General Medical Emergencies Flashcards

1
Q

Types of hemophilia that only men have

A

Hemophilia A (factor VIII) (most common)
Hemophilia B (fact IX)

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2
Q

Type of hemophilia that both men and women can have

A

Von Willebrand (common)

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3
Q

What common medications do patients with hemophilia have to avoid? (2)

A

Aspirin + NSAIDs

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4
Q

If a hemophiliac has decreased LOC following a head injury, what must you obtain immediately?

A

Head CT

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5
Q

What is the treatment for hemophiliacs following a traumatic injury of any kind?

A

-replace clotting factor
-administer cryo of FFP
-ice, compression, elevation, immobilization

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6
Q

What is the treatment for lacerations in a hemophiliac?

A

-replace clotting factor
-topical thrombin
-observation for 4 hours post suturing

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7
Q

How long do you need to hold pressure on a hemophiliac following IV insertion or phleb draw?

A

5 minutes manual pressure

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8
Q

What are some common causes of DIC?

A

sepsis, trauma, pancreatitis, HELLP in OB

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9
Q

S/s of DIC

A

bruising, petechia, purpura, hematuria, excessive bleeding, end-organ failure

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10
Q

Dx of DIC (4)

A

-low hemoglobin, hematocrit, platelets, fibrinogen
-prologed coags

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11
Q

Tx of DIC

A

-treat underlying cause
-control bleeding
-antifibrinolytic agents (Amicar + TXA)
-Transfuse platelets, FFP

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12
Q

Causes of anemia

A

-blood loss
-low iron
-low vitamin B12
-low folic acid

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13
Q

Tx for anemia

A

-stop blood loss
-oral iron replacement
-replace vitamin B12

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14
Q

Side effects of oral iron replacement

A

-dark stools
-constipation

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15
Q

What is polycythemia?

A

Excessive red blood cells

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16
Q

What is secondary polycythemia?

A

increased RBC d/t high altitude or hypoxia seen in COPD

17
Q

Tx for polycythemia vera

A

phleb to remove whole blood and infuse saline
-chemotherapy to decrease blood cell production

18
Q

What is polycythemia vera?

A

Overactive bone marrow which results in a hematocrit over 55% and results in crease in RBC, WBC, and platelets

19
Q

What organs are potentially enlarged in polycythemia vera?

A

Spleen + liver

20
Q

What is sickle cell disease?

A

congenital hemolytic anemia causes sickilg of RBCs

21
Q

What is treatment for sickle cell anemia? How does it work?

A

Hydroxyurea | Works by decreasing sickling + producing more hemoglobin

22
Q

What should acute chest syndrome be triaged as?

A

ESI 2

23
Q

What is acute chest syndrome?

A

Chest pain and dyspnea, high mortality rate

24
Q

Why do sickle cell patients often have abdominal pain when in crisis?

A

Sequestration of cell in the spleen

25
Q

What is the most common s/s of vaso-occlusive crisis?

A

Priaprism

26
Q

What are common triggers for sickle cell disease?

A

-low 02 saturation
-infection
-dehydration
-exposure to cold

27
Q

What kind of ischemia is seen in acute chest syndrome?

A

Cardiac

28
Q

Splenic ischemia in sickle cell crisis increases….

A

risk of infection

29
Q

Main s/s of sickle cell disease

A

Excruciating, sudden, exposive pain in abdomen, chest, back, and joints

30
Q

Dx of sickle cell anemia

A

CBC to detect infection, dehydration, reticuloyte count

31
Q

Tx for sickle cell crisis

A

-high flow 02
-IVF for rehydration
-antibiotics for infection
-opioids for pain
-early stem cell transplantation is goal