Variable | Risk ratio | 95% CI | P value |
All-cause hospitalisations* | |||
Per 1000 DMT dispensations | 0.994 | 0.992 to 0.996 | <0.0001 |
Calendar year | 0.978 | 0.974 to 0.983 | <0.0001 |
MS-specific hospitalisations* | |||
Per 1000 DMT dispensations | 0.909 | 0.880 to 0.938 | <0.0001 |
Calendar year | 0.940 | 0.924 to 0.957 | <0.0001 |
All-cause hospitalisations† | 1.000 | 1.000 to 1.000 | 0.090 |
All-cause mean length of stay (days)‡ | |||
Per 1000 DMT dispensations | 1.077 | 1.024 to 1.132 | 0.004 |
Calendar year | 0.999 | 0.993 to 1.005 | 0.781 |
All-cause physician claims* | |||
Per 1000 DMT dispensations | 1.006 | 0.990 to 1.022 | 0.477 |
Calendar year | 0.982 | 0.977 to 0.987 | <0.0001 |
MS-specific physician claims* | |||
Per 1000 DMT dispensations | 0.962 | 0.910 to 1.016 | 0.165 |
Calendar year | 0.954 | 0.935 to 0.975 | <0.0001 |
*Negative binomial regression fitted with generalised estimating equation (GEE).
†Adjusted for all-cause hospitalisations in the Saskatchewan general population to account for changes in hospitalisation trends.
‡Poisson regression fitted with GEE.
DMT, disease-modifying therapy; MS, multiple sclerosis.