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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
2.
Darko Antic; Natasa Milic; Thomas Chatzikonstantinou; Lydia Scarfò; Vladimir Otasevic; Nina Rajovic; David Allsup; Alejandro Alonso Cabrero; Martin Andres; Monica Baile Gonzales; Antonella Capasso; Rosa Collado; Raul Cordoba; Carolina Cuéllar-García; Juan Gonzalo Correa; Lorenzo De Paoli; Maria Rosaria De Paolis; Giovanni Del Poeta; Maria Dimou; Michael Doubek; Maria Efstathopoulou; Shaimaa El-Ashwah; Alicia Enrico; Blanca Espinet; Lucia Farina; Angela Ferrari; Myriam Foglietta; Alberto Lopez-Garcia; José A. García-Marco; Rocío García-Serra; Massimo Gentile; Eva Gimeno; Maria Gomes Silva; Odit Gutwein; Yervand K. Hakobyan; Yair Herishanu; José Ángel Hernández-Rivas; Tobias Herold; Gilad Itchaki; Ozren Jaksic; Ann Janssens; Оlga B. Kalashnikova; Elżbieta Kalicińska; Arnon P. Kater; Sabina Kersting; Maya Koren-Michowitz; Jorge Labrador Gomez; Deepesh Lad; Luca Laurenti; Alberto Fresa; Mark-David Levin; Carlota Mayor Bastida; Lara Malerba; Roberto Marasca; Monia Marchetti; Juan Marquet; Biljana Mihaljevic; Ivana Milosevic; Fatima Mirás; Marta Morawska; Marina Motta; Talha Munir; Roberta Murru; Raquel Nunes; Jacopo Olivieri; Miguel Arturo Pavlovsky; Inga Piskunova; Viola Maria Popov; Francesca Maria Quaglia; Giulia Quaresmini; Gianluigi Reda; Gian Matteo Rigolin; Amit Shrestha; Martin Šimkovič; Svetlana Smirnova; Martin Špaček; Paolo Sportoletti; Oana Stanca; Niki Stavroyianni; Doreen Te Raa; Kristina Tomic; Sanne Tonino; Livio Trentin; Ellen Der Spek; Michel Gelder; Marzia Varettoni; Andrea Visentin; Candida Vitale; Vojin Vukovic; Ewa Wasik-Szczepanek; Tomasz Wróbel; Lucrecia Yáñez San Segundo; Mohamed Yassin; Marta Coscia; Alessandro Rambaldi; Emili Montserrat; Robin Foà; Antonio Cuneo; Marc Carrier; Paolo Ghia; Kostas Stamatopoulos.
researchsquare; 2022.
Preprint in English | PREPRINT-RESEARCHSQUARE | ID: ppzbmed-10.21203.rs.3.rs-1571423.v1

ABSTRACT

Background: Patients with chronic lymphocytic leukemia (CLL) may be more susceptible to COVID-19 related poor outcomes, including thrombosis and death, due to the advanced age, the presence of comorbidities, and the disease and treatment-related immune deficiency. In this retrospective multicenter study, conducted by ERIC, the European Research Initiative on CLL, we assessed the risk of thrombosis and bleeding in patients with CLL affected by severe COVID-19.Methods: The study included patients from 79 centers across 22 countries. Data collection was conducted between April and May 2021.Results: A total of 793 patients from 79 centers were included in the study with 593 being hospitalized (74.8%). Among these, 518 were defined as having severe COVID: 162 were admitted to the ICU while 356 received oxygen supplementation outside the ICU. Most patients (90%) were receiving thromboprophylaxis. During COVID-19 treatment, 8.8% developed a thromboembolic event, while 4.8% experienced bleeding. Thrombosis developed in 20.5% of patients who were not receiving thromboprophylaxis, but only in 8.1% of patients who were on thromboprophylaxis. Bleeding episodes were more frequent in patients receiving intermediate/therapeutic versus prophylactic doses of low-molecular-weight heparin (LWMH) (11.1% vs. 4.2%, respectively) and in elderly. In multivariate analysis, peak D-dimer level was a poor prognostic factor for thrombosis occurrence (OR=1.020, 95%CI 1.006‒1.033), while thromboprophylaxis use was protective (OR=0.194, 95%CI 0.061‒0.614). Age and LMWH intermediate/therapeutic dose administration were prognostic factors in multivariate model for bleeding (OR=1.055, 95%CI 1.013-1.103 and OR=2.490, 95%CI 1.044-5.935, respectively). Conclusions: Patients with CLL affected by severe COVID-19 are at a high risk of thrombosis if thromboprophylaxis is not used, but also at increased risk of bleeding under the LMWH intermediate/therapeutic dose administration.  


Subject(s)
COVID-19
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
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