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ISRN Vascular Medicine
Volume 2013 (2013), Article ID 546709, 7 pages
Tumour Thrombi in the Suprahepatic Inferior Vena Cava: The Cardiothoracic Surgeons’ View
Division of Surgery, Department of Surgery and Cancer, Imperial College London, London SW7 3SS, UK
Received 9 August 2013; Accepted 27 September 2013
Academic Editors: S. Takebayashi, Y. Watanabe, and Z. Yang
Copyright © 2013 Aristotle D. Protopapas et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Background. Retroperitoneal tumours propagate intrathoracic caval tumour thrombi (ICTT) of which we consider two subgroups: ICTT-III (extracardiac) and ICTT-IV (intracardiac). Methods. Case series review. Results. 29 series with 784 patients, 453 with extracardiac and 331 with intracardiac ICTT. Average age was 59 years. 98% of the tumours were RCC, 1% adrenal and Wilms’ tumours, and 1% transitional cell carcinomas. The prevalent incision was rooftop with or without sternotomy. Mortality was 10% (5% for ICTT-III, 15% for ICTT-IV). Morbidity was 56% (36% for ICTT-III, 64% for ICTT-IV) and reoperation for bleeding was the commonest complication (14%). Mean Blood loss was 2.6 litres for ICTT-III and 3.7 litres for ICTT-IV. Mean blood product use was 2.4 litres for ICTT-III and 3.5 litres for ICTT-IV. Operative and anaesthetic times exceeded 5 hours. Hospital stay averaged 13 days. Variations in perioperative care included preoperative embolisation, perioperative transoesophageal echo, surgical incisions, and extracorporeal circulation. Brief Summary. Surgery for ICTT has high transfusion, operating/anaesthetic time, and in-hospital stay requirements, and intracardiac ICTT also attract higher risk. Preoperative tumour embolisation is controversial. The cardiothoracic team offers proactive optimisation of blood loss and preemptive management of intracardiac thrombus impaction: we should always be involved in the management the ICTT.
Tumour thrombus, as opposed to bland (i.e., blood) thrombus, is a collective term for intravascular metastases with thrombotic elements. Tumour thrombi propagate in the Inferior Vena Cava (IVC) from retroperitoneal primaries such as renal cell carcinoma (RCC). 10% of the 50,000 RCC diagnosed internationally every year  present with IVC thrombosis . Similar caval tumour thrombi are found in less common retroperitoneal primaries such as Wilms’ tumour  and various adrenal, uterine, and bladder tumours. The Levels of tumour thrombi have been defined by Neves and Zincke of Mayo Clinic . Level I, extension into the renal vein; Level II, extension into the infrahepatic IVC; Levels III, IVC, extension to the level of hepatic veins but below the diaphragm; and Levels IV, IVC, extension above the diaphragm and into the right atrium or beyond.This classification (not to be confused with the MAYO scoring system for metastases) has been more or less established in the literature with small minutiae in definitions [5–8].
As a whole, the management from the general and urological points of view has recently been reviewed [6, 7, 9], yet the role of the cardiothoracic team can be further discussed specifically in the 1% that tumour thrombi extend into the intrathoracic (supradiaphragmatic and suprahepatic) IVC .
These intrathoracic caval tumour thrombi (ICTT) pose an even more complex surgical problem .
In search of anatomical boundaries to guide the complex bicoelomic radical resection, we consider hereby two ICTT subgroups mirroring the Levels III and IV of the comprehensive “Neves and Zincke” classification : ICTT-III and ICTT-IV, respectively.
We sought the perioperative evidence on ICTT surgery with curative intent. We reflected on relevant data as we sought to define the role of the cardiothoracic surgeon as a member of the multidisciplinary team.
2. Materials and Methods
Ethical issues were not raised; therefore, ethical approval was not sought. Absence of conflict of interest is declared.
2.1. PubMed Search
For clinical studies with at least 10 patients published between 1965 and March 31, 2011 in English, search keywords “cava*” AND “bypass” AND “nephrectomy” were limited to “human subjects.” Articles were also identified using the function “related articles" in PubMed and cross-validated by hand search so that overlapping cohorts were appropriately merged. We reanalysed pooled data from these studies. The data were thus tabulated (Table 1) in order to formulate our cohortial endpoints.
2.2. Perioperative Considerations
(i)Imaging.(a)Echocardiography: in addition to abdominal ultrasound (standard imaging modality for RCC), nine tenths of the cohort had pre- or perioperative cardiac ultrasound (echo) with an increasing use of transoesophageal modality (TOE or TEE). The benefit from TOE is real-time assessment of potentially mobile tumour thrombi in risk of intracardiac impaction, when preemptive use of extracorporeal perfusion is indicated.(b)Embolisation of the (renal) tumour through angiography/cavography. The embolisation aims primarily to limit vascularity and thence haemorrhage upon surgical dissection and decrease the engorged renal hilum .(ii)Surgical access and incisions . Incisions were abdominal and thoracic. The original approaches were based on midline laparotomy or chevron (roof-top, bilateral Kocher) incisions affording only transdiaphragmatic access to the IVC and right atrium . Later in the series, abdominal incisions were combined with sternotomy or thoracotomy. This involved the cardiothoracic surgeon the preoperative planning.(iii)Cavotomy and reconstruction of the IVC. The perioperative management of the IVC is based on principles influenced by hepatic transplantation : resection with curative intent, avoidance of narrowing the lumen, and control of the tumour thrombus. It is evident that the options are(a)cavotomy and direct closure, where 50% of the lumen can be preserved ;(b)patch closure or resection with interposition graft. Occasionally, the IVC lumen has been surgically obliterated, yet this option is rather dated and not routinely used. IVC Filters are used in circumstances of growth occluding the lumen and history of proximal emboli . Sequential clamping of the IVC  may lead to hypotension, managed (in the absence of CPB) with preemptive Trendelenburg position and liberal volume expansion.(iv)Surgical bleeding and transfusion requirements. Extensive retroperitoneal dissection and cardiovascular sub procedures predispose to considerable bleeding, especially from engorged collateral phrenic veins. The management of intravascular volume is paramount to a favourable outcome (see also the previous paragraph on IVC clamping). It also accounts for the considerable perioperative transfusions .(v)Use of perfusion techniques.(vi)Mortality.(vii)Morbidity.(viii)Length of hospital stay.
3. Results and Analysis (Table 1)
29 series [2, 8, 10–36] with 784 patients from the last four decades offer cumulated perioperative data; 453 cases of ICTT-III and 331 of ICTT-IV were scrutinised. We included follow-up papers with the understanding that although their focus veered away from the perioperative period, their data for surgery were relevant to our review.
Average age at operation was 59 years. 62% of the patients were male. 98% tumours were RCC. The remaining were Wilms’, adrenal, and bladder tumours. 64% of primaries were in the right side, 36% on the left. There were no primary tumours from the anatomical midline. The laterality of tumour is relevant to operative planning as a left sided tumour presents a different pathological anatomy of the thrombus and the necessary intraabdominal dissection.
It is paramount to determine the extent of the IVC growth in order to plan the bicoelomic access and dissection [6, 37]. 29% of patients had had preoperative tumour embolization via cavography as a measure to decrease the tumour burden and, importantly for the surgical team, reduce the expected blood loss by rending the culprit primary lesion and the organ (in 98% cases the kidney) relatively avascular. The contrast cavogram affords also a preoperative assessment of the extension of the thrombus.
3.3. Surgical Access and Incisions
The prevalent access was that of chevron (rooftop) incision with (27%) or without (34%) sternotomy.
37% of the patients were operated through the anatomical midline and 11% just by a median laparotomy.
3% of patients had some form of lateral thoracoabdominal incision. 86% of ICTT-IV had undergone sternotomy in combination with chevron (46%) or midline laparotomy (38%). The two teams operating on intracardiac extensions without opening the chest are also the “champions” of avoiding (albeit in small samples) CPB [10, 16].
The abdominal dissection has often been based on controlling of the porta hepatis (Pringle manoeuvre, with vascular loops under intermittent tension or soft vascular clamps) and the dissection of the liver known as “piggy-back” with minimal dissection of the IVC [10, 38].
3.4. Cavotomy and IVC Reconstruction
12% of patients had resection of IVC and interposition graft. 55% of patients had a partial occlusion clamp on their preserved IVC, and 22% had cross-clamping of the preserved IVC.
There was variability in most setups. Most surgeons retorted to invest in the (presumed expensive) perfusion techniques for ICTT-IV ; 88% of these intracardiac cases were operated with some form of bypass, reflecting the incidence of sternotomy in this subgroup. Moreover, circulatory arrest was used in 60% of ICTT-IV whilst in only 10% of ICTT-III. A small number of patients (5%) had only veno-venous bypass.
Average cardiopulmonary bypass time was 103 minutes (88 minutes for ICTT-III and 106 minutes for ICTT-IV). HCA times averaged 25 minutes (23 in ICTT-III and 26 in ICTT-IV).
3.6. Operating and Anaesthetic Times
The former average was 352 and the latter 362 minutes. The respective times for each subgroup were 339/331 minutes for ICTT-III and 378/396 minutes for ICTT-IV. We comment on these data.
3.7. Blood Loss and Transfusions
The magnitude of the operations can be appreciated by the considerable average blood loss and transfusion volumes: 2.6 L of blood loss and 2.4 L of blood products for ICTT-III and 3.7 L of blood loss and 3.5 L of blood products for ICTT-IV (Table 1).
This was 10% (5% for ICTT-III and 15% for ICTT-IV).
Any-or-none morbidity was 56% (36% for ICTT-III, 64% for ICTT-IV). Most common complications were related either to perioperative bleeding (and reexploration) or thromboembolism (Table 1). Incidence of acute renal failure was 4%.
3.10. Length of Hospital Stay
That was 13 days. This is an important outcome measure that has to be weighed against variation of health policies and balance of tertiary to primary care worldwide.
The authorship of the various series includes primarily noncardiothoracic surgeons . The ample literature is skewed towards the urological/general surgical point of view, and our paper aspires to balance this.
4.1. Choice of Incision and the Cardiothoracic Surgeon
The contrast of opinion on choice of incision is germane to the involvement of the cardiothoracic surgeon in ICTT. Incisions vary between surgeons and relate to the extracardiac or intracardiac level of thrombus [22, 27, 30, 31, 33]. The debate is akin to that of en bloc or trans hiatal oesophagectomies. The abdominal approach has a lot in common with hepatic transplantation . The risk of cardiac impaction of thrombus during such transdiaphragmatic procedures, especially during the manoeuvres of “milking” the IVC retrogradely , has in fact led to earlier involvement of cardiothoracic surgeons; a thoracic incision preempts the need for intracardiac disimpaction of tumour thrombus . It is noted that the two teams reporting no CPB whatsoever have small total numbers and only four patients with ICTT-IV. It was expected that most surgeons would consider perfusion for all the ICTT-IV  and some ICTT-III , especially where preoperative imaging could not exclude intracardiac thrombus. It is evident that assessment of the cranial extent of the thrombus by preoperative imaging can be inaccurate [40–43]. It follows that preemptive involvement of the cardiothoracic specialists, including anaesthetists and perfusionists, is prudent, especially where they are not available on site.
The sternotomy offers the facile option of central cannulation for cardiopulmonary bypass with either of Ross basket, “two-stage,” or bicaval cannulation depending on preference and extend of thrombus. The peripheral (femoral or axillary ) cannulation is of course available when there are concerns for the extent of thrombus around the possible IVC cannulation areas. Preemptive hypothermic circulatory arrest  necessitates sternotomy. CPB can, according to one well-presented school of thought , only be avoided with caution in the presence of a free-floating thrombus.
That is how the risk of intraoperative tumour embolization (that has being reported as cause of death [28, 30]) is managed efficiently. The Sloan-Kettering group had previously pursued a very well described transabdominal technique , possibly because of the limited access to inhouse cardiac surgery, yet they have changed recently.
We note that the HCA times were reasonable and no HCA-attributable incidents were recorded in any of the subjects. Of note also is the potential of HCA to create a “bloodless field” of dissection  and facilitate the intra-atrial manoeuvring of the thrombus in relation to the outflow cannula.
4.2. Blood Conservation
We further note the need of massive transfusions (replacement of body blood volume in 24 hours or half of blood volume in 4 hours). Heparinisation for CPB, even after completing the abdominal dissection , would account for the 26% bleeding morbidity in ICTT-IV, where CPB was used in almost 9 out of 10 patients. On the other hand, the cost and implications could drive a reexpansion of the indications of aprotinin  or utilising tranexamic acid . By the same token, cell saving techniques will be of relevance; some of the shed blood can be returned to the patient through the Intraoperative perfusion circuit or the cell saver apparatus. Procoagulant and blood conservation strategies, including biological and synthetic glues, may reduce the need for transfusion; the patients’ intact immunocompetence is important in the primary diagnosis of malignancy. The presence of an anaesthetic team with experience in cardiovascular anaesthesia is essential .
4.3. Preoperative Embolisation
Stark contrasting on opinions is noted [46–48]. Its strong critics  proffer nonrandomised retrospective data of two groups with 30% difference in presence of ICTT. There is one propensity-matched study in favour of embolisation . This technique also relates inversely to use of preemptive HCA. We note the emerging capabilities of diffusion weighted magnetic resonance, especially in accurate definition of the level and nature of the thrombotic lesions .
4.4. Morbidity and Mortality
Complications are to be expected in more than half of patients. We found that morbidity and mortality varied between lower and higher levels of tumour; intracardial extension rends surgery three times riskier, yet tumour extension has not always been found to affect long-term survival [32, 35, 50]. Acute renal failure and renal support appear as a relatively rare complication, given that 98% of patients had a nephrectomy and three out of ten had their left cancerous kidney removed.
The times recorded indicate long procedures (exceeding 5 hours in average) and also unveiling a weakness in recording operating and anaesthetic times; these appear similar instead of at least 30 minutes difference, affording time for anaesthetic induction and insertion of multiple monitoring lines .
Close multidisciplinary collaboration has led to acceptable operative risks for ICTT. We propose that it is achieved more efficiently in hospitals with on-site cardiothoracic teams. We consider the following advantages of such policy:(i)management of blood loss, with the expertise in preempting and correcting the circulatory events inevitable to such extensive cardiovascular procedures and haemostasis, with experience in all aspects of adjuncts (glues and other technologies ),(ii)risk management of fracture thrombi , with the advantage of preemptive extracorporeal perfusion.A standard of care for ICTT is emerging. The cardiothoracic surgeon is increasingly involved [19, 37] were previously excluded from their management [10, 16, 51]. We believe that preemptive cardiothoracic consultation is instrumental in developing such standard of care. In the United Kingdom, the National Institute for Clinical Excellence has already mandated the preemptive referral to the cardiothoracic team for all ICTT in at least one region (to Wythenshawe Hospital, Manchester, UK). A streamlined procedure plan would be especially advantageous if technical performance was to be scored  in order to convince the stakeholders where the local setup is reluctant to change ; a marginal analysis  would recommend reallocating resources to increase efficiencies.
Retrospective reviews have to be interpreted cautiously; limitations have been previously outlined in a small self-reporting multicentre review of ICTT-IV .
We further note that potential causes of bias are(i)reporting bias(ii)control for comorbidities, which influence mortality and unbalance any attempt to compare interventions,(iii)missing variables, especially in relation with the morbidity,(iv)nonuniform definition of complications between centres , and(v)lack of detailed perioperative patient information for series that focus on followup rather than the surgery itself.
The corresponding author is grateful to Mr. Keith Buchan FRCS, Consultant Cardiothoracic Surgeon, North of Scotland Cardiothoracic Unit, United Kingdom, for valuable input in the clinical and academic minutiae of the operative techniques.
- L. Lipworth, R. E. Tarone, and J. K. McLaughlin, “The epidemiology of renal cell carcinoma,” The Journal of Urology, vol. 176, no. 6, pp. 2353–2358, 2006.
- F. F. Marshall, D. D. Dietrick, W. A. Baumgartner, and B. A. Reitz, “Surgical management of renal cell carcinoma with intracaval neoplastic extension above the hepatic veins,” The Journal of Urology, vol. 139, no. 6, pp. 1166–1172, 1988.
- A. Lall, K. Pritchard-Jones, J. Walker et al., “Wilms' tumor with intracaval thrombus in the UK Children's Cancer Study Group UKW3 trial,” Journal of Pediatric Surgery, vol. 41, no. 2, pp. 382–387, 2006.
- R. J. Neves and H. Zincke, “Surgical treatment of renal cancer with vena cava extension,” British Journal of Urology, vol. 59, no. 5, pp. 390–395, 1987.
- A. Vaidya, G. Ciancio, and M. Soloway, “Surgical techniques for treating a renal neoplasm invading the inferior vena cava,” The Journal of Urology, vol. 169, no. 2, pp. 435–444, 2003.
- F. Pouliot, B. Shuch, J. C. Larochelle, A. Pantuck, and A. S. Belldegrun, “Contemporary management of renal tumors with venous tumor thrombus,” The Journal of Urology, vol. 184, no. 3, pp. 833–841, 2010.
- S. M. Lawindy, T. Kurian, T. Kim et al., “Important surgical considerations in the management of renal cell carcinoma (RCC) with inferior vena cava (IVC) tumour thrombus,” BJU International, vol. 110, no. 7, pp. 926–939, 2012.
- J. C. Nesbitt, E. R. Soltero, C. P. N. Dinney et al., “Surgical management of renal cell carcinoma with inferior vena cava tumor thrombus,” Annals of Thoracic Surgery, vol. 63, no. 6, pp. 1592–1600, 1997.
- C. Wotkowicz, J. A. Libertino, A. Sorcini, and A. Mourtzinos, “Management of renal cell carcinoma with vena cava and atrial thrombus: Minimal access vs median sternotomy with circulatory arrest,” BJU International, vol. 98, no. 2, pp. 289–297, 2006.
- G. Ciancio, A. S. Livingstone, and M. Soloway, “Surgical management of renal cell carcinoma with tumor thrombus in the renal and inferior vena cava: the university of miami experience in using liver transplantation techniques,” European Urology, vol. 51, no. 4, pp. 988–995, 2007.
- A. S. M. Ali, N. Vasdev, S. Shanmuganathan et al., “The surgical management and prognosis of renal cell cancer with IVC tumor thrombus: 15-Years of experience using a multi-specialty approach at a single UK referral center,” Urologic Oncology, 2011.
- M. Al Otaibi, T. A. Youssif, A. Alkhaldi et al., “Renal cell carcinoma with inferior vena caval extention: impact of tumour extent on surgical outcome,” BJU International, vol. 104, no. 10, pp. 1467–1470, 2009.
- M. Ayati, A. Nikfallah, P. Jabalameli, T. V. Najjaran, M. Noroozi, and H. Jamshidian, “Extensive surgical management for renal tumors with inferior vena cava thrombus,” The Journal of Urology, vol. 3, no. 4, pp. 212–215, 2006.
- B. Chiappini, C. Savini, G. Marinelli et al., “Cavoatrial tumor thrombus: single-stage surgical approach with profound hypothermia and circulatory arrest, including a review of the literature,” Journal of Thoracic and Cardiovascular Surgery, vol. 124, no. 4, pp. 684–688, 2002.
- M. Jibiki, T. Iwai, Y. Inoue et al., “Surgical strategy for treating renal cell carcinoma with thrombus extending into the inferior vena cava,” Journal of Vascular Surgery, vol. 39, no. 4, pp. 829–835, 2004.
- M. G. Kaag, C. Toyen, P. Russo et al., “Radical nephrectomy with vena caval thrombectomy: a contemporary experience,” BJU International, vol. 107, no. 9, pp. 1386–1393, 2011.
- M. S. Kalkat, A. Abedin, S. Rooney et al., “Renal tumours with cavo-atrial extension: surgical management and outcome,” Interactive Cardiovascular and Thoracic Surgery, vol. 7, no. 6, pp. 981–985, 2008.
- R. J. Karnes and M. L. Blute, “Surgery insight: management of renal cell carcinoma with associated inferior vena cava thrombus,” Nature Clinical Practice Urology, vol. 5, no. 6, pp. 329–339, 2008.
- J. G. Lubahn, A. I. Sagalowsky, D. H. Rosenbaum et al., “Contemporary techniques and safety of cardiovascular procedures in the surgical management of renal cell carcinoma with tumor thrombus,” Journal of Thoracic and Cardiovascular Surgery, vol. 131, no. 6, pp. 1289–1295, 2006.
- A. C. Novick, M. C. Kaye, D. M. Cosgrove et al., “Experience with cardiopulmonary bypass and deep hypothermic circulatory arrest in the management of retroperitoneal tumors with large vena caval thrombi,” Annals of Surgery, vol. 212, no. 4, pp. 472–477, 1990.
- D. J. Parekh, M. S. Cookson, W. Chapman et al., “Renal cell carcinoma with renal vein and inferior vena caval involvement: clinicopathological features, surgical techniques and outcomes,” The Journal of Urology, vol. 173, no. 6, pp. 1897–1902, 2005.
- J. Parra, S. J. Drouin, V. Hupertan, E. Comperat, M. O. Bitker, and M. Rouprêt, “Oncological outcomes in patients undergoing radical nephrectomy and vena cava thrombectomy for renal cell carcinoma with venous extension: a single-centre experience,” European Journal of Surgical Oncology, vol. 37, no. 5, pp. 422–428, 2011.
- B. Shuch, P. L. Crispen, B. C. Leibovich et al., “Cardiopulmonary bypass and renal cell carcinoma with level IV tumour thrombus: can deep hypothermic circulatory arrest limit perioperative mortality?” BJU International, vol. 107, no. 5, pp. 724–738, 2011.
- S. Yazici, K. Inci, C. Y. Bilen et al., “Renal cell carcinoma with inferior vena cava thrombus: the Hacettepe experience,” Urologic Oncology, vol. 28, no. 6, pp. 603–609, 2010.
- C. Yamashita, T. Azami, M. Okada et al., “Usefulness of cardiopulmonary bypass in reconstruction of inferior vena cava occupied by renal cell carcinoma tumor thrombus,” Angiology, vol. 50, no. 1, pp. 47–53, 1999.
- A. Welz, N. Schmeller, C. Schmitz, B. Reichart, and A. Hofstetter, “Resection of hypernephromas with vena caval or right atrial tumor extension using extracorporeal circulation and deep hypothermic circulatory arrest: a multidisciplinary approach,” European Journal of Cardio-Thoracic Surgery, vol. 12, no. 1, pp. 127–132, 1997.
- G. J. Wang, J. P. Carpenter, R. M. Fairman et al., “Single-center experience of caval thrombectomy in patients with renal cell carcinoma with tumor thrombus extension into the inferior vena cava,” Vascular and Endovascular Surgery, vol. 42, no. 4, pp. 335–340, 2008.
- Y. Tsuji, A. Goto, I. Hara et al., “Renal cell carcinoma with extension of tumor thrombus into the vena cava: surgical strategy and prognosis,” Journal of Vascular Surgery, vol. 33, no. 4, pp. 789–796, 2001.
- J. R. Stewart, J. A. Carey, W. S. McDougal, W. H. Merrill, M. O. Koch, and H. W. Bender Jr., “Cavoatrial tumor thrombectomy using cardiopulmonary bypass without circulatory arrest,” The Annals of Thoracic Surgery, vol. 51, no. 5, pp. 717–722, 1991.
- G. Staehler and D. Brkovic, “The role of radical surgery for renal cell carcinoma with extension into the vena cava,” The Journal of Urology, vol. 163, no. 6, pp. 1671–1675, 2000.
- F. Manassero, A. Mogorovich, G. Di Paola et al., “Renal cell carcinoma with caval involvement: contemporary strategies of surgical treatment,” Urologic Oncology, vol. 29, no. 6, pp. 745–750, 2011.
- T. Klatte, A. J. Pantuck, S. B. Riggs et al., “Prognostic factors for renal cell carcinoma with tumor thrombus extension,” The Journal of Urology, vol. 178, no. 4, pp. 1189–1195, 2007.
- D. C. Vergho, A. Loeser, A. Kocot, M. Spahn, and H. Riedmiller, “Tumor thrombus of inferior vena cava in patients with renal cell carcinoma-clinical and oncological outcome of 50 patients after surgery,” BMC Research Notes, vol. 5, p. 5, 2012.
- P. Sweeney, C. G. Wood, L. L. Pisters et al., “Surgical management of renal cell carcinoma associated with complex inferior vena caval thrombi,” Urologic Oncology, vol. 21, no. 5, pp. 327–333, 2003.
- A. Haferkamp, P. J. Bastian, H. Jakobi et al., “Renal cell carcinoma with tumor thrombus extension into the vena cava: prospective long-term followup,” The Journal of Urology, vol. 177, no. 5, pp. 1703–1708, 2007.
- J. Rigaud, J.-F. Hetet, G. Braud et al., “Surgical care, morbidity, mortality and follow-up after nephrectomy for renal cancer with extension of tumor thrombus into the inferior vena cava: retrospective study since 1990s,” European Urology, vol. 50, no. 2, pp. 302–310, 2006.
- C. Wotkowicz, M. F. Wszolek, and J. A. Libertino, “Resection of renal tumors invading the vena cava,” Urologic Clinics of North America, vol. 35, no. 4, pp. 657–671, 2008.
- D. I. Swierzewski, M. J. Swierzewski, and J. A. Libertino, “Radical nephrectomy in patients with renal cell carcinoma with venous, vena caval, and atrial extension,” The American Journal of Surgery, vol. 168, no. 2, pp. 205–209, 1994.
- B. Shuch, J. C. Larochelle, T. Onyia et al., “Intraoperative thrombus embolization during nephrectomy and tumor thrombectomy: critical analysis of the University of California-Los Angeles experience,” The Journal of Urology, vol. 181, no. 2, pp. 492–499, 2009.
- P. Sharma, R. Kumar, H. Singh et al., “Imaging thrombus in cancer patients with FDG PET-CT,” Japanese Journal of Radiology, vol. 30, no. 2, pp. 95–104, 2012.
- N. Mollard and H. Liu, “Right atrial thrombus from renal cancer,” Journal of Clinical Anesthesia, vol. 22, no. 6, pp. 484–485, 2010.
- H. Takayama, T. Kinouchi, N. Meguro et al., “Renal vein thrombosis misdiagnosed as a renal cell carcinoma with a tumor thrombus in the inferior vena cava,” International Journal of Urology, vol. 5, no. 1, pp. 94–95, 1998.
- P. J. Hallscheidt, C. Fink, A. Haferkamp et al., “Preoperative staging of renal cell carcinoma with inferior vena cava thrombus using multidetector CT and MRI: prospective study with histopathological correlation,” Journal of Computer Assisted Tomography, vol. 29, no. 1, pp. 64–68, 2005.
- D. Pagano, N. J. Howell, N. Freemantle et al., “Bleeding in cardiac surgery: the use of aprotinin does not affect survival,” Journal of Thoracic and Cardiovascular Surgery, vol. 135, no. 3, pp. 495–502, 2008.
- J. Shi, G. Wang, H. Lv et al., “Tranexamic acid in on-pump coronary artery bypass grafting without clopidogrel and aspirin cessation: randomized trial and 1-year follow-up,” The Annals of Thoracic Surgery, vol. 95, no. 3, pp. 795–802, 2013.
- M. J. Schwartz, E. B. Smith, D. W. Trost, and E. D. Vaughan Jr., “Renal artery embolization: clinical indications and experience from over 100 cases,” BJU International, vol. 99, no. 4, pp. 881–886, 2007.
- V. S. Subramanian, A. J. Stephenson, D. A. Goldfarb, A. F. Fergany, A. C. Novick, and V. Krishnamurthi, “Utility of preoperative renal artery embolization for management of renal tumors with inferior vena caval thrombi,” Urology, vol. 74, no. 1, pp. 154–159, 2009.
- H. Zielinski, S. Szmigielski, and Z. Petrovich, “Comparison of preoperative embolization followed by radical nephrectomy with radical nephrectomy alone for renal cell carcinoma,” American Journal of Clinical Oncology, vol. 23, no. 1, pp. 6–12, 2000.
- O. A. Catalano, G. Choy, A. Zhu, P. F. Hahn, and D. V. Sahani, “Differentiation of malignant thrombus from bland thrombus of the portal vein in patients with hepatocellular carcinoma: application of diffusion-weighted MR imaging,” Radiology, vol. 254, no. 1, pp. 154–162, 2010.
- B. Wagner, J.-J. Patard, A. Méjean et al., “Prognostic value of renal vein and inferior vena cava involvement in renal cell carcinoma,” European Urology, vol. 55, no. 2, pp. 452–460, 2009.
- R. Ayyathurai, M. Garcia-Roig, M. A. Gorin et al., “Bland thrombus association with tumour thrombus in renal cell carcinoma: analysis of surgical significance and role of inferior vena caval interruption,” BJU International B, vol. 110, pp. E449–E455, 2012.
- M. Nathan, J. M. Karamichalis, H. Liu, et al., “Surgical technical performance scores are predictors of late mortality and unplanned reinterventions in infants after cardiac surgery,” The Journal of Thoracic and Cardiovascular Surgery, vol. 144, no. 5, pp. 1095.e7–1101.e7, 2012.
- A. Tsourapas and E. Frew, “Evaluating 'success' in programme budgeting and marginal analysis: a literature review,” Journal of Health Services Research and Policy, vol. 16, no. 3, pp. 177–183, 2011.