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1. Executive Summary
2. Introduction
3. Healthcare Structures in Europe
- 3.1 Belgium and the Netherlands
- 3.2 France
- 3.3 Germany
- 3.4 Italy
- 3.5 United Kingdom
- 3.6 Scandinavia
- 3.7 Spain
4. Hospital Financing and the shift to DRG-based reimbursement for services
- 4.1 Benelux
- Legislative reform and business implications
- 4.2 France
- Legislative reform and business implications
- 4.3 Germany
- Legislative reform and business implications
- 4.4 Italy
- Legislative reform and business implications
- 4.5 United Kingdom
- Legislative reform and business implications
- 4.6 Sweden
- Legislative reform and business implications
5. The impact of DRGs on reimbursement in selected disease/treatment areas
- 5.1 Implantable cardioverter defibrillators
- 5.1.1 ICD therapy in the treatment of arrhythmia and complications
- 5.1.2 The role of ICDs in prophylaxis of SCD
- 5.1.3. Cost-effectiveness assessments
- 5.1.4 DRG and reimbursement impact on ICD implantation rates-US Recommendations
- 5.1.5. European ICD Implant Rates
- 5.2 Drug-Eluting Stents
- 5.2.1 Creation of new DRGs to cover stent reimbursement and encourage utilization
- 5.3 End stage renal disease (ESRD)
- 5.3.1 Prevalence and socio-economic aspects of chronic kidney disease
- 5.3.2 Home vs Hospital Haemodialysis – an assessment of UK guidelines
6. Health Technology Assessment (HTA) – its expanding role in medical device diffusion.
- 6.1 HTA activity in Europe
- 6.1.1 Benelux
- 6.1.2 France
- 6.1.3 Germany
- 6.1.4 Italy
- 6.1.5 Spain
- 6.1.6 United Kingdom
- 6.1.7 Scandinavia
- 6.2 Relevant case studies – The NICE approach and impact
7. The anticipated impact of DRG implementation in Germany
- 7.1 DRGs in the USA and Australia – Any lessons to be learnt for device manufacturers?
8. Corporate Strategies – Positioning in an era of increasing reform |