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124
Ó. R. Faba et al.

Preoperative Workup

All candidates should be discussed in multidisci­plinary committee with the same work-up for muscle-invasive bladder cancer. This comprises a complete blood test, a CT scan of the abdomen and pelvis with intravenous contrast, and thoracic CT.If there is any suspicious for bone metastasis, then a bone scan should also be indicated. Random bladder biopsies should also be per­formed priory to surgery to exclude multifocal disease and/or CIS. Moreover, a cystoscopy might be part of the preoperative workup to assess the location of the tumor and the bladder capacity.
Special consideration should be taken in the diagnosis and management of urachal tumors as it can be difcult to distinguish between urachal and nonurachal bladder adenocarcinomas. While various criteria have been established to rule-out in this differentiation, a practical approach was reported by Johnson etal. The clinic and patho­logic characteristics required for a diagnosis include an enteric-type adenocarcinoma in the midline of the bladder, location within the blad­der wall, sharp demarcation between tumor and normal urothelium, and exclusion of a primary adenocarcinoma located elsewhere that has spread secondarily to the bladder [6]. Urachal cancers may express detectable serum levels of tumor markers as carcinoembryonic antigen (CEA), cancer antigen (CA) 125, and cancer antigen (CA) 19-9, especially in the setting of locally advanced or peritoneal carcinomatosis [7, 8].

Surgical Technique

The surgical technique for an open PC has been well-described in the literature over the years by different authors [3]. A lower midline incision is made from the pubic symphysis to the level of the umbilicus. PC may be performed either transperi­toneally or extraperitoneally. Dissection pro­gresses down through the fascia, after which the peritoneum and the Retzius space are opened. To
open the surgical eld, the vascular pedicles might be divided on one side. The colon is par­tially mobilized on each side to partially expose the retroperitoneum. The ureters are carefully identied and swept medially. A surgical retrac­tor of the surgeon’s choice is recommended to be placed at this point. The pelvic lymph nodes should be removed from the obturator fossa to the common iliac vessels. After the lymphade­nectomy, the bladder tumor is resected. The blad­der is opened away from the site of the tumor, preferably on the anterior bladder wall. The tumor is identied intravesically and then excised with a 1–2-cm margin. Alternatively, a exible cystoscope can be inserted to identify the loca­tion of the tumor or perform rst step endoscopic approach to delineate endoscopically the location of the tumor. Next, the bladder is closed in two layers and lled to conrm that the closure is watertight. A closed suction drain is placed, and the abdominal incision is closed [9].
Robotic surgery has some advantages over open and laparoscopic surgery. It provides the surgeon with superior optics with three­dimensional visualization of the surgical eld as well as improved dexterity that allows for precise intracorporeal suturing. Furthermore, patients who undergo robot-assisted PC (RAPC) could potentially benet from earlier postoperative recovery, improved postoperative cosmesis, and reduced postoperative pain [10]. But it has been reported the increased risk of cell seeding and implantation in urothelial cell carcinoma [11].
Partial Cystectomy forUrachal Tumors
The open surgical approach for urachal adeno­carcinoma proceeds in much the same way as it does for urothelial carcinoma. However, because the urachus may be involved with the tumor any­where along its course, an “en bloc” resection of the entire urachus as well as umbilicus is required.
There is not much evidence on how to manage urachal tumors in an adult population. When a urachal mass is detected incidence of malignancy
12 Partial Cystectomy
ranges from 51 to 64% [12]. The surgical tech­nique for treating a symptomatic urachal remnant includes excision of the urachus and its tract, including the portion that is attached to the blad­der dome. Open partial cystectomy is the most widely used technique for urachal disease. Robotic partial cystectomy has been described for the management of both pediatric and adult urachal disease with good results [13].
The advantage of complete excision of the urachal tract, including umbilectomy to achieve a negative surgical margin, has been described to be an important oncological aspect. The fail­ure to perform umbilectomy is an independent predictor of increased cancer-specic mortality [14]. In other reports, the authors did not nd umbilectomy to be a statistically signicant fac­tor associated with survival [15] (Figs.12.1 and
12.2).
125
Fig. 12.1 Partial cystectomy for urachal tumor
Fig. 12.2 Partial cystectomy for urachal tumor

Complications

Apart from oncological issues (recurrence, pro­gression), the complication rate of PC ranges from 11–29% [1]. It is important to consider that lower complication and mortality rates have been reported at high-volume centers. Specically, no cases of intrahospital mortality were identied among hospitals performing at least ve PC pro­cedures in a year [5]. Kates etal. [5] analyzed more than 10, 000 patients who underwent PC for BC (2002–2008). PC represented 13.9% of all cystectomies performed. The complications rate was 15.8%, with a mortality rate of 1.8%. Results revealed that patients who died had higher comorbidity status and were signicantly older when compared to patients undergoing rad­ical cystectomy (74.1 vs. 70.4years; P<0.001), and therefore likely represent a population. It is important to consider that a complication rate of
126
Ó. R. Faba et al.
15.8% is markedly decreased when compared to that of radical cystectomy; 67% of radical cystec­tomy patients experienced an in-hospital compli­cation and 13% had Clavien grade 3–5 complications [16].
Common complications of partial cystectomy include bleeding, infection, reduction of bladder capacity, and urinary stula. Less commonly, some patients develop stulas (vesicocutaneous, vesicovaginal, colovesical). Other complications include those that are possible in any major sur­gery: myocardial infarction, pulmonary embolus, congestive heart failure, upper gastrointestinal hemorrhage, and death [3].
The implementation of laparoscopic and robotic surgical approaches to PC represents a signicant advancement and promises to further reduce the length of hospital stay, surgical mor­bidity, and complication rates [17]. Robotic PC results have been reported in small, single-center studies, including a heterogenous patient popula­tion. Global results report a median hospital length of stay of 1 day and an overall 90-day complication rate of 24.1% (all Clavien grades I–II) [1, 18]. Complications of robotic PC for muscle-invasive BC have been explained in detail in a retrospective series of 35 patients. Any grade complications (ileus, pneumonia, and urethral stricture) were reported in 4 patients. After 1year, seven patients presented with recurrence; ve of those patients died of their disease, and the other two died of unrelated causes [10].

Oncological Outcomes

There are not randomized trials comparing radi­cal and partial cystectomy in the contemporary literature. Nevertheless, the retrospective data report that in selected patients who t the prole, PC may be a good alternative.
Capitanio et al. analyzed PC and RC after matching at a ratio of 1:4 for tumor grade, pT stage, pN stage, age, race, and year of surgery. A second matched analysis was performed after adding the number of removed lymph nodes to the matching criteria. In the rst analysis, the overall survival (OS) and cause-specic survival
(CSS) estimates at 5 years were 57.2% and
76.4%, respectively, for PC patients and 50.2% and 65.8%, respectively, for RC patients (P<0.001). In the second analysis, the OS and CSS estimates were 56.0% and 73.5%, respec­tively, for PC patients and 50.9% and 67.5%, respectively, for RC patients (P = 0.03 and P<0.001 for both). When the number of removed lymph nodes was included in the third analysis, the 5-year OS and CSS estimates were 57.2% and 70.3%, respectively, for PC patients and
54.6% and 69.2%, respectively, for RC patients [19].
To assess the role of neoadjuvant chemother­apy in this eld, 60 patients who achieved cT0 after receiving MVAC (methotrexate, vinblas­tine, doxorubicin, and cisplatin) chemotherapy followed by transurethral resection of a bladder tumor (TURBT) were studied. Fifteen of these patients subsequently underwent PC and 17 underwent RC.The 10-year metastasis-free sur­vival (MFS) was 73% for those who underwent PC and 65% for those who underwent RC. Furthermore, 53% of patients in the PC group had intact bladders [20]. Knoedler et al. performed a matched-control analysis to com­pare RC with PC.Patients submitted to PC had a single tumor without CIS. They were matched based on age, gender, pathological stage, and neoadjuvant chemotherapy. The results revealed that patients undergoing PC were less likely to have multifocal bladder tumors on the nal pathology as compared to those undergoing RC (15.1% vs. 32.9%). In all, 38% of patients who underwent PC developed intravesical recurrence. Five percent of PC patients experienced pelvic recurrence. At a mean follow-up of 6.2 years, 81% of patients maintained an intact bladder. Most signicantly, no differences existed between PC and RC with regard to 10-year MFS (61% vs. 66%), CSS (58% vs. 63%), and OS (36% vs. 36%) [21].
Koga etal. developed a much stricter protocol. Patients received as rst step a debulking TURBT with random biopsy and were subsequently con­sidered for PC if they had intravesical circum­scribed tumors 25% of the bladder area and no involvement of the bladder neck or trigone. They
12 Partial Cystectomy
Table 12.1 Oncological outcomes PC
Author N (PC) F-U (months) Outcomes (y; %) Characteristics Capitanio [19] 1573 64 DSS(5y): 76.4
OS(5y):57.2
Herr [20] 15 120 MFS (10y): 73 Neoadj MVAC
Knoedler [21] 86 74 MFS (10y):61
DSS (10y):58 OS (10y);36
Koga [22] 46 45 MFS (10y): 100
DSS(5y):100
Golombos [18] 29 37 RFS (5y): 68
OS (5y): 79
DSS Disease free survival, OS Overall Survival, RFS Recurrence free survival, MFS Metastasis free survival
SEER database T1-4, N0-2, M0; RC vs.PC
RC vs. PC (T0) RC vs.PC
Pior TURBT
Robotic
127
were then submitted to radiotherapy and two cycles of cisplatin, before being restaged 4–6weeks later. To be included as a PC candi­date, the restaged TURBT must show no evi­dence of disease or small residual non-muscle-invasive disease. Of their initial cohort of 183 patients, 65 met the criteria, of which 46 underwent PC. Seven patients devel­oped intravesical recurrence, all of which was supercial. Five-year CSS for this cohort was 100% [22].
One of the largest robotic PC series included 29 patients who underwent robotic PC. With a median follow-up of 37months, the 5-year OS and recurrence-free survival (RFS) rates were 79% and 68%, respectively. Seven patients (24%) had a recurrence, three of which were local and four of which were regional or distant. Two local recurrences were managed with TURBT because there was no muscle invasion. The third local recurrence was muscle-invasive and was thus managed with a cystectomy [18] (Table12.1).

Conclusions

• Approximately 5.8–18.9% of patients with
muscle-invasive bladder cancer are suitable
candidates for partial cystectomy.
• PC is indicated in patients with a normally
functioning bladder with good capacity and a
solitary tumor located where a 1–2-cm resec-
tion margin is possible.
• For high-risk tumors, a multimodal approach with neoadjuvant or adjuvant chemotherapy and possible radiotherapy may be needed.
• Absolute contraindications include carcinoma in situ (CIS) elsewhere in the bladder and mul­tifocal tumors.
• After surgery, ongoing surveillance, including imaging, cystoscopy, and cytology, is impor­tant because the local recurrence rate is high (37–78%).
• Patients who have undergone partial cystec­tomy for bladder cancer should have cystos­copy and urinary cytological examination every 3months for at least 2years. Regular CT scans of the pelvis and abdomen are rec­ommended in the rst several years of follow-up.
• With proper patient selection, long-term, bladder- sparing survival rates with partial cys­tectomy range from 35 to 70%.

References

1. Knoedler J, Frank I.Organ-sparing surgery in urology: partial cystectomy. Curr Opin Urol. 2015;25:111–5.
2. Holzbeierlein JM, Lopez-Corona E, Bochner BH, Herr HW, Donat SM, Russo P, et al. Partial cys­tectomy: a contemporary review of the Memorial Sloan-Kettering Cancer Center experience and recommendations for patient selection. J Urol. 2004;172:878–81.
3. Sweeney P, Kursh ED, Resnick MI. Partial cystec­tomy. Urol Clin North Am. 1992;19:701–11.
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4. Gray PJ, Fedewa SA, Shipley WU, Efstathiou JA, Lin CC, Zietman AL, etal. Use of potentially curative therapies for muscle-invasive bladder cancer in the United States: results from the National Cancer Data Base. Eur Urol. 2013;63:823–9.
5. Kates M, Gorin MA, Deibert CM, Pierorazio PM, Schoenberg MP, McKiernan JM, et al. In-hospital death and hospital-acquired complications among patients undergoing partial cystectomy for blad­der cancer in the United States. Urol Oncol. 2014;32(53):e9–14.
6. Johnson DE, Hodge GB, Abdul-Karim FW, Ayala AG.Urachal carcinoma. Urology. 1985;26:218–21.
7. Kikuno N, Urakami S, Shigeno K, Shiina H, Igawa M.Urachal carcinoma associated with increased car­bohydrate antigen 19-9 and carcinoembryonic anti­gen. J Urol. 2001;166:604.
8. Guarnaccia S, Pais V, Grous J, Spirito N. Adenocarcinoma of the urachus associated with elevated levels of CA 125. J Urol. 1991;145:140–1.
9. Peak TC, Hemal A.Partial cystectomy for muscle­invasive bladder cancer: a review of the literature. Transl Androl Urol. 2020;9:2938–45.
10. Alanee S, El-Zawahry A.Robotic-assisted partial cys­tectomy for muscle invasive bladder cancer: contem­porary experience. Int J Med Robot. 2022;18:e2390.
11. Carrion A, Huguet J, Garcia-Cruz E, Izquierdo L, Mateu L, Musquera M, et al. Intraoperative prog­nostic factors and atypical patterns of recurrence in patients with upper urinary tract urothelial carcinoma treated with laparoscopic radical nephroureterectomy. Scand J Urol. 2016;50:305–12.
12. Ashley RA, Inman BA, Routh JC, Rohlinger AL, Husmann DA, Kramer SA.Urachal anomalies: a lon­gitudinal study of urachal remnants in children and adults. J Urol. 2007;178:1615–8.
13. Kim DK, Lee JW, Park SY, Kim YT, Park HY, Lee TY. Initial experience with robotic-assisted laparo­scopic partial cystectomy in urachal diseases. Korean J Urol. 2010;51:318–22.
14. Ashley RA, Inman BA, Sebo TJ, Leibovich BC, Blute ML, Kwon ED, etal. Urachal carcinoma: clinicopath-
ologic features and long-term outcomes of an aggres­sive malignancy. Cancer. 2006;107:712–20.
15. Siefker-Radtke AO, Gee J, Shen Y, Wen S, Daliani D, Millikan RE, etal. Multimodality management of urachal carcinoma: the M.D. Anderson cancer center experience. J Urol. 2003;169:1295–8.
16. Shabsigh A, Korets R, Vora KC, Brooks CM, Cronin AM, Savage C, etal. Dening early morbidity of radi­cal cystectomy for patients with bladder cancer using a standardized reporting methodology. Eur Urol. 2009;55:164–74.
17. Bailey GC, Frank I, Tollefson MK, Gettman MT, Knoedler JJ.Perioperative outcomes of robot-assisted laparoscopic partial cystectomy. J Robot Surg. 2018;12:223–8.
18. Golombos DM, O’Malley P, Lewicki P, Stone BV, Scherr DS.Robot-assisted partial cystectomy: periop­erative outcomes and early oncological efcacy. BJU Int. 2017;119:128–34.
19. Capitanio U, Isbarn H, Shariat SF, Jeldres C, Zini L, Saad F, etal. Partial cystectomy does not undermine cancer control in appropriately selected patients with urothelial carcinoma of the bladder: a population­based matched analysist. Urology. 2009;74:858–64.
20. Herr HW, Bajorin DF, Scher HI. Neoadjuvant che­motherapy and bladder-sparing surgery for invasive bladder cancer: ten-year outcome. J Clin Oncol. 1998;16:1298–301.
21. Knoedler JJ, Boorjian SA, Kim SP, Weight CJ, Thapa P, Tarrell RF, etal. Does partial cystectomy compro­mise oncologic outcomes for patients with bladder cancer compared to radical cystectomy? A matched case-control analysis. J Urol. 2012;188:1115–9.
22. Koga F, Kihara K, Yoshida S, Yokoyama M, Saito K, Masuda H, et al. Selective bladder-sparing protocol consisting of induction low-dose chemoradiotherapy plus partial cystectomy with pelvic lymph node dis­section against muscle-invasive bladder cancer: onco­logical outcomes of the initial 46 patients. BJU Int. 2012;109:860–6.
Complications ofRadical Cystectomy
KellyR.Pekala andBernardH.Bochner
13

Introduction

Radical cystectomy in women (with hysterec­tomy, bilateral salpingectomy, +/ oophorec­tomy, +/ anterior vaginectomy and urethral excision) and pelvic lymphadenectomy with sub­sequent urinary diversion are the gold-standard operation for women with invasive bladder can­cer [1]. When performed for bladder cancer the average age of women undergoing cystectomy is 68years, with two thirds having a prior history of extensive smoking. Owing to advanced age, mul­tiple comorbidities, and the extent of the proce­dure, complications are common. In a series of 1142 radical cystectomy patients at a large cancer center, in which complications were recorded prospectively, 64% of patients were observed to have a complication of any grade (1–5) at 90-days. Approximately two thirds experienced a complication during the initial hospital admis­sion and 58% following postoperative discharge. Importantly, of these complications, only 13% were of high grade (grades 3–5) with a 30-day mortality rate of 1.5% [2]. These are consistent with more contemporary series, in which the rate of grade 3–5 complications was 14.4% at 30days and 21.7% at 90days [3].
K. R. Pekala · B. H. Bochner (*) Urology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA e-mail: bochnerb@mskcc.org
There is retrospective evidence that women undergoing radical cystectomy may experience more complications than men in patients under­going radical cystectomy for reasons other than bladder cancer. In one analysis of the National Surgical Quality Improvement Program Data­base, after propensity matching, there was an increased risk of readmission, supercial surgical wound infection, and transfusion in women com­pared with men. The addition of organ sparing to radical cystectomy in women did not increase the complication rates [4].
Herein, we review the common complications following radical cystectomy.

Surgical Approach

Historically, the majority of radical cystectomy series encompassed patients undergoing open surgery. The use of robotic cystectomy, with intra- or extracorporeal diversion, is increasing, with a recent analysis of the national cancer data­base revealing that 40.6% of cystectomies were performed robotically in 2015 [5]. There have been several randomized controlled trials (RCTs) comparing robotic with open cystectomy. The MSKCC trial was the initial RCT, with a primary endpoint of 90-day complication rates of open versus robotic techniques. The robotic group underwent robotic extirpative surgery and the diversion was performed as open surgery. Overall
© The Author(s), under exclusive license to Springer Nature Switzerland AG 2025 M. Hoffman et al. (eds.), Major Complications of Female Pelvic Surgery,
https://doi.org/10.1007/978-3-031-66772-5_13
129
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K. R. Pekala and B. H. Bochner
complications of 62% and 66% were observed in the robot-assisted radical cystectomy (RARC) and open radical cystectomy (ORC) patients respectively (p=0.7). Operative time was longer with RARC but resulted in a lower intraoperative blood loss. The RAZOR trial had a primary end­point of 3-year cancer recurrence. Similar to the MSKCC study, it compared open and robotic approaches with extracorporeal diversion and found no difference in rates of overall complica­tions or rates of major grade 3–5 complications. There were higher rates of urinary tract infection (35% vs 26%) and similar rates of postoperative ileus (22% vs 20%) in the robotic group versus the open group [6]. The recently published iROC study, a randomized controlled trial that com­pared robotic cystectomy plus intracorporeal diversion with open radical cystectomy found no differences in overall complications, or high­grade complications. Closer evaluation of spe­cic categories of complications found that wound complications (17.3% vs 5.6%) and thromboembolic events (8.3% vs 1.9%) showed a higher trend in the open surgical groups. Readmission rates of 32% in the open and 22% in the robotic cohort were observed; however, most readmissions were short with a median readmis­sion time of 0days [7].
Table 13.1 Early and overall complications within 90days following radical cystectomy and urinary diver­sion
30-day complications (N=149)
GU 24% GU 28% Infectious 20% Infectious 23% Pulmonary 11% GI 9% Cardiac 10% Cardiac 9% DVT/PE 9% Pulmonary 9%
Reproduced with permission from Ref. [2] GU genitourinary, GI gastrointestinal, DVT deep vein thrombosis, PE pulmonary embolism
Overall complications within 90days (N=199)
leakage (4.3% vs 2.6%) amongst the robotic group [7]. Renal failure occurred in 5–7% of patients in the iROC study [7] and 11–13% in the RAZOR trial [6]. However, these data contradict rates of new renal failure or worsening of CKD, which was noted to be ~3% in an MSKCC pro­spectively recorded database that included over 1100 patients [2]. Renal failure can be managed expectantly postoperatively by assessment for the presence or absence of hydronephrosis and sub­sequent placement of appropriate nephrostomy tubes, with concomitant management of electro­lyte disturbances.

Infection

Complications by Category

The most common complications by category following radical cystectomy include genitouri­nary, infectious, gastrointestinal, cardiac, and pulmonary complications (Table13.1).

Genitourinary

There is an 11% rate of genitourinary (GU) com­plications found in ORC and RARC patients undergoing cystectomy [2, 7]. The most common GU complications are typically urinary diversion related and include ureteral obstruction, renal failure, and urine leaks. The iROC study found that there were higher rates of ureteroenteric anastomotic strictures (2.5% vs 0.6%) and urine
Infectious complications are another major cate­gory of complications and are seen in one quarter to one third of all patients undergoing ORC [2]. Randomized trial data demonstrated rates of infection of 24–38% and 29–33% in the RARC vs ORC cohorts in the iROC and MSKCC studies [7, 8]. Rates of infection types were similar, with the exception of wound infections, seen more fre­quently in the open cohorts of both trials [7, 8]. Common sources of infection are urinary (pyelo­nephritis, urosepsis, urinary tract infections), abdominal uid collections, wound infections, or rarer infections such as pulmonary, bowel leaks, or osteomyelitis of the pubic bone.
Careful assessment and treatment of preop­erative positive urine cultures and administra­tion of antibiotics that cover likely organisms to include skin ora, S. aureus, Gram-negative
13 Complications ofRadical Cystectomy
131
rods, possibly Enterococcus, and anaerobic coverage is recommended by American Uro­logical Association guidelines, depending on the type of planned urinary diversion and use of the small or large bowel [9].

Gastrointestinal

As radical cystectomy is accompanied by a uri­nary diversion using a segment of the gastrointes­tinal tract, gastrointestinal complications are a common postoperative complication. The most common gastrointestinal complications include ileus or small bowel obstruction. Less common gastrointestinal-associated complications include anastomotic bowel leak and gastrointestinal bleeding. In the randomized controlled trials of open versus robotic cystectomy, the MSKCC trial found 23% vs 29% gastrointestinal complications in ORC versus RARC, whereas the iROC study found similar rates of gastrointestinal complica­tions within 90days of 28%, similar rates of ileus of around 10%, and small bowel obstruction of 3% [7]. These ndings are echoed by smaller real world series that report that ileus is the most com­mon reason for readmission within 30days (11%), whereas small bowel obstruction was a common reason for readmissions within 90days (5%). [10]
There have been several efforts to improve on gastrointestinal complications over the years. The enhanced recovery after surgery (ERAS) approach, originally designed for colorectal sur­gery, has been adopted for radical cystectomy and is detailed in another chapter in this textbook. ERAS typically consists of alterations to histori­cal management in the preoperative phase (bowel preparation, preoperative fasting), intraoperative phase (intravenous uid management, alterations to analgesia with minimization of opioids), and postoperative phase (alteration of diet advance­ment and use of nasogastric tubes). There have been three randomized controlled trials of ERAS for cystectomy. Two trials found no difference in 30-day postoperative complications [11, 12], with improved time to bowel function and length of stay group in the ERAS group. One trial found that patients who received alvimopan (Entereg)
had a statistically signicantly faster recovery of bowel function than those who received placebo (5.5days vs 6.8days), shorter length of stay (7.4 vs 10.1 days), and fewer postoperative ileus­related morbidity (8.4% vs 29.1%) [13]. A sys­tematic review and meta-analysis performed a multivariable analysis of individual ERAS fac­tors associated with length of stay and found that omitting the nasogastric tube (8.7days) and the use of local anesthetic blocks (−3.29 days) reduced the duration of hospital stay [14].

Cardiopulmonary

Cardiopulmonary complications such as cardiac arrhythmia, congestive heart failure, hyperten­sion, hypotension, myocardial infarction, atelec­tasis, pleural effusion, pneumothorax, and pneumonia are relatively rare but certainly pos­sible in patients with pre-existing comorbidities. In these cases, postoperative cardiac monitoring should be performed, at least in the initial periop­erative setting, with early evaluation by Cardiology as indicated. Pre- and postoperative use of incentive spirometry and early ambulation can reduce the risk of pulmonary complications.

Bleeding/Thromboembolic

Although bleeding is a common surgical risk for radical cystectomy, prospective series demon­strate average intraoperative blood loss of 500 vs 680cc (MSKCC), 300 vs 700cc (RAZOR), 200 vs 550cc (iROC) for robotic versus open respec­tively [68]. Transfusion rates in large open series of approximately 8% have been reported [2]. Open versus robotic comparisons have consis­tently noted a lower estimated blood loss (EBL) in RARC-treated patients; however, this is not nec­essarily associated with a lower transfusion rate of 12% vs 7% in the iROC study. Still, major bleeding complications (0.6%), wound hemato­mas (0%), and postoperative bleeding (0%) remain rare amongst both the open and robotic cohorts. Other clinical characteristics associated with increased EBL come from real- world data
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K. R. Pekala and B. H. Bochner
using the NSQIP database. Propensity matching and multivariable analysis note that women were twice as likely to require postoperative blood transfusion for anemia (53% vs 38%) [4].
In one, the largest radical cystectomy analysis of complications, there was a 8% risk of thrombo­embolic events, with deep vein thrombosis (5%) and pulmonary embolism (3%) the most common events. This was conrmed by the RAZOR trial, which found a 8% versus 5% thromboembolic event rate (deep vein thrombosis, DVT) in open versus robotic and similar rates of pulmonary embolism (PE; 3%). These data contrast with the iROC study, in which thromboembolic events such as DVT (0.6% vs 0%), PE (7.1% vs 1.9%) were higher in the open cohort [7].
Postoperative thromboembolic prevention is a mainstay for patients undergoing major abdominal and pelvic surgery, with a large Cochrane review that demonstrated a reduction of thromboembolic events from 13.2% to 5.3%, without an associated increase in bleeding complications or mortality [15]. In the cystectomy setting, it typically consists of sequential compression devices, early ambula­tion, pre- and post-operative administration of subcutaneous heparin during the perioperative inpatient hospital stay and discharge with 30days of anticoagulation (commonly subcutaneous enoxaparin), with emerging evidence for the use of oral anticoagulation with apixaban [16].
the MSKCC series and similar rates of delirium of approximately 3% in both the open and robotic cohorts in the iROC study [7]. Efforts to reduce delirium, such as reduced night-time sleep dis­ruptions for unnecessary vital signs, ensuring adequate sunlight during the day, and efforts to reorient patients, are recommended to reduce the risk of hospital-induced delirium. There are also low-risk pharmacological interventions, such as melatonin or ramelteon, that can be used at night, and in a recent systematic review of randomized controlled trials signicantly reduced hospital delirium by 49% in surgical patients [18].

Miscellaneous

Lymphocele
Pelvic lymph node dissection performed for radi­cal cystectomy is associated with a risk of lym­phocele of approximately 3% that has been reported in randomized controlled trials [6]. These can present with lower-extremity swelling, DVT, or abdominal uid collections. Management may consist of needle aspiration or drain place­ment in selected cases, depending on whether or not there are signs of infection or other related symptoms. Extending the pelvic lymphadenec­tomy to the level of the aortic bifurcation can increase the risk of lymphocele formation [19].

Neurological

Cerebrovascular Accident/Stroke
Cerebrovascular accident/stroke are uncommon complications following radical cystectomy (<1%) [2], but are more common in older patients. Octogenarians have a signicantly higher rate of neurological complications than patients aged <80years (10.3% vs 3.9%) [17].
Delirium/Agitation
As radical cystectomy patients have an average age of 68years old and spend several days in the hospital recovering, they are at particular risk of hospital-induced delirium, with disturbed sleep/ wake cycles. There was a 2% rate of delirium in
Unique Complications forWomen
The concept of radical cystectomy for women has evolved over time with uterus-, fallopian tube-, ovary-, and vagina-sparing cystectomy entering the treatment paradigm to maintain the oncologi­cal outcomes while attempting to preserve gyne­cological organs of importance to women for endocrine and sexual function [20]. Patients must be appropriately selected for pelvic organ sparing, taking into consideration bimanual examination, tumor location, gynecological history, and rele­vant cervical cancer screening, menopausal sta­tus, sexual function, and family history (BRCA 1 or 2 mutation or Lynch syndrome) [21].
13 Complications ofRadical Cystectomy
133

Organ-Sparing Cystectomy (Uterus-, Fallopian Tube-, Ovary-Sparing)

The rationale for organ-sparing approaches includes the low incidence of involvement of gynecological organs by direct exten­sion, with a rate of 2.5–7.5%, improved sexual function, reduction in neobladder– vaginal fistula, and improved voiding for the neobladder. [22] Series have demon­strated that in the well-selected patient, there are equivalent oncological outcomes and excellent urinary and sexual functional outcomes [21].

Ovary Removal Risks (Bone Loss, Fracture Risk, Cardiac Events, Cognitive Decline, Mortality)

Bilateral oophorectomy has been based on the risk of bladder cancer presence or recurrence within the ovaries and risk of ovarian primary malignancy. However, ovarian involvement of cancer is rare, with one retrospective study that found 4% ovarian involvement and 2.5% involve­ment of the fallopian tubes with urothelial carci­noma and no primary gynecological malignancies [23]. After excluding patients with advanced dis­ease, women with pT2 had a 0% rate of ovarian involvement.
There have been several large prospective studies that have found that women who undergo bilateral salpingo-oophorectomy as part of a hysterectomy had a 13% increase in overall mortality [24], particularly in women up to the age of 50–65, where the risk of mortality related to oophorectomy was similar to other compet­ing risks [25, 26]. Even in the postmenopausal setting, ovaries continue to secrete hormones, which has a variety of benets, including car­diac, cognitive, bone, sexual, and health [2731]. Gynecologists recognizing the benets of leaving the ovary in situ in younger women, have adopted a practice of prophylactic bilateral salpingectomies as there is evidence that most ovarian cancers originate in the fallopian tubes [32, 33].

Vaginal Complications

There are many possible vaginal complications following removal of the anterior vaginal wall and subsequent closure, including vaginal pro­lapse, stula, dyspareunia, cuff dehiscence, and subsequent bowel evisceration. In a study that evaluated SEER-Medicare, which includes patients 65 and older including 481 women, there was a 20% rate of vaginal complications within 2 years of radical cystectomy. They found that cuff dehiscence was the most common vaginal complication (10.2%), followed by stula (6.9%), prolapse (4.5%), and dyspareunia (2.3%). However, only 26% of these women went on to have an intervention [34]. In a systematic review that reviewed the same topic with an inclusive cohort that included younger patients, a neoblad­der vaginal stula rate of 3–6% at high- volume centers with risk factors for stula such as poor vascularity, overlapping suture lines, prior radia­tion, and tumor recurrence [35]. There are several techniques to counter the potential for neoblad­der vaginal stula including organ preservation of the uterus and omental interposition.

References

1. Brown KG, Solomon MJ, Latif ER, et al. Uro­logical complications after cystectomy as part of pelvic exenteration are higher than that after cys­tectomy for primary bladder malignancy. J Surg Oncol. 2017;115(3):307–11. https://doi.org/10.1002/
jso.24511.
2. Shabsigh A, Korets R, Vora KC, etal. Dening early morbidity of radical cystectomy for patients with bladder cancer using a standardized reporting meth­odology. Eur Urol. 2009;55(1):164–74. https://doi.
org/10.1016/j.eururo.2008.07.031.
3. Knorr JM, Ericson KJ, Zhang JH, etal. Comparison of major complications at 30 and 90 days following radical cystectomy. Urology. 2021;148:192–7. https://
doi.org/10.1016/j.urology.2020.08.038.
4. Bukavina L, Mishra K, Mahran A, et al. Gender disparity in cystectomy postoperative outcomes: propensity score analysis of the National Surgical Quality Improvement Program Database. Eur Urol Oncol. 2021;4(1):84–92. https://doi.org/10.1016/j.
euo.2019.04.004.
5. Elshabrawy A, Wang H, Dursun F, etal. Diffusion of robot-assisted radical cystectomy: Nationwide trends, predictors, and association with continent urinary