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Tracheal tubes provide a means of securing the patienťs airway, allowing spontaneous and controlled ventilation. These disposable plastic tubes are made of polyvinyl chloride (PVC), which could be clear, ivory or siliconized. As plastic is not radio-opaque, tracheal tubes have a radio-opaque line running along their length, which enables their position to be determined on chest X-rays. The siliconized PVC aids the passage of suction catheters through the tube. In the past, tracheal tubes used to be made of rubber, allowing them to be reused after cleaning and autoclaving.
The ‘size’ of a tracheal tube refers to its internal diameter (ID), which is marked on the outside of the tube in millimetres. Narrower tubes increase the resistance to gas flow, therefore the largest possible ID should be used. This is especially important during spontaneous ventilation in which the patienťs own respiratory effort must overcome the tube’s resistance. A size 4-mm tracheal tube has 16 times more resistance to gas flow than a size 8-mm tube. Usually, a size 8.5–9-mm ID tube is selected for an average size adult male and a size 7.5–8-mm ID tube for an average size adult female. Paediatric sizes are determined on the basis of age and weight ( Table 5.1 ). Tracheal tubes have both ID and outside diameter (OD) markings. There are various methods or formulae used to determine the size of paediatric tracheal tubes. A commonly used formula is:
Age | Weight (kg) | Size, ID (mm) | Length (cm) |
---|---|---|---|
Neonate | 2–4 | 2.5–3.5 | 10–12 |
1–6 months | 4–6 | 4.0–4.5 | 12–14 |
6–12 months | 6–10 | 4.5–5.0 | 14–16 |
1–3 years | 10–15 | 5.0–5.5 | 16–18 |
4–6 years | 15–20 | 5.5–6.5 | 18–20 |
7–10 years | 25–35 | 6.5–7.0 | 20–22 |
10–14 years | 40–50 | 7.0–7.5 | 22–24 |
The length (taken from the tip of the tube) is marked in centimetres on the outside of the tube. The tube can be cut down to size to suit the individual patient. If the tube is cut too long, there is a significant risk of it advancing into one of the main bronchi (usually the right one [ Fig. 5.2 ]). Black intubation depth markers located 3 cm proximal to the cuff can be seen in some designs (see Fig. 5.1 ). These assist in the accurate placement of the tracheal tube tip within the trachea. The vocal cords should be at the black mark in tubes with one mark or should be between marks if there are two such marks. However, these are only rough estimates, and correct tracheal tube position depth should always be confirmed by auscultation.
More recent designs have a small integrated high-resolution camera ( Fig. 5.3 ) positioned at the tip of the tube, allowing continuous visual monitoring during intubation and positioning of the tube throughout the whole procedure.
The bevel is left-facing and oval in most tube designs. A left-facing bevel improves the view of the vocal cords during laryngoscopy and intubation as the tube is inserted from the right-hand side.
Some designs incorporate a side hole just above and opposite the bevel, called a Murphy’s eye. This enables ventilation to occur should the bevel become occluded by secretions, blood or the wall of the trachea ( Fig. 5.4 ).
Tracheal (oral or nasal) tubes can be either cuffed or uncuffed. The cuff, when inflated, provides an air-tight seal between the tube and the tracheal wall ( Fig. 5.5 ). This air-tight seal protects the patienťs airway from aspiration and allows efficient ventilation during intermittent positive pressure ventilation (IPPV). The cuff is connected to its pilot balloon, which has a self-sealing valve for injecting air. The pilot balloon also indicates whether the cuff is inflated or not. After intubation, the cuff is inflated until no gas leak can be heard during IPPV.
The narrowest point in the adulťs airway is the glottis (which is hexagonal). In order to achieve an air-tight seal, cuffed tubes are used in adults.
The narrowest point in a child’s airway is the cricoid cartilage. Since this is essentially circular, a correctly sized uncuffed tube will fit well. Because of the narrow upper airway in children, post-extubation subglottic oedema can be a problem. In order to minimize the risk, the presence of a small leak around the tube at an airway pressure of 15 cm H 2 O is desirable.
Cuffs can be either:
high pressure/low volume
low pressure/high volume.
These can prevent the passing of vomitus, secretions or blood into the lungs.
At the same time, they exert a high pressure on the tracheal wall. If left in position for long periods, they may cause necrosis of the tracheal mucosa ( Fig. 5.6 ).
These exert minimal pressure on the tracheal wall as the pressure equilibrates over a wider area ( Fig. 5.7 ). This allows the cuff to remain inflated for longer periods.
They are less capable of preventing the aspiration of vomitus or secretions. This is due to the possibility of wrinkles forming in the cuff.
The pressure in the cuff should be checked at frequent and regular intervals ( Figs. 5.8 and 5.9 ), maintaining a pressure of 15–20 mmHg (20–30 cm H 2 O). The pressure may increase mainly because of diffusion of nitrous oxide into the cuff. Expansion of the air inside the cuff due to the increase in its temperature from room to body temperature and the diffusion of oxygen from the anaesthetic mixture (about 33%) into the air (21%) in the cuff can also lead to increase in the intracuff pressure. An increase in pressure of about 10–12 mmHg is expected after 30 minutes of anaesthesia with 66% nitrous oxide. Some designs use cuff material (Soft Seal, Portex) that allows minimum diffusion of nitrous oxide into the cuff with a pressure increase of 1–2 mmHg only. The pressure may decrease because of a leak in the cuff or the pilot balloon’s valve.
Recent designs allow suction above the cuff ( Fig. 5.10 ). A designated suction port runs along the wall of the tube to remove secretions above the cuff. This can reduce the incidence of ventilator-associated pneumonia.
Tubes can be inserted orally or nasally ( Fig. 5.11 ).
The indications for nasal intubation include:
surgery where access via the mouth is necessary, e.g. maxilla-facial procedures.
long-term ventilated patients in intensive care units. Patients tolerate a nasal tube better and cannot bite on the tube. However, long-term nasal intubation may cause sinus infection.
Nasal intubation is usually avoided, if possible, in children up to the age of 8–11 years. Hypertrophy of the adenoids in this age group increases the risk of profuse bleeding if nasal intubation is performed.
Ivory PVC nasotracheal tubes cause less trauma to the nasal mucosa.
These connect the tracheal tubes to the breathing system (or catheter mount). Various designs and modifications ( Fig. 5.12 ) are available. They are made of plastic or metal and should have an adequate ID to reduce the resistance to gas flow.
On the breathing system end, the British Standard connector has a 15-mm diameter at the proximal end. An 8.5-mm diameter version exists for neonatal use. On the tracheal tube end, the connector has a diameter that depends on the size of the tracheal tube. Connectors designed for use with nasal tracheal tubes have a more acute angle than the oral ones (e.g. Magill’s connector). Some designs have an extra port for suction.
Obstruction of the tracheal tube by kinking, herniation of the cuff, occlusion by secretions, foreign body or the bevel lying against the wall of the trachea.
Oesophageal or bronchial intubation.
Trauma and injury to the various tissues and structures during and after intubation.
Usually made of plastic.
Oral or nasal (avoid nasal intubation in children).
Cuffed or uncuffed.
The cuff can be low pressure/high volume or high pressure/low volume.
Recent designs incorporate high-definition camera and facility for suction above the cuff.
It is important to understand the difference between low-pressure/high-volume and high-pressure/low-volume cuffs and their potential risks/benefits in clinical practice.
Armoured tracheal tubes are made of plastic or silicone rubber ( Fig. 5.13 ). The walls of the armoured tube are thicker than ordinary tracheal tubes because they contain an embedded spiral of metal wire or tough nylon. They are used in anaesthesia for head and neck surgery. The spiral helps to prevent the kinking and occlusion of the tracheal tube when the head and/or neck is rotated or flexed, so giving it strength and flexibility at the same time. An introducer stylet is used to aid intubation.
Because of the spiral, it is not possible to cut the tube to the desired length. This increases the risk of bronchial intubation. Two markers, situated just above the cuff, are present on some designs. These indicate the correct position for the vocal cords.
The north-facing polar or the Ring, Adair and Elwyn (RAE) tube is a preformed nasal cuffed or uncuffed tracheal tube ( Fig. 5.14 ). It is used mainly during anaesthesia for maxillofacial procedures as it does not impede surgical access. Because of its design and shape, it lies over the nose and the forehead. It can be converted to an ordinary nasal tracheal tube by cutting it at the scissors mark just proximal to the pilot tube and reconnecting the 15-mm connector. An oral version of the polar tube exists. They can be made of ivory PVC or clear polyurethane.
The south-facing polar or RAE tube has a preformed shape to fit the mouth without kinking. It has a bend located just as the tube emerges, so the connections to the breathing system are at the level of the chin and not interfering with the surgical access. Such tubes can be either cuffed or uncuffed.
Because of its preformed shape, there is a higher risk of bronchial intubation than with ordinary tracheal tubes. The cuffed tracheal tube has one Murphy eye, whereas the uncuffed version has two eyes. Since the uncuffed version is mainly used in paediatric practice, two Murphy eyes ensure adequate ventilation should the tube prove too long.
The tube can be temporarily straightened to insert a suction catheter.
These tubes are used in anaesthesia for laser surgery on the larynx or trachea ( Fig. 5.15 ). They are designed to withstand the effect of carbon dioxide and potassium-titanyl-phosphate (KTP) laser beams, avoiding the risk of fire or damage to the tracheal tube. One design has a flexible stainless steel body. Reflected beams from the tube are defocused to reduce the accidental laser strikes to healthy tissues. Other designs have a laser-resistant metal foil wrapped around the tube for protection ( Fig. 5.16 ). The cuff is filled with methylene blue–coloured saline. If the laser manages to damage the cuff, the colouring will help identify rupture and the saline will help prevent an airway fire.
Some designs have two cuffs. This ensures a tracheal seal should the upper cuff be damaged by laser. An air-filled cuff, hit by the laser beam, may ignite and so it is recommended that the cuffs are filled with saline instead of air.
Laser is an acronym for “ l ight a mplification by the s timulated e mission of r adiation.”
These tubes are used in a number of surgical procedures that have the risks of damage to nerves, e.g. thyroid surgery. Bipolar stainless steel contact electrical electrodes are embedded in the tracheal tubes above the cuff where they are in contact with the vocal cords. These electrodes are connected to a nerve stimulator. An additional earth electrode is attached to the skin of the patient.
The use of such tubes allows continuous nerve monitoring throughout surgery providing visual and audible warnings.
This tube allows better exposure and surgical access to the larynx. It has a small diameter (usually a 5-mm ID) with an adult-sized cuff ( Fig. 5.18 ). Its length is sufficient to allow nasal intubation if required. The tube is made of ivory PVC to reduce trauma to the nasal mucosa.
This anatomically L-shaped tracheal tube is used in anaesthesia for head and neck surgery because it is non-kinking ( Fig. 5.19 ). The tube can be made of rubber or plastic and can be cuffed or uncuffed. The bevel is oval and faces posteriorly, and an introducing stylet is supplied to aid the insertion of the tube. Its thick wall adds to the tube’s external diameter, making it wider for a given ID. This is undesirable especially in paediatric anaesthesia.
The distance from the bevel to the curve of the tube is fixed. If the tube is too long, the problem cannot be corrected by withdrawing the tube and shortening it because this means losing its anatomical fit.
This tube is not widely used in the current anaesthetic practice.
These are curved plastic tubes usually inserted through the second, third and fourth tracheal cartilage rings ( Fig. 5.20 ).
An introducer is used for insertion.
Wings are attached to the proximal part of the tube to fix it in place with a ribbon or suture. Some designs have an adjustable flange to fit the variable thickness of the subcutaneous tissues ( Fig. 5.21 ).
They can be cuffed or uncuffed. The former has a pilot balloon.
The proximal end can have a standard 15-mm connector.
The tip is usually cut square rather than bevelled. This decreases the risk of obstruction by lying against the tracheal wall.
Some designs have an additional suctioning lumen, which opens just above the cuff. The cuff shape is designed to allow the secretions above it to be suctioned effectively through the suctioning lumen ( Fig. 5.22 ).
In patients with a difficult anatomy, some designs use a reinforced tube to prevent kinking ( Fig. 5.23 ).
Some tubes have an inner cannula. Secretions can collect and dry out on the inner lumen of the tube, leading to obstruction. The internal cannula can be replaced instead of changing the complete tube in such cases. The cannula leads to a slight reduction of the ID of the tube.
Different sizes of tracheostomy tubes are available to fit neonates to adults.
Older uncuffed metal tracheostomy tubes made of a non-irritant and bactericidal silver are rarely used in current practice. Some designs have a one-way flap valve and a window at the angle of the tube to allow the patient to speak.
Long-term ventilation.
Upper airway obstruction that cannot be bypassed with an oral/nasal tracheal tube.
Maintenance of an airway and to protect the lungs in patients with impaired pharyngeal or laryngeal reflexes and after major head and neck surgery (e.g. laryngectomy).
Long-term control of excessive bronchial secretions especially in patients with a reduced level of consciousness.
To facilitate weaning from a ventilator. This is due to a reduction in the sedation required, as the patients tolerate tracheostomy tubes better than tracheal tubes. Also there is a reduction in the anatomical dead space.
Increased patient comfort.
Less need for sedation.
Improved access for oral hygiene.
Possibility of oral nutrition.
Bronchial suctioning aided.
Reduced dead space.
Reduced airway resistance.
Reduced risk of glottic trauma.
Surgical tracheostomy has a mortality rate of <1% but has a total complications rate as high as 40%. The complications rate is higher in the intensive care unit and emergency patients.
The complications can be divided into:
Immediate:
haemorrhage
tube misplacement (e.g. into a main bronchus)
occlusion of tube by cuff herniation
occlusion of the tube tip against carina or tracheal wall
pneumothorax.
Delayed:
blockage of the tube by secretions, which can be sudden or gradual; this is rare with adequate humidification and suction
infection of the stoma
overinflation of the cuff leads to ulceration and distension of the trachea
mucosal ulceration because of excessive cuff pressures, asymmetrical inflation of the cuff or tube migration
surgical emphysema, pneumothorax and pnuemomediastinum.
Late:
tracheal stenosis
granulomata of the trachea may cause respiratory difficulty after extubation
persistent sinus at the tracheostomy site
tracheal dilatation
tracheal stenosis at the cuff site
scar formation.
The fenestration (window) in the greater curvature channels air to the vocal cords, allowing the patient to speak.
After deflation of the cuff, the patient can breathe around the cuff and through the fenestration as well as through the stoma. This reduces airway resistance and assists in weaning from tracheostomy in spontaneously breathing patients.
Some tubes have a fenestrated inner cannula.
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