Extreme arousal, irritability, excess motor activity driven by internal sense of discomfort such as disease, pain, anxiety and delirium

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Agitated patient in ICUapproach & management Arjun Srinivasan

Agitation Extreme arousal, irritability, excess motor activity driven by internal sense of discomfort such as disease, pain, anxiety and delirium Acute Ongoing

Why bother? Harm to self & staff Prolonged & inadequate ventilation Inappropriate & overuse of sedation Increased ICU cost, morbidity & mortality

Approach Onset & organ dysfunction Etiology & reversibility Therapy

Etiology

Ventilator dyssynchrony Agitation

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

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

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

Strategies for Optimizing trigger synchrony

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

Pulled down pressure tracing

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

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

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)

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

What if no cause is identified? Structured ICU sedation algorithm Target specified, patient focused Incorporating scales for assessing Pain Sedation need Delirium

Pain Whether present? If yes, then why? Management

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)

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

Behavioral Pain Scale Tool Score of 3 = no pain & 12 = maximum pain

Critical Care Pain Observation Tool (CPOT)

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

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)

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

Chemically Increased ddopamine Decreased acetyl choline Serotonin imbalance DELIRIUM Endorphin hyperactivity

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

Can these scales be implemented?

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

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

Pharmacotherapy Opiate analgesics Sedatives Anti psychotics

Analgesics

Sedation Which drug? How to titrate?

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

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

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

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

Recent meta analysis of 24 studies Decreased ICUstay Trend towards decreased mortality & delirium Heterogeneity of data Higher incidence of bradycardia

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

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

Co sedation / A1 strategy

Delirium

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

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

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