Publications by authors named "COHN C"

Background: Low titer group O whole blood (LTOWB) is commonly used for severe bleeding in trauma patients. LTOWB may also benefit young children requiring cardiac surgery with cardiopulmonary bypass (CPB) at risk of severe bleeding.

Study Design And Methods: In this retrospective study, children <2 years old who underwent cardiac surgery with CPB were included.

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The optimum number of units of blood and the associated number of blood donors required to meet a given population's needs remain undetermined globally. Typically, a whole blood donation rate of ten donations per 1000 population, at a minimum, is necessary to meet a country's blood needs. This rate is attributed to a WHO recommendation that 1% of a given country's population should donate blood to ensure a blood supply that is sufficient to meet clinical needs.

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Background: Drugs such as daratumumab (Darzalex, anti-CD38) and Hu5F9-G4 (magrolimab, anti-CD47) may interfere with red blood cell compatibility testing as CD38 and CD47 are expressed on red blood cells.

Study Design And Methods: A survey of AABB member transfusion services was undertaken to understand their experiences of managing patients taking therapeutic monoclonal antibodies that are known to interfere with blood grouping and compatibility testing.

Results: The survey was distributed to the contact person at US-based AABB member transfusion services.

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Patients treated with antineoplastic therapy often develop thrombocytopenia requiring platelet transfusion, which has potential to exacerbate pulmonary injury. This study tested the hypothesis that amotosalen-UVA pathogen-reduced platelet components (PRPCs) do not potentiate pulmonary dysfunction compared with conventional platelet components (CPCs). A prospective, multicenter, open-label, sequential cohort study evaluated the incidence of treatment-emergent assisted mechanical ventilation initiated for pulmonary dysfunction (TEAMV-PD).

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Background: The Mirasol® Pathogen Reduction Technology System was developed to reduce transfusion-transmitted diseases in platelet (PLT) products.

Study Design And Methods: MiPLATE trial was a prospective, multicenter, controlled, randomized, non-inferiority (NI) study of the clinical effectiveness of conventional versus Mirasol-treated Apheresis PLTs in participants with hypoproliferative thrombocytopenia. The novel primary endpoint was days of ≥Grade 2 bleeding with an NI margin of 1.

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Article Synopsis
  • Red blood cell transfusions can be beneficial but come with potential risks, necessitating guidelines for their use in both adults and children.
  • Studies involved numerous randomized controlled trials which found that restrictive transfusion strategies (transfusing at lower hemoglobin thresholds) generally do not harm patient outcomes for most populations.
  • Recommendations include using restrictive strategies for stable adult patients, advising transfusions at hemoglobin levels below 7 g/dL, with some exceptions based on specific patient conditions like cardiac or orthopedic surgeries.
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Article Synopsis
  • The Association for the Advancement of Blood and Biotherapies' Clinical Transfusion Medicine Committee (CTMC) annually summarizes significant advances in transfusion medicine, publishing their findings in the journal *Transfusion*.
  • For 2022, CTMC selected and summarized key research publications in various transfusion medicine topics, such as blood component therapy, infectious diseases, and patient blood management, among others.
  • The compiled report serves as an educational resource, although it is not a systematic review and may not include all relevant publications.
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Coronavirus disease 2019 (COVID-19) convalescent plasma (CCP) is a safe and effective treatment for COVID-19 in immunocompromised (IC) patients. IC patients have a higher risk of persistent infection, severe disease, and death from COVID-19. Despite the continued clinical use of CCP to treat IC patients, the optimal dose, frequency/schedule, and duration of CCP treatment has yet to be determined, and related best practices guidelines are lacking.

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Article Synopsis
  • - The BLOODSAFE Program was created to address the critical shortage of blood supply in Sub-Saharan Africa, aiming to improve access to safe blood transfusions through collaborative research efforts.
  • - Research teams in Ghana, Kenya, and Malawi are tackling various challenges related to blood donation, including iron deficiency among donors, blood donation workflows, and donor retention strategies in schools.
  • - The initiative fosters collaboration among the teams and a data coordinating center, working together to understand donor motivations and outcomes, ultimately leading to sustainable improvements in blood access and enhancing research capabilities in the region.
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Description: Coronavirus disease 2019 convalescent plasma (CCP) has emerged as a potential treatment of COVID-19. However, meta-analysis data and recommendations are limited. The Association for the Advancement of Blood and Biotherapies (AABB) developed clinical practice guidelines for the appropriate use of CCP.

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Simulation-based training (SBT) programs are commonly employed by organizations to train individuals and teams for effective workplace cognitive and psychomotor skills in a broad range of applications. Distributed cognition has become a popular cognitive framework for the design and evaluation of these SBT environments, with structured methodologies such as used for analysis. However, the analysis and evaluations generated by such distributed cognition frameworks require extensive domain-knowledge and manual coding and interpretation, and the analysis is primarily qualitative.

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Background: Anticoagulation requires urgent reversal in cases of life-threatening bleeding or invasive procedures.

Study Design And Methods: Network meta-analysis for comparing the safety and efficacy of warfarin reversal strategies including plasma and prothrombin complex concentrates (PCCs).

Results: Seven studies including 594 subjects using reversal agents plasma, 3-factor-PCC (Uman Complex and Konyne), and 4-factor-PCC (Beriplex/KCentra, Octaplex, and Cofact) met inclusion criteria.

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Background: Convalescent plasma has been one of the most common treatments for COVID-19, but most clinical trial data to date have not supported its efficacy.

Research Question: Is rigorously selected COVID-19 convalescent plasma with neutralizing anti-SARS-CoV-2 antibodies an efficacious treatment for adults hospitalized with COVID-19?

Study Design And Methods: This was a multicenter, blinded, placebo-controlled randomized clinical trial among adults hospitalized with SARS-CoV-2 infection and acute respiratory symptoms for < 14 days. Enrolled patients were randomly assigned to receive one unit of COVID-19 convalescent plasma (n = 487) or placebo (n = 473).

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Background: Platelet transfusion carries risk of transfusion-transmitted infection (TTI). Pathogen reduction of platelet components (PRPC) is designed to reduce TTI. Pulmonary adverse events (AEs), including transfusion-related acute lung injury and acute respiratory distress syndrome (ARDS) occur with platelet transfusion.

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Article Synopsis
  • The AABB Clinical Transfusion Medicine Committee creates an annual synopsis that highlights significant, clinically relevant studies in transfusion medicine, published since 2018.
  • For the 2020-2021 period, committee members selected original manuscripts based on their relevance and originality, discussing their findings and summarizing each topic in pairs before compiling the final document.
  • The synopsis covers various important topics such as blood products, convalescent plasma, donor testing, and patient blood management, serving as a valuable educational resource for professionals in the field.
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Article Synopsis
  • This study evaluated the safety and tolerability of solvent/detergent-treated (S/D) plasma in children needing therapeutic plasma exchange (TPE).
  • It involved 41 pediatric patients aged 2 to 20 years, who underwent a total of 102 TPE procedures, with most showing excellent safety outcomes.
  • The results indicated that S/D plasma is well tolerated, with only a few mild adverse reactions, supporting its use in pediatric plasma exchange therapy.
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As the coronavirus disease (COVID-19) pandemic led to a global health crisis, there were limited treatment options and no prophylactic therapies for those exposed to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Convalescent plasma is quick to implement, potentially provides benefits, and has a good safety profile. The therapeutic potential of COVID-19 convalescent plasma (CCP) is likely mediated by antibodies through direct viral neutralization and Fc-dependent functions such as a phagocytosis, complement activation, and antibody-dependent cellular cytotoxicity.

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Background: The SARS-CoV-2 pandemic disrupted hospital operations, affected the blood supply, and challenged the health care system to develop new therapeutic options, including convalescent plasma (CCP). The aim of this study is to describe and analyze blood supply fluctuations and the use of convalescent plasma in 2020.

Methods: AABB distributed a weekly and biweekly questionnaire through email to hospital-based members (HBM).

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Article Synopsis
  • - The AABB Clinical Transfusion Medicine Committee (CTMC) creates an annual overview of significant advancements in transfusion medicine, with a manuscript published since 2018.
  • - Committee members review and discuss TM-related research papers from late 2019 to late 2020, selecting topics based on their relevance and originality before drafting synopses.
  • - The final synopsis includes key subjects such as COVID-19's impacts on blood supply, convalescent plasma, adult and pediatric transfusion practices, and advances in cellular therapy, serving as a helpful educational resource.
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