• No results found

Objectives. Important Principles

N/A
N/A
Protected

Academic year: 2021

Share "Objectives. Important Principles"

Copied!
12
0
0

Loading.... (view fulltext now)

Full text

(1)

Management of the Intubated

Management of the Intubated

Patient

Patient

Christopher J Edwards PharmD BCPS Christopher J. Edwards, PharmD, BCPS Clinical Pharmacist - Emergency Medicine March 19th, 2013

REPS EC SAG 2

Objectives

Describe the rationale for post intubation

analgesia and sedation

Compare and contrast various sedatives

commonly used in mechanically ventilated

patients

Design the optimum regimen of sedation and

analgesia for the recently intubated patient

Important Principles

Events prior to intubation can be painful

Intubation is painful

Procedures done after intubation are painful

Analgesia is the cornerstone of post intubation

care

(2)

Pain from Endotracheal Intubation

Rotondi AJ, et al. Patient’s recollections of

stressful experiences while receiving prolonged

mechanical ventilation in an intensive care unit.

Crit Care Med 2002

Crit Care Med 2002

Endotracheal tube pain , 0–10 scale (25

th

and 75

th

percentile)

ETT pain at its worst = 8 (6, 10) ETT pain at its least = 5 (3, 7)

Negative Effects of Poor Pain Control

Patients who recalled pain had higher

incidence of chronic pain, PTSD symptoms,

and lower health related quality of life

Schelling et al. CCM. 1998

Pain response increases catecholamine release,

impairs tissue perfusion

Deleterious effects on immune response

Post-Intubation Analgesia and Sedation in

the Emergency Department

Weingart GS et al. Estimates of sedation in patients

undergoing intubation in US EDs. 2013. Am J of EM

1,071,000 patients included, 46.4% received sedatives and/or opiates

Jordan, B et al. Inadequate provision of postintubation

Jordan, B et al. Inadequate provision of postintubation

anxiolysis and analgesia in the ED. 2008. Am J of EM

117 patients, 33% received no anxiolysis, 53% received no analgesia

Of 70 patients who received vecuronium, 4% received adequate anxiolysis or analgesia

(3)

Paralytic Choice and Time to Sedation

Early initiation of analgesia and sedation is

particularly important when long acting

paralytics are used

Watt JM, et al. Effect of paralytic type on time

to post-intubation sedative use in the ED. EMJ.

2012.

Significantly greater time between intubation and initiation of sedation in patients receiving rocuronium compared to succinylcholine

Emergency Pharmacists Can Help!

Endpoint

Before EPh After EPh

p – value

Rate of post

intubation analgesia

8 (20%)

20 (49%)

p = 0.005

Sedative or anxiolytic 30 (73%)

y

21 (51%)

p = 0.04

without analgesia

(

)

(

)

p

Time to analgesia

after intubation

98 minutes

45 minutes

N/A

Robey-Gavin, E and Abukar, L. Impact of clinical pharmacists on initiation of post-intubation analgesia in the emergency department. Poster presented at ASHP’s Midyear Clinical Meeting. 2012

SCCM Guidelines for Management of

Pain, Agitation, and Delirium in ICU

Barr J, et al. Critical Care Medicine. 2013.

Preemptive analgesia

Opiate based regimens

Light level sedation

Non-benzodiazapines first line

(4)

The ED is not the ICU

Procedures often performed immediately after

intubation

Central line placement

R di l i l i i

Radiological imaging

Lumbar puncture

Orthopedic reduction

Etc, etc, etc…

Higher nurse to patient ratios

Much shorter length of stay

Pain Assessment in Mechanically

Ventilated Patients

Pain Scales

BPS – Behavioral Pain Scale

CPOT – Critical Care Pain Observation Tool

Vit l i

h ld

t f th

l ti

Vital signs should prompt further evaluation

Respiratory rate

Tachycardia

Hypertension

Diaphoresis

Richmond Agitation Sedation Scale

(RASS)

Score Term Description

+ 4 Combative Overtly combative, violent, immediate danger to staff + 3 Very Agitated Pulls or removes tube(s) or catheter(s); aggressive + 2 Agitated Frequent non-purposeful movement, fights ventilator + 1 Restless Anxious but movements not aggressive vigorous 0 Alert and Calm

-1 Drowsy Not fully alert, but has sustained awakening (eye-opening/eye contact) to voice (>10 seconds) -2 Light sedation Briefly awakens with eye contact to voice (<10 seconds) -3 Moderate sedation Movement or eye opening to voice (but no eye contact) -4 Deep sedation No response to voice, but movement or eye opening

to physical stimulation

(5)

Important Concept

Bolus when patient acutely agitated

Titrating drip without bolus leads to slow resolution of agitation

Leads to aggressive titration

Leads to aggressive titration

Leads to over sedation\adverse effects

Leads to discontinuation of sedation

Leads to acute agitation

Rinse and repeat

Analgesia

Opiates

Who should receive

Almost anyone who is currently intubated

Who should not receive

Patients currently on naloxone

Certain patients intubated for oversedation/intoxication

Precautions

(6)

Fentanyl

Onset: 30 - 60 seconds with bolus dosing

Elimination Half-Life

0.5 - 1 hour for bolus doses

Extended with prolonged infusion, hepatic impairment

Dosing

Bolus dosing: 0.5 – 1 mcg/kg

Continuous infusion starting rate: 0.5-1 mcg/kg/hr

Less hypotension compared to morphine

Potential for chest wall rigidity

Hydromorphone

Onset: 5 - 15 minutes with bolus dosing

Elimination Half-Life

2 – 3 hours for bolus doses

Dosing

Intermittent bolus dosing: 0.2 – 1 mg every 1 - 2 hours

Continuous infusion rate: 0.5 – 3 mg/hr

Less hypotension compared to morphine

Morphine

Onset: 5 - 10 minutes with bolus dosing

Elimination Half-Life

3 - 4 hours for bolus doses

D i

Dosing

Intermittent bolus dosing: 2 - 4 mg every 1 - 2 hours

Continuous infusion rate: 2 – 30 mg/hr

Accumulation of active metabolite in renal

failure

(7)

Opiates

Opiate Equi-Analgesic Dose Onset Elimination Half-Life

Bolus Dose Initial Infusion Rate Fentanyl 0.1 mg (100 mcg) 30 – 60 sec 0.5 – 1 hr 0.5-1 mcg/kg q 0.5 – 1 hr 0.5-1 mcg/kg/hr H d h 1 5 5 15 i 2 3 h 0 5 1 0 5 3 /h Hydromorphone 1.5 mg 5 – 15 min 2 – 3 hr 0.5 – 1 mg q 1 – 2 hr 0.5 – 3 mg/hr Morphine 10 mg 5 – 10 min 3 – 4 hr 2 – 4 mg q 1 – 2 hr 2 – 30 mg/hr

Sedatives

Propofol

Non-benzodiazepine sedative

Sedative, hypnotic, anxiolytic, amnestic, antiemetic, and anticonvulsant properties

NO analgesic effects

Who should get it

Patients requiring frequent neurologic examinations

Patients with traumatic brain injury

Precautions/contraindications

(8)

Propofol

Onset: 30-60 seconds with bolus dosing

Elimination Half-Life

3-12 hours with continuous infusion

Duration extended with prolonged infusion, higher rate of infusion, excessive lipid stores, older patients

Duration decreased in younger patients

Dosing

Bolus dosing: 0.5 – 1 mg/kg

Continuous infusion: 5 – 70 mcg/kg/min Typical starting rate: 20 mcg/kg/min

Benzodiazepines

GABA-A activation leading to sedative effects

Anxiolytic, amnestic, hypnotic, and anticonvulsant properties

NO analgesic effect

Who should receive

Patients who cannot tolerate propofol

Patients who cannot tolerate propofol

Patients who do not require frequent awakening

Precautions

Patients with hepatic failure (prolonged duration)

Chronic alcohol/benzo users may require higher doses

Midazolam

Onset: 2 – 5 minutes after bolus

Elimination Half-Life

3 – 11 hours

Extended with prolonged infusion, higher rate of infusion, older patients, hepatic failure, renal insufficiencyp , p , y

Dosing

Bolus dosing: 0.05 – 0.1 mg/kg

Initial infusion rate: 0.02 – 0.1 mg/kg/hr

Concerns

Accumulation of active metabolite in renal insufficiency

(9)

Lorazepam

Onset: 3 – 10 minutes after bolus

Elimination Half-Life

8-15 hours

Duration extended with prolonged infusion, higher rate of infusion, older patients, hepatic failure, renal insufficiency

Dosing

Bolus dosing: 0.02 – 0.04 mg/kg q 6 hrs prn

Infusion rate: 0.01 – 0.1 mg/kg/hr

Preferred benzodiazepine in hepatic failure

Concern for propylene glycol toxicity

Dexmedetomidine

Selective

α

2-receptor agonist

Sedative, analgesic, sympatholytic properties

Lacks amnestic and anticonvulsant properties

Wh

h ld

i

Who should receive

Patients requiring short term, low level sedation

Patients who are difficult to wean off of mechanical ventilation

Precautions

Hemodynamic instability (bradycardia, hypotension)

No amnestic effects

Dexmedetomidine

Onset: 15 minutes after initiation of infusion

Elimination Half-Life

1.8-3.1 hours

Extended in hepatic insufficiency

Dosing

Bolus not recommended due to adverse hemodynamic effects

(10)

Sedatives

Agent Onset After Bolus Elimination Half-Life

Bolus Dose Maintenance

Dosing Propofol 0.5 - 1min 3 - 12 hr

(Short term use)

0.5 – 1 mg/kg 5 – 70 mcg/kg/ min

Dexmedetomidine N/A 1 8 – 3 1 hr Not recommended 0 2-0 7 mcg/kg/hr Dexmedetomidine N/A 1.8 3.1 hr Not recommended 0.2 0.7 mcg/kg/hr

Midazolam 2 – 5 min 3 – 11 hr 0.05 -0.1 mg/kg 0.02-0.1 mg/kg/hr Lorazepam 3 – 10 min 8 – 15 hr 0.02 – 0.04 mg/kg (2 mg max) 0.01 – 0.1 mg/kg/hr (max 10 mg/hr)

Ketamine

NMDA receptor antagonist

Dissociative anesthetic with analgesic, sympathomimetic, and brochodilatory effects

Who should receive

Who should receive

Patients in status asthmaticus

Opioid tolerant patients with uncontrolled pain

Precautions

May lead to ICU delirium

Intracranial and intraocular pressure

Ketamine

Onset: 30 – 60 seconds after bolus dose

Elimination Half-Life

2 – 3 hours

Extended in hepatic insufficiency

Dosing

Bolus dosing: 0.1-0.5 mg/kg

(11)

Non-Pharmacologic Measures

Talk to the patient!

Optimize ventilator settings

Minimize disruptions (if possible)

p

( p

)

Soft restraints

Other Concepts in Post Intubation

Management

Prevention of ventilator associated pneumonia

Oral care early and often

Elevate head of the bed at least 30 degrees

OG/NG tube placement gastric suctioning

OG/NG tube placement, gastric suctioning

Ocular care

Stress ulcer prophylaxis

Mechanical ventilation > 48 hours

Coagulopathy

Conclusions

Analgesia and sedation are key to ensuring

patient and provider comfort after intubation

Keep patient’s clinical picture and trajectory in

mind when designing regimen

Post intubation management is an easy way for

emergency pharmacists to make a big impact!

(12)

Further Reading

Barr J, Fraser GL, Puntillo K, Ely EW, Gelinas

C, Dasta JF, et al. Clinical practice guidelines

for the management of pain, agitation, and

d li i

i

d l

i

i

h i

i

delirium in adult patients in the intensive care

unit. Critical Care Med. 2013; 41:263-306

References

Related documents

 All  other  necessary  chemicals  and  lab  supplies   were  obtained  from  Sigma  (St.   Mineral   deposition  of  osteogenically  induced  cells  was  confirmed

In this short paper we have tried to extend the traditional Blinder-Oaxaca decomposition of wage differences to take account of (a) discrimination at point of entry to the

The high proportion of shrub and canopy cover related to the literature range suggests that without proper, effective habitat management, the area may degrade to unsuitable habitat

After preparation of impure paracetamol followed by recrystallisation, the student actually obtained 4.07 g of pure paracetamol.. Calculate the mass of impure paracetamol expected

ASEAN Jepang mengalami keuntungan akibat terjadinya trade creation yang berdampak pada peningkatan pendapatan pemerintah dari tarif yang di terima pemerintah dari

Speci fi c objectives were to: (1) determine the 5-year prevalence in paediatric admissions and characteristics of unplanned hospital readmissions; (2) examine the time interval

We tested the hypothesis for an involvement of partly segregated cortico-subcortical structures between phonologic and semantic fluency by examining with a voxel-based lesion

Figure 19 Reaction time evaluation in optimum conditions (means with same letter do not differ each other at Tukey test with 95% of confidence).. The reaction in US system seems