{"id":1417591,"date":"2022-10-13T16:13:18","date_gmt":"2022-10-13T14:13:18","guid":{"rendered":"https:\/\/staging-wp-int.laboklin.com\/imha\/"},"modified":"2024-07-22T13:08:26","modified_gmt":"2024-07-22T11:08:26","slug":"imha","status":"publish","type":"post","link":"https:\/\/laboklin.com\/se\/imha\/","title":{"rendered":"Which tests can help me diagnose an immune-mediated hemolytic anemia (IMHA) and which samples should I take?"},"content":{"rendered":"

[vc_row][vc_column width=”2\/3″][vc_column_text]<\/p>\n

When to suspect hemolysis?<\/h3>\n

We suspect hemolysis especially in regenerative anemia when blood loss has been excluded (Fig. 1).<\/p>\n

In most cases, hemolytic anemia are severe and show stronger signs of regeneration than blood loss anemia. In case of hemolysis, erythrocytes are destroyed. In addition to primary IMHA (referred to as non-associative IMHA), a variety of underlying diseases can cause hemolysis (Fig. 2).<\/p>\n

Which tests should be performed?<\/h3>\n

Requested material for the diagnosis of IMHA are listed in Fig. 3.<\/p>\n

CBC\/cytomorphology (blood smear):<\/strong><\/p>\n

Provides information regarding regeneration and is useful as a first overview, e.g. to detect infectious agents. Erythrocyte morphology can also provide important information regarding the cause of anemia. At Laboklin, a reticulocyte count is included in every canine and feline CBC. The CBC should be measured from EDTA blood as soon as possible after blood collection as the erythrocyte fragility of dogs with IMHA is increased.<\/p>\n

Blood chemistry:<\/strong> Measurement of serum bilirubin and total protein to identify the cause of anemia can help to differentiate between hemolysis and hemorrhages.<\/p>\n

Urinalysis:<\/strong> In some cases of hemolysis, bilirubinuria or hemoglobinuria may be present. Please note that in dogs \u2013 especially in male dogs \u2013 a weakly positive test result can be physiological.<\/p>\n

Infectious agents t<\/strong>o detect infectious agents such as babesia and haemotropic mycoplasma in acute phases, molecular analysis (PCR) is recommended. Additionally, pathogens such as ehrlichia and anaplasma should be excluded. For ehrlichia, an additional antibody titer determination is useful.
\n<\/strong><\/p>\n

Tests to diagnose immune-mediated destruction<\/h3>\n

Spherocytes:<\/strong> The presence of so-called spherocytes (Fig. 4) in the blood smear can provide valuable information about an immunemediated destruction of the erythrocytes. The sample material required for their detection are two to three blood smears directly made in the practice.<\/strong><\/p>\n

Autoagglutination:<\/strong> By looking at the EDTA sample, one may notice the presence of an unspecific autoagglutination. This finding should be followed by a saline agglutination test and a Coombs’ test.<\/p>\n

Coombs’ test:<\/strong> Suitable to detect the presence of autoantibodies on the surface of erythrocytes. Sample material: Fresh EDTA blood. If the sample is kept refrigerated, the test can be evaluated up to 5 days from collection.<\/p>\n

FAQs on assessing the Coombs’ test<\/h3>\n

What is the principle of the Coombs’ test?<\/strong><\/p>\n

The Coombs\u2019 test, also named DAT (Direct Antiglobulin Test), is testing for the presence of antibodies on the surface of the red blood cells (Fig. 5).<\/p>\n

Different test methods are available on the market: gel test, strip test, flow cytometry test, the well-known microtiter plate test, and more. All the mentioned tests are adequate for the diagnosis of IMHA in humans and dogs. Some tests are also available on the market for cats and horses.<\/p>\n

What is the principle of the microtiter plate method?<\/strong><\/p>\n

In veterinary medicine, the microtiter plate is the most commonly used method. The antiglobulin (Coombs’ reagent) is gradually diluted (1:2, 1:4, 1:8, 1:16, etc.), then washed erythrocytes are added and incubated for at least 30 minutes. If no reaction occurs, the blood cells will sediment at the bottom of the wells and only a tiny red point will be observed after incubation: the test result for this well is negative. If the test is positive, the added antiglobulins bind the erythrocytes, refraining them from falling to the bottom of the well. The erythrocytes cover the well completely, or almost completely. If only the two first wells (1:2 and 1:4) show positivity, the test is still considered negative, because these low titers are considerated unspecific. Titers from 1:8 are considerate positive. It is not rare to see titers above 1:1024 in IMHA.<\/p>\n

What is a prozone effect?
\n<\/strong>The prozone effect is a phenomenon observed in highly positive samples. The high concentration of anti-erythrocyte antibodies inhibits the positive reaction. An example is pictured below (Fig. 6).<\/p>\n

The EDTA-blood sample presents a blood clot, can the Coombs’ test overcome this?
\n<\/strong>Unfortunately no. The presence of intact red blood cells is mandatory for the performance of a correct Coombs’ test. However, it is important to know the difference between a blood clot and an agglutination. The blood clot is the result of the physiological coagulation, and can occur when the sample is not correctly mixed with EDTA-anticoagulant. The blood clot is irreversible. To avoid this: after sampling, gently repeatedly invert the sample. The agglutination can be caused by different factors. In most cases, the agglutination is reversible, e.g. by warming up the sample in your hand, or by washing the cells.
\n<\/strong>[\/vc_column_text][\/vc_column][vc_column width=”1\/3″][vc_column_text]<\/p>\n\n\t\t\t