Evidence map›Paper›PMID 40453534›Full record

ArticleEClinicalMedicine2025

The DESTINIES Study: an online Delphi study to build international consensus on the medical conditions and procedures that confer immunosuppression and their respective COVID-19 risk profiles.

Meredith Leston, José M Ordóñez-Mena, Mark Joy, F D Richard Hobbs, Simon de Lusignan, Benjamin W Teh, Ingrid de Groot, Iain McInnes, Hana M El Sahly, John Isaacs and 13 more

Abstract read
In one paragraph

Article in EClinicalMedicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

23 authors.

Meredith LestonNuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, United Kingdom.
José M Ordóñez-MenaNuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, United Kingdom.
Mark JoyNuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, United Kingdom.
F D Richard HobbsNuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, United Kingdom.
Simon de LusignanNuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, United Kingdom.
Benjamin W TehDepartment of Infectious Diseases, Peter MacCallum Cancer Centre, 305 Grattan Street, Melbourne, VIC, 3000, Australia.
Ingrid de GrootSpierziekten Nederland, Dutch Myositis Working Group, Lt.Gen van Heutszlaan 6, 3743JN, Baarn, Netherlands.
Iain McInnesMVLS College Office, Wolfson Medical School Building, University of Glasgow, University Avenue, Glasgow, United Kingdom.
Hana M El SahlyDepartments of Molecular Virology and Microbiology and Medicine, Baylor College of Medicine, Houston, TX, USA.
John IsaacsWilliam Leech Building, Medical School, Framlington Place, Newcastle Upon Tyne, United Kingdom.
Monique AnderssonNuffield Division of Clinical Laboratory Science, Radcliffe Department of Medicine, University of Oxford, Oxford, United Kingdom.
Francois RaffiDepartment of Infectious and Tropical Diseases and CIC 1413, INSERM, University Hospital, Nantes, 44093, France.
Wei Shen LimNottingham University Hospitals, City Hospital Campus, Hucknall Road, Nottingham, United Kingdom.
Richard ConwayRobert Mayne Clinic & Rheumatology Day Centre, St James' Hospital, Dublin, Ireland.
Stefan SiebertSchool of Infection & Immunity, University of Glasgow, University Place, Glasgow, United Kingdom.
Iain BuchanInstitute of Population Health, Waterhouse Building, Block B Brownlow Street, Liverpool, United Kingdom.
Martin UnderwoodWarwick Clinical Trials Unit, Warwick Medical School, University of Warwick, Coventry, United Kingdom.
David LoweUCL Institute of Immunity & Transplantation, The Pears Building, Pond Street, London, United Kingdom.
Michael HoergerTulane Cancer Center, Tulane University, 1700 Tulane Ave, New Orleans, LA, 70112, USA.
Christopher E M GriffithsDermatology Centre, Hope Hospital, University of Manchester, Manchester, United Kingdom.
Alessia AlunnoDepartment of Life, Health and Environmental Sciences, University of L'Aquila, Internal Medicine and Nephrology Division, ASL-1 Avezzano-Sulmona-L'Aquila, L'Aquila, Italy.
Lennard Y W LeeDepartment of Oncology, University of Oxford, Old Road Campus Research Building, Roosevelt Drive, Oxford, OX3 7DQ, United Kingdom.
DESTINIES Consortium

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The lack of international consensus on defining and categorising immunosuppression has undermined disease surveillance and patient care, particularly during the COVID-19 pandemic. To address this, a global expert panel was recruited to join the eDElphi STudy to fully defiINe and COVID-risk stratify ImmunosupprESsion (DESTINIES) and develop a COVID risk-stratified digital phenotype for 'adult immunosuppression' (the DESTINIES phenotype). Methods: Panellists were presented with all medical diagnoses and procedures cited in prevailing immunosuppressed definitions; they evaluated their appropriateness for the DESTINIES phenotype and their risks for severe COVID-19 outcomes through anonymous online questionnaires and discussion. Panel agreement with a series of clinical statements were also assessed; statements incorporated longstanding disputes, including variables that could reverse immunosuppression. Each round of data collection informed and refined a draft phenotype until final ratification. This study was active between May and September 2024. Findings: Sixty-four experts from four continents and 12 international agencies completed two rounds of consensus questionnaire, a discussion group and ratifying vote. Panellists identified candidates posing higher (e.g. Transplantation, Primary Immunodeficiency) and lower COVID-19 risk (e.g. Anorexia nervosa, Cerebral spinal fluid leak) but disagreed on the categorisation of others (e.g. Asplenia, Immune-mediated Inflammatory Disease). Consensus was reached on ten clinical statements, notably removing Drug-managed HIV and Cancer remission from consideration as immunosuppressed. The DESTINIES phenotype was ratified with near unanimous support (94%) for implementation in surveillance. Interpretation: Pending validation, the DESTINIES phenotype provides a clinically meaningful, internationally ratified and digitally practical method for identifying and COVID-19 risk-stratifying adult immunosuppressed patients in healthcare data. Funding: This work was funded by the UK Medical Research Council and EMIS Health.

Indexed as

ConsensusCOVID-19DelphiDigital healthDisease surveillanceImmunosuppressedImmunosuppressionInclusion healthInoculationPersonalised medicinePharmacovigilancePolicyPolicymakingPrecision healthPublic healthVaccine

Identifiers

PMID40453534
PMCPMC12124667

What OpenQuestion holds

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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.