Abstract
Objective:
The objective for the research was to evaluate the direct healthcare costs for Crohn’s disease (CD) patients categorized by adherence status.
Methods:
Adult patients with ≥1 claim for infliximab and ≥2 claims for CD who were continuously insured for 12 months before and after their first infliximab infusion (index date) were identified in a 2006–2009 US managed care database. Patients were excluded if they had rheumatoid arthritis claims, received infliximab billed as a pharmacy benefit, or received another biologic drug. Patients were categorized as being either adherent or intermittently adherent to infliximab using a pre-defined algorithm. Total and component direct costs, CD-related costs, rates of surgery, and days of hospitalization were estimated for the 360-day post-index period. Propensity weighted generalized linear models were used to adjust the cost estimates for potential confounding variables.
Results:
The total propensity weighted cost for infliximab adherent patients was $40,425 (95% CI = [$38,686, $42,242]), compared to $41,082 (95% CI = [$38,163, $44,223]) for the intermittently adherent (p = 0.71). However, adherent patients had lower total direct medical costs, exclusive of infliximab, that were $13,097 (95% CI = [$12,141, $14,127]) compared with $20,068 (95% CI = [$17,676, $22,784]) for intermittently adherent patients as a result of substantially lower hospital and outpatient costs (p < 0.0001).
Conclusions:
Greater drug-related costs for infliximab adherent patients were offset by lower costs from hospitalization and outpatient visits. These findings indicate that adherent patients have improved clinical outcomes, at a similar aggregate cost, than patients who are only intermittently adherent to therapy.
Transparency
Declaration of funding
Research funding was provided by Janssen Scientific Affairs, LLC.
Declaration of financial/other relationships
Employees of Janssen Scientific Affairs, LLC (JSA) participated in the design of the study, the analysis of the data, and the preparation of the paper. CK and TS received research funding from JSA. BF was a paid study consultant who has received research funding from JSA and GW and WO are employees of Janssen a member of Johnson & Johnson family of companies. JME peer reviewers on this manuscript have no relevant financial or other relationships to disclose.
Acknowledgments
The authors thank Tecca Wright for assistance in the preparation of the manuscript. This manuscript was presented in part as an oral presentation at the International Society for Pharmacoeconomics & Outcomes Research Annual Meeting, June 2–6, 2012, Washington, DC.