COVID-19 Among Patients With Inflammatory Rheumatic Diseases.
Adult
Aged
Ambulatory Care
Antirheumatic Agents
/ adverse effects
COVID-19
/ complications
Cohort Studies
Comorbidity
Critical Care
Female
Glucocorticoids
/ adverse effects
Hospitalization
Humans
Male
Middle Aged
Multivariate Analysis
Oxygen Inhalation Therapy
Regression Analysis
Rheumatic Diseases
/ complications
Turkey
COVID-19
DMARDs
SARS CoV-2
biologic DMARDs
rheumathoid diseases
Journal
Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960
Informations de publication
Date de publication:
Historique:
received:
10
01
2021
accepted:
26
03
2021
entrez:
3
5
2021
pubmed:
4
5
2021
medline:
15
5
2021
Statut:
epublish
Résumé
The course of novel coronavirus disease 2019 (COVID-19) has been of special concern in patients with inflammatory rheumatic diseases (IRDs) due to the immune dysregulation that may be associated with these diseases and the medications used for IRDs, that may affect innate immune responses. In this cohort study, we aimed to report the disease characteristics and variables associated with COVID-19 outcome among Turkish patients with IRDs. Between April and June, 2020, 167 adult IRD patients with COVID-19 were registered from 31 centers in 14 cities in Turkey. Disease outcome was classified in 4 categories; (i) outpatient management, (ii) hospitalization without oxygen requirement, (iii) hospitalization with oxygen requirement, and (iv) intensive care unit (ICU) admission or death. Multivariable ordinal logistic regression analysis was conducted to determine variables associated with a worse outcome. 165 patients (mean age: 50 ± 15.6 years, 58.2% female) were included. Twenty-four patients (14.5%) recovered under outpatient management, 141 (85.5%) were hospitalized, 49 (30%) required inpatient oxygen support, 22 (13%) were treated in the ICU (17 received invasive mechanic ventilation) and 16 (10%) died. Glucocorticoid use (OR: 4.53, 95%CI 1.65-12.76), chronic kidney disease (OR: 12.8, 95%CI 2.25-103.5), pulmonary disease (OR: 2.66, 95%CI 1.08-6.61) and obesity (OR: 3.7, 95%CI 1.01-13.87) were associated with a worse outcome. Biologic disease-modifying antirheumatic drugs (DMARDs) do not seem to affect COVID-19 outcome while conventional synthetic DMARDs may have a protective effect (OR: 0.36, 95%CI 0.17-0.75). Estimates for the associations between IRD diagnoses and outcome were inconclusive. Among IRD patients with COVID-19, comorbidities and glucocorticoid use were associated with a worse outcome, while biologic DMARDs do not seem to be associated with a worse outcome.
Sections du résumé
BACKGROUND
BACKGROUND
The course of novel coronavirus disease 2019 (COVID-19) has been of special concern in patients with inflammatory rheumatic diseases (IRDs) due to the immune dysregulation that may be associated with these diseases and the medications used for IRDs, that may affect innate immune responses.
OBJECTIVE
OBJECTIVE
In this cohort study, we aimed to report the disease characteristics and variables associated with COVID-19 outcome among Turkish patients with IRDs.
METHODS
METHODS
Between April and June, 2020, 167 adult IRD patients with COVID-19 were registered from 31 centers in 14 cities in Turkey. Disease outcome was classified in 4 categories; (i) outpatient management, (ii) hospitalization without oxygen requirement, (iii) hospitalization with oxygen requirement, and (iv) intensive care unit (ICU) admission or death. Multivariable ordinal logistic regression analysis was conducted to determine variables associated with a worse outcome.
RESULTS
RESULTS
165 patients (mean age: 50 ± 15.6 years, 58.2% female) were included. Twenty-four patients (14.5%) recovered under outpatient management, 141 (85.5%) were hospitalized, 49 (30%) required inpatient oxygen support, 22 (13%) were treated in the ICU (17 received invasive mechanic ventilation) and 16 (10%) died. Glucocorticoid use (OR: 4.53, 95%CI 1.65-12.76), chronic kidney disease (OR: 12.8, 95%CI 2.25-103.5), pulmonary disease (OR: 2.66, 95%CI 1.08-6.61) and obesity (OR: 3.7, 95%CI 1.01-13.87) were associated with a worse outcome. Biologic disease-modifying antirheumatic drugs (DMARDs) do not seem to affect COVID-19 outcome while conventional synthetic DMARDs may have a protective effect (OR: 0.36, 95%CI 0.17-0.75). Estimates for the associations between IRD diagnoses and outcome were inconclusive.
CONCLUSIONS
CONCLUSIONS
Among IRD patients with COVID-19, comorbidities and glucocorticoid use were associated with a worse outcome, while biologic DMARDs do not seem to be associated with a worse outcome.
Identifiants
pubmed: 33936073
doi: 10.3389/fimmu.2021.651715
pmc: PMC8086428
doi:
Substances chimiques
Antirheumatic Agents
0
Glucocorticoids
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
651715Investigateurs
Ayse Cefle
(A)
Ali Karakas
(A)
Derya Kaskari
(D)
Samet Karahan
(S)
Dilek Tezcan
(D)
Abdurrahman Tufan
(A)
Ayse Ayan
(A)
Levent Kılıc
(L)
Salim Donmez
(S)
Mustafa Erdogan
(M)
Veli Yazisiz
(V)
Edip Gokalp Gok
(EG)
Ahmet Eftal Yucel
(AE)
Elif Dincses Nas
(ED)
Gezmiş Kimyon
(G)
Gunay Sahin Dalgic
(GS)
Hakan Erdem
(H)
Kerem Yigit Abacar
(KY)
Ridvan Mercan
(R)
Omer Karadag
(O)
Onay Gercik
(O)
Suleyman Ozbek
(S)
Sebnem Gider
(S)
Semih Gulle
(S)
Sibel Osken
(S)
Sedat Kiraz
(S)
Timucin Kasifoglu
(T)
Fatma Alibaz-Oner
(F)
Izzet Fresko
(I)
Ali Akdogan
(A)
Neslihan Yilmaz
(N)
Informations de copyright
Copyright © 2021 Esatoglu, Tascilar, Babaoğlu, Bes, Yurttas, Akar, Pehlivan, Akleylek, Tecer, Seyahi, Yuce-Inel, Alpay-Kanitez, Bodakci, Tekgoz, Colak, Bolek, Koca, Kalyoncu, Icacan, Ugurlu, Oz, Hamuryudan, Hatemi and the Turkish Society for Rheumatology COVID-19 Registry Investigators.
Déclaration de conflit d'intérêts
KT has served as a speaker for Gilead. GH has received grant/research support from Celgene and has served as a speaker for AbbVie, Celgene, Novartis, and UCB Pharma. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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