Also called American trypanosomiasis, Chagas disease can infect anyone. Left untreated, Chagas disease later can cause serious heart and digestive problems. During the acute phase of infection, treatment of Chagas disease focuses on killing the parasite.
People who have Chagas disease can be found anywhere in the world. However, transmission of the disease by kissing bugs (vectorborne transmission), only occurs in the Americas. Most people with Chagas disease became infected in rural areas of Mexico, Central America, and South America.
In the chronic phase of the disease, the parasite gets inside your heart muscle. This is why later symptoms often involve the heart. Symptoms of Chagas disease in the acute phase (the first few weeks or months) are: Mild flu-like symptoms, such as fever, fatigue, body aches, and headaches.
Chagas disease, whose etiological agent is Trypanosoma cruzi, presents severe clinical manifestations in humans, including pathological dysfunctions of the heart, oesophagus and colon that may be present in single or combined form during the chronic phase. The protozoan T.
The pathology of Chagas disease is based in an inmunoinflammatory reaction producing fibrosis and remodelling, mainly in the myocardium. In many cases these mechanisms result in a dilated cardiomyopathy with HF and reduced ejection fraction, frequent cardiac arrhythmias and different types of heart block.
Chagas disease is related to several chronic gastrointestinal disorders resulting from damage to both excitatory and inhibitory enteric motor innervations, leading to megaesophagus, megacolon, megasmall intestine, megagallbladder, megacholedochus, achalasia of the cardia, changes in gastric receptive relaxation, fast ...
Chagas disease is an emerging disease in Australia. GPs are best placed to offer opportunistic Chagas disease screening to those at risk from endemic regions as they are likely to be the first point of contact.
The large reservoir of T. cruzi parasites in wild animals of the Americas means that the infection cannot be eradicated. Instead, the control targets are elimination of the transmission to humans and early health-care access of the infected people. There is no vaccine to prevent Chagas disease.
Pathophysiology of Chagas Disease
The parasites invade macrophages at the site of entry and transform into amastigotes that multiply by binary fission; the amastigotes develop into trypomastigotes, enter the bloodstream and tissue spaces, and infect other cells.
Triatomine bugs are a type of reduviid bug that can carry Trypanosoma cruzi, the parasite that causes Chagas disease.
Texas, New Mexico, and Arizona are the states with the most different species and most findings of kissing bugs. Scientists have found that about 50% of kissing bugs are infected with the Chagas parasite. Kissing bugs are a 'vector' because they can carry a parasite that can make people and animal sick.
You're most at risk for Chagas disease if you have visited or traveled in rural Latin America or if you have been exposed to the blood products or received organs from someone infected with Chagas disease. The symptoms may be mild at first and then disappear for years or even decades.
Trypanosoma cruzi, the etiological agent of Chagas' disease, causes an intense inflammatory response in several tissues, including the liver. Since this organ is central to metabolism, its infection may be reflected in the outcome of the disease.
In rare cases, young children or immunosuppressed people infected with Chagas disease develop life-threatening complications, including: Myocarditis (severe inflammation and infection of the heart muscle). Meningoencephalitis (severe inflammation and infection of the brain).
The involvement of the central nervous system (CNS) during human acute and chronic Chagas disease (CD) has been largely reported. Meningoencephalitis is a frequent finding during the acute infection, while during chronic phase the CNS involvement is often accompanied by behavioral and cognitive impairments.
Chronic Chagas disease affects mostly the heart and the digestive tract. Arrhythmias and congestive heart failure are ominous signs of the disease.
Up to a third of people with Chagas will suffer heart damage that becomes evident only many years later and can lead to progressive heart failure or sudden death. Chagas kills more people in Latin America each year than any other parasitic disease, including malaria.
African trypanosomiasis, or sleeping sickness, is caused by Trypanosoma brucei parasites in sub-Saharan Africa and is transmitted by the tsetse fly? (Glossina). American trypanosomiasis, or Chagas disease, is caused by Trypanosoma cruzi parasites in Latin America and is transmitted by the triatomine or 'kissing' bug.
In Australia there were 116,430 persons born in endemic regions in 2011, a 46% increase since 1997, not including adoptees, visitors or second-generation immigrants. Epidemiological models suggest that 2000–3000 persons could be infected but 95% of cases remain undiagnosed.
Background: Chagas disease, resulting from the protozoan Trypanosoma cruzi, is an important cause of heart failure, stroke, arrhythmia, and sudden death.
Symptoms of chagas
In the acute stage - the first few weeks after infection - only mild symptoms show which are common in many other diseases. These can range from body aches and fatigue to fever and vomiting. After the acute phase, chagas goes into remission and no other symptoms may appear for many years.
Chagas disease has an acute and a chronic phase. If untreated, infection is lifelong. Acute Chagas disease occurs immediately after infection, and can last up to a few weeks or months. During the acute phase, parasites may be found in the circulating blood.
Life Cycle:
An infected triatomine insect vector (or “kissing bug”) takes a blood meal and releases trypomastigotes in its feces near the site of the bite wound. Trypomastigotes enter the host through the wound or through intact mucosal membranes, such as the conjunctiva .
The diagnosis of Chagas disease can be made by observation of the parasite in a blood smear by microscopic examination.