https://issuesinsights.com/2020/04/12/one-more-regulation-for-reform-to-keep-you-safe-during-this-pandemic/
As the deadly coronavirus takes its toll on countless families, healthcare workers are doing their best to get patients the medicine and equipment they desperately need.
But medical devices can do more harm than good unless properly sterilized and disinfected by applying agents such as Ethylene Oxide (EtO) gas. And, because of deeply flawed federal studies and subsequent state and local actions based on this shoddy science, production of sterilizing agents such as EtO has been put on the backburner. Policymakers must examine all the evidence at hand and keep patients safe from COVID-19 contamination.
As any of the nearly 500,000 coronavirus patients in the U.S. can attest, COVID-19 is highly contagious and can spread easily on shared surfaces, making sterilization critical. The Advanced Medical Technology Association notes, “Ethylene Oxide (EtO) gas is the most common way to sterilize medical devices, a process which is critical for preventing infections and ensuring patients have safe surgeries and medical treatments…For many medical devices, due to their size, shape, complexity or material composition, EtO is the only option for sterilization.”
Hospitals need ample supplies of sterilized equipment now more than ever. But hospitals face the prospect of shortages due to irresponsible Environmental Protection Agency (EPA) risk reporting.
The culprit behind the shortage and misinformation is an obscure research program within the agency called the Integrated Risk Information System (IRIS) which monitors the risks associated with a host of chemicals and issues reports on toxicity.
In 2016, IRIS found that EtOs start to pose harm to human health at the infinitesimally low level of 100 parts per quadrillion, or approximately 19,000 times lower than the amount of EtO found in the human body.