Impact of pain associated with the subcutaneous administration of adalimumab.


Journal

Gastroenterologia y hepatologia
ISSN: 0210-5705
Titre abrégé: Gastroenterol Hepatol
Pays: Spain
ID NLM: 8406671

Informations de publication

Date de publication:
Jan 2020
Historique:
received: 21 03 2019
revised: 01 05 2019
accepted: 14 06 2019
pubmed: 8 9 2019
medline: 31 10 2020
entrez: 8 9 2019
Statut: ppublish

Résumé

There is limited information regarding the impact of patients' perception of injection pain on adherence to treatments, specifically in inflammatory bowel disease (IBD) patients. Therefore, we aimed to determine the impact of the pain associated with the subcutaneous administration of adalimumab in patients with IBD treated with the old formulation and the new low-volume/citrate-free formulation. A specifically-designed questionnaire was completed by 76 patients with IBD, who started treatment with adalimumab before the availability of the low-volume/citrate-free formulation and were switched to this new formulation. Intensity of pain was measured by using visual analog scales (VAS). A total of 62 patients (82%) experienced injection-related pain with the initial formulation. The perception of pain was associated with a decreased adherence to the treatment (37%), an increase in pre-administration anxiety (25%) or, as a consequence, the patient required someone else to carry out the injection (21%). Younger age was the only factor associated with pain perception. After switching to the new formulation, perception of pain persisted only in 2 patients (3%). Among those who felt pain with the initial formulation, pre-administration anxiety disappeared in 44%; 32% and 42% stated that the new formulation eased adherence and self-administration. The perception of pain related to the subcutaneous administration of therapy negatively impacts on treatment adherence in IBD patients. Improved formulations for subcutaneous administration of drugs can positively impact patients' convenience and adherence.

Sections du résumé

BACKGROUND BACKGROUND
There is limited information regarding the impact of patients' perception of injection pain on adherence to treatments, specifically in inflammatory bowel disease (IBD) patients. Therefore, we aimed to determine the impact of the pain associated with the subcutaneous administration of adalimumab in patients with IBD treated with the old formulation and the new low-volume/citrate-free formulation.
METHODS METHODS
A specifically-designed questionnaire was completed by 76 patients with IBD, who started treatment with adalimumab before the availability of the low-volume/citrate-free formulation and were switched to this new formulation. Intensity of pain was measured by using visual analog scales (VAS).
RESULTS RESULTS
A total of 62 patients (82%) experienced injection-related pain with the initial formulation. The perception of pain was associated with a decreased adherence to the treatment (37%), an increase in pre-administration anxiety (25%) or, as a consequence, the patient required someone else to carry out the injection (21%). Younger age was the only factor associated with pain perception. After switching to the new formulation, perception of pain persisted only in 2 patients (3%). Among those who felt pain with the initial formulation, pre-administration anxiety disappeared in 44%; 32% and 42% stated that the new formulation eased adherence and self-administration.
CONCLUSIONS CONCLUSIONS
The perception of pain related to the subcutaneous administration of therapy negatively impacts on treatment adherence in IBD patients. Improved formulations for subcutaneous administration of drugs can positively impact patients' convenience and adherence.

Identifiants

pubmed: 31492425
pii: S0210-5705(19)30175-X
doi: 10.1016/j.gastrohep.2019.06.008
pii:
doi:

Substances chimiques

Anti-Inflammatory Agents 0
Adalimumab FYS6T7F842

Types de publication

Journal Article

Langues

eng spa

Sous-ensembles de citation

IM

Pagination

9-13

Informations de copyright

Copyright © 2019 Elsevier España, S.L.U. All rights reserved.

Auteurs

Cristina Gely (C)

Hospital Santa Creu i Sant Pau, Barcelona, Catalonia, Spain.

Laura Marín (L)

Hospital Universitari Germans Trias i Pujol, Badalona, Catalonia, Spain.

Jordi Gordillo (J)

Hospital Santa Creu i Sant Pau, Barcelona, Catalonia, Spain.

Míriam Mañosa (M)

Hospital Universitari Germans Trias i Pujol, Badalona, Catalonia, Spain; Centro de Investigación Biomédica en Red Enfermedades Hepáticas y Digestivas (Ciberehd), Spain.

Federico Bertoletti (F)

Hospital Santa Creu i Sant Pau, Barcelona, Catalonia, Spain.

Fiorella Cañete (F)

Hospital Universitari Germans Trias i Pujol, Badalona, Catalonia, Spain; Centro de Investigación Biomédica en Red Enfermedades Hepáticas y Digestivas (Ciberehd), Spain.

Carlos González-Muñoza (C)

Hospital Santa Creu i Sant Pau, Barcelona, Catalonia, Spain.

Margalida Calafat (M)

Hospital Universitari Germans Trias i Pujol, Badalona, Catalonia, Spain.

Eugeni Domènech (E)

Hospital Universitari Germans Trias i Pujol, Badalona, Catalonia, Spain; Centro de Investigación Biomédica en Red Enfermedades Hepáticas y Digestivas (Ciberehd), Spain. Electronic address: eugenidomenech@gmail.com.

Esther Garcia-Planella (E)

Hospital Santa Creu i Sant Pau, Barcelona, Catalonia, Spain.

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Classifications MeSH