Question 1
Question
What does the term "haemorrhage by rhexis" mean?
Answer
-
A substantial tear in a blood vessel or a tear in a heart chamber --> rapid escape of a substantial
volume of blood
-
The escape of red blood cells one by one through minute or microscopically imperceptible defects
in vessel walls
-
Escape of blood from the cardiovascular system
-
Haemorrhage into a synovial joint
Question 2
Question
What does the term "haemorrhage by diapedesis" mean?
Answer
-
A substantial tear in a blood vessel or a tear in a heart chamber --> rapid escape of a substantial
volume of blood
-
The escape of red blood cells one by one through minute or microscopically imperceptible defects
in vessel walls
-
haemorrhage into the pleural cavity
-
The escape of blood from the cardiovascular system
Question 3
Question
[blank_start]haemothorax[blank_end] = haemorrhage into the pleural cavity
[blank_start]haemopericardium[blank_end] = haemorrhage into the pericardial sac
[blank_start]haemoperitoneum[blank_end] (haemabdomen or haemoabdomen) = haemorrhage into the peritoneal cavity
[blank_start]haemarthrosis[blank_end] = haemorrhage into a synovial joint
[blank_start]haematuria[blank_end] = haemorrhage into urine
[blank_start]haemoptysis[blank_end] = coughing of blood
[blank_start]haematemesis[blank_end] = vomiting of blood
[blank_start]haematochezia[blank_end] = passage of fresh blood in faeces (typically over the surface of stools)
[blank_start]dysentery[blank_end] = diarrhoea containing blood
[blank_start]melaena[blank_end] = diffuse, dark red-black discolouration of faeces due to upper alimentary tract haemorrhage or swallowing of blood from the respiratory tract
[blank_start]epistaxis[blank_end] = bleeding from the nose
[blank_start]hyphaema[blank_end] = haemorrhage into the anterior chamber of the eye
Answer
-
haemothorax
-
haemopericardium
-
haemoperitoneum
-
haemarthrosis
-
haematuria
-
haemoptysis
-
haematemesis
-
haematochezia
-
dysentery
-
melaena
-
epistaxis
-
hyphaema
Question 4
Question
[blank_start]petechiae[blank_end] = tiny, pinpoint foci of haemorrhage, 1-2 mm in diameter, typically found in skin and on mucosal and serosal membranes
[blank_start]purpura[blank_end] = slightly larger haemorrhages ≥ 3 mm in diameter
[blank_start]ecchymoses[blank_end] = larger foci of haemorrhage, 2-3 cm in diameter; usually blotchy and of irregular shape
[blank_start]paintbrush (or suffuse or suffusive)[blank_end] haemorrhages = linear or streaky haemorrhages, especially over serosal or mucosal membranes, as if a brush dipped in red paint has been hastily splashed across the tissues
[blank_start]haematoma[blank_end] = a palpable, discrete, space-occupying mass of clotted blood within tissues, small "" are common at sites of difficult venipuncture
Question 5
Question
The gross colour of haemorrhage depends on whether the blood was arterial or venous, the volume of extravasated blood and the time elapsed since haemorrhage occurred. What colour does the bruise appear during the acute, sub-acute and chronic stages and what is the molecule causing this colouration?
In the acute phase, bruises appear [blank_start]red-blue[blank_end] due to the presence of poorly oxygenated [blank_start]haemoglobin[blank_end]
In the subacute phase, bruises appear [blank_start]blue-green[blank_end] due to the formation within macrophages of [blank_start]biliverdin and bilirubin[blank_end] (derived from the porphyrin component of haemoglobin)
In the chronic phase, bruises appear [blank_start]gold-brown[blank_end] due to the formation of [blank_start]haemosiderin[blank_end] and, to a lesser extent, haematoidin +/- lipofuscin pigments
Answer
-
red-blue
-
haemoglobin
-
blue-green
-
biliverdin and bilirubin
-
gold-brown
-
grey-black
-
haemosiderin
Question 6
Question
What happens to a haematoma from 5-7 days after onset?
Answer
-
They become enveloped by granulation tissue - following phagocytosis of the extravasated blood
-
The cavity of a haematoma is ultimately filled in by scar tissue (fibrosis)
-
Haemosiderin colouration of the haematoma
Question 7
Question
[blank_start]haemosiderin[blank_end] (composed of ferritin micelles (iron + apoferritin) derived from the iron component of haemoglobin) first appears microscopically within macrophages by 24-48 hours after the onset of haemorrhage. Sufficient "" accumulation to cause gross yellow discolouration is not expected until 2-3 days after haemorrhage.
[blank_start]Haematoidin[blank_end] is a bright golden extracellular pigment composed of precipitates of bilirubin complexed with tissue proteins
[blank_start]Lipofuscin[blank_end] is an intracellular yellow-brown pigment derived from peroxidation of phospholipids of membranes of damaged cells in the area
Answer
-
haemosiderin
-
Haematoidin
-
Lipofuscin
Question 8
Question
What factor(s) determine the clinical significance of haemorrhage?
(select the answer or answers that are correct)
Answer
-
Location of haemorrhage
-
Rate of blood loss
-
Volume of blood loss
Question 9
Question
[blank_start]internal haemorrhage[blank_end] (haemorrhage into tissues or body cavities) --> reutilisation of plasma
proteins and iron
[blank_start]external haemorrhage[blank_end] (e.g. from the skin or gastrointestinal, respiratory, urinary or reproductive tracts) --> if recurrent or prolonged= hypoproteinaemia and iron deficiency anaemia
Answer
-
internal haemorrhage
-
external haemorrhage
Question 10
Question
What is the most common cause of haemorrhage in domestic animals?
Question 11
Question
What is the clinical sign this horse is exhibiting?
Answer
-
epistaxis
-
haemoptysis
-
haematemesis
-
hyphaema
Question 12
Question
What is the correct terminology for each of these poo/faeces samples?
Answer
-
melaena
-
haematochezia
-
dysentery
-
haematuria
-
haematemesis
Question 13
Question
What is the correct terminology for each of these forms of haemorrhage?
Answer
-
haemothorax
-
haemoperitoneum
-
haemoptysis
-
haemarthrosis
-
haemopericardium
-
hyphaema
-
epistaxis
Question 14
Question
How would you correctly describe each of these haemorrhagic lesions?
Answer
-
petechiae
-
ecchymoses
-
purpura
-
paintbrush
-
haematoma
-
hyphaema
Question 15
Question
Below are two lists of possible "features" or "symptoms relating to primary or secondary haemostasis, which list belongs to primary haemostasis and which to secondary haemostasis?
[blank_start]Secondary haemostasis[blank_end]
•delayed bleeding after venipuncture
•large volume bleeds
•petechiae rare
•haematomas common
•bleeding into muscles, joints and/or body cavities
•bleeding may be localised
•+/- mucosal bleeding
[blank_start]Primary Haemostasis[blank_end]
•bleeding immediately after venipuncture
•small volume bleeds
•petechiae common
•haematomas uncommon
•bleeding from mucous membranes
•bleeding from multiple sites
Answer
-
Secondary haemostasis
-
Primary Haemostasis
Question 16
Question
Disseminated intravascular coagulation (DIC) is a combined disorder of both Primary and Secondary Haemostasis.
Question 17
Question
Match the below words with the correct definition
[blank_start]Thrombocytopenia[blank_end]- deficiency of platelets in the blood. Can result in bleeding into the tissues, bruising, and slow blood clotting after injury.
[blank_start]Haemorrhagic diatheses[blank_end]- clinical disorders of haemostasis characterised by a bleeding tendency
[blank_start]Myelophthisis[blank_end] - replacement of haemopoietic bone marrow by neoplastic tissue (e.g. leukaemia), collagen (myelofibrosis), bone (osteosclerosis) or inflammatory exudate (e.g. chronic granulomatous osteomyelitis in systemic fungal infections)
[blank_start]Thrombocytopathy[blank_end]- platelet dysfunction
Answer
-
Thrombocytopenia
-
Haemorrhagic diatheses
-
Myelophthisis
-
Thrombocytopathy
-
Thrombocytosis
Question 18
Question
Which of the below are disorders of Primary Haemostasis?
Answer
-
platelet deficiency (thrombocytopenia)
-
platelet dysfunction (thrombocytopathy, thrombopathy or thrombopathia)
-
von Willebrand’s disease (deficiency of von Willebrand factor)
-
damage to small blood vessels
-
inherited deficiency of one or more coagulation factors
-
decreased coagulation factor synthesis due to severe acute or chronic hepatic parenchymal disease
-
excessive fibrinolysis or fibrinogenolysis
Question 19
Question
Which of the below are disorders of Secondary Haemostasis?
Answer
-
excessive fibrinolysis or fibrinogenolysis
-
decreased coagulation factor synthesis due to severe acute or chronic hepatic parenchymal disease
-
decreased coagulation factor activity due to vitamin K antagonism or deficiency
-
inherited deficiency of one or more coagulation factors
-
damage to small blood vessels
-
platelet deficiency (thrombocytopenia)
Question 20
Question
Disorders of secondary haemostasis provoke multiple short-lived bleeds that cease once the coagulation cascade generates fibrin
Question 21
Question
What is the most common acquired haemostatic disorder in dogs and cats?
Question 22
Question
What is the MOST COMMON mechanism responsible for clinically significant thrombocytopenia in cats?
Question 23
Question
What is/are the most common mechanisms of decreased platelet production in cats that lead to thrombocytopenia?
Answer
-
Retroviral infection (especially feline leukaemia virus (FeLV))
-
Myeloproliferative or lymphoproliferative disease
-
Megakaryocytic hypoplasia
-
Hypothermia
Question 24
Question
Of the below which can cause marrow aplasia or panhypoplasia?
Answer
-
Ionising radiation
-
Viral infection eg. canine and feline parvovirus, FeLV, feline immunodeficiency virus (FIV), equine infectious anaemia (EIA) virus
-
Toxins eg. aflatoxins, stachybotryotoxin, bracken fern, benzene
-
Drug cytotoxicity - chemotherapeutic agents, chloramphenicol, sulphadiazine, oestrogen (dogs and ferrets), griseofulvin (cats), methimazole (cats)
-
Other infectious agents - late stages of infection with Ehrlichia canis and other rickettsial species
-
Immune mediated destruction of platelets
-
Massive external haemorrhage
Question 25
Question
Which is the correct order of cell lifespan (from longest to shortest)?
Answer
-
erythrocytes > platelets > neutrophils
-
erythrocytes > neutrophils > platelets
-
neutrophils > erythrocytes > platelets
-
neutrophils > platelets > erythrocytes
-
platelets > erythrocytes > neutrophils
-
platelets > neutrophils > erythrocytes
Question 26
Question
What is the most common mechanism of thrombocytopenia in dogs?
Question 27
Question
What is the most common cause of platelet destruction in dogs?
Answer
-
Immune-mediated destruction
-
Infectious viral agents
-
Infectious bacterial agents
-
Infectious parasitic agents
Question 28
Question
Platelet consumption due to formation of numerous microthrombi is typical of disseminated intravascular coagulation (DIC)
Question 29
Question
In health what percentage of platelets are located in the spleen?
Answer
-
30-40%
-
10-20%
-
70-80%
-
5-10%
Question 30
Question
In most circumstances, does sequestration of platelets cause a mild, moderate or severe thrombocytopenia?
Question 31
Question
Why does massive acute haemorrhage usually only cause a mild subclinical thrombocytopenia?
Answer
-
because of the large splenic platelet reservoir
-
because platelets are rapidly made in the bone marrow (faster than any form of bleed)
-
because of the large liver platelet reservoir
Question 32
Question
Define Thrombopathia
Answer
-
rare autosomal-recessive genetic form of haemophilia
-
rare autosomal-dominant genetic form of haemophilia
-
common autosomal-recessive genetic form of haemophilia
-
common autosomal-dominant genetic form of haemophilia
Question 33
Question
Which is the most common inherited bleeding disorder of dogs?
Question 34
Question
What is the role of the large glycoprotein von Willebrand factor?
Answer
-
Mediates the adhesion of platelets to exposed subendothelial collagen via their surface GpIb receptors. Prevents platelets being dislodged by blood flow.
-
Activates the zymogen prothrombin by converting it into the serine protease thrombin
-
Forms a mesh, enforcing the platelet plug making it stronger
-
is an intracellular yellow-brown pigment derived from peroxidation of phospholipids of membranes of damaged cells in the area
-
Prevents the adhesion of platelets to exposed subendothelial collagen via their surface GpIb receptors and so prevents platelets being lodged in vessels during blood stasis.
Question 35
Question
Where can von Willebrand's factor expressed and/or stored?
Question 36
Question
Determine which is type 1, type 2 and type 3 von Willebrand's disease forms from the below lists of information
[blank_start]Type 1 vWD[blank_end]
- the most common form of vWD in dogs (> 90% of cases)
- all of the various multimer chains of vWf are present but in reduced plasma concentrations (< 50% of normal)
- e.g. doberman pinscher (in the not so distant past, approximately 60% of dobermans in Australia were thought to be carriers of the trait), Welsh corgis, German shepherd dogs, golden retrievers, and poodles
- may be subclinical or cause mild to moderate bleeding
- bleeding does not usually occur until the plasma vWf concentration falls below 20% of normal
[blank_start]Type 3 vWD[blank_end]
- there is virtually negligible vWf in plasma, with all multimers absent
- Scottish terriers (the main breed affected in Australia), Shetland sheepdogs, Chesapeake Bay retrievers and Dutch kooikers
- trauma in homozygotes --> severe haemorrhage
[blank_start]Type 2 vWD[blank_end]
- decreased plasma vWf concentration is associated with a disproportionate loss of the large high m.w. multimers
- can be responsible for severe haemorrhage
- rare but reported in German short-haired and wire-haired pointers
- also reported in horses
Answer
-
Type 1 vWD
-
Type 3 vWD
-
Type 2 vWD
Question 37
Question
Dogs with vWD will often bleed spontaneously