Severe manifestations of SARS-CoV-2 in children and adolescents: from COVID-19 pneumonia to multisystem inflammatory syndrome: a multicentre study in pediatric intensive care units in Spain

被引:116
作者
Garcia-Salido, Alberto [1 ]
de Carlos Vicente, Juan Carlos [2 ]
Belda Hofheinz, Sylvia [3 ]
Balcells Ramirez, Joan [4 ]
Slocker Barrio, Maria [5 ]
Leoz Gordillo, Ines [1 ]
Hernandez Yuste, Alexandra [6 ]
Guitart Pardellans, Carmina [7 ]
Cuervas-Mons Tejedor, Maite [8 ]
Huidobro Labarga, Beatriz [9 ]
Vazquez Martinez, Jose Luis [10 ]
Gutierrez Jimeno, Miriam [11 ]
Oulego-Erroz, Ignacio [12 ]
Trastoy Quintela, Javier [13 ]
Medina Monzon, Carmen [14 ]
Medina Ramos, Laura [15 ]
Holanda Pena, Maria Soledad [16 ]
Gil-Anton, Javier [17 ]
Sorribes Orti, Clara [18 ]
Flores Gonzalez, Jose Carlos [19 ]
Hernandez Palomo, Rosa Maria [20 ]
Sanchez Ganfornina, Inma [21 ]
Fernandez Romero, Emilia [22 ]
Garcia-Besteiro, Maria [23 ]
Lopez-Herce Cid, Jesus [5 ]
Gonzalez Cortes, Rafael [5 ]
机构
[1] Hosp Infantil Univ Nino Jesus, Madrid, Spain
[2] Hosp Univ Son Espases, Palma De Mallorca, Spain
[3] Hosp Univ 12 Octubre, Madrid, Spain
[4] Hosp Univ Vall DHebron, Barcelona, Spain
[5] Hosp Gen Univ Gregorio Maranon, Paediat Intens Care Unit, Calle Doctor Castelo 47, Madrid 28007, Spain
[6] Hosp Reg Univ Malaga, Malaga, Spain
[7] Hosp Univ St Joan de Deu, Esplugas de Llobregat, Spain
[8] Hosp Univ Burgos, Burgos, Spain
[9] Hosp Univ Virgen Salud, Toledo, Spain
[10] Hosp Univ Ramon Y Cajal, Madrid, Spain
[11] Clin Univ Navarra, Pamplona, Spain
[12] Complejo Asistencial Univ Leon, Leon, Spain
[13] Complejo Hosp Univ Santiago, Santiago De Compostela, Spain
[14] Hosp Gen Univ Albacete, Albacete, Spain
[15] Hosp Gen Univ Alicante, Alicante, Spain
[16] Hosp Univ Marques Valdecilla, Santander, Spain
[17] Hosp Univ Cruces, Baracaldo, Spain
[18] Hosp Univ Joan XXIII, Tarragona, Spain
[19] Hosp Univ Puerta del Mar, Cadiz, Spain
[20] Hosp Univ Quironsalud Madrid, Pozuelo De Alarcon, Spain
[21] Hosp Univ Virgen Rocio, Seville, Spain
[22] Hosp Univ Virgen Macarena, Seville, Spain
[23] Parc Tauli Hosp Univ, Sabadell, Spain
关键词
SARS-CoV-2; Pediatric multisystem inflammatory syndrome temporally associated with COVID-19; Kawasaki disease; Toxic shock syndrome; Children; Critical care; Shock; DISEASE; SHOCK;
D O I
10.1186/s13054-020-03332-4
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background Multisystem inflammatory syndrome temporally associated with COVID-19 (MIS-C) has been described as a novel and often severe presentation of SARS-CoV-2 infection in children. We aimed to describe the characteristics of children admitted to Pediatric Intensive Care Units (PICUs) presenting with MIS-C in comparison with those admitted with SARS-CoV-2 infection with other features such as COVID-19 pneumonia. Methods A multicentric prospective national registry including 47 PICUs was carried out. Data from children admitted with confirmed SARS-CoV-2 infection or fulfilling MIS-C criteria (with or without SARS-CoV-2 PCR confirmation) were collected. Clinical, laboratory and therapeutic features between MIS-C and non-MIS-C patients were compared. Results Seventy-four children were recruited. Sixty-one percent met MIS-C definition. MIS-C patients were older than non-MIS-C patients (p = 0.002): 9.4 years (IQR 5.5-11.8) vs 3.4 years (IQR 0.4-9.4). A higher proportion of them had no previous medical history of interest (88.2% vs 51.7%, p = 0.005). Non-MIS-C patients presented more frequently with respiratory distress (60.7% vs 13.3%, p < 0.001). MIS-C patients showed higher prevalence of fever (95.6% vs 64.3%, p < 0.001), diarrhea (66.7% vs 11.5%, p < 0.001), vomits (71.1% vs 23.1%, p = 0.001), fatigue (65.9% vs 36%, p = 0.016), shock (84.4% vs 13.8%, p < 0.001) and cardiac dysfunction (53.3% vs 10.3%, p = 0.001). MIS-C group had a lower lymphocyte count (p < 0.001) and LDH (p = 0.001) but higher neutrophil count (p = 0.045), neutrophil/lymphocyte ratio (p < 0.001), C-reactive protein (p < 0.001) and procalcitonin (p < 0.001). Patients in the MIS-C group were less likely to receive invasive ventilation (13.3% vs 41.4%, p = 0.005) but were more often treated with vasoactive drugs (66.7% vs 24.1%, p < 0.001), corticosteroids (80% vs 44.8%, p = 0.003) and immunoglobulins (51.1% vs 6.9%, p < 0.001). Most patients were discharged from PICU by the end of data collection with a median length of stay of 5 days (IQR 2.5-8 days) in the MIS-C group. Three patients died, none of them belonged to the MIS-C group. Conclusions MIS-C seems to be the most frequent presentation among critically ill children with SARS-CoV-2 infection. MIS-C patients are older and usually healthy. They show a higher prevalence of gastrointestinal symptoms and shock and are more likely to receive vasoactive drugs and immunomodulators and less likely to need mechanical ventilation than non-MIS-C patients.
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