Paeds - Respiratory (Acute Conditions) Flashcards

1
Q

Severities of Asthma Exacerbation

Mild
Moderate
Severe
Life-Threatening

A
  1. ) Mild - peak expiratory flow rate (PEFR) >75%
    - signs of respiratory distress: SOB, tachypnoea,
    - expiratory wheeze on auscultation, ↓air entry

2.) Moderate - PEFR 50-75%

  1. ) Severe - any one of the following:
    - PEFR 33-50% of best or predicted
    - unable to talk properly or feed
    - SATS <92%
    - over 5s: RR >30, HR > 125
    - under 5s: RR >40, HR > 140
    - still hyperventilating so pCO2 should be reduced
    - risk factors: previous asthma admissions or near-fatal asthma, repeated attendances to ED for asthma care, needing 3+ classes of asthma medication, heavy use of SABA, brittle asthma
  2. ) Life-Threatening - any one of the following:
    - PEFR < 33% of best or predicted
    - sats <92% or ABG pO2 < 8kPa
    - normal pCO2 (4.8-6kPA) indicates reduced resp effort
    - exhaustion, cyanosis, hypoventilation, silent chest
    - hypotension, altered consciousness or confusion
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2
Q

Management of Asthma Exacerbation

Mild
Moderate to Severe
Stepping Down Treatment
Discharge After an Exacerbation

A
  1. ) Mild - can be managed as an outpatient
    - regular salbutamol inhalers with a spacer (4-6 puffs every 4 hours)
    - PO prednisolone for 3 days for all patients with any severity of an asthma attack
  2. ) Moderate to Severe - steps in order:
    - INH salbutamol w/ spacer: start w/ 10puffs per 2hrs
    - first line: NEB salbutamol + ipratropium bromide AND PO prednisolone( 1mg/kg OD for 3 days)
    - second line: IV hydrocortisone –> IV magnesium sulphate –> IV salbutamol –> IV aminophylline
    - call anaesthetist and ITU for potential intubation and ventilation
  3. ) Stepping Down Treatment
    - review before next dose of their bronchodilator, if well, consider stepping down no and frequency e.g.
    - stepping down INH salbutamol: 10puffs 2hrly –> 10puffs 4hrly –> 6puffs 4hrly –> 4puffs 6hrly
    - consider monitoring serum potassium when on high doses of salbutamol as it can cause hypokalaemia
  4. ) Discharge After an Exacerbation
    - considered when the child is well on 6puffs 4hrly of INH salbutamol which can be lowered after discharge to 4puffs 6hrly after 2days then 2-4puffs as required
    - must finish the course of steroids (typically 3 days)
    - provide an individualised written asthma action plan
    - provide safety-netting info for when to seek help
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3
Q

Community-Acquired Pneumonia in Children

Aetiology
Clinical Features
CAP Severity in Infants (and Older Children)

A
  1. ) Aetiology - bacterial and/or viral infection
    - newborns: organisms from mother’s genital tract e.g. group B strep, g-ve enterococci and bacilli
    - infants and young children: resp viruses (RSV common), S.pneumoniae, H.influenzae
    - children >5yrs: S.pneumoniae, Mycoplasma pneumonaie, Chlamydia pneumoniae
  2. ) Clinical Features
    - cough: may be associated w/ vomiting in young kids
    - high-grade fever (>38.5), difficulty breathing/SOB
    - localised pain (chest, neck, abdo), delirium
    - signs: ↑RR, ↑HR, hypoxia, hypotension, confusion
    - bacterial: >2yrs, >38.5ºC, no rhinorrhoea or wheeze, presence of localised pain (pleuritic irritation)
    - viral: <2yrs, low fever, rhinorrhoea, wheeze, no pain
    - chest signs: bronchial breathing, coarse crackles, dullness to percussion
  3. ) CAP Severity in Infants (and Older Children)
    - mild: RR<50 (<35), CRT <2s, mild recessions (mild breathlessness, full feeds
    - mod: RR 50-70 (35-50), CRT≈2s, mod recessions, reduced feeds
    - severe: RR>70 (>50), CRT>2s, unable to feed, signs of resp distress: nasal flaring, intermittent apnea, grunting (unable to complete sentences, severe recessions, signs of dehydration)
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4
Q

Management of CAP in Children

Investigations
Management
Investigating Recurrent LRTIsin

A
  1. ) Investigations
    - CXR: only used in severe/complicated cases
    - sputum cultures and throat swabs for bacterial cultures and viral PCR to establish causative organism
    - capillary blood gas (ABG in children)
    - septic screen for very unwell children
  2. ) Management - oral antibiotics (IV if severe)
    - Abx: amoxicillin +/- macrolide (atypical pneumonia)
    - mild: managed in community w/ safety netting
    - mod: admission, may need O2, or support w/ feeds
    - severe: bloods, CXR, IV fluids, IV antibiotics
  3. ) Investigating Recurrent LRTIs
    - underlying conditions: reflux, aspiration, neurological disease, heart disease, asthma, cystic fibrosis, primary ciliary dyskinesia and immune deficiency
    - investigations inc: FBC, CXR, serum immunoglobulins, test IgG to previous vaccines, sweat test (CF), HIV test
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5
Q

Bronchiolitis

Pathophysiology
Clinical Features
Signs of Respiratory Distress
Differential Diagnoses

A
  1. ) Pathophysiology - inflammation and infection in the bronchioles, the small airways of the lungs (LRTI)
    - usually caused by the respiratory syncytial virus (RSV)
    - very common in winter
    - occurs in children <1yr (<6mths most common), rare in children up to 2 years (often premature babies)
    - the smallest obstruction in airways in infants as a significant effect on infants’ breathing ability
    - RF: breastfed < 2mths, smoke exposure, siblings in school, chronic lung disease due to prematurity
  2. ) Clinical Features
    - SOB, tachypnoea, apnoeic episodes (stop breathing)
    - poor feeding, mild fever (<39), coryzal sx (viral URTI): runny nose, sneezing, mucus in throat (can cause drooling), watery eyes
    - signs of respiratory distress
    - auscultation: expiratory wheeze, fine inspiratory crackles (not always present)
  3. ) Signs of Respiratory Distress
    - raised respiratory rate, cyanosis (due to low sats)
    - use of accessory muscles: SCM, abdo, intercostal
    - intercostal and subcostal recessions, inflated chest
    - nasal flaring, head bobbing, tracheal tugging
    - abnormal airway noises: inspiratory crackles, expiratory wheeze, grunting, stridor
  4. ) Differential Diagnoses
    - pneumonia, croup, cystic fibrosis
    - heart failure, bronchitis
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6
Q

Sequelae of Bronchiolitis

Typical RSV/Bronchiolitis Course
Admission Criteria
Complications of Bronchiolitis

A
  1. ) Typical RSV/Bronchiolitis Course
    - usually starts as a URTI w/ coryzal sx then 50% get chest sx over the first 1-2 days after onset of coryzal sx
    - sx generally at their worst on day 3/4 and often last 7-10 days total and most fully recover within 2-3wks
    - can have a cough for up to 6 weeks and are more likely to have viral-induced wheeze during childhood
  2. ) Admission Criteria - managed at home unless:
    - aged < 3mths, clinical dehydration, RR >70, O2 <92%
    - signs of mod-severe respiratory distress, apnoeas
    - poor feeding: <75% of their normal milk intake
    - poor oral fluid intake: <50% of normal fluid intake
    - any pre-existing condition: prematurity, Downs, CF, congenital heart disease e.g. VSD
    - parents not confident in managing at home
  3. ) Complications of Bronchiolitis
    - bronchiolitis obliterans: airways become permanently damaged due to inflammation and fibrosis
    - respiratory failure, hypoxia, dehydration, fatigue
    - persistent cough or wheeze (very common, parents should be counselled that it can last for several weeks)
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7
Q

Management of Bronchiolitis

Admission Criteria
Supportive Management
Ventilatory Support
Palivizumab

A

1.) Supportive Management - only required for most
- adequate intake: PO/NG/IV depending on severity, avoid overfeeding as a full stomach restricts breathing
- supplementary O2: if the O2 sats remain below 92%
- nasal decongestion: NEB 3% saline or saline nasal drops or nasal suctioning, particularly prior to feeding
- ventilation is assessed using capillary blood gases: assess acidosis
- other investigations: nasopharyngeal aspirate or throat swab for RSV rapid testing and viral cultures, FBC, blood/urine culture if pyrexic, CXR

  1. ) Ventilatory Support - used when a child is exhausted and needs support to maintain their breathing, this is stepped up until they are adequately ventilated:
    - Positive End-Expiratory Pressure (PEEP): helps maintain airways after expiration, high-flow humidified O2 via a nasal cannula to deliver continuous air+O2 w/ some pressure to prevent the airway collapse
    - CPAP: similar to ^^ but can deliver higher pressures
    - intubation and ventilation: inset ET tube into trachea
  2. ) Palivizumab - MAB that targets the RSV virus
    - a monthly injection is given as prevention to high-risk babies: ex-premature, congenital heart disease
    - not a true vaccine as it only provides passive protection until the virus is encountered
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8
Q

Croup (acute laryngotracheobronchitis)

Pathophysiology
Clinical Features
Severities of Croup
Differential Diagnoses

A
  1. ) Pathophysiology - viral URTI –> inflammation in the mucosa anywhere between the nose and trachea
    - barking cough: impaired movement of the VCs
    - causative organisms inc: parainfluenza (common), RSV, adenovirus, rhinovirus, influenza, measles
    - peak incidence at 2yrs but range is 3mths to 3yrs
    - risk factors: male, genetics (specific gene variant)
  2. ) Clinical Features
    - hx of a 1-4 day non-specific cough, rhinorrhoea, mild fever, progressing to a barking cough & hoarseness
    - symptoms are often worse at night
    - signs: high-pitched stridor, normal/reduced chest sounds, signs of respiratory distress e.g. ↑RR, intercostal recession etc.
  3. ) Severities of Croup
    - mild: occasional barking cough, no audible stridor at rest, no suprasternal or intercostal recession, the child is happy and will drink, eat & play
    - moderate: frequent barking cough, audible stridor at rest, suprasternal and sternal wall retraction at rest, the child will still show interest in its surroundings
    - severe: marked sternal wall retractions, the child will appear distressed/agitated or lethargic or restless, tachycardia may occur if more severe obstructive symptoms are present which can result in hypoxemia
  4. ) Differential Diagnoses
    - epiglottitis: onset w/in hours, fever >38.5, can’t E+D, no barking cough, soft stridor, weak/silent voice,
    - acute anaphylaxis, angioedema,
    - bacterial tracheitis (high fever+HR), diphtheria
    - laryngomalacia, vocal cord paralysis
    - peritonsillar abscess, retropharyngeal abscess
    - inhaled foreign body or noxious substance
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9
Q

Management of Croup

Investigations
Management at Home
Admission Criteria
Treatment

A
  1. ) Investigations - CLINICAL DIAGNOSIS
    - additional tests can make the child more distressed
    - do not examine the throat due to risk of obstruction
    - bloods: FBC, CRP, U&Es
    - CXR: to identify other possible causes (foreign body)
    - laryngoscopy if the illness is atypical or another cause of airway obstruction is suspected
  2. ) Management at Home - most kids with mild croup
    - sx usually resolve w/in 48hrs but may last 1 week
    - explain no abx needed as it’s a viral illness
    - paracetamol/ibuprofen to control pain and fever
    - ensure that the child has an adequate fluid intake
    - avoid infection spread: hand washing, no school
    - safety netting: worsening, intermittent stridor at rest, high fever, high HR, signs of respiratory failure
  3. ) Admission Criteria
    - mod/severe croup or impending respiratory failure
    - hx of severe airway obstruction, <6 months of age
    - inadequate fluid intake, poor response to initial tx
    - uncertain diagnosis, immunocompromised
    - suspect serious differential: peritonsillar abscess, laryngeal diphtheria, foreign body, angioedema
    - there is significant parental anxiety
  4. ) Treatment
    - 1 dose of PO dexamethasone (0.15mg/kg) OR pred
    - O2 as required, steam inhalation is not advised
    - NEB adrenaline/budesonide for temporary relief of sx in severe croup
    - keep the child calm as continuing crying increases oxygen demand & causes respiratory muscle fatigue
    - call ENT/anaesthetist if airway support is needed (I+V)
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10
Q

Epiglottitis

Pathophysiology
Aetiology
Clinical Features
Differential Diagnoses

A
  1. ) Pathophysiology - inflammation of the epiglottis leading to an airway obstruction (life-threatening)
    - VCs have a tightly bound epithelium which restricts the progression of swelling –> ↑pressure in small area
    - children are more at risk as their tongue is larger and epiglottis is more floppy, broader, longer and angled more obliquely to the trachea
  2. ) Aetiology
    - bacterial: H. influenza (main), S. pneumoniae, group A/C strep, S.aureus, and other respiratory bacteria
    - viral: HSV, parainfluenza, VZV, HIV, EBV
    - candida or aspergillus in immunocompromised
    - non-infective: trauma, thermal/chemical injury
    - risk factors: unvaccinated from HiB (must have high suspicion) male, immunocompromised
  3. ) Clinical Features
    - 4Ds: dyspnoea, dysphagia, drooling, dysphonia
    - onset is within hours and children appear toxic with a high-grade fever, sore throat and dehydration
    - sx last <12hrs, no cough, soft inspiratory stridor and a muffled voice
    - tripod position: leans forward on outstretched arms with neck extended and tongue out (to open airway)
  4. ) Differential Diagnoses
    - croup, inhaled foreign body, retropharyngeal abscess
    - tonsillitis/peritonsillar abscess, diphtheria
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11
Q

Management of Epiglottitis

General Management
Investigations
Management
Complications and Prognosis

A
  1. ) General Management
    - avoid unnecessary observations or examinations as agitation increases the risk of airway obstruction
    - secure airway before any further investigations
    - maintain a calm environment, keep with their parents
    - avoid supine position, visualise epiglottis in theatre
    - intubation equipment should always be kept nearby
  2. ) Investigations
    - throat swabs: bacterial and viral swabs taken on intubation to aid diagnosis and management
    - bloods (once airway secured): FBC, cultures, CRP
    - lateral neck X-Ray (used to exclude not diagnose): thumb-print sign (swollen epiglottis, thickened aryepiglottic folds, ↑opacity of the larynx and VCs
    - CT/MRI: if patient isn’t responding to initial therapy
  3. ) Management - step by step actions:
    - secure the airway: call anaesthetist or ENT registrar
    - oxygen: parent can hold the mask near child’s face
    - NEB adrenaline: ↓oedema of upper airway mucosa, used whilst awaiting definitive airway management
    - IV Abx: cefotaxime/ceftriaxone (cover H.influenzae), can convert to oral once stable and extubated
    - IV steroids: reduces supraglottic inflammation
    - resus+maintenance: keep NBM until airway improves
  4. ) Complications - epiglottic abscess
    - mediastinitis: if the infection spreads to the retro-pharyngeal space (rare but severe with 50% mortality)
    - DNSI: para/retropharyngeal cellulitis/abscess
    - pneumonia: especially following intubation
    - meningitis: complication in any HiB infection
    - sepsis/bacteraemia, death (now rare)
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12
Q

Whooping Cough (Bordetella Pertussis)

Pathophysiology
Vaccination
Clinical Features
Differential Diagnoses

A
  1. ) Pathophysiology - URTI caused by a g-ve bacillus that impairs the clearance of resp secretions
    - attaches to the resp epithelium and produce toxins that paralyse the cilia and promote inflammation
    - highly contagious (up to 90% of household contacts), spread via aerosolised droplets from coughing
    - more common in >15s but ↑mortality in infants
    - risk factors: non-vaccination and infection exposure
  2. ) Vaccination
    - pertussis vaccine is given at 2/3/4mths then a booster at 3yrs and 4mths, the immunity lasts 5-10 years
    - vaccination of pregnant women provides passive immunity in the first few months of life
  3. ) Clinical Features
    - catarrhal phase w/ mild coryzal sx followed by the paroxysmal severe coughing episode phase and then the convalescent phase where the cough reduces
  4. ) Differential Diagnoses
    - bronchiolitis/viral respiratory infection
    - pneumonia: bacterial/viral/mycoplasma
    - asthma, tuberculosis
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13
Q

Clinical Features/Phases of Whooping Cough

Catarrhal Phase
Paroxysmal Phase
Convalescent Phase

A
  1. ) Catarrhal Phase - lasts 1 to 2 weeks
    - sx: low-grade fever, dry cough, sore throat, irritability, rhinitis, conjunctivitis
    - general URTI sx means it’s rarely diagnosed at this stage
  2. ) Paroxysmal Phase - lasts for 2 to 8 weeks
    - recurrent episodes of severe coughing followed by an inspiratory gasp producing the ‘whoop’ sound
    - coughing episodes are worse at night, often followed by vomiting and may cause cyanosis (if severe)
    - examination: low-grade fever, facial petechiae and conjunctival haemorrhages may be present due to vigorous coughing, chest auscultation is usually normal
  3. ) Convalescent Phase - can last up to 3 months
    - cough gradually decreases in frequency and severity
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14
Q

Management of Whooping Cough

Investigations
Admission Criteria
General Management 
Management
Complications
A
  1. ) Investigations
    - nasopharyngeal swab/aspirate if cough is < 2wks
    - anti-pertussis toxin IgG serology if cough is >2wks and the child is <5yrs (vaccine can produce false +ve)
    - anti-pertussis toxin detection in oral fluid if 5-17yrs
    - FBC: lymphocytosis (+/- elevated white cell count)
  2. ) Admission Criteria
    - under 6 months of age and acutely unwell
    - significant breathing difficulties: respiratory distress, apnoeic episodes, cyanosis, severe coughing
    - feeding difficulties
    - complications: pneumonia, seizures
  3. ) General Management
    - a notifiable disease so must inform Public Health
    - advise cough can take up to 3mths to resolve and safety netting for complications
    - avoid school until they have had the cough for 21 days or have had antibiotics for 5 days

3.) Management - macrolides
- clarithromycin (<1mth), or azithromycin (if >1mth)
- Co-trimoxazole if macrolides are contra-indicated
- antibiotics can reduce the period of infectivity if given early (duration of cough is less than 21 days)
- supportive: paracetamol +/- ibuprofen, fluid intake
- prophylactic abx for vulnerable close contacts:
pregnant women, unvaccinated infants or healthcare workers w/ contact with children or pregnant women

  1. ) Complications
    - bacterial pneumonia, bronchiectasis, otitis media
    - seizures, encephalopathy (rare)
    - worse prognosis in unvaccinated young infants
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