The author describes how toilet flushes aerosolize germs sending them airborne to soar around and infect their next victim(s) because bathrooms are designed backwards. Learn novel ways to control and clean bathroom air to help control airborne disease transmission problems. So feel free to hold your nose as you learn about how you can help protect people’s health within your client’s buildings.
M ethicillin Resistant Staphylococcus Aureus (MRSA), Clostridium-Difficile (C-Difficile), and Norovirus (NV) are floating around your hospital and won’t stop infecting your patients, staff, and even visitors with those dreaded hospital-acquired infections (HAIs). Your infection control people have hit a brick wall and can’t stop the infection rates nor prevent periodic outbreaks that can last several months. The hospital’s CFO is tearing his hair out because major insurance companies and Medicaid/Medicare are no longer reimbursing for HAIs. Ouch. By focusing on what impact HVAC systems, pressurization, filtration, and sterilization technologies can have on airborne germs, you can proactively (or reactively) address these problems. There are rather simple explanations to previously flummoxing airborne disease problems, so relax and read on.
AIRBORNE MRSA, C-DIFFICILE, AND NOROVIRUS: THE FEARSOME THREESOMEThe pestilences swarming hospitals worldwide are ever-mutating super-bacteria like MRSA and C-Diff. NV is a highly infective virion (virus), and studies have shown that you only need one NV virion to get infected. Many infection prevention specialists continue to be thwarted in reducing these pathogen’s infection rates because the current guidelines are to wash your hands and to wear gloves and a gown in order to have protected contact with patients, all of which do not directly address airborne disease transmission.
The critical questions to slice and dice on airborne disease transmission are:
- How do infected humans shed bacteria and virions?
- How do germs like MRSA, C-Diff, and NV become airborne?
- How do humans breathe in these germs to make them sick?
- How do toilet flushes aerosolize these germs?
- How do airborne germs move between rooms?
- What technologies and strategies are available to help drive down airborne infections rates?
WASH OR SANITIZE YOUR HANDSOn June 3, 2009, I briefed1 the EPA’s Federal Interagency Committee on Indoor Air Quality2 and showed how the pandemic H1N1 airborne influenza flu virions can easily land in your lungs to replicate and infect you. I minimized the importance of handwashing thusly: “No matter how sterile your hands are, you’ll still be fully exposed to airborne Influenza virions entering and depositing into your lungs to cause disease.”
This controversial position was (and still is) contrary to the Center for Disease Control’s (CDC) advice that washing or sanitizing your hands is the best method to prevent yourself from being infected. A CNN reporter pressed the CDC to produce the science backing their handwashing/sanitizing recommendation and forced the CDC to admit that handwashing to prevent influenza flu transmission was not supported by any peer-reviewed, published papers anywhere3. Handwashing for preventing staph infections already was weakening in 2008 when Professor Beggs showed4 that vigilant hand washing may only lower staph infections by around 20%, and additional handwashing protocols have less additional disease reduction impact. This leaves airborne transmission as the next empire to conquer.
HOW MRSA, C-DIFF, AND NV GET AIRBORNEMRSA, C-Diff, and NV are not traditional respiratory diseases, which are easily coughed or sneezed out, sending them airborne. Since C-Diff and NV are primarily intestinal diseases, they cause vomiting and diarrhea (think of it as reverse vomiting) and both these events can launch and aerosolize C-Diff and NV5,6,7 germs into indoor air spaces. In addition, intestinally infected MRSA patients can also aerosolize their germs by these means. MRSA, C-Diff, and NV can grow in your perineal region and surrounding private areas and their airborne dispersal in a bathroom exacerbates the total impact of toilet aerosolization. Staph species also thrive in many healthy peoples’ noses, and many asymptomatic carriers have no clue about their condition. Sneezing was documented as the most efficient way to aerosolize nasal MRSA8 when a sneezy doctor on rounds infected many of his patients with his nasal MRSA, thereby jeopardizing his bedside manner reputation.
HOW AIRBORNE MRSA, C-DIFF, AND NV INFECT USWhen unlucky humans breathe in airborne MRSA, C-Diff, and NV, those germs can impale themselves on the mucus layer that lines our entire respiratory system (from nose to lungs) which is your very own airborne disease filtration system. Your tiny cilia (hairs) undulate the mucus’s new prisoners back up through your trachea (windpipe) into your pharynx (area behind your tongue) where you swallow them down your esophagus. Once they snuggle into our stomachs, most diseases are killed by our stomach acids but these monsters thwart that and quickly amplify (grow) to start wreaking havoc throughout the intestinal tract. They either exit out our bottom or through our mouths and that’s where properly designing bathroom ventilation, supply, and exhaust vent placement, room pressurization, filtration, sterilization, and more can ground their flight as airborne infectious diseases.
TOILETS FLUSHES AS EXPLOSIVE GERM-LAUNCHING EVENTSA toilet flushing event to a bacteria or virion is like millions of ping pong balls riding down Niagara Falls and being whipped up in the frothing undercurrent which then launches them airborne9. Once airborne, these germs are usually riding on a water droplet that is being sucked upwards at supersonic speeds (to a germ) by the bathroom fan’s vacuum power. That droplet quickly evaporates (in less than a second) and the remaining naked germs are called “droplet nuclei,” which can stay airborne for hours if not days depending on the air movement within the room. All toilet-aerosolized droplet nuclei lifted up into the breathing zone allow unsuspecting people to breathe them in. Eventually bacteria and virions fall (plate out) like party confetti, dusting every single surface in the bathroom and then spill over into the patient rooms coating them and eventually out their doors into the hospital:
- Making it nearly impossible to kill them all10
- Providing infinite opportunities for anyone to infect themselves though hand inoculation.
Their experiments successfully captured airborne bacteria up to 4 ft above the toilet due to flushing aerosolization concluding, “Experiments have demonstrated that flushing a washdown type of water closet (toilet) can produce a bacterial aerosol. The size of the particles is such that bacteria tend to persist in the air and may reach the lower respiratory tract. Aerosol formation was not prevented by closing the lid before flushing. It was still produced after the closet had been flushed twice in succession.”
It took Professors Gerba12 in 1975 and Barker13 in 2005 to show how bacteria and virions bore into porous ceramic toilet surfaces to be pulled out on each successive flush and aerosolized for up to seven flushes and even hours or days later. Barker showed that a diarrhea event “seeds” 10 billion bacteria and virions into the toilet water. Barker captured aerosolized germs that equated to 1.2 million airborne bacteria and 2.4 million airborne virions per cubic meter above the toilet. Professor Wilcox14 found C-Diff spores all over the bathrooms surfaces and adjoining patient rooms from the toilet aerosolization explosions.
These facts diminish fecal-oral transmission as the only way that MRSA, C-Diff, and NV can infect patients and others. Since the 1930s, scientists have found bacteria and virions in every nook and cranny all over hospitals whose surfaces were sampled especially when MRSA, C-Diff, and NV patients were shedding these missiles nearby. Since patients don’t crawl all over the bathroom, their room, or the entire hospital touching every single surface to spread their fecal germs, it must be airborne transmission, right?
New C-Diff airborne transmission studies by Beggs15 in 2008 and Wilcox16 in 2010 found that C-Diff patients are surrounded by their own airborne C-Diff spores, which infection prevention specialists labeled as a “fecal cloud.” (No one defined it, so I gave it a go17.) How did this cloud magically appear like Finnegan’s rainbow? Here are the likely suspects:
- Rubbing and friction
- Underwear removal
- Bed changing
- Toilet flush aerosolization
MRSA, C-Diff, and NV happily living on human skin can easily become airborne when the skin they’re nesting on silently flakes off and goes airborne. Since patients are always rubbing their legs against each other, this liberates germ infested skin flakes contributing to their fecal cloud. Anyone in the area, including the patient, can breathe and then eventually swallow those grenades, thereby reinfecting themselves or newly infecting others breathing their fecal cloud. Lastly, toilet aerosolization and flatulence can cover the entire patient with their own disease known as a “fecal veneer,” which infects those who touch it or breathe it when the fecal veneer goes airborne.
EPIDEMIC VALIDATION OF TOILET AEROSOLIZATIONToilet aerosolization was the key factor in spreading the 2003 SARS epidemic around the world. A SARS-infected Chinese doctor stayed at the Metropole Hong Kong hotel and had diarrhea events in his bathroom located next to the room’s entry door. Since his room was positively pressurized to the hallway, his aerosolized SARS virions were pushed out into the hallway creating a SARS fecal cloud. As 15 unlucky guests and visitors passed through his SARS fecal cloud on the ninth-floor common areas, they became infected and:
- Flew worldwide spawning multiple infections (the World Health Organization
[WHO] shut down travel to Hong Kong and Toronto);
- Went to local hospitals, infecting patients, staff, and visitors,causing the largest recorded hospital superspreaing HAI event,20 which infected a visiting dialysis patient named Wang Kaix and 98 others.
Post-facto, University of Hong Kong Professor Yuguo Li elegantly documented22 the unprecedented Amoy superspreading events using computational fluid dynamics and scaled mock-ups of the Amoy Garden apartments, illustrating Wang’s fecal clouds flowing from his brother’s 16th floor bathroom. I’ve written23 about both these SARS events and problems with the resulting WHO reports.
I met with Dr. Li in Orlando at ASHRAE 2009 and he generously gave me his 2004 Powerpoint presentation showing how his investigations found that 34.5% of hospital rooms tested were contaminated by airborne infiltration from neighboring bathrooms. It also showed how a SARS toilet aerosolization hospital HAI outbreak in Beijing resulted from a SARS patient’s bathroom who dumped his toilet aerosolized fecal cloud into a shared bathroom ventilation shaft. That fecal cloud rose up through the shaft and infected four new patients whose bathrooms were connected to the same shaft. The aerosolized SARS viral fecal cloud(s) penetrated into their upper floor bathrooms and may have moved into the adjacent rooms, thereby anonymously infecting these unsuspecting victims. Clearly there was no fecal-oral vector in that outbreak.
BATHROOM VENTILATION IS BACKWARDSMost bathroom air is vented up through a ceiling exhaust duct, and Figure 1 illustrates why it’s the exact wrong design to properly control toilet flush aerosolization. Ceiling exhaust exacerbates toilet flush aerosolization supporting how MRSA, C-Diff, and especially NV hosts re-infect themselves and many persons who use their bathroom after their diarrhea event. It explains why MRSA, C-Diff, and NV epidemics continue long after the hospital or cruise ship has been thoroughly “cleaned” with disinfectants, which clearly failed since 20% of cleaned toilets are still infected.
Anytime asymptomatic hospital staff or crew members have a diarrhea or flatulence event(s) they start the infection cycle all over again. There are many studies documenting how asymptomatic infected patients are still shedding their germs within their diarrhea, which may make them able to aerosolize germs for months or years (10+) later. This explains why many MRSA, C-Diff, and NV patients return back to the hospital: they re-infect themselves with every flush or flatulence event. Aerosolizing millions of the fearsome threesome, when it only takes a couple of them to infect you, creates Vegas odds that anyone can appreciate.
AIRBORNE-GERM ENGINEERED BATHROOMSIn order to minimize the impact of toilet aerosolization and shedding in bathrooms, consider the following
from the top down. (Figure 2) Bathroom supply vents must be at the
ceiling, and return vents should be behind-the-toilet and below the seat level.
are source contamination sites. Engineer behind-the-toilet exhaust
flows to meet a +500 fpm velocity at the vent opening to produce enough suction
to remove toilet aerosolized germs. The ceiling supply duct must provide enough
CFM to negatively pressurize the bathroom to prevent aerosolized germs
exfiltration into the adjacent patient room and further. These high volume
ventilation systems must be on whenever the bathroom is occupied.
(“clean”) airborne germs. Bathroom air must be cleaned before it is
exhausted outdoors, in order to prevent airborne virions and bacteria from
re-entering through the building’s fresh air ducts to infect others. All
outside and supply air must be totally cleaned before it is circulated indoors
(Figure 2). Your weapons of choice are
16+ filters. Install the highest MERV rated filter you system can
handle and ensure that the filters are correctly sealed.
light systems. Start with a 12,000 microwatts seconds per square
standard. A 2011 UV study showed that treating the supply air helped drop
ventilator-assisted pneumonia infection rates in a Neonate ICU by 40%24. UV effectiveness
depends on wattage, exposure time, distance, reflectivity, temperature, air
velocity, and more. It’s widely accepted to install UV lights downstream of
cooling coils to sterilize them, the drain pans, and the airstream passing
- MERV 16+ filters. Install the highest MERV rated filter you system can handle and ensure that the filters are correctly sealed.
While I’m prevented from disclosing my bioterrorism project specifications, the Air Force has publicly specified 12,000 µWs/cm2 of UV photons for airborne infectious disease control. Figure 3 illuminates another specification in a UV kill graph from a 2003 study done by Research Triangle Institute26 showing +99% kill rates using 10,000 µWs/cm2 of UV photons on airborne bacteria and their spores (with some fungi thrown in for garnish).
A 2010 study27 provides impressive UV kill rates of C-Diff, MRSA, and VRE using 12,000 and 22,000 µW/cm2 of reflected UV light providing yet more specification reference points. Since virions have no exoskeleton (outer shell) like bacteria or their spores, virions typically require 50% or less UV power for sterilization, so by killing/sterilizing +99% of airborne bacteria you’ll easily get +99% of airborne virions. It’s critical that radiometers be installed to monitor each and every UV light’s photon output, as these fail-safe devices will alert your BAS system if a lamp fails.
Make sure you have an independent expert calculate the final UV wattage needed to meet your specification, since many factors must be custom-calculated both for the specific airborne germ you want to neutralize and each AHU configuration that UV systems will be mounted in. Make sure that you specify sealed and encapsulated UV lamps in case of accidental drops. A 12,000 µWs/cm2 spec could require high output UV lamps (not standard) spaced less than 4 in. on center, so make sure you have the properly custom calculated data to support the specification.
Second generation needlepoint cold plasma systems. Cold plasma devices (with nearly non-detectable ozone levels) are now widely installed so you can add them as a bioterrorism tool to your weapons cache. While the sun makes plasma, down here on earth I’ve seen national lab tests which verify a needlepoint cold plasma system’s 90% airborne MRSA kill rate in 24 min with 99% of MRSA killed after 60 min28. Since cold plasma energy can be delivered into any indoor space, flooding occupied bathrooms with cold plasma may lower airborne MRSA transmission rates.
- Delay timer and safety devices (Figure 2). Patients push a 30-s econd delay toilet flush button and quickly leave the bathroom to wash their hands outside. A mounted closed-door safety switch with a backup bathroom-mounted heat sensor will redundantly ensure that the UV lights are not on when someone is in the room. The UV lights should produce 12,000 µW/cm2 with light placement and tile reflectivity playing a large role in any specification.
Cited Works1. GreenCleanAir.com website
4. Beggs, Clive. “How does healthcare worker hand hygiene behaviour impact upon the transmission of MRSA between patients?: An analysis using a Monte Carlo model.” BMC Infectious Diseases. 2008, v8:114.
5. Caul, EO. “Evidence for transmission of transmission of a Norwalk-Like virus in a hotel restaurant.” Epidemiology and Infection. 2000, v124:481.
6. Chadwick, PR. “Transmission of a small round structured virus by vomiting during a hospital outbreak of gastroenteritis.” Journal of Hospital Infection. 1994, v26:251.
7. Kimura, H. A. “Norovirus outbreak associated with environmental contamination at a hotel.” Epidemiology and Infection. Feb. 2010, v139:317.
8. Boyce, J.M. “Spread of methicillin-resistant Staphylococcus aureus in a hospital after exposure to a health care worker with chronic sinusitis.” Ann Intern Med. 1993, v17:496.
10. Manian FA, et al. “Isolation of Acinetobacter baumannii Complex and Methicillin-Resistant Staphylococcus aureus from Hospital Rooms Following Terminal Cleaning and Disinfection: Can We Do Better?” Infect Control Hosp Epidem. July 2011, Vol. 32, No. 7:667-672.
11. Darlow & Bale. “Infective Hazards Of Water-Closets.” The Lancet. 1959:1196.
12. Gerba, Charles. “Microbiological Hazards of Household Toilets: Droplet Production and the Fate of Residual Organisms.” Applied Microbiology. Aug., 1975: 229.
13. Barker, J. “The potential spread of infection caused by aerosol contamination of surfaces after flushing a domestic toilet.” Journal of Applied Microbiology. 2005, v99:339.
14. Wilcox, Mark. “Comparison of the effect of detergent versus hypochlorite cleaning on environmental contam-ination and incidence of Clostridium Difficile infection.” Journal of Hospital Infection. 2003, v54: 109.
15. Beggs, Clive. “Aerial Dissemination of Clostridium difficile spores.” BMC Infectious Diseases. 2008, v8:7.
16. Wilcox, Mark. “The Potential for Airborne Dispersal of Clostridium difficile from Symptomatic Patients.” Clinical Infectious Diseases. 2010, v50:1450.
18. Sherertz, Robert. “A cloud adult: the Staphylococcus aureus virus interaction revisited.” Ann Intern Med. 1996, v124:539.
19. Eichenwald H., O. Kotsevalov, and L.A. Fasso. “The “cloud baby:” An example of bacterial-viral interaction.” Am J Dis Child. 1960, v100:161-73.
20. Yuguo Li. “Role of air distribution in SARS transmission during the largest nosocomial outbreak in Hong Kong.” Indoor Air. 2004, v15:83.
21. Yuguo Li. “Evidence of Airborne Transmission of the Severe Acute Respiratory Syndrome Virus.” New England J Med. 2003, v350:17.
23. GreenCleanAir.com website.
24. Ryan, R. “Effect of Ultraviolet germicidal irradiation in the heating, ventilation and air conditioning system on ventilator associated pneumonia in a neonatal intensive care unit.” Journal of Perinatology. 2011:1–8.
25. Keikavousi, Firouz. “UVC: Florida Hospital Puts HVAC Under a New Light,” Engineered Systems, February 2003.
26. GreenCleanAir.com website.
27. Nerandzic, et al. “Evaluation of an automated ultraviolet radiation device for decontamination of Clostridium Difficile and other healthcare-associated pathogens in hospital rooms.” BMC Infectious Diseases. 2010, v10:197.
28. EMSL Laboratories. Cinnaminson, NJ. 2007.
29. Chuaybamroong, Paradee. “Performance of photocatalytic lamps on reduction of culturable airborne micro-organism concentration.” Chemosphere. 2011, v83:730.
31. Engineered Systems. January 2010, February 2010, May 2010, June 2011.