6. Respiratory / ENT major Flashcards

1
Q

What is the most common respiratory disorder in children?

A

-Asthma (>10%)
-Severe asthma = most common reason for PICU admission
-Many childhood asthmas improve / resolve with age

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2
Q

What is the pathophysiology of asthma?

A

-Airway hypersensitivity
-Increased airway inflammation / mucosal oedema
-Bronchoconstriction
-Hyper-secretion of mucus

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3
Q

What risk factors are there for developing asthma?

A

-Personal / FHx of atopy
-Antenatal factors eg maternal smoking, viral infection
-LBW / pre-term birth
-Not breast fed
-Hygiene hypothesis
-Male sex

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4
Q

What features make a diagnosis of asthma more / less likely?

A

MORE LIKELY
-Cough + wheeze
-Hx of atopy
-Wheeze on auscultation
-Responsive to therapy
LESS LIKELY
-Symptoms with colds only
-Moist / isolated cough
-Normal examination
-Non-responsive to therapy

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5
Q

What tests can be done to confirm an asthma diagnosis?

A

-PEFR
-Spirometry - FEV1/FVC (usually reduced)
-FeNO (fractional exhaled nitric oxide)

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6
Q

What signs indicate acute severe asthma vs life-threatening asthma?

A

ACUTE SEVERE
-PEFR 33-50% best / predicted
-HR >140 in 2-5yrs / >125 in >5yrs
-RR >40 in 2-5 yrs / >30 in >5yrs
-Unable to complete sentences in 1 breath / too breathless to talk
LIFE-THREATENING
-PEFR <33% predicted
-Silent chest, cyanosis, hypotension, exhaustion, poor respiratory effort
BOTH
-Sats <92%

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7
Q

How would you manage acute asthma?

A

-A-E + oxygen
-SALBUMATOL NEBS
–<5 - 2.5mg every 20-30mins back to back
–>5 - 5mg
-IPRATROPIUM BROMIDE NEBS
–250mcg every 5 mins
-PREDNISOLONE PO
–<2 = 10mg, 2-5 = 20mg, >5 = 30-40mg
NO RESPONSE?
-+ MAGNESIUM SULFATE to each neb
-Aminophylline / IV salbutamol (specialist)
-Hydrocortisone IV (50/100mg)
INFECTIVE?
-Amoxicillin
–250mg TDS PO for 5 days

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8
Q

How should asthma be managed in children <12yrs?

A
  1. Inhaled SABA
  2. Regular preventer (ICS / LTRA <5yrs)
    –200-400mcg/day
  3. Add Inhaled LABA >5yrs / ICS <5yrs
    –Increase ICS (+ stop LABA if no benefit) 400mcg/day
  4. Increase ICS to 800mcg / add theophylline + refer
  5. Daily oral steroids
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9
Q

How should asthma be managed in children >12yrs?

A
  1. Inhaled SABA / ICS
    –2-800mcg/day
  2. Add inhaled LABA +/- ICS
    –Increasing ICS (+ stop LABA) if limited benefit
  3. Addition of LTRA / theophylline
  4. Daily oral steroids
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10
Q

What is bronchiolitis and what causes it?

A

-Acute LRTI usually following a viral URTI
-Small airway obstruction caused by infection
-1 in 3 children will get it in 1st year of life
-80% caused by respiratory syncytial virus, rest caused by adenovirus, influenza

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11
Q

How does bronchiolitis present and what are red flag symptoms potentially requiring admission?

A

Typically a 9 day illness (peaks day 5-7):
-3 days prodrome with cold + harsh cough
-3 days ill with fever, high-pitched wheeze, fine inspiratory crackles, SOB
-3 days recovering
-Cough can last for up to 2-3 weeks
RED FLAGS
-Disrupted breathing
-Central cyanosis
-No wet nappy for 12h

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12
Q

How should you investigate bronchiolitis?

A

-None needed in mild cases
-In severe cases:
–Capillary blood gas (respiratory acidosis)
–CXR
–Nasal swab for virus type
-Admit in cases of:
–Dehydration / intake <50% normal
–RR >70 / marked recession
–Apnoeic episodes
–Sats <92
–Exhaustion

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13
Q

How should you manage bronchiolitis?

A

MILD = minimal distress, feeding ok, o2 fine
-Home with safety netting
MODERATE = increased work of breathing, low o2, poor feeding
-Admit for feeding + support +/- oxygen (40L/min through nasal cannula)
SEVERE = worsening distress, respiratory acidosis, apnoea, dehydration
-HDU/PICU
-CPAP / ventilation + IV fluids

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14
Q

Who is at risk of severe bronchiolitis?

A

-Infants born at or <35 weeks (up to 6months)
-Chronic lung disease / significant congenital heart disease (up to 2yrs)
-Previous episode of wheeze
-PALIVIZUMAB given as prophylaxis - monthly IM for 6months during winter months

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15
Q

What is croup and what causes it?

A

-Acute viral laryngo-tracheo-bronchitis (URTI)
-Most cases caused by parainfluenza virus (can be caused by RSV, influenza, adenovirus)
-Peak incidence = 6m-3yrs

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16
Q

How does croup present compared to epiglottis?

A

CROUP
-Very common, can be mild to severe
-STRIDOR, hoarse voice
-Fever
-Barking cough
-Drooling not seen
EPIGLOTTITIS
-Rapid onset, intensely painful throat, emergency
-Unable to speak or swallow
-Muffled voice
-Soft, inspiratory stridor
-Drooling

17
Q

How should croup vs epiglottis be managed?

A

CROUP
-Parental advice eg ibuprofen/paracetamol, increase fluid intake
-Admission required if moderate-severely ill or high risk
-Oral dexamethasone 0.15mg/kg
-Inhaled budesonide nebs 2mg OR IM dexamethasone
-Nebulised adrenaline in severely ill
EPIGLOTTITIS
-Do not distress child - urgent ENT / anaesthetics referral
-Single dose of oral dexamethasone
-IV abx +/- intubation (caused by H. influenza)

18
Q

What can cause pneumonia in children of different ages?

A

-1/3 are viral (RSV, parainfluenza, adenovirus, rhinovirus)
-Bacterial causes:
–NEONATES = GBS, E. coli, listeria, chlamydia
–INFANTS = strep pneumonia, H.influenza
–CHILDREN = strep pneumonia, H.influenza, GAS, mycoplasma pneumoniae

19
Q

How is mild pneumonia managed?

A

AT HOME
-1st line = amoxicillin
-2nd line = macrolides if no response or if mycoplasma / chlamydia suspected
-Fluids + temp control advice
-Safety net

20
Q

How is moderate-severe pneumonia managed?

A

ADMISSION
-Oxygen to maintain sats >93
-IV co-amoxiclav if influenza-associated
-Cefotaxime / cefuroxime
-Fluids
-Close observation

21
Q

What complications can arise from pneumonia?

A

-Pleural effusion
-Sepsis
-Bronchiectasis
-Empyema
-Lung abscess

22
Q

What would indicate a bacterial URTI?

A

CENTOR CRITERIA
-Purulent exudate on tonsils
-Tender cervical lymphadenopathy
-History of fever
-Absence of cough
If 3 or more of the above present, 40-60% chance GBS is causative organism

23
Q

How should bacterial sore throat / tonsillitis be managed?

A

-Phenoxymethylpenicillin (erythromycin if penicillin-allergic) for 7-10 days
-Avoid amoxicillin as may cause a rash if actually caused by EBV
-Treat if 3+ centor criteria or Hx of rheumatic fever, immunodeficiency

24
Q

When can a tonsillectomy be considered?

A

-If 5+ recurrent episodes a year, disabling + prevents normal functioning
-If causing obstructive sleep apnoea / stridor / dysphagia
-Quinsy (= unilateral peritonsilar abscess, complication of tonsillitis)

25
What does a wheeze indicate?
-Wheeze = breath sound heard during expiration -Indicates obstruction to airflow within thorax -High or low-pitched -Monophonic or polyphonic (multiple airway involvement)
26
What are the main broad categories for wheeze differentials?
-Extrinsic lower airway compression -Intrinsic change in lower airway -Intraluminal lower airway obstruction
27
What are some differentials for wheeze?
NB top differential for children >5 = asthma EXTRINSIC LOWER AIRWAY COMPRESSION -Pneumonia, pulmonary oedema -Enlarged LA compressing left main bronchus -Enlarged hilar nodes -Scoliosis INTRINSIC CHANGE IN LOWER AIRWAY -Asthma, bronchiolitis, bronchitis, bronchiectasis -CF, ciliary disease -Haemangioma, polyps, tracheobronchomalacia INTRALUMINAL LOWER AIRWAY OBSTRUCTION -Aspiration of food due to reflux, foreign body inhalation -Mucus, pus, blood
28
What causes cystic fibrosis?
-Autosomal recessive inheritance -Caused by a defect in the CTFR gene on chromosome 7 -Codes for a cAMP-regulated chloride channel, leading to impaired transport -Leads to airway lining liquid depletion --> increased Na+ absorption + net water absorption across cells -Causes mucus to be more sticky and defective mucociliary clearance
29
What are the clinical features of cystic fibrosis?
RESPIRATORY -Cough + wheeze -Recurrent chest infections + sinusitis -Nasal polyps -Decline in lung function GI -Failure to thrive + ravenous appetite due to fat malabsorption + pancreatic insufficiency -Meconium ileus at birth in 10% -Steatorrhoea -Weight loss GENERAL -CF-related bone disease -Delayed puberty -Male infertility / female sub fertility
30
What investigations can be done to confirm a CF diagnosis?
1. SWEAT TEST (gold standard) -Chloride levels >60mmols from 2 tests indicates CF 2. GENETIC TESTING 3. NEWBORN SCREENING -Raised immunoreactive trypsin on newborn bloodspot card 4. CXR -Hyperinflation, peribronchial thickening, bronchiectasis 5. LUNG FUNCTION -Obstructive defect seen 6. SPUTUM SAMPLE -H.influenzae, staph aureus, pseudomonas, E. coli, klebsiella 7. FAT-SOLUBLE VITAMINS -A, D, E 8. FAECAL ELASTASE -<200 indicates pancreatic insufficiency
31
How is cystic fibrosis managed by the MDT?
1.MEDICAL -Seen every 6-8 weeks by: --Paediatrician (prophylactic abx - azithromycin) --Endocrinology (pancreatic enzyme supplements) --Respiratory, GP, genetics, transplant team, vaccines 2. NURSING 3. PHYSIO -Twice daily - manual techniques, deep breathing -Nebulised DNAase (breaks down mucus) / hypertonic saline -Vest therapy 4.DIETICIANS -High calorie high fat diet -Vitamin + salt supplements, may need laxatives 5. Education, psychosocial support, isolation from other CF patients
32
What is assessed in an annual review for a CF patient?
-BLOODS (haematology, vitamin levels, glucose control, LFTs, immunology) -RADIOLOGY (CXR, USS, DEXA, LFTs) -MORBIDITY assessment eg no. of admissions, no. of abx courses -REVIEW of meds, physio etc