5. Cardiovascular System Pathologies Flashcards

1
Q

Anaemia

A

• A deficiency in haemoglobin given the persons age, sex and geographical location.

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2
Q

Anaemia: Signs and Symptoms

A

SYMPTOMS:
* Feeling fatigued: lack of oxygen being delivered to various tissues -> the cells cannot make energy if they don’t get enough oxygen.
* Shortness of breath on exertion (= effort, strain)
* Palpitations (= heart racing): the heart desperately tries to
move enough blood around the body to
deliver sufficient oxygen to the tissues.
* Irritability and fainting: because of a lack of oxygen in the
brain.
• SIGNS:
* Tachycardia: fast heart rate
* Thin & thready (= weak) pulse: because of the heart
racing
* Pallor skin/conjunctiva (= tissue on the inside of the eye
lids, that covers the white of the eye) -> result of not
enough oxygen to the tissues there.

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3
Q

Normal Haemoglobin ranges

A

Males 13 - 18 g/dl
Females 11.5 - 16.5 g/dl
Pregnanct >11 g/dl

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4
Q

Iron-Deficiency Anaemia

A

• The most common cause of anaemia worldwide.
• Iron deficiency: leads to hypochromic (= low in colour,
paler) microcytic (= small) erythrocytes (= red blood cells).

-> Not enough iron available we cannot make haemoglobin in erythrocytes causing them to appear paler & smaller. Hence iron deficiency anaemia is a ‘hypochromic microcytic anaemia’.

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5
Q

Iron-Deficiency Anaemia: Causes

A
  • Deficient dietary intake (e.g. low dark leafy vegetables).
  • Malabsorption: you need sufficient stomach acid and a healthy digestive system to absorb iron correctly. Low stomach acid because of coeliac, Crohn’s disease (=malabsorption diseases) can lead to iron-deficiency anaemia.
  • Excessive blood loss (i.e. from menses (=menstruation) /GIT bleed (=Gastro Intestinal bleeding).
  • Excess requirements (extra iron is needed) e.g. Pregnancy, rapid growth with children.
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6
Q

Iron-Deficiency Anaemia: Signs and Symptoms

A

SIGNS & SYMPTOMS:
• General anaemia signs & symptoms.
• Key signs: * Koilonychia: Spoon shaped nails
* angular stomatitis: cracking on the outside
of the mouth
* glossitis: a soar red tongue
* brittle hair
* tachycardia (=abnormal rapid heart beat)
• Blood tests: Low RBCs & Hb, low ferritin. Ferritin stores iron. If we recently had to rapidly make a lot of red blood cells, our store of iron is going to be low.

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7
Q

Iron-Deficiency Anaemia: Treatment

A

TREATMENT:
• Treat cause!
• Also: Herbs (Withania), beetroot, dark green leafy vegetables, pumpkin and sunflower seeds. Iron supplementation (gentle organic ones that don’t upset the stomach)

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8
Q

Megaloblastic Anaemia

A
  • Megaloblastic anaemia is characterised by large, immature and dysfunctional red blood cells.
  • Happens because of a lack of folate or vitamin B12
  • The maturation of red blood cells relies on having enough folate and B12 available. If they are short in supply the ability to make the red blood cells is compromised.
    What happens? That DNA replication slows but the cell division continues -> results in the production of immature blood cells. Some of them might still have their nucleus in and they will be bigger than normal.
    They will get more easily damaged as they circulate around the body. They have a shorter life circle.
    => With Megaloblastic Anaemia the erythrocytes are described as macrocytic (they are larger than normal).
  • Diagnosis by blood test: ‘MCV’>97 fL. MCV = Mean corpuscular volume. This volume is larger than normal in Megablastic Anaemie.
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9
Q

Megaloblastic Anaemia: Causes

A

• Deficient dietary intake of folate (folic acid) &/or vitamin B12 (rare, except in vegans). Vitamin B12 we find especially in animal products.
• Lack of intrinsic factor:
Intrinsic factor = a protein that is created by the stomach. Is required to absorb enough B12. This factor is a little bit like the guide document for the B12. If there is no intrinsic factor available the B12 just passes through the intestines completely ignored. When the intrinsic factor is there it will bind on to the B12 and helps to carry it into the bloodstream.
People with autoimmune disease (pernicious Anaemia), gastrectomy (=medical procedure where all or part of the stomach is surgically removed), chronic gastritis (=inflammation of the stomach lining), stomach cancer, Coeliac’s disease have a lack of intrinsic factor.
• Malabsorption in Crohn’s disease, surgical excision.
• Drugs–‘methotrexate ’is a folate antagonist -> Drug used for certain autoimmune diseases. It can create Megaloblastic Anaemia.
• In order for folate to function in the body, it must be modified (changed) by an enzyme that requires Vitamin B12.
• The liver has abundant stores of B12. B12 can be stored up for 2 to 4 years in the liver. Folate is only stored for max 4 months in the body. Is not stored in the fat tissues of the body.
=> we need to figure out which nutrient is missing. Folate or B12? And why? So that we can address that dietary and absorption in balance to correct the problem.

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10
Q

Megaloblastic Anaemia: Signs & Symptoms

A

SIGNS & SYMPTOMS:
• General anaemia signs & symptoms.
• Enlarged red sore shiny tongue.
• Neurological symptoms only with B12 deficiency: Tingling, numbness, weakness, loss of co-ordination, burning sensations, tinnitus, depression
=> you can get all strange symptoms within the nervous system when you lack B12. Reason: production and maintenance of the myelin sheath (= fatty cover over the nerve fibres) stops. The neurons stop cross firing, stop communicating with each other.
-> If you don’t have enough B12 you cannot make that protective myelin fatty sheet.

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11
Q

Megaloblastic Anaemis: Treatment

A

TREATMENT:
• B12 Deficiency: Increase Vitamin B12 with supplements or B12 injection for people with an absorption problem.
• Folate Deficiency: Folate supplementation and rich folate food like green leafy vegetables.

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12
Q

Aplastic Anaemias

A

• A rare and potentially life-threatening failure of haematopoiesis -> failure of production of all 3 blood types
(Red blood cells, White blood cells and platelets)
=> Result is ‘Pancytopenia’ (lack of all three blood cell types) and hypocellular bone marrow (few or no cells).

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13
Q

Aplastic Anaemias: Causes

A

• Congenital (condition that you are born with)
“Fanconi’s anaemia”
• Idiopathic (unknown cause).
• Can be secondary to drugs (naproxen, diclofenac etc.), chemicals, radiation, cancer, hepatitis/EBV.

Chemotherapy or radiation therapy for cancer can cause Aplastic Anaemias. These treatments are so heavy on the body that they actually suppress the bone marrow to the point where it is not producing sufficient levels of red blood cells, white blood cells and platelets.

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14
Q

Aplastic Anaemias: Signs and Symptoms

A

• Anaemia (pallor, headache, dyspnoea (shortness of breath or breathlessness), palpitations etc).
• Multiple infections (due to low white blood cell count)
• Easy bleeding (due to low thrombocyte count).
Most common cause of death is sepsis (blood poisoning), then haemorrhage (heavy blood loss)

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15
Q

Aplastic Anaemias: Treatment

A
  • Treat the cause.
  • Bone marrow stem cell transplant.
  • Platelet transfusion/blood transfusion: in order to keep blood cell numbers up to prevent these nasty complication.
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16
Q

Haemolytic Anaemias

A
  • Anaemia resulting from excessive breakdown of erythrocytes, when bone marrow activity cannot compensate for the loss of RBC’s.
  • Erythrocyte life span can become as low as 5 days.
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17
Q

Haemolytic Anaemias: Causes

A
  • Genetic e.g. sickle cell, thalassemia. Thalassemia is the name for a group of inherited conditions that affect haemoglobin. People with thalassaemia produce either no or too little haemoglobin.
  • Rhesus factor incompatibility (blood transfusion problem)
  • Malaria: The parasites of Malaria enter the red blood cells and also mature inside the red blood cells. Then the parasites bursts the cells open and damage the cells. Causing the red blood cells to be removed from the circulation. Malaria untreated can lead to Anaemia very quickly.
  • Some drugs, chemicals, autoimmune diseases, radiation
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18
Q

Haemolytic Anaemias: Signs and Symptoms

A
  • Same general signs & symptoms of anaemia.
  • Jaundice: excess bilirubin production -> when we breakdown red blood cells, we recycle the globin and the iron. We turn the haem into bilirubin which we then conjugate and get rid of through the bile. If there is excessive destruction of red blood cells we are going to get more bilirubin produced then we can easily get rid of. As bilirubin is yellow in colour it can start to generate to yellow colour of the skin and white of the eyes.
  • Splenomegaly: excess haemolysis (breakdown of the red blood cells) in the spleen causes it to enlarge, leading to abdominal distention (swollen from internal pressure) and a feeling of fullness quickly whilst eating.
  • Gallstones: because of the increase of bilirubin going out in the bile
  • Vascular occlusions (complete or partial blockage of a blood vessel): If the Haemolytic Anaemias is characterized by badly shaped red blood cells it is also possible that these might become occlusions. They might become blockages in blood vessels leading to a lack of oxygenated red blood cells in certain areas of the body.
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19
Q

Sickle Cell Anaemia

A
  • Sickle cell anaemia causes a deficiency of the 2-alpha 2-beta formation of haemoglobin and causes it to sickle up.
  • > The 2 alpha an 2 beta formation of haemoglobin is incorrect. When the cells let go of that oxygen the haemoglobin changes shape and causes the red blood cells to create ‘like a crescent moon shape’. Instead of being flat bi-concave discs they become curved over like sickle shaped. The problem with sickle shaped cells is that they rupture easily. They also can get more easily stuck in blood vessels causing concussions (stretch and bruise nerves and blood vessels).
  • These cells rupture easily. Even though erythropoiesis is stimulated, it cannot keep up with the rate of haemolysis.
  • The sickle trait (characteristic) protects against malaria because it causes sickle formation and potassium leakage out of erythrocytes.
  • Sickle cell is an inherited recessive condition (substitution chromosome 21), affecting African and Caribbean populations.
  • > Is a certain immunity against malaria.
20
Q

Sickle Cell Anaemia: Signs and Symptoms

A
  • Usually begins 3-6 months of age as HbF falls: This is when the foetal haemoglobin is changing over to the adult haemoglobin. But in some sickle cell anaemia this adult haemoglobin will be the incorrect shape.
  • General signs and symptoms of anaemia.
  • Splenomegaly and jaundice.
  • Can also occlude (obstruct) vessels and cause ischaemic pain: this is pain caused by lack of blood flow to an area. The sickle shaped cells tend to pile up and get stuck in the smaller blood vessels. Stopping the blood flowing in a particular tissue. This can lead to things like pain in the extremities -> fingers
  • Can also cause: placental infarction (interruption in blood flow between the placenta and the baby), strokes, renal colic (pain that occurs due to a stone in the urinary tract)
21
Q

Sickle Cell Anaemia: Diagnosis and Treatment

A

BLOOD TEST:
• FBC (Full Blood Count) and blood film. Hb is 6-8g/dL.

TREATMENT:
• Analgesics (pain relievers), fluid therapy, blood transfusion, bone marrow transplant.

22
Q

Thalassaemia

A

• Thalassaemia describes a defect in synthesis of either the alpha or beta Hb chains.
HbA (2-alpha and 2-beta)
HbF (2-alpha and 2-gamma)
• An inherited recessive disease -> 2 copies of the mutation are needed to cause the disease. Healthy gen is the boss.

23
Q

Thalassaemia: Signs and Symptoms

A

• B-Thalassaemia -> Starts when HbA production begins and gamma chain ceases (comes to an end) usually later part of first year. Causes ‘failure to thrive’ (lack of growth) and anaemia in younger people.
• A-Thalassaemia -> Can be lethal in utero in severe cases (‘major’). Signs/symptoms of anaemia, jaundice, splenomegaly, hepatomegaly: enlarged spleen and liver because the bone marrow and liver haven’t accompensate for the spleen’s ability to brake down red bloods cells because it is such an excessive requirement.
To compensate haemolysis: bone marrow proliferation (increase in the number of hematopoietic cells in the bone marrow) -> mostly skull/ribs).

24
Q

Haemolytic Disease of the Newborn

A
  • Can happen during pregnancy when the mother has Rhesus - and the child Rhesus + that she is carrying
  • Occurs when the mother produces Anti-Rhesus antibodies that cross the placenta.
    • The antibodies bind to the foetal rhesus antigens, causing agglutination & haemolysis -> all the red blood cells stick together inside the baby and then start to be braking down. This can obviously be fatal for the child.
    • Sensitisation (cause to change) occurs with the first baby that the mother is producing maternal antibodies against rhesus.
    • The greatest possibility of sensitisation occurs at delivery or when there is a complication during the pregnancy. When blood from mother and child gets mixed. The first born child is normally unaffected.
    • Anti-Rhesus antibodies (D injections) can be given during pregnancy to bind to Rhesus antigens and block them.
25
Q

Polycythaemia

A
  • Polycythaemia describes an excessive production of erythrocytes resulting in increased blood viscosity, reduced blood flow and an increased risk of thrombosis.
  • Also known as ‘erythrocytosis’.
26
Q

Polycythaemia: Causes

A
  • Physiological: occurs at high altitude.

* Pathological:unknown/genetic

27
Q

Polycythaemia: Signs and Symptoms

A
  • Mild cases may cause no symptoms.
  • Arterial thrombosis: Myocardial infarction (heart attack), pulmonary embolism, stroke.
  • Venous thrombosis: Deep vein thrombosis (DVT).
  • Hypertension, red skin, headaches, dizziness, pruritus.
28
Q

Granulocytopenia

A
  • Marked reduction in the number of granulocyte leukocytes.

* I.e. ‘neutropenia’ (normal neutrophil count is 2.5 -7.5 x10^9/L. “Severe neutropenia” if <0.5.

29
Q

Granulocytopenia: Causes

A
  • Drug toxicity & radiation.
  • Bone marrow diseases.
  • Severe infections, HIV & AIDS
30
Q

Granulocytopenia: Signs and Symptoms

A
  • Severe illness.
  • Malaise.
  • Necrosis of mucous tissues
31
Q

Granulocytopenia: Treatment

A
  • Treat the cause.
  • Support immunity i.e. herbs (Echinacea, Andrographis) and nutrients (vitamin C, zinc, vitamin A, vitamin D) as well as life-style (e.g. stress management).
  • Acupuncture & homeopathy
32
Q

Leukocytosis

A

• Leukocytosis describes a marked increase in the number of all leukocytes.

33
Q

Leukocytosis: Causes

A
  • Response to infections (physiological).

* Leukaemia (uncontrolled production of leukocytes in bone marrow due to cancer).

34
Q

Leukaemia

A

• ‘Leukaemia’ describes a group of bone marrow cancers, characterised by an abnormal over production of leukocytes.
• This uncontrolled proliferation results in supressed erythrocyte production (= anaemia) and thrombocytes (= thrombocytopenia).
Divided into:
• Acute leukaemia’s: Rapid onset, more aggressive course. Immature cells (>20% -blast cells in bone marrow).
• Chronic leukaemia’s:Insidious onset and more differentiated cells.

35
Q

Acute Leukaemia

A
Age: All ages
Onset: Sudden
Leukaemiccells: Immature (-blasts)
Anaemia: Prominent
Thrombocytopenia: Prominent
Leukocyte count: Variable
Lymph node enlargement: Mild
Splenomegaly: Mild
36
Q

Chronic Leukaemia

A
Age: Usually Adults
Onset: Insidious
Leukaemiccells: Mature
Anaemia: Mild
Thrombocytopenia: Mild
Leukocyte count: Increased
Lymph node enlargement: Prominent
Splenomegaly: Prominent
37
Q

Leukaemia: Types

A
  1. Acute myelogenous leukaemia (AML)
  2. Acute lymphocytic leukaemia (ALL)
  3. Chronic myeloid leukaemia (CML)
  4. Chronic lymphocytic leukaemia (CLL)
38
Q

Leukaemia: Signs and Symptoms

A
  • Malaise, anaemia (fatigue, pallor etc.), frequent infections, easy bleeding/bruising.
  • Fever, weight loss.
  • Splenomegaly (abdominal swelling/discomfort).
  • Lymph node enlargement.
39
Q

Leukaemia: Diagnosis and Treatment

A

• Full Blood Count: anaemia, low thrombocytes, variable leukocyte count.
• Blood film (viewing sample of blood)
• Bone marrow biopsy.
ALLOPATHIC TREATMENT:
• Chemotherapy, bone marrow transplant, radiotherapy (relapse is common).

40
Q

Thrombocytopenia

A

• Reduction in the thrombocyte count

41
Q

Thrombocytopenia: Signs and Symptoms

A
  • Excessive bleedingand bruising. Prolonged bleeding times (spontaneous bleeding occurs when count is less than 30).
  • Petechiae (micro-haemorrhagesin the skin).
  • Haematuria, vomiting blood, bleeding gums.
  • Post-partum haemorrhage.
42
Q

Thrombocytopenia: Causes

A
  • Leukaemia.
  • Congenital (e.g. Fanconi’s anaemia).
  • Radiation, drugs, chemotherapy.
  • Viral infections (EBV, hepatitis, HIV, MMR).
  • Autoimmune destruction.
43
Q

Haemophilia

A

• A Deficiency of clotting factors:
 Haemophilia A: Deficiency of clotting factor VIII (8).
 Haemophilia B:Deficiency of clotting factor IX (9).

44
Q

Haemophilia: Causes

A

• Genetic: X-Linked recessive disorder (usually affects males. Females normally carriers. 1 in 5000 males).

45
Q

Haemophilia: Signs & Symptoms

A
  • Severe disease:Excessive and easy bleeding, GIT/mucosal haemorrhage, haematuria, haemarthrosis(causing inflammation and pain).
  • Moderate disease:Easy bleeding.
  • Mild disease:Bleeding after major trauma.
46
Q

Haemophilia: Treatment

A

• Replacement of clotting factors/blood transfusion. Avoid contact sports. Herbs, Homeopathy, Nutrition.