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Baseline Comorbidities in a Population-Based Cohort of Rheumatoid Arthritis Patients Receiving Biological Therapy: Data from the Australian Rheumatology Association Database
Aims. To describe the baseline characteristics of an Australian population-based cohort of rheumatoid arthritis (RA) patients commencing biological therapy. Methods. Descriptive analysis from the Australian Rheumatology Association Database (ARAD). Results. Up to October 2006, there were 681 RA pati...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2814100/ https://www.ncbi.nlm.nih.gov/pubmed/20130803 http://dx.doi.org/10.1155/2009/861481 |
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author | Briggs, Andrew M. March, Lyn Lassere, Marissa Reid, Christopher Henderson, Lyndall Murphy, Bridie van den Haak, Rosemarie Rischin, Adam Staples, Margaret Buchbinder, Rachelle |
author_facet | Briggs, Andrew M. March, Lyn Lassere, Marissa Reid, Christopher Henderson, Lyndall Murphy, Bridie van den Haak, Rosemarie Rischin, Adam Staples, Margaret Buchbinder, Rachelle |
author_sort | Briggs, Andrew M. |
collection | PubMed |
description | Aims. To describe the baseline characteristics of an Australian population-based cohort of rheumatoid arthritis (RA) patients commencing biological therapy. Methods. Descriptive analysis from the Australian Rheumatology Association Database (ARAD). Results. Up to October 2006, there were 681 RA patients taking biologics enrolled in ARAD. Baseline data were available for 624 (72% female, mean (SD) age 57.0 (12.5) years). Of these, 59.5% reported at least one comorbid condition, most commonly hypertension (35.7%) and osteoporosis (30.4%); 61 (9.8%) had a history of malignancy (35 nonmelanoma skin, 5 breast, 4 bowel, 5 cervix, 3 melanoma, 3 prostate and 1 each of lip, lung, myeloma, testis, uterus, vagina). Self-reported infections within the previous 6 months were common (71.5%). Conclusions. History of comorbidities, including recent infections, is common among Australian RA patients commencing biologics, and 10% have a history of malignancy. This may impact future evaluations of health outcomes among this population, including attribution of adverse events of biologic therapy. |
format | Text |
id | pubmed-2814100 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-28141002010-02-03 Baseline Comorbidities in a Population-Based Cohort of Rheumatoid Arthritis Patients Receiving Biological Therapy: Data from the Australian Rheumatology Association Database Briggs, Andrew M. March, Lyn Lassere, Marissa Reid, Christopher Henderson, Lyndall Murphy, Bridie van den Haak, Rosemarie Rischin, Adam Staples, Margaret Buchbinder, Rachelle Int J Rheumatol Clinical Study Aims. To describe the baseline characteristics of an Australian population-based cohort of rheumatoid arthritis (RA) patients commencing biological therapy. Methods. Descriptive analysis from the Australian Rheumatology Association Database (ARAD). Results. Up to October 2006, there were 681 RA patients taking biologics enrolled in ARAD. Baseline data were available for 624 (72% female, mean (SD) age 57.0 (12.5) years). Of these, 59.5% reported at least one comorbid condition, most commonly hypertension (35.7%) and osteoporosis (30.4%); 61 (9.8%) had a history of malignancy (35 nonmelanoma skin, 5 breast, 4 bowel, 5 cervix, 3 melanoma, 3 prostate and 1 each of lip, lung, myeloma, testis, uterus, vagina). Self-reported infections within the previous 6 months were common (71.5%). Conclusions. History of comorbidities, including recent infections, is common among Australian RA patients commencing biologics, and 10% have a history of malignancy. This may impact future evaluations of health outcomes among this population, including attribution of adverse events of biologic therapy. Hindawi Publishing Corporation 2009 2009-09-01 /pmc/articles/PMC2814100/ /pubmed/20130803 http://dx.doi.org/10.1155/2009/861481 Text en Copyright © 2009 Andrew M. Briggs et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Study Briggs, Andrew M. March, Lyn Lassere, Marissa Reid, Christopher Henderson, Lyndall Murphy, Bridie van den Haak, Rosemarie Rischin, Adam Staples, Margaret Buchbinder, Rachelle Baseline Comorbidities in a Population-Based Cohort of Rheumatoid Arthritis Patients Receiving Biological Therapy: Data from the Australian Rheumatology Association Database |
title | Baseline Comorbidities in a Population-Based Cohort of Rheumatoid
Arthritis Patients Receiving Biological Therapy: Data from the
Australian Rheumatology Association Database |
title_full | Baseline Comorbidities in a Population-Based Cohort of Rheumatoid
Arthritis Patients Receiving Biological Therapy: Data from the
Australian Rheumatology Association Database |
title_fullStr | Baseline Comorbidities in a Population-Based Cohort of Rheumatoid
Arthritis Patients Receiving Biological Therapy: Data from the
Australian Rheumatology Association Database |
title_full_unstemmed | Baseline Comorbidities in a Population-Based Cohort of Rheumatoid
Arthritis Patients Receiving Biological Therapy: Data from the
Australian Rheumatology Association Database |
title_short | Baseline Comorbidities in a Population-Based Cohort of Rheumatoid
Arthritis Patients Receiving Biological Therapy: Data from the
Australian Rheumatology Association Database |
title_sort | baseline comorbidities in a population-based cohort of rheumatoid
arthritis patients receiving biological therapy: data from the
australian rheumatology association database |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2814100/ https://www.ncbi.nlm.nih.gov/pubmed/20130803 http://dx.doi.org/10.1155/2009/861481 |
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