion holds

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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.