Liver Cancer Open Access
Copyright ©The Author(s) 2003. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Oct 15, 2003; 9(10): 2194-2197
Published online Oct 15, 2003. doi: 10.3748/wjg.v9.i10.2194
Total vascular exclusion technique for resection of hepatocellular carcinoma
Zhen-Yu Yin, Ning Li, Jie-Shou Li, Institute of General Surgery, School of Medicine, Nanjing University, Nanjing 210093, Jiangsu Province, China
Zhen-Yu Yin, Xiao-Ming Wang, Ren-Xiang Yu, Bai-Meng Zhang, Ke-Ke Yu, Department of General Surgery, Zhongshan Hospital, Xiamen 361004, Fujian Province, China
Author contributions: All authors contributed equally to the work.
Correspondence to: Zhen-Yu Yin, Department of General Surgery, Zhongshan Hospital, Xiamen 361004, Fujian Province, China. davidmd@sohu.com
Telephone: +86-592-2292045 Fax: +86-592-2212328
Received: May 13, 2003
Revised: May 25, 2003
Accepted: June 2, 2003
Published online: October 15, 2003

Abstract

AIM: To improve the low resection rate, poor prognosis and to control the massive hemorrhage during operation, total vascular exclusion (TVE) technique was used in hepatectomies of advanced and complicated hepatocellular carcinomas (HCCs).

METHODS: Five hundred and thirty patients with HCCs were admitted in our hospital. They were divided into TVE technique group (group A: n = 78), Pringle maneuver method group (group B: n = 176) and unresectable group (group C: n = 276). The clinical, operative, pathological parameters and outcome of the patients were statistically evaluated.

RESULTS: Group A had a significantly higher resection rate than group B (accounting for 47.92% and 33.21% respectively). There was no significant difference in blood loss, blood transfusion and perioperative mortality between groups A and B. Both groups had the similar median disease free survival time (14.6 vs 16.3 months) and 1 year survival rate (92.9% vs 95.5%). The TVE group had a medial survival time of 40.5 months and its 5-year survival rate was 34.6%.

CONCLUSION: As compared with Pringle maneuver method, the total vascular exclusion is a safe and effective technique to increase the total resection rate of advanced and complicated HCCs.




INTRODUCTION

At present, operations including tumor resection and liver transplantation offer the only chance of cure for the patients with HCCs[1], and hepatectomy remains the normal choice when liver transplantation is not available. HCCs we met were mostly advanced with a low resection rate and had a high risk of lethal blood loss during operation as well as a high mortality after operation especially when the liver was affected by chronic hepatitis or cirrhosis[2-7]. To avoid excessive bleeding and blood transfusion, several methods to limit bleeding have been developed since hepatic portal clamping was successfully performed by Pringle in 1908, which led to the development of total vascular exclusion (TVE) of the liver by Heaney in 1966. Since then, Huguet and his colleagues have better characterized and widely advocated the use of TVE, which can greatly reduce the risk of massive hemorrhage and air embolism[8].

Pringle maneuver method is routinely used in hepatectomy to control blood loss during HCCs operation, TVE is there fore controversial. To the present, no study has documented its safety and efficacy as compared with Pringle maneuver method in resection of HCCs. This study was review our experiences with resection of HCCs by TVE and Pringle maneuver methods.

MATERIALS AND METHODS
Patients

From January 1994 to January 2002, 530 patients with HCCs were admitted in our hospital, they were divided into 3 groups. Group A: 78 patients with complicated HCCs underwent total vascular exclusive hepatectomies. Group B: 176 patients with HCCs underwent Pringle maneuver hepatectomies. Group C: 276 patients with unresectable HCCs underwent conservative treatments such as transhepatic artery embolization.

Diagnosis and vascular exclusion selection

HCCs were diagnosed by examinations such as serum tumor marker α-fetal protein, B-type ultrasound, plain or enhanced spiral computed tomography, magnetic resonance imaging before operation. The diagnosis was confirmed by pathologic examination after operation.

Pringle maneuver method was routinely used in the hepatectomy in our center, and the TVE was only used in advanced and complicated HCC patients such as massive tumors needing major hepatectomy, tumor closing or invading the major blood vessels of liver, tumor in the caudate lobe and multiple tumors.

Perioperative care and treatment

Preoperative care: A venous catheter was introduced one week before operation for routine parenteral nutrition to improve the patient’s liver function, nutritional status and coagulation condition. During perioperative care period, frozen plasma should be infused and blood transfusion must be strictly controlled. Blood loss and ascites production during the operation were balanced by infusing fresh frozen plasma. Intraoperative blood transfusion was given only if the hematocrit value was below 0.30. To prevent bleeding, hemostatic drugs such as fibrinogen and thrombinogen were always intravenously given. The main aim during the first few postoperative days was to restore the liver function and prevent hepatic failure. We used 20% human albumin 100-200 mL/day to maintain the serum protein level. Glucose solution was given for the energy, and short-term antibiotics, histamine blockers were also administered. Appropriate oral intake was restored as soon as possible. The blood discharge from the drain was carefully monitored. When bleeding exceeded 100 mL/h, an emergency laparotomy was performed. The patients were taken care of in an intensive care unit for the first 24 to 48 hrs with their the life signs inspected. Immediate postoperative treatments included hemostasis, prophylaxis antibiotic treatment and total parental nutritional support.

Operative technique

The surgical technique was described previously[2,8]. In general, a bilateral subcostal incision with or without an upward midline extension was used, and intraoperative ultrasound was routinely used to determine location of the tumor, or possible tumor modules in the contralateral lobe and the exact relationship between the tumor and the major liver blood vessels. In group A, all the hepatic ligaments were divided to allow complete mobilization of the liver and exposure of the whole retrohepatic vena cava. TVE was prepared by carefully dissecting the suprahepatic and infrahepatic vena cava, and right adrenal veins and accessory hepatic veins were ligated if necessary to allow complete venous control during clamping. Clamps were always applied in the following sequence: hepatoduodenal ligament, infrahepatic vena cava and suprahepatic vena cava. During transection of the liver, 5 min interval was always allowed in every 15-20 min TVE until the transection was over. After the resection was completed, the clamps were removed in reverse order of their application. Pringle maneuver method was applied in group B at the time of liver transection and consisted of cross-clamping the hepatoduodenal ligament until the liver transection was completed. If the time was more than 20 min, the clamp was released for about 5 min until the operation was completed. Hemostasis of the raw surface of the liver was assured by biological fibrin glue and exact suture. Closed drainage was routinely used before closure of the incision.

Data collection and analysis

All medical records of the patients of the three groups were reviewed retrospectively. Major hepatectomy was defined as resection of two or more liver segments according to Goldsmith and Woodburne, while minor hepatectomy was defined as resection of only one segment[2]. Tumor closing or invading the major liver blood vessels was defined as the distance between them which was less than 1 cm.

The values were expressed as median (range) and cases (percent). The overall survival after hepatic resection was calculated by the Kaplan-Meier method. Statistical evaluations were performed by using unpaired Student t test and chi-spuare analysis, and comparison was made by log rank analysis. Statistical significance was determined by a P value of less than 0.05. Calculations were made with SPSS computer software (Chicago, IL).

RESULTS

As shown in Table 1, the two groups (groups A and B) of patients were similar in terms of age, sex. Both groups had similar high HBV infectious rate. Although the operative time and blood exclusive time were long in TVE group, no significant difference was found in blood loss and blood transfusion between groups A and B. More major hepatectomies and caudate lobe hepatectomies were performed in group A than in group B.

Table 1 General clinical data.
Clinical parametersGroup A (n = 78)Group B (n = 176)
Age (yr)51.72 (36-71)49.66 (14-74)
Male69 (88.64%)147 (83.52%)
HbsAg (+)67 (85.89%)151 (85.79%)
Child-Push grade
Grade A41 (52.54%)a124 (70.45%)
Grade B28 (35.90%)a38 (21.59%)
Grade C9 (11.53%)14 (8.0%)
Total resection rate47.92% (254/530)a33.21% (176/530)
Procedure time (min)268 (150-325)a178 (128-356)
Blood exclusion time (min)25.4 (12-55)a14.2 (8-28)
Blood loss (mL)818 (250-2800)725 (180-2400)
Blood transfusion (mL)690 (0-2400)620 (0-2600)
Total hospital stay time (d)29.4 (12-35)19.8 (10-39)
Re-operation11 (14.10%)16 (9.09%)
Emergency operation5 (6.41%)9 (5.11%)
Local hepatectomy12 (15.38%)a48 (27.28%)
Minor hepatectomy21 (26.92%)a96 (54.55%)
Major hepatectomy45 (57.69%)a32 (18.19%)
Caudate lobe hepatectomy4 (5.13%)a0 (0)

The pathologic data are shown in Table 2. There was a significant difference in the size of tumors between groups A and B. From the data, the rate of tumor closing or invading the major liver blood vessels in group A was higher than that in group B. The patients with HCCs in group A had a higher probability in their advanced stage, about 70% of the patients were TNM stage 3 or 4 in group A, while only about 32% in group B. Although higher cirrhosis rate, multiple tumor possibility, more caudate lobe location and higher risk of tumor rupture were found during operation in group A than in group B, the possibilities of tumor free resection margin in the two groups were similar.

Table 2 Pathologic data.
Clinical parametersGroup A (n = 78)Group B (n = 176)
The mass
Median diameter (cm)11.58 (6.2-24.6)a6.25 (1.8-12.7)
> or = 5 cm72 (92.30%)a118 (67.05%)
> or = 10 cm53 (67.95%)a28 (15.90%)
Close or invade vana cana23 (29.49%)a17 (9.65%)
Close or invade major21 (26.92%)a13 (7.39%)
hepatic vein
Close or invade major bile duct11 (14.10%)a8 (4.55%)
Close or invade major port vein32 (41.03%)a22 (12.5%)
TNM tumor stage
Stage 16 (7.69%)a49 (27.84%)
Stage 212 (15.38%)a71 (40.34%)
Stage 336 (46.15%)a32 (18.19%)
Stage 4a20 (25.64%)a22 (12.5%)
Stage 4b4 (5.13%)a2 (1.14%)
Cirrhosis59 (75.64%)120 (68.18%)
Multiple tumor8 (10.25%)a6 (3.41%)
Caudate lobe tumor4 (5.13%)a0 (0)
Tumor free resection margin74 (94.87%)173 (98.3%)
Tumor rupture during operation11 (14.10%)a13 (7.39%)

Bleeding was most common short-term complication after hepatectomy, but there was no significant difference between the two groups, accounting for 20.5% and 16.48%, respectively. Although the complications in group A including bile leakage, ascites, pleural effusion, jaundice, hepatic failure were significantly higher than those in group B, the reoperation rate within 24 h after operation and perioperative mortality were similar in the two groups. The data are shown in Table 3.

Table 3 Postoperative complications.
Clinical parametersGroup AGroup B
Bleeding16 (20.51%)29 (16.48%)
Bile leakage6 (7.69%)a8 (4.55%)
Infection (including abscess)12 (15.38%)23 (13.68)
Pleural effusion31 (39.74%)a34 (19.32%)
Reoperation within 24 h3 (3.85%)6 (3.40%)
after operation
Ascites16 (20.51%)a20 (11.36%)
Jaundice6 (7.69%)a5 (2.84%)
Hepatic failure6 (7.69%)a5 (2.84%)
Total morbidity40 (51.28%)a45 (25.57%)
Perioperative mortality2 (2.56%)5 (2.84%)

The prognostic data are shown in Table 4. As compared with Pringle maneuver technique, the hepatectomy of TVE might lead to similar median disease-free survival time and short-term survival rate (92.3% vs 95.5% of one year survival rate, P > 0.05). The median survival time and long-term survival rate in group A were significantly lower than those in group B, but obviously higher than those in group C. The results showed that the Pringle maneuver group had a higher incidence of remote metastasis than the other two groups.

Table 4 Outcome after hepatic resection.
Clinical parametersGroup AGroup BGroup C
Median disease-free14.6 (8-25)16.3 (9-37)-
survival (m)
Median survival (m)40.5 (28-52)57.6 (33-84)8.8 (5-31)
Cumulative survival rate
1 year survival92.3%b95.5%b29.9%
3 year survival51.3%ab69.6%b2.9%
5 year survival34.6%ab48.0%b0
Remote metastasis rate16.27%a23.9%b14.8%
DISCUSSION

With the advances in surgical technique, the mortality rate of hepatectomy today is less than 5%[2]. Despite of the satisfactory outcome of hepatectomy for HCC[9], hepatectomy of advanced and complicated HCC remains a major surgical challenge, especially when underlying liver cirrhosis is present[10-12]. HCC is mostly resulted from hepatitis virus infection and liver cirrhosis, and the conventional approach used in hepatcetomy will always lead to excessive bleeding and high risk of perioperative mortality[13,14]. Perioperative transfusion has been found to promote recurrence of HCC and to result in short disease-free and overall survivals[15], the highlight of surgery of advanced and complicated HCC is thus to prevent massive bleeding and blood transfusion in hepatectomies[2]. HCCs we met were always in their terminal stage with a diameter larger than 10 cm. Since the Pringle maneuver method does not prevent hepatic venous bleeding or air embolism, new ways of vascular exclusion has to be devised. The TVE technique has been widely accepted in resection of advanced and complicated HCCs since it was introduced by Heaney in 1966 and modified in clinical practice[3,7,8,16]. In general, the TVE technique is used predominantly for major resections or centrally placed lesions or in cases with blood vessels involved.

TVE technique means the total vascular block of the liver during hepatectomy. Though bleeding is decreased in the operation, the TVE technique will prolong the warm ischemia time of the liver, so we must emphasize its safety. Complications were noted in the total vascular exclusive group, which was regarded to be corresponded to the higher incidence of complex resections[17]. Berney and his colleagues showed that the risk factors for postoperative complications were the duration of surgery and the amount of blood transfused[3]. The frequency of perihepatic infected fluid collections has been reported to be 2% to 20%, biliary fistulas occurrence was up to 8% of patients[18]. Brancatisano showed similar perioperative mortality (2.5%) in radical major hepatic surgery by TVE but with a lower postoperative complication rate (about 46%) than that of ours[19].

At present, it is generally accepted that liver resection performed under intermittent warm ischema is a safe and well-tolerated modality in patients with and without cirrhotic livers[20]. Huguet and others showed that hepatocytes could tolerate normothermic ischemia in excess of 1 hour, and ischemia up to 2 hour without major detrimental effects other than transient hepatic failure has never been reported[21,22]. Others suggested that the risks related to hemorrhage were of greater concern than those related to the time of ischemia. Thus, for advanced and complicated HCC, it is safer to continue vascular exclusion, within 1 h, until complete resection is achieved, rather than take the risk of significant bleeding for the sake of a shorter period of ischemia. A prospective randomized trial showed that the postoperative outcome of patients who underwent liver resection with Pringle maneuver method was better than that of those who underwent operation with other methods[2]. The results of our data showed that although the TVE group had a high hepatic failure rate and complication occurrence than the Pringle maneuver group, but the perioperative mortality was not significantly higher, suggesting that the hepatic failure and complication occurrence might be transient and recoverable.

Another major problem of TVE is the hemodynamic change during TVE. As reported before, hemodynamic tolerance to TVE was excellent in most patients[3], and we also found that the patients could adapt well and quickly to the haemodynamic changes observed after total vascular exclusion. On the bases of the reported complications of spinal cord ischemia, renal failure or aortic injury after routine aortic clamping[23] and the excellent hemodynamic tolerance obtained without aortic occlusion, we applied the modified TVE without aortic exclusion.

Advanced and complicated HCCs were formerly regarded as contraindications of operation for their high mortality and postoperative recurrent rate, the resection rate of advanced and complicated HCCs was extremely low. It was reported that the resection rate of HCCs was 12%-28%[18,24,25]. After the use of TVE technique, the resection rate of HCCs increased remarkably, which was also confirmed in our retrospective analysis.

Untreated patiens with HCCs had a median survival time of 6 months, no 5-year survival has been reported. But the surgical treatment prolonged the median survival to 42 months and the 5-year survival to 32% in some center[26]. Good results could be obtained through an aggressive surgical approach for patients with advanced and complicated HCCs, even for those with tumor thrombi in the portal trunk and vena cava invasion[27]. Comparatively, our perioperative mortality of the patients with advanced and complicated HCCs by TVE was similar to the hepatectomy by Pringle maneuver method and the 5-year survival rate of TVE group after resection was similar to others[28]. The shorter long-term survival rate and median survival time of complicated HCCs by TVE compared with Pringle maneuver group might be resulted from their poorer conditions such as inflammatory activity, hepatic reserve and tumor characteristics, advanced TNM stage, higher possibility of introgenic tumor rupture, higher rate of metachronous and multicentric liver carcinogenesis[29-31]. However, the long-term survival rate and median survival time of the TVE group were remarkably higher than those of the unresectable group. By the way, the remote metastasis rate of the Pringle maneuver group was higher than that of the TVE group and unresectable group, and this result needs to be further studied. In addition, the potentially harmful effect on the metabolic function of hepatocytes should be mentioned in future study.

In summary, hepatectomy by TVE is a safe and effective technique in surgical treatment of advanced and complicated HCC as compared with Pringle maneuver technique. It can increase the resection rate of HCCs, reduce the massive bleeding during operation and increase the survival rate of advanced and complicated HCCs. This series of HCCs demonstrate that an aggressive policy of liver resection by TVE can be adopted as a feasible therapeutic option without excess mortality.

Footnotes

Edited by Wang XL

References
1.  Wakabayashi H, Yachida S, Maeba T, Maeta H. Indications for portal vein embolization combined with major hepatic resection for advanced-stage hepatocellular carcinomas. A preliminary clinical study. Dig Surg. 2000;17:587-594.  [PubMed]  [DOI]  [Cited in This Article: ]
2.  Man K, Fan ST, Ng IO, Lo CM, Liu CL, Wong J. Prospective evaluation of Pringle maneuver in hepatectomy for liver tumors by a randomized study. Ann Surg. 1997;226:704-711; discussion 711-713.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 324]  [Cited by in F6Publishing: 331]  [Article Influence: 12.3]  [Reference Citation Analysis (0)]
3.  Berney T, Mentha G, Morel P. Total vascular exclusion of the liver for the resection of lesions in contact with the vena cava or the hepatic veins. Br J Surg. 1998;85:485-488.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 61]  [Cited by in F6Publishing: 67]  [Article Influence: 2.6]  [Reference Citation Analysis (0)]
4.  Shimada M, Matsumata T, Akazawa K, Kamakura T, Itasaka H, Sugimachi K, Nose Y. Estimation of risk of major complications after hepatic resection. Am J Surg. 1994;167:399-403.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 94]  [Cited by in F6Publishing: 96]  [Article Influence: 3.2]  [Reference Citation Analysis (0)]
5.  Torzilli G, Makuuchi M, Inoue K, Takayama T, Sakamoto Y, Sugawara Y, Kubota K, Zucchi A. No-mortality liver resection for hepatocellular carcinoma in cirrhotic and noncirrhotic patients: is there a way? A prospective analysis of our approach. Arch Surg. 1999;134:984-992.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 344]  [Cited by in F6Publishing: 373]  [Article Influence: 14.9]  [Reference Citation Analysis (0)]
6.  Rui JA, Wang SB, Chen SG, Zhou L. Right trisectionectomy for primary liver cancer. World J Gastroenterol. 2003;9:706-709.  [PubMed]  [DOI]  [Cited in This Article: ]
7.  Qin LX, Tang ZY. The prognostic significance of clinical and pathological features in hepatocellular carcinoma. World J Gastroenterol. 2002;8:193-199.  [PubMed]  [DOI]  [Cited in This Article: ]
8.  Huguet C, Addario-Chieco P, Gavelli A, Arrigo E, Harb J, Clement RR. Technique of hepatic vascular exclusion for extensive liver resection. Am J Surg. 1992;163:602-605.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 112]  [Cited by in F6Publishing: 97]  [Article Influence: 3.0]  [Reference Citation Analysis (0)]
9.  Makuuchi M, Takayama T, Kubota K, Kimura W, Midorikawa Y, Miyagawa S, Kawasaki S. Hepatic resection for hepatocellular carcinoma -- Japanese experience. Hepatogastroenterology. 1998;45 Suppl 3:1267-1274.  [PubMed]  [DOI]  [Cited in This Article: ]
10.  Capussotti L, Polastri R. Operative risks of major hepatic resections. Hepatogastroenterology. 1998;45:184-190.  [PubMed]  [DOI]  [Cited in This Article: ]
11.  Farges O, Malassagne B, Flejou JF, Balzan S, Sauvanet A, Belghiti J. Risk of major liver resection in patients with underlying chronic liver disease: a reappraisal. Ann Surg. 1999;229:210-215.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 212]  [Cited by in F6Publishing: 223]  [Article Influence: 8.9]  [Reference Citation Analysis (0)]
12.  Tang ZY. Hepatocellular carcinoma--cause, treatment and metastasis. World J Gastroenterol. 2001;7:445-454.  [PubMed]  [DOI]  [Cited in This Article: ]
13.  Liu CL, Fan ST, Lo CM, Tung-Ping Poon R, Wong J. Anterior approach for major right hepatic resection for large hepatocellular carcinoma. Ann Surg. 2000;232:25-31.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 153]  [Cited by in F6Publishing: 156]  [Article Influence: 6.5]  [Reference Citation Analysis (0)]
14.  Tjandra JJ, Fan ST, Wong J. Peri-operative mortality in hepatic resection. Aust N Z J Surg. 1991;61:201-206.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 24]  [Cited by in F6Publishing: 28]  [Article Influence: 0.8]  [Reference Citation Analysis (0)]
15.  Hanazaki K, Kajikawa S, Shimozawa N, Shimada K, Hiraguri M, Koide N, Adachi W, Amano J. Hepatic resection for large hepa-tocellular carcinoma. Am J Surg. 2001;181:347-353.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 49]  [Cited by in F6Publishing: 53]  [Article Influence: 2.3]  [Reference Citation Analysis (0)]
16.  Stephen MS, Gallagher PJ, Sheil AG, Sheldon DM, Storey DW. Hepatic resection with vascular isolation and routine supraceliac aortic clamping. Am J Surg. 1996;171:351-355.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 26]  [Cited by in F6Publishing: 26]  [Article Influence: 0.9]  [Reference Citation Analysis (0)]
17.  Buell JF, Koffron A, Yoshida A, Hanaway M, Lo A, Layman R, Cronin DC, Posner MC, Millis JM. Is any method of vascular control superior in hepatic resection of metastatic cancers? Longmire clamping, pringle maneuver, and total vascular isolation. Arch Surg. 2001;136:569-575.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 32]  [Cited by in F6Publishing: 32]  [Article Influence: 1.4]  [Reference Citation Analysis (0)]
18.  Fong Y, Brennan MF, Brown K, Heffernan N, Blumgart LH. Drainage is unnecessary after elective liver resection. Am J Surg. 1996;171:158-162.  [PubMed]  [DOI]  [Cited in This Article: ]
19.  Brancatisano R, Isla A, Habib N. Is radical hepatic surgery safe? Am J Surg. 1998;175:161-163.  [PubMed]  [DOI]  [Cited in This Article: ]
20.  Wu CC, Hwang CR, Liu TJ, P'eng FK. Effects and limitations of prolonged intermittent ischaemia for hepatic resection of the cirrhotic liver. Br J Surg. 1996;83:121-124.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 71]  [Cited by in F6Publishing: 75]  [Article Influence: 2.7]  [Reference Citation Analysis (0)]
21.  Huguet C, Gavelli A, Chieco PA, Bona S, Harb J, Joseph JM, Jobard J, Gramaglia M, Lasserre M. Liver ischemia for hepatic resection: where is the limit? Surgery. 1992;111:251-259.  [PubMed]  [DOI]  [Cited in This Article: ]
22.  Hannoun L, Borie D, Delva E, Jones D, Vaillant JC, Nordlinger B, Parc R. Liver resection with normothermic ischaemia exceeding 1 h. Br J Surg. 1993;80:1161-1165.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 78]  [Cited by in F6Publishing: 82]  [Article Influence: 2.6]  [Reference Citation Analysis (0)]
23.  Emre S, Schwartz ME, Katz E, Miller CM. Liver resection under total vascular isolation. Variations on a theme. Ann Surg. 1993;217:15-19.  [PubMed]  [DOI]  [Cited in This Article: ]
24.  Makuuchi M, Mori T, Gunvén P, Yamazaki S, Hasegawa H. Safety of hemihepatic vascular occlusion during resection of the liver. Surg Gynecol Obstet. 1987;164:155-158.  [PubMed]  [DOI]  [Cited in This Article: ]
25.  Hu RH, Lee PH, Yu SC, Dai HC, Sheu JC, Lai MY, Hsu HC, Chen DS. Surgical resection for recurrent hepatocellular carcinoma: prognosis and analysis of risk factors. Surgery. 1996;120:23-29.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 69]  [Cited by in F6Publishing: 68]  [Article Influence: 2.4]  [Reference Citation Analysis (0)]
26.  Nagorney DM, van Heerden JA, Ilstrup DM, Adson MA. Primary hepatic malignancy: surgical management and determinants of survival. Surgery. 1989;106:740-748; discussion 740-748.  [PubMed]  [DOI]  [Cited in This Article: ]
27.  Madariaga JR, Fung J, Gutierrez J, Bueno J, Iwatsuki S. Liver resection combined with excision of vena cava. J Am Coll Surg. 2000;191:244-250.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 49]  [Cited by in F6Publishing: 51]  [Article Influence: 2.1]  [Reference Citation Analysis (0)]
28.  Buell JF, Rosen S, Yoshida A, Labow D, Limsrichamrern S, Cronin DC, Bruce DS, Wen M, Michelassi F, Millis JM. Hepatic resection: effective treatment for primary and secondary tumors. Surgery. 2000;128:686-693.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 36]  [Cited by in F6Publishing: 38]  [Article Influence: 1.6]  [Reference Citation Analysis (0)]
29.  Takata M, Yamanaka N, Tanaka T, Yamanaka J, Maeda S, Okamoto E, Yasojima H, Uematsu K, Watanabe H, Uragari Y. What patients can survive disease free after complete resection for hepatocellular carcinoma? A multivariate analysis. Jpn J Clin Oncol. 2000;30:75-81.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 19]  [Cited by in F6Publishing: 23]  [Article Influence: 1.0]  [Reference Citation Analysis (0)]
30.  Sakon M, Umeshita K, Nagano H, Eguchi H, Kishimoto S, Miyamoto A, Ohshima S, Dono K, Nakamori S, Gotoh M. Clinical significance of hepatic resection in hepatocellular carcinoma: analysis by disease-free survival curves. Arch Surg. 2000;135:1456-1459.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 104]  [Cited by in F6Publishing: 105]  [Article Influence: 4.4]  [Reference Citation Analysis (0)]
31.  Hanazaki K, Kajikawa S, Shimozawa N, Mihara M, Shimada K, Hiraguri M, Koide N, Adachi W, Amano J. A 15-year retrospective study of hepatic resection for stage IV-A hepatocellular carcinoma shows value in hepatitis B negative patients. Am J Surg. 2002;183:89-94.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 3]  [Cited by in F6Publishing: 3]  [Article Influence: 0.1]  [Reference Citation Analysis (0)]