Medical Oxygen
SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
COMPRESSED MEDICAL OXYGEN
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Compressed Medical Oxygen Specification
Compressed Medical Oxygen cylinders are supplied to the European Pharmacopoeia (1998) specification which includes:
Compressed Medical Oxygen Purity 99.5%
Maximum Impurity Levels Carbon Monoxide 5 vpm
Carbon dioxide 300 vpm
Moisture 50 vpm
3. PHARMACEUTICAL FORM
Medicinal gas, compressed.
4 CLINICAL PARTICULARS
4.1 Therapeutic indications
Medical Oxygen is widely used in clinical practice to:
■ provide a basis for most modern anaesthetic techniques including pre and postoperative management.
■ restore the tissue oxygen tension towards normal by improving oxygen availability in a wide range of conditions such as:
• cyanosis of recent origin as a result of cardio-pulmonary disease
• surgical trauma, chest wounds and rib fracture
• shock, severe haemorrhage and coronary occlusion
• carbon monoxide poisoning
• hyperpyrexia
• major trauma, i.e. road traffic accidents and gunshot wounds
• in the management of sudden cardiac and respiratory arrest, whether drug induced or traumatic
■ aid in the resuscitation of the critically ill, when the circulation is impaired
■ aid in neo-natal resuscitation
■ treat acute severe headache in adults diagnosed with cluster headache
4.2 Posology and method of administration
Medical Oxygen is administered by inhalation through the lungs. The major exception is when a metered supply is fed into the oxygenator of an extracorporeal circulation of a cardio-pulmonary by-pass system.
For cluster headache, oxygen should be administered as soon as possible after the onset of the attack, via a non-rebreathing facemask at a flow of 6 to 12 l/min for approximately 15 minutes.
4.3 Contraindications
There are no absolute contraindications to the use of Compressed Medical Oxygen, but the inspired concentration should be limited in the case of premature infants and those patients with chronic bronchitis and emphysema.
4.4 Special warnings and precautions for use
Special care is needed when Medical Oxygen is administered:
• to neonates where the inspired concentration should not exceed 40% because of the risk of retrolenticular fibroplasia
• to elderly chronic bronchitic patients in whom the inspired concentration should only be raised in stages of 1% and probably should not exceed 30%
• in hyperbaric chambers in the management of conditions such as carbon monoxide poisoning, anaerobic infections and acute ischaemic disease. Convulsions may occur at 3 bar (g) after a few hours.
Careful monitoring of oxygen levels on the breath, blood and tissue is required to ensure that appropriate concentrations are not exceeded.
Where the patient has been exposed to agents which are toxic to the lungs, such as Paraquat, the use of gases containing more than 21% oxygen should be avoided.
Compressed Medical Oxygen is non flammable but strongly supports combustion and should not be used near sources of ignition.
Compressed Medical Oxygen Cylinders should be set up and tested before placing near the patient. Do not place the cylinder on the patient’s bed unless there is no suitable alternative for retaining the cylinder.
Smoking should be prohibited when using Compressed Medical Oxygen.
Under no circumstances should oils or grease be used to lubricate any part of the Compressed Medical Oxygen cylinder or the associated equipment used to deliver the gas to the patient.
Where moisturising creams are required for use with a facemask or in nasal passages, oil based creams should not be used.
Check that hands are clean and free from any oils or grease.
Where alcohol gels are used to control microbiological cross-contamination ensure that all alcohol has evaporated before handling Compressed Medical Oxygen cylinders or equipment.
4.5 Interaction with other medicinal products and other forms of interaction
The use of higher levels of oxygen can increase the risk of pulmonary toxicity in patients who have been administered Bleomycin, Amiodarone and Nitrofurantoin or similar antibiotics. In these cases oxygen should be administered with caution and at levels kept as low as possible.
4.6 Pregnancy and Lactation
Compressed Medical Oxygen does not adversely affect pregnancy and lactation.
4.7 Effects on Ability to Drive and Use Machines
In normal circumstances, Compressed Medical Oxygen does not interfere with the conscious level but patients who require continuous Oxygen support are obviously not fit either to drive or to operate machinery.
4.8 Undesirable effects
Compressed Medical Oxygen toxicity can occur as manifested by:
• retrolenticular fibroplasia in premature infants exposed to oxygen concentrations greater than 40%
• convulsions appear after a few hours exposure to Medical Oxygen at pressures above 3 bar(g)
• retrosternal soreness associated with coughing and breathing difficulties,
made worse by smoking and exposure to cold air after breathing pure Medical Oxygen at atmospheric pressure for several hours.
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via The Yellow Card System. www.mhra.gov.uk/yellowcard
4.9 Overdose
Overdose effects for Compressed Medical Oxygen are as detailed in 'Undesirable Effects'.
5 PHARMACOLOGICAL PROPERTIES
5.1 Pharmacodynamic properties
The characteristics of Compressed Medical Oxygen are:
Odourless, colourless gas
Molecular weight 32
Boiling point -183.1°C (at 1 bar (g))
Density 1.355 kg/m3 (at 15°C)
Oxygen is present in the atmosphere at 21% and is an absolute necessity for life.
The basal Oxygen consumption in man is about 250mm/min for a body surface of 1.8m2. It is reduced by about 10% during anaesthesia and natural sleep and by about 50% for a 10°C fall in body temperature.
Alveolar air contains about 14% Oxygen (105mm Hg) and the arterial blood has an Oxygen tension of 97mm Hg. The difference, known as the alveolar-arterial Oxygen tension gradient, increases with age. The difference may be as great as 30mm Hg in a healthy, elderly individual.
Oxygen in the blood is mostly combined with haemoglobin. 1.34ml per 9ml to give a maximum capacity of 20ml per 100ml of blood. A small amount, 0.3ml, exists in solution in the same volume of blood.
The concept of Oxygen availability first described by Richards in 1943 and later elaborated by Freeman and Nunn has been used to quantify the amount of Oxygen available to the body. It can be expressed as the product of the cardiac output and the Oxygen content of the blood.
Available Oxygen is calculated by: (cardiac output) x Hb conc x 1.34 x (% saturation)
Substituting normal values for Available Oxygen the amount is:
Available Oxygen: ((5000ml) 15/100 x 1.34 x 95/100) = 950ml
The average healthy individual with a basal Oxygen consumption has no more than four minutes supply of Oxygen in the blood.
5.2 Pharmacokinetic Properties
The uptake of Compressed Medical Oxygen by the blood in the lungs and discharge to the tissues is determined by the Oxygen dissociation curve. The characteristic sigmoid shape ensures that, at tensions between 40 and 15mm Hg the Oxygen carried in the blood from the lungs can be readily given up to the tissues.
The uptake from the lungs is rapid, because blood flow through the capillaries, where exchange takes place, occurs in about 0.5 seconds. The uptake of Oxygen is favoured by the simultaneous loss of carbon dioxide which is then excreted in the expired air. Conversely the entry of carbon dioxide into the blood from the tissues facilitates Oxygen transfer to the cells.
At rest, mixed venous blood returning to the lungs contains 13-14ml of Oxygen per 100ml, but with severe exercise, the Oxygen content may fall to 34ml. In very active tissue, almost complete extraction occurs.
5.3 Preclinical Safety Data
None stated
6. PHARMACEUTICAL PARTICULARS 6.1 List of Excipients
None.
6.2 Incompatibilities
Compressed Medical Oxygen strongly supports combustion and will cause substances to burn vigorously, including some materials that will not normally burn in air. It is highly dangerous in the presence of oils, greases, tarry substances and many plastics due to the risk of spontaneous combustion in the presence of Medical Oxygen in relatively high concentrations.
Shelf-Life
6.3
36 months
6.4 Special Precautions for Storage
Compressed Medical Oxygen cylinders should be :
• stored under cover, preferably inside, kept dry and clean and not subjected to extremes of heat or cold away from stocks of material.
• not stored near stocks of combustible materials or near sources of heat.
• stored separately from industrial and other non-medical cylinders
• stored to maintain separation between full and empty cylinders.
• used in rotation so that cylinders with the earliest filling dates are used first.
• Stored separately from other medical cylinders within the store.
Warning notices prohibiting smoking and naked lights must be posted clearly in the cylinder storage area and the Emergency Services should be advised of the location of the cylinder store.
6.5 Nature and contents of container
A summary of Compressed Medical Oxygen cylinders, their size and construction, type of valve fitted and valve outlet pressure is detailed below:
|
Cylinder Details |
Valve details | ||||
|
Size |
Gas Content (litres) |
Water Capacity (Litres) |
Material of Construction |
Valve Type Filling Port Outlet Connections Outlet Flowrates |
Nominal Valve Outlet Pressure Bar(g) |
|
AZ |
170 |
1.2 |
Aluminium |
Valve Type Non Regulated Outlet Pin Index (BS Outlet EN 850) |
137 |
|
ZA |
300 |
1.0 |
Aluminium (Carbon Fibre hoop wrapped) |
Integral Valve Type Regulated „ . ISO 5145 Fini„g port (Oxygen) Outlet 6 mm Fir Tree |
4 |
|
Cylinder Details |
Valve details | ||||
|
Size |
Gas Content (litres) |
Water Capacity (Litres) |
Material of Construction |
Valve Type Filling Port Outlet Connections Outlet Flowrates |
Nominal Valve Outlet Pressure Bar(g) |
|
0.1 - 15 Flowrate litres/min | |||||
|
D |
340 |
2.32 |
Steel |
Valve Type Non Regulated outlet Pin Index (BS Outlet EN 850) |
137 |
|
CD |
460 |
2.0 |
Aluminium (Kevlar hoop wrapped) |
Integral Valve Type Regulated „... „ . ISO 5145 F‘ll‘ng Port (Oxygen) Outlet (1) 6 mm Fir Tree Flowrate 1 - 15 litres/min ^ . ,r,x BS 5682 Outlet (2) Schrader T-ii . 40 litres/min Flowrate ( (max) |
4 |
|
DD |
460 |
2.0 |
Steel |
Integral Valve Type Regulated „... „ . ISO 5145 F‘ll‘ng Port (Oxygen) Outlet 6 mm Fir Tree Flowrate 2, 4 litres/min |
4 |
|
ZD |
605 |
2.0 |
Aluminium (Carbon Fibre hoop wrapped) |
Integral Valve Type Regulated „... „ . ISO 5145 Mhng port (Oxygen) Outlet (1) 6 mm Fir Tree Flowrate 1 - 15 litres/min n BS 5682 Outlet (2) Schrader |
4 |
|
T-ii . 40 litres/min Flowrate ( (max) | |||||
|
Cylinder Details |
Valve details | ||||
|
Size |
Gas Content (litres) |
Water Capacity (Litres) |
Material of Construction |
Valve Type Filling Port Outlet Connections Outlet Flowrates |
Nominal Valve Outlet Pressure Bar(g) |
|
E |
680 |
4.68 |
Steel |
Valve Type Non Regulated Outlet Pin Index (BS EN 850) |
137 |
|
F |
1360 |
9.43 |
Steel |
w T MPR Non Valve Type Regulated ~ +1 . BS 341 No 3 (Top) |
137 |
|
AF |
1360 |
9.43 |
Aluminium / Steel |
w T MPR Non Valve Type Regulated ~ . BS 341 No 3 (Top) |
137 |
|
DF |
1360 |
9.43 |
Aluminium / Steel |
Integral Valve Type Regulated tth- td w ISO 5145 F‘ll‘ng Port (Oxygen) Outlet 6 mm Fir Tree Flowrate 2, 4 litres/min |
4 |
|
IQX |
2000 |
10.0 |
Steel |
Valve Type Reggrated Filling Port (Oxygen5 Outlet (1) 6 mm Fir Tree „ + 0.5 - 15 Flowrate . litres/min n „ t ^ BS 5682 Outlet (2) Schrader x 40 litres/min Flowrate . N (max) |
4.5 |
|
HX |
2300 |
10.0 |
Steel |
Valve Type Slid |
4 |
|
Cylinder Details |
Valve details | ||||
|
Size |
Gas Content (litres) |
Water Capacity (Litres) |
Material of Construction |
Valve Type Filling Port Outlet Connections Outlet Flowrates |
Nominal Valve Outlet Pressure Bar(g) |
|
Fl"lng p°rt (Oxygen) Outlet (1) 6 mm Fir Tree Flowrate 1 - 15 litres/min n „ t ^ BS 5682 Outlet (2) Schrader x 40 litres/min Flowrate . . (max) | |||||
|
ZH |
2400 |
8.0 |
Steel (Carbon Fibre hoop wrapped) |
Valve Type RegUated Filling Port JO^ Outlet (1) 6 mm Fir Tree Flowrate 1 - 15 litres/min n „ t ^ BS 5682 Outlet (2) Schrader 40 litres/min Flowrate (max) |
4 |
|
ZX |
3040 |
10.0 |
Steel (Carbon Fibre hoop wrapped) |
Integral Valve Type RegUlated „... „ . ISO 5145 Filling Port (Oxygen) Outlet (1) 6 mm Fir Tree Flowrate 1 - 15 litres/min n BS 5682 Outlet (2) Schrader T-ii . 40 litres/min Flowrate ( (max) |
4 |
|
G |
3400 |
23.6 |
Steel |
w T MPR Non Valve Type Regulated ~ +1 . BS 341 No 3 (Top) |
137 |
|
Cylinder Details |
Valve details | ||||
|
Size |
Gas Content (litres) |
Water Capacity (Litres) |
Material of Construction |
Valve Type Filling Port Outlet Connections Outlet Flowrates |
Nominal Valve Outlet Pressure Bar(g) |
|
J |
6800 |
47.2 |
Steel |
MPR Non Valve Type Regulated Outlet Pin IndeX (BS Outlet EN 850) |
137 |
|
W |
11300 |
46.6 |
Steel |
Valve Type Non Regulated ISO 5145 Outlet (Oxygen) |
230 |
Cylinders
All cylinders used for the storage of Compressed Medical Oxygen are manufactured from either high tensile steel or aluminium.
The AZ, D, E, F, AF, DF, G and J size cylinders are designed with working pressure of at least 137 bar(g)
The CD, DD, IQX, HX and W size cylinders are designed with a maximum working pressure of 230 bar (g).
The ZA, ZD, ZH and ZX size cylinder are designed with a maximum working pressure of 300 bar (g).
The colour coding of the shoulders of Compressed Medical Oxygen cylinders is white (RAL 9010).
The colour coding of the cylinder body is white (RAL 9010). Cylinders also carry the oxygen name on the body of the cylinder.
For a limited period, cylinders may have black bodies. These cylinders do not have the name oxygen on the body of the cylinder.
The programme to convert all Compressed Medical Oxygen cylinders to white bodies will be completed by 2025.
Cylinder Valves
Compressed Medical Oxygen cylinders are supplied with two main types of cylinder valves, dependent upon the cylinder filling pressure and the type of application.
Conventional cylinder valves are fitted to AZ, D, E, F, AF, G and J cylinders which are designed to be used with a pressure regulator. All of these cylinders are fitted with valves with outlet connections that conform to either ISO 407 (pin index) or BS 341 (5/8” BSP F) and are filled to 137 bar (g). The cylinder valves are constructed from high tensile brass with a steel spindle fitted with a Nylon 6.6 insert.
ZA, ZD, CD, DD, DF, ZH, HX, and ZX cylinders are fitted with valves that have an integral pressure regulator, with an outlet pressure of 3 or 4 bar(g). These regulated valves are fitted with an ISO 5145 product specific filling connection and a product specific BS 5682 Schrader outlet connection and a standard 6mm fir tree outlet. Integral cylinder valves are constructed from high tensile brass with a steel spindle fitted with a Nylon 6.6 insert.
The IQX package utilises the LIV IQ medical device system manufactured by Linde. The device incorporates a valve with an integral pressure regulator with an outlet pressure of 4.5 bar(g) to a 10 litre cylinder. These regulated valves are fitted with an ISO 5145 product specific filling connection and a product specific BS 5682 Schrader outlet connection and a standard 6mm fir tree outlet. The valve is constructed from high tensile brass with a steel spindle fitted with a Nylon 6.6 insert.
In addition the IQX valve has an electronic pressure gauge and display providing real time information regarding flowrate, length of time remaining for therapy (at the current flowrate) as well as providing visual and audible alarms / warnings for the user.
The side outlet hand wheel valve fitted to W cylinders has an ISO 5145 product specific valve outlet. The valve design incorporates a residual pressure device to prevent the cylinder from being fully emptied and prevent the cylinder from being contaminated should the valve be left open. The valve is constructed from brass and is fitted with a brass spindle with a Nylon 6.6 insert. The residual pressure device is fitted with EDPM O-ring seals.
The internal valve components in the valves are made from oxygen compatible materials, designed to not produce poisonous fumes if the cylinder is subjected to high temperatures, causing ignition of any of the valve components.
6.6 Special precautions for disposal
All personnel handling Compressed Medical Oxygen cylinders should have adequate knowledge of:
• properties of the gas
• correct operating procedures for the cylinder
• precautions and actions to be taken in the event of an emergency.
Preparation for Use
Cylinders used with a pressure regulator Sizes AZ, D, E, F, AF, G, J and W
To prepare the cylinder for use, before placing near the patient:
• remove the tamper evident seal and the valve outlet protection cap. Ensure the cap is retained so that it can be refitted after use.
• ensure the batch label fitted to the cylinder is not removed or discarded
• ensure that an appropriate Compressed Medical Oxygen regulator or manifold tailpipe is selected for connection to the cylinder.
• ensure the connecting face on the regulator is clean and the sealing washer fitted is in good condition.
• connect the regulator or tailpipe, using moderate force only and where appropriate connect the tubing to the regulator / flowmeter outlet. Only the appropriate regulator should be used for the particular gas concerned.
• open the cylinder valve slowly and check for any leaks.
Cylinders with an integral regulated valve
Sizes ZA, ZD, CD, DD, DF, ZH, HX, and ZX
To prepare the cylinder for use, before placing near the patient
• check the cylinder contents gauge on the cylinder valve to ensure that there is sufficient gas contents in the cylinder.
• remove the tamper evident seal and cover fitted over the valve outlets.
• ensure the batch label fitted to the cylinder is not removed or discarded
• ensure that the correct equipment is selected for connection to the cylinder. Connect as appropriate either:
• the appropriate sized tubing to the fir tree outlet or
• the Medical Oxygen Schrader probe to the Schrader outlet (where fitted)
• open the cylinder valve slowly and check for any leaks
Size IQX
To prepare the cylinder for use, before placing near the patient
• check the cylinder contents indicator on the electronic display to ensure that there is sufficient gas contents in the cylinder.
• remove the tamper evident seal and cover fitted over the valve outlets.
• ensure the batch label fitted to the cylinder is not removed or discarded
• ensure that the correct equipment is selected for connection to the cylinder. Connect as appropriate either:
• the appropriate sized tubing to the fir tree outlet or
• the Medical Oxygen Schrader probe to the Schrader outlet
• open the cylinder valve slowly and check for any leaks
Leaks
Cylinders used with a pressure regulator Sizes AZ, D, E, F, AF, G, J and W
Having connected the regulator or manifold yoke/connector to the cylinder check the connections for leaks using the following procedure:
• should leaks occur this will usually be evident by a hissing noise.
• if a leak occurs between the valve outlet and the regulator or manifold yoke/connector, depressurise and remove the fitting and fit an approved replacement sealing washer. Reconnect the fitting to the valve with moderate force only, fitting a replacement regulator or manifold tailpipe as required.
• sealing or jointing compounds must never be used to cure a leak.
• never use excessive force when connecting equipment to cylinders.
• if leak persists, label cylinder and return to BOC
Cylinders with an integral regulated valve
Sizes ZA, ZD, CD, DD, DF, ZH, IQX, HX, and ZX
Check the connection for leaks using the following procedure:
• Should leaks occur this will usually be evident by a hissing noise.
• Close valve, remove connection, check and refit.
• Never use excessive force when connecting equipment to cylinders
• If leak persists, label cylinder and return to BOC
Use of Cylinders
When Compressed Medical Oxygen cylinders are in use ensure that they are:
• only used for medicinal purposes.
• turned off, when not in use, using only moderate force to close the valve
• only moved with the appropriate size and type of trolley or handling device.
• handled with care and not knocked violently or allowed to fall.
• used with an appropriately designed cylinder support to hold the cylinder whilst in use adjacent to the patient. Do not place the cylinder on the patient’s bed unless there is no suitable alternative for retaining the cylinder
• not allowed to have any markings, labels or batch labels obscured or removed
• not used in the vicinity of persons smoking or near naked lights.
After use
Cylinders used with a pressure regulator
Sizes AZ, D, E, F, AF, G, J and W
When the Compressed Medical Oxygen cylinders are empty ensure that the:
• cylinder valve is closed using moderate force only and the pressure in the regulator or tailpipe released.
• valve outlet cap, where fitted, is replaced
Cylinders with an integral regulated valve Sizes ZA, ZD, CD, DD, DF, ZH, HX, and ZX
When the Compressed Medical Oxygen cylinders are turned off or empty ensure that the:
• cylinder valve is closed slowly using moderate force
• valve is allowed to vent before turning the flow selector to zero
• equipment is disconnected
• valve outlet cap, where fitted, is replaced
Size IQX
When the Compressed Medical Oxygen cylinders are turned off or empty ensure that the:
• flow selector is turned to zero
• cylinder valve is closed slowly using moderate force
• Valve is allowed to vent by selecting a flow
• flow selector is turned to zero again
• equipment is disconnected
• valve outlet cap, where fitted, is replaced
Empty cylinders must be returned immediately to an empty cylinder storage area for return to BOC.
7. MARKETING AUTHORISATION HOLDER
BOC Limited.
The Priestley Centre 10 Priestley Road The Surrey Research Park GUILDFORD Surrey, GU2 5XY.
8.
MARKETING AUTHORISATION NUMBER(S)
PL 00735/5000R
9. DATE OF FIRST AUTHORISATION / RENEWAL OF THE
AUTHORISATION
Date First Granted: 01/09/1972
Date of Renewal: 21/07/1997
10 DATE OF REVISION OF THE TEXT
02/11/2016