3 minute read
Immunosuppression (other than HIV
466 | CovidReference.com
Hoffmann C, Casado JL, Härter G, et al. Immune deficiency is a risk factor for severe COVID-19 in people living with HIV. HIV Med. 2020 Dec 27. PubMed: https://pubmed.gov/33368966.
Full-text: https://doi.org/10.1111/hiv.13037 Inciarte A, Gonzalez-Cordon A, Rojas J, et al. Clinical characteristics, risk factors, and inci-
dence of symptomatic COVID-19 in adults living with HIV: a single-center, prospec-
tive observational study. AIDS. 2020 Aug 7. PubMed: https://pubmed.gov/32773471. Fulltext: https://doi.org/10.1097/QAD.0000000000002643 Jewell BL, Mudimu E, Stover J, et al. Potential effects of disruption to HIV programmes in sub-
Saharan Africa caused by COVID-19: results from multiple mathematical models.
Lancet HIV. 2020 Sep;7(9):e629-e640. PubMed: https://pubmed.gov/32771089. Full-text: https://doi.org/10.1016/S2352-3018(20)30211-3 Richardson S, Hirsch JS, Narasimhan M, et al. Presenting Characteristics, Co-morbidities, and
Outcomes Among 5700 Patients Hospitalized With COVID-19 in the New York City Ar-
ea. JAMA. 2020 Apr 22:e206775. PubMed: https://pubmed.gov/32320003. Full-text: https://doi.org/10.1001/jama.2020.6775 Sanchez TH, Zlotorzynska M, Rai M, Baral SD. Characterizing the Impact of COVID-19 on Men
Who Have Sex with Men Across the United States in April, 2020. AIDS Behav. 2020 Apr 29:1-9. PubMed: https://pubmed.gov/32350773. Full-text: https://doi.org/10.1007/s10461020-02894-2 U.S. Department of Health and Human Services. Interim Guidance for COVID-19 and Persons with HIV. https://aidsinfo.nih.gov/guidelines/html/8/covid-19-and-persons-with-hiv-interim-guidance-/554/interim-guidance-for-covid-19-and-persons-with-hiv
Immunosuppression may bear a higher risk for SARS-CoV-2 infection and severe COVID-19. But the story is not that simple. Neither is it clear what immunosuppression actually means, nor are the available data sufficient to draw any conclusion. We just don’t know enough. Nevertheless, some authors are trumpeting the news that there is an increased risk. A bad example? A systematic review and meta-analysis on 8 studies and 4007 patients came to the conclusion that “immunosuppression and immunodeficiency were associated with increased risk of severe COVID-19 disease, although the statistical differences were not significant” (Gao 2020). The authors also state that “in response to the COVID-19 pandemic, special preventive and protective measures should be provided.” There is null evidence for this impressive statement. The total number of patients with immunosuppression in the study was 39 (without HIV: 11!), with 6/8 studies describing less than 4 patients with different modalities of immunosuppression. Despite the large absence of data, numerous viewpoints and guidelines have been published on how to manage immunosuppressed patients that may be more susceptible to acquire COVID-19 infection and develop severe courses. There are recommendations for intranasal corticosteroids in allergic rhinitis (Bousquet 2020), immunosuppressants for psoriasis and other cutaneous diseases (Conforti 2020, Torres 2020), rheumatic diseases (Favalli 2020, FigueroaParra 2020) or inflammatory bowel diseases (Kennedy 2020, Pasha 2020). The
Co-morbidities | 467
bottom line of these heroic attempts to balance the risk of immune-modifying drugs with the risk associated with active disease: what is generally needed, has to be done (or to be continued). Exposure prophylaxis is important. However, several studies have indeed found evidence for deleterious effects of glucocorticoids, indicating that these drugs should be given with particular caution these days. • In 600 COVID-19 patients with rheumatic diseases from 40 countries, multivariate-adjusted models revealed a prednisone dose ≥ 10 mg/day to be associated with higher odds of hospitalization. There was no risk with conventional disease-modifying anti-rheumatic drugs (DMARD) alone or in combination with biologics and Janus kinase (JAK) inhibitors (https://doi.org/10.1136/annrheumdis-2020-217871). • In 525 patients with inflammatory bowel disease (IBD) from 33 countries (Brenner 2020), risk factors for severe COVID-19 included systemic corticosteroids (adjusted odds ratio 6,9, 95% CI: 2,3-20,5), and sulfasalazine or 5-aminosalicylate use (aOR 3,1). TNF antagonist treatment was not associated with severe COVID-19.
• In 86 patients with IBD and symptomatic COVID-19, among them 62 receiving biologics or JAK inhibitors, hospitalization rates were higher in patients treated with oral glucocorticoids, hydroxychloroquine and methotrexate but not with JAK inhibitors (Haberman 2020). • In a large French database, including patients with inflammatory rheumatic and musculoskeletal diseases (iRMD), of 694 adults, 438 (63%) developed mild (not hospitalized), 169 (24%) moderate (hospitalized non-
ICU) and 87 (13%) severe (ICU/deceased) disease. In multivariable imputed analyses, the variables associated with severe infection were age, male gender, hypertension and higher BMI. Use of corticosteroids (OR = 1,97), mycophenolate mofetil (OR = 6,6) and rituximab (OR = 4,21) were also risk factors.
References
Bousquet J, Akdis C, Jutel M, et al. Intranasal corticosteroids in allergic rhinitis in COVID-19 infected patients: An ARIA-EAACI statement. Allergy. 2020 Mar 31. PubMed: https://pubmed.gov/32233040. Full-text: https://doi.org/10.1111/all.14302 Brenner EJ, Ungaro RC, Gearry RB, et al. Corticosteroids, But Not TNF Antagonists, Are
Associated With Adverse COVID-19 Outcomes in Patients With Inflammatory Bowel
Diseases: Results From an International Registry. Gastroenterology. 2020
Aug;159(2):481-491.e3. PubMed: https://pubmed.gov/32425234. Full-text: https://doi.org/10.1053/j.gastro.2020.05.032 Conforti C, Giuffrida R, Dianzani C, Di Meo N, Zalaudek I. COVID-19 and psoriasis: Is it time to limit treatment with immunosuppressants? A call for action. Dermatol Ther. 2020