Bruising and Bleedign Flashcards

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

A

HSP

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
Q

The onset of HSP typically follows an upper

respiratory tract infection including a _____

A

group A

streptococcal tonsillopharyngitis

26
Q

HSP

The bleeding time, coagulation time and platelet
counts are ______ The prognosis is ___

A

normal.

good; most
recover fully in a few months

27
Q

Association of HSP

1
2
3
4

A
• Kidney involvement—deposition of IgA immune
complex (a serious complication)
• Melaena
• Intussusception
• Scrotal involvement
28
Q

Tx of HSP

• Short course of steroids for \_\_\_\_\_\_ (if
intussusception excluded)
• If \_\_\_\_\_\_\_: follow-up urine microscopy
and kidney function especially if no
resolution
A

abdominal pain

haematuria

29
Q

The purpura associated with severe infections, such
as ______ and other septicaemias, is
due primarily to a severe angiitis

A

meningococcaemia

30
Q

Abnormal bleeding in the elderly

The outstanding causes are ____ and ______. The cause in both instances
is atrophy of the vascular supporting tissue.

A

senile purpura and

purpura due to steroids

31
Q

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

A
Simple purpura (easy bruising
syndrome
32
Q

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.

A

Factitial purpura

33
Q

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

A

post-viral

autoimmune disorder,

34
Q

Acute thrombocytopenia of
childhood:

This is caused by a reaction to a virus infection
resulting in the production of _____

A

cross-reacting

antibodies against platelets

35
Q

Chronic ITP is a relapsing illness that rarely undergoes
spontaneous remission and may require treatment
with _______

A

prednisolone or biological agents e.g. rituximab

36
Q

This is an uncommon life-threatening syndrome
of haemolytic anaemia, thrombocytopenia and
extremely high LDH

A

TTP

37
Q

defect in TTP

A

The defect is in the absence of a specific protease in

the plasma.

38
Q

The features are:
• ecchymoses
• haemarthrosis and muscle haematomas
• usually traumatic and delayed

A

COAGULATION DISORDERS

39
Q

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

A

von Willebrand disease

40
Q

von Willebrand disease

______ inheritance (common types
Prolonged_____
Defective platelet adhesion at site of trauma
combined with _____

A

Autosomal dominant

bleeding time

factor VIII deficiency

41
Q

von Willebrand disease labs

  • _____prolonged
  • Positive ______ antigen
A

APTT

vW factor

42
Q

menorrhagia + bruising + increased

bleeding —1. incisions 2. dental 3. mucosal

A

VWD

43
Q

Tx of VWD

A

Preparations that help include desmopressin
acetate (DDAVP), factor VIII concentrates and
tranexamic acid

44
Q

• Spontaneous haemarthroses, especially knees,
ankles and elbows, are almost pathognomic
• X-linked recessive pattern of inheritance
• Invariably only males affected

A

Haemophilia A

45
Q

Haemophilia A

• Deficiency of\_\_\_\_\_\_
• \_\_\_\_\_ prolonged
• Normal\_\_\_\_\_\_\_
• Many seropositive for HIV, hepatitis B or C
(factor VIII concentrate transmission)
A

factor VIII

APTT

prothrombin time and fibrinogen

46
Q

Tx of Haemophilia A

A

• Infusion of recombinant factor VIII concentrates

47
Q

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
A

Haemophilia B (Christmas disease)

48
Q

Tx of Haemophilia B (Christmas disease)

A

Treatment is with recombinant factor IX

concentrates

49
Q
Main indications for Splenectomy
1
2
3
4
5
A
• immune thrombocytopenic purpura
• haemolytic anaemias especially hereditary
spherocytosis
• hypersplenism
• trauma
• Hodgkin/non-Hodgkin lymphoma
50
Q

Problem immediately after splenectomy

A

Immediate problem is thrombocytosis (↑ platelets
to 600–1000 × 10 9 /L) for 2–3 weeks with risk of
thromboembolism

51
Q

Long-term risk is overwhelming infection
(pneumococcus [especially] ________ and ___________, especially in young children
in the first 2 years post-splenectomy

A

Haemophilus influenzae

and meningococcus)

52
Q

Post splenectomy MX

For elective surgery give _____ at least 2 weeks before surgery

A

immunisation

53
Q

Think of __________
in any acutely ill patient with abnormal bleeding
from sites such as the mouth or nose, venepuncture
or with widespread ecchymoses

A

disseminated intravascular coagulation (DIC)

54
Q

Clinical situations of DIC

A

The clinical
situations are numerous, such as septicaemia,
obstetric emergencies, disseminated malignant
disease, falciparum malaria and snake bites

55
Q

The main differential diagnoses of ACS include

A

aortic dissection, pericarditis, oesophageal reflux
and spasm, biliary colic and hyperventilation with
anxiety.