CF
Around the bed:
- Medications (Creon tablets, nebuliser equipment, antibiotics, overnight NG feeds, laxatives)
- Sputum pots
From the end of the bed with top off/open:
- Small for age
- PICC/Portacath/Hickmann
- PEG/gastrosomy
- Old well healed abdominal scars (think about previous intestinal obstruction or meconium ileus)
- Ask patient to COUGH and then HUFF (huffing is important – if they know what that means then you know you’re on to the right diagnosis as the patient must have some form of bronchiectasis to know what this is)
Systematically examining child:
- Clubbing
- Scars on hand and ACF
- Neck scars
- Mouth/nose – look for polyps
- Chest – first check where the apex beat is – DO NOT MISS KARTAGENERS SYNDROME!! Adequate chest expansion, ausculation – bibasal crepitations occasional wheeze, productive cough, may have some dulness in bases
- Abdomen – looking for gastostomy, scars, liver size
To complete examination
- Plot height and weight, examine anal passage for polyps, review recent CXR, sputum cultures
Asthma
Around the bed:
- Inhalers, spacers, nebuliser equipment, peak flow meters
From the end of the bed, inspect child with top off:
- Are they comfortable? signs of respiratory distress-check respiratory rate, attached to sats monitor?
- Harrisons’s sulcus
- Signs of long term steroid use (Cushing’s syndrome)
- Small for age (is there nutritional compromise)
Examining the patient:
- Hands and arms -scars from previous cannulas, signs of eczema
- Face – check mouth – signs of candida from poor inhalation technique of steroids)
- Chest – tracheal position, check where apex beat is, expansion (may be hyperinflated), auscultation – clear or may have scattered wheeze if recovering from acute deterioration (don’t just say ‘wheeze’ – is this just expiratory is there a prolonged expiratory phase, is it low pitched, high pitched and is it polyphonic in nature). Chest expansion and auscultate on posterior as well as anterior chest.
To complete examination:
- Growth chart, peak flow record (if >5yrs), review medications, review recent CXR, review history for atopy
Kartageners
As for CF but important to note following differences:
- Check apex beat!!!
- Check side of liver (to confirm that this isn’t a case of situs invertus with CF – rare but potentially possible!)
Chronic lung disease
Around the bed:
- Home oxygen, nasal cannulae, inhalers, spacer (especially if aged 3-5yrs – may have been an ex-prem who now has frequent viral induced wheeze episodes)
From the end of the bed:
- Child <18 months with nasal cannulae
- +/-Soft subcostal recessions
- Signs of being ex-prem (may be small considering the age given), abdominal scars following NEC
Examining the child:
- Multiple scars on the hand from cannulas whilst on NICU
- Bruising (if on steroids)
- Round face (long term steroid use)
- Plagiocephaly
- Nasal cannulae in situ
- Chest – equal air entry, may be generally reduced or a little quiet, no wheeze unless intercurrent illness
To complete the examination
- Plot height and weight, review oxygen requirement/night time oxygen requirement, review medications, review CXR, developmental examination, check glucose levels ( if signs of Cushing’s syndrome)
TOF
From the end of the bed:
- Well looking child, usually without any signs of respiratory distress
- ALWAYS, ALWAYS ALWAYS ask patients to put hands on hips and really check the axillary regions so you don’t miss a scar
- Is there an additional scar on the left side of the praecordium. This can be due to aortopexy following the initial TF repair. If there is a scar, then check the radial pulses bilaterally! The aortopexy will often reduce blood flow to the left radial artery.
- The most important aspect of this exam is to ASK THE PATIENT TO COUGH! You’ll hear a harsh, grunting-like cough, which is caused from the collapse of the non-cartilage containing part of the trachea formed following repair of the TOF
- Any other thoracic/abdominal scars
Examining the child:
- Usually very well looking
- Hands – may have healed scar marks
- Neck – central line scars
- Face – +/-syndromic
- Chest – scar in either right or left axillary region, equal chest expansion, equal air entry, normal vesicular breath sounds, resonant percussion note
To complete your examination
- Plot height and weight, oxygen sats, review recent CXR
- Ask about the neonatal period (taken immediately to NICU), discovered during infancy following recurrent aspiration
Thoracotomy scars
Around the end of the bed:
- Inhalers, nebulisers, supplemental oxygen
Looking at the patient from the end of the bed:
- Pink or cyanosed? midline sternotomy scars (need to think about whether this is a BT shunt scar), stats probe attached (may have sats target of around 75% if palliative procedure for hypoplastic left/right heart)
- Appears syndromic?
- Ask patient to put hands on hips before examining to make sure you don’t miss scar in axilla skin fold
- Ask patient to cough (TOF cough)
Examining the patient:
- Hands – assess for clubbing, peripheral cyanosis, small scars on hands
- Check radial pulse bilaterally, may be absent on side of BT repair (unless a modified BT shunt in which case the pulse is usually still present)
- Neck – scars from central lines
- Face – syndromic appearance? central cyanosis
- Praecordium – midline sternotomy, axillary scars, posteriolateral thoracotomy scars (pneumonectomy following unilateral lung disease/lobar emphysema/CCAM)
- Listen for a murmur – may be part of staged palliative repair and therefore child has had a BT shunt inserted. Note if a BT shunt, then usually a continuous mumrur will be heard under either the right of left clavicle depending on side or surgery
- Air entry usually vesicular, but may be reduced depending on extent of lung removal)
- Abdomen – feel for hepatomegly (especially if there is pulmonary fibrosis or element of cardiac failure)
To complete your examination
- Growth charts, observations (RR, saturations and BP), review recent CXR or HRCT if one has been performed, review medications (are they on immunosuppressants for pulmonary fibrosis), full neonatal history



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