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A retrospective study assessing the characteristics of COVID-19 convalescent plasma donors and donations.
Del Fante, Claudia; Franchini, Massimo; Baldanti, Fausto; Percivalle, Elena; Glingani, Claudia; Marano, Giuseppe; Mengoli, Carlo; Mortellaro, Cristina; Viarengo, Gianluca; Perotti, Cesare; Liumbruno, Giancarlo Maria.
Afiliação
  • Del Fante C; Immunohematology and Transfusion Service, IRCCS Policlinico San Matteo, Pavia, Italy.
  • Franchini M; Department of Hematology and Transfusion Medicine, Carlo Poma Hospital, Mantova, Italy.
  • Baldanti F; Italian National Blood Centre, Rome, Italy.
  • Percivalle E; Molecular Virology Unit, Microbiology and Virology Department, IRCCS Policlinico San Matteo, Pavia, Italy.
  • Glingani C; Molecular Virology Unit, Microbiology and Virology Department, IRCCS Policlinico San Matteo, Pavia, Italy.
  • Marano G; Department of Hematology and Transfusion Medicine, Carlo Poma Hospital, Mantova, Italy.
  • Mengoli C; Italian National Blood Centre, Rome, Italy.
  • Mortellaro C; Italian National Blood Centre, Rome, Italy.
  • Viarengo G; Immunohematology and Transfusion Service, IRCCS Policlinico San Matteo, Pavia, Italy.
  • Perotti C; Immunohematology and Transfusion Service, IRCCS Policlinico San Matteo, Pavia, Italy.
  • Liumbruno GM; Immunohematology and Transfusion Service, IRCCS Policlinico San Matteo, Pavia, Italy.
Transfusion ; 61(3): 830-838, 2021 03.
Article em En | MEDLINE | ID: mdl-33231325
ABSTRACT

BACKGROUND:

Although many trials are currently investigating the safety and efficacy of convalescent plasma (CP) in critically ill COVID-19 patients, there is a paucity of ongoing and published studies evaluating the CP donors' side. This retrospective study reports the first Italian experience on CP donors' selection and donations.

METHODS:

Patients aged 18-68 years who had recovered from COVID-19 at least 2 weeks previously were recruited between March 18 and June 30, 2020 in a study protocol at the Italian hospitals of Pavia and Mantova.

RESULTS:

During the study period, 494 of 512 donors recruited were judged eligible and underwent 504 plasmapheresis procedures. Eighty-five percent (437/512) of the CP donors were males. The average time between symptom recovery and CP donation was 36.6 (±20.0) days. Four hundred and eighty-eight plasmapheresis procedures (96.8%) were concluded and each unit was divided into two subunits (total 976) with an average volume of 316.2 (±22.7) mL. Ninety-three percent (460/494) of CP donors at the time of plasma donation had a neutralizing IgG titer ≥180. Plasmapheresis-related adverse reactions occurred in 2.6% (13/504) of cases; all the reactions were mild and none required therapeutic intervention. Donors' age and COVID-19 severity were positively associated with greater antibody responses.

CONCLUSION:

This study demonstrates the feasibility and safety of a pilot CP program conducted in Italy. The identification of factors (ie, age and severity of COVID-19) positively associated with higher neutralizing antibody titers at the time of donation may help to optimize the selection of CP donors.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doadores de Sangue / Seleção do Doador / COVID-19 Tipo de estudo: Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doadores de Sangue / Seleção do Doador / COVID-19 Tipo de estudo: Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Ano de publicação: 2021 Tipo de documento: Article