Department of Anesthesiology, Academic Hospital Paramaribo, Paramaribo, Suriname.
Department of Intensive Care, Academic Hospital Paramaribo, Paramaribo, Suriname.
mBio. 2023 Apr 25;14(2):e0337922. doi: 10.1128/mbio.03379-22. Epub 2023 Feb 23.
Convalescent plasma is a promising therapy for coronavirus disease 2019 (COVID-19), but its efficacy in intensive care unit (ICU) patients in low- and middle-income country settings such as Suriname is unknown. Bedside plasma separation using the HemoClear device made convalescent plasma therapy accessible as a treatment option in Suriname. Two hundred patients with severe SARS-CoV-2 infection requiring intensive care were recruited. Fifty eight patients (29%) received COVID-19 convalescent plasma (CCP) treatment in addition to standard of care (SOC). The CCP treatment and SOC groups were matched by age, sex, and disease severity scores. Mortality in the CCP treatment group was significantly lower than that in the SOC group (21% versus 39%; Fisher's exact test = 0.0133). Multivariate analysis using ICU days showed that CCP treatment reduced mortality (hazard ratio [HR], 0.35; 95% confidence interval [CI], 0.18 to 0.66; = 0.001), while complication of acute renal failure (creatinine levels, >110 mol/L; HR, 4.45; 95% CI, 2.54 to 7.80; < 0.0001) was independently associated with death. Decrease in chest X-ray score in the CCP treatment group (median -3 points, interquartile range [IQR] -4 to -1) was significantly greater than that in the SOC group (median -1 point, IQR -3 to 1, Mann-Whitney test = 0.0004). Improvement in the PaO/FiO ratio was also significantly greater in the CCP treatment group (median 83, IQR 8 to 140) than in the SOC group (median 35, IQR -3 to 92, Mann-Whitney = 0.0234). Further research is needed for HemoClear-produced CCP as a therapy for SARS-CoV-2 infection together with adequately powered, randomized controlled trials. This study compares mortality and other endpoints between intensive care unit COVID-19 patients treated with convalescent plasma plus standard of care (CCP), and a control group of patients hospitalized in the same medical ICU facility treated with standard of care alone (SOC) in a low- and middle-income country (LMIC) setting using bedside donor whole blood separation by gravity (HemoClear) to produce the CCP. It demonstrates a significant 65% survival improvement in HemoClear-produced CCP recipients (HR, 0.35; 95% CI, 0.19 to 0.66; = 0.001). Although this is an exploratory study, it clearly shows the benefit of using the HemoClear-produced CCP in ICU patients in the Suriname LMIC setting. Additional studies could further substantiate our findings and their applicability for both LMICs and high-income countries and the use of CCP as a prepared readiness method to combat new viral pandemics.
恢复期血浆是治疗 2019 年冠状病毒病(COVID-19)的一种很有前途的疗法,但在苏里南等中低收入国家的重症监护病房(ICU)患者中的疗效尚不清楚。床边使用 HemoClear 设备进行血浆分离,使恢复期血浆治疗成为苏里南的一种治疗选择。我们招募了 200 名需要重症监护的严重 SARS-CoV-2 感染患者。58 名患者(29%)在接受标准治疗(SOC)的基础上接受了 COVID-19 恢复期血浆(CCP)治疗。CCP 治疗组和 SOC 组在年龄、性别和疾病严重程度评分方面相匹配。CCP 治疗组的死亡率明显低于 SOC 组(21%比 39%;Fisher 确切检验 = 0.0133)。使用 ICU 天数进行的多变量分析表明,CCP 治疗降低了死亡率(危险比[HR],0.35;95%置信区间[CI],0.18 至 0.66; = 0.001),而急性肾衰竭并发症(肌酐水平,>110 μmol/L;HR,4.45;95%CI,2.54 至 7.80; < 0.0001)与死亡独立相关。CCP 治疗组的胸部 X 线评分下降(中位数-3 分,四分位距[IQR]-4 至-1)明显大于 SOC 组(中位数-1 分,IQR-3 至 1,Mann-Whitney 检验 = 0.0004)。CCP 治疗组的 PaO/FiO 比值改善也明显大于 SOC 组(中位数 83,IQR 8 至 140)(中位数 35,IQR-3 至 92,Mann-Whitney = 0.0234)。需要进一步研究使用 HemoClear 生产的 CCP 作为 SARS-CoV-2 感染的治疗方法,并进行适当的、随机对照试验。本研究比较了在中低收入国家(LMIC)环境中,使用床边供体全血重力分离(HemoClear)生产 CCP 的 COVID-19 重症监护病房患者(CCP 治疗组)与接受标准治疗(SOC)的对照组患者之间的死亡率和其他终点。它证明了 HemoClear 生产的 CCP 接受者的生存率显著提高了 65%(HR,0.35;95%CI,0.19 至 0.66; = 0.001)。尽管这是一项探索性研究,但它清楚地表明,在苏里南的中低收入国家环境中,使用 HemoClear 生产的 CCP 对 ICU 患者有益。进一步的研究可以进一步证实我们的发现及其在中低收入国家和高收入国家的适用性,以及使用 CCP 作为对抗新病毒大流行的准备就绪方法。