Introduction
Digestive endoscopy procedures require gas insufflation to allow the progression of
the endoscope and proper examination of the mucosa.
Room air is the most common gas used in standard endoscopic settings, however, subsequent
distension of the bowel often causes abdominal discomfort because of air slow re-absorption
[1]. Therefore, employment of carbon dioxide (CO2) instead of air is increasing. In fact, it is well established that CO2 causes less abdominal discomfort because it is absorbed faster (160 times) than air
from the gut and then expired through the lungs [2]. Several studies demonstrated that CO2 insufflation induces less abdominal discomfort than air during colonoscopy, endoscopic
retrograde cholangiopancreatography (ERCP) and enteroscopy [3]
[4]
[5]
[6]
Endoscopic ultrasonography (EUS) matches endoscopic and ultrasound view to investigate
pancreatic and biliary diseases, stage gastrointestinal tumors and diagnose submucosal
lesions and lymph nodes [7]
[8]
[9]
[10]
[11].
Instrumentation consists of a dedicated echoendoscope with a high-frequency ultrasound
transducer on its tip. Gas pockets may persist between the probe and the target organ
as a consequence of insufflation; thereby acoustic coupling is impaired, generating
visual artifacts that can hamper diagnostic accuracy. As a consequence, endosonographers
need to activate multiple suctions in attempt to reduce bowel gas throughout the entire
procedure.
We hypothesized that CO2 insufflation could influence not only patients’ discomfort but also the quality of
EUS images. To our knowledge, the outcomes of CO2 insufflation in EUS have not been evaluated in a clinical study so far. Therefore,
to date, no recommendation is available regarding the choice of gas insufflation for
EUS (air or CO2).
The main aim of this study was to compare the effects of CO2 vs. air insufflation on abdominal discomfort in patients undergoing EUS. The secondary
outcomes were to ascertain the effects of CO2 on dose of sedation, EUS image quality and presence of visual gas artifacts.
Patients and methods
This was a prospective, controlled, single-blind, observational study. Consecutive
patients who were scheduled for EUS in our center from April 2016 to January 2017
were eligible. The trial was approved by the local ethic committee and registered
at www.clinicaltrials.gov (NCT02773563).
Exclusion criteria were:
Patients enrolled were allocated to either of two groups:
Two endoscopic rooms were available for EUS during the study period, of which one
was equipped with a CO2 delivery system and another one with a standard air-insufflation system. At the time
of reservation, patients were randomly allocated in one of these two rooms according
to the availability of booking slots.
All the procedures were performed by one of three experienced operators (PF, AL, MS).
Before starting enrollment, all endoscopists met to come to agreement related to the
study standards of care and definitions. Moreover, at the end of each examination,
all the images were reviewed collectively by the three endosonographers in order to
share quality evaluation by consensus and not only based on the judgment of a single
operator.
Procedures and data collection
All the procedures were performed either with a radial (GF-UE160, Olympus Medical
Systems Corp., Tokyo, Japan) or with a curvilinear-array echoendoscope (GF-UTC180,
Olympus Medical Systems Corp., Tokyo, Japan). Study data were directly collected by
the endosonographers and recorded in a case report form. Abdominal discomfort intensity
was assessed before the procedure, and 1 and 3 hours post-procedure and recorded as
a visual analogue scale (VAS) ranging from 0 to 10 (0: no pain, 10: maximum pain).
All the patients were blinded as to which gas was used. The endosonographers showed
a printed numeric scale to the patients before and after examinations (at 1 and 3
hours post-procedure). By doing so, a verbal explanation was also provided to the
patients during each administration of the VAS.
Image quality assessment was performed at four standard stations (second part of the
duodenum, duodenal bulb, stomach, and esophagus) and recorded as optimal, suboptimal,
poor, and impossible. Optimal was defined as a clean EUS view of the target organ
with adequate resolution; suboptimal was defined as a minimal loss in image resolution,
but still adequate for diagnosis; poor was defined as a significant loss in image
quality barely adequate for diagnosis; impossible was defined as inadequate for diagnosis.
Visual artifacts were defined as white convex shadows between the probe and the target
organ impairing acoustic coupling. Need for suction was considered as the frequency
of gas aspiration from the lumen in order to remove the gas pockets. Dosage and type
of sedation were also recorded.
CO2 delivery system
The CO2 regulator available in our Unit was the Olympus UCR, connected by tubing to the CO2 central supply of our hospital. The gas flow setting was 1.5 L/min.
Statistical analysis
Continuous variables were reported as mean ± standard deviation or median (range).
Categorical variables were reported as number (percentage). The Mann-Whitney test
was used for comparison of continuous variables. Fisher’s exact test or Chi-square
test was used for the comparison of categorical variables. To compare the effects
of CO2 vs. air insufflation in patients undergoing EUS, the subjects were randomized to
treatment, and the two-sided two-sample Mann Whitney test was used. To achieve 90 %
power of test, at significance levels of 0.01, the sample size required for each patient
group was calculated to be 94 units; we hypothesized up to 10 % of incomplete examinations,
therefore we planned to enroll 200 patients. All the analyses were performed using
STATA version 14.0 software (Stata Corporation, College Station, Texas).
Results
From April 2016 to January 2017, 200 patients were enrolled. Two patients were excluded
because of the premature interruption of the procedure, one due to esophageal stenosis,
one due to status post-gastric surgery that was previously unknown.
The two groups were well balanced with regard to demographic characteristics ([Table 1]). Ninety-four patients were enrolled in the CO2 group and 104 patients were enrolled in the air group. Indications and results of
EUS are also reported in [Table 1]. There were no statistically significant differences between group A and B concerning
the duration of exams.
Table 1
Baseline characteristics of the study population.
Patient characteristics
|
Total (no. 198)
|
Age (years)
|
64 (21 – 90)
|
Gender (male)
|
97 (48.9 %)
|
EUS indication
|
Biliary tree
|
72 (36.4 %)
|
Pancreatic parenchyma
|
86 (43.4 %)
|
Gastric cancer
|
30 (15.2 %)
|
Subepithelial tumor
|
10 (5.1 %)
|
Fine needle aspiration
|
49 (24.7 %)
|
Echoendoscope type
|
Curvilinear array
|
113 (57.1 %)
|
Radial scanning
|
85 (42.9 %)
|
EUS, endoscopic ultrasound; CO2, carbon dioxide; SD, standard deviation.
Abdominal discomfort
There was no statistically significant difference between the two groups concerning
abdominal discomfort before EUS (1.04 ± 1.82 vs. 1.03 ± 1.83). We observed a trend
to a reduced discomfort in the CO2 group at 1 hour after the procedure compared to the air group (1.17 ± 1.68 vs. 1.54 ± 1.77;
P = 0.112). Interestingly, a significant reduction in abdominal discomfort in the CO2 group compared to the air group was seen at 3 hours after EUS (0.88 ± 1.57 vs. 1.17 ± 1.54;
P = 0.048) ([Table 2]).
Table 2
Comparison between CO2 and air insufflation.
|
CO2 Group
(mean ± SD)
|
Air Group
(mean ± SD)
|
P value
|
Abdominal discomfort – VAS 0 – 10[1]
|
Before EUS
|
1.04 ± 1.82
|
1.03 ± 1.83
|
0.956
|
1 hour after EUS
|
1.17 ± 1.68
|
1.54 ± 1.77
|
0.112
|
3 hours after EUS
|
0.88 ± 1.57
|
1.17 ± 1.54
|
0.048
|
Image quality assessment[2]
|
Duodenum – second portion
|
1.31 ± 0.55
|
1.72 ± 0.68
|
< 0.0001
|
Duodenum – bulb
|
1.30 ± 0.55
|
1.74 ± 0.69
|
< 0.0001
|
Stomach – celiac trunk
|
1.42 ± 0.60
|
1.87 ± 0.75
|
< 0.0001
|
Esophagus – mediastinum
|
1.53 ± 0.69
|
1.98 ± 0.82
|
0.0001
|
Visual artifacts[3]
|
0.54 ± 0.67
|
0.96 ± 0.67
|
< 0.0001
|
Need of suction[4]
|
0.15 ± 0.36
|
0.48 ± 0.50
|
< 0.0001
|
EUS duration (minutes)
|
22.56 ± 10.87
|
21.18 ± 10.93
|
0.310
|
Sedation
|
Fentanyl dose (mcg)
|
107.98 ± 23.54
|
107.69 ± 25.85
|
0.868
|
Midazolam dose (mg)
|
4.26 ± 1.74
|
4.13 ± 1.82
|
0.723
|
P value from the comparison between CO2 vs. air group, made with the Mann-Whitney test.
1 Abdominal discomfort was recorded as a Visual Analogue Scale ranging from 0 (no pain)
to 10 (maximum pain).
2 Image quality assessment was recorded as optimal (1), suboptimal (2), poor (3) or
impossible (4).
3 Visual artifacts were recorded as none (0), few (1) or several (2).
4 Need of suction was recorded as infrequent (0) or frequent (1).
Image quality and visual artifacts
Analysis of our data showed that the quality of EUS images was significantly superior
in each single station (second part of the duodenum, duodenal bulb, stomach, esophagus)
with CO2 insufflation (P < 0.001) compared to air insufflation ([Fig. 1], [Fig. 2]). There was also a statistically significant difference with respect to visual artifacts
and need of gas suction, with CO2 correlating with less artifacts and requiring less gas aspiration from the lumen
of the gut (P < 0.001).
Fig. 1 Typical image showing visual artifacts from the second portion of the duodenum (asterisk).
The image also shows a stone (green arrow) and aerobilia (arrowhead) in the common
bile duct.
Fig. 2 An example of optimal imaging from the second portion of the duodenum. No visual artifacts
are seen. The image shows a small stone in the common bile duct (arrow) and large
stones in the gallbladder (asterisk).
Sedation
There were no statistically significant differences between group A and B concerning
the amount of sedation. In particular we administered on average/pro patient 107.9 mcg
of fentanyl in the CO2 group and 107.6 mcg in the air group, and 4.2 mg of midazolam in the CO2 group and 4.1 mg in the air group ([Table 2]).
Discussion
To the best of our knowledge, this is the first study investigating the role CO2 insufflation on abdominal discomfort after EUS. The main finding of this study consisted
in the significant association between CO2 insufflation and lower abdominal discomfort scores at 3 hours after the procedure,
compared to air insufflation. However, no statistically significant differences were
found between CO2 and air before and 1 hour after the procedure, although a trend to a reduced discomfort
in the CO2 group was seen at the latter stage. A possible explanation for the lack of benefit
in the CO2 group 1 hour after EUS can be found in the ongoing impact of sedation drugs on the
perception of abdominal discomfort. On the other hand, we may assume that the effect
of conscious sedation on the perception of visceral pain had completely vanished 3
hours after the procedure when the statistically significant difference between air
and CO2 was detected. Meanwhile, the amount of administered sedation was similar between
the two groups and no association between CO2 insufflation and reduced need of sedation was found.
Moreover, we showed a better quality of the EUS images obtained with CO2 vs. air insufflation evaluated at different scanning points, including transduodenal,
transgastric and transesophageal. Similarly, visual air artifacts and need of suction
were lower when CO2 was used in comparison to air. We hypothesize that use of CO2 contributed significantly to improvement in image quality, thanks to its quick reabsorption
that may be 160 times faster than air [2]. In particular the beneficial effect of CO2 might be related not only to suction of gas pockets during EUS but also to less gas
distension of intervening bowel loops.
As far as the safety of CO2 is concerned, Bretthauer et al. enrolled 103 patients in a randomized study evaluating
whether CO2 insufflation leads to CO2 retention in both sedated and unsedated patients undergoing colonoscopy, in comparison
to air insufflation. Data analysis showed a slight increase of end-tidal CO2 in sedated patients but the type of gas insufflated was not relevant. They also administered
a questionnaire to record abdominal pain at 1, 3 and 6 hours after the procedure.
The results indicated a significant lower abdominal pain in the CO2 group [12].
The role of CO2 vs. air insufflation for colonoscopy was also the subject for a meta-analysis by
Wu et al. (9 studies, 1577 patients). Despite significant heterogeneity for some major
results, data showed that CO2 insufflation was associated with a significant decrease in abdominal pain during
and 1, 6 and 24 hours after the procedure [13].
A prospective, randomized, double blind study evaluated the degree of abdominal discomfort
post ERCP in 116 patients insufflated with CO2 vs. air. Mean pain scores were significantly reduced in the CO2 group at 1, 3 and 24 hours after ERCP [14]. Another study on ERCP showed favorable results for CO2 insufflation. The primary outcome was to compare immediate post-procedure abdominal
pain where the CO2 group showed a statistically lower VAS score than the air group. The authors also
described a statistically significant reduction in abdominal distension at 3 and 24
hours post ERCP; no effect was seen with respect to nausea [15].
Intubation depth and total enteroscopy rate in single balloon enteroscopy were evaluated
in a Chinese study comparing 214 patients sorted in 2 groups (air vs. CO2). They also recorded abdominal pain/distension at 1, 2, 3 and 6 hours post-enteroscopy.
In the CO2 group, a higher total enteroscopy rate was observed and the VAS score for pain and
distension were milder, although not statistically significant [16].
Recently, the American Society for Gastrointestinal Endoscopy issued a review on the
use of CO2 in gastrointestinal endoscopy. CO2 use was described in colonoscopy, ERCP, balloon-assisted enteroscopy and endoscopic
submucosal dissection. As a conclusion of the review, a big amount of data indicated
that CO2 insufflation in many types of digestive endoscopy procedures is safe and associated
with less abdominal pain compared with air insufflation [17].
Our study has limitations. First, no validated criteria for image quality and visual
artifacts were available. As a result, the evaluation of EUS image quality may have
been operator-dependent. However, we developed rigorous criteria for image analysis,
which were shared by three experienced endosonographers who subsequently performed
all the exams. Second, the operator was aware of the type of gas being used during
the procedures, with a potential risk for an evaluation bias. However, all the endosonographers
reviewed images and videos after each procedure to give an objective evaluation of
the parameters of image quality and artifacts. Our study was conducted in patients
who underwent EUS with conscious sedation. We acknowledge that results may change
with deep sedation as far as patient satisfaction scores are concerned. On the other
hand, we believe that the results concerning image quality evaluation are not related
to the type of sedation used.
If our results are confirmed by future studies, it may be speculated that CO2 insufflation should become a standard for diagnostic EUS to improve the quality of
imaging, potentially leading to even more accurate diagnosis. Similarly, as the number
of operative and therapeutic EUS procedures is steadily increasing, CO2 insufflation should be the standard of care similarly to other types of therapeutic
endoscopy.
Conclusion
In conclusion, we showed that CO2 insufflation for EUS provided better scores for abdominal discomfort at 3 hours after
the procedure. No differences were found in the amount of sedation administered in
the CO2 group compared to the air group. We also showed that EUS image quality, visual artifacts
and need of suction were improved using CO2 insufflation compared to air. Future studies are warranted to ascertain whether CO2 insufflation should be regarded as standard of care for both diagnostic and therapeutic
EUS.