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Emergency physicians and nurses should all be trained to provide effective procedural sedation in the emergency department (ED).
Plan and prepare yourself, and assess the risk-benefit of each individual procedure.
Assess the timing and nature of recent oral intake, medications, available staff to assist, other simultaneous activity in the ED and patient comorbidities.
Determine the safe limit of targeted depth and duration of the sedation.
Sedation is a continuum. It is not always possible to predict how an individual will respond or at which point airway reflexes may be jeopardized.
Sedative agents should be titrated to clinical end points, rather than delivered in a cookbook fashion using generic mg/kg doses.
Each procedural situation should be based on its individual merits, balanced against the available resources of both the ED and the health service at that moment in time.
Procedural sedation is a core competency for the emergency physician, for the performance of brief, but painful procedures, and has become standard emergency medicine practice. Emergency department procedural sedation (EDPS) refers to the technique of administering sedatives or dissociative agents, with or without analgesics, to induce a state that allows the patient to tolerate unpleasant or anxiety-provoking therapeutic or diagnostic procedures, while maintaining cardio-respiratory function.
However, significant variation exists in the practice of EDPS in relation to the approach, choice and combination of agent/s given. Paediatric patients in particular represent a significant challenge; children are often frightened when in pain, and their presentation to the hospital disrupts the family’s functioning. Medical staff underestimate and undertreat pain in children. Painful procedures in the ED are remembered vividly by children, their parents and adult patients. Denial of relief from pain that is proportionate to the expressed need for such relief must be judged as an unjustified harm and amounts to substandard and unethical medical practice.
The Australasian College for Emergency Medicine (ACEM), the Royal College of Emergency Medicine, American College of Emergency Physicians (ACEP) and the Canadian Association of Emergency Physicians (CAEP) have all published on the underlying principles for successful procedural sedation and analgesia. All guidelines cover presedation preparation and assessment, presedation fasting, physician skills, staffing, equipment and environment, patient monitoring, documentation and postsedation care. There has been a gradual change in the perception accorded to EDPS being performed in EDs over the past decade, and the use of intravenous ‘anaesthetic agents’ for EDPS is widely accepted and is now part of mainstream emergency medicine specialist training.
Best practice guidelines require that two medical attendants, one of whom should be a specialist or advanced trainee with sedation competency, be present. Nursing staff are also required, and the procedure must be performed in a resuscitation-capable area of the ED. Physiologic monitoring is mandated during the procedure and extending into the recovery phase. The practitioner must understand the agents available and choose based on the procedure being performed (e.g. the potential for pain, the likely duration of sedation and pain relief required and staff familiarity with the agent and its effects).
The optimal end point of any sedation episode depends on the procedure being performed and patient’s characteristics. Sedation state classification ranging from minimal sedation (anxiolysis) through moderate sedation (formerly conscious sedation), deep sedation and general anaesthesia. Dissociative sedation is a separate state induced by ketamine. The exact characteristics of respiratory and/or airway reflex depression in relation to depth of sedation are not well defined and can be quite variable.
Titration of drug and constant verbal and tactile reassessment of the patient reduce the risk of oversedation. Some degree of responsiveness to painful stimuli should indicate preservation of airway reflexes, decreasing the risk of aspiration if vomiting occurs.
The duration of sedation is largely determined by the choice and dose of agent used and the procedure itself, as to whether this will be brief (e.g. shoulder reduction) or longer (e.g. compound scrub, or manipulation of fractures), with most ED procedures taking less than 20 minutes. The longer the sedation, the greater the risk of an adverse event.
Indications include, but are not limited to, fracture and dislocation reduction, incision and drainage of abscesses and cardioversion. Less painful but anxiety-provoking procedures in children will also be facilitated by the use of dissociative sedation (e.g. lumbar puncture, suturing, ocular or auditory canal FB removal or IV cannulation in an uncooperative and anxious child).
All departments that perform EDPS should have written guidelines, standardized data collection and suitably trained staff. Patient selection is informed by the pre-procedural risk assessment, by available departmental resources to successfully and safely perform the procedure and the sedation without jeopardizing patient care elsewhere in the department and by the ability to monitor and safely discharge the patient.
Preprocedural assessment is of critical importance before embarking on EDPS. Adverse outcomes are associated with advanced age of patient, deep sedation, high BMI and intra-procedural use of fentanyl in combination with either propofol or midazolam. Procedure type and fasting status do not appear associated with adverse intra-procedural adverse respiratory events. However, procedural failure is related to patient weight greater than 100 kg and to certain procedure types, notably prosthetic hip reductions and digit and temporomandibular joint (TMJ) relocations. In terms of agents used, ketamine has a lower rate of respiratory adverse events but has the overall highest procedural success rate.
Each procedural sedation situation should be critically assessed by the treating ED physician, with particular consideration given to:
A young patient’s level of anxiety and cooperation will depend upon past medical experiences, anxiety of the parent/s and the reassurance given by medical staff.
Children often present the challenge of initial lack of cooperation with the sedation process. Elderly patients, whilst mostly cooperative, may have underlying impairment of cardiorespiratory reserve and are at greater risk of respiratory depression or hypotension.
The American Society of Anesthesiologists (ASA) classification system is a global score used to classify the physical status of patients before planned surgery ( Box 22.3.1 ). ASA class I and ASA II patients are usually preferred as candidates for procedural sedation in the ED. If an ASA class III patient requires sedation out of necessity, this should not preclude performance of the procedure. The management of respiratory depression becomes a more active issue with increasing ASA in all age groups.
An adverse past anaesthetic history or a focussed airway assessment with attention to mouth opening, pharyngeal visualization (Mallampati score), neck movement, thyromental distance and dentition may signal potential difficulty should active airway intervention be required. An airway assessment checklist can be found in Box 22.3.2 and Fig. 22.3.1 .
Some conditions predispose to gastro-oesophageal reflux (such as pregnancy or hiatus hernia), raising the theoretical risk of aspiration events during deep sedation. Unstable acute medical/neurological conditions (with the exception of arrhythmia requiring cardioversion) may carry too high a risk to justify proceeding with EDPS. Allergies to any agent in the past precludes use of that agent, and egg and/or soy allergy will preclude the use of propofol in particular.
Occasionally a patient with significant comorbidities will present for a procedure requiring sedation. A careful assessment of the patient, the urgency of the procedure and the available alternatives, in consultation with anaesthetic or ICU colleagues, would be appropriate. Often only very small doses or sedation are required in the elderly to safely perform procedures in a painless fashion.
ED patients, particularly children, undergoing urgent EDPS are commonly not fasted on presentation, nor at the time of the procedure. Furthermore, holding a patient for 6 hours in an overcrowded ED to achieve a goal of fasting time is impractical if an urgent procedure needs to be performed. Fasting guidelines are consensus based, not evidence based. The ASA recommends, by extrapolation, at least 2 hours and 6 hours from last intake of fluid and food, respectively, prior to an ED sedation, despite a lack of evidence. In fact, prolonged preprocedural fasting has been shown to increase the rate of vomiting in the recovery period.
The risk of aspiration is low. Fasting status is just one consideration when individualizing decisions about choice of agent, approach to dosing, desired depth of sedation or even referral to the operating theatre. EDPS does not use volatile inhalational anaesthetics or involve pharyngeal instrumentation which can induce emesis; however, there is a risk. There is no association between fasting status and adverse events during procedural sedation in the ED for a range of agents, including ketamine, midazolam/fentanyl, chloral hydrate, pentobarbital or nitrous oxide. A recent large retrospective observational study of paediatric propofol sedation outside of the operating theatre environment revealed only four cases of aspiration pneumonitis in almost 50,000 cases, all of whom recovered with conservative measures.
Those patients at high risk of aspiration may benefit from an alternative approach or different technique.
This usually occurs well into the recovery period. Postprocedure vomiting is more common with ketamine or narcotics than it is with propofol or benzodiazepines.
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