Home Reduction in deep organ-space infection in gynecologic oncology surgery with use of oral antibiotic bowel preparation: a retrospective cohort analysis
Article Open Access

Reduction in deep organ-space infection in gynecologic oncology surgery with use of oral antibiotic bowel preparation: a retrospective cohort analysis

  • Kathryn Kennedy , Jennifer Gaertner-Otto ORCID logo EMAIL logo and Eav Lim
Published/Copyright: October 9, 2024

Abstract

Context

Deep organ-space infection (OSI) following gynecologic surgery is a source of patient morbidity and mortality. There is currently conflicting evidence regarding the use of bowel preparation prior to gynecologic surgery to reduce the rates of infection. For the additional purpose of improving patient recovery at our own institution, a retrospective cohort study compared the rate of deep OSI in patients who received oral antibiotic bowel preparation per Nichols–Condon bowel preparation with metronidazole and neomycin.

Objectives

The primary aim of this study was to compare the rate of deep organ-space surgical site infection in gynecologic surgery before and after institution of an oral antibiotic bowel preparation, thus assessing whether the preparation is associated with decreased infection rate. The secondary objective was to identify other factors associated with deep organ-space site infection.

Methods

A retrospective cohort study was performed. Demographic and surgical data were collected via chart review of 1,017 intra-abdominal surgeries performed by gynecologic oncologists at a single institution from April 1, 2019 to December 1, 2021. Of these, 778 met the inclusion criteria; 444 did not receive preoperative oral antibiotic bowel preparation, and 334 did receive preoperative bowel preparation. Odds ratios (ORs) were calculated, and a logistic regression model was utilized for categorical variables. Multivariable regression analysis was performed.

Results

A total of 778 patients were included. Deep OSI rate in patients who did not receive oral antibiotic bowel preparation was 2.3 % compared to 0.3 % (OR 0.13, confidence interval [CI] 0.06–1.03, p=0.02) in patients who did. Receiving oral antibiotic bowel preparation predicted absence of deep OSI (OR 0.04, CI 0.00–0.87, p=0.04). Laparotomy (OR 20.1, CI 1.6–250.2, p=0.02) and Asian race (OR 60.8, CI 2.6–1,380.5, p=0.01) were related to increased rates of deep OSI.

Conclusions

Oral antibiotic bowel preparation predicts a reduced risk of deep OSI. This preparation is inexpensive and low-risk, and thus these clinically significant results support a promising regimen to improve surgical outcomes, and provide guidance for prospective larger studies.

Deep organ-space infection (OSI) is a major source of patient morbidity and mortality following gynecologic surgery. The National Healthcare Safety Network of the Centers for Disease Control and Prevention (NHSN/CDC) divides it into superficial incisional, deep incisional, or deep OSI, with deep OSI carrying the greatest clinical consequences. These include a high likelihood of readmission and intervention, reduced quality of life, and increased healthcare costs including from prolonged hospitalization, antibiotic course, or drain placements [1]. In addition, readmission for deep OSI within 30 days is reportable and can affect a hospital’s Centers for Medicare & Medicaid Services (CMS) star rating, which can affect reimbursements. Due to these implications, this study focused on deep OSIs. Entry into the bowel is a known risk factor for deep OSI, and in gynecologic oncology, 20–50 % of patients undergoing cytoreductive surgery will require bowel resection [2], [3], [4]. Surgeons as early as the 19th century recommended mechanical bowel preparations to reduce risks of infection in bowel surgery; however, mechanical preparations decrease stool burden without affecting the high stool bacterial concentration [5], [6], [7], [8]. Oral antibiotic bowel preparation was first proposed in 1971, and since then, the use of oral antibiotic bowel preparation has been shown to decrease deep OSI rates in colorectal surgery by nearly 60 % [9], [10], [11]. Avoiding mechanical bowel preparation also improves patient satisfaction, reduces preoperative dehydration and electrolyte imbalances, and decreases the risk of postoperative ileus [12], 13].

In gynecologic oncology surgery, existing evidence on bowel preparation is conflicting. A database analysis of 224,687 hysterectomy patients failed to show that any type of bowel preparation protects against all deep OSI. However, among these patients, only 3.2 % had bowel resection, and 2.9 % had oral antibiotic bowel preparation alone [14]. This does not reflect the overall gynecologic oncology population or provide guidance regarding oral antibiotic bowel preparation specifically. Single-institution experiences with oral antibiotic bowel preparations do suggest a benefit. At Memorial Sloan Kettering, the infection rate for any type of deep OSI for gynecologic oncology patients undergoing colon resection decreased from 37 to 12 % (p≤0.001) with the use of a perioperative bundle that included preoperative oral antibiotics with optional mechanical bowel preparation [15]. At Johns Hopkins, an initiative that included preoperative oral antibiotics in conjunction with mechanical bowel preparation before ovarian debulking surgery resulted in a reduction in all types of deep OSI from 33 to 7 % (p<0.001), specifically for patients undergoing bowel resection, and from 20 to 30 % in the group overall (p<0.001) [16]. Other institutions have had similar findings; however, these interventions were implemented simultaneously with Enhanced Recovery After Surgery (ERAS) protocols and similar bundles, so the impact of oral antibiotic bowel preparation alone has not been definitively shown [17].

Our institution implemented ERAS protocols in 2017 (Table 1), but the deep OSI rate remained higher than expected based on NHSN/CDC guidelines. This drastically affected our hospital’s CMS rating along with a decrease in patient satisfaction with care, outcome, and reimbursement. Therefore, as a quality and patient improvement practice, the division of gynecologic oncology was tasked to evaluate and improve our perioperative care for the major gynecologic oncology surgeries. The gynecologic oncology division instituted antibiotic bowel preparation prior to intra-abdominal surgery on August 1, 2020, with the prescription of 1 g of neomycin and 500 mg of metronidazole taken at 2, 3, and 9 pm the day before surgery. The specific bowel regimen is based on the Nichols–Condon bowel preparation, a well-studied and established preparation in colorectal surgery [18]. Metronidazole has been shown to have improved tolerability, excellent anaerobic coverage, and proven clinical efficacy, and was therefore selected over the authors’ original erythromycin base [9], 19], 20]. If a patient were to report a history of allergy to one or both medications, that drug or the complete preparation would have been omitted, although this issue did not arise in the time frame of the study. Following ERAS protocol, patients preoperatively received 2 g or 3 g cefotetan based on body mass index (BMI), and the surgical site was prepped with ChloraPrep (2 % chlorhexidine gluconate in 70 % isopropyl alcohol), and/or vaginal prep with povidone iodine solution unless patient allergies dictated otherwise. Patients were draped in normal sterile fashion, and no Ioban was utilized.

Table 1:

The enhanced recovery after surgery (ERAS) protocol.

Day before surgerya
  1. Clear liquid diet until midnight day before surgery

  2. Twenty-ounce Gatorade to be consumed and completed 2 hours prior to scheduled surgery

PACU
  1. Tylenol 975 mg PO x1 dose

  2. Cefotetan 2 g IV (3 g for higher BMI patients)

  3. Body wipes

  4. Nasal wipes

  5. Heparin 5,000 subcutaneous

Intraoperative
  1. Volume monitoring for euvolemia

  2. Temperature monitoring for normothermia

  3. TAP block (physician preference)

Postoperative
  1. Sequential compression stockings

  2. Lovenox 40 mg subcutaneous injection 24 h post-surgery

  3. Early ambulation encouraged

  4. Clear liquid diet

  5. Discontinue IV fluids when tolerating oral fluid intake

  6. Discontinuation of Foley catheter

  7. Gum chewing encouraged

  8. Toradol 15 mg every 6 h for 5 days

  9. Tylenol and oral motrin

  10. Gabapentin 300 mg at bedtime (qHS)

  11. Magnesium oxide

  1. aOn the day before surgery, in addition to adhering to ERAS protocol, patients received Neomycin and Flagyl at 2, 3, and 9 pm. BMI, body mass index; ERAS, enhanced recovery after surgery; IV, intravenous; PACU, postanesthesia care unit; TAP, transverse abdominis plane.

The primary objective of this study was to compare the rate of deep OSI in patients who received oral antibiotic bowel preparation with the rate in those who did not. We hypothesized that the use of oral antibiotic bowel preparation would be associated with reduced rates of infection.

Methods

A retrospective cohort study was performed via chart review. The protocol was reviewed by the WellSpan Institutional Review Board (IRB) and met the criteria for exemption because it involved only information collection and analysis involving the authors’ use of identifiable health information (exemption category 45 CFR 46.104(d)). The study was approved for waiver of consent. It was registered with ClinicalTrials.gov under Identifier NCT05210556.

The electronic medical record was reviewed from April 1, 2019 to December 1, 2021. The review was completed in January 2022 via direct examination of the surgical schedule and operative reports by the research team. The patients who underwent scheduled intra-abdominal surgery with a gynecologic oncologist were identified. Patients aged 18 years and older were included, and patients who underwent unplanned urgent or emergent surgery were excluded. The patient’s chart was reviewed for demographic data including age, race, and BMI. Patient comorbidities, type of surgery, and presence or absence of malignancy on final pathology were recorded by research team members as they were observed in the medical record. Race, as reported by the patient upon intake into the health system, was recorded as it was documented in the electronic medical record. It was pertinent to include race in this study given that racial disparities in the surgical and overall outcomes for gynecologic cancer patients have been reported [18], 21].

If patients received a prescription for the full regimen of neomycin and metronidazole, and there was no documentation regarding failure to administer or acquire the antibiotic, they were noted to have received oral antibiotic bowel preparation. Patients were asked and verbally acknowledged taking the oral antibiotic bowel preparation on the morning of the procedure. Patients with OSI were identified based on the NHSN/CDC definition of deep OSI: infection occurring within 30 days of the procedure, and infection involving any part of the body deeper than the fascia [1]. Evidence of infection could include the following: purulent drainage from a drain that is placed into the organ/space, organisms identified on culture or microbiological testing from aseptically obtained fluid or tissue in the organ-space, an abscess or other evidence of infection involving the organ/space on gross anatomical or histopathologic examination, or imaging consistent with infection [1]. Data entry was performed by the authors and verified by the principal investigator (E.L.).

Sample size determination was made based on the primary outcome of rate of deep OSI. The institutional predicted rate of infection at the time that the study was conducted was 2.5 % [22]. Based on existing literature, a decrease of up to 50–60 % could be anticipated, to a rate of 1–1.25 %. Thus, the study was designed to detect a decrease to 1.12 %. At a power of 80 % and alpha=0.05, 773 cases were needed. The time selected allowed for approximately equivalent numbers of patients before and after institution of the standard oral antibiotic bowel preparation. The duration of time pre- and post-institution of the bowel prep are approximately equivalent, and an adequate number of cases were assessed to satisfy the power as above. However, the number of cases did decrease slightly in the latter portion of the study during the COVID-19 pandemic.

The observed frequency of deep OSI for patients who did and did not receive oral antibiotic bowel preparation was computed. Patient characteristics were analyzed for both groups utilizing t tests and chi-square tests. The association between these factors with the presence of OSI was then tested utilizing t tests and chi-square tests. Logistic regression was performed to identify categorical variables that were predictors of deep OSI. Multivariable logistic regression was then performed to compare the effects of utilizing an oral antibiotic bowel preparation compared to the other risk factors for OSI identified. STATA SE 17.0 and SPSS 25 software were utilized.

Results

There were 1,017 surgical cases, including minimally invasive surgeries and laparotomies, performed by this institution’s fellowship-trained gynecologic oncologists between April 1, 2019 and December 1, 2021. Among these, 778 cases met the criteria of scheduled intra-abdominal surgery and were included. A total of 444 patients did not receive a preoperative oral antibiotic bowel preparation, while 334 patients did receive preoperative antibiotic bowel preparation. There were no patients who underwent surgery after August 1, 2020 who were ineligible for the oral antibiotic bowel preparation due to a documented allergy (Figure 1). Demographic and surgical data were compared between the two groups (Table 2).

Figure 1: 
Flow diagram of patient identification, eligibility criteria review, and inclusion or exclusion from the study.
Figure 1:

Flow diagram of patient identification, eligibility criteria review, and inclusion or exclusion from the study.

Table 2:

Patient demographic, clinical, and surgical characteristics by group.

Bowel preparation
No bowel prep (n=444) Received bowel prep (n=334)
Mean age: 58.4 ± 14.7 years Mean age: 57.9 ± 14.2 years
Mean BMI: 33.6 ± 9.5 kg/m2 Mean BMI: 32.7 ± 9.1 kg/m2
Count % Count % p-Value
Race White 421 94.8 % 304 91.0 % 0.091
Black 20 4.5 % 24 7.2 %
Asian 3 0.7 % 6 1.8 %
Ethnicity Non-Hispanic 421 94.8 % 322 96.4 % 0.290
Hispanic 23 5.2 % 12 3.6 %
Deep pelvic infection No infection 434 97.7 % 333 99.7 % 0.022
Infection 10 2.3 % 1 0.3 %
Type of surgery MIS 311 70.0 % 245 73.4 % 0.312
Laparotomy 133 30.0 % 89 26.6 %
Transfusion No 421 94.8 % 323 96.7 % 0.203
Yes 23 5.2 % 11 3.3 %
GI tract entry No 346 77.9 % 275 82.3 % 0.129
Yes 98 22.1 % 59 17.7 %
Current smoker No 399 89.9 % 296 88.6 % 0.579
Yes 45 10.1 % 38 11.4 %
Diabetic No 343 77.3 % 255 76.3 % 0.767
Yes 101 22.7 % 79 23.7 %
GYN malignancy on final pathology Benign 234 52.7 % 188 56.3 % 0.321
Malignant 210 47.3 % 146 43.7 %
  1. GYN, gynecology; MIS, minimally invasive surgery.

Among the demographic and surgical characteristics, only the length of surgery differed significantly, with the average surgical time for those not receiving a bowel preparation significantly longer at 157.3 (±85.7) minutes than those who did receive a bowel preparation at 133.9 (±70.7) minutes (p<0.001). The full list of patient characteristics and demographics for those who experience deep organ-space pelvic infection are outlined in Table 3.

Table 3:

Patient characteristics with deep organ-space pelvic infection.

Patient 1 2 3 4 5 6 7 8 9 10 11
Received bowel prep? No No No No No No No No No No Yes Mean Mean (no bowel prep)
Age, mean 79 66 64 58 66 84 59 47 48 65 67 64 64
BMI, kg/m 2 29.96 37.1 25.3 32.9 34.6 30.8 33.4 42.3 23.8 28.5 28.5 32 32
Race
 White x x x x x x x x x 82 % 90 %
 Black x 9 % 10 %
 Asian x 9 % 0 %
Ethnicity
 Non-Hispanic x x x x x x x x x x x 100 % 100 %
 Hispanic 0 % 0 %
Smoking status
 Smoker x 9 % 10 %
 Nonsmoker x x x x x x x x x x 91 % 90 %
Diabetes status
 Diabetics 0 % 0 %
 Nondiabetics x x x x x x x x x x x 100 % 100 %
Cancer on final pathology
 Gynecologic malignancy x x x x x x x x 73 % 70 %
 Benign x x x 27 % 30 %
Type of surgery
aMinimally invasive x 9 % 10 %
 Laparotomy x x x x x x x x x x 91 % 90 %
Length of surgery, minutes 67 198 70 202 112 421 450 294 245 165 190 219 222
Estimated blood loss, ml 40 350 150 150 130 500 1,200 500 250 650 200 375 392
Intraoperative blood transfusion No No No No No No No No Yes No No 9 % 10 %
GI tract entry Yes No Yes Yes No Yes Yes No Yes Yes Yes 73 % 70 %
  1. aMinimally invasive includes robotic-assisted, laparoscopic, and transvaginal hysterectomy/surgery. BMI, body mass index; GI, gastrointestinal.

For the primary outcome of deep OSI rate, only 1 patient (0.3 %) who received antibiotic bowel preparation developed an infection, compared with 10 patients (2.3 %) who did not receive antibiotic bowel preparation (OR 0.13, CI 0.06–1.03, p=0.02). Several additional factors were demonstrated to be associated with deep OSI (Table 4).

Table 4:

Patient demographic, clinical, and surgical factors associated with organ-space infection.

Patient factors No infection (n=767) Organ-space infection (n=11) p-Value
White 716 (93.4 %) 9 (81.8 %) 0.04
Black 43 (5.6 %) 1 (9.01 %)
Asian 8 (1.0 %) 1 (9.01 %)
Received oral antibiotic bowel prep 333 (43.4 %) 1 (9.1 %) 0.022
Did not receive oral antibiotic bowel prep 434 (56.6 %) 10 (90.9 %)
Laparotomy 212 (27.6 %) 10 (90.9 %) <0.001
MIS (laparoscopic, robotic) 555 (72.4 %) 1 (9.1 %)
Length of surgery, mean, SD 146.2 (79.2) min 219.5 (127.2) min 0.003
Estimated blood loss, mean, SD 154.8 (325.6) mL 374.6 (332.8) mL 0.027
GI tract entry 618 (80.6 %) 3 (27.3 %) <0.001
No GI tract entry 149 (19.4 %) 8 (72.7 %)
  1. GI, gastrointestinal; MIS, minimally invasive surgery; SD, standard devation.

In the initial analysis, factors associated with a greater risk of OSI included Black or Asian race (p=0.04), longer surgical time (p=0.003), higher estimated blood loss (p=0.027), laparotomy rather than a minimally invasive approach (p<0.001), and entry into the gastrointestinal (GI) tract (p<0.001). Factors for which no association was identified included age (p=0.18), BMI (p=0.55), ethnicity (p=0.46), smoking (p=0.86), diabetes (p=0.06), malignant pathology (p=0.07), and receipt of blood transfusion (p=0.4). Multivariable regression analysis was then performed to properly compare the effects of utilizing an oral antibiotic bowel preparation compared to the other risk factors for SSI identified (Table 3). This allowed for accurate determination of the effect size of the oral antibiotic bowel preparation. Receiving an oral antibiotic bowel preparation was suggestive of an absence of OSI with an OR 0.04 (CI 0.00–0.87, p=0.04). In contrast, surgery via laparotomy (OR 20.1, CI 1.6–250.2, p=0.02) and Asian race (OR 60.8, CI 2.6–1,380.5, p=0.01) were both indicative of increased occurrence of deep OSI. Length of surgery, estimated blood loss, and GI tract entry were not related to OSI on multivariable analysis.

Discussion

Summary of main results

This study demonstrates that the use of this oral antibiotic bowel preparation in gynecologic oncology surgeries is indicative of reduced deep OSI rate on multivariable regression analysis. Factors that increased the risk for deep OSI included Asian race and laparotomy approach. However, due to the low number of Asian patients included in this analysis, it would be prudent to view the statistical significance with caution, and specifics cannot be generalized without increasing the number of Asian patients included in future studies.

Results in the context of published literature

This was a unique opportunity to investigate the impact of oral antibiotic bowel preparation given that there were no further changes to institutional policies, surgeons, or ERAS bundles since implementation. The previously mentioned large database study and single institution reports were unable to pinpoint the effects of oral antibiotic bowel preparation on deep OSI specifically, as other interventions were bundled simultaneously. This single-institution study therefore provides more granular information on the use of oral antibiotic bowel preparation and confirms the potential of this regimen to reduce deep OSI.

It is worth noting that certain factors historically noted to be associated with OSI were not found to be significant: high BMI, smoking, diabetes on initial analysis, length of surgery, estimated blood loss, and GI tract entry on multivariable analysis. This result is quite interesting and could be due to several explanations. For instance, our minimally invasive approach was 72.4 % for the entire cohort. It is known that minimally invasive surgery has improved outcomes in terms of postoperative recovery [23]. Further, there is a possibility that improvements in perioperative care including ERAS protocol, tight glycemic control, normothermia, adherence to sterile technique, and antibiotic use minimized these traditionally seen differences for this patient sample. However univariate analysis showed no significant association between diabetes, blood loss, and smoking on deep OSI, and although the study was not powered to determine an association, it can be assumed that a larger study with greater numbers of patients would reveal consistency with these previously established associations, which was not the goal of this research.

Strengths and weaknesses

The study was substantiated by including patients from both groups within the same institution, and all patients underwent the same ERAS protocol (Table 1). No major changes in surgical technique occurred over the duration of the study period. The same surgeons operated on patients both before and after August 1, 2020 when the oral antibiotic bowel preparations were standardized. The study was further strengthened by the accessibility of metronidazole and neomycin, which are low-risk and inexpensive antibiotics, allowing this regimen to be highly generalizable. The oral antibiotic bowel preparation utilized in this study held both statistically and clinically meaningful results that impacted both individual patients in terms of individual morbidity, and overall health system by decreasing the NHSN/CDC reportable rates of infection. Metronidazole and neomycin are inexpensive in comparison to hospitalization for a deep OSI: $12.21 for the medications vs. an average of $60,000 in this hospital system at the time of the study [24]. These antibiotics are also safe, with the literature only having case reports of hypersensitivity reactions to oral administration of either one [25], [26], [27]. Therefore, the authors [21] recommended adding this oral antibiotic regimen as part of the armamentarium to reduce deep OSIs. In the future, a multi-institution randomized controlled trial would be beneficial to remove the limitations of this study’s retrospective and single-institution approach. A thorough cost analysis would also be indicated.

Potential confounders to the study are innate to that of a retrospective study. Certain information of interest was not previously documented. For instance, adverse effects of oral antibiotic bowel preparation were not consistently noted, and no scoring system for the severity of any adverse effects was instituted. There were several patient reports of mild nausea and mild diarrhea after oral antibiotic administration, but more detailed information was not gathered. Similarly, while verbal compliance with bowel preparation was confirmed the morning of surgery, there is always the possibility that compliance was not perfect, and there was no verification via chemical or lab testing. If the patient experienced emesis after bowel preparation, they were documented as not receiving the antibiotic bowel prep. One additional confounder between the two arms is that of surgical time (Table 4); the group that did not receive antibiotic bowel preparation had a significantly longer mean surgical time (157.3 ± 85.7 min) than the group receiving antibiotic bowel preparation (133.9 ± 70.7 min, p<0.001). Although other characteristics between groups were well-balanced, this could have affected the rate of deep OSI for the group of patients who did not receive antibiotic bowel preparation.

Implications for practice and future research

Instituting an oral antibiotic bowel preparation before major gynecologic oncology surgery with neomycin and metronidazole demonstrated a statistically significant reduction in deep OSIs. The results suggest an inexpensive and feasible regimen that may definitively improve surgical outcomes in future, prospective, larger studies.

Conclusions

These results support utilizing an inexpensive, low-risk oral antibiotic bowel preparation regimen to improve surgical outcomes and to reduce the risk of deep OSI, and these results provide a basis for pursuing larger-scale prospective studies.


Corresponding author: Jennifer Gaertner-Otto, DO, Division of Gynecologic Oncology, WellSpan York Hospital, 1001 S. George Street, York, PA 17402, USA, E-mail:

  1. Research ethics: The protocol was reviewed by the WellSpan Institutional Review Board and met criteria for exemption as it involved only information collection and analysis involving the authors’ use of identifiable health information (exemption category 45 CFR 46.104(d)). The study was approved for waiver of consent. It was registered with ClinicalTrials.gov under Identifier NCT05210556.

  2. Informed consent: The study was approved for waiver of consent. It was registered with ClinicalTrials.gov under Identifier NCT05210556.

  3. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  4. Use of Large Language Models, AI and Machine Learning Tools: None declared.

  5. Conflict of interest: None declared.

  6. Research funding: None declared.

  7. Data availability: Data sharing was performed via deidentified demographic and surgical data is shared on Mendeley Data, V1, DOI: 10.17632/zm3sb7s3by.1. Data was published June 14, 2022, and will be available in perpetuity to the public online via search of the DOI above for review and research purposes.

References

1. Surgical Site Infection Event. National healthcare safety network. Centers for Disease Control and Prevention; 2017. https://www.cdc.gov/nhsn/pdfs/pscmanual/9pscssicurrent.pdf [Accessed May 2022].Search in Google Scholar

2. Budker, RL, Rudasill, SE, Mardock, AL, Nyakudarika, NC, Benharash, P, Cohen, JG. Predictors of 30-day readmission among ovarian cancer patients undergoing surgery. J Women’s Health Dev 2021;4:64–77. https://doi.org/10.26502/fjwhd.2644-28840061.Search in Google Scholar

3. Cai, HB, Zhou, YF, Chen, HZ. The role of bowel surgery with cytoreduction for epithelial ovarian cancer. Clin Oncol (RCR) 2007;19:757–62. https://doi.org/10.1016/j.clon.2007.06.015.Search in Google Scholar PubMed

4. Jones, NL, Chen, L, Chatterjee, S, Tergas, AI, Burke, WM, Hou, JY, et al.. National trends in extended procedures for ovarian cancer debulking surgery. Int J Green Comput 2018;28:19–25. https://doi.org/10.1097/IGC.0000000000001132.Search in Google Scholar PubMed PubMed Central

5. Halsted, WS. Circular suture of the intestine – an experimental study. AJMS 1887;188:436–60. https://doi.org/10.1097/00000441-188710000-00010.Search in Google Scholar

6. Lei, P, Ruan, Y, Yang, X, Wu, J, Hou, Y, Wei, H, et al.. Preoperative mechanical bowel preparation with oral antibiotics reduces surgical site infection after elective colorectal surgery for malignancies: results of a propensity matching analysis. World J Surg Oncol 2020;11:35. https://doi.org/10.1186/s12957-020-1804-4.Search in Google Scholar PubMed PubMed Central

7. Jung, B, Matthiessen, P, Smedh, K, Nilsson, E, Ransjö, U, Påhlman, L. Mechanical bowel preparation does not affect the intramucosal bacterial colony count. Int J Colorectal Dis 2010;25:439–42. https://doi.org/10.1007/s00384-009-0863-3.Search in Google Scholar PubMed

8. Fa-Si-Oen, PR, Verwaest, C, Buitenweg, J, Putter, H, de Waard, JW, van de Velde, C, et al.. Effect of mechanical bowel preparation with polyethyleneglycol on bacterial contamination and wound infection in patients undergoing elective open colon surgery. Clin Microbiol Infection 2005;11:158–60. https://doi.org/10.1111/j.1469-0691.2004.01012.Search in Google Scholar

9. Stone, HH, Hooper, CA, Kolb, LD, Geheber, CE, Dawkins, EJ. Antibiotic prophylaxis in gastric, biliary and colonic surgery. Ann Surg 1976;184:443–52. https://doi.org/10.1097/00000658-197610000-00007.Search in Google Scholar PubMed PubMed Central

10. Nelson, RL, Glenny, AM, Song, F. Antimicrobial prophylaxis for colorectal surgery. CDSR 2009;1:CD001181. https://doi.org/10.1002/14651858.CD001181.pub3.Search in Google Scholar PubMed

11. Morris, MS, Graham, LA, Chu, DI, Cannon, JA, Hawn, MT. Oral antibiotic bowel preparation significantly reduces surgical site infection rates and readmission rates in elective colorectal surgery. Ann Surg 2015;261:1034–40. https://doi.org/10.1097/SLA.0000000000001125.Search in Google Scholar PubMed

12. Bellows, CF, Mills, KT, Kelly, TN, Gagliardi, G. Combination of oral non-absorbable and intravenous antibiotics versus intravenous antibiotics alone in the prevention of surgical site infections after colorectal surgery: a meta-analysis of randomized controlled trials. Tech Colproctol 2011;15:385–95. https://doi.org/10.1007/s10151-011-0714-4.Search in Google Scholar PubMed

13. McSorley, ST, Steele, CW, McMahon, AJ. Meta-analysis of oral antibiotics, in combination with preoperative intravenous antibiotics and mechanical bowel preparation the day before surgery, compared with intravenous antibiotics and mechanical bowel preparation alone to reduce surgical-site infections in elective colorectal surgery. BJS Open 2018;2:185–94. https://doi.org/10.1002/bjs5.68.Search in Google Scholar PubMed PubMed Central

14. Kalogera, E, Van Houten, HK, Sangaralingham, LR, Borah, BJ, Dowdy, SC. Use of bowel preparation does not reduce postoperative infectious morbidity following minimally invasive or open hysterectomies. AJOG 2020;223:231.e1–e12. https://doi.org/10.1016/j.ajog.2020.02.035.Search in Google Scholar PubMed

15. Schiavone, MB, Moukarzel, L, Leong, K, Zhou, QC, Afonso, AM, Iasonos, A, et al.. Surgical site infection reduction bundle in patients with gynecologic cancer undergoing colon surgery. J Gynecol Oncol 2021;147:115–19. https://doi.org/10.1016/j.ygyno.2017.07.010.Search in Google Scholar PubMed PubMed Central

16. Lippitt, MH, Fairbairn, MG, Matsuno, R, Stone, RL, Tanner, EJ, Wick, EC, et al.. Outcomes associated with a five-point surgical site infection prevention bundle in women undergoing surgery for ovarian cancer. Obstet Gynecol 2017;130:756–64. https://doi.org/10.1097/AOG.0000000000002213.Search in Google Scholar PubMed

17. Johnson, MP, Kim, SJ, Langstraat, CL, Jain, S, Habermann, EB, Wentink, JE, et al.. Using bundled interventions to reduce surgical site infection after major gynecologic cancer surgery. Obstet Gynecol 2016;127:1135–44. https://doi.org/10.1097/AOG.0000000000001449.Search in Google Scholar PubMed

18. Nichols, RL, Broido, P, Condon, RE, Gorbach, SL, Nyhus, LM. Effect of preoperative neomycin-erythromycin intestinal preparation on the incidence of infectious complications following colon surgery. Ann Surg 1973;178:453–62. https://doi.org/10.1097/00000658-197310000-00008.Search in Google Scholar PubMed PubMed Central

19. Lewis, RT, Allan, CM, Goodall, RG, Lloyd-Smith, WC, Marien, B, Park, M, et al.. Preventing anaerobic infection in surgery of the colon. Can J Surg 1981;24:139–41, 184.Search in Google Scholar

20. Coppa, GF, Eng, K, Gouge, TH, Ranson, JH, Localio, S. Parenteral and oral antibiotics in elective colon and rectal surgery. A prospective, randomized trial. Am J Surg 1983;145:62–5. https://doi.org/10.1016/0002-9610(83)90167.Search in Google Scholar

21. Srivastava, SK, Ahmad, A, Miree, O, Patel, GK, Singh, S, Rocconi, RP, et al.. Racial health disparities in ovarian cancer: not just black and white. J Ovarian Res 2017;10:58. https://doi.org/10.1186/s13048-017-0355-y.Search in Google Scholar PubMed PubMed Central

22. WellSpan Hospital Acquired Conditions Committee, as per CDC Calculation Guidelines. The NHSN standardized infection ratio (SIR). Updated April 2022. Available from: https://www.cdc.gov/nhsn/pdfs/ps-analysis-resources/nhsn-sir-guide.pdf.Search in Google Scholar

23. Scarpelli, E, Armano, G, Monfardini, L, Valenti, A, Barresi, G, De Finis, A, et al.. Minimally invasive surgery in gynecological cancers: update and systematic review. CEOG 2022;49:88. https://doi.org/10.31083/j.ceog4904088.Search in Google Scholar

24. WellSpan York Hospital Outpatient Pharmacy, as per WellSpan Health Pharmacy Database. Oral communication. York PA: WellSpan Hospital; 2022.Search in Google Scholar

25. Sanchez-Borges, M, Thong, B, Blanca, M, Ensina, LFC, González-Díaz, S, Greenberger, PA, et al.. Hypersensitivity reactions to non-beta-lactam antimicrobial agents, a statement of the WAO special committee on drug allergy. WAO J 2013;6:18. https://doi.org/10.1186/1939-4551-6-18.Search in Google Scholar PubMed PubMed Central

26. García-Rubio, I, Martínez-Cócera, C, Santos Magadán, S, Rodríguez-Jiménez, B, Vázquez-Cortés, S. Hypersensitivity reactions to metronidazole. Allergol Immunopathol Suppl (Madr) 2006;34:70–2. https://doi.org/10.1157/13086750.Search in Google Scholar PubMed

27. Carnicle, JM, Tran, TV, McKissack, SS. Systemic contact dermatitis following oral neomycin therapy. Proc (Bayl Univ Med Cent). 2020;34:89–90. https://doi.org/10.1080/08998280.2020.18056.Search in Google Scholar

Received: 2024-05-16
Accepted: 2024-09-06
Published Online: 2024-10-09

© 2024 the author(s), published by De Gruyter, Berlin/Boston

This work is licensed under the Creative Commons Attribution 4.0 International License.

Downloaded on 17.11.2025 from https://www.degruyterbrill.com/document/doi/10.1515/jom-2024-0099/html
Scroll to top button