Table I.
Baseline characteristics | OnabotulinumtoxinA (N = 735) |
---|---|
Male, n (%) | 394 (54) |
Age at index date, mean (SD) | 60.7 (13.9) |
Insurance type, n (%) | |
Commercial | 479 (65.2) |
Medicare | 256 (34.8) |
Patients with stroke diagnosis prior to first onabotulinumtoxinA claima (index date), n (%) | 542 (73.7) |
≤ 180 days | 181 (33.4) |
> 180 days | 361 (66.6) |
≤ 365 days | 420 (77.5) |
> 365 days | 122 (22.5) |
Charlson comorbidities within 12 months of index date, n (%) | |
Cerebrovascular diseaseb | 735 (100) |
Hemiplegiab | 694 (94.4) |
Diabetes without chronic complication | 214 (29.1) |
Peripheral vascular disease | 176 (23.9) |
Chronic pulmonary disease | 139 (18.9) |
Congestive heart failure | 128 (17.4) |
Diabetes with chronic complication | 65 (8.8) |
Any malignancy | 65 (8.8) |
Renal disease | 61 (8.3) |
Myocardial infarction | 60 (8.2) |
Mild liver disease | 32 (4.4) |
Dementia | 31 (4.2) |
Peptic ulcer disease | 16 (2.2) |
Rheumatic disease | 11 (1.5) |
Metastatic solid tumour | 9 (1.2) |
Moderate or severe liver disease | 3 (0.4) |
AIDS/HIV | 1 (0.1) |
For the remainder of patients (26%), it was not possible to confirm stroke diagnosis based on medical history despite diagnosis of post-stroke spasticity and, therefore, they were omitted from sensitivity analysis.
These components of the Charlson Comorbidity Index were also represented among the International Classification of Diseases, Tenth Revision, Clinical Modification (ICD-10-CM) Codes for inclusion in this study.
SD: standard deviation.