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Does timing matter on tocilizumab administration? Clinical, analytical and radiological outcomes in COVID-19.
Moreno Diaz, Raquel; Amor García, Miguel Angel; Teigell Muñoz, Francisco Javier; Saldaña Perez, Leonardo Ernesto; Mateos Gonzalez, María; Melero Bermejo, Jose Antonio; López Hernández, Alberto; Reyes Marquez, Laura; De Guzman García-Monge, Maria Teresa; Perez Quero, Jose Luis; Homez Guzman, Marcela Patricia.
Afiliação
  • Moreno Diaz R; Pharmacy, Hospital Universitario Infanta Cristina, Parla, Spain rmorenod@salud.madrid.org.
  • Amor García MA; Pharmacy, Hospital Universitario Infanta Cristina, Parla, Spain.
  • Teigell Muñoz FJ; Internal Medicine, Infanta Cristina University Hospital, Parla, Spain.
  • Saldaña Perez LE; Neumology, Getafe University Hospital, Getafe, Madrid, Spain.
  • Mateos Gonzalez M; Internal Medicine, Infanta Cristina University Hospital, Parla, Spain.
  • Melero Bermejo JA; Internal Medicine, Infanta Cristina University Hospital, Parla, Spain.
  • López Hernández A; Pharmacy, Hospital Universitario Infanta Cristina, Parla, Spain.
  • Reyes Marquez L; Radiologist, Hospital Universitario Infanta Cristina, Parla, Madrid, Spain.
  • De Guzman García-Monge MT; Internal Medicine, Infanta Cristina University Hospital, Parla, Spain.
  • Perez Quero JL; Internal Medicine, Infanta Cristina University Hospital, Parla, Spain.
  • Homez Guzman MP; Critical Care, Hospital Universitario Infanta Cristina, Parla, Madrid, Spain.
Eur J Hosp Pharm ; 29(6): 340-345, 2022 Nov.
Article em En | MEDLINE | ID: mdl-33627476
ABSTRACT

INTRODUCTION:

While there are no pharmacological treatments with proven efficacy for coronavirus disease 2019 (COVID-19), tocilizumab has emerged as a candidate therapy. Some aspects of this therapy are still unknown, including the optimal timing of administration.

OBJECTIVE:

This observational study aimed to compare the 90-day mortality in two cohorts of patients when the drug was administered within the first 10 days from onset of symptoms or after day 11.

METHODS:

Patients hospitalised with severe COVID-19 pneumonia who had received tocilizumab were divided into two groups according to when the medication was administered. The primary outcome was 90-day mortality. Secondary outcomes were 30-day mortality, clinical improvement on a 6-item scale by day 6, biomarker improvement by day 6, radiological image improvement by day 10 and SaO2 quotient by day 6. The results in the two groups were compared. Additionally, adverse events relating to tocilizumab were recorded.

RESULTS:

A total of 112 patients were analysed. Both groups were epidemiologically comparable. The results obtained in the primary efficacy variable of the study (90-day mortality) showed a statistically significant difference in the subgroups according to the time of administration of tocilizumab (18.6% vs 5.0%, p=0.048). There was clinical improvement in 24.1% of patients at 6 days, with similar behaviour in both subgroups. No statistically significant differences were found in the percentage of patients who achieved radiological improvement at 10 days or in the other inflammatory parameters, with the exception of significant reductions in lactate dehydrogenase and C-reactive protein. Administration of tocilizumab was not associated with relevant adverse events.

CONCLUSION:

To our knowledge, this is the first report of data regarding the timing of administration of tocilizumab in patients with COVID-19 pneumonia. A strategy involving tocilizumab administration after 10 days from onset of symptoms may decrease mortality. Further randomised controlled trials are needed to confirm this emerging hypothesis.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anticorpos Monoclonais Humanizados / Tratamento Farmacológico da COVID-19 Tipo de estudo: Clinical_trials / Observational_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anticorpos Monoclonais Humanizados / Tratamento Farmacológico da COVID-19 Tipo de estudo: Clinical_trials / Observational_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article