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Position Statement

Paediatric advanced life support
The Australian Resuscitation Council Guidelines

The Advanced Life Support Committee of the Australian Resuscitation Council

MJA 1996; 165: 199-206

Basic cardiorespiratory resuscitation - Advanced life support - Techniques in paediatric advanced life support - Medications and fluids used in paediatric advanced life support - Management after resuscitation - Cessation of cardiopulmonary resuscitation - Contributors - References - Register to be notified of new articles by email - Current contents list

These guidelines by the Australian Resuscitation Council (ARC) provide brief step-by-step outlines of the management of common life-threatening emergencies in infants and children. The guidelines are similar, but not identical, to guidelines published by the American Heart Association 1 and the European Resuscitation Council. 2 An international liaison committee (including representation from the ARC) is attempting to resolve differences and will in due course publish common advisory statements.

The current guidelines are specifically for advanced life support, but some essential techniques of basic life support are presented. Further details of basic life support for infants and children 3 and specific guidelines for resuscitation of asphyxiated newborn infants have been published. 4,5


Basic cardiorespiratory resuscitation

Cardiorespiratory arrest should be suspected when the infant or child loses consciousness, appears pale or cyanosed, or is apnoeic or pulseless (see definitions in Box 1).

Assess airway and breathing by observing movement of the chest and feeling for expired breath. Position the head and neck to maintain an open airway. Movement of the chest without expiration implies an obstructed airway. If the obstruction is not relieved by backward head tilt and chin lift or by forward jaw thrust, the pharynx should be inspected with a laryngoscope and cleared of any secretions, vomitus or blood with a sucker (Yankauer). Forceps (Magill) may be needed to extract a foreign body. If spontaneous ventilation is not immediately resumed, artificial ventilation is commenced with mouth-to-mask expired air, a self-inflating resuscitation bag or an oxygen-inflated bag and mask circuit. Supplemental 100% oxygen should be added. Insertion of an oropharyngeal airway (Guedel) may facilitate ventilation.

Assess the circulation by palpating the carotid, brachial or femoral pulse. Commence external cardiac compression (ECC) if a pulse is not palpable or it is:

  • < 80 beats per minute (bpm) in a newborn or infant;
  • < 60 bpm in a small child;
  • < 40 bpm in a large child.

Precede ECC with 2-5 slow breaths to reinflate the lungs. The patient should be placed on a firm surface, and compression directed to the lower sternum to a depth approximating a third of the anteroposterior diameter of the chest, or at a

  • depth of 2-3 cm and rate of 100/min for a newborn or infant;
  • depth of 3-4 cm and rate of 100/min for a small child;
  • depth of 4-5 cm and rate of 80-100/min for a large child.

ECC for a newborn or infant can be performed with two fingers, although a better technique is to encircle the chest with both hands, compressing the sternum anteriorly with the thumbs while stabilising the vertebral column posteriorly with the fingers. The rescuer's hands must encircle the chest freely and not restrict chest expansion. ECC for a small child can be performed with the heel of one hand and, for a large child or teenager, with two hands. A cycle should be 50% chest compression and 50% relaxation.

Combine ECC and assisted ventilation in an infant or small child in a ratio of 5 : 1. For a large child or teenager in whom a two-handed technique of ECC is required, a single rescuer may achieve better circulation and ventilation with a ratio of compression to ventilation of 15 : 2. If a mask is used, breaths should be delivered between successive compressions to allow adequate expansion of the lungs, but if an endotracheal tube is used coordination is less crucial as effective ventilation can be given against the resistance imposed by ECC. For the asphyxiated newborn, ECC should be at a rate of 120/minute and ventilation at 40-60/min (i.e., in a ratio of 3 : 1). 5,6


Advanced life support

Advanced life support implies a patent airway by endotracheal intubation, mechanical ventilation with oxygen, the treatment of cardiac arrhythmias, the treatment of the cause of cardiorespiratory arrest and of complications arising from its management.

When several rescuers are in attendance, tracheal intubation and ventilation, display of the electrocardiograph (ECG) and access to the circulation should be attempted simultaneously. Thereafter treatment should be guided by the cardiac rhythm (see Flowchart in Box 2).

Tracheal intubation is the first priority. This establishes and maintains a patent airway, facilitates mechanical ventilation with 100% oxygen, minimises pulmonary aspiration, enables suctioning of the trachea and provides a route for the administration of selected drugs. If intubation cannot be accomplished easily, ventilate and oxygenate the patient using a mask before reattempting intubation.

Assess the cardiac rhythm by displaying the ECG via chest leads or the defibrillator paddles. Proceed with drug therapy or immediate direct current (DC) shock (Box 2), while maintaining ECC and mechanical ventilation with supplemental 100% oxygen.

Secure access to the circulation with a peripheral intravenous (IV) cannula. If cannulation is difficult, do not waste time (more than 90 seconds) with repeated unsuccessful attempts -- instead use the intraosseous (IO) route or the (less effective) respiratory tract via the endotracheal tube (ETT). 7 All drugs and resuscitative fluids may be given via the IO route but only adrenaline, atropine and lignocaine may be given via the ETT. Central venous cannulation of the subclavian or internal jugular veins should not be attempted initially as it wastes time and is potentially hazardous. However, cannulation of an external jugular or femoral vein may be easily accomplished. Surgical cutdown onto a vein may be required. Intracardiac injection should not be attempted unless all alternative methods of access to the circulation are impossible.

The doses of drugs, DC shock and fluid therapy are based on body weight, which may be estimated according to age if the weight is unknown:

  • Newborn: 3.5 kg
  • 1 year: 10 kg
  • 1-9 years: (age in years x 2) + 8 kg
  • 10 years and over: age in years x 3.3 kg.

Doses may also be prescribed on the basis of height. 8,9 Drug doses according to the 50th percentiles of weight and height for age are given in Box 3.

Asystole or severe bradycardia
If the cardiac rate is unresponsive to ventilation with 100% oxygen, asystole or pulseless severe bradycardia ( < 80 bpm in an infant, < 60 bpm in a small child, < 40 bpm in a large child or teenager) should be treated with adrenaline (10 µg/kg IV or IO, or 100 µg/kg via the ETT). The subsequent dose of adrenaline by any route is up to 100 µg/kg. If sinus rhythm cannot be restored, sodium bicarbonate (1 mmol/kg IV or IO) and/or atropine (20 µg/kg IV, IO or ETT), with additional doses of adrenaline, may be successful. If facilities are available, cardiac pacing (via the oesophageal, transcutaneous, transvenous or epicardial routes) may be effective.

Ventricular fibrillation and pulseless ventricular tachycardia
The only effective treatment of ventricular fibrillation (VF) or pulseless ventricular tachycardia (VT) is DC shock. If the onset of VF is recent or is observed, a precordial thump may be given (although its efficacy has not been proven) and defibrillation should be attempted before any other treatment.

The initial DC shock treatment of VF or pulseless VT is 2 J/kg, increasing to a maximum of 4 J/kg 10,11 in a series of three shocks. If sinus rhythm does not occur, give adrenaline (10 µg/kg IV or IO, or 100 µg/kg ETT) and a further three shocks of 4 J/kg. Persistent or refractory VF or VT may be treated with lignocaine (1 mg/kg IV, IO or ETT) followed by another series of up to three shocks of 4 J/kg. If the VF or VT remains refractory, alternative agents (bretylium tosylate 5 mg/kg, sodium bicarbonate 1 mmol/kg, magnesium sulfate 0.05-0.1 mmol/kg) may be tried, in combination with adrenaline (100 µg/kg IV, IO or ETT) and a series of three shocks of 4 J/kg. However, no drug has been conclusively proven to improve the efficacy of DC shock.

Electromechanical dissociation (pulseless electrical activity)
Electromechanical dissociation exists if pulses are absent despite relatively normal coordinated electrical activity on the ECG. It may be due to poor intrinsic myocardial contractility or secondary to a number of remediable causes, including hypoxaemia, hypovolaemia, severe acidosis, tension pneumothorax, pericardial tamponade, hyperkalaemia, hypocalcaemia, poisoning with a calcium channel blocker or hypothermia. It may also be due to massive pulmonary embolism.

Treatment is with adrenaline, 10 µg/kg IV or IO or 100 µg/kg ETT initially, with subsequent doses up to 100 µg/kg by any route. If the electromechanical dissociation is persistent, consider hypovolaemia or severe acidosis and give a bolus of crystalloid or colloid fluid (20 mL/kg IV or IO) and/or sodium bicarbonate (1 mmol/kg). An underlying cause should be sought by clinical examination and investigations, including a chest x-ray, 12-lead ECG and echocardiograph if possible.

Supraventricular tachycardia
Supraventricular tachycardia (SVT) may cause severe hypotension or pulselessness. Synchronised DC shock (0.5-1 J/kg) should be given immediately to a pulseless patient. If blood pressure is adequate, vagal stimulation or drug therapy may be used. Adenosine is the drug of first choice. Alternatives are digoxin, a beta-blocker or a calcium channel blocker. Calcium channel blockers should not be used to treat SVT in infants because their negative inotropic effect may be fatal.

Techniques in Paediatric advanced life support are given in Box 4.

Medications and fluids used in paediatric advanced life support are summarised in Box 5.



Management after resuscitation
The cause of cardiorespiratory arrest should be sought and specifically treated. Complications of the resuscitation procedure should also be sought, especially if secondary deterioration occurs. This includes a chest x-ray to check the position of the endotracheal tube, to exclude pneumothorax, lung collapse or aspiration and to check the cardiac silhouette, and a blood sample for estimation of the haemoglobin level, pH, gas tensions and electrolyte and glucose concentrations.

Supportive therapy should be provided until there is recovery of function of vital organs. This may include oxygen therapy, mechanical ventilation, inotropic infusion and renal support for several days or longer. Recovery in infants and children is usually slow because cardiorespiratory arrest is often secondary to prolonged global hypoxaemia and ischaemia with prior damage of other organs. Particular care should be taken to ensure adequate cerebral perfusion with well oxygenated blood and adequate blood pressure.



Cessation of cardiopulmonary resuscitation
The decision to cease cardiopulmonary resuscitation should be based on a number of factors, including the patient's pre-arrest condition, response to resuscitation, remediable factors, likely outcome and the opinions of experienced medical personnel.


References
  1. Emergency Cardiac Care Committee and Subcommittees of the American Heart Association. Guidelines for cardiopulmonary resuscitation and emergency cardiac care. JAMA 1992; 268: 2171-2302.
  2. Paediatric Life Support Working Party of the European Resuscitation Council. Guidelines for paediatric life support. BMJ 1994; 308: 1349-1355.
  3. Manual Australian Resuscitation Council. Policy Statements. Policies 12.1-12.9, November 1995. (Located at the Royal Australasian College of Surgeons, Spring Street, Melbourne.)
  4. Emergency Cardiac Care Committee and Subcommittee of the American Heart Association. Guidelines for cardio resuscitation and emergency cardiac care. JAMA 1992; 268: 2276-2281.
  5. Roy RN, Betheras FR. The Melbourne chart -- a logical guide to neonatal resuscitation. Anaesth Intens Care 1990; 18: 348-357.
  6. The Advanced Life Support Committee of the Australian Resuscitation Council. Adult advanced life support. The Australian Resuscitation Council Guidelines. Med J Aust 1993; 159: 616-621.
  7. Tibballs J. Endotracheal and intraosseous drug administration for paediatric CPR. Aust Fam Physician 1992; 21: 1477-1480.
  8. Lubitz SL, Seidel JS, Chameides L, et al. A rapid method for estimating weight and resuscitation drug dosages from length in the pediatric age group. Ann Emerg Med 1988; 17: 576-581.
  9. Oakley P, Phillips B, Molyneux E, Mackway-Jones K. Updated standard reference chart. BMJ 1993; 306: 1613.
  10. Chameides L, Brown GE, Raye JR, et al. Guidelines for defibrillation in infants and children. Report of the American Heart Association Target Activity Group: cardiopulmonary resuscitation in the young. Circulation 1977; 56 (suppl): 502A-503A.
  11. Gutgesell HP, Tacker HA, Geddes LA, et al. Energy dose for ventricular defibrillation of children. Pediatrics 1976; 58: 898-901.
  12. Rogers FB. Technical note: a quick and simple method of obtaining venous access in traumatic exsanguination. J Trauma 1993; 34: 142-143.
  13. Hornchen U, Schuttler J, Stoeckel H, et al. Endobronchial instillation of epinephrine during cardiopulmonary resuscitation. Crit Care Med 1987; 15: 1037-1039.
  14. Jasani MS, Nadkarni VM, Finkelstein MS, et al. Effects of different techniques of endotracheal epinephrine administration in pediatric porcine hypoxic-hypercarbic cardiopulmonary arrest. Crit Care Med 1994; 22: 1174-1180.
  15. Patterson M, Boenning D, Klein B. High dose epinephrine in pediatric cardiopulmonary arrest (CPA). Pediatric Emerg Care 1994; 10: 310.
  16. Goetting MG, Paradis NA. High-dose epinephrine improves outcome from pediatric cardiac arrest. Ann Emerg Med 1991; 20: 22-26.

Contributors This document was drafted and revised by Dr James Tibballs at the request of the Australian Resuscitation Council.

Submissions were received from members of the Advanced Life Support Committee of the ARC and from Dr R Henning, Dr F Shann, Ms S Kinney (Melbourne); Dr A Duncan (Perth); Dr J McEniery, Dr G Delbridge, Dr B Lister (Brisbane); Dr B Wilkins, Dr R Choong, Dr B Duffy, Dr T Gratten-Smith, Dr I Alexander, Dr M Schindler, Dr J Gillis, Dr A O'Connell, Dr D Schell, Dr O Miller (Sydney); Dr S R Keeley, Dr A J Slater, Dr G M Shaw, Dr J Raftos (Adelaide); Dr E R Segedin (Auckland); Dr L Quan (Seattle); and Dr D Zideman (London).

Members of the Advanced Life Support Committee:
Dr M Allen (ARC South Australian Branch).
Dr R A Capps (Australian Defence Force).
A/Prof V Callanan (ARC Chairman; and Australian and New Zealand College of Anaesthetists).
Ms J Dennett (Confederation of Australian Critical Care Nurses).
Mr M Draheim (ARC Tasmanian Branch).
Ms J Finn (Royal College of Nursing, Australia).
Dr L Grigg (Cardiac Society of Australia and New Zealand; and National Heart Foundation).
Mr A Hadj (Royal Australasian College of Surgeons).
Mr J Hall (Institute of Ambulance Officers, Australia).
Mr K Hambrecht (Co-opted member).
Prof G A Harrison (Chairman, ARC Advanced life Support Committee; and Australian and New Zealand College of Anaesthetists).
Dr I Jacobs (ARC Western Australian Branch).
Mr O Juul (ARC New South Wales Branch).
Mr S Leahy (Surf Lifesaving Association of Australia).
Ms J Maclean (Royal Lifesaving Society, Australia).
Dr P Morley (ARC Victorian Branch).
Dr J O'Callaghan (Co-opted member).
Dr A Phillips (Royal Australian College of General Practitioners).
Mr C Smith (ARC Queensland Branch).
Dr J Taylor (Co-opted member).
Dr J Tibballs (Australian and New Zealand Intensive Care Society).
Mrs E P Tyler (Australian Red Cross Society).
Dr J Wassertheil (Australasian College for Emergency Medicine).
Dr J Williamson (St John Ambulance Australia).

No reprints will be available.
Correspondence: Dr J Tibballs, Intensive Care Unit, Royal Children's Hospital, Flemington Road, Parkville, Melbourne, VIC 3052.

©MJA 1996


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4: Techniques in paediatric advanced life support

Endotracheal intubation

Select the correct size ETT and insert to the correct depth ( Boxes 3 and 4.1), to avoid accidental extubation or endobronchial intubation. Secure the tube with cotton tape tied around the neck or affix it to the face with adhesive tape.

Venous access
In newborns, scalp veins are accessible and the umbilical vein can be used up to about a week after birth. Cannulation of an external jugular vein is facilitated when the patient is intubated and the head is turned to the opposite side. Cannulation of the femoral vein is an option in the pulseless patient if bony landmarks are familiar. Surgical cutdown onto the long saphenous vein, saphenofemoral junction 12 or basilic vein is sometimes required in cases of traumatic exsanguination.

Intraosseous injection of drugs and infusion of fluids
Drugs injected into the bone marrow are distributed as fast and attain the same blood concentrations as if injected intravenously. Aspirated bone marrow may be used for biochemical and haematological analysis. Contraindications to the use of the IO route are local trauma or infection.

The upper or lower anteromedial surfaces of the tibia are suitable puncture sites. Insert a special intraosseous needle (a short lumbar puncture needle may suffice) perpendicularly to the bone surface, using a rotary action to traverse the cortex until a loss of resistance signals entry to the marrow. Confirm correct positioning of the needle by aspiration of bone marrow or injection of saline without extravasation. Any fluid may then be administered with the aid of gravity, or infused under pressure or with a syringe.

Endotracheal administration of drugs
The endotracheal route is an alternative for administration of adrenaline (Box 4.2), atropine and lignocaine, if intravenous or intraosseous access is not available; it may be the first route for drug administration at the start of resuscitation. Although these drugs are absorbed from the respiratory tree into the circulation, the optimum doses are unknown in humans (although in an animal model the dose was 10 times the standard intravenous dose). 13 Drugs should be injected directly into the endotracheal tube, or into the trachea beyond the tip of the endotracheal tube with the aid of a catheter or feeding tube, 14 and dispersed throughout the respiratory tract with vigorous bagging.
DC shock
Defibrillators for infants and small children should have paddles with cross-sectional areas of 12-20 cm 2 to allow full skin contact and to prevent physical contact between paddles when on the chest (adult-sized paddles are 50-80 cm 2 ). Variable energy levels should enable delivery of 1-4 J/kg. To deliver a shock, place one paddle in the middle of the left axilla opposite the xiphisternum or nipple, the other to the right of the upper sternum. Adequate conductive gel (confined to the area beneath the paddles) and firm pressure are required to deliver optimum energy through the heart and to avoid skin burns.

Rescuers should be prepared to deliver an uninterrupted series of up to three shocks by maintaining the paddles on the chest while the defibrillator is recharged. The series of three shocks decreases impedance and increases transit of energy through the heart. The dose for VF and pulseless VT is 2 J/kg progressing to a third dose of 4 J/kg (unsynchronised mode), and for SVT is 0.5-1 J/kg (synchronised mode). In the treatment of refractory arrhythmias, an anteroposterior position of the paddles (one over the cardiac apex, the other over the left scapula) may be more efficacious than the standard positions. Dextrocardia may be present in patients with congenital heart disease and the position of the paddles should be altered accordingly.

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5: Medications and fluids used in paediatric advanced life support

Adrenaline
Indications: Asystole, severe bradycardia, ventricular fibrillation and electromechanical dissociation.

Dose: 10 µg/kg IV or IO initially, up to 100 µg/kg subsequently. 15 Although controversial, doses of 200 µg/kg for children have been used with some success. 16 Instead of repeated bolus doses, a continuous venous infusion of approximately 0.1-1 µg/kg per min may be given. Although unproven, all endotracheal doses are 100 µg/kg.

Lignocaine
Indications: VF, VT, ventricular ectopy.

Dose: 1 mg/kg IV or IO or ETT initially. A subsequent infusion of 20-50 µg/kg per min may be used to suppress ventricular ectopy.

Sodium bicarbonate

Indications: Severe metabolic acidosis (pH < 7.1) or prolonged arrest.

Dose: 1 mmol/kg IV or IO after adequate ventilation with 100% oxygen and ECC have been established.

Atropine

Indications: Bradycardia initiated by vagal stimulation. (Bradycardia caused by hypoxaemia should be treated by ventilation with oxygen. Severe bradycardia with or without hypotension should be treated with oxygen and adrenaline.)

Dose: 20 µg/kg IV or IO.

Bretylium tosylate

Indications: Refractory VF or pulseless VT.

Dose: 5 mg/kg IV or IO initially, second dose 10 mg/kg.

Magnesium sulfate

Indications: VF and pulseless VT of any cause; hypomagnesaemia (which may cause life-threatening ventricular tachyarrhythmia, particularly when associated with hypokalaemia).

Dose: 0.05-0.1 mmol/kg IV or IO initially, followed by an infusion of 0.3 mmol/kg over 4 hours.

Potassium

Indications: Hypokalaemia (which may cause life-threatening tachyarrhythmia).

Dose: 0.03-0.07 mmol/kg of potassium chloride IV or IO by slow injection. An infusion of 0.2-0.5 mmol/kg per hour to a maximum of 1 mmol/kg may be required to correct deficiency states.

Calcium

Indications: Often used erroneously in cardiorespiratory resuscitation -- it has no place in the management of arrhythmias unless caused by hyperkalaemia, hypocalcaemia or hypermagnesaemia. It is an antidote to hypotension caused by a calcium channel blocker.

Dose: 0.2 mL/kg of 10% calcium chloride (20 mg/kg) or 0.65 mL/kg of 10% calcium gluconate.

Fluid therapy

Indications: Hypovolaemia; flushing drugs to ensure that they enter the circulation and do not precipitate or become inactivated (e.g., when sodium bicarbonate mixes with calcium, or with adrenaline).

Dose: 20 mL/kg of crystalloid or colloid fluid initially, with additional boluses titrated against the response. Small boluses for flushing drugs.

Glucose

Indications: Hypoglycaemia (in critical illness, particularly in infants).

Dose: 0.5 g/kg IV or IO.

Adenosine

Indication: SVT.

Dose: 0.05 mg/kg, increasing successively to 0.25 mg/kg by rapid IV or IO bolus.