Lactate: the Black Peter in high-risk gastrointestinal surgery patients

Lactate: the Black Peter in high-risk gastrointestinal surgery patients

Patrick M. Honore, Rita Jacobs, Inne Hendrickx, Elisabeth De Waele, Herbert D. Spapen

ICU Department, Universitair Ziekenhuis Brussel, Vrije Universiteit Brussel, Brussels, Belgium

Correspondence to: Prof. Patrick M. Honore, MD, PhD, FCCM. Professor of Intensive Care Medicine, Deputy Head of Research Unit, ICU Department, Universitair Ziekenhuis Brussel, Vrije Universiteit Brussel, 101, Laarbeeklaan, 1090 Jette, Brussels, Belgium. Email:

Submitted Mar 08, 2016. Accepted for publication Mar 16, 2016.

doi: 10.21037/jtd.2016.03.80

Lactate arises from metabolisation of glucose to pyruvate. Pyruvate either is transformed to or from lactate in the cytosol or converted by pyruvate dehydrogenase in mitochondria to acetyl coenzyme A which enters the Krebs cycle to produce energy for cellular metabolism. Any switch to anaerobic metabolism will reduce activity of the highly oxygen-dependent Krebs cycle and shunt “redundant” pyruvate towards lactate (1).

Why is this seemingly trifle lactate molecule so important in the intensive care unit (ICU)? Increased blood lactate concentrations are dreaded by ICU physicians since they are almost invariably linked to the presence or persistence of inadequate tissue perfusion and oxygenation. Hyperlactatemia at a cut-off value between 2 and 4 mmol/L is associated with worse outcome in all types of shock. As such, the blood lactate level has become a powerful “biomarker” to predict morbidity and mortality as well as a tool to guide resuscitation in hemodynamically compromised critically ill patients (2). However, lactate may also be produced independently from tissue hypoxia in conditions characterized by decreased pyruvate dehydrogenase activity (e.g., thiamine deficiency), modification of the cellular redox potential (e.g., ketoacidosis, ethanol abuse), or accelerated glycolytic flux (e.g., induced by drugs such as catecholamines and biguanides) (3).

Monitoring lactate has been progressively introduced in the postoperative setting. Blood lactate concentration proved to be an indispensable and accurate marker of mortality at both individual patient and patient cohort level after cardiac surgery (4). An early lactate increase was also found to predict complications after elective pancreatic (5) and extensive liver surgery (6). However, the association between lactate concentrations and mortality with regard to type of gastrointestinal (GI) surgery (emergency vs. elective) remained unexplored. Hyperlactatemia following elective GI surgery was intuitively accepted as a relatively “physiological” reaction to surgical stress. Indeed, a GI surgical intervention itself will cause activation of coagulation and inflammatory pathways which can be further accentuated by procedure-related gut manipulation, temporary ischemia, and eventual bacterial translocation and shedding. In contrast, elevated lactate during emergency GI surgery was traditionally linked to a more frequent occurrence of peri-operative hemodynamic instability and resuscitation-associated ischemia-reperfusion disorders.

Li et al. studied dynamic postoperative changes in blood lactate levels during the first 24 h after elective major abdominal surgery. They found that time-weighted average lactate at a cut-off level as low as 1.5 mmol/L was independently predictive of both overall and major postoperative complications observed in nearly half of the patients (7). These findings have now been corroborated and expanded by the recently published study of Creagh-Brown et al. in Critical Care Medicine. These investigators showed that the highest lactate level obtained on the first day after ICU admission in patients who underwent major GI surgery was independently associated with increased morbidity and in-hospital mortality. This association was not related to the type of intervention (emergency vs. elective) and also continued down into the “normal lactate concentration” range (8). The key message of Creagh-Brown et al. is that any increase in postoperative lactate after high-risk GI surgery is a “bad” prognostic sign. It can be assumed that the increase in lactate after major GI surgery is related either to an overt imbalance between oxygen delivery and consumption (as in shock accompanying emergency surgery) or to a systemically occult deficit in tissue oxygen handling (as in elective surgery). Microcirculatory alterations that hamper gut oxygen extraction have been incriminated as the main culprit to explain insidious tissue oxygen debt during elective surgery. Increased blood lactate levels have indeed been shown to reflect microcirculatory dysfunction after general or thoracic surgery (9). However, changes in microcirculation during abdominal surgery were found to be rather modest and not correlated with peri-operative lactate levels (10).

The findings of Creagh-Brown et al. do have important clinical implications. Interventions aimed at increasing gut perfusion or altering glycolytic flux during GI surgery should be promptly implemented in an attempt to lower deleterious lactate levels. The question is how this can be adequately and safely achieved. Glycolytic flux could be modulated by insulin administration but such treatment is controversial and may have significant and often unwarranted effects on glucose homeostasis (11). Lactate elimination in GI surgery patients could be enhanced by boosting oxygen delivery with a combination of intravenous fluids and inotropes. However, results of such “goal-directed” therapy after major surgery are conflicting (12,13) and probably benefit only those patients with the highest risk profile (14). Also, pursuing lactate normalization at all costs in the absence of other signs of tissue hypoperfusion may expose patients to the toxicity of over-resuscitation without any clear benefit. Nevertheless, lactate-driven adjustment of intravenous fluid administration intra-operatively and in the early postoperative period allowed early detection and correction of inadequate tissue perfusion and significantly decreased the overall complication rate after elective surgery for GI malignancy (15).

The study of Creagh-Brown et al. has some important limitations. First, the authors measured peak lactate levels within 24 h after ICU admission. Lactate levels result from a dynamic balance between lactate production and clearance. Therefore, serial lactate sampling is preferable to a single value since changes in lactate concentration may significantly lag behind clinical interventions, a transient increase in blood lactate does not necessarily predict poor clinical outcome, and sustained hyperlactatemia is associated with an even worse prognosis (16). Second, resuscitation policy (in emergency surgery) and routine surgical and anesthesiology procedures (in elective surgery) may have differed substantially between hospitals, hence introducing potential bias into the lactate/outcome relationship. For instance, artificial colloids can augment the risk of peri-operative hemorrhage by more than 50% (17) while a sustained positive fluid balance in the early postsurgical period may significantly increase infectious complications and mortality in critically ill surgical patients (18). Also, the grade of intestinal mucosal damage and corresponding high lactate concentrations have been found to be directly correlated with the duration of surgery (19). Third, the study results were adjusted for age, severity of illness, and cardiopulmonary resuscitation status. However, in-hospital mortality may be determined by other variables that were not registered such as co-morbidity and complications either related (e.g., suture detachment or leakage necessitating revision), or unrelated to surgery (e.g., ICU-acquired infection or organ failure).

Despite these shortcomings, the study of Creagh-Brown et al. underscores that occurrence of increased blood lactate in the immediate postoperative period after major GI surgery is an ominous sign that requires close monitoring and adequate therapeutic anticipation. Future research must determine which intervention(s) best counteract hyperlactatemia after planned or acute GI surgery without harming the patient.




Provenance: This is an invited Commentary commissioned by the Section Editor Zhongheng Zhang (Department of Critical Care Medicine, Jinhua Municipal Central Hospital, Jinhua Hospital of Zhejiang University, Jinhua, China).

Conflicts of Interest: The authors have no conflicts of interests to declare.

Commentary on: Creagh-Brown BC, De Silva AP, Ferrando-Vivas P, et al. Relationship between peak lactate and patient outcome following high-risk gastrointestinal surgery: influence of the nature of their surgery: elective versus emergency. Crit Care Med 2016;44:918-25.


  1. Kraut JA, Madias NE. Lactic acidosis. N Engl J Med 2014;371:2309-19. [Crossref] [PubMed]
  2. Bakker J, Nijsten MW, Jansen TC. Clinical use of lactate monitoring in critically ill patients. Ann Intensive Care 2013;3:12. [Crossref] [PubMed]
  3. Suetrong B, Walley KR. Lactic acidosis in sepsis: it's not all anaerobic: implications for diagnosis and management. Chest 2016;149:252-61. [Crossref] [PubMed]
  4. Badreldin AM, Doerr F, Elsobky S, et al. Mortality prediction after cardiac surgery: blood lactate is indispensible. Thorac Cardiovasc Surg 2013;61:708-17. [Crossref] [PubMed]
  5. De Schryver N, Wittebole X, Hubert C, et al. Early hyperlactatemia predicts pancreatic fistula after surgery. BMC Anesthesiol 2015;15:109. [Crossref] [PubMed]
  6. Vibert E, Boleslawski E, Cosse C, et al. Arterial lactate concentration at the end of an elective hepatectomy is an early predictor of the postoperative course and a potential surrogate of intraoperative events. Ann Surg 2015;262:787-92; discussion 792-3. [Crossref] [PubMed]
  7. Li S, Peng K, Liu F, et al. Changes in blood lactate levels after major elective abdominal surgery and the association with outcomes: a prospective observational study. J Surg Res 2013;184:1059-69. [Crossref] [PubMed]
  8. Creagh-Brown BC, De Silva AP, Ferrando-Vivas P, et al. Relationship between peak lactate and patient outcome following high-risk gastrointestinal surgery: influence of the nature of their surgery: elective versus emergency. Crit Care Med 2016;44:918-25. [PubMed]
  9. Yeh YC, Wang MJ, Chao A, et al. Correlation between early sublingual small vessel density and late blood lactate level in critically ill surgical patients. J Surg Res 2013;180:317-21. [Crossref] [PubMed]
  10. Bansch P, Flisberg P, Bentzer P. Changes in the sublingual microcirculation during major abdominal surgery and post-operative morbidity. Acta Anaesthesiol Scand 2014;58:89-97. [Crossref] [PubMed]
  11. NICE-SUGAR Study Investigators, Finfer S, Chittock DR, et al. Intensive versus conventional glucose control in critically ill patients. N Engl J Med 2009;360:1283-97. [Crossref] [PubMed]
  12. Pearse R, Dawson D, Fawcett J, et al. Early goal-directed therapy after major surgery reduces complications and duration of hospital stay. A randomised, controlled trial Crit Care 2005;9:R687-93. [ISRCTN38797445]. [Crossref] [PubMed]
  13. Sandham JD, Hull RD, Brant RF, et al. A randomized, controlled trial of the use of pulmonary-artery catheters in high-risk surgical patients. N Engl J Med 2003;348:5-14. [Crossref] [PubMed]
  14. Cecconi M, Corredor C, Arulkumaran N, et al. Clinical review: goal-directed therapy-what is the evidence in surgical patients? The effect on different risk groups. Crit Care 2013;17:209. [Crossref] [PubMed]
  15. Wenkui Y, Ning L, Jianfeng G, et al. Restricted peri-operative fluid administration adjusted by serum lactate level improved outcome after major elective surgery for gastrointestinal malignancy. Surgery 2010;147:542-52. [Crossref] [PubMed]
  16. Kruse O, Grunnet N, Barfod C. Blood lactate as a predictor for in-hospital mortality in patients admitted acutely to hospital: a systematic review. Scand J Trauma Resusc Emerg Med 2011;19:74. [Crossref] [PubMed]
  17. Rasmussen KC, Johansson PI, Højskov M, et al. Hydroxyethyl starch reduces coagulation competence and increases blood loss during major surgery: results from a randomized controlled trial. Ann Surg 2014;259:249-54. [Crossref] [PubMed]
  18. Barmparas G, Liou D, Lee D, et al. Impact of positive fluid balance on critically ill surgical patients: a prospective observational study. J Crit Care 2014;29:936-41. [Crossref] [PubMed]
  19. Gulam D, Dmitrović B, Kvolik S, et al. Integrity of gut mucosa during anaesthesia in major abdominal surgery. Coll Antropol 2011;35:445-51. [PubMed]
Cite this article as: Honore PM, Jacobs R, Hendrickx I, De Waele E, Spapen HD. Lactate: the Black Peter in high-risk gastrointestinal surgery patients. J Thorac Dis 2016;8(6):E440-E442. doi: 10.21037/jtd.2016.03.80

Download Citation