Anaemia -CVR Flashcards

(41 cards)

1
Q

what demographic of people can have symptoms of anaemia even though their Hb and Hct are normal?

A

Those with chronic respiratory disease and those with malnutrition

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2
Q

what are the most common SYMPTOMS of anaemia

A

Dyspnea WITH exertion and AT REST

Fatigue

Hyperdynamic state like bounding pulses

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3
Q

what are the boundaries for microcytic, normocytic or macrocytic anaemia?

A
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4
Q

what are the overall mechanisms of anaemia

*Yr 1*

A
  • Reduced production of red cells/haemoglobin in the bone marrow
  • Reduced survival of red cells in the circulation - haemolysis
  • Loss of blood from the body
  • Pooling of red cells in a very large spleen
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5
Q

what are the 4 main causes of Microcytic anaemia

A

Iron def anaemia

Thalassaemia (alpha and beta)

  • Anaemia of chronic disease*
  • sideroblastic*
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6
Q

For Iron deficiency anaemia, what are the parameters for:

  • iron
  • ferritin
  • Transferrin or TIBC
  • Transferrin sats
A

Ferritin- iron stores

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7
Q

what are the causes of IRON deficiency anaemia

A

People with chronic slow bleeding like:

  • Heavy menstruation ore postmenopausal bleeding
  • Colon cancer- rectal bleeding

Diet- vegans etc

Pregnancy

IBS

Celiac disease

H.pylori infection

Meds like NSAIDs or aspirin

GI symptoms like dysphagia, haematemesis, maleana

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8
Q

if a pt result shows iron deficiency anaemia, what investigations should perform to determine it’s causing?

A
  • Feacal Immunochemical test for blood in the stool
  • GI investigations like:
    • Upper GI endoscopy
    • Duodenal endoscopy
    • Colonoscopy
  • Coeliac antibody testing
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9
Q

what are the treatments of iron deficiency anaemia?

A

Oral iron supplements with orange juice: it can have S/E like nausea, diarrhoea

if the supplement isn’t tolerated then use IV iron

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10
Q

what are the results of the blood count, blood film and iron tests for a pt with Anaemia of chronic disease

A

ESR is high due to inflammation

MCV may be normal

Ferritin is high (body likes to store iron during systemic inflammation)

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11
Q

what are the common causes (diseases associated) of Anaemia of chronic disease?

A

Occur in people with:

  • Infections like TB or HIV
  • Rheumatoid arthritis or other autoimmune disorders like SLE
  • Cancers

Hence anaemia of chronic disease will resolve once the underlying condition resolves.

it occurs with other disease

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12
Q

why is ferritin high in anaemia of chronic disease

A

In inflammatory states, hepcidin production is increased.

Hepcidin blocks the release of iron from liver and absorption fro GI

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13
Q

Describe the pathophysiology of Anaemia of chronic disease

A

Pro-inflammatory cytokines like IL-1, IL-6 and TNFa are released

These cytokines:

  • reduces erythropoietin
  • stimulates the production of hepcidin
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14
Q

what is the blood results of thalassaemia

A

Everything is normal

Problem is with globin synthesis

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15
Q

Contrast the two types of thalassaemia and what are the severity of symptoms for each mutation

A

alpha- mutation in alpha chain (found in fetal and adult)

Beta- only found in adult haemoglobin

there are 4 alpha genes and 2 beta genes

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16
Q

what are the treatment for thalassaemia?

A

blood transfusion

Iron chelating agents (sweep iron away through faces or urine)

Pts with thalassaemia present with it from brith

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17
Q

Summarise sideroblastic anaemia

A

There is too many sideroblasts (in bone marrow)

The unused iron build up in blood and bind to trasnferrin

A ring is seen on blood film (iron-binding to mitochondria)

18
Q

what are the causes of sideroblastic anaemia and what is the result of bone marrow biopsy?

what is the treatment

A

Congenital

Acquired:

  • alcohol, copper or Vit b6 def
  • myelodysplastic syndrome

BM biopsy: ringed sideroblasts

Treatment depends on the cause

19
Q

One of the causes of macrocytic anaemia is Megaloblastic anaemia.

what are the results of it on a blood film.

A

Macrocytes

Hypersegmented neutrophils

20
Q

what is the mechanism underlying formation of megaloblasts in megaloblastic anaemia?

A

Impaired DNA synthesis,

Hence impaired nuclear maturation and cell division

21
Q

what are the causes of Megaloblastic anaemia

A

Most common are; Vit B12 and/Or Folate deficiency

Others are secondary to agents or mutations that impair DNA synthesis like:

  • Drugs: azathioprine, cytotoxic chemotherapy
  • Folate antagonists: methotrexate
  • BM cancers: myelodysplastic syndrome
22
Q

what are the importance of Vitamin B12 and folate

A

Vit B12

  • DNA synthesis
  • The integrity of the nervous system- hence can cause neurological symptoms if deficient.

Folic acid is required for

  • DNASynthesis
  • Homocysteine metabolism
23
Q

When b12 or folate test is not conclusive enough, what other tests can you do to discern the cause of megaloblastic anaemia

A

Homocysteine and Methylmalonic acid

24
Q

what are the causes of Vit B12 deficiency and give corresponding treatments?

B12 can be stored for years

A

N.B: Test for pernicious anaemia using anti IF antibody test or endoscopy)

25
What are the causes of Folate deficiency and give corresponding treatments. Folate only stored for 6 weeks.
Very common in pregnant women (hence just take oral folate supplements)
26
what are the neurological disorders for vit B12 and folate deficiency?
Vitamin B12; * Dementia and SACD (sub-acute combined degeneration) of spinal cord Folic acid: * Developmental neural tube defects * It doesn't cause any neurological disorders if you developed normally
27
what are the causes of non-megaloblastic macrocytic anaemia
chronic alcohol intake liver disease hypothyroidism myelodysplastic syndrome some drugs
28
what are the causes of normocytic anaemia when reticulocyte count is normal?
Bone marrow suppression- * malignancy * drugs * infection CKD: * rReduces EPO * Signs show elevated creatinine levels * treat with erythropoiesis-stimulating agents
29
Haemolytic anaemia shows a high MCV on a blood film, what are the results of a blood test that suggests haemolytic anaemia LDH? Bili? hap?
High LDH High unconjugated bilirubin Low haptoglobin Blood smear shows abnormal RBCs (reticulocyte)
30
what are the causes of acquired haemolytic anaemia?
Could be RBC defect or problem with the environment.
31
what are the immune and non-immune environmental factors that can damage RBCs? (heamolysis)
32
what tests confirm an immune mechanism in acquired haemolysis?
Direct antiglobulin test (postive)
33
Summarise the pathology of autoimmune hemolytic anaemia. Give treatments and what does the blood result show
blood film shows spherocytes it can be IgM (cold) or IgG (HOT) Use coombs test to determine which
34
Summarise Hereditary spherocytosis (a cause of haemolytic anaemia) what is the defect and how do you diagnose it
Defect in ankyrin, band 3, spectrin Use Coomb's test to rule out autoimmune hemolytic anaemia Use osmotic fragility test Treat; splenectomy
35
give examples of inherited causes of haemolytic anaemia
* Abnormal red cell membrane- hereditary spherocytosis * Abnormal Hb: Sickle cell * Defect in the **glycolytic pathway: pyruvate kinase deficiency** * Defect in enzymes of pentose shunt,e.g. G6PD deficiency.
36
what is the role of G6PD? it converts G6P to 6-phosphoglyconolactone
A key enzyme in the pentose shunt Protects the **RBC from oxidative stressors** like fava beans, infections etc
37
how common is G6PDD and in what demographic what is the inheritance?
X-linked recessive Very common in Africa (mild variant) Severe variant found in the Mediterranean
38
what will a blood film **characteristic for G6PDD** show and explain why
**Heinz body**- when haemoglobin gets damaged by oxidative stress **Bite cell** (irregularly contracted cells): when splenic macrophages try to destroy RBC due to damaged haem. Ghost cell (intravascular haemolysis)- haemoglobin disappeared Hemighost
39
what is a reliable time in which the levels of G6PD in the blood can be used to diagnose G6PDD
8 weeks after the attack; it should be low levels are unreliable during an attack
40
what advice should you pts with G6PDD in order to prevent attacks? what is the treatment for it
Avoid triggers like: * oxidant drugs (quinine rich) * Don't eat fava beans in broad bean * Avoid naphthalene Be aware that it can be precipitated by infections Treatment * Blood transfusions * Splenectomy
41
Summarise the clinical reasoning for anaemia