Fig. 27.1
Richmond Agitation-Sedation Scale (© Vanderbilt University)
Table 27.1
The ICU pain, agitation, and delirium care bundle
Component | Pain | Agitation | Delirium |
---|---|---|---|
Assess | Assess ≥4×/shift and prn NRS if patient can report pain BPS or CPOT if patient cannot report | Assess ≥4×/shift and prn RASS or SAS if not paralyzed Brain function monitor if paralyzed | Assess delirium each shift and prn CAM-ICU or ICDSC |
Treat | Treat pain then reassess Non-pharmacologic (relaxation) IV opioids +/− non-opioids for non-neuropathic pain Gabapentin or carbamazepine for neuropathic pain | Targeted sedation and/or daily SATs to achieve goal of RASS −1 to 0 or SAS 3 to 4 If undersedated, use non-benzodiazepine sedatives as needed If oversedated, hold sedatives | Treat pain as needed Reorient patients; provide eyeglasses, hearing aids as needed Avoid benzodiazepines unless alcohol or benzodiazepine withdrawal Avoid rivastigmine Avoid antipsychotics if QTc is high |
Prevent | Preprocedural analgesia Relaxation therapy | Treat pain before using sedation Consider daily SBTs and early mobility unless contraindicated EEG if high ICP warrants burst suppression or high risk for seizures | Identify delirium risk factors Avoid benzodiazepines Early mobility Promote sleep Restart baseline psychiatric medications if indicated |
The SCCM guidelines (Table 27.1) also recommend monitoring ICU patients for delirium using one of two validated tools: the CAM-ICU [7] (Fig. 27.2; used in this case) or the Intensive Care Delirium Screening Checklist (ICDSC) [8]. Delirium, which is frequently hypoactive (i.e., characterized by somnolence rather than agitation) in the ICU, is easily overlooked when a validated assessment tool is not used. Use of the CAM-ICU or ICDSC, therefore, can improve detection and management of delirium.
Fig. 27.2
CAM-ICU (© 2002 Vanderbilt University)
Minimizing Sedation
Oversedation is common and harmful in the ICU, where heavily sedated patients remain on the ventilator longer and have higher mortality rates than their less sedated counterparts [9]. Patients who require sedatives during critical illness should therefore be managed with light rather than heavy sedation (barring a specific, time-limited indication for the latter, e.g., neuromuscular blockade, open abdomen, etc.). Use of a validated sedation scale (see section on “Sedative Choice”) is an important part of efforts to maintain light sedation, since frequent, reliable data regarding actual vs. targeted level of sedation can prompt changes in sedative choice, dose, and/or frequency. In addition to use of sedation scales, strategies that can improve outcomes by minimizing sedation include treating pain adequately before using sedatives [10], avoiding benzodiazepines in favor of other sedatives (e.g., propofol, dexmedetomidine, and/or an opioid) [11], using a sedation protocol [5], and interrupting sedatives on a daily basis with SATs [12, 13].
Risk Factors for Delirium
Though questions remain regarding the most effective strategies to prevent and treat delirium (see Prevention of Delirium and Antipsychotics sections), studies have identified a number of modifiable risk factors for delirium that should be addressed whenever possible when managing patients who are high risk as well as those already delirious. Numerous observational and interventional studies have found benzodiazepines (used initially in this case) increase delirium risk [14, 15], whereas dexmedetomidine does not [16, 17]. This may be because benzodiazepine pharmacokinetics make them prone to cause oversedation—drug-induced coma, regardless of which medication is the culprit, is a delirium risk factor—or because of their mechanism of action in the brain (GABA agonism). Infection, acute kidney injury, metabolic acidosis, mechanical ventilation, and high severity of illness are also risk factors for delirium that, in many cases, can be addressed [18].
In addition to the modifiable risk factors listed herein, many risk factors for delirium are not modifiable but an awareness of these factors may prompt clinicians to monitor high-risk patients more closely for delirium. These include advanced age and hypertension (both present in this case) as well as preexisting cognitive impairment, emergency surgery, and trauma.
Evidence Contour
This case highlights a number of evidence gaps and areas of controversy that remain despite the growing body of evidence regarding sedation and delirium in the ICU.
Sedative Choice
Dozens of randomized controlled trials have examined whether sedative choice affects outcomes in the ICU. Most compared a benzodiazepine (typically midazolam), the class of sedatives used most frequently in the ICU for several decades, with a non-benzodiazepine sedative, and the large majority of these trials found non-benzodiazepine sedation resulted in better outcomes (Table 27.2). A recent meta-analysis, in fact, found that benzodiazepine sedation (compared with sedation using propofol or dexmedetomidine) delays extubation and discharge from the ICU [11]. These data led the SCCM guidelines [4] to recommend non-benzodiazepines for sedation in the ICU, but questions remain regarding which drug(s) should be preferred. Dexmedetomidine has the benefit of facilitating light sedation and reducing delirium risk [16, 17], but costs remain high and the patient population that benefits the most from this agent has not yet been clearly defined. Propofol is less expensive than dexmedetomidine and less prone to cause oversedation than benzodiazepines but its use in some patients is limited by hemodynamic effects. Other drugs, including opioids, clonidine, haloperidol, and atypical antipsychotics are sometimes used to manage agitation in the ICU, but evidence of benefit in randomized trials is needed before use of these agents can be widely recommended.
Table 27.2
Randomized trials comparing benzodiazepines with alternative sedatives in the ICU
First author | Year | Population | Outcome(s) improved |
---|---|---|---|
Benzodiazepines vs. propofol | |||
Trials finding better outcomes with propofol | |||
Grounds RM | 1987 | Cardiac surgery | Faster awakening |
Aitkenhead AR | 1989 | General ICU | More consistent awakening, faster weaning |
McMurray TJ | 1990 | Cardiac surgery | Faster awakening |
Carrasco G | 1993 | General ICU | More accurate sedation, faster awakening, lower costs |
Roekaerts PM | 1993 | Cardiac surgery | Faster awakening, earlier extubation |
Ronan KP | 1995 | Surgical ICU | Faster awakening |
Sherry KM | 1996 | Cardiac surgery | Lower costs |
Chamorro C | 1996 | General ICU | Better ventilator synchrony, faster awakening |
Barrientos-Vega R | 1997 | General ICU | Earlier extubation |
Weinbroum AA | 1997 | General ICU | Faster awakening |
Sanchez-Izquierdo-Riera JA | 1998 | Trauma ICU | Faster awakening |
McCollam JS | 1999 | Trauma ICU | Less oversedation |
Hall RI | 2001 | Mixed ICU | More accurate sedation, earlier extubation |
Carson SS | 2006 | Medical ICU | Fewer ventilator days |
Trials finding no differences in outcomes | |||
Searle NR | 1997 | Cardiac surgery | None |
Kress JP | 2000 | Medical ICU | None |
Huey-Ling L | 2008 | Cardiac surgery | None |
Trials finding better outcomes with the benzodiazepine | |||
None | |||
Benzodiazepines vs. remifentanil | |||
Trials finding better outcomes with remifentanil | |||
Breen D | 2005 | Mixed ICU | Shorter duration of mechanical ventilation |
Muellejans B | 2006 | Cardiac surgery | Earlier extubation and ICU discharge |
Rozendaal FW | 2009 | Mixed ICU | Lighter sedation, shorter weaning time |
Trials finding no differences in outcomes | |||
None
Full access? Get Clinical TreeGet Clinical Tree app for offline access |