Efficacy and safety of convalescent plasma therapy in patients with moderate-to-severe COVID-19: A non-randomized comparative study with historical control in a referral hospital in Indonesia

被引:3
|
作者
Kurnianda, Johan [1 ]
Hardianti, Mardiah S. [1 ]
Triyono, Teguh [2 ]
Thobari, Jarir A. [3 ]
Trisnawati, Ika [4 ]
Wisudarti, Calcarina F. R. [5 ]
Sukorini, Usi [2 ]
Anshori, Fuad [2 ]
Setiawan, Syahru A. [1 ]
Ucche, Meita [1 ]
Farahnaz, Abrid [1 ]
Suryani, Yana [1 ]
机构
[1] Univ Gadjah Mada, Fac Med Publ Hlth & Nursing, Dept Internal Med, Div Hematol & Med Oncol,Dr Sardjito Hosp, Jl Kesehatan 1, Yogyakarta 55281, Indonesia
[2] Univ Gadjah Mada, Fac Med Publ Hlth & Nursing, Dept Clin Pathol & Lab Med, Dr Sardjito Hosp, Yogyakarta 55281, Indonesia
[3] Univ Gadjah Mada, Fac Med Publ Hlth & Nursing, Dept Pharmacol & Therapy, Yogyakarta 55281, Indonesia
[4] Univ Gadjah Mada, Fac Med Publ Hlth & Nursing, Dept Internal Med, Div Pulmonol,Dr Sardjito Hosp, Yogyakarta 55281, Indonesia
[5] Univ Gadjah Mada, Fac Med Publ Hlth & Nursing, Dept Anesthesiol & Intens Care, Dr Sardjito Hosp, Yogyakarta 55281, Indonesia
关键词
Convalescent plasma; COVID-19; Moderate; Severe; INFECTION; MORTALITY;
D O I
10.1016/j.jiph.2021.10.028
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: Studies to confirm the efficacy and safety of convalescent plasma (CP) as an adjunctive treatment for COVID-19 are still required especially for the countries where standard treatments are unevenly distributed.Methods: A non-randomized comparative study was done from June - September 2020 in Dr. Sardjito Hospital, Yogyakarta, Indonesia. Plasma with anti-SARS-CoV-2 specific IgG titer of > 1:320 were used. Primary end points were clinical and laboratory parameters outcome including BGA, chest X-ray, CT value, CRP, procalcitonin, IL-6, D-Dimer and ALC examined on day 1, 2 and 7 post-transfusion.Results: The experimental arm of this study consisted of 15 patients who received CP: 3 (20%) with moderate COVID-19 and 12 (80%) with severe COVID-19. There were 15 historical controls in this study. Ten recipients survived and 5 deceased (survival rate was 66.7%). There were higher rate of pneumonia resolution (OR 1.54, CI95% 0.33-7.23), ARDS resolution (OR 1.20, CI95% 0.25-5.84) and shorter median length of stay (20 vs 22 days, p = 0.41) among recipients compared to controls. Lower mortality rate was observed in recipients vs controls (33.3% vs 46.7% (OR 0.75, CI95% 0.17-3.33)). Median death onset was longer in recipient vs control (7(th) vs 1(st) day, p = 0.13). Survival analysis showed protective effect of CP (HR 0.69, CI 95% 0.21-2.27, p = 0.545). Higher CT value improvement (p = 0.51) and negative conversion rate (OR1.20, CI95% 0.25-5.84) were observed in recipients compared to controls. Sub-analysis showed more number of comorbidities, higher procalcitonin and higher D-Dimer among CP recipients who did not survive (p = 0.02 and p = 0.02 respectively). Lower CRP and procalcitonin, and higher ALC were found in survivors compared to non-survivors (p = 0.0437; p = 0.0049; and p = 0.0002 respectively). Conclusion: This study showed promising results for CP marked by improvements in clinical outcome, as well as significant reduction of inflammatory markers among recipients.(c) 2021 The Author(s). Published by Elsevier Ltd on behalf of King Saud Bin Abdulaziz University for Health Sciences. This is an open access article under the CC BY license (http://creativecommons.org/ licenses/by/4.0/).
引用
收藏
页码:100 / 108
页数:9
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