A Systematic Review on Outcomes of Patients with Heatstroke and Heat Exhaustion

Abstract

Introduction

Heatstroke (HS) is a severe form of heat-related illness (HRI) associated with high morbidity and mortality, representing a condition that includes long-term multiorgan dysfunction and susceptibility to further heat illness.

Methods

In a systematic review searching Medline PubMed from the studies conducted between 2009 and 2020, 16 papers were identified.

Results

A hallmark symptom of heat stroke is CNS dysfunction (a hallmark sign of HS) which manifests as mental status changes, including agitation, delirium, epilepsy, or coma at the time of the collapse. Acute kidney injury (AKI), gut ischemia, blood clots in the stomach and small intestine, cytoplasmic protein clumps in the spleen, and injury of skeletal muscle (rhabdomyolysis) are all characteristics of peripheral tissue damage. Severe heat stroke tends to be complicated by rhabdomyolysis, especially in patients with exertional heat stroke. Rhabdomyolysis may lead to systemic effects, including the local occurrence of compartment syndrome, hyperkalemic cardiac arrest, and/or lethal disseminated intravascular coagulopathy. Untreated heat stroke might exacerbate psychosis, lactic acidosis, consumptive coagulopathy, hematuria, pulmonary edema, renal failure, and other metabolic abnormalities. Core body temperature and level of consciousness are the most significant indicators to diagnose the severity of heat stroke and prevent unfavorable consequences. Heatstroke is a life-threatening illness if not promptly recognized and effectively treated.

Discussion

This review highlighted that core body temperature and white blood cell count are significant contributing factors affecting heat stroke outcomes. Other factors contributing to the poor outcome include old age, low GCS, and prolonged hospital stay. The prevalence of both classic and exertional heatstroke can be reduced by certain simple preventive measures, such as avoiding strenuous activity in hot environments and reducing exposure to heat stress.

Introduction

Heat-related illnesses (HRIs) have a substantial impact on a considerable number of individuals annually and are emerging as a significant health-related issue in light of the notable increase in global temperatures.¹ Based on the findings of the study, it has been observed that the occurrence of severe heat stroke poses a significant risk to the mental well-being of affected individuals. Prolonged exposure to elevated temperatures in the surrounding environment has the potential to induce hypothermia, a condition characterized by an abnormal decrease in body temperature. This physiological response can subsequently impact mental well-being and result in dehydration.² The factors that contribute to an individual’s susceptibility to HRIs encompass a range of elements. These include a medical history that includes prior instances of illness or HRI, the presence of cardiovascular disease, individuals with a high body mass index (BMI), the use of certain medications, tobacco consumption, a low level of physical fitness, and the presence of the sickle cell trait (SCT) (Figure 1).³

Figure 1.

Flow diagram for the searches and inclusion criteria in the study.

Heat exhaustion (HE) and heat stroke (HS) are considered to lie on the same heat spectrum with the former considered to be a milder form of HRI. It is an extremely important step to recognize heat exhaustion which has the potential to progress into more serious heat stroke.⁴ The condition of hyperthermia which is characterized by heat stroke causes the dysregulation of the nervous system. If physical treatment has not been provided for heat events this will significantly lead to morbidity, in most cases, cardiac arrest is the most common circumstance.

HS is categorized into two classes based on the presence or absence of exertion. Exertional HS is present in able-bodied individuals, such as athletes, soldiers, or laborers, or those performing rigorous physical activities, while non-exertional heat stroke is observed in people with low-level physical activities such as elderly, ambulatory individuals with co-morbidities such as diabetes, hypertension, heart disease, renal disease, dementia, and alcoholism.⁵

The research identifies that there are worse impacts of comorbid heat-related illness and common illnesses on that patient which are in more use of hospital resources. The factors which are the number of hours stayed in hospitals, length of stay, number of visits, discharge status or death condition, and having the symptom of the heat-related illness or common illness are all associated with the increase of disease. Many of them suffer from respiratory problems when heat stroke increases. The study reported that heat stroke has an indication of multiple health hazards like renal and diabetic problems are all linked with the illness of heat stroke. The multiple cases and the symptom of the HRI have a worse outcome and cause a higher risk of death among respiratory and cardiac disease patients.⁶ According to the climate report, it has been observed that for the last two decades, there had been reported record-breaking heat waves which have increased class heat stroke which affects the epidemic form of the globe and its facilities the heat-related illness to 9–37%, whereas external heat stroke badly affected young adults. The mortality reaches up to 26.5% in the intensive care units; however, 63.2% includes external and classic heat stroke. The survivor of heat stroke also suffers long-term damage in the cell injury and causes inflammation and thrombosis with the experience of neurological and cardiovascular complications. This leads to the persistent risk of death. No specific therapy or sure has been identified. The phenomena have proved that heat stroke contributes to physiological and morphological complications⁷ The significant effects caused by classical heat stroke and exertional heat stroke encompass a range of symptoms such as headache, weakness, dizziness, nausea and vomiting, diarrhea, irritability, coordination loss, tachycardia/hypotension, and preserved cognitive function. The primary demographic affected by this phenomenon consists of individuals who are particularly susceptible to its effects, such as street children who are regularly exposed to direct sunlight, as well as adults who remain inside sun-exposed enclosed vehicles during periods of intense heat.⁸

The facilities of the heat techniques which are immensely used and found effective are ice water immersion, augmentation of ice packs which can diffuse in the body easily, and provide the primary cooling supplement of chilled intravenous fluid. Applying the ice packs directly on the neck, axilla, and groin and cooling blankets are not recommended as the basic method of cooling to control heat stroke.⁶ The researchers define HS based on pathophysiology which stated

it as a form of hyperthermia accompanied by a systemic inflammatory response (SIR) resulting in multiorgan failure including rhabdomyolysis, renal failure, hepatitis, or coagulation disorder, particularly encephalopathy (Table 1 and Table 2).⁹

Table 1.

The Outcome of HS Patients in Various Studies

S. No	Author	Year	Study Design	Sample Size	Mean Age (Year)	Gender	Affected System	Findings	HS/HE/ HRI
1	Wei-Ta Chen et al14	2012	Case report	-	39	M	CVS	ST elevation, stress-induced cardiomyopathy	HS
2	Mimish et al27	2012	Case-control	HS/HE/Control- 34/28/21 (n=83)	59	M/F	CVS	1. Mean core temp: 41.7/38.7/37.1	HS and HE
								2. HR: 120/97/74
								3.Mean BP:76/102/92
								4.Mean PR interval:158/152/159
								5. Mean QT interval: 314/326/364
								6. Pathological Q-waves: 0/2/0
3	Yang et al30	2017	Retrospective cohort	117	22	M/F	CNS	Incidence of a neurologic sequel: 24.4%	EHS
								GCS: 6 (4–9), GCS (3 in alive and 6 in expired)
								Deep coma: 37.6%
4	Satirapoj et al33	2016	Retrospective cohort	66	22.1	M	Renal	(Renal loss: potassium loss; 54.2%, phosphate loss; 86.7%, sodium loss; 64.7% and magnesium loss; 83.3%).	Nonexertional HS
								AKI in 90.9% of cases,
								Expired: 3%
								Received dialysis: 16.7%
5	Erarslan et al47	2012	Case report	-	63	M	Hepatic	Acute liver failure: Total bilirubin (max): 7.8mg/dl on day 6
								Direct bilirubin (max): 5.7mg/dl on day 6
								AST (max): 3450 IU/L on day 5
								ALT (max): 2600 IU/L
							Renal	Acute renal failure: Urea (max): 122mg/dl on day 3, creatinine: 7.7 mg/dl on day 7
6	Wu et al65	2015	Case report		35	Male	Multiple organ failure	Urea nitrogen: 1.55 Serum creatinine:35.6 Prothrombin Ratio: 54 C-Reactive Protein 72	Exertional heat stroke
7	Abriat et al28	2014	Retrospective study	182	26	Male	Multiple organ failure	Renal failure in 31.3% of the subjects, liver insufficiency in 12%, and disseminated intravascular coagulation in 1%	Exertional heatstroke
8	Li et al29	2015			59	Male	Neurological problem	Remarkable symmetric lesions in the cerebellar peduncles, restricted water diffusion in the bilateral dentate nuclei	Heat stroke
9	Jilma et al34	2012	Retrospective study	66	22.1		Renal system failure	Hypokalemia in 71.2%, hypophosphatemia in 59.1%, hyponatremia in 53.0%, hypocalcemia in 51.5%, and hypomagnesemia in 34.9% of cases. 90.9% of patients suffered from AKI with 16.7% receiving acute dialysis	Exertional heatstroke
10	Hifumi et al40	2018	Randomized controlled study	705	68	Male	Coagulation system failure	Hospital mortality was significantly associated with the presence of DIC (odds ratio [OR], 2.16; 95% confidence interval [CI], 1.09–4.27; p=0.028)	Heat stroke
11	Carvalho et al48	2016	Case report		25	Male	Acute liver failure	Acute kidney injury with creatinine 2.2 mg/ dL	Exertional heat stroke
12	Salathé et al53	2015	Case report		36	Male	Acute liver failure	Raised Aspartate aminotransferase [AST], Phosphate, and Factor V	Exertional heat stroke
13	Castro et al57	2018	Case report		35	Male	Fulminant liver failure	D-dimer (ng/mL): 8801 Activated partial thromboplastin time: 89, Total bilirubin (mg/dL):2.5, Creatinine: 1.7	Heat stroke
14	Yoshizawa et al58	2016	Case report		34	Male	Bimodal rhabdomyolysis	Creatinine phosphokinase (CPK) level increased to 8832 IU/L	Heat stroke
15	Thongprayoon et al60	2020	Cohort study	3372	20–39 (median)	Male	Rhabdomyolysis	Rhabdomyolysis was significantly associated with an increased risk of hyponatremia, hypernatremia, hyperkalemia, hypocalcemia, serum phosphorus and magnesium derangement, metabolic acidosis, sepsis, ventricular arrhythmia or cardiac arrest, renal failure, respiratory failure, liver failure, neurological failure, hematologic failure, and in-hospital mortality
16	Azzopardi et al47	2012	Case report		25	Male	Acute liver impairment, Hypoxic Hepatitis, and Rhabdomyolysis	Glasgow Coma Score of 10. He had a temperature of 105.4°F on admission and he was sweaty, tachycardic (heart rate of 160 bpm), and had a systolic blood pressure of 90 mm Hg, creatinine phosphokinase (CPK) level (178,850 U/l)

Table 2.

HS Cases with Rhabdomyolysis

No	Report	Year	Age	Sex	Trigger	Peak Day	CPK Max	HD	Outcome
1	Wu65	2015	27	Male	Exercise	2	55,650	Yes	Survival
2	Asserraji66	2014	35	Male	Marathon	5	91,596	Yes	Survival
3	Raj67	2013	11	Male	Jog	1	4326	Yes	Death
4	Horseman47	2013	22	Male	Walking	1	649,530	Yes	Survival
5	Azzopard68	2012	25	Male	Marathon	2	178,850	No	Survival
6	Muriz74	2011	15	Male	Football	2	39,954	No	Survival
7	Trujilo38	2011	14	Female	Exercise	3	36,243	Yes	Survival
8	Lin22	2011	11	Female	Jogging	2	21,351	No	Survival
9	Miura69	2010	38	Male	Marathon	3	84,612	No	Death
10	Lee70	2010	57	Male	Ko spring	3	9565	Yes	Death
11	Niu71	2009	47	Male	Labor	1	4682	No	Survival

A rise in the body temperature leads to sympathetic cutaneous vasodilation activation which causes thermal sweating but also results in a reduction in the intra-vascular volume leading to heat syncope. Several strategies are used by sports athletes which uses to reduce the risk factors of the dangers which come from exercise done in the heat condition. Nutritional intervention is one of the major sources to vasodilate the cutaneous process and also expand the plasma volume which will be helpful to improve cardiovascular activity and helps in optimizing the hydration status by fluid replacement beverages. The more consumption of sodium and glucose can improve and provide betterment water retention and absorption.¹⁰

The nonspecific symptom of heat exhaustion is headache, malaise, and nausea. All the first aid or treatment including the monitoring of liquid intake by the patient and the surrounding environment have cooling impacts. If heat exhaustion is not treated priory, it may lead to damage to the central nervous system like coma and heatstroke leading the cardiac arrest. Now the researcher is focusing more on physicians and the public health department.¹¹

Several studies are associated with heat-related illnesses describing the risk factors and their illness symptoms with cardiovascular diseases. The association of heat stroke represents that the risk of cardiovascular diseases increases with the increased ratio of heat stroke. The symptom has equal control on the population in different comparisons of age, sex, and comorbidity-matched patients.^12,13 The outcomes of HRIs include cause rhabdomyolysis, coma with acute and even permanent vital organ damage, and multiple organ failure (MOF).^14,15

The heat waves have provoked the global warming condition, damaging the greenhouse effect which threatens the survival of human beings. The ability to absorb heat has deteriorated the skin of the body and led to skin problems. This thermal change has aided the sweating and the cutaneous flow in the body, although it also affects the physiological and pathological condition of the body. Thus, more identification is required to protect the skin of the body, and more care is required for the patient.¹⁶ In heat stroke, there is further impairment of thermoregulation due to a reduction in cutaneous vasodilation as a result of shunting of the blood from the central circulation to the muscles and skin, leading to MOF.¹⁷

Although previous studies have examined the associations between climate variability and the outcomes of patients with heatstroke and heat exhaustion, none of these studies have specifically investigated the impact of different climate zones on these outcomes. Consequently, we conduct a comprehensive and methodical examination of the existing epidemiological data about the impacts of heat exposure on patient outcomes. This is accomplished through a thorough and current review of the relevant literature, followed by an evaluation of the quality and robustness of the evidence.

Materials and Methods

This systematic review was executed to identify and extract all relevant and potential studies emphasizing the outcome of patients with heat stroke and exhaustion. The literature search was conducted using the “PubMed: MEDLINE” database. The search screened articles published from 2009 to 2020 and possibly qualified articles were searched manually through reference list screening. The preferred language for this research is English, while the keywords selected to search algorithms in the database are “Heatstroke” “Heat-related illness” “Heat exhaustion” or “Heat stress”. The inclusion criteria of this study were to enroll the adult population who have experience visiting hospitals in heat stroke or heat exhaustion conditions. This review considers the application domain including disease diagnosis and the outcome. International Classification of Diseases (ICD) was followed. The exclusion criteria were to reject the articles which were not in English, studies related to heat impact on the animal, and articles without full text.

Two researchers conducted initial screenings of articles, employing a double-blind and independent approach. These screenings encompassed the evaluation of titles, abstracts, and full texts. The relevant data from the chosen studies were recorded in a spreadsheet, which included details such as the author’s name, publication year, study design, sample size, age range, gender distribution, affected system, findings, and evaluation of health economics, health systems, and health research and innovation. This information was then reviewed and verified by the investigators.

The present study employed a systematic review methodology, thus statistical analysis was not performed. The data was synthesized using a narrative approach. The assessment of study quality and bias was conducted using a combination of the Downs and Black scale and the Newcastle-Ottawa Scale. These scales consist of 11 items, as described by Downs et al¹⁸ and Wells et al,¹⁹ and are organized into four themes: reporting, external validity, internal validity for bias, and internal validity for confounding. This approach was employed to encompass both observational and experimental study designs.

The data for each included study consisted of the following details author and year of publication.

Results

A total of 869 citations were identified through electronic searches. Titles and abstracts were screened for relevance (stage 1 screening), then study duplications were identified, resulting in 280 relevant citations being retained. The full texts of these articles were obtained. Then applying inclusion criteria to these full-text articles (stage 2 selection), 264 citations were excluded, which were not according to the inclusion criteria. Sixteen citations were therefore included in the systematic review.

Mortality

ICU mortality was due to MOF present early after admission to ICU, as reflected by circulatory shock, renal failure, hemostasis disorders, deep coma, and a high admission SAPS II score. Furthermore, it is very likely that neurologic sequelae largely contributed to death in the hospital after ICU discharge, as previously reported.^19,20 Misset et al¹⁷ reported a mortality rate of 20% mortality (n = 58) of patients and these patients had much more severe heatstroke as reflected by the lower Glasgow Coma Scale score.²¹ Several factors independently associated with mortality, including high body temperature and prolonged prothrombin time, were present within the first 24 hrs after ICU admission. This is consistent with the current knowledge of the pathophysiology of heatstroke, including the diffuse cell damage induced by higher temperatures,²² the production of cytokines²³ and nitric oxide,²⁴ and endothelial cell injury.²⁵ Although older age, cardiac, respiratory, or neurologic co-morbidity, preexisting use of neuroleptics or diuretics, and alcohol abuse commonly predispose to the occurrence of heatstroke,²⁶ Misset et al¹⁹ observed none of these factors was an independent predictor of mortality in declared heatstroke.

Cardiovascular Damage

A case–control study conducted by Mimish²⁷ observed that electrocardiographic abnormalities occur with a high frequency in patients with HS and HE, with sinus tachycardia and ischemic changes. In Group 1, 18 were females and 16 males with mean ages of 59 ± 11 years.²⁷ Their mean heart rate was 120 ± 24 per minute. Only 5/34 ECGs were completely normal. Sinus tachycardia was present in 79% of patients, with ischemic changes in 9/34 ECGs. In group 2, 24 were males and four females with age 47 ± 15 years, mean heart rate was 97 ± 160 per minute. In group 2, 21/28 (75%) had some abnormalities. None had ischemic changes. The control group (group 3), was five females and 26 males, the mean age was 38 ± 15 years, and 22/31 (71%) had normal ECGs. All had normal sinus rhythm, and mean beats were 74 ± 11 per minute. Nine patients had some electrocardiographic abnormalities, but none of them had ischemic changes.

Findings on ECG described in patients with HRI include sinus tachycardia, conduction defects, QT interval prolongation, diffuse ST-T changes, as well as ST-T changes localized to the distribution of a coronary artery.²⁷ Although previous research had attributed most of the ECG changes to electrolyte imbalances associated with heat stroke, subsequent studies done on a larger cohort have failed to evaluate any clear correlation.²⁷

Previous studies reported conduction defects including non-specific intraventricular conduction delay, which have been attributed to multiple factors including a change in the conduction rate of the repercussions of the right bundle branch due to the potential involvement of heat shock proteins in ion channel trafficking in the cell membrane and elevated right ventricle pressure (resulting in incomplete RBBB).²⁷

Neurological Damage

With the brain being sensitive to extremely high temperatures, the impairment of CNS is considered one of the most serious complications of HS. This impairment has been reported in 80.3 to 100% of HS patients admitted to ICUs during the heat waves in America and Europe and 100% of soldiers.²⁸ Another important finding observed in HS patients is the presence of neurological sequelae such as cerebellar ataxia, dysarthria, cognitive disorders, and anterograde amnesia) in 20–30% of patients within a few days, weeks, or months of heat stroke even with timely aggressive clinical intervention initiation which includes lowering of core body temperature and support of organ function.²⁹

The Glasgow Coma Scale (GCS) is the most commonly used clinical scoring system for the assessment of the severity of CNS deterioration severity, which ranges as follows: mild (GCS 13–15), moderate (GCS 9–12), or severe (GCS 3–8).³⁰ Yang et al³⁰ study reported HS patients were classified into 2 groups, ie, severe (GCS 3–8) and moderate (GCS 9–15) depending on CNS injury extent. The period of CNS injury spanned from the time of admission in the hospital until the point at which the patient’s condition had improved such that s/he could open the eyes in response to the speech, exhibit improved conversational ability, and attain a GCS score of at least 12. Since HS patients were discharged, neurological sequelae such as cerebellar ataxia, dysarthria, cognitive disorders, and/or anterograde amnesia that developed later were also observed.

Of one hundred and seventeen patients, for axillary temperature, 46 patients (39.3%), 44 (37.6%), 25 (21.3%), and 1 (0.8%) exhibited axillary temperatures between 39 and 40 °C; 40.1 and 41 °C; 41.1 and 42 °C; and greater than 42 °C, respectively. Forty-five (38.5%) patients exhibited signs of hypotension (mean arterial pressure <65 mm Hg). 79.5% had severe (GCS 3–8) CNS injuries, while 22.5% did not have severe (GCS 9–15) CNS injuries. Forty-four (37.6%) patients experienced deep coma (GCS = 3). The extent of CNS injury extent was significantly more severe in expired (median GCS-3; IQR 3–4.5) than in alive patients (median GCS: 6; IQR 4–9). Of the 21 patients with neurological sequelae, 42.9% patients were found to have developed cerebellar ataxia, 28.6% had dysarthria and 19.0% had cognitive disorders and anterograde amnesia.³⁰

Another study conducted by Yamamoto et al³¹ retrospectively analyzed various predictive factors for hospitalization amongst patients who presented with mild to moderate heat illness in the emergency department (ED) of Yamaguchi Prefecture, Japan. It was found that a significant difference was observed in the GCS between inpatient and outpatient groups (inpatient GCS median 15 (IQR 14–15), outpatient GCS median 15 (IQR 15–15).

A case report was published about a Japanese man who collapsed due to non-exertional HS on a hot and humid day.³² On presentation, the patient had a GCS of 6/15, altered consciousness, and a core body temperature of 40.6°C. He had a deranged hepatic and renal profile with evidence of severe rhabdomyolysis (CPK – 1163 U/L). Due to low GCS, the patient was intubated and cooled aggressively with the intravascular balloon-catheter system. The patient was discharged on day 5 with no evidence of any neurological sequelae and a GCS of 15/15.³³

Renal System Failure

A retrospective cohort study³⁴ included 66 subjects (mean age 22.1 years) with EHS. Hypokalemia was observed in 71.2%, hypophosphatemia in 59.1%, hyponatremia in 53.0%, hypocalcemia in 51.5%, and hypomagnesemia in 34.9% of cases. Electrolyte depletion was confirmed as renal loss (potassium loss; 54.2%, phosphate loss; 86.7%, sodium loss; 64.7%, and magnesium loss; 83.3%). During hospitalization ranging from 2 to 209 days, 90.9% of patients suffered from AKI with 16.7% receiving acute dialysis, and 3% of patients died. At discharge, AKI and electrolyte abnormalities had dramatically improved. The prognosis factors for AKI receiving dialysis were identified as neurological status, renal function, and serum muscle enzyme at the time of admission.

Coagulation System Failure

HS has also been reported to result in the activation of the coagulation pathway and fibrin formation which is manifested as disseminated intravascular coagulation (DIC).³⁵ The occurrence of DIC in the case of HS has been reported in original research studies,³⁶ three case series^37,38 and numerous case reports^6,9–41 over the past 50 years. Hifumi et al⁴⁰ reported the DIC in 708 HS patients. The diagnosis of DIC was made according to JAAM DIC diagnostic criteria⁴¹ The score consisted of systemic inflammatory response syndrome, platelet counts, prothrombin time, and fibrinogen/fibrin degradation products or D-dimer levels, and a total score of ≥4 established the diagnosis of DIC. It was reported that patients with scores ≥4 had higher odds of mortality during hospital stay (OR, 2.16; 95% CI, 1.09–4.27; p = 0.028). Another important finding was the increase in the mortality rate to 10% in patients who had a DIC score of 2. It was further reported that anti-thrombin levels were found to be significantly reduced in expired patients in comparison to alive patients (median [IQR]: 77%^38,42–63 vs 98%,^47,64–71 p = 0.02).

A study conducted by Ward et al⁴⁴ reported the time-resolved progression of clinical laboratory disturbances days following an exertional heat stroke (EHS) in 2216 patients experiencing a total of 2529 HS episodes. The study participants were US Active-Duty Service Members (US Army, Navy, Air Force, and Marine Corps) serving from 2008 to 2014. It was reported that prothrombin times were found to be elevated 4 days after injury and remained outside the reference range from days 1–16 days. Corresponding decreases in hemoglobin, hematocrit, and red blood cells were observed from day 1 after injury and then persisted below the lower levels of normal for 6 days. Thirty-five percent of patients were found to have platelets below the lower levels of normal on 2nd day.

Hepatic System Damage

Hepatocellular injury is a well-documented complication of heat stroke, but few case reports [45–52] have described an association with acute liver injury or failure (ALI/ALF). Weigand et al reported two cases of liver failure associated with EHS, suggesting that HS and exhaustion were underestimated causes of liver failure.⁵² Garcin et al⁵² concluded that 22.7% of 110 patients progressed with liver failure.^53–57 Recently, the ALF Study Group identified eight patients with HS in a prospective American cohort of 2675 patients with ALI.⁵⁶ Hepatocellular necrosis is consequent to thermal and circulatory shock, endotoxemia, and cytokines with increased concentration and acute-phase proteins.⁵⁵ However, the only predictor for the occurrence of liver failure was hypophosphatemia.^55–57 There must be no evidence that hypophosphatemia is the cause of liver dysfunction. A report from the Acute Liver Failure Study Group found that 25% of deaths in patients with liver failure secondary to heat stroke were diagnosed between January 1988 and April 2015 in the United States.¹⁰ Varghese et al⁵⁸ followed 28 HS victims and concluded that the high mortality of these cases is due to multiple organic dysfunctions.

Rhabdomyolysis

Severe heat stroke tends to be complicated by rhabdomyolysis, especially in patients with exertional heat stroke.⁵⁹ Rhabdomyolysis may lead to systemic effects, including the local occurrence of compartment syndrome, hyperkalemic cardiac arrest, and/or lethal disseminated intravascular coagulopathy.⁶⁰

Yoshizawa et al⁶¹ reported a case of a 34 years old male patient, found lying unconscious (GCS of 10) on the road after participating in a half marathon in the spring with a temperature of 24.2°C. A sedative was administered, and tracheal intubation was performed. On the second day of hospitalization, a blood analysis was compatible with a diagnosis of acute hepatic failure; thus, he received fresh frozen plasma and a platelet transfusion was performed, following plasma exchange and continuous hemodiafiltration. The patient’s creatinine phosphokinase (CPK) level increased to 8832 IU/L on the fifth day of hospitalization and then showed a tendency to transiently decrease. The patient was extubated on the 8th day of hospitalization. On the 9th day, rehabilitation was initiated gradually. His CPK level increased with pain in his legs again. Despite the cessation of all drugs and rehabilitation, his CPK level increased from 105 to 945 IU/L on the 15th day.⁶²

Systemic Inflammatory Response Syndrome (SIRS) Criteria

The preliminary cardiovascular reaction to heat exposure or heat stroke is an elevation in skin blood flow that increases heat loss and deteriorates the level of heat exposure from the surrounding. Elevated skin blood flow is convoyed by a reduced splanchnic blood flow as an alternative mechanism for maintaining blood pressure. Reduced cerebral blood flow is further correlated with hyperthermia, ac-counting for CNS impairments, and presyncopal indications.⁶³ The SIRS is classified as a reply to bacterial infection that follows disruption to the gut and other organs, ensuing elevated mitigations in splanchnic blood flow. Nitrosative and oxidative stress are promoted through the resultant ischemic environment that results in stricter gut junctions becoming leaky. Gram-positive and -negative bacteria are then aided for freely crossing the stricter junction restriction and entering into the systemic circulation.^{24–38,40–64}

Risk Factors

Previous studies have compared risk factors among survival and non-survival heat stroke cases and found prolonged hospital stay in non-survival cases (p-value ‎<0.001)‎, significantly low mean among non-survived patients (p-value = 0.001), high core body temperature, ie, ‎42.454‎ ± ‎1.082‎°C (p-value = 0.001), increased mean lactate, ie, ‎8.756‎ ±‎ (p-value = 0.001, increased mean white blood cells (WBCs) values ‎of ‎19.623‎ ±‎ 7.612‎ (p-value = 0.001), increased mean creatinine (3.992 ± 2.263) and BUN (46.325 ± 27.940), increased AST (1445.125‎ ±‎ 2829.278) and AST (810.174‎ ±‎ 1566.975) among non-survival patients. While the heart rate (HR), respiratory rate (RR), systolic blood pressure (SBP), and diastolic blood pressure (DBP) had no significant effect on the prognosis of ‎heat stroke patients. The results have shown no significant value in the ‎outcome of the patients based on PT, PTT, INR, and CK-CPK.‎

Conclusion

This study concludes that HS is a life-threatening condition marked by neurological disorders, damage in the hepatic system, renal system, coagulation failure, muscular-skeletal system, and cardiovascular system. Untreated heat stroke might exacerbate psychosis, lactic acidosis, consumptive coagulopathy, haematuria, pulmonary edema, renal failure, and other metabolic abnormalities. This review elucidated that core body temperature and white blood cell count are pivotal determinants influencing the outcomes of heat stroke. Certain simple preventive measures can effectively reduce the prevalence of both classic and exertional heatstroke. These measures include refraining from engaging in strenuous physical activity in hot environments and minimizing exposure to heat stress. In contrast, there is a significant lack of understanding regarding the pathophysiology of heat stroke and its relationship to systemic inflammatory response syndrome (SIRS), which is crucial for comprehending the factors that contribute to mortality and morbidity. It is crucial to recognize the significance of novel biotechnologies in advancing our understanding of the pathophysiology of heat stroke. The utilization of these technologies will play a crucial role in enhancing comprehension of Systemic Inflammatory Response Syndrome (SIRS) and devising innovative approaches to mitigate the mortality and morbidity associated with heat stroke. This will be achieved through the integration of novel in vitro, in silico, and in vivo models. One of the limitations inherent in our study was the relatively brief duration of the study period, coupled with a predominance of case reports. However, it was observed through case presentations that males exhibited a higher susceptibility to heat stroke and were more significantly impacted by its associated complications.

Disclosure

The author declares no competing interest.