Evidence map›Paper›PMID 31100075›Full record

ArticlePloS one2019

Heart rate variability as a marker of recovery from critical illness in children.

Lauren E Marsillio, Tomas Manghi, Michael S Carroll, Lauren C Balmert, Mark S Wainwright

Registry-linked trialOpen access · goldAbstract 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. It is linked to trial NCT05312333 (Holter Monitoring of Critically-ill Childern in PICU at Sohag University Hospital), which is not on this map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.6field-weighted citation impact, top 9% 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.

NCT05312333 unknown statusnot on this mapstarted 2022, after this paper: background citation

Holter Monitoring of Critically-ill Childern in PICU at Sohag University Hospital

TypeobservationalSponsorSohag UniversityRan2022 to 2023Enrolled100ConditionsCritically Ill Childern in PICU
3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 24 citations in OpenAlex.

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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 at 4 institutions in 1 country.

Lauren E MarsillioDivision of Critical Care Medicine, Department of Pediatrics, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, United States of America.ORCID 0000-0003-3166-6318
Tomas ManghiDepartment of Pediatrics, Yale School of Medicine, New Haven, CT, United States of America.
Michael S CarrollData Analytics and Reporting, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, United States of America.
Lauren C BalmertDepartment of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, United States of America.
Mark S WainwrightDivision of Pediatric Neurology, Department of Neurology, University of Washington, Seattle, WA, United States of America.
Lurie Children's Hospital · USNorthwestern University · USUniversity of Washington · USYale University · US

Funding

Northwestern University Clinical and Translational Science Institute (NUCATS)UL1TR001422 · NCATS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI D'AQUILA, RICHARD · 2015 to 2023
$56.8M
NCATS NIH HHS UL1 TR001422
6 · The paper itself

Abstract

objectivesThe purpose of this study was to Identify whether changes in heart rate variability (HRV) could be detected as critical illness resolves by comparing HRV from the time of pediatric intensive care unit (PICU) admission with HRV immediately prior to discharge. We also sought to demonstrate that HRV derived from electrocardiogram (ECG) data from bedside monitors can be calculated in critically-ill children using a real-time, streaming analytics platform.

methodsThis was a retrospective, observational pilot study of 17 children aged 0 to 18 years admitted to the PICU of a free-standing, academic children's hospital. Three time-domain measures of HRV were calculated in real-time from bedside monitor ECG data and stored for analysis. Measures included: root mean square of successive differences between NN intervals (RMSSD), percent of successive NN interval differences above 50 ms (pNN50), and the standard deviation of NN intervals (SDNN).

resultsHRV values calculated from the first and last 24 hours of PICU stay were analyzed. Mixed effects models demonstrated that all three measures of HRV were significantly lower during the first 24 hours compared to the last 24 hours of PICU admission (p<0.001 for all three measures). In models exploring the relationship between time from admission and log HRV values, the predicted average HRV remained consistently higher in the last 24 hours of PICU stay compared to the first 24 hours.

conclusionHRV was significantly lower in the first 24 hours compared to the 24 hours preceding PICU discharge, after resolution of critical illness. This demonstrates that it is feasible to detect changes in HRV using an automated, streaming analytics platform. Continuous tracking of HRV may serve as a marker of recovery in critically ill children.

Indexed as

Critical IllnessHeart RateRecovery of FunctionAdolescentBiomarkersChildChild, PreschoolFemaleHumansInfantInfant, NewbornIntensive Care UnitsMaleRetrospective StudiesBiomarkers

Identifiers

PMID31100075
PMCPMC6524820
OpenAlexW2946792289

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.