Understanding and Controlling the Hazards of Surgical Smoke
The following article was originally published in Preventing Infection in Ambulatory Care, the quarterly e-publication from the Association for Professionals in Infection Control and Epidemiology (APIC). To learn more about receiving this resource and joining APIC, visit www.apic.org/ambulatorynewsletter. To learn more about APIC, visit www.apic.org.
More than 500,000 workers are exposed to surgical smoke every year; numerous studies have documented dangerous atmospheric agents in surgical smoke causing a range of adverse health symptoms and effects.[1,2,3] Hazardous air quality in the operating room has been an occupational concern since the mid 1970s.
Research and workplace studies conducted over long periods of time confirm that surgical smoke, also known as surgical plume, contains hazardous substances including respiratory irritants and carcinogens that have been linked to asthma and infectious agents such as human papilloma virus (HPV). This article will discuss why the proper use of local exhaust ventilation (LEV) augmented by the use of properly fitted filtering facepiece respirators are the recommended and effective controls to reduce surgical smoke exposures.
The composition and exposure hazards associated with surgical smoke depend on a variety of factors such as the type of surgical procedure and device (i.e. laser, electrosurgical, ultrasonic); type and infectious nature of the tissue; extent of tissue ablation; the duration of surgery; and the worker's proximity to the surgical field. The hazards reported to be associated with exposure to surgical smoke are substantiated by the following research evidence.
Ninety-five percent of surgical smoke is made up of water, but the remaining 5% contains potentially hazardous particles including blood fragments, bacteria, viruses and lung-damaging dust.[3,5] Within 5 minutes of beginning an electrocautery procedure, during breast reduction surgery, the baseline measurement of particulate matter was found to increase from approximately 60,000 particles per cubic foot to more than 1 million particles per cubic foot. Additionally, it took approximately 20 minutes for particle concentrations to return to baseline levels once the surgical procedure was completed. However, most startling is a laboratory study finding that the burning of 1 gram of tissue can release the same level of mutagenic contaminants as three to six cigarettes.
In recent years, electrocautery has been commonly used for the treatment of genital warts caused by HPV and cervical neoplasia in patients infected with human immunodeficiency virus (HIV). Although electrocautery is potentially less hazardous than laser smoke as a route of disease transmission, intact virions (HIV, Hepatitis, HPV) have been shown to be present in electrocautery smoke, and their infectivity has been demonstrated.
The National Institute for Occupational Safety and Health (NIOSH) recommends a combination of the specified operating room (OR) air exchanges and LEV as the first line of protection for controlling surgical smoke. The Association for periOperative Registered Nurses (AORN) recommends that OR air exchanges should be maintained at a minimum of 15 air exchanges per hour. The ASHRAE/ASHE ventilation standard for new construction of healthcare facilities requires a minimum total air exchange rate of 20 air exchanges per hour.
Smoke evacuators and room (wall) suction systems are the two LEV control methods recommended to reduce surgical smoke levels. Smoke evacuators should incorporate high efficiency particulate air (HEPA) or ultra low particulate air (ULPA) filters to effectively trap particulates in the air, and be highly efficient at removing airborne particles with a capture velocity of 100 to 150 ft/min at the inlet nozzle.[10,11]
In addition to OR ventilation and use of smoke evacuators, wall suction systems are another option for controlling small amounts of smoke. Room (wall) suction systems pull at a much lower rate; smoke evacuators and wall suction must be kept within 2 inches of the surgical site to efficiently capture the generated contaminants. Wall unit suction devices are considered a less effective method of capturing smoke plume and only should be used with adequate room air ventilation.
Because of higher capture velocity, smoke evacuators should be used in high plume situations. To ensure optimal function, LEV and room ventilation systems must be properly maintained, cleaned, and monitored according to manufacturer's recommendations. Healthcare personnel should consider used filters, tubing and wands as biohazards and handle them properly.figu
Every facility should establish guidelines for dealing with surgical smoke. Figure 1 provides a sample of a facility's OR procedures for smoke evacuation and includes examples of low and high plume generating surgical procedures. In addition to NIOSH, the Occupational Safety and Health Administration (OSHA), AORN, Laser Institute of America (LIA), ANSI, and The Joint Commission (TJC) recommend that surgical smoke be filtered and evacuated through the use of room ventilation and LEV methods. Despite these recommendations, a 2007 survey of 623 AORN members indicated weak compliance by healthcare facilities.
Due to the inconsistent use of smoke mitigation systems and the variability in smoke production during a surgical procedure, one may need additional sources of protection. A secondary form of protection is the appropriate respiratory protection used in conjunction with properly functioning OR ventilation and LEVs.
While the type of respirators used in the OR has been a controversial issue, the proper selection and use of personal protective equipment (PPE) can also reduce or prevent exposure to smoke plume. Various degrees of protection are associated with different types of PPE.
Surgical and laser (high filtration) masks create a barrier that protects the wearer's face from large droplets and splashes of blood and other body fluids during medical procedures. They also function to some extent to limit the spread of contamination from the wearer to the patient, although this is a subject of debate. Surgical and laser masks do not protect wearers from airborne particles small enough to be inhaled through the larynx and into the lungs. Additionally, surgical and laser masks are designed with a wide range of filter media. Research findings reveal that the performance of surgical masks for capturing particles varies widely.[14,15]
A study conducted with particles the size of viruses and bacteria (0.04 – 1.3μm) found that of the nine surgical masks tested, none provided the minimum level of protection recommended by OSHA. Correspondingly, small particles, less than 1.1μm in diameter, constitute 77% of the particulate matter generated in surgical smoke. Most significant and perhaps easily misunderstood is the fact that surgical and laser masks do not seal to the face and thereby allow contaminants to enter the worker's breathing zone through gaps between the wearer's face and the mask.
For these reasons, NIOSH recommends the use of properly fitted, filtering facepiece respirators rather than surgical and laser masks. Filtering facepiece respirators with an N95 filter class designation prevent all sizes of particles from passing through the filter media and entering the wearer's breathing zone. Even taking some facepiece seal leakage around the respirator into account, a properly fitted N95 reduces the wearer's exposure against a range of very small particles (less than 1μm) to large droplet sized particles (> 60μm) by at least 10-fold. Thus, healthcare personnel should wear respiratory protection at least as protective as a fit-tested N95 filtering facepiece respirator when working with known disease transmissible cases (i.e., HPV) and/or during aerosol-generating procedures or with aerosol transmissible diseases (i.e., TB, varicella, rubeola). Furthermore as a precautionary measure, it is recommended that respiratory equipment as protective as a fit-tested N95 be worn in the absence of properly functioning smoke control measures (ie, OR exchanges, LEV).
The choice is yours to advocate for workplace safety practices (i.e., OR ventilation, LEV and respiratory protective equipment) that best protect you from the known hazardous exposures of smoke plume. For more information on this topic see Figure 2 for a list of selected web-based references. Let's protect ourselves by clearing the air we breathe in the OR!
*Disclaimer: The findings and conclusions in this report are those of the authors and do not necessarily represent the views of the National Institute for Occupational Safety and Health.
1. Alp E, Bijl D, Bleichrodt R P, Hansson B, Voss A. Surgical smoke and infection control. Journal of Hospital Infection. 2006; 62:1-5.
2. Ortolano G A, Cervia J S, Canonica F P. Surgical smoke: a concern for infection control practitioners. Managing Infection Control. March 2009, 48-54.
3. Ulmer B C. The hazards of surgical smoke. AORN J. April 2008; 87(4):721-734.
4. Barrett W L and Garber S M. Surgical smoke: a review of the literature. Surg Endosc. 2003; 17:979-987.
5. Wentzell J M, Robinson J K, Wetzell J M Jr, Scwartz D E and Carlson S E. Physical properties of aerosols produced by dermabrasion. Archives of Dermatology. 1989; 125:1637-1643.
6. Brandon H J and Young V L. Characterization and removal of electrosurgical smoke. Surgical Services Management. March 1997; 3(3):14-16.
7. Tomita Y,Mihashi S,Nagata K, et al. Mutagenicity of smoke condensates induced by CO2-laser irradiation and electrocauterization. Mutation Research. 1981; 89:145–149.
8. AORN. Recommended practices for a safe environment of care. 2010 Perioperative standards and recommended practices.2009; 217-240.
9. American Society of Heating, Refrigerating and Air-Conditioning Engineers, Inc. Ventilation of health care facilities. ANSI/ASHRAE/ASHE addendum to ANSI/ASHRAE/ASHE Standard 170-2008, 2008.
10. AORN. Recommended practices for electrosurgery. 2010 Perioperative standards and recommended practices.2009; 105-126.
11. National Institute for Occupational Safety and Health Hazard Control HC-11. Control of smoke from laser/electric surgical procedures. http://www.cdc.gov/niosh/hc11.html
12. American National Standards Institute. American National Standard for Safe use of Lasers, ANSI Z136.1-2007.
13. Edwards B E and Reiman R E. Results of a survey on current surgical smoke control practices. AORN J April 2008; 87(4):739-749.
14. Oberg T and Brosseau L M. Surgical mask filter and fit performance. AJIC. May 2008; 36(4):276-282.
16. Lee S, Grinshpun S, and Reponen T. Respiratory performance offered by N95 respirators and surgical mask: human subject evaluation with NaCl aerosol representing bacterial and viral particle size range. Ann. Occup. Hyg. 2008; 52(3):177-185.
17. Kunachak S, Sobhon P. The potential alveolar hazard of carbon dioxide laser-induced smoke. J Med Assoc Thai. 1998; 81(4):278-282.
© Copyright ASC COMMUNICATIONS 2017. Interested in LINKING to or REPRINTING this content? View our policies by clicking here.
- Ambulatory Surgical Center Quality and Access Act of 2017 introduced in House: 5 key notes
- GI leader to know: Dr. Saleem Desai of Los Angeles Gastroenterology Institute
- Brookings Ambulatory Surgery Center earns AAAHC accreditation: 3 notes
- Capital Digestive Care adds Dr. Darryn Potosky: 3 notes
- Adults with disabilities screened less often for colorectal cancer: 4 study insights