Paediatric procedural sedation within the emergency department


Essentials

  • 1

    Procedural sedation has mirrored the development of paediatric emergency medicine as a subspecialty.

  • 2

    Local (departmental, hospital, state and national) governance and educational programmes must be developed to facilitate safe sedation practice. Ask ‘Can we do this procedure?’ before considering sedation.

  • 3

    Develop a sedation plan that includes patients, families/carers and staff.

  • 4

    Organise staff, equipment and the environment to allow the procedure to occur in a timely yet controlled fashion.

  • 5

    Remember rapport building and nonpharmacological approaches to anxiolysis.

  • 6

    Become familiar with medications: dose, administration and potential complications.

  • 7

    Combining drugs without detailed knowledge and training increases risk.

  • 8

    Aim to minimise the number of drugs used.

Introduction

Emergency department (ED) attendances due to acute pain are very common in children. The Paediatric Research in Emergency Departments International Collaborative (PREDICT) reported on 314 025 attendances around Australia and New Zealand, and 28 123 attendances to Royal Darwin Hospital. , In both cohorts, forearm fractures and lacerations were among the most common diagnoses. Pain can be the trigger for ED presentation but may also be the consequence of necessary medical management within the ED.

The development of procedural sedation (PS) parallels the development of paediatric emergency medicine as a subspecialty. As clinicians developed confidence in managing the sedated child, procedures previously performed in the operating theatre have migrated to the ED. ED performance of PS allows more rapid discharge, reduces costs, and increases clinician skills and job satisfaction, while making unpleasant procedures more tolerable to children and their families. ,

The goal of procedural sedation

The ultimate goal of PS is to safely achieve a level of sedation that allows successful completion of the necessary procedure, a return to consciousness and discharge home within a reasonable time frame. However, it is not enough to safely sedate a child. A practitioner competent in the procedure that is deemed necessary must be available. If there is doubt, then ED PS may be inappropriate.

Collaborative planning between the ED staff and other specialists may be required. The procedure may need to be done in an operating theatre or may still be achieved with the ED practitioner taking responsibility for safe sedation and a relevant proceduralist undertaking the procedure. One clinician must remain responsible for, and focus on, safe PS, whether or not the procedure is undertaken by an ED clinician or another specialist.

Although serious adverse events are rare, sedation providers should be prepared to intervene should complications occur. Coté and Hoffman demonstrated that patient selection, adherence to a prescribed process and minimisation of the number of sedating agents were important in reducing PS risks. Sedation registries have provided data accumulated over many thousands of sedation events. The Pediatric Sedation Research Consortium ( www.pedsedation.org ) in the United States receives data from over 30 centres that perform PS. No deaths, one cardiac arrest (requiring CPR) and one aspiration event were reported by Cravero et al. in a cohort who represented 30 000 PS episodes. Unplanned intervention was needed in 336 PS episodes (111.9 per 10 000 PS episodes), with bag-valve-mask ventilation (63.9 per 10 000 PS episodes) and intubation (9.7 per 10 000 PS episodes) the most invasive. Hertzog et al. reported anaphylaxis risk of PS at 1:37 972 with ketamine, midazolam, methohexital and morphine more likely than other medications to cause this rare event.

The phases and the tasks involved in PS can be divided as follows: preprocedure, intraprocedure and postprocedure ( Fig. 3.2.1 ). This division provides a framework to build one’s practice upon.

Fig. 3.2.1, The phases and tasks of procedural sedation.

Preprocedure

Ensuring safe governance, training of staff and preprocedure preparedness reduces adverse events during PS. , , Prior to a PS episode there should be careful risk assessment, preparation of staff and environment as well as a decision on use of the most appropriate pharmacological and nonpharmacological methods for the particular patient and procedure. COVID-19 risks to ED staff and patients must be considered. For example, nitrous oxide administration is a low risk aerosol generating procedure (AGP). The location of nitrous oxide must be in either a negative pressure room or in a room where the door is closed and only essential staff wearing high level personal protective equipment (N95 mask, eye protection, hair coverings, gown and gloves) are permitted in the room. It is also important to note, before any avoidance of nitrous oxide is considered, that crying due to procedural distress poses a risk of aerosol generation, perhaps greater than appropriate sedation.

Governance

Governance that include guideline development, education and credentialing improve practice in PS , with a reduction in adverse events. This is the foundation for safe PS practice and should occur before any child is sedated. In Victoria, Australia, over the last decade, the development and dissemination of a PS programme , (handbook, presentations for trainers, practical train-the-trainer sessions and testing materials) has provided a structure for teaching and providing practical experience. Hospital networks and EDs all play a role in the establishment and maintenance of PS education and procedural systems.

Patient selection and risk assessment

Appropriate patient selection reduces the risk of PS. Assigning risks as potential threats to airway, breathing, circulation, neurological and other factors can assist in developing a structure to assessment ( Table 3.2.1 ). Sedation risk is higher in younger children. For example, children under 12 months, and especially those under 6 months, have an increased risk of apnoea. , Airway interventions, such as bag-valve-mask ventilation and/or endotracheal intubation, if needed, is more complicated in infants. Intercurrent illness such as active asthma and upper respiratory tract infection can complicate general anaesthesia and may also have an adverse effect on PS.

Table 3.2.1
Factors to consider in assessing risk for procedural sedation
Modified from Paediatric Procedural Sedation; ED Manual. Victorian Department of Health (ECIICN, Royal Children’s Hospital, VMIA) 2013 and Daud YN, Carlson DW. Pediatric sedation. Pediatr Clin North Am 2014;61(4):703–717.
Active medical problems Past history
Airway Croup
Foreign body
Head and facial trauma
Previous airway surgery
Laryngomalacia
Craniofacial abnormalities
Risk of vomiting (e.g. bowel obstruction, gastrooesophageal reflux)
Breathing Respiratory tract infection
(e.g. pneumonia, bronchiolitis)
Asthma
Sleep apnoea
Circulation Shock (e.g. hypovolaemia, sepsis)
Arrhythmia
Congenital cardiac disease
(e.g. cardiac failure, pulmonary hypertension)
Neurological Altered level of consciousness (seizure, meningitis, trauma)
Space-occupying lesion
Unstable epilepsy
Neuromuscular disease
Other Unstable psychiatric disorder History of sedation failure
History of anaesthetic reaction
Family history of anaesthetic reaction

As with any ED attendance a history of current medications and allergies is required. Physical examination must document patient weight, vital signs, an assessment of conscious state, airway evaluation (e.g. Mallampati score) with assessment of cardiac and respiratory systems. A Mallampati score of Class 3 or 4 suggests more difficult bag-valve-mask ventilation and risk of airway obstruction. The Mallampati score requires a degree of cooperation that may not be possible in younger infants.

Fasting

The association between fasting time, vomiting and aspiration is not well supported by evidence, although fasting remains a powerful principle in anaesthesia. Babl noted vomiting in 162 of 2002 (8%) children undergoing PS with either nitrous oxide or ketamine, while Cravero et al., reporting on the Pediatric Sedation Research Consortium data, identified 142 vomiting events out of 30 037 PS (0.47%) episodes. Bellolio et al., as part of a metaanalysis, reported 498 vomiting events out of 7865 (6.33%) PS episodes. Given conflicting reports, a pragmatic sedation plan will recognise the patient’s medical, surgical and anaesthetic history (where relevant), the nature of the last meal eaten and the urgency of the procedure required. ,

Consent

Informed consent should include general risks associated with PS and the procedure being undertaken. In addition, the specific effects of the chosen sedation plan must be discussed. For example, if ketamine were the chosen pharmacological agent, discussion regarding vomiting (± aspiration), hyperlacrimation, hypersalivation, hiccups and emergence phenomena should be initiated. Preprepared information sheets for specific, and common, PS plans can be useful.

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