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CORYLUS UK: A retrospective observational cohort study of the impact of COVID-19 on systemic lupus erythematosus patients in England using data from linked primary and secondary care databases

Safe People

Organisation name

Health IQ

Organisation sector

Commercial

Applicant name(s)

Jay Were - Chief Investigator - Health iQShea O'Connell - Corresponding Applicant - Health iQArchie Farrer - Collaborator - Health iQBoglarka Kovacs - Collaborator - Health iQGulsah Akin Unal - Collaborator - Health iQJudith Ruzangi - Collaborator - Health iQMico Hamlyn - Collaborator - Health iQ

Safe Projects

Project ID

CPRD696

Lay summary

Systemic lupus erythematosus (SLE) is a complicated and chronic autoimmune disease where a patient’s own immune system can attack any part of their body. SLE has a huge range of symptoms from rash and hair loss, through to heart disease and serious brain and nerve problems from constant immune activity. Commonly prescribed medications include steroids and immunosuppressants that leave patients in an immunocompromised state, depending on the severity of their disease and medication dosage.

Technical summary

Systemic lupus erythematosus (SLE) is a chronic autoimmune disease characterised by autoantibodies, systemic inflammation and lymphopenia. There is no cure for SLE, and treatment depends on severity, including non-steroidal anti-inflammatories (NSAIDs), corticosteroids, immunosuppressants, and antimalarial agents such as chloroquine or hydroxychloroquine. Whilst corticosteroids are rapidly effective for suppressing flares, long term use has considerable side-effects[1].

Latest approval date

09/03/2021

Safe Data

Dataset(s) name

HES Accident and Emergency

HES Admitted Patient Care

HES Outpatient

ONS Death Registration Data

Safe Setting

Access type

Release