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Which opioids are the cornerstone of treatment for pain for patients in the ICU?
fentanyl and hydromorphone
Which opioid is most commonly used for pain in the ICU?
fentanyl
A/E for opioids
- oversedation
- respiratory depression
- delirium
- hypotension
- decreased GI motility
Potential components of multimodal approach to pain treatment
- APAP
- NSAIDs
- lidocaine
- ketamine
- neuropathic pain medications (pregabalin, gabapentin)
Non-pharmacist therapy for pain in the ICU
- music
- pet therapy
- massage
- temperature control
- relaxation techniques
What is used for sedation if anxiety/agitation is not relieved by analgosedation in mechanically ventilated patients?
- benzodiazepines
- propofol
- dexmedetomidine
Which agents do the PADIS guidelines recommend to maintain a light goal of sedation and to minimize delirium?
propofol and dexmedetomidine
Lorazepam onset
15-20 minutes
Lorazepam duration
6-8 hours
ADRs: lorazepam
- anterograde amnesia
- CNS effects (drowsiness, sedation)
- paradoxical reactions
- withdrawal syndrome
Monitoring: lorazepam
- respiratory and CV status
- BP, HR
- symptoms of anxiety
- mental alertness
Pearls: lorazepam
intermittent dosing preferred to continuous infusion
Propofol onset
30 seconds
Propofol duration
3-10 minutes
ADRs: propofol
- hypertriglyceridemia
- pancreatitis
- propofol-related infusion syndrome
- hyperkalemia
- hepatomegaly
Monitoring: propofol
- BP
- oxygen saturation
- S/sx of propofol related infusion syndrome
- CNS function
Dexmedetomidine onset
5-10 minutes
Dexmedetomidine duration
1-2 hours
ADRs: dexmedetomidine
- hypotension
- bradycardia
- tachyphylaxis
Monitoring: dexmedetomidine
- level of sedation
- HR
- RR
- heart rhythm
- BP
MOA: dexmedetomidine
alpha 2 agonist with anesthetic and sedative properties
Delirium
- disturbed level of consciousness
- reduced ability to focus, sustain, or shift attention
- change in cognition
- development of perceptual disturbances
True or false: there are several FDA approved treatments for delirium
False
Management strategies for preventing delirium
- reducing BZD utilization
- patient reorientation
- improving sleep hygiene
- early mobilization
- lighter sedation strategies
What can be done to improve sleep for patients in the ICU?
minimize noise and light disturbances
Blood glucose target for patients in ICU
Guideline recommendation for insulin therapy in ICU
initiate insulin therapy after two consecutive blood glucose values greater than 180 mg/dL to reach a goal of less than 180 mg/dL
How often should glucose be checked in an ICU setting when patient is given insulin?
every 1-2 hours
What patients are considered high risk for clinically important upper GI bleeds?
- coagulopathy (platelets
- shock
- chronic liver disease
- neurocritical care adults
Prophylaxis for stress-induced UGIB
H2RAs and PPIs (PPIs preferred), oral route
When should stress ulcer prophylaxis (SUP) be discontinued?
once the risk factor is resolved
Nonmodifiable risk factors for VTE
- factor V Leiden or hematological disorders
- age >40 years
- familial hx of thrombosis
- oncological disorders
- male sex
Modifiable risk factors for VTE
- immobility
- medications
- obesity
- transfusion related
- surgery or trauma
- PICC lines
What risk assessment is used to evaluate risk of VTE in hospitalized patients?
Padua score
UFH dose/route/frequency for VTE prevention
5000 units subQ 2-3x/day
CrCl adjustment for UFH
none
Monitoring: UFH
- prothrombin time (PT)
- activation partial thromboplastin time (aPTT)
- s/sx of bleeding
- hematocrit
- hemoglobin
- platelet count (for HIT)
LMWH dose/route/frequency for VTE prevention
40 mg subQ daily
CrCl adjustment for LMWH
30 mg subQ daily
Monitoring: LMWH
- platelet count
- hemoglobin
- hematocrit
- s/sx of bleeding
- serum creatinine
Fondaparinux dose/route/frequency for VTE prevention
2.5 mg subQ daily
CrCl adjustment for fondaparinux
- Caution 30-50 mL/min
- C/I
Monitoring: fondaparinux
- CBC
- platelet count
- serum creatinine
- s/sx bleeding
What agents are recommended for critically ill patients to treat or prevent constipation?
PEG, bisacodyl, senna, metoclopramide
Preload
volume in the left ventricle at the end of diastole
Contractility
force of the heart
Afterload
overall resistance to blood flow leaving the heart
Mean arterial pressure (MAP)
monitoring parameter in shock
Goal MAP in shock
>/= 65
MAP equation
MAP = (SBP + 2*DBP)/3
Hypovolemic shock causes
- bleeding
- diarrhea
- vomiting
- diuretic use
- diabetic ketoacidosis
- diabetes insipidus
- damaged skin
Hypovolemic shock alteration in hemodynamic variables
decreased preload
Cardiogenic shock causes
- MI
- CHF
- arrhythmias
- septal wall rupture
Cardiogenic shock alteration in hemodynamic variables
decreased myocardial contractility
Distributive shock causes
- sepsis
- anaphylaxis
- neurogenic
Distributive shock alteration in hemodynamic variables
decreased after load (and increase in contractility)
Sepsis
- life-threatening organ dysfunction caused by a dysregulated host response to infection
- response to infection which manifests as systemic inflammation, coagulation, and tissue hypo perfusion, potentially leading to organ dysfunction
Septic shock
subset of sepsis with circulatory and cellular/metabolic dysfunction associated with a higher risk of mortality
General approach to treatment of sepsis
1. prompt recognition of septic patient and early implementation of therapies
2. fluid therapy, using crystalloids, to restore intravascular volume depletion
3. early administration of broad-spectrum anti-microbial therapy
4. vasopressor therapy, using NE initially, to maintain hemodynamic stability in patients with septic shock refractory to fluid resuscitation
5. IV hydrocortisone may be considered for patients who remain hemodynamically unstable despite adequate fluid and vasopressor support
6. glycemic control via infusion of regular insulin to maintain glucose levels between 140 and 180 mg/dL
Adjunctive therapies for sepsis
- blood product administration
- analgesia
- sedation
- neuromuscular blockade
- renal replacement therapy
- sodium bicarbonate therapy
- VTE prophylaxis
- stress ulcer prophylaxis
- nutrition
Examples of crystalloid solutions
- 0.9% sodium chloride
- lactated ringer solution
Examples of colloid solutions
- albumin 5%
- albumin 25%
Which type of fluid is preferred in septic shock?
crystalloids
ADRs: crystalloid fluids
- fluid overload
- edema
- electrolyte imbalances
- dilution of coagulation factors
Initial resuscitation: crystalloids
30 mL/kg over first 3 hours
Initial resuscitation: colloids
500-1000 mL
Alpha receptor action
vasoconstriction in periphery
B1 receptor action
Chronotropic (cardiac rate) and inotropic (myocardial contractility)
Dopaminergic receptor action
increase renal blood flow
Norepinephrine receptors/effects
alpha adrenergic agonist (vasoconstriction in periphery)
What is the first line pressor in septic shock?
NE
ADRs: NE
- extravasation --> tissue necrosis
- bradycardia
- arrhythmias (less than DA)
Normal vasopressin action
normally increased during hypotension to maintain blood pressure by vasoconstriction
Vasopressin in septic shock
shock causes depletion of vasopressin
Vasopressin receptors/effects
direct vasoconstrictor without inotropic or chronotropic effects
ADRs: vasopressin
- Afib
- bradycardia
- decreased cardiac output
- ischemic skin lesions
- hyponatremia
Note about DA as a pressor
receptors and effect are dose-dependent
Generally, what does DA do in shock
increases stroke volume and HR
1-5 mcg/kg/min of DA in shock
improve renal blood flow (not appropriate)
5-10 mcg/kg/min of DA in shock
B1 and mild B2 and DA effects
10-20 mcg/kg/min of DA in shock
alpha effects
ADRs: DA
- tachycardia
- arrhythmias
- N/V
- anxiety
- HA
Epinephrine receptors/effects
nonspecific alpha and beta adrenergic agonist that can increase cardiac index and produce significant peripheral vasoconstriction
ADRs: epinephrine
- arrhythmias
- chest pain
- HTN
- tachycardia
- hyperglycemia
- insulin resistance
- N/V
- anxiety
Phenylephrine receptors/effects
- fast-acting and short-acting pure alpha 1 agonist
- least likely to cause tachycardia, but may decrease stroke volume
When do we use phenylephrine in shock?
only in patients with high cardiac output in whom tachycardia or ischemia limits use of other vasopressors
ADRs: phenylephrine
- arrhythmias
- HTN
- ischemia
- low cardiac output
- diaphoresis
- N/V
- blurred vision
Dobutamine receptors/effects
beta-adrenergic inotropic agent that is used for improvement of cardiac output and oxygen delivery
When do we use dobutamine?
- septic pts with adequate filling pressure and BP, but low cardiac index
- if used in hypotensive pt, combine with vasopressor therapy
ADRs: dobutamine
- chest pain
- tachycardia
- HTN
- palpitations
Angiotensin II receptors/effects
hormone in renin-angiotensin-aldosterone system --> causes vasoconstriction and increases release of aldosterone (increases BP)
ADRs: angiotensin II
- DVT
- tachycardia
- peripheral ischemia
- thrombocytopenia
- metabolic acidosis
- fungal infection
- delirium
When are pressors recommended in septic shock?
pts with systolic BP