Evidence map›Paper›PMID 36814045›Full record

ArticleDiabetes therapy : research, treatment and education of diabetes and related disorders2023

The Effect of the COVID-19 Pandemic on HbA1c Testing: Prioritization of High-Risk Cases and Impact of Social Deprivation.

David Holland, Adrian H Heald, Fahmy F W Hanna, Mike Stedman, Pensée Wu, Julius Sim, Christopher J Duff, Helen Duce, Lewis Green, Jonathan Scargill and 9 more

Abstract read
In one paragraph

Article in Diabetes therapy : research, treatment and education of diabetes and related disorders, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–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.

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

7 citing papers in PubMed.

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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

19 authors.

David HollandThe Benchmarking Partnership, Alsager, Cheshire, UK.
Adrian H HealdDepartment of Diabetes and Endocrinology, Salford Royal Hospital, The Northern Care Alliance NHS Foundation Trust, Salford, UK.ORCID http://orcid.org/0000-0002-9537-4050
Fahmy F W HannaDepartment of Diabetes and Endocrinology, University Hospitals of North Midlands NHS Trust, Stoke-On-Trent, Staffordshire, UK.ORCID http://orcid.org/0000-0001-5800-1442
Mike StedmanRes Consortium, Andover, UK.ORCID http://orcid.org/0000-0002-0491-7823
Pensée WuDepartment of Obstetrics & Gynaecology, University Hospitals of North Midlands NHS Trust, Stoke-On-Trent, Staffordshire, UK.ORCID http://orcid.org/0000-0003-0011-5636
Julius SimSchool of Medicine, Keele University, Keele, Staffordshire, ST5 5BG, UK.ORCID http://orcid.org/0000-0002-1816-1676
Christopher J DuffSchool of Medicine, Keele University, Keele, Staffordshire, ST5 5BG, UK.ORCID http://orcid.org/0000-0002-3753-0043
Helen DuceDepartment of Clinical Biochemistry, North Midlands and Cheshire Pathology Services, University Hospitals of North Midlands NHS Trust, Stoke-On-Trent, Staffordshire, UK.
Lewis GreenDepartment of Clinical Biochemistry, St. Helens & Knowsley Teaching Hospitals NHS Trust, Whiston Hospital, Prescot, UK.ORCID http://orcid.org/0000-0001-5792-5408
Jonathan ScargillDepartment of Clinical Biochemistry, The Royal Oldham Hospital, The Northern Care Alliance NHS Foundation Trust, Manchester, UK.
Jonathon D HoweDepartment of Clinical Biochemistry, Salford Royal Hospital, The Northern Care Alliance NHS Foundation Trust, Manchester, UK.
Sarah RobinsonDepartment of Clinical Biochemistry, North Midlands and Cheshire Pathology Services, University Hospitals of North Midlands NHS Trust, Stoke-On-Trent, Staffordshire, UK.
Ian HalsallDepartment of Clinical Biochemistry, Cambridge University Hospitals NHS Foundation Trust, Addenbrooke's Hospital, Cambridge, UK.
Neil GaskellDepartment of Pathology, Warrington & Halton Teaching Hospitals NHS Foundation Trust, Warrington, UK.
Andrew DavisonDepartment of Clinical Biochemistry & Metabolic Medicine, Liverpool Clinical Laboratories, Liverpool University Hospital NHS Foundation Trust, Liverpool, UK.
Mark SimmsDepartment of Clinical Biochemistry, Wirral University Teaching Hospital NHS Foundation Trust, Birkenhead, Wirral, UK.
Angela DennyDepartment of Clinical Biochemistry, Wirral University Teaching Hospital NHS Foundation Trust, Birkenhead, Wirral, UK.
Martin LanganPathology Directorate, Countess of Chester Hospital NHS Foundation Trust, Chester, UK.
Anthony A FryerSchool of Medicine, Keele University, Keele, Staffordshire, ST5 5BG, UK. a.a.fryer@keele.ac.uk.ORCID http://orcid.org/0000-0001-8678-0404

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionStudies show that the COVID-19 pandemic disproportionately affected people with diabetes and those from disadvantaged backgrounds. During the first 6 months of the UK lockdown, > 6.6 M glycated haemoglobin (HbA1c) tests were missed. We now report variability in the recovery of HbA1c testing, and its association with diabetes control and demographic characteristics.

methodsIn a service evaluation, we examined HbA1c testing across ten UK sites (representing 9.9% of England's population) from January 2019 to December 2021. We compared monthly requests from April 2020 to those in the equivalent 2019 months. We examined effects of (i) HbA1c level, (ii) between-practice variability, and (iii) practice demographics.

resultsIn April 2020, monthly requests dropped to 7.9-18.1% of 2019 volumes. By July 2020, testing had recovered to 61.7-86.9% of 2019 levels. During April-June 2020, we observed a 5.1-fold variation in the reduction of HbA1c testing between general practices (12.4-63.8% of 2019 levels). There was evidence of limited prioritization of testing for patients with HbA1c > 86 mmol/mol during April-June 2020 (4.6% of total tests vs. 2.6% during 2019). Testing in areas with the highest social disadvantage was lower during the first lockdown (April-June 2020; trend test p < 0.001) and two subsequent periods (July-September and October-December 2020; both p < 0.001). By February 2021, testing in the highest deprivation group had a cumulative fall in testing of 34.9% of 2019 levels versus 24.6% in those in the lowest group.

conclusionOur findings highlight that the pandemic response had a major impact on diabetes monitoring and screening. Despite limited test prioritization in the > 86 mmol/mol group, this failed to acknowledge that those in the 59-86 mmol/mol group require consistent monitoring to achieve the best outcomes. Our findings provide additional evidence that those from poorer backgrounds were disproportionately disadvantaged. Healthcare services should redress this health inequality.

Indexed as

COVID-19Diabetes mellitusGlycated haemoglobinHbA1cIndex of multiple deprivationMonitoringPandemicRecovery

Identifiers

PMID36814045
PMCPMC9946287

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.