苏里南icu收治的COVID-19患者经重力过滤获得恢复期血浆治疗后死亡率降低

Rosita Bihariesingh, Rakesh Bansie, Janeri Froberg, N. Ramdhani, Rishi Mangroo, Debra Bustamente, Ernesto Diaz, I. Thakoer, Stephen Vreden, Zaheeb Choudhry, Wouter Jansen Klomp, Dimitri Diavatopoulos, Arno Nierich
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A pre-planned interim analysis is reported in 78 PCR-confirmed COVID-19 patients admitted to the ICU with severe or lifethreatening symptoms. CP in combination with standard treatment (n = 28) was compared to standard treatment alone (control) (n = 50), stratified by disease severity. The primary endpoint was 28-day ICU mortality. Secondary (exploratory) endpoints were changes two days after treatment initiation in pulmonary oxygen exchange capacity (PF ratio) and chest xray (CXR) score. Findings The median age of patients was 52 years with 43 [55.1%] being male. Twenty-eight day mortality occurred in 18% (5/28) of the CP group vs 36% (18/50) of the control group. Survival probability was significantly higher in the CP group compared to the control group with standard care (P=0.027). When stratifying into disease severity, the survival probability was the lowest for the control group with life-threatening disease (P=0.0051). CP treatment of severe COVID-19 resulted in a higher probability of survival, with a hazard ratio (HR) of 0.22 (95% CI, 0.074-0.067), correcting for age, the presence of diabetes and COVID-19 severity. Age significantly increased the mortality risk (HR, 1.08 [95%CI, 1.022-1.14]; P =0.006). In the severe group, CP resulted in an improved CXR score (P =0.0013) and increase in PF ratio (P = 0.011) as compared to standard therapy. The gravity-based plasmapheresis method used for CP production was well-tolerated and no adverse events were observed in the donors. Interpretation Among patients with severe or life-threatening COVID-19, CP therapy in combination with standard treatment resulted in 78% reduction of 28-day ICU mortality (HR = 0.22) compared to standard treatment alone. Both CXR-score and PF ratio changes represent indicators of treatment effect of CP after two days and can easily be implemented in low-resource settings. 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引用次数: 4

摘要

背景虽然恢复期血浆治疗是COVID-19患者的一种潜在治疗选择,但缺乏来自低资源环境的研究数据。评价苏里南重症监护病房(ICU)新冠肺炎患者CP治疗的疗效和安全性。采用一种新的基于重力的过滤方法获得CP。该设计是一项开放标签、多中心、非随机前瞻性临床试验,于2020年6月至2020年12月在苏里南的两家医院进行。据报道,对78名经pcr确诊的COVID-19患者进行了预先计划的中期分析,这些患者有严重或危及生命的症状。将CP联合标准治疗(n = 28)与单独标准治疗(对照)(n = 50)进行比较,按疾病严重程度分层。主要终点是28天ICU死亡率。次要(探索性)终点是治疗开始后2天肺氧交换容量(PF比率)和胸部x线片(CXR)评分的变化。发现患者中位年龄52岁,男性43例(55.1%)。CP组28天死亡率为18%(5/28),对照组为36%(18/50)。与标准护理对照组相比,CP组患者的生存概率显著提高(P=0.027)。按疾病严重程度分层时,危重疾病对照组的生存率最低(P=0.0051)。重症COVID-19的CP治疗导致更高的生存概率,危险比(HR)为0.22 (95% CI, 0.074-0.067),校正了年龄、糖尿病的存在和COVID-19严重程度。年龄显著增加死亡风险(HR, 1.08 [95%CI, 1.022-1.14];P = 0.006)。重症组与标准治疗组相比,CP改善了CXR评分(P =0.0013),增加了PF比率(P = 0.011)。重力血浆置换法制备CP耐受性良好,供体无不良反应。在重症或危及生命的COVID-19患者中,与单独标准治疗相比,CP治疗联合标准治疗可使28天ICU死亡率降低78% (HR = 0.22)。两天后,cxr评分和PF比率的变化都是衡量CP治疗效果的指标,在资源匮乏的环境下很容易实现。这种新型的CP生产方法是有效的,为中低收入国家在当地生产CP提供了一种切实可行的解决方案。虽然解释受到试验的非随机设计的限制,但这些结果为在低收入国家更广泛地实施CP治疗提供了一条潜在的途径。
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Mortality reduction in ICU-admitted COVID-19 patients in Suriname after treatment with convalescent plasma acquired via gravity filtration
Background Although convalescent plasma (CP) treatment is a potential therapeutic option for patients with COVID-19, there is a paucity of data from studies in low-resource settings. The efficacy and safety of CP therapy in intensive care unit (ICU) patients with COVID-19 in Suriname was evaluated. A novel gravity-based filtration method was used to obtain CP. The design was an open-label, multi-centre, non-randomized prospective clinical trial performed in two hospitals in Suriname, from June 2020, to December 2020. A pre-planned interim analysis is reported in 78 PCR-confirmed COVID-19 patients admitted to the ICU with severe or lifethreatening symptoms. CP in combination with standard treatment (n = 28) was compared to standard treatment alone (control) (n = 50), stratified by disease severity. The primary endpoint was 28-day ICU mortality. Secondary (exploratory) endpoints were changes two days after treatment initiation in pulmonary oxygen exchange capacity (PF ratio) and chest xray (CXR) score. Findings The median age of patients was 52 years with 43 [55.1%] being male. Twenty-eight day mortality occurred in 18% (5/28) of the CP group vs 36% (18/50) of the control group. Survival probability was significantly higher in the CP group compared to the control group with standard care (P=0.027). When stratifying into disease severity, the survival probability was the lowest for the control group with life-threatening disease (P=0.0051). CP treatment of severe COVID-19 resulted in a higher probability of survival, with a hazard ratio (HR) of 0.22 (95% CI, 0.074-0.067), correcting for age, the presence of diabetes and COVID-19 severity. Age significantly increased the mortality risk (HR, 1.08 [95%CI, 1.022-1.14]; P =0.006). In the severe group, CP resulted in an improved CXR score (P =0.0013) and increase in PF ratio (P = 0.011) as compared to standard therapy. The gravity-based plasmapheresis method used for CP production was well-tolerated and no adverse events were observed in the donors. Interpretation Among patients with severe or life-threatening COVID-19, CP therapy in combination with standard treatment resulted in 78% reduction of 28-day ICU mortality (HR = 0.22) compared to standard treatment alone. Both CXR-score and PF ratio changes represent indicators of treatment effect of CP after two days and can easily be implemented in low-resource settings. The novel CP production method was effective and represents a practical solution for low and middle income countries (LMICs) to produce CP locally. Although interpretation is limited by the non-randomised design of the trial, these results offer a potential route for broader implementation of CP treatment in LMICs.
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