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10.1016/j.intimp.2020.106873

http://scihub22266oqcxt.onion/10.1016/j.intimp.2020.106873
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suck abstract from ncbi


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pmid32795897      Int+Immunopharmacol 2020 ; 88 (ä): 106873
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  • Thymosin alpha1 therapy in critically ill patients with COVID-19: A multicenter retrospective cohort study #MMPMID32795897
  • Wu M; Ji JJ; Zhong L; Shao ZY; Xie QF; Liu ZY; Wang CL; Su L; Feng YW; Liu ZF; Yao YM
  • Int Immunopharmacol 2020[Nov]; 88 (ä): 106873 PMID32795897show ga
  • BACKGROUND: COVID-19 characterized by refractory hypoxemia increases patient mortality because of immunosuppression effects. This study aimed to evaluate the efficacy of immunomodulatory with thymosin alpha1 for critical COVID-19 patients. METHODS: This multicenter retrospective cohort study was performed in 8 government-designated treatment centers for COVID-19 patients in China from Dec. 2019 to Mar. 2020. Thymosin alpha1 was administrated with 1.6 mg qd or q12 h for >5 days. The primary outcomes were the 28-day and 60-day mortality, the secondary outcomes were hospital length of stay and the total duration of the disease. Subgroup analysis was carried out according to clinical classification. RESULTS: Of the 334 enrolled COVID-19 patients, 42 (12.6%) died within 28 days, and 55 (16.5%) died within 60 days of hospitalization. There was a significant difference in the 28-day mortality between the thymosin alpha1 and non-thymosin alpha1-treated groups in adjusted model (P = 0.016), without obvious differences in the 60-day mortality and survival time in the overall cohort (P > 0.05). In the subgroup analysis, it was found that thymosin alpha1 therapy significantly reduced 28-day mortality (Hazards Ratios HR, 0.11, 95% confidence interval CI 0.02-0.63, P=0.013) via improvement of Pa0(2)/FiO(2) (P = 0.036) and prolonged the hospital length of stay (P = 0.024) as well as the total duration of the disease (P=0.001) in the critical type patients, especially those aged over 64 years, with white blood cell >6.8x10(9)/L, neutrophil >5.3x10(9)/L, lymphocyte < 0.73 x 10(9)/L, PaO(2)/FiO(2) < 196, SOFA > 3, and acute physiology and chronic health evaluation (APACHE) II > 7. CONCLUSION: These results suggest that treatment with thymosin alpha1 can markedly decrease 28-day mortality and attenuate acute lung injury in critical type COVID-19 patients.
  • |APACHE[MESH]
  • |Adjuvants, Immunologic/administration & dosage/adverse effects/*therapeutic use[MESH]
  • |Aged[MESH]
  • |Betacoronavirus[MESH]
  • |COVID-19[MESH]
  • |China/epidemiology[MESH]
  • |Cohort Studies[MESH]
  • |Coronavirus Infections/*drug therapy/immunology/mortality[MESH]
  • |Critical Care/*methods[MESH]
  • |Critical Illness[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Mortality/trends[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/*drug therapy/immunology/mortality[MESH]
  • |Proportional Hazards Models[MESH]
  • |Retrospective Studies[MESH]
  • |SARS-CoV-2[MESH]


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