Haematological Conditions & Infectious Diseases Flashcards
What is the composition of blood
55% Plasma
45% Red blood cells (erythrocytes)
0.1% White blood cells (leukocytes)
0.17% Platelets (thrombocytes)
What is plasma made up of
91% water
7% proteins
2% other solutes
What is the formed elements of blood made up of
Platelets
White blood cells
Red blood cells
Explain: Plasma
liquid part of blood
- pale yellow
- is a colloid solution
Contains:
- albumin
- globulins
- fibrinogen
Describe: Ethryrocytes
- no nucleaus
- made up of hemoglobin, lipids, ATP and carbonic anhydrase
- They transport oxygen from lungs to tissues and carbon dioxide from tissues to lungs
Describe: Hemaglobin
Consists of:
- 4 globin molecules: Transport carbon dioxide (carbonic anhydrase involved), nitric oxide
- 4 heme molecules: Transport oxygen
- Iron is required for oxygen transport
Define: Erythropoiesis
is the process by which new erythrocytes are made.
- It is stimulated by a decrease in oxygen in the blood
- detected by the kidneys
- kidney’s then secrete hormone erythropoiesis.
List types of Leukocytes
Neutrophils: Eosinophils: Basophils: Lymphocytes: Monocytes:
Define: Hemostasis
is the process by which bleeding is stopped, which prevents excessive blood loss
What are the 3 steps on Hemostasis
Vascular spasm: smooth muscle of blood vessel contracts and pinches off blood supply to area injured
Platelet plug formation: Platelets detect and adhere to injured site, band together and release contents, ADP makes platelets sticky so other platelets stick to existing ones creating a platelet plug
Coagulation or blood clotting: aim is to contain blood into a gel.
What determines the a blood groups Rh
If a D antigen is present: Rh Positive (85% population)
Id D antigen is not present: Rh Negative (15% population)
Explain: Beta-Thalamassaemia
a group of hereditary disorders characterised by a genetic deficiency in the synthesis of beta-globin chain
Symptoms: Pallor Lethargy Poor appetite Developmental delay Failure to thrive Irritability, difficulty settling Splenomegaly, growth failure with bone changes, fractures and leg ulcers also develop during childhood Haemolytic anaemia Carriers for β-thalassaemia are usually asymptomatic but may have mild hypochromic anaemia
Explain: Alpha-Thalassaemia
is caused my a mutation in the alpha gene of the hemaglobin molecule
If a woman tests positive for thalassaemia or has a known family history, what needs to happen
She needs genetic counselling
Partner needs to be tested
Explain: Sickle Cell Disease
is an autosomal receptive condition caused by a mutation in both copies of the β-(beta) globin genes
- carriers have 50% chance of passing the mutated gene onto their infant
- Most common inherited conditions of hemoglobin worldwide
Symptoms: • Anaemia • Failure to thrive • Repeated infections • Painful swelling of the hands or feet • Infarction • Asplenia • Abdominal pain • Chest pain
Explain: Sickle cell trait
(term to describe the carrier state) is caused by a mutation in one copy of the β-globin
- carriers are usually healthy
Explain: Sickle cell pregnancy, labour/birth and postantal management
The risk in pregnancy depends on whether the woman has sickle cell disease or the sickle cell trait
Pregnancy
- Sickle cell trait women- not at risk of significant pregnancy problems.
- Specialist management
- Iron deficient anaemia, need suppliment
- May experience frequent UTI.
- Hyperemesis may cause dehydration
- U/S (IUGR)
Labour/Birth
- IV fluids
- pain relief
- At risk: premature birth, placental abruption
- Mobilisation (immobility can cause sickle cell crises)
- PPH risk
Postnatal
- Monitor for PPH, dehydration, sickle cell crises
- Baby: screening for SC
What are 3 causes of Anaemia
- Inadequate production of erythrocytes: dietary, low bone marrow production, autoimmune reaction or disease
Rapid destruction of erythroctes: liver disease, lupus, sickle cell disease, malaria
Blood loss: gastrointestinal bleeding, haemophilia, haemorrhoids
Define: Coagulopathy
is any condition where there is impaired clotting ability
- inc. reduced ability or inability to clot and an extra ability to clot
What are the 2 main types of coagulopathy
Inherited: Autosomal dominant deficiencies
Aquired: occur in chronic disease state, after severe infection/viral infection, or with VitK deficiency
What is the diagnostic criteria for Thrombocytopaenia
Normal range: 150 000 to 450 000/ per microLitre
Diagnostic: <50 000 Signs and symptoms: Petichiea Bleeding gums Nosebleeds Malaise
Define: Thrombocytopaenia
is an abnormally low amount of thrombocytes (platelets)
What are some cause of Thrombocytopaenia
Decreased platelet production: Leukaemia, anaemia, viral infections, HIV
Increased destruction: Autoimmune diseases, Blood borne bacterial infection
Medication induced: Quinine, alcohol abuse, interferon, chemotherapy, sulphur antibiotics