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1.
Tommaso Francesco Aiello; Jon Salmanton-Garcia; Francesco Marchesi; Barbora Weinbergerova; Andreas Glenthoj; Jens Van Praet; Francesca Farina; Julio Davila-Valls; Sonia Martín-Pérez; Shaimaa El-Ashwah; Martin Schönlein; Iker Falces-Romero; Jorge Labrador; Uluhan Sili; Caterina Buquicchio; Antonio Vena; Gaetan Plantefeve; Verena Petzer; Monika M. Biernat; Tobias Lahmer; Ildefonso Espigado; Jaap A. van Doesum; Ola Blennow; Klára Piukovics; Carlo Tascini; Michael Samarkos; Yavuz M. Bilgin; Luana Fianchi; Federico Itri; Toni Valkovic; Nicola S. Fracchiolla; Michelina Dargenio; Moraima Jimenez; Ferenc Magyari; Alberto Lopez-Garcia; Lucia Prezioso; Natasa Čolovic; Evgenii Shumilov; Ghaith Abu-Zeinah; Esperanza Lavilla-Rubira; Mario Virgilio Papa; Tomás-José Lopez-Gonzalez; László Imre Pinczes; Fatih Demirkan; Natasha Ali; Caroline Besson; Guillemette Fouquet; Alessandra Romano; Jose Angel Hernández-Rivas; Maria Ilaria del Principe; Avinash Aujayeb; Maria Merelli; Sylvain Lamure; Joyce Marques De Almeida; Maria Gomes da Silva; Noha Eisa; Joseph Meletiadis; Ikhwan Rinaldi; Olimpia Finizio; Ozren Jakšić; Mario Delia; Summiya Nizamuddin; Monia Marchetti; Marina Machado; Martin Cernan; Nicola Coppola; Eleni Gavriilaki; Chiara Cattaneo; Ana Groh; Zlate Stojanoski; Nurettin Erben; Nikola Pantic; Gustavo-Adolfo Mendez; Roberta Di Blasi; Stef Meers; Cristina De Ramon; Nathan C. Bahr; Ziad Emarah; Gina Varricchio; Milche Cvetanoski; Ramón Garcia-Sanz; Mirjana Mitrovic; Raphaël Lievin; Michaela Hanakova; Zdeněk Racil; Maria Vehreschild; Athanasios Tragiannidis; Raquel Nunes Rodrigues; Daniel Garcia-Bordallo; Raul Cordoba; Alba Cabirta; Anna Nordlander; Emanuele Ammatuna; Elena Arellano; Dominik Wolf; Romane Prin; Alessandro Limongelli; Martina Bavastro; Gökçe Melis Çolak; Stefanie K. Grafe; Ditte Stampe Hersby; Laman Rahimli; Oliver A. Cornely; Carolina Garcia-Vidal; Livio Pagano.
ssrn; 2023.
Preprint in English | PREPRINT-SSRN | ID: ppzbmed-10.2139.ssrn.4473151
3.
Francesco Marchesi; Jon Salmanton-Garcia; Ziad EMARAH; Klára PIUKOVICS; Marcio Nucci; Alberto Lopez-Garcia; Zdenek Racil; Francesca Farina; Marina POPOVA; Sofia ZOMPI; Ernesta Audisio; Marie-Pierre Ledoux; Luisa VERGA; Barbora Weinbergerova; Tomas Szotkowski; Maria Silva; Nicola Stefano Fracchiolla; Nick DE JONGE; Graham Collins; Monia Marchetti; Gabriele MAGLIANO; Carolina GARCÍA-VIDAL; Monika M. BIERNAT; Jaap van Doesum; Marina MACHADO; Fatih Demirkan; Murtadha Al Khabori; Pavel Zak; Benjamin Visek; Igor STOMA; Gustavo-Adolfo MÉNDEZ; Johan Maertens; Nina KHANNA; Ildefonso Espigado; Giulia DRAGONETTI; Luana Fianchi; Maria Ilaria Del Principe; Alba CABIRTA; Irati ORMAZABAL-VÉLEZ; Ozren Jaksic; Caterina BUQUICCHIO; Valentina BONUOMO; Josip Batinić; Ali S. OMRANI; Sylvain Lamure; Olimpia Finizio; Noemí FERNÁNDEZ; Iker FALCES-ROMERO; Ola BLENNOW; Rui BERGANTIM; Natasha Ali; Sein WIN; Jens VAN PRAET; Maria Chiara Tisi; Ayten SHIRINOVA; Martin SCHÖNLEIN; Juergen PRATTES; Monica PIEDIMONTE; Verena Petzer; Milan NAVRÁTIL; Austin Kulasekararaj; Pavel Jindra; Jiří SRAMEK; Andreas Glenthøj; Rita FAZZI; Cristina de Ramón; Chiara Cattaneo; Maria CALBACHO; Nathan C. BAHR; Shaimaa Saber EL-ASHWL; Raúl Córdoba; Michaela HANAKOVA; Giovanni ZAMBROTTA; Mariarita Sciumè; Stephen Booth; Raquel NUNES-RODRIGUES; Maria Vittoria SACCHI; Nicole GARCÍA-POUTÓN; Juan-Alberto MARTÍN-GONZÁLEZ; Sofya KHOSTELIDI; Stefanie GRÄFE; Laman RAHIMLI; alessandro busca; Paolo Corradini; Martin HOENIGL; Nikolai KLIMKO; Philipp Koehler; Antonio PAGLIUCA; Francesco Passamonti; Oliver Cornely; Livio pagano.
researchsquare; 2022.
Preprint in English | PREPRINT-RESEARCHSQUARE | ID: ppzbmed-10.21203.rs.3.rs-1323457.v1

ABSTRACT

Patients with acute myeloid leukemia (AML) are at high risk of mortality from coronavirus disease 2019 (COVID-19). The optimal management of AML patients with COVID-19 has not been established. Our multicenter study included 388 adult AML patients with COVID-19 diagnosis between February 2020 and October 2021. The vast majority were receiving or had received AML treatment in the prior 3 months. COVID-19 was severe in 41.2% and critical in 21.1% of cases. The chemotherapeutic schedule was modified in 174 patients (44.8%), delayed in 68 and permanently discontinued in 106. After a median follow-up of 325 days, 180 patients (46.4%) had died. Death was attributed to COVID-19 (43.3%), AML (26.1%) or to a combination of both (26.7%). Active disease, older age, and treatment discontinuation were associated with death, whereas AML treatment delay was protective. Seventy-nine patients had a simultaneous AML and COVID-19 diagnosis, with an improved survival when AML treatment could be delayed. Patients with COVID-19 diagnosis between January and August 2020 had a significantly lower survival. COVID-19 in AML patients was associated with a high mortality rate and modifications of therapeutic algorithms. The best approach to improve survival was to delay AML treatment.


Subject(s)
COVID-19
4.
researchsquare; 2021.
Preprint in English | PREPRINT-RESEARCHSQUARE | ID: ppzbmed-10.21203.rs.3.rs-505561.v1

ABSTRACT

Background Patients with rheumatic diseases have been considered at risk of COVID-19. A significant percentage of infections in children are asymptomatic or mild and can go unnoticed. This study aims to describe the seroprevalence of SARS-CoV-2 in a cohort of children with rheumatic diseases and assess possible risk factors. Methods: A cross-sectional study was performed in a pediatric rheumatology unit from a reference hospital in Madrid, from September 2020 to February 2021. Serology of SARS-CoV-2 was performed at the same time as their routine laboratory tests, and a specific questionnaire was completed by parents. Demographics, treatment and disease activity from laboratory-confirmed COVID-19 patients were compared to the data of patients without laboratory-confirmed COVID-19.Findings A total of 105 children were included. SARS-CoV-2 infection was demonstrated in 27 patients (25.7%): 6 PCR and 21 positive IgG serology. The mean age was 11.8 years , and the majority of the patients were females (72.4%). Most of the children were diagnosed with juvenile idiopathic arthritis (JIA) (70.3%; 19/27), followed by PFAPA (11.1%; 3/27). Immunosuppresive treatment was given in 88% of cases (24/27). Overall, 44.4% (12/27) of infected patients were asymptomatic. Three patients required hospital admission because of COVID-19, however none of them required oxygen supplementation. A total of 66.7% (18/27) of patients did not require any treatment or medical assistance. The seroprevalence in our cohort was 20% in contrast to the 7.7% population seroprevalence observed during the same study period in Spanish children. SARS-CoV-2 confirmed children with positive IgG or PCR were less frequently in remission (52% vs 72%; p 0.014). Moderate disease activity and treatment with oral corticosteroids were associated with higher risk for COVID-19 (OR 5.05; CI 95%: 1.56 - 16.3 and OR 4.2; CI 95%: 1.26 - 13.9 respectively).                            Conclusions In a cohort of pediatric patients with rheumatic disease and immunosuppressive therapy, moderate disease activity and oral corticosteroids were associated with COVID-19 positive patients. Seroprevalence was significantly higher compared to the same age healthy population. The clinical manifestations were mild and there were no severe infections among the patients.


Subject(s)
COVID-19
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