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COMPARE

Population Size

29,021

People

Population Size statistic card

Years

2016 - 2017

Years statistic card

Associated BioSamples

DNA

Plasma

...see more

Associated BioSamples statistic card

Geographic coverage

United Kingdom

England

Geographic coverage statistic card

Lead time

2-6 months

Lead time statistic card

Summary

The COMPARE bioresource comprises 30,000 English blood donors, on whom genetic and blood cell trait data have been generated.

Documentation

The COMPARE dataset comprises of genomic and blood data from the COMPARE clinical trial run by the University of Cambridge and NHS Blood and Transplant.

Background: To safeguard donors, blood services measure haemoglobin concentration in advance of each donation. NHS Blood and Transplant's (NHSBT) customary method have been capillary gravimetry (copper sulphate), followed by venous spectrophotometry (HemoCue) for donors failing gravimetry. However, NHSBT's customary method results in 10% of donors being inappropriately bled (ie, with haemoglobin values below the regulatory threshold).

Methods: We compared the following four methods in 21 840 blood donors (aged ≥18 years) recruited from 10 NHSBT centres in England, with the Sysmex XN-2000 haematology analyser, the reference standard: (1) NHSBT's customary method; (2) "post donation" approach, that is, estimating current haemoglobin concentration from that measured by a haematology analyser at a donor's most recent prior donation; (3) "portable haemoglobinometry" (using capillary HemoCue); (4) non-invasive spectrometry (using MBR Haemospect or Orsense NMB200). We assessed sensitivity; specificity; proportion who would have been inappropriately bled, or rejected from donation ("deferred") incorrectly; and test preference.

Results: Compared with the reference standard, the methods ranged in test sensitivity from 17.0% (MBR Haemospect) to 79.0% (portable haemoglobinometry) in men, and from 19.0% (MBR Haemospect) to 82.8% (portable haemoglobinometry) in women. For specificity, the methods ranged from 87.2% (MBR Haemospect) to 99.9% (NHSBT's customary method) in men, and from 74.1% (Orsense NMB200) to 99.8% (NHSBT's customary method) in women. The proportion of donors who would have been inappropriately bled ranged from 2.2% in men for portable haemoglobinometry to 18.9% in women for MBR Haemospect. The proportion of donors who would have been deferred incorrectly with haemoglobin concentration above the minimum threshold ranged from 0.1% in men for NHSBT's customary method to 20.3% in women for OrSense. Most donors preferred non-invasive spectrometry.

Conclusion: In the largest study reporting head-to-head comparisons of four methods to measure haemoglobin prior to blood donation, our results support replacement of NHSBT's customary method with portable haemoglobinometry.

Dataset type

, ,

Dataset population size

29021

Keywords

Observations

Observed Node

Disambiguating Description

Measured Value

Measured Property

Observation Date

Persons

29021

Count

01 Jan 2016

Provenance

Purpose of dataset collection

Trial

Source of data extraction

EPR, Electronic survey, Other

Collection source setting

Cohort, study, trial

Patient pathway description

Blood donors in England were invited to take part in the study. The inclusion and exclusion criteria were as follows: Key inclusion criteria 1. Age &ampampampampge18 years and fulfilling all normal criteria for blood donation with the exception of pre-donation haemoglobin levels measured using the current NHSBT methods

  1. Willing to undergo additional haemoglobin measurement
  2. Willing to donate an extra blood sample for measurement of haemoglobin using an automated cell counter
  3. Willing to come back for a subsequent appointment at standard donation interval (ie 12-wk and 16-wk for men and women respectively) Key exclusion criteria 1. Participants who do not have internet access and/or are not willing to provide an email address for study correspondence (as the study will aim to be almost &ampampampampldquopaper-less&ampampampamprdquo and will involve remote web-based data collection)
  4. Donors already enrolled in the INTERVAL randomised trial will be excluded

Image contrast

Not stated

Biological sample availability

DNA,Plasma,Serum,Whole blood

Structural Metadata

Details

Publishing frequency

Other

Version

1.0.0

Modified

08/10/2024

Citation Requirements

COMPARE must be acknowledged in all publications using these data. Further details will be issued through the Data Access Committee.

Coverage

Start date

02/01/2016

End date

20/03/2017

Time lag

Not applicable

Geographic coverage

United Kingdom, England

Minimum age range

18

Maximum age range

80

Follow-up

Other

Accessibility

Language

en

Data Access Request

Dataset pipeline status

Not available

Time to dataset access

2-6 months

Access request cost

Cost recovery.

Access method category

TRE/SDE

Access service description

Researchers around the world can enquire about accessing the data from COMPARE which forms part of the Blood Donors Studies BioResource for their own research projects. Access to all samples and de-identified data (without any identifiable details such as the participant's name or date of birth) is strictly controlled by a formal Data Access Committee, comprising individuals responsible for the studies and members of the public. Full information on how to access the dataset can be found on the Donor Health website: https://www.donorhealth-btru.nihr.ac.uk/research/blood-donors-bioresource/

Data use limitation

General research use

Data use requirements

Not for profit use,Return to database or resource,User-specific restriction

Data Controller

The University of Cambridge

Data Processor

The University of Cambridge

Demographics

Dataset Types: Omics, Lifestyle, Measurements/Tests


Collection Sources: Cohort, study, trial

Publications about this dataset

Comparison of four methods to measure haemoglobin concentrations in whole blood donors (COMPARE): A ...Bell S, Sweeting M, Ramond A, Chung R, Kaptoge S, ...

Transfusion medicine (Oxford, England)

Published - 2021