Skill 14-9 | Suctioning an Endotracheal Tube: Open System | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
The purpose of suctioning is to maintain a patent airway and remove pulmonary secretions, blood, vomitus, or foreign material from the airway. When suctioning via an endotracheal tube, the goal is to remove secretions that are not accessible to cilia bypassed by the tube itself. Tracheal suctioning can lead to hypoxemia, cardiac dysrhythmias, airway trauma, atelectasis, hyperinflation, infection, bleeding, and pain. Therefore, it is imperative to be diligent in maintaining aseptic technique and in following best practice and facility guidelines and procedures to prevent potential hazards. Tracheal suctioning should be performed only when clinically indicated based on assessment and not routinely (AARC, 2010; Burns & Delgado, 2019; Hess et al., 2021; Morton & Fontaine, 2018). Indications for the need for suctioning include audible and/or visible secretions, reduced oxygen saturation, presence of coarse crackles over the trachea, deterioration of arterial blood gas values, reduced breath sounds, the patient's inability to generate an effective spontaneous cough, acute respiratory distress, and suspected aspiration of secretions (AARC, 2010; Patton, 2019). Because suctioning removes secretions not accessible to bypassed cilia, the recommendation is to insert the catheter only as far as the end of the endotracheal tube. Catheter contact and suction can cause tracheal mucosal damage, loss of cilia, edema, and fibrosis and increase the risk of infection and bleeding. Insertion of the suction catheter to a predetermined distance, no more than the tip of the artificial airway to no more than 1 cm past the length of the endotracheal tube (adults) and 0.5 cm (pediatric patients) (Boroughs & Dougherty, 2015; Hess et al., 2021; Kendrick, 2020), avoids contact with the trachea and carina, reducing the effects of tracheal mucosal damage (Boroughs & Dougherty, 2015; Hahn, 2010; Ireton, 2007; Pasrija & Hall, 2020; Pate & Zapata, 2002). Box 14-2 outlines several methods for determining the appropriate suction catheter depth. The suction catheter should be small enough not to occlude the airway being suctioned but large enough to remove secretions; use a suction catheter that occludes less than 50% of the lumen of the endotracheal tube (AARC, 2010; Pasrija & Hall, 2020). Tracheal suctioning is an uncomfortable procedure at a minimum, and it can be a very painful and/or distressing experience. Individualized pain management must be performed in response to the patient's needs (Arroyo-Novoa et al., 2008; Chaseling et al., 2014; Wrona et al., 2021; Düzkaya & Kuğuoğlu, 2015). Anticipate the administration of pharmacologic (analgesic medication) and use of nonpharmacologic interventions for the patient before suctioning. As mentioned previously, perform suctioning only when clinically necessary because of the many potential risks, including hypoxia, infection, tracheal tissue damage, dysrhythmias, and atelectasis. Open-system suctioning and closed-system suctioning are equally effected at secretion clearance (Hess et al., 2021). The open suctioning system requires disconnection of the endotracheal or tracheostomy tube from the ventilator or oxygen therapy source and insertion of a suction catheter each time the patient requires suctioning (Burns & Delgado, 2019), but it is associated with gas exchange deterioration and hypoxia (Burns & Delgado, 2019), potential contamination (Hess et al., 2021), and bioaerosol exposure risk for caregivers (Imbriaco & Monesi, 2021). In closed-system suction, a sterile multiple-use catheter enclosed in a plastic sheath is connected to the ventilation circuit and allows periodic insertion of the suction catheter without disconnection of the endotracheal or tracheostomy tube from the ventilator or oxygen therapy source (Burns & Delgado, 2019; Hess et al., 2021; Pasrija & Hall, 2020). Closed-system suctioning prevents gas exchange deterioration, atelectasis, and hypoxia; is cost-effective because only one catheter is used daily; and reduces bioaerosol exposure risk for caregivers and contamination of the surrounding environment (Hess et al., 2021; Imbriaco & Monesi, 2021; Yazdannik et al., 2019). Closed-system suctioning is recommended for use with patients who are mechanically ventilated; refer to facility policies for specifics of use (AARC, 2010; Morton & Fontaine, 2018; Pasrija & Hall, 2020; Raimundo et al., 2021). Refer to Skill 14-10 for guidelines related to closed-system suctioning. Delegation Considerations Suctioning an endotracheal tube is not delegated to assistive personnel (AP). Depending on the state's nurse practice act and the organization's policies and procedures, suctioning of an endotracheal tube in a stable situation, such as long-term care and other community-based care settings, may be delegated to licensed practical/vocational nurses (LPN/LVNs). The decision to delegate must be based on careful analysis of the patient's needs and circumstances as well as the qualifications of the person to whom the task is being delegated. Refer to the Delegation Guidelines in Appendix A. Equipment
Assessment Assess for indications for the need for suctioning: audible and/or visible secretions, reduced oxygen saturation, presence of coarse crackles over the trachea, deterioration of arterial blood gas values, reduced breath sounds, the patient's inability to generate an effective spontaneous cough, acute respiratory distress, or suspected aspiration of secretions (AARC, 2010; Patton, 2019; Sole et al., 2015). Assess lung sounds. Wheezes, coarse crackles, gurgling or diminished breath sounds may indicate the need for suctioning. Assess for the presence of visualized secretions in the artificial airway, audible secretions, and ineffective coughing (Morton & Fontaine, 2018; Sole et al., 2015). Assess the oxygen saturation level. Deterioration in oxygen desaturation may be an indication of the need for suctioning (AARC, 2010). Assess respiratory status, including respiratory rate and depth. Patients may become tachypneic when they need to be suctioned. Assess the patient for signs of respiratory distress, such as nasal flaring, retractions, or grunting. Assess for pain and the potential to cause pain during the intervention (Arroyo-Novoa et al., 2008; Chaseling et al., 2014; Wrona et al., 2021; Düzkaya & Kuğuoğlu, 2015). Anticipate the administration of pharmacologic (analgesic medication) and use of nonpharmacologic interventions for the patient before suctioning (Arroyo-Novoa et al., 2008; Düzkaya & Kuğuoğlu, 2015). Assess the appropriate suction catheter depth. Refer to Box 14-2. Assess the characteristics and amount of secretions while suctioning. Actual or Potential Health Problems and Needs Many actual or potential health problems or issues may require the use of this skill as part of related interventions. An appropriate health problem or issue may include: Outcome Identification and Planning The expected outcome to achieve is that the patient will exhibit a clear, patent airway. Other outcomes that may be appropriate include that the patient will exhibit an oxygen saturation level within acceptable parameters, will demonstrate a respiratory rate and depth within acceptable parameters, and will remain free from any signs of respiratory distress and adverse effect. Implementation
Evaluation The expected outcomes have been met when the patient has exhibited a clear, patent airway; an oxygen saturation level within acceptable parameters; and a respiratory rate and depth within acceptable parameters; and the patient has remained free from any signs of respiratory distress and adverse effect. Documentation Guidelines Document the time of suctioning, assessments before and after interventions, the reason for suctioning, oxygen saturation levels, and the characteristics and amount of secretions. Sample Documentation 9/1/25 1850 Tan secretions noted in ET tube; coarse crackles noted to auscultation over trachea. Lung sounds coarse in lower lobes. Respirations 24 breaths/min, regular rhythm. Intercostal retractions noted. Endotracheal tube suctioning completed with 12-Fr catheter. Small amount of thin, tan secretions obtained. Specimen for culture collected and sent. After suctioning, no secretions noted in ET tube, auscultation over trachea clear, lung sounds clear, respirations 18 breaths/min, no intercostal retractions noted.Developing Clinical Reasoning and Clinical Judgment Unexpected Situations and Associated Interventions
Special Considerations General Considerations
Infant and Child Considerations
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