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Wednesday, August 13, 2025

Sickle Cell Crisis

Card A — Ketamine + Dexmedetomidine (Precedex) for Acute Sickle Cell Pain

Opioid-sparing analgesia for moderate to severe vaso-occlusive pain not controlled with standard therapy. Intended for step-down or ICU monitoring. Follow local protocols and pharmacy guidance.

No intubation required at analgesic doses

Quick start (no bolus)

Drug Starting infusion Titration Typical max (analgesic range) Notes
Ketamine 0.1 to 0.3 mg per kg per hour Increase by 0.05 to 0.1 mg per kg per hour every 30 to 60 minutes 0.5 mg per kg per hour Optional slow bolus 0.1 to 0.3 mg per kg over at least 10 minutes if protocol allows
Dexmedetomidine 0.2 to 0.4 microgram per kg per hour Increase by 0.1 to 0.2 microgram per kg per hour every 20 to 30 minutes 0.7 to 1.0 microgram per kg per hour per local policy No loading dose; avoid rapid bolus to reduce bradycardia and hypotension

Monitoring and targets

  • Continuous pulse oximetry; noninvasive blood pressure every 15 minutes during titration, then every hour
  • Cardiac monitoring during initiation and dose changes
  • Assess pain and sedation at least hourly
Target RASSMeaning
0 to minus 20 = alert and calm; minus 1 = drowsy but sustained eye contact; minus 2 = light sedation, briefly awakens to voice

Expected effects and airway considerations

  • Both agents preserve spontaneous ventilation at analgesic doses
  • Dexmedetomidine may cause bradycardia or hypotension
  • Ketamine may cause mild increase in heart rate and blood pressure; dissociation possible

Adjuncts to continue

  • Acetaminophen scheduled if not contraindicated
  • NSAID if no acute kidney injury or bleeding risk
  • Rescue opioid for breakthrough pain
  • Bowel regimen, antiemetic, incentive spirometry, hydration and trigger management

Cautions

  • Dexmedetomidine: caution in significant bradycardia or higher-degree heart block without pacer
  • Ketamine: caution in uncontrolled hypertension, active ischemia, or acute psychosis; consider lower start in severe hepatic impairment

Disclaimer: Adult reference; verify doses and maximums with local policies and pharmacy.

Card B — Complete Analgesia Options for Acute Sickle Cell Crisis

Multimodal approach: treat pain aggressively while preserving breathing, prevent acute chest syndrome, and address triggers. Use clinical judgment and local order sets.

Pharmacologic and non-pharmacologic

Opioids (first line for moderate to severe pain)

Agent Typical IV bolus for titration Common PCA settings (opioid naive) Notes
Morphine 2 to 4 mg IV every 10 to 15 minutes as needed Demand 1 to 2 mg; lockout 6 to 10 minutes; no basal initially Reduce dose in renal impairment; histamine release may cause pruritus
Hydromorphone 0.2 to 0.4 mg IV every 10 to 15 minutes as needed Demand 0.1 to 0.3 mg; lockout 6 to 10 minutes; no basal initially Often preferred when renal dysfunction or morphine intolerance
Fentanyl 25 to 50 microgram IV every 5 to 10 minutes as needed Demand 10 to 25 microgram; lockout 6 to 10 minutes Short acting; hemodynamically stable option if hypotension limits others

Mini PCA setup cheat sheet

Patient profile Suggested starting PCA (choose one agent) Basal infusion Safety notes
Opioid naive, normal kidney function Morphine demand 1 to 2 mg, lockout 6 to 10 minutes
or Hydromorphone demand 0.1 to 0.2 mg, lockout 6 to 10 minutes
or Fentanyl demand 10 to 25 microgram, lockout 6 to 10 minutes
None at start Assess pain and sedation every 1 hour during first 4 to 6 hours
Opioid tolerant (taking daily opioids before admission) Use higher end of demand ranges above; consider shorter lockout (6 minutes)
Example: Hydromorphone demand 0.2 to 0.3 mg
Consider low basal only if clearly tolerant and monitored:
Morphine 0.5 to 1 mg per hour, or
Hydromorphone 0.1 to 0.3 mg per hour, or
Fentanyl 25 to 50 microgram per hour
Confirm tolerance; continuous pulse oximetry recommended
Renal impairment or high risk for oversedation (elderly, low BMI, OSA) Prefer Hydromorphone or Fentanyl over Morphine; use lower demand dose:
Hydromorphone 0.05 to 0.1 mg; lockout 8 to 10 minutes
None at start Avoid basal early; reassess frequently; consider capnography if available
Persistent severe pain despite above Keep PCA for rescue None or minimal basal unless clearly tolerant Add multimodal infusions (Ketamine or Dexmedetomidine) per Card A

Always individualize based on age, kidney and liver function, and prior opioid exposure. Basal infusions increase risk of respiratory depression—use only with clear tolerance and close monitoring.

Non-opioid analgesics and adjuvants

Class Agent Adult dosing Key cautions
Acetaminophen PO or IV 650 to 1000 mg every 6 to 8 hours; max 3000 mg per day in most adults (up to 4000 mg per day if low risk and per policy) Reduce max dose in liver disease or with alcohol use disorder
NSAID Ketorolac IV 15 mg IV every 6 hours in older or renally at risk; 30 mg IV every 6 hours in low risk; limit 5 days Avoid in acute kidney injury, bleeding risk, platelets low, peptic ulcer, or recent surgery
Gabapentinoid Gabapentin Start 100 to 300 mg by mouth three times daily; titrate as tolerated; adjust for kidney function Sedation, dizziness; renal dose adjustment required
Gabapentinoid Pregabalin 50 to 75 mg by mouth two or three times daily; adjust for kidney function Sedation, edema; renal dose adjustment required
Antidepressant (chronic overlay) Duloxetine 30 mg daily, then 60 mg daily if tolerated Not for rapid acute relief; avoid in severe liver disease
Antidepressant (chronic overlay) Amitriptyline 10 to 25 mg at bedtime Anticholinergic effects; avoid in prolonged QT

Analgesic infusions beyond opioids

Agent Starting infusion Titration and typical max Monitoring Notes
Ketamine 0.1 to 0.3 mg per kg per hour Titrate by 0.05 to 0.1 mg per kg per hour; typical max 0.5 mg per kg per hour Cardiac and oximetry monitoring Preserves breathing; may cause mild dissociation
Dexmedetomidine 0.2 to 0.4 microgram per kg per hour Titrate by 0.1 to 0.2 microgram per kg per hour; typical max 0.7 to 1.0 microgram per kg per hour Cardiac and blood pressure monitoring No loading dose to reduce bradycardia and hypotension
Lidocaine IV Optional bolus 1 mg per kg over 10 minutes, then 0.5 to 1.5 mg per kg per hour Titrate within 0.5 to 2 mg per kg per hour per protocol Continuous ECG and neurologic checks Avoid in significant heart block without pacer, severe hepatic failure, or seizure disorder; use institutional protocols
Clonidine 0.1 mg by mouth every 8 to 12 hours Patch 0.1 to 0.2 mg per day weekly if oral not feasible Blood pressure and heart rate Adjunct for analgesia and anxiety; caution hypotension and bradycardia

Non-pharmacologic and supportive measures

Measure How it helps Practical notes
Heat packs and gentle positioning Muscle relaxation and local comfort Protect skin; avoid burns; limit continuous heat time
Incentive spirometry and early mobilization Prevents atelectasis and acute chest syndrome Set hourly reminders; document volumes and effort
Hydration and trigger management Addresses dehydration and acidosis that worsen vaso-occlusion Avoid overhydration if cardiac or renal dysfunction present
Cognitive and behavioral strategies Reduces anxiety and pain amplification Brief coaching: breathing exercises, guided imagery, reassurance
Sleep hygiene and quiet environment Improves rest and reduces sympathetic tone Cluster care at night; dim lights; limit alarms if safe

Disease-modifying therapy such as hydroxyurea or transfusion strategies may reduce future crises but do not treat acute pain directly; manage triggers and complications in parallel.

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