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10.1159/000512063

http://scihub22266oqcxt.onion/10.1159/000512063
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33486496!7900459!33486496
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suck abstract from ncbi

pmid33486496      Respiration 2021 ; 100 (2): 116-126
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  • Early Use of Corticosteroid May Prolong SARS-CoV-2 Shedding in Non-Intensive Care Unit Patients with COVID-19 Pneumonia: A Multicenter, Single-Blind, Randomized Control Trial #MMPMID33486496
  • Tang X; Feng YM; Ni JX; Zhang JY; Liu LM; Hu K; Wu XZ; Zhang JX; Chen JW; Zhang JC; Su J; Li YL; Zhao Y; Xie J; Ding Z; He XL; Wang W; Jin RH; Shi HZ; Sun B
  • Respiration 2021[]; 100 (2): 116-126 PMID33486496show ga
  • BACKGROUND: There is still no clinical evidence available to support or to oppose corticosteroid treatment for coronavirus disease 2019 (COVID-19) pneumonia. OBJECTIVE: To investigate the efficacy and safety of corticosteroid given to the hospitalized patients with COVID-19 pneumonia. METHODS: This was a prospective, multicenter, single-blind, randomized control trial. Adult patients with COVID-19 pneumonia who were admitted to the general ward were randomly assigned to either receive methylprednisolone or not for 7 days. The primary end point was the incidence of clinical deterioration 14 days after randomization. RESULTS: We terminated this trial early because the number of patients with COVID-19 pneumonia in all the centers decreased in late March. Finally, a total of 86 COVID-19 patients underwent randomization. There was no difference of the incidence of clinical deterioration between the methylprednisolone group and control group (4.8 vs. 4.8%, p = 1.000). The duration of throat viral RNA detectability in the methylprednisolone group was 11 days (interquartile range, 6-16 days), which was significantly longer than that in the control group (8 days [2-12 days], p = 0.030). There were no significant differences between the 2 groups in other secondary outcomes. Mass cytometry discovered CD3+ T cells, CD8+ T cells, and NK cells in the methylprednisolone group which were significantly lower than those in the control group after randomization (p < 0.05). CONCLUSIONS: From this prematurely closed trial, we found that the short-term early use of corticosteroid could suppress the immune cells, which may prolong severe acute respiratory syndrome coronavirus 2 shedding in patients with COVID-19 pneumonia. TRIAL REGISTRATION: ClinicalTrials.gov, NCT04273321.
  • |*COVID-19 Drug Treatment[MESH]
  • |*Hospitalization[MESH]
  • |*Virus Shedding[MESH]
  • |Adult[MESH]
  • |Aged[MESH]
  • |Anti-Bacterial Agents/therapeutic use[MESH]
  • |Antiviral Agents/therapeutic use[MESH]
  • |CD3 Complex[MESH]
  • |CD8-Positive T-Lymphocytes[MESH]
  • |COVID-19 Nucleic Acid Testing[MESH]
  • |COVID-19/blood/therapy/transmission[MESH]
  • |Disease Progression[MESH]
  • |Early Medical Intervention[MESH]
  • |Extracorporeal Membrane Oxygenation[MESH]
  • |Female[MESH]
  • |Glucocorticoids/*therapeutic use[MESH]
  • |Humans[MESH]
  • |Killer Cells, Natural[MESH]
  • |Lymphocyte Count[MESH]
  • |Male[MESH]
  • |Methylprednisolone/*therapeutic use[MESH]
  • |Middle Aged[MESH]
  • |Oxygen Inhalation Therapy[MESH]
  • |Patients' Rooms[MESH]
  • |Pharynx/*chemistry/virology[MESH]
  • |Proportional Hazards Models[MESH]
  • |RNA, Viral/*isolation & purification[MESH]
  • |Respiration, Artificial[MESH]
  • |SARS-CoV-2[MESH]
  • |Single-Blind Method[MESH]
  • |T-Lymphocyte Subsets[MESH]
  • |T-Lymphocytes[MESH]
  • |Time Factors[MESH]


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