- Case report
- Open Access
A rapid and accurate new bedside test to assess maximal liver function: a case report
© Müller et al.; licensee BioMed Central Ltd. 2013
- Received: 13 February 2013
- Accepted: 17 April 2013
- Published: 25 April 2013
In liver surgery, appropriate preoperative evaluation and preparation of the patient is of cardinal importance. The up-to-date, preoperative prediction of residual liver function has thus far been limited. As post-hepatectomy liver failure is a major cause of mortality, a new and simple bedside test (LiMAx) has been developed to predict postoperative liver function in conjunction with preoperative volumetric analysis of the liver.
A 45-year-old patient presented with a cecal carcinoma and a large synchronous liver metastasis for major liver surgery. Liver function was determined by the LiMAx-test for the enzymatic capacity of cytochrome P450 1A2, which is ubiquitously and solely active in the liver. A solution of 2 mg/kg body weight 13C-labeled methacetin was injected as a bolus into an intravenous catheter and, thereafter, was metabolized into acetaminophen and 13CO2 and pulmonarily exhaled. The analysis of the 13CO2/12CO2 ratio was performed using online breath sampling over a period of maximally 60 minutes. Based on this test, a value of more than 315 μg/kg/h represents normal liver function. A laparoscopic right hemihepatectomy was planned during virtual resection with a residual liver volume of 48% and a preoperative anticipated residual LiMAx of 301 μg/kg/h. After successful resection, the initial postoperative LiMAx value was 316 μg/kg/h, indicating good liver function and a correct prediction of the outcome.
In the presented patient, residual liver function could be accurately predicted preoperatively using a combination of the new LiMax test with CT-volumetry. This test might significantly improve preoperative evaluation and postoperative outcomes in liver surgery.
- Liver function
- Liver volumetry
- Liver resection
- Liver function measurement
Improvements in surgical techniques, anesthetic protocols, and perioperative care have decreased morbidity and mortality and have contributed to an increase in extended liver resections. This more aggressive approach inevitably leads to smaller remnant livers with a substantially elevated risk of post-resectional liver failure (PLF) [1–3]. It was demonstrated that 80% of deaths caused by PLF occur after resecting more than 50% of the liver volume [4–6], and the PLF incidence increases with the number of resected segments . Therefore, accurate preoperative volumetric calculation of total and partial liver volumes based on preoperative imaging and resection planning is crucial in the assessment of hepatic functional reserve and resectability, especially in cases of major liver resection and patients with underlying parenchymal disease . Liver steatosis and steatohepatitis, for example, are associated with an increased risk of PLF after partial liver resection, especially after neoadjuvant chemotherapy, or in living donor liver transplantation . Traditional methods estimating the hepatic functional reserve, such as liver enzyme tests and Child-Pugh classification, have clinical and practical limitations . The major disadvantage of most quantitative liver function tests, such as the indocyanine green clearance test and the galactose elimination capacity, is that they are influenced by several factors such as hepatic blood flow and hyperbilirubinemia . Moreover, no reliable cutoffs and guidelines could be defined. Consequently, clinical decisions mainly rely on the surgeon’s experience . Until now no biological marker or score has been able to reliably measure total liver function or predict the postoperative outcome. Here, we present the LiMAx-test, which has been developed at the Department of General, Visceral and Transplantation Surgery at the Charité in Berlin . The test has been successfully evaluated in many patients undergoing liver surgery and liver transplantation since 2003 [11, 12]. This test is now used in all patients with planned liver resection in our surgical department and in several other European centers.
This breath test is based on the hepatocyte-specific metabolism of the cytochrome P450 1A2 enzyme, which is active throughout the liver. After 3 hours of fasting, patients are placed in a resting horizontal position. The activity of the enzyme is measured by i.v. bolus injection of non-radioactive 13C-methacetin (2 mg/kg body weight). Ten minutes prior to the injection with 13C-methacetin, the baseline 13CO2/12CO2 ratio is recorded. 13C-methacetin (Euriso-top, Saint-Aubin, Cedex, France) is metabolized into acetaminophen and 13CO2, which is pulmonarily exhaled. The exhaled air is collected using a face mask (Humedics GmbH, Berlin Germany), and the 13CO2/12CO2 ratio in the air is determined using a modified nondispersive isotope-selective infrared spectroscopy (FANci2-db16, Fischer Analysen Instumente, Leipzig, Germany, Humedics GmbH, Berlin, Germany) [11, 13]. Based on the 13CO2/12CO2 ratio and the body weight, the cytochrome P450 1A2 activity is determined using the so-called LiMAx value with the unit μg/kg/h (μg methacetin/kg body weight/hour). The analysis of the 13CO2/12CO2 ratio is performed over a period of 20 to 60 minutes. For normal liver function, a LiMAx value over 315 μg/kg/h is required. In healthy volunteers, the normal range of LiMAx was found to be 425 ± 67 μg/kg/h (range 311-575 μg/kg/h). Furthermore, the correlation between repeated measurements was found to be 0.82 .
After successful resection, the initial postoperative LiMAx value on postoperative day one was 316 μg/kg/h, indicating good liver function and correct prediction of the outcome. After an uneventful postoperative course, the patient was discharged on postoperative day six. Eight days later, an uneventful laparoscopic right hemicolectomy was performed to remove the primary tumor.
As impressively demonstrated by the presented case, the LiMAx-test in combination with a CT-based liver volumetry can reliably predict the postoperative liver function. Therefore, we adopted these preoperative tests as a standard procedure for every patient undergoing liver resection at our institution.
In 2010, Stockmann et al. published the LiMAx algorithm, which is an easily applicable clinical decision tree for preoperative resection planning . This allows effective preoperative surgical risk evaluation to prevent major complications or even liver failure-related death. Normal liver function (LiMAx >315 μg/kg/h) allows the resection of up to four liver segments without further consideration. By contrast, patients with strongly impaired liver function (LiMAx <140 μg/kg/h, indicating significant hepatic injury) are not eligible for surgery as they are prone to developing postoperative liver failure even after minor liver resection. Patients with limited hepatic impairment and a preoperative LiMAx-value between 140–315 μg/kg/h are the most challenging ones. In these patients, precise liver volumetry is mandatory for a planned major liver resection (>four liver segments). Resections with an expected residual LiMAx value less than 80 μg/kg/h should be avoided because they are associated with a high mortality of up to 40%. Planned resections with a predicted residual LiMAx value between 80–100 μg/kg/h are considered critical (10.5% postoperative mortality), and thus alternative therapies or additional preoperative procedures should be considered (i.e., portal vein embolization, neo-adjuvant chemotherapy to downstage tumors). Liver resections with expected residual LiMAx values of >100 μg/kg/h can safely be performed.
The LiMAx test can clearly help to avoid post-resectional liver failure. Thus, one could expect a relevant impact on health care costs. Recently, Lock et al. published a study examining 45 patients after major liver resection . Eight patients developed postoperative liver failure, seven of these died in the postoperative course. Patients developing post-resectional liver failure generated higher costs than patients without post-resectional liver failure (82,199 € [95%CI: 42,812 – 21,586 €] vs. 25,980 € [95%CI: 9,559 – 42,401 €]; p = 0.013) . The proportion of intensive-care unit cost relative to total costs increased from 30% to more than 50%, and the cost for blood tests and products from the blood bank increased more than eightfold from 819 € [95%CI: 0 – 1,837 €] to 6,953 € [95%CI: 4,512 – 9,395 €]; p ≤ 0.001). In covariate analysis, overall costs related to post-resectional liver failure were 56,219 € [95%CI: 12,327 – 100,066 €]. Routinely applying the LiMAx test, we can achieve an optimized and individualized treatment for patients scheduled for liver resections. This ultimately leads to economic savings by significantly decreasing morbidity and mortality and the overall length of hospital stay.
In the presented patient, residual liver function could be accurately predicted preoperatively by the combination of the new LiMax test with CT-volumetry. Considering the existing literature, the LiMAx test significantly improves preoperative evaluation and postoperative outcomes in liver surgery.
Written informed consent was obtained from the patient for the publication of this case report.
- Schneider PD: Preoperative assessment of liver function. Surg Clin North Am. 2004, 84 (2): 355-373. 10.1016/S0039-6109(03)00224-X.View ArticlePubMedGoogle Scholar
- Belghiti J, Hiramatsu K, Benoist S, Massault P, Sauvanet A, Farges O: Seven hundred forty-seven hepatectomies in the 1990s: an update to evaluate the actual risk of liver resection. J Am Coll Surg. 2000, 191 (1): 38-46. 10.1016/S1072-7515(00)00261-1.View ArticlePubMedGoogle Scholar
- Clavien P-A, Petrowsky H, DeOliveira ML, Graf R: Strategies for safer liver surgery and partial liver transplantation. N Engl J Med. 2007, 356 (15): 1545-1559. 10.1056/NEJMra065156.View ArticlePubMedGoogle Scholar
- 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 (4): 698-708.PubMed CentralPubMedGoogle Scholar
- Schindl MJ, Redhead DN, Fearon KCH, Garden OJ, Wigmore SJ: The value of residual liver volume as a predictor of hepatic dysfunction and infection after major liver resection. Gut. 2005, 54 (2): 289-296. 10.1136/gut.2004.046524.PubMed CentralView ArticlePubMedGoogle Scholar
- Hammond JS, Guha IN, Beckingham IJ, Lobo DN: Prediction, prevention and management of postresection liver failure. Br J Surg. 2011, 98 (9): 1188-1200. 10.1002/bjs.7630.View ArticlePubMedGoogle Scholar
- Pianka F, Baumhauer M, Stein D, Radeleff B, Schmied BM, Meinzer H-P, Müller SA: Liver tissue sparing resection using a novel planning tool. Langenbecks Arch Surg. 2011, 396 (2): 201-208. 10.1007/s00423-010-0734-y.View ArticlePubMedGoogle Scholar
- Veteläinen R, van Vliet A, Gouma DJ, van Gulik TM: Steatosis as a risk factor in liver surgery. Ann Surg. 2007, 245 (1): 20-30. 10.1097/01.sla.0000225113.88433.cf.PubMed CentralView ArticlePubMedGoogle Scholar
- Mullin EJ, Metcalfe MS, Maddern GJ: How much liver resection is too much?. Am J Surg. 2005, 190 (1): 87-97. 10.1016/j.amjsurg.2005.01.043.View ArticlePubMedGoogle Scholar
- Stehr A, Ploner F, Traeger K, Theisen M, Zuelke C, Radermacher P, Matejovic M: Plasma disappearance of indocyanine green: a marker for excretory liver function?. Intensive Care Med. 2005, 31 (12): 1719-1722. 10.1007/s00134-005-2826-7.View ArticlePubMedGoogle Scholar
- Stockmann M, Lock JF, Riecke B, Heyne K, Martus P, Fricke M, Lehmann S, Niehues SM, Schwabe M, Lemke AJ, Neuhaus P: Prediction of postoperative outcome after hepatectomy with a new bedside test for maximal liver function capacity. Ann Surg. 2009, 250 (1): 119-125. 10.1097/SLA.0b013e3181ad85b5.View ArticlePubMedGoogle Scholar
- Lock JF, Schwabauer E, Martus P, Videv N, Pratschke J, Malinowski M, Neuhaus P, Stockmann M: Early diagnosis of primary nonfunction and indication for reoperation after liver transplantation. Liver Transpl. 2010, 16 (2): 172-180. 10.1002/lt.21973.View ArticlePubMedGoogle Scholar
- Riecke B, Neuhaus P, Stockmann M: Major influence of oxygen supply on 13CO2:12CO ratio measurement by nondispersive isotope-selective infrared spectroscopy. Helicobacter. 2005, 10 (6): 620-622. 10.1111/j.1523-5378.2005.00357.x.View ArticlePubMedGoogle Scholar
- Pearce NW, Di Fabio F, Teng MJ, Syed S, Primrose JN, Abu Hilal M: Laparoscopic right hepatectomy: a challenging, but feasible, safe and efficient procedure. Am J Surg. 2011, 202 (5): e52-e58. 10.1016/j.amjsurg.2010.08.032.View ArticlePubMedGoogle Scholar
- Stockmann M, Lock JF, Malinowski M, Niehues SM, Seehofer D, Neuhaus P: The LiMAx test: a new liver function test for predicting postoperative outcome in liver surgery. HPB (Oxford). 2010, 12 (2): 139-146. 10.1111/j.1477-2574.2009.00151.x.View ArticleGoogle Scholar
- Lock JF, Reinhold T, Malinowski M, Pratschke J, Neuhaus P, Stockmann M: The costs of postoperative liver failure and the economic impact of liver function capacity after extended liver resection–a single-center experience. Langenbecks Arch Surg. 2009, 394 (6): 1047-1056. 10.1007/s00423-009-0518-4.View ArticlePubMedGoogle Scholar
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