blood Flashcards

(27 cards)

1
Q

erythropoiesis process

A

SC - erythroblast - reticulocyte - erythrocyte

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

lifespan of RBC

A

120 days

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

cause of Fe def anemia

A
  1. ↓ iron rich foods
    (eg red meat, beans, leafy veg)
  2. ↓ GI absorption
    Due to ↓ stomach acid production or inflammation of GIT
  3. ↑ body dd - children, pregnancy & lactation
  4. ↑ loss due to acute hemorrhage, chronic slow bleeding, ↑ hemolysis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what is hypochromic anemia

A

RBC appear paler than normal

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

what is microcytic anemia

A

smaller RBC

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

what is anisocytosis

A

unequally shaped RBC

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

signs/ symptoms of Fe def anemia

A

Sore tongue/ glossitis/ angular cheilitis/ yellowing of eyes
Pallor
Koilonychia
Pica

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

diagnosis for Fe def anemia

A

blood test
1. CBC - ↓ RBC, reticulocyte # (may show increase to compensate) & Hb
2. MCV - ↓
3. ↓ Fe & ferritin, ↑ TIBC, transferrin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

treatment for Fe def anemia

A
  1. ↑ Fe intake
  2. IV Fe, IM Fe dextran
  3. severe - blood transfusion
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

coagulation process

A
  1. temporary plug at site of injury
  2. platelet plug attracts clotting factors
  3. activation of factor X to Xa, which activates prothrombin to thrombin
  4. thrombin converts fibrinogen to fibrin
  5. which then activates plasminogen to plasmin, causing fibrinolysis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

cause of DIC

A
  1. sepsis
  2. cancer
  3. toxin
  4. obstetric complications (amniotic fluid embolism, placental abruption)
  5. blood complications (incompatible organ, blood transfusion)
  6. trauma
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

treatment for DIC

A
  1. ↓ bleeding - heparin (anticoagulant)
  2. treat underlying cause
    - sepsis - microbial agents
  3. fresh frozen plasma & platelets, blood pdts, IV fluids
  4. supplemental O2
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

signs/ symptoms of DIC

A
  1. uncontrollable bleeding (mouth, gum, nose, stools, urine, puncture sites)
  2. hypoxia - ischemia - necrosis - stroke/ MI/ organ failure/ DVT/ PE
  3. bluish discoloration in nailbed/ fingers/ lip
  4. deep tissue bleeding - altered mental status, angina, dyspnea, palpitations, tachycardia, shock
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

signs/ symptoms of polycythemia

A
  • headache, dizziness, tinnitus, blurred vision
  • itchy skin after a hot shower
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what causes pri polycythemia

A

spontaneous mutation of gene

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

what causes sec polycythemia

A

tissue hypoxia (increased EPO)
- increased altitude
- lung - copd
- cyanotic HD
- meds eg EPO analogs, testosterone
- EPO-secreting tumours

17
Q

RF of pri polycythemia

18
Q

RF of sec polycythemia

A

obesity, smoking, alc, HTN

19
Q

complications of polycythemia

A
  • risk of thrombosis/ blood clots (cause DVT, PE, MI, stroke)
  • risk of more RBC breakdown (gout, k stones)
  • splenomegaly, hepatomegaly
20
Q

treatment of polycythemia

A
  • phlebotomy (500ml drawn every wk)
  • IV fluids to decrease viscosity
  • meds eg myelosuppressive agents, allopurinol, aspirin
  • sec polycythemia: treat underlying condition eg stop smoking, remove EPO-secreting tumour
21
Q

causes of thrombocytopenia

A
  1. ↓ Thrombocyte production (BM)
  2. ↑ Thrombocyte destruction (non-immune/ immune)
    - non-immune (thrombocytic thrombocytopenia purpura, DIC)
    - immune-mediated (heparin-induced thrombocytopenia, immune thrombocytopenia purpura)
  3. ↓ Distribution of thrombocytes
    - hypersplenism
    - blood transfusion
22
Q

signs/ symptoms of thrombocytopenia

A
  1. bruising easily
  2. petechiae/ purpura/ ecchymoses
  3. mucosal bleeding eg gum
  4. hypoxia/ ischemia/ necrosis/ stroke/ MI/ DVT/ PE
23
Q

RF of thrombocytopenia

A
  1. meds eg heparin, aspirin
  2. immune diseases eg lupus, RA, infections, cancers
  3. alc
24
Q

treatment for thrombocytopenia

A
  1. plasma xchange (TTP)
  2. discontinue heparin (HIT) , aspirin (since prolong bleeding)
  3. glucocorticoids (anti-inflammatory), IV immunoglobulin, splenectomy (ITP)
  4. platelet transfusion (severe haemorrhage)
  5. pt care - avoid BP cuffs, injections, rectal temp
25
diagnosis for thrombocytopenia
1. CBC → platelet count < 150 000 (severe < 50 000) 2. Coagulation studies - Normal prothrombin & partial thromboplastin time 3. Peripheral blood smear → scarce platelets 4. Fecal occult blood testing & urinalysis → blood in stool/ urine 5. Bone marrow biopsy - Abnormal megakaryocytes → platelet problems - Scarce amts of all blood cells & precursors → aplastic anemia 6. Immune-mediated thrombocytopenia → detection of autoimmune Ab
26
when are myelosuppressive agents given?
pri polycythemia (mutation of gene)
27
why arent fresh frozen plasma given to pts w thrombocytopenia?
fresh frozen plasma to replenish clotting factors that have been used - DIC plasma xchange to remove harmful ones and replace - TTP