Tick transmitted diseases Flashcards
What are 3 mechanisms for a fever and lymph node enlargement?
Infection, Neoplasia, Autoimmune
What can cause pale mucous membranes?
Poor perfusion, Anemia
What etiologies can result in petechiae?
Thrombocytopenia, Thrombocytopathia, Endothelial dysfunction (vasculitits)
*Coagulopathy more likely to cause large bruises or cavitary bleeding
How low does a platelet count need to be before you see petechiae?
<50,000
-varies a bit from case to case, but generally this is the range that you worry about spontaneous bleeding
What abnormalities are most likely to be seen on the chemistry of a patient with systemic inflammation?
Hypoalbuminemia and hyperglobulinemia
What are the main mechanisms that can result in thrombocytopenia?
Sequestration, Consumption, Decreased production, Destruction (IMTP)
- severe thrombocytopenia more likely to be due to destruction or decreased production
What would make you put bone marrow disease higher on your differential list for a patient with thrombocytopenia?
If the other cell lines are also reduced (pancytopenia)
What are the main causes of thrombocytopenia due to decreased production (bone marrow disease)?
-infection (ehrlichia canis or histoplasmosis)
-neoplasia (multiple melanoma, lymphoma, leukemia)
-immune mediated (aplastic anemia)
-toxins or drugs (estrogens, chemotherapy drugs, azothiaprine, phenobarbital)
What tick borne disease is the most likely to target the bone marrow?
Ehrlichia canis
What abnormality can be seen on a blood smear of a patient with ehrlichia canis?
A morulae in the cytoplasm of monocytes
- specific but not very sensitive - cant rule out the disease if you don’t see this
-evaluation of buffy coat smears, lymph node aspirates or splenic aspirates increases sensitivity
What is the other name for infection with Ehrlichia canis? What is the tick that transmits this disease?
Also known as canine monocytic ehrlichiosis
-primarily transmitted by the brown dog tick
-found throughout the US but prefers warm climates (southeastern and southwestern states)
Describe the 3 potential phases of ehrlichia canis infection
Acute phase (8-20 days after innoculation): patients often will be febrile, lethargic, innapetant, with potential lymphadenopathy and hepatosplenomegaly. There may be peripheral edema present (due to vasculitits), as well as potentially uveitis and retinal disease. Thrombocytopenia/pathia are common findings. More rarely there may be neuro signs (meningeal inflammation and or CNS hemorrhage). May spontaneously recover after 2-4 weeks without vet intervention, or may become subclinical
Subclinical phase: will show up positive on snap test, but will have no appreciated clinical signs
Chronic phase: similar signs to acute phase plus maybe bone marrow hypoplasia (pancytopenia), protein losing nephropathy, polymyositis, marked lymphocytosis (can look like lymphoma or lymphocytic leukemia) and bone marrow plasmacytosis leading to hyperglobulinemia (can look like multiple myeloma)
What are the downsides to antibody testing for E canis?
-there is cross reactivity with ehrlichia ewingii and e chaffeensis
-indicates exposure to the organism but not necessarily active infection
-potential for false negative results with acute infections
What is the serological gold standard for Ehrlichia testing?
Indirect immunofluorescent antibody test (IFA)
-looks for IgG antibodies
-if acute exposure is suspected, take two consecutive tests 7-14 days apart- 4 fold increase is suggestive of acute and active infection (unlikely to change with chronic infection)
-be aware that IgG antibodies may persist for several months to years after treatment and elimination of E canis
Describe the ELISA snap test for diagnosis of E canis
-point of care test that allows for a quick qualitative measurement of IgG antibodies against E canis
-sensitivity is 97% (great), comparable to IFA
Describe PCR for diagnosis of E canis
-quantitative real time PCR that is frequently used
-detects E canis DNA as early as 4-10 days post inoculation (likely represents true infection and organism can be detected prior to seroconversion)
-whole blood PCR is more sensitive for acute infections but serology is more sensitive for chronic infections
-antimicrobial treatment at the time of blood collection may lead to false negative results
*take blood sample before starting antibiotics to avoid risk of false negative