Category: Paeds

Brief Resolved Unexplained Event (BRUE)

Brief Resolved Unexplained Event (BRUE) is now the recommended term for ALTE (Apparent Life Threatening Event).

Definition:

BRUE is defined as an episode in an infant less than 12 months old characterized by: 

  • < 1 minute duration (typically 20-30s)
  • Followed by return to baseline state
  • Not explained by identifiable medical conditions

Includes one or more of the following:  

  • Central cyanosis/pallor
  • Absent, decreased or irregular breathing
  • Marked change in tone (hyper or hypotonia)
  • Altered level of consciousness

Read more

EMBRACE & Paediatric Critical Care

In our trust we don’t have paediatric critical care beds. However, in our region we use EMBRACE (a paediatric critical care transport team), who can transfer critically  ill children to specialist centers (in or out of region).

EMBRACE

Y&H Paed Critical Care

Drugs:

  • Trust guide
  • Remember: Midazolam 10mg/2ml is used(not the 5mg/5ml we have  in ED)

 

Limping Child

This is a relatively common  presentation within the ED that has a myriad of possible diagnoses ranging from sprain to malignancy. One thing to remember is that patients and relatives will look for a traumatic reason for limb pain, and may link it to minor injuries that would not have caused it.  Read more

Paediatric Asthma / Wheeze Guideline for over 1s

Severity Assessment

Asthma and Wheeze-2 (4)

Life threatening Asthma (1)

Inital Therapy

  1. Administer oxygen to maintain SpO₂ >94%.
  2. Nebulised Salbutamol:
    • <5 years: 2.5 mg
    • ≥5 years: 5 mg
  3. Nebulised Ipratropium Bromide:
    • <12 years: 250 micrograms
    • ≥12 years: 500 micrograms
  4. Steroids: (Oral Prednisolone)
    • <2 years – 10mg
    • 2-5 years – 20mg
    • >5 years – 30-40mg
    • ≥12 years: 40–50 mg daily for 3–5 days
    • Needs to be given within 1 hour of admission
    • If oral route not tolerated: IV Hydrocortisone 4 mg/kg QDS (max 100 mg)
  5. Reassess after initial treatment.

Escalate care if poor response: IV access, VBG, U&E, theophylline level if relevant.

Nebulised magnesium sulphate can be considered in severe asthma attacks at 150mcg per administration and is added to the salbutamol and ipratropium inhalers. It should not be used under 2 years and should not delay escalation to IV therapy if required.

Second-Line Management – Paediatric Senior must be involved

Any patient needing or may need second line management should be discussed with the Paediatric team. All such patients after stabilisation will need admission or a period of observation in SDEC/Children’s ward.

Be mindful of next steps – do you need anaesthetic support.

IV Magnesium Sulfate:

  • 40 mg/kg (max 2 g) over 20 minutes
  • Use separate IV line from salbutamol/aminophylline
  • Adverse effects – Bradycardia and Hypotension.
  • Monitor HR, BP every 15 mins.
  • Contraindicated in renal failure and heart block

IV Aminophylline:

  • Loading dose: 5 mg/kg over 20 mins (omit if on theophylline)
    Infusion: 1–12 yrs: 1 mg/kg/hr, ≥12 yrs: 0.5–0.7 mg/kg/hr
  • Should be nursed in Enhance Care Area
  • Monitor theophylline levels 4-6 hours after starting treatment (target 10–20 mg/L)
  • Adjust IV fluids to account for infusion volume
  • IV Aminophylline is compatible with fluids containing potassium.
  • IV Aminophylline is NOT COMPATIBLE to run in the same line as IV Salbutamol.
  • Dose should be calculated on the basis of ideal weight for height in obese patients to avoid toxicity.  Ideal weight can be inferred from the height centile using a standard WHO growth chart  (Moore’s method) – Check height centile on growth chart – check corresponding weight for that centile and age and use this weight – more information can be found at: UKMIQA-drug-dosing-in-childhood-obesity.pdf .
  • If no height is available then the approximate weights can be used in the BNF online ‘Approximate Conversions and Units’ section
  • For further information please see CHFT guideline – ‘Guidance For Use of Aminophylline Infusion 1mg/1ml In Children’

IV Salbutamol:

  • Inform the on-call consultant if IV Salbutamol is being started.
  • Continue mixed nebulisers (Salbutamol/Ipratropium) every 30-60 minutes for first 2-3 hours.
  • Loading dose:
    • <2 years: 5mcg/kg over 5 mins
    • 2-18 year: 15 mcg/kg (max 250 mcg) over 5 mins and reassess. Dose to be calculated on actual body weight.
    • Infusion: 1–5 mcg/kg/min

Discuss with Embrace/PICU if >2 mcg/kg/min required

  • Consider chest X-Ray if on IV Salbutamol.
  • Close monitoring of Heart rate and Blood pressure is needed.
  • Monitor potassium on U+E/Blood gas
  • Watch for lactic acidosis

Oxygen and Vapotherm

  • Maintain saturation >94%
  • If deterioration despite second line measures Nasal High Flow Oxygen can be considered but this is a consultant decision – evidence base is limited for High Flow in asthma.
  • Acute Asthma patients on high flow need to be monitored carefully for deterioration, pneumothorax and/or air trapping
  • CXR should be performed for any children/young people managed on high flow
  • Administer nebulisers via Aerogen chamber

Monitoring

  • All patients who need IV treatment should be on continuous cardiac monitoring.
  • Observations: BP every 15 mins (1st hr), then 30 mins, then hourly if stable
  • Clinical review every 30 mins for first 2 hrs
  • U&E and glucose at the start and every 6 hours on IV therapy- Hypokalaemia and Hyperglycaemia are common side effects on treatment with Salbutamol.
  • Blood gases as clinically indicated– beware of lactic acidosis with prolonged use Salbutamol (both nebulized and IV treatment).
  • Theophylline level 4–6 hours after infusion start (Target level between 10 – 15 mg/L).

Special Considerations

SVT with beta-agonists:

  • Stop IV salbutamol if SVT suspected
  • Alert senior staff, inform on-call consultant – Anaesthetics and ICU presence to be considered early.
  • Attempt vagal manoeuvres
  • Ensure has two sites of IV access.
  • DC cardioversion under sedation (Propofol has bronchodilator effect, to be guided by the anaesthetics/ICU team) if needed- 1st shock: 1 J/kg – if needed 2nd shock: 2 J/kg

Adenosine is contraindicated in life-threatening asthma as Adenosine causes bronchoconstriction, worsen inflammation and increases airway plasma exudation.

 

Observe in-hospital for at least 24 hours after IVs have been stopped due to the risk of rebound

 

Discharge checklist:

  • Normal HR, RR
  • Off oxygen ≥6 hrs
  • Sustained good response to inhaled Bronchodilator – on pMDI and spaced to at least 4 hours between inhalers and needing 6 puffs or less.
  • After discharge do not recommend regular salbutamol puffs (weaning plan), instead advise use of salbutamol or MART inhaler doses as required and as per PAAP (Personalised Asthma Action Plan) – these are available on the ward or on the childrens’ drive for both MART and salbutamol.

For those on MART regime:

  • Once ready to space to 6 puffs 4 hourly Salbutamol – give 1 puff of Symbicort (MART reliever dose), then observe for 4 hours – if the child/young person remains well they can be discharged home with use of Symbicort as required as per their MART PAAP.

 

Follow Up:

  • Any child/young person with >1 admission for wheeze should be followed up in clinic
  • If known asthma please message Dr Houston on EPR for asthma clinic follow up
  • If recurrent viral wheeze picture follow up in general paediatric clinic

Trust Guide Here

Paediatric ECG

Use the following chart as a quick checklist to review what’s normal and what’s not in a paediatric ECG. 

Remember:

  • Lead V4R in under5’s
  • Manually calculate QTc
  • WPW needs referral for ablation – increase risk of sudden death

If in any doubt discuss with paediatric registrar/senior. If in need of urgent interven:on then contact the paediatric cardiology team in LGI.

This website interpretation tool makes this even easier!

1. Placement of Leads: Precordial Leads

In young children, the right ventricle normally extends to the right side of the sternum. To appropriately display right ventricular potentials, ECGs for children in the under five-year age group must include an alternate lead (‘V4R’) on the right side of the chest at a point analogous to the left sided V4.

2. P Waves:

3. Axis:

In utero- high pulmonary pressures and a relatively thick Right Ventricle (RV) -> Initial Right Axis on ECG is normal and resolves after the first 6 months of life

QRS Axis Deviation

  • Chest leads in wrong position

     

RAD:

  • Newborns
  • RVH secondary to Right ventricular outflow tract obstruction eg: Pulmonary
    Stenosis ,Tetralogy Of Fallot, Noonans (characterized by mildly unusual facial features, short stature, heart defects, bleeding problems, skeletal malformations, and many others)
  • RBBB

 

LAD:

  • LBBB
  • LVH secondary to LVOTO (Left Ventricular Outflow Tract Obstruction) e.g. Aortic Stenosis, HOCM

 

Superior Axis

  • AVSD (Atrio ventricular septal defect – Trisomy 21)
4. QTc:
  • Infants less than 6 months = < 0.49 seconds.
  • Older than 6 months = < 0.44 seconds.

QTc is prolonged in:

  • Hypocalcaemia
  • Myocarditis
  • Long QT syndromes such as Romano-Ward Drugs

QTc is short in:

  • Hypercalcaemia
  • Congenital short QT syndrome
5. Ventricular Hypertrophy

6. T waves:
  • The precordial T-wave configuration changes over time
  • For the first week of life, T waves are upright throughout the precordial leads.
  • After the first week, the T waves become inverted in V1-3 (= the “juvenile T-wave pattern”)
  • This T-wave inversion usually remains until ~ age 8; thereafter the T waves become upright in V1-3.
  • However, the juvenile T-wave pattern can persist into adolescence and early adulthood (= “persistent juvenile T waves”).

Tall, peaked T waves are seen in:

Hyperkalaemia, Dilated LV (volume overload), Benign early repolarisation

 

Flat T waves are seen in:

Normal newborns, Hypothyroidism, Hypokalaemia, Pericarditis, Myocarditis

7. ST Segment:

Some ST changes may be normal:

  • Limb lead ST depression or elevation of up to 1mm (up to 2mm in the left precordial leads).

  • J-point depression: the J point is depressed without sustained ST depression, i.e. upsloping ST depression

  • Benign early repolarisation in adolescents: the ST segment is elevated and concave in leads with an upright T wave.

 

 

Others are pathological:

  • A downward slope of the ST followed by a inverted T.

  • A sustained horizontal ST segment depression

     

 

Pathological ST segment changes are commonly associated with T wave changes and occur in:

  • Pericarditis.

  • Myocardial ischaemia or infarction.

  • Severe ventricular hypertrophy (ventricular strain pattern)

Thanks to the paediatric dept for supplying the guidance –  trust PDF here