Success Flashcards

1
Q

What does SCAPE stand for?

And other names?

A

Sympathetic Crashing Acute Pulmonary Edema

Flash pulmonary edema, hypertensive cardiogenic pulmonary edema, hypertensive acute heart failure, acute pulmonary edema.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What does FOSPE stand for?

A

Fluid Overload Subacute Pulmonary Edema

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is another name for FOSPE?

A

Congestive heart failure exacerbation, Decompensated heart failure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What is the acuity of SCAPE?

A

Occurs rapidly (within minutes to hours)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What is the acuity of FOSPE?

A

Gradual onset over days

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What is the key physiological problem in SCAPE?

A

Volume status

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is the key physiological problem in FOSPE?

A

Fluid overload

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What type of congestion is associated with SCAPE?

A

Systemic congestion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What type of congestion is associated with FOSPE?

A

Hypertensive cardiogenic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What are common treatments for SCAPE?

A

CPAP or BIPAP, Nitroglycerine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What are common signs of FOSPE?

A

Ascites and/or peripheral edema are more commonly seen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is the blood pressure status in SCAPE?

A

May be hypotensive, normotensive, or hypertensive

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is the characteristic ECG change associated with digitalis effect?

A

Downsloping ST depression with characteristic ‘sagging’ appearance

# flattened , inverted or biphasic T WAVE
# Shortened QT interval

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is a common effect of acute digoxin overdose?

A

Marked bradycardia with PR and QRS prolongation

Acute overdose effects can significantly alter heart rate and conduction.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What arrhythmias may occur due to digoxin toxicity?

A

Sinus arrest, varying degrees of AV block, paroxysmal atrial tachycardia with AV block, junctional tachycardia, frequent ventricular ectopics, bigeminy

These arrhythmias can complicate the clinical picture of digoxin toxicity.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What severe complications can arise from digoxin toxicity?

A

Ventricular tachycardia and ventricular fibrillation

These are critical conditions that may necessitate immediate medical intervention.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Clinical features of digitalis toxicity

A

Clinical features :

General features (may develop within 1 -2 hours of acute overdose) : Nausea, vomiting, diarrhoea and general malaise

CNS features : Anorexia, headache, weakness and rarely blurred vision or alteration in colour perception (classically xanthopsia)

Cardiac effects (may take 6 hours or more to develop) :Marked bradycardia, hypotension, arrhythmias

Metabolic effects : Hyperkalaemia (common in severe poisoning), metabolic acidosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

four recognised temporal patterns of anaphylaxis

A

*Uniphasic anaphylaxis — Uniphasic anaphylactic reactions are the most common type, accounting for an estimated 80 to 94 percent of all episodes. A uniphasic response typically peaks within hours after symptom onset and then either resolves spontaneously or after treatment, usually within several hours.

*Protracted anaphylaxis — A protracted or persistent anaphylactic reaction lasts hours to days without clearly resolving completely. The exact frequency of protracted episodes of anaphylaxis is unknown, although they appear to be uncommon. The literature consists only of case reports and small series.

*Refractory anaphylaxis — Refractory anaphylaxis can be defined as continued symptoms of anaphylaxis despite appropriate epinephrine dosing and symptom-directed treatment (e.g. intravenous fluids for hypotension).

*Biphasic anaphylaxis — Biphasic reactions are characterised by an initial reaction that meets criteria for anaphylaxis, followed by an asymptomatic period of one hour or more, and then a subsequent return of symptoms meeting the criteria for anaphylaxis without further exposure to antigen. Biphasic reactions have been reported with an array of allergens, including ingested, injected, and intravenously administered substances, as well as in idiopathic anaphylaxis. The time period between the resolution of the first reaction and the start of the second can range from 1 hour to up to 48 hours. The severity of recurrent symptoms in biphasic reactions is unpredictable. In most patients, recurrent symptoms are less severe than the initial symptoms. However, in a minority of patients, recurrent symptoms are more severe or even fatal.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

What is the location of the Dorsal columns?

A

Posteromedial aspect of cord

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

What is the function of the Dorsal columns?

A

Transmits ipsilateral proprioception, vibration and fine-touch sensation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

What is the location of the Spinothalamic tract?

A

Anterolateral aspect of cord

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

What is the function of the Spinothalamic tract?

A

Transmits contralateral pain, crude-touch and temperature sensation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

What is the location of the Lateral corticospinal tract?

A

Posterolateral aspect of cord

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

What is the function of the Lateral corticospinal tract?

A

Controls ipsilateral motor power

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

What are the types of spinal cord syndromes?

A

Central cord syndrome, anterior cord syndrome, Brown-Séquard syndrome, complete cord transection, posterior cord syndrome.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

What is the mechanism of complete cord transection?

A

Major trauma.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
27
Q

What tracts are affected in complete cord transection?

A

All tracts.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
28
Q

What is Brown-Séquard syndrome?

A

Hemitransection due to penetrating trauma or unilateral compression of the cord.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
29
Q

What tracts are affected in Brown-Séquard syndrome?

A

All tracts on one side.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
30
Q

What are the clinical features of Brown-Séquard syndrome?

A

Ipsilateral hemiparesis, ipsilateral loss of proprioception/vibration/touch sensation, contralateral loss of touch/pain/temperature sensation.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
31
Q

What is central cord syndrome?

A

Involves the corticospinal tract and spinothalamic tract.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
32
Q

What are the clinical features of central cord syndrome?

A

Quadriplegia (above C), paraplegia (below C), varying degrees of motor and sensory loss, greater loss in upper than lower limbs.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
33
Q

What is anterior cord syndrome?

A

Caused by occlusion of anterior spinal artery with infarction of anterior cord.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
34
Q

What tracts are affected in anterior cord syndrome?

A

Corticospinal, spinothalamic, and spinocerebellar tracts.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
35
Q

What are the clinical features of anterior cord syndrome?

A

Bilateral motor loss, loss of pain and temperature sensation, preserved proprioception and vibration sense.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
36
Q

What is posterior cord syndrome?

A

Caused by penetrating trauma to the back or hyperextension injury associated with vertebral arch fractures.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
37
Q

What tracts are affected in posterior cord syndrome?

A

Dorsal column.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
38
Q

What are the clinical features of posterior cord syndrome?

A

Bilateral loss of proprioception/vibration/touch sensation.

39
Q

What is neurogenic shock?

A

Neurogenic shock results in the loss of vasomotor tone and sympathetic innervation to the heart.

40
Q

What causes neurogenic shock?

A

Injury to the cervical or upper thoracic spinal cord (T1 and above) can cause impairment of the descending sympathetic pathways.

41
Q

What are the physiological effects of neurogenic shock?

A

The resultant loss of vasomotor tone causes vasodilation of visceral and peripheral blood vessels, pooling of blood, and hypotension.

42
Q

How does neurogenic shock affect heart rate?

A

Loss of sympathetic innervation to the heart can cause bradycardia or the inability to mount a tachycardic response to hypovolaemia.

43
Q

Is fluid resuscitation effective in neurogenic shock?

A

The physiologic effects of neurogenic shock are not reversed with fluid resuscitation alone.

44
Q

What can massive fluid resuscitation lead to in neurogenic shock?

A

Massive resuscitation can result in fluid overload and/or pulmonary oedema.

45
Q

What treatments may be required after moderate volume replacement in neurogenic shock?

A

Judicious use of vasopressors may be required after moderate volume replacement.

46
Q

What medication can be used to counteract significant bradycardia in neurogenic shock?

A

Atropine may be used to counteract haemodynamically significant bradycardia.

47
Q

Why is dobutamine not used in neurogenic shock?

A

Dobutamine is not used in neurogenic shock because of its peripheral vasodilatory properties and potential reflex bradycardia.

48
Q

What are the causative agents of Neuroleptic Malignant Syndrome?

A

Dopamine antagonists

Commonly associated with antipsychotic medications.

49
Q

What is the onset time for Neuroleptic Malignant Syndrome?

A

Gradual (days)

Symptoms can develop over several days.

50
Q

List some similar features of Neuroleptic Malignant Syndrome and Serotonin Syndrome.

A
  • Hypertension
  • Tachycardia
  • Hyperthermia (> 40°C)
  • Hypersalivation
  • Diaphoresis

Both syndromes share several autonomic symptoms.

51
Q

What are some distinct features of Neuroleptic Malignant Syndrome?

A
  • Encephalopathy, stupor, coma
  • Hyporeflexia
  • ‘Lead-pipe’ rigidity
  • Normal pupils
  • Reduced, sluggish bowel sounds

These features help differentiate it from Serotonin Syndrome.

52
Q

What are the lab findings associated with Neuroleptic Malignant Syndrome?

A
  • Increased creatine kinase
  • Leucocytosis
  • Low serum iron
  • Acidosis

Lab findings can indicate muscle breakdown and other metabolic changes.

53
Q

What is the management for Neuroleptic Malignant Syndrome?

A
  • Dantrolene
  • Amantadine
  • Bromocriptine

These medications help to counteract the effects of dopamine antagonism.

54
Q

What are the causative agents of Serotonin Syndrome?

A

Serotonergic agents

Commonly associated with antidepressants and certain recreational drugs.

55
Q

What is the onset time for Serotonin Syndrome?

A

Rapid (hours)

Symptoms can appear within hours of exposure to serotonergic agents.

56
Q

List some distinct features of Serotonin Syndrome.

A
  • Agitation
  • Hypervigilance
  • Delirium
  • Hyperreflexia
  • Rigidity with clonus
  • Dilated pupils
  • Hyperactive bowel sounds

These features are indicative of increased serotonergic activity.

57
Q

What are the lab findings associated with Serotonin Syndrome?

A

More commonly no lab findings

Unlike Neuroleptic Malignant Syndrome, lab tests are often unremarkable.

58
Q

What is the management for Serotonin Syndrome?

A
  • Benzodiazepines
  • Cyproheptadine

These treatments help alleviate symptoms and counteract serotonin effects.

59
Q

What does DOACS stand for?

A

DOACS stands for apixaban, dabigatran, edoxaban, and rivaroxaban

60
Q

What is the mode of action of DOACS?

A

DOACS are anticoagulants with a novel mode of action

61
Q

Which DOACS are direct and reversible inhibitors of factor Xa?

A

Apixaban, edoxaban, and rivaroxaban

62
Q

What is the effect of inhibiting factor Xa?

A

Inhibition of factor Xa prevents thrombin generation and thrombus development

63
Q

What type of inhibitor is dabigatran?

A

Dabigatran is a reversible inhibitor of free thrombin, fibrin-bound thrombin, and thrombin-induced platelet aggregation

64
Q

Reversible agents of

-) heparin

-) dabigatrin

-) apixaban, riveroxaban

A

Heparin = protamine sulfate

Dabigatran = Idarucizumab

Apixaban = Andexanet alfa

65
Q

Acyanotic CHDs

A

ASD
VSD
AORTIC STENOSIS
COARCTATION OF AORTA

66
Q

Cyanotic CHDs

A

5T’s

Truncus arteriosus
Transposition of great arteries
Tricuspid atresia
Tetrology of fallot
Total anamolus pulmonary venous return

67
Q

Dosage of IM adrenaline for Children > 12 years and adults

A

500 mcg (0.5 mL)

68
Q

Dosage of IM adrenaline for Children 6 - 12 years

A

300 mcg (0.3 mL)

69
Q

Dosage of IM adrenaline for Children 6 months - 6 years

A

150 mcg (0.15 mL)

70
Q

Dosage of IM adrenaline for Children < 6 months

A

100-150 mcg (0.1 - 0.15 mL)

71
Q

Trifasicular block includes?

A

RBBB
LAD ( left ant.fascicular block )
First degree AV block

Nothing but bifascicular block + AV block

72
Q

What concentration should intravenous insulin infusion start at in dka

73
Q

What is the fixed rate for insulin infusion in dka

A

0.1 units/kg/hour

74
Q

How is the insulin infusion made up in dka?

A

Using 50 units human soluble insulin (Actrapid® or Humulin S®) made up to 50 ml with 0.9% sodium chloride solution.

75
Q

What should happen to blood ketone concentration during treatment in dka

A

It should fall by at least 0.5 mmol/litre/hour OR bicarbonate should rise by at least 3 mmol/L/hour and blood glucose concentration should fall by at least 3 mmol/litre/hour.

76
Q

When should the insulin infusion be continued in dka?

A

Until blood ketone concentration is below 0.6 mmol/litre, blood pH is above 7.3 and/or venous bicarbonate is over 18 mmol/L.

77
Q

What are the criteria for moderate severity in asthma?

A

Increasing symptoms
PEFR > 50 - 75% of best or predicted
No features of acute severe asthma

78
Q

What are the criteria for severe asthma?

A

Any one of:
PEFR 33 - 50% of best or predicted
Respiratory rate ≥ 25 breaths/minute
Heart rate ≥ 110 beats/minute
Inability to complete sentences in one breath

79
Q

What are the criteria for life-threatening asthma?

A

Any one of the following in a patient with severe asthma:
Clinical signs
Altered conscious level
Exhaustion
Arrhythmia
Hypotension
Cyanosis
Silent chest
Poor respiratory effort
Measurements
PEFR < 33% of best or predicted
Oxygen saturations < 92%
PaO2 < 8 kPa
Normal PaCO2 (4.6 - 6.0 kPa)

80
Q

What indicates a near-fatal asthma condition?

A

Raised PaCO2 and/or requiring mechanical ventilation with raised inflation pressures

81
Q

Wells score for PE

82
Q

Maintenance fluids in children calculation

83
Q

What does the Mental Health Act (2007) allow?

A

Compulsory admission of people who have a mental disorder that warrants assessment or treatment in hospital and need to be admitted for their own health or safety, or for the protection of others.

84
Q

What is Section 2 of the Mental Health Act?

A

Allows compulsory admission for up to 28 days for assessment.

85
Q

What is Section 3 of the Mental Health Act?

A

Allows compulsory admission for up to 6 months for treatment.

86
Q

What is required for admission under Sections 2 and 3?

A

An application from an approved mental health professional (AMHP) or the person’s nearest relative, and written recommendations from two doctors, one of whom must be section 12 approved.

87
Q

What happens if there is no obvious second medical recommendation for Section 2?

A

Another section 12-approved doctor is usually asked to assess the individual, but if impractical, any registered medical practitioner may provide the second recommendation without conflicts of interest.

88
Q

What is Section 4 of the Mental Health Act?

A

Used in exceptional cases to permit compulsory admission for up to 72 hours if there is urgent necessity.

89
Q

What is required for admission under Section 4?

A

An application from an AMHP or the person’s nearest relative and just one medical recommendation.

90
Q

What happens after a compulsory admission under Section 4?

A

This section is usually converted to a Section 2, requiring further involvement of the GP.

91
Q

What is Section 5 of the Mental Health Act?

A

Permits emergency holding powers for admitted patients to provide temporary restraint while awaiting assessment by a psychiatrist.

92
Q

What are the holding powers under Section 5?

A

Section 5 (2) allows a doctor holding power for 72 hours, and Section 5 (4) allows a registered mental health nurse holding power for 6 hours.

93
Q

What is Section 136 of the Mental Health Act?

A

Allows police to take people from a public place to a place of safety for examination by a registered medical practitioner and interview by an AMHP.

94
Q

What is the rule for young people aged 16 or 17 regarding hospital admission?

A

They cannot be admitted or kept in hospital for treatment for a mental disorder based on their parents’ consent if they have the capacity to consent but refuse.