Bruising and Bleedign Flashcards

(55 cards)

1
Q

_______ = petechiae + ecchymoses

A

Purpura

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2
Q
Abnormal bleeding is basically the result of
disorders of 
1
2
3
A
(1) the platelet, (2) the coagulation
mechanism or (3) the blood vessel
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3
Q

The commonest cause of an acquired bleeding

disorder is______

A
drug therapy (e.g. aspirin, NSAIDs,
cytotoxics and oral anticoagulants
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4
Q
The three major mechanisms of systemic bleeding
disorders are (the Virchow triad):
A

1 coagulation deficiencies (reduction or inhibition
of circulatory coagulation factors)
2 platelet abnormalities: of platelet number or
function
3 vascular defects: of vascular endothelium

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5
Q

___________ disorders which are the
most common include von Willebrand disease
(vWD), thrombocytopenia and platelet function
disorders.

A

Primary haemostatic

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6
Q

Examples of disorders of secondary

haemostasis are disorders of _____

A

fibrin formation and

the haemophilias

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7
Q

_______ present as early bleeding

following trauma

A

Platelet abnormalities

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8
Q

______ present with
delayed bleeding after initial haemostasis is
achieved by normal platelets

A

Coagulation factor deficiencies

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9
Q

A normal response to previous coagulation
stresses (e.g. dental extraction, circumcision or
pregnancy) indicates an ________

A

acquired problem

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10
Q

Drugs and their responses

__________:
— prednisolone/other steroids

A

vascular purpura

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11
Q

Drugs and their responses

______________

— cytotoxic drugs
— carbamazepine
— gold
— sodium valproate
— heparin
— ranitidine
— sulphonamides
A

thrombocytopenia

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12
Q

Drugs and their responses

functional platelet abnormalities:
1
2

A

— aspirin

— NSAIDs

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13
Q

The initial choice of investigations depends upon the
bleeding pattern.

If coagulation defect suspected
1
2
3
4
A
  • prothrombin time (PT), i.e. INR
  • activated partial thromboplastin time (APTT)
  • fibrinogen level
  • thrombin time (TT)
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14
Q

The initial choice of investigations depends upon the
bleeding pattern.

If platelet pathology suspected:
1
2
3

A
  • platelet count
  • skin bleeding time (of doubtful value)
  • platelet function analyser (PFA-100)
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15
Q

The initial choice of investigations depends upon the
bleeding pattern.

If inherited disorders suspected:

1
2
3

A
  • factor VIII
  • vW factor activity
  • vW factor antigen
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16
Q

The _______ as a screening test
of haemostasis has been shown recently to be severely
limited by its lack of specificity and sensitivity

A

skin-bleeding time

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17
Q

Laboratory investigation checklist for the easy

bruiser

A
Full blood count
Platelet count
Prothrombin time (INR)
Thrombin time (TT)
Activated partial thromboplastin time
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18
Q

A common condition is ______________ which is a self-limiting disease usually
presenting on the second or third day of life because of a
deficiency of coagulation factors dependent on vitamin
K.

A

haemorrhagic disease of

the newborn,

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19
Q

What Tx has eliminated HDN

A

Vit K at birth

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20
Q

________is the commonest of the primary platelet
disorders in children. Both acute and chronic forms
have an immunological basis

A

Idiopathic (immune) thrombocytopenic purpura

ITP

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21
Q

Prognosis of ITP

A

Spontaneous remission within 4 to 6

weeks occurs with acute ITP in childhood

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22
Q

The commonest vascular defects in childhood are:
1
2
3

A

• anaphylactoid (Henoch–Schönlein) purpura
• infective states
• nutritional deficiency (usually inadequate dietary
vitamin C)

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23
Q

_______is the commonest vasculitis of children. It affects
small vessels, producing a leucocytoclastic vasculitis
with a classic triad of non-thrombocytopenic purpura,
large joint arthritis and abdominal pain

24
Q

Distribution of HSP

A

over the lower limbs,
extending onto the buttocks, but it can
also involve the upper limbs, trunk and even the face

25
The onset of HSP typically follows an upper | respiratory tract infection including a _____
group A | streptococcal tonsillopharyngitis
26
HSP The bleeding time, coagulation time and platelet counts are ______ The prognosis is ___
normal. good; most recover fully in a few months
27
Association of HSP 1 2 3 4
``` • Kidney involvement—deposition of IgA immune complex (a serious complication) • Melaena • Intussusception • Scrotal involvement ```
28
Tx of HSP ``` • Short course of steroids for ______ (if intussusception excluded) • If _______: follow-up urine microscopy and kidney function especially if no resolution ```
abdominal pain haematuria
29
The purpura associated with severe infections, such as ______ and other septicaemias, is due primarily to a severe angiitis
meningococcaemia
30
Abnormal bleeding in the elderly The outstanding causes are ____ and ______. The cause in both instances is atrophy of the vascular supporting tissue.
senile purpura and | purpura due to steroids
31
This is a benign disorder occurring in otherwise healthy women usually in their 20s or 30s. The feature is bruising on the arms, leg and trunk with minor trauma
``` Simple purpura (easy bruising syndrome ```
32
Unexplained bruising or bleeding may represent selfinflicted abuse or abuse by others. In self-inflicted abuse the bruising is commonly on the legs or areas within easy reach of the patient.
Factitial purpura
33
ITP The two distinct types caused by immune destruction of the platelets are: • acute thrombocytopenia of childhood—usually in children, usually_____ • chronic ITP—_______ usually in adult women; all cases should be referred to a specialist unit
post-viral autoimmune disorder,
34
Acute thrombocytopenia of childhood: This is caused by a reaction to a virus infection resulting in the production of _____
cross-reacting | antibodies against platelets
35
Chronic ITP is a relapsing illness that rarely undergoes spontaneous remission and may require treatment with _______
prednisolone or biological agents e.g. rituximab
36
This is an uncommon life-threatening syndrome of haemolytic anaemia, thrombocytopenia and extremely high LDH
TTP
37
defect in TTP
The defect is in the absence of a specific protease in | the plasma.
38
The features are: • ecchymoses • haemarthrosis and muscle haematomas • usually traumatic and delayed
COAGULATION DISORDERS
39
This is the most common disorder of haemostasis (incidence 1% of population) and is usually a mild problem with an excellent prognosis. There are about 22 types
von Willebrand disease
40
von Willebrand disease ______ inheritance (common types Prolonged_____ Defective platelet adhesion at site of trauma combined with _____
Autosomal dominant bleeding time factor VIII deficiency
41
von Willebrand disease labs * _____prolonged * Positive ______ antigen
APTT vW factor
42
menorrhagia + bruising + increased | bleeding —1. incisions 2. dental 3. mucosal
VWD
43
Tx of VWD
Preparations that help include desmopressin acetate (DDAVP), factor VIII concentrates and tranexamic acid
44
• Spontaneous haemarthroses, especially knees, ankles and elbows, are almost pathognomic • X-linked recessive pattern of inheritance • Invariably only males affected
Haemophilia A
45
Haemophilia A ``` • Deficiency of______ • _____ prolonged • Normal_______ • Many seropositive for HIV, hepatitis B or C (factor VIII concentrate transmission) ```
factor VIII APTT prothrombin time and fibrinogen
46
Tx of Haemophilia A
• Infusion of recombinant factor VIII concentrates
47
What bleeding DO * Identical clinical features to haemophilia A * Also an X-linked recessive hereditary disorder * Incidence of 1 in 30 000 * Deficiency of coagulation factor IX
Haemophilia B (Christmas disease)
48
Tx of Haemophilia B (Christmas disease)
Treatment is with recombinant factor IX | concentrates
49
``` Main indications for Splenectomy 1 2 3 4 5 ```
``` • immune thrombocytopenic purpura • haemolytic anaemias especially hereditary spherocytosis • hypersplenism • trauma • Hodgkin/non-Hodgkin lymphoma ```
50
Problem immediately after splenectomy
Immediate problem is thrombocytosis (↑ platelets to 600–1000 × 10 9 /L) for 2–3 weeks with risk of thromboembolism
51
Long-term risk is overwhelming infection (pneumococcus [especially] ________ and ___________, especially in young children in the first 2 years post-splenectomy
Haemophilus influenzae | and meningococcus)
52
Post splenectomy MX For elective surgery give _____ at least 2 weeks before surgery
immunisation
53
Think of __________ in any acutely ill patient with abnormal bleeding from sites such as the mouth or nose, venepuncture or with widespread ecchymoses
disseminated intravascular coagulation (DIC)
54
Clinical situations of DIC
The clinical situations are numerous, such as septicaemia, obstetric emergencies, disseminated malignant disease, falciparum malaria and snake bites
55
The main differential diagnoses of ACS include
aortic dissection, pericarditis, oesophageal reflux and spasm, biliary colic and hyperventilation with anxiety.