Can Peripheral Venous Lactate Levels Substitute for Arterial Lactate Levels in The Emergency Department? An Observational Study

2020 ◽  
Author(s):  
Yasufumi Oi ◽  
Kosuke Mori ◽  
Hidehiro Yamagata ◽  
Ayako Nogaki ◽  
Tomoaki Takeda ◽  
...  

Abstract Background: Arterial lactate (AL) level is an important parameter used to predict patients’ prognosis. AL and peripheral venous lactate (PVL) in blood gas analysis have a low concordance rate, and PVL cannot be used as a substitute for AL. However, if the AL range can be predicted from PVL, PVL may be an alternative method of predicting patient prognosis, and the risk of arterial puncture complications with AL may be reduced. This could become a safe and rapid test method.Methods: This was a retrospective observational study of 143 cases in which blood gas analysis was performed on both arterial blood and venous blood in an emergency department. Spearman's rank correlation coefficient (r) and Bland–Altman analysis were performed. Sensitivity, specificity, and the area under the curve (AUC) were calculated for PVL to predict AL < 2 mmol/L or < 4 mmol/L.Results: The median [interquartile range] AL and PVL were 1.82 [1.25–2.58] vs 2.09 [1.57–3.29], respectively, r was 0.799 (p<0.0001), and a strong correlation was observed; however, Bland–Altman analysis showed disagreement. When AL < 2 mmol/L was used as the outcome, AUC was 0.974, the PVL cutoff value was 2.55 mmol/L, sensitivity was 87.9%, and specificity was 94.1%. If PVL < 2 mmol/L was the outcome, the sensitivity for AL < 2 mmol/L was 100%, and for PVL levels ≥ 3 mmol/L, the specificity was 100%. When AL < 4 mmol/L was used as the outcome, AUC was 0.970, the PVL cutoff value was 3.4 mmol/L, sensitivity was 100%, and specificity was 84.5%. When PVL < 3.5 mmol/L was the outcome, the sensitivity for AL < 4 mmol/L was 100%, and for PVL levels ≥ 4 mmol/L, the specificity was 93.8%.Conclusions: This study revealed that PVL and AL levels in the same critically ill patients do not perfectly agree with each other but are strongly correlated. Furthermore, the high accuracy for predicting AL ranges from PVL levels explains why PVL levels could be used as a substitute for AL level ranges.

Critical Care ◽  
2011 ◽  
Vol 15 (3) ◽  
pp. R145 ◽  
Author(s):  
Emanuel Burri ◽  
Mihael Potocki ◽  
Beatrice Drexler ◽  
Philipp Schuetz ◽  
Alexandre Mebazaa ◽  
...  

2021 ◽  
Vol 20 (3) ◽  
pp. 178-182
Author(s):  
Ram Kirubakar Thangaraj ◽  
Hari Hara Sudhan Chidambaram ◽  
Melvin Dominic ◽  
V.P. Chandrasekaran ◽  
Karthik Narayan Padmanabhan ◽  
...  

Author(s):  
Michael Bernhard ◽  
Stephanie Döll ◽  
Andre Kramer ◽  
Lorenz Weidhase ◽  
Thomas Hartwig ◽  
...  

Abstract Background Elevated blood lactate levels were reported as useful predictors of clinical outcome and mortality in critically ill patients. To identify higher-risk patients, this investigation evaluated the relationship between patient mortality and admission lactate levels during the management of non-trauma critically ill patients in the emergency department (ED). Methods In this prospective, single centre observational study in a German university ED, all adult patients who were admitted to the ED resuscitation room were evaluated between September 1, 2014 and August 31, 2015. Blood samples for blood gas analysis, including lactate levels, were obtained immediately at admission. Study endpoint was 30-day mortality. Results During the study period, 532 patients were admitted to the resuscitation room of the ED. The data of 523 patients (98.3%) were available. The overall 30-day mortality was 34.2%. Patients presenting to the resuscitation room with admission lactate levels < 2.0 mmol/l had a 30-day mortality of 22.7%, while admission lactate levels above 8.0 mmol/l were associated with higher mortality (8.0–9.9 mmol/l: OR: 2.83, 95%CI: 1.13–7.11, p = 0.03, and ≥ 10 mmol/l: OR: 7.56, 95%CI: 4.18–13.77, p < 0.001). Conclusion High lactate levels at admission are associated with an increased 24-h and 30-day mortality. These measurements may be used not only to predict mortality, but to help identify patients at risk for becoming critically ill. The breakpoint for mortality may be an ALL ≥8.0 mmol/l.


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