TY - JOUR
T1 - Long-Term Opioid Therapy Among Patients With Systemic Lupus Erythematosus in the Community
T2 - A Lupus Midwest Network (LUMEN) Study
AU - Figueroa-Parra, Gabriel
AU - Jeffery, Molly M.
AU - Dabit, Jesse Y.
AU - Chevet, Baptiste
AU - Valenzuela-Almada, Maria O.
AU - Hocaoglu, Mehmet
AU - Osei-Onomah, Shirley Ann
AU - Kurani, Shaheen
AU - Vallejo, Sebastian
AU - Achenbach, Sara J.
AU - Hooten, W. Michael
AU - Barbour, Kamil E.
AU - Crowson, Cynthia S.
AU - Duarte-García, Alí
N1 - Funding Information:
The Lupus Midwest Network (LUMEN) project is supported by the Centers for Disease Control and Prevention (CDC) of the US Department of Health and Human Services (HHS) under grant number U01 DP006491 as part of a financial assistance award totaling US $1,750,000 with 100% funded by CDC/HHS. The contents are those of the authors and do not necessarily represent the official views of, nor an endorsement by, CDC/HHS or the US Government. The Rochester Epidemiology Project was supported by the National Institute on Aging of the National Institutes of Health (NIH) under award number R01AG034676 and grant number UL1 TR002377 from the National Center for Advancing Translational Sciences, a component of the NIH. The content is solely the authors’ responsibility and does not necessarily represent the official views of the NIH. ADG is supported by the Rheumatology Research Foundation Scientist Development Award and the Robert D. and Patricia E. Kern Center for the Science of Health Care Delivery. In the past 3 years, MMJ has received unrelated grant funding from the Agency for Healthcare Research and Quality; the National Institute on Drug Abuse; the National Heart, Lung, and Blood Institute; the American Cancer Society; and the US Food and Drug Administration for the Yale-Mayo Clinic Center for Excellence in Regulatory Science and Innovation program. 1G. Figueroa-Parra, MD, J.Y. Dabit, MD, MS, M.O. Valenzuela-Almada, MD, M. Hocaoglu, MD, S.A. Osei-Onomah, MPH, S. Vallejo, MD, Division of Rheumatology, Mayo Clinic, Rochester, Minnesota, USA; 2M.M. Jeffery, PhD, Division of Health Care Delivery Research, Mayo Clinic, Rochester, Minnesota, USA; 3B. Chevet, MD, Division of Rheumatology, Mayo Clinic, Rochester, Minnesota, USA, and Division of Rheumatology, Brest Teaching Hospital, LBAI, UMR1227, Univ Brest, Inserm, CHU de Brest, Brest, France; 4S. Kurani, PhD, Robert D. and Patricia E. Kern Center for the Science of Health Care Delivery, Mayo Clinic, Rochester, Minnesota, USA; 5S.J. Achenbach, MS, Department of Quantitative Health Sciences, Mayo Clinic, Rochester, Minnesota, USA; 6W.M. Hooten, MD, Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, Rochester, Minnesota, USA; 7K.E. Barbour, PhD, MPH, MS, Division of Population Health, National Center for Chronic Disease Prevention and Health Promotion, Centers for Disease Control and Prevention, Atlanta, Georgia, USA; 8C.S. Crowson, PhD, Division of Rheumatology, Mayo Clinic, and Department of Quantitative Health Sciences, Mayo Clinic, Rochester, Minnesota, USA; 9A. Duarte-García, MD, MSc, Division of Rheumatology, Mayo Clinic, and Robert D. and Patricia E. Kern Center for the Science of Health Care Delivery, Mayo Clinic, Rochester, Minnesota, USA. The authors declare no conflicts of interest relevant to this article. Address correspondence to Dr. A. Duarte-García, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA. Email: duarte.ali@mayo.edu. Accepted for publication October 24, 2022.
Funding Information:
The Lupus Midwest Network (LUMEN) project is supported by the Centers for Disease Control and Prevention (CDC) of the US Department of Health and Human Services (HHS) under grant number U01 DP006491 as part of a financial assistance award totaling US $1,750,000 with 100% funded by CDC/HHS. The contents are those of the authors and do not necessarily represent the official views of, nor an endorsement by, CDC/HHS or the US Government. The Rochester Epidemiology Project was supported by the National Institute on Aging of the National Institutes of Health (NIH) under award number R01AG034676 and grant number UL1 TR002377 from the National Center for Advancing Translational Sciences, a component of the NIH. The content is solely the authors' responsibility and does not necessarily represent the official views of the NIH. ADG is supported by the Rheumatology Research Foundation Scientist Development Award and the Robert D. and Patricia E. Kern Center for the Science of Health Care Delivery. In the past 3 years, MMJ has received unrelated grant funding from the Agency for Healthcare Research and Quality; the National Institute on Drug Abuse; the National Heart, Lung, and Blood Institute; the American Cancer Society; and the US Food and Drug Administration for the Yale-Mayo Clinic Center for Excellence in Regulatory Science and Innovation program. The study team would like to thank Barbara Abbott for her support in accessing the Rochester Epidemiology Project data.
Publisher Copyright:
© 2023 The Journal of Rheumatology. This is an Open Access article, which permits use, distribution, and reproduction, without modification, provided the original article is correctly cited and is not used for commercial purposes.
PY - 2023/4/1
Y1 - 2023/4/1
N2 - Objective. There is little information about the epidemiology and factors associated with opioid therapy in systemic lupus erythematosus (SLE). We aimed to assess the prevalence of opioid therapy and explore factors associated with long-term opioid therapy (LTOT) in patients with SLE. Methods. Patients with SLE were matched with controls without SLE in a population-based cohort on January 1, 2015. We captured demographics, manifestations of SLE, comorbidities (ie, fibromyalgia, mood disorders, osteoarthritis, chronic low back pain [CLBP], chronic kidney disease (CKD), avascular necrosis, osteoporosis, fragility fractures, and cancer), and the Area Deprivation Index (ADI). Opioid prescription data were used to assess the prevalence of LTOT, defined as contiguous prescriptions (gaps of < 30 days between prescriptions) and receiving opioid therapy for ≥ 90 days or ≥ 10 prescriptions before the index date. Results. A total of 465 patients with SLE and 465 controls without SLE were included. In total, 13% of patients with SLE and 3% of controls without SLE were receiving opioid therapy (P < 0.001), and 11% of patients with SLE were on LTOT vs 1% of controls without SLE. Among patients with SLE, acute pericarditis (odds ratio [OR] 3.92, 95% CI 1.78-8.66), fibromyalgia (OR 7.78, 95% CI 3.89-15.55), fragility fractures (OR 3.72, 95% CI 1.25-11.07), CLBP (OR 4.00, 95% CI 2.13-7.51), and mood disorders (OR 2.76, 95% CI 1.47-5.16) were associated with LTOT. We did not find an association between opioid therapy and ADI. Conclusion. Patients with SLE are more likely to receive LTOT than controls. Among patients with SLE, LTOT was associated with pericarditis and several comorbidities. However, LTOT was not associated with CKD despite the limited pain control options among these patients.
AB - Objective. There is little information about the epidemiology and factors associated with opioid therapy in systemic lupus erythematosus (SLE). We aimed to assess the prevalence of opioid therapy and explore factors associated with long-term opioid therapy (LTOT) in patients with SLE. Methods. Patients with SLE were matched with controls without SLE in a population-based cohort on January 1, 2015. We captured demographics, manifestations of SLE, comorbidities (ie, fibromyalgia, mood disorders, osteoarthritis, chronic low back pain [CLBP], chronic kidney disease (CKD), avascular necrosis, osteoporosis, fragility fractures, and cancer), and the Area Deprivation Index (ADI). Opioid prescription data were used to assess the prevalence of LTOT, defined as contiguous prescriptions (gaps of < 30 days between prescriptions) and receiving opioid therapy for ≥ 90 days or ≥ 10 prescriptions before the index date. Results. A total of 465 patients with SLE and 465 controls without SLE were included. In total, 13% of patients with SLE and 3% of controls without SLE were receiving opioid therapy (P < 0.001), and 11% of patients with SLE were on LTOT vs 1% of controls without SLE. Among patients with SLE, acute pericarditis (odds ratio [OR] 3.92, 95% CI 1.78-8.66), fibromyalgia (OR 7.78, 95% CI 3.89-15.55), fragility fractures (OR 3.72, 95% CI 1.25-11.07), CLBP (OR 4.00, 95% CI 2.13-7.51), and mood disorders (OR 2.76, 95% CI 1.47-5.16) were associated with LTOT. We did not find an association between opioid therapy and ADI. Conclusion. Patients with SLE are more likely to receive LTOT than controls. Among patients with SLE, LTOT was associated with pericarditis and several comorbidities. However, LTOT was not associated with CKD despite the limited pain control options among these patients.
KW - comorbidity
KW - long-term opioid therapy
KW - opioids
KW - pain management
KW - systemic lupus erythematosus
UR - http://www.scopus.com/inward/record.url?scp=85151380184&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85151380184&partnerID=8YFLogxK
U2 - 10.3899/JRHEUM.220822
DO - 10.3899/JRHEUM.220822
M3 - Article
C2 - 36379579
AN - SCOPUS:85151380184
SN - 0315-162X
VL - 50
SP - 504
EP - 511
JO - Journal of Rheumatology
JF - Journal of Rheumatology
IS - 4
ER -