Index
Module 17 • PADIS
Pain, Agitation/Sedation, Delirium, Immobility & Sleep
5%
Learning Objectives
Pain, Agitation/Sedation, Delirium, Immobility & Sleep
Joanna L. Stollings ~3 min read Module 17 of 20
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Pain, Agitation/Sedation, Delirium, Immobility, Sleep Disruption, and Neuromuscular Blockade

Learning Objectives

1

Develop a management strategy for the preven-

tion and treatment of pain, agitation/sedation, and

delirium, immobility, and sleep disruption (PADIS)

in an intensive care unit (ICU) patient with various

comorbidities.

2Discuss relevant pharmacokinetic and pharmacody-

namic considerations of PADIS medications as they

pertain to disturbances in critical care physiology.

3

Identify relevant adverse effects, drug interactions,

and drug withdrawal syndromes in the management

of PADIS.

4

Evaluate patients in the ICU for PADIS using a vali-

dated screening tool.

5

Construct a plan for the management of delirium.

6

Identify the long-term effects of critical illness in

adult ICU patients.

7

Create a management strategy for PADIS-related

medications that are continued beyond ICU dis-

charge.

8

Describe a treatment and monitoring plan for criti-

cally ill patients receiving neuromuscular blockade.

Abbreviations in This Chapter
ARDS

Acute respiratory distress syndrome

BPS

Behavioral Pain Scale

CAM-ICUConfusion assessment method for the

intensive care unit

CPOT

Critical-Care Pain Observation Tool

GABA

ฮณ-Aminobutyric acid

ICDSC

Intensive Care Delirium Screening

Checklist

ICP

Intracranial pressure

ICU

Intensive care unit

NMBA

Neuromuscular blocking agent

PAD

Pain, agitation, and delirium

PADIS

Pain, agitation/sedation, delirium,

immobility, and sleep disruption

PRIS

Propofol-related infusion syndrome

RASS

Richmond Agitation Sedation Scale

SAS

Sedation-Agitation Scale

SAT

Spontaneous awakening trial

SBT

Spontaneous breathing trial

SCCM

Society of Critical Care Medicine

TOF

Train of four

Self-Assessment Questions

Answers and explanations to these questions may be

found at the end of this chapter.

1

P.J. has been receiving propofol 50โ€“60 mcg/kg/

minute and fentanyl 75โ€“100 mcg/hour for 4 days.

She has no significant medical history. Laboratory

results today show that transaminases have

increased to 5 times baseline, lactate is increased to

5 mmol/L, and triglyceride concentration is 450 mg/

dL. No new medications have been added. Given

these laboratory values, which complication would

be most appropriate to address?

A.Deep venous thrombosis (DVT).
B.Critical illness-induced polyneuropathy.
C.Intensive care unit (ICU) delirium.
D.Propofol-related infusion syndrome (PRIS).
2T.I. is a 35-year-old man admitted to the ICU for

severe alcohol withdrawal. His medical history is

otherwise unknown. Laboratory values are within

normal limits on admission. He has been receiv-

ing a lorazepam infusion 6โ€“8 mg/hour for active

alcohol withdrawal. On day 4, his blood pressure is

130/75 mm Hg, oxygen saturation is 98% on 2 L

of oxygen, blood urea nitrogen (BUN) is 50 mg/dL,

and serum creatinine (SCr) is 2.0 mg/dL; he has a

new anion gap of 20 mEq/L, an osmolar gap of 18

mmol/L H2O, and a fractional excretion of sodium

of 0.2. Which is the most likely cause for his clinical

presentation?

A.Acute respiratory distress syndrome (ARDS).
B.Propylene glycol toxicity.
C.Delirium tremens.
D.Acute tubular necrosis.
3

R.B. is a 25-year-old man admitted to the ICU for

acute pancreatitis and sepsis. He is intermittently

agitated on hydromorphone 2 mg/hour and mid-

azolam 6 mg/hour (Richmond Agitation-Sedation

Scale [RASS] score of โ€“1 to +2) and is not oxygen-

ating adequately after adjustments on the ventilator.

The physician would like to initiate therapeutic

paralysis. Which is the next best step in the treat-

ment of this patient?

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