Factors associated with the severity of COVID-19 outcomes in people with neuromuscular diseases: Data from the International Neuromuscular COVID-19 Registry.
Factors associated with the severity of COVID-19 outcomes in people with neuromuscular diseases: Data from the International Neuromuscular COVID-19 Registry.
复制标题
DOI:
10.1111/ene.15613
复制
发表时间:
2023-02
影响因子:
5.1
通讯作者:
Machado, Pedro M.
中科院分区:
文献类型:
--
作者:
Pizzamiglio, Chiara;Pitceathly, Robert D. S.;Lunn, Michael P.;Brady, Stefen;De Marchi, Fabiola;Galan, Lucia;Heckmann, Jeannine M.;Horga, Alejandro;Molnar, Maria J.;Oliveira, Acary S. B.;Pinto, Wladimir B. V. R.;Primiano, Guido;Santos, Ernestina;Schoser, Benedikt;Servidei, Serenella;Souza, Paulo V. Sgobbi;Venugopalan, Vishnu;Hanna, Michael G.;Dimachkie, Mazen M.;Machado, Pedro M.
Clinical outcome information on patients with neuromuscular diseases (NMDs) who have been infected with SARS‐CoV‐2 is limited. The aim of this study was to determine factors associated with the severity of COVID‐19 outcomes in people with NMDs. Cases of NMD, of any age, and confirmed/presumptive COVID‐19, submitted to the International Neuromuscular COVID‐19 Registry up to 31 December 2021, were included. A mutually exclusive ordinal COVID‐19 severity scale was defined as follows: (1) no hospitalization; (2) hospitalization without oxygenation; (3) hospitalization with ventilation/oxygenation; and (4) death. Multivariable ordinal logistic regression analyses were used to estimate odds ratios (ORs) for severe outcome, adjusting for age, sex, race/ethnicity, NMD, comorbidities, baseline functional status (modified Rankin scale [mRS]), use of immunosuppressive/immunomodulatory medication, and pandemic calendar period. Of 315 patients from 13 countries (mean age 50.3 [±17.7] years, 154 [48.9%] female), 175 (55.5%) were not hospitalized, 27 (8.6%) were hospitalized without supplemental oxygen, 91 (28.9%) were hospitalized with ventilation/supplemental oxygen, and 22 (7%) died. Higher odds of severe COVID‐19 outcomes were observed for: age ≥50 years (50–64 years: OR 2.4, 95% confidence interval [CI] 1.33–4.31; >64 years: OR 4.16, 95% CI 2.12–8.15; both vs. <50 years); non‐White race/ethnicity (OR 1.81, 95% CI 1.07–3.06; vs. White); mRS moderately severe/severe disability (OR 3.02, 95% CI 1.6–5.69; vs. no/slight/moderate disability); history of respiratory dysfunction (OR 3.16, 95% CI 1.79–5.58); obesity (OR 2.24, 95% CI 1.18–4.25); ≥3 comorbidities (OR 3.2, 95% CI 1.76–5.83; vs. ≤2; if comorbidity count used instead of specific comorbidities); glucocorticoid treatment (OR 2.33, 95% CI 1.14–4.78); and Guillain–Barré syndrome (OR 3.1, 95% CI 1.35–7.13; vs. mitochondrial disease). Among people with NMDs, there is a differential risk of COVID‐19 outcomes according to demographic and clinical characteristics. These findings could be used to develop tailored management strategies and evidence‐based recommendations for NMD patients.
登录
查看更多内容
DOI:
10.1056/nejmoa2022926
发表时间:
2020-11-19
期刊:
The New England journal of medicine
影响因子:
--
作者:
RECOVERY Collaborative Group;Horby P;Mafham M;Linsell L;Bell JL;Staplin N;Emberson JR;Wiselka M;Ustianowski A;Elmahi E;Prudon B;Whitehouse T;Felton T;Williams J;Faccenda J;Underwood J;Baillie JK;Chappell LC;Faust SN;Jaki T;Jeffery K;Lim WS;Montgomery A;Rowan K;Tarning J;Watson JA;White NJ;Juszczak E;Haynes R;Landray MJ
通讯作者:
Landray MJ
DOI:
10.1016/j.clim.2020.108651
发表时间:
2021-03
期刊:
Clinical immunology (Orlando, Fla.)
影响因子:
--
作者:
Gasmi A;Peana M;Pivina L;Srinath S;Gasmi Benahmed A;Semenova Y;Menzel A;Dadar M;Bjørklund G
通讯作者:
Bjørklund G
影响因子:
3.9
作者:
Dresser L;Wlodarski R;Rezania K;Soliven B
通讯作者:
Soliven B
影响因子:
27.4
作者:
Alunno, Alessia;Najm, Aurelie;Mariette, Xavier
通讯作者:
Mariette, Xavier
DOI:
10.1002/art.41567
发表时间:
2021-03
期刊:
Arthritis & rheumatology (Hoboken, N.J.)
影响因子:
--
作者:
Gianfrancesco MA;Leykina LA;Izadi Z;Taylor T;Sparks JA;Harrison C;Trupin L;Rush S;Schmajuk G;Katz P;Jacobsohn L;Hsu TY;D'Silva KM;Serling-Boyd N;Wallwork R;Todd DJ;Bhana S;Costello W;Grainger R;Hausmann JS;Liew JW;Sirotich E;Sufka P;Wallace ZS;Machado PM;Robinson PC;Yazdany J;COVID-19 Global Rheumatology Alliance
通讯作者:
COVID-19 Global Rheumatology Alliance