Journal of Hospital Infection: Forced-Air Warming An Infection-Control "Hazard" in Implant Surgery

StopSurgicalInfections.org recently submitted a press release regarding a review article published by Journal of Hospital Infection.  The press release is as follows:

Surgical-infection experts have unambiguously concluded that forced-air warming “...does contaminate ultra-clean air ventilation….” in the operating room. Their advice: Use air-free warming during implant surgery.

PRLog - Nov. 12, 2014 - MINNEAPOLIS -- “Infection Control Hazards Associated with the Use of Forced-air Warming in Operating Theatres," appears in the scientific publication of the Healthcare Infection Society, Journal of Hospital Infection. The article, in press, can be found on-line at www.journalofhospitalinfection.com/article/S0195-6701%2814%2900245-X/abstract?showall=true=

The authors, including surgeon D.L. Leaper, chair of the committee that drafted the UK’s surgical-site infection guidelines, summarized the findings of 10 peer-reviewed, published studies regarding the infection risks of forced-air warming.  Their conclusions:

• No studies have shown that forced-air warming (“FAW”) reduces surgical infections—other than in colorectal surgery.
• In implant surgery, even minor contamination of the operative field can be catastrophic.
• FAW devices contaminate the operative field.

Patient Advocate Warns Against Forced-Air Warming

A well-known patient advocate now urges surgical patients to avoid forced-air warming—even to change hospitals if necessary.

The advocate, Rosie Bartel, speaks from experience. Infected with MRSA during a knee-replacement procedure at a hospital using forced-air warming, Bartel has undergone 27 subsequent operations— including amputation of her leg to the hip. The MRSA remains active.

After researching how the pathogens rose from the floor of the operating room into the sterile field, Bartel concluded that Bair Hugger warming blew particles into her wound, causing the MRSA infection. 

Bartel has a website (www.RosiesDream.com) to share her findings and give her advice to patients. Click on the video below. She has some powerful things to say.

A former educator, Bartel works closely with Partnership for Patients and the Institute for Healthcare Improvement. She will be co-chair of IHI’s national conference this year.

Infection Risk from Forced-air Warming Considered; Study on Bacterial Contamination Recommended

International Orthopedic Consensus 

“We recognize the theoretical risk posed by forced air warming blankets,” concluded the Consensus Statement recently released by the International Consensus on Periprosthetic Joint Infection.  While not urging a change in practice, the Consensus Statement recommended that further studies be undertaken regarding the safety of forced-air warming (“FAW”) in orthopedic implant surgery.
Delegates from more than 50 countries and 80 different societies met in August 2013 to evaluate scientific literature and identify areas for further research.  Among the other conclusions relating to periprosthetic joint infections and the risk of airborne contamination:
 
1. Airborne particulate bacteria are a major source of contamination in the operating room.  The number of airborne bacteria around the wound is correlated to the incidence of periprosthetic joint infections.  Bacteria “circulate through the operating room via air currents.”

“Legg et al,” the Consensus Statement noted, “found increased particles above the surgical site when using FAW compared to radiant warming.” To be precise, the Legg study, published in Bone & Joint Journal, found 2,000 times more contaminant particles in the air over the wound with Bair Hugger forced-air warming than with air-free HotDog conductive warming.  With HotDog patient warming, only 1,000 particles per cubic meter of air were present. With Bair Hugger warming, the particle count was 2,174,000 per cubic meter, an increase of 217,300%.

Nursing Journal: Forced-Air Warmers May Allow Pathogens to Contact Surgical Wounds

October 10, 2013

   

AORN Journal, noting concerns about infection risk from forced-air warmers, called for multi-center, randomized, controlled trials. Evidence of bacteria in the air-flow paths of forced-air warmers; authors ask manufacturers to consider redesign.

In a continuing-education review article in the October issue of AORN Journal, published by the Association of Operating Room Nurses, the authors examined 192 sources.  Their conclusions included the following:

• “Clinicians should take steps to prevent health care–associated infections from the use of forced-air warmers….”  Such steps include “routinely and meticulously” cleaning the devices.

•  Forced-air warmers may interrupt the flow of filtered air toward the area of the wound and may allow dust particles containing pathogenic organisms to come into contact with the wound.

•  Five separate studies suggested that forced-air warmers could be harboring bacteria or bacteria-containing particles.

Among the research considered by the authors was “Forced-air warming and ultra-clean ventilation do not mix: an investigation of theatre ventilation, patient warming and joint replacement infection in orthopaedics,” by UK orthopedic surgeon PD McGovern et al and published in the Journal of Bone & Joint Surgery.  The research included 1,437 patients undergoing hip or knee replacement.  The “Finding and comments” of the AORN Journal authors included:

“High risk of developing deep infections for subjects warmed with forced-air warming systems (odds ratio, 3.8; P=.024).”

Recent A & A study: “These findings warrant future research into the effects of forced air warming…during contamination-sensitive surgery.”

August 2013
 
Research in the August edition of Anesthesia & Analgesia, a publication of the International Anesthesia Research Society, and appearing under the name of the Anesthesia Patient Safety Foundation stated:

 “[F]orced air warming was found to establish convection currents that mobilized resident air from nonsterile areas (under the anesthesia drape) upward and into the surgical site.”

The clinical concern, according to the article, is that the convection currents created by Bair Hugger will mobilize contaminants and/or impede the ventilation systems’ ability to clear contaminants from the surgical site.  The concerns, they stated, “are most relevant for smaller airborne particles…such as free-floating bacteria and skin cell fragments.”

The study compared the impact of Bair Hugger warming with air-free HotDog conductive fabric warming.  No convective currents were detected when HotDog warming was applied.  In explanation, the scientists stated:

 “Because conductive blankets (like HotDog) are localized in their application, they tend to have higher thermal efficiencies and contribute less excess heat to the environment than forced air.”

In contrast, Bair Hugger “was found to have a significant disruptive impact on clean airflow patterns over the surgical site….”

Infection Guidance: Air Turbulence in Operating Room Increases Risk of Orthopedic Infection

In its Guide to the Elimination of Orthopedic Surgical Site Infections, the Association of Professionals in Infection Control and Epidemiology (APIC) states, “If airflow is interrupted, rapid air turbulence can stir settled particles, enabling them to become airborne thus increasing the risk for wound contamination.” By applying recent research to APIC’s Guidance, StopSurgicalInfections.org found that forced-air warming systems violate APIC’s Guidance “by drawing potentially contaminated particles from below the operating table into the surgical site.”   

Minneapolis, MN July 25, 2013

According to the Association of Professionals in Infection Control (APIC), the maintenance of uninterrupted, downward airflow during orthopedic surgery is “vitally important.” Several recent articles published in top peer-reviewed medical journals, however, confirm that forced-air patient warming, such as 3M’s Bair Hugger, produces rising, turbulent convection currents that can mobilize floor-level contaminants.

The printing and distribution of APIC’s Guide was sponsored by 3M.  APIC, of course, neither endorses nor is affiliated with this press release.

“The APIC guidance,” says Dr. Scott Augustine, inventor of Bair Hugger, “ summarizes the reason that researchers have questioned the safety of forced-air patient warming (“FAW”) in orthopedic implant and other ultra-clean surgeries.  I believe the research is conclusive—the largest study involved a retrospective analysis of 1,437 hip or knee replacements. It showed a 74.6% decrease in deep joint infection when FAW was discontinued and replaced with air-free warming.”

The Paradox of Forced-Air Patient Warming

Studies show that forced-air warming (FAW) reduces soft-tissue surgical infections. How can FAW be linked to increased deep-joint infections?

The paradox is easy to explain: BIOFILM.  A bacterium that lands on a prosthetic implant can secrete a coating of biofilm that protects it from both antibodies and antibiotics. Bacteria in soft-tissue cannot form effective biofilm coatings.

Secretion of biofilm allows a single airborne germ to cause a deep infection of a joint implant (Lidwell, 1983).  When the germ lands on the new implant, it protects itself in a biofilm coating and then sprouts weeks-to-months later as a catastrophic deep joint infection.  The increased airborne contamination from FAW vastly increases the chances of an airborne bacterium landing on the new implant.

In contrast, without biofilm protection, the germs in soft-tissue are susceptible to antibiotics and to an immune system activated by heat.  As a result, the creation of soft-tissue surgical infections require large inoculums of more than 100,000 germs (Elek & Cohen, 1957).

This also explains why soft-tissue surgical infections may not be increased by contaminated FAW air, while blowing even one germ into the surgical site during implant surgery can have significant negative concequences.

Watch this terrific video about bacterial biofilms 

produced by the Arthroplasty Patient Foundation:

Here is another interesting video about bacterial biofilms 

and orthopedic implants produced by the Arthroplasty Patient Foundation: