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Coxsackie B virus belongs to the Picornavirus family and can cause a variety of diseases, including gastrointestinal illness, myocarditis, pneumonia, aseptic meningitis, encephalitis, and hepatitis. This activity describes the evaluation and treatment of coxsackie group B infection and highlights the role of the interprofessional team in improving care for patients with this condition. Objectives: Describe the etiology of coxsackie group B viral infections. Review the symptoms of infection with viruses in the coxsackie B group. Summarize the appropriate treatment for coxsackie Group B viral infections. Explain how the interprofessional team should be aware of the severe complications that can occur and anticipate the need for supportive care in such situations. Access free multiple choice questions on this topic.

Coxsackievirus Group B is a member of the family Picornaviridae, genus Enterovirus. The enterovirus (EV) is a positive-sensed, single-stranded RNA virus named for its enteric or gastrointestinal route of transmission.[1] Before being reclassified as EV A-D, the enteroviruses were categorized according to their pathogenesis in humans and laboratory animals into four groups: polioviruses, coxsackie A viruses (CA), coxsackie B viruses (CB), and echoviruses.[2] The species of enterovirus that cause disease in human beings include enterovirus A-D and rhinovirus A-C. Coxsackieviruses are non-enveloped viruses with linear single-stranded RNA. Group A coxsackieviruses were noted to cause flaccid paralysis, which was caused by generalized myositis. In contrast, group B coxsackieviruses were observed to cause spastic paralysis because of the degeneration of neuronal tissue and focal muscle injury. At least twenty-three serotypes (1-22, 24) of group A and six serotypes (1-6) of group B are recognized: CV-B1, CV-B2, CV-B3, CV-B4, CV-B5, and CV-B6.[3] Group B coxsackieviruses cause infection of the heart, pleura, pancreas, and liver, causing pleurodynia, myocarditis, pericarditis, and hepatitis.[4] It also causes systemic neonatal disease.[5] This article will focus on coxsackievirus subgroup B.

Coxsackie group B virus is responsible for several syndromes: Viral prodrome including fever, fatigue, malaise, myalgia, gastrointestinal upset such as nausea, vomiting, diarrhea and abdominal pain Exanthema Aseptic meningitis Encephalitis Pleurodynia Myopericarditis Pancreatitis leading to beta-cell destruction and type one diabetes mellitus.[1][6][7]

Coxsackie group B affects males and females equally and can occur worldwide. Infection usually occurs during warm summer months.[8][9] In general, population trends are studied according to presenting disease syndromes rather than specific serotypes. For 2 to 3 years, coxsackievirus B1 was the predominant serotype. Infections due to coxsackievirus B4 were associated with higher mortality than other serotypes. The age of the patient seems to play a role in the development of the different types of manifestations of the infection.[10] Children and adults tend to have a milder disease course with less likelihood of severe complications than neonates.[11][6] Enteroviruses are the predominant cause of viral meningitis in adults, but most of the cases occur in infants and children less than five years old.[12][13][14] Encephalitis occurs in all ages, with a modest inclination for children and young adults. Pleurodynia is most common among adults.[10] Out of the 21 viruses that can cause cardiovascular disease, the coxsackie B virus is the major cause of viral myocarditis, especially in neonates and younger children.[15][16]

The pathogenesis of coxsackieviruses depends upon specific virus-receptor interactions. These interactions determine the location and the origin of the primary infection and also influence the viral spread to other organs during the post viremic stage. The coxsackievirus-adenovirus receptor (CAR) and the decay-accelerating factor (DAF) are the notable receptor proteins that play an important role in the pathogenesis of Coxsackie B virus infections. DAF is expressed in epithelial and endothelial cells. CAR is present in intercalated discs, which are structures that link the myocardial cells and relay signals between cells. Interactions with these receptors facilitate Coxsackie B virus entry into the myocardial cells, eventually leading to myocarditis.[17] CNS infections may occur by hematogenous spread or by axonal transport. Viral replication or activation of the autoimmune system can lead to injury of CNS tissues. While the exact mechanisms that cause cell injury and death remain unknown, viral inhibition of cellular macromolecular production, the toxicity of viral proteins, and virus-induced apoptosis are thought to play a role.[18]

Symptoms of infection with viruses in the Coxsackie B grouping include headache, fever, sore throat, gastrointestinal distress, extreme fatigue, chest pain, and myalgia. The severity of infection varies depending on the host's age, and immune status as well as the presenting disease syndrome and organ system attacked. The incubation period also varies within syndromes, and maximum transmission occurs within the first two weeks of infection.[19] Exanthema presents as maculopapular eruptions surrounded by an erythematous halo. They appear on the face and neck and then spread to the trunk and extremities within twenty-four hours. The lesions spare the palms and soles. They can be associated with petechiae and cervical adenopathy.[20][21] Aseptic meningitis presents as fever and irritability in infants and as fever, headache, stiff neck, nausea, and vomiting in children or adults.[22][23] Encephalitis presents with confusion and or seizures. Severity can range from mild to fatal disease. Coxsackieviruses are known to be associated with epidemic pleurodynia or Bornholm disease. Pleurodynia is characterized by chest pain that worsens with breathing and can often be confused with myocardial infarction. The pain can last from two days to two weeks. Many patients have associated fever, abdominal pain, and tender muscles of the trunk and extremities.[20] Myopericarditis causes inflammation of the subepicardial myocardium and pericardium. Patients present with shortness of breath, chest pain, and an irregular heartbeat. The illness can last for a few hours up to a few months. Severity varies from asymptomatic to fulminant heart failure due to dilated cardiomyopathy and sometimes cardiac arrest.[24] Pancreatitis presents with abdominal pain, nausea, vomiting, and elevated pancreatic enzymes amylase and lipase. Severe pancreatitis due to Coxsackie group B can lead to pancreatic beta-cell destruction and the development of type one diabetes mellitus.[7]

Usually, a clinical diagnosis is all that is required due to the self-limiting course of the infection. However, more severe cases such as myocarditis, aseptic meningitis, encephalitis, and neonatal infection can sometimes require the identification of the specific organism. Furthermore, laboratory diagnosis can be epidemiologically useful, especially during epidemics. Enterovirus infection is diagnosed mainly through RT-PCR, viral cultures, or serological tests. RT-PCR is the most commonly used modality.[25] It can detect Enterovirus RNA in respiratory secretions, urine, serum, and CSF. While RT-PCR is a quick and sensitive test, it is unable to identify the serotype.[26][27] Viral cultures allow typing of an isolate, but they are time-consuming and sixty-five to seventy-five percent sensitive.[28] Serological tests are reserved for the diagnosis of an enterovirus infection when a particular serovar is suspected.[29] Other appropriate investigations include: CBC Comprehensive metabolic profile Erythrocyte sedimentation rate Chest X-ray Abdominal CT Head CT Lumbar puncture for CSF cell count, culture and sensitivity, Gram stain, protein, and glucose, viral PCR Lactic acid Procalcitonin

The virus is self-limited with no specific recommended treatment. Symptomatic and supportive care for the associated syndromes is appropriate. Patients with neurological complications may need antiepileptics for seizures and sedation for delirium.[30] Initial supportive measures for myocarditis include supplemental oxygen and fluid resuscitation. Furthermore, patients may also require heart failure therapy and treatment of arrhythmias.

Overlap of symptoms occurs among various viral infections. There are several important viruses to keep in mind that mimic Coxsackie Group B. These may have targeted treatment plans or other severe complications. These include: Human immunodeficiency virus Hepatitis B and C predispose to hepatocellular carcinoma JCV causes progressive multifocal leukoencephalopathy Measles causes subacute sclerosing panencephalitis Herpes simplex virus encephalitis Rabies encephalitis Poliomyelitis Epstein Barr virus causes splenomegaly and possible splenic rupture Cytomegalovirus

Infections are usually self-limited. Most syndromes result in complete recovery, with a few exceptions. While aseptic meningitis due to Enterovirus has an excellent prognosis, some patients may experience malaise and fatigue for a couple of weeks. Infants and children who suffer from aseptic meningitis may have mild intellectual complications. Myocardial syndromes can sometimes lead to poor outcomes.[30]

Complications arise from infections that target the central nervous system, leading to aseptic meningitis and encephalitis, as well as cardiac involvement, leading to viral myopericarditis and fulminant heart failure.[1][6]

Since no treatment or vaccine protects against Coxsackie B virus infection, healthcare professionals must emphasize promoting infection control strategies like maintaining effective hand and environmental hygiene.[31] Pregnant women can develop perinatal complications like a severe neonatal disease if exposed to persons with an enterovirus infection and, hence, should avoid contact with anyone with suspected infection.[6]

To improve the outcome of enterovirus infections, the interprofessional team should be aware of the severe complications that can occur and anticipate the need for supportive care in such situations. It is also paramount to practice effective handwashing and to maintain good sanitization to reduce disease transmission among patients.