Abstract
Background
Unexpected death within 24 hours of admission is a real challenge for the clinician in the emergency room. How to diagnose these patients and the right approach to prevent sudden death with 24 hours is still an enigma. The aims of our study were to find the independent factors that may affect the clinical outcome in the first 24 hours of admission to the hospital.
Methods
We performed a retrospective study defining unexpected death within 24 hours of admission in our Department of Medicine in the last 6 years. We found 43 patients who died within 24 hours of admission, and compared their clinical and biochemical characteristics to 6055 consecutive patients who were admitted in that period of time and did not die within the first 24 hours of admission. The parameters that were used include gender, age, temperature, clinical and laboratory criteria for SIRS, arterial blood lactate, and arterial blood pH.
Results
Most of the patients who died within 24 hours had sepsis with SIRS. These patients were older (78.6±14.7 vs. 65.2±20.2 years [p<.0001]), had higher lactate levels (8.0±4.8 vs. 2.1±1.8mmol/L [p<.0001]), and lower pH (7.2±0.2 vs. 7.4±0.1 [p<.0001]). Logistic regression analysis found that lactate was the strongest independent parameter to predict death within 24 hours of admission (OR 1.366 [95% CI 1.235–1.512]), followed by old age (OR 1.048 [95% CI 1.048–1.075] and low arterial blood pH (OR 0.007 [CI <0.001–0.147]). When gender was analyzed, pH was not an independent variable in females (only in males).
Conclusions
The significant independent variable that predicted death within 24 hours of admission was arterial blood lactate level on admission. Older age was also an independent variable; low pH affected only males, but was a less dominant variable. We suggest use of arterial blood lactate level on admission as a bio-marker in patients with suspected sepsis admitted to the hospital for risk assessment and prediction of death within 24 hours of admission.
Keywords: Lactate, SIRS
1 Background
Death within the first 24 hours of admission in the medical ward is still an enigma. We expect grave prognosis for patients who are admitted with an acute myocardial infarction (AMI) or severe septic shock, but patients who are admitted without these extreme conditions and die within the first 24 hours are still an unsolved mystery for the clinician in the emergency department and in the department of medicine.
Several studies investigated different scores that could predict 28-day mortality and the ability to use them in the emergency department. In a study where the mortality in emergency department sepsis (MEDS), confusion, urea, respiratory rate, blood pressure, age>65 (CURB-65), acute physiology and chronic health evaluation II (APACHE II), rapid acute physiology score (RAPS), and rapid emergency medicine score (REMS) scores were studied, it was found that MEDS and CURB-65 scores were the most adequate and feasible tools for the prediction of 28-day mortality [1]. Another study tried to predict mortality by using emergency department sepsis score for in-hospital mortality and did not find definite results [2]. The effectiveness of the APACHE II, SAPS, and SOFA scoring systems was evaluated to predict death in hematological patients admitted to the ICU and found that SAPS II score was the only independent risk factor of patients’ in-hospital deaths in multivariate analysis [3].
We decided to study those patients who died within the first 24 hours of admission and were admitted to the general internal medicine department without an AMI or septic shock, and try to define clinical and biochemical characteristics that could define those patients in order to find a bio-marker that would warn the clinician in the emergency department that this specific individual is at high risk of death within 24 hours and should get special monitoring and be admitted in the ICU.
2 Methods
This was a retrospective study that investigated death within 24 hours of admission to the general internal medicine ward. We found 43 patients who were admitted to the department and died unexpectedly within 24 hours of admission. In order to find the independent variables that could characterize them and distinguish them from other patients, we compared their clinical and laboratory data to 6055 patients who were admitted to the general internal medicine ward in the last 3 years and survived the first 24 hours of hospitalization.
We used statistical tests such as Chi-square test and logistic regression analysis to predict death within 24 hours.
Ethical approval
The research related to human use has been complied with all the relevant national regulations, institutional policies and in accordance the tenets of the Helsinki Declaration, and has been approved by the my institutional review board.
3 Results
Patients who died within the first 24 hours were older (78.6±14.7 vs. 65.2±20.2 years [p<.0001]), had higher lactate levels (8.0±4.8mmol/L vs. 2.1±1.8mmol/L [p<.0001]), and a more acidic pH (7.2±0.2 vs. 7.4±0.1 [p<.001]).
Most of the patients who died in the first 24 hours had an infection with a positive systemic inflammatory response syndrome (SIRS) (86% of all patients), most had coronary artery disease (CAD) documented by an old MI or coronary intervention (93%), many were hypertensive per history (67%), had type 2 diabetes mellitus (DM) (37%), half had renal failure (53%), and 58% had recurrent hospitalizations in the last year.
Thirty-eight patients (88%) had high levels of lactate and 28 patients (65%) had pH lower than 7.1 (Table 1).
Table 1.
Unexpected Death within 24 Hours; Clinical and Biochemical Data.
Males (%) | Females (%) | p value | |
---|---|---|---|
Number | 29 | 14 | |
Age | 75.9±15.0 | 84.2±12.7 | .04 |
SIRSa | 25 (86%) | 12 (86%) | NS |
CADb | 23 (79%) | 12 (86%) | NS |
DMc | 11 (38%) | 5 (36%) | NS |
HTNd | 18 (62%) | 11 (78%) | NS |
RFe | 17 (58%) | 6 (42%) | .05 |
RHf | 18 (62%) | 7 (50%) | NS |
Lactate>2 | 25 (85%) | 13 (93%) | NS |
pH<7.1 | 20 (69%) | 8 (57%) | NS |
SIRS – systemic inflammatory response syndrome
CAD – coronary artery disease
DM – diabetes mellitus
HTN – hypertension
RF – renal failure
RH – recurrent hospitalization
No gender differences were observed in this group of patients except for age (females were older – 84.2±12.7 years, males 75.9±15.0; p=.04). No gender difference was observed in relation to temperature, heart rate, lactate, pH, and blood pressure measurements. No significant difference was observed between genders in relation to SIRS, CAD, type 2 DM, HTN, renal failure, recurrent hospitalizations, lactate level, and pH.
Comparing the group of patients who died within the first 24 hours to controls, we found that patients who died in the first 24 hours were older (males 75.9±15.0 vs. 63.5±19.9 years [p=.0009]; females 84.2±12.7 vs. 66.9±20.3 years [p=.0002]). Lactate level was higher in those patients (males 7.6±4.3 vs. 2.2±1.8mmol/L [p<.0001]), females 8.6±5.7 vs. 2.1±1.8mmol/L [p=.0008]), and the pH level was lower (males 7.2±0.2 vs. 7.4±0.1 [p<.0001]), females 7.2±0.2 vs. 7.4±0.1 [p=.011]). Interestingly, the pCO2 was 55.6±25.4 in men and 48.7±20.6 in women (p=0.172).
Logistic regression analysis showed that the strongest independent variable that could predict death within 24 hours of admission was blood lactate (for male patients Odds Ratio (OR) 1.325 [95% Confidence Interval (CI) 1.176–1.495], for female patients 1.548 [95% CI 1.376–1.740]); then old age (for males OR 1.043 [95% CI 1.013–1.075], for females 1.085 [95% CI 1.023–1.151]); and pH (for males OR of <0.001 [95% CI <0.001–0.015]). pH did not have any independent effect in females (Table 2).
Table 2.
Analysis of Difference between Patients by Outcome and Gender.
Males | Females | |||
---|---|---|---|---|
Survivors | Died | Survivors | Died | |
Number | 3118 | 29 | 2937 | 14 |
p value | <.0001 | <.0001 | ||
Age | 63.5±19.9 | 75.9±15.0 | 66.9±20.3 | 84.2±12.7 |
p value | .0009 | .0002 | ||
Lactate | 2.2±1.8 | 7.6±4.3 | 2.1±1.8 | 8.6±5.7 |
p value | <.0001 | <.0008 | ||
pH | 7.4±0.1 | 7.2±0.2 | 7.4±0.1 | 7.2±0.2 |
p value | <.0001 | .0115 |
Odds Ratios
Age | 1.043 (95% CI 1.013–1.075) | 1.085 (95% CI 1.023–1.151) |
Lactate | 1.325 (95% CI 1.176–1.495) | 1.548 (95% CI 1.376–1.740) |
pH | <0.001 (95% CI <0.001–0.015) |
4 Discussion
The most significant independent variable that could predict death within 24 hours of admission to the general internal medicine department was lactate level. Levels higher than 2 mmol/L (the cutoff point in our study) predicted a grave outcome; the higher the level the worse the outcome and a higher probability of death within 24 hours of admission. The second significant independent variable was old age. Old age could predict a worse outcome according to our study. Blood pH (pH lower than 7.1) had a predictive value only in male patients, not in females, and showed that male patients admitted with sepsis and SIRS who also had a pH level lower than 7.1 had a high chance to die within 24 hours of admission. It could be that the mechanism is a more complex acid base disturbance in this group of patients, and it could be that the real culprit here is not the lactic acidosis but the mixed respiratory and metabolic acidosis that could explain the independent variable of pH in men but not in women.
The purpose of this study was to try to define a biomarker that could guide the clinician in the emergency room and in the general ward that there is a high risk patient who is now in danger and should be treated more aggressively and should be transferred to the intensive care department.
Blood lactate concentration reflects a balance between production and uptake of lactate in tissues, and the normal level is between 0.5 and 1.8mM. It is formed by reduction of pyruvate, and metabolized by oxidation to pyruvate in a reaction catalyzed by the cytosolic NAD-dependent lactate dehydrogenase. Pyruvate is metabolized to carbon dioxide and water in the mitochondria by oxidation and it is part of the energy production of the respiratory chain. If pyruvate production exceeds the capacity of oxidative metabolism, pyruvate is diverted to lactate. Lactate is released from tissues with a proton, and excessive lactate production may cause lactic acidosis. Uptake of lactate occurs mainly in the heart, where it is used for energy purposes, and the liver, where it is a precursor for glucose formation.
A meta-analysis that reviewed the literature found that blood lactate monitoring is useful for risk assessment in patients admitted acutely to the hospital and the trend is especially valuable in predicting in-hospital mortality [4]. The main difference between this study and ours is the research population. In this study patients were already hospitalized in the ICU. In our study all patients who died within 24 hours were admitted to the general medicine ward and their death was unexpected. On admission they were not considered “patients at high risk” and were not transferred to the ICU. Another study examined lactate clearance for death prediction in severe sepsis or septic shock patients during the first 24 hours in ICU after initial resuscitation [5]. Even though we aren’t talking about the same population of patients, still it is important to learn that in those intensive care septic shock patients who had already been treated intensively, lactate clearance was the best parameter associated with 28-day mortality and the authors of this study recommended that a protocol of lactate clearance directed therapy should be considered in septic patients even after the golden hours [5]. Among undifferentiated children with SIRS, early hyperlactemia (>4 mmol/L) was significantly associated with increased risk of organ dysfunction, resuscitative therapies, and critical illness. Adding lactate level to the current clinical assessment may improve early identification of pediatric patients with sepsis requiring intensive care, and thus may prevent death in high risk patients [6].
Admission lactate >2mM was found to be an independent predictor of mortality in adults admitted to the ICU [7]. Odds Ratio (OR) for mortality increased from 1.94 to 10.89 dependent on the level of lactate (in comparison to patients with lactate level lower than 2mmol/L). Another study supported these findings and demonstrated a significant effect of elevated lactate level on admission (above 2.0mmol/L) on mortality in unselected ICU patients [8,9]. Other studies have shown the importance of elevated admission lactate on in-hospital mortality [10–20].
Blood lactate monitoring for risk assessment in the critically ill patient is still controversial. Some of the inconsistent data relates to the different screening methods – one measurement, several measurements, arterial or venous blood, peripheral or capillary blood. Sustained high lactate levels in ICU patients demonstrated by serial measurements have shown to be predictive of in hospital mortality [20–22]. In most of the studies the cut-off point was 2.0mmol/L. Jansen et al. assessed blood lactate at the site of injury and at the hospital, and found that mortality was higher in patients with lactate >3.5mmol/L at the site of injury or at admission to the hospital compared to patients with lactate level below 3.5mmol/L [11]. Prehospital lactate level had a better predictive prognostic value than vital signs such as blood pressure [23]. More than that, lactate-guided treatment (by giving erythrocytes, dobutamine, and fluids) lowered the in-hospital mortality significantly [24]. No significant difference was observed between peripheral arterial and venous blood lactate; the highest correlation was found between the radial artery and a peripheral vein. 20 Other studies supported these findings [24, 25].
5 Summary
Our study, evaluated by logistic regression, analyzed the independent variables that could predict death within 24 hours of admission for patients admitted with an infectious disease but without septic shock or severe sepsis. If we have to choose the most important and significant variable, then lactate level on admission higher than 2mmol/L predicted death within 24 hours of admission. The higher the lactate level, the higher the probability to die within 24 hours.
We also found that old age is another independent variable for death within 24 hours of admission.
We suggest measuring lactate level in the emergency department in order to improve the risk assessment and triage of patients admitted with an infectious disease, especially in older patients (older than 70 years).
Acknowledgements
We would like to thank the Research Galilee Center headed by Dr. Nadya Lisovoder for the statistical analysis and for secretarial editing of the paper.
Footnotes
Conflict of interest: Authors state no conflict of interest
References
- 1.Hilderink MJ, Roest AA, Hermans M, et al. Predictive accuracy and feasibility of risk stratification scores for 28-day mortality of patients with sepsis in an emergency department. Eur J Emerg Med. 2014 Aug 20; doi: 10.1097/MEJ.0000000000000185. Epub ahead of print. [DOI] [PubMed] [Google Scholar]
- 2.Jones AE, Saak K, Kline JA. Performance of the mortality in emergency department sepsis score for predicting hospital mortality among patients with severe sepsis and septic shock. Am J Emerg Med. 2008;26(6):689–692. doi: 10.1016/j.ajem.2008.01.009. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Sawicka W, Owczuk R, Wujtewicz MA, Wujtewicz M. The effectiveness of the APACHE II, SAPS II, and SOFA prognostic scoring systems in patients with haematological malignancies in the intensive care unit. Anaesthesiol Intensive Ther. 2014;46(3):166–170. doi: 10.5603/AIT.2014.0030. [DOI] [PubMed] [Google Scholar]
- 4.Kruse O, Grunnet N, Barford C. Blood lactate as a predictor for in hospital mortality in patients admitted acutely to hospital: a systemic review. Scandinavian Journal of Trauma, Resuscitation and Emergency Medicine. 2011;19:74–86. doi: 10.1186/1757-7241-19-74. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Marty P, Roquilly A, Vallée F, et al. Lactate clearance for death prediction in severe sepsis or septic shcok patients during the first 24 hours in intensive care unit: an observational study. Annals of Intensive Care. 2013;3:3–10. doi: 10.1186/2110-5820-3-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Scott HF, Donoghue AJ, Gaieski DF, et al. The utility of early lactate testing in undifferentiated pediatric systemic inflammatory response syndrome. Academic Emergency Medicine. 2012;19:1276–1280. doi: 10.1111/acem.12014. [DOI] [PubMed] [Google Scholar]
- 7.Khosravani H, Shahpori R, Stelfox HT, et al. Occurrence and adverse effect on outcome of hyperlactemia in the critically ill. Crit Care. 2009;13(3):R90. doi: 10.1186/cc7918. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Nichol AD, Egi M, Pettila V, et al. Relative hyperlactemia and hospital mortality in critically ill patients: a retrospective multi-centre study. Crit Care. 2010;14(1):R25. doi: 10.1186/cc8888. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Smith I, Kumar P, Molloy S, et al. Base excess and lactate as prognostic indicators for patients admitted to intensive care. Intensive Care Med. 2001;27(1):74–83. doi: 10.1007/s001340051352. [DOI] [PubMed] [Google Scholar]
- 10.Del Portal DA, Shofer F, Mikkelsen ME, et al. Emergency department lactate is associated with mortality in older adults admitted with and without infections. Acad Emerg Med. 2010;17(3):260–268. doi: 10.1111/j.1553-2712.2010.00681.x. [DOI] [PubMed] [Google Scholar]
- 11.Jansen TC, van BJ, Mulder PG, et al. The prognostic value of blood lactate levels relative to that of vital signs in the pre-hospital setting: a pilot study. Crit Care. 2008;12(6):R160. doi: 10.1186/cc7159. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Kaplan LJ, Kellum JA. Initial pH, base deficit, lactate, anion gap, strong ion difference, and strong ion gap predict outcome from major vascular injury. Crit Care Med. 2004;32(5):1120–1124. doi: 10.1097/01.ccm.0000125517.28517.74. [DOI] [PubMed] [Google Scholar]
- 13.Pal JD, Victorino GP, Twomey P, et al. Admission serum lactate levels do not predict mortality in the acutely injured patient. J Trauma. 2006;60(3):583–587. doi: 10.1097/01.ta.0000205858.82575.55. [DOI] [PubMed] [Google Scholar]
- 14.Vandromme MJ, Griffin RL, Weinberg JA, et al. Lactate is a better predictor than systolic blood pressure for determining blood requirement and mortality: could pre-hospital measures improve trauma triage? J Am Coll Surg. 2010;210(5):861–869. doi: 10.1016/j.jamcollsurg.2010.01.012. [DOI] [PubMed] [Google Scholar]
- 15.Arnold RC, Shapiro NI, Jones AE, et al. Multicenter study of early lactate clearance as a determinant of survival in patients with presumed sepsis. Shock. 2009;32(1):35–39. doi: 10.1097/shk.0b013e3181971d47. [DOI] [PubMed] [Google Scholar]
- 16.Guyette F, Suffoletto B, Castillo JL, et al. Pre hospital serum lactate as a predictor of outcomes in trauma patients: a retrospective observational study. J Trauma. 2011;70(4):782–786. doi: 10.1097/TA.0b013e318210f5c9. [DOI] [PubMed] [Google Scholar]
- 17.Trzeciak S, Dellinger RP, Chansky ME, et al. Serum lactate as a predictor of mortality in patients with infection. Intensive Care Med. 2007;33(6):970–977. doi: 10.1007/s00134-007-0563-9. [DOI] [PubMed] [Google Scholar]
- 18.Kaplan LJ, Kellum JA. Comparison of acid base models for prediction of hospital mortality after trauma. Shock. 2008;29(6):662–666. doi: 10.1097/shk.0b013e3181618946. [DOI] [PubMed] [Google Scholar]
- 19.Lavery RF, Livingston DH, Tortella BJ, et al. The utility of venous lactate to triage injured patients in the trauma center. J Am Coll Surg. 2000;190(6):656–664. doi: 10.1016/s1072-7515(00)00271-4. [DOI] [PubMed] [Google Scholar]
- 20.Nguyen HB, Rivers EP, Knoblich BP, et al. Early lactate clearance is associated with improved outcome in severe sepsis and septic shock. Crit Care Med. 2004;32(8):1637–1642. doi: 10.1097/01.ccm.0000132904.35713.a7. [DOI] [PubMed] [Google Scholar]
- 21.Claridge JA, Crabtree TD, Pelltier SJ, et al. Persistent occult hypoperfusion is associated with a significant increase in infection rate and mortality in major trauma patients. J Trauma. 2000;48(1):8–14. doi: 10.1097/00005373-200001000-00003. [DOI] [PubMed] [Google Scholar]
- 22.Jansen TC, van BJ, Mulder PG, et al. Prognostic value of blood lactate levels: does the clinical diagnosis at admission matter? J Trauma. 2009;66(2):377–385. doi: 10.1097/TA.0b013e3181648e2f. [DOI] [PubMed] [Google Scholar]
- 23.Jansen TC, van BJ, Schoonderbeek FJ, et al. Early lactate guided therapy in intensive care unit patients: a multicenter, open-label, randomized controlled trial. Am J Respire Crit Care Med. 2010;182(6):752–761. doi: 10.1164/rccm.200912-1918OC. [DOI] [PubMed] [Google Scholar]
- 24.Gallagher EJ, Rodriguez K, Touger M. Agreement between peripheral venous and arterial lactate levels. Annals Emerg Med. 1997;29(4):479–483. [PubMed] [Google Scholar]
- 25.Younger JG, Falk JL, Rothrock SG. Relationship between arterial and peripheral venous lactate levels. Acad Emerg Med. 1996;3(7):730–734. doi: 10.1111/j.1553-2712.1996.tb03502.x. [DOI] [PubMed] [Google Scholar]