Clinical Research Open Access
Copyright ©The Author(s) 2003. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Feb 15, 2003; 9(2): 364-367
Published online Feb 15, 2003. doi: 10.3748/wjg.v9.i2.364
Changes in the level of serum liver enzymes after laparoscopic surgery
Min Tan, Feng-Feng Xu, Jun-Shen Peng, Dong-Ming Li, Liu-Hua Chen, Bao-Jun Lv, Zhen-Xian Zhao, Chen Huang, Chao-Xu Zheng, Department of General Surgery, the First Affiliated Hospital of Zhong Shan University, 58 Zhongshan 2 Road Guangzhou 510080, Guangdong Province China
Author contributions: All authors contributed equally to the work.
Correspondence to: Dr Min Tan, Department of General Surgery, the First Affiliated Hospital of Sun Yat-sen University, 58 Zhongshan 2 Road Guangzhou 510080, Guangdong Province China. tommyt@vip.163.com
Telephone: +86-20-87766335 Fax: +86-20-87750632
Received: June 29, 2002
Revised: July 4, 2002
Accepted: July 24, 2002
Published online: February 15, 2003

Abstract

AIM: The purpose of this study was to investigate the effect of laparoscopic surgery on liver function in humans and the possible mechanisms behind such effect.

METHODS: Blood samples from 286 patients who underwent laparoscopic cholecystectomy (LC) and 40 patients who underwent open cholecystectomy (OC) were tested for liver function by measuring the level of serum alanine aminotrasferase (ALT) and aspartate aminotrasferase (AST) before and after the operations. The same tests were also applied to 18 laparoscopic colorectal cancer resection (LCR) patients and 23 open colorectal cancer resection (OCR) patients to determine whether CO2 pneumoperitoneum could alter the serum liver enzymes.

RESULTS: The level of serum ALT and AST increased significantly during the first 48 h post operations in both LC and LCR patients. However, no significant change of the serum liver enzymes was detected in both OC and OCR patients. As a result, there was statistically significant difference in change of both ALT and AST levels between LC and OC patients and LCR and OCR patients, respectively. By the 7th day post operation, the level of both enzymes returned to normal values in LC, OC and OCR patients except LCR patients whose enzymes remained at a higher level.

CONCLUSION: Transient elevation of hepatic transaminases occurred after laparoscopic surgery. The major causative factor seemed to be the CO2 pneumoperitoneum. In most of the laparoscopic surgery patients, the transient elevation of serum liver enzymes showed no apparent clinical implications. However, if preoperative liver function was very poor, laparoscopic surgery may not be the best choice for the treatment of patients with certain abdominal diseases.




INTRODUCTION

The introduction of laparoscopic surgery has profoundly changed the way for the management of patients with both gallbladder disease and common bile duct stone, and the laparoscopic cholecystectomy (LC) has become the “gold standard” in the treatment of benign gallbladder diseases such as gallbladder stone and cholecystitis[1-4]. However, little attention has been paid to effects on liver function by laparoscopic surgery. We noticed in clinical practice that, following laparoscopic surgery, the level of certain serum liver enzymes rose markedly in most patients who had shown normal preoperative liver function tests. This clinical observation raises several questions. Are these changes of any clinical significance? What is the mechanism responsible for these changes? Do other laparoscopic operations cause the same changes? To address these questions, we conducted a prospective study to compare changes in serum liver enzymes before and after operations between LC and open cholecystectomy (OC) and laparoscopic colorectal cancer resection (LCR) with open colorectal resection (OCR).

MATERIALS AND METHODS

A total of 286 patients (102 men and 184 women with mean age of 48.6 years and range of 21-89 years) underwent elective LC from February 2001 to April 2002. During the same period, 40 patients (18 men and 22 women with mean age of 51.2 years and range of 29-86 years) with symptomatic cholelithiasis, gallbladder stone or gallbladder polypus underwent OC and were included for the study. For comparison, 18 LCR (10 men and 8 women with mean age of 62.8 years and range of 43-85 years) and 23 OCR patients (16 men and 7 women with mean age of 61.6 years and range of 39-76 years) were also selected for the study. The LCR cases included 2 descending colon cancers, 7 sigmoid colon cancers and 9 rectal cancers. The OCR patients included 4 ascending colon cancers, 6 transverse colon cancers, 1 descending colon cancers, 6 sigmoid colon cancers and 6 rectal cancers.

All patients selected for the study had normal values of serum liver enzymes prior to the operations. The following patients were excluded from the study: those who had undergone endoscopic retrograde cholangiopancreatography (ERCP) and endoscopic sphincterotomy (EST) within one week before laparoscopic operation. The cases who developed complications such as bile duct injury, obstruction, infection, leakage and high fever by any reason were also excluded. All colorectal cancer patients included for the study had no evidence of cancer metastasis to liver by B-ultrasonic and CT scan.

Serum liver enzymes alanine amino transferase (ALT) and aspartate aminotransferase (AST) were measured before operations and 1, 2 and 7 d post operation to assess liver function except for LC patients. The LC patients were randomly divided into two groups before the operation, with group A of 143 LC patients tested for the liver function postoperatively on days 1 and 7 and group B of 143 patients tested for the liver function postoperatively on days 2 and 7. All LC and LCR patients received operation by one surgeon. The OC operations were performed by 3 surgeons from the same Division. The OCR operations were performed by the same team of surgical staff. All patients received general anesthesia except OC patients who received local anesthesia. The operations on LC and LCR patients were performed with four-cannula technique. During laparoscopic surgery, the intra-abdominal pressure (IAP) was maintained at a range of 12-14 mmHg. Monopolar diathermy was used in LC and OC patients to dissect the gallbladder from the liver beds. Ultrasonic scissors and bipolar diathermy were used in LCR to dissect the mesenteric vessels.

All data were expressed as the mean ± standard deviation. Student t test was used to analyse the difference in level of serum liver enzymes before and after LC, OC, LCR and OCR. The P value less than 0.05 was considered to be statistically significant.

RESULTS

Postoperative liver failure or mortality did not occur in any of the patients studied, and all the patients were hemodynamically stable during the perioperative period.

The level of serum ALT and AST increased significantly within 24-48 h following operations in LC and LCR patients compared with those in OC and OCR patients (Table 1). In details, the mean pre- and post operation serum levels of ALT were respectively 23.3 U·L-1 and 38.8 U·L-1 in LC patients of group A (P < 0.05), 21.5 U·L-1 and 44.2U·L-1 in LC patients of group B (P < 0.01), and 22.6 U·L-1 and 45.7 U·L-1 in LCR patients (P < 0.01). In contrast, ALT only increased from a preoperative mean of 21.8 U·L-1 to 28.2 U·L-1 in OC patients (P > 0.05) and from 22.2 U·L-1 to 30.6 U·L-1 in OCR patients (P > 0.05). The degree of change in ALT following the operations was greater in LC patients than that in OC patients (P < 0.05, D1), P < 0.01, D2), so was the change between LCR and OCR patients (P < 0.05, D1 and D7), P < 0.01, D2).

Table 1 Preoperative and postoperative level of serum liver enzymes.
nPreoperationD1D2D7
ALT
LC (a)14323.3 ± 11.638.8 ± 15.2ac25.1 ± 14.3
LC (b)14321.5 ± 12.944.2 ± 14.5bc26.3 ± 11.7
OC4021.8 ± 16.728.2 ± 13.727.3 ± 18.324.2 ± 11.1
LCR1822.6 ± 10.939.3 ± 13.4ac45.7 ± 17.2bd37.2 ± 18.1ac
OCR2322.2 ± 17.329.6 ± 11.830.6 ± 15.527.1 ± 11.2
AST
LC (a)14328.4 ± 20.241.5 ± 24.7ac29.1 ± 18.7
LC (b)14327.1 ± 18.848.7 ± 20.8bd29.6 ± 15.4
OC4025.2 ± 17.631.8 ± 22.132.6 ± 21.127.9 ± 16.6
LCR1827.3 ± 16.140.7 ± 27.3ac45.5 ± 22.2bc38.6 ± 20.3ac
OCR2326.8 ± 19.530.2 ± 25.132.9 ± 24.628.5 ± 18.6

Similar changes were observed in the mean value of serum AST. The AST increased significantly after operation in LC patients (from 28.4 to 41.5 U·L-1, P < 0.05, D1) and 27.1 up to 48.7 U·L-1, P < 0.01, D2) and LCR patients (from 27.3 to 40.7 U·L-1, P < 0.05, D1) and to 45.5 U·L-1, P < 0.01, D2). In OC and OCR patients, however, the AST showed only a small degree of increase (Table 1). The change of AST due to the operations was also greater in LC patients than that in OC patients (P < 0.05, D1), P < 0.01, D2), and so was the change between LCR and OCR (P < 0.05, D1 and D7), P < 0.01, D2).

Seven days following the operations, both enzymes returned to normal value in LC, OC and OCR patients except in LCR patients whose enzymes, although lower than day 2 level, remained higher (ALT 37.2 U·L-1, D7, P < 0.05) and AST 38.6 U·L-1(D7, P < 0.05) (Table 1).

In this study, we also tested other liver function indice such as total bilirubin (TBIL), direct bilirubin (DBIL), alkaline phosphatase (ALP), lactic dehydrogenase (LDH), total protein (TP) and gamma glutamyl transferase (GGT) (data not shown). In general, TBIL and DBIL showed a slight increase within 24-48 h following operation in some patients, but the changes were within normal range, and these values returned to preoperative levels. Other liver function test indice did not show significant alteration.

DISCUSSION

Changes in serum levels of liver enzymes in LC rather than OC patients had been reported before[5-9]. In order to understand whether or not CO2 pneumoperitoneum could cause these changes, we tested the liver function of patients who received LCR or OCR. Our present studies suggest that these transient postoperative hypertransaminases in LC and LCR patients might be attributed to the following possible factors.

The first factor of consideration was CO2 pneumoperitoneum. Both LC and LCR patients were subject to CO2 pneumoperitoneum during the operations and they showed significant changes in serum liver enzymes after operation. In contrast, both OC and OCR patients were under the operation conditions similar to those of LC and LCR patients except that they were not subject to CO2 pneumoperitoneum and they showed no apparent change in the level of serum liver enzymes. This finding is consistent with other studies that showed similar changes in liver function clearance test after pneumoperitoneum[10-16]. Because an intra-abdominal pressure (IAP) of 12-14 mmHg used in the present laparoscopic surgery was higher than the normal portal blood pressure of 7-10 mmHg, this operation might, therefore, reduce portal blood flow and cause alteration in liver function[17-20]. On the other hand, the elevation and depression of IAP in a short time during laparoscopic operation might be causative as well. During laparoscopic procedure, the sudden alteration of IAP could cause the undulation of portal blood flow. This undulation and “re-irrigation” of organs blood flow may give rise to “ischemia and re-irrigation” damage of tissues and organs, especially the Kupffer and the endothelial cells of the hepatic sinusoids[21]. The mesothelial cells were bulging up and the intercellular clefts thereby increased in size, and the underlying basal lamina became visible[22]. During LC, an IAP of 8 mmHg was found to decrease the hepatic microcirculation significantly[23,24]. Therefore, the elevation of IAP caused by CO2 pneumoperitoneum may be the main reason behind these changes.

A second possible mechanism for alterations of serum liver enzymes after LC is the “squeeze” pressure effect on the liver. The traction of the gallbladder may free these enzymes into the blood stream. But in our study, 40 OC were performed with a small wound within 6 cm. There should be the same or more “squeeze” pressure effect on the liver in these patients, yet the change of serum liver enzymes was different between LC and OC patients. In addition, the same changes occurred in LCR patients. This mechanism remains to be determined in animal models.

The third possibility may be the local effect of prolonged use of diathermy to the liver surface and spread of heat to liver parenchyma. This hypothesis is supported by some other studies[25-31]. However, similar type and intensity of diathermy were used in both OC and LC patients and it remains to be explained why the serum liver enzyme level increased in LCR patients whose focus was far from liver. While the thermal damage to liver by diathermy is generally recognized, there are no references available in the literature that compared the postoperative enzyme levels between cholecystectomies performed with and without the use of diathermy in humans.

In addition, transient liver dysfunction occurs in patients after some general anesthesia[32-41]. This complication is associated with anesthesia-induced changes in splanchnic blood flow and oxygen consumption. However, the anesthesia-induced hepatic hypoperfusion may not be the cause of elevation of transaminases after LC and LCR as the same anesthesia protocols was used in our 23 OCR patients who did not show marked postoperative change in serum liver enzymes. It seems that the anesthesia could not acted exclusively to cause these changes. Other studies have also shown similar liver function test results in both LC and OC cases with general anesthesia[42].

Another possible mechanism of alterations of serum liver enzymes that had been considered was the inadvertent clipping of the right branch of the hepatic artery or any other aberrant arterial branch supplying blood to the liver. When Calot's triangle has dense or cicatricial adhesion, the related arterial branch could be easily injured. This, however, should be followed by a massive increase in liver enzymes and usually has clinical implications[43-45]. Nevertheless, the LCR hardly gave rise to any chance to injure the right branch of the hepatic artery, yet the LCR patients showed marked elevation of ALT and AST postoperatively. Therefore, arterial branch injury could be ruled out in almost LC patients.

In summary, our present studies demonstrated that transient elevation of hepatic transaminases could occur after laparoscopic procedures. These changes might be attributed to hepatocellular dysfunction secondary to one or combination of CO2 pneumoperitoneum, diathermy, extruding liver, branch of the hepatic artery injured and general anesthesia. Based on our findings, the CO2 pneumoperitoneum might be one of the main reasons for the change of serum liver enzymes. However, the transient elevation of hepatic transaminases showed no apparent clinical implication in most patients who received laparoscopic surgery according to follow-up observations and feedback from these patients. Nevertheless, these results indicate that, if the patient's preoperative liver function was very poor, laparoscopic surgery might not be the optimal choice for treating certain abdominal diseases[46].

Footnotes

Edited by Liu HX

References
1.  Cuschieri A. Laparoscopic cholecystectomy. J R Coll Surg Edinb. 1999;44:187-192.  [PubMed]  [DOI]  [Cited in This Article: ]
2.  Himal HS. Minimally invasive (laparoscopic) surgery. Surg Endosc. 2002;16:1647-1652.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 59]  [Cited by in F6Publishing: 63]  [Article Influence: 2.9]  [Reference Citation Analysis (0)]
3.  Suter M, Meyer A. A 10-year experience with the use of laparoscopic cholecystectomy for acute cholecystitis: is it safe. Surg Endosc. 2001;15:1187-1192.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 64]  [Cited by in F6Publishing: 70]  [Article Influence: 3.0]  [Reference Citation Analysis (0)]
4.  Kiely JM, Brannigan AE, Foley E, Cheema S, O'Brien W, Delaney PV. Day case laparoscopic cholecystectomy is feasible. Ir J Med Sci. 2001;170:98-99.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 9]  [Cited by in F6Publishing: 9]  [Article Influence: 0.4]  [Reference Citation Analysis (0)]
5.  Giraudo G, Brachet Contul R, Caccetta M, Morino M. Gasless laparoscopy could avoid alterations in hepatic function. Surg Endosc. 2001;15:741-746.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 34]  [Cited by in F6Publishing: 32]  [Article Influence: 1.4]  [Reference Citation Analysis (0)]
6.  Morino M, Giraudo G, Festa V. Alterations in hepatic function during laparoscopic surgery. An experimental clinical study. Surg Endosc. 1998;12:968-972.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 71]  [Cited by in F6Publishing: 77]  [Article Influence: 3.0]  [Reference Citation Analysis (0)]
7.  Sala-Blanch X, Fontanals J, Martínez-Palli G, Taurá P, Delgado S, Bosch J, Lacy AM, Visa J. Effects of carbon dioxide versus helium pneumoperitoneum on hepatic blood flow. Surg Endosc. 1998;12:1121-1125.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 33]  [Cited by in F6Publishing: 35]  [Article Influence: 1.3]  [Reference Citation Analysis (0)]
8.  Kotake Y, Takeda J, Matsumoto M, Tagawa M, Kikuchi H. Subclinical hepatic dysfunction in laparoscopic cholecystectomy and laparoscopic colectomy. Br J Anaesth. 2001;87:774-777.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 29]  [Cited by in F6Publishing: 31]  [Article Influence: 1.3]  [Reference Citation Analysis (0)]
9.  Andrei VE, Schein M, Margolis M, Rucinski JC, Wise L. Liver enzymes are commonly elevated following laparoscopic cholecystectomy: is elevated intra-abdominal pressure the cause. Dig Surg. 1998;15:256-259.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 43]  [Cited by in F6Publishing: 47]  [Article Influence: 2.0]  [Reference Citation Analysis (0)]
10.  Sato K, Kawamura T, Wakusawa R. Hepatic blood flow and function in elderly patients undergoing laparoscopic cholecystectomy. Anesth Analg. 2000;90:1198-1202.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 59]  [Cited by in F6Publishing: 59]  [Article Influence: 2.5]  [Reference Citation Analysis (1)]
11.  Takagi S. Hepatic and portal vein blood flow during carbon dioxide pneumoperitoneum for laparoscopic hepatectomy. Surg Endosc. 1998;12:427-431.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 91]  [Cited by in F6Publishing: 99]  [Article Influence: 3.8]  [Reference Citation Analysis (0)]
12.  Richter S, Olinger A, Hildebrandt U, Menger MD, Vollmar B. Loss of physiologic hepatic blood flow control (“ hepatic arterial buffer response”) during CO2-pneumoperitoneum in the rat. Anesth Analg. 2001;93:872-877.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 51]  [Cited by in F6Publishing: 55]  [Article Influence: 2.4]  [Reference Citation Analysis (0)]
13.  Perner A, Bugge K, Lyng KM, Schulze S, Kristensen PA, Bendtsen A. Changes in plasma potassium concentration during carbon dioxide pneumoperitoneum. Br J Anaesth. 1999;82:137-139.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 10]  [Cited by in F6Publishing: 10]  [Article Influence: 0.4]  [Reference Citation Analysis (0)]
14.  Tuñón MJ, González P, Jorquera F, Llorente A, Gonzalo-Orden M, González-Gallego J. Liver blood flow changes during laparoscopic surgery in pigs. A study of hepatic indocyanine green removal. Surg Endosc. 1999;13:668-672.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 36]  [Cited by in F6Publishing: 38]  [Article Influence: 1.5]  [Reference Citation Analysis (0)]
15.  Klopfenstein CE, Morel DR, Clergue F, Pastor CM. Effects of abdominal CO2 insufflation and changes of position on hepatic blood flow in anesthetized pigs. Am J Physiol. 1998;275:H900-H905.  [PubMed]  [DOI]  [Cited in This Article: ]
16.  Schäfer M, Sägesser H, Reichen J, Krähenbühl L. Alterations in hemodynamics and hepatic and splanchnic circulation during laparoscopy in rats. Surg Endosc. 2001;15:1197-1201.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 35]  [Cited by in F6Publishing: 40]  [Article Influence: 1.7]  [Reference Citation Analysis (0)]
17.  Schmandra TC, Kim ZG, Gutt CN. Effect of insufflation gas and intraabdominal pressure on portal venous flow during pneumoperitoneum in the rat. Surg Endosc. 2001;15:405-408.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 32]  [Cited by in F6Publishing: 39]  [Article Influence: 1.7]  [Reference Citation Analysis (0)]
18.  Glantzounis GK, Tselepis AD, Tambaki AP, Trikalinos TA, Manataki AD, Galaris DA, Tsimoyiannis EC, Kappas AM. Laparoscopic surgery-induced changes in oxidative stress markers in human plasma. Surg Endosc. 2001;15:1315-1319.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 104]  [Cited by in F6Publishing: 112]  [Article Influence: 4.9]  [Reference Citation Analysis (0)]
19.  Tsugawa K, Hashizume M, Migou S, Tanoue K, Kishihara F, Kawanaka H, Sugimachi K. The effect of carbon dioxide pneumoperitoneum on the portal hemodynamics in a portal-hypertensive rat model. Surg Laparosc Endosc Percutan Tech. 1999;9:338-347.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 6]  [Cited by in F6Publishing: 6]  [Article Influence: 0.3]  [Reference Citation Analysis (0)]
20.  Bendet N, Morozov V, Lavi R, Panski M, Halevy A, Scapa E. Does laparoscopic cholecystectomy influence peri-sinusoidal cell activity. Hepatogastroenterology. 1999;46:1603-1606.  [PubMed]  [DOI]  [Cited in This Article: ]
21.  Volz J, Köster S, Spacek Z, Paweletz N. Characteristic alterations of the peritoneum after carbon dioxide pneumoperitoneum. Surg Endosc. 1999;13:611-614.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 99]  [Cited by in F6Publishing: 106]  [Article Influence: 4.2]  [Reference Citation Analysis (0)]
22.  Gutt CN, Schmandra TC. Portal venous flow during CO (2) pneumoperitoneum in the rat. Surg Endosc. 1999;13:902-905.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 47]  [Cited by in F6Publishing: 57]  [Article Influence: 2.3]  [Reference Citation Analysis (0)]
23.  Jakimowicz J, Stultiëns G, Smulders F. Laparoscopic insufflation of the abdomen reduces portal venous flow. Surg Endosc. 1998;12:129-132.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 204]  [Cited by in F6Publishing: 189]  [Article Influence: 7.3]  [Reference Citation Analysis (0)]
24.  Dessole S, Rubattu G, Capobianco G, Caredda S, Cherchi PL. Utility of bipolar electrocautery scissors for abdominal hysterectomy. Am J Obstet Gynecol. 2000;183:396-399.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 5]  [Cited by in F6Publishing: 6]  [Article Influence: 0.3]  [Reference Citation Analysis (0)]
25.  Raut V, Bhat N, Kinsella J, Toner JG, Sinnathuray AR, Stevenson M. Bipolar scissors versus cold dissection tonsillectomy: A prospective, randomized, multi-unit study. Laryngoscope. 2001;111:2178-2182.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 48]  [Cited by in F6Publishing: 50]  [Article Influence: 2.2]  [Reference Citation Analysis (0)]
26.  Tulikangas PK, Smith T, Falcone T, Boparai N, Walters MD. Gross and histologic characteristics of laparoscopic injuries with four different energy sources. Fertil Steril. 2001;75:806-810.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 54]  [Cited by in F6Publishing: 52]  [Article Influence: 2.3]  [Reference Citation Analysis (0)]
27.  Capelluto E, Champault G. [Variations in intraperitoneal temperature during laparoscopic cholecystectomy]. Ann Chir. 2000;125:259-262.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 9]  [Cited by in F6Publishing: 10]  [Article Influence: 0.4]  [Reference Citation Analysis (0)]
28.  Barrat C, Capelluto E, Champault G. Intraperitoneal thermal variations during laparoscopic surgery. Surg Endosc. 1999;13:136-138.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 12]  [Cited by in F6Publishing: 12]  [Article Influence: 0.5]  [Reference Citation Analysis (0)]
29.  Shamiyeh A, Schrenk P, Tulipan L, Vattay P, Bogner S, Wayand W. A new bipolar feedback-controlled sealing system for closure of the cystic duct and artery. Surg Endosc. 2002;16:812-813.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 30]  [Cited by in F6Publishing: 31]  [Article Influence: 1.4]  [Reference Citation Analysis (0)]
30.  Yang W, Benjamin IS, Sherwood R, Alexander B. Correlation of endothelium-dependent and -independent vasodilatation with liver function tests during prolonged perfusion of the rat liver. J Pharmacol Toxicol Methods. 1998;40:227-234.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 6]  [Cited by in F6Publishing: 6]  [Article Influence: 0.2]  [Reference Citation Analysis (0)]
31.  Berger M, Jünemann K, Schramm H. [Danger of monopolar current in laparoscopic gallbladder surgery]. Zentralbl Chir. 2001;126:591-595.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 6]  [Cited by in F6Publishing: 5]  [Article Influence: 0.2]  [Reference Citation Analysis (0)]
32.  Scapa E, Pinhasov I, Eshchar J. Does general anesthesia affect sinusoidal liver cells as measured by beta-N-acetyl hexosaminidase serum activity level. Hepatogastroenterology. 1998;45:1813-1815.  [PubMed]  [DOI]  [Cited in This Article: ]
33.  Shimamoto A, Tanaka E, Mizuno D, Misawa S. Age- and sex-related changes in toluene metabolism by rat hepatic microsomes in vitro. Res Commun Mol Pathol Pharmacol. 1999;104:265-276.  [PubMed]  [DOI]  [Cited in This Article: ]
34.  Zamparelli M, Eaton S, Quant PA, McEwan A, Spitz L, Pierro A. Analgesic doses of fentanyl impair oxidative metabolism of neonatal hepatocytes. J Pediatr Surg. 1999;34:260-263.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 14]  [Cited by in F6Publishing: 14]  [Article Influence: 0.6]  [Reference Citation Analysis (0)]
35.  Tanaka E, Yamazaki K, Misawa S. Update: the clinical importance of acetaminophen hepatotoxicity in non-alcoholic and alcoholic subjects. J Clin Pharm Ther. 2000;25:325-332.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 28]  [Cited by in F6Publishing: 30]  [Article Influence: 1.3]  [Reference Citation Analysis (0)]
36.  Obata R, Bito H, Ohmura M, Moriwaki G, Ikeuchi Y, Katoh T, Sato S. The effects of prolonged low-flow sevoflurane anesthesia on renal and hepatic function. Anesth Analg. 2000;91:1262-1268.  [PubMed]  [DOI]  [Cited in This Article: ]
37.  Ichinose K, Yanagi F, Higashi K, Kozuma S, Akasaka T. [Recurrent transient increases in liver enzymes specifically after isoflurane anesthesia]. Masui. 1999;48:421-423.  [PubMed]  [DOI]  [Cited in This Article: ]
38.  Nishiyama T, Yokoyama T, Hanaoka K. Liver function after sevoflurane or isoflurane anaesthesia in neurosurgical patients. Can J Anaesth. 1998;45:753-756.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 23]  [Cited by in F6Publishing: 23]  [Article Influence: 0.9]  [Reference Citation Analysis (0)]
39.  McEwen MM, Gleed RD, Ludders JW, Stokol T, Del Piero F, Erb HN. Hepatic effects of halothane and isoflurane anesthesia in goats. J Am Vet Med Assoc. 2000;217:1697-1700.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 20]  [Cited by in F6Publishing: 20]  [Article Influence: 0.8]  [Reference Citation Analysis (0)]
40.  Darling JR, Sharpe PC, Stiby EK, McAteer JA, Archbold GP, Milligan KR. Serum mitochondrial aspartate transaminase activity after isoflurane or halothane anaesthesia. Br J Anaesth. 2000;85:195-198.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 9]  [Cited by in F6Publishing: 9]  [Article Influence: 0.4]  [Reference Citation Analysis (0)]
41.  Feierman DE. The effect of paracetamol (acetaminophen) on fentanyl metabolism in vitro. Acta Anaesthesiol Scand. 2000;44:560-563.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 24]  [Cited by in F6Publishing: 24]  [Article Influence: 1.0]  [Reference Citation Analysis (0)]
42.  Saber AA, Laraja RD, Nalbandian HI, Pablos-Mendez A, Hanna K. Changes in liver function tests after laparoscopic cholecystectomy: not so rare, not always ominous. Am Surg. 2000;66:699-702.  [PubMed]  [DOI]  [Cited in This Article: ]
43.  Kayaalp C, Nessar G, Kaman S, Akoglu M. Right liver necrosis: complication of laparoscopic cholecystectomy. Hepatogastroenterology. 2001;48:1727-1729.  [PubMed]  [DOI]  [Cited in This Article: ]
44.  Balsara KP, Dubash C, Shah CR. Pseudoaneurysm of the hepatic artery along with common bile duct injury following laparoscopic cholecystectomy. A report of two cases. Surg Endosc. 1998;12:276-277.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 35]  [Cited by in F6Publishing: 36]  [Article Influence: 1.4]  [Reference Citation Analysis (0)]
45.  Mathisen O, Søreide O, Bergan A. Laparoscopic cholecystectomy: Bile duct and vascular injuries: management and outcome. Scand J Gastroenterol. 2002;37:476-481.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 41]  [Cited by in F6Publishing: 46]  [Article Influence: 2.1]  [Reference Citation Analysis (0)]
46.  Tsuboi S, Kitano S, Yoshida T, Bandoh T, Ninomiya K, Baatar D. Effects of carbon dioxide pneumoperitoneum on hemodynamics in cirrhotic rats. Surg Endosc. 2002;16:1220-1225.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 11]  [Cited by in F6Publishing: 13]  [Article Influence: 0.6]  [Reference Citation Analysis (0)]