Air Quality in IVF laboratories is far more critical than in any other medical room.
30 May 2010
Air Quality in IVF laboratories is far more critical than in any other medical room.
Growing embryos can be very frustrating. Sometimes we just can't find any logical explanation why rates of success are dropping. Embryos are extremely sensitive. A deep concern should be involved when they are exposed to lab environment.
Here are some points for concern:
VOC - is responsible for lack of success during the first years of any lab life. "Off-gas" process along with a proper ventilation pattern could dramatically reduce the negative effects of VOC on embryo survival.
Ultra Violet Radiation: fluorescent lamps, the microscope lamp, sun light are all "contaminated" with UV light spectrum. UV is an excellent disinfectant, but we do not want to disinfect our embryos... Replacing the lamps with truly "UV free" lamps can solve this problem.
CO2 quality: compressed gases contain dangerous levels of organic (VOC) contamination. Use of pre –filtered CO2 VOC free, is essential.
Magnetic flux: Is probably responsible for many failures in the" In vitro fertilization" process. Modern equipment contains heavy electronic circuits. Electronic heaters and fans increase dramatically the magnetic flux in incubators and on laminar work stations. Studies showed that embryos in their first 24 hours are most sensitive to magnetic radiation from heated work surfaces and incubators. The DNA might be damaged at as low as 0.1 A/M magnetic field , while the magnetic flux inside incubators reaches levels as strong as 10 A/M. Until manufacturers will be more aware of that problem you can use a" Safety Box" that stops the magnetic flux and gives embryos a better chance to live.
Bio-Safe shields embryos against the strong magnetic flux found in most IVF equipment.
A major source of disease and contamination in hospitals and clinics lays in the air-conditioning systems and in the quality of air. Sore throat, red eyes, headaches, “lack of air syndrome" acquired diseases, are all part of the same problem.
Airborne concentrations of microbes and nano particles pose a hazard both to patients and staff. In many hospitals this source of contamination looks like a new, unfamiliar science. A simple air sample usually reveals contamination that has been associated with human health problems in indoor environments.
Base maintenance personnel have no regular access to provide periodic professional disease preventive maintenance (PM) on the hospital Heating, Ventilation and Air Conditioning (HVAC) systems.
Periodical examination and tests for "IVF CLINICS"
1. Air quality measurements
1.1. monitoring of air cleanliness according to ISO14644-1;
2. Measuring and evaluating the effective number of air changes in the room
2.1. evaluating the tightness factor;
3. Evaluating sterile qualities of the room and surroundings
3.1. evaluating airborne microorganisms in the room;
4. Physical environment hazards
4.1. monitoring the intensity of electromagnetic fields in the room;
These series of tests, which last no more than a few hours, provide a clear and accurate picture of the room and of the maintenance quality. There after one can determine what measures have to be taken in order to bring the room condition to an acceptable level. These series of tests determine the Room Grade according to the EN GMP.
We can learn a lot from monitoring the air for small particles.
When one has the proper measuring devices the monitoring is quick and gives a clear picture of the condition of a room. Following are the cases in which it is recommended to monitor particles in the air:
• In a new room: "particles’ counting" is required for an immediate feedback regarding the quality of the air system.
• During renovation and maintenance monitoring should be repeatedly done to make sure that the job is improving the air quality and not vice versa.
• During adjusting "air changes per hour", repeated "particles’counting" monitoring is to be done to regulate the optimum number of changes required.
In the following table, the max. number of particles’ concentration according to ISO 14644-1, sorted by size, is shown. The common levels for hospitals are
Class 5: IVF laboratories, operating theaters - orthopedics (bones), open chest and cranium;
Class 6 : other operating theaters ;
Class 7 : intensive care units, sterile material storage rooms, air locks and sterile corridors and rooms.
The "Tightness Factor" (T.F) measurements for medical clean rooms
Keeping up the tightness factor dramatically improves the performance of medical clean rooms, improves the filtration process, the humidity and temperature control.
When tightness is poor, every opening of the door, little cracks or holes cause a purge of contaminated air into the room.
Standard tightness factor is reached in a room where pressure loss rate from 160 pascal to 60 pascal lasts more then 12 seconds . In this case the outside air penetration rate is smaller than 0.5 percent of the room volume in one minute and the filtration recovery system can cope with this amount of contamination and keep the room clean.
A clean room is a room that maintains a high tightness factor and the rate of filtration is higher than the rate of contamination per minute
Air flow pattern
Clean air should reach the operation field in the shortest and most direct way. It should not cross through equipment or stuff. It should always move in the room from up to down. Any other flow pattern might cause cross contamination.
Positive Ion monitoring
Positive ions in the air are a common source of stuff and patients’ complaints of head ackes, feel of lack of air, sore throat and running eyes. The sources of ions are the ionization devices that are sometimes part of the air filtration systems.
Common causes of contamination in clinics
• The corridor that connects the operating rooms is not treated as a clean room, thus every door opening into the operating room causes a flow of contaminated air into the room;
• Medical and assistance stuff do not fulfill the hygiene instructions for operating rooms;
• Doors are left partially open during and after operations;
• Shuttting down the air-conditioning system ("because it is too cold") actually stops the filtering process;
• Servicing of the AHU and replacement of filters done by an unqualified technician and without strict regulations causes an enormous amount of dirt entering the room;
• Each room should have its own AHU. A common AHU might transfer contamination from one room to another. Furthermore, using a common AHU might influence the overpressure. Opening the door of one room brings down the overpressure from all other rooms;
• Without the ability to regularly monitor concentrations of particles in the air one cannot really determine when to change filters or if the room is a "clean" room.
• The source for fresh air is critical to the quality of the clean room. Hospitals have a hostile environment and contaminated air. The source for fresh air should be from the highest point possible and far from all obnoxious toxic contaminated discharges emitted by other departments.
• The HVAC system and tunnels are natural places for growing microorganism. They are the second most important cause for disease spread in hospitals. The first cause is the stuff itself. Decontamination measures should be done several times a year to reduce the risk.
Effective Decontamination methods for sterile rooms
Ozone ( O3 ) in gas state is a highly effective decontamination means for the room surface and HVAC systems. The gas ozone reaches every little corner and crack that is unreachable or has been skipped by the cleaning team. In the attached photos you can see the results of air samples for bacteria presence in the air before and after the ozone treatment .
About the Author
Mr. Lehrmann has earned a nationwide reputation in Israel designing and implementing new methods and standards for CleanRooms
He holds an exclusive international patent for ‘Gas-tight Ventilation System’ and this, together with his many years of experience constructing gas-tight buildings, gained him the CTCB "PROFESSIONAL certification.
Mr. Lehmann applied his unique knowledge in the design and operation of ‘clean rooms’ to hospital operating theatres, IVF laboratories and isolation rooms throughout Israel. In fact he has set new standards in his approach to controlling and maintaining clean air – particularly with regard to the "Tightness Factor" parameter and the linkage between ‘Tightness and Air quality’.
As a result of his experience and many innovations, Mr. Lehrmann was invited to represent his work at the prestigious ‘Clean-Room Contamination Control Technology’ conference recently held at the world trade centre in Boston, MA, USA.
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