Decreasing incidence of venous thromboembolic events after radical cystectomy: are we finally improving?
Editorial

Decreasing incidence of venous thromboembolic events after radical cystectomy: are we finally improving?

Benjamin T. Harper1, Christopher J. D. Wallis2, Zachary Klaassen1,3

1Department of Surgery, Division of Urology, Medical College of Georgia at Augusta University, Augusta, GA, USA;2Department of Surgery, Division of Urology, University of Toronto, Toronto, ON, Canada;3Georgia Cancer Center, Augusta University, Augusta, GA, USA

Correspondence to: Zachary Klaassen, MD. Assistant Professor of Surgery/Urology, Division of Urology, Department of Surgery, Medical College of Georgia at Augusta University, 1120 15th Street, BA-8414, Augusta, GA 30912, USA. Email: zklaassen19@gmail.com.

Provenance: This is an invited Editorial commissioned by Section Editor Xiao Li (Department of Urology, Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research & Nanjing Medical University Affiliated Cancer Hospital, Nanjing, China).

Comment on: Lyon TD, Tollefson MK, Shah PH, et al. Temporal trends in venous thromboembolism after radical cystectomy. Urol Oncol 2018;36:361.e15-e21.


Submitted Aug 07, 2018. Accepted for publication Aug 13, 2018.

doi: 10.21037/tau.2018.08.17


Radical cystectomy (RC) is associated with significant postoperative morbidity, including venous thromboembolism (VTE). Current reports suggest that the incidence of symptomatic VTE after RC ranges widely, from 2.6% to 11.6% (1-4), based on patient characteristics and variation between studies. However, current data suggests that this risk is essentially unchanged regardless of surgical approach: the VTE risk for open RC has been estimated in a prior review to be 2.9%, 5.8%, and 11.6% for low, intermediate and high-risk patients, respectively; for robotic RC the corresponding VTE risk was 2.6%, 5.2%, and 10.3% (1). As such, there has been several reports advocating for increased awareness of this potentially modifiable complication and for adherence to guidelines for extended VTE prophylaxis for patients undergoing high-risk abdominal oncologic procedures, such as RC (5).

In a recently published article, Lyon et al. (6) critically assessed a contemporary population-based cohort of RC patients treated between 2011 and 2016, noting for the first time a decreasing incidence of VTE over time. Using data from the American College of Surgeons National Surgical Improvement Program (NSQIP) database, among 8,241 patients who underwent RC, Lyon et al. noted a significant decrease in VTE incidence rates from 5.1% in 2011 to 2.8% in 2016 (Cochran-Armitage test for trend, P=0.001). Furthermore, this trend held when VTE events were sub-stratified into deep vein thromboses (DVT, 3.6–1.9%, P=0.008) and pulmonary embolism (PE, 3.0–1.3%, P=0.005).

Multivariable logistic regression analysis demonstrated that body mass index (BMI) ≥35 kg/m2 (OR 1.64, 95% CI, 1.15–2.35), preoperative congestive heart failure (OR 3.11, 95% CI, 1.37–7.04), increased operative time (OR 1.71, 95% CI, 1.23–2.37), continent urinary diversion (OR 1.47, 95% CI, 1.10–1.97), receipt of a perioperative blood transfusion (OR 1.32, 95% CI, 1.06–1.65), and postoperative infection (OR 1.74, 95% CI, 1.33–2.37) or sepsis (OR 2.37, 95% CI, 1.77–3.16) were associated with an increased likelihood of post-operative VTE. Furthermore, the authors report that nearly half of VTE events occurred following hospital discharge, consistent with prior literature (5). The authors appropriately noted several limitations of the NSQIP database, including poor reporting of neoadjuvant chemotherapy [which increases risk of VTE (5)], preoperative VTE incidence [which may be as high as 14% for subclinical VTE (7)], and receipt of VTE prophylaxis.

These data are notable as, to our knowledge, this is the first population-level analysis to suggest a decreasing incidence of VTE over time for patients undergoing RC. A previous study using the NSQIP database assessing VTE incidence among all thoraco-abdominopelvic oncologic surgeries, including RC, from 1999 to 2009 found increasing rates of VTE over time (8), paralleling other studies over the same time frame that looked at overall VTE rates in the United States (9,10). The discrepancy between these studies and the work of Lyon et al. may be explained, optimistically, as a true change in outcome which simply did not begin occurring until after these prior analyses had ceased inclusion or, less optimistically, as a form of detection bias (with prior increases simply reflecting changing scrutiny for these complications) or ecological fallacy (due to changes in the captured population). As mentioned by Lyon et al. (6), there has been increasing numbers of RC cases included in the NSQIP database (2,065 cases between 2005 and 2012, and 8,241 cases between 2011 and 2016), suggesting improved participation among registered institutions. When comparing older RC VTE studies using NSQIP to the current study, patient demographics and comorbidities appear to be comparable, suggesting that the observed improvement in VTE incidence rates in more recent years (6) may represent true improvement.

While improvement, in any surgical outcome, is to be welcomed, a better understanding of the factors underpinning the changes in VTE incidence offers the opportunity to potentiate such improvements. Unfortunately, due to the limitations in data abstracted in the NSQIP database, it is not possible to assess the utilization or type of VTE prophylaxis patients received. However, there are two protocols for RC patients that may explain a decrease in VTE incidence rates. First, the Enhanced Recovery After Surgery (ERAS) protocol recommends patients undergoing RC to receive VTE chemoprophylaxis for 4 weeks postoperatively, beginning one day preoperatively (11). While there is evidence to suggest that ERAS has utility for decreasing hospital length of stay and associated healthcare costs without increasing morbidity, there is limited evidence suggesting that ERAS protocols decrease VTE rates (12-16). A limitation of ERAS studies is the inconsistent reporting of VTE rates, considering that evaluation of VTE event rates were not these study’s primary or secondary outcome. Clinically, we believe that implementation of ERAS protocols should assist with decreasing VTE incidence rates, considering that extended VTE prophylaxis is included in the protocol, and that a main feature of ERAS is early mobility and return to preoperative function, both of which should contribute to VTE prevention. Since the ERAS protocol became widely accepted during the study period of the Lyon et al. report, conceivably this may at least partially explain a drop in VTE rates. Second, the European Association of Urology (EAU) Guidelines recommend 4 weeks of postoperative VTE prophylaxis for RC patients (17), and similar recommendations are made by the American College of Chest Physicians for high risk postoperative patients, including RC (18). Additionally, there have been several RCTs demonstrating a significant risk reduction in patients who receive extended VTE chemoprophylaxis compared to short term prophylaxis following major oncologic abdominopelvic surgery (19-22).

Despite this level-1 evidence among non-RC patients advocating for extended VTE chemoprophylaxis, as well as guideline recommendations (1) and institutional studies (2) demonstrating benefit, there has been resistance to adopting these clinical measures (5). A 2013 survey of American Urologic Association (AUA) members showed only 67.9% of responders endorsed frequently or always using VTE prophylaxis (of any duration) in their patients undergoing RC (23). In that survey, factors associated with more consistent use of VTE prophylaxis included younger age, self-reported sub-specialization in either oncology or laparoscopic/robotics, and awareness of the AUA Best Practice Statement on VTE prophylaxis. Interestingly, this Best Practice Statement from 2009 does not specifically recommend a time-frame or duration of chemoprophylaxis, but does note that RC is one of the most high-risk routinely performed surgery by urologists and should strongly consider multiple methods of VTE prophylaxis (24).

While it is reassuring for urologic oncologists that rates of VTE following RC appear to be falling, there is much work left to do. The present data do not allow us to assess the role of VTE prophylaxis in these changes and prior work has shown that adherence in quite low. As has been consistently reported, more than half of patients experiencing a VTE event do so after discharge from the hospital. Previous work has further suggested that the cumulative incidence of VTE may continue to rise for months following RC (25). Thus, extended thromboprophylaxis is likely warranted for nearly all patients undergoing RC. Further studies exploring barriers to such care are likely to assist in future declines in the rates of VTE.


Acknowledgements

None.


Footnote

Conflicts of Interest: The authors have no conflicts of interest to declare.


References

  1. Tikkinen KAO, Craigie S, Agarwal A, et al. Procedure-specific Risks of Thrombosis and Bleeding in Urological Cancer Surgery: Systematic Review and Meta-analysis. Eur Urol 2018;73:242-51. [Crossref] [PubMed]
  2. Pariser JJ, Pearce SM, Anderson BB, et al. Extended Duration Enoxaparin Decreases the Rate of Venous Thromboembolic Events after Radical Cystectomy Compared to Inpatient Only Subcutaneous Heparin. J Urol 2017;197:302-7. [Crossref] [PubMed]
  3. Doiron RC, Booth CM, Wei X, et al. Risk factors and timing of venous thromboembolism after radical cystectomy in routine clinical practice: a population-based study. BJU Int 2016;118:714-22. [Crossref] [PubMed]
  4. VanDlac AA, Cowan NG, Chen Y, et al. Timing, incidence and risk factors for venous thromboembolism in patients undergoing radical cystectomy for malignancy: a case for extended duration pharmacological prophylaxis. J Urol 2014;191:943-7. [Crossref] [PubMed]
  5. Klaassen Z, Arora K, Goldberg H, et al. Extended Venous Thromboembolism Prophylaxis after Radical Cystectomy: A Call for Adherence to Current Guidelines. J Urol 2018;199:906-14. [Crossref] [PubMed]
  6. Lyon TD, Tollefson MK, Shah PH, et al. Temporal trends in venous thromboembolism after radical cystectomy. Urol Oncol 2018;36:361.e15-e21. [Crossref] [PubMed]
  7. Schomburg JL, Krishna S, Cotter KJ, et al. Preoperative Incidence of Deep Venous Thrombosis in Patients With Bladder Cancer Undergoing Radical Cystectomy. Urology 2018;116:120-4. [Crossref] [PubMed]
  8. Trinh VQ, Karakiewicz PI, Sammon J, et al. Venous thromboembolism after major cancer surgery: temporal trends and patterns of care. JAMA Surg 2014;149:43-9. [Crossref] [PubMed]
  9. Deitelzweig SB, Johnson BH, Lin J, et al. Prevalence of clinical venous thromboembolism in the USA: current trends and future projections. Am J Hematol 2011;86:217-20. [Crossref] [PubMed]
  10. Stein PD, Matta F, Dalen JE. Is the campaign to prevent VTE in hospitalized patients working? Chest 2011;139:1317-21. [Crossref] [PubMed]
  11. Cerantola Y, Valerio M, Persson B, et al. Guidelines for perioperative care after radical cystectomy for bladder cancer: Enhanced Recovery After Surgery (ERAS((R))) society recommendations. Clin Nutr 2013;32:879-87. [Crossref] [PubMed]
  12. Azhar RA, Bochner B, Catto J, et al. Enhanced Recovery after Urological Surgery: A Contemporary Systematic Review of Outcomes, Key Elements, and Research Needs. Eur Urol 2016;70:176-87. [Crossref] [PubMed]
  13. Pang KH, Groves R, Catto JWF. Reply to Mark C. Kendall's Letter to the Editor re: Karl H. Pang, Ruth Groves, Suresh Venugopal, Aidan P. Noon, James W.F. Catto. Prospective Implementation of Enhanced Recovery After Surgery Protocols to Radical Cystectomy. Eur Urol 2018;74:e66. [Crossref] [PubMed]
  14. Altobelli E, Buscarini M, Gill HS, et al. Readmission Rate and Causes at 90-Day after Radical Cystectomy in Patients on Early Recovery after Surgery Protocol. Bladder Cancer 2017;3:51-6. [Crossref] [PubMed]
  15. Semerjian A, Milbar N, Kates M, et al. Hospital Charges and Length of Stay Following Radical Cystectomy in the Enhanced Recovery After Surgery Era. Urology 2018;111:86-91. [Crossref] [PubMed]
  16. Tyson MD, Chang SS. Enhanced Recovery Pathways Versus Standard Care After Cystectomy: A Meta-analysis of the Effect on Perioperative Outcomes. Eur Urol 2016;70:995-1003. [Crossref] [PubMed]
  17. Tikkinen KAO, Cartwright R, Gould MK. EAU guidelines on thromboprophylaxis. Available online: http://uroweb.org/course/eau-guidelines-on-thromboprophylaxis/
  18. Gould MK, Garcia DA, Wren SM, et al. Prevention of VTE in nonorthopedic surgical patients: Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines. Chest 2012;141:e227S-e77S.
  19. Bergqvist D, Agnelli G, Cohen AT, et al. Duration of prophylaxis against venous thromboembolism with enoxaparin after surgery for cancer. N Engl J Med 2002;346:975-80. [Crossref] [PubMed]
  20. Rasmussen MS, Jorgensen LN, Wille-Jorgensen P, et al. Prolonged prophylaxis with dalteparin to prevent late thromboembolic complications in patients undergoing major abdominal surgery: a multicenter randomized open-label study. J Thromb Haemost 2006;4:2384-90. [Crossref] [PubMed]
  21. Kakkar VV, Balibrea JL, Martinez-Gonzalez J, et al. Extended prophylaxis with bemiparin for the prevention of venous thromboembolism after abdominal or pelvic surgery for cancer: the CANBESURE randomized study. J Thromb Haemost 2010;8:1223-9. [Crossref] [PubMed]
  22. Fagarasanu A, Alotaibi GS, Hrimiuc R, et al. Role of Extended Thromboprophylaxis After Abdominal and Pelvic Surgery in Cancer Patients: A Systematic Review and Meta-Analysis. Ann Surg Oncol 2016;23:1422-30. [Crossref] [PubMed]
  23. Sterious S, Simhan J, Uzzo RG, et al. Familiarity and self-reported compliance with American Urological Association best practice recommendations for use of thromboembolic prophylaxis among American Urological Association members. J Urol 2013;190:992-8. [Crossref] [PubMed]
  24. Forrest JB, Clemens JQ, Finamore P, et al. AUA Best Practice Statement for the prevention of deep vein thrombosis in patients undergoing urologic surgery. J Urol 2009;181:1170-7. [Crossref] [PubMed]
  25. Wallis CJD, Magee D, Satkunasivam R, et al. Long term incidence of venous thromboembolic events following cystectomy: a population-based analysis. J Clin Oncol 2017.35. abstract 288.
Cite this article as: Harper BT, Wallis CJ, Klaassen Z. Decreasing incidence of venous thromboembolic events after radical cystectomy: are we finally improving? Transl Androl Urol 2018;7(Suppl 6):S747-S750. doi: 10.21037/tau.2018.08.17

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