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Clinical and experimental immunology · 2022

Outcomes following SARS-CoV-2 infection in patients with primary and secondary immunodeficiency in the UK.

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Shields Adrian M, Anantharachagan Ariharan, Arumugakani Gururaj, Baker Kenneth, Bahal Sameer, Baxendale Helen, Bermingham William, Bhole Malini, Boules Evon, Bright Philip, Chopra Charu, Cliffe Lucy, Cleave Betsy, Dempster John, Devlin Lisa, Dhalla Fatima, Diwakar Lavanya, Drewe Elizabeth, Duncan Christopher, Dziadzio Magdalena, Elcombe Suzanne, Elkhalifa Shuayb, Gennery Andrew, Ghanta Harichandrana, Goddard Sarah, Grigoriadou Sofia, Hackett Scott, Hayman Grant, Herriot Richard, Herwadkar Archana, Huissoon Aarnoud, Jain Rashmi, Jolles Stephen, Johnston Sarah, Khan Sujoy, Laffan James, Lane Peter, Leeman Lucy, Lowe David M, Mahabir Shanti, Lochlainn Dylan James Mac, McDermott Elizabeth, Misbah Siraj, Moghaddas Fiona, Morsi Hadeil, Murng Sai, Noorani Sadia, O'Brien Rachael, Patel Smita, Price Arthur, Rahman Tasneem, Seneviratne Suranjith, Shrimpton Anna, Stroud Catherine, Thomas Moira, Townsend Katie, Vaitla Prashantha, Verma Nisha, Williams Anthony, Burns Siobhan O, Savic Sinisa, Richter Alex G

Аннотация

In March 2020, the United Kingdom Primary Immunodeficiency Network (UKPIN) established a registry of cases to collate the outcomes of individuals with PID and SID following SARS-CoV-2 infection and treatment. A total of 310 cases of SARS-CoV-2 infection in individuals with PID or SID have now been reported in the UK. The overall mortality within the cohort was 17.7% (n = 55/310). Individuals with CVID demonstrated an infection fatality rate (IFR) of 18.3% (n = 17/93), individuals with PID receiving IgRT had an IFR of 16.3% (n = 26/159) and individuals with SID, an IFR of 27.2% (n = 25/92). Individuals with PID and SID had higher inpatient mortality and died at a younger age than the general population. Increasing age, low pre-SARS-CoV-2 infection lymphocyte count and the presence of common co-morbidities increased the risk of mortality in PID. Access to specific COVID-19 treatments in this cohort was limited: only 22.9% (n = 33/144) of patients admitted to the hospital received dexamethasone, remdesivir, an anti-SARS-CoV-2 antibody-based therapeutic (e.g. REGN-COV2 or convalescent plasma) or tocilizumab as a monotherapy or in combination. Dexamethasone, remdesivir, and anti-SARS-CoV-2 antibody-based therapeutics appeared efficacious in PID and SID. Compared to the general population, individuals with PID or SID are at high risk of mortality following SARS-CoV-2 infection. Increasing age, low baseline lymphocyte count, and the presence of co-morbidities are additional risk factors for poor outcome in this cohort.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты