Unit 2 Flashcards
In 2nd and 3rd degree AV block, what part of the ECG wave is dropped?
QRS complex
what are the 5 main leukocytes?
neutrophils
monocytes/macrophages
lymphocytes
eosinophils
basophils
neutrophils
“marine”
makes up ~60-70% of total WBC count
granulocytic segmented cells that are first to response to an immune signal, especially bacterial infections
- phagocytosis
- degranulation
- release of neutrophil extracellular traps (NETS)
monocytes/macrophages
“general”/”clean up crew”
phagocytic process of using acidic ph to kill microbes and inhibit bacterial protein synthesis
monocytes = blood; macrophages = tissues
boost immune response by presenting antigens on surface to other cells of immune system
3-8% of leukocyte count but largest one
lymphocytes
originates in bone marrow and moves to lymphoid tissue, develops into T and B cells
- cell mediated immunity (t cells)
- humoral immunity (b cells)
T cells
cell mediated immunity
form many lymphocytes to destroy foreign antigens and infected cells
cytotoxic, memory, or helper
B cells
humoral immunity
make antibodies to signal other cells to attack
agglutination, precipitation, neutralization, or lysis
plasma or memory
cytotoxic T cells
receptors bind to specific receptors that activate cells to release toxic substances into foreign cells
helper T cells
most numerous, helps activate cytotoxic T cells and B cells, amplifying response
memory T cells
long lived and respond to antigens later
plasma B cells
produce antibodies to attach to antigens and signal for destruction
memory B cells
similar to memory T cells
long lived, respond to antigens later
immune mediated hemolytic anemia (IMHA)
immune system attacks its own RBCs and signals for their destruction
too many RBCs are tagged with antibodies for destruction
what causes IMHA?
usually is idiopathic, can be trauma, infection, toxins, or neoplasia
extravascular IMHA
antibody coated RBCs are recognized and phagocytosed by macrophages
intravascular IMHA
antibody/complement on RBC surface directly leads to cell lysis in circulation
clinical signs of IMHA
pale/icteric gums
lethargy
collapse and exercise intolerance
anorexia
dark orange/brown urine
tachypnea
vomiting
fever
necrosis of distal extremities
risk factors of IMHA
basenjis, beagles, westies, cairn terries, abyssinian and somali cats
dogs 2-8 years old
4x more likely in females
PE for IMHA
depressed/obtunded
weak
tachycardia/tachypnea
bounding pulses +/- grade II left systolic murmur
jaundice
hemoglobinemia/hemoglobinuria
diagnostics for IMHA
CBC/chem: severe anemia (<15% HCT/PCV)
RET elevated
Leukocytosis + neutrophilia
Thrombocytopenia
TBIL, ALT elevated
UA: r/o hematuria and other kidney damage
smear to look at RBC structure and r/o infectious causes such as mycoplasma or bartonella
autoagglutination test: add small sample of blood on slide and add sterile saline, then move sample around on slide looking for clumping
other tests for IMHA
coomb’s test looks for antibodies and complement that sticks to RBCs
imaging
bone marrow biopsy to r/o neoplasia
PCR test for infectious disease
treatment for IMHA
hospitalize with IVF and blood transfusion if PCV < 15%
Dexamethasone IV BID
chronic care on oral steroids (predniso (lo) ne
other immunosuppressive medications such as azathioprine, mycophenolate, or cyclosporine
prognosis for IMHA
guarded; 30-40% if in crisis, with tx
relapse rate is 11%
immune mediated thrombocytopenia
destruction of platelets on liver, spleen, or bone marrow
usually idiopathic, but may be due to drugs, neoplasia, or infection
clinical signs of IMTP
lethargy
weak
petechia and ecchymotis hemorrhage (bruising)
melena (upper GI blood in stool)
epistaxis (nose bleed)
pale MM
PE for IMTP
QAR-obtunded
petechiation
epistaxis
splenomegaly
fever
hemorrhage in eyes
heart murmurs edema or erythema
lymph node enlargement
diagnostics for IMTP
cbc/chem: thrombocytopenia (<40,000), anemia
PROT, ALB low
BUN elevated
clotting factor tests usually normal
rads can r/o other issues (splenic mass)
AUS looks for lesions on liver/spleen and can allow aspirates
PCR/ELISA test for infectious disease
tx for IMTP
hospitalization with IVF to improve volume and plasma transfusion
chronic care on immunosuppressive drugs (prednisone, azatioprine, cyclosporine)
monitor PLT count q 2 weeks until stable
prognosis for IMTP
fair, better than IMHA
16% mortality rate + 10% relapse rate
increased BUN, melena, CNS bleeds indicate - prognosis
immune mediated polyarthritis (IMPA)
diseases that cause joint pathology and systemic illness, affecting at least 2 joints with no infectious component, responsive to immunosuppressive tx
erosive IMPA
radiographic evidence of cartilage and subchrondal bone destruction in 1+ joints; rare = 1%
frequent in smaller breeds, age 2-6 yrs, stiff, intermittent lameness, swelling of joints, fever, lethargy, inappetence, lymphadenopathy
genetic form in greyhounds
nonerosive IMPA
no radiographic evidence of destruction
most common
types:
1. not associated w distant disease, most common
2. associated w infectious or chronic inflammatory disease
3. associated w chronic GI disease
4. associated w distant neoplasia
clinical signs of IMPA
difficulty walking/lameness
joint swelling and pain
vomiting
decreased appetite
fever
pitting edema
diagnostics for IMPA
synovial fluid analysis
CBC/chem: neutrophilic leukocytosis mild thrombocytopenia and anemia, elevated ALP and UPC ratio, low hypoalbuminemia
antinuclear antibodies test: helps identify autoimmune conditions
rads to r/o other causes of lameness, determine if erosive
PCR/ELISA to r/o vector borne or infectious causes
tx for IMPA erosive
prednisone, azatioprine, cyclophosphamide
disease modifying agents such as gold salts, hydroxychloroquine, penicillamine, methotrexate, leflunomide
tx for IMPA nonerosive
prednisone, azathioprine, cyclophosphamide, levamisole
how can you monitor the progression of IMPA?
recheck CBC q 3-6 mo to ensure not oversuppressing immune system
CHEM to monitor liver/kidney values
repeat synovial fluid analysis PRN
prognosis good is caught before permanent damage
what two breeds have specific IMPA?
akita and shar peis
nasal cavity
mucus lined airway with bony turbinates to help humidify inhaled air
pharynx
area containing structures at back of throat
larynx
opening to the trachea, with epiglottis, glottis, and arytenoid cartilage
epiglottis
triangle shaped fold that cover the opening to the trachea
what are the 4 layers of the trachea?
mucosa, submucosa, musculocartilaginous, adventitia
bronchi
first branches from the trachea into each lung lobe
contains less cartilage, muscle, and goblet cells
with clara cells to produce surfactant
bronchioles
further branching from bronchi
no cartilage or goblet cells, less muscle
alveolar sacs
terminal ends of respiratory tract, made of pneumocytes 1/2 and alveolar macrophages/dust cells
pneumocytes type 1
perform gas exchange with pulmonary capillaries
pneumocytes type 2
produce surfactant to reduce surface tension
alveolar macrophages/dust cells
clear out particles not cleared by URT
eosinophilic bronchopneumopathy
eosinophil infiltration of lower respiratory tract (especially bronchial mucosa), due to a hypersensitivity, parasites, chronic bacterial/fungal infections, viruses, external antigens, or allergens
eosinophils
related to allergies, hypersensitivities, and parasites
what breeds are predisposed to eosinophilic bronchopneumopathy?
huskies, malamutes, labs, gsd, belgian shepherds, fox/jack russels
rare in mini/giant breeds
avg 4-6 years
clinical signs of eosinophilic bronchopneumopathy
cough
gagging/retching
dyspnea
nasal d/c
exercise intolerance
lethargy
anorexia
PE for eosinophilic bronchopneumopathy
BAR-QAR, sometimes NSF
tachypnea w/ dyspnea
increased lung sounds, wheezing, crackles
+/- serous/mucous discharge
what diagnostics for eosinophilic bronchopneumopathy?
cbc: eosinophilia, leukocytosis, neutrophilia, basophilia
chem: nsf
rads: r/o other causes
elisa/pcr tests for VFT, HWT, etc
additional ($$$) diagnostics for eosinophilic bronchopneumopathy
bronchoscopy, bronchial lavage, or CT scan
treatment for eosinophilic bronchopneumopathy
treat co infections first with antibiotics, anti-fungals, anti-parasitics
pred chronically
what causes feline asthma?
scents or other allergens, cats are very sensitive
immune cells trigger inflammatory substances, decreasing the diameter of airways and allowing mucus to accumulate within the passages
what breeds are predisposed to feline asthma?
siamese
4-5 yrs
what are the clinical signs for feline asthma?
dyspnea
wheezing
tachypnea
coughing/hacking
open mouth breathing
vomiting
PE for feline asthma
increased tracheal sensitivity
harsh lung sounds, crackles, wheezes
abdominal breathing
may present w extreme dyspnea, cyanosis, open mouth
hunched with extended neck