Bleeding Symptoms Flashcards

1
Q

It is the excessive bleeding that requires medical or physical intervention

A

Hemorrhage

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2
Q

Type of bleeding may result from primary (platelet- related) or secondary (coagulation factor-related) hemostasis disorders or from unregulated fibrinolysis in which clots are rapidly metabolized.

A

Congenital Bleeding

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3
Q

Bleeding from a single location usually indicates injury, infection, tumor, or an isolated blood vessel defect and is called

A

Localized bleeding or Localized hemorrhage

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4
Q

Give and example of localized bleeding

A

Inadequately cauterized or ineffectively sutured surgical site or an arteriovenous malformation (AVM)

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5
Q

This is a reduced platelet count (thrombocytopenia), or a coagulation factor deficiency cause systemic and not localized bleeding

A

Qualitative platelet defect

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6
Q

Bleeding from multiple sites, spontaneous and recurring bleeds, or a hemorrhage that requires physical intervention is called

A

Generalized bleeding

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7
Q

It is a potential evidence for a disorder of primary hemostasis such as a blood vessel or platelet defect or thrombocytopenia; or secondary hemostasis characterized by single or multiple coagulation factor deficiencies or uncontrolled fibrinolysis.

A

Generalized bleeding

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8
Q

Generalized bleeding may exhibit either _ or _

A

Mucutaneous (typically in skin or at body orifices) or anatomic (soft tissue, muscle, joints, deep tissue)

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9
Q

Red pin points (<3mm)

A

Petechiae

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10
Q

Purple skin lesions (3mm to 1cm)

A

Purpura

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11
Q

Greater than 1 cm, typically seen after trauma

A

Ecchymoses (bruises)

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12
Q

Other symptoms of a primary hemostasis defect include:

A
  • Bleeding from the gums,
  • Epistaxis (uncontrolled nosebleed)
  • Hematemesis (vomiting of blood),
  • Blood in the urine or stool
  • Menorrhagia (profuse menstrual flow)
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13
Q

Mucocutaneous hemorrhage is most likely to be associated with

A
  • Thrombocytopenia (platelet count less than 150,000/uL
  • Qualitative platelet dsd.
  • vWF dse.
  • Vascular dsd. (scurvy or telangiectasia)
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14
Q

Seen in acquired or congenital defects in secondary hemostasis such as plasma coagulation factor deficiencies (coagulopathies)

A

Anatomic Hemorrhage

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15
Q

Examples of anatomic bleeding include:

A
  • Recurrent or excessive bleeding after minor trauma
  • Dental extraction
  • Surgical procedure.
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16
Q

Bleeds that are internal, such as bleeds into joints, body cavities, muscles, or the central nervous system, and may have few initially discernible signs.

A

Anatomic bleeds

17
Q

Cause swelling and acute pain; may not be immediately perceived as hemorrhages,

A

Joint bleeds (Hemathroses)

18
Q

Cause inflammation that may culminate in permanent cartilage damage that immobilizes the joint.

A

Recurrent hemarthroses

19
Q

May cause nerve compression and subsequent temporary or permanent loss of function

A

Bleeds into soft tissues such as muscle or fat

20
Q

Bleeds into the kidney may present as hematuria and may be associated with

A

Acute Renal Failure

21
Q

This test isessential whenever a generalized mucocutaneous or anatomic bleed is detected

A

Hemostasis laboratory testing

22
Q

Assess anemia associated with chronic bleeding or a hemolytic anemia; bone marrow response

A

Hemoglobin, Hematocrit, Reticulocyte count

23
Q

Assesses thrombocytopenia

A

Platelet count

24
Q

Assess clotting time prolonged in deficiencies of
factors II (prothrombin), V, VII, or X

A

Prothrombin Time (PTT)

25
Q

Assess clotting time prolonged in deficiencies of all
factors except VII and XIII

A

Partial thromboplastin time (PTT)

26
Q

Assess prolonged by unfractionated heparin therapy, dysfibrinogenemia, hypofibrinogenemia, and afibrinogenemia; qualitative

A

Thrombin Time (TT)

27
Q

Reduced in dysfibrinogenemia, hypofibrinogenemia, and afibrinogenemia; quantitative result

A

Fibrinogen assay (FG)

28
Q

Are coagulometers that measure whole blood clotting, a process called global hemostasis. Both report clot onset dynamics, clot strength, and fibrinolysis in 15 to 30 minutes

A

Thromboelastograph (TEG) or thromboelastometry (TEM)

29
Q

Are uncommon, occurring in fewer than 1 per 100 people, and are usually diagnosed in infancy or during the first years of life

A

Congenital Hemorrhagic disorder

30
Q

Lead to recurrent hemorrhages that may be spontaneous or may occur after minor injury or in unexpected locations, such as joints, body cavities, retinal veins and arteries, or the central nervous system

A

Congenital Bleeding disorders

31
Q

May have no symptoms until they reach adult- hood or experience some physical challenge, such as trauma, dental extraction, or a surgical procedure.

A

Mild congenital hemorrhagic disorders

32
Q

The most common congenital deficiencies are:

A
  • vWD
  • factor VIII (FVIII, hemophilia A)
  • factor IX deficiencies (FIX, hemophilia B)
  • platelet function disorders