Pall Corporation Homepage: Filtration, Separations, Purification, and Environmental Technology
Home
1.800.645.6578 (USA)
CONTACT US



You need to upgrade your Flash Player
Click here to intall latest Flash Player

Surgical Gas and Smoke Filtration Products and Technologies

Insufflation Gas Safety in Diagnostic
and Surgical Endoscopy

The gases used in laparoscopy are supplied via an insufflation system, which consists of a CO2 cylinder, an insufflation pump and an application set. The commonly accepted rules for the handling of sterile surgical products are followed cautiously for all parts of this system that are reaching into the sterile surgical field. In contrast to these high level precautions the insufflation gases may often be directed to the sterile body cavity of the patient from a non-sterile gas cylinder or insufflation pump.

Insufflation equipment has been shown to be contaminated with particles and micro-organisms1,2,3. Contamination by back flow of patient fluids and blood, may pose an additional risk for potential cross contamination4,5,6. Back flow of fluids into the pump may also cause damage to the insufflation machine and put the technical staff at risk of contamination, when these products have to be repaired6.

PALL Insufflator Gas Filters

The Pall IGF Insufflator Gas Line Filters are validated to retain airborne bacterial and viral contamination. They provide a total
 





barrier to potentially contaminated patient liquids and blood, and prevent the back flow of patient fluids into the insufflation pump. Pall IGF filters are available in a range of set variants that allow adaption of the concept of hydrophobic filtration to any clinical insufflation set up and to the various flow requirements.

1. Public Health Laboratory Services, Disease Report Weekly, 1999;9(16):133
2. Ott DE. APIC Conference 1993
3. Saxena A.K. Effects of Insufflation. In Essentials of Pediatric Endoscopic Surgery, Chapter 6, p 59-62, Springer, 2008
4. Muscarella LF. J Gynecol Surg. 1994;10:51-53
5. Medical Device Agency. MDA Safety Notice SN9602. 1996
6. ECRI Problem Reporting System. Health Devices 1992;21(2):180-181