In this post, I link to and excerpt from The Candian Paediatric Society’s Position Statement “Recommendations for procedural sedation in infants, children, and adolescents“. Posted: Mar 12, 2021.
All that follows is from the above resource.
This statement provides best practice guidance for the development of institutional standards surrounding safe procedural sedation for infants, children and adolescents (Figure 1).
The term ‘procedural sedation’ refers here to the administration of any pharmacologic agent(s) for the purpose of sedation. Guidance in this document does not necessarily apply to patients receiving medications for anxiolytic purposes or analgesic drugs for pain. Such cases are described in another Canadian Paediatric Society statement on managing pain and distress in children undergoing brief diagnostic and therapeutic procedures.
Clinician skills, training, and credentialing
Procedural sedation can be safely administered by non-anesthesiologist clinicians in both tertiary care and community hospitals [8]-[11][14]. Safety and effectiveness relate primarily to individual clinicians’ skills [15], and a practitioner competent in airway management and the resuscitation and stabilization of critically ill paediatric patients must be immediately available at all times [12].
The clinician responsible for administering sedation must be prepared to manage emergency situations including aspiration, airway obstruction, laryngospasm, apnea, hypoventilation, hypoxia, hypotension, bradycardias, arrhythmias, cardiac arrest, seizures, allergic reactions, and paradoxical reactions [6][8][9][11][12].
There is significant institutional variation in credentialing requirements for clinicians who provide procedural sedation [16]. Many institutions have developed formal training programs demonstrating improvements in the quality and safety of sedation services [17]–[20]. Participation in a formal training course is likely more effective in improving physician knowledge than self-directed learning [21]. Recommended core competencies can be found at http://www.pedsedation.org/resources/quality-safety/core-competencies. High-fidelity simulation team-based training may assist in training and maintaining the skills of health care providers (HCPs) to respond more effectively in emergency situations that could arise [22]–[24].
Table 1. Key elements of the pre-sedation evaluation
Demographic data
name, age, weight Details of procedure
type, duration, urgency Past medical history
acute medical conditions/current illnesses comorbid medical conditions review of systems previous sedations/anesthetics Allergies Medications Family history of anesthetic complications Social history Fasting status
current or provide recommendations before procedure Physical examination
baseline vital signs airway assessment for features of a difficult airway (e.g., craniofacial anomalies, abnormal neck mobility, small oral aperture or cavity, large tongue, neck masses, laryngeal and subglottic abnormalities) cardiopulmonary examination Other investigations as required Summary
ASA physical status assessment sedation plan and rationale planned disposition Informed consent ASA American Society of Anesthesiologists
Table 2. American Society of Anesthesiologists (ASA) Physical Status Classification System Definition Examples* ASA I Healthy, normal child ASA II Child with mild systemic disease Controlled asthma, controlled diabetes ASA III Child with severe systemic disease Active wheezing, diabetes with complications, heart disease that limits activity ASA IV Child with severe systemic disease that is a constant threat to life Status asthmaticus, severe bronchopulmonary dysplasia, sepsis ASA V Child who is moribund who is not expected to survive 24 h with or without an operative procedure Severe traumatic brain injury, septic shock * Modified from reference [28] to provide paediatric-specific examplesASA American Society of AnesthesiologistsAlthough recent studies have demonstrated no statistically significant association between pre-procedural fasting of any duration and any type of adverse event in children who undergo procedural sedation in the emergency department (ED) [34][35], ASA fasting guidelines recommend a minimum fasting period of 1 h for clear liquids, 4 h for human milk, and 6 h for infant formula, nonhuman milk, and light meals [36]. Children undergoing procedural sedation should be fasted according to institution-specific general anesthesia fasting guidelines and practices.
Emergency preparedness
Most adverse events are preventable, provided that patients have been appropriately selected, prepared, monitored, and managed in emergency situations [12]. Before commencing procedural sedation, the clinician should ensure the availability of:
- Appropriate personnel
- Monitoring equipment
- Emergency equipment and rescue medications
1) Appropriate personnel
Procedural sedation should only occur in the presence of at least two HCPs, including a clinician skilled in procedural sedation and advanced airway management and resuscitation. One HCP must be dedicated to continuously monitoring the patient and responding to physiological changes. When the clinician responsible for the sedation is also performing the procedure, continuous patient monitoring and directed administration of medications should be delegated to another highly qualified HCP, such as another physician, a nurse practitioner, an anesthesia assistant, or a nurse with advanced resuscitation skills (e.g., several years of experience in ED, intensive care, or post-anesthetic recovery).
2) Monitoring equipment
Monitoring should include continuous pulse oximetry and intermittent noninvasive blood pressure monitoring every 5 minutes. The AAP and the ASA recommend the use of continuous 3-lead electrocardiography (ECG) and end-tidal carbon dioxide monitoring (i.e., capnography) for moderate sedation because this technique is superior to clinical monitoring alone [1][37]. Pulse oximetry is essential but insufficient because normal saturations may be maintained after the onset of inadequate ventilation. Hypoventilation can be masked by the maintenance of normal saturations. Although ECG electrodes allow for transthoracic impedance monitoring, chest wall movement may continue to be interpreted as “normal” during episodes of obstructive apnea or laryngospasm. Air flow is best assessed by auscultation. The ability to immediately detect ventilatory failure secondary to hypoventilation, apnea, upper airway obstruction, or laryngospasm allows for timely intervention and avoidance of progression to cardiac arrest [12]. Hospitals should ensure that the necessary equipment and HCP skills required to perform and interpret capnography are available for moderate to deep procedural sedations.
3) Emergency equipment and rescue medications
Regardless of the anticipated level of sedation, age- and size-appropriate emergency equipment (Table 3) and rescue medications (Table 4) should be immediately available. The clinician administering the sedation and HCPs who are assisting must ensure familiarity with the location and functioning of equipment and weight-based doses of rescue medications, including those required for cardiopulmonary resuscitation and reversal agents.
Table 3. Emergency equipment (SOAPME) S = suction catheters and apparatusO = oxygen supply and delivery equipment (e.g., flow meters, tubing, prongs)A = airway equipment (e.g., face masks, nasopharyngeal/oropharyngeal airways, laryngoscope handles and blades, endotracheal tubes, stylets)P = positive-pressure delivery system (i.e., bag-valve-mask ventilation)M = monitors (e.g., pulse oximetry, end-tidal carbon dioxide, ECG leads, noninvasive blood pressure)E = emergency cart with alternate airways (e.g., laryngeal mask airway), supplies for vascular access, and resuscitation drugs
Table 4. Rescue medications Dose range and route Comments Atropine 0.02 mg/kg IV (maximum 0.5 mg) May repeat dose once (maximum total dose 1 mg for child; 3 mg for adolescent) Epinephrine (0.1 mg/mL)
0.01 mg/kg IV (maximum 1 mg) May repeat dose every 3 to 5 minutes Flumazenil (benzodiazepine reversal)
0.01 mg/kg IV (maximum 0.2 mg) May repeat every 1 minute to a maximum total cumulative dose of 0.05 mg/kg or 1 mg total, whichever is less Contraindicated in patients with underlying seizure disorder
Naloxone (opioid reversal)
0.1 mg/kg IV (maximum 2 mg) Dilute and titrate to effect May repeat every 2 to 3 minutes
Contraindicated in patients with chronic opioid exposure
Succinylcholine 1 to 2 mg/kg IV (maximum 150 mg) 2 to 4 mg/kg IM
Essential rescue medication that should be drawn up for the treatment of severe laryngospasm and to facilitate rapid intubation, when needed. Repeat doses increase risk for bradycardia