DEMOGRAPHICS, CLINICAL CHARACTERISTICS, AND TREATMENT PATTERNS OF PATIENTS NEWLY STARTED ON PROSTACYCLIN THERAPY FOR PULMONARY ARTERIAL HYPERTENSION
Author(s)
Rotella P1, Schneider G1, Raspa S2, Berger A1, Pruett J2, Murphy B1, Lickert C2, Drake W2
1Evidera, Lexington, MA, USA, 2Actelion Pharmaceuticals, Inc., South San Francisco, CA, USA
OBJECTIVES: Describe demographics, clinical characteristics and treatment patterns (i.e., discontinuation, switching, or augmentation) of patients with pulmonary arterial hypertension (PAH) initiating prostacyclin (PGI2) therapy. METHODS: Using Truven® Commercial and Medicare Databases (2010–2014), two non-mutually exclusive cohorts were constituted. The first consisted of initiators of parenteral PGI2 (P-PGI2); the second, non-parenteral PGI2 (NP-PGI2). All patients were required to have evidence of PAH (i.e., ≥1 claims with a PAH diagnosis or ≥1 pharmacy claims for PAH-specific medications). Demographics and clinical characteristics were assessed during the three months prior to PGI2 initiation. Treatment patterns were assessed until switch/discontinuation, or end of follow-up. RESULTS: Of the 12,306 PAH patients identified during the study period, 1,569 (12.7%) were new initiators of PGI2 (755 [6.1%] for P-PGI2 and 1,003 [8.2%] for NP-PGI2). Approximately 70% of each cohort was female. P-PGI2 patients were nominally younger than NP-PGI2 patients (54.2 vs. 59.4 years), yet, had more comorbidities, hospitalizations, emergency room visits and mean (standard deviation [SD]) PAH-related medical costs than NP-PGI2 patients ($46,038 [$72,208] vs. $28,210 [$58,386]) during the three months before PGI2 initiation. P-PGI2 patients had less other PAH medication use than NP-PGI2 patients prior to PGI2 initiation (43% vs. 67%). Twenty-seven percent and 19% of P-PGI2 and NP-PGI2 patients, respectively, discontinued initial PGI2; mean (SD) weeks to discontinuation was 22 (35) and 20 (23). Only 7% of P-PGI2 and 11% of NP-PGI2 patients switched; mean (SD) weeks to switch was approximately 8 (12.5) in both groups. Augmentation with another PAH medication occurred among 36% and 50% of P-PGI2 and NP-PGI2 patients, respectively; mean (SD) weeks to augmentation were 7 (15) and 3 (8). CONCLUSIONS: Use of other PAH therapies prior to PGI2 is common, particularly among NP-PGI2. Our findings suggest that parenteral PGI2 may be reserved for more severe PAH patients.
Conference/Value in Health Info
2015-11, ISPOR Europe 2015, Milan, Italy
Value in Health, Vol. 18, No. 7 (November 2015)
Code
PCV32
Topic
Epidemiology & Public Health
Topic Subcategory
Safety & Pharmacoepidemiology
Disease
Cardiovascular Disorders, Respiratory-Related Disorders