Chapter 7 Equipment for the inhalation of oxygen and other gasses
Introduction
The benefits of supplemental oxygen are:
• as a treatment for hypoxaemia due to hypoventilation, or due to gas transfer or ventilation/perfusion abnormalities (e.g. heart failure, anaesthesia)
• to improve oxygen supply to tissues, when a disease process causes oxygen demand to outstrip delivery (e.g. severe sepsis, malignant hyperpyrexia)
• as a specific treatment for certain conditions, e.g. carbon monoxide poisoning, postoperative nausea and vomiting
• to allow humans to survive at very low atmospheric pressure, e.g. mountaineering and high altitude flying.
Normobaric oxygen therapy
There are almost as many devices that deliver oxygen as there are indications for its use. These devices may be classified by the extent to which the patient relies upon them to correct any deficiency in oxygen delivery (Table 7.1).
CPAP, continuous positive airway pressure; NIPPV, non-invasive positive pressure ventilation; IPPV, intermittent positive pressure ventilation
Low dependency systems
Variable performance devices
With these devices, the oxygen concentration delivered to the upper airway varies with the phase and pattern of respiration (as well as the selected oxygen flow rate). As an example, consider a standard oxygen mask applied to the face (Fig. 7.1). Oxygen flows into the facemask from a continuous supply and quickly fills the relatively small volume of the mask (approximately 200 ml) at the end of an exhaled breath. The oxygen then begins to escape through the mask’s vents and where the seal against the face is imperfect.
The complex interplay between the factors that determine FIO2 (Table 7.2) means that most oxygen delivery devices deliver a variable FIO2. The extent of this variability is difficult to quantify as normal methods of measuring breathing pattern are impractical in clinical practice. The latter require a mouthpiece that interferes with oxygen flow in the mask, and subjects are not able to breathe with a fixed respiratory pattern long enough for accurate measurements to be recorded. These difficulties explain why the factors most influential in determining FIO2 are still unclear.
No capacity oxygen delivery devices
Traditionally, nasal cannulae (also known as nasal prongs or specs) deliver unhumidified oxygen to the nasopharynx (Fig. 7.2). They are more comfortable and less claustrophobic than facemasks, allowing talking, eating and drinking, and making them the most suitable means of delivering long-term oxygen therapy for chronic conditions, especially at home. The main drawback is that an unhumidified oxygen flow greater than 2 L min−1 can cause discomfort and drying of the nasal mucosa. Thus unhumidified oxygen therapy in association with the tiny capacity of the nasal cannulae leads to variable FIO2. Clinical and laboratory studies in this context have shown an enormous variability with respiratory pattern, FIO2 ranging between 0.26 and 0.90.2,3 A further design is the nasal sponge (tipped) catheter, which is lodged in one nostril and again effectively uses the nasopharynx as a small reservoir during the respiratory pause (Fig. 7.3). Devices permitting humidified oxygen therapy via nasal cannulae are now available (Fig. 7.4), allowing oxygen flow rates up to 60 L min−1 to be tolerated for long periods. As a result, consistently higher, more reliable FIO2 can be achieved with this form of high flow humidified oxygen therapy.4 However, warm humidified gas is a good medium for bacterial growth; therefore, it is mandatory that any disinfection and infection control procedures deemed necessary by manufacturers and regulatory authorities are adhered to. The other point to note is that delivering high flows into the nasopharynx generates a small amount of positive end expiratory pressure (PEEP) depending on the flow used and if the mouth is open or closed. Pharyngeal pressures of up to 4 cm H2O have been recorded with a flow of 60 L min−1 with the mouth open, increasing to nearly 10 cm H2O with the mouth closed.5 As such, high flow humidified oxygen therapy delivered via nasal cannulae should be regarded as a medium dependency device (see below). Its role in the management of acutely breathless patients is becoming increasingly appreciated.
Low capacity oxygen delivery devices (capacity <100 ml)
Facemasks for children, or tracheostomy masks (Fig. 7.5) have a volume of approximately 70–100 ml. Tracheostomy masks, especially, do not provide humidification without extra equipment, and so are best suited for short-term use. In long-term use, oxygen may be humidified by using a ‘Swedish nose’ device (Fig. 7.6) (see also Chapter 11, Humidifiers). This is a small, light heat and moisture exchanger that connects to the tracheostomy tube by means of a 15 mm International Organization for Standards (ISO) connector. Supplemental oxygen can be administered into this via a clip-on device. A ‘Swedish nose’ may also provide 2.5–5 cm H2O of PEEP.
Medium capacity oxygen delivery devices (capacity 100–250 ml)
Standard adult facemasks are designed to cover the nose and mouth and have a capacity of approximately 175–200 ml (Fig. 7.1); there are a multitude of different designs. They are, almost without exception, made of transparent soft plastic with an elastic strap to secure the mask in place. Some incorporate a short deformable metal bar allowing the mask to be shaped around the nose to achieve a closer fit. Oxygen flow rates of 2–15 l min−1 result in a highly variable and unpredictable FIO2. Rebreathing of CO2 can occur with O2 flow rates of less than 2 L O2 min−1 or if minute ventilation is very high.6 A more recent design (Intersurgical, UK) fits filters in the expiratory ports, in an attempt to reduce infection risk from aerosolized pathogens emitted from the patient’s airway.
High capacity oxygen delivery devices (capacity 250–2500 ml)
Air is only entrained into a facemask when the patient’s inspiratory flow rate exceeds the oxygen supply rate. To achieve a FIO2 near 1.0 (100% oxygen) by providing sufficient oxygen flow alone, rates in excess of 60 l min−1 would be required (in order to exceed the patient’s peak inspiratory flow rate) which is clearly impractical. Increasing mask size simply increases the risk of rebreathing CO2. However, a great deal of oxygen delivered to the facemask is lost to the atmosphere whenever the patient’s inspiratory flow rate is (a) less than the oxygen supply rate and (b) during exhalation. High-capacity masks are designed to store some of this wasted oxygen in a reservoir bag (usually of >1 litre volume) attached to the facemask, thus providing a higher FIO2 (Fig. 7.7). With these devices, oxygen flows directly into the reservoir bag, which fills during exhalation and whenever the patient’s inspiratory flow rate is less than the flow rate of delivered oxygen. The patient inhales oxygen preferentially from the reservoir bag: provided the mask makes a reasonable seal to the face. Expiratory flap valves are incorporated on the vents or in piping below the mask to prevent air entrainment from these sites. However, ambient air will still be entrained if there are leaks between the mask and the face.7 Some manufacturers include a one-way valve between mask and reservoir bag, reducing rebreathing of CO2. However, higher oxygen supply rates are required as oxygen in the exhaled dead space of the mask, pharynx and upper trachea is prevented from entering the reservoir bag and is wasted. A valveless device is, therefore, most suitable when oxygen supplies are limited, but a valve is desirable if rebreathing of CO2 would be detrimental, for example after head injury.
One example of a high-capacity mask (Fig. 7.8) uses a sequential gas delivery system incorporated in a small circuit below the mask with a one-way valve to prevent re-breathing, an expiratory valve and a third valve to allow entrainment of room air should the reservoir bag become exhausted. This design is reputed to allow FIO2 close to 1.0 to be given, although again attention to the seal between the mask and the face and the oxygen flow rate is required to achieve this.8 A more recent high capacity mask (Intersurgical, UK) again incorporates a one-way valve from the reservoir bag but designed such that it also allows entrainment of room air if the bag is emptied (Fig. 7.9). This and the expiratory one way valve are neatly arranged within the front of the mask itself. Additionally this device is made of non-PVC materials, in an attempt to reduce the impact on the environment during disposal.
Generally, it is accepted that facemasks with reservoir bags probably deliver an FIO2 between 0.6 and 0.8;9,10 however, in reality there is likely to be considerable variation around these values due to leak between the mask and face combined with variable respiratory patterns. Best results will be achieved by using an O2 flow rate adequate for the patient’s needs such that the reservoir bag empties by no more than a third during inspiration and by achieving the best seal possible between the mask and the face. Some masks incorporate additional features, for example a small chimney containing a red polystyrene ball that moves up and down with respiration so that a patient’s respiratory effort can be visualized and respiratory rate can easily be measured (Fig. 7.10).11
A reservoir bag may also be attached to airway maintenance devices to improve the FIO2 delivered during emergence from anaesthesia. The T-Bag (Ultimate Medical Pty Ltd, Australia) (Fig. 7.11