Treatment of coagulopathies Flashcards

(38 cards)

1
Q

Treatment of immune mediated haemolytic anaemia

A

Immunosupression
- glucocorticoids (reduces chemotaxis and endothelial adhesion, reduces arachidonic acid release, reduced T cell activation, suppersses cytokine production and macrophage activity)
- Ciclosporin (calcineurin inhibitor, inhibits T-cell activation, proliferation, and IL-2)
- Azathioprine (inhibits purine biosynthesis- humoral immunity)
- Mycophenolate (inhibits purine synthesis, alternative to azathioprine)
- IV immunoglobulin

Tansfusion if severely affected

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2
Q

Side effects of glucocorticoids

A

Common

Iatrogenic hyperadrenocorticim

PUPD

Polyphagia

Muscle weakness/wasting

Poor hair growth

Skin thinning

Elevated liver enzymes (esp ALP)

Diabetogenic

Can increase the risk of secondary infections (UTIs, skin infections)

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3
Q

What is the risk of combining NSAIDs and corticosteroids?

A

GI ulceration

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4
Q

Main indications for using alterantive immunosuppressive agents

A

Absolute contraindication for use of glucocorticoids, meaning others can be used as first line

Failure of treatment with glucocorticoids

‘Steroid sparing’ to reduce the dose of glucocorticoids needed/taper them off more quickly - due to side effects, either present or anticipated

Severe disease to ensure that effective treatment is not delayed

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5
Q

Ciclosporin

A

Calcineurin inhibitor, inhibits T cell activation, proliferation, and secretion of IL-2

Immunosuppression takes 1-2 wees to be fully effective

Not myelosuppressive

Expensive!

Severe side effects uncommon, can cause V+ and D+ (mild and transient)

Hypertrichosis common

Can also cause gingival hyperplasia and nephrotoxicity

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6
Q

Azathioprine

A

Not licensed

Can cause severe bone marrow suppression in cats - use is not recommended

Purine analogue

Acts on humoral mediated immunity

Adverse effects: bone marrow suppression, hepatotoxicity

Monitored with routine haem and biochem every 1-2weeks initially and then every 1-2mo

Can take several weeks to achiece adequate immunosuppression

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7
Q

Mycophenolate mofetil

A

Not licensed for use in dogs or cats

Inhibits purine systhesis, alternative to azathioprine

Main adverse effects: GI (nausea, vomiting, diarrhoea), can also cause bone marrow supression

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8
Q

Intravenous immunoglobulin (IVIG)

A

Not licensed in cats or dogs

Very expensive

Pooled human immunoglobulins

Act through macrophage Fc receptor signalling

Given as single transfusion

Beneficial in some cases with severe, refractory disease

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9
Q

Anti-thrombotic therapy in IMHA

A

Used off license

Thromboembolism is the most common cause of death in IMHA cases.

Improves outcomes - best therapy not known

Clopidogral unless thromboembolic disease has already occurred.

Thromboprophylaxis should be used in all dogs with IMHA unless they have severe thrombocytopenia (<30 x109 cells/l).

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10
Q

Possible anticoagulants for IMHA

A

Heparin - inhibits coagulation casacade via activation of anti-thrombin III, needs monitoring due to risk of coagulopathy

Rivaroxaban - direct Xa inhibitor, can be administered orally, less monitoring needed

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11
Q

Platelet inhibition in IMHA

A

Aspirin - NSAID, COX inhibition, prevents platelet activation. Risk of GI ulceration with high doses

Clopidogrel - inhibits ADP receptors on platelets, works as well as aspirin with less risk of GI ulceration

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12
Q

Immunosuppressive dose tapering and monitoring in IMHA

A

Length of treatment needed unknown

Reduce corticosteroid dose by about 25% every 3-4 weeks to stop medication after around 6mo

Any additional immunosuppressives should be stopped after the glucocorticoids unless cost or side effects inhibit

Need to monitor to ensure clinical remission is maintained - PCV/haematology - some will need ongoing immunosuppressive therapy

Thrombophylaxis should be continued until remission has been achieved and steroids stopped (or after 6mo)

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13
Q

What % of dogs relapse (IMHA)

A

About 15-20%

Either while on treatment or after treatment discontinued

After relapse dose tapering should be significantly slowed

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14
Q

Emergency assessment and treatment of clotting disorders

A

Point of care ultrasound to assess bleeding

PCV - will not immediately fall, important to assess
Serum total protein

Crystalloid or colloid fluid therapy to maintain circulating volume

Blood product transfusion

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15
Q

Treatment for immune mediated thrombocytopaenia

A

Braodly the same immunosuppressives as IMHA

No effective way to rapidly increase platelet counts - fresh whole blood has them but lifespan is short

Vincristine can also improve response (alongside steroids)

Mycophenolate can be used as a sole agent if glucocorticoids contraindicated

Prognosis good

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16
Q

Treatment of vonWillebrands disease

A

Depends on severity of signs

Use of drugs that inhibit platelet function should be avoided e.g. NSAIDs

Desmopressin used before surgery to increase vWF and reduce bleeding (for type 1 vWD)

Transfusion of cryoprecipitate or fresh frozen plasma will provide vWF in an emergency situation - can be used bfore surgery for dogs with severe type 2 or 3 vWD

17
Q

Treatment for rodenticide toxicity

A

Parenteral, followed by enteral, vitamin K1 therapy, continued for at least 3-4 weeks

PT should be checked 36-48hrs after stopping treatment

Activation of vitamin K dependent factors will take several hours - only appropriate for stable, well dogs

Coagulation factors can be immediately replaced with frozen plasma

18
Q

Treatment of Haemophilia A and B

A

Replacement of clotting factors using blood products when required

19
Q

Angiostrongylus vasorum

A

Should always be considered in a coagulopathic dog

Signs: coughing, exercise intolerance, clotting defect

DIC or hyperfibrinolysis

Diagnosis: faecal testing, serology, ELISA SNAP (none 100% sensitive)

Treatment: moxidectin/imidacloprid (advacate), mibemycin/praziquantel (milbemax), fenbendazole (panacur)

20
Q

Blood transfusions

A

Obtained through donation or from a blood bank

Provides RBCs and plasma

Second choice for IMHA after pRBCs (increases blood volume which you normally dont want in IMHA)

Currently no blood bank for cats

21
Q

Packed Red Blood Cells

A

Does not contain clotting factors

Produced by blood bank (good screening of donors)

Can be combined with other components

Better for euvolaemic animals e.g. IMHA

22
Q

Fresh whole blood

A

Includes red cells and clotting factors (and some platelets)

Collected in practice (faster, cheaper?)

Best for haemorrhage

23
Q

When to consider transfusion

A

If PCV below 15-20% (20% if having GA/sedation)

Severity
Chronicity and rapidity
Existing co-morbidities
Physical examination findings (HR, pulse quality, degree of weakness/lethargy)
other markers of impaired oxygen delivery
safety for further interventions

24
Q

Requirements for canine blood donors

A

Healthy, fully vaccinated, no travel, appropriate temperament

No previous transfusion

> 25kg dogs

1-8yo

Normal PCV: ideally >40%

Ideally DEA 1.1. negative

Collect aseptically into a closed blood giving set containing anticoagulant

25
Requirements for feline blood donors
Blood types - need to have both A and B on register Healthy, fully vaccinated, no travel, (appropriate temperament) Infectious disease screening - FIV/FeLV negative No previous transfusion >4kg 1-8yo Normal OCV, ideally >40%
26
Storage of red cell products
Store packed cells or whole blood @ 4C. Never freeze Ensure stored in a good fridge with good monitoring of temperature control. Rock bag every 3-4 days to agitate PRBCs for up to 35-42 days (will have expiry date) Whole Blood for 28 days Should only store for maximum 24h after opening bag (4C); 4-6hours at room temperature
27
Storage of platelet blood products
Shelf life only 72hrs Storage at room temp with frequent agitation Must be used within 4hrs once broached
28
Storage of plasma products
Stored at -20 degrees until use
29
Most important blood type in dogs
DEA 1 If positive can recieve eithe +ve or -ve blood If negative can only recieve -ve
30
Most important blood types in cats
A/B typing A type cats have week anti-B alloantibodies B type cats have strong anti-A alloantibodies ALL cats must be blood types prior to transfusion
31
Monitoring patients during blood product transfusion
At least every 5 mins for 30mins, and then every 15-30mins Demeanour Rectal temp (any increase of >1 degree) Pulse rate and character (increased RR) MM colour and CRT +/- blood pressure (plasma and urine colour)
32
Acute transfusion reactions
Acute haemolytic transfusion reaction Acute allergic and anaphylactic non-haemolytic transfusion reaction Febrile non-haemolytic transfusion reaction Other potential acute transfusion reactions - thromboembolism - electrolyte disturbances - volume overload
33
Acute haemolytic transfusion reactions
Most common in DEA 1 sensitised dogs Can lead to death Type II hypersensitivity of recipient plasma to the donor cells IV haemolysis - fever, vomiting, tachycardia, hypotension, haemoglobinaemia and haemoglobinuria Can lead to shock, DIC, acute kidney injury
34
Acute allergic or anaphylactic non-haemolytic transfusion reaction
Immunologic: Typically IgE mediated (Type I hypersensitivity) Variable severity o May be relatively mild - urticaria, vomiting, pruritus o Or more severe – dyspnoea, upper airway oedema & obstruction, hypotension & circulatory collapse. Can be difficult to differentiate from haemolytic reaction If severe can treat with corticosteroids and antihistamines, or if mild just slow transfusion
35
Febrile non-haemolytic transfusion reaction
Temperature increase by >1oC without any obvious reason Need to rule out AHTR & Bacterial Contamination (Discolouration & Gram stain) Typically caused by white cells & platelets (leukodepletion filter can help) Can last 24 hours
36
Fresh frozen plasma
Contains all clotting factors, immunoglobulins, albumin Stable for 1 year
37
Frozen plasma
Fresh frozen plasma that is 1-5 years old Reduced concentrations of Factors V and VIII, and vWF compared to fresh frozen plasma Suitable for replacement of vit K dependent factors
38
Cryoprecipitate
Allows transfusion of fibrinogen, FVIII & vWF in much smaller volumes than if using plasma, with significant advantages in using this smaller volume.