Carbon dioxide insufflation reduces residual gas in the gastrointestinal tract following colorectal endoscopic submucosal dissection

  • Authors:
    • Tomohiko Sugiyama
    • Hiroshi Araki
    • Noritaka Ozawa
    • Jun Takada
    • Masaya Kubota
    • Takashi Ibuka
    • Masahito Shimizu
  • View Affiliations

  • Published online on: January 17, 2018     https://doi.org/10.3892/br.2018.1044
  • Pages: 257-263
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Abstract

Quantitative examinations evaluating the effects of CO2 insufflation on residual gas in the gastrointestinal tract following colorectal endoscopic submucosal dissection (ESD) are lacking. The present study aimed to assess whether CO2 insufflation could decrease the amount of residual gas in the gastrointestinal tract following ESD in patients with colorectal neoplasms. Computed tomography (CT) was used to objectively examine whether CO2 insufflation during colorectal ESD reduced residual gas levels in the gastrointestinal tract following ESD. A total of 83 patients who underwent colorectal ESD between January and December 2009 at Gifu University Hospital (Gifu, Japan) were enrolled. Following exclusion of 17 patients with chronic pulmonary dysfunction, 66 patients were randomized into a CO2 insufflation group (n=34) and an air insufflation group (n=32). The level of residual gas and the presence of transmural and free‑air leaks following ESD were evaluated in both groups using CT. Transcutaneous CO2 tension (PtcCO2) and ESD‑related complications were also compared between the groups. CT measurements of the major and minor axes of the cecal lumen, and of the terminal ileum diameter, indicated the level of residual gas following ESD to be significantly reduced in the CO2 insufflation group compared with the air insufflation group (P<0.001). Neither the incidences of ESD‑related complications, including post‑procedure hemorrhage and air leak, nor the abnormalities in vital signs differed between the groups. No significant between‑group differences were identified in the baseline and peak PtcCO2 levels during ESD or in the median PtcCO2 following ESD. In conclusion, CO2 insufflation during colorectal ESD was effective in reducing residual gas in the gastrointestinal tract following ESD.

Introduction

Colorectal cancer is among the most prevalent malignancies worldwide, and therefore effective and minimally invasive procedures are required to reduce the incidence rate of this malignancy (1,2). More recently, utilization of colorectal endoscopic submucosal dissection (ESD) as a minimally invasive treatment for en bloc resection of large superficial neoplasms has become a favored method (3). However, the risk of complication is higher than in gastric ESD as the wall of the colon is thin and operability is limited. In addition, colorectal ESD generally requires a long procedure time due to its technical difficulty (4,5). Therefore, a high level of gas enters the colonic lumen. This is associated with aggravation of subjective symptoms, such as abdominal pain, discomfort and distention, and an increased risk of severe problems, including pneumoderma, pneumothorax, abdominal compartment syndrome and air embolism (614).

The safety and efficacy of CO2 insufflation during ESD for lesions of the esophagus and stomach have been demonstrated in several randomized controlled trials (1521). A pilot study also reported that CO2 insufflation was safe and effective during colorectal ESD (15). As CO2 is absorbed faster than air and is rapidly eliminated through the lungs, CO2 insufflation is expected to reduce residual gas in both the small and large bowels following ESD, and consequently reduce the abdominal symptoms and complications associated with ESD (15,2230). However, to the best of our knowledge, detailed and quantitative examinations evaluating the effects of CO2 insufflation on residual gas in the gastrointestinal tract following colorectal ESD have not been performed.

The aim of the present study was to assess whether CO2 insufflation could decrease the level of residual gas in the gastrointestinal tract following ESD in patients with colorectal neoplasms. All patients received an abdominal computed tomography (CT) examination immediately following colorectal ESD, and the level of residual gas in the gastrointestinal tract following ESD was objectively evaluated by measuring the axes of the cecal lumen and the diameter of the terminal ileum lumen. The safety of CO2 insufflation was also assessed by measuring the levels of transcutaneous CO2 tension (PtcCO2) and evaluating the development of ESD-related complications such as air leaks.

Materials and methods

Patients

Between January and December 2009, all consecutive patients undergoing colorectal ESD at Gifu University Hospital (Gifu, Japan), were screened for the present study. Colorectal ESD was indicated for lesions that required endoscopic en bloc resection, despite this technique being difficult to use for endoscopic mucosal resection or polypectomy.

Patients with one or more of the following conditions were excluded: (i) They exhibited chronic pulmonary dysfunction defined as a forced expiratory volume in 1.0 sec/forced vital capacity of <70% or a vital capacity of <80%; (ii) they were unable to understand the consent information required for participation; and/or (iii) they refused to participate in the study. The study protocol was approved by the institutional Ethics Committee of Gifu University Hospital (ethical approval no. 28-104). All eligible individuals provided written informed consent prior to study enrollment. Randomization was conducted using a random number list, and patients were divided into two groups, namely a CO2 insufflation group (CO2 group) and an air insufflation group (air group).

ESD procedures and examination schedule for study events prior to and following ESD

ESD was conducted in the afternoon on the day of admission. Prior to inserting the colonoscope, 5.0–10.0 mg diazepam (Cercine®; Takeda Pharmaceutical Company, Ltd., Tokyo, Japan), 7.5–15.0 mg pentazocine (Pentagin®; Daiichi Sankyo Co., Ltd., Tokyo, Japan) and 12.5–25.0 mg hydroxyzine (Atarax-P®; Phizer Japan, Inc., Tokyo, Japan) were injected intravenously for induction of anesthesia and analgesia. As necessary, 5.0 mg diazepam or 7.5 mg pentazocine and 12.5 mg hydroxyzine were administered repeatedly for deep sedation; when patients opened their eyes or moved their body, the patients were considered to be out of deep sedation and received the additional injections. The ESD procedures were performed using a colonoscope and water jet (PCF-Q260J; Olympus Medical Systems; Olympus Corporation, Tokyo, Japan). The colorectal lesions were resected using either a DualKnife (KD-650Q) or FlexKnife (KD-630L; both from Olympus Corporation). A 0.4% high-molecular-weight hyaluronic acid solution containing 0.001% epinephrine was injected into the submucosal layer to raise the lesion. The mucosal layer around the lesion was cut circumferentially; subsequently, the submucosal layer was directly dissected with the DualKnife or FlexKnife. If possible, the post-ESD ulcer was closed using clips; otherwise, exposed blood vessels were clipped to reduce the risk of active bleeding. Circulation vitals, including systolic and diastolic blood pressures, heart rate and transcutaneous oxygen saturation (SpO2) were measured with a bedside monitor (BSM-4101; Nihon Kohden Corporation, Tokyo, Japan) at the start of the procedure, every 5 min during the procedure, and at the end of the procedure. On the second hospital day, blood tests for white blood cell (WBC) count and C-reactive protein (CRP) were performed, and the highest axillary temperature during the total hospital stay was recorded. WBC count was measured with an automated hematology analyzer (XE-2100; Sysmex Corporation, Kobe, Japan) and CRP was measured with an automatic biochemical analyzer (JCA-BM2250; JEOL, Ltd., Tokyo, Japan) with use of a CRP kit (CRP Latex X2 NX®; Denka Seiken Co. Ltd., Tokyo, Japan), according to the manufacturer's instructions.

CO2 insufflation and transcutaneous gas analysis

CO2 was administered using a CO2 regulation unit (OLYMPUS UCRTM; Olympus Corporation). PtcCO2 was continuously measured from the time of insertion of the colonoscope until the end of the procedure by using a CO2 sensor kit (TOSCA measurement system and TOSCA 500 monitor; Linde Medical Sensors Ag, Basel, Switzerland). The low-flow gas tube (MAJ-1742, Olympus Corporation) of the UCR was used for CO2 insufflation, which was set at a constant rate of 1.4 l/min for all patients, as reported previously (31).

Evaluation of CT examination

CT examination of the abdomen and pelvis was performed immediately following ESD using a 16-MDCT device (LightSpeed 16; GE Healthcare Life Sciences, Little Chalfont, UK) with a fixed tube voltage of 120 kVp and an automatic tube current modulation program (3D mA modulation; GE Healthcare Life Sciences). The operational parameters of the scanner were set to noise index, 10.0 HU at 5 mm slice thickness; collimation, 1.25 mm; detector configuration, 16×1.25 mm; table feed, 27.5 mm/rotation; pitch, 1.37:1; field of view, 32×32 cm; gantry rotation time, 0.5 sec; acquisition time, 12.7 sec. All transverse CT images were reconstructed at 5 mm section thickness with a standard reconstruction algorithm. CT images were analyzed using Advantage Workstation v4.6 software (GE Healthcare Life Sciences). To evaluate the amount of residual gas in the gastrointestinal tract following ESD, a scan was performed at the level of the ileocecal valve, and the major and minor axes of the cecal lumen and the diameter of the terminal ileum lumen were measured. A small level of focal free air close to the colonic wall of the resected lesion was defined as a transmural air leak and a high level of free air reaching the surface of the liver was defined as free air (32,33).

Definitions of outcome parameters and complications

The operation time was measured from the start of injection into the submucosal layer until the end of the procedure. A diagnosis of perforation was made by direct endoscopic observation during ESD. Post-procedure hemorrhage was diagnosed with clinical evidence of bleeding following ESD, as shown by repetitive bloody bowel discharges that required endoscopic treatment.

Statistical analysis

All the variables in the present study are described as the number of patients (%) or the median (range). Fisher's exact test was used to compare differences in categorical variables between the two groups when required, and the non-parametric Mann-Whitney U test was used to compare continuous variables. Two-sided P<0.05 was considered to indicate statistically significant differences for all tests. All statistical analyses were performed using JMP v12 (SAS Institute, Inc., Cary, NC, USA).

Results

Patient and procedure characteristics

A total of 83 patients underwent colorectal ESD during the study period. Among them, 17 patients were excluded due to presentation of chronic pulmonary dysfunction; the remaining 66 patients were enrolled in the present study. The enrolled subjects were randomized into two groups: A total of 34 patients received CO2 insufflation (CO2 group) and 32 patients received air insufflation (air group; Fig. 1).

Baseline characteristics and related factors for each group are listed in Table I. The median age was 65.0 (34.0–87.0) years in the CO2 group and 65.5 (34.0–86.0) years in the air group. No significant differences in age, sex, en bloc resection rate, location of the colorectal lesion, histopathological type, tumor size, histological depth, resection size or histopathologically curative resection rate between the groups were identified. The median procedure time was 35 (10–163) and 30 (9–94) min and the rate of clip closure for the post-ESD ulcer was 44.1 and 53.1% in the CO2 and air groups, respectively; neither of these differed significantly between the groups.

Table I.

Patient and procedure characteristics.

Table I.

Patient and procedure characteristics.

VariablesCO2 group (n=34)Air group (n=32)P-value
Age, years65.0 (34.0–87.0)65.5 (34.0–86.0)0.78
Sex, male/female, n18/1617/151.00
Location of lesion, C/A/T/D/S/R, n2/3/7/0/5/173/6/5/1/5/120.58
En bloc resection, n (%)33 (97.1)31 (96.9)1.00
Histopathological type, tub1/tub2/adenoma/carcinoid/hyperplastic/endocrine carcinoma, n14/1/13/5/0/111/1/14/5/1/00.71
Histological depth, M/SM, n25/825/71.00
Histopathologically curative resection, n (%)30 (88.2)31 (96.9)0.36
Tumor size, mm30 (12–72)30 (12–47)0.93
Resection size, mm23 (7–62)24 (3–46)0.73
Procedure time, min35 (10–163)30 (9–94)0.57
Prophylactic clip closure, n (%)15 (44.1)17 (53.1)0.62

[i] Continuous variables are presented as the median (range). C, cecum; A, ascending colon; T, transverse colon; D, descending colon; S, sigmoid colon; R, rectum; tub, tubular; M, intramucosal; SM, submucosal.

Presence of residual gas in the gastrointestinal tract evaluated by CT examination

Representative CT images of patients in the two groups are presented in Fig. 2. In the air group, marked intestinal dilatation of the cecum and terminal ileum was observed compared with the CO2 group. The findings of the CT examination following ESD are summarized in Table II. The median major (21.8 vs. 56.3 mm, P<0.001) and minor (13.4 vs. 36.6 mm, P<0.001) axes of the cecal lumen at the level of the ileocecal valve were significantly lower in the CO2 group compared with the air group. In addition, the median diameter of the terminal ileum lumen was significantly lower in the CO2 group compared with that in the air group (5.0 vs. 16.4 mm, P<0.001). These findings demonstrated the effects of CO2 insufflation on the diminution of residual gas in the bowel following colorectal ESD.

Table II.

Post-ESD computed tomography results.

Table II.

Post-ESD computed tomography results.

VariablesCO2 group (n=34)Air group (n=32)P-value
Major axis of cecal lumen after ESD, mm21.8 (6.1–59.0)56.3 (28.9–126.9)<0.001
Minor axis of cecal lumen after ESD, mm13.4 (4.2–39.8)36.6 (11.9–62.3)<0.001
Diameter of terminal ileum lumen after ESD, mm5.0 (0.0–15.9)16.4 (3.5–28.1)<0.001
Free air after ESD, n (%)1 (2.9)3 (9.4)0.340
Transmural air leak after ESD, n (%)8 (23.5)2 (6.3)0.080

[i] Continuous variables are presented as the median (range). ESD, endoscopic submucosal dissection.

The presence of free air was indicated in 1 patient (2.9%) in the CO2 group and 3 patients (9.4%) in the air group. Transmural air leak was also observed in 8 patients (23.5%) in the CO2 group and 2 patients (6.3%) in the air group; however, no significant differences were identified in the incidence rates of these air leaks between the groups.

PtcCO2 and vital signs prior to and following ESD

The PtcCO2 and vital signs (blood pressure, heart rate and SpO2) of patients recorded during ESD are listed in Table III. The median PtcCO2 prior to and following ESD was 38.5 (22.0–51.0) and 46.5 (30.0–58.0) mmHg in the CO2 group and 40.0 (27.0–48.0) and 47.0 (36.0–55.0) mmHg in the air group, respectively; no significant differences in these values between the groups were determined. The median peak PtcCO2 during ESD was 49.0 (34.0–111.0) mmHg in the CO2 group and 49.0 (40.0–55.0) mmHg in the air group; no significant difference was observed between these values.

Table III.

PtcCO2 and vital signs during ESD.

Table III.

PtcCO2 and vital signs during ESD.

VariablesCO2 group (n=34)Air group (n=32)P-value
Baseline PtCO2, mmHg38.5 (22.0–51.0)40.0 (27.0–48.0)0.13
PtCO2 after ESD, mmHg46.5 (30.0–58.0)47.0 (36.0–55.0)0.38
Peak PtCO2, mmHg49.0 (34.0–111.0)49.0 (40.0–55.0)0.95
Baseline systolic blood pressure, mmHg132.5 (94.0–187.0)133.5 (98.0–180.0)0.78
Systolic blood pressure after ESD, mmHg134.5 (100.0–180.0)135.5 (85.0–174.0)0.83
Maximum systolic blood pressure, mmHg150.5 (112.0–229.0)145.0 (102.0–182.0)0.80
Maximum systolic blood pressure elevation value, mmHg3.5 (0.0–92.0)4.5 (0.0–42.0)0.64
Baseline diastolic blood pressure, mmHg74.0 (38.0–103.0)69.5 (50.0–95.0)0.48
Diastolic blood pressure after ESD, mmHg74.5 (56.0–104.0)75.0 (45.0–94.0)0.89
Maximum systolic blood pressure, mmHg84.0 (64.0–121.0)83.0 (53.0–112.0)0.90
Maximum systolic blood pressure elevation value, mmHg7.5 (0.0–43.0)7.5 (0.0–34.0)0.73
Baseline heart rate, n/min76.5 (51.0–125.0)71.0 (50.0–116.0)0.30
Heart rate after ESD, n/min72.0 (53.0–97.0)69.5 (53.0–93.0)0.31
Maximum heart rate, n/min87.5 (61.0–125.0)80.0 (57.0–125.0)0.07
Maximum heart rate elevation value, n/min3.5 (0.0–48.0)1.5 (0.0–37.0)0.74
Minimum SpO2, %98.0 (94.0–100.0)98.5 (95.0–100.0)0.81

[i] Values are presented as the median (range). ESD, endoscopic submucosal dissection; PtCO2, transcutaneous CO2 tension.

Circulation vitals, including systolic and diastolic blood pressures and heart rate prior to and following ESD, did not differ significantly between the groups. In addition, significant elevation or lowering of blood pressures and heart rate during ESD was not observed in either group. The median minimum SpO2 levels did not differ significantly between the groups, being 98.0 (94.0–100.0) % in the CO2 group and 98.5 (95.0–100.0) % in the air group (Table III).

Incidence of post-ESD complications and hospital stay

ESD-related complications and the length of hospital stay are summarized in Table IV. No significant differences were observed in body temperature, incidence of post-ESD hemorrhage or the length of stay between the CO2 and air groups. Furthermore, no significant differences were identified in serum CRP levels or WBC counts on day 1 after ESD. A patient in the CO2 group presented a complication of perforation during ESD, but the lesion was closed using clips. The patient did not require emergency surgery and was discharged 4 days after ESD. No cases of cardiopulmonary adverse events occurred in either group.

Table IV.

ESD-related complications and length of hospital stay.

Table IV.

ESD-related complications and length of hospital stay.

VariablesCO2 group (n=34)Air group (n=32)P-value
Body temperature, °C36.8 (36.3–38.5)36.8 (36.3–38.4)0.94
Post-procedure hemorrhage, n (%)2 (5.9)1 (3.1)1.00
WBC on day 1 after ESD, n/µl6,800 (4,220–14,890)7,500 (3,940–18,900)0.80
CRP on day 1 after ESD, mg/dl0.27 (0.02–6.17)0.20 (0.02–11.03)0.98
Perforation, n (%)1 (2.9)0 (0)1.00
Emergency surgery, n (%)0 (0)0 (0)1.00
Hospital stay, days3 (2–9)3 (2–10)0.34

[i] Continuous variables are presented as the median (range). CRP, C-reactive protein; ESD, endoscopic submucosal dissection; WBC, white blood cell count.

Discussion

ESD of colorectal tumors can provide clinical benefits as it enables en bloc resection of large superficial neoplasms (32,34). However, one of the problems with this procedure is the severe intraoperative and post-operative abdominal discomfort and distention caused by air infusion (15). CO2 is absorbed by the bowel mucosa approximately 100 times faster than air and is rapidly eliminated through the lungs (35). This may be associated with the superior recovery quality of CO2 insufflation compared with room air insufflation in colonoscopy (36). Therefore, when compared with air insufflation, CO2 insufflation is expected to reduce the volume of residual gas following ESD, which is a primary cause of patient discomfort associated with this procedure, and consequently prevent the development of abdominal symptoms and problems associated with ESD (5,2230).

The results of the present randomized trial indicated that CO2 insufflation during colorectal ESD significantly reduced the volume of residual bowel gas compared with air insufflation. Several studies have reported the efficacy of CO2 insufflation during various types of endoscopic procedures (24,25,28,37,38). However, few studies have objectively evaluated the level of residual bowel gas following this procedure. Chen et al (39), observed that CO2 insufflation significantly reduced the volume of residual bowel gas compared with air insufflation following colonoscopy by using abdominal radiography. To the best of our knowledge, the present study is the first to objectively evaluate the degree of bowel distention following colorectal ESD using CT examination. The present study identified the median major and minor axes of the cecal lumen at the level of the ileocecal valve to be significantly lower in the CO2 group than in the air group (P<0.001). In addition, the median diameter of the terminal ileum lumen was significantly lower in the CO2 group than in the air group (P<0.001). These findings suggest that CO2 insufflation significantly reduced the volume of residual bowel gas compared with air insufflation following colorectal ESD.

In the present study, there was no significant difference in the peak PtCO2, which is a useful marker for evaluating CO2 retention (40), between the CO2 and air insufflation groups. No marked adverse events, such as CO2 narcosis, air embolism, SpO2 depression or hemodynamic abnormality, occurred in either group. In addition, post-procedure CT demonstrated no significant difference in the incidence of free air or transmural air leak between the groups. As CO2 insufflation can reduce the volume of residual bowel gas, it may avoid an increase in intra-bowel pressure and improve patient safety. These results suggest that CO2 insufflation during colorectal ESD is a safer alternative to air insufflation.

In the present study, patients with chronic pulmonary dysfunction were excluded, as the safety of CO2 insufflation during colorectal ESD has not been established for such patients. However, a recent study demonstrated that CO2 insufflation during gastric ESD was safe for patients with pulmonary dysfunction under conscious sedation (31). CO2 insufflation during colorectal ESD is also safe for patients with obstructive ventilatory disturbance (41). The number of patients, particularly elderly patients, suffering from complications including chronic pulmonary dysfunction is increasing; therefore, a clinical trial that clarifies the safety and efficacy of CO2 insufflation during colorectal ESD in such patients should be conducted.

The present study had a number of limitations. First, the study was a single-center study with a relatively small sample size. Therefore, multi-center studies with larger sample sizes should be performed to confirm the present results. These studies may also be useful for assessing whether CO2 insufflation may reduce the risk of ESD-related complications, such as transmural air leak and perforation, compared with conventional air insufflation. It should be also verified in future studies whether CO2 insufflation relieved abdominal pain and improved the degree of patients satisfaction. Second, the volume of insufflated gas during the ESD procedure could not be measured. However, it is probable that there was not much difference in the volume of insufflated gas between the CO2 and air groups since the flow volume was the same (1.4 L/min) in both groups and no significant difference was observed in the median procedure time between the groups.

Despite these limitations, it should be emphasized that reduction of the patient's residual gastrointestinal gas following ESD can decrease abdominal fullness; this is associated with a high level of patient satisfaction (35). In conclusion, the present results suggest that CO2 insufflation during colorectal ESD is effective, as it may significantly reduce residual gas in the gastrointestinal tract and therefore increase the satisfaction and comfort of patients who have undergone ESD.

Acknowledgements

Not applicable.

Funding

No funding was received.

Availability of data and materials

The analyzed data sets generated during the study are available from the corresponding author on reasonable request.

Authors contributions

TS and HA contributed to the study design, acquisition and interpretation of data, and in the writing of the manuscript; NO and JT acquired the data; MK and TI analyzed and interpreted the data; MS wrote the manuscript and approved the final contents of the manuscript. The final version of the manuscript has been read and approved by all authors.

Ethics approval and consent to participate

The study protocol was approved by the institutional ethics committee of Gifu University Hospital (ethical approval code: 28-104). All eligible individuals provided written informed consent prior to study enrollment.

Consent for publication

Not applicable.

Competing interests

The authors declare no competing interests.

References

1 

Zauber AG, Winawer SJ, O'Brien MJ, Lansdorp-Vogelaar I, van Ballegooijen M, Hankey BF, Shi W, Bond JH, Schapiro M, Panish JF, et al: Colonoscopic polypectomy and long-term prevention of colorectal-cancer deaths. N Engl J Med. 366:687–696. 2012. View Article : Google Scholar

2 

Rex DK, Johnson DA, Lieberman DA, Burt RW and Sonnenberg A: American College of Gastroenterology: Colorectal cancer prevention 2000: Screening recommendations of the American College of Gastroenterology. Am J Gastroenterol. 95:868–877. 2000. View Article : Google Scholar

3 

Saito Y, Kawano H, Takeuchi Y, Ohata K, Oka S, Hotta K, Okamoto K, Homma K, Uraoka T, Hisabe T, et al: Current status of colorectal endoscopic submucosal dissection in Japan and other Asian countries: Progressing towards technical standardization. Dig Endosc. 24 Suppl 1:67–72. 2012. View Article : Google Scholar

4 

Fujishiro M: Endoscopic submucosal dissection for colorectal neoplasms. World J Gastrointest Endosc. 1:32–38. 2009. View Article : Google Scholar

5 

Saito Y, Uraoka T, Yamaguchi Y, Hotta K, Sakamoto N, Ikematsu H, Fukuzawa M, Kobayashi N, Nasu J, Michida T, et al: A prospective, multicenter study of 1111 colorectal endoscopic submucosal dissections (with video). Gastrointest Endosc. 72:1217–1225. 2010. View Article : Google Scholar

6 

Morley AP, Lau JY and Young RJ: Tension pneumothorax complicating a perforation of a duodenal ulcer during ERCP with endoscopic sphincterotomy. Endoscopy. 29:3321997. View Article : Google Scholar

7 

Katzgraber F, Glenewinkel F, Fischler S and Rittner C: Mechanism of fatal air embolism after gastrointestinal endoscopy. Int J Legal Med. 111:154–156. 1998. View Article : Google Scholar

8 

Rai A and Iftikhar S: Tension pneumothorax complicating diagnostic upper endoscopy: A case report. Am J Gastroenterol. 94:845–847. 1999. View Article : Google Scholar

9 

Nayagam J, Ho KM and Liang J: Fatal systemic air embolism during endoscopic retrograde cholangio-pancreatography. Anaesth Intensive Care. 32:260–264. 2004.

10 

Green BT and Tendler DA: Cerebral air embolism during upper endoscopy: Case report and review. Gastrointest Endosc. 61:620–623. 2005. View Article : Google Scholar

11 

Stabile L, Cigada M, Stillittano D, Morandi E, Zaffroni M, Rossi G and Lapichino G: Fatal cerebral air embolism after endoscopic retrograde cholangiopancreatography. Acta Anaesthesiol Scand. 50:648–649. 2006. View Article : Google Scholar

12 

Bisceglia M, Simeone A, Forlano R, Andriulli A and Pilotto A: Fatal systemic venous air embolism during endoscopic retrograde cholangiopancreatography. Adv Anat Pathol. 16:255–262. 2009. View Article : Google Scholar

13 

Finsterer J, Stöllberger C and Bastovansky A: Cardiac and cerebral air embolism from endoscopic retrograde cholangio-pancreatography. Eur J Gastroenterol Hepatol. 22:1157–1162. 2010. View Article : Google Scholar

14 

van Boxel GI, Hommers CE, Dash I, Goodman AJ, Green J and Orme RM: Myocardial and cerebral infarction due to massive air embolism following endoscopic retrograde cholangiopancreatography (ERCP). Endoscopy. 42 Suppl 2:E80–E81. 2010. View Article : Google Scholar

15 

Saito Y, Uraoka T, Matsuda T, Emura F, Ikehara H, Mashimo Y, Kikuchi T, Kozu T and Saito D: A pilot study to assess the safety and efficacy of carbon dioxide insufflation during colorectal endoscopic submucosal dissection with the patient under conscious sedation. Gastrointest Endosc. 65:537–542. 2007. View Article : Google Scholar

16 

Nonaka S, Saito Y, Takisawa H, Kim Y, Kikuchi T and Oda I: Safety of carbon dioxide insufflation for upper gastrointestinal tract endoscopic treatment of patients under deep sedation. Surg Endosc. 24:1638–1645. 2010. View Article : Google Scholar

17 

Maeda Y, Hirasawa D, Fujita N, Obana T, Sugawara T, Ohira T, Harada Y, Yamagata T, Suzuki K, Koike Y, et al: A prospective, randomized, double-blind, controlled trial on the efficacy of carbon dioxide insufflation in gastric endoscopic submucosal dissection. Endoscopy. 45:335–341. 2013. View Article : Google Scholar

18 

Kikuchi T, Fu KI, Saito Y, Uraoka T, Fukuzawa M, Fukunaga S, Sakamoto T, Nakajima T and Matsuda T: Transcutaneous monitoring of partial pressure of carbon dioxide during endoscopic submucosal dissection of early colorectal neoplasia with carbon dioxide insufflation: A prospective study. Surg Endosc. 24:2231–2235. 2010. View Article : Google Scholar

19 

Suzuki T, Minami H, Komatsu T, Masusda R, Kobayashi Y, Sakamoto A, Sato Y, Inoue H and Serada K: Prolonged carbon dioxide insufflation under general anesthesia for endoscopic submucosal dissection. Endoscopy. 42:1021–1029. 2010. View Article : Google Scholar

20 

Kim SY, Chung JW, Park DK, Kwon KA, Kim KO and Kim YJ: Efficacy of carbon dioxide insufflation during gastric endoscopic submucosal dissection: A randomized, double-blind, controlled, prospective study. Gastrointest Endosc. 82:1018–1024. 2015. View Article : Google Scholar

21 

Li X, Dong H, Zhang Y and Zhang G: CO2 insufflation versus air insufflation for endoscopic submucosal dissection: A meta-analysis of randomized controlled trials. PLoS One. 12:e01779092017. View Article : Google Scholar

22 

Hussein AM, Bartram CI and Williams CB: Carbon dioxide insufflation for more comfortable colonoscopy. Gastrointest Endosc. 30:68–70. 1984. View Article : Google Scholar

23 

Stevenson GW, Wilson JA, Wilkinson J, Norman G and Goodacre RL: Pain following colonoscopy: Elimination with carbon dioxide. Gastrointest Endosc. 38:564–567. 1992. View Article : Google Scholar

24 

Church J and Delaney C: Randomized, controlled trial of carbon dioxide insufflation during colonoscopy. Dis Colon Rectum. 46:322–326. 2003. View Article : Google Scholar

25 

Sumanac K, Zealley I, Fox BM, Rawlinson J, Salena B, Marshall JK, Stevenson GW and Hunt RH: Minimizing postcolonoscopy abdominal pain by using CO2 insufflation: A prospective, randomized, double blind, controlled trial evaluating a new commercially available CO2 delivery system. Gastrointest Endosc. 56:190–194. 2002. View Article : Google Scholar

26 

Rogers BH: The safety of carbon dioxide insufflation during colonoscopic electrosurgical polypectomy. Gastrointest Endosc. 20:115–117. 1974. View Article : Google Scholar

27 

Bretthauer M, Lynge AB, Thiis-Evensen E, Hoff G, Fausa O and Aabakken L: Carbon dioxide insufflation in colonoscopy: Safe and effective in sedated patients. Endoscopy. 37:706–709. 2005. View Article : Google Scholar

28 

Bretthauer M, Thiis-Evensen E, Huppertz-Hauss G, Gisselsson L, Grotmol T, Skovlund E and Hoff G: NORCCAP (Norwegian colorectal cancer prevention): A randomised trial to assess the safety and efficacy of carbon dioxide versus air insufflation in colonoscopy. Gut. 50:604–607. 2002. View Article : Google Scholar

29 

Nakajima K, Lee SW, Sonoda T and Milsom JW: Intraoperative carbon dioxide colonoscopy: A safe insufflation alternative for locating colonic lesions during laparoscopic surgery. Surg Endosc. 19:321–325. 2005. View Article : Google Scholar

30 

Wu J and Hu B: The role of carbon dioxide insufflation in colonoscopy: A systematic review and meta-analysis. Endoscopy. 44:128–136. 2012. View Article : Google Scholar

31 

Takada J, Araki H, Onogi F, Nakanishi T, Kubota M, Ibuka T, Shimizu M and Moriwaki H: Safety of carbon dioxide insufflation during gastric endoscopic submucosal dissection in patients with pulmonary dysfunction under conscious sedation. Surg Endosc. 29:1963–1969. 2015. View Article : Google Scholar

32 

Tamegai Y, Saito Y, Masaki N, Hinohara C, Oshima T, Kogure E, Liu Y, Uemura N and Saito K: Endoscopic submucosal dissection: A safe technique for colorectal tumors. Endoscopy. 39:418–422. 2007. View Article : Google Scholar

33 

Coriat R, Leblanc S, Pommaret E, Chryssostalis A, Prat F and Chaussade S: Transmural air leak following endoscopic submucosal dissection: A non-useful computed tomography finding. Endoscopy. 42:1117, author reply 11182010. View Article : Google Scholar

34 

Terasaki M, Tanaka S, Oka S, Nakadoi K, Takata S, Kanao H, Yoshida S and Chayama K: Clinical outcomes of endoscopic submucosal dissection and endoscopic mucosal resection for laterally spreading tumors larger than 20 mm. J Gastroenterol Hepatol. 27:734–740. 2012. View Article : Google Scholar

35 

Saltzman HA and Sieker HO: Intestinal response to changing gaseous environments: Normobaric and hyperbaric observations. Ann N Y Acad Sci. 150(1 Gastrointesti): 1–39. 1968. View Article : Google Scholar

36 

Wang WL, Wu ZH, Sun Q, Wei JF, Chen XF, Zhou DK, Zhou L, Xie HY and Zheng SS: Meta-analysis: The use of carbon dioxide insufflation vs. room air insufflation for gastrointestinal endoscopy. Aliment Pharmacol Ther. 35:1145–1154. 2012. View Article : Google Scholar

37 

Dellon ES, Velayudham A, Clarke BW, Isaacs KL, Gangarosa LM, Galanko JA and Grimm IS: A randomized, controlled, double-blind trial of air insufflation versus carbon dioxide insufflation during ERCP. Gastrointest Endosc. 72:68–77. 2010. View Article : Google Scholar

38 

Hirai F, Beppu T, Nishimura T, Takatsu N, Ashizuka S, Seki T, Hisabe T, Nagahama T, Yao K, Matsui T, et al: Carbon dioxide insufflation compared with air insufflation in double-balloon enteroscopy: A prospective, randomized, double-blind trial. Gastrointest Endosc. 73:743–749. 2011. View Article : Google Scholar

39 

Chen SW, Hui CK, Chang JJ, Lee TS, Chan SC, Chien CH, Hu CC, Lin CL, Chen LW, Liu CJ, et al: Carbon dioxide insufflation during colonoscopy can significantly decrease post-interventional abdominal discomfort in deeply sedated patients: A prospective, randomized, double-blinded, controlled trial. J Gastroenterol Hepatol. 31:808–813. 2016. View Article : Google Scholar

40 

Chhajed PN, Kaegi B, Rajasekaran R and Tamm M: Detection of hypoventilation during thoracoscopy: Combined cutaneous carbon dioxide tension and oximetry monitoring with a new digital sensor. Chest. 127:585–588. 2005. View Article : Google Scholar

41 

Yoshida M, Imai K, Hotta K, Yamaguchi Y, Tanaka M, Kakushima N, Takizawa K, Matsubayashi H and Ono H: Carbon dioxide insufflation during colorectal endoscopic submucosal dissection for patients with obstructive ventilatory disturbance. Int J Colorectal Dis. 29:365–371. 2014. View Article : Google Scholar

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March-2018
Volume 8 Issue 3

Print ISSN: 2049-9434
Online ISSN:2049-9442

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Spandidos Publications style
Sugiyama T, Araki H, Ozawa N, Takada J, Kubota M, Ibuka T and Shimizu M: Carbon dioxide insufflation reduces residual gas in the gastrointestinal tract following colorectal endoscopic submucosal dissection. Biomed Rep 8: 257-263, 2018
APA
Sugiyama, T., Araki, H., Ozawa, N., Takada, J., Kubota, M., Ibuka, T., & Shimizu, M. (2018). Carbon dioxide insufflation reduces residual gas in the gastrointestinal tract following colorectal endoscopic submucosal dissection. Biomedical Reports, 8, 257-263. https://doi.org/10.3892/br.2018.1044
MLA
Sugiyama, T., Araki, H., Ozawa, N., Takada, J., Kubota, M., Ibuka, T., Shimizu, M."Carbon dioxide insufflation reduces residual gas in the gastrointestinal tract following colorectal endoscopic submucosal dissection". Biomedical Reports 8.3 (2018): 257-263.
Chicago
Sugiyama, T., Araki, H., Ozawa, N., Takada, J., Kubota, M., Ibuka, T., Shimizu, M."Carbon dioxide insufflation reduces residual gas in the gastrointestinal tract following colorectal endoscopic submucosal dissection". Biomedical Reports 8, no. 3 (2018): 257-263. https://doi.org/10.3892/br.2018.1044