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International Journal of Surgical Oncology
Volume 2014 (2014), Article ID 419712, 5 pages
http://dx.doi.org/10.1155/2014/419712
Clinical Study

Incisional Surgical Site Infection after Elective Open Surgery for Colorectal Cancer

1Department of Plastic and Reconstructive Surgery, Hokkaido University Graduate School of Medicine, Kita 15, Nishi 7, Kita-ku, Sapporo 060-8638, Japan
2Department of Surgery, Keiyukai Sapporo Hospital, Kita 1-1, Hondori 14, Shiroishi-ku, Sapporo 003-0027, Japan

Received 3 January 2014; Accepted 4 March 2014; Published 27 March 2014

Academic Editor: Steven Heys

Copyright © 2014 Kosuke Ishikawa et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background. The purpose of this study was to clarify the incidence and risk factors for incisional surgical site infections (SSI) in patients undergoing elective open surgery for colorectal cancer. Methods. We conducted prospective surveillance of incisional SSI after elective colorectal resections performed by a single surgeon for a 1-year period. Variables associated with infection, as identified in the literature, were collected and statistically analyzed for their association with incisional SSI development. Results. A total of 224 patients were identified for evaluation. The mean patient age was 67 years, and 120 (55%) were male. Thirty-three (14.7%) patients were diagnosed with incisional SSI. Multivariate analysis suggested that incisional SSI was independently associated with TNM stages III and IV (odds ratio [OR], 2.4) and intraoperative hypotension (OR, 3.4). Conclusions. The incidence of incisional SSI in our cohort was well within values generally reported in the literature. Our data suggest the importance of the maintenance of intraoperative normotension to reduce the development of incisional SSI.

1. Introduction

Surgical site infections (SSI) are the most common nosocomial infection in surgical patients, contributing to perioperative morbidity, prolonged postoperative hospital length of stay, and increased hospital costs [13]. The colorectal surgery has been associated with the highest risk of SSI [1], predominately because of the heavy bacterial load of the colon and rectum. The incidence of incisional SSI following colorectal surgery has been reported to range from 5% to 26% [48]. Although various risk factors for incisional SSI have been reported [1, 46], there has been no clear consensus on the risk factors contributing to incisional SSI following colorectal surgery. To clarify the incidence and risk factors for incisional SSI, we conducted prospective surveillance of incisional SSI and analyzed plausible factors in patients undergoing elective open surgery for colorectal cancer, performed by a single surgeon.

2. Materials and Methods

2.1. Subjects

This prospective observational study was conducted at Keiyukai Sapporo Hospital from January 1, 2009, to December 31, 2009. All patients undergoing elective laparotomy with colorectal resection for cancer by a single board-certified colon and rectal surgeon (Takaya Kusumi) were registered in this cohort. Patients were excluded if the surgical wound was not closed primarily. Also excluded were patients undergoing laparoscopy or simple ostomy creation or closure with associated wedge or segmental resection. The resident surgeon (Kosuke Ishikawa) completed a prospective infection surveillance form for each patient, recording date of identification of incisional SSI. We collected demographic and clinical variables on a standardized form from electronic medical records and operating room records. Approval for this study was obtained from the institutional review board.

The diagnosis of SSI was strictly made based on the definitions stated in the guidelines issued by the Center for Disease Control and Prevention (CDC) [2]. Therefore, wounds with tenderness, swelling, or redness were diagnosed as incisional SSI. The primary outcome measures for this study were the incidence and risk factors for incisional SSI. Secondary outcome measures included number of days to the identification of infection, postoperative length of stay, and microbiology of the infections.

2.2. Perioperative Management

Mechanical bowel preparation (MBP) was performed with an oral cathartic agent and an electrolyte solution that did not contain antibiotics in the preoperative period for 1 or 2 days. In case preoperative bowel obstruction was severe, MBP was not performed. Antimicrobial prophylaxis was administered to all patients via intravenous infusion of 1 g of cefmetazole sodium. The exact time for antibiotic infusion was recorded by the anesthesiologist. Antimicrobial prophylaxis was continued postoperatively for up to 48 hours. Anesthesia induction and perioperative care were standardized across all patients. Perioperative normothermia was maintained with standardized use of forced-air heaters.

For surgical site preparation, povidone-iodine scrub was used exclusively. We placed a polyurethane wound protector (the Alexis wound retractor manufactured by Applied Medical) in close contact with a wound margin immediately after making an incision in the abdomen. Our standard anastomotic procedures were functional end-to-end anastomosis [9] using four GIA linear staplers for colectomy, abdominal stapled side-to-end anastomosis [10] using a circular stapler and a TA55 for sigmoid anterior resection, and transanal stapled end-to-end anastomosis [11] using a TA55 or a linear stapler and a circular stapler (double stapling technique [12]) for rectal anterior resection. After completing the anastomosis, approximately 2 L saline lavage of the peritoneal cavity was conducted. After closure of the fascia, we conducted pressure irrigation of the subcutaneous fat tissue with 400 mL of saline solution, using a 20 mL syringe with an intravenous catheter. Abdominal incisions were closed primarily using interrupted absorbable or nonabsorbable sutures for the fascia and nonabsorbable sutures for the skin. A subcutaneous closed-suction drain was placed. Postoperative blood glucose level was evaluated at least once a day until postoperative day 2. All wounds were observed by attending surgeons every day, and, after discharge, the operator observed all wounds in the outpatient setting for at least 30 days postoperatively.

2.3. Measures

Patient characteristic data collected included age, gender, body mass index, presence of comorbid medical conditions (diabetes mellitus, cardiovascular disease, and chronic obstructive pulmonary disease), history of prior laparotomy, smoking status, preoperative albumin level, preoperative hemoglobin level, physical status according to the American Society of Anesthesiologists (ASA) score, weight loss of more than 10% body weight within 6 months before the operation, and stage of cancer according to the TNM staging system. Operative variables collected included MBP, timing of prophylactic antibiotic use, type of procedure, type of anastomosis, additional surgical procedures (ostomy creation and multiple organ resection), length of operation, surgical wound classification dichotomized as clean-contaminated (without unusual contamination; class II) or contaminated (gross spillage from the gastrointestinal tract; class III), depth and length of incisional site, intraoperative hypotension (systolic blood pressure <80 mmHg continued more than 5 minutes), estimated blood loss, use of perioperative blood transfusion, and postoperative maximum glucose level. All variables were divided into categorical variables (Tables 1 and 2).

tab1
Table 1: Patient characteriscics.
tab2
Table 2: Perioperative/operative variables.
2.4. Statistical Analyses

The univariate relation between each independent variable and incisional SSI was evaluated using Pearson’s test for categorical variables. The variables with a value <0.2 in the univariate analysis were entered into the multivariate logistic regression model, using a Wald statistic backward stepwise selection. The results of the logistic regression were reported as odds ratios (OR) with 95% confidence intervals (CI). All values were two-tailed, and was considered to indicate statistical significance. All statistical analyses in this study were performed using JMP software (SAS Institute Inc., Cary, NC).

3. Results

A total of 224 patients met the inclusion criteria for this study during the 1-year period. The mean patient age was 67 years (interquartile ranges [IQR], 60 to 75), and 120 (55%) were male. Of 224 patients, 33 (14.7%) had a diagnosis of incisional SSI. All were inpatients at diagnosis. The median time to the identification of incisional SSI was 9 days (IQR, 8 to 10). Of 27 infected patients without other postoperative complications, the median postoperative length of stay was 14 days (IQR, 12 to 19) compared with uninfected patients (median, 14 days; IQR, 12 to 18.5; ).

Tables 1 and 2 summarize the patients’ characteristics, perioperative/operative variables, and the incidence of SSI according to the factors. By univariate analysis, patients who developed incisional SSI were more likely to have a higher ASA score and TNM stage. When evaluating the perioperative/operative variables, length of incisional site and intraoperative hypotension were associated with the development of incisional SSI. Table 3 summarizes the results from the multivariate analysis. For our cohort, factors associated independently with incisional SSI were TNM stage III, TNM stage IV (odds ratio [OR], 2.4), and intraoperative hypotension (OR, 3.4).

tab3
Table 3: Multivariate analysis of risk factors for incisional SSI.

Cultures were obtained from 14 of the 33 (42.4%) surgical sites, which resulted in 8 isolates. The bacteria isolated were Enterococcus spp. (71.4%), methicillin-resistant Staphylococcus aureus (14.3%), Staphylococcus epidermidis (7.1%), and Pseudomonas aeruginosa (7.1%).

4. Discussion

There has been wide discrepancy in the reported incidence of incisional SSI following colorectal surgery, ranging from 5% to 26% [48]. Most of this variation is probably due to modification of CDC definitions of SSI and differing personnel performing the assessments for infection. This study attempted to address these potential sources of variation by adopting strict CDC definitions and having prospective infection assessments performed by a single surgeon. We adopted intraoperative antiseptic measures, including wound protector placement [13], syringe pressure irrigation of subcutaneous fat tissue [14], and subcutaneous closed-suction drainage [15]. On this condition, the incidence of incisional SSI was 14.7%, well within values generally reported in the literature (roughly 15%) [68, 16, 17].

A further objective of this study was to identify potential risk factors that independently predict development of incisional SSI. Various risk factors for incisional SSI after colorectal surgery have been reported, including a high BMI [4, 16], blood transfusion [5, 18], and ostomy creation [5, 16]. National Nosocomial Infections Surveillance system identified three independent risk factors for SSI: ASA score of 3, 4, or 5, surgical wound classification of contaminated or dirty-infected, and duration of operation lasting more than 3 hours [1]. In our analysis, none of these were identified as risk factors.

By multivariate analysis, we identified TNM stage III and TNM stage IV as a risk factor. This correlation may be due to extent of lymph node dissection. However, a recent study did not identify stage of colorectal cancer as a risk factor for incisional SSI [7]. In our multivariate analysis, we also identified intraoperative hypotension as an operative risk factor. Smith et al. [4] also reported intraoperative hypotension as a risk factor and they theorized the contribution of poor wound tissue perfusion related to hypotension. These data suggest the importance of the maintenance of intraoperative normotension in the reduction of SSI. However, intraoperative hypotension may also be a surrogate marker for other factors that were not identified in the variables studied.

The degree of bacterial contamination is fundamental to the risk of SSI. In the colorectal surgery, we hypothesized that the procedures of anastomosis were associated with contamination of the surgical site, because of the heavy bacterial load of the colon and rectum. There was a trend toward developing incisional SSI if the patient underwent functional end-to-end anastomosis for colectomy and end-to-end anastomosis for rectal anterior resection compared to no anastomosis (i.e., abdominoperineal resection and Hartmann’s procedure). However, Konishi et al. [6] reported the higher incidence of incisional SSI in rectal surgery than in colonic surgery. Because surgery for rectal cancer is often associated with ostomy formation, preoperative radiation and total mesorectal excision with anastomosis close to the anal verge, all of which could lead to surgery that lasts longer and has greater bacterial contamination.

The use of prophylactic antimicrobial in colorectal surgery has been proven to reduce the infection rate when compared with no-treatment controls [19]. The Surgical Infection Prevention Project developed 3 performance measures: (1) antimicrobial prophylaxis initiated within 1 hour before incision, (2) prophylactic antimicrobial regimen consistent with published guidelines, and (3) prophylactic antimicrobial discontinued within 24 hours after surgery end time [20]. Weber et al. [21] reported that the prophylactic administration 30 to 59 minutes before incision was more effective than administration during the last half hour. In our cohort, administration of prophylactic antimicrobial was conducted 15 to 50 minutes before skin incision in all cases. There was no significant difference between 15 to 29 and 30 to 50 minutes before incision in the development of incisional SSI. In Japan, 2 or 3 days of prophylaxis with parenteral antibiotics for gastroenterologic surgery was the widely accepted standard. Therefore, intravenous antimicrobial prophylaxis was administered postoperatively for up to 48 hours.

Our median time to the identification of incisional SSI was close to other studies [4, 8, 16]. Unlike other studies [7, 22], we could detect no additional postoperative length of stay related to incisional SSI. However, our postoperative length of stay with uninfected patients was longer than other studies of colorectal surgery [7, 16], which masked the influence of infections on hospital stay. We believe that careful observation of wounds for early identification and treatment is important to minimize the influence of incisional SSI.

The microbiology of the infections in the present study was similar to that reported in other studies [16, 17]. Gram-positive aerobic cocci (Enterococcus spp. and Staphylococcal spp.) accounted for the majority of the isolates. Cefmetazole sodium was active against most of the bacteria identified in the present study.

Because all operations were performed by a single surgeon in an institute, we could minimize interhospital variations, including observer differences, differences in perioperative management, and different environmental factors. We believe that the present study accurately reflects the incidence of incisional SSI in this cohort. However, a larger study is necessary to provide definitive evidence of risk factors for incisional SSI.

5. Conclusions

The incidence of incisional SSI in patients undergoing elective open surgery for colorectal cancer in our cohort was well within values generally reported in other studies. The present study identified a higher TNM stage and intraoperative hypotension as risk factors for incisional SSI following elective colorectal resection. Our data suggest the importance of the maintenance of intraoperative normotension to reduce the development of incisional SSI.

Conflict of Interests

The authors declare no financial or any other type of support.

References

  1. National Nosocomial Infections Surveillance System, “National Nosocomial Infections Surveillance (NNIS) System Report, data summary from January 1992 through June 2004, issued October 2004,” The American Journal of Infection Control, vol. 32, no. 8, pp. 470–485, 2004.
  2. A. J. Mangram, T. C. Horan, M. L. Pearson, L. C. Silver, and W. R. Jarvis, “Guideline for prevention of surgical site infection, 1999. Centers for Disease Control and Prevention (CDC) Hospital Infection Control Practices Advisory Committee,” The American Journal of Infection Control, vol. 27, no. 2, pp. 97–132, 1999. View at Scopus
  3. T. Anthony, J. Long, L. S. Hynan et al., “Surgical complications exert a lasting effect on disease-specific health-related quality of life for patients with colorectal cancer,” Surgery, vol. 134, no. 2, pp. 119–125, 2003. View at Publisher · View at Google Scholar · View at Scopus
  4. R. L. Smith, J. K. Bohl, S. T. McElearney et al., “Wound Infection after elective colorectal resection,” Annals of Surgery, vol. 239, no. 5, pp. 599–607, 2004. View at Publisher · View at Google Scholar · View at Scopus
  5. R. Tang, H. H. Chen, Y. L. Wang 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,” Annals of Surgery, vol. 234, no. 2, pp. 181–189, 2001. View at Scopus
  6. T. Konishi, T. Watanabe, J. Kishimoto, and H. Nagawa, “Elective colon and rectal surgery differ in risk factors for wound infection: results of prospective surveillance,” Annals of Surgery, vol. 244, no. 5, pp. 758–763, 2006. View at Publisher · View at Google Scholar · View at Scopus
  7. T. Nakamura, H. Mitomi, A. Ihara et al., “Risk factors for wound infection after surgery for colorectal cancer,” World Journal of Surgery, vol. 32, no. 6, pp. 1138–1141, 2008. View at Publisher · View at Google Scholar · View at Scopus
  8. M. Kobayashi, Y. Mohri, Y. Inoue, Y. Okita, C. Miki, and M. Kusunoki, “Continuous follow-up of surgical site infections for 30 days after colorectal surgery,” World Journal of Surgery, vol. 32, no. 6, pp. 1142–1146, 2008. View at Publisher · View at Google Scholar · View at Scopus
  9. F. M. Steichen, “The use of staplers in anatomical side-to-side and functional end-to-end enteroanastomoses,” Surgery, vol. 64, no. 5, pp. 948–953, 1968. View at Scopus
  10. J. W. Baker, “Low end to side rectosigmoidal anastomosis; description of technic,” Archives of Surgery, vol. 61, no. 1, pp. 143–157, 1950. View at Scopus
  11. C. D. Knight and F. D. Griffen, “An improved technique for low anterior resection of the rectum using the EEA stapler,” Surgery, vol. 88, no. 5, pp. 710–714, 1980. View at Scopus
  12. Z. Cohen, E. Myers, B. Langer, B. Taylor, R. H. Railton, and C. Jamieson, “Double stapling technique for low anterior resection,” Diseases of the Colon & Rectum, vol. 26, no. 4, pp. 231–235, 1983. View at Scopus
  13. T. Horiuchi, H. Tanishima, K. Tamagawa et al., “Randomized, controlled investigation of the anti-infective properties of the Alexis retractor/protector of incision sites,” The Journal of Trauma—Injury, Infection and Critical Care, vol. 62, no. 1, pp. 212–215, 2007. View at Publisher · View at Google Scholar · View at Scopus
  14. C. R. Cervantes-Sánchez, R. Gutiérrez-Vega, J. A. Vázquez-Carpizo, P. Clark, and C. Athié-Gutiérrez, “Syringe pressure irrigation of subdermic tissue after appendectomy to decrease the incidence of postoperative wound infection,” World Journal of Surgery, vol. 24, no. 1, pp. 38–42, 2000. View at Publisher · View at Google Scholar · View at Scopus
  15. E. Kaya, E. Paksoy, E. Ozturk, D. Sigirli, and H. Bilgel, “Subcutaneous closed-suction drainage does not affect surgical site infection rate following elective abdominal operations: a prospective randomized clinical trial,” Acta Chirurgica Belgica, vol. 110, no. 4, pp. 457–462, 2010. View at Scopus
  16. J. Blumetti, M. Luu, G. Sarosi et al., “Surgical site infections after colorectal surgery: do risk factors vary depending on the type of infection considered?” Surgery, vol. 142, no. 5, pp. 704–711, 2007. View at Publisher · View at Google Scholar · View at Scopus
  17. K. M. F. Itani, S. E. Wilson, S. S. Awad, E. H. Jensen, T. S. Finn, and M. A. Abramson, “Ertapenem versus cefotetan prophylaxis in elective colorectal surgery,” The New England Journal of Medicine, vol. 355, no. 25, pp. 2640–2651, 2006. View at Publisher · View at Google Scholar · View at Scopus
  18. E. C. Vamvakas, J. H. Carven, and P. L. Hibberd, “Blood transfusion and infection after colorectal cancer surgery,” Transfusion, vol. 36, no. 11-12, pp. 1000–1008, 1996. View at Scopus
  19. A. M. Glenny and F. Song, “Antimicrobial prophylaxis in colorectal surgery,” Quality in Health Care, vol. 8, no. 2, pp. 132–136, 1999. View at Scopus
  20. D. W. Bratzler and D. R. Hunt, “The surgical infection prevention and surgical care improvement projects: national initiatives to improve outcomes for patients having surgery,” Clinical Infectious Diseases, vol. 43, no. 3, pp. 322–330, 2006. View at Publisher · View at Google Scholar · View at Scopus
  21. W. P. Weber, W. R. Marti, M. Zwahlen et al., “The timing of surgical antimicrobial prophylaxis,” Annals of Surgery, vol. 247, no. 6, pp. 918–926, 2008. View at Publisher · View at Google Scholar · View at Scopus
  22. K. B. Kirkland, J. P. Briggs, S. L. Trivette, W. E. Wilkinson, and D. J. Sexton, “The impact of surgical-site infections in the 1990s: attributable mortality, excess length of hospitalization, and extra costs,” Infection Control and Hospital Epidemiology, vol. 20, no. 11, pp. 725–730, 1999. View at Publisher · View at Google Scholar · View at Scopus