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The SPOTLIGHT Study

Population Size

0

People

Population Size statistic card

Years

2023

Years statistic card

Associated BioSamples

Availability to be confirmed

Associated BioSamples statistic card

Geographic coverage

England

Geographic coverage statistic card

Lead time

Data only
Lead time statistic card

Summary

The Severn Pleural Disease Outcomes: Long term insight (SPOTLight) study is a prospective cohort study which aims to improve our understanding of factors influencing patient outcomes in pleural disease.

Documentation

Patients presenting with radiologically confirmed pleural disease including (but not limited to) pneumothorax, pleural effusion, pleural thickening or pleural cancer (mesothelioma) to North Bristol NHS Trust will be screened and invited to participate by a member of the study team. The team will collect data on the patient’s demographics, past medical history and history of current illness, smoking status including cannabis, asbestos and other inhalational exposures, clinical frailty score (CFS) and performance status (PS). The team will also collect data related to their condition and its management, for example, radiological and thoracic ultrasound appearances, the number and type of interventions undertaken and digital measurements of air leaks in the case of pneumothorax. For patients with pleural effusions, if blood or pleural fluid samples are collected as part of their routine care, additional research samples will also be collected for use in current or future studies. For patients who undergo a pleural biopsy procedure following enrolment, additional tissue samples may be obtained and retained for research purposes if felt appropriate by the operator. These data and sample collections are not study-specific procedures but are performed as part of the participants’ routine clinical care. At enrolment patients will be asked to complete 2 routine questionnaires to provide patient-reported outcome measures. These are study-specific, not part of the patient’s routine care. Where necessary, additional PROMS relevant to a specific sub-study the patient may be eligible for may also be collected during the baseline assessment. Further data will be collected from the patient’s medical records at 4 months and 12 months post enrolment, to encompass the patient’s length of stay, number and type of interventions, and mortality. These two timepoints allow for the collection of complete data sets, acknowledging that some patients may have a prolonged diagnostic pathway or require recurrent procedures to manage their symptoms. A final diagnosis will be recorded after 12 months, based on the diagnosis of their treating clinician, and ratified by a second pleural specialist.

Dataset type

Health and disease

Provenance

Purpose of dataset collection

Research cohort

Source of data extraction

Other

Collection source setting

Cohort, study, trial, Secondary care - Outpatients, Secondary care - In-patients

Biological sample availability

Availability to be confirmed

Details

Publishing frequency

Irregular

Version

1.0.0

Modified

30/04/2026

Coverage

Start date

02/05/2023

Time lag

Less than 1 week

Geographic coverage

England

Minimum age range

16

Maximum age range

150

Follow-up

6 - 12 Months

Accessibility

Language

en

Alignment with standardised data models

OTHER

Controlled vocabulary

OTHER

Data Access Request

Dataset pipeline status

Not available

Data Controller

NIHR Bristol Biomedical Research Centre

Data Processor

NIHR Bristol Biomedical Research Centre

Demographics

Dataset Types: Health and disease


Collection Sources: Cohort, study, trial, Secondary care - Outpatients, Secondary care - In-patients