Evidence map›Paper›PMID 30859371›Full record

Observational studyPurinergic signalling2019

Point-of-care measurements reveal release of purines into venous blood of stroke patients.

Nicholas Dale, Faming Tian, Ravjit Sagoo, Norman Phillips, Chris Imray, Christine Roffe

Registry-linked trialAbstract readObservational Study
In one paragraph

Observational study in Purinergic signalling, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02308605 (A Field Deployable Blood Test for Stroke, Capable of Detecting Brain Ischaemia From the Earliest Stages of Pathology), which is not on this map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–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.

NCT02308605 completednot on this map

A Field Deployable Blood Test for Stroke, Capable of Detecting Brain Ischaemia From the Earliest Stages of Pathology

TypeobservationalSponsorUniversity Hospitals Coventry and Warwickshire NHS TrustRan2014 to 2015Enrolled217ConditionsStrokeArmsSMARTCap
3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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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

6 authors.

Nicholas DaleSchool of Life Sciences, University of Warwick, Coventry, UK. n.e.dale@warwick.ac.uk.ORCID 0000-0003-2196-2949
Faming TianSarissa Biomedical Ltd, Unit 4b Vanguard Centre, Sir William Lyons Road, Coventry, UK.
Ravjit SagooUniversity Hospitals of Coventry and Warwickshire, Clifford Bridge Road, Coventry, UK.
Norman PhillipsPatient Representative, University Hospitals of Coventry and Warwickshire, Clifford Bridge Road, Coventry, UK.
Chris ImrayUniversity Hospitals of Coventry and Warwickshire, Clifford Bridge Road, Coventry, UK.
Christine RoffeUniversity Hospital of North Midlands, Stoke-on-Trent, and Keele University, Keele, UK.

Funding

Department of Health II-LA-0313-20002
6 · The paper itself

Abstract

Stroke is a leading cause of death and disability. Here, we examine whether point-of-care measurement of the purines, adenosine, inosine and hypoxanthine, which are downstream metabolites of ATP, has potential to assist the diagnosis of stroke. In a prospective observational study, patients who were suspected of having had a stroke, within 4.5 h of symptom onset and still displaying focal neurological symptoms at admission, were recruited. Clinical research staff in the Emergency Departments of two hospitals used a prototype biosensor array, SMARTCap, to measure the purines in the venous blood of stroke patients and healthy controls. In controls, the baseline purines were 7.1 ± (SD) 4.2 μM (n = 52), while in stroke patients, they were 11.6 ± 8.9 μM (n = 76). Using the National Institutes for Stoke Scale (NIHSS) to band the severity of stroke, we found that minor, moderate and severe strokes all gave significant elevation of blood purines above the controls. The purine levels fall over 24 h. This was most marked for patients with haemorrhagic strokes (5.1 ± 3.6 μM, n = 9 after 24 h). The purine levels measured on admission show a significant correlation with the volume of affected brain tissue determined by medical imaging in patients who had not received thrombolysis or mechanical thrombectomy. ClinicalTrials.gov Identifier: NCT02308605.

Indexed as

Biosensing TechniquesPoint-of-Care TestingAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedPoint-of-Care SystemsProspective StudiesPurinesStrokePurinesBiosensorCerebral ischemiaPoint of carePurinesStroke

Identifiers

PMID30859371
PMCPMC6635545

What OpenQuestion holds

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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.