Evidence map›Paper›PMID 34688611›Full record

Trial reportClinical biochemistry2022

Evaluation of heparinized syringes for measuring newborn metabolites in neonates with a central arterial line.

Kelli K Ryckman, Abhismitha Ramesh, Hyunkeun Cho, Scott P Oltman, Elizabeth E Rogers, John M Dagle, Laura L Jelliffe-Pawlowski

Open access · greenAbstract readClinical Trial
In one paragraph

Trial report in Clinical biochemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 77% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

7 authors at 2 institutions in 1 country.

Kelli K RyckmanUniversity of Iowa, Department of Epidemiology, United States. Electronic address: Kelli-ryckman@uiowa.edu.
Abhismitha RameshUniversity of Iowa, Department of Epidemiology, United States.
Hyunkeun ChoUniversity of Iowa, Department of Biostatistics, United States.
Scott P OltmanUniversity of California, San Francisco, Department of Epidemiology & Biostatistics, United States; UCSF California Preterm Birth Initiative, United States.
Elizabeth E RogersUCSF California Preterm Birth Initiative, United States; University of California San Francisco, Department of Pediatrics, United States.
John M DagleUniversity of Iowa, Department of Pediatrics, United States.
Laura L Jelliffe-PawlowskiUniversity of California, San Francisco, Department of Epidemiology & Biostatistics, United States; UCSF California Preterm Birth Initiative, United States.
University of Iowa · USUniversity of California, San Francisco · US

Funding

Targeted metabolic profiling to predict major morbidity in very preterm newbornsR01HD102381 · NICHD · UNIVERSITY OF IOWA · PI JELLIFFE-PAWLOWSKI, LAURA LEE, ROGERS, ELIZABETH E · 2020 to 2024
$3.1M
Can an Evidence-Based Mental Health Intervention be Implemented into Preexisting Home Visiting Programs using Implementation Facilitation?R01MH134474 · NIMH · UNIVERSITY OF IOWA · PI Elissa Z Faro, KELLI K. RYCKMAN · 2024 to 2026
$2.4M
NICHD NIH HHS R01 HD102381NIMH NIH HHS R01 MH134474
6 · The paper itself

Abstract

Newborn metabolic screening is emerging as a novel method for predicting neonatal morbidity and mortality in neonates born very preterm (<32 weeks gestation). The purpose of our study was to determine if blood collected by an electrolyte-balanced dry lithium heparin syringe, as is routine for blood gas measurements, affects targeted metabolite and biomarker levels. Two blood samples (one collected with a heparinized syringe and the other with a non-heparinized syringe) were obtained at the same time from 20 infants with a central arterial line and tested for 49 metabolites and biomarkers using standard procedures for newborn screening. Overall, the median metabolite levels did not significantly differ by syringe type. However, there was wide variability, particularly for amino acids and immunoreactive trypsinogen, for individual paired samples and therefore, consideration should be given to sample collection when using these metabolites in prediction models of neonatal morbidity and mortality.

Indexed as

Blood Specimen CollectionCentral Venous CathetersNeonatal ScreeningSyringesBiomarkersFemaleHeparinHumansInfant, NewbornMaleBiomarkersHeparinHeparinMetabolitesSample collection

Identifiers

PMID34688611
PMCPMC8671267
OpenAlexW3210644005

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.