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The aim of this guideline is to ensure that:
This guideline is for general use within all general wards and departments. Where specific clinical guidelines are required for oxygen administration within specialist areas, such as PICU and NICU, they must be approved via the appropriate forum. They should reflect wherever possible the principles within this policy. Patients transferring from specialist areas must be transferred with a prescription for their oxygen therapy utilising target saturation, if the clinical indication is ongoing. If a patient transfers from an area not utilising the target saturation system, their oxygen should be administered as per the transferring area’s prescription until the patient is reviewed and transferred over to the target saturation scheme, which should occur as soon as possible.
It is the responsibility of all staff to ensure oxygen is prescribed and administered in accordance with the guideline as outlined below.
An NPSA rapid response report ‘Oxygen safety in hospitals’ in 2009 reported 281 serious incidents from Dec 2004 to June 2009 relating to oxygen therapy and that poor oxygen management caused 9 deaths and contributed to a further 35. This report placed an obligation on hospitals to introduce measures to reduce avoidable harm associated with administration of oxygen.
In 2008 the British Thoracic Society (BTS) published guidelines on ‘Emergency Oxygen use in adult patients’ which are evidence based and set out good practice recommendations for oxygen prescription and delivery. There are regular national audits undertaken in adults.
(a) Prescribe oxygen with a target saturation range on preprinted section on front of drug kardex
(b) Choose most appropriate delivery device
METHOD |
CONCENTRATION |
COMMENTS |
Nasal prongs |
Up to 3L/min can be delivered comfortably |
No need for humidification, cold humidification routine practice in RHSC |
Simple Oxygen Mask |
High concentrations can be delivered safely |
Flow below 4 litres could potentially result in carbon dioxide retention (Bell, 1995) |
High Concentration Oxygen Masks |
10-15 litres required |
For use in emergency situations |
Humidified |
26%-65% FiO2 (approx 4-10L/min) |
|
Wafting |
30%-40% with 10 litres oxygen per minute |
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(c) Follow flow chart for administration and monitoring of oxygen in non emergency situation
(d) Follow flow chart for titration of oxygen
Stop oxygen. If not tolerated try 0.5L/min or decrease more gradually with low flow meter. |
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Nasal cannulae 1L/min | Seek medical advice if patient has increasing need for oxygen or if there is a rising CEWS score |
Nasal cannulae 2L/min | |
Nasal cannulae up to 3L/min |
Signs of respiratory deterioration:
SEEK MEDICAL ADVICE |
Simple face mask 4-6L/min (humidified) |
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Simple face mask 7-10L/min (humidified) |
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Reservoir (non rebreathe) mask 15L/min (If required seek senior medical input immediately) |
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If difficulty maintaining saturations on increasing |
The administration of supplemental oxygen is an essential element of appropriate management for a wide range of clinical conditions; however oxygen is a drug and therefore requires prescribing in all but emergency situations. ‘Oxygen must be considered as a medication and use of oxygen must be documented for each patient’. (Royal Pharmaceutical Society of Great Britain, 2005)
Failure to administer oxygen appropriately can result in serious harm to the patient. The safe implementation of oxygen therapy with appropriate monitoring is an integral component of the Healthcare Professional’s role.
The rationale for oxygen therapy is prevention of cellular hypoxia, caused by hypoxaemia (low PaO2), and thus prevention of potentially irreversible damage to vital organs.
Therefore the most common reasons for oxygen therapy to be initiated are:
Other indications include:
There are no absolute contraindications to oxygen therapy if indications are judged to be present. The goal of oxygen therapy is to achieve adequate tissue oxygenation using the lowest possible FiO2.
Some congenital heart defects can lead to an unbalanced circulation which may be made worse by administration of oxygen due to pulmonary vasodilation and subsequent systemic ischaemia. This should be considered in a baby who presents unwell in the first two weeks of life with absent or weak femoral pulses and a heart murmur and is not improving with oxygen.
Supplemental O2 should be administered with caution in patients suffering from paraquat poisoning (BNF 2005) and with acid inhalation or previous bleomycin lung injury.
In patients with chronic carbon dioxide retention, oxygen administration may cause further increases in carbon dioxide and respiratory acidosis. Children with chronic neuromuscular disorders, chest wall deformities, cystic fibrosis, morbid obesity and chronic lung disease of prematurity are at risk. Evidence has also shown high concentration oxygen can cause a clinically significant increase in CO2 in patients with severe exacerbations of asthma (2).
An oxygen section on the drug chart has been designed to assist prescription and administration. Oxygen should be prescribed by a doctor in the designated section of the hospital prescription card and the appropriate target saturation should be circled on the chart.
Once the target saturation has been identified and prescribed, guidance regarding the most appropriate delivery system to reach and maintain the prescribed saturation is provided for those administering oxygen.
ACTION |
RATIONALE |
All patients requiring oxygen therapy will have a prescription for oxygen therapy recorded on the patients drug prescription chart. N.B exceptions- see emergency situations |
Oxygen should be regarded as a drug and should be prescribed. BTS National guidelines (2008). British National Formulary (2008). |
The prescription will incorporate a target saturation that will be identified by the clinician prescribing the oxygen. |
Certain groups of patients require different target ranges for their oxygen saturation |
Patients should have their oxygen saturation observed immediately after starting oxygen for at least five minutes, after one hour and then four hourly depending on the clinical status of the patient. Oxygen saturations should be recorded on the CEWS chart. |
To identify if oxygen therapy is maintaining the target saturation or if an increase or decrease in oxygen therapy is required |
The oxygen flow rate should be recorded alongside the oxygen saturation on the bedside observation (CEWS) chart. |
To provide an accurate record and allow trends in oxygen therapy and saturation levels to be identified. |
Oxygen saturations must always be interpreted alongside the patient’s clinical status incorporating the early warning score (CEWS). |
To identify early signs of clinical deterioration, e.g. elevated respiratory rate |
If the patient falls outside the target saturation range, the oxygen therapy will be adjusted accordingly.Saturations should then be monitored continuously for at least 5 minutes and recorded on the CEWS chart after any increase or decrease in oxygen dose to ensure that the patient acheives the desired saturation range. |
To maintain the saturation in the desired range. |
Saturation higher than target specified or >98% for an extended period of time. |
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The patient will require weaning down from current oxygen delivery system. |
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The patients clinical condition may have improved negating the need for supplementary oxygen |
Saturation lower than target specified |
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To assess the patients response to oxygen increase and to review the cause of deteriorating oxygen level. Consider need to check capillary blood gas for CO2 level. |
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Patient safety |
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In most instances a fall in oxygen saturation is due to deterioration of the patient however equipment faults should be checked for. |
Saturation within target specified |
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(The change may be made in stable patients due to patient preference or comfort). |
The selection of an appropriate oxygen delivery system must take into account, clinical condition, the patient's size, needs and therapeutic goals (6)
Supplied in children sizes but children do not always tolerate them (7). There are two types of facemasks and selection depends on the condition of the child (8):
Vents in the mask allow for the dilution of oxygen (9).
Guide to oxygen concentration:
5- 6 lpm = 35-50%
6 -10 lpm = 50-60%
10 - 12 lpm = 60-65%
Used for emergency situations (Advanced Life Support Group, 1997) due to a large reservoir that allows oxygen only to be breathed in by the child. This prevents the inhalation of mixed gases. The approximate inspired oxygen received is 99% (10).
Nasal cannula device capable of giving high flows up to 8L/min in infants and 40L/min in older children and adults without drying secretions as the oxygen is warmed to body temperature and saturated with water vapour. Please see separate guidelines for ward use in bronchiolitis and PICU use.
Humidification
Humidified oxygen should be used when high concentration of oxygen is required for prolonged periods and in those with chronic respiratory illness to prevent drying of the mucosa and secretions (9). Although there is no evidence that nasal cannula oxygen needs to be humidified our current policy in RHSC is to use cold humidification at all flow rates.
Wafting
When conventional delivery methods are not tolerated, wafting of oxygen via a face mask has been shown to deliver concentrations of 30% - 40% with 10 litres oxygen per minute, to an area of 35 x 32cms from top of the mask. Wafting via green oxygen tubing has been assessed as appropriate for short- term use only, i.e., whilst feeding. A standard paediatric oxygen mask placed on the chest can give significant oxygen therapy with minimal distress to the patient (11).
Via nebulisation
Nebulisers should be delivered via oxygen and not air.
Tracheostomy
Oxygen can be delivered via a tracheostomy mask (4-15L/min) or Swedish nose (0.125-4L/min). Consider child’s individual needs.
Nasal Cannula
Can be used for long-term oxygen use, whilst allowing the child to vocalise and eat. The concentration is often not controlled resulting in a low inspiratory oxygen concentration. The use of nasal cannulae can cause dermatitis and mucosal drying (Joint Formulary Committee, 2006). Nasal cannula oxygen does not need to be humidified.
Via a ventilation circuit
Accurate measurement of inspired oxygen is difficult and pulse oximetry must be maintained. Can be delivered at various points throughout the ventilation circuit (12).
Via an Ayres T piece – open ended bag
Used frequently by anaesthetists and gives a reliable impression of the state of the lungs. This technique allows manual application of PEEP (Positive End-Expiratory Pressure). It is completely reliant on an effective oxygen source (Advanced Life Support Group, 2003).
Bag valve mask
Come in three sizes: 250 mls, 500 mls and 1500 mls. The smallest one is ineffective even at birth. Two smallest bags have a pressure-limiting valve set at 4.41 kPa (45 cm H20) to protect the lungs from barotrauma (Damage caused to tissues by a change in pressure inside and outside the body). The reservoir bag enables the delivery of oxygen concentrations up to 98%. Without the reservoir bag it is not possible to supply more than 50% oxygen
(Advanced Life Support Group, 2003)
The patient's oxygen saturation and oxygen flow rate should be recorded on the bedside observation chart alongside other physiological variables.
All patients on oxygen therapy should have regular pulse oximetry measurements. The frequency of oximetry measurements will depend on the condition being treated and the stability of the patient.
In the emergency situation an oxygen prescription is not required. Oxygen should be given to the patient immediately without a formal prescription or drug order but documented later in the patient’s record.
All peri-arrest and critically ill patients should be given 100% oxygen (15 l/m reservoir mask) whilst awaiting immediate medical review. Patients with risk factors for hypercapnia who develop critical illness should have the same initial target saturations as other critically ill patients pending the results of urgent blood gas results after which these patients may need controlled oxygen therapy or supported ventilation if there is severe hypoxaemia and/or hypercapnia with respiratory acidosis.
All patients who have had a respiratory arrest or cardiac arrest should have 100% oxygen provided along with basic/advanced life support.
A subsequent written record must be made of what oxygen therapy has been given to every patient alongside the recording of all other emergency treatment.
Any qualified nurse/ health professional can commence oxygen therapy in an emergency situation.
Patients admitted to specialist areas with a specialised oxygen prescribing policy eg. PICU, NICU
Patients who are transferred from one area to another must have clear documentation of their ongoing oxygen requirements and documentation of their oxygen saturation. If a patient transfers from an area not utilising the target saturation system (see specialist areas above) their oxygen should be administered as per the transferring areas prescription until the patient is reviewed and transferred over to the target saturation scheme, which should occur as soon as possible.
Patients requiring oxygen therapy whilst being transferred from one area to another should be accompanied by a trained member of the nursing staff wherever possible. If this does not occur, clear instructions must be provided for personnel involved in the transfer of the patient, which must include delivery device and flow rate.
The usual procedure for prescribing oxygen therapy in these areas should be adhered to, utilising the target saturation. If a patient is transferred back to the ward on oxygen therapy and is not on the target saturation system, the need for ongoing oxygen therapy should be reviewed as soon as possible. If oxygen therapy is to be continued, it should be prescribed using the target saturation scheme unless there is an alternative time-limited instruction which is part of the Directorate’s Post-Operative care policy for selected patients.
All nurses, nursing assistants and other healthcare professionals involved in prescribing or administrating oxygen will be taught on the oxygen guideline. A record of all those who have been taught will be kept.
All doctors will be taught about the oxygen guideline at induction.
Audits will be performed in all clinical areas.
The guideline will be reviewed if the proposed BTS guideline with a paediatric section on oxygen prescription is released. It will then be reviewed on a three yearly basis.
1. Inform patients and carers about the combustibility of oxygen |
Oxygen supports combustion, there is always a danger of fire when oxygen is being used. |
2. Oxygen should be stored in an area designated as no smoking. |
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3. Electrical appliances should be kept at least five feet away from the source of oxygen. |
Oxygen can be potentially dangerous when in contact with sources of ignition and flame. |
4. Avoid grease or cooking oil coming into contact with apparatus. |
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5. Store unused cylinders in a dry well ventilated place. |
METHOD |
CONCENTRATION |
COMMENTS |
Nasal prongs |
Up to 3L/min can be delivered comfortably |
No need for humidification, cold humidification routine practice in RHSC |
Simple Oxygen Mask |
High concentrations can be delivered safely |
Flow below 4 litres could potentially result in carbon dioxide retention (Bell, 1995) |
High Concentration Oxygen Masks |
10-15 litres required |
For use in emergency situations |
Humidified |
26%-65% FiO2 (approx 4-10L/min) |
|
Wafting |
30%-40% with 10 litres oxygen per minute |
|
Stop oxygen. If not tolerated try 0.5L/min or decrease more gradually with low flow meter. |
|
Nasal cannulae 1L/min | Seek medical advice if patient has increasing need for oxygen or if there is a rising CEWS score |
Nasal cannulae 2L/min | |
Nasal cannulae up to 3L/min |
Signs of respiratory deterioration:
SEEK MEDICAL ADVICE |
Simple face mask 4-6L/min (humidified) |
|
Simple face mask 7-10L/min (humidified) |
|
Reservoir (non rebreathe) mask 15L/min (If required seek senior medical input immediately) |
|
If difficulty maintaining saturations on increasing |
Last reviewed: 04 March 2020
Next review: 04 March 2023
Author(s): Louise Thomson
Version: 3
Approved By: Paediatric Drugs & Therapeutics Committee