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- Table of Contents
Diagnostic and Therapeutic Endoscopy
Volume 2012 (2012), Article ID 692532, 4 pages
Carbon Dioxide Insufflation in Colonoscopy Is Safe: A Prospective Trial of 347 Patients
1Gastroenterologie Wettingen, Rosengartenstrasse 2, 5430 Wettingen, Switzerland
2Department of Oncology, Kantonsspital, 9007 St. Gallen, Switzerland
3Department of Visceral Surgery and Medicine, University Hospital Bern, 3010 Bern, Switzerland
4Department of Gastroenterology, University Hospital, 4031 Basel, Switzerland
Received 1 June 2012; Revised 16 August 2012; Accepted 29 August 2012
Academic Editor: Jean-Marc Dumonceau
Copyright © 2012 M. Geyer et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Available evidence suggests that the use of CO2 insufflation in endoscopy is more comfortable for the patient. The safety of CO2 use in colonoscopy remains contentious, particularly in sedated patients. The objective of the present prospective trial was to assess the safety of CO2 colonoscopies. Methods. 109 patients from our previous randomized CO2 colonoscopy study and an additional 238 subsequent consecutive unselected patients who had a routine colonoscopy performed in a private practice were enrolled from April 2008 through September 2008. All but 2 patients were sedated. All patients were routinely monitored with transcutaneous CO2 measurement. Volumes of CO2 administered were correlated with capnographic measurements from transcutaneous monitoring. Results. Of the 347 patients examined, 57% were women; mean (SD) age of participants was of 60.2 years (12.8). Mean propofol dosage was 136 mg (64 mg). Mean CO2 values were 34.7 mm Hg (5.3) at baseline, 38.9 mm Hg (5.5) upon reaching the ileum, and 36.9 mm Hg (5.0) at examination's end. Mean maximum increase of CO2 was 4.5 mm Hg (3.6). No correlation was observed between volume of CO2 administered and increase in level of CO2 (correlation coefficient: 0.01; P value: 0.84). No complications were observed. Conclusions. The present prospective study, which was based on one of the largest sedated patient sample reported to date in this setting, provides compelling evidence that CO2 insufflation in colonoscopy is safe and unassociated with relevant increases in transcutaneously measured levels of CO2.
For almost 2 decades, CO2 insufflation with carbon dioxide (CO2) has been widely used in laparoscopic surgery. In contrast, insufflation with room air has remained the standard of care in the vast majority of endoscopy centers in both Europe and North America. Unfortunately, many patients still experience pain and discomfort after colonoscopy with room air insufflation. Studies [1–5] and one review  indicate that insufflation with CO2 can reduce periprocedural pain in different endoscopic settings (e.g., endoscopic retrograde cholangio-pancreatography , balloon enteroscopy , and endoscopic submucosal dissection ). However, in the setting of colonoscopy, current scientific data with regard to the safety of CO2 insufflation are limited. Small patient populations have characterized most studies, including those with sedated patients, and many physicians remain concerned that CO2 insufflation might lead to CO2 retention. In a previous randomized, controlled, double-blinded trial, we randomly allocated 219 patients to colonoscopy with CO2 versus room air, patients in the CO2 group experienced significantly less pain and bloating and a higher overall satisfaction score . However, this study was not designed to definitively demonstrate the safety of CO2 insufflation in colonoscopy. In the present study, we sought to prospectively assess the safety of CO2 colonoscopy in a larger sample of patients.
2. Patients and Methods
This trial included all 109 patients from our previous CO2 colonoscopy study  plus 238 subsequent, consecutive, nonselected, patients who had a routine colonoscopy performed in a private Swiss gastroenterology practice and were enrolled from April 2008 through September 2008. All patients who were deemed medically fit for an ambulatory colonoscopy were included in this study. In order to maximize the generalizability (external validity) of our study, we did not initially apply exclusion criteria, although one exclusion criterion emerged (due to a small earlap, CO2 measurement was not possible in 4 patients, which were excluded). All colonoscopies were done by the first author (M. G.) and carried out with standard Pentax endoscopes (EC-3885K and EC-380FKp) (Pentax Medical, Pentax of America, Inc., Montvale, NJ, USA) with an EPK 1000 processor. For CO2 insufflation, the CO2-Efficent Insufflator device (EZEM Company, Westbury, NY, USA) was used. The insufflator was connected to a 10-litre CO2 bottle and supplied over a tubing set connected with a branch connection to the water bottle tube, which was itself directly connected to the endoscope. The flow rate (basal flow rate 0.5 L/min, increasing to 3 L/min maximum) can be controlled on demand over the standard air valve. Oxygen was delivered to patients if the saturation dropped below 90% at a flow rate of 4 liters per minute.
All but 2 patients were sedated with propofol using standard procedures previously described . The total dose of propofol was registered for later analysis. A level of conscious sedation (“moderate sedation”) was targeted. All patients were routinely monitored with transcutaneous CO2 measurement on the ear, with the exception of those patients who were excluded due to insufficient earlap (). CO2 measurement was performed with the SenTec capnograph (SenTec AG, 4106 Therwil, Switzerland) as described by Heuss et al. . Our measurement technique followed that recommended by SenTec; internal validation was not performed as the system has been previously extensively validated [12–14]. Sensors were calibrated according to mandatory procedure and placed on the earlap after cleaning with 70% isopropyl alcohol solution and application of contact liquid on the sensor membrane.
In previous validation studies, correlation of partial pressure of CO2 (paCO2) and transcutaneous CO2 measurement was as follows: ; intraclass correlation coefficient [ICC] = 0.92; for arterial saturation of oxygen (SaO2/SpO2), ; ICC = 0.73 . Data for continuous transcutaneous CO2 measurements were analyzed, as were baseline characteristics including age, propofol use, and CO2 volume administered. To ensure validity of our measurements, we analyzed and compared the 238 consecutive patients separately, with the 109 patients derived from our earlier CO2 study using an unpaired t-test. Additionally the correlation of the insufflated amount of CO2 with a possible increase of transcutaneously measured CO2 was assessed using Spearman correlations. Statistical analyses were performed using SPSS, v. 11.0 (IBM Corp., Armonk, NY, USA).
The first sample of 109 patients who received CO2 insufflation for colonoscopy was drawn from our previous study, which was conducted from April to June of 2008. All subsequent patients referred for colonoscopy at this single practice were routinely examined with CO2, with the result that from June 2008 through September 2008, an additional 238 patients (second sample) were examined using CO2 insufflation, for a final study population of 347. Of the 347 patients examined, 198 (57%) were female; the mean (SD) age was 60 years (12.8). Mean (SD) propofol dosage was 136 mg (64) (Table 1); mean (SD) duration of endoscopy procedures was 24 minutes (7.5). All but 2 patients in the second sample were sedated. Mean (SD) value for baseline CO2 measurement was 34.7 mm Hg (5). Mean (SD) pressure of CO2 recorded reaching the ileum was 38.9 mm Hg (5) and 36.9 mm Hg (5) at the end of the examination (Figure 1). Mean maximum increase of CO2 pressure was 4.4 mm Hg (Figure 2).
Four patients in the second sample experienced transient pCO2 values in excess of 50 mm Hg (three when reaching the ileum and one at the end of the examination), but these patients showed no signs of respiratory distress or O2 desaturation and O2 substitution was not deemed necessary. These four patients did not receive a higher propofol dosage or volume of CO2 insufflated.
Among the total study sample, no correlation was observed between volume of CO2 administered and an increase of CO2 (correlation coefficient: 0.01; -value: 0.84) (Figure 3). Parameters did not significantly differ between the first and second samples. None of the patients required ventilation or mechanical airway support, and no other complications (bleeding, perforation, loss of consciousness, hospital admission) were observed.
The present prospective study, which was based on one of the largest sample of sedated patients to date, provides compelling evidence that CO2 insufflation colonoscopy is safe and is not associated with an increase in transcutaneously measured CO2 or with adverse respiratory effects. Our findings add to mounting scientific evidence demonstrating the safety and superiority of CO2 colonoscopy over room air [6, 10]. Given these findings, we believe that CO2 colonoscopy should be considered the procedure of choice.
Although CO2 insufflation has been used for different endoscopic procedures [1–9] and was found to be associated with less postprocedural pain and bloating [10, 15], most endoscopy units continue to use room air for screening colonoscopies and are unaware of the benefits of this relatively new technique .
In our first double-blinded randomized study—hitherto the largest reported sample of sedated and CO2 monitored patients—239 patients were randomly allocated in a 1 : 1 ratio to colonoscopy with CO2 versus room air. This study, which represented the first examination of sedated, unselected, and consecutive patients in this setting, yielded encouraging results: no difference in transcutaneous CO2 values was observed with continuous capnography between groups, and there was no evidence of advanced hypercapnia as a possible problem with this technique . However, we felt that this initial experience from our group needed to be confirmed in a study with larger sample size. By incorporating patients randomized to CO2 insufflation in that previous study and an additional 238 consecutive patients, we achieved an even larger patient population, providing compelling evidence for the safety of CO2 insufflation in sedated and monitored patients undergoing colonoscopy. Only 4 patients experienced a partial pressure of CO2 in excess of 50 mm Hg (max. paCO2 52.8 mm Hg).
Our study shows that sedated patients had a small increase in CO2 during colonoscopy until the terminal ileum was reached, after which CO2 levels fell. We speculate from these observations that sedation per se, but not CO2 insufflation in particular, appears to be the primary cause of the observed CO2 increase during colonoscopy.
Many patients with severe chronic obstructive pulmonary disease (COPD) experience CO2 retention, an inherent phenomenon of this disease. Until now, no studies have been performed to assess whether CO2 is also safe to use in this high-risk population. But although COPD patients included in our study suffered no relevant adverse outcomes, they constituted only a small percentage of the study population and larger studies of CO2 insufflation in patients with COPD should be performed to confirm its safety in this subset of patients.
A particularly noteworthy finding of this study is the lack of correlation between volume of insufflated CO2 and the increase of CO2 as measured by transcutaneous monitoring. Because CO2 is very quickly exhaled, paCO2 never reached clinically toxic value. It might be influenced more by individual factors not yet fully understood than by the amount of insufflated CO2.
Because CO2 is absorbed into the bloodstream 150 times faster than room air and also exhaled with an elimination of 0.2 L per minute , higher volumes of gas (e.g., 51 L [±14 L]) are usually needed when using CO2 for colonoscopy insufflation, compared with room air . Some physicians who are already using CO2 insufflation for colonoscopy believe that briefly switching from CO2 to room air to obtain a faster and better colonic distension can be useful in certain circumstances. This may be due to the fact that the flow rates of all commercial available CO2 insufflators are still below the usual rates achieved with air insufflators.
From a practical point of view, there are no clinically relevant problems in handling CO2 insufflation with modern insufflators; further, we believe that no safety concerns remain in patients devoid of COPD.
The present prospective study, which was based on one of the largest sedated patient sample reported to date, provides compelling evidence that colonoscopy with CO2 insufflation is safe in patients devoid of COPD. Neither a relevant increase in transcutaneously measured CO2 nor adverse respiratory effects were detected.
The authors thank Jonathan McCall, M. S., for critically reviewing this paper and making many valuable suggestions.
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