Adverse drug events in rheumatoid arthritis and osteoarthritis ambulatory patients

Aim: We aimed to determine the prevalence and characteristics of adverse drug events (ADE) in rheumatoid arthritis (RA) and (osteoarthritis) OA patients. Method: A cross-sectional study at rheumatology clinics, was performed by random selection of RA and OA out-patients by a research pharmacist. All...

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Main Authors: Pramote Tragulpiankit, Suvatna Chulavatnatol, Ticha Rerkpattanapipat, Suchela Janwityanujit, Suthatip Somjarit, Uamporn Sirikhedgon
Other Authors: Faculty of Pharmacy
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Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/14766
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spelling th-mahidol.147662018-06-11T12:09:41Z Adverse drug events in rheumatoid arthritis and osteoarthritis ambulatory patients Pramote Tragulpiankit Suvatna Chulavatnatol Ticha Rerkpattanapipat Suchela Janwityanujit Suthatip Somjarit Uamporn Sirikhedgon Faculty of Pharmacy Mahidol University Medicine Aim: We aimed to determine the prevalence and characteristics of adverse drug events (ADE) in rheumatoid arthritis (RA) and (osteoarthritis) OA patients. Method: A cross-sectional study at rheumatology clinics, was performed by random selection of RA and OA out-patients by a research pharmacist. All suspected ADEs occurring during the last hospital visit and the subjects were identified by retrospective chart review and direct patient interview. ADE characteristics, including causative drug groups, affected organ severity and patient outcomes, were recorded. Results: One hundred and forty-three patients consisting of 129 RA and 14 OA were recruited. The patients' mean ages were 54.3 ± 14.3 years and 121 (84.6%) patients were female. A total of 68 ADEs were detected in 51 patients. The prevalence and rate of ADE were 35.7% and 47.6 events per 100 patients, respectively. Thirty out of 68 ADEs (44.1%) were preventable. Disease-modifying anti-rheumatic drugs and non-steroidal anti-inflammatory drugs resulted in ADEs by 41 (59.4%) and 10 (14.5%) events, respectively. Common affected organs were skin, gastrointestinal tract and eyes which accounted for 20 (29.4%), 18 (26.5%) and eight events (11.6%), respectively. Continuation of the suspected drug was noted in 42 ADEs (61.8%), classified as severity level 1 and 2a-b, and 43 ADEs (63.2%) were completely or partially resolved during the study period. Conclusion: ADEs are common in RA and OA patients with prevalence of 35.7%. High exposure to potentially harmful drugs might explain the higher rate of ADE in these patients. © 2012 Asia Pacific League of Associations for Rheumatology and Blackwell Publishing Asia Pty Ltd. 2018-06-11T05:09:41Z 2018-06-11T05:09:41Z 2012-06-01 Article International Journal of Rheumatic Diseases. Vol.15, No.3 (2012), 315-321 10.1111/j.1756-185X.2012.01716.x 1756185X 17561841 2-s2.0-84862520517 https://repository.li.mahidol.ac.th/handle/123456789/14766 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84862520517&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Medicine
spellingShingle Medicine
Pramote Tragulpiankit
Suvatna Chulavatnatol
Ticha Rerkpattanapipat
Suchela Janwityanujit
Suthatip Somjarit
Uamporn Sirikhedgon
Adverse drug events in rheumatoid arthritis and osteoarthritis ambulatory patients
description Aim: We aimed to determine the prevalence and characteristics of adverse drug events (ADE) in rheumatoid arthritis (RA) and (osteoarthritis) OA patients. Method: A cross-sectional study at rheumatology clinics, was performed by random selection of RA and OA out-patients by a research pharmacist. All suspected ADEs occurring during the last hospital visit and the subjects were identified by retrospective chart review and direct patient interview. ADE characteristics, including causative drug groups, affected organ severity and patient outcomes, were recorded. Results: One hundred and forty-three patients consisting of 129 RA and 14 OA were recruited. The patients' mean ages were 54.3 ± 14.3 years and 121 (84.6%) patients were female. A total of 68 ADEs were detected in 51 patients. The prevalence and rate of ADE were 35.7% and 47.6 events per 100 patients, respectively. Thirty out of 68 ADEs (44.1%) were preventable. Disease-modifying anti-rheumatic drugs and non-steroidal anti-inflammatory drugs resulted in ADEs by 41 (59.4%) and 10 (14.5%) events, respectively. Common affected organs were skin, gastrointestinal tract and eyes which accounted for 20 (29.4%), 18 (26.5%) and eight events (11.6%), respectively. Continuation of the suspected drug was noted in 42 ADEs (61.8%), classified as severity level 1 and 2a-b, and 43 ADEs (63.2%) were completely or partially resolved during the study period. Conclusion: ADEs are common in RA and OA patients with prevalence of 35.7%. High exposure to potentially harmful drugs might explain the higher rate of ADE in these patients. © 2012 Asia Pacific League of Associations for Rheumatology and Blackwell Publishing Asia Pty Ltd.
author2 Faculty of Pharmacy
author_facet Faculty of Pharmacy
Pramote Tragulpiankit
Suvatna Chulavatnatol
Ticha Rerkpattanapipat
Suchela Janwityanujit
Suthatip Somjarit
Uamporn Sirikhedgon
format Article
author Pramote Tragulpiankit
Suvatna Chulavatnatol
Ticha Rerkpattanapipat
Suchela Janwityanujit
Suthatip Somjarit
Uamporn Sirikhedgon
author_sort Pramote Tragulpiankit
title Adverse drug events in rheumatoid arthritis and osteoarthritis ambulatory patients
title_short Adverse drug events in rheumatoid arthritis and osteoarthritis ambulatory patients
title_full Adverse drug events in rheumatoid arthritis and osteoarthritis ambulatory patients
title_fullStr Adverse drug events in rheumatoid arthritis and osteoarthritis ambulatory patients
title_full_unstemmed Adverse drug events in rheumatoid arthritis and osteoarthritis ambulatory patients
title_sort adverse drug events in rheumatoid arthritis and osteoarthritis ambulatory patients
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/14766
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