Abstract
Introduction:
We report the contemporary outcomes of radical cystectomy (RC) in patients with bladder cancer using a national, prospective perioperative database specifically developed to assess the quality of surgical care.
Methods:
The National Surgical Quality Improvement Program (NSQIP) database was queried from 2006 to 2011 for RC. Data on postoperative complications, operative time, length of stay, blood transfusions, readmission, and mortality within 30 days from surgery were abstracted.
Results:
Overall, 1094 patients undergoing RC were identified. Rates of overall complications, transfusions, prolonged length of hospitalization, readmission, and perioperative mortality were 31.1%, 34.4%, 25.9%, 20.2%, and 2.7%, respectively. Body mass index represented an independent predictor of overall complications on multivariate analysis (p = 0.04). Baseline comorbidity status was associated with increased odds of postoperative complications, prolonged operative time, transfusion, prolonged hospitalization, and perioperative mortality. In particular, patients with cardiovascular comorbidities were 2.4 times more likely to die within 30 days following cystectomy compared to their healthier counterparts (p = 0.04). Men had lower odds of prolonged operative time and blood transfusions (p ≤ 0.03). Finally, the receipt of a continent urinary diversion was the only predictor of readmission (p = 0.02). Our results are limited by their retrospective nature and by the lack of adjustment for hospital and tumour volume.
Conclusions:
Complications, transfusions, readmission, and perioperative mortality remain relatively common events in patients undergoing RC for bladder cancer. In an era where many advocate the need for prospective multi-institutional data collection as a means of improving quality of care, our study provides data on short-term outcomes after RC from a national quality improvement initiative.
Introduction
Open radical cystectomy (RC) currently represents the standard of care for the treatment of muscle-invasive bladder cancer.1 Despite refinements in surgical technique and perioperative management, RC has been associated with a substantial risk of postoperative morbidity and mortality, where the rates of short-term complications and mortality.1–7
Identifying determinants of postoperative outcomes is crucial for individual risk-adjustment prior to RC. Several studies have reported predictors of complications, perioperative mortality, and readmission. However, these data are usually obtained from tertiary referral centres,2,5–7 and therefore may not be generalizable to the American population. Recent population-based studies have reported nationwide outcomes for patients treated with RC for bladder cancer.8–10 Despite their larger sample sizes, such studies are inherently limited by pre-selection bias, as well as errors in data collection, procedure classification and coding.11,12
To overcome these limitations, we sought to identify determinants of significant endpoints, such as postoperative complications, blood transfusions, prolonged operative time (pOT), prolonged length of stay (pLOS), perioperative mortality, and readmission using the American College of Surgeons (ACS) National Surgery Quality Improvement Program (NSQIP) database. The NSQIP was specifically developed to assess the quality of surgical care, and prospectively collects perioperative data on preoperative risk factors, intraoperative variables, and 30-day postoperative mortality and morbidity for patients undergoing major surgical procedures in the United States. This database reliably detects complications and mortality in comparison to administrative databases or institutional series.13–15
Methods
Data source
The current study relied on the ACS NSQIP database. Per protocol, 252 Health Insurance Portability and Accountability Act (HIPAA)-compliant variables were collected for each encounter. These included patient demographic information, preoperative comorbidities risk factors, and laboratory results, intraoperative proceedings, as well as postoperative morbidity and mortality data for the subsequent 30-day period, where about 50% of complications occurred. Trained surgical clinical reviewers prospectively collected the data.
Study population
Overall, 1094 patients undergoing RC (Current Procedural Terminology [CPT] codes: 51590, 51595, and 51596) for bladder cancer (International Classification of Diseases 9th edition [ICD-9] codes: 188.x) between 2006 and 2011 were identified.
Covariates
For each patient, age at surgery, gender, body mass index (BMI), race, smoking status, alcohol consumption, preoperative comorbidity status, preoperative creatinine, albumin, hematocrit, receipt of neoadjuvant chemotherapy within 30 days before surgery, and type of urinary diversion were available. The Charlson comorbidity index (CCI) was calculated according to previously described methodology.16,17 The glomerular filtration rate (GFR) was calculated using the Cockcroft-Gault equation. Multiple imputation was used to analyze missing data for the following covariates: BMI (n = 5), preoperative hematocrit (n = 31), and serum creatinine (n = 43).
Outcomes
Postoperative complications were classified under the following categories: cardiovascular (postoperative cardiac arrest, myocardial infarction, or cerebrovascular accident), pulmonary (pneumonia, need for postoperative reintubation, and need for ventilatory support >48 hours), thromboembolic (deep venous thrombosis and pulmonary embolism), septic (sepsis and septic shock), renal (acute renal failure and progressive renal insufficiency), urinary tract infections, and wound complications (superficial, deep, and organ space surgical site infections, and dehiscence), according to previously reported methodology.18 Additional outcomes consisted of intraoperative transfusions, pOT, pLOS, readmission, and perioperative mortality. Postoperative transfusions were defined as any transfusion given from the time the patient left the operating room to 72 hours postoperatively. Prolonged operative time was defined as an operative time greater than the 75th percentile (≥422 minutes). Similarly, pLOS was defined as a LOS beyond the 75th percentile (≥11 days). Perioperative mortality was defined as death within 30 days after surgery. Data on the occurrence of 30-day readmission after surgery was only available for procedures performed on or after January 1, 2011.19
Statistical analyses
Descriptive statistics of categorical variables focused on frequencies and proportions. Means, medians and interquartile ranges were reported for continuously coded variables.
Multivariable logistic regression models tested the association between preoperative covariates and overall complications, pLOS, pOT, transfusion, and readmission rates. Covariates consisted of age at surgery, race, gender, BMI, smoking status, baseline comorbidities, GFR, albumin, hematocrit, neoadjuvant chemotherapy, and type of diversion. All statistical tests were performed using the R statistical package (version 3.0.2), with a two-sided significance level set at p < 0.05.
The Institutional Review Board exempted this study for review since it includes de-identified patients.
Results
Baseline characteristics
Overall, 1094 patients underwent RC at NSQIP participating hospitals between 2006 and 2011 (Table 1). The median age at surgery was 69 (interquartile range [IQR]: 61–76). Most patients were men (80.0%) and Caucasian (83.5%). Overall, 240 patients (21.9%) received continent diversion.
Table 1.
Total (n = 1094) | |
---|---|
Age at diagnosis | |
Median (IQR) | 69 (61–76) |
Gender, n (%) | |
Female | 219 (20.0) |
Male | 875 (80.0) |
BMI, n (%) | |
<25 | 340 (31.1) |
25–30 | 406 (37.1) |
>30 | 348 (31.8) |
Race, n (%) | |
White | 914 (83.5) |
Other | 180 (16.5) |
Smoking status, n (%) | |
Non smoker | 818 (74.8) |
Current smoker | 276 (25.2) |
Alcohol, n (%) | |
<2 drinks/day | 1063 (97.2) |
>2 drinks/day | 31 (2.8) |
Preoperative comorbidities, n (%) | |
No comorbidities | 337 (30.8) |
Diabetes mellitus | 204 (18.4) |
Hypertension | 650 (59.4) |
Cardiovascular disease | 134 (12.2) |
Dyspnea | 117 (10.7) |
Other medical comorbidities | 160 (14.6) |
CCI | |
0 | 772 (70.6) |
1 | 278 (25.4) |
≥2 | 44 (4.0) |
Preoperative creatinine (mg/dL), n (%) | |
<1.2 | 764 (69.8) |
≥1.2 | 330 (30.2) |
Preoperative albumin (g/dL, n (%) | |
<3.0 | 75 (6.9) |
≥3.0 | 1019 (93.1) |
Preoperative hematocrit (%), n (%) | |
<30 | 91 (8.3) |
30–45 | 905 (82.7) |
>45 | 98 (9.0) |
Glomerular filtration rate (mL/min/1.73m2), n (%) | |
≥60 | 763 (69.7) |
30–59 | 288 (26.3) |
<30 | 43 (3.9) |
Neoadjuvant chemotherapy | 48 (7.6) |
Diversion, n (%) | |
Continent Diversion | 240 (21.9) |
Other | 854 (78.1) |
BMI: body mass index; IQR: interquartile range; CCI: Charlson comorbidity index.
Short-term outcomes
Overall, 340 (31.1%) patients experienced at least 1 complication within 30 days. The most common postoperative complications were sepsis (14.2%), urinary tract infection (10.3%), and wound complications (10.3%). The median operative time was 331 minutes (IQR: 256–422). Overall, 425 (38.8%) patients received intraoperative blood transfusions. The median length of stay was 8 days (IQR: 7–11). Overall, 29 patients (2.7%) died within 30 days of surgery. Finally, 128 (20.2%) patients required readmission (Table 2).
Table 2.
Overall | ||
---|---|---|
Postoperative complications, n (%) | ||
Overall | 340 | (31.1) |
Cardiovascular | 15 | (1.4) |
Pulmonary | 71 | (6.5) |
Thromboembolic | 65 | (5.9) |
Septic | 155 | (14.2) |
Renal failure | 45 | (4.1) |
UTI | 113 | (10.3) |
Wound | 113 | (10.3) |
Median operative time (minutes; IQR) | 331 | (256–422) |
Transfusions, n (%) | 425 | (38.8) |
Median length of stay (days; IQR) | 8 | (7–11) |
Readmission*, n (%) | 128 | (20.2) |
Postoperative mortality, n (%) | 29 | (2.7) |
Readmission data only available for the year 2011 (n = 633); UTI: Urinary tract infections; IQR: Interquartile range.
Multivariate analyses
Table 3 shows the multivariable logistic regression analyses evaluating the association between preoperative variables and postoperative outcomes.
Table 3.
Overall complications OR (95% CI) | p value | Prolonged operative time OR (95% CI) | p value | Transfusion OR (95% CI) | p value | Prolonged LOS OR (95% CI) | p value | Readmission* OR (95% CI) | p value | Perioperative mortality OR (95% CI) | p value | |
---|---|---|---|---|---|---|---|---|---|---|---|---|
Age at surgery | 0.99 (0.98–1.01) | 0.5 | 0.97 (0.96–0.99) | <0.001 | 1.01 (0.98–1.01) | 0.9 | 1.04 (1.02–1.05) | <0.001 | 0.98 (0.96–1.01) | 0.06 | 1.04 (1.01–1.1) | 0.03 |
Race | ||||||||||||
White | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | ||||||
Other | 1.11 (0.78–1.59) | 0.5 | 1.50 (1.03−2.19) | 0.03 | 1.11 (0.78–1.58) | 0.6 | 1.61 (1.12–2.31) | 0.01 | 0.61 (0.32–1.13) | 0.1 | 1.33 (0.51–3.46) | 0.5 |
Gender | ||||||||||||
Female | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | ||||||
Male | 1.24 (0.85–1.75) | 0.2 | 0.65 (0.45–0.94) | 0.02 | 0.70 (0.51–0.97) | 0.03 | 0.84 (0.59–1.19) | 0.3 | 0.97 (0.58–1.62) | 0.9 | 0.58 (0.24–1.38) | 0.2 |
BMI | ||||||||||||
<25 | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | ||||||
25–30 | 1.04 (0.73–1.46) | 0.9 | 1.08 (0.74–1.58) | 0.4 | 0.80 (0.58–1.11) | 0.2 | 1.14 (0.80–1.63) | 0.4 | 1.12 (0.66–1.91) | 0.6 | 0.71 (0.25–1.99) | 0.5 |
>30 | 1.67 (1.16–2.42) | 0.01 | 1.40 (1.01−2.09) | 0.04 | 0.78 (0.54–1.13) | 0.2 | 1.26 (0.85–1.88) | 0.2 | 1.44 (0.81–2.57) | 0.2 | 1.54 (0.55–4.28) | 0.4 |
Smoking status | ||||||||||||
Non–smoker | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | ||||||
Current smoker | 1.11 (0.80–1.54) | 0.5 | 0.91 (0.64–1.29) | 0.6 | 0.70 (0.51–1.01) | 0.1 | 1.07 (0.75–1.52) | 0.7 | 0.93 (0.56–1.54) | 0.7 | 0.80 (0.27–2.34) | 0.6 |
Preoperative comorbidities (Yes vs. No) | ||||||||||||
Diabetes | 1.28 (0.91–1.80) | 0.2 | 1.06 (0.72–1.55) | 0.8 | 1.03 (0.73–1.45) | 0.8 | 0.87 (0.60–1.26) | 0.5 | 1.12 (0.66–1.90) | 0.6 | 0.63 (0.21–1.92) | 0.4 |
Hypertension | 0.81 (0.61–1.09) | 0.2 | 1.49 (1.08–2.06) | 0.01 | 1.14 (0.86–1.52) | 0.3 | 1.00 (0.74–1.36) | 0.9 | 1.21 (0.78–1.89) | 0.4 | 0.56 (0.25–1.26) | 0.1 |
Cardiovascular | 1.02 (0.67–1.54) | 0.9 | 1.02 (0.65–1.63) | 0.9 | 0.63 (0.41–0.96) | 0.03 | 0.89 (0.57–1.38) | 0.6 | 0.73 (0.29–1.83) | 0.5 | 2.41 (1.01–6.17) | 0.04 |
Dyspnea | 1.69 (1.11–2.59) | 0.01 | 1.03 (0.65–1.62) | 0.9 | 1.27 (0.83–1.96) | 0.3 | 1.59 (1.08–2.33) | 0.1 | 0.88 (0.39–1.49) | 0.4 | 1.09 (0.34–3.44) | 0.8 |
Other | 1.10 (0.74–1.60) | 0.6 | 1.18 (0.77–1.82) | 0.6 | 0.86 (0.58–1.26) | 0.4 | 1.58 (1.08–2.33) | 0.02 | 0.76 (0.38–1.49) | 0.3 | 0.69 (0.22–2.16) | 0.6 |
Glomerular filtration rate | ||||||||||||
≥60 | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | ||||||
30–59 | 1.27 (0.89–1.82) | 0.2 | 0.76 (0.49–1.18) | 0.2 | 1.28 (0.91–1.80) | 0.1 | 1.21 (0.84–1.74) | 0.3 | 0.97 (0.55–1.70) | 0.9 | 1.44 (0.53–3.95) | 0.4 |
<30 | 1.33 (0.64–2.76) | 0.4 | 0.83 (0.34–2.02) | 0.7 | 0.91 (0.44–1.87) | 0.8 | 0.80 (0.36–1.79) | 0.6 | 1.06 (0.27–4.11) | 0.9 | 1.32 (0.15–11.82) | 0.8 |
Preoperative albumin (g/dL) | ||||||||||||
≥3.0 | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | ||||||
<3.0 | 1.06 (0.57–1.96) | 0.8 | 0.75 (0.35–1.63) | 0.5 | 0.99 (0.54–1.81) | 0.9 | 1.35 (0.72–2.54) | 0.4 | 1.18 (0.42–3.29) | 0.7 | 1.72 (0.42–6.99) | 0.6 |
Unknown | 0.64 (0.48–0.85) | 0.01 | 0.80 (0.59–1.09) | 0.1 | 0.93 (0.70–1.22) | 0.6 | 0.82 (0.61–1.11) | 0.2 | 0.91 (0.59–1.40) | 0.7 | 1.47 (0.61–3.01) | 0.9 |
Hematocrit | ||||||||||||
<30 | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | ||||||
30–45 | 0.72 (0.44–1.16) | 0.1 | 1.05 (0.59–1.85) | 0.8 | 0.52 (0.33–0.82) | 0.01 | 0.81 (0.49–1.34) | 0.4 | 0.94 (0.42–2.09) | 0.8 | 1.47 (0.32–6.99) | 0.6 |
>45 | 0.83 (0.43–1.59) | 0.6 | 1.11 (0.52–2.35) | 0.7 | 0.24 (0.12–0.51) | <0.001 | 0.81 (0.39–1.65) | 0.5 | 1.12 (0.39–3.21) | 0.8 | 0.92 (0.1–11.22) | 0.9 |
Neoadjuvant chemotherapy | ||||||||||||
No | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | ||||||
Yes | 0.71 (0.46–1.11) | 0.1 | 1.65 (0.95–2.88) | 0.1 | 1.14 (0.67–1.94) | 0.1 | 0.57 (0.29–1.13) | 0.1 | 0.76 (0.35–1.67) | 0.5 | 1.10 (0.2–5.11) | 0.9 |
Diversion | ||||||||||||
Other | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | 1 (ref) | ||||||
Continent | 1.21 (0.86–1.72) | 0.2 | 2.16 (1.53–3.05) | <0.001 | 0.76 (0.53–1.08) | 0.1 | 1.38 (0.95–2.02) | 0.1 | 1.49 (1.03–2.41) | 0.02 | 0.58 (0.16–2.13) | 0.5 |
Readmission data only available for the year 2011 (n = 633); OR: Odds Ratio; CI: Confidence Interval; BMI: Body Mass Index; LOS: length of stay.
Preoperative BMI, dyspnea, and unknown albumin were the only independent predictors of postoperative complications (p = 0.01). In particular, patients with a BMI >30 were 1.7 times more like to have postoperative complications compared to those with a BMI <25 (p = 0.01). Similarly, patients with dyspnea were 1.7 times more likely to experience complications compared to their counterparts without dyspnea (p = 0.01).
Age, race, BMI, hypertension, and continent diversion were significant predictors of the pOT (p ≤ 0.04). Of note, patients receiving a continent diversion were 2.2 times more likely to have pOT compared to those receiving other diversions (p < 0.001).
Gender, preoperative hematocrit, and the presence of cardiovascular comorbidities were significant predictors of postoperative transfusion (p ≤ 0.03). Men had a lower odds of blood transfusion compared to women (p = 0.03). Additionally, patients with cardiovascular comorbidity were 57% less likely to receive postoperative transfusion compared to their counterparts without cardiovascular comorbidities (p = 0.03).
Age at diagnosis, race, and the presence of comorbidities defined as other were the only predictors of pLOS (p ≤ 0.01).
Urinary diversion type was the only predictor of read-mission after discharge. Particularly, patients receiving a continent diversion were 49% more likely to be readmitted when compared to those patients who had other diversions (p = 0.02).
Finally, age at surgery and cardiovascular comorbidities were significant predictors of mortality within 30 days of surgery (p ≤ 0.04). Specifically, patients with cardiovascular comorbidities were 2.4 times more likely to die within 30 days compared to their counterparts without cardiovascular comorbidities (p = 0.04).
Discussion
In the current study, we evaluated the contemporary rates and predictors of postoperative complications, pOT, transfusions, pLOS, readmission, and short-term mortality in a large cohort of patients included in the NSQIP database.
Several of our results are notable. First, we show that the risk of postoperative complications after RC for bladder cancer remains high in a contemporary cohort (up to 30%). This is consistent with complication rates reported in previous studies,1,2,6,8,20 and corroborates the need for accurate identification of preoperative risk factors for potentially avoidable adverse events. Our results suggest that preoperative BMI represents a significant predictor of overall postoperative complications. Previous studies have linked increased BMI to a substantially higher risk of wound infection and dehiscence,2,20 while others have suggested that construction of either urinary diversions or orthotopic bladder substitutions in patients with higher BMIs poses a much greater technical difficulty.21,22 Although we do not advocate that obesity should be considered a contraindication for surgery, these patients may do better in the care of an experienced urologist. Additionally, modifying surgical technique and using the appropriate surgical instruments are essential to minimizing the risk of adverse short-term outcomes in obese patients.21 Finally, recent data supporting the use of multi-modal chemotherapy and radiation in selected patients with muscle-invasive bladder cancer suggest that these patients need to be properly counselled of their alternatives before electing to undergo extirpative surgery.23
The high rate of readmission following cystectomy is another notable finding derived from this study. Specifically, more than 20% of the patients necessitated a hospital readmission within 30 days of surgery. This result complements those recently reported by Stimson and colleagues; these authors showed that most readmissions after RC occurred within 30 days (19.7%).5 In multivariable analyses, type of urinary diversion was the only independent predictor of hospital readmission after hospital discharge in our cohort. Specifically, patients receiving a continent diversion were 1.5 times more likely to require readmission compared to those who underwent other diversions. However, the type of diversion was not associated with increased odds of 30-day overall complications. Thus, we hypothesized that patients receiving a continent diversion may be considered at higher risk of late postoperative complications, and thus of readmission after hospital discharge.
Another noteworthy finding was that comorbidity status was a significant predictor of perioperative complications, pOT, transfusion, pLOS, and mortality. Specifically, patients with dyspnea had higher odds of postoperative complications. Additionally, patients with cardiovascular comorbidities were 2.4 times more likely to die within 30 days following surgery compared to individuals without baseline cardiovascular diseases. Surprisingly, cardiovascular comorbidities were associated with lower odds of receiving blood transfusion. However, we suspect that this finding reflects more aggressive preoperative preparation of these patients.
When looking at the impact of baseline comorbidity status in published series, while the vast majority of the studies relied on the American Society for Anesthesiologists score, only a few studies comprehensively reported the impact of patient comorbidities on short-term outcomes after RC.2,24 In the current study, the NSQIP database facilitated more accurate identification of the type of comorbidities, thus providing more clinically relevant information. For example, we were able to determine which specific comorbidities were associated with postoperative outcomes, instead of the overall comorbidity status as determined by a score relying on administrative data.
Our analyses failed to show a significant association between neoadjuvant chemotherapy and adverse postoperative outcomes. Several investigators have suggested that the underutilization of neoadjuvant chemotherapy prior to RC resides in patient and physician concerns regarding the increased risk of postoperative adverse outcomes.25 However, our results together with recently published data suggest that efforts should be made to increase guideline compliant care with regard to the use of this therapeutic approach.26,27
It should also be noted that women were had higher odds of pOT and transfusions. This is in line with previous studies,20,28 and highlights that RC might be more challenging in women.
Finally, we confirmed the unfavourable impact of older age on short-term postoperative outcomes. These observations may be explained by the established correlation between age and failure to rescue (i.e., death after the occur-rence of a complication) in the context of RC.29 Indeed, one may hypothesize that although advancing age is not associated with increased odds of complications, older and sicker patients are unable to recover when a complication does occur.29
From a practical perspective, our findings may be useful to develop preoperative strategies aimed at reducing perioperative morbidity and mortality in patients undergoing RC for bladder cancer. Indeed, reducing adverse events represents an important objective in the current state of health care, and would likely result in decreased expenditures related to the management of complications, transfusions, and readmissions following RC. In this context, individual preoperative risk assessment may facilitate better case selection, finally resulting in a decrease of adverse short-term outcomes.
The current study has its limitations. First, the lack of hospital and payer characteristic prevented assessment of the impact of hospital volume or other socioeconomic factors, such as insurance status on outcomes, as previously described.30 Second, the NSQIP did not provide data on disease characteristics, such as tumour histology and stage, and therefore we could not adjust for these variables. However, previous studies failed to show higher complication rates for advanced diseases compared to localized tumours.2,3,5,7 Nonetheless, further investigations are needed to comprehensively address this issue. Additionally, the NSQIP database lacked information regarding gastrointestinal complications, which has been shown to occur in a substantial proportion of patients after RC.2,3,10,20 Nonetheless, the NSQIP data has been shown to reliably identify those complications that are most predictive of mortality. The lack of data beyond 30 days is another limitation.5 Finally, the voluntary participation in NSQIP requires resources, which may select for larger, high-volume institutions, which are known to have lower rates of complications and readmission after RC.8,29,30 For this reason, our results might not be generalizable to small rural hospitals.
Conclusion
Complications, transfusion, readmission, and mortality are relatively common events within 30 days following RC for bladder cancer. Age, baseline comorbidity status, BMI, and type of urinary diversion represent significant determinants of these outcomes. In an era where many advocate the need for prospective multi-institutional data collection as a means of improving quality of care, our study provides data on short-term outcomes after RC from a national quality improvement initiative.
Acknowledgments
The American College of Surgeons National Surgical Quality Improvement Program and the hospitals participating in the ACS NSQIP are the source of the data used herein; they have not verified and are not responsible for the statistical validity of the data analysis or the conclusions derived by the authors. This work is supported by the Professor Walter Morris-Hale Distinguished Chair in Urologic Oncology at Brigham and Women’s Hospital.
Footnotes
Competing interests: Dr. Gandaglia, Dr. Varda, Dr. Sood, Dr. Pucheril, Dr. Konijeti, Dr. Sammon, Dr. Sukumar, Dr. Menon, Dr. Sun, Dr. Chang, Dr. Montorsi and Dr. Kibel all declare no competing financial or personal interests. Dr. Trinh has received consultant fees from Intuitive Surgical Inc.
This paper has been peer-reviewed.
References
- 1.Gakis G, Efstathiou J, Lerner SP, et al. ICUD-EAU International Consultation on Bladder Cancer 2012: Radical cystectomy and bladder preservation for muscle-invasive urothelial carcinoma of the bladder. Eur Urol. 2013;63:45–57. doi: 10.1016/j.eururo.2012.08.009. [DOI] [PubMed] [Google Scholar]
- 2.Roghmann F, Trinh QD, Braun K, et al. Standardized assessment of complications in a contemporary series of European patients undergoing radical cystectomy. Int J Urol. 2014;21:143–9. doi: 10.1111/iju.12232. . Epub 2013 Aug 1. [DOI] [PubMed] [Google Scholar]
- 3.Novara G, De Marco V, Aragona M, et al. Complications and mortality after radical cystectomy for bladder transitional cell cancer. J Urol. 2009;182:914–21. doi: 10.1016/j.juro.2009.05.032. [DOI] [PubMed] [Google Scholar]
- 4.Lowrance WT, Rumohr JA, Chang SS, et al. Contemporary open radical cystectomy: Analysis of perioperative outcomes. J Urol. 2008;179:1313–8. doi: 10.1016/j.juro.2007.11.084. discussion 1318. [DOI] [PubMed] [Google Scholar]
- 5.Stimson CJ, Chang SS, Barocas DA, et al. Early and late perioperative outcomes following radical cystectomy: 90-day readmissions, morbidity and mortality in a contemporary series. J Urol. 2010;184:1296–300. doi: 10.1016/j.juro.2010.06.007. [DOI] [PubMed] [Google Scholar]
- 6.Hollenbeck BK, Miller DC, Taub D, et al. Identifying risk factors for potentially avoidable complications following radical cystectomy. J Urol. 2005;174:1231–7. doi: 10.1097/01.ju.0000173923.35338.99. discussion 1237. [DOI] [PubMed] [Google Scholar]
- 7.De Nunzio C, Cindolo L, Leonardo C, et al. Analysis of radical cystectomy and urinary diversion complications with the Clavien classification system in an Italian real life cohort. Eur J Surg Oncol. 2013;39:792–8. doi: 10.1016/j.ejso.2013.03.008. [DOI] [PubMed] [Google Scholar]
- 8.Roghmann F, Sukumar S, Ravi P, et al. Radical cystectomy in the elderly: National trends and disparities in perioperative outcomes and quality of care. Urol Int. 2014;92:27–34. doi: 10.1159/000353091. . Epub 2013 Sep 19.2013. [DOI] [PubMed] [Google Scholar]
- 9.Bianchi M, Trinh QD, Sun M, et al. Impact of academic affiliation on radical cystectomy outcomes in North America: A population-based study. Can Urol Assoc J. 2012;6:245–50. doi: 10.5489/cuaj.12032. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Kim SP, Boorjian SA, Shah ND, et al. Contemporary trends of in-hospital complications and mortality for radical cystectomy. BJU Int. 2012;110:1163–8. doi: 10.1111/j.1464-410X.2012.10990.x. [DOI] [PubMed] [Google Scholar]
- 11.Jollis JG, Ancukiewicz M, DeLong ER, et al. Discordance of databases designed for claims payment versus clinical information systems. Implications for outcomes research. Ann Intern Med. 1993;119:844–50. doi: 10.7326/0003-4819-119-8-199310150-00011. [DOI] [PubMed] [Google Scholar]
- 12.Lawthers AG, McCarthy EP, Davis RB, et al. Identification of in-hospital complications from claims data. Is it valid? Medical Care. 2000;38:785–95. doi: 10.1097/00005650-200008000-00003. [DOI] [PubMed] [Google Scholar]
- 13.Davenport DL, Holsapple CW, Conigliaro J. Assessing surgical quality using administrative and clinical data sets: A direct comparison of the University HealthSystem Consortium Clinical Database and the National Surgical Quality Improvement Program data set. Am J Med Qual. 2009;24:395–402. doi: 10.1177/1062860609339936. [DOI] [PubMed] [Google Scholar]
- 14.Cima RR, Lackore KA, Nehring SA, et al. How best to measure surgical quality? Comparison of the Agency for Healthcare Research and Quality Patient Safety Indicators (AHRQ-PSI) and the American College of Surgeons National Surgical Quality Improvement Program (ACS-NSQIP) postoperative adverse events at a single institution. Surgery. 2011;150:943–9. doi: 10.1016/j.surg.2011.06.020. [DOI] [PubMed] [Google Scholar]
- 15.Koch CG, Li L, Hixson E, et al. What are the real rates of postoperative complications: Elucidating inconsistencies between administrative and clinical data sources. JAMA. 2012;214:798–805. doi: 10.1016/j.jamcollsurg.2011.12.037. [DOI] [PubMed] [Google Scholar]
- 16.Sundararajan V, Henderson T, Perry C, et al. New ICD-10 version of the Charlson comorbidity index predicted in-hospital mortality. J Clin Epidemiol. 2004;57:1288–94. doi: 10.1016/j.jclinepi.2004.03.012. [DOI] [PubMed] [Google Scholar]
- 17.Charlson ME, Pompei P, Ales KL, et al. A new method of classifying prognostic comorbidity in longitudinal studies: Development and validation. J Chronic Dis. 1987;40:373–83. doi: 10.1016/0021-9681(87)90171-8. [DOI] [PubMed] [Google Scholar]
- 18.Liu JJ, Maxwell BG, Panousis P, et al. Perioperative outcomes for laparoscopic and robotic compared with open prostatectomy using the National Surgical Quality Improvement Program (NSQIP) database. Urology. 2013;82:579–83. doi: 10.1016/j.urology.2013.03.080. [DOI] [PubMed] [Google Scholar]
- 19.Sellers MM, Merkow RP, Halverson A, et al. Validation of new readmission data in the American College of Surgeons National Surgical Quality Improvement Program. J Am Coll Surg. 2013;216:420–7. doi: 10.1016/j.jamcollsurg.2012.11.013. [DOI] [PubMed] [Google Scholar]
- 20.Lawrentschuk N, Colombo R, Hakenberg OW, et al. Prevention and management of complications following radical cystectomy for bladder cancer. Eur Urol. 2010;57:983–1001. doi: 10.1016/j.eururo.2010.02.024. [DOI] [PubMed] [Google Scholar]
- 21.Stewart SB, Freedland SJ. Influence of obesity on the incidence and treatment of genitourinary malignancies. Urol Oncol. 2011;29:476–86. doi: 10.1016/j.urolonc.2009.12.011. [DOI] [PubMed] [Google Scholar]
- 22.Lee CT, Dunn RL, Chen BT, et al. Impact of body mass index on radical cystectomy. J Urol. 2004;172:1281–5. doi: 10.1097/01.ju.0000138785.48347.aa. [DOI] [PubMed] [Google Scholar]
- 23.Mitin T, Hunt D, Shipley WU, et al. Transurethral surgery and twice-daily radiation plus paclitaxel-cisplatin or fluorouracil-cisplatin with selective bladder preservation and adjuvant chemotherapy for patients with muscle invasive bladder cancer (RTOG 0233): A randomised multicentre phase 2 trial. Lancet. 2013;14:863–72. doi: 10.1016/S1470-2045(13)70255-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Bostrom PJ, Kossi J, Laato M, et al. Risk factors for mortality and morbidity related to radical cystectomy. BJU Int. 2009;103:191–6. doi: 10.1111/j.1464-410X.2008.07889.x. [DOI] [PubMed] [Google Scholar]
- 25.Johar RS, Hayn MH, Stegemann AP, et al. Complications after robot-assisted radical cystectomy: Results from the International Robotic Cystectomy Consortium. Eur Urol. 2013;64:52–7. doi: 10.1016/j.eururo.2013.01.010. [DOI] [PubMed] [Google Scholar]
- 26.Clark PE, Agarwal N, Biagioli MC, et al. Bladder cancer. J Natl Compr Canc Netw. 2013;11:446–75. doi: 10.6004/jnccn.2013.0059. [DOI] [PubMed] [Google Scholar]
- 27.Gandaglia G, Popa I, Abdollah F, et al. The effect of neoadjuvant chemotherapy on perioperative outcomes in patients who have bladder cancer treated with radical cystectomy: A population-based study. Eur Urol. 2014;66:561–8. doi: 10.1016/j.eururo.2014.01.014. [DOI] [PubMed] [Google Scholar]
- 28.Lee KL, Freiha F, Presti JC, Jr, et al. Gender differences in radical cystectomy: Complications and blood loss. Urology. 2004;63:1095–9. doi: 10.1016/j.urology.2004.01.029. [DOI] [PubMed] [Google Scholar]
- 29.Trinh VQ, Trinh QD, Tian Z, et al. In-hospital mortality and failure-to-rescue rates after radical cystectomy. BJU Int. 2013;112:E20–7. doi: 10.1111/bju.12214. [DOI] [PubMed] [Google Scholar]
- 30.Sun M, Ravi P, Karakiewicz PI, et al. Is there a relationship between leapfrog volume thresholds and perioperative outcomes after radical cystectomy? Urol Oncol. 2014;32:27, e7–13. doi: 10.1016/j.urolonc.2012.09.012. . Epub 2013 Feb 10. [DOI] [PubMed] [Google Scholar]