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European Market Report for Infusion Pumps 2017 - MedCore

European Market Report for Infusion Pumps 2017 - MedCore

  • August 2017
  • 255 pages
  • ID: 5076663
  • Format: PDF
  • By iData Research, Inc.


Table of Contents

General Report Contents
- Market Analyses include: Unit Sales, ASPs, Market Value & Growth Trends
- Market Drivers & Limiters for each chapter segment
- Competitive Analysis for each chapter segment
- Section on recent mergers & acquisitions

When patients begin to receive medical treatment, they may require an infusion of fluids at some point. These fluids can contain medication for disease management or pain control, and/or nutrients to compensate for a deficiency, facilitating a faster recovery. Before infusion pumps, fluids would be infused by using a bag and an intravenous (IV) set that used the force of gravity to introduce the fluids into the vasculature through a drip chamber. This was commonly referred to as gravity drip.

While this method is effective in administering fluids, it is not always practical for several reasons. Fluids administered via the gravity method have a maximum rate of infusion that may not be ideal when large volumes of fluid need to be infused. Gravity pumps also have a minimum infusion rate that may be too large for certain types of medications. Finally, infusion rates may have to vary depending on the time of day; maintaining an acceptable degree of accuracy with a gravity drip can be difficult.

Because of these gravity drip method drawbacks, infusion pumps were introduced and have been used in some capacity since the early 20th century. Since then, infusion pumps have become the dominant method of fluid administration. Several specific infusion pump designs have branched off in order to manage specific needs and concerns during medical treatment.

While the use of pumps has provided the added benefit of increasing accuracy, recurrent hardware and software problems have led to concerns over patient safety during infusions. Several warnings of product recalls have been issued that led to the replacement of all pumps installed by a leading manufacturer and cessation of new pump sales by another leading supplier.
The Committee for Medicinal Products for Human Use (CHMP), the division of the European Medicines Agency’s committee responsible for elaborating the agency’s opinions on all issues regarding medicinal products for human use, has a report outlining key areas that need to be addressed in order to improve infusion processes and devices.

This market includes large volume, syringe, electronic ambulatory and disposable ambulatory infusion pump segments. Growth in the total market will be driven primarily by increases in unit sales of electronic ambulatory infusion pumps which have a higher than average ASP. Market growth will be hindered by overall reduction in ASP as a result of intensified competition for less frequent tenders.


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