Hematology Flashcards

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1
Q

Regarding autoimmune hemolytic anemia, what are the causes of warm agglutinin, and which immunoglobulin is it associated with?

A

IgG

  • SLE (lupus)
  • Malignancies (CLL, non-Hodgkin’s lymphoma)
  • Viruses (EBV, HIV)
  • Congenital immune abnormalities
  • Drugs
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2
Q

Regarding autoimmune hemolytic anemia, what are the causes of cold agglutinin, and which immunoglobulin is it associated with?

A

IgM

  • CLL
  • Mycoplasma infection
  • Infectious mononucleosis (EBV)
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3
Q

What are the three main steps to platelet stimulation/platelet plug formation?

A
  1. Adhesion
  2. Activation
  3. Aggregation
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4
Q

What are some of the contents in platelets? Name 6

A
  • vWF
  • Fibrinogen
  • Thrombin
  • Cyclooxygenase
  • Thromboxane A2
  • ADP
  • Calcium
  • PDGF
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5
Q

What are the possible causes of disseminated intravascular coagulopathy (DIC)?

A

STOP Making New Thrombi

  • Sepsis (Gram-negative)
  • Trauma
  • Obstetric complications
  • acute Pancreatitis
  • Malignancy
  • Nephrotic syndrome
  • Transfusion
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6
Q

What are some examples of ADP-receptor antagonists?

A
  • Clopidogrel
  • Ticlopidine
  • Prasugrel
  • Ticagrelor
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7
Q

What are some examples of GPIIb/IIIa inhibitors?

A
  • Abciximab
  • Eptifibatide
  • Tirofiban
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8
Q

What are the indications for aspirin usage?

A
  • Antipyrexia
  • Analgesia
  • Anti-inflammatory
  • Anti-platelet
    &raquo_space; Acute MI/ACS
    &raquo_space; Acute thrombotic stroke
    &raquo_space; MI prevention
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9
Q

What are the side effects of aspirin?

A
  • Gastric bleeding/Peptic ulcers
  • Bleeding
  • Hyperventilation&raquo_space; Respiratory alkalosis&raquo_space; Metabolic acidosis
  • Reye syndrome in children
    &raquo_space; Liver failure
    &raquo_space; Encephalopathy
    &raquo_space; Hypoglycemia
  • Tinnitus
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10
Q

What is a specific side effect of ticlopidine, and which class of drug is ticlopidine?

A
  • ADP receptor inhibitor

- Neutropenia

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11
Q

What are the laboratory findings of a patient with DIC?

A
  • Decreased PLT
  • Increased BT
  • Increased PT
  • Increased aPTT
  • Increased D-dimers
  • Decreased fibrinogen
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12
Q

What is the mode of inheritance of von Willebrand disease?

A

Autosomal dominant

- The most common inherited bleeding disorder, albeit mild

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13
Q

What is the common investigation used to the diagnosis of von Willebrand disease?

A

Ristocetin cofactor assay

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14
Q

What is the treatment for von Willebrand disease?

A

DDAVP: releases vWF stored in the endothelium

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15
Q

Name four common platelet disorders.

A

Quantitative (low platelet count)

  • Immune thrombocytopenic purpura (anti-GpIIb/IIIa Abs)
  • Thrombotic thrombocytopenic purpura (deficiency of ADAMTS 13 to cleave vWF into smaller functional units)

Qualitative (platelet dysfunction)

  • Bernard-Soulier syndrome: GpIb deficiency
  • Glanzmann thrombocytopenia: GpIIb/IIIa deficiency
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16
Q

What is the pentad for thrombotic thrombocytopenic purpura (TTP)?

A
  • Hemolytic anemia (microangiopathic)
  • Uremia/Acute kidney failure
  • Thrombocytopenia
  • Neurological symptoms
    &raquo_space; Confusion
    &raquo_space; Headaches
    &raquo_space; Coma
    &raquo_space; Seizures
    &raquo_space; Focal neurological symptoms/signs
  • Fever
17
Q

What is the hallmark of platelet abnormalities?

A

Microhemorrhages

  • Petechiae/purpura
  • Epistaxis
  • Mucous membrane bleeding