Evidence map›Paper›PMID 37984960›Full record

ArticleBMJ open2023

Predictors of outcome in sciatica patients following an epidural steroid injection: the POiSE prospective observational cohort study protocol.

Siobhan Stynes, Kym Ie Snell, Richard D Riley, Kika Konstantinou, Andrea Cherrington, Noor Daud, Raymond Ostelo, John O'Dowd, Nadine E Foster

Open access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in BMJ open, 2023. 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
0.3field-weighted citation impact, top 35% 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, 1 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

9 authors at 6 institutions in 3 countries.

Siobhan StynesSchool of Medicine, Keele University, Keele, Staffordshire, UK s.stynes@keele.ac.uk.ORCID 0000-0002-5117-9034
Kym Ie SnellCollege of Medical and Dental Sciences, University of Birmingham Institute of Applied Health Research, Birmingham, UK.ORCID 0000-0001-9373-6591
Richard D RileyCollege of Medical and Dental Sciences, University of Birmingham Institute of Applied Health Research, Birmingham, UK.ORCID 0000-0001-8699-0735
Kika KonstantinouSchool of Medicine, Keele University, Keele, Staffordshire, UK.ORCID 0000-0003-4228-9386
Andrea CherringtonSchool of Medicine, Keele University, Keele, Staffordshire, UK.
Noor DaudSchool of Medicine, Keele University, Keele, Staffordshire, UK.
Raymond OsteloDepartment of Health Sciences, VU Amsterdam Faculty of Sciences, Amsterdam, The Netherlands.ORCID 0000-0001-7679-7210
John O'DowdHampshire Hospitals NHS Foundation Trust, Hampshire, UK.
Nadine E FosterSchool of Medicine, Keele University, Keele, Staffordshire, UK.ORCID 0000-0003-4429-9756
Keele University · GBMidlands Partnership NHS Foundation Trust · GBUniversity of Birmingham · GBAmsterdam University Medical Centers · NLHampshire Hospitals NHS Foundation Trust · GBThe University of Queensland · AU

Funding

Department of Health NIHR300441
6 · The paper itself

Abstract

introductionSciatica can be very painful and, in most cases, is due to pressure on a spinal nerve root from a disc herniation with associated inflammation. For some patients, the pain persists, and one management option is a spinal epidural steroid injection (ESI). The aim of an ESI is to relieve leg pain, improve function and reduce the need for surgery. ESIs work well in some patients but not in others, but we cannot identify these patient subgroups currently. This study aims to identify factors, including patient characteristics, clinical examination and imaging findings, that help in predicting who does well and who does not after an ESI. The overall objective is to develop a prognostic model to support individualised patient and clinical decision-making regarding ESI.

methodsPOiSE is a prospective cohort study of 439 patients with sciatica referred by their clinician for an ESI. Participants will receive weekly text messages until 12 weeks following their ESIand then again at 24 weeks following their ESI to collect data on leg pain severity. Questionnaires will be sent to participants at baseline, 6, 12 and 24 weeks after their ESI to collect data on pain, disability, recovery and additional interventions. The prognosis for the cohort will be described. The primary outcome measure for the prognostic model is leg pain at 6 weeks. Prognostic models will also be developed for secondary outcomes of disability and recovery at 6 weeks and additional interventions at 24 weeks following ESI. Statistical analyses will include multivariable linear and logistic regression with mixed effects model. ETHICS AND DISSEMINATION: The POiSE study has received ethical approval (South Central Berkshire B Research Ethics Committee 21/SC/0257). Dissemination will be guided by our patient and public engagement group and will include scientific publications, conference presentations and social media.

Indexed as

Intervertebral Disc DisplacementSciaticaHumansObservational Studies as TopicPainProspective StudiesSteroidsTreatment OutcomeSteroidsBack painEPIDEMIOLOGYPAIN MANAGEMENTPatientsPrognosisSpine

Identifiers

PMID37984960
PMCPMC10660415
OpenAlexW4388835459

What OpenQuestion holds

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LicenceCC BY-NC
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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.