Dengue is a prevalent arthropod-borne viral disease in tropical and subtropical areas of the globe. Dengue clinical manifestations include asymptomatic infections; undifferentiated fever; dengue fever, which is characterized by fever, headache, retroorbital pain, myalgia, and arthralgia; and a severe form of the disease denominated dengue hemorrhagic fever/dengue shock syndrome, characterized by hemoconcentration, thrombocytopenia, and bleeding tendency. However, atypical manifestations, such as liver, central nervous system, and cardiac involvement, have been increasingly reported. called expanded dengue syndrome. We report a 40 years old gentleman with atypical and rare presentation of dengue disease marked by a dramatic and fatal acute cardiac failure due to acute myocarditis. Condition improved after five days of conservative treatment. Cardiac complications in dengue are now increasingly observed with the most common case ismyocarditis. The main mechanism of dengue myocarditis is still unknown though both directviral infection and immune mediated damage have been suggested to be the cause ofmyocardial damage. The low incidence of dengue myocarditis is because it’s asymptomaticand diagnosis is easily missed. Almost all cases of dengue myocarditis are self-limiting andsevere myocarditis leading to dilated cardiomyopathy is extremely rare. To avoid otherwise preventable morbidity and mortality, physicians should have a highindex of suspicion for cardiac complications in patients with dengue illness and should manage thisaccordingly.

Dengue, an arthropod-borne viral infection of humans, is endemic to tropical and subtropical regions of the world and represents an important public health problem. Dengue viruses are transmitted by the bite of the Aedesaegypti mosquito infected by the one of the four dengue virus serotypes: dengue-1, -2, -3, and -4. More recently, dengue disease has spread geographically to many previously unaffected areas and, as travelling around the world has become more accessible, physicians in temperate areas are more likely to see returning travelers with dengue infection.1,2

World Health Organization (WHO) classification of symptomatic dengue infection, continuously evolved, first in 1997 it divided into dengue fever (DF), dengue hemorrhagic fever (DHF) and dengue shock syndrome (DSS). In 2009 it improved into dengue with or without warning signs and severedengue.[3]

However, in 2011, WHO Regional Office for South East Asia (SEARO) revised and further improving the classification, divided into DF, DHF without shock or with shock (DSS) characterized by increased vascular permeability, thrombocytopenia (platelets <100,000), bleeding tendency, and, in a small percentage of patients, circulatory shock.[4,5,6,7]and expanded dengue syndrome.[8]

Expanded dengue syndrome is a new entity added to the classification system to incorporate a wide spectrum of unusual manifestations of dengue infection affecting various organ systems that had been reported including gastrointestinal, hepatic, neurological, cardiac, pulmonary and renal systems.8Of note, a variety of cardiac complications have been reported indengue-affected patients, which include atrioventricular conductiondisorders,9supraventricular arrhythmia,10and myocarditis11,12. The most commoncomplication is myocarditis. However, the study of myocarditis in dengue is still very lacking. The pathogenesis of myocarditis in dengue is still not clear. Clinical manifestation of myocarditis dengueis varied. Endomyocardial biopsy (EMB) is a deterministic diagnostic method but difficult topopularize. According to the ESC (European Society of Cardiologist) New Criteria, the combination of symptoms, electrocardiography, cardiac enzyme marker and cardiac imaging can use to diagnosethe dengue hemorrhagic fever patient with myocarditis. The fatal complications of dengue myocarditis are arrhythmias, heart failure, cardiogenic shock until death.[13]

Although reports of a more severe disease with progression to cardiogenic shock and death have been increasingly described,[14,15,16] the pathogenesis of myocardial lesions has not been elucidated. We present a rare case of a fulminant and fatal myocarditis leading to acute heart failure caused by dengue.

A 40-year-old gentleman was admitted to Ad-din Women’s Medical College Hospital, Dhaka, Bangladesh with a history of progressive dyspnoea in the last 3 days that had recently evolved to dyspnoea at rest and orthopnoea, atypical chest pain and palpitation. Eight days prior the admission, he complained of fever, headache, retro-orbital pain, generalized bodyache and weakness for 6 days followed by afebrile for last 2 days. There are spontaneous bleeding complaints in the form of nosebleeds 1-day prior admission to hospital His past medical history was positive only for a diagnosis of primary hypothyroidism for last four years for which he was taking tablet thyroxin 50 mcg daily regularly. From the previous history of disease did not get the history of dengue fever, diabetes mellitus, bronchial asthma, hypertension and heart disease. Patients do not smoke and do not consume alcohol. 

On clinical examination, he was in severe condition, agitated, dyspnoeic  with signs of poor peripheral perfusion, such as cold extremities and cyanosis. Heart rate was 105 bpm, blood pressures 60/30 mm of Hg, respiratory rate 28 breaths/min, axillary temperature 98.2ºF. SaO2 was 85% in room air. Bi pedal edema was present. Haemorrhagic suffusions or other skin lesions were absent except right subconjuctival hemorrhage and positive rumple leed test. On examination of the head and neck, there is no anemia or  jaundice. No enlargement of lymph nodes nor increased jugular venous pressure. On precordial examination there was gallop with no murmur. On abdominal examination, there was no ascites with normal bowel sounds, liver and spleen were not palpable. On chest examination, Bi basal mid to late inspiratory coarse rales were present over both lung base with no rhonchi. Breath sound was vesicular. 

On laboratory investigations, hemoglobin 11.1 g/dL, leukocyte 5600/μL with normal differentials, platelet 45,000/μL, HCT 33.8%, SGPT 66U/L( normal less than 40U/L), Alb 4.8g/dL,  serum creatinine 0.75mg/L, sodium 132mmol/L, potassium 3.6mmol/L, chloride 101mmol/L,HCO3 20 mmol/L. HbsAg (non-reactive), CKMB 77U/L (normal 7.0-25.0U/L) and troponin I 2.71ng/mL (normal <0.02 ng/mL). IgM Anti dengue antibody came positive. Chest x ray revealed bilateral opacities extending from both hilum with bat wing appearance suggestive of pulmonary edema(Figure 1). USG of whole abdomen revealed thickened GB wall with mild ascites. Urine routine examination was normal. NT-Pro BNP was 27332 pg/ml(normal less than 400 pg/ml). The 12-lead electrocardiogram detected diffuse ST-segment elevation(figure 2). Emergency transthoracic echocardiography was performed at bedside and showed mild pericardial effusion, without signs of cardiac tamponade, dilated left ventricle with diffuse hypokinesia of left ventricular wall. There was severe left ventricular dysfunction with ejection fraction was 36%. Interventricular septum was normal. So diagnosis of dengue hemorrhagic fever with dengue myocarditis with acute pulmonary edema was made as a part of expanded dengue syndrome.

Resuscitation with intravenous frusemide, sodium bicarbonate, vasoactive drugs and digoxin were promptly initiated. Dopamine was used in progressive doses up to 20 µg/kg/min along with frusemide infusion 15 mg/hour along with high flow, high concentration oxygen. He continued receiving intravenous frusemide and dopamine for a further 2 days. With treatment his condition improved with decreasing shortness of breath. On 4th day dopamine infusion was stopped and frusemide infusion was substituted by bolus injection.

Figure 1and 2: showing chest x-ray suggestive of pulmonary edema and ECG with diffuse ST elevation respectively.

On 7th day of admission, his condition further improved with no shortness of breath even on exertion. Repeat CKMB 17U/L (normal 7.0-25.0U/L), troponin I 0.7ng/mL (normal <0.02 ng/mL), NT-Pro BNP was 996 pg/ml(normal less than 400 pg/ml). He was discharged on 9th day of admission with stable hemodynamic condition with no clinical signs of heart failure. He was advised to follow up on outpatient door after 2 weeks.

Discussion: Dengue is a worldwide public health problem and causes innumerous deaths. More than 40% of the world’s population lives in dengue endemic areas, and the World Health Organization estimates that about 2.5 billion people in 100 countries are at risk of infection and that as many as 100 million people are infected by dengue viruses every year. In the majority of infected people, dengue is an auto-limited disease that resolves in 5–7 days. However, approximately 500,000 people develop a severe form, leading to about 20,000 deaths annually. Consequently, approximately 0.5% of dengue patients develops a severe form and requires a specialized treatment. [2,17]

Dengue virus infection is a disease that found in children and adults with the main symptoms of fever, muscle and joint pain that usually worsens after the first three days. This disease is an acute febrile illness accompanied by bleeding manifestations with potential shocking and can lead to death in children<15 years, but not likely to attack adults.[18] Signs of this disease are sudden high fever 2 to 7 days with no obvious cause, weakness, lethargy, anxiety, heartburn, accompanied by signs of bleeding in the skin (petechiae), bruising (ecchymosis) or rash (purpura). Sometimes there are other spontaneous bleeding manifestations such as nosebleeds, bleeding gums to dysentery. Severe symptoms can lead to decreased awareness or shock.[19]

Laboratory results in dengue fever are found in thrombocytopenia (20% of the baseline on dengue hemorrhagic fever is a sign of plasma. Serological tests results in dengue are influenced by the type of dengue infection, whether it is the primary/first, or secondary/reinfection. IgM antibodies are detectable by days 3–5 after the onset of illness, rise quickly in two weeks and decline to undetectable levels after 2–3 months, because this late appearance, the first five days of clinical illness are usually negative of IgM. In dengue secondary infection, the rise of IgM are not as high as primary infection, and sometimes absent / undetectable completely.[20]

IgG antibodies in primary infection, evolves relatively slow, with low titres 8-10 days after fever onset, increase subsequently and remain for many years, whereas in secondary infection it evolves rapidly, with high titres soon after fever onset and persist to a lifelong period. Hence, a ratio of IgM/IgG is commonly used to differentiate between primary and secondary dengue infections. Ratio of IgM/IgG titre less than 1.2 is considered a secondary dengue infection. But to be noted, titre ratio only could be validly use as a data if the IgG/IgM serological test is using pure quantitative means, not by qualitative or semi-quantitative.[21]

NS1 antigen detection is widely used and cost-effective, NS1 could be detected from day 1-8 of fever onset, unaffected by a primary or secondary dengue infection. In conclusion, by combining the serological (IgG and IgM) and NS1 tests, clinicians could rapidly assess the dengue diagnosis with its types (primary or secondary infection) and applies the best treatment.[22]

In 2011, based on many reports of cases with dengue-related unusual manifestations and organ complications, WHO-SEARO further improved and revised 2009 WHO guidelines by adding a new entity, that is expanded dengue syndrome (unusual/atypical manifestation of dengue), these include neurological, hepatic, renal, cardiac and other isolated organ involvement, that could be explained as complications of severe, profound shock or associated with underlying host conditions/diseases or coinfections. [8]

The incidence of cardiac complications in patients with dengue illness varies greatly from one series to another. From India, Agarwal et al. reported that only one of 206 patients subjected to cardiovascular evaluation experienced cardiac symptoms;23Wali et al., reported that 70% of 17 patients with DHF/DSS who underwent myocardial scintigraphic study suffered diffuse left ventricular hypokinesis with a mean ejection fraction of 40%;24 and Kabra et al., reported that 16.7% of 54 children with dengue illness had a decreased left ventricular ejection fraction of<50A>

The clinical manifestations of cardiac complications in dengue illness vary considerably.[9-12,14,24,25] At one end of the clinical spectrum, patients are asymptomatic or have mild cardiac symptoms despite relative bradycardia, transient atrioventricular block, and/or ventricular arrhythmia.[9,10,24,27,28.] At the other severe end, patients may experience acute pulmonary edema and/or cardiogenic shock due to severe myocardial cell damage with left ventricular failure.[6,9,11,12,14,24,29] Myocarditis can masquerade as acute myocardial infarction.29,30.Clinical presentation in myocarditis is varied. The sign and symptoms are chest pain, dyspnea at rest or exercise, palpitation, syncope, cardiac shock and sudden cardiac death.13Cardiac arrhythmias are other clinical manifestations of myocarditis. Various arrhythmias have been described during dengue virus infection such as atrial fibrillation, ventricular tachycardia and even atrioventricular blocks. These arrhythmias are associated to syncope and even sudden death[10,27.]

According to the diagnostic criteria from European Society of Cardiology 2013, dengue patients were subjected to electrocardiogram (ECG), echocardiography and cardiac enzyme test (CET) to make the diagnosis of myocarditis. Myocarditis was diagnosed if 1 or more clinical presentation and 1 or more auxiliary diagnosis method; 2 or more auxiliary diagnosis method should be met if the patient is asymptomatic. 12 leads ECG was considered abnormal with any of following, such as sinus arrest, AV-block, bundle branch block, atrial fibrillation, ST wave change (ST elevation, ST depression, T inversion), abnormal Q waves. Based on echocardiography usually found functional and structural abnormalities such as ventricular dilatation, increased wall thickness, diastolic function abnormality, pericardial effusion, left ventricular ejection fraction less than 55%, valvular regurgitation or vegetation. The cardiac enzyme was considered to be elevated and abnormal if CK-MB more than 25U/L and/or cTnI more than 0.02ng/m and/or NT-proBNP more than 450ng/L (age 75 years). The gold standard to diagnose myocarditis is EMB (Endomyocardial Biopsy), but it is not performed regularly.13 As for the cardiac complication in this reported patient, the differential diagnosis included acute myocardial infarction and acute myocarditis; the former is characterized by a blockage of the coronary arteries, while the latter has patent coronary arteries. However, rapid clinical improvement after the development of hypotension and acute pulmonary edema unequivocally indicated that this was a case of myocarditis.

The pathogenesis myocarditis in dengue patient is still unclear. The mechanism of myocardial damage in dengue could be the release of inflammatory mediators and the direct action of the virus on cardiomyocytes, as seen in acute myocarditis caused by other viruses31. Using immunofluorescence confocal microscopy in heart tissue, Salgado et al 32reported that myotubes were infected by dengue virus in one child with fatal DHF, although the myocardium sections appeared morphologically normal, with minimal cellular, infiltrates.

Figure 2: Pathogenesis myocarditis in dengue infection virus 34

The gold standard of myocarditis in dengue patient is Endomyocardial Biopsy, the fulminant course of clinical dengue myocarditis was associated with intense interstitial edema, several multifocal areas of necrosis, and diffuse inflammatory infiltration. Interestingly, the myocytolitic necrotic areas were replete with virus particles; therefore providing detailed histological evidence of a possible dengue direct action in cardiomyocytes. Further clinical and experimental studies are necessary to better understand the molecular mechanism of dengue virus-induced lesions on the myocardium33.

With respect to volume replacement for DHF patients with a 20% increase in hematocrit, the World Health Organizationrecommends intravenous infusion with 5% glucose in physiological saline at 6 ml/h/kg for the initial 1–2 h, followed by 3–5 ml/h/kg, which may be discontinued at 24 to 48 h depending on the normalization of hematocrit, pulse rate, and blood pressure. Overhydration may lead to fluid overload, resulting in respiratory distress in patients with dengue. In the present case, despite improvement in the serial hematocrit after fluid therapy, hypotension developed on the third day of treatment suggesting that this resulted from cardiac dysfunction rather than insufficient intravenous fluid replacement, thus indicating that the patient’s pulmonary edema was cardiogenic due to impairment of left ventricular function.[35]

Myocardial dysfunction has been reported to be more severe inpatients with DSS when compared to those with DF or non-shock DHF.36The pathophysiology of myocardial cell injury in dengue illness is not yet fully understood. Myocardial involvement in dengue may result either from direct DEN invasion of the cardiac muscles or a cytokine-mediated immunological response, or both.37,38The upsurge in serum tumor necrosis factor-a, interleukins 6, 13 and 18, and cytotoxic factors in patients with dengue illness lead to increased vascular permeability and shock;39,40whether these cytokines play a role in the development ofmyocardial cell injury is unknown. Of note, only DEN-2 and DEN-3 were reported to be the culprit viruses in dengue patients with cardiac complications where the DEN serotype was mentioned.9,14,24,25Further studies are needed to clarify the role that DEN serotypeplays, if any, in cardiac complications in dengue-affected patients.

Our review shows that cardiac complications are not uncommonin dengue illness. Although it was self-limiting in our patient under supportive treatment, acute myocarditis in dengue may be clinically severe to such an extent that it has a fatal outcome.6,29 Early recognition of myocardial involvement in dengue illness, prompt restoration of hemodynamic instability while avoiding fluid overload, and sparing unnecessary invasive management are important in treating dengue-affected patients with severe myocarditis.

Dengue virus can produce atypical manifestations as acute myocarditis leading to cardiogenic shock and death by a possible direct virus action on cardiomyocytes. Physicians taking care of dengue patients should be aware of this possible complication. Early recognition of myocardial involvement in dengue illness, prompt restoration of hemodynamic instability while avoiding fluid overload, and sparing unnecessary invasive management are important in treating dengue-affected patients with severe myocarditis.

None declared