Blood I Flashcards

1
Q

function of blood

A
  • transport: O2, nutrients, CO2 and waste products

- immune response

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2
Q

what is the composition of blood

A

plasma (55%)

cells (40-45%)

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3
Q

when does haemopoisis begin
then 6 wks-6 months
6 months-birth
adult life

A

in yolk sac at 3rd week of gestation
6 wks–6 mo: liver, spleen (extramedullar)
6 mo–birth: bone marrow taking over (medullary)
In adult life: bone marrow

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4
Q

how do mature cells form

A

pluripotent stem cells–> myeloid or lymphoid cells–> committed stem cells–> earliest recognisable precursors–> mature cells

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5
Q

how is MCV mean cell volume calculated

A

PCV/RBC count

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6
Q

how is mean cell Hb calculated

A

Hb (g/dl)/RBC count

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7
Q

how is mean cell Hb conc calculated

A

Hb g/dl/ PCV

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8
Q

what are the essential diatary constituents of blood

A
  • iron
  • vit B12
  • folic acid
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9
Q

what is anaemia

A

haemiglobin lower than ref level for age and gender
reduction in red cell mass
classified in terms of RED CELL INDICES (MCV)

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10
Q

what are the 3 major types of anaemia

A
  • hypochromic microcytic with low MCV
  • normochromic normocytic with a normal MCV
  • macrocytic with a high MCV
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11
Q

what are the pathological consequences of anaemia

A

tissue hypoxia

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12
Q

what are the clinical manifestations of anaemia

A
  • can be asymptomatic
  • fatugue
  • headaches
  • faintness
  • pallor of conjuctiva
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13
Q

what is anisocytosis in anaemia

A

variation in size

eg low VitB12

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14
Q

what is poikilocytosis

A

variation in shape

eg sickle cell

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15
Q

what is anisochromasia

A

variation in haemoglobinisation

eg low Fe

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16
Q

what are the causes of anaemia

A
  • dec production
    (suppressed proliferation, defective maturation)
  • inc destruction/loss
    (haemorrhage, haemolysis)
17
Q

describe Fe deficiency

A
  • causes microcytic and hypochromic anaemia
  • most common cause of anaemia
  • iron status controlled by absorption
  • stored ferritin and haemosiderin
18
Q

what causes Fe deficiency

A
  • inc demands
  • chronic blood loss
  • poor diet
  • malabsorption
19
Q

how to treat Fe deficient anaemia

A
  • find and treat underlying cause
  • Fe to correct anaemia
  • monitored by RETICULOCYTE count and Hb
  • oral Fe
20
Q

what happens if Fe therapy doesn’t work

what could be the cause

A
  • non-compliance
  • incorrect diagnosis
  • mixed deficiency eg thalassamia
  • chronic inflammation eg TB, malaria INFECTIOUS, and rheumatoid arthiritis
  • malignant disease eg carcinoma, sarcoma, lymphoma
21
Q

what is megaloblastic anaemia

A
  • eg macrocytic, normo/hypochromic
  • characterised by megaloblasts in bone marrow eg erythroblasts with delayed nucleus formation
  • large oval RBCs
  • hypersegmented neutrophils
22
Q

what are the causes of megaloblastic

A
  • deficiency of VitB12 and folate
  • abnormal metabolism of B12 and folate
  • other defects of DNA synthesis
23
Q

dietary folate i sessential for what

A

DNA synthesis

as it provides methylation to form DNA

24
Q

where is B12

A
  • meat
  • fish
  • dairy produce
  • not in plants
25
Q

where is B12 absorbed

A

in terminal ileum, Intrinsic Factor req

26
Q

what is the function of B12

A

methylation for DNA synth

27
Q

what are the causes of B12 deficiency

A
  • low dietary inate
  • malabsoption: gastric (pernicious anaemia, congenital lack of IF, gastrectomy)
  • intestinal: Crohn’s, blind loop syndrome, ileal resection
28
Q

folate is from where

A
  • meat
  • greens
    (present as polyglutamates)
29
Q

how is folate metabolised

A

converted to MONOGLUTAMATE during absorption

30
Q

what are the causes of folate deficiency

A
  • nutritional (poor diet, overcooking food)
  • malabsorption (tropical sprue, coeliac, Crohn’s)
  • excess utilisation (pregnancy, lactation, malignancy, haemolytic anaemia)
  • drugs (alcohol, anti-convulsants)