IDI - Irish Decontamination Institute...

IDI - Irish Decontamination Institute

NOTE: These WFHSS web archive pages are not maintained anymore. Please visit for current WFHSS affairs.
/ IDI - Irish Decontamination Institute / Publications / Periodicals / Central Service / Central Service Archive / Central Service 3/2007
Central Service - Issue 3/2007

Central Service - Issue 3/2007


WFHSS Congress


  • What's New in Standardisation: Instrument Disinfectants
  • Joint OEGSV/WFHSS Congress. Baden/Vienna, 3 - 5 May 2007
  • The Latest on Low-Temperature Sterilisation. Johnson & Johnson Satellite Symposium, 3 May 2007, Baden/Vienna
  • Sparkling Egg Award 2007. Awarded at the WFHSS Conference in Baden near Vienna
  • The 29th French National Sterilisation Meeting - Just Short of the Jubilee Mark. 25 - 26 April 2007, Lyon
  • Performance Requalification of Validated Cleaning and Disinfection Processes on Changing Process Chemicals. Supplementary Memorandum by the AKI on the Guideline for Validation and Routine Monitoring of Cleaning and Disinfection Processes for Heat-Resistant Medical Devices
  • Patchwork Europe: Still no Uniform Regulations for Decontamination of Medical Devices
  • Dr. Meinrad Lugan New Chairman of BVMed Board of Directors


T. Friedrich, K. Roth, J. Gauer, P. Heeg:
Binding Properties and Other Important Considerations when Interpreting Results Obtained with the Radionuclide Method
(Zentr Steril 2007; 15 (3): 191-200)

The stability of the Tc99m-albumin complex, in addition to standardisation of the measured values, is a decisive factor when evaluating the results of the radionuclide method (RNM).
Methods and Aim:
On using specific protein precipitation methods and varying the temperature, acidity, alkalinity and combinations of the latter parameters, it is possible to identify these binding characteristics. Testing also included an investigation of the physical conditions related to the gamma camera: homogeneity, measurement constancy and temporal parameters.
Radionuclide-albumin binding is shown to be largely stable, even in worst-case scenarios. Only minor fluctuations in gamma camera measurements are noted for repeat measurements.
Key Words
radionuclide method, binding stability, verification of cleaning

S. Terzaki*, K. Amazian, L. Dhidah, S. Sekkat, T. Abdelmoumène, M. Njah, J. Fabry und Mitgleider des NosoMed network:
Quality of the Organization of Sterilization: an Audit in Euro-Mediterranean Hospitals
(Zentr Steril 2007; 15 (3): 201-211)

Management of sterilization in a health care facility is a sensitive aspect of infection control (IC) and of the quality of care in many countries. In the context of NosoMed, an EU-funded Euro-Mediterranean project, an audit tool was developed to assess the quality of this function in the hospitals of this region. It was tested in different hospitals in Algeria, Egypt, Morocco and Tunisia.
The observation tool was designed by IC practitioners having been trained in sterilization methods. It was tested in 21 hospitals who had volunteered. Observation and data collection were carried out by an external observer who was trained in sterilization management. International (France, UK) and national official recommendations were used where available. Data collection covered hospital characteristics, sterilization scheme, staff, premises, equipment, processes and quality control.
Among the 21 hospitals audited, 14 had an exclusive central sterilization unit (six in Egypt, seven in Morocco and one in Tunisia). For some of the items, the results conformed to the recommendations, particularly with respect to the availability of trained managers and staff, the practice of regular quality control and with respect to the sterilization cycle.
Some aspects, however, were insufficient and should be improved. These concerned mainly architecture and equipment:
1. insufficient barrier between dirty, clean and sterile areas in 3 SU
2. insufficient space for cleaning of trolleys and maintenance of equipment in 4 US
3. lack of air filtration, pressure gradient and even "natural ventilation" in most facilities; condition of sterilizers: 16/65 (25%) of the sterilizers in use being classified as insufficiently reliable; staff clothing for reception and transport; frequent overloading of sterilizers; unprotected storage of sterile items: storage in cupboards or containers in 4 CSSDs only.
The NosoMed audit tool for sterilization quality was globally found to be easy to use. The results from Egypt show that NICC support (by training) succeeded in implementing recommended procedures, but that hospitals still have to improve their physical environment and their equipment. The Euro-Mediterranean countries need more support in training and improvement in the equipment provided and implementation of recommended procedures.
Key Words
sterilisation, data collection, infection control, Euro-Mediterranean

Quality Management in the CSSD - Standard Surgical Instruments (4):
Visual Inspection and Functional Testing of Standard Forceps


Requirements for Construction or Conversion of a Hospital Central Sterile Supply Department

Information on this page provided with kind permission of: mhp-verlag GmbH
Address: Marktplatz 13
65183 Wiesbaden
Phone: +49-(0)611-50593 0
Fax: +49-(0)611-50593 11

mhp stands for publications in medicine, hygiene and prevention. For more than 20 years, the mhp publishing house has devoted itself to supporting developments aiming for a better standard of hygiene and infection control in hospitals and other medical facilities.

Free Access to Central Service E-Paper
Since 2008 Central Service has also been available as electronic E-Paper version. Subscriptions are possible to the print issue only, the online E-Paper issue only, or as a combined subscription to both. A free E-Paper version of back issues of Central Service is now available for subscribers to the print issue (starting from Volume 16, 2008). Please contact to order your free E-Paper access code.