Pelvic drain after colorectal anastomosis: useful or useless
Editorial

Pelvic drain after colorectal anastomosis: useful or useless

Varut Lohsiriwat

Colorectal Surgery Unit, Division of General Surgery, Department of Surgery, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand

Correspondence to: Varut Lohsiriwat, MD. PhD. Department of Surgery, Faculty of Medicine Siriraj Hospital, Mahidol University, 2 Wang Lung Road, Bangkok 10700, Thailand. Email: bolloon@hotmail.com.

Comment on: Denost Q, Rouanet P, Faucheron JL, et al. To Drain or Not to Drain Infraperitoneal Anastomosis After Rectal Excision for Cancer: The GRECCAR 5 Randomized Trial. Ann Surg 2016. [Epub ahead of print].


Submitted Nov 29, 2016. Accepted for publication Dec 02, 2016.

doi: 10.21037/tcr.2016.12.48


Strategies for rectal cancer surgery have been evolved and total mesorectal excision (TME) now becomes a standard treatment for middle to low rectal cancer (1). In suitable cases, surgeon will perform bowel restoration after rectal removal with TME because patient with sphincter-saving operation had a better quality of life than those with abdominoperineal excision (2). However, TME has been shown to be associated with high anastomotic leakage, particularly in those receiving neoadjuvant chemoradiation (3). According to the definition of anastomotic leakage proposed by the International Study Group of Rectal Cancer in 2010, anastomotic leakage is defined as a defect of the intestinal wall at the anastomotic site—including suture and staple lines of neorectal reservoirs which leads to a connection between intraluminal compartment and extraluminal compartment (4).

Since the pelvic cavity is a fix and dependent non-peritonized space, a fluid collection in this area after rectal dissection is possible. Some surgeons have advocated to use prophylactic pelvic drain because they believe that fluid collection in the pelvis could be a potential source of contamination and thereby weakening anastomotic integrity and healing. Meanwhile pelvic drain may help detecting anastomotic leakage and may reduce risk of reoperation. Recently, the French Research Group of Rectal Cancer Surgery conducted a large, multicenter, open-label, randomized superiority phase III clinical trial comparing pelvic drainage after infraperitoneal anastomosis after rectal excision for cancer to no pelvic drainage, named the GRECCAR 5 randomized trial (5). The primary endpoint of the study was postoperative pelvic sepsis within 30 postoperative days including anastomotic leakage, pelvic abscess and peritonitis. Secondary endpoints were postoperative morbidities, rate of reoperation, length of hospitalization and rate of stoma closure at 6 months. Comparing 236 with drain and 233 without, there was no significant difference in the rate of postoperative pelvic sepsis (16.1% vs. 18.0%; P=0.58). There was also no difference in postoperative morbidities (18.7% vs. 25.3%; P=0.83), rate of reoperation (16.6% vs. 21.0%; P=0.22), length of hospitalization (12.2 vs. 12.2 days; P=0.99) and rate of stoma closure (80.1% vs. 77.3%; P=0.53) between the two groups.

Of note, 73% of patients enrolled in the GRECCAR 5 trial received neoadjuvant chemoradiation and average anastomotic height was 3.5 cm from the anal verge. Ninety four percent underwent laparoscopic surgery and 76% had diverting stoma. It is worth noting that 27 patients (12%) in arm without drain finally had suction pelvic drain because of pelvic bleeding, difficult TME, or surgeon’s misinterpretation of randomization. As stated in the protocol, suction pelvic drain was placed behind the anastomosis in the presacral area and was removed when the drain output was clear and less than 100 mL per day. In average, pelvic drain was removed on 5.6 days postoperatively and the diagnosis of pelvic sepsis was documented on 7.8 days after an operation.

Similar to other prospective studies, including a large multicenter study by French association for surgical research in 1999, with a total sample size of 653 (6-8), the GRECCAR 5 trial of 494 patients clearly showed that pelvic drain did not decrease the incidence of pelvic sepsis and anastomotic leakage. On the other hand, many studies indicated that pelvic drain was associated with an increased risk of anastomotic dehiscence. For example, a review of 1,014 patients with stapled colorectal anastomosis from the Cleveland Clinic, Ohio, USA noted an increased rate of anastomotic leakage in those with pelvic drain (9). Another review of 978 patients undergoing anterior resection for primary rectal cancer in Taiwan found that an irrigation-suction drain was an independent risk factors for anastomotic leakage [odds ratio of 9.13; 95% confidence interval (CI): 1.16–71.76] (10). Therefore, a prophylactic placement of pelvic drain after colorectal anastomosis is not justified and should be discouraged because it does not reduce the incidence of anastomotic leakage and, in fact, it may increase risk of anastomotic dehiscence. However, it is difficult to determine whether type of pelvic drain is related to colorectal anastomotic leakage because there are a large number of drains used in the literature such as irrigation-suction drain, closed-suction drain and Penrose drain.

In a view of enhanced recovery after surgery (ERAS) protocol (11,12), pelvic drain should not be used routinely as it may cause patient discomfort and prolong hospitalization (13). Drain itself is also a potential site of infection especially if open or passive drainage system is used. From a single-center prospective study of 2,809 patients undergoing open elective colorectal excision, presence of drain was one of significant risk factors for developing surgical site infection (14).

Since pelvic drain seems to be not beneficial (or even harmful) to the development of colorectal anastomotic leakage and surgical site infection, many surgeons refrain from using pelvic drain but still perform diverting stoma to prevent or minimize such a potentially fatal complication. A recent meta-analysis of 13 studies including 8,002 patients undergoing infraperitoneal colorectal anastomosis indicated that diverting stomas significantly reduced the rate of anastomotic leakage and reoperation with the pooled risk ratios of 0.47 (95% CI: 0.33–0.68) and 0.36 (95% CI: 0.28–0.46), respectively (15). However, a diverting stoma itself was a significant risk factor for permanent stoma (16). Thus, diverting stoma should be performed selectively in those with at high risk of leakage e.g., those with difficult pelvic dissection, those receiving neoadjuvant chemoradiation, and those with coloanal anastomosis. Both diverting stoma and pelvic drainage might be unnecessary if surgeons achieve an overall leak rate below 8% (17). A review of 170 sphincter-saving operations form a university hospital in Thailand showed that the operation can be performed safely in the vast majority of rectal cancer patients without a diverting stoma and pelvic drain (18). Tumor height within 5 cm from the anal verge was an independent risk factor for anastomotic leakage.

Another possible rationale of using pelvic drain after TME is to detect leakage and to reduce a need of re-laparotomy. However, the GRECCAR 5 randomized trial failed to show any advantage of pelvic drain on these purposes. One explanation is that the sensitivity of pelvic drain in detecting anastomotic leakage was modest (between 5% and 71%) (19,20), which was mainly dependent on the location of drain and timing of drain removal. Although colorectal anastomotic leakage typically and clinically appeared on postoperative day 4th to 8th, it may present as late as on postoperative day 20th or beyond (21,22). As reported in the GRECCAR 5 randomized trial that the diagnosis of pelvic sepsis was documented on approximately 8 days after an operation but pelvic drain was earlier removed on postoperative day 6th, the beneficial effect of pelvic drain in detecting leakage and reducing reoperation may not be seen.

Recently, new concepts of pelvic drain have been proposed as diagnostic tool for detecting “early” anastomotic leakage using intraperitoneal cytokines and biomarkers. Using intraabdominal exudate obtained from drain, two exploratory studies showed a significant rise in intraperitoneal interleukin-1, interleukin-6 and tumor necrosis factor-α level in patients developing symptomatic anastomotic leakage before clinical symptoms were evident (23,24). Meanwhile, a high intraperitoneal lactate/pyruvate ratio may be an additional biomarker of “early” intraabdominal complication after colorectal surgery (23). An elevated level of intraperitoneal matrix metalloprotienases-8 and -9 was evident as early as 4 hours after rectal cancer surgery in those developing anastomotic leakage (25). Future studies should focus on preclinical detection of anastomotic leakage using such intraperitoneal cytokines and biomarkers from pelvic drain i.e., periodical fluid collection rather than observation of drain content. On condition that several and large studies show consistent and positive results, the driving effect of pelvic drain to detect early anastomotic leakage may become reality and could be applied into daily clinical practice.

In conclusion, based on the published literature, the author believes that there has not been sufficient evidence to use pelvic drain after colorectal anastomosis. In cases pelvic drain is required such as difficult pelvic dissection, massive intraoperative bleeding and surgery beyond TME planes, pelvic drain other than irrigation-suction should be considered. Future studies should focus on preclinical detection of anastomotic leakage using biomarkers of intraperitoneal fluid from drain (if any).


Acknowledgments

Funding: None.


Footnote

Provenance and Peer Review: This article was commissioned and reviewed by the Section Editor Mu-Xing Li (Department of Abdominal Surgical Oncology, Cancer Hospital, Chinese Academy of Medical Sciences (CAMS) and Peking Union Medical College (PUMC), Beijing, China).

Conflicts of Interest: The author has completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/tcr.2016.12.48). The author has no conflicts of interest to declare.

Ethical Statement: The author is accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.


References

  1. Heald RJ, Husband EM, Ryall RD. The mesorectum in rectal cancer surgery--the clue to pelvic recurrence? Br J Surg 1982;69:613-6. [Crossref] [PubMed]
  2. Konanz J, Herrle F, Weiss C, et al. Quality of life of patients after low anterior, intersphincteric, and abdominoperineal resection for rectal cancer--a matched-pair analysis. Int J Colorectal Dis 2013;28:679-88. [Crossref] [PubMed]
  3. Lee WS, Yun SH, Roh YN, et al. Risk factors and clinical outcome for anastomotic leakage after total mesorectal excision for rectal cancer. World J Surg 2008;32:1124-9. [Crossref] [PubMed]
  4. Rahbari NN, Weitz J, Hohenberger W, et al. Definition and grading of anastomotic leakage following anterior resection of the rectum: a proposal by the International Study Group of Rectal Cancer. urgery 2010;147:339-51.
  5. Denost Q, Rouanet P, Faucheron JL, et al. To Drain or Not to Drain Infraperitoneal Anastomosis After Rectal Excision for Cancer: The GRECCAR 5 Randomized Trial. Ann Surg 2016; [Epub ahead of print]. [Crossref] [PubMed]
  6. Sagar PM, Hartley MN, Macfie J, et al. Randomized trial of pelvic drainage after rectal resection. Dis Colon Rectum 1995;38:254-8. [Crossref] [PubMed]
  7. Merad F, Hay JM, Fingerhut A, et al. Is prophylactic pelvic drainage useful after elective rectal or anal anastomosis? A multicenter controlled randomized trial. French Association for Surgical Research. Surgery 1999;125:529-35. [Crossref] [PubMed]
  8. Brown SR, Seow-Choen F, Eu KW, et al. A prospective randomised study of drains in infra-peritoneal rectal anastomoses. Tech Coloproctol 2001;5:89-92. [Crossref] [PubMed]
  9. Vignali A, Fazio VW, Lavery IC, et al. Factors associated with the occurrence of leaks in stapled rectal anastomoses: a review of 1,014 patients. J Am Coll Surg 1997;185:105-13. [Crossref] [PubMed]
  10. Yeh CY, Changchien CR, Wang JY, et al. Pelvic drainage and other risk factors for leakage after elective anterior resection in rectal cancer patients: a prospective study of 978 patients. Ann Surg 2005;241:9-13. [PubMed]
  11. Lohsiriwat V. Enhanced recovery after surgery vs conventional care in emergency colorectal surgery. World J Gastroenterol. 2014;20:13950-5. [Crossref] [PubMed]
  12. Nygren J, Thacker J, Carli F, et al. Guidelines for perioperative care in elective rectal/pelvic surgery: Enhanced Recovery After Surgery (ERAS®) Society recommendations. Clin Nutr 2012;31:801-16. [Crossref] [PubMed]
  13. Puleo FJ, Mishra N, Hall JF. Use of intra-abdominal drains. Clin Colon Rectal Surg 2013;26:174-7. [Crossref] [PubMed]
  14. Tang R, Chen HH, Wang YL, et al. Risk factors for surgical site infection after elective resection of the colon and rectum: a single-center prospective study of 2,809 consecutive patients. Ann Surg 2001;234:181-9. [Crossref] [PubMed]
  15. Gu WL, Wu SW. Meta-analysis of defunctioning stoma in low anterior resection with total mesorectal excision for rectal cancer: evidence based on thirteen studies. World J Surg Oncol 2015;13:9. [Crossref] [PubMed]
  16. Rutegård M, Boström P, Haapamäki M, et al. Current use of diverting stoma in anterior resection for cancer: population-based cohort study of total and partial mesorectal excision. Int J Colorectal Dis 2016;31:579-85. [Crossref] [PubMed]
  17. The Association of Coloproctology of Great Britain and Ireland. Guidelines for the Management of Colorectal Cancer. 3rd edition. 2007. Available online: http://www.acpgbi.org.uk/content/uploads/2007-CC-Management-Guidelines.pdf
  18. Lohsiriwat V, Lohsiriwat D, Boonnuch W, et al. Outcomes of sphincter-saving operation for rectal cancer without protective stoma and pelvic drain, and risk factors for anastomotic leakage. Dig Surg 2008;25:191-7. [Crossref] [PubMed]
  19. Urbach DR, Kennedy ED, Cohen MM. Colon and rectal anastomoses do not require routine drainage: a systematic review and meta-analysis. Ann Surg 1999;229:174-80. [Crossref] [PubMed]
  20. Tsujinaka S, Kawamura YJ, Konishi F, et al. Pelvic drainage for anterior resection revisited: use of drains in anastomotic leaks. ANZ J Surg 2008;78:461-5. [Crossref] [PubMed]
  21. Shin US, Kim CW, Yu CS, et al. Delayed anastomotic leakage following sphincter-preserving surgery for rectal cancer. Int J Colorectal Dis 2010;25:843-9. [Crossref] [PubMed]
  22. Maeda H, Okamoto K, Namikawa T, et al. Rarity of late anastomotic leakage after low anterior resection of the rectum. Int J Colorectal Dis 2015;30:831-4. [Crossref] [PubMed]
  23. Matthiessen P, Strand I, Jansson K, et al. Is early detection of anastomotic leakage possible by intraperitoneal microdialysis and intraperitoneal cytokines after anterior resection of the rectum for cancer? Dis Colon Rectum 2007;50:1918-27. [Crossref] [PubMed]
  24. Yamamoto T, Umegae S, Matsumoto K, et al. Peritoneal cytokines as early markers of peritonitis following surgery for colorectal carcinoma: a prospective study. Cytokine 2011;53:239-42. [Crossref] [PubMed]
  25. Pasternak B, Matthiessen P, Jansson K, et al. Elevated intraperitoneal matrix metalloproteinases-8 and -9 in patients who develop anastomotic leakage after rectal cancer surgery: a pilot study. Colorectal Dis 2010;12:e93-8. [PubMed]
Cite this article as: Lohsiriwat V. Pelvic drain after colorectal anastomosis: useful or useless. Transl Cancer Res 2016;5(Suppl 7):S1404-S1407. doi: 10.21037/tcr.2016.12.48

Download Citation