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Serum arterial lactate concentration predicts mortality and organ dysfunction following liver resection

Perioperative Medicine volume 2, Article number: 21 (2013) Cite this article

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Abstract

Background

The aim of this study was to determine if the post-operative serum arterial lactate concentration is associated with mortality, length of hospital stay or complications following hepatic resection.

Methods

Serum lactate concentration was recorded at the end of liver resection in a consecutive series of 488 patients over a seven-year period. Liver function, coagulation and electrolyte tests were performed post-operatively. Renal dysfunction was defined as a creatinine rise of >1.5x the pre-operative value.

Results

The median lactate was 2.8 mmol/L (0.6 to 16 mmol/L) and was elevated (≥2 mmol/L) in 72% of patients. The lactate concentration was associated with peak post-operative bilirubin, prothrombin time, renal dysfunction, length of hospital stay and 90-day mortality (P < 0.001). The 90-day mortality in patients with a post-operative lactate ≥6 mmol/L was 28% compared to 0.7% in those with lactate ≤2 mmol/L. Pre-operative diabetes, number of segments resected, the surgeon’s assessment of liver parenchyma, blood loss and transfusion were independently associated with lactate concentration.

Conclusions

Initial post-operative lactate concentration is a useful predictor of outcome following hepatic resection. Patients with normal post-operative lactate are unlikely to suffer significant hepatic or renal dysfunction and may not require intensive monitoring or critical care.

Background

Despite advances in both operative technique and peri-operative care, liver resection is associated with post-operative mortality rates of 0% to 22% (median 3.7%) [1] and morbidity rates of 12.5% to 66% including liver dysfunction [2, 3], renal dysfunction [4] and bile leak [5, 6]. Factors associated with peri-operative complications and death include patient age [7, 8] and gender [9, 10], hospital annual number of liver resections undertaken [9, 11], pathologic origin of liver tumour [9, 11], pre-operative liver and renal dysfunction [8, 10], diabetes [12, 13], chronic liver disease [7, 9], and the peripheral neutrophil to lymphocyte ratio (NLR) [14]. Operative factors associated with outcome include blood loss [8, 10] and transfusion [15, 16], extent of liver resection [15, 17], duration of surgery [18], simultaneous extrahepatic procedures [15, 19], and the use of the Pringle manoeuvre [16, 20].

Therefore, many factors affect outcome after liver surgery which have not been incorporated into a single scoring system. The American Society of Anesthesiologists (ASA) grade and Portsmouth Physiologic and Operative Severity Score for the enUmeration of Mortality and morbidity (P-POSSUM) scores are used in the risk prediction of many types of surgery [21, 22] including liver surgery [23]. However, these scores may not be applicable to the unique stresses of liver resection. One of the main reported causes of mortality following liver resection is post-hepatectomy liver failure (PHLF) [24]. Although the ‘50-50 criteria’ of serum bilirubin of >50 μmol/L and prothrombin index (laboratory’s calculated mean normal prothrombin time (PT) divided by the patient’s observed PT) of <50% measured on the fifth post-operative day have been shown to be associated with death due to PHLF [2], an earlier prediction system may be clinically more useful in guiding therapy. Furthermore, failure of multiple organ systems may contribute to death following liver resection and there is a need for a global peri-operative measure to predict the risk of developing significant post-operative morbidity and death.

Lactic acid is a by-product of anaerobic metabolism that is subsequently metabolised in the liver during gluconeogenesis [25]. Hyperlactataemia has been shown to be associated with increased mortality and morbidity in a critical care setting [26, 27], in patients with liver failure [28], sepsis [29] and following trauma [30]. Similar relationships have been shown in the post-operative setting following pancreatic resection [31] and other major abdominal surgery [32], cardiac surgery [33] and after hepatic transplantation [34].

The primary aim of this study was to determine if the first post-operative arterial lactate concentration (‘initial lactate’) is associated with adverse outcomes following liver resection including 90-day mortality, length of hospital stay (LOS), and renal and hepatic dysfunction. The secondary aim was to determine which pre- and intra-operative risk factors are associated with initial lactate concentration following liver resection.

Methods

This study was a retrospective analysis of a prospectively maintained database of all patients undergoing liver resection since July 2005. Routine patient characteristics, laboratory data and intra-operative details were retrieved. Pre-operative liver-directed chemotherapy was administered to selected patients following discussion at a regional multidisciplinary team meeting. A period of recovery of at least six weeks was allowed following cessation of chemotherapy before undertaking surgery. The P-POSSUM scoring system was used to calculate the physiological score [21]. Prior to resection, the operating surgeon makes a visual assessment of the condition of the liver parenchyma and records this as normal or abnormal. Liver resections were performed using standard techniques with a Cavitron Ultrasonic Surgical Aspirator™ (CUSA; Tyco Healthcare, Mansfield, MA, USA) dissector. Hepatic inflow occlusion was used in a minority of cases where there was excessive blood loss. Anaesthetic techniques include the routine use of invasive arterial blood pressure monitoring, central venous pressure monitoring (CVP) (using a target CVP of <5 cm H20) and epidural anaesthesia. Liver resections were defined according to the Brisbane classification [35] and the number of removed segments recorded. Intravenous fluid replacement was minimised during the resection phase to decrease venous pressure. After removal of the surgical specimen, a pause in surgical activity is routinely planned to allow haemostasis and intravenous volume replacement with 0.9% saline or Hartmann’s solution at the anaesthetist’s discretion. Patients are usually returned to the High Dependency Unit (HDU) after surgery with full invasive monitoring, except for minor resections in fit patients who are returned to the general ward.

The serum lactate was recorded from an arterial blood sample taken immediately prior to abdominal closure or immediately on arrival in the HDU. The arterial lactate in the normal population is below 1.6 mmol/L whereas in a critical care setting <2 mmol/L is more commonly accepted in acutely stressed patients [36].

Serum biochemistry tests and coagulation assays were performed on all patients in the first 24 hours post-operatively and the tests repeated according to clinical course. The peak measurement of bilirubin and PT were recorded and used for analysis. A PT index of <50% corresponds to a PT >24 s. Similarly peak post-operative creatinine levels were obtained and renal dysfunction was defined according to the Risk, Injury, Failure, Loss, and End-stage kidney disease (RIFLE) criteria [37]. Renal dysfunction in categorical analyses was defined as any increase in serum creatinine of ≥1.5-fold from the pre-operative baseline. The length of hospital stay was measured from day of surgery to day of discharge and was expressed as a natural logarithm. Ninety-day mortality was recorded.

The association between initial serum lactate concentration and continuous outcomes was investigated using a multiple linear regression model as well as Spearman’s rank correlation. To overcome increasing variance with the mean a natural log transformation was used. Binary variables were investigated using univariate regression. Potential associations between initial lactate concentration and pre- and intra-operative factors were tested using univariate regression or chi-square test at the level of P < 0.25 [38], as appropriate. Significant variables in the univariate analysis were included in the multivariate regression model and were considered to be significant if P < 0.05. All analyses were carried out using the statistical package R 2.1.14 [39].

Confirmation was obtained from the South West Health Research Authority that under the harmonised Guidance Approval for Research Ethics Committees (REC), REC review was not required because patient data was collected in the course of their normal hospital care and was anonymised for research purposes. No patient consent was required for this study.

Results

In the study period 501 patients underwent liver resection for whom an initial lactate measurement was available in 488. The indications for surgery, pre-operative and operative details are shown in Table 1. Results of blood tests are shown in Table 2 and the main post-operative outcome measures are summarised in Table 3. The median number of biochemistry tests performed per patient in the first five post-operative days was 4 (0 to 6) and coagulation assays was 3 (0 to 6). It was not necessary to administer clotting factors to any surviving patients between postoperative days 1 to 5. Peak abnormalities in PT and bilirubin usually occurred early in the post-operative course and tended to improve over five days (Table 2). Post-operatively, 118 patients (24.1%) had a serum bilirubin ≥50 μmol/L. Minor abnormalities in PT were commonly noted, though only 15 patients (3.1%) developed a PT >24 s. Although a small number of patients remained jaundiced at the time of discharge, only one patient fulfilled the ‘50-50 criteria’ at day five. The median length of hospital stay was seven days (range 2 to 78) with 90% of patients having a LOS between two and 15 days. Twelve patients (2.5%) died within 30 days of surgery and 23 died within 90 days of surgery (4.7%). The most common cause of death was liver failure, which occurred in 11 of 23 patients. Four patients died from ongoing malignancy (of whom three had undergone non-curative resections) and two patients died from sepsis without evidence of liver failure. The remaining deaths were attributed to pulmonary embolus, heart failure, anastomotic leak following colonic resection, bleeding peptic ulcer, strangulated hernia and peritonitis.

Table 1 Pre-operative and intra-operative characteristics of 488 patients undergoing liver resection
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Table 2 Post-operative blood tests for 488 patients undergoing liver resection
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Table 3 Post-operative outcomes for 488 patients undergoing liver resection
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The median initial lactate concentration was 2.8 mmol/L (inter-quartile range = 1.9 to 3.9) and 350 patients (72%) had an elevated serum lactate concentration (≥2 mmol/L) (Figure 1). There was no difference in the lactate concentration taken prior to abdominal closure (n = 380, median 2.8 mmol/L, range 0.6 to 16.0) or immediately on arrival in the HDU (n = 108, median 2.8 mmol/L, range 0.6 to 14.0). The initial lactate concentration was noted to be associated with all recorded outcome measures (Table 4). Although major abnormalities of serum bilirubin and PT were rare in our series there was a weak correlation with initial lactate for both bilirubin (coefficient 0.41, P < 0.001) and PT (coefficient 0.37, P < 0.001), which was stronger for bilirubin. Similarly, there was a weak correlation with length of hospital stay (coefficient 0.28, P < 0.001). Of note the values for length of hospital stay include only survivors, and therefore exclude some patients who are likely to have high post-operative lactate levels. Renal dysfunction after liver resection was rare in this series (7.0%) but there was a correlation with lactate concentration (Table 4). Three of 137 patients (2.2%) with an initial lactate concentration less than 2 mmol/L who had creatinine measured developed renal dysfunction (negative predictive value (NPV) = 0.98) compared to 8 of 29 (27.5%) patients with an initial lactate greater than 6 mmol/L (positive predictive value (PPV) = 0.28) (P = < 0.001) (Figure 2). In 322 patients with a lactate concentration ≥2 and <6 mmol/L 23 developed renal dysfunction (7.1%).

Figure 1
figure1

Distribution of arterial lactate concentration in 488 patients at the end of liver resection.

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Table 4 Univariate analysis of the association between lactate and postoperative outcomes for 488 patients undergoing liver resection
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Figure 2
figure2

Probability of renal dysfunction after liver resection according to lactate concentration in 484 patients.

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Similarly, there was a correlation between mortality in the 90-day period following liver resection and initial lactate concentration (Table 4). One of 138 patients (0.7%) with an initial lactate concentration <2 mmol/L died within this period, due to an anastomotic leak following colonic resection (NPV = 0.99), compared to eight of 29 patients with initial lactate ≥6 mmol/L (PPV = 0.28) (P = < 0.001) (Figure 3). The deaths in patients with lactate ≥6 mmol/L were due to liver failure in four patients, sepsis without liver failure in two patients, cardiac failure in one patient and ongoing malignancy in the other. Of the remaining 322 patients with lactate concentration ≥2 and <6 mmol/L there were 14 deaths within 90 days of surgery (4.3%).

Figure 3
figure3

Probability of 90-day mortality after liver resection according to lactate concentration in 488 patients.

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Comparison of patients with initial lactate concentrations <2 mmol/L and ≥6 mmol/L revealed there were significantly more major resections performed (P < 0.001) and more patients with pre-operative diabetes (P < 0.001) in patients with a lactate concentration ≥6 mmol/L (Table 5). There was no significant difference in the use of pre-operative chemotherapy between these two groups (P = 0.351). The proportion of patients with both renal dysfunction and who died within 90 days was significantly higher in those with lactate concentrations ≥6 mmol/L (P < 0.001).

Table 5 Distribution of risk factors and outcomes in 138 patients with lactate <2 mmol/L and 29 patients with lactate ≥6 mmol/L undergoing liver resection
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Regression analysis revealed that a pre-operative diagnosis of diabetes mellitus, the number of liver segments resected, the operating surgeon’s assessment of the health of the liver parenchyma, the operative blood loss and number of units of red cells transfused were all independently associated with initial lactate concentration at closure (Table 6). The only pre-operative factor associated with the post-operative lactate concentration was the presence of diabetes. On average, this increased the post-operative lactate concentration at any level by 20% compared to non-diabetics.

Table 6 Univariate and multivariate analysis of pre- and intra-operative factors associated with serum lactate concentration following liver resection in 488 patients
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Discussion

The principal findings of this study are that higher initial serum lactate concentration after liver resection is associated with an increased risk of mortality and renal and liver dysfunction. Both the 90-day mortality rate and the rate of renal dysfunction in patients with initial lactate concentrations greater than 6 mmol/L were 28% compared to those patients with initial lactate concentrations less than 2 mmol/L where they were 0.7% and 2.2% respectively. Similarly, higher lactate concentration was associated with higher post-operative peaks in serum bilirubin concentration and PT, as well longer lengths of hospital stay.

These findings support and extend those of an earlier study [40] by demonstrating the association of post-operative lactate with renal and hepatic dysfunction and length of hospital stay in addition to mortality. Pre-operative diabetes mellitus, the surgeon’s assessment of the liver at laparotomy, the extent of liver resection, blood loss and the number of units of blood transfused are also shown to be associated with post-operative serum lactate concentration.

During cellular hypoxia pyruvate is diverted from the citric acid cycle and converted to lactate, reducing the amount of adenosine triphosphate (ATP) generated. This occurs in all metabolically active tissues including muscle, gut, liver, brain, erythrocytes and skin [41–43] and is exacerbated by intra-operative stresses including blood loss [42], endogenous release of stress hormones [44] and administration of pressor agents [45]. Liver ischaemia induced by handling of the liver during surgery and temporary inflow occlusion has been shown to lead to a rise in lactate [46]. Serum lactate can also be increased by transfusion of stored blood, which contains a higher concentration of lactate than fresh blood depending on length of storage [47]. Administration of Hartmann’s solution has been shown to have a small effect on serum lactate concentration [48]. A potential weakness of this study is that details of pressor agents were not recorded, which could affect the lactate concentration. Similarly precise details regarding intravenous fluid type and volume of fluid (colloid and crystalloid) were not recorded.

In addition to being a potential source of lactate the liver is the principle location of lactate metabolism, where it is converted back to glycogen, accounting for 70% of whole body lactate clearance [42]. No change in lactate metabolism has been demonstrated following recovery from partial hepatectomy in either rats [49] or humans [25], implying that the liver has a large functional reserve under physiological conditions of lactate production. However, the effects of intra-operative stress on hepatic glucose homeostasis have not been assessed, particularly when in combination with an extended hepatectomy. It is possible that inflow occlusion during resection and intra-operative handling of the liver lead to a temporary impairment of the ability of the liver to metabolise lactate. The finding of an association between the number of liver segments resected and the initial post-operative lactate supports this hypothesis. Diabetes is also known to be associated with impaired lactate metabolism via gluconeogenesis [42] and may account for the strong association with post-operative lactate in this series. Furthermore, the use of metformin in non-insulin-dependent diabetes has also been shown to increase lactate concentration [50]. The rise in serum lactate at the end of liver resection therefore may be due to a failure of lactate metabolism in addition to increased production during surgery.

Significantly, the use of pre-operative chemotherapy was not shown to be associated with elevation of post-operative lactate. This may be due to a policy of allowing a period of recovery after completion of pre-operative chemotherapy before undertaking surgery. Interestingly, the operating surgeon’s assessment of the liver parenchyma was associated with the post-operative lactate concentration. This finding suggests that patient co-morbidity was a more common cause of abnormal liver parenchyma than the use of liver-directed chemotherapy.

An important observation of this study is the relative rarity of major hepatic dysfunction following liver resection in this series with only one patient fulfilling the ‘50-50’ criteria [2], who subsequently recovered. Despite the infrequency of major disturbances of post-operative bilirubin and PT, there was an independent association with increasing concentration of post-operative lactate, demonstrating that even a minor degree of liver injury can lead to impaired lactate clearance or increase its production.

Renal dysfunction was also rare in this series, affecting 34 patients (7%) compared to 15% in a similar series [51]. The risk factors for post-operative renal dysfunction are likely to be similar to those in other forms of abdominal surgery, including blood loss and sepsis, which are also initiating factors for anaerobic metabolism and lactate production. This supports the value of initial lactate as an early predictor of renal dysfunction. Of note, the risk of renal dysfunction appeared to rise more rapidly when the post-operative lactate rose above 5 mmol/L (Figure 2). This suggests that the kidneys are able to tolerate a degree of oxidative stress to a threshold level beyond which the risk of damage rises rapidly.

There was a weak association between initial lactate concentration and length of hospital stay in the study (Table 4). However, this may also be affected by other factors such as post-operative complications, particularly bile leaks, and degree of social support.

The strongest association demonstrated was between lactate concentration and the risk of mortality. In a similar manner to renal dysfunction, there seems to be a threshold level of post-operative lactate of approximately 6 mmol/l above which the risk of 90-day mortality rises rapidly (Figure 3). Organ dysfunction was a major contributor to mortality in the series and initial lactate concentration is a valuable global marker of poor organ function in the early post-operative period, including cardiovascular, renal and hepatic dysfunction.

Conclusions

These findings are of value in clinical practice as it may be possible to use the initial post-operative lactate concentration to determine the patient pathway in the early post-operative period. Patients with an initial post-operative lactate of less than 2 mmol/L have low rates of mortality and organ dysfunction and we are currently evaluating this criterion as a determinant of the need for post-operative critical care. In addition the correlation of post-operative lactate with subsequent organ dysfunction and mortality may allow its use as a single measure of the impact of innovations in operative technique or peri-operative care.

Authors’ information

M.G. Wiggans and T. Starkie: joint first authors.

Abbreviations

ASA:

American society of anesthesiologists

ATP:

Adenosine triphosphate

CUSA:

Cavitron ultrasonic surgical aspirator

CVP:

Central venous pressure

HDU:

High dependency unit

LOS:

Length of stay

NLR:

Neutrophil to lymphocyte ratio

NPV:

Negative predictive value

PHLF:

Post-hepatectomy liver failure

P-POSSUM:

Portsmouth physiologic and operative severity score for the enUmeration of mortality and morbidity

PPV:

Predictive value

PT:

Prothrombin time

REC:

Research ethics committee

RIFLE:

Risk, injury, failure, loss, and end-stage kidney disease.

References

  1. 1.

    Mann CD, Palser T, Briggs CD, Cameron I, Rees M, Buckles J, Berry DP: A review of factors predicting perioperative death and early outcome in hepatopancreaticobiliary cancer surgery. HPB. 2010, 12: 380-388. 10.1111/j.1477-2574.2010.00179.x.

  2. 2.

    Balzan S, Belghiti J, Farges O, Ogata S, Sauvanet A, Delefosse D, Durand F: The “50-50 criteria” on postoperative day 5: an accurate predictor of liver failure and death after hepatectomy. Ann Surg. 2005, 242: 824-829. 10.1097/01.sla.0000189131.90876.9e.

  3. 3.

    Schreckenbach T, Liese J, Bechstein WO, Moench C: Posthepatectomy liver failure. Dig Surg. 2012, 29: 79-85. 10.1159/000335741.

  4. 4.

    Saner F: Kidney failure following liver resection. Transplant Proc. 2008, 40: 1221-1224. 10.1016/j.transproceed.2008.03.068.

  5. 5.

    Savage AP, Malt MD: Elective and emergency hepatic resection determinants of operative mortality and morbidity. Ann Surg. 1991, 214: 689-695. 10.1097/00000658-199112000-00008.

  6. 6.

    Koch M, Garden OJ, Padbury R, Rahbari NN, Adam R, Capussotti L, Fan ST, Yokoyama Y, Crawford M, Makuuchi M, Christophi C, Banting S, Brooke-Smith M, Usatoff V, Nagino M, Maddern G, Hugh TJ, Vauthey J-N, Greig P, Rees M, Nimura Y, Figueras J, DeMatteo RP, Büchler MW, Weitz J: Bile leakage after hepatobiliary and pancreatic surgery: a definition and grading of severity by the International Study Group of Liver Surgery. Surgery. 2011, 149: 680-688. 10.1016/j.surg.2010.12.002.

  7. 7.

    Alfieri S, Carrierio C, Caprino P, Di Giorgio A, Sgadari A, Crucitti F, Doglietto G: Avoiding early postoperative complications in liver surgery. A multivariate analysis of 254 patients consecutively observed. Dig Liv Dis. 2001, 33: 341-346. 10.1016/S1590-8658(01)80089-X.

  8. 8.

    Jarnagin WR, Gonen M, Fong Y, DeMatteo RP, Ben-Porat L, Little S, Corvera C, Weber S, Blumgart LH: Improvement in perioperative outcome after hepatic resection: analysis of 1,803 consecutive cases over the past decade. Ann Surg. 2002, 236: 397-406. 10.1097/00000658-200210000-00001.

  9. 9.

    Dixon E, Schneeweiss S, Pasieka JL: Mortality following liver resection in US medicare patients: does the presence of a liver transplant program affect outcome?. J Surg Oncol. 2007, 95: 194-200. 10.1002/jso.20645.

  10. 10.

    Melendez J, Ferri E, Zwillman M, Fischer M, DeMatteo R, Leung D, Jarnagin W, Fong Y, Blumgart LH: Extended hepatic resection: a 6-year retrospective study of risk factors for perioperative mortality. J Am Coll Surg. 2001, 192: 47-53. 10.1016/S1072-7515(00)00745-6.

  11. 11.

    Dimick J, Cowan J, Knol J, Upchurch G: Hepatic resection in the United States: indications, outcomes, and hospital procedural volumes From a nationally representative database. Arch Surg. 2003, 138: 185-191. 10.1001/archsurg.138.2.185.

  12. 12.

    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. 10.1016/0002-9610(94)90124-4.

  13. 13.

    Shimada M, Takenaka K, Fujiwara Y, Gion T, Shirabe K, Yanaga K, Sugimachi K: Risk factors linked to postoperative morbidity in patients with hepatocellular carcinoma. Br J Surg. 1998, 85: 195-198. 10.1046/j.1365-2168.1998.00567.x.

  14. 14.

    Halazun KJ, Aldoori A, Malik HZ, Al-Mukhtar A, Prasad KR, Toogood GJ, Lodge JPA: Elevated preoperative neutrophil to lymphocyte ratio predicts survival following hepatic resection for colorectal liver metastases. Eur J Surg Oncol. 2008, 34: 55-60. 10.1016/j.ejso.2007.02.014.

  15. 15.

    Poon RT, Fan ST, Lo CM, Liu CL, Lam CM, Yuen WK, Yeung C, Wong J: Improving perioperative outcome expands the role of hepatectomy in management of benign and malignant hepatobiliary diseases: analysis of 1222 consecutive patients from a prospective database. Ann Surg. 2004, 240: 698-708. discussion 708–710

  16. 16.

    Benzoni E, Cojutti A, Lorenzin D, Adani GL, Baccarani U, Favero A, Zompicchiati A, Bresadola F, Uzzau A: Liver resective surgery: a multivariate analysis of postoperative outcome and complication. Langenbecks Arch Surg. 2007, 392: 45-54. 10.1007/s00423-006-0084-y.

  17. 17.

    Bolder U, Brune A, Schmidt S, Tacke J, Jauch KW, Löhlein D: Preoperative assessment of mortality risk in hepatic resection by clinical variables: a multivariate analysis. Liver Transpl Surg. 1999, 5: 227-237. 10.1002/lt.500050302.

  18. 18.

    Redaelli CA, Dufour J-F, Wagner M, Schilling M, Hüsler J, Krähenbühl L, Büchler MW, Reichen J: Preoperative galactose elimination capacity predicts complications and survival after hepatic resection. Ann Surg. 2002, 235: 77-85. 10.1097/00000658-200201000-00010.

  19. 19.

    Karoui M, Penna C, Amin-Hashem M, Mitry E, Benoist S, Franc B, Rougier P, Nordlinger B: Influence of preoperative chemotherapy on the risk of major hepatectomy for colorectal liver metastases. Ann Surg. 2006, 243: 1-7. 10.1097/01.sla.0000193603.26265.c3.

  20. 20.

    Benzoni E, Lorenzin D, Baccarani U, Adani GL, Favero A, Cojutti A, Bresadola F, Uzzau A: Resective surgery for liver tumor: a multivariate analysis of causes and risk factors linked to postoperative complications. Hepatobiliary Pancreat Dis Int. 2006, 5: 526-533.

  21. 21.

    Copeland GP, Jones D, Walters M: POSSUM: a scoring system for surgical audit. Br J Surg. 1991, 78: 355-360. 10.1002/bjs.1800780327.

  22. 22.

    Whiteley M, Prytherch D, Higgins B, Weaver P, Prout W: An evaluation of the POSSUM surgical scoring system. Br J Surg. 1996, 83: 812-815. 10.1002/bjs.1800830628.

  23. 23.

    Lam CM, Fan ST, Yuan AW, Law WL, Poon K: Validation of POSSUM scoring systems for audit of major hepatectomy. Br J Surg. 2004, 91: 450-454. 10.1002/bjs.4515.

  24. 24.

    Van den Broek MAJ, OldeDamink SWM, Dejong CHC, Lang H, Malagó M, Jalan R, Saner FH: Liver failure after partial hepatic resection: definition, pathophysiology, risk factors and treatment. Liver Int. 2008, 28: 767-780. 10.1111/j.1478-3231.2008.01777.x.

  25. 25.

    Chioléro R, Tappy L, Gillet M, Revelly JP, Roth H, Cayeux C, Schneiter P, Leverve X: Effect of major hepatectomy on glucose and lactate metabolism. Ann Surg. 1999, 229: 505-513. 10.1097/00000658-199904000-00009.

  26. 26.

    Husain FA, Martin MJ, Mullenix PS, Steele SR, Elliott DC: Serum lactate and base deficit as predictors of mortality and morbidity. Am J Surg. 2003, 185: 485-491. 10.1016/S0002-9610(03)00044-8.

  27. 27.

    Khosravani H, Shahpori R, Stelfox HT, Kirkpatrick AW, Laupland KB: Occurrence and adverse effect on outcome of hyperlactatemia in the critically ill. Crit Care. 2009, 13: R90-10.1186/cc7918.

  28. 28.

    Macquillan GC, Seyam MS, Nightingale P, Neuberger JM, Murphy N: Blood lactate but not serum phosphate levels can predict patient outcome in fulminant hepatic failure. Liver Transpl. 2005, 11: 1073-1079. 10.1002/lt.20427.

  29. 29.

    Bernardin G, Pradier C, Tiger F, Deloffre P, Mattei M: Blood pressure and arterial lactate level are early indicators of short-term survival in human septic shock. Intensive Care Med. 1996, 22: 17-25. 10.1007/BF01728326.

  30. 30.

    Manikis P, Jankowski S, Zhang H, Kahn RJ, Vincent JL: Correlation of serial blood lactate levels to organ failure and mortality after trauma. Am J Emerg Med. 1995, 13: 619-622. 10.1016/0735-6757(95)90043-8.

  31. 31.

    Gruttadauria S, Marino IR, Vitale CH, Mandala L, Scott VL, Doria C: Correlation between peri-operative serum lactate levels and outcome in pancreatic resection for pancreatic cancer, preliminary report. J Exp Clin Cancer Res. 2002, 21: 539-545.

  32. 32.

    Li SH, Liu F, Zhang YT: [Initial serum lactate level as predictor of morbidity after major abdominal surgery]. Zhonghua Yi Xue Za Zhi. 2008, 88: 2470-2473.

  33. 33.

    Murtuza B, Wall D, Reinhardt Z, Stickley J, Stumper O, Jones TJ, Barron DJ, Brawn WJ: The importance of blood lactate clearance as a predictor of early mortality following the modified Norwood procedure. Eur J Cardiothorac Surg. 2011, 40: 1207-1214.

  34. 34.

    Nishimura A, Hakamada K, Narumi S, Totsuka E, Toyoki Y, Ishizawa Y, Umehara M, Yoshida A, Umehara Y, Sasaki M: Intraoperative blood lactate level as an early predictor of initial graft function in human living donor liver transplantation. Transplant Proc. 2004, 36: 2246-2248. 10.1016/j.transproceed.2004.08.051.

  35. 35.

    IHPBA: The Brisbane 2000 terminology of hepatic anatomy and resections. HPB. 2000, 2: 333-339.

  36. 36.

    Mizock BA: Lactic acidosis. Dis Mon. 1989, 35: 233-300.

  37. 37.

    Bellomo R, Ronco C, Kellum JA, Mehta RL, Palevsky P: Acute renal failure - definition, outcome measures, animal models, fluid therapy and information technology needs: the second international consensus conference of the Acute Dialysis Quality Initiative (ADQI) group. Crit Care. 2004, 8: R204-R212. 10.1186/cc2872.

  38. 38.

    Agresti A: An Introduction to Categorical Data Analysis Second Edition. 2002, Hoboken, New Jersey: John Wiley & Sons

  39. 39.

    R Foundation for Statistical Computing. http://www.r-project.org/,

  40. 40.

    Watanabe I, Mayumi T, Arishima T, Takahashi H, Shikano T, Nakao A, Nagino M, Nimura Y, Takezawa J: Hyperlactemia can predict the prognosis of liver resection. Shock. 2007, 28: 35-38. 10.1097/shk.0b013e3180310ca9.

  41. 41.

    Handy J: Lactate - the bad boy of metabolism, or simply misunderstood?. Curr Anaesth Crit Care. 2006, 17: 71-76. 10.1016/j.cacc.2006.05.006.

  42. 42.

    Phypers B, Pierce JM: Lactate physiology in health and disease. Contin Educ Anaesth Crit Care Pain. 2006, 6: 128-132. 10.1093/bjaceaccp/mkl018.

  43. 43.

    Theodoraki K, Arkadopoulos N, Fragulidis G, Voros D, Karapanos K, Markatou M, Kostopanagiotou G, Smyrniotis V: Transhepatic lactate gradient in relation to liver ischemia/reperfusion injury during major hepatectomies. Liver Transpl. 2006, 12: 1825-1831. 10.1002/lt.20911.

  44. 44.

    James JH, Luchette FA, McCarter FD, Fischer JE: Lactate is an unreliable indicator of tissue hypoxia in injury or sepsis. Lancet. 1999, 354: 505-508. 10.1016/S0140-6736(98)91132-1.

  45. 45.

    Luchette FA, Jenkins WA, Friend LA, Su C, Fischer JE, James JH: Hypoxia is not the sole cause of lactate production during shock. J Trauma. 2002, 52: 415-419. 10.1097/00005373-200203000-00001.

  46. 46.

    Pietsch UC, Herrmann ML, Uhlmann D, Busch T, Hokema F, Kaisers UX, Schaffranietz L: Blood lactate and pyruvate levels in the perioperative period of liver resection with Pringle manoeuver. Clin Hemorheol Microcirc. 2010, 44: 269-281.

  47. 47.

    Uvizl R, Klementa B, Adamus M, Neiser J: Biochemical changes in the patient’s plasma after red blood cell transfusion. Signa Vitae. 2011, 6: 64-71.

  48. 48.

    Shin WJ, Kim YK, Bang JY, Cho SK, Han SM, Hwang GS: Lactate and liver function tests after living donor right hepatectomy: a comparison of solutions with and without lactate. Acta Anaesthesiol Scand. 2011, 55: 558-564. 10.1111/j.1399-6576.2011.02398.x.

  49. 49.

    Petenusci SO, Freitas TC, Roselino ES, Migliorini RH: Glucose homeostasis during the early stages of liver regeneration in fasted rats. Can J Physiol Pharmacol. 1983, 61: 222-228. 10.1139/y83-034.

  50. 50.

    Davis TM, Jackson D, Davis WA, Bruce DG, Chubb P: The relationship between metformin therapy and the fasting plasma lactate in type 2 diabetes: The Fremantle Diabetes Study. Br J Clin Pharmacol. 2001, 52: 137-144. 10.1046/j.0306-5251.2001.01423.x.

  51. 51.

    Slankamenac K, Breitenstein S, Held U, Beck-Schimmer B, Puhan MA, Clavien P-A: Development and validation of a prediction score for postoperative acute renal failure following liver resection. Ann Surg. 2009, 250: 720-728. 10.1097/SLA.0b013e3181bdd840.

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Acknowledgements

Thanks to Dr. C. Seavell, Dr. P. Davis and Dr. D. Lunn (Consultant Anaesthetists) for their work in study design and collecting lactate data.

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Author notes

    Affiliations

    1. Hepatobiliary Surgery, Plymouth Hospitals NHS Trust, Derriford Hospital, Derriford Road, Plymouth, Devon, PL6 8DH, UK
      • Matthew G Wiggans
      • , Matthew J Bowles
      • , Somaiah Aroori
      •  & David A Stell
    2. Peninsula College of Medicine and Dentistry, University of Exeter and Plymouth University, Research Way, Plymouth, Devon, PL6 8BU, UK
      • Matthew G Wiggans
      •  & David A Stell
    3. Department of Anaesthetics, Plymouth Hospitals NHS Trust, Derriford Hospital, Derriford Road, Plymouth, Devon, PL6 8DH, UK
      • Tim Starkie
      • , Tom Woolley
      • , David Birt
      • , Paul Erasmus
      •  & Ian Anderson
    4. Centre for Health Statistics, Tamar Science Park, Davy Road, Plymouth, Devon, PL6 8BX, UK
      • Golnaz Shahtahmassebi
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    Corresponding author

    Correspondence to David A Stell.

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    Competing interests

    The authors declare that they have no competing interests.

    Authors’ contributions

    MW and TS designed the study, collected data, analysed the data and drafted the manuscript. GS participated in the design of the study and performed the statistical analysis. TW, DB, PE, IA, SA and MB participated in the design of the study, collected data and drafted the manuscript. DS conceived the study, supervised its design and coordination and helped to draft the manuscript. All authors read and approved the final manuscript.

    Matthew G Wiggans, Tim Starkie contributed equally to this work.

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    Wiggans, M.G., Starkie, T., Shahtahmassebi, G. et al. Serum arterial lactate concentration predicts mortality and organ dysfunction following liver resection. Perioper Med 2, 21 (2013). https://doi.org/10.1186/2047-0525-2-21

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    Keywords

    • Liver
    • Hepatectomy
    • Post-operative care

    Perioperative Medicine

    ISSN: 2047-0525