key: cord-0014759-ruqidr4e
authors: Nguyen, Kevin A.; Le, Danny Q.; Bui, Yvonne T.; Advani, Sonali D.; Renzulli, Joseph; Kenney, Patrick A.; Leapman, Michael S.
title: Incidence, risk factors, and outcome of Clostridioides difficile infection following urological surgeries
date: 2021-01-20
journal: World J Urol
DOI: 10.1007/s00345-020-03551-y
sha: a834e7dd1104a67fafce889cfd4722e166d41eed
doc_id: 14759
cord_uid: ruqidr4e

PURPOSE: To assess the incidence, risk factors, and clinical outcomes associated with (Clostridioides difficile infection) CDI following urological surgery, which is the leading cause of nosocomial diarrhea and a growing public health burden. METHODS: We queried the National Surgical Quality Improvement Program (NSQIP) to identify patients undergoing urological surgery in 2015–2016. We evaluated the 30-day incidence and factors associated with postoperative CDI and 30-day hospital readmission and length of stay as secondary outcomes. Among the subset of patients undergoing radical cystectomy with urinary diversion (surgery with highest CDI incidence) we used multivariable logistic regression analysis to evaluate independent clinical and demographic factors associated with postoperative CDI. RESULTS: We identified 98,463 patients during the study period. The overall 30-day incidence of CDI was 0.31%, but varied considerably across surgery type. The risk of CDI was greatest following radical cystectomy with urinary diversion (2.72%) compared to all other urologic procedures (0.19%) and was associated with increased risk of hospital readmission (p < 0.0001), re-operation (p < 0.0001), and longer mean length of stay (p < 0.0001) in this cohort. Among patients undergoing radical cystectomy with urinary diversion, multivariable logistic regression revealed that preoperative renal failure (OR: 5.30, 95% CI 1.13–24.9, p = 0.035) and blood loss requiring transfusion (OR: 1.67, 95% CI 1.15–2.44, p = 0.0075) were independently associated with CDI. CONCLUSIONS: In a nationally representative cohort, the incidence of CDI was low but varied substantially across surgery types. CDI was most common following radical cystectomy and associated with potentially modifiable factors such as blood transfusion and significantly longer length of stay. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00345-020-03551-y.

Clostridioides difficile (C. difficile), formerly known as Clostridium difficile, is a spore-forming, gram-positive anaerobic bacillus that colonizes the human gut and is one of the leading causes of opportunistic nosocomial infection in the United States [1, 2] . C. difficile infection (CDI) can cause a wide spectrum of clinical features ranging from asymptomatic colonization to diarrhea, hemorrhage, pseudomembranous colitis, and death [3, 4] . Although there have been significant advancements in infection prevention, the incidence of CDI has substantially increased since the early 2000s with the emergence of a hypervirulent strain of C. difficile ribotype 027 that releases much higher toxin levels earlier in the growth phase than other variants [2] .

There has been increasing awareness of the impact of CDI on perioperative outcomes. Several risk factors for CDI identified in the general surgery literature include use of broad-spectrum antibiotics, advanced age, and immunosuppression [5] . In addition, prior publications have indicated that CDI is associated with decreased patient reported quality of life measures, increased hospital length of stay, intensive care unit (ICU) admissions, postoperative emergency room utilization, and readmissions [4, 6, 7] . In cost analyses, CDI contributed an additional $21,000 in costs per patient, resulting in an estimated national burden of $7 billion per year [8] . Given direct clinical and economic burdens of CDI, it is increasingly important to understand and address the issues surrounding CDI prevention.

Nosocomial infections are significant contributors to adverse patient outcome and increased healthcare expenditure after urological surgery [9] . Yet, little information exists in the literature regarding the effects of CDI after urological surgery. Previous retrospective, single-institution studies have begun to characterize the risk of CDI after urologic surgeries of larger scale, such as radical cystectomy [9] . However, to our knowledge, no cross-sectional national analyses have been performed to study this question across the span of common urological surgeries. Therefore, we aimed to comprehensively evaluate the incidence, risk factors, and postoperative complications associated with CDI following urological surgery using the American College of Surgeons National Surgical Quality Improvement Project (NSQIP).

The American College of Surgeons National Surgical Quality Improvement Program (NSQIP) was queried to identify records from 2015 through 2016. NSQIP consolidates clinical data from patients undergoing surgical procedures in the United States at more than 200 hospitals. The data collected encompass more than 200 variables, which include pre-operative, perioperative/intraoperative, postoperative complications, demographic, comorbidity, and mortality outcomes 30 days after surgery. Surgical staff reviewers at each hospital site curate the data using a standardized protocol and regularly audit participating sites. Patients were diagnosed with any of the following diagnostic laboratory tests: stool culture, glutamate dehydrogenase enzyme immunoassay or latex agglutination, PCR assay, stool cytotoxin test, or enzyme immunoassay for toxins A and B. All patients diagnosed with CDI were treated by either oral and/or IV antibiotics, fecal enemas, or surgical management for fulminant/ uncontrolled C. diff. colitis.

We included patients who underwent urological surgery between January 1, 2015 and December 31, 2016, based on the availability of CDI coding within NSQIP. We used common procedural terminology (CPT) codes to classify major procedures (Supplementary Table 1 ). The primary outcome of interest was CDI infection as documented within 30-days of the procedure.

Clinicopathologic and demographic variables including age, sex, operative time, total length of stay duration, race, comorbidities (history of bleeding disorder, ascites, congestive heart failure, chronic obstructive pulmonary disease, diabetes, hypertension, smoking, steroid/immunosuppressant usage), preoperative conditions (renal failure, dialysis, transfusion), sex, American Society of Anesthesiology (ASA) Class, disseminated cancer status, intraoperative bleeding requiring transfusion, mortality, 30-day readmission, and 30-day reoperation records were evaluated. A preplanned subgroup analysis was then performed to assess differences in clinicopathologic, demographic, and outcome measurements in patients who received radical cystectomy due to the high incidence of CDI in this population documented in the literature [10] .

We used the chi-square test and Student t-tests to evaluate differences in demographic and clinicopathologic characteristics between patients who developed CDI and those who did not. The Anderson-Darling test was used to verify normality of distribution. Given the substantially higher incidence of CDI in patients undergoing radical cystectomy, we constructed multivariable logistic regression models in forward-step fashion to evaluate independent predictors of developing postoperative CDI in this patient subset. We applied a Bonferroni correction to account for multiple comparisons. Data analysis was performed using JMP Pro v.11.1 statistical software (SAS Institute Inc., Cary, NC, USA) and R version 3.5.1.

Of 98,463 patients undergoing urological surgery within NSQIP, we identified 306 (0.31%) cases of postoperative CDI (Table 1 ). CDI was more common after radical cystectomy with urinary diversion (2.72%) compared to all 

Among patients who underwent radical cystectomy with urinary diversion, those with postoperative CDI had longer mean lengths of stay (14.6 vs. 9.4 days, p < 0.0001), however there were no differences in 30-day readmission (24.4% vs. 20.5%, p = 0.302) or re-operation (7.3% vs. 5.4%, p = 0.382). On univariate analysis, CDI after radical cystectomy was associated with intraoperative/ postoperative bleeding requiring transfusion (52.0% vs. 36.2%, p < 0.0001) and female sex (33.3% vs. 24.2%, p = 0.041) (Supplementary Table 2 ). On multivariable logistic regression analysis evaluating for determinants of CDI in patients receiving radical cystectomy, preoperative renal failure (OR: 5.30, 95% CI 1.13-24.9, p = 0.035), intraoperative/postoperative bleeding requiring transfusion (OR: 1.67, 95% CI 1.15-2.44, p = 0.0075), and ventilator dependence (OR: 17.9 (1.69-189, p = 0.017) were associated with the development of postoperative CDI (Supplementary Table 3 ). 

Using national hospital data, we evaluated the incidence, risk factors, and complications associated with CDI following urological surgery. Compared to previous literature, we found that the overall incidence of CDI was relatively low across all types of urological surgery; however, the incidence was more than ten-fold greater following radical cystectomy with urinary diversion. Moreover, cystectomy was associated with substantially higher incidence relative to other major oncologic surgeries. Controlling for surgery type, CDI was associated with both patient related factors, including female sex, and history of renal failure, ascites, bleeding disorders, hypertension, steroid/ immunosuppressant use, and systemic sepsis and treatment related factors such as longer operative time and receipt of blood transfusion. CDI after radical cystectomy with urinary diversion was associated with longer length of stay but not risk for readmission. By offering the largest crosssectional evaluation of CDI after urological surgery, this work provides additional information and external validity regarding the scope and potentially modifiable factors associated with this outcome. CDI is well known to be associated with antibiotics use as well as other host factors that increase risk in the postoperative period [11] . The 'normal' human colonic flora offers protection against C. difficile over growth and, thereby, opportunistic infection. Use of antibiotics, especially betalactams or clindamycin, disrupts the typical state of the colonic microbiome and creates a susceptible environment for CDI, especially in the presence of risk factors [12] . Our data also reveal that specific clinical conditions were associated with higher risk of postoperative CDI including higher ASA class status and higher intraoperative/postoperative blood loss. Among the subset of patients undergoing radical cystectomy, risk factors associated with CDI included prior renal failure, ventilation dependence, and blood transfusions, a finding which has not yet been demonstrated in the urological literature [1, 13, 14] . Evidence from mouse models indicate that antibiotic treatment disrupts the microbiome of stable murine carriers, leading to development of a spore shedding state and increased transmission to other mice [15] . Stopping antibiotic treatment in mice led to suppression of C. difficile levels and recovery of the microbiome, which supports early cessation of prophylactic antibiotic treatment for all patients particularly those at highest risk. This data also raise a greater emphasis on modifiable provider interventions, such as prompt diagnosis with sensitive screening and subsequent confirmatory tests, handwashing with soap and water instead of alcohol-based agents, and contact precautions for at risk individuals.

Other proposed theories include direct effects on gut flora and antitoxin production that protect hosts against CDI [16] . As renal failure and ventilator dependence are indicative of serious systemic illness, it is plausible that altered immunological responses could be contributors [17, 18] . Moreover, blood transfusion may also suppress immunological responses increasing the risk of CDI [19] . Perioperative transfusion has been associated with an increased risk of surgical site infections (SSI), largely due to transfusionrelated immunomodulation. Perioperative blood transfusion may increase risk of postoperative CDI in a similar manner by modulating and suppressing the host immune system, especially circulating lymphocytes, as well as increased antibiotic exposure from higher incidence of SSI [20] . Thus, efforts such as preoperative control of anemia; the use of judicious transfusion thresholds; the minimization of intraoperative blood loss and the use of autologous blood products should be made to implement measures to avoid unnecessary transfusions [21] .

These findings also suggest that careful considerations be noted toward interventions to where the risk is greatest, in particular radical cystectomy with urinary diversion [22] . The current AUA and EUA guidelines recommend perioperative antibiotic prophylaxis in cystectomy, which may encompass a second or third generation cephalosporin in addition to metronidazole [23, 24] . Given the significant risk of developing postoperative CDI with the use of prolonged cephalosporins [25] , our findings imply the need for greater scrutiny when assessing the length of antibiotic use. While the AUA and EUA guidelines recommend 24 h of antibiotic coverage, the American College of Surgeons guidelines recommend stopping perioperative antibiotics after skin closure [26] . This recommendation can be applied in high risk individuals to reduce the risk of developing postoperative CDI. In radical cystectomy, the higher incidence of CDI may be related to the complex nature of the operation, bowel preparation, prolonged hospitalization, use of perioperative broader spectrum antibiotics, and intestinal diversion. Approximately 76% of postoperative CDI in the United States occur after hospital discharge, and the incidence of CDI may be linked to the observation that slower growth rates correlate with increased disease severity [27, 28] . Initiatives to reduce CDI rates with judicious antibiotic use are warranted, and we identified potentially modifiable factors that were associated with CDI after radical cystectomy including length of operation and blood loss/transfusion. Although we cannot imply a simple causal relationship, these factors have also been identified in other studies as associated with surgical site infections and appear to warrant additional investigation [29] .

We found that CDI is independently associated with other adverse perioperative outcomes, including length of stay and readmission, which is consistent with previous literature [30] . Financial analysis of healthcare expenditures associated with CDI has demonstrated that direct health care costs and increased length of stay were the main hospital cost drivers.2 Therefore, preventative measures could reduce national annual hospital-associated costs of CDI, which now approach 7 billion dollars.8 In addition to direct financial costs, CDI has been shown to negatively impact patient-reported health status in regard to physical, mental and social well-being [2] .

In this nationally representative study, we identified a lower incidence of CDI than reported in smaller single institutional cohort studies. Among nearly 5000 patients undergoing cystectomy with urinary diversion, we found that the incidence of CDI was 2.6%. This rate is lower than prior studies which reported a rate of 8.8% in a series of 522 patients and 11.7% in a series of 350 patients and may reflect a more representative national sample [9, 10] . However, a lower incidence may also relate to methodological differences in capturing CDI which is limited to 30 days after surgery within NSQIP. Underreporting of CDI may also stem from differences in methodology of data abstraction and breadth of available diagnostic tests. In our cohort, stool culture, glutamate dehydrogenase enzyme immunoassay or latex agglutination, PCR assay, stool cytotoxin test, or enzyme immunoassay for toxins A and B were all available modalities; however, they all present with different sensitivities and specificities, which may contribute to institutional variations in reported rates. In studies evaluating the quality of data from NSQIP compared to other national surgical outcomes databases, NSQIP mortality and complication rates were lower than comparable databases, which likely are attributed to how these hospitals systematically monitor their surgical outcomes to attenuate complication rates. This discrepancy in outcome may also be attributed to the possibility that nurse abstractors exclude complication rates or mortality rates not directly attributable to a procedure, which is not true of other databases [31] . These differences may also relate to the larger sample size, drawing from over 200 institutions which increases diversity of patient and procedural complexity and reduces variations in local institutions attributed to antibiotic prophylaxis practices, clinical volume, and patient morbidity. A large number of studies regarding CDI rates are nonrandomized and as such, selection bias may contribute to the variability in reported CDI rates [30] . Given these limitations, our study aims to minimize selection bias by including all NSQIP patients undergoing urological surgery for a two-year period from 2015 to 2016. Although this is the largest national analysis of postoperative CDI after urologic surgery there are several limitations that require attention. Most notably, through the use of national administrative data, we are unable to account for antibiotic use, as well as type and dosage, both prior to surgery and in the perioperative period. Furthermore, information regarding the outcome of CDI treatment and a prior history of CDI were unavailable. As CDI is highly contagious within healthcare delivery systems, we are unable to incorporate the local incidence rates at the hospital-level that may further modify postoperative risk. Although the incidence was greatest after radical cystectomy with urinary diversion, we were unable to account for effects that may further alter the host microbiome including the use of neoadjuvant chemotherapy, type of urinary diversion during radical cystectomy, mechanical or antibiotic bowel preparations. Additionally, there are other factors that are not recorded by NSQIP such as the identity of the surgeon, local antibiotic resistance or antibiogram, or hand hygiene that may further modify these outcomes.

The overall incidence of CDI after urological surgery was low (0.31%) but varied substantially by surgery type and was highest after radical cystectomy with urinary diversion (2.72%). postoperative CDI was associated with both patient factors, including renal failure and aggregate measures of comorbidity, as well as surgical factors including use of blood transfusion. CDI was associated with significantly longer length of stay.

Author contributions KN: protocol/project development, data collection or management, data analysis, manuscript writing/editing, DL: protocol/project development, manuscript writing/editing, YB: protocol/project development, manuscript writing/editing, SR: protocol/ project development, manuscript writing/editing, JK: protocol/project development, manuscript writing/editing, PK: protocol/project development, manuscript writing/editing, ML: protocol/project development, data collection or management, manuscript writing/editing.

The authors declared that they have no conflicts of interest.

Ethics approval IRB exemption.

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