Cargando…
Adverse events in patients with ankylosing spondylitis treated with TNF inhibitors: a cross-sectional study
Background Although TNF inhibitors are well established in ankylosing spondylitis treatment, the majority of studies on TNF inhibitors safety have been performed in rheumatoid arthritis patients. Meanwhile, it seems that TNF inhibitors in ankylosing spondylitis may present a better safety profile th...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6677866/ https://www.ncbi.nlm.nih.gov/pubmed/31172410 http://dx.doi.org/10.1007/s11096-019-00859-7 |
_version_ | 1783440970335911936 |
---|---|
author | Wroński, Jakub Fiedor, Piotr Głuszko, Piotr |
author_facet | Wroński, Jakub Fiedor, Piotr Głuszko, Piotr |
author_sort | Wroński, Jakub |
collection | PubMed |
description | Background Although TNF inhibitors are well established in ankylosing spondylitis treatment, the majority of studies on TNF inhibitors safety have been performed in rheumatoid arthritis patients. Meanwhile, it seems that TNF inhibitors in ankylosing spondylitis may present a better safety profile than we thought. Objective The aim of our study was to retrospectively investigate the occurrence of adverse events in ankylosing spondylitis patients treated with TNF inhibitors. Setting A single referral center in Poland. Methods Detailed medical history of ankylosing spondylitis patients was obtained during the interview with the patient and by reviewing electronic medical records. Patients treated with TNF inhibitors and patients without TNF inhibitors treatment were compared. Main outcome measure The incidence of adverse events during the 3 months period before the interview. Results A total of 150 patients, 103 in the treatment group and 47 in the control group, were included in the study. There were no differences in the incidence of adverse events, serious adverse events, infections and opportunistic infections between both groups. However, in the treatment group, noninfectious adverse events were significantly less frequent than in control group (RR 0.39, 95% CI 0.23–0.66), with abdominal pain as the most common noninfectious adverse event (RR 0.20, 95% CI 0.07–0.63). The differences in incidence rates of specific infections were not significant, except acute infectious diarrhea which also was less frequent in patients treated with TNF inhibitors (RR 0.17, 95% CI 0.03–0.85). The female gender was significantly associated with any adverse event occurrence (OR 2.36, 95% CI 1.15–4.83). Conclusion TNF inhibitors show a good safety profile in ankylosing spondylitis patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11096-019-00859-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6677866 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-66778662019-08-16 Adverse events in patients with ankylosing spondylitis treated with TNF inhibitors: a cross-sectional study Wroński, Jakub Fiedor, Piotr Głuszko, Piotr Int J Clin Pharm Research Article Background Although TNF inhibitors are well established in ankylosing spondylitis treatment, the majority of studies on TNF inhibitors safety have been performed in rheumatoid arthritis patients. Meanwhile, it seems that TNF inhibitors in ankylosing spondylitis may present a better safety profile than we thought. Objective The aim of our study was to retrospectively investigate the occurrence of adverse events in ankylosing spondylitis patients treated with TNF inhibitors. Setting A single referral center in Poland. Methods Detailed medical history of ankylosing spondylitis patients was obtained during the interview with the patient and by reviewing electronic medical records. Patients treated with TNF inhibitors and patients without TNF inhibitors treatment were compared. Main outcome measure The incidence of adverse events during the 3 months period before the interview. Results A total of 150 patients, 103 in the treatment group and 47 in the control group, were included in the study. There were no differences in the incidence of adverse events, serious adverse events, infections and opportunistic infections between both groups. However, in the treatment group, noninfectious adverse events were significantly less frequent than in control group (RR 0.39, 95% CI 0.23–0.66), with abdominal pain as the most common noninfectious adverse event (RR 0.20, 95% CI 0.07–0.63). The differences in incidence rates of specific infections were not significant, except acute infectious diarrhea which also was less frequent in patients treated with TNF inhibitors (RR 0.17, 95% CI 0.03–0.85). The female gender was significantly associated with any adverse event occurrence (OR 2.36, 95% CI 1.15–4.83). Conclusion TNF inhibitors show a good safety profile in ankylosing spondylitis patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11096-019-00859-7) contains supplementary material, which is available to authorized users. Springer International Publishing 2019-06-06 2019 /pmc/articles/PMC6677866/ /pubmed/31172410 http://dx.doi.org/10.1007/s11096-019-00859-7 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Research Article Wroński, Jakub Fiedor, Piotr Głuszko, Piotr Adverse events in patients with ankylosing spondylitis treated with TNF inhibitors: a cross-sectional study |
title | Adverse events in patients with ankylosing spondylitis treated with TNF inhibitors: a cross-sectional study |
title_full | Adverse events in patients with ankylosing spondylitis treated with TNF inhibitors: a cross-sectional study |
title_fullStr | Adverse events in patients with ankylosing spondylitis treated with TNF inhibitors: a cross-sectional study |
title_full_unstemmed | Adverse events in patients with ankylosing spondylitis treated with TNF inhibitors: a cross-sectional study |
title_short | Adverse events in patients with ankylosing spondylitis treated with TNF inhibitors: a cross-sectional study |
title_sort | adverse events in patients with ankylosing spondylitis treated with tnf inhibitors: a cross-sectional study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6677866/ https://www.ncbi.nlm.nih.gov/pubmed/31172410 http://dx.doi.org/10.1007/s11096-019-00859-7 |
work_keys_str_mv | AT wronskijakub adverseeventsinpatientswithankylosingspondylitistreatedwithtnfinhibitorsacrosssectionalstudy AT fiedorpiotr adverseeventsinpatientswithankylosingspondylitistreatedwithtnfinhibitorsacrosssectionalstudy AT głuszkopiotr adverseeventsinpatientswithankylosingspondylitistreatedwithtnfinhibitorsacrosssectionalstudy |