key: cord-0914162-lbt965o7
authors: Kamel, Hany
title: We stand ready … Blood collection organizations and the COVID‐19 pandemic
date: 2021-05-09
journal: Transfusion
DOI: 10.1111/trf.16400
sha: ba0bcaecb25f0757601055bd6887601ec8e03816
doc_id: 914162
cord_uid: lbt965o7

See article on page 1471–1478, in this issue

With every emergent pathogen, an immediate concern to blood collection organizations (BCOs) is to determine if the new agent represents a risk to the safety of the blood supply. If suspected, prompt efforts are introduced to prevent the spread of infection to blood transfusion recipients. This is done initially by setting donor eligibility criteria, modifying donor educational materials, introducing new questions to the medical history questionnaire, encouraging donors to report post-donation illness, and finally by implementing blood donor screening tests if warranted along with lookback procedures. When severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) first emerged in late 2019/early 2020, it was believed based on our experiences with severe acute respiratory syndrome (SARS) and Middle East respiratory syndrome (MERS) that there was no risk to the blood supply and that SARS-CoV-2 would only minimally impact BCOs and transfusion services. We soon realized such wishful thinking was far from the truth. Although coronavirus disease 2019 (COVID-19) presents primarily as a lower respiratory tract infection transmitted via air droplets, increasing evidence points to multiorgan involvement in infected patients. This systemic involvement is postulated to be mainly related to SARS-CoV-2 binding to angiotensin-converting enzyme 2 (ACE2) receptors located on several different human cells. 1 Consequently, hematology services 2,3 had to manage patients with COVID-19-associated immune thrombocytopenia, 4 hyperviscosity, 5 and coagulopathy. [6] [7] [8] With the arrival of the first COVID-19 case into Washington State on January 21, 2020, Pagano, et al. were first to give a glimpse into what became the norm at hospitals, transfusion services, and blood centersthat is, preparing to adapt to changes in the blood supply and transfusion support during the pandemic. 9 One aim of this piece is to demonstrate the resilience and readiness of BCOs facing the COVID-19 pandemic.

The history of serum therapy or convalescent plasma therapy dates to the 1890s, when the German physician Emil von Behring intentionally exposed horses to the toxic bacteria that causes diphtheria. 10 After the animals had recovered, Behring used their antibody-rich blood to successfully immunize humans against the deadly disease. For this work, Behring won the first Nobel Prize in Physiology or Medicine in 1901. 11 Afterwards, in the late 19th and early 20th century, convalescent serum or plasma was used to treat measles, Spanish influenza, and many other diseases. Interest in this therapy waned in the antibiotic era but remained on stand-by for resurrection when an infectious agent emerged for which there was no match in our therapeutic armamentarium, e.g., influenza, SARS, MERS, etc. 12 COVID-19 convalescent plasma (CCP) took center stage worldwide in the current pandemic due to our lack of directly effective antiviral medications or other therapies.

The SARS-CoV-2 pandemic forced significant changes to BCOs. Every mitigation measure to curb the spread of infection directly impacted BCO operations. Stay-at-home orders and school and business closures immediately constrained the size of the donor pool. Blood collection, processing, and distribution activities were modified to accommodate enhanced personal protective equipment, social distancing, sanitizing collection areas, and screening individuals for elevated temperature prior to entry to facilities. While aided by the substantial elimination of elective surgeries, the fewer donations collected were barely adequate to meet the decreasing demand.

Then came the need to collect convalescent plasma from patients who had recently recovered from COVID-19 infections. Faced with a rapidly increasing demand, BCOs had limited time to establish a complex process: from recruiting patients/donors, to screening donors for eligibility, to collecting and processing plasma, to distributing CCP to transfusion services. All activities had to follow strict clinical trial criteria and regulatory requirements. This required developing new processes with all that entails, from creating computer controls, writing procedures, and training staff to establishing screening tests for SARS-CoV-2 antibodies to donor notifications. In addition, BCOs had to keep up with the frequent regulatory updates made before and after the emergency use authorization issued on August 23, 2020; some required almost immediate implementation (Figure 1) .

In this issue of TRANSFUSION, Lasky et al., describe the American Red Cross's experience with establishing a CCP donor/donation program in response to information favoring the efficacy of this therapeutic modality in managing hospitalized patients with COVID-19 infection. 13 The analysis covers an approximately 14-week period. The study describes CCP donor characteristics; the majority (56.2%) were first-time donors in contrast to standard plasma/platelet apheresis (SA) or whole blood (WB) donor populations. The proportion of female donors was 12 percentage points higher than in the SA donor group. Older (>65 years) and younger (16-19 years) individuals were comparatively underrepresented among CCP donors. Presenting CCP donations had deferral rates and Quantity Not Sufficient rates of 10.2 and 6.4%, respectively, compared to 8.2 and 1.1% for SA donations. HLA antibody reactivity comprised the most frequent cause of product loss for CCP donations versus SA donations (9.6 vs. 1.3%). Acute adverse events also occurred at a higher rate among both first-time and repeat CCP donations compared to SA. The overall pattern of reaction rates between both first-time and repeat CCP and SA donors were similar, with small hematomas and prefaint reactions being the most common reactions. Two points of interest may warrant additional exploration. First, the CCP donor racial profile was similar to that of SA and WB donors but differed from that of COVID-19 patient populations. The second is the higher rate of reactions observed in both first-time and repeat CCP donors compared to first-time and repeat SA donors. A small previous study showed a higher frequency of mild adverse reactions in CCP donors with a perdonation volume of >8 ml/kg body weight or ≥600 ml, <100 mm Hg in pre-donation systolic blood pressure, or less than 28 days from the onset of COVID-19 symptoms. There was no correlation with donation history, weight, sex, ABO blood type, pre-donation diastolic blood pressure, pulse, or hemoglobin level. 14 This manuscript is a welcome addition to the many multifaceted manuscripts related to COVID-19 already published in TRANSFUSION over the past year: from how to establish a program 15, 16 to donor studies, [17] [18] [19] [20] to transfusion optimization, [21] [22] [23] to CCP. 24, 25 The collection and distribution of CCP ramped up steadily, peaking in December 2020 and January 2021, before starting to decline in February 2021 (Figure 2) . Multiple studies and meta-analyses of CCP have been performed that overall have failed to show significant benefits in patient outcomes. 26, 27 If anything, the observation made by von Behring more than 130 years ago (see quote) remains valid. The earlier the administration of CCP, the betterin one randomized trial, early administration of high-titer CCP (within 72 h after the onset of mild Covid-19 symptoms) to mildly ill infected older adults reduced the progression of Covid-19. 28, 29 At present, the Infectious Diseases Society of America Guidelines on the Treatment and Management of Patients with COVID-19 recommendations state, "Among patients who have been admitted to the hospital with COVID-19, the IDSA guideline panel recommends COVID-19 convalescent plasma only in the context of a clinical trial". 30 Are there lessons learned? 31 Recent convalescent plasma trials to treat Ebola, SARS, and MERS were criticized as being small, non-randomized trials. A search for Covid-19 convalescent plasma on clinicalTrials.gov returned 146 (49 in the United States) registered trials at various stages of completion. Will these trials provide the answer or will they create new questions?

Before closing, it would be remiss not to mention the significant role BCOs across the globe are playing to further our understanding of the epidemiology and the immunologic response to SARS-CoV-2 by introducing various serological testing for SARS-CoV-2 antibodies. [32] [33] [34] What is next? Will the pandemic regress with the development of vaccines and the population reaching herd immunity? Will a new wave of the pandemic emerge with the spread of the ever-increasing variants along with the relaxation of restrictions by various states and localities? Will there be a resurgence of CCP with neutralizing antibodies against variants resistant to current CCP inventory? 35 Will BCOs successfully retain most of the first-time CCP donors as blood donors supporting the community blood supply postpandemic? Regardless, there are reasons to assure the public that BCOs will be standing ready to meet the challenges of the next crisis.

The author thanks Dr. Ralph Vassallo for reviewing the editorial and contributing Figure 1 (The CCP Regulatory Timeline). 

Organ-specific manifestations of COVID-19 infection

A review on how to do hematology consults during COVID-19 pandemic

The hematology laboratory's response to the COVID-19 pandemic: a scoping review

Outcomes and management of immune thrombocytopenia secondary to COVID-19: Cleveland clinic experience

Therapeutic plasma exchange for COVID-19-associated hyperviscosity

Coagulopathy in COVID-19

A proposal for staging COVID-19 coagulopathy

ISTH interim guidance on recognition and management of coagulopathy in COVID-19

Prepare to adapt: blood supply and transfusion support during the first 2 weeks of the 2019 novel coronavirus (COVID-19) pandemic affecting Washington State

The peculiar 100-plus-year history of convalescent plasma

Convalescent plasma: therapeutic hope or hopeless strategy in the SARS-CoV-2 pandemic

COVID-19 convalescent plasma donor characteristics, product disposition, and comparison with standard apheresis donors

Donor tolerability of convalescent plasma donation

Rapid establishment of a COVID-19 convalescent plasma program in a regional health care delivery network

How did we rapidly implement a convalescent plasma program?

Pandemic blood donor demographics -do changes impact blood safety? Transfusion. 2021;1-5

The effect of COVID-19 on blood donation habits

A retrospective study assessing the characteristics of COVID-19 convalescent plasma donors and donations

Screening donors for COVID-19 convalescent plasma

Blood component utilization in COVID-19 patients in New York City: transfusions do not follow the curve

Transfusion support in COVID-19 patients: impact on hospital blood component supply during the outbreak

Blood transfusion utilization in hospitalized COVID-19 patients

Convalescent plasma to treat coronavirus disease 2019 (COVID-19): considerations for clinical trial design

Characterization of 100 sequential SARS-CoV-2 convalescent plasma donations

Convalescent plasma in 2 patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, openlabel, platform trial. medRxiv

Association of convalescent plasma treatment with clinical outcomes in patients with COVID-19 a systematic review and meta-analysis

Earlier the better: convalescent plasma

Early high-titer plasma therapy to prevent severe Covid-19 in older adults

Infectious Diseases Society of America Guidelines on the Treatment and Management of Patients with COVID-19. Please check website for most updated version of these guidelines. www.idsociety.org/COVID19guidelines

Emerging lessons from COVID-19 for the US clinical research enterprise

Estimation of SARS-CoV-2 infection fatality rate by realtime antibody screening of blood donors

Serosurveillance for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) incidence using global blood donor populations

Seroprevalence of antibodies to SARS-CoV-2 in US blood donors

Multiple SARS-CoV-2 variants escape neutralization by vaccine-induced humoral immunity