Pain Management Analgesia: Comparison
Please note this is a comparison between Version 1 by Samuel Huang and Version 2 by Catherine Yang.

Effective pain management in hospitalized patients involves a multimodal approach tailored to the severity and type of pain (mild, moderate, or severe) and the patient's clinical condition. The goal is to provide adequate pain relief while minimizing side effects and preventing complications like opioid dependence or gastrointestinal and renal issues from NSAIDs.

  • Mild Pain: Managed with non-opioid analgesics such as acetaminophen or NSAIDs. Topical agents like lidocaine patches or capsaicin cream may be used for localized pain.

  • Moderate Pain: Combines non-opioid analgesics with low-potency opioids (e.g., tramadol). Adjuncts like topical therapies or neuropathic pain medications (e.g., gabapentin) may also be employed.

  • Severe Pain: Requires short-acting opioids (e.g., morphine, hydromorphone) often administered via scheduled dosing or patient-controlled analgesia. Long-acting opioids are reserved for chronic conditions like cancer-related pain.

Special considerations include adjusting treatment for patients with chronic pain, hepatic or renal dysfunction, or risk factors for adverse drug reactions. Preventive measures, such as bowel regimens for opioid-induced constipation, and regular reassessment of pain control are critical components of care.

The approach prioritizes not just the relief of pain but also the functional improvement and safety of patients. Consultation with pain management or palliative care teams is advised for complex or refractory cases.

  • critical care
  • analgesia
  • multimodal
  • emergency medicine

1. Pain Management Regimens: Mild, Moderate, Severe Pain with Breakthrough Pain Options

Pain Management Regimens: Mild, Moderate, Severe Pain with Breakthrough Pain Options

Mild Pain

  • Acetaminophen (Tylenol):
    • PRN: 650 mg q4hr or 1000 mg q6hr as needed.
    • Scheduled: Consider for patients with uncontrolled mild pain.
    • Max Doses:
      • 4g/day in patients with normal liver function.
      • 2g/day in those with liver dysfunction or cirrhosis.
    • Routes: Oral or rectal preferred; IV is available but expensive.
  • NSAIDs:
    • Use cautiously in patients at risk for GI bleeding or acute kidney injury.
    • Ibuprofen: 400 mg PO every 6–8 hours.
    • Naproxen: 250–500 mg PO every 12 hours.
    • Ketorolac (IV/IM): 10–15 mg q6hr (limit use to 48 hours to reduce risks).
    • Consider topical NSAIDs (e.g., Diclofenac gel) for localized musculoskeletal pain.

Moderate Pain

  • Combination Therapy:

    • Acetaminophen ± NSAIDs for additive effects.
  • Topical Analgesics:

    • Lidocaine Patch: Apply up to 3 patches; remove after 12 hours.
    • Capsaicin Cream: Effective for neuropathic and osteoarthritis pain.
  • Low-Potency Opioids:

    • Tramadol: 50 mg PO q4–6hr PRN.
      • Avoid in patients with seizure history.
    • Consider consultation for opioid-sparing strategies if chronic pain.

Severe Pain

  • Opioid Therapy:

    • Short-acting Opioids: First-line for acute severe pain.
      • Oxycodone: 5 mg PO q4–6hr PRN.
      • Hydromorphone (Dilaudid): 1–2 mg IV q4–6hr PRN.
      • Morphine: IV or PO options; adjust for renal impairment.
      • Fentanyl (IV): Short half-life, for acute episodes.
    • Use conversion charts for switching opioids; start at 75% of equianalgesic dose when rotating.
  • Adjuncts:

    • Ketamine: Consult pain service. Useful for opioid-sparing.
    • Methadone: Requires specialist involvement for titration.
  • Neuropathic Pain:

    • Duloxetine or Venlafaxine.
    • Gabapentin: Start at 100–300 mg PO nightly, titrate.

Breakthrough Pain

  • PRN Opioids:
    • 10–15% of total daily opioid dose, every 2–4 hours as needed.
    • Ensure opioid conversion and rescue dosing are appropriately calculated.

General Considerations

  • Prevent Constipation with Opioids:
    • Prophylaxis: Senna and docusate or polyethylene glycol (Miralax).
  • Multimodal Pain Control:
    • Combine pharmacologic and non-pharmacologic options (e.g., warm compresses, physical therapy).
  • Consult Services:
    • Pain management or palliative care for complex cases or refractory pain.

2. Summary: Management of Vaso-Occlusive Crisis in Sickle Cell Disease

 

 

Summary: Management of Vaso-Occlusive Crisis in Sickle Cell Disease

Nonnarcotic Analgesics for Mild Pain

  • Acetaminophen (Tylenol): 500–1,000 mg q4–6 hours (Max < 4,000 mg/day).
  • Aspirin: 650–1,000 mg q4–6 hours (Max < 4,000 mg/day).
  • NSAIDs:
    • Ibuprofen: 200–400 mg q4–6 hours.
    • Naproxen: 500 mg initially, then 250 mg q6–8 hours.
    • Ketoprofen: 25–75 mg q6–8 hours (Max < 300 mg/day).

Narcotic Analgesics for Moderate Pain

  • Weak opioids like codeine and oxycodone can be titrated for moderate pain control.
  • Avoid prolonged use due to dose-limiting side effects (e.g., sedation, nausea, vomiting).

Opioids for Severe Pain

  • AdministWer strongerak opioids parenterally or via patient-controlledlike analgesia (PCA) for severe pain:
    • Morphine:
      • Oral: 15–30 mg q4 hours.
      • IV: 0.1–0.15 mg/kg q3–4 hours.
    • Hydromorphone (Dilaudid):
      • Oral: 2–4 mg q4–6 hours.
      • IV: 1–2 mg q4–6 hours.
    • Avoid Meperidine due to short half-life, risk of neurotoxicity, and complications with repetitive dosing.
    codeine and oxycodone can be titrated for moderate pain control.
  • Avoid prolonged use due to dose-limiting side effects (e.g., sedation, nausea, vomiting).

BOpioids foreakthrough Severe Pain

  • Administer 1/4 sto 1/2 of the maintenance dose based on sedation level.ronger opioids parenterally or via patient-controlled analgesia (PCA) for severe pain:
    • Morphine:
      • Oral: 15–30 mg q4 hours.
      • IV: 0.1–0.15 mg/kg q3–4 hours.
    • Hydromorphone (Dilaudid):
      • Oral: 2–4 mg q4–6 hours.
      • IV: 1–2 mg q4–6 hours.
    • Avoid Meperidine due to short half-life, risk of neurotoxicity, and complications with repetitive dosing.
  • If 3+ rescue doses are needed in 24 hours, increase maintenance dose by 25–50%.

Breakthrough Pain

  • Administer 1/4 to 1/2 of the maintenance dose based on sedation level.
  • If 3+ rescue doses are needed in 24 hours, increase maintenance dose by 25–50%.

Supportive Care

  • Fluids:
    • Oral hydration for mild crises; IV fluids for severe dehydration or vomiting.
    • Use balanced solutions (e.g., 5% dextrose in 0.25% normal saline) after correcting deficits.
  • Oxygen:
    • Only for hypoxemia; unnecessary in normoxic patients.
    • Use arterial blood gas if pulse oximetry is unreliable.

Hydroxyurea

  • Indicated for patients with severe recurrent crises.
  • Dosage: Start at 500 mg/day, titrate to 1,000–2,000 mg/day.
  • Monitor blood counts every 4–6 weeks.

Nonpharmacologic Strategies

  • HeIndicat application, physical therapy, TENS, distraction techniques, and self-hypnosised for patients with severe recurrent crises.
  • Dosage: Start at 500 mg/day, titrate to 1,000–2,000 mg/day.
  • Monitor blood counts every 4–6 weeks.

Key MNonphanagement Principlrmacologic Strategies

  • AvHeat applicatioid delays in analgesian, physical therapy, TENS, distraction techniques, and self-hypnosis.
  • Prefer scheduled dosing over PRN.
  • Regular reassessment of pain, sedation, and vital signs.
  • Transition to oral analgesics as pain resolves and taper doses gradually.
  • Provide a prescription for pain control upon discharge if needed.

3.Key Management Principles

  • Avoid delays in analgesia.
  • Prefer scheduled dosing over PRN.
  • Regular reassessment of pain, sedation, and vital signs.
  • Transition to oral analgesics as pain resolves and taper doses gradually.
  • Provide a prescription for pain control upon discharge if needed.

 

Opioid Overdose Order Set

3.1. Monitoring and Initial Assessment

  • Vitals Monitoring:

    • Continuous pulse oximetry, cardiac telemetry.
    • Capnography if available (preferred for assessing hypoventilation).
    • Measure respiratory rate and mental status every 15 minutes until stable, then every hour.
  • Labs:

    • Arterial blood gas (ABG) or venous blood gas (VBG) to assess CO2 retention.
    • Basic metabolic panel (BMP) to check for acidosis or hyperkalemia.
    • Serum glucose to rule out hypoglycemia as a contributor.
    • Urine toxicology screen.
    • Blood ethanol level if history or suspicion of concurrent alcohol ingestion.

3.2. Airway and Breathing

  • AVirway Supporttals Monitoring:

    • EConsure airway patency; initiate bag-mask ventilation if respiratory rate < 8/min or oxygen saturation < 92% despite oxygentinuous pulse oximetry, cardiac telemetry.
    • Capnography if available (preferred for assessing hypoventilation).
    • Measure respiratory rate and mental status every 15 minutes until stable, then every hour.
  • SupplementLal Oxygenbs:

    • Adminisrter 2–6 L/min via nasal cannula or non-rebreather mask as needed to maintain oxygen saturation > 92%ial blood gas (ABG) or venous blood gas (VBG) to assess CO2 retention.
    • Basic metabolic panel (BMP) to check for acidosis or hyperkalemia.
    • Serum glucose to rule out hypoglycemia as a contributor.
    • Urine toxicology screen.
    • Blood ethanol level if history or suspicion of concurrent alcohol ingestion.

32.3. Naloxone Administratio Airway and Breathing

  • InAitial Dosingrway Support:

    • Naloxone (Narcan):
      • IV Route: 0.04 mg IV bolus initially; repeat every 2–3 minutes, titrate up to 2 mg as needed for adequate respiratory effort.
      • IM/SC Route: 0.4 mg; may repeat every 2–3 minutes.
      • Intranasal Route: 4 mg in one nostril, may repeat after 3–5 minutes if no response.
      Ensure airway patency; initiate bag-mask ventilation if respiratory rate < 8/min or oxygen saturation < 92% despite oxygen.
  • CoSupplemensider Infusiotal Oxygen:

    • FoAdminister long-acting opioid overdoses or recurrent respiratory depression:
      • Naloxone Infusion: Start at 0.02–0.1 mg/hour; titrate to effect (based on respiratory rate and oxygenation).
      2–6 L/min via nasal cannula or non-rebreather mask as needed to maintain oxygen saturation > 92%.

3.4. Supportive MeasuresNaloxone Administration

  • IVnitial FluidsDosing:

    • Start Normal Saline (0.9% NaCloxone (Narcan) 1 L bolus if hypotension is present.:
      • IV Route: 0.04 mg IV bolus initially; repeat every 2–3 minutes, titrate up to 2 mg as needed for adequate respiratory effort.
      • IM/SC Route: 0.4 mg; may repeat every 2–3 minutes.
      • Intranasal Route: 4 mg in one nostril, may repeat after 3–5 minutes if no response.
  • HypCoglycemia Managementnsider Infusion:

    • IfFor blood glucose < 70 mg/dL, administerlong-acting opioid overdoses or recurrent respiratory depression:
      • DeNaloxtrose 50% (D50)one Infusion: 1Start amp (25–50 mL) IV push, repeat as neededt 0.02–0.1 mg/hour; titrate to effect (based on respiratory rate and oxygenation).
  • Bicarbonate Therapy:

    • If severe acidosis (pH < 7.2):
      • Sodium bicarbonate: 1 amp IV, repeat based on ABG results.

34.5. Observation and Tapering Supportive Measures

  • Observe patients for at least 2–4 hours after last naloxone dose for signs of recurrent respiratory depression.

    IV Fluids:

    • Start Normal Saline (0.9% NaCl) 1 L bolus if hypotension is present.
  • Extend observation to 6–12 hours for long-acting opioids (e.g., methadone, extended-release formulations).

    Hypoglycemia Management:

    • If blood glucose < 70 mg/dL, administer:
      • Dextrose 50% (D50): 1 amp (25–50 mL) IV push, repeat as needed.
  • Bicarbonate Therapy:

    • If severe acidosis (pH < 7.2):
      • Sodium bicarbonate: 1 amp IV, repeat based on ABG results.

35.6. Educ Observation and PreventioTapering

  • AObssess for opioid use disorder (OUD) and consider initiating treatment:
    • Buprenorphine for withdrawal management.
    • Referral to addiction medicine or pain management.
    erve patients for at least 2–4 hours after last naloxone dose for signs of recurrent respiratory depression.
  • PExtend observation to 6–12 hourescribe as for long-acting opioids (e.g., methadone, naloxone kit for discharge with education on overdose prevention and response.extended-release formulations).

36.7. Documentat Education and Prevention

  • RAssecord time, dose, and route of naloxone administration.ss for opioid use disorder (OUD) and consider initiating treatment:
    • Buprenorphine for withdrawal management.
    • Referral to addiction medicine or pain management.
  • Document patient’s Presponse to treatment, including changes in respiratory rate, oxygenation,cribe a and mental status.naloxone kit for discharge with education on overdose prevention and response.
  • Note any complications (e.g., withdrawal symptoms, agitation).

7. Documentation

  • Record time, dose, and route of naloxone administration.
  • Document patient’s response to treatment, including changes in respiratory rate, oxygenation, and mental status.
  • Note any complications (e.g., withdrawal symptoms, agitation).
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