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- Posted in Research & Development | April 17, 2013 | Comments (0)
- By: Daniel Prince, Ph.D., Jozef Mastej, Diana Easton, Ph. D., Isabel Hoverman and Raja Chatterjee
The design, validation and regulatory review of orthopaedic trays and instruments are a sophisticated challenge. Many U.S. companies successfully compete in this industry in part because of the helpful guidance available from FDA, United States Pharmacopeia (USP) and ISO. Contract laboratories play an important role in this process. This case study, “Sterilization by Moist Heat Sterilization at 132C of Reusable Device and Tray System,” systematically investigates the role of steam, heat and load configuration in the validation of moist heat sterilization and drying.
The orthopaedic instrument system comprised six different reusable instruments. The first step was to determine whether or not the instrument system could be successfully steam sterilized under worst case conditions according to ST79.1 The validation was performed in a validated hospital sized gravity and pre-vacuum autoclave, with FDA-cleared approved 510(k) sterilizer.2 Heat penetration studies were performed on each reusable instrument by placing a National Institute of Standards and Technology thermocouple inside each instrument. Pre- and post-thermocouple calibration was performed. The instruments were individually wrapped with 24 x 24 inch Convertors Bio-Shield Sterilization wrap, and pulsed pre-vacuum and gravity-displacement sterilization cycles were performed. The instruments were placed in the steam sterilizer’s previously-determined cold spot.3, 4 To assess sterilization effectiveness, half-cycle sterilization at 132C for two minutes and 7.5 minutes were performed for pulsed pre-vacuum and gravity-displacement sterilization cycles, respectively, as delineated in Table 1.
Biological challenges were performed to verify half-cycle sterilization cycles’ effectiveness under both maximum and minimum load configurations. (Refer to Exhibits 1 and 2) Geobacillus stearothermophilus at 2x106 spores per indicator, having a D121-value of 2.2 minutes and a Z value of 9C, were used.4 One biological indicator was inserted into multiple locations of each instrument. These locations were non-surface portions of the instrument, so as to achieve maximum retention of and barrier effects to the biological indicator. The maximum load comprised three trays and three baskets each fully loaded with surgical instruments. The six test instruments were placed in the immediate proximity of the cold spot at the back right-hand top shelf of the chamber. The minimum load configuration was six reusable instruments, individually wrapped and placed on the right side of the top shelf at the back of the chamber. After the cycle, the biological indicators were aseptically removed and cultured at 55-60°C for seven days in USP soybean casein digest broth.5
Full cycle sterilization runs were performed to assess whether the ST79 requirements of dryness were met, as delineated in Table 2.
The thermocouples used for thermal mapping conformed to the pre- and post-calibration requirements of ± 0.5°C.6 The cold spot inside the reusable instruments at the sterilization chamber’s cold spot was determined by thermocouple mapping. As indicated in Table 3, TC06 was the found to be the cold spot for the pulsed pre-vacuum sterilization process, and TC05, TC06 were found to be the cold spots for the gravity-displacement sterilization process.7
For five of the six instruments in all of the half-cycle sterilization processes, all of the Biological Indicators (BIs) were sterilized. One instrument (#4) could not be sterilized by the pulsed pre-vacuum sterilization process. The positive BI control and negative media control were positive and negative, respectively, for growth as expected. (See Table 4.) The failed instrument was retested with more space available in the area of the BI by not having the handle completely closed, as illustrated in Exhibit 3; 0/2 BI were positive upon retest, as shown in Table 5.
The label claim population of the BIs conformed to the USP specifications of not less than 0.30 log10 and not more than 0.48 log10 of Label Claim. The log number of spores per carrier at 48 hours is equal to or greater than the log number after 24 hours.5
All Positive BIs were found by gram stain as Gram Positive Bacillus, and further identified to the expected species level using Vitek Compact 2.
Moisture was not observed on wrap, or Reusable Instruments wrapped individually in double 24” x 24” Convertors Bio-Shield Sterilization Wrap for the three full-cycles for pulsed pre-vacuum and gravity-displacement sterilization processes, as delineated in Tables 6 and 7.
Orthopaedic instruments are complex, with multiple locations in which tissue-related organic material may become embedded, such as in a groove or cannulated area. Sterilization of the outer surface of the instrument is not adequate to protect the patient from exposure to infectious material. In the work described here, worst case conditions were employed in the moist heat sterilization validation scheme. Specifically, (1) relatively resistant bacterial spores were inserted into the instrument at locations judged to create the greatest barrier to the penetration by steam, (2) half the anticipated sterilization exposure time was used to determine spore death and (3) maximum and minimum loads were separately sterilized.
It is not well-known whether moist heat sterilization is more readily achieved under maximum or minimum load configurations. The maximum load was a fully-loaded chamber containing three trays and three fill-in baskets each containing the six instruments. The BIs were located in the tray positioned in the chamber’s coldest spot. For the minimum load, the chamber contained only six instruments located in the immediate proximity of the chamber’s coldest spot and there were no trays or baskets. More BI failures were observed in the pulsed pre-vacuum minimum load than the corresponding maximum load (Refer to Table 4.). The failure was common to a single instrument, #4. This instrument is of a type that can be actuated to an open and closed position. Initially, it was tested in the closed position and failed. When it was tested in the open position, it passed.
Thermal mapping of this location demonstrated that the exposure temperature setting of 132°C was slightly exceeded for this and all of the other five instruments. Interestingly, the overall time of the half-cycle was much longer for the maximum versus minimum load configurations, 29.7 minutes and 19.9 minutes, respectively. Accordingly, the failure was due to the fact that the location of the BI was such that insufficient steam could access it. The failure was only apparent from the biological testing, as F0 heat lethality alone is not predictive of the results obtained. Therefore, it is apparent from this case study that biological testing is an essential component of a validation plan. The failure was easily overcome by creating more steam access channels, as demonstrated in Exhibit 3. An exaggerated minimum load half-cycle comprising the failed instrument and one other instrument positioned at the chamber’s coldest spot, rather than six instruments, was also successfully sterilized. In this study, the minimum pulsed pre-vacuum load was a more stringent sterilization condition; however, we have observed the opposite in other studies.8 Accordingly, this result is not a universal finding, but is a distinct possibility revealing that a physical determination may not necessarily supersede a biological determination in validation studies as reported here.
No failure was observed in any of the Gravity-displacement sterilization processes. (Refer to Table 4.) Comparing the full-cycles of the Pulsed pre-vacuum to the Gravity-displacement, the calculated F0 values were five minutes and 18 minutes 40 seconds, respectively consistent with the results obtained. It is noted that the 7.5-minute half-cycle was substantially longer than the two-minute pulsed pre-vacuum exposure.
Drying was achieved for all full-cycle sterilization processes. (Refer to Tables 6 and 7.) There was no evidence of moisture on the sterilization wraps or reusable instrument following the exposure to the full-cycle sterilization processes. In addition, with respect to moisture retention following sterilization, (1) the wrap weight did not increase by more than 3% relative to its weight before sterilization (ANSI/AAMI ST79 and (AAMI TIR 12) and 4 the wrapped tray did not increase by more than 0.2% relative to its weight before sterilization (EN 868-8).9
1. ANSI/AAMI ST79:2010 and A1:2010 – Comprehensive guide to steam sterilization and sterility assurance in health care facilities.
2. ANSI/AAMI ST8-2008 Hospital Steam Sterilizers.
3. ANSI/AAMI ST 46-2002. Good Hospital Practice: Steam Sterilization and Sterility Assurance.
4. AAMI TIR 12-2010 Designing, testing and labeling reusable medical devices for reprocessing in health care facilities: A guide for medical device manufacture.
5. Current United States Pharmacopeia Chapter <55> Biological Indicators-Resistance Performance Tests.
6. ANSI/AAMI/ISO 18472: 2006(R) 2010 - Sterilization of health care products – Biological and chemical indicators – test equipment.
7. ANSI/AAMI ST77: 2006/(R) 2010. Containment devices for reusable medical device sterilization.
8. Gibraltar Laboratories, Inc. # 319605/1.409
9. EN 868-8:2009. Packaging materials for terminally sterilized medical devices Part 8: Re-usable sterilization containers for steam sterilizers conforming to EN 285 - Requirements and test methods. European Committee for Standardization, Brussels, Belgium.