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Impact of the Adalimumab Patient Support Program on Clinical Outcomes in Ankylosing Spondylitis: Results from the COMPANION Study.
Bessette, Louis; Lebovic, Gerald; Millson, Brad; Charland, Katia; Donepudi, Krishna; Gaetano, Tania; Remple, Valencia; Latour, Martin G; Gazel, Sandra; Laliberté, Marie-Claude; Thorne, Carter.
Affiliation
  • Bessette L; Department of Medicine, Laval University, Quebec, QC, Canada. louis.bessette@crchudequebec.ulaval.ca.
  • Lebovic G; Applied Health Research Centre, St. Michael's Hospital, Toronto, ON, Canada.
  • Millson B; Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, ON, Canada.
  • Charland K; QuintilesIMS, Kirkland, Quebec, Canada.
  • Donepudi K; QuintilesIMS, Kirkland, Quebec, Canada.
  • Gaetano T; QuintilesIMS, Kirkland, Quebec, Canada.
  • Remple V; AbbVie Corporation, St. Laurent, Quebec, Canada.
  • Latour MG; AbbVie Corporation, St. Laurent, Quebec, Canada.
  • Gazel S; AbbVie Corporation, St. Laurent, Quebec, Canada.
  • Laliberté MC; AbbVie Corporation, St. Laurent, Quebec, Canada.
  • Thorne C; AbbVie Corporation, St. Laurent, Quebec, Canada.
Rheumatol Ther ; 5(1): 75-85, 2018 Jun.
Article in En | MEDLINE | ID: mdl-29633196
INTRODUCTION: Adalimumab (ADA) is a tumor necrosis factor (TNF)-alpha inhibitor indicated for the treatment of inflammatory autoimmune diseases, including ankylosing spondylitis (AS). Patients receiving ADA in Canada are eligible to enroll in the AbbVie Care™ patient support program (AC-PSP), which provides personalized services, including care coach calls (CCCs). We estimated the likelihood of controlled disease in a cohort of AS patients treated with ADA enrolled in the AC-PSP and who received CCCs versus those who did not. METHODS: A longitudinal analysis using de-identified aggregate-level data collected through the AC-PSP was performed. A probabilistic matching algorithm was used to link patient-level records from the AC-PSP database to records from the QuintilesIMS longitudinal prescription transactions database. Patients were indexed on the date of their first prescription of ADA between January 2010 and October 2015. The AC-PSP database included patient assessments of the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI), a measure of disease activity. Eligible patients had a baseline BASDAI assessment performed between 90 days before and 30 days after the index date, and a follow-up BASDAI assessment 6-18 months later. Poisson regression was used to estimate the adjusted relative risk (RR) of controlled disease (BASDAI < 4) at the time of follow-up, comparing patients who received CCCs with those who did not. RESULTS: In total 249 AS patients met eligibility criteria, and 123 (49%) received CCCs. Of the 249 patients, 184 (74%) had controlled disease (BASDAI < 4) at follow-up assessment, 98 (80%) in the CCC group and 86 (68%) in the no CCC group. Multivariable regression analysis demonstrated a 23% increased likelihood of controlled disease in patients who received CCCs relative to those who did not (RR = 1.23; 95% confidence interval, 1.06-1.42; p = 0.0055). CONCLUSION: AS patients receiving tailored services through the AC-PSP in the form of CCCs have an increased likelihood of controlled disease within 6-18 months. FUNDING: AbbVie.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Etiology_studies / Prognostic_studies Language: En Journal: Rheumatol Ther Year: 2018 Type: Article Affiliation country: Canada

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Etiology_studies / Prognostic_studies Language: En Journal: Rheumatol Ther Year: 2018 Type: Article Affiliation country: Canada