Incremental economic and clinical burden of illness among adults with chronic inflammatory demyelinating polyneuropathy in the United States


Topic:

Other

Poster Number: P380

Author(s):

Cecile Blein, PhD, argenx, Swapna Karkare, MS, argenx, Arash Mahajerin, MD, MSCR, argenx, Rucha Kulkarni, MPH, ZS Associates, Tania Banerji, MPH, ZS Associates, Namith Dharani, ZS Associates, Aazim Ajmal Shaukathali, ZS Associates, Anthony Nguyen, PhD, ZS Associates, Amit Goyal, MBA, ZS Associates

Objective: To evaluate the incremental economic and clinical burden among patients with chronic inflammatory demyelinating polyneuropathy (CIDP) in the United States (US) compared to matched controls without CIDP.

Methods: This retrospective cohort study was conducted using Optum Market Clarity data from January 2016 – December 2023. CIDP patients were selected based on: (1) ≥2 claims with CIDP, ≥30-≤365 days apart (first claim is index), (2) ≥1 nerve conduction test ≤90 days before or after index, with ≥1 CIDP claim following it within 365 days, (3) continuous enrollment 1 year pre- and 2 years post-index date. CIDP patients were 1:3 propensity score (PS)-matched to controls without CIDP. Outcomes, including all-cause healthcare resource utilization (HCRU) and costs, and clinical characteristics over the two-year follow-up period were compared between cohorts using generalized linear models.

Results: Among 1,435 CIDP patients and 4,305 controls, CIDP patients had over 3x greater mean all-cause healthcare costs over a two-year follow-up period ($170,275 vs. $49,486; p<0.001), primarily driven by prescription and drug administration cost ($93,126 vs. $11,529; p<0.001). CIDP cohort also had more HCRU across all care settings, with outpatient care being the largest contributor. CIDP patients more frequently utilized CIDP-specific treatments like steroids (62% vs. 43%), immunoglobulins (54% vs 0%) and other medications including anti-convulsants (58% vs. 20%), opioids (53% vs. 38%) and anti-depressants (48% vs. 30%) relative to controls (all p<0.0001) over the follow-up. CIDP patients also had a higher comorbidity burden during follow-up, with increased prevalence of neuropathic pain (100% vs 41%), back pain (71% vs. 45%), osteoarthritis (54% vs 47%), sleep disorders (46% vs 33%), peripheral vascular disease (34% vs 24%) and cerebrovascular disease (29% vs 18%). Conclusions: Based on US claims data, CIDP has a substantial incremental economic and clinical burden compared to matched controls without CIDP.