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?

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
What is the most common s/s of vaso-occlusive crisis?
Priaprism
26
What are common triggers for sickle cell disease?
-low 02 saturation -infection -dehydration -exposure to cold
27
What kind of ischemia is seen in acute chest syndrome?
Cardiac
28
Splenic ischemia in sickle cell crisis increases....
risk of infection
29
Main s/s of sickle cell disease
Excruciating, sudden, exposive pain in abdomen, chest, back, and joints
30
Dx of sickle cell anemia
CBC to detect infection, dehydration, reticuloyte count
31
Tx for sickle cell crisis
-high flow 02 -IVF for rehydration -antibiotics for infection -opioids for pain -early stem cell transplantation is goal