Table 2.
Relative Treatment Effects for LMWH/VKA and Placebo versus Apixaban§
| Initial LMWH/VKAa | 95% Confidence Interval | Extended Placebob | 95% Confidence Interval | Extended VKAsc | 95% Confidence Interval | |
|---|---|---|---|---|---|---|
| Relative risks | ||||||
| Recurrent VTE and VTE-related death | 1.18 | 0.83–1.66 | 5.33 | 3.02–9.40 | 0.42 | 0.16–1.06 |
| Major bleed | 3.26 | 1.84–5.79 | 2.07* | 0.38–11.24 | 7.7 | 1.09–76.40 |
| CRNM bleed | 2.09 | 1.66–2.63 | 0.78 | 0.43–1.40 | 3.84 | 1.55–9.38 |
| Other treatment discontinuation | 1.07§ | 0.85–1.35§ | - | 1.33 | 0.75–1.87 | |
*Absolute event rates for major bleed, apixaban: 0.0024, placebo: 0.0048
§The resulting risks for placebo and LMWH/VKA are detailed in the Additional file 2
Source:
aAMPLIFY [12]
bAMPLIFY-EXT [13]
cNMA (presented in the Additional file 2)
§Data on file: Secondary Analysis of AMPLIFY (CV185-056) to Support Apixaban Cost Effectiveness Modeling for the Indication of Treatment of Deep Vein Thrombosis and Pulmonary Embolism in Venous Thromboembolisim (OR APIX 025). 2014