Haematology Flashcards

1
Q

What is atrial fibrillation?

A
  • AF happens when electrical impulses in the atria of the heart fire irregularly
  • Causes an irregular/ fast heart beat.
  • Can create blood clots in the heart which may lead to stroke
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2
Q

What is diabetes?

A
  • Pancreas no longer able to make insulin/ body becomes insensitive to insulin causing abnormal blood glucose levels.
  • Chronic high blood glucose levels associated with tissue damage and organ failure (cataracts, neuropathy)
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3
Q

What are the dental implications of diabetes?

A
  • Poor wound healing
  • Xerostomia
  • Oral dysesthesia (burning mouth syndrome)
  • Periodontal disease
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4
Q

What is hypertension?

A
  • High blood pressure
  • Can lead to heart attack/ stroke, kidney failure, vascular dementia.
  • Arteries lose stretch and become narrow, easier for a thrombus to occlude lumen.
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5
Q

What is frusemide?

A
  • loop diuretic (for hypertension)
  • decreases fluid in body
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6
Q

What is metformin?

A
  • Anti-hyperglycaemic drug - enhances insulin sensitivity
  • Can reduce vitamin B12 levels (anaemia risk)
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7
Q

What is a side effect of sulfonylureas?

A

Reduced factor VIII and reduced platelet aggregation

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8
Q

How is pseudomembranous candidiasis managed?

A
  • Assess risk factors - diabetic control, medications, anaemia, ill fitting denture
  • Denture hygiene advice
  • Antifungal medication - miconazole contraindicated with warfarin, nystatin safe to use for warfarin
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9
Q

Why is joint swelling significant in haemophilia patients?

A
  • Swelling is likely to be a haemarthrosis - bleeding into joint space (associated with haemophilia)
  • This can cause damage to articular cartilage in joint- bone resorption and cyst formation.
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10
Q

What is haemophilia A?

A

Deficiency in factor VIII (most common)

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11
Q

What is haemophilia B?

A

Deficiency in factor IX

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12
Q

What procedures are safe for haemophilia patients?

A
  • Treatment which doesn’t require manipulation of mucosa
  • ID block contraindication (articaine infil instead)
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13
Q

What is DDVAP?

A
  • Desmopressin
  • Releases factor VIII that has been bound to endothelial cells, giving a temporary boost
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14
Q

What is tranexamic acid?

A

Inhibitor of fibrinolysis (keeps clot formed)

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15
Q

How are patients with severe haemophilia classed and managed?

A

<1% of factor
Recombinant factor

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16
Q

Haemophilia A is a deficiency of which factor?

A

VIII

17
Q

Apixiban inhibits which factor?

A

Factor Xa

18
Q

A person with moderate haemophilia has what percentage of normal factor in their blood?

A

1-5%

19
Q

Von Willibrands type 2 is normally managed with which product to manage bleeding?

A

Factor VIII concentrate

20
Q

Augmentation of factor levels is required for which of the inherited bleeding conditions
-Moderate Haemophilia B
-Type 3 Von Willebrand’s Disease
-Mild Haemophilia A
-Type 2a Von Willebrand’s Disease
-All of the above

A

All of the above

21
Q

Takes the medication warfarin with associated blood testing every week and requires a single tooth extraction.

What is the most appropriate management strategy?

A

INR required within 24 hours

22
Q

Takes the medications aspirin and clopidogrel following a STEMI two weeks ago and requires the extraction of two asymptomatic teeth.

What is the most appropriate management strategy?

A

Delay extractions until 6 month point

23
Q

Takes the medication Rivaroxaban once a day in the morning and requires the extraction of 5 teeth at 0900 in the morning.

What is the most appropriate management strategy?

A

Delay the morning dose and take it four hours after haemostatis has been achieved

24
Q

Takes the medication Dabigatran and requires the surgical extraction of two teeth at 0900 in the morning

Most appropriate management?

A

Miss the morning dose of medication and take the evening dose as usual

25
Q

Takes the medication Apixaban and requires a single extraction

Most appropriate management?

A

Do not change drug regime

26
Q

The prothrombin time (PT) would be deranged in…

A

Liver disease or warfarin therapy

27
Q

The activated partial thromboplastin time (APTT) would be deranged in…

A

Haemophilia

28
Q

Activated partial thromboplastin time (APTT) measures…

A
  • Factors V, VIII, IX, X, XI, XII
  • prothrombin
  • fibrinogen
29
Q

Prothrombin time (PT) measures..

A
  • Factors V, VII, X
  • prothrombin
  • fibrinogen
30
Q

A patient with moderate haemophilia A requires factor coverage for supra-gingival scaling true or false?

A

False

31
Q

Topical miconazole for the management of oral candidosis presents a risk for patients prescribed Warfarin by potentiating bleeding.

A

True

32
Q

What kind of inheritance pattern do haemophilia A and B follow?

A
  • Sex linked recessive
  • Defective gene on the X chromosome - males are affected and females are the carries.
  • Unusual for females to have both X chromosomes affected
33
Q

What is considered a normal INR?

A

1

34
Q

What are the important platelet count numbers?

A
  • 100 to take out tooth in GDP
  • 50 in hospital
35
Q

What is the INR?

A
  • international normalised ratio
  • prothrombin time of pt and dividing it by reference PT plasma value
36
Q

What neutrophil count is required for dental treatment?

A
  • over 1 for GDP
  • under is high infection risk
  • consider antibiotic prophylaxis or post operative antibiotics