High-dose corticosteroid pulse therapy increases the survival rate in COVID-19 patients at risk of hyper-inflammatory response

被引:46
作者
Lopez Zuniga, Miguel Angel [1 ,2 ]
Moreno-Moral, Aida
Ocana-Granados, Ana [3 ]
Padilla-Moreno, Francisco Andres [4 ]
Castillo-Fernandez, Alba Maria [4 ]
Guillamon-Fernandez, Dionisio [5 ]
Ramirez-Sanchez, Carolina [6 ]
Sanchez-Palop, Maria [7 ]
Martinez-Colmenero, Justo [2 ,4 ]
Pimentel-Villar, Maria Amparo [8 ]
Blazquez-Rosello, Sara [9 ]
Moreno-Sanchez, Jose Juan [4 ]
Lopez-Vilchez, Maria [4 ]
Prior-Sanchez, Inmaculada [10 ]
Jodar-Moreno, Rosario [11 ]
Lopez Ruz, Miguel Angel [1 ]
机构
[1] Hosp Univ Virgen Nieves, Infect Dis Unit, Granada, Spain
[2] Univ Jaen, Grp Invest CTS 990 GEAPACECP, Jaen, Spain
[3] Complejo Hosp Jaen, Allergol Serv, Jaen, Spain
[4] Complejo Hosp Jaen, Internal Med Serv, Jaen, Spain
[5] Hosp Univ San Cecilio, Otorhinolaryngol Serv, Granada, Spain
[6] Hosp Univ Virgen Victoria, Pathol Anat Serv, Malaga, Spain
[7] Pneumol Serv Complejo Hosp Jaen, Jaen, Spain
[8] Complejo Hosp Jaen, Haematol Serv, Jaen, Spain
[9] Complejo Hosp Jaen, Nephrol Serv, Jaen, Spain
[10] Complejo Hosp Jaen, Endocrinol Serv, Jaen, Spain
[11] Complejo Hosp Jaen, Otorhinolaryngol Serv, Jaen, Spain
关键词
D O I
10.1371/journal.pone.0243964
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Objective Test whether high dose corticosteroid pulse therapy (HDCPT) with either methylprednisolone or dexamethasone is associated with increased survival in COVID-19 patients at risk of hyper-inflammatory response. Provide some initial diagnostic criteria using laboratory markers to stratify these patients. Methods This is a prospective observational study, 318 met the inclusion criteria. 64 patients (20.1%) were treated with HDCPT by using at least 1.5mg/kg/24h of methylprednisolone or dexamethasone equivalent. A multivariate Cox regression (controlling for co-morbidities and other therapies) was carried out to determine whether HDCPT (among other interventions) was associated with decreased mortality. We also carried out a 30-day time course analysis of laboratory markers between survivors and non-survivors, to identify potential markers for patient stratification. Results HDCPT showed a statistically significant decrease in mortality (HR = 0.087 [95% CI 0.021-0.36]; P < 0.001). 30-day time course analysis of laboratory marker tests showed marked differences in pro-inflammatory markers between survivors and non-survivors. As diagnostic criteria to define the patients at risk of developing a COVID-19 hyper-inflammatory response, we propose the following parameters (IL-6 > = 40 pg/ml, and/or two of the following: C-reactive protein > = 100 mg/L, D-dimer > = 1000 ng/ml, ferritin > = 500 ng/ml and lactate dehydrogenase > = 300 U/L). Conclusions HDCPT can be an effective intervention to increase COVID-19 survival rates in patients at risk of developing a COVID-19 hyper-inflammatory response, laboratory marker tests can be used to stratify these patients who should be given HDCPT. This study is not a randomized clinical trial (RCT). Future RCTs should be carried out to confirm the efficacy of HDCPT to increase the survival rates of COVID-19.
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