v
Search
Advanced Search

Publications > Journals > Journal of Clinical and Translational Hepatology > Article Full Text

  • Original Article
  • OPEN ACCESS

Characteristics and Outcome of Exertional Heatstroke Patients Complicated by Acute Hepatic Injury: A Cohort Study

  • Jingjing Ji1,# ,
  • Jinghua Gao1,#,
  • Conglin Wang1,
  • Leifang Ouyang1,
  • Zheying Liu1 and
  • Zhifeng Liu1,2,* 
 Author information  Cite
Journal of Clinical and Translational Hepatology   2021;9(5):655-660

doi: 10.14218/JCTH.2021.00084

Abstract

Background and Aims

Exertional heatstroke (EHS) is associated with strenuous physical activity in hot environments. The present study aimed to investigate dynamic changes of hepatic function indices in EHS patients and determine risk factors for death.

Methods

This single-center retrospective cohort study considered all patients with EHS admitted to the intensive care unit at the General Hospital of Southern Theater Command of PLA from October 2008 to May 2019. Data on general characteristics, organ function parameters, and the 90-day outcome of enrolled patients were collected. Hepatic indices were collected dynamically, and patients with acute hepatic injury (AHI) were identified by plasma total bilirubin (TBIL) ≥34.2 µmol/L and an international normalized ratio ≥1.5, or with any grade of hepatic encephalopathy.

Results

In patients who survived, TBIL, alanine aminotransferase and aspartate aminotransferase were increased at 24 h, peaked at 2–3 days, and began to decrease at 5 days. In non-survivors, TBIL continuously increased post-admission. The area under the receiver operating characteristic curve for the prediction of mortality based on sequential organ failure assessment (SOFA) scores was 89.8%, and the optimal cutoff value was 7.5. Myocardial injury and infection were identified as independent risk factors for death in EHS patients with AHI.

Conclusions

In EHS patients, hepatic dysfunction usually occurred within 24 h. Patients with AHI had more severe clinical conditions, and significantly increased 90-day mortality rates. SOFA scores over 7.5, complicated with myocardial injury or infection, were found to be risk factors for death in EHS patients with AHI.

Keywords

Exertional heatstroke, Acute hepatic injury, Mortality, TBIL, SOFA

Introduction

Heatstroke is a life-threatening condition involving a significant elevation of core body temperature with central nervous system dysfunction, and includes symptoms such as combativeness, delirium, seizures, or even a comatose state.1,2 It has been reported that at least 3,332 deaths can be attributed to heatstroke between the years of 2006 to 2010 in the USA.3 As global warming worsens, the morbidity of heatstroke has increased, and it has been predicted that heatstroke-related deaths could increase to nearly 2.5 times the current annual baseline by 2050.4 Based on the underlying cause, heatstroke can be classified as either classical heatstroke (CHS) or exertional heatstroke (EHS). In both types, the increased core body temperature is attributed to excessive heat accumulation. CHS involves exposure to heat from the environment with poor heat dissipation, whereas EHS is associated with strenuous physical activity in hot environments and excessive production of metabolic heat that overwhelms physiological heat loss.5 It is still unclear whether the different mechanisms of initiation result in unique pathophysiological disease processes, but organ dysfunction may differ between these two types of heatstroke patients. EHS is usually observed in young, healthy men, most of whom have few underlying diseases. However, the incidence rate of hepatocellular insufficiency in EHS patients is higher compared to that in CHS patients.1,6 For EHS patients with severe acute liver failure, the hepatic injury due to EHS can result in death that occurs approximately 1 week after the onset of heatstroke, unless a liver transplant is performed.7,8

EHS remains a major problem for individuals who regularly meet strenuous physical demands, such as athletes, firefighters, and agricultural workers. The current knowledge regarding EHS patients complicated by acute hepatic injury (AHI) is limited. In the present study, the clinical and prognostic data of heatstroke patients admitted to the intensive care unit (ICU) at a single center in China over a 10-year period were retrospectively collected. The aim was to investigate the dynamic changes of hepatic function indices in EHS patients and determine the risk factors for death in these patients.

Methods

Study design and participants

Patients diagnosed with EHS in the ICU of the General Hospital of Southern Theater Command in China from October 2008 to May 2019 were considered for inclusion. The inclusion criteria9 consisted of 1) ≥ 18 years of age, and 2) met the diagnostic criteria of EHS. These diagnostic criteria included a history of strenuous activity (with or without exposure to hot and humid weather), concurrent hyperthermia (central temperature above 40°C), and neurological dysfunction (such as delirium, cognitive disorders, or disturbed consciousness). The exclusion criteria consisted of 1) existing irreversible underlying diseases affecting mortality, and 2) pregnant or breastfeeding women. The study was approved by the Research Ethics Commission of General Hospital of Southern Theater Command of PLA and the requirement for informed consent was waived by the Ethics Commission.

Research procedure

Patient characteristics, organ function parameters, and 90-day outcomes for all enrolled patients were collected. Scores according to the Acute Physiology and Chronic Health Evaluation II (APACHE II), the sequential organ failure assessment (SOFA), and the Glasgow coma scale (GCS) were also collected. The dynamic changes to hepatic indices, including total bilirubin (TBIL), alanine transaminase (ALT), aspartate transaminase (AST), and the international normalized ratio (INR) were evaluated. The time points included admission and 24 h, 2 d, 3 d, 5 d and 7 d after admission. Patients with AHI were identified by plasma levels of TBIL ≥34.2 µmol/L and an INR ≥1.5, or with any grade of hepatic encephalopathy. Myocardial injury was defined by plasma cardiac troponin I >0.2 µg/mL, and kidney injury was defined by serum creatinine >176 µmol/L. Rhabdomyolysis was defined by creatine kinase (CK) >1,000 IU, and patients with procalcitonin (PCT) >2 ng/mL and a white blood cell (WBC) count >10 × 109/L were considered to have an infection. Lymphopenia was defined by a lymphocyte count <0.8 × 109/L. Patients with a GCS score <8 were considered to have a central nervous system (CNS) disorder.1 The primary outcome was 90-day mortality, and the secondary outcome was the ICU length of stay.

Statistical analysis

Categorical data were summarized as numbers and percentages, and inter-group comparisons were performed using either Mann-Whitney U, χ2 or Fisher’s exact tests. Continuous variables were expressed as the median with interquartile range (IQR) and analyzed using a Wilcoxon rank-sum test, since most continuous variables did not show a Gaussian distribution. Kaplan-Meier survival curves and the log-rank test were used for survival analysis. To determine the independent risk factors of 90-day mortality in severe heatstroke patients with AHI, the Cox proportional hazards model was used. Significant indicators were identified using single-factor analysis, and those with a p-value <0.1 were included in the multifactor Cox regression model. The odds ratio (OR) and 95% confidence interval (CI) levels were presented. Statistical analysis was performed using R, version 3.4.0. A two-tailed p-value <0.05 was considered statistically significant.

Results

Dynamic changes of hepatic function indices in patients with EHS: Comparison of survivors and non-survivors

Data from a total of 189 patients were collected. Three cases were excluded due to missing data, and 186 cases were included for analysis. All 186 patients were male, with a median age of 21 years (IQR: 19–27) and without any underlying diseases prior to the onset of heatstroke. At admission, the concentration of TBIL in survivors was normal, but TBIL in non-survivors was slightly increased (Table 1). In patients who survived, TBIL was increased at 24 h, reached a peak between 2–3 days, and began to decrease after day 5. The concentrations of ALT and AST also showed similar changes to TBIL. In non-survivors, the levels of TBIL continuously increased following admission. ALT and AST levels were remarkably increased at 24 h until day 3 (Table 1). Though ALT and AST also decreased 5 days after admission, this did not indicate that the liver injury was alleviated; the decreased ALT and AST may have been due to considerable hepatocyte death. In both survivors and non-survivors, INRs increased immediately after the onset of heatstroke. INRs began to decrease after 24 h in the survival group, but remained high in the non-survival group. These results indicate that if hepatic function indices of an EHS patient are slightly increased between 24 h and 3 days following the onset of heatstroke, and the serum levels of TBIL continuously increase, the patient may have a higher risk of mortality.

Table 1

Dynamic changes of the hepatic function indexes in the survivor and non-survivor patients with EHS

Overall (n=186)Survivor (n=164)Non-survivor (n=22)p
TBIL in µmol/L
  Ad15.85 [10.10, 29.40]14.75 [9.80, 25.47]29.90 [14.98, 118.08]0.002
  24 h27.10 [15.45, 55.65]23.70 [15.07, 47.85]95.60 [53.53, 176.45]<0.001
  2 d36.65 [17.20, 87.28]28.90 [15.70, 55.70]176.00 [96.05, 198.20]<0.001
  3 d32.60 [17.60, 97.10]24.50 [16.40, 59.75]233.45 [166.45, 373.32]<0.001
  5 d23.85 [10.20, 83.05]18.90 [9.80, 36.10]390.30 [328.10, 422.00]<0.001
  7 d20.90 [12.20, 73.60]16.10 [9.70, 28.85]400.20 [251.33, 424.70]<0.001
ALT in U/L
  Ad34.50 [20.00, 222.75]32.00 [19.00, 149.50]170.50 [61.50, 1,648.25]<0.001
  24 h234.50 [56.25, 956.25]174.50 [47.25, 652.00]1,530.00 [792.75, 2,649.50]<0.001
  2 d383.00 [134.00, 1,389.50]355.00 [134.00, 1,112.50]1,660.00 [460.00, 3,474.00]0.017
  3 d468.00 [164.25, 1,431.00]407.50 [144.75, 1,094.75]2,573.50 [1,228.50, 4,911.50]<0.001
  5 d373.50 [129.00, 666.00]348.00 [110.00, 609.00]488.00 [370.50, 870.50]0.077
  7 d192.00 [106.00, 309.00]205.00 [94.50, 312.00]148.50 [115.75, 217.50]0.726
AST in U/L
  Ad66.50 [34.75, 228.00]62.00 [33.50, 163.50]356.00 [110.00, 1,645.00]<0.001
  24 h214.00 [60.00, 751.75]166.00 [57.00, 559.00]2,545.00 [631.00, 5,690.00]<0.001
  2 d278.00 [91.50, 947.50]250.00 [89.00, 625.00]2,635.00 [421.75, 5,159.00]<0.001
  3 d183.00 [70.50, 568.50]162.00 [66.50, 462.00]1,629.50 [359.50, 5,276.75]0.001
  5 d118.50 [59.00, 219.00]116.00 [56.00, 190.00]220.00 [101.00, 355.00]0.058
  7 d67.50 [39.25, 101.50]58.50 [34.50, 80.75]102.50 [75.00, 126.50]0.003
INR
  Ad1.29 [1.09, 1.76]1.24 [1.09, 1.47]3.22 [1.86, 4.82]<0.001
  24 h1.29 [1.09, 1.70]1.19 [1.07, 1.54]2.76 [2.20, 3.28]<0.001
  2 d1.14 [1.04, 1.65]1.10 [1.02, 1.32]2.82 [2.04, 3.59]<0.001
  3 d1.05 [0.97, 1.70]1.02 [0.96, 1.21]3.10 [2.07, 3.53]<0.001
  5 d1.01 [0.93, 1.21]0.98 [0.93, 1.11]3.02 [2.08, 4.04]<0.001
  7 d1.07 [0.99, 1.33]1.03 [0.98, 1.11]2.38 [1.53, 2.57]<0.001

d, day.

Characteristics and outcomes of EHS patients: Comparison of patients with and without AHI

To further investigate the characteristics of patients with AHI, all patients were divided into either the AHI group or non-AHI group. Among the 186 cases, 69 showed increased TBIL (≥34.2 µmol/L) and INR (≥1.5) and were placed in the AHI group (Table 2). Compared with the non-AHI group, patients in the AHI group showed increased WBC and neutrophil counts, and decreased lymphocyte and platelet counts. In addition, other organ dysfunction indices were also increased in the AHI group, including kidney (urea nitrogen, serum creatinine), muscle (rhabdomyolysis; creatine kinase (CK), CK-Mb), and cardiac (CTNI) injuries. Patients in the AHI group also showed decreased GCS, and increased APACHE II and SOFA scores compared to the non-AHI group. In addition, patients with AHI had increased ICU length of stays and 90-day mortality rates (Table 3). The 90-day mortality of EHS patients with AHI was 27.5% (19/69) but was only 2.6% (3/117) for patients without AHI. The survival times of EHS patients with AHI were also significantly lower compared to those without AHI (Fig. 1).

Table 2

Comparison of the characteristics between the EHS patients in the non-AHI group and AHI group

Overall (n=186)Non-AHI (n=117)AHI (n=69)p
Age21.00 [19.00, 27.00]20.00 [19.00, 27.00]23.00 [19.00, 27.00]0.263
WBC, ×109/L11.34 [8.72, 14.62]10.39 [8.61, 14.25]12.13 [9.04, 15.82]0.057
Neutrophil, ×109/L8.86 [6.54, 12.44]8.26 [5.80, 11.41]10.14 [7.42, 13.22]0.003
Lymphocyte, ×109/L1.11 [0.58, 1.89]1.35 [0.79, 2.12]0.73 [0.40, 1.63]<0.001
Monocyte, ×109/L0.68 [0.38, 0.99]0.68 [0.40, 0.97]0.66 [0.35, 1.00]0.581
PLT, ×109/L165.0 [82.00, 219.0]185.5 [148.8, 232.25]80.00 [35.00, 132.0]<0.001
BUN in mmol/L5.75 [4.50, 7.60]5.20 [4.20, 6.50]6.80 [5.40, 8.70]<0.001
SCR in μmol/L127.5 [92.00, 162.3]107.0 [82.00, 137.0]159.0 [128.0, 201.0]<0.001
CK in U/L904.0 [346.75, 2,537.0]572.0 [244.0, 1,810.0]1,452.0 [853.0, 4,573.0]<0.001
PT in s15.90 [14.10, 20.58]14.70 [13.70, 16.10]23.40 [18.80, 35.00]<0.001
APTT in s38.95 [33.52, 49.45]36.10 [32.60, 40.90]50.60 [39.20, 91.20]<0.001
Fib in g/L2.50 [2.00, 2.80]2.60 [2.30, 3.10]2.00 [1.58, 2.60]<0.001
D.D in mg/L1.86 [0.51, 7.00]0.70 [0.36, 2.16]9.49 [3.51, 14.55]<0.001
CK-Mb in ng/mL469.40[128.9, 1,000.0]239.1 [64.75, 594.5]1,000.0 [381.5, 1,000.0]<0.001
CTNI in ng/mL110.00 [21.40, 432.45]50.00 [10.00, 143.22]410.0 [125.90, 1,407.5]<0.001
CRP in mg/dL3.30 [1.48, 5.98]3.18 [0.67, 6.86]3.38 [3.14, 5.27]0.3
PCT in ng/mL1.70 [0.76, 4.14]1.43 [0.56, 3.97]2.05 [1.08, 4.69]0.083
GCS12.00 [7.00, 14.00]12.00 [9.00, 14.00]8.00 [6.00, 13.00]0.005
SOFA score3.00 [2.00, 6.00]3.00 [2.00, 4.00]6.00 [4.00, 9.00]<0.001
APACHE II score10.50 [8.00, 15.75]9.00 [7.00, 13.00]15.00 [10.00, 21.00]<0.001

APACHE, acute physiology and chronic health evaluation; APTT, activated partial thromboplastin time; BUN, blood urea nitrogen; CK, creatine kinase; CK-Mb, creatine kinase-Mb; CTNI, cardiac troponin I; CRP, C-reactive protein; D.D, D-dimer; GCS, glasgow coma scale; PCT, procalcitonin; PLT, platelets; PT, prothrombin time; SOFA, sequential organ failure assessment; SCR, serum creatinine; WBC, white blood cell.

Table 3

Comparison of the outcome between the EHS patients in Non-AHI group and AHI group

Overall (n=186)Non-AHI (n=117)AHI (n=69)p
ICU time in days5.00 [3.00, 9.00]4.00 [3.00, 7.00]8.00 [5.00, 14.00]<0.001
Outcome, %<0.001
  Survive164 (88.2)114 (97.4)50 (72.5)
  Death22 (11.8)3 (2.6)19 (27.5)
Survival curves of 90-day mortality rate in the AHI group and non-AHI group.
Fig. 1  Survival curves of 90-day mortality rate in the AHI group and non-AHI group.

Risk factors for EHS patients with AHI

To further determine the risk factors for death in EHS patients with AHI, the organ function indices of the survivors and non-survivors were compared (Table 4). The non-survivors had more severe disease conditions compared to survivors, as evidenced by higher levels of serum creatinine, CK, CTNI, PCT etc. at the time of admission. The non-survivors also had higher SOFA scores. The area under the receiver operating characteristic curve for the prediction of mortality based on the SOFA scores at the time of admission was 89.8%, and the optimal cutoff value was 7.5 (sensitivity of 90.0%, specificity of 80.6%; Fig. 2). Among the patients in the AHI group, 44 cases had myocardial injuries, 32 cases had injury to the kidney, 57 cases were experiencing rhabdomyolysis, 18 cases had a CNS disorder, 45 cases had an infection, and 54 cases showed signs of lymphopenia. Single variable analysis showed that complications due to myocardial injuries, a CNS disorder or infection were risk factors for death in patients with AHI (Table 5). The ORs were 13.10 (95% CI: 1.74, 98.26; p=0.012), 2.86 (95% CI: 1.15, 6.96; p=0.024) and 6.14 (95% CI: 1.42, 26.62; p=0.025), respectively. In the multi-variate analysis, myocardial injury and infection were found to be independent risk factors for death in EHS patients with AHI, with ORs of 12.169 (95% CI: 1.526, 94.806; p=0.023) and 5.637 (95% CI: 1.219, 26.064; p=0.027), respectively.

Table 4

Comparison of the characteristics between the survivors and non-survivors in the AHI group

Overall (n=69)Survivor (n=50)Non-survivor (n=19)p
Age23.00 [19.00, 27.00]23.00 [20.00, 27.00]21.00 [18.00, 23.50]0.103
WBC, ×109/L12.13 [9.04, 15.82]12.22 [9.37, 15.71]10.56 [8.46, 15.48]0.648
Neutrophil, ×109/L10.14 [7.42, 13.22]10.61 [7.95, 13.71]8.86 [6.38, 13.18]0.323
Lymphocyte, ×109/L0.73 [0.40, 1.63]0.73 [0.51, 1.55]0.67 [0.33, 2.81]0.909
Monocyte, ×109/L0.66 [0.35, 1.00]0.64 [0.36, 1.00]0.73 [0.26, 0.90]0.92
PLT, ×109/L80.00 [35.00, 132.00]85.50 [42.25, 167.00]72.00 [29.00, 89.00]0.097
BUN in mmol/L6.80 [5.40, 8.70]6.55 [5.40, 8.10]8.10 [6.30, 9.25]0.209
SCR, μmol/L159.00 [128.00, 201.00]146.00 [125.50, 171.50]228.00 [189.00, 280.00]<0.001
CK in U/L1,452.0 [853.00, 4,573.0]1,278.0 [803.00, 3,769.0]3,220.0 [1,014.0, 7,931.5]0.076
PT in s23.40 [18.80, 35.00]21.25 [16.33, 26.90]37.50 [25.70, 45.00]<0.001
APTT in s50.60 [39.20, 91.20]44.90 [37.68, 68.18]91.20 [77.35, 122.85]<0.001
Fib in g/L2.00 [1.58, 2.60]2.20 [1.70, 2.60]1.30 [0.90, 1.90]0.001
D.D in mg/L9.49 [3.51, 14.55]5.32 [1.61, 13.06]10.27 [10.00, 20.00]0.001
CK-Mb in ng/mL1,000.0 [381.48, 1,000.0]789.00 [264.90, 1,000.0]1,000.0 [967.55, 1,000.0]0.088
CTNI in ng/mL410.00 [125.90, 1,407.50]230.00 [100.00, 699.90]1,530.0 [952.80, 2,930.0]<0.001
CRP in mg/dL3.38 [3.14, 5.27]3.37 [2.13, 5.37]3.38 [3.30, 3.58]0.668
PCT in ng/mL2.05 [1.08, 4.69]2.02 [0.97, 4.08]2.95 [1.46, 5.81]0.263
GCS8.00 [6.00, 13.00]10.00 [6.00, 14.00]5.50 [3.00, 7.00]0.003
SOFA score6.00 [4.00, 9.00]5.00 [3.00, 7.00]11.50 [9.25, 13.75]<0.001
APACHE II score15.00 [10.00, 21.00]14.00 [8.00, 16.50]22.50 [18.50, 23.75]0.001
Receiver operating characteristic curve analysis of SOFA to predict the 90-day mortality of patients with AHI.
Fig. 2  Receiver operating characteristic curve analysis of SOFA to predict the 90-day mortality of patients with AHI.
Table 5

Risk factors for the EHS patients with AHI

VariableUnivariate
Multivariate
OR (95 % CI)pOR (95 % CI)p
Myocardial injury13.10 (1.744, 98.26)0.01212.169 (1.562, 94.806)0.023
Kidney injury1.156 (0, Inf)0.997
Rhabdomyolysis2.077 (0.476, 9.992)0.328
CNS disorder2.862 (1.147, 6.96)0.0241.106 (0.425, 2.879)0.837
Infection6.143 (1.418, 26.62)0.1535.637 (1.219, 26.064)0.027
Lymphopenia28.78 (0, Inf)0.998

Inf, infinity.

Discussion

The present retrospective cohort study revealed that hepatic dysfunction usually occurred within 24 h after admission in EHS patients. The patients with AHI had more severe clinical conditions, significantly increased 90-day mortality rates, and shorter survival times. Complications with myocardial injuries or infection were found to be independent risk factors for death in EHS patients with AHI.

The time course of liver damage was found to differ from the damage-associated markers of other organs, since liver damage was often not detected at the onset of heatstroke.10 These results revealed that TBIL levels were increased at 24 h, peaked at 2–3 days, and began to decrease after day 5 in the survivors, while the non-survivors showed continuously increased levels of TBIL after admission. An animal heatstroke model has indicated that heat stress leads to extensive hepatocyte ballooning degeneration and necrosis.11 Data from patient autopsies have revealed that EHS-associated liver damage is characterized by centrilobular degeneration and necrosis with parenchymal damage.1,12 Previous studies have also found that the inhibition of inflammatory mediators, such as high-mobility group box 1 (HMGB1), could alleviate liver injury in a rat model of heatstroke, as evidenced by decreased levels of ALT and AST.11,13 The modulation of coagulation by thrombomodulin was also shown to improve liver function.14 Therefore, the hepatocyte damage in heatstroke patients is thought to be caused by a multifactorial damaging effect, including hyperthermia in combination with hypoxia, inflammatory stimuli, ischemia, and disseminated intravascular coagulation.15,16

Liver dysfunction is not usually detected at the onset of heatstroke, unlike damages to other organs that can be detected much earlier, such as injury to the myocardia or coagulation dysfunction. Currently, the liver is regarded as one of the first organs that becomes injured during heatstroke. Heat stress and the subsequent inflammatory response and coagulation dysfunction could lead to the damage of hepatocytes as well as liver sinusoidal endothelial cells and intrahepatic biliary epithelial cells, characterized by an increase in aminopherase and bilirubin. However, since liver compensatory mechanisms can maintain liver function, the dysfunction indices do not always directly correlate with damage to the liver. In addition, the secondary factors of heat stress, such as the systemic inflammatory response or liver ischemia, could further aggravate liver damage. These factors might also contribute to the delayed detection of liver damage. In the current study, non-survivor EHS patients had concentrations of TBIL over 2-fold higher at 24 h after admission, and these levels continuously increased, suggesting that a dramatic and continuous increase of TBIL may indicate a poor prognosis. Notably, since the liver plays a significant role in the synthesis of coagulation factors, INR was also regarded as a major index for liver function. However, during the pathological process of heatstroke, coagulation dysfunction occurs at an early stage due to the activation of endothelial cells. Therefore, INR was increased at the onset of heatstroke, which differed from other liver function indices.

During the pathophysiological process of heatstroke, the primary cell damage was due to heat-induced necrotic and apoptotic cell death. In later stages, thermoregulatory failure combined with an inflammatory reaction results in multiorgan failure that can cause death. Autopsy studies show that end-organ failure following heatstroke is accompanied by widespread microthrombosis, hemorrhage, and inflammatory injury.5,17,18 In the current study, EHS patients with AHI showed a higher all-cause mortality compared to those without AHI. Hepatocyte damage could result in a weakened detoxification process and decreased protein synthesis, which further increases the risk of infection and coagulation dysfunction. In addition, another explanation could be that EHS patients with AHI were in a more severe condition. Compared to patients in the non-AHI group, the organ dysfunction indices were increased in the AHI group, including those that indicate kidney injury, rhabdomyolysis, and cardiac injury.

To further clarify the risk factors for EHS patients with AHI, since most EHS patients in the AHI group were also experiencing dysfunction of other organs, a Cox hazard analysis was used to investigate the risk factors for death. A single variable analysis showed that complications with myocardial injuries, CNS disorders or infection were risk factors for death. In the multi-variate analysis, myocardial injuries and infection were found to be independent risk factors for death in EHS patients with AHI. In healthy individuals, bacteria are rarely cultured from the systemic circulation, and the liver plays an important role in eliminating micro-organisms from the blood.19 As a result, AHI may contribute to increased circulating endotoxin levels in heatstroke patients due to decreased bacterial clearance function. In EHS patients with AHI and myocardial injury or infection, the circulatory stability was affected. Unstable circulation may aggravate injuries of other organs due to hypoperfusion, leading to an increased risk of death, especially in the acute phase.

Conclusions

In EHS patients, hepatic dysfunction usually occurred 24 h after onset. EHS patients with AHI had more severe clinical conditions, significantly increased 90-day mortality rates, and shorter survival times. Complications of myocardial injuries and infection were found to be independent risk factors for death in EHS patients with AHI.

Abbreviations

AHI: 

acute hepatic injury

ALT: 

alanine transaminase

APACHE: 

acute physiology and chronic health evaluation

APTT: 

Activated Partial Thromboplastin Time

AST: 

aspartate transaminase

BUN: 

Blood Urea Nitrogen

CHS: 

classical heatstroke

CK: 

creatine kinase

CK-Mb: 

creatine kinase-Mb

CNS: 

central nervous system

CTNI: 

cardiac troponin I

CRP: 

C-reactive protein

D.D: 

D-dimer

EHS: 

exertional heatstroke

GCS: 

glasgow coma scale

ICU: 

intensive care unit

INR: 

international normalized ratio

IQR: 

interquartile range

OR: 

odds ratio

PCT: 

procalcitonin

PLT: 

platelets

PT: 

prothrombin time

SOFA: 

sequential organ failure assessment

SCR: 

serum creatinine

TBIL: 

total bilirubin

WBC: 

white blood cell

Declarations

Data sharing statement

The data sets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Funding

This work was supported by grants from the National Natural Science Foundation of China [No. 82072143], the Natural Science Foundation of Guangdong Province of China [No. 2021A1515010170], and the PLA Logistics Research Project of China [Nos. 18CXZ030, BLJ20J006].

Conflict of interest

The authors have no conflict of interests related to this publication.

Authors’ contributions

Study concept and design (ZfL, JJ), data collecting (JG, CW, LO, ZyL), statistical analysis (ZfL, JJ), manuscript drafting (JJ, JG, ZfL).

References

  1. Leon LR, Bouchama A. Heat stroke. Compr Physiol 2015;5(2):611-647 View Article
  2. Bouchama A, Knochel JP. Heat stroke. N Engl J Med 2002;346(25):1978-1988 View Article
  3. Gaudio FG, Grissom CK. Cooling methods in heat stroke. J Emerg Med 2016;50(4):607-616 View Article
  4. Argaud L, Ferry T, Le QH, Marfisi A, Ciorba D, Achache P, et al. Short- and long-term outcomes of heatstroke following the 2003 heat wave in Lyon, France. Arch Intern Med 2007;167(20):2177-2183 View Article
  5. Epstein Y, Yanovich R. Heatstroke. N Engl J Med 2019;380(25):2449-2459 View Article
  6. Abriat A, Brosset C, Brégigeon M, Sagui E. Report of 182 cases of exertional heatstroke in the French Armed Forces. Mil Med 2014;179(3):309-314 View Article
  7. Bi X, Deising A, Frenette C. Acute liver failure from exertional heatstroke can result in excellent long-term survival with liver transplantation. Hepatology 2020;71(3):1122-1123 View Article
  8. Hassanein T, Razack A, Gavaler JS, Van Thiel DH. Heatstroke: its clinical and pathological presentation, with particular attention to the liver. Am J Gastroenterol 1992;87(10):1382-1389
  9. Hifumi T, Kondo Y, Shimizu K, Miyake Y. Heat stroke. J Intensive Care 2018;6:30 View Article
  10. Deutsch M, Koskinas J, Emmanuel T, Kountouras D, Hadziyannis S. Heat stroke and multi-organ failure with liver involvement in an asylum-seeking refugee. J Emerg Med 2006;31(3):255-257 View Article
  11. Geng Y, Ma Q, Liu YN, Peng N, Yuan FF, Li XG, et al. Heatstroke induces liver injury via IL-1β and HMGB1-induced pyroptosis. J Hepatol 2015;63(3):622-633 View Article
  12. Malamud N, Haymaker W, Custer RP. Heat stroke; a clinico-pathologic study of 125 fatal cases. Mil Surg 1946;99(5):397-449
  13. Tong H, Tang Y, Chen Y, Yuan F, Liu Z, Peng N, et al. HMGB1 activity inhibition alleviating liver injury in heatstroke. J Trauma Acute Care Surg 2013;74(3):801-807 View Article
  14. Kawasaki T, Okamoto K, Kawasaki C, Sata T. Thrombomodulin improved liver injury, coagulopathy, and mortality in an experimental heatstroke model in mice. Anesth Analg 2014;118(5):956-963 View Article
  15. Kew M, Bersohn I, Seftel H, Kent G. Liver damage in heatstroke. Am J Med 1970;49(2):192-202 View Article
  16. Kew MC, Minick OT, Bahu RM, Stein RJ, Kent G. Ultrastructural changes in the liver in heatstroke. Am J Pathol 1978;90(3):609-618
  17. Bouchama A, Roberts G, Al Mohanna F, El-Sayed R, Lach B, Chollet-Martin S, et al. Inflammatory, hemostatic, and clinical changes in a baboon experimental model for heatstroke. J Appl Physiol (1985) 2005;98(2):697-705 View Article
  18. Roberts GT, Ghebeh H, Chishti MA, Al-Mohanna F, El-Sayed R, Al-Mohanna F, et al. Microvascular injury, thrombosis, inflammation, and apoptosis in the pathogenesis of heatstroke: a study in baboon model. Arterioscler Thromb Vasc Biol 2008;28(6):1130-1136 View Article
  19. Nolan JP. Endotoxin, reticuloendothelial function, and liver injury. Hepatology 1981;1(5):458-465 View Article
Copyright © 2021 Authors. This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 4.0 License (CC BY-NC 4.0), permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
  • Journal of Clinical and Translational Hepatology
  • pISSN 2225-0719
  • eISSN 2310-8819

Article Options

Metrics

Cite this Article

  • © 2024 Xia & He Publishing Inc.
  • Total visits : 2642816
  • Visits today : 1630
Back to Top

Characteristics and Outcome of Exertional Heatstroke Patients Complicated by Acute Hepatic Injury: A Cohort Study

Jingjing Ji, Jinghua Gao, Conglin Wang, Leifang Ouyang, Zheying Liu, Zhifeng Liu
  • Reset Zoom
  • Download TIFF