MSRA 10 Flashcards

1
Q

What tool is used to diagnosed acute rheumatic fever?
What are its major and minor criteria?

A

Revised Jones criteria

Major - migratory polyarthritis, Carditis, Sydenham Chorea, subcutaneous nodules, erythema marginatum

Minor - high fever, polyarthritis, esr >60 crp>30, ecg showing prolonged PR

2majors
1major and 2minor

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2
Q

What are the rheumatic fever effects on the heart valve?

A

Pancarditis
Mitral valvulitis
(Acute mutral regurgitation)
(Chronic mitral stenosis) or mixed
Aortic stenosis or regurgitation

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3
Q

What is aortic sclerosis

A

Aortic valve sclerosis occurs without aortic stenosis in its early stages, but can progress to aortic stenosis once signs of LVOT obstruction begin to occur.

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4
Q

Which genetic condition cause a bicuspid aortic valve?

A

Turner syndrome

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5
Q

What is Reye syndrome

A

A rare but potentially life-threatening condition in children < 19 years that generally develops after treating a viral illness (e.g., influenza, varicella) with salicylates like aspirin. The viral infection alters the metabolism of salicylates and leads to accumulation of metabolites in the liver, which causes hepatic mitochondrial injury that prevents hepatic ATP production. The result is hepatic failure (hyperammonemia, metabolic acidosis, and hepatic steatosis) that manifests with acute hepatic encephalopathy.

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6
Q

At what age does paediatric BLS be used from?

A

1month to 18 yeats

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7
Q

When are signs of life assessed for after 5rescue breathes in paediatric BLS and what would be the next step in the

A

During rescue breathes, if no signed of life then 15:2 chest compressions

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8
Q

How is a UTI investigated if it shows an atypical organism or if is under 6 months?

A

Ultrasound kidneys during the infection

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9
Q

How should a treated UTI in an under 6month be managed if they responded to antibiotics?

A

US within 6 weeks

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10
Q

How do you manage a uti in under 3months?

A

Urgent referral

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11
Q

What are the APGAR readings?

A

Activity - Nothing 0 / Some flexion 1 / Active 2
Pulse - Nothing 0 / under 100 1 / over 100 2
Grimace - No reactio 0 / Reactive 1 / cough, sneezing, cry 2
Appearance - Blue 0 / Blue hands, feet 1 / Good colour 2
Respiration - Nothing 0 / weak 1 / strong 2

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12
Q

What are the CI for 5-flouracil cream and what can be given instead?

A

Diclifenac gel

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13
Q

What is bacterial exanthem?

A

Scarlet fever

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14
Q

What would you give to treat the cosmetic appearance in mild psoriasis plaques in a child

A

Vit D cream

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15
Q

What is pustules on the hands with eczema that improved with steroids with widespread rash?

A

Scabies incognito

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16
Q

Is cefelexane safe in pregnancy

A

Yes, it is a cephalosporon and cephalosporin is safe in pregnancy

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17
Q

Which is always the preferred option for emergency contraception?

A

IUD

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18
Q

Can you sterilise at the same time as a continuous section?

A

Yes

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19
Q

What does a broken foot with lots of swelling in a cast signify? What treatment does it need?

A

Compartment syndrome, remove the cast

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20
Q

What is the antimitochondrial antibody associated with?

A

PBC

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21
Q

How is Salmonella spread?

A

Faecol oral route

22
Q

What is Hoagland sign

A

Eye lid swelling in EBV infections

23
Q

Which nerve is affected in Ramsey hunt syndrome

A

Trigeminal nerve

24
Q

What is a shower of floater characteristic of?
What are the risk factors for it?

A

Retinal tear
Myopia, cataract surgery

25
Retrobulbar haemorrhage risks what complication? How quickly can this complication occur?
Oribtal compartment syndrome OCS can cause irreversible loss of vision within 1–2 hours.
26
What is a rhabdomyoscarcoma
Most common soft tissue sarcoma and malignant orbital tumor in children
27
What are the features of fragile X
Second commonest cause of intellectual disability after trisomy 21 X-linked dominant Hypermobile joints, mitral valve prolapse, seizures
28
How do you differentiate between Edward and Patau?
Edwards has a prominent occiput
29
What are the cardiac feature of Turner's syndrome?
COA and bicuspid aorta
30
What is the commonest cause of male hypogonadism?
Klinerfelter
31
Which adenoma is the commonest pituitary adenoma?
Prolactinoma
32
Is ibuprofen associated with cardiovascular events?
No
33
What would an insulinoma be associated with? (with genetic condition)
MEN a
34
What are the tools to assess for possible FH?
Use the Simon Broome criteria or the Dutch Lipid Clinic Network (DLCN)
35
When would you suspect FH and when would you make a clinical diagnosis?
A total cholesterol level greater than 7.5 mmol/L and/or A personal or family history of premature coronary heart disease (CHD, an event before 60 years in an index person or first-degree relative [parents, siblings, children]). Take two measurements of low-density lipoprotein (LDL) cholesterol concentration. Consider a clinical diagnosis of homozygous FH in adults with LDL cholesterol concentration greater than 13 mmol/L. Consider a clinical diagnosis of homozygous FH in a child or young person (up to 15 years of age) with an LDL cholesterol concentration greater than 11 mmol/L.
36
Which drug must you not co-prescribe with erythromycin?
Using simvastatin, tolterodine, mizolastine, amisulpride, astemizole, terfenadine, domperidone, cisapride, pimozide, ergotamine, or lomitapide.
37
What is rubeosis iridis
a condition in which abnormal blood vessels form on the surface of the iris
38
What is enteric fever
Caused by invasive diarrhoea Caused by Salmonella enterica serotypes Typhi and Paratyphi. Manifestations include fever, abdominal pain, and rose spots on the trunk and abdomen.
39
What are the features of Yersinia?
Causes pseudopancreatitis. Caught from mil and pork. A condition that presents with signs and symptoms classically associated with appendicitis (e.g., right lower quadrant pain, fever, vomiting, leukocytosis). Caused by mesenteric lymphadenitis, typically as a complication of Yersinia infection. Management involves antibiotic therapy to eradicate the underlying infection.
40
Which DI does Lithium cause?
Nephrogenic diabetes insipidus
41
What is Troisier's sign
Troisier's sign, also known as the Virchow node, is a clinical sign that indicates an enlarged left supraclavicular lymph node.
42
What are the big SE of cholchicine?
Diarrhoea
43
What is Epiphora
Epiphora is the medical term for watery eyes,
44
Give 3 characteristic features of open angle glaucoma
Impaired adaptation to darkness Generally bilateral, progressive visual field loss (from peripheral to central) Arcuate scotoma: arch-shaped scotoma that starts from the blind spot
45
What are the risk factors for open angle glaucoma
Age > 40 years Increased IOP European or African descent Diabetes mellitus Familial predisposition Myopia Steroid use
46
What should you not do in acute angle glaucoma
Do not use mydriatic drugs (e.g., atropine and epinephrine) during ophthalmologic examination in patients with acute angle-closure glaucoma! Moreover, do not cover the eye, since darkness induces mydriasis and worsens the condition!
47
What is the normal optic disc cup ratio?
The normal optic disc cup-to-disc ratio is less than 0.5. A ratio of 0.6 or greater is generally considered suspicious for glaucoma, but there are other factors to consider:
48
What are the features of gonorrhoea conjunctivitis?
Hyperacute conjunctivitis Marked eye swelling Profuse purulent discharge Preauricular lymphadenopathy Possibly, corneal infiltrates or ulcers
49
What are features of chlamydia conjunctivitis?
Inflamed upper tarsal conjunctiva Conjunctival scarring Corneal ulcers and opacities Superficial neovascularization with cellular infiltration (corneal pannus) Entropion Trichiasis
50
What are the three gross motor delay findings needing urgent referral?
not sitting by 8 months (corrected for gestational age) not walking by 18 months (corrected for gestational age) early asymmetry of hand function (hand preference) before 1 year (corrected for gestational age).
51
When should a child with difficulty walking be referred?
Delayed walking after 15 months of age for girls or 18 months for boys. Waddling gait, enlarged muscle bulk, or proximal muscle weakness (consider muscular dystrophies). Frequent falls or clumsiness. Delay or regression of milestones (for example speech, communication, and feeding). A family history of delayed walking or muscle disease.