Klein Tovah, Elue Rita, Ikegami Sachie, Mikkelson Christopher, Wright Gregory, Mallek Jessica, Kang Jason, Sullivan David J, Gniadek Thomas J
NorthShore University HealthSystem, Evanston, IL, USA.
Department of Pathology and Laboratory Medicine, NorthShore University HealthSystem, Evanston, IL, USA.
Acad Pathol. 2021 Feb 10;8:2374289520987236. doi: 10.1177/2374289520987236. eCollection 2021 Jan-Dec.
The effort to collect convalescent plasma from individuals who recovered from COVID-19 began in earnest during the spring of 2020. Either whole blood or apheresis donations were obtained, the latter yielding higher numbers of units per donor per collection and more frequent collections. The NorthShore University HealthSystem blood donor center purchased 2 Alyx (Fresenius Kabi) apheresis plasma collection devices and quickly implemented them in order to collect COVID-19 convalescent plasma. Apheresis-experienced and inexperienced phlebotomists operated the instruments. Donors were collected >14 days from symptom resolution and all donors were negative by SARS-CoV-2 nasopharyngeal swab. Both internal metrics of performance as well as a post donation survey were used to evaluate the feasibility implementing this collection program. During the first 100 days of the collection program, 650 plasma units were collected. In particular, during the first week of the program, 38 units were collected and distributed to hospitals under the emergency investigational new drug and expanded access program. Fifty-one donors (15%) were deferred due to vital signs out of range or donor screening questions. Thirty-one donors (10%) were deferred due to positive nasopharyngeal swab. Lower than target yield occurred in 16.6% of collections due to donor reactions or flow errors. Donors rated the overall program lower, but not the staff, when they reported symptoms related to collection. In conclusion, a hospital-based apheresis convalescent plasma collection program can be rapidly implemented. Donor reaction rates and vein infiltration rates should be carefully monitored for each phlebotomist.
从新冠康复者中采集恢复期血浆的工作于2020年春季正式开始。采集的是全血或单采血浆,后者每次采集每个献血者可获得更多单位的血浆,且采集频率更高。北岸大学医疗系统血液中心购买了2台Alyx(费森尤斯卡比公司)单采血浆采集设备,并迅速投入使用,以采集新冠恢复期血浆。有单采经验和无单采经验的采血技师操作这些仪器。在症状缓解14天以上采集献血者血液,且所有献血者的新冠病毒鼻咽拭子检测均为阴性。通过内部绩效指标以及献血后调查来评估实施该采集项目的可行性。在采集项目的前100天,共采集了650个血浆单位。特别是在项目的第一周,采集了38个单位的血浆,并根据紧急研究性新药和扩大使用项目分发给了医院。51名献血者(15%)因生命体征超出范围或献血者筛查问题而被推迟献血。31名献血者(10%)因鼻咽拭子检测呈阳性而被推迟献血。由于献血者反应或流程错误,16.6%的采集出现了低于目标产量的情况。当献血者报告与采集相关的症状时,他们对整个项目的评价较低,但对工作人员的评价不低。总之,基于医院的单采恢复期血浆采集项目可以迅速实施。应对每位采血技师的献血者反应率和静脉渗透率进行仔细监测。