es va demostrar que no hi havia difer\u00e8ncies significatives en la taxa d\u2019hospitalitzaci\u00f3 entre el grup experimental (22 de 188 participants, 12%) i el grup control (21 de 188 participants, 11%). Tampoc es van veure difer\u00e8ncies entre els grups quant a la reducci\u00f3 de la c\u00e0rrega viral als 7 dies, <\/strong>en la durada dels s\u00edmptomes, la necessitat d\u2019ingr\u00e9s a l\u2019UCI, ni els par\u00e0metres inflamatoris pron\u00f2stics en sang. El reclutament de pacients va tenir lloc des de novembre de 2020 fins a maig de 2021, amb seguiment fins al juliol de 2021.<\/p>\nEls investigadors de l\u2019estudi han afirmat que \u201cels resultats d\u2019aquest estudi no descarten definitivament l\u2019\u00fas d\u2019aquesta ter\u00e0pia que encara podria ser efectiva si es millora la dosis i l\u2019afinitat dels anticossos i els procediments per processar el producte. Per una banda, un producte amb major quantitat d\u2019anticossos, i que aquests fossin espec\u00edfics per a la variant circulant podria incrementar l\u2019efic\u00e0cia. Per altra banda, el plasma a Catalunya se sotmet a un proc\u00e9s d\u2019inactivaci\u00f3 de pat\u00f2gens amb blau de metil\u00e8 que podria degradar els anticossos, i per tant \u00e9s necessari un canvi en el processament per assegurar-ne la integritat\u201d.<\/em><\/p>\n","protected":false},"excerpt":{"rendered":"L\u2019estudi demostra que no hi ha difer\u00e8ncies a l\u2019hora de presentar complicacions que requereixin hospitalitzaci\u00f3 entre les persones amb COVID-19 que van rebre la infusi\u00f3 endovenosa de plasma i les que no la van 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