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ORIGINAL ARTICLE
Year : 2015  |  Volume : 10  |  Issue : 3  |  Page : 190-194

Hypocalcemia as a prognostic factor in mortality and morbidity in moderate and severe traumatic brain injury


1 Department of Neurosurgery, Evangelic Hospital Oldenburg, Medical Campus University of Oldenburg, Germany
2 Department of Clinical Epidemiology, Faculty of Medicine, San Luis Potosi, Mexico
3 Department of Neurosurgery Bathildis Krankenhaus, Bad Pyrmont, Germany

Date of Web Publication22-Jul-2015

Correspondence Address:
Sanchez-Aguilar Martin
Clinic of Neurosurgery, Evangelisches Krankenhaus Oldenburg, Oldenburg
Mexico
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Source of Support: Nil, Conflict of Interest: None declared.


DOI: 10.4103/1793-5482.161171

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  Abstract 

Objectives: Our main objective was to evaluate whether serum hypocalcaemia (defined as <2.1 mmol/L [8.5 mg/dL]) and ionized serum calcium (defined as <1.10 mmol/L [4.5 mg/dL]) is a prognostic factor for mortality and morbidity (defined as Glasgow outcome score [GOS] ≤3) in early moderate and severe traumatic brain injury (TBI).
Materials and Methods: We developed a retrospective study and evaluated clinical profiles from included patients from January 2004 to December 2012. Patients were between 16 and 87 years old and had a Glasgow coma scale of 3–13 points following TBI, with demonstrable intracranial lesions in cranial computed tomography.
Results: We found a significant statistical difference (P < 0.008) in the ionized serum calcium levels on the 3rd day of admission between the groups: GOS ≤3 and >3 (disability/death). According with the receiving operative curves analysis, we found that the best level of higher sensitivity (83.76%) and specificity (66.66%) of hypocalcaemia of serum ionized calcium on 3rd day was the value of 1.11 mmol/L, with an odds ratio value of 6.45 (confidence intervals 95%: 2.02–20.55).
Conclusions: The serum levels of ionized calcium on day 3 could be useful for the prediction of mortality and disability in patients with moderate and severe TBI.

Keywords: Glasgow outcome score, hypocalcemia, ionized serum calcium, prognostic factor, traumatic brain injury


How to cite this article:
Manuel VRJ, Martin SA, Juan SRJ, Fernando MAL, Frerk M, Thomas K, Christian H. Hypocalcemia as a prognostic factor in mortality and morbidity in moderate and severe traumatic brain injury. Asian J Neurosurg 2015;10:190-4

How to cite this URL:
Manuel VRJ, Martin SA, Juan SRJ, Fernando MAL, Frerk M, Thomas K, Christian H. Hypocalcemia as a prognostic factor in mortality and morbidity in moderate and severe traumatic brain injury. Asian J Neurosurg [serial online] 2015 [cited 2020 Sep 27];10:190-4. Available from: http://www.asianjns.org/text.asp?2015/10/3/190/161171


  Introduction Top


Traumatic brain injury (TBI) is one of the most common disorders within the vast neurological field. The incidence of TBI in Germany is approximately 332 per 100,000, in comparison to 182 per 100,000 for strokes.[1] The effects from TBI can result in severe disability or death[2],[3] and have an important social and economic impact.[4] Despite of advances in technology and increasing knowledge about its pathophysiology, there are few predictors for outcome after TBI, with magnetic resonance imaging (MRI) findings being the most important.[4],[5]

Recent adoption of high throughput technologies and a change in focus from the identification of markers has fostered new optimism in this direction.[6]

Different markers have been studied, particularly bivalent cations as magnesium Mg (2+) and calcium.[6][7][8]

Objective

Our objective was to evaluate whether serum hypocalcemia (defined as <2.1 mmol/L [8.5 mg/dL]) and hypocalcemia of ionized serum calcium (defined as <1.10 mmol/L [4.5 mg/dL]) is a prognostic factor for mortality and morbidity (defined as Glasgow outcome score [GOS] ≤3) in early moderate and severe TBI.


  Materials and Methods Top


We developed a retrospective study evaluating clinical profiles from included patients from January 2004 to December 2012. Patients were between 16 and 87 years old and had a Glasgow coma scale (GCS) of 3–13 points following TBI, with demonstrable intracranial lesions in cranial computed tomography. The retrospective evaluated patients were included from the registries from the University Clinic Evangelisches Krankenhaus, Oldenburg, Germany.

Patients with the following characteristics were excluded:

  • TBI older as 3 days
  • Intake of medicaments, conditions or diseases affecting calcium metabolism (such as hyperparathyroidism, acute pancreatitis, massive blood transfusion, and treatment with hydrochlorothiazide)
  • Multisystem trauma, exposed fracture, lacerated spleen, liver, great vessels or hypovolemic shock III-IV
  • Lesions in the brainstem as an isolated finding
  • Previous treatment in another clinic
  • Pregnancy
  • Hyperphosphatemia (>1.32 mmol/L)
  • Hypomagnesemia (<0.61 mmol/L)
  • Alcoholism
  • Hypoalbuminemia at the hospitalary admittance
  • Prior disability to TBI.
Management and intervention

The patients were admitted to the emergency room and handled according to the guidelines of Advanced Trauma Life Support. Once the patients were stabilized, blood samples for hematic biometry, blood chemistry and serum electrolytes (sodium, potassium, calcium, ionized calcium), and arterial blood gases were taken.

The routine treatment included a crystalloid solution, gastric protector, analgesic and sedative in case of agitation. For intubation purposes, we used propofol plus rocuronium.

Clinical variables at hospital admittance consisted of age, sex, seizures, and pupillary reaction assessment. We measured respiratory and cardiac frequency, as well as, arterial systolic, diastolic, and mean arterial pressures.

Statistical analysis

We utilized the program JMP.[7][8][9] We completed an analysis of descriptive statistics, obtaining the measures of central tendency and dispersion of all the variables. For the comparative analysis, we used the Student’s t-test for continuous variables with normal distribution and the Wilcoxon/Kruskal–Wallis test for continuous variables without normal distribution. For categorical variables, the Chi-squared test was applied and for tables with boxes <5, the Fisher’s exact test was utilized. Statistical significance was considered with a value of P < 0.05. We calculated the odds ratio (OR) with of confidence intervals (CI) of 95%. We made an analysis of logistic regression with the variables that showed a significant difference (P < 0.05) in the bivariate analysis. In the final model, they were expressed with OR (CI 95%), as well as with multiple coefficient correlation R2. We also made an analysis of receiving operative curves (ROC) in order to determine the level of higher sensitivity and specificity. There were calculated sensitivity, specificity, predicted positive value, and predicted negative value for different points of clinical interest.


  Results Top


We compiled data from 99 patients with moderate and severe TBI that fulfilled the inclusion criteria with a median age of 42 years old (range: 16–87). From the studied patients, 67 (67.67%) were of male gender and 32 (32.32%) of female gender. Fifty-two (52.52%) patients had a GOS ≤3 and 47 (47.47%) had a GOS >3. The demographic and clinical variables, basal pH levels, and number of days in the intensive care unit are shown in [Table 1].
Table 1: Demographic and clinical variables, basal pH levels, intubation days, and number of admittance days in the ICU

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After evaluation of the hospitalization variables, it could be seen that most of them did not show a significant difference, with the exception of GCS at the admittance (0.041), mean arterial pressure at admittance (0.018) and GCS at discharge (<0.001) known to be risk factors associated with poor prognosis. In our study, there were no differences in the demographic variables, basal pH levels, and number of days in the intensive care unit and days of intubation [Table 1], as well as in the blood cellularity measures and serum electrolyte levels at hospital admittance [Table 2]. Therefore, we consider the variables at the beginning of our study as nonhomogenous especially regarding GCS upon arrival. The GCS at the admittance was analyzed in each group separately due to the marked difference between the groups in order to avoid a statistical bias, mean arterial pressure, and Hemoglobin at day 3 was considered in the analysis of logistic regression as a potential confounding factor [Table 3].
Table 2: Chemistry variables and blood cellularity at0 and 3days

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Table 3: Logistic regression model: GOS≤3

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The comparison in the GCS at the discharge between groups is statistical significant (P < 0.001) this is explained because of the bad prognosis of the second group [Table 1].

We found a significant statistical difference (P < 0.008) in the ionized serum calcium levels on the 3rd day of admission between the groups: GOS ≤3 and >3 (disability/death) [Table 2]. In the serum sodium levels on the 7th day, we also found a statistical difference (P < 0.047) between groups [Table 2].

We calculated an OR of 6.6 (95% CI: 2.28–40.36) (P < 0.009) for the association of hypocalcemia of ionized serum calcium (<1.10 mmol/L) on 3rd day and the disability/death group.

The best logistic regression model included: Absent pupillary reactivity, hypocalcemia of ionized serum calcium (<1.10 mmol/L) on day 3, and serum sodium dysregulation on day 7. These variables substantiated poor GOSs in 28.08% (R2 = 0.2808, P < 0.002) [Table 3].

In our model, we have attempted to analyze the studied variables in order to establish which of them influence the dependent variable, GOS.

It appears that in the included cases, pupillary reactivity, hypocalcemia of ionized serum calcium on day 3 and serum sodium dysregulation on day 7 following trauma were significant factors in our study. However, in comparison to our initial results, GCS at admittance (analyzed separately in each group in order to avoid a statistical bias as mentioned before), mean arterial pressure at admittance and hemoglobin at day 3 was nonsignificant and thereby potential confusing factors.

According with the ROC analysis, we found that the best level of higher sensitivity (83.76%) and specificity (66.66%) of ionized serum calcium on 3rd day was the value of 1.11 mmol/L), with an OR value of 6.45 (CI 95%: 2.02–20.55). Other levels of clinical importance can also be seen in [Table 4].
Table 4: Levels of ionized serum calcium on 3rd day of clinical importance

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  Discussion Top


We found ionized calcium values in serum on the third posttraumatic day to be a prognostic factor for mortality and morbidity in moderate/severe TBI, with a level of significance of P < 0.008 in our study. A similar result was seen in our previous study demonstrating a significant difference for serum hypocalcemia at day 3 after TBI between survivors and nonsurvivors.[7]

The role of hypocalcemia in moderate/severe TBI still remains unclear. However, based on the initially proposed pathophysiological mechanism hypocalcemia could interfere with the development of cerebral edema due to neuronal death [Figure 1]. As an indirect sign patients with bad outcome had an impaired pupillary reactivity. The latter is a crucial clinical sign for intracranial elevated pressure with imminent risk of cerebral herniation/cerebral ischemia correlating with bad prognosis.[10],[11]
Figure 1: Proposed pathophysiological mechanism

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Although the role of hypocalcemia is poorly understood, in our study there was an association of hypocalcemia at 3rd day in ionized calcium after moderate/severe TBI with bad outcome (GOS ≤3).

A variety of mechanisms have been postulated to be involved in TBI such as neuroinflammation, neuronal hypoxia, loss of cerebral vessel autoregulation, and brain edema with MRI as a reliable prognostic marker.[12][13][14][15] In the following their role in hypocalcemia following TBI will be discussed.

We described that depending on the level of hypocalcemia, the risk for the patient to die or suffer moderate/severe disability varies significantly. A worst or poor outcome, defined as death or moderate/severe disability respectively, was evident in all patients with a level of hypocalcemia of 0.95 mmol/L or lower. In addition, our results demonstrated that 83.76% of patients had an unfavorable outcome, consisting of death or moderate/severe disability when the serum hypocalcemia level was lower than 1.11 mmol/L.

The association of hypocalcemia with morbidity and mortality after TBI could be the diminution of ionized calcium due to the sudden influx of intracellular ionized calcium. This could induce neuronal postischemic damage.[16] As mentioned above an increase of intracellular calcium plays a role in apoptotic processes due to inhibition of mitochondrial enzymatic processes and lipase activation.[16]

Moreover, the chemical binding of ionized calcium to proinflammatory proteins/molecules might play a role. These are elevated following trauma due to tissue hypo-oxygenation and increase of the catabolic and proinflammatory processes.[12],[17]

Secondary hypoxia after TBI promotes adverse outcomes in patients with TBI. One cause might be the loss of cerebrovascular autoregulation, as a consequence of hypoxia and neuroinflammation.[15],[17] Different study groups discovered that TBI combined with hypoxia enhances cerebral cytokine production.[15][16][17]

At the beginning of our analysis, the GCS values at admittance demonstrated a significant difference between the groups of patients. Later according to the logistic regression analysis, the GCS at admittance was not significant in explain the difference between the group of patients in ionized serum calcium on day 3, becoming a confounding bias. Herewith GCS at admittance cannot be considered a significant determinator in our study.

The pupillary reactivity was not significant in the comparative analysis between patients with a GOS ≤3 and those with a GOS >3. Considering the fact that pupillary reactivity is a well-known and important clinical sign for highly elevated intracranial pressure and, therefore, a prognostic factor for outcome, we included it into our calculations.

We found pupillary reactivity to be significant in the final regression model, confirming its role as a crucial prognostic factor for mortality.

Retrospective data collection could limit the validity of our findings because of possible inherent bias. In our study, this possibly can be attributed to diverse primary clinical documentation or inconsistencies in data registration and the fact that data were collected by the first Author only (JMVR).

It is necessary to perform additional prospective and controlled studies with a larger population and a longer follow-up period in order to improve the statistical significance of the obtained data avoiding the possible source of bias such as missing information or discrepancies in patient’s data.


  Conclusion Top


As seen in our study, the serum levels of ionized calcium on day 3 as well as impaired pupillary reactivity are significantly associated with higher mortality and disability rates in patients with moderate and severe TBI. We believe that the value of ionized serum calcium of 1.11 mmol/L can be utilized as a reliable cut-off point.

Therefore, hypocalcemia should alert the treating physician and make him aware of the severity of the on-going pathophysiological process.



 
  References Top

1.
Health report for Germany; 2006. Available from: http:// www.gbe-bund.de/ .  Back to cited text no. 1
    
2.
Müller K, Ingebrigtsen T, Wilsgaard T, Wikran G, Fagerheim T, Romner B, et al. Prediction of time trends in recovery of cognitive function after mild head injury. Neurosurgery 2009;64:698-704.  Back to cited text no. 2
    
3.
Willemse-van Son AH, Ribbers GM, Verhagen AP, Stam HJ. Prognostic factors of long-term functioning and productivity after traumatic brain injury: A systematic review of prospective cohort studies. Clin Rehabil 2007;21:1024-37.  Back to cited text no. 3
    
4.
Heegaard W, Biros M. Traumatic brain injury. Emerg Med Clin North Am 2007;25:655-78, viii.  Back to cited text no. 4
    
5.
Woischneck D, Lerch K, Kapapa T, Skalej M, Firsching R. Predictive quality of the injury severity score in the systematic use of cranial MRI. Z Orthop Unfall 2010;148:548-53.  Back to cited text no. 5
    
6.
Di Battista AP, Rhind SG, Baker AJ. Application of blood-based biomarkers in human mild traumatic brain injury. Front Neurol 2013;4:44.  Back to cited text no. 6
    
7.
Vinas-Rios JM, Sanchez-Aguilar M, Sanchez-Rodriguez JJ, Gonzalez-Aguirre D, Heinen C, Meyer F, et al. Hypocalcaemia as a prognostic factor of early mortality in moderate and severe traumatic brain injury. Neurol Res 2014;36:102-6.  Back to cited text no. 7
    
8.
Hästbacka J, Pettilä V. Prevalence and predictive value of ionized hypocalcemia among critically ill patients. Acta Anaesthesiol Scand 2003;47:1264-9.  Back to cited text no. 8
    
9.
JMP®, Version <x>. SAS Institute Inc., Cary, NC, 1989-2007.  Back to cited text no. 9
    
10.
Dickerson RN, Morgan LM, Martin A. Croce treatment of moderate to severe acute hypocalcemia in critically trauma patients. JEPN J Parenter Nutr 2007;31:228.  Back to cited text no. 10
    
11.
Zivin JR, Gooley T, Zager RA, Ryan MJ. Hypocalcemia: A pervasive metabolic abnormality in the critically ill. Am J Kidney Dis 2001;37:689-98.  Back to cited text no. 11
    
12.
Dias CR, Leite HP, Nogueira PC, Brunow de Carvalho W. Ionized hypocalcemia is an early event and is associated with organ dysfunction in children admitted to the intensive care unit. J Crit Care 2013;28:810-5.  Back to cited text no. 12
    
13.
Murillo-Rodriguez. Head trauma in the child and teenager. Moderate Traumatic Brain Injury. 1st ed. México, D.F: McGrawhill; 2007. p. 46-7.  Back to cited text no. 13
    
14.
Buriticá E, Villamil L, Guzmán F, Escobar MI, García-Cairasco N, Pimienta HJ. Changes in calcium-binding protein expression in human cortical contusion tissue. J Neurotrauma 2009;26:2145-55.  Back to cited text no. 14
    
15.
Lucas SM, Rothwell NJ, Gibson RM. The role of inflammation in CNS injury and disease. Br J Pharmacol 2006;147 Suppl 1:S232-40.  Back to cited text no. 15
    
16.
Balbino M, Capone Neto A, Prist R, Ferreira AT, Poli-de-Figueiredo LF. Fluid resuscitation with isotonic or hypertonic saline solution avoids intraneural calcium influx after traumatic brain injury associated with hemorrhagic shock. J Trauma 2010;68:859-64.  Back to cited text no. 16
    
17.
Zhang M, Shan H, Gu Z, Wang D, Wang T, Wang Z, et al. Increased expression of calcium/calmodulin-dependent protein kinase type II subunit d after rat traumatic brain injury. J Mol Neurosci 2012;46:631-43.  Back to cited text no. 17
    


    Figures

  [Figure 1]
 
 
    Tables

  [Table 1], [Table 2], [Table 3], [Table 4]


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