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Position Statement
Paediatric advanced life support
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 -
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Current contents list
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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 | |||
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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:
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
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 | |||
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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:
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
Ventricular fibrillation and pulseless ventricular tachycardia
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)
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
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 | |||
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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 |
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| 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: No reprints will be available. ©MJA 1996
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| 4: Techniques in paediatric advanced life support | |||
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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. |
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Venous access
Intraosseous injection of drugs and infusion of fluids 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 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).
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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. |