U1 O3 - Emergency diagnostics Flashcards
What is the normal PCV for cats and dogs?
Normal dogs have a PCV of 37-55% and cats 30-45%.
What are reticulocytes?
Reticulocytes are immature, non-nucleated red blood cells that are found in the circulation in increased numbers in regenerative responses.
What is the mean cell volume (MCV) in haematology?
➢ Mean cell (corpuscular) volume (MCV) The mean cell volume provides information about the average size of red blood cells. Cells may be: • macrocytic (bigger than normal), • normocytic (normal size) • microcytic (smaller than normal).
Why would a patient have large circulating erythrocytes?
RBCs become smaller as they develop in the bone marrow- so if immature are released early into the bloodstream e.g. following haemorrhage, they will be relatively large. In regenerative anaemia, immature cells are often released into the circulation and are relatively larger than mature erythrocytes.
Why would a patient have small circulating erythrocytes?
If a patient, has iron deficiency anaemia, the circulating red blood cells are smaller than normal as they have spent longer developing in the bone marrow, due to the lack of iron.
What us the mean cell haemoglobin concentration (MCHC) in haemoatology?
➢ Mean cell (corpuscular) haemoglobin concentration (MCHC)
This is a measurement of the average haemoglobin concentration per red blood cell. Depending on the haemoglobin levels in RBCs, they will be
• normochromic (normal colour = normal haemoglobin concentration)
• hypochromic (paler than normal = reduced haemoglobin).
Immature RBCs contain less haemoglobin- thus regenerative anaemia will usually be hypochromic; whereas non-regenerative anaemia will be normochromic.
What is a white blood cell count made up of?
The white blood cell count is made up of neutrophils, lymphocytes, eosinophils and basophils.
What can a leucogram assist with identifying?
The character of the leucogram (i.e. what combination of white cells is present) can assist in identifying an underlying cause e.g. stress leucogram, inflammatory leucogram etc.
What is an increase in neutrophils usually associated with?
Explain what a left shift is and what a degenerative left shift is?
Neutrophils: an increase in the number of neutrophils is most commonly associated with infection or inflammation. Immature neutrophils are called band cells - an increase in the number of immature neutrophils in the circulation is known as ‘a left shift’. This is seen where neutrophils are involved in an active inflammatory or infectious process; or where there is abnormal neutrophil production. In a normal regenerative response, the number of mature neutrophils will outnumber the band neutrophils- indicating that the immune response is working well. However, if band neutrophils outnumber the mature neutrophils, this indicates that the mature neutrophils are being consumed/destroyed- the immune response is not working as well as we would like or is being overwhelmed. This is called a degenerative left shift.
What is lymphopaenia? and what is it associated with?
Lymphopaenia (decreased circulating lymphocyte numbers) can be seen in association with acute infection or chronic stress e.g. chronic disease or corticosteroid therapy etc. Lymphocytosis (increased numbers of circulating lymphocytes) can be seen with hypoadrenocorticism, leukaemia or prolonged antigenic stimulation. It may also be seen with an acute stress response.
What are lymphocytes T and B associated with?
Lymphocytes (T and B lymphocytes) are associated with the immune response.
What are eosinophils associated with?
Eosinophils are present in relatively small numbers. They are associated with allergic disease and parasitism. Increased numbers may also be seen with specific conditions such as pulmonary infiltration with eosinophilia (PIE) or neoplasia. Eosinopaenia may be a stress response or secondary to corticosteroid treatment.
How common are basophil abnormalities?
Basophils abnormalities in basophil numbers are rarely identified.
What do monocytes develop in to? and what are large number associated with?
Monocytes these large cells are only present in blood for a short time before leaving and developing into macrophages. Increased numbers can be associated with chronic, intracellular infections or a stress response
What is haemostasis?
Haemostasis is the process of stopping bleeding
How can haemostasis occur?
- vasoconstriction
- primary haemostasis - formation of an initial platelet plug
- secondary haemostasis/ clot formation - the platelet plug is stabilised by cross-linked fibrin- clot
- thrombolysis- clot break-down.
What can happen to platelets when a patient is thrombocytopaenic?
thrombocytopaenia can arise due to:
• Increased platelet destruction e.g. immune-mediated thrombocytopaenia (IMHA)
• Increased platelet ‘consumption’: platelets have been used up secondary to haemorrhage or inflammation.
What is primary haemostasis?
Primary Haemostasis
Platelets are required for primary haemostasis (the start of clot formation). Alterations in the platelet numbers occur for many reasons and with various diseases.
What is the monolayer segment of a smear and what is it composed of?
Oil immersion fields are examined in the monolayer segment of the smear. The monolayer segment lies between the feathered edge of the smear and the main body of the smear - it is composed of a single layer of cells.
How many platelets should be seen per field on average on a normal blood smear? What would be considered as dangerously low level of platelets?
Each one platelet, seen in an oil immersion (x100) field, is roughly equivalent to 15x109 platelets/l. Therefore, a normal blood smear should have 11-15 platelets per field on average. Dangerously low levels of platelets would be indicated by less than 3 platelets per oil immersion field (equivalent to 0-45x109/l). A patient with a platelet count of <5 per field should be closely monitored for evidence of bleeding.
What equipment would you need to carry out a true platelet count?
A true platelet count may be done, manually, using a haemocytometer, commercial diluting fluid and a microscope
How do you carry out a true platelet count?
A commercial ammonium oxalate diluent pipette system should be used (e.g. ‘Unopette Micro-collection System for WBC and Platelet Determination’ produced by Becton-Dickinson, Oxford UK). This is filled as directed and lyses the red cells after ~ 10 minutes. A Neubauer modified haemocytometer is then filled with the mixture and left in a humid environment (a small covered dish with a layer of wet filter paper in the bottom) for 5-10 minutes, to allow the platelets to settle to the floor of the haemocytometer.
A platelet count is then performed by examining the haemocytometer microscopically. Platelets can be differentiated from white cells by their smaller size and refractile nature. The total number of platelets, in the central major square on each side of the haemocytometer, is counted. This square is divided into 25 smaller squares, each of which contains 16 further squares. The average of the two major square counts is then the total platelet count in 109/l. Normal values for dogs are 200-700x109/l and for cats are 300-800 x109/l.
Clinically what is the best way to perform platelet function assessment?
Platelet function can be assessed in a laboratory using specific analysers. Clinically, however, the best way is to perform a buccal mucosal bleeding time (BMBT).
How do you carry out a Buccal mucosal bleeding time test?
Buccal mucosal bleeding time - The BMBT requires the use of a commercial device that produces two standardised cuts to the buccal mucosa of the upper lip - 5mm long and 1mm deep. The patient is placed in lateral recumbency, the upper lip is reflected to expose the mucosal surface and held in place by a gauze tape lightly applied around the maxilla, enough to partially block venous return (Oakley, 2007). The BMBT device is then placed on the mucosa and activated. The incisions are then left alone until bleeding stops- the time taken should be recorded. This is assessed by using a swab or filter paper placed near to the incisions (3-4 mm below), but not touching them. Bleeding is judged to have stopped when blood stops being taken up by the clean edge of the swab/filter paper. The BMBT is taken as the mean bleeding time of the two incisions and should normally be less than 4 minutes. The BMBT evaluates primary haemostasis by assessing platelet and vascular aspects of haemostasis.