Extreme arousal, irritability, excess motor activity driven by internal sense of discomfort such as disease, pain, anxiety and delirium
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1 Agitated patient in ICUapproach & management Arjun Srinivasan
2 Agitation Extreme arousal, irritability, excess motor activity driven by internal sense of discomfort such as disease, pain, anxiety and delirium Acute Ongoing
3 Why bother? Harm to self & staff Prolonged & inadequate ventilation Inappropriate & overuse of sedation Increased ICU cost, morbidity & mortality
4 Approach Onset & organ dysfunction Etiology & reversibility Therapy
5 Etiology
6 Ventilator dyssynchrony Agitation
7 Patient ventilator dyssynchrony Ventilator should cycle in synchrony with pt s respiratory drive Indirectly proportional degree of support Dyssynchrony arises frequently Trigger Rest of inspiration (flow dependent) Cycle End of expiration
8 Physical signs Failed trigger Chest wall & abdominal effort in spite of no breath thdli delivery Trigger delay Appreciable delay between effort & breath delivery PEEPi Inward chest wall movement persisting up to next inspiration Audible expiratory sound during next inspiration
9 Trigger dyssynchrony Too little Inappropriate setting Dynamichyperinflation & PEEPi Decreased effort / drive Increased resistance ( ET tube / tubing / pt s respiratory mechanics) Time delay Ventilator t design anomaly Too much Inappropriate setting Water / secretions in tubing Leak / expiratory valve fault
10
11 Strategies for Optimizing trigger synchrony
12 Flow dyssynchrony Frequently due to low fixed flow setting in volume cycled flow controlled ventilation Pt has breath to breath variability Mismatch especially in cases of ARDS & COPD Patient s requirement may exceed set parameters Minute ventilation Tidal volume Hypoxemia Flow rate Elicits sensation of dyspnea & increases WOB
13 Pulled down pressure tracing
14 Strategies for optimizing flow Increase flow rate Pros synchrony Decreases inspiratory time Allows more expiratory time Decreases dynamic hyperinflation & PEEPi Cons Increases PIP Causes tachypnea Increase MVe & TV Not always possible Decrease CO2 production Treating fever & sepsis
15 Cycle dyssynchrony Cycling Parameter determining the switch from inspiration to expiration It is volume / time in ACMV & flow in PSV Synchrony Patient s Ti (neural Ti) = machine Ti Dyssynchrony Neural Ti > machine Ti or neural Ti < machine Ti
16 Does cycle dyssynchrony occur in PSV? ll Usually no Can occur in presence of severe obstruction Ventilators use flow for cycling in PSV Usually < 25% of PF or 5 Ltrs/min Rate of decrease of flow is slow & inspiratory time prolonged Tackled by Increasing inspiratory rise time % or changing cycling parameters Decreasing PS ( may increase WOB)
17 Last difficult to ventilate pt needed. 18 days of ventilation ~ 5 grams of midazolam ~ 12 grams of propofol p ~ 4 grams of vecuronium ~ 200 mg of haloperidol ~100 mg of morphine
18 What if no cause is identified? Structured ICU sedation algorithm Target specified, patient focused Incorporating scales for assessing Pain Sedation need Delirium
19 Pain Whether present? If yes, then why? Management
20 Whether present? Omnipresent Day to day procedures ( suctioning / dressing changes / turning ) Improper positioning Immobilization Full bladder Post operative / wound site pain Cardiac / visceral pain (constipation / ileus)
21 Able to communicate How to detect? Verbal or non verbal localization Quantification by appropriate scales Visual analog scale Numeric scales Verbal descriptive rating Unableto communicate Inferred by observable behaviors & vital parameters Limited by lack of specificity BPS & CPOT have been used and validated recently
22 Behavioral Pain Scale Tool Score of 3 = no pain & 12 = maximum pain
23 Critical Care Pain Observation Tool (CPOT)
24 Agitation sedation scales First used by Ramsay et al in 1974 Titrate sedation target specific end points Shown to decrease Over sedation & costs Dose of sedatives & analgesics Duration of mechanical ventilation & early weaning Nosocomial infections
25 Various scales in use Ramsay Sedation Scale (RSS) Richmond Agitation Sedation Scale (RASS) Sedation Agitation Scale (SAS) Motor Atiit Activity Assessment tscale (MAAS) Adaptation to the Intensive Care Environment (ATICE) instrument Minnesota Sedation Assessment Tool (MSAT) Vancouver interaction and calmness scale (VICS)
26 Delirium Present in 35 80% of critically ill patients Independent predictor longer hospital stay Higher hospital costs Higher mortality Not easily recognized by treating physicians Caused by interplay of multiple factors
27 Chemically Increased ddopamine Decreased acetyl choline Serotonin imbalance DELIRIUM Endorphin hyperactivity
28 IATROGENIC/ENVIRONMENTAL Sedative/ analgesic use Immobilization (restraint, catheters) TPN Sleep deprivation Malnutrition Anemia (phlebotomy) Delirium in the ICU HOST FACTORS Underlying co morbidities(liver, renal, diabetes, hypertension) Elderly Pre existing cognitive impairment/ dementia Hearing/ vision impairment Neurologic disease (stroke, seizure) Alcoholism, smoking ACUTE ILLNESS. Severe sepsis ARDS MODS Drug overdose/ illicit drugs Nosocomial infection Metabolic disturbance
29 Can these scales be implemented?
30 General measures Reassurance (for fear, anxiety) Writing board if unable to communicate Re positioning the patient Repositioning ET > 2 cms from carina Treatment of withdrawal state Correcting metabolic tbli derangements Catheterization Music therapy Hypnosis
31 How drug use in ICU is different? Advanced age Malnutrition Altered renal & liver function Effects of underlying disease Polypharmacy Slowed metabolism High body water/ increased volume of distribution Decreased protein binding
32 Pharmacotherapy Opiate analgesics Sedatives Anti psychotics
33 Analgesics
34 Sedation Which drug? How to titrate?
35 Midazolam vs. lorazepam Midazolam Faster onset of action bolus dosing Less duration of action repeated doing Accumulates in renal / hepatic dysfunction Expensive ( 10 mg ~ Rs 50 ) Lorazepam Long duration of action ( 4 6hrs) prolonged therapy Cheaper ( 4 mg ~ Rs 15) Carrier toxicity ( propylene glycol anion gap acidosis ) Time to come off sedation Data conflicting
36 Propofol The active ingredient in Propofol is 2,6 diisopropylphenol l in 10% soybean oil, 2.25% glycerol, and 1.2% purified egg phosphatide. Disodium EDTA (0.05 mg/ml) or sodium metabisulfite (0.25 mg/ml) is added to inhibit bacterial growth. Is hepatically modified & renally excreted Key benefits include Rapid onset & offset of action Easy titration Metabolism independent of hepatic & renal function Sedative hypnotic with anxiolytic & amnestic properties Bronchodialtor, anti epileptic,muscle relaxant and anti oxidant
37 Adverse events Hypotension Hypertriglyceridemia Sepsis due to contamination Pancreatitis Metabolic acidosis Adrenal insufficiency Immune dysfunction PRIS Is very expensive Practically no benefit over Midazolam in terms of earlier extubation and shorter stay
38 Dexmedetomidine Is an α2 2 agonist it Increasing role, especially in post operative operative patients Advantages include Maintenance of respiratory drive Rapid awakenings Analgesia Amnesia Good hemodynamic tolerance Decreased requirement for other medications
39 Recent meta analysis of 24 studies Decreased ICUstay Trend towards decreased mortality & delirium Heterogeneity of data Higher incidence of bradycardia
40 How to give sedation? Intermittent tboluses preferred Consider continuous infusion Requirement more frequent than every 2 hours Unable to achieve target sedation Checkfor pain / delirium If on continuous infusion Titrate dose to target Reassess every few hours Daily interruption of sedation (DIS) & restart at half dose Empiric downward titration after 48 hrs
41 DIS Wake up & breathe protocol Earlier extubation Less morbidity Less cost No increase in adverse events (PTSD, recall or cardiac events) Should be practiced in all except pt s with increased risk for cardiac events
42 Co sedation / A1 strategy
43 Delirium
44 Haloperidol Starting ti doses are 2 10 mg (5 mg) bolus over 5 10 minutes. Repeat every 20 minutes till end point achieved 25% of the cumulative dose q6 hourly for maintenance Block 60% of the D2 receptor while avoiding side effectseffects associated with complete D2 blockade Once calm, smaller doses can be used Adverse events Extrapyramidal symptoms Malignant hyperthermia Torsade de pointe
45
46 AGITATION in the ICU PAIN & ANXIETY ILLNESS VENTILATOR DYSSYNCHRO NY DELIRIUM Specific measures Anti psychotics py Sedatives, analgesics Dangerous agitation Pain lightly deeply unresponsive agitation dyssynchrony anxiety sedated sedated
47 Aitti Agitation is a distressing i issue in ICU Look around before reaching for syringe Patient focused & target based sedation Reassess on a daily basis for pain & delirium Wake up & breathe
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