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Journal of Healthcare Engineering
Volume 1 (2010), Issue 2, Pages 155-168
Research Article

A New Approach in the Design of High-Risk Infusion Technology

Robert Murphy1 and Steven Wilcox2

1Faculty of Engineering, Manukau Institute of Technology, Auckland, New Zealand
2Faculty of Advanced Technology, Glamorgan University, Pontypridd, UK

Copyright © 2010 Hindawi Publishing Corporation. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. L. Dougherty and S. E. Lister, Eds., The Royal Marsden Hospital Manual of Clinical Nursing Procedures, Wiley-Blackwell, Hoboken, 6th edition, 2004, 264.
  2. J. D. Bronzino, Ed., Medical Devices and Systems, Taylor & Francis, London, 3rd edition, 2006, 68–2.
  3. MDA London, Infusion Systems - Device Bulletin, DB 2003(02) March 2003, ISBN 1 84182 6898.
  4. British Standards Institution, Medical electrical equipment - particular requirements for the safety of infusion pumps and controllers, BS EN 60601-2-24:1998, BS 5724-2.124:1998, IEC 60601-2-24: 1998.
  5. Bath Institute of Medical Engineering,, accessed Sept. 2009.
  6. T. A. Neff, C. Fellmann, R. M. Fuechslin, A. C. Gerber, and M. Weiss, “The Panomat P-10 micro-volumetric infusion pump is suitable for continuous drug administration at minimal flow rates,” Can J Anaesth., vol. 49, pp. 1048–1052, 2002. View at Google Scholar
  7. M. Weiss, S. Gerber, R. M. Füchslin, and T. A. Neff, “Accurate continuous drug delivery at low infusion rate with a novel microvolumetric infusion pump (MIVP): pump design, evaluation and comparison to the current standard,” Anaesthesia, vol. 59, pp. 1133–1137, 2004. View at Google Scholar
  8. R. S. Murphy and S. J. Wilcox, “High risk infusions—accuracy compromised by changes in patient venous pressure,” Journal of Medical Engineering & Technology, vol. 33, no. 6, pp. 470–474, 2009. View at Google Scholar
  9. K. H. Krauskopf, J. Rauscher, and L. Brandt, “Disturbance of continuous, pump administration of cardiovascular drugs by hydrostatic pressure,” Der Anaesthesist, vol. 45, no. 5, pp. 449–52, 1996 May. View at Google Scholar
  10. H. Kern, A. Kuring, U. Redlich et al., “Downward movement of syringe pumps reduces syringe output,” Br J Anaesth, vol. 86, pp. 828–31, 2001. View at Google Scholar
  11. T. A. Neff, J. E. Fischer, G. Schulz, O. Baenziger, and M. Weiss, “Infusion pump performance with vertical displacement: effect of syringe pump and assembly type,” Intensive Care Med., vol. 27, no. 1, pp. 287–91, 2001 Jan. View at Google Scholar
  12. M. Weiss, M. I. Hug, T. Neff, and J. Fischer, “Syringe size and flow rate affect delivery from syringe pumps,” Can J Anaesth., vol. 47, no. 10, pp. 929–35, 2000 Oct. View at Google Scholar
  13. D. Murray, “Another central line complication: failure of inotrope delivery due to equipment incompatibility,” Anaesthesia, vol. 58, p. 715, 2003. View at Google Scholar
  14. T. A. Neff, J. Fischer, S. Fehr, O. Banziger, and M. Weiss, “Start-up delays of infusion syringe pumps,” Paediatr Anaesth, vol. 11, no. 5, pp. 561–565, 2001. View at Google Scholar
  15. M. Weiss, O. Baenziger, T. Neff, and S. Fanconi, “Influence of infusion line compliance on drug delivery rate during acute line loop formation,” Intensive Care Med., vol. 26, pp. 776–779, 2000. View at Google Scholar
  16. M. Weiss, T. Neff, A. C. Gerber, and J. Fischer, “Impact of infusion line compliance on syringe pump performance,” Paediatr Anaesth., vol. 10, pp. 595–599, 2000. View at Google Scholar
  17. R. M. Fuechslin, M. Weiss, R. Duenkel et al., United States Patent Nr 7,614,857 B2 Nov 2009 Assignee: Medinnovation AG Zurich (CH).