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Convalescent Plasma as Adjunctive Therapy for Hospitalized Patients with COVID-19: The Co-CLARITY Trial.
Gauiran, Deonne Thaddeus V; Dumagay, Teresita E; Ang, Mark Angelo C; Dungog, Cecile C; Climacosa, Fresthel Monica M; Maganito, Sandy Chiong; Alfonso, Rachelle N; Quero, Anne Kristine H; Lucero, Josephine Anne C; Cortez, Carlo Francisco N; Evasan, Agnes Lorrainne M; King, Ruby Anne Natividad; Heralde, Francisco M; Bonifacio, Lynn B; Castillo, German J; Escasa, Ivy Mae S; Santos, Maria Clariza M; Malundo, Anna Flor G; Mondragon, Alric V; Salamat, Saubel Ezreal A; Veloso, Januario D; Carnate, Jose M; Tagayuna, Pedrito Y; Lim, Jodor A; Alejandria, Marissa M; Mirasol, Ma Angelina L.
Afiliación
  • Gauiran DTV; Division of Hematology, Department of Medicine, Philippine General Hospital, University of the Philippines Manila.
  • Dumagay TE; Division of Hematology, Department of Medicine, Philippine General Hospital, University of the Philippines Manila.
  • Ang MAC; Department of Laboratories, Philippine General Hospital, University of the Philippines Manila.
  • Dungog CC; Department of Laboratories, Philippine General Hospital, University of the Philippines Manila.
  • Climacosa FMM; Biomedical Innovations Research for Translational Health Science (BIRTHS) Laboratory, Department of Biochemistry and Molecular Biology, College of Medicine, University of the Philippines Manila.
  • Maganito SC; Department of Medical Microbiology, College of Public Health, University of the Philippines Manila.
  • Alfonso RN; Biomedical Innovations Research for Translational Health Science (BIRTHS) Laboratory, Department of Biochemistry and Molecular Biology, College of Medicine, University of the Philippines Manila.
  • Quero AKH; Division of Hematology, Department of Medicine, Philippine General Hospital, University of the Philippines Manila.
  • Lucero JAC; Division of Hematology, Department of Medicine, Philippine General Hospital, University of the Philippines Manila.
  • Cortez CFN; Division of Hematology, Department of Medicine, Philippine General Hospital, University of the Philippines Manila.
  • Evasan ALM; Division of Hematology, Department of Medicine, Philippine General Hospital, University of the Philippines Manila.
  • King RAN; Division of Infectious Diseases, Department of Medicine, Philippine General Hospital, University of the Philippines Manila.
  • Heralde FM; Biomedical Innovations Research for Translational Health Science (BIRTHS) Laboratory, Department of Biochemistry and Molecular Biology, College of Medicine, University of the Philippines Manila.
  • Bonifacio LB; Molecular Diagnostics and Multi-omics Laboratory (MDML), Department of Biochemistry and Molecular Biology, College of Medicine, University of the Philippines Manila.
  • Castillo GJ; Division of Hematology, Department of Medicine, Philippine General Hospital, University of the Philippines Manila.
  • Escasa IMS; Division of Hematology, Department of Medicine, Philippine General Hospital, University of the Philippines Manila.
  • Santos MCM; Division of Hematology, Department of Medicine, Philippine General Hospital, University of the Philippines Manila.
  • Malundo AFG; Division of Hematology, Department of Medicine, Philippine General Hospital, University of the Philippines Manila.
  • Mondragon AV; Division of Infectious Diseases, Department of Medicine, Philippine General Hospital, University of the Philippines Manila.
  • Salamat SEA; Division of Allergy and Immunology, Department of Medicine, Philippine General Hospital, University of the Philippines Manila.
  • Veloso JD; Department of Veterinary Paraclinical Sciences, College of Veterinary Medicine, University of the Philippines Los Baños.
  • Carnate JM; Division of Hematology, Department of Medicine, Philippine General Hospital, University of the Philippines Manila.
  • Tagayuna PY; Department of Pathology, College of Medicine, University of the Philippines Manila.
  • Lim JA; Department of Laboratories, Philippine General Hospital, University of the Philippines Manila.
  • Alejandria MM; Division of Infectious Diseases, Department of Medicine, Philippine General Hospital, University of the Philippines Manila.
  • Mirasol MAL; Division of Infectious Diseases, Department of Medicine, Philippine General Hospital, University of the Philippines Manila.
Acta Med Philipp ; 58(2): 5-15, 2024.
Article en En | MEDLINE | ID: mdl-38966161
ABSTRACT
Background and

Objective:

Convalescent plasma therapy (CPT) may reduce the risk of disease progression among patients with COVID-19. This study was undertaken to evaluate the efficacy and safety of CPT in preventing ICU admission among hospitalized COVID-19 patients.

Methods:

In this open-label randomized controlled trial, we randomly assigned hospitalized adult patients with COVID-19 in a 11 ratio to receive convalescent plasma as an adjunct to standard of care or standard of care alone. The primary endpoint was ICU admission within first 28 days of enrolment. Primary safety endpoints include rapid deterioration of respiratory or clinical status within four hours of convalescent plasma transfusion and cumulative incidence of serious adverse events during the study period including transfusion-related acute lung injury (TRALI), transfusion-associated circulatory overload (TACO), severe allergic reactions, and transfusion-related infections.

Results:

A total of 22 patients were assigned to receive convalescent plasma as an adjunct to standard of care and 22 to receive standard of care alone. The median time from onset of COVID-19 symptoms to study enrolment was eight days (IQR, 4 to 10). Two patients (9.1%) in the CPT group and one patient (4.5%) in the control group were admitted to the ICU. The primary outcome measure, ICU admission, was not different between the two groups (q-value >0.9). No patient who received convalescent plasma had rapid deterioration of respiratory/clinical status within four hours of transfusion and none developed TRALI, TACO, anaphylaxis, severe allergic reactions, or transfusion-related infections. There was also no significant difference in the secondary outcomes of 28-day mortality (two patients in the CPT group and none in the control group, q-value >0.90), dialysis-free days, vasopressor-free days, and ICU-free days.

Conclusions:

Among hospitalized COVID-19 patients, no significant differences were observed in the need for ICU admission between patients given CPT as adjunct to standard of care and those who received standard of care alone. Interpretation is limited by early termination of the trial which may have been underpowered to detect a clinically important difference.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Acta Med Philipp Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Acta Med Philipp Año: 2024 Tipo del documento: Article