Respiratory Flashcards

1
Q

Croup epidemiology and features

A

Croup is a form of upper respiratory tract infection seen in infants and toddlers. It is characterised by stridor which is caused by a combination of laryngeal oedema and secretions. Parainfluenza viruses account for the majority of cases.

Epidemiology

  • peak incidence at 6 months - 3 years
  • more common in autumn

Features

  • stridor
  • barking cough (worse at night)
  • fever
  • coryzal symptoms
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2
Q

Croup classification and reasons for admission

A

Admit with moderate/severe croup and other admission factors:

  • <6 months of age
  • known UA abnormalities (e.g. laryngomalacia, Down’s syndrome)
  • uncertainty about diagnosis (e.g. epiglottitis, bacterial tracheitis, peritonsillar abscess and foreign body inhalation)
  • pallor, cyanosis, decreased consciousness, RR>70, fatigue, asyncrhonous chest well and abdominal movement, sternal/intercostal recession
  • increasing UA obstruction
  • *Mild croup**: barking cough
  • *Moderate**: + stridor/sternal recession at rest
  • *Severe:** + agitation/lethargy, sternal/intercostal recession

Westley croup severity score (in image)

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3
Q

Croup Ix

A

clinical Dx

if CXR done:

  • PA view = subglottic narrowing aka ‘steeple sign’
  • Lateral view = swelling of epiglottis aka ‘thumb sign’

ix:

  • Basic obs
  • Examination
  • Urine catch (hard to get)
  • CXR = not usually done, steeple sign

tripod stance

NEVER examine a child’s throat (unsettles child)

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4
Q

Croup Mx

A

All severities croup:

  • Oral dexamethasone (0.15 mg/kg)
  • if not possible = inhaled beclomethasone (2mg) or IM dexamethasone (0.6/kg)
  • can give while transported to hospital for admission
  • incorporate paediatrician, nurses, anaesthetist → airway support STAT,
  • provide analgesics

Hospital

  • A to E, reduce temperature, start steroids, supportive care (fluids)
  • then talk about community care

Mild croup:

  • admission NOT required
  • Advise to take child to hospital if continuous stridor heard or skin between ribs pulling in with every breath
  • call ambulance if = pale/blue/grey for more than few seconds, unusually sleep or not responding, having a lot of trouble breathing, upset (agitated/restless) while struggling to breathe and cannot be calmed down quickly, unable to talk/drooling/trouble swallowing

Moderate croup:

  • oxygen

Severe croup:

  • oxygen (high flow via non-rebreathe mask)
  • nebuliser adrenaline (1 in 1000 (1mg/ml)) = RISK OF REBOUND 2h later so needs close monitoring, observe on day unit until respiratory distress settles
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5
Q

Causes of stridor in children

A
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6
Q

What is laryngomalacia? features and ix, complications

A

Congenital abnormality of the larynx cartilage which predisposes to dynamic supraglottic collapse during inspiration of respiration → results in upper airway obstruction and stridor.

Most frequent congenital stridor in infants and cause ‘noisy breathing’ in infancy.

  • 2-6 weeks old with noisy respiration and inspiratory stridor – worse supine, when feeding or if agitated
  • ± association with GORD
  • ± feeding difficulties, slow, ↑ cough/choking, ↑ respiratory noise
  • Normal cry → no abnormality with vocal cords
  • Not present at birth
  • Baby is otherwise comfortable despite thenoise

Ix:

  • monitor sats + laryngoscopy if diagnostic difficulty to assess anatomy and comorbidities

Complications = respiratory distress, failure to thrive, cyanosis

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7
Q

Laryngomalacia mx

A
  • Manage conservatively with close observation
  • Regular review and monitoring of growth
  • Tend to resolve by 18-24 months (although
  • may initially worsen with age, max at 6-8 months) – 70% resolve by 1 year old

Endoscopic supraglottoplasty if airway compromise or feeding disrupted sufficiently to prevent normal growth.

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8
Q

Asthma medical management for children aged 5 to 16

A
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9
Q

What is bronchiolitis, causes and epidemiology, more serious with…

A

Bronchiolitis is a condition characterised by acute bronchiolar inflammation. Respiratory syncytial virus (RSV) is the pathogen in 75-80% of cases.

OTHER CAUSES = mycoplasma, adenoviruses, 2o to bacterial infection

More serious if bronchopulmonary dysplasia (e.g. premature), congenital heart disease or CF

Epidemiology

  • most common cause of a serious lower respiratory tract infection in < 1yr olds (90% are 1-9 months, with a peak incidence of 3-6 months). Maternal IgG provides protection to newborns against RSV
  • higher incidence in winter
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10
Q

Features of bronchiolitis

A

coryzal symptoms (including mild fever) precede:

  • dry cough
  • increasing breathlessness
  • wheezing, fine inspiratory crackles (not always present)
  • feeding difficulties associated with increasing dyspnoea are often the reason for hospital admission
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11
Q

Bronchiolitis: when to make immediate referral and consider referring to hospital

A

‘consider’ referring to hospital if any of the following apply:

  • a respiratory rate of over 60 breaths/minute
  • difficulty with breastfeeding or inadequate oral fluid intake (50-75% of usual volume ‘taking account of risk factors and using clinical judgement’)
  • clinical dehydration.

immediate referral (usually by 999 ambulance) if they have any of the following:

  • apnoea (observed or reported)
  • child looks seriously unwell to a healthcare professional
  • severe respiratory distress, for example grunting, marked chest recession, or a respiratory rate of over 70 breaths/minute
  • central cyanosis
  • persistent oxygen saturation of less than 92% when breathing air.
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12
Q

How do we investigate bronchiolitis

A

clinical

immunofluorescence of nasopharyngeal secretions may show RSV

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13
Q

Bronchiolitis management and prevention

A

Infection control measures are required in the ward the patient is placed as RSV is highly infectious

Palivizumab (monoclonal antibody against RSV) reduces the number of hospital admissions in high-risk preterm infants

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14
Q

Nephrotic

A
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15
Q

Bronchiolitis vs Viral Episodic Wheeze

A

Bronchiolitis = crackles

VEW = wheeze

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16
Q

2 types of pre-school wheeze in children

A
  • episodic viral wheeze: only wheezes when has a viral upper respiratory tract infection (URTI) and is symptom free inbetween episodes (not associated with asthma in later life)
  • multiple trigger wheeze: as well as viral URTIs, other factors appear to trigger the wheeze such as exercise, allergens and cigarette smoke (a lot fo children with this end up with asthma)
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17
Q

Management of pre-school wheeze in children

A

Parents who are smokers should be strongly encouraged to stop.

Episodic viral wheeze

  • treatment is symptomatic only
  • first-line is treatment with short acting beta 2 agonists (e.g. salbutamol) or anticholinergic via a spacer
  • next step is intermittent leukotriene receptor antagonist (montelukast), intermittent inhaled corticosteroids, or both
  • there is now thought to be little role for oral prednisolone in children who do not require hospital treatment

Multiple trigger wheeze

  • trial of either inhaled corticosteroids or a leukotriene receptor antagonist (montelukast), typically for 4-8 weeks
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18
Q

How do we diagnose Cystic Fibrosis?

A

On day 5 of life, newborns have the heel prick test. They are tested for cystic fibrosis (CF), congenital hypothyroidism, sickle cell disease, and a number of other metabolic diseases. For CF, the levels of IRT (immune reactive trypsinogen) are tested, and if they are raised that can indicate CF. The baby should then undergo the sweat test, and if this is raised, this confirms a diagnosis of CF.

Sweat test

  • patient’s with CF have abnormally high sweat chloride
  • normal value < 40 mEq/l, CF indicated by > 60 mEq/l
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19
Q

Causes of a false positive sweat test (and also false negative)

A

Causes of false positive sweat test

  • malnutrition
  • adrenal insufficiency
  • glycogen storage diseases
  • nephrogenic diabetes insipidus
  • hypothyroidism, hypoparathyroidism
  • G6PD
  • ectodermal dysplasia

The most common reason for false negative tests is skin oedema, often due to hypoalbuminaemia/ hypoproteinaemia secondary to pancreatic exocrine insufficiency.

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20
Q

What causes whooping cough? (pertussis) when infants vaccinated?

A

G-ve Bordetella pertussis

Imms at 2,3,4 months and 3-5 years (infection/imms does not result in lifelong protection)

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21
Q

Features of whooping cough (pertussis)

A

Diagnosis criteria:

Acute cough >14 days w/o another apparent cause, and one or more of the following:

  • paroxysmal cough (CATARRHAL PHASE)
  • inspiratory whoop
  • post-tussive vomiting
  • undiagnosed apnoea attacks in young infants

2-3 days coryza precede onset of:

  • coughing bouts = worse at night/after feeding, ended by vomiting, associated central cyanosis
  • inspiratory whoop = forced inspiration against closed glottis
  • apnoea spells
  • persistent coughing → subconjunctival haemorrhages or anoxiasyncope/seizures
  • sx’s 10 - 14 weeks and more severe in infants (→ CONVALESCENT PHASE)
  • marked lymphocytosis
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22
Q

Whooping cough diagnostic ix

A

Per nasal swab culture for Bordetella pertussis = takes several days/weeks to come back

PCR + serology increasingly used as more available

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23
Q

Complications of pertussis

A

subconjunctival haemorrhage

pneumonia

bronchiectasis

seizures

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24
Q

Management of whooping cough

A

Notify HPU

Admit if:

  • <6m or acutely unwell
  • significant breathing difficulties (apnoea, severe paroxysms, cyanosis)
  • complications (seizures, pneumonia)

Pharm = if NOT admitted, onset within 21 days (as does not shorten course but affects infectivity)

  • <1m = clarithromycin
  • >1m and not pregnant = azithromycin
  • if pregnant = erythromycin (from 36 wk GA w/o vaccination to reduce risk of transmission to newborn)
  • if macrolides CI → co-trimoxazole (do NOT use in pregnant/infants <6wks of age)

Advice:

  • rest, adequate fluid intake, paracetamol/ibuprofen for sx relief
  • inform parents, despite abx tx, disease likely to cause protracted non-infectious cough that may take weeks to resolve
  • children avoid nursery until 48 hours of abx tx has been completed, or until 21 days after onset of cough if not treated with abx
  • once acute illness dealt with, advise parents to complete any outstanding imms
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25
Q

Assessment of acute asthma attacks

A
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26
Q

Management of life-threatening/severe asthma attack

salbutamol x3 = 10 puffs, 10 minute break, 10 puffs, 10 minutes break, 10 puffs

A

nebulised

IV salbutamol, IV aminophylline, IV magnesium sulfate second line

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27
Q

Moderate exacerbation of asthma requiring admission mx

A

inhaler with space

no magnesium sulfate

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28
Q

Mild exacerbation or moderate exacerbation not requiring admission

A

no hospital admission

inhaler with spacer

no ipratropium bromide, no magnesium sulfate

return to SABA up to 4x a day

consider initiating montelukast in children >2 years old

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29
Q

Follow up of asthma exacerbation

A
30
Q

Prenisolone doses in mild/moderate asthma attack

A
31
Q

When can you give pertussis vaccine in pregnant women?

A

16 - 32 weeks of pregnancy

o provide maternal antibodies to the foetus when it is delivered and to prevent the spreading of pertussis which can cause severe illness and death in a newborn.

32
Q

What is cow’s milk protein intolerance/allergy and what are it’s features and two types

A

Cow’s milk protein intolerance/allergy (CMPI/CMPA) occurs in around 3-6% of all children and typically presents in the first 3 months of life in formula-fed infants, although rarely it is seen in exclusively breastfed infants.

Both immediate up to 2 hours (IgE mediated) and delayed 2-72 hours (non-IgE mediated) reactions are seen. The term CMPA is usually used for immediate reactions and CMPI for mild-moderate delayed reactions.

Features

  • regurgitation and vomiting
  • diarrhoea (has a lot of mucus in it)
  • urticaria, atopic eczema
  • ‘colic’ symptoms: irritability, crying
  • wheeze, chronic cough
  • rarely angioedema and anaphylaxis may occur
33
Q

Ix of CMPI/A

A

Diagnosis is often clinical (e.g. improvement with cow’s milk protein elimination). Investigations include:

  • skin prick/patch testing
  • total IgE and specific IgE (RAST) for cow’s milk protein
34
Q

CMPI/A mx

A

formula fed/mixed feeding = eHF (extensively hydrolysed formula) → eAAF (elementary amino acid formula)

breastfed =

  • exclusion of all cow’s milk protein from mother’s diet
  • mother to take calcium and vitamin D supplements

Milk Ladder

35
Q

CMPI/A prognosis

A

CMPI usually resolves in most children

  • in children with IgE mediated intolerance around 55% will be milk tolerant by the age of 5 years
  • in children with non-IgE mediated intolerance most children will be milk tolerant by the age of 3 years
  • a challenge is often performed in the hospital setting as anaphylaxis can occur.
36
Q

stridor condition timelines

A

laryngomalacia = commonest cause of stridor in neonate

bronchiolitis = stridor 3-6 months

epiglottitis = 2-4 years

37
Q

What causes acute epiglottitis

features of acute epiglottis

A

HiB → airway obstruction

2-4 years old

Features:

  • rapid onset
  • high temperature, generally unwell
  • stridor
  • drooling of saliva
  • ‘tripod’ position
38
Q

How do we diagnose acute epiglottitis?

A

direct visualisation (only by senior/aitway trained staff)

XR if concern about foreign body = ‘THUMB’ sign

39
Q

How do we manage acute epiglottitis?

A

urgent hospital admission to ICU for tx → involve seniors esp. for away support (e.g. anaesthetics, ENT)

secure airway → endotracheal intubation and give oxygen

IV ceftriaxone for 7-10 days

Oral co-amoxiclav once stable and extubated

Rifampicin to close contacts

  • steroids + adrenaline (in some patients to reduce inflammation)

most children recover within 2-3 days

40
Q

Causes of stridor in children

A
41
Q

Features of sudden onset inhaled foreign body

where does it go if aspirated

A
  • coughing
  • choking
  • vomiting
  • stridor

If aspirated, foreign bodies are most likely to be found in the right main bronchus as it is wider, shorter and more vertical than the left.

42
Q

How do we manage foreign body inhalation?

A

Conscious

encourage coughing

external manoeuvres (back blows x5, Heimlich x5) = do NOT do Heimlich on infants and very young children (chest thrusts x5 instead)

removal of foreign body = flexible/rigid bronchoscopy

  • rigid → stridor, asphyxia, radio-opaque object on CXR, foreign body aspiration hx associated with unilateral decreased breath sounds, localising wheeze, obstructive hyper-inflation, or atelectasis
  • flexible → all other cases
  • done under conscious sedation or GA
  • 2nd line = surgery, thoracotomy

Unconscious

Secure airway immediately (endotracheal intubation)

  • unless foreign body can be seen and removed from upper airway
  • may need to do a cricothyroidectomy

Removal of foreign body

43
Q

Asthma mx in children less than 5 years

A
  1. SABA
  2. SABA + 8wk trial MODERATE ICS

Sx do not resolve → consider alternative diagnosis

Sx resolved then reoccured within 4 weeks of stopping ICS tx → restart ICS at LOW-DOSE as 1st line maintenance therapy

Sx resolved but reoccured beyond 4 weeks of stopping ICS tx → repeat 8wk trial

  1. SABA + low-dose ICS + LTRA
  2. stop LTRA and refer to a paediatric asthma specialist
44
Q

Non-pharamacological asthma management

A
  • assess baseline asthma status (Asthma Control Questionnaire or Lung Function Test aka spirometry)
  • provide self-mx education and personalised asthma action plan (from Asthma UK)
  • ensure child is UTD with imms
  • provide source of support (Asthma UK)
  • Advise trigger avoidance (allergens, smoke, b-blockers, NSAIDs)
  • assess for presence of anxiety and depression
  • give patient town peak flow meter
  • explain how to use inhalers

At review:

  • confirm adherence with medication
  • review inhaler technique
  • review if tx needs to be changed
  • ask about occupational asthma and triggers
45
Q

Non-pharamacological asthma management

A
  • assess baseline asthma status (Asthma Control Questionnaire or Lung Function Test aka spirometry)
  • provide self-mx education and personalised asthma action plan (from Asthma UK)
  • ensure child is UTD with imms
  • provide source of support (Asthma UK)
  • Advise trigger avoidance (allergens, smoke, b-blockers, NSAIDs)
  • assess for presence of anxiety and depression
  • give patient town peak flow meter
  • explain how to use inhalers

At review:

  • confirm adherence with medication
  • review inhaler technique
  • review if tx needs to be changed
  • ask about occupational asthma and triggers
46
Q

When do we go straight to step on asthma ladder (SABA PLUS ICS)

A

Newly-diagnosed asthma with symptoms ≥3/week or night-time waking

47
Q

Causes of snoring children

A

Causes

  • obesity
  • nasal problems: polyps, deviated septum, hypertrophic nasal turbinates
  • recurrent tonsillitis
  • Down’s syndrome
  • hypothyroidism
48
Q

Give an example of a low dose ICS

A

beclometasone diproprionate

49
Q

acute otitis media causes

A

URTI precedes otitis media, mostly 2o to bacteria (Step pneumoniae, Hib, Moraxella cararrhalis, RSV, rhinovirus), 6-12 months

Viral URTI disturbs nasopharyngeal microbiome → allows bacteria infect middle ear via Eustachian tube (tube short and function poorly)

50
Q

Acute otitis media features

A

Features

  • Otalgia (rub/tug ear)
  • Fever (50%)
  • Hearing loss
  • Recent viral URTI sx common (e.g. coryza)
  • Ear discharge may occur if tympanic membrane perforates (+effusions = glue ear)

Criteria (3) =

  • acute onset symptoms, (otalgia)
  • presence of middle ear effusion
  • inflammation of tympanic membrane
51
Q

Investigation findings for acute otitis media

A

Otoscopy =

  • bulging tympanic membrane → loss of light reflex
  • opacification
  • erythema of tympanic membrane
  • perforation with purulent otorrhoea
52
Q

Mx of acute otitis media

A

Mx:

  • Analgesia (paracetamol/NSAID)
  • Seek help if sx don’t resolve after 3 days/deterioration
  • Admit = complications, systemically unwell, children <3m with temperature >38dc, ENT referral/advice, hearing test, developmental assessment

Abx → + <2y bilateral, perforation/discharge, immcomp

  • None = most cases resolve
  • Back-up = abx NOT needed immediately, but should be used if sx’s have not improved after 3 days/worsened
  • Immediate = sx worsen rapidly, systemically unwell, seek medical help
  • Amoxicillin 5-7d → allergy then clarithromycin, erythromycin, 2nd line co-amoxiclav
53
Q

Allergic rhinitis features

A
  • Intermittent vs persistence
  • Mild vs severe
  • Seasonal vs perennial

Features

  • Coryza, conjunctivitis, chronically blocked nose, sleep disturbance, impaired daytime behaviour/concentration
  • Sleep disturbance, impaired daytime behaviour/concentration
54
Q

Investigations for allergic rhinitis

A
  • Identify causative allergen
  • Assess for atopy, asthma, allergic conjunctivitis, eczema
  • Look for signs of nasal congestion (mouth breathing, cough, halitosis)
  • Examine nose = nasal polyps, deviated septum, mucosal swelling/depressed, wide nasal bridge
55
Q

Mx of allergic rhinitis

A
  • Mild-mod = allergen avoidance, nasal irrigation, intranasal antihistamines/PO non-sedating antihistamines (e.g. loratadine/cetirizine). 2nd line intranasal chromone
  • Mod-severe = as above, + intranasal corticosteroid, short course PO corticosteroids
  • Add-ons for ineffective therapy= intranasal decongestants (ephedrine/xylometazoline), intranasal anticholinergic, SL/SC immunotherapy

f/u 2-4 weeks

56
Q

Food allergy features

A

Primary and secondary “oral allergy syndrome”

Ask for personal/FHx of atopy, details of food avoidance, feeding history *age of weaning, breast/formula)

Similar features to CMPA

With rash, erythema, urticaria, angioedema, colicky abdominal pain, sneezing, rhinorrhoea, congestion, cough, tightness, wheeze

  • Anaphylaxis in 10-15 minutes
57
Q

Food allergy investigations

A

Ix:

  • Skin prick allergy testing and RAST
  • Trial elimination of suspected allergen then reintroduce
  • Consider endoscopy, intestinal biopsy
58
Q

Food allergy mx

A

Diet

  • Exclusion of offeding food from diet
  • Paed dietician referral
  • Dietary exclusion in mother if breastfeeding

Drug

  • Mild (no cardioresp sx) = non-sedating anti-histamine (diphenhydramine)
  • Severe (cardio, laryngeal, bronchial) = IM adrenaline/EpiPEN, salbutamol for bronchospasm

Education = allergy action plan

  • Training and self-management
  • Epi-Pen use (2 doses at all times)

Food challenge

  • After 6-12m sx free
  • If previous reaction severe (do in hospital)
59
Q

Principles of upper airway mx (REMEMBER THIS ORDER)

A
  1. step away from the child = do NOT examine the throat
  2. give oxygen
  3. Get people you need in the room (anaesthetics, ENT, paediatrics)
  4. reduce the inflammation = adrenaline nebulisers (repeat as necessary), dexamethasone orally, budesonide nebuliser
60
Q

Bacterial tracheitis summary

A
61
Q

3 years old, presents with stridor and spreading rash after returning from a plane

A
62
Q

salbutamol toxicity signs

A

nausea + vomiting

low potassium

lactic acidosis

tremors

63
Q

Causes of snoring in children

A
  • Obesity
  • Nasal problems (polyps, deviated septum, hypertrophic nasal turbinates)
  • Recurrent tonsillitis
  • Down’s syndrome
  • Hypothyroidism
64
Q

Scarlet fever: pathogen, epidemiology, physiology and features

A

Scarlet fever is a reaction to erythrogenic toxins produced by Group A haemolytic streptococci (usually Streptococcus pyogenes). It is more common in children aged 2 - 6 years with the peak incidence being at 4 years.

Scarlet fever is spread via the respiratory route by inhaling or ingesting respiratory droplets or by direct contact with nose and throat discharges, (especially during sneezing and coughing).

Scarlet fever has an incubation period of 2-4 days and typically presents with:

  • fever: typically lasts 24 to 48 hours
  • malaise, headache, nausea/vomiting
  • sore throat
  • ‘strawberry’ tongue
  • rash
    • fine punctate erythema (‘pinhead’) which generally appears first on the torso and spares the palms and soles
    • children often have a flushed appearance with circumoral pallor. The rash is often more obvious in the flexures
    • it is often described as having a rough ‘sandpaper’ texture
    • desquamination occurs later in the course of the illness, particularly around the fingers and toes
65
Q

Scarlet fever diagnosis and management

A

Diagnosis = throat swab, BUT abx commenced immediately rather than waiting for the results

Management:

  • notify HPU
  • Abx = penicillin V (QDS 10 days) OR azithromycin (if penicillin allergy)
  • 10 days to prevent complications such s acute glomerulonephritis and rheumatic fever
  • stay away from nursery/school for 24 hours after starting abx
  • paracetamol/ibuprofen given for symptomatic relief
  • symptoms should settle down after 1 week
66
Q

Scarlet fever complications

A
  • otitis media: the most common complication
  • rheumatic fever: typically occurs 20 days after infection
  • acute glomerulonephritis: typically occurs 10 days after infection
  • invasive complications (e.g. bacteraemia, meningitis, necrotizing fasciitis) are rare but may present acutely with life-threatening illness
67
Q

Inhaled corticosteroid doses

A
  • <200 is low dose
  • 200 - 400 is moderate dose
  • >400 is high dose
68
Q

Cystic fibrosis features

A

Main features

  • Neonatal = meconium ileus, less commonly prolonged jaundice
  • Recurrent chest infections
  • Malabsorption = steatorrhea, FTT
  • Liver disease

Other features = Short stature, DM, delayed puberty, rectal prolapse (from bulky stools), nasal polyps, male infertility, female subfertility, USI, muscle pains, arthralgia

Pulmonary = pneumonia, nasal polyps, sinusitis

GI = underweight, malnutrition, intussusception, meconium ileus

69
Q

Cystic fibrosis epidemiology and aetiology

A

AR, defect in CFTR, delta F508 on Chr7, mutation mainly, increased viscosity of secretions (e.g. lungs, pancreas), 1 in 25 carrier rate, 1 in 2500 births, 5% diagnosed after 18 years old

Organisms:

S. AUREUS, P.AERUGINOSA, BURHOLDERIA CEPACIA, ASPERGILLUS

70
Q

CXR in cystic fibrosis

A

CXR =hyperinflation, peribronchial shadowing, bronchial wall thickening, ring shadows

71
Q

Cystic fibrosis Management

A

MDT = paeds, physio, GP, dieticians, specialist nurses, primary care team, teachers, psychologists, social workers, annual review in specialist centre, psych and educational support, routine reviews

DF508 mutation = lumacaftor/ivacaftor

Pulmonary, infection, nutrition, psychosocial

Pulmonary:

  • airway clearance techniques + mucoactive agents  1) rhDNase 2) hypertonic NaCl +/- rhDNase 3) mannitol dry powder for inhalation
  • S. aureus pneumonia  flucloxacillin (prophylaxis)
  • P. aeruginosa pneumonia Acute = PO/inhaled abx, chronic/persistent = 1) colistimethate sodium + PO/IV abx 2) tobramycin DPI
  • Immunomodulatory agents for deteriorating lung function: azithromycin, oral corticosteroids

GI: high calorie diet, Creon, H2 receptor antagonist/PI, UDA (only for abnormal LFTs, stop when recovers) for liver disease, distal intestinal obstruction syndrome  diatrizoate meglumine + diatrizoate sodium solution (Gastrografin)