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Videosurgery and Other Miniinvasive Techniques
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Original paper

Does elevated intra-abdominal pressure during laparoscopic colorectal surgery cause acute gastrointestinal injury?

Zhenghao Cai
,
Manu L.N.G. Malbrain
,
Jing Sun
,
Ruijun Pan
,
Junjun Ma
,
Bo Feng
,
Feng Dong
,
Minhua Zheng

Videosurgery Miniinv 2015; 10 (2): 161–169
Online publish date: 2015/06/15
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Introduction

Acute gastrointestinal injury (AGI) was proposed by the Working Group on Abdominal Problems (WGAP) of the European Society of Intensive Care Medicine (ESICM) in 2012 [1]. According to the severity, a grading system of AGI was established for clinical and research purposes [1]. Similar symptoms of gastrointestinal dysfunction, including ileus, diarrhea and vomiting, can be observed in postoperative patients after abdominal surgery [2]. These symptoms are AGI grade I according to the ESICM WGAP recommendations [1].
Though technical improvements of laparoscopic colorectal surgery and perioperative care in recent years [3–5] have significantly reduced the incidence of AGI correlated symptoms, resulting in improved clinical recovery after colorectal surgery [6–8], continuous insufflation of CO2 into the peritoneal cavity still results in elevated intra-abdominal pressure (IAP) for several hours during surgery. Traditionally insufflation pressures are limited to an IAP of 15 mm Hg and are generally between 12 and 15 mm Hg, corresponding with intra-abdominal hypertension (IAH) grade I [9]. Furthermore, this level of IAH has been associated with AGI grade II, which means gastrointestinal dysfunction more severe than might be expected in relation to standard abdominal procedures and surgery [1]. Moreover, in analogy to other intra-abdominal organs (like the liver, kidneys and spleen), the gut also suffers from a reduction of blood flow during IAH. A splanchnic ischemia-reperfusion (IR) injury is induced by the insufflation and desufflation of CO2 pneumoperitoneum while IAP increases up to 12 mm Hg [10, 11], with postoperative AGI correlated symptoms observed in animal models of IR injury [12].
Most clinical trials on this regard has not examined the IAP level during CO2 pneumoperitoneum. Moreover, Kronberg et al. did not introduce IAP into their novel predictive score evaluating possible risk factors for postoperative ileus (POI) after laparoscopic colorectal surgery [13]. Kozlik et al. had indicated the development of oxidative stress performed at high pressure pneumoperitoneum in a clinical study, but they focused mainly on the duration of laparoscopy, not on the intra-abdominal pressure [14]. Therefore, it remained to be discussed whether the level of IAP during laparoscopic surgery was related to the incidence of postoperative AGI. If this is the case, then the IAP induced by CO2 pneumoperitoneum during laparoscopic surgery should be set below a critical threshold in the future.
In addition, POI, a common symptom of AGI, is considered to be a major determining factor related to increased hospital stay and increased recovery time after surgery [15, 16]. Various pathogenic mechanisms have been suggested in relation to POI, including inflammatory mediators such as interleukin-6 (IL-6) and tumor necrosis factor  (TNF-) [17]. These cytokine levels have been reported to increase in patients with high IAP induced by CO2 pneumoperitoneum during laparoscopic surgery, and IL-6 and TNF- levels may be elevated for more than 1 day [18]. In this study we compared the degree of increase of these cytokines caused by different levels of IAP. We hypothesized that IAP levels and cytokine levels correlate with the incidence of POI.

Aim

The aim of the study was to assess the impact of increased IAP during laparoscopic CO2 pneumoperitoneum on the incidence of postoperative AGI. To verify the safety of laparoscopic colorectal surgery performed with IAP up to 15 mm Hg.

Material and methods

Ethics

The Ethics Committee of Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China, approved the protocol of this study. The project was registered at the Chinese Clinical Trial Registry (Registration Number: ChiCTR-TRC-13003292) in accordance with the ethical standards of the 1964 Declaration of Helsinki and its later amendments. Out of 84 consecutive patients who met the study inclusion criteria, 66 (78.6%) agreed to participate after signed informed consent was obtained.

Sample size calculation

The standardized formula N = 0(1 – 0)(Z + Z)2/2 was used to calculate the sample size ( = 0.05, 1 –  = 0.2, Z = 1.6449, Z = 1.2816; 0 refers to the population rate of endpoint;  refers to the expected significant difference of sample rate). In a preliminary experiment before this study, we observed 13 eligible patients who met the inclusion criteria within 30 days. Five (38.5%) patients presented AGI correlated symptoms. On the other hand, a reduction of incidence of AGI by 50% was considered clinically significant. Thus, 0 = 38.5%,  = 0/2. The theoretical sample size (N) hence is 54.76. With a loss to follow-up probability of about 0.2, the actual sample size was calculated at (1 + 0.2) × N = 65.71 ≈ 66 in this study.

Patients and eligibility

Patients from Shanghai Minimally Invasive Surgery Center, Shanghai, China were enrolled for this study. Inclusion criteria were as follows: age between 40 and 80 years; American Society of Anesthesiologists (ASA) score I or II; a biopsy proven histological diagnosis of colorectal carcinoma; no clinical evidence of metastasis; undergoing laparoscopic colorectal surgery. Exclusion criteria were: contraindication of laparoscopic surgery (e.g. extensive intra-abdominal adhesion); emergency procedure; evidence of bowel ileus/obstruction before surgery; unresectable mass; a planned stoma (e.g. abdominoperineal resection of rectal carcinoma, protective ileal stoma); an unexpected stoma; conversion to open surgery; short-term re-operation; postoperative opioid analgesic usage; or persistent uncorrected severe fluid and electrolyte imbalance (e.g. hypokalemia, hypomagnesemia) [19].

Study design and intervention

The eligible patients were randomized into 3 groups using Microsoft Excel software (Redmond, WA, USA), in which the IAP of CO2 pneumoperitoneum during laparoscopic surgery was set at three levels in different groups: group 1: 10 mm Hg; group 2: 12 mm Hg; and group 3: 15 mm Hg. The fixed IAP was set and monitored via the CO2 pneumoperitoneum insufflation system (STORZ Thermoflator, KARL STORZ GmbH & Co. KG, Tuttlingen, Germany) by an anesthesiologist.
The laparoscopic procedures were standardized and performed by an identical surgical team in all groups. Right hemicolectomy was performed in a supine position with the head of the bed raised 30°, while sigmoid colectomy and anterior resection of the rectum were performed in a modified lithotomy position (head-down tilt). Left hemicolectomy required an alteration between these two positions. A small incision with a varying size corresponding to the resection specimen was performed in order to accomplish the anastomosis. The nasogastric tube (NG tube) was inserted before the anesthesia induction and was removed immediately when the patients regained consciousness in order to avoid anesthetic accidents (inhalation of vomit).

Blinding

A double-blind method was adopted in this study. Patients, operating surgeon or surgeons taking care of patients were not informed about the IAP level applied during the surgery; only the anesthesiologist was aware, keeping the IAP level fixed during laparoscopy.

End-points and outcomes

The first flatus/defecation, the first bowel movement (the sense of bowel sound before flatus/defecation) and the occurrence of vomiting/diarrhea were self-reported by the patient and recorded in the study files. Patients were visited at least once daily after surgery by an experienced surgeon evaluating clinical recovery, including the tolerance of semi-liquid food, other postoperative intra-abdominal complications such as anastomotic leak, surgical site oozing, etc, and finally the discharge time. The anesthesiologist recorded the duration of surgery and CO2 pneumoperitoneum and the intra-operative blood loss. At the onset of the CO2 pneumoperitoneum and at 6 a.m. on postoperative day 1 (POD1), serum interleukin-6 (IL-6) and TNF- levels were measured.
Criteria for allowing semi-liquid food were: normothermia; no adverse reactions with liquid food; normal defecation/free-flow of stoma. Discharge criteria included: tolerance of semi-liquid food for more than 24 h; normothermia; normal defecation/free-flow of stoma.
Postoperative ileus (POI) was defined as absence of flatus/defecation or bowel movement before POD2 according to Vather et al. [2]. The AGI was considered to occur in patients who presented: nausea/vomiting unrelated to anesthetic reaction; diarrhea (three or more loose or liquid stools per day) for more than 1 day; postoperative ileus (POI).

Statistical analysis

The data collection was done using EpiData 3.1 software (freeware available at www.epidata.dk, Odense, Denmark), while all statistical analysis was performed with the IBM Statistical Package for the Social Sciences (SPSS 13.0, Chicago, IL, USA). Continuous data were expressed by mean ± SD, and intergroup differences were determined by one-way analysis of variance (ANOVA) analyses (represented asx ± s). Categorical data were expressed as frequency distributions and/or percentages, and the 2 test or Fisher’s exact test was used to determine intergroup differences. For other variables, a non-parametric test was used (represented as median and quartiles). Two-sided p values < 0.05 were considered to indicate statistical significance.

Results

Patient demographics

All 66 enrolled patients were analyzed, and each group consisted of randomly assigned 22 patients. No statistically significant differences in baseline characteristics were noted between patients in the 3 groups (Table I). Tumor location, type of surgery, duration of surgery, duration of CO2 pneumoperitoneum, intra-operative blood loss, and removal of NG tube within 6 h after surgery were not significantly different between the 3 groups (Table I). The postoperative anatomopathologic staging (based on the TNM classification system, 2010, 7th edition) was also not statistically significantly different (p = 0.44). The length of follow-up ranged from 7 to 14 days after surgery and 4 (6.1%) patients presented with early postoperative intra-abdominal complications other than AGI: one chylous fistula, one anastomotic leak and two cases of surgical site oozing. However, we could not determine a statistical correlation between IAP and early postoperative intra-abdominal complications other than AGI (p = 0.17).

Postoperative AGI incidence

Of the 66 enrolled patients, 11 patients were excluded from the AGI analysis (respectively 3, 3 and 5 in groups 1, 2 and 3). The reasons for exclusion were as follows: 4 patients underwent an unexpected stoma; the other 6 received opioid analgesia after surgery; and finally in 1 patient from group 1, the surgeon changed the IAP level (from 10 to 15 mm Hg) during surgery.
Of the 55 remaining patients, 15 (27.3%) patients presented with postoperative AGI correlative symptoms (respectively 6, 3 and 6 in groups 1, 2 and 3), of which 8 cases were regarded as AGI grade I and 7 cases were classified as AGI grade II. Neither the incidence nor the grade of AGI showed a statistically significant difference between the 3 groups (p = 0.41, and p = 0.36 respectively). Recovery of gastrointestinal function was not significantly improved in patients receiving a low IAP level (group 1) compared with those having received higher IAP levels (groups 2 and 3) during laparoscopy. The level of IAP elevation was not related to increased occurrence of AGI symptoms, neither POI (p = 0.92) nor diarrhea (p = 0.67). Postoperative hospital stay was similar in the 3 groups (p = 0.27) (Table II).
Compared with the 55 patients included in the AGI analysis, the use of opioid analgesia and the application of the stoma did not alter the time to the first flatus/defecation, the time to the first bowel movement or the post-operative hospital stay (Table III). However, patients with a protective ileal stoma achieved earlier tolerance of semi-liquid food than others (p < 0.001, Mann-Whitney U-test).

Serum cytokine levels

The patients in the 3 groups had equal serum IL-6 and TNF- levels at the onset of CO2 pneumoperitoneum (Table IV). At 6 a.m. on POD 1, serum IL-6 levels were increased (p < 0.001, Wilcoxon’s test) while TNF- levels remained virtually unchanged compared to the pre-operative levels (p = 0.17, Wilcoxon’s test). However, the increase in IL-6 levels was not significantly different in the 3 groups (p = 0.27) (Table IV). The 11 POI cases did not have a significantly increase in IL-6 levels compared to other patients (p = 0.98, Mann-Whitney U-test).

Discussion

For the past 20 years, CO2 pneumoperitoneum during laparoscopic surgery has been considered to compromise cardiopulmonary functions due to the increased IAP during the procedure [20]. Hemodynamic changes such as a decrease in cardiac index, an increase in mean arterial blood pressure (MAP), systemic vascular resistance (SVR) and central venous pressure (CVP) have been observed previously, while alterations in respiratory function include reduced compliance and a transient reduction in lung volumes and capacities [20–22]. Increased IAP may result in neuroendocrine alterations with an increase in plasma concentration of renin, aldosterone, cortisol, adrenalin and noradrenalin in various degrees [20–22].
However, little is known about acute gastrointestinal dysfunction caused by CO2 pneumoperitoneum during laparoscopic surgery. Possible reasons include the variety of definitions and classification of GI dysfunction [23], the lack of reliable biomarkers for assessing GI function [24], and the underestimated GI injury in post-laparoscopic patients [25, 26].
The consensus and recommendations about acute gastrointestinal injury (AGI) [1] allowed us to investigate these issues. The gastrointestinal symptoms of AGI, including nausea/vomiting [27], diarrhea (three or more loose or liquid stools per day) [28, 29], paralysis of the lower GI tract (paralytic ileus) [15], and abnormal bowel sound [30] can be observed frequently in post-operative patients undergoing laparoscopic colorectal surgery. Thus far, there has been no published study indicating whether the elevated IAP during laparoscopic surgery (generally between 12 and 15 mm Hg) is associated with postoperative AGI or is related to increased occurrence of the above-mentioned GI symptoms.
Our present prospective randomized controlled study indicates no significant correlation between the level of elevated intra-abdominal pressure during surgery and the incidence of postoperative AGI. Out of the total 66 enrolled patients, 11 (16.7%) were excluded from the AGI analysis in accordance with the exclusion criteria, which corresponded to the loss to follow-up probability of about 20%. The incidence of AGI was 35.3% in group 3 (IAP = 15 mm Hg), similar to the result of the preliminary experiment (38.5%). The standard deviation (SD) of the other end-points in this study was 18.9 h (time to the first bowel movement), 21.6 h (time to the first flatus/defection) and 18.8 h (time to tolerance of semi-liquid food) respectively, which was in line with the results of Muller et al. [31].
The strengths of the present study are as follows. First, a blinded surgeon was appointed to visit the patients after surgery and to decide the discharge time, limiting bias. The operating surgeon was also blinded with regard to the level of IAP applied during laparoscopy to avoid bias. Second, the serum inflammatory mediators were measured with the same testing method and the same lab machine. Third, in order to avoid a confounding bias, opioid analgesia was avoided if other analgesics were sufficiently effective (protocol for postoperative analgesics: level I: paracetamol; level II: nefopam, phloroglucinol; level III: tramadol or subcutaneous morphine). Fourth, fluid and electrolyte imbalances were adjusted as soon as possible, especially hypokalemia and hypomagnesemia, as these have been reported to aggravate bowel ileus [18]. Finally, other confounding factors such as the duration of surgery and the duration of CO2 pneumoperitoneum were similar among the three groups.
The limitations of our study are as follows: First, the lack of objective serum biomarkers for GI function/dysfunction does not permit a quantitative integrative analysis. We could only compare the occurrence and recovery of GI symptoms separately. Second, the incidence of AGI in our study was low, so that statistically significant differences may not be detected due to a small sample size and possibly low statistical power. Third, although some possible confounding factors, such as type of surgery, duration of surgery and CO2 pneumoperitoneum, and removal of the NG tube within 6 h after surgery, were equally balanced between the three study groups, the results could have been more convincing if we had done a stratified analysis on these factors in a larger sample size. Fourth, the IAP was not measured postoperatively, to check whether a postoperative IAP increase was related to AGI.
With regard to inflammatory mediators that play a role in POI, such as IL-6 and TNF- [17, 32], previous studies have reported increased serum levels after laparoscopic surgery [18, 33–35]. The elevated IAP in this study did not attenuate the immune response, but the test frequency was restricted. Previous studies have shown a dose-response effect in relation to IAP elevation and serum cytokine levels. Hence dynamic monitoring of these cytokines would have provided more information reflecting the real postoperative immune status.

Conclusions

The incidence of postoperative AGI in patients undergoing laparoscopic colorectal surgery is not correlated with the level of elevated intra-abdominal pressure during CO2 pneumoperitoneum. These “negative” results need to be validated in a multi-centre randomized controlled trial with a larger sample size.

Conflict of interest

The authors declare no conflict of interest.

References

1. Reintam Blaser A, Malbrain ML, Starkopf J, et al. Gastrointestinal function in intensive care patients: terminology, definitions and management. Recommendations of the ESICM Working Group on Abdominal Problems. Intensive Care Med 2012; 38: 384-94.
2. Vather R, Trivedi S, Bissett I. Defining postoperative ileus: results of a systematic review and global survey. J Gastrointest Surg 2013; 17: 962-72.
3. Wilmore DW, Kehlet H. Management of patients in fast track surgery. BMJ 2001; 322: 473-6.
4. Kehlet H, Wilmore DW. Multimodal strategies to improve surgical outcome. Am J Surg 2002; 183: 630-41.
5. Kehlet H, Wilmore DW. Evidence-based surgical care and the evolution of fast-track surgery. Ann Surg 2008; 248: 189-98.
6. Chen HH, Wexner SD, Iroatulam AJ, et al. Laparoscopic colectomy compares favorably with colectomy by laparotomy for reduction of postoperative ileus. Dis Colon Rectum 2000; 43: 61-5.
7. Kang CY, Chaudhry OO, Halabi WJ, et al. Outcomes of laparoscopic colorectal surgery: data from the Nationwide Inpatient Sample 2009. Am J Surg 2012; 204: 952-7.
8. van Bree SH, Vlug MS, Bemelman WA, et al. Faster recovery of gastrointestinal transit after laparoscopy and fast-track care in patients undergoing colonic surgery. Gastroenterology 2011; 141: 872-80.
9. Kirkpatrick AW, Roberts DJ, De Waele J, et al. Intra-abdominal hypertension and the abdominal compartment syndrome: updated consensus definitions and clinical practice guidelines from the World Society of the Abdominal Compartment Syndrome. Intensive Care Med 2013; 39: 1190-206.
10. Nickkholgh A, Barro-Bejarano M, Liang R, et al. Signs of reperfusion injury following CO2 pneumoperitoneum: an in vivo microscopy study. Surg Endosc 2008; 22: 122-8.
11. Eleftheriadis E, Kotzampassi K, Papanotas K, et al. Gut ischemia, oxidative stress, and bacterial translocation in elevated abdominal pressure in rats. World J Surg 1996; 20: 11-6.
12. Moore-Olufemi SD, Kozar RA, Moore FA, et al. Ischemic preconditioning protects against gut dysfunction and mucosal injury after ischemia/reperfusion injury. Shock 2005; 23: 258-63.
13. Kronberg U, Kiran RP, Soliman MS, et al. A characterization of factors determining postoperative ileus after laparoscopic colectomy enables the generation of a novel predictive score. Ann Surg 2011; 253: 78-81
14. Koźlik J, Przybyłowska J, Mikrut K, et al. Selected oxidative stress markers in gynecological laparoscopy. Videosurgery Miniinv 2015; 10: 92-100.
15. Story SK, Chamberlain RS. A comprehensive review of evidence-based strategies to prevent and treat postoperative ileus. Dig Surg 2009; 26: 265-75.
16. Lubawski J, Saclarides T. Postoperative ileus: strategies for reduction. Ther Clin Risk Manag 2008; 4: 913-7.
17. Behm B, Stollman N. Postoperative ileus: etiologies and interventions. Clin Gastroenterol Hepatol 2003; 1: 71-80.
18. Han C, Ding Z, Fan J, et al. Comparison of the stress response in patients undergoing gynecological laparoscopic surgery using carbon dioxide pneumoperitoneum or abdominal wall-lifting methods. J Laparoendosc Adv Surg Tech A 2012; 22: 330-5.
19. Carroll J, Alavi K. Pathogenesis and management of postoperative ileus. Clin Colon Rectal Surg 2009; 22: 47-50.
20. Wahba RW, Beique F, Kleiman SJ. Cardiopulmonary function and laparoscopic cholecystectomy. Can J Anaesth 1995; 42: 51-63.
21. O’Leary E, Hubbard K, Tormey W, et al. Laparoscopic cholecystectomy: haemodynamic and neuroendocrine responses after pneumoperitoneum and changes in position. Br J Anaesth 1996; 76: 640-4.
22. Andersson L, Lindberg G, Bringman S, et al. Pneumoperitoneum versus abdominal wall lift: effects on central haemodynamics and intrathoracic pressure during laparoscopic cholecystectomy. Acta Anaesthesiol Scand 2003; 47: 838-46.
23. Rombeau JL, Takala J. Summary of round table conference: gut dysfunction in critical illness. Intesive Care Med 1997; 23: 476-9.
24. Piton G, Manzon C, Cypriani B, et al. Acute intestinal failure in critically ill patients: is plasma citrulline the right marker? Intesive Care Med 2011; 37: 911-7.
25. van der Voort M, Heijnsdijk EA, Gouma DJ. Bowel injury as a complication of laparoscopy. Br J Surg 2004; 91: 1253-8.
26. Bishoff JT, Allaf ME, Kirkels W, et al. Laparoscopic bowel injury: incidence and clinical presentation. J Urol 1999; 161: 887-90.
27. Fujii Y. The utility of antiemetics in the prevention and treatment of postoperative nausea and vomiting in patients scheduled for laparoscopic cholecystectomy. Curr Pharm Des 2005; 11: 3173-83.
28. Wiesen P, Van Gossum A, Preiser JC. Diarrhoea in the critically ill. Curr Opin Crit Care 2006; 12: 149-54.
29. Hassel DA, Smith PA, Nieto JE, et al. Di-tri-octahedral smectite for the prevention of post-operative diarrhea in equids with surgical disease of the large intestine: results of a randomized clinical trial. Vet J 2009; 182: 210-4.
30. Baid H. A critical review of auscultating bowel sounds. Br J Nurs 2009; 18: 1125-9.
31. Muller SA, Rahbari NN, Schneider F, et al. Randomized clinical trial on the effect of coffee on postoperative ileus following elective colectomy. Br J Surg 2012; 99: 1530-8.
32. Schmidt J, Stoffels B, Chanthaphavong RS, et al. Differential molecular and cellular immune mechanisms of postoperative and LPS-induced ileus in mice and rats. Cytokine 2012; 59: 49-58.
33. Bellon JM, Manzano L, Larrad A, et al. Endocrine and immune response to injury after open and laparoscopic cholecystectomy. Int Surg 1998; 83: 24-7.
34. Madureira FA, Manso JE, Madureira Filho D, et al. Inflammation in laparoendoscopic single-site surgery versus laparoscopic cholecystectomy. Surg Innov 2013; 21: 263-8.
35. Kang SH, Kim YS, Hong TH, et al. Effects of dexmedetomidine on inflammatory responses in patients undergoing laparoscopic cholecystectomy. Acta Anaesthesiol Scand 2013; 57: 480-7.

Received: 10.03.2015, accepted: 12.05.2015.
Copyright: © 2015 Fundacja Videochirurgii This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
  
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