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Apixaban for the prevention of venous thromboembolism in people ...

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5 COST EFFECTIVENESS<br />

5.1 ERG comment on manufacturer’s review <strong>of</strong> cost-effectiveness evidence<br />

5.1.1 State objective <strong>of</strong> cost effectiveness review. Provide description <strong>of</strong> manufacturers search<br />

strategy and comment on whe<strong>the</strong>r <strong>the</strong> search strategy was appropriate. If <strong>the</strong> manufacturer did<br />

not per<strong>for</strong>m a systematic review, was this appropriate?<br />

The objective was to per<strong>for</strong>m a systematic review <strong>of</strong> economic evaluations <strong>for</strong> <strong>in</strong>terventions <strong>for</strong> <strong>the</strong><br />

prophylaxis <strong>of</strong> <strong>venous</strong> <strong>thromboembolism</strong> (VTE) <strong>in</strong> patients undergo<strong>in</strong>g elective total knee and hip<br />

replacement.<br />

5.1.2 State <strong>the</strong> <strong>in</strong>clusion/exclusion criteria used <strong>in</strong> <strong>the</strong> study selection and comment on<br />

whe<strong>the</strong>r <strong>the</strong>y were appropriate.<br />

The <strong>in</strong>clusion criteria <strong>for</strong> <strong>the</strong> literature review were:<br />

Patients undergo<strong>in</strong>g hip and/or knee replacement or, <strong>in</strong> a mixed population, where <strong>in</strong><strong>for</strong>mation<br />

was reported specifically <strong>for</strong> <strong>the</strong> hip and/or knee replacement patient population.<br />

Graduated elastic compression stock<strong>in</strong>gs / anti-embolism stock<strong>in</strong>gs (GCS)<br />

Intermittent pneumatic compression (IPCD) devices<br />

Foot pumps or foot impulse devices (FID)<br />

Vena cava filters<br />

Aspir<strong>in</strong> or antiplatelet <strong>the</strong>rapy<br />

Low-dose unfractionated hepar<strong>in</strong> adm<strong>in</strong>istered subcutaneously (UFH)<br />

Low molecular weight hepar<strong>in</strong> (LMWH)<br />

The syn<strong>the</strong>tic pentasaccharide, Fondapar<strong>in</strong>ux<br />

Vitam<strong>in</strong> K Antagonists (For example, warfar<strong>in</strong>, coumar<strong>in</strong>)<br />

Early mobilisation<br />

Foot elevation<br />

Hydration<br />

New oral anticoagulants licensed dur<strong>in</strong>g <strong>the</strong> guidel<strong>in</strong>e development period (rivaroxaban and<br />

dabigatran)<br />

Papers not meet<strong>in</strong>g <strong>the</strong> <strong>in</strong>clusion criteria above or published <strong>in</strong> a language o<strong>the</strong>r than English were<br />

excluded.<br />

5.1.3 What studies were <strong>in</strong>cluded <strong>in</strong> <strong>the</strong> cost effectiveness review and what were excluded?<br />

Where appropriate, provide a table <strong>of</strong> identified studies. Please identify <strong>the</strong> most important cost<br />

effectiveness studies.<br />

Based on <strong>the</strong> search and <strong>the</strong> <strong>in</strong>clusion and exclusion criteria, <strong>the</strong> cost effectiveness review <strong>in</strong>cluded 96<br />

studies.In total 14 UK studies were <strong>in</strong>cluded:<br />

eight publications (Davies et al, 36 Davies and Saltzman, 37 Drummond et al, 38 Gordois et al, 39<br />

McCullagh et al 40 , Nicolaides and Bosanquet, 41 Wolowacz et al, 42 Wolowacz et al 43 ).<br />

three abstracts (Diamantopoulos, 44 Diamantopoulos, 45 Ryttberg 46 )<br />

three UK HTA documents (Dabigatran STA 47, 48 Rivaroxaban STA, 34, 49 NICE guidel<strong>in</strong>es 2010 3 ).<br />

33<br />

Copyright 2011 Queen’s Pr<strong>in</strong>ter and Controller <strong>of</strong> HMSO. All rights reserved.

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