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Clinical effects of dexamethasone among patients with sickle cell disease hospitalized with COVID-19: Outcomes from a single academic health system

Garneau et al., PLOS ONE, doi:10.1371/journal.pone.0313289
Nov 2024  
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Mortality -31% Improvement Relative Risk ICU admission -423% Hospitalization time -155% Dexamethasone  Garneau et al.  LATE TREATMENT Is late treatment with dexamethasone beneficial for COVID-19? Retrospective 30 patients in the USA (June 2020 - June 2022) Higher ICU admission (p=0.14) and longer hospitalization (p=0.063), not sig. c19early.org Garneau et al., PLOS ONE, November 2024 Favorsdexamethasone Favorscontrol 0 0.5 1 1.5 2+
Retrospective 30 hospitalized patients with sickle cell disease (SCD) showing increased risk of venous thromboembolism (VTE) with dexamethasone treatment for COVID-19. There were also trends towards increased ICU admission and longer hospital stays with dexamethasone, without statistical significance.
Standard of Care (SOC): SOC for COVID-19 in the study country, the USA, is very poor with very low average efficacy for approved treatments1. Only expensive, high-profit treatments were approved. Low-cost treatments were excluded, reducing the probability of treatment—especially early—due to access and cost barriers, and eliminating complementary and synergistic benefits seen with many low-cost treatments.
risk of death, 30.8% higher, RR 1.31, p = 1.00, treatment 1 of 13 (7.7%), control 1 of 17 (5.9%).
risk of ICU admission, 423.1% higher, RR 5.23, p = 0.14, treatment 4 of 13 (30.8%), control 1 of 17 (5.9%).
hospitalization time, 154.5% higher, relative time 2.55, p = 0.06, treatment 13, control 17.
Effect extraction follows pre-specified rules prioritizing more serious outcomes. Submit updates
Garneau et al., 26 Nov 2024, retrospective, USA, peer-reviewed, median age 33.7, 6 authors, study period 1 June, 2020 - 26 June, 2022. Contact: william.garneau@jhmi.edu, jhmeirb@jhmi.edu.
This PaperMiscellaneousAll
Clinical effects of dexamethasone among patients with sickle cell disease hospitalized with COVID-19: Outcomes from a single academic health system
William M Garneau, Matthew J Lankiewicz, Catherine R Lesko, Ashley P Lauriello, Kelly A Gebo, Sophie M Lanzkron
PLOS ONE, doi:10.1371/journal.pone.0313289
Background Dexamethasone is a steroid used in the treatment of hospitalized patients with severe COVID-19. However, the effect of dexamethasone in patients with SCD remains unclear given that steroids may precipitate vaso-occlusive crisis (VOC) in patients with SCD. Methods and findings We performed a retrospective analysis of patients with SCD who were hospitalized at Johns Hopkins Health System between June 1, 2020 and June 26, 2022. We reviewed individual charts to assess severity of illness and eligibility for dexamethasone treatment. The exposure of interest was treatment with dexamethasone. Outcomes of interest included incident VTE, length of hospital stay, ICU admission, follow up-VOC and mortality. We identified 30 patients with SCD and COVID-19 who were eligible for dexamethasone treatment, 13 of whom received dexamethasone. Dexamethasone was associated with an increased risk of incident VTE (risk difference = 36%; 95% CI 8%, 66%) after adjustment for high-risk genotypes, >3 hospitalizations, and receipt of anticoagulation. There was an increase in the risk difference of ICU admission and an increased length of stay in crude and adjusted analyses however these associations were not statistically significant. Conclusions We analyzed outcomes among patients with SCD who were hospitalized for COVID-19 and eligible for dexamethasone. Our study suggests that in this population, treatment with dexamethasone increases the risk of incident VTE. There was a suggestion of an increased risk
Author Contributions Conceptualization: William M. Garneau, Matthew J. Lankiewicz, Ashley P. Lauriello, Kelly A. Gebo, Sophie M. Lanzkron. Data curation: William M. Garneau, Matthew J. Lankiewicz, Kelly A. Gebo, Sophie M. Lanzkron. Formal analysis: William M. Garneau, Catherine R. Lesko, Kelly A. Gebo, Sophie M. Lanzkron. Investigation: William M. Garneau, Matthew J. Lankiewicz, Catherine R. Lesko, Ashley P. Lauriello, Kelly A. Gebo, Sophie M. Lanzkron. Methodology: William M. Garneau, Matthew J. Lankiewicz, Catherine R. Lesko, Kelly A. Gebo, Sophie M. Lanzkron. Project administration: William M. Garneau, Sophie M. Lanzkron. Resources: William M. Garneau, Kelly A. Gebo. Software: William M. Garneau, Catherine R. Lesko. Supervision: William M. Garneau, Kelly A. Gebo, Sophie M. Lanzkron. Validation: William M. Garneau, Matthew J. Lankiewicz, Catherine R. Lesko, Kelly A. Gebo. Visualization: William M. Garneau. Writing -original draft: William M. Garneau, Matthew J. Lankiewicz, Kelly A. Gebo, Sophie M. Lanzkron. Writing -review & editing: William M. Garneau, Matthew J. Lankiewicz, Catherine R. Lesko, Ashley P. Lauriello, Kelly A. Gebo, Sophie M. Lanzkron.
References
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Arlet, Lionnet, Khimoud, Joseph, Montalembert et al., Risk factors for severe COVID -19 in hospitalized sickle cell disease patients: A study of 319 patients in France, Am J Hematol, doi:10.1002/ajh.26432
Balanchivadze, Kudirka, Askar, Almadhoun, Kuriakose et al., Impact of COVID-19 Infection on 24 Patients with Sickle Cell Disease. One Center Urban Experience, Hemoglobin, doi:10.1080/03630269.2020.1797775
Calderwood, Sabir, Rao, Baker, Balasa et al., SARS-CoV-2 Infection Presenting as Acute Chest Syndrome in a Child With Hemoglobin SD-Los Angeles Disease: A Case Report and Review of Literature, J Pediatr Hematol Oncol, doi:10.1097/MPH.0000000000002546
Christian, Lanzkron, Naik, COVID-19 outcomes in sickle cell disease and sickle cell trait, Best Pract Res Clin Haematol, doi:10.1016/j.beha.2022.101382
Clift, Saatci, Coupland, Dambha-Miller, Cox, Sickle Cell Disorders and Severe COVID-19 Outcomes: A Cohort Study, Ann Intern Med, doi:10.7326/M21-1375
Cohen, Klings, Systemic Steroids and the Risk of Vasoocclusive Events in Patients with Sickle Cell Disease, Ann Am Thorac Soc
Efron, Tibshirani, An Introduction to the Bootstrap
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Hoogenboom, Fleysher, Soby, Mirhaji, Mitchell et al., Individuals with sickle cell disease and sickle cell trait demonstrate no increase in mortality or critical illness from COVID-19a fifteen hospital observational study in the Bronx, New York, Haematologica, doi:10.3324/haematol.2021.279222
Marshall, Murthy, Diaz, Adhikari, Angus et al., A minimal common outcome measure set for COVID-19 clinical research, Lancet Infect Dis, doi:10.1016/S1473-3099%2820%2930483-7
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DOI record: { "DOI": "10.1371/journal.pone.0313289", "ISSN": [ "1932-6203" ], "URL": "http://dx.doi.org/10.1371/journal.pone.0313289", "abstract": "<jats:sec id=\"sec001\">\n<jats:title>Background</jats:title>\n<jats:p>Dexamethasone is a steroid used in the treatment of hospitalized patients with severe COVID-19. However, the effect of dexamethasone in patients with SCD remains unclear given that steroids may precipitate vaso-occlusive crisis (VOC) in patients with SCD.</jats:p>\n</jats:sec>\n<jats:sec id=\"sec002\">\n<jats:title>Methods and findings</jats:title>\n<jats:p>We performed a retrospective analysis of patients with SCD who were hospitalized at Johns Hopkins Health System between June 1, 2020 and June 26, 2022. We reviewed individual charts to assess severity of illness and eligibility for dexamethasone treatment. The exposure of interest was treatment with dexamethasone. Outcomes of interest included incident VTE, length of hospital stay, ICU admission, follow up-VOC and mortality. We identified 30 patients with SCD and COVID-19 who were eligible for dexamethasone treatment, 13 of whom received dexamethasone. Dexamethasone was associated with an increased risk of incident VTE (risk difference = 36%; 95% CI 8%, 66%) after adjustment for high-risk genotypes, &gt;3 hospitalizations, and receipt of anticoagulation. There was an increase in the risk difference of ICU admission and an increased length of stay in crude and adjusted analyses however these associations were not statistically significant.</jats:p>\n</jats:sec>\n<jats:sec id=\"sec003\">\n<jats:title>Conclusions</jats:title>\n<jats:p>We analyzed outcomes among patients with SCD who were hospitalized for COVID-19 and eligible for dexamethasone. Our study suggests that in this population, treatment with dexamethasone increases the risk of incident VTE. 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Late treatment
is less effective
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