Medical environments, are a place where Volatile Organic Compounds (VOCs) need to be monitored, whether it be to meet regulations such as the Human Fertilisation and Embryology (HFEA) regulations for air quality in tissue laboratories, or ensuring that harmful gases used to sterilise tools and equipment used in hospitals has been removed to permitted levels
A common gas for sterilisation of equipment destined for medical usage is Ethylene Oxide (EtO) Ethylene Oxide has a EH40 Time weighted average of 1 part per million (PPM) and is a capable of causing cancer and/or heritable genetic damage and also can be absorbed through the skin for which there are concerns that dermal absorption will lead to systemic toxicity.
For many medical devices, sterilisation with ethylene oxide may be the only method that effectively sterilises and does not damage the device during the sterilisation process. Medical devices made from certain polymers (plastic or resin), metals, or glass, or that have multiple layers of packaging or hard-to-reach places (for example, catheters) are likely to be sterilised with ethylene oxide. About fifty percent of all sterile medical devices in the U.S. are sterilised with ethylene oxide. The types of devices that are sterilised with ethylene oxide range from devices used in general health care practices such as wound dressings to more specialised devices used to treat specific areas of the body e.g. stents.
For ethylene oxide sterilisation, two voluntary consensus standards exist, these are ANSI AAMI ISO 11135:2014 and ANSI AAMI ISO 10993-7:2008(R)2012. These standards describe how to develop, validate, and control ethylene oxide sterilisation processes for medical devices and the acceptable levels of residual left on a device after it has undergone sterilisation. These standards help ensure levels of ethylene oxide on medical devices are within safe limits since long-term and occupational exposure to ethylene oxide has been linked to cancer.