- Research article
- Open Access
Surveillance cultures of samples obtained from biopsy channels and automated endoscope reprocessors after high-level disinfection of gastrointestinal endoscopes
© Chiu et al.; licensee BioMed Central Ltd. 2012
- Received: 26 July 2012
- Accepted: 22 August 2012
- Published: 3 September 2012
The instrument channels of gastrointestinal (GI) endoscopes may be heavily contaminated with bacteria even after high-level disinfection (HLD). The British Society of Gastroenterology guidelines emphasize the benefits of manually brushing endoscope channels and using automated endoscope reprocessors (AERs) for disinfecting endoscopes. In this study, we aimed to assess the effectiveness of decontamination using reprocessors after HLD by comparing the cultured samples obtained from biopsy channels (BCs) of GI endoscopes and the internal surfaces of AERs.
We conducted a 5-year prospective study. Every month random consecutive sampling was carried out after a complete reprocessing cycle; 420 rinse and swabs samples were collected from BCs and internal surface of AERs, respectively. Of the 420 rinse samples collected from the BC of the GI endoscopes, 300 were obtained from the BCs of gastroscopes and 120 from BCs of colonoscopes. Samples were collected by flushing the BCs with sterile distilled water, and swabbing the residual water from the AERs after reprocessing. These samples were cultured to detect the presence of aerobic and anaerobic bacteria and mycobacteria.
The number of culture-positive samples obtained from BCs (13.6%, 57/420) was significantly higher than that obtained from AERs (1.7%, 7/420). In addition, the number of culture-positive samples obtained from the BCs of gastroscopes (10.7%, 32/300) and colonoscopes (20.8%, 25/120) were significantly higher than that obtained from AER reprocess to gastroscopes (2.0%, 6/300) and AER reprocess to colonoscopes (0.8%, 1/120).
Culturing rinse samples obtained from BCs provides a better indication of the effectiveness of the decontamination of GI endoscopes after HLD than culturing the swab samples obtained from the inner surfaces of AERs as the swab samples only indicate whether the AERs are free from microbial contamination or not.
- Surveillance culture monitoring
- Gastrointestinal scope
- Automated endoscope reprocessor
- High-level disinfection reprocessing
Flexible endoscopes are complex reusable instruments, and according to the British Society of Gastroenterology guidelines (February 2008) for decontamination of equipment used for gastrointestinal (GI) endoscopy, special care must be taken when decontaminating endoscopes. In addition to the external surfaces of GI endoscopes, their internal channels for air and water aspiration and other accessories are exposed to body fluids and other contaminants . In our experience, instrument contamination can occur even after a complete reprocessing cycle using high-level disinfection (HLD). For example, a relief valve in the water supply system of an automated endoscope reprocessor (AER) may be damaged and disconnected . Therefore, surveillance culture may help in monitoring the effectiveness of GI endoscope disinfection. The first step in decontamination of the GI endoscopes is thorough manual cleaning using a compatible enzymatic detergent; all accessible channels should be brushed with the detergent and then flushed with sterile distilled water, before automatic disinfection using an AER. We conducted this prospective study to assess the effectiveness of a complete reprocessing cycle in decontaminating GI endoscopes. To this end, we performed culture studies on the samples obtained from biopsy channels (BCs) of the upper (gastroscope) and lower (colonoscope) of the GI endoscopes and from the internal surfaces of the AERs.
The X2 test was used for statistical analysis of independent and paired samples. Statistical analyses were performed using the Statistical Package for the Social Sciences (SPSS) version 14.0 for Windows (Chicago, IL, USA). A p value <0.05 was considered statistically significant.
The number of positive bacterial cultures obtained from rinse samples from biopsy channels of gastroscopes and colonoscopes and from swab samples obtained from automated endoscope reprocessors used for the decontamination of gastroscopes and colonoscopes
BC No. (%)
AER No. (%)
Gastroscope, n = 300
Colonoscope, n = 120
Total, n = 420
Bacterial flora of the culture-positive rinse samples obtained from the biopsy channels of gastroscopes and colonoscopes after reprocessing
Single species No. (%)
Multiple species No. (%)
Gastroscope, n = 32
Colonoscope, n = 25
Total, n = 57
Organisms identified from cultures of samples collected from the biopsy channels of gastroscopes and colonoscopes and from swab cultures of samples obtained from automated endoscope reprocessors
Organisms in the cultures of rinse samples obtained from biopsy channels
3c, d, f
Total number of bacteria
Total number of positive cultures
Organisms in swab cultures of samples obtained from automated endoscope reprocessors#
Total number of positive cultures
AERs subjected to HLD are widely used for the decontamination of endoscopes. The guidelines of the British Society of Gastroenterology emphasize the benefits of manual brushing of endoscope channels in addition to automated decontamination . We aimed to determine whether adequate decontamination of AERs and GI endoscopes was achieved after complete reprocessing. This 5-year prospective study showed that the number of culture-positive samples obtained from the BCs (13.6% [57/420]) of GI endoscopes was significantly higher than those obtained from swab samples taken from the internal surfaces of AERs (1.7% [7/420]) after HLD (p < 0.0001). This finding may be due to the fact that the structure of an endoscope is more complicated than that of an AER. GI endoscopes are complex reusable instruments that require special care during decontamination. Contamination of the AER samples may have been underestimated because the structures of the GI endoscopes and that of the AERs differ. Endoscopes are complicated instruments with multiple internal channels (air, water, suction, and biopsy channels) with many dead air spaces and complete disinfection is difficult to achieve. BCs are easily contaminated by patient body fluids, blood, or tissue. The finding of a higher contamination rate in BCs compared with AERs was also true for the rinse samples obtained from the BCs and the swab samples obtained from the AERs reprocess to the gastroscope (10.7% [32/300] vs. 2.0% [6/300]; p < 0.0001) and colonoscope (20.8% [25/120] vs. 0.8% [1/120]; p < 0.0001) AERs. Most updated guidelines emphasize adequate decontamination of endoscopes [1, 4–7]. There was greater contamination in 160 m long colonoscopes than in the 100 cm long colonoscopies (p = 0.00585); decontamination of a gastroscope was easily achieved after HLD reprocessing. Endoscopes inserted via the anal route are reportedly more contaminated than those inserted orally, and a 200 cm long endoscope is more difficult to decontaminate than a 100 cm long endoscope .The surveillance resulting consensus document defines invasive procedures in detail and provides endoscopists with practical advice on how to avoid contamination of BCs by lymphoid tissue during endoscopic biopsy and other therapeutic procedures. BCs are the most complicated components of GI endoscopes and they are difficult to disinfect when they become contaminated with highly infectious material, such as that associated with fine needle puncture biopsy of lymphoid tissue. Sheathed biopsy forceps may be introduced to improve the safety of biopsies in at-risk individuals and to avoid BC contamination of GI endoscopes. This change is intended to address concerns about a new variant of Creutzfeldt-Jakob disease (vCJD) and is emphasized by the British Society of Gastroenterology guidelines (February 2008). The length of the endoscope is an important factor that adds to the difficulty of disinfection . In addition, adequate manual pre-cleaning of long endoscopes with complicated internal channels, such as BCs, is difficult. Therefore, contamination of AERs may be a consequence of their design and is not necessarily a result or by-product of the design of GI endoscopes or the quality of reprocessing. The inner surfaces of the BCs may not be sufficiently decontaminated even after a complete reprocessing cycle. Regular monitoring of reprocessing is important for ensuring quality and patient safety . Our results suggest that culturing samples obtained by rinsing the BCs is one of the best methods for performing regular monitoring. A review of recent reports highlights cost concerns along with the importance of monitoring the microbial content of rinse samples from BCs . Regular monitoring of GI endoscopes and HLD decontamination is important for ensuring patient safety and should not be reserved for infectious disease outbreaks. Our data indicates that the culturing of rinse samples from BCs of GI endoscopes (compared with AER samples) and from colonoscopes (compared with gastroscopes) is the best indicator of the effectiveness of the decontamination process.
An interesting finding with regard to the samples obtained from the BCs of gastroscopes (93.75% [30/32]) and colonoscopes (84.0% [21/25]) after reprocessing was that most samples were colonized by a single bacterial species. Sporadic contamination by multiple species was observed in only 2 gastroscope (6.25% [2/32]) and 4 colonoscope (16.0% [4/25]) samples. This incidence did not differ significantly between samples obtained from gastroscopes and colonoscopes, and the difference was approximately 10%. The detection of bacterial colonization (particularly by multiple species) after abdominal surgery is indicative of a complicated and potentially unsafe surgical environment. Contamination with commensal gut bacteria can also lead to pathogenic conditions that may be life threatening . The bacterial profiles of samples cultured from the BCs were diverse with most colonies belonging to a single Gram-negative species (Table 3). In our study, the number of culture-positive samples obtained from colonoscopes was 2-fold higher than those obtained from gastroscopes, and almost 90% of the samples from both endoscopes showed colonization by a single species. Therefore, HLD of GI endoscopes is very important. In terms of the severity of contamination, colonization by multiple species is indicative of greater contamination. In fact, standard reprocessing with HLD is an effective method for decontaminating GI endoscopes according to the current guidelines; 100% decontamination of all GI endoscopes after HLD reprocessing may be impossible, and a culture-positive sample identified as a single species colonization event that is not associated with a clinical outbreak is considered acceptable. In contrast, the bacterial profiles of culture-positive samples obtained from the BCs were diverse, with most samples showing colonization by a single species and most strains were aerobic. Although routine sampling of surfaces within a healthcare facility is generally not recommended by the Centers for Disease Control and Prevention, the Association for the Advancement of Medical Instrumentation, and several healthcare organizations, the practice is recommended by some organizations . We also believed that everything to be too late as clinically required during an outbreak investigation. Dr. Lawrence Muscarella suggested that bacterial growth in a collected sample indicates contamination of the sampled channel, and if no bacterial growth is detected from a surveillance culture this does not necessarily mean that the channel is sterile. Indeed, endoscope sampling is prone to false-negative results and provides data, albeit potentially erroneous data, specific only to the sampled surface . Anyway, our results suggest that culturing samples obtained by rinsing BCs is one of the best methods for performing regular monitoring.
More than 68.4% of the organisms identified were GNGN bacteria, which are associated with a wide range of infections, predominantly those of nosocomial origin. Such infections usually develop in patients with identifiable deficiencies of local and/or systemic immunity. These GNGN bacteria can be isolated from a wide variety of environmental sources, and can cause infection via contaminated medical devices or “pseudoinfections” due to their survival/growth in blood sample tubes or laboratory media. Pseudomonas aeruginosa is a GNGN rod-shaped bacterium that is most commonly associated with human infection. Earlier, most species of GNGN bacteria were thought to be contaminants when they were cultured from human specimens, but many have now been shown to be opportunistic pathogens in humans . However, in veterinary medicine, GNGN bacterial species are not considered animal pathogens. Most veterinary microbiology laboratories do not routinely identify GNGN bacteria other than P. aeruginosa, Bordetella bronchiseptica, and Moraxella bovis[14–16]. Even our laboratory unit does not routinely identify GNGN bacteria. If GNGN bacterial species are not considered contaminants of AERs after HLD, the percentage of culture-positive rinse samples obtained from the BCs in our study would be reduced to 3.3% (10/300) for gastroscopes and 8.8% (10/120) for colonoscopes. Furthermore, we believe that the primary source of these GNGN is the patient. Although this would suggest that the endoscope cleaning was ineffective, no clinical outbreak occurred because most of these bacteria are not of clinical significance. According to the British Society of Gastroenterology guidelines (February 2008), manual brushing is emphasized for endoscope cleaning and disinfection. If manual brushing was performed correctly, the complete reprocessing cycle after HLD would have been excellent. Rinsing and drying after HLD are essential for the removal of chemical solutions and for preventing bacterial colonization during storage of GI endoscopes . In our study, 42.8% (3/7) of the culture-positive swab samples obtained from AERs showed fungal contamination. This finding highlights the importance of daily forced-air drying of AERs . Therefore, surveillance culturing for both GI endoscopes and AERs is an effective means of monitoring the effectiveness of HLD of GI endoscopes after manual pre-cleaning and decontamination by AER. AERs are effective for decontamination of the outer surfaces of GI endoscopes; however, manual pre-cleaning of all working channels is essential for decontamination of the internal surfaces and should be a high priority.
For endoscope sampling, the BCs were flushed with 50 ml of sterile distilled water, which is an appropriate irrigation solution for bacterial culture in case of the obstruction of external biliary drainage or urinary bladder tube in the general practice. It is a very simple sampling for bacterial culture and also has vigorous results in our previous study [2, 8] before ISO 11737–1:2006 documentation. According to the data published, the absence of neutralizing agent in the sampling solution may lead to an underestimation of endoscope contamination levels [18, 19]. Both of the references were the experimental contamination and design for the microbiological testing of the sampling solutions. Of course, the results are provided a higher culture-positive rate. Indeed, the sterile distill water is used to washout the possible contaminated material from the BC of the GI endoscopy. The important consideration is the culture agar as blood agar, MacConkey agar, and Lowenstein–Jensen medium in our studies. According to ISO 11737–1:2006 for the sterilization of medical devices, both of the content including determination of a population of microorganisms on product and tests of sterility performed in the validation of a sterilization process was not determined as our practical culture method which was designed before the documentation of ISO 11737–1 and ISO 15883–4. For AER sampling, we swabbed the surface of the AER chamber. This method is not the method recommended in ISO 15883–4 for AER sampling and is not accurate enough. ISO 15883–4 is provided for washer disinfection and emphasized that the methods, instrumentation and instructions required for type testing, works testing, validation (installation, operational and performance qualification on first installation), routine control and monitoring and re-validation, periodically and after essential repairs. We also reported the limitation in our recent reported . The AER sampling result should be used to describe the AER with a high-level disinfection process is enough or not. Therefore, we provided this monitoring method both of the BC sampling and AER swab culture for the patient safety in re-usable medical devices. For the patient safety, regular monitoring the medical devices in daily medical used is very important and a best way to avoid infectious disease outbreak in the hospital. Further clinical studies are warranted to further evaluate our findings as there are no publications documenting any increased risk of infection transmission for endoscopes processed using glutaraldehyde as the HLD.
In conclusion, culturing samples from GI endoscopes is more effective for monitoring the effectiveness of reprocessing after HLD than culturing swab samples from AERs. Our data suggest that culturing rinse samples from BCs can better indicate the effectiveness of decontamination of GI endoscopes after HLD than culturing swab samples from AERs, which can only indicate whether AERs are free from microbial contamination.
This study was supported by the Gastrointestinal Endoscopy unit of Chang Gung Memorial Hospital (Kaohsiung), Taiwan. We thank Miss Ching-Yin Huang for her help with data collection, culture processing, and automatic endoscope reprocessing.
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