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The April 1997 issue of Antech News summarized current views on the
diagnosis of feline heartworm disease. Feline heartworm antibody and antigen testing are both available, although
the indications, specificity and sensitivity of these tests vary with the case presentation and different test kits
used. Filarial antibody tests typically become positive 2-3 months after infection, whereas antigen tests detect
current infections with adult heartworms and not larval or previous infections. Most cats that test antigen positive
have occult infections with significant pathology in the lungs and heart. A negative antibody test
strongly suggests that no heartworms are present in the cat's heart, lungs or pulmonary vessels. If the cat is
heartworm antigen negative and has symptoms of heartworm disease, additional testing with heartworm
antibody, radiographs, blood profile and ultrasonography may be indicated.
Accurate diagnostic testing is especially important given the low prevalence of heartworm disease in cats, frequent
lack of symptoms, or variable nonspecific clinical signs of pulmonary, neurologic or other disease. Results of a recently
completed assessment of results from 3 laboratories are summarized below:
Sensitivity and specificity of several feline heartworm serologic tests were compared using serum samples collected
serially from 42 laboratory cats experimentally infected with heartworms (n = 33), gastrointestinal hematodes (n = 6) or
lungworms (n = 3). The 33 cats with Dirofilaria immitis infection were sampled before and 1, 2, 3, 5 and 6-9
months afterwards. The 6 cats with GI parasites (tapeworms, roundworms and hookworms in a staggered infection) were
tested beforehand and 4 times afterwards, whereas the 3 cats infected with lungworms were assessed prior to and 1 and 2
months afterwards. Three sets of split serum samples from 233 bleedings of these cats were submitted for in-house feline
heartworm antibody and antigen testing to laboratories A, B and C*.
All three laboratories detected heartworm antibody with a high degree of sensitivity (97-100% at
three months post-infection, and 100% thereafter). At two months post-infection, lower sensitivity results were found.
[85% (lab C), 64% (lab B) and 27% (lab A)]. Only the tests measured at labs C and B detected infection at one month,
and the rates were low range, (24-30%). Of the 42 preinfection samples, all were negative with each of the three test
labs, indicating 100% specificity for these antibody tests in the absence of parasite infection. None of the samples
from cats infected with GI parasites or lungworms were positive at lab C, and none of the six lungworm infected samples
were positive at labs A and B. However, 1 of 23 samples from cats with GI parasites was positive at both labs A and B,
indicating decreased sensitivity.
With respect to heartworm antigen, antibody positive samples were measured for antigen at labs A
and B only. Results were influenced greatly by the presence or absence of heartworms at necropsy. Detection rates for
cats with heartworms at necropsy varied from 0, 0, 5 and 63% at the last four post-infection collection points for lab A,
and fluctuated from 19, 86, 43, 52 and 100% for lab B. For cats with no heartworms at necropsy, none of the 40 samples
tested at lab A was antigen-positive, whereas 4 of 42 were positive at lab B. Also, none of the pre-infection, GI parasites
or lungworm infected cat samples were positive for heartworm antigen.
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