Table 1.
Baseline demographics and clinical characteristics | Overall (N = 690) | Patients aged 18–64 yr (n = 634) | Patients aged ≥65 yr (n = 56) |
Age, yr, mean (SD) | 48.0 (14.7) | 45.7 (12.8) | 74.4 (7.1) |
Sex, n (%) | |||
Female | 604 (87.5) | 563 (88.8) | 41 (73.2) |
Male | 86 (12.5) | 71 (11.2) | 15 (26.8) |
Charlson Comorbidity Index,a mean (SD) | 0.5 (1.0) | 0.5 (1.0) | 1.1 (1.5) |
Initial dose of prucalopride, mg, mean (SD) | 1.9 (0.3) | 1.9 (0.3) | 1.8 (0.4) |
1.0 mg, n (%) | 76 (11.0) | 66 (10.4) | 10 (17.9) |
2.0 mg, n (%) | 614 (89.0) | 568 (89.6) | 46 (82.1) |
Any constipation-related comparator treatment any time before the index date,b n (%) | 436 (63.2) | 399 (62.9) | 37 (66.1) |
Index drugs,c n (%) | |||
Prucalopride monotherapy | 507 (73.5) | 464 (73.2) | 43 (76.8) |
Prucalopride combination therapy | 183 (26.5) | 170 (26.8) | 13 (23.2) |
Prucalopride and lubiprostone | 26 (3.8) | 24 (3.8) | 2 (3.6) |
Prucalopride and linaclotide | 118 (17.1) | 110 (17.4) | 8 (14.3) |
Prucalopride and plecanatide | 28 (4.1) | 26 (4.1) | 2 (3.6) |
Prucalopride and >1 other constipation-related prescription medication | 11 (1.6) | 10 (1.6) | 1 (1.8) |
The Charlson Comorbidity Index was defined based on criteria by Charlson et al (21) and adapted by Quan et al (22).
The index date was defined as the first prucalopride prescription fill date. Constipation-related comparator medications included lubiprostone, linaclotide, or plecanatide.
Constipation-related prescription medications taken concurrently with the index drug included lubiprostone, linaclotide, or plecanatide.