Evaluation of the safety and satisfaction of rheumatic patients with accelerated infliximab infusion

Abstract Introduction Infliximab infusion generally occurs in 2–4 h. Recent studies have suggested the possibility of accelerated infusion (1 h) of this drug. Objective To evaluate the safety of accelerated infliximab infusion in patients with rheumatic diseases. In addition, patient satisfaction wa...

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Main Authors: Jozélio Freire de Carvalho, Maria Natividade Pereira dos Santos, Joyce Meyre Vieira de Oliveira, Andrea Nogueira S. Lanty Silva, Roberto Paulo Correia de Araujo, Juliana Bahia Cardozo
Format: Article
Language:English
Published: BMC 2018-08-01
Series:Advances in Rheumatology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s42358-018-0016-x
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spelling doaj-c4cfe5915a1f435583edd33c24d2e4482020-11-25T01:39:02ZengBMCAdvances in Rheumatology2523-31062018-08-015811310.1186/s42358-018-0016-xEvaluation of the safety and satisfaction of rheumatic patients with accelerated infliximab infusionJozélio Freire de Carvalho0Maria Natividade Pereira dos Santos1Joyce Meyre Vieira de Oliveira2Andrea Nogueira S. Lanty Silva3Roberto Paulo Correia de Araujo4Juliana Bahia Cardozo5SOS Vida, Rheumatology UnitSOS Vida, Rheumatology UnitSOS Vida, Rheumatology UnitSOS Vida, Rheumatology UnitSOS Vida, Rheumatology UnitSOS Vida, Rheumatology UnitAbstract Introduction Infliximab infusion generally occurs in 2–4 h. Recent studies have suggested the possibility of accelerated infusion (1 h) of this drug. Objective To evaluate the safety of accelerated infliximab infusion in patients with rheumatic diseases. In addition, patient satisfaction was also assessed. Methods A prospective, single-center, non-randomized study with 34 patients with rheumatic diseases was conducted from July to November 2016. Patients with the following were excluded: history of allergic reaction to biologics, asthma or severe atopy. All patients previously received a 2- to 3-h infliximab infusion. The infusion rate was accelerated to 1 h, and premedication was excluded. The infusion was monitored in all patients. Results A total of 34 patients were included in the study [rheumatoid arthritis (n = 16), ankylosing spondylitis (n = 15), psoriatic arthritis (n = 2) and enteropathic arthropathy (n = 1)], with an average age of 48.7 ± 18.6 years; 55.5% of the patients were female, and 29.4% were white. The duration of disease was 9.5 ± 9.2 years, and the duration of infliximab use was 38.9 ± 27.6 months, with a mean dose per infusion of 414.2 ± 158.1 (range, 200–800) mg. The mean infliximab infusion time prior to the study was 2.2 ± 0.4 h. A total of 6 (17.6%) patients received premedication. The premedication was suspended. There were no adverse effects during or after infusion. Ninety-seven percent of the patients and 100% of the health workers were satisfied with the accelerated infusion. Conclusion Our data support the safe use of accelerated infliximab infusion in rheumatic patients, with high satisfaction among patients and health workers.http://link.springer.com/article/10.1186/s42358-018-0016-xInfliximabInfusionImmunobiologicsRheumatoid arthritisAnkylosing spondylitisPsoriatic arthritis
collection DOAJ
language English
format Article
sources DOAJ
author Jozélio Freire de Carvalho
Maria Natividade Pereira dos Santos
Joyce Meyre Vieira de Oliveira
Andrea Nogueira S. Lanty Silva
Roberto Paulo Correia de Araujo
Juliana Bahia Cardozo
spellingShingle Jozélio Freire de Carvalho
Maria Natividade Pereira dos Santos
Joyce Meyre Vieira de Oliveira
Andrea Nogueira S. Lanty Silva
Roberto Paulo Correia de Araujo
Juliana Bahia Cardozo
Evaluation of the safety and satisfaction of rheumatic patients with accelerated infliximab infusion
Advances in Rheumatology
Infliximab
Infusion
Immunobiologics
Rheumatoid arthritis
Ankylosing spondylitis
Psoriatic arthritis
author_facet Jozélio Freire de Carvalho
Maria Natividade Pereira dos Santos
Joyce Meyre Vieira de Oliveira
Andrea Nogueira S. Lanty Silva
Roberto Paulo Correia de Araujo
Juliana Bahia Cardozo
author_sort Jozélio Freire de Carvalho
title Evaluation of the safety and satisfaction of rheumatic patients with accelerated infliximab infusion
title_short Evaluation of the safety and satisfaction of rheumatic patients with accelerated infliximab infusion
title_full Evaluation of the safety and satisfaction of rheumatic patients with accelerated infliximab infusion
title_fullStr Evaluation of the safety and satisfaction of rheumatic patients with accelerated infliximab infusion
title_full_unstemmed Evaluation of the safety and satisfaction of rheumatic patients with accelerated infliximab infusion
title_sort evaluation of the safety and satisfaction of rheumatic patients with accelerated infliximab infusion
publisher BMC
series Advances in Rheumatology
issn 2523-3106
publishDate 2018-08-01
description Abstract Introduction Infliximab infusion generally occurs in 2–4 h. Recent studies have suggested the possibility of accelerated infusion (1 h) of this drug. Objective To evaluate the safety of accelerated infliximab infusion in patients with rheumatic diseases. In addition, patient satisfaction was also assessed. Methods A prospective, single-center, non-randomized study with 34 patients with rheumatic diseases was conducted from July to November 2016. Patients with the following were excluded: history of allergic reaction to biologics, asthma or severe atopy. All patients previously received a 2- to 3-h infliximab infusion. The infusion rate was accelerated to 1 h, and premedication was excluded. The infusion was monitored in all patients. Results A total of 34 patients were included in the study [rheumatoid arthritis (n = 16), ankylosing spondylitis (n = 15), psoriatic arthritis (n = 2) and enteropathic arthropathy (n = 1)], with an average age of 48.7 ± 18.6 years; 55.5% of the patients were female, and 29.4% were white. The duration of disease was 9.5 ± 9.2 years, and the duration of infliximab use was 38.9 ± 27.6 months, with a mean dose per infusion of 414.2 ± 158.1 (range, 200–800) mg. The mean infliximab infusion time prior to the study was 2.2 ± 0.4 h. A total of 6 (17.6%) patients received premedication. The premedication was suspended. There were no adverse effects during or after infusion. Ninety-seven percent of the patients and 100% of the health workers were satisfied with the accelerated infusion. Conclusion Our data support the safe use of accelerated infliximab infusion in rheumatic patients, with high satisfaction among patients and health workers.
topic Infliximab
Infusion
Immunobiologics
Rheumatoid arthritis
Ankylosing spondylitis
Psoriatic arthritis
url http://link.springer.com/article/10.1186/s42358-018-0016-x
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