Difference between revisions of "Dirofilaria immitis"

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[[Image:Dirofilaria immitus.jpg|thumb|right|250px|''Dirofilaria immitis'' - Courtesy of the Laboratory of Parasitology, University of Pennsylvania School of Veterinary Medicine]]
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Also known as: heartworm disease.
  
Also known as: '''Heartworm Disease — Dirofilariasis
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Do not confuse with: ''Angiostrongylus vasorum'', angiostrongylosis.
  
Beware confusing with: ''[[Angiostrongylus vasorum]]'', [[angiostrongylosis]].
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==Description==
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[[Image:Dirofilaria immitus.jpg|thumb|right|150px|''Dirofilaria immitus'' - Courtesy of the Laboratory of Parasitology, University of Pennsylvania School of Veterinary Medicine]]
  
==Introduction==
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''Dirofilaria immitis'' is a nematode parasite that causes heartworm disease in dogs, cats and ferrets. Heartworm
''Dirofilaria immitis'' is a nematode parasite that causes heartworm disease in dogs, cats and ferrets. Heartworm disease is transmitted by [[Culicidae|mosquito]] bites and there are more than 70 species of mosquito that are able to transmit infection; ''Aedes, Anopheles'' and ''Culex'' are the most common vector species. Heartworm disease has been reported in many countries with temperate climate and is particularly prevalent in the USA, Canada, and southern Europe. The introduction of the PETS travel scheme has increased the concern over Dirofilariasis in the UK.
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disease is transmitted by mosquito bites and there are more than 70 species of mosquito that are able to transmit infection; Aedes, Anopheles and Culex are the most common vector species. Heartwoem disease has been reported in many countries with temperate and is particularly prevalent in the USA, Canada, and southern Europe. The introduction of the PETS travel scheme has increased the concern over Dirofilariasis in the UK.
  
''Dirofilaria'' does have zoonotic potential: infected mosquitos can transmit ''D. immitis'' to humans, but the infection does not become patent. The infective larvae instead reach the lungs, become encapsulated, and die causing granulomatous reactions called "coin lesions" in the process. These are only important because they may be confused with neoplastic metastasis to the lungs on radiography<sup>1</sup>.
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Dirofilarias does have zoonotic potential: infected mosquitos can transmit ''Dirofilaria immitis'' to humans, but the infection does not become patent. The infective larvae instead reach the lungs, become encapsulated, and die causing granulomatous reactions called "coin lesions" in the process. These are only imporant because they may be confused with neoplastic metastasis to the lungs on radiography<sup>1</sup>.
  
 
==Life Cycle==
 
==Life Cycle==
''Dirofilaria immitis'' adults reach maturity and sexually reproduce in the '''pulmonary arteries''' and '''right ventricle'''. Adult males are around 15cm in length, and females are around 25cm<sup>1</sup>. After mating, female worms release larvae known as microfilariae (or L1) into the circulation. When a mosquito takes a blood meal from the infected dog or cat, microfilariae are ingested. Mosquitoes are true intermediate hosts for ''Dirofilaria immitis'', since microfilariae require a period of maturation to L2 then L3 in the vector. The duration of this development depends upon environmental conditions. For example, maturation at 30&deg;C takes around 8 days, but when temperatures are down to 18&deg;C, this takes around one month<sup>2</sup>. Below 14&deg;C, development is halted and resumes when temperatures rise. In cooler climates, this means that transmission of heartworm disease to new canine or feline hosts can only occur in warmer months.  
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''Dirofilaria immitis'' adults reach maturity and sexually reproduce in the pulmonary arteries and right ventricle. Adult males are around 15cm in length, and females are around 25cm<sup>1</sup>. After mating, female worms release larvae known as microfilariae (or L1) into the circulation. When a mosquito takes a blood meal from the infected dog or cat, microfilariae are ingested. Mosquitos are true intermediate hosts for ''Dirofilaria immitis'', since microfilariae require a period of maturation to L2 then L3 in the vector. The duration of this development depends upon environmental conditions. For example, maturation at 30&deg;C takes around 8 days, but when temperatures are down to 18&deg;C, this takes around one month<sup>2</sup>. Below 14&deg;C, development is halted and resumes when temperatures rise. In cooler climates, this means that transmission of heartworm disease to new canine or feline hosts can only occur in warmer months.  
  
 
Once matured, L3 in the mosquito migrate to the labium, from which they erupt onto the host's skin as the mosquito feeds. Larvae then migrate into the bite wound and, as most dogs are highly susceptible to heartworm disease, most L3 then establish infection. It takes 2-3 days for L3 to moult to L4, which remain in the subcutaneous tissues for up to two months before becoming young adults (L5) and migrating to the pulmonary arteries.  
 
Once matured, L3 in the mosquito migrate to the labium, from which they erupt onto the host's skin as the mosquito feeds. Larvae then migrate into the bite wound and, as most dogs are highly susceptible to heartworm disease, most L3 then establish infection. It takes 2-3 days for L3 to moult to L4, which remain in the subcutaneous tissues for up to two months before becoming young adults (L5) and migrating to the pulmonary arteries.  
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==Pathogenesis==
 
==Pathogenesis==
Heartworm disease primarily affects the cardiopulmonary system and the severity and extent of lesions depends on several factors. These include the number and location of adult worms<sup>1, 2</sup>, the duration of infection, and the level of activity of the host<sup>1</sup>. Parasites in the pulmonary arteries cause mechanical irritation, leading to endothelial damage, proliferation of the intima and perivascular cuffing with inflammatory cells. This results in narrowing and occlusion of the vessels which in turn causes pulmonary hypertension. A combination of pulmonary hypertension and inflammatory mediators can lead to an increase in the permeability of pulmonary vessels, giving periarterial oedema and intersitial and alveolar infiltrates. Eventually, irreversible interstitial fibrosis arises.
 
  
Sequelae to heartworm infection include pulmonary thromboembolism, which can either occur due to the death and metastasis of adult worms, or due to platelet aggregation induced by the parasite. In severe cases, live nematodes can migrate to the right ventricle, right atrium and caudal vena cava. The resulting incompetence of the tricuspid valve, augmented by concurrent pulmonary hypertension, leads to signs of right-sided heart failure. Flow of erythrocytes through the mass of parasites formed can also cause haemolysis and thus haemoglobinaemia. This combination of acute right-sided heart failure and intravascular haemolysis is referred to as "caval syndrome", which in severe cases can also be characterised by thromboembolic events and [[Disseminated Intravascular Coagulation|disseminated intravascular coagulation]]. Due to the smaller numbers of adult worms, caval syndrome is less common in cats<sup>2</sup>.
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Heartworm disease primarily affects the cardiopulmonary system and the severity and extent of lesions depends several factors. These include the number and location of adult worms<sup>1, 2</sup>, the duration of infection, and the level of activity of the host<sup>1</sup>. Parasites in the pulmonary arteries cause mechanical irritation, leading to endothelial damage, proliferation of the intima and perivascular cuffing with inflammatory cells. This results in narrowing and occlusion of the vessels which in turn causes pulmonary hypertension. A combination of pulmonary hypertension and inflammatory mediators can lead to in an increase in the permeability of pulmonary vessels, giving periarterial oedema and intersitial and alveolar infiltrates. Eventually, irreversible interstitial fibrosis arises.
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Sequelae to heartworm infection include pulmonary thromboembolism, which can either occur due to the death and metastasis of adult worms, or due to platelet aggregation induced by the parasite. In severe cases, live nematodes can migrate to the right ventricle, right atrium and caudal vena cava. The resulting incompetence of the tricuspid valve, augmented by concurrent pulmonary hypertension, leads to signs of right-sided heart failure. Flow of erythrocytes through the mass of parasites formed can also cause haemolysis and thus haemoglobinaemia. This combination of acute right-sided heart failure and intravascular haemolysis is referred to as "caval syndrome", which in severe cases can also be characterised by thromboembolic events and disseminated intravascular coagulation. Due to the smaller numbers of adult worms, caval syndrome is less common in cats<sup>2</sup>.
  
 
In cats, heartworm disease generally causes a diffuse pulmonary infiltrate and an eosinophilic pneumonia<sup>2</sup>. Adult worms may die and embolise to the lungs, resulting in severe haemorrhage and oedema of the affected lobe. Immature nematodes have also been known to migrate to sites other than the pulmonary arteries and heart such as the CNS, eye and subcutaneous tissues. These ectopic infections are far more common in cats than in dogs, suggesting that ''D. immitis'' is not well adapted to feline hosts.
 
In cats, heartworm disease generally causes a diffuse pulmonary infiltrate and an eosinophilic pneumonia<sup>2</sup>. Adult worms may die and embolise to the lungs, resulting in severe haemorrhage and oedema of the affected lobe. Immature nematodes have also been known to migrate to sites other than the pulmonary arteries and heart such as the CNS, eye and subcutaneous tissues. These ectopic infections are far more common in cats than in dogs, suggesting that ''D. immitis'' is not well adapted to feline hosts.
  
 
==Signalment==
 
==Signalment==
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''Dirofilaria immitis'' infection affects dogs more commonly than cats, and risk is greatest in outdoor animals. Dogs of any age may be affected, but infections are most common in 3 to 8 year old dogs, and medium and large breeds are over-represented<sup>1, 3</sup>. In cats, there are no breed or age predispositions, but males are more frequently affected<sup>3</sup>. Ferrets may also contract dirofilariasis; there are no age or sex predilections<sup>1</sup>.
 
''Dirofilaria immitis'' infection affects dogs more commonly than cats, and risk is greatest in outdoor animals. Dogs of any age may be affected, but infections are most common in 3 to 8 year old dogs, and medium and large breeds are over-represented<sup>1, 3</sup>. In cats, there are no breed or age predispositions, but males are more frequently affected<sup>3</sup>. Ferrets may also contract dirofilariasis; there are no age or sex predilections<sup>1</sup>.
  
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===Clinical Signs===
 
===Clinical Signs===
  
In dogs, historical findings at the time of presentation can vary. Some animals are asymptomatic, or cough only occasionally. In countries where heartworm is endemic, animals may be routinely tested for dirofilariasis six months after the end of the high-risk season<sup>3</sup>. Therefore, positive laboratory testing may be the first indication of disease<sup>1</sup>. More obvious signs may be seen depending on the severity of disease. Generally, the onset of heartworm disease is insidious, and clinical signs are related either to a high parasite burden, or to an allergic response to the parasite<sup>2</sup>. Affected dogs most often show coughing, and dyspnoea/tachypnoea, exercise intolerance, loss of condition and syncope may also be seen. In severe cases the pulmonary vessels may rupture, leading to haemoptysis or epistaxis. There is a tendency for signs to only manifest during exercise, and so patients with a sedentary lifestyle may never show overt disease. Right-sided congestive heart failure may ensue when worm burden is high, and signs can include jugular distension, ascites, marked exercise intolerance and hepatomegaly. A systolic murmur is sometimes audible on cardiac auscultation.
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In dogs, historical findings at the time of presentation can vary. Some animals are asymptomatic, or cough only occasionally. In countries where heartworm is endemic, animals may be routinely tested for dirofilariasis at the end of the high-risk season, when weather becomes cooler<sup>3</sup>. Therefore, positive laboratory testing may be the first indication of disease<sup>1</sup>. More obvious signs may be seen depending on the severity of disease. Generally, the onset of heartworm disease is insidious, and clinical signs are related either to a high parasite burden, or to an allergic response to the parasite<sup>2</sup>. Affected dogs most often show coughing, and dyspnoea/tachypnoea, exercise intolerance, loss of condition and syncope may also be seen. In severe cases the pulmonary vessels may rupture, leading to haemoptysis or epistaxis. There is a tendency for signs to only manifest during exercise, and so patients with a sedentary lifestyle may never show overt disease. Right-sided congestive heart failure may ensue when worm burden is high, and signs can include jugular disension, ascites, marked exercise intolerance and hepatomegaly. A systolic murmur is sometimes audible on cardiac auscultation.
  
 
A classification system for the presentation of heartworm disease exists<sup>1</sup>, outlined in the table below.
 
A classification system for the presentation of heartworm disease exists<sup>1</sup>, outlined in the table below.
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  !width="92%"|<center><u>'''Clinical Signs'''</u></center>  
 
  !width="92%"|<center><u>'''Clinical Signs'''</u></center>  
 
  |-
 
  |-
  |<center>'''Class I'''</center>   
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  |<center>'''Class 1'''</center>   
 
  |'''Asymptomatic or mild disease'''  
 
  |'''Asymptomatic or mild disease'''  
 
*Weight loss, reduced exercise tolerance or an occasional cough may be seen.  
 
*Weight loss, reduced exercise tolerance or an occasional cough may be seen.  
 
*No radiographic signs or laboratory abnormalities.
 
*No radiographic signs or laboratory abnormalities.
 
  |-
 
  |-
  |<center>'''Class II'''</center>  
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  |<center>'''Class 2'''</center>  
 
  |'''Moderate disease'''
 
  |'''Moderate disease'''
 
*Animal coughs occasionally and shows mild-to-moderate exercise intolerance.  
 
*Animal coughs occasionally and shows mild-to-moderate exercise intolerance.  
*Lung sounds may be increased
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*Lung sounds may be increasd
 
*Radiography may show mild-to-moderate changes, e.g. right ventricular enlargement.  
 
*Radiography may show mild-to-moderate changes, e.g. right ventricular enlargement.  
*Anaemia and proteinuria may be present.  
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*Anemia and proteinuria may be present.  
 
  |-
 
  |-
  |<center>'''Class III'''</center>  
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  |<center>'''Class 3'''</center>  
 
  |'''Severe disease'''
 
  |'''Severe disease'''
*Signs are variable but may include weight loss, exercise intolerance, tachypnoea, dyspnoea, severe/persistent coughing, haemoptysis, syncope, or ascites.
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*Signs are variable but may include weight loss, exercise intolerance, tachypnoea, dyspnoea, severe/persistent coughing, hemoptysis, syncope, or ascites.
 
*Radiographs appear abnormal: right ventricular hypertrophy, enlargement of the main pulmonary artery, and diffuse pulmonary densities. ECG often shows right ventricular hypertrophy.  
 
*Radiographs appear abnormal: right ventricular hypertrophy, enlargement of the main pulmonary artery, and diffuse pulmonary densities. ECG often shows right ventricular hypertrophy.  
 
*Anaemia, thrombocytopenia, and proteinuria are seen.
 
*Anaemia, thrombocytopenia, and proteinuria are seen.
 
  |-
 
  |-
  |<center>'''Class IV'''</center>  
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  |<center>'''Class 4'''</center>  
 
  |'''Caval syndrome'''
 
  |'''Caval syndrome'''
 
*Sudden onset of collapse, haemoglobinuria, and respiratory distress.  
 
*Sudden onset of collapse, haemoglobinuria, and respiratory distress.  
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  |}
 
  |}
  
'''Caval syndrome''' is a very severe form of heartworm disease that can occur in dogs and cats. It is characterised by respiratory distress, signs of right-sided heart failure, intravascular haemolysis and haemoglobinuria. Disseminated intravascular coagulation frequently occurs, and the syndrome is often fatal.
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Caval syndrome is a very severe form of heartworm disease that can occur in dogs and cats. It is characterised by respiratory distress, signs of right-sided heart failur, intravascular haemolysis and haemoglobinuria. Disseminated intravascular coagulation frequently occurs, and the syndrome is often fatal.
  
In cats, most infections are asymptomatic. However, sudden death can occasionally occur. This may be preceded by an acute respiratory crisis, thought to be due to parasitic thromboembolism and obstruction of a major pulmonary artery<sup>1, 2</sup>. When clinical signs are less acute, they are vague and may include anorexia, weight loss and lethargy. Intermittent coughing and dyspnoea can appear similar to feline asthma. Syncope may also occur, and cats may vomit. The cause of this vomiting is undetermined<sup>3</sup>.
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In cats, most infections are asymptomatic. However, sudden death can occasionally occur. This may be preceded by an acute respiratory crisis, thought to be due to parasitic thromboembolism and obstruction of a major pulmonary artery<sup>1, 2</sup>. When clinical signs are less acute, they are vague and may include anorexia, weight loss and letheargy. Intermittent coughing and dyspnoea can appear similar to feline asthma. Syncope may also occur, and cats may vomit. The cause of this vomiting is undetermined<sup>3</sup>.
  
 
===Radiography===
 
===Radiography===
In dogs, thoracic radiography provides good information on disease severity and is useful for screening dogs showing clinical signs compatible with ''D. immitis'' infection<sup>1</sup>. However, thoracic radiograph do not necessarily reflect the current worm burden: radiographic signs of advanced disease can persist long after an infection has run its course<sup>4</sup>. Conversely, dogs with high burdens may be inactive and thus show few clinical signs or radiographic changes. Radiographic signs are mild-to-moderate in class II disease, but become more obvious in class III infections. The main pulmonary artery is enlarged<sup>1, 4</sup>, and the caudal lobar vessels appear tortuous<sup>1</sup>. Ill-defined, fluffy infiltrates are apparent, and often surround the caudal lobar vessels. Right-sided cardiomegaly may be appreciated, and pleural and peritoneal effusions can be noted in right-sided congestive heart failure<sup>4</sup>.
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In dogs, thoracic radiography provides good information on disease severity and is useful for screening dogs showing clinical signs compatible with ''D. immitis'' infection<sup>1</sup>. However, thoracic radiograph do not neccessarily reflect the current worm burden: radiographic signs of advanced disease can persist long after an infection has run its course<sup>4</sup>. Conversely, dogs with high burdens may be inactive and thus show few clinical signs or radiographic changes. Radiographic signs are mild-to-moderate in class II disease, but become more obvious in class III infections. The main pulmonary artery is enlarged,sup>1, 4</sup>, and the caudal lobar vessels appear tortuous<sup>1</sup> Ill-defined, fluffy infiltrates are apparent, and often surroung in the caudal lobar vessels. Right-sided cardiomegaly may be appreciated, and pleural and peritoneal effusions can be noted if right-sided congestive heart failure occurs<sup>4</sup>.
  
Cardiac changes on thoracic radiography are less common in cats than dogs. The caudal lobar veins are enlarged (greater than 1.5 times the width of the ninth rib), and the pulmonary arteries are blunted and tortuous<sup>3, 5</sup>. Patchy parenchymal infiltrates may be seen in the region of vessels in animals showing respiratory signs<sup>1, 3</sup>. Enlargement of the main pulmonary artery cannot normally be seen in cats, as it has a relatively midline position and is thus obscured by the cardiac silhouette<sup>1, 5</sup>. Right-sided cardiomegaly is not considered a typical finding in the cat<sup>5</sup>.
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Cardiac changes on thoracic radiography are less common in cats than dogs. The caudal lobar veins are enlarged (greater than 1.5 times the width of the ninth ribe), and the pulmonary arteries are blunted and tortuous<sup>3, 5</sup>. Patchy parenchymal infiltrates may be seen in the region of vessels in animals showing respiratory signs<sup>1, 3</sup>. Enlargement of the main pulmonary artery cannot normally be seen in cats, as it is has a relatively midline position and is thus obscured by the cardiac silhouette<sup>1, 5</sup>. Right-sided cardiomegaly is not considered a typical finding in the cat<sup>5</sup>.
  
 
===Echocardiography===
 
===Echocardiography===
In dogs, echocardiography is not particularly useful as a diagnostic tool for heartworm disease. In severe, chronic pulmonary hypertension, right ventricular hypertrophy, septal flattening, underloading of the left heart, and high-velocity tricuspid and pulmonic regurgitation may be seen<sup>1</sup>. With caval syndrome or high-burden infections, worms may be visualised in the right heart and vena cava.
 
  
Echocardiography is more important in cats than dogs because of the increased difficulty of diagnosis and the fact that this test can have a high sensitivity depending on operator experience<sup>1</sup>. Specificity is 100%<sup>5</sup>, and the test can help exclude or confirm other primary cardiac diseases such as hypertrophic cardiomyopathy<sup>3</sup>. Worms can be visualised as parallel hyperechoic lines<sup>1</sup>, and are seen in the right atrium and ventricle and main pulmonary artery<sup>1, 3, 5</sup>.
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In dogs, echocardiography is not particularly useful as a diagnostic tool for heartworm disease. In severe, chronic pulmonary hypertansion,  right ventricular hypertrophy, septal flattening, underloading of the left heart, and high-velocity tricuspid and pulmonic regurgitation may be seen<sup>1</sup>. With caval syndrome or high-burden infections, worms may be visualised in the right heart and vena cava.
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Echocardiography is more important in cats than dogs because of the increased difficulty of diagnosis and the fact that this test can have a high sensitivity depending on operater experience<sup>1</sup>. Specificity is 100%<sup>5</sup>, and the test can help exclude or confirm other primary cardiac diseases such as hypertrophic cardiomyopathy<sup>3</sup>. Worms can usually be visualised as parallel hyperechoic lines<sup>1</sup>, and are seen in the right atrium and ventricle and main pulmonary artery<sup>1, 3, 5</sup>.
  
 
===Electrocardiography===
 
===Electrocardiography===
The ECG of infected dogs is usually normal. Right ventricular hypertrophy patterns may be seen in chronic ,severe pulmonary hypertension and are associated with impending or apparent right-sided congestive heart failure<sup>4</sup>. Arrhythmias do not normally occur, buy atrial fibrillation is is occasionally seen in Class III disease.
 
  
Electrocardiography is less useful in the cat, as involvement of the heart chambers does not occur as frequently as in the dog<sup>5</sup>.
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The ECG of infected dogs is usually normal. Right ventricular hypertrophy patterns are seen when there is severe, chronic pulmonary hypertension and are associated with overt or impending right-sided CHF (ascites). Heart rhythm disturbances are usually absent or mild, but atrial fibrillation is an occasional complication in dogs with Class III disease.
  
 
===Laboratory Tests===
 
===Laboratory Tests===
In both dogs and cats, '''routine haematology, biochemistry and urinalysis''' should be performed. Most parameters are usually within normal limits, but an anaemia can often be seen. Eosinophilia and basophilia are also common<sup>1, 3</sup>. Eosinophilia peaks as L5 enter the pulmonary arteries and subsequently varies. An inflammatory leukogram is possible<sup>3</sup>. Hyperglobulinaemia due to antigenic stimulation is an inconsistent finding<sup>1, 3</sup>. Right-sided heart failure or immune-complex glomerulonephritis can lead to hypoalbuminaemia and, very occasionally, nephrotic syndrome<sup>1</sup>. Because of this, it is possible for urinalysis to reveal proteiunuria<sup>1, 3</sup>. Haemoglobinaemia and haemoglobinuria are associated with caval syndrome<sup>3</sup>.
 
  
[[Image:dirofilariasis.jpg|right|thumb|200px|Dirofilariasis. Courtesy of T. Scase]]
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In both dogs and cats, routine haematology, biochemistry and urinalysis should be performed. Most parameters are usually within normal limits, but an anaemia can often be seen. Eosinophilia and basophilia are also common, and when seen together suggests occult dirofilariasis or allergic lung disease <sup>1, 3</sup>. Eosinophilia peaks as L5 enter the pulmonary arteries and subsequently varies. An inflammatory leukogram is also possible<sup>3</sup>. Hyperglobulinemia due to antigenic stimulation is an inconsistent finding<sup>1, 3</sup>. Right-sided heart failure or immune-complex glomerulonephritis can lead to hypoalbuminaemia and, very occasionally, nephrotic syndrome<sup>1</sup>. Because of this, it is possible for urinalysis to reveal proteiunuria<sup>1, 3</sup>. Haemoglobinaemia and haemoglobinuria are associated with caval syndrome<sup>3</sup>.  
There are several methods for the specific demonstration of ''Dirofilaria immitis'' in the animal. Firstly, direct '''microscopic examination''' allows rapid identification of microfilariae in a drop of fresh blood, as their movements can vigorously displace the surrounding red blood cells<sup>2</sup>. Despite being quick, simple and inexpensive, this test is not sufficiently sensitive to provide a definitive diagnosis, particularly when there is a low concentration of microfilariae in the bloodstream. '''Filtration methods''' therefore exist to facilitate the microscopic demonstration of microfilariae<sup>2, 3</sup>. These include the '''modified Knott's test''', which involves haemolysis, centrifugation and staining with methylene blue before direct examination. Tests such as this are more sensitive than merely examining a drop of blood, and the morphology of microfilariae can be clearly seen. However, sensitivity in comparison to other methods is still low and so microfilarial identification tests are often reserved for confirmation of weak positive antigen tests and determination of microfilarial status prior to treatment with a microfilaricide<sup>3</sup>. Cats frequently lack circulating microfilariae, and so direct microscopic examination is of little use in this species.
 
[[Image:dirofilariasis 2.jpg|right|thumb|200px|'''Dirofilariasis'''. Courtesy of T. Scase]]
 
Tests exist to detect ''D. immitis'' antigens. '''ELISAs''' specific for proteins released from the reproductive tract of adult female worms are available for in-house use<sup>2</sup>. Sensitivity and specificity are excellent, but small worm burdens and the presence of immature female- or male-only infections can give low antigen titres hence false negatives. This is especially common in cats. '''Specific agglutination and immunochromatography''' techniques are also available for use in dogs. Any antigen test performed in the first six months of infection may give false negative results as levels of circulating antigen are initially low while female worms mature. '''In-house tests''' are also available to detect antibody against ''Dirofilaria immitis''. The presence of antibodies confirms exposure, but does not necessarily provide information about current infection. These tests are therefore most useful for ruling out infection. ''D. immitis'' antibody tests have a low specificity<sup>2</sup> and so have largely been superceded by tests for antigen.
 
  
'''PCR-based tests''' are highly sensitive and specific for the diagnosis of immature and adult heartworms, and are especially useful in unconventional (e.g. wildlife) hosts<sup>2</sup>. At present, these tests are not widely available for the diagnosis of ''Dirofilaria immitis''.
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he antigen detection test is the preferred diagnostic method for asymptomatic dogs or when seeking verification of a suspected HW infection. This is the most sensitive diagnostic method available to veterinary practitioners. Even in areas where the prevalence of HW infection is high, ~20% of infected dogs may not be microfilaremic. Also, monthly macrolide prophylaxis induces embryo stasis in female dirofilariae.
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Available antigen detection tests are very sensitive and specific. To determine when testing might become useful, it is advisable to add a predetection period to the approximate date on which infection may have been possible. A reasonable interval is 7 mo. There is generally no need to test a dog for antigen or microfilariae prior to ~7 mo of age. The level of antigenemia is directly related to the number of mature female worms present. At least 90% of dogs harboring ≥3 adult females will test positive. In general, strong-quick positive reactions correlate with relatively high worm burdens. For low-burden suspects, commercial laboratory-based microwell titer tests are the most sensitive.
  
 
===Pathology===
 
===Pathology===
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[[Image:dirofilariasis.jpg|right|thumb|150px|<small><center>'''Dirofilariasis'''. Courtesy of T. Scase</center></small>]]
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[[Image:dirofilariasis 2.jpg|right|thumb|150px|<small><center>'''Dirofilariasis'''. Courtesy of T. Scase</center></small>]]
  
On post-mortem examination, ''Dirofilaria immitis'' worms are apparent in the pulmonary artery and possibly the right side of the heart. The right side of the heart is found to be enlarged and there is proliferation of the pulmonary arterial myointima. Pulmonary thromboembolism and haemorrhage may be seen. If right-sided congestive heart failure was present in life, hepatomegaly and hepatic congestion will be apparent.
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On post-mortem examination, the right side of the heart is found to be enlarged. There is proliferation of the pulmonary arterial myointima, as well as pulmonary thromboembolism and haemorrhage. If right-sided congestive heart failure was present in life, the hepatomegaly and hepatic congestion will be seen.
  
 
==Treatment==
 
==Treatment==
Animals with right-sided congestive heart failure require stablisation with diuretics, ACE inhibitors and cage rest before treatment for heartworm disease is implemented. Animals with severe respiratory signs also require stabilisation with oxygen supplementation, anti-inflammatory doses of corticosteroid and anti-thrombotic drugs.
 
 
The specific adulticidal treatment for ''Dirofilaria immitis'' is '''melarsomine dihydrochoride''', a new generation arsenical compound. Melarsomine is administered intramuscularly into the epaxial muscles, and pressure should be applied during and after needle withdrawal<sup>3</sup>. A "graded-kill" protocol is recommended: an initial injection is followed one month later with two injections at an interval of 24 hours, given on opposite sides<sup>1-4</sup>. This spreads the killing effects over two treatments, with an aim to reducing the occurrence of thromboembolism after parasite death. Cage rest and anti-inflammatory doses of corticosteroids in the week following melarsomine treatment can also reduce the likelihood of pulmonary thromboembolism. Antigen testing four months after adulticidal treatment will determine whether it is necessary to repeat the therapy<sup>3</sup>.
 
  
Adulticidal treatment may be declined by the owner, owing to the risk of thromboembolism. Alternatively, it may not be possible to implement adulticidal treatment if the patient is suffering renal or hepatic failure<sup>3</sup>. In these cases, monthly administration of prophylactic doses of ivermectin is a reasonable treatment option, as it prevents further infection and may kill some adult nematodes<sup>2</sup>.
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===Adulticidal Treatment===
  
Even low grade infections in cats may result in pulmonary thromboembolism with adulticidal treatment. Because of this, symptomatic treatment of sick cats may be followed by surgical or catheter-based extraction of nematodes once the patient is stable<sup>3</sup>. Stablisation is similar to that for feline asthma, and can include cage rest, oxygen supplementation, bronchodilators (e.g. theophylline), tapering doses of prednisolone, and balanced fluid therapy if indicated<sup>3</sup>. Heartworms have a much shorter life-span in cats, and spontaneous remission is seen in some cases. Regular monitoring may therefore be the best course of action in clinically well cats.
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Decisions in the treatment of heartworm disease are dependent on the severity of infection. A scheme exists to classify patients in terms of disease severity<sup>2</sup>. Class one patients have subclinical heartworm disease, and carry an excellent prognosis following treatment wiht adulticidal drugs. Class two animals show mild to moderate clinical signs and similar radiographic changes. These animals may respond positively to treatment. Dogs with class 3 disease have severe clinical signs, such as persistent coughing, dyspnoea, right-sided heart failure or haemoptysis, and these are reflected by severe radiographic signs. These cases have a high risk of pulmonary thromboembolism and so prognosis is guarded and the benefits of adulticidal treatment should be considered carefully.  
  
In '''caval syndrome''', surgery is the treatment of choice. Worms are removed from the right side of the heart and the main pulmonary artery using flexible crocodile or basket-type retrieval forceps<sup>2</sup>. This procedure is complex and requires general anaesthesia and fluoroscopic imaging, but reduces the risk of thromboembolism following subsequent adulticidal treatment. Symptomatic and supportive therapy to stabilise the patient should be continued for around one month after surgery before adulticidal treatment is administered<sup>3</sup>.
+
Even low grade infections in cats may result in pulmonary thromboembolism with adulticidal treatment, and spontaneous remission is seen in some cats. Because of this, symptomatic treatment (cage rest, oxygen supplementation, fluid therapy, bronchodilators and dexamethasone) may be more appropriate in sick cats, and clinically well cats can merely be monitored regularly for remission. Adulticidal treatment should only be considered in cats that fail to respond to supportive treatments but are in a stable condition.
  
'''No drugs are specifically approved for microfilaricidal treatment''' of ''Dirofilaria immitis'', and successful elimination of adult worms should result in the demise of circulating microfilariae four to six weeks later<sup>2</sup>. '''Single doses of ivermectin, milbemycin oxime, moxidection or selamectin''' are, however, effective at removing microfilariae from the circulation. The sudden death of large numbers of microfilariae may invoke an anaphylactic response, and oral prednisolone may be administered with microfilaricides to help prevent this.
+
Adulticidal treatment involves the administration of
+
a new generation arsenical compound, melarsomine dihydrochloride
Heartworm prophylaxis should be implemented in all cats and dogs living in or visiting areas in which ''Dirofilaria immitis'' is endemic. Ivermectin or milbemycin oxime can be given ''per os'' on a monthly basis, and selemectin spot-on is effective when applied each month. If animals have already been exposed to ''Dirofilaria immitis'' it may be wise to perform an antigen test before starting treatment. In endemic countries, routine antigen testing six months after the end of the previous heartworm season will detect infections that have slipped through the net, and enable treatment during the mild, early stages of disease<sup>3</sup>.
+
(Immiticide, Merial; this product is not
 +
licensed for use in the UK). Melarsomine is less nephrotoxic
 +
and hepatotoxic than its predecessor thiacetarsamide,
 +
and has a higher efficacy. Melarsomine is injected
 +
intramuscularly into the lumbar muscles at a recommended
 +
dose of 2-5 mg/kg, repeated after 24 hours. However,
 +
only a single dose should be administered to class 3 dogs,
 +
to kill just a proportion of worms and hence minimise
 +
the risk of pulmonary thromboembolism. If the patient
 +
remains stable, the standard adulticidal protocol can be
 +
administered one month later. In the week following the
 +
administration of melarsomine, the likelihood of pulmonary
 +
thromboembolism can be minimised with cage
 +
rest and corticosteroids at anti-inflammatory doses.
 +
If adulticidal treatment is declined by the owner,
 +
monthly administration of prophylactic doses of ivermectin
 +
may represent a reasonable option because it will prevent
 +
further infection and may kill some adult nematodes.
 +
Patients with severe caval syndrome may benefit from
 +
physical removal of worms from the right side of the
 +
heart and the main pulmonary artery using flexible crocodile
 +
or basket-type retrieval forceps. This procedure is
 +
complex, requires general anaesthesia and fluoroscopic
 +
imaging, but may reduce the risk of thromboembolism
 +
following subsequent adulticidal treatment.
  
==Prognosis==
+
===Microfilaricidal Treatment===
  
In mildly symptomatic  or asymptomatic animals, the course of dirofilariasis is usually uneventful following treatment and the prognosis is excellent<sup>3</sup>. Animals with severe infection carry a guarded prognosis with a higher risk of complications.
+
No drugs are specifically approved for microfilaricidal treatment of ''Dirofilaria immitis'', and successful elimination of adult worms should results in the demise of circulating microfilariae four to six weeks later<sup>2</sup>. Single doses of ivermectin, milbemycin oxime, moxidection or selamectin are, however, effective at removing microfilariae from the circulation. The sudden death of large numbers of microfilariae may invoke an anaphylactic response, and oral prednisolone may be administered with microfilaricides to help prevent this.
  
{{Learning
+
===Prevention===  
|literature search = [http://www.cabdirect.org/search.html?rowId=1&options1=AND&q1=%22Dirofilaria+immitis%22&occuring1=title&rowId=2&options2=AND&q2=&occuring2=freetext&rowId=3&options3=AND&q3=&occuring3=freetext&x=21&y=6&publishedstart=2000&publishedend=yyyy&calendarInput=yyyy-mm-dd&la=any&it=any&show=all Dirofilaria immitis publications since 2000]
 
|full text = [http://www.cabi.org/cabdirect/FullTextPDF/2010/20103181752.pdf '''A review of American heartworm society guidelines for the management of heartworm infections in cats.''' Guerrero, J.; The North American Veterinary Conference, Gainesville, USA, Small animal and exotics. Proceedings of the North American Veterinary Conference, Orlando, Florida, USA, 16-20 January 2010, 2010, pp 1173-1176, 1 ref.]
 
  
[http://www.cabi.org/cabdirect/FullTextPDF/2008/20083097550.pdf '''Epidemiology and prevention of ''Dirofilaria'' infections in dogs and cats.''' Genchi, C.; Guerrero, J.; McCall, J. W.; Venco, L.; Veterinary Parasitology and Parasitic Diseases, Naples, Italy, Mappe Parassitologiche, 2007, 8, pp 145-161, many ref.]
+
Heartworm prophylaxis should be implemented in all cats and dogs living in or visiting areas in which ''Dirofilaria immitis'' is endemic. In the UK, milbemycin oxime and selamectin are licensed for the prevention of heartworm disease and should be administered on a monthly basis as they are capable of killing migrating larvae up to week six post-infection. In the event of non-compliance or a missed dose, it may be necessary to test the animal for ''Dirofilaria immitis'' six months later if they are likely to have been exposed to infection during the time they were unprotected. Drugs that persist in the long term, such as injectable moxidectin, can help overcome this issue.
  
[http://www.cabi.org/cabdirect/FullTextPDF/2006/20063226177.pdf ''' Heartworm of dog - its aetiopathogenesis, diagnosis, treatment and prevention.''' Kundu, P.; Intas Pharmaceuticals Ltd, Ahmedabad, India, Intas Polivet, 2006, 7, 1, pp 106-110, 16 ref.]
+
==Prognosis==
 
 
[http://www.cabi.org/cabdirect/FullTextPDF/2005/20053201370.pdf ''' The utility of echocardiography in the diagnosis of feline heartworm disease: a review of published reports.''' Defrancesco, T. C.; Atkins, C. E.; Seward, R. L.; Knight, D. H.; American Heartworm Society, Batavia, USA, Recent advances in heartworm disease: Symposium '98, Tampa, Florida, USA, 1-3 May, 1998, 1998, pp 103-106, 20 ref.]
 
 
 
|Vetstream = [https://www.vetstream.com/canis/search?s=nematode Nematodes]
 
}}
 
  
 
+
In mildly symptomatic  or asymptomatic animals, the course of dirofilariasis is usually uneventful following treatment and the prognosis is excellent<sup>3</sup>. Animals with severe infection carry a guarded prognosis with a higher risk of complications.
{{Chapter}}
 
{{Mansonchapter
 
|chapterlink = http://www.mansonpublishing.co.uk/book-images/9781840760576_sample.pdf
 
|chaptername = Cardiopulmonary Dirofilariasis
 
|book = Arthropod-borne Infectious Diseases of the Dog and Cat
 
|author = Susan E. Shaw, Michael J. Day
 
|isbn = 9781840760576
 
}}
 
  
 
==Links==
 
==Links==
 
*[http://www.merckvetmanual.com/mvm/index.jsp?cfile=htm/bc/11300.htm The Merck Veterinary Manual - Heartworm Disease]
 
*[http://www.dogheartworm.org/ dogheartworm.org]
 
*[http://www.defra.gov.uk/foodfarm/farmanimal/diseases/vetsurveillance/dactari/ DEFRA - Dog and Cat Travel and Risk Information]
 
 
 
==References==
 
==References==
  
Line 154: Line 159:
 
#Venco, L (2007) Heartworm (Dirofilaria immitis) disease in cats. ''Dirofilaria immitis and D. repens in dog and cat and human infections'', 126-132.
 
#Venco, L (2007) Heartworm (Dirofilaria immitis) disease in cats. ''Dirofilaria immitis and D. repens in dog and cat and human infections'', 126-132.
 
#Ridyard, A (2005) Heartworm and lungworm in dogs and cats in the UK, ''In Practice'', '''27(3)''', 147-153.
 
#Ridyard, A (2005) Heartworm and lungworm in dogs and cats in the UK, ''In Practice'', '''27(3)''', 147-153.
 
 
{{review}}
 
 
==Webinars==
 
<rss max="10" highlight="none">https://www.thewebinarvet.com/parasitology/webinars/feed</rss>
 
  
 
[[Category:Filarioidea]]
 
[[Category:Filarioidea]]
 
[[Category:Dog_Nematodes]]
 
[[Category:Dog_Nematodes]]
 
[[Category:Cat_Nematodes]]
 
[[Category:Cat_Nematodes]]
[[Category:Zoonoses]]
+
[[Category:To_Do_-_Parasites]]
[[Category:Cardiovascular Diseases - Dog]]
+
 
[[Category:Cardiovascular Diseases - Cat]]
+
 
 
[[Category:Respiratory Parasitic Infections]]
 
[[Category:Respiratory Parasitic Infections]]
 
+
[[Category:To_Do_-_Lizzie]]
[[Category:Expert_Review]]
 
[[Category:Cardiology Section]]
 

Revision as of 09:04, 26 August 2010



Also known as: heartworm disease.

Do not confuse with: Angiostrongylus vasorum, angiostrongylosis.

Description

Dirofilaria immitus - Courtesy of the Laboratory of Parasitology, University of Pennsylvania School of Veterinary Medicine

Dirofilaria immitis is a nematode parasite that causes heartworm disease in dogs, cats and ferrets. Heartworm disease is transmitted by mosquito bites and there are more than 70 species of mosquito that are able to transmit infection; Aedes, Anopheles and Culex are the most common vector species. Heartwoem disease has been reported in many countries with temperate and is particularly prevalent in the USA, Canada, and southern Europe. The introduction of the PETS travel scheme has increased the concern over Dirofilariasis in the UK.

Dirofilarias does have zoonotic potential: infected mosquitos can transmit Dirofilaria immitis to humans, but the infection does not become patent. The infective larvae instead reach the lungs, become encapsulated, and die causing granulomatous reactions called "coin lesions" in the process. These are only imporant because they may be confused with neoplastic metastasis to the lungs on radiography1.

Life Cycle

Dirofilaria immitis adults reach maturity and sexually reproduce in the pulmonary arteries and right ventricle. Adult males are around 15cm in length, and females are around 25cm1. After mating, female worms release larvae known as microfilariae (or L1) into the circulation. When a mosquito takes a blood meal from the infected dog or cat, microfilariae are ingested. Mosquitos are true intermediate hosts for Dirofilaria immitis, since microfilariae require a period of maturation to L2 then L3 in the vector. The duration of this development depends upon environmental conditions. For example, maturation at 30°C takes around 8 days, but when temperatures are down to 18°C, this takes around one month2. Below 14°C, development is halted and resumes when temperatures rise. In cooler climates, this means that transmission of heartworm disease to new canine or feline hosts can only occur in warmer months.

Once matured, L3 in the mosquito migrate to the labium, from which they erupt onto the host's skin as the mosquito feeds. Larvae then migrate into the bite wound and, as most dogs are highly susceptible to heartworm disease, most L3 then establish infection. It takes 2-3 days for L3 to moult to L4, which remain in the subcutaneous tissues for up to two months before becoming young adults (L5) and migrating to the pulmonary arteries.

Cats differ from dogs in that they are more resistant to infection with Dirofilaria immitis. A lower percentage of exposed cats develop adult infections, and when this does occur the burden is usually low1. L5 in the pulmonary arteries also have a relatively short (2 year) survival time in cats.

Pathogenesis

Heartworm disease primarily affects the cardiopulmonary system and the severity and extent of lesions depends several factors. These include the number and location of adult worms1, 2, the duration of infection, and the level of activity of the host1. Parasites in the pulmonary arteries cause mechanical irritation, leading to endothelial damage, proliferation of the intima and perivascular cuffing with inflammatory cells. This results in narrowing and occlusion of the vessels which in turn causes pulmonary hypertension. A combination of pulmonary hypertension and inflammatory mediators can lead to in an increase in the permeability of pulmonary vessels, giving periarterial oedema and intersitial and alveolar infiltrates. Eventually, irreversible interstitial fibrosis arises.

Sequelae to heartworm infection include pulmonary thromboembolism, which can either occur due to the death and metastasis of adult worms, or due to platelet aggregation induced by the parasite. In severe cases, live nematodes can migrate to the right ventricle, right atrium and caudal vena cava. The resulting incompetence of the tricuspid valve, augmented by concurrent pulmonary hypertension, leads to signs of right-sided heart failure. Flow of erythrocytes through the mass of parasites formed can also cause haemolysis and thus haemoglobinaemia. This combination of acute right-sided heart failure and intravascular haemolysis is referred to as "caval syndrome", which in severe cases can also be characterised by thromboembolic events and disseminated intravascular coagulation. Due to the smaller numbers of adult worms, caval syndrome is less common in cats2.

In cats, heartworm disease generally causes a diffuse pulmonary infiltrate and an eosinophilic pneumonia2. Adult worms may die and embolise to the lungs, resulting in severe haemorrhage and oedema of the affected lobe. Immature nematodes have also been known to migrate to sites other than the pulmonary arteries and heart such as the CNS, eye and subcutaneous tissues. These ectopic infections are far more common in cats than in dogs, suggesting that D. immitis is not well adapted to feline hosts.

Signalment

Dirofilaria immitis infection affects dogs more commonly than cats, and risk is greatest in outdoor animals. Dogs of any age may be affected, but infections are most common in 3 to 8 year old dogs, and medium and large breeds are over-represented1, 3. In cats, there are no breed or age predispositions, but males are more frequently affected3. Ferrets may also contract dirofilariasis; there are no age or sex predilections1.

Diagnosis

Clinical Signs

In dogs, historical findings at the time of presentation can vary. Some animals are asymptomatic, or cough only occasionally. In countries where heartworm is endemic, animals may be routinely tested for dirofilariasis at the end of the high-risk season, when weather becomes cooler3. Therefore, positive laboratory testing may be the first indication of disease1. More obvious signs may be seen depending on the severity of disease. Generally, the onset of heartworm disease is insidious, and clinical signs are related either to a high parasite burden, or to an allergic response to the parasite2. Affected dogs most often show coughing, and dyspnoea/tachypnoea, exercise intolerance, loss of condition and syncope may also be seen. In severe cases the pulmonary vessels may rupture, leading to haemoptysis or epistaxis. There is a tendency for signs to only manifest during exercise, and so patients with a sedentary lifestyle may never show overt disease. Right-sided congestive heart failure may ensue when worm burden is high, and signs can include jugular disension, ascites, marked exercise intolerance and hepatomegaly. A systolic murmur is sometimes audible on cardiac auscultation.

A classification system for the presentation of heartworm disease exists1, outlined in the table below.

Class
Clinical Signs
Class 1
Asymptomatic or mild disease
  • Weight loss, reduced exercise tolerance or an occasional cough may be seen.
  • No radiographic signs or laboratory abnormalities.
Class 2
Moderate disease
  • Animal coughs occasionally and shows mild-to-moderate exercise intolerance.
  • Lung sounds may be increasd
  • Radiography may show mild-to-moderate changes, e.g. right ventricular enlargement.
  • Anemia and proteinuria may be present.
Class 3
Severe disease
  • Signs are variable but may include weight loss, exercise intolerance, tachypnoea, dyspnoea, severe/persistent coughing, hemoptysis, syncope, or ascites.
  • Radiographs appear abnormal: right ventricular hypertrophy, enlargement of the main pulmonary artery, and diffuse pulmonary densities. ECG often shows right ventricular hypertrophy.
  • Anaemia, thrombocytopenia, and proteinuria are seen.
Class 4
Caval syndrome
  • Sudden onset of collapse, haemoglobinuria, and respiratory distress.
  • Usually fatal without immediate surgery.

Caval syndrome is a very severe form of heartworm disease that can occur in dogs and cats. It is characterised by respiratory distress, signs of right-sided heart failur, intravascular haemolysis and haemoglobinuria. Disseminated intravascular coagulation frequently occurs, and the syndrome is often fatal.

In cats, most infections are asymptomatic. However, sudden death can occasionally occur. This may be preceded by an acute respiratory crisis, thought to be due to parasitic thromboembolism and obstruction of a major pulmonary artery1, 2. When clinical signs are less acute, they are vague and may include anorexia, weight loss and letheargy. Intermittent coughing and dyspnoea can appear similar to feline asthma. Syncope may also occur, and cats may vomit. The cause of this vomiting is undetermined3.

Radiography

In dogs, thoracic radiography provides good information on disease severity and is useful for screening dogs showing clinical signs compatible with D. immitis infection1. However, thoracic radiograph do not neccessarily reflect the current worm burden: radiographic signs of advanced disease can persist long after an infection has run its course4. Conversely, dogs with high burdens may be inactive and thus show few clinical signs or radiographic changes. Radiographic signs are mild-to-moderate in class II disease, but become more obvious in class III infections. The main pulmonary artery is enlarged,sup>1, 4, and the caudal lobar vessels appear tortuous1 Ill-defined, fluffy infiltrates are apparent, and often surroung in the caudal lobar vessels. Right-sided cardiomegaly may be appreciated, and pleural and peritoneal effusions can be noted if right-sided congestive heart failure occurs4.

Cardiac changes on thoracic radiography are less common in cats than dogs. The caudal lobar veins are enlarged (greater than 1.5 times the width of the ninth ribe), and the pulmonary arteries are blunted and tortuous3, 5. Patchy parenchymal infiltrates may be seen in the region of vessels in animals showing respiratory signs1, 3. Enlargement of the main pulmonary artery cannot normally be seen in cats, as it is has a relatively midline position and is thus obscured by the cardiac silhouette1, 5. Right-sided cardiomegaly is not considered a typical finding in the cat5.

Echocardiography

In dogs, echocardiography is not particularly useful as a diagnostic tool for heartworm disease. In severe, chronic pulmonary hypertansion, right ventricular hypertrophy, septal flattening, underloading of the left heart, and high-velocity tricuspid and pulmonic regurgitation may be seen1. With caval syndrome or high-burden infections, worms may be visualised in the right heart and vena cava.

Echocardiography is more important in cats than dogs because of the increased difficulty of diagnosis and the fact that this test can have a high sensitivity depending on operater experience1. Specificity is 100%5, and the test can help exclude or confirm other primary cardiac diseases such as hypertrophic cardiomyopathy3. Worms can usually be visualised as parallel hyperechoic lines1, and are seen in the right atrium and ventricle and main pulmonary artery1, 3, 5.

Electrocardiography

The ECG of infected dogs is usually normal. Right ventricular hypertrophy patterns are seen when there is severe, chronic pulmonary hypertension and are associated with overt or impending right-sided CHF (ascites). Heart rhythm disturbances are usually absent or mild, but atrial fibrillation is an occasional complication in dogs with Class III disease.

Laboratory Tests

In both dogs and cats, routine haematology, biochemistry and urinalysis should be performed. Most parameters are usually within normal limits, but an anaemia can often be seen. Eosinophilia and basophilia are also common, and when seen together suggests occult dirofilariasis or allergic lung disease 1, 3. Eosinophilia peaks as L5 enter the pulmonary arteries and subsequently varies. An inflammatory leukogram is also possible3. Hyperglobulinemia due to antigenic stimulation is an inconsistent finding1, 3. Right-sided heart failure or immune-complex glomerulonephritis can lead to hypoalbuminaemia and, very occasionally, nephrotic syndrome1. Because of this, it is possible for urinalysis to reveal proteiunuria1, 3. Haemoglobinaemia and haemoglobinuria are associated with caval syndrome3.

he antigen detection test is the preferred diagnostic method for asymptomatic dogs or when seeking verification of a suspected HW infection. This is the most sensitive diagnostic method available to veterinary practitioners. Even in areas where the prevalence of HW infection is high, ~20% of infected dogs may not be microfilaremic. Also, monthly macrolide prophylaxis induces embryo stasis in female dirofilariae. Available antigen detection tests are very sensitive and specific. To determine when testing might become useful, it is advisable to add a predetection period to the approximate date on which infection may have been possible. A reasonable interval is 7 mo. There is generally no need to test a dog for antigen or microfilariae prior to ~7 mo of age. The level of antigenemia is directly related to the number of mature female worms present. At least 90% of dogs harboring ≥3 adult females will test positive. In general, strong-quick positive reactions correlate with relatively high worm burdens. For low-burden suspects, commercial laboratory-based microwell titer tests are the most sensitive.

Pathology

Dirofilariasis. Courtesy of T. Scase
Dirofilariasis. Courtesy of T. Scase

On post-mortem examination, the right side of the heart is found to be enlarged. There is proliferation of the pulmonary arterial myointima, as well as pulmonary thromboembolism and haemorrhage. If right-sided congestive heart failure was present in life, the hepatomegaly and hepatic congestion will be seen.

Treatment

Adulticidal Treatment

Decisions in the treatment of heartworm disease are dependent on the severity of infection. A scheme exists to classify patients in terms of disease severity2. Class one patients have subclinical heartworm disease, and carry an excellent prognosis following treatment wiht adulticidal drugs. Class two animals show mild to moderate clinical signs and similar radiographic changes. These animals may respond positively to treatment. Dogs with class 3 disease have severe clinical signs, such as persistent coughing, dyspnoea, right-sided heart failure or haemoptysis, and these are reflected by severe radiographic signs. These cases have a high risk of pulmonary thromboembolism and so prognosis is guarded and the benefits of adulticidal treatment should be considered carefully.

Even low grade infections in cats may result in pulmonary thromboembolism with adulticidal treatment, and spontaneous remission is seen in some cats. Because of this, symptomatic treatment (cage rest, oxygen supplementation, fluid therapy, bronchodilators and dexamethasone) may be more appropriate in sick cats, and clinically well cats can merely be monitored regularly for remission. Adulticidal treatment should only be considered in cats that fail to respond to supportive treatments but are in a stable condition.

Adulticidal treatment involves the administration of a new generation arsenical compound, melarsomine dihydrochloride (Immiticide, Merial; this product is not licensed for use in the UK). Melarsomine is less nephrotoxic and hepatotoxic than its predecessor thiacetarsamide, and has a higher efficacy. Melarsomine is injected intramuscularly into the lumbar muscles at a recommended dose of 2-5 mg/kg, repeated after 24 hours. However, only a single dose should be administered to class 3 dogs, to kill just a proportion of worms and hence minimise the risk of pulmonary thromboembolism. If the patient remains stable, the standard adulticidal protocol can be administered one month later. In the week following the administration of melarsomine, the likelihood of pulmonary thromboembolism can be minimised with cage rest and corticosteroids at anti-inflammatory doses. If adulticidal treatment is declined by the owner, monthly administration of prophylactic doses of ivermectin may represent a reasonable option because it will prevent further infection and may kill some adult nematodes. Patients with severe caval syndrome may benefit from physical removal of worms from the right side of the heart and the main pulmonary artery using flexible crocodile or basket-type retrieval forceps. This procedure is complex, requires general anaesthesia and fluoroscopic imaging, but may reduce the risk of thromboembolism following subsequent adulticidal treatment.

Microfilaricidal Treatment

No drugs are specifically approved for microfilaricidal treatment of Dirofilaria immitis, and successful elimination of adult worms should results in the demise of circulating microfilariae four to six weeks later2. Single doses of ivermectin, milbemycin oxime, moxidection or selamectin are, however, effective at removing microfilariae from the circulation. The sudden death of large numbers of microfilariae may invoke an anaphylactic response, and oral prednisolone may be administered with microfilaricides to help prevent this.

Prevention

Heartworm prophylaxis should be implemented in all cats and dogs living in or visiting areas in which Dirofilaria immitis is endemic. In the UK, milbemycin oxime and selamectin are licensed for the prevention of heartworm disease and should be administered on a monthly basis as they are capable of killing migrating larvae up to week six post-infection. In the event of non-compliance or a missed dose, it may be necessary to test the animal for Dirofilaria immitis six months later if they are likely to have been exposed to infection during the time they were unprotected. Drugs that persist in the long term, such as injectable moxidectin, can help overcome this issue.

Prognosis

In mildly symptomatic or asymptomatic animals, the course of dirofilariasis is usually uneventful following treatment and the prognosis is excellent3. Animals with severe infection carry a guarded prognosis with a higher risk of complications.

Links

References

  1. Merck & Co (2008) The Merck Veterinary Manual (Eighth Edition), Merial.
  2. Ferasin, L (2004) Disease risks for the travelling pet: Heartworm disease, In Practice, 26(6), 350-357.
  3. Tilley, L P and Smith, F W K (2004) The 5-minute Veterinary Consult (Fourth Edition),Blackwell.
  4. Venco, L (2007) Heartworm (Dirofilaria immitis) disease in dogs. Dirofilaria immitis and D. repens in dog and cat and human infections, 117-125.
  5. Venco, L (2007) Heartworm (Dirofilaria immitis) disease in cats. Dirofilaria immitis and D. repens in dog and cat and human infections, 126-132.
  6. Ridyard, A (2005) Heartworm and lungworm in dogs and cats in the UK, In Practice, 27(3), 147-153.