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    Acute Pain Management in Adults

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    Apr.19.2024

    Acute Pain Management in Adults

    Summary

    Key Points

    • Identification and treatment of the underlying cause is important in the treatment of acute pain
    • Acute pain should be treated using a multimodal approach including nonpharmacologic strategies, medications, and procedures
    • Nonpharmacologic approaches include ice/heat, rehabilitation psychology support, cognitive strategies (eg, guided imagery, music therapy, relaxation, distraction), physical therapy, massage, use of TENS unit, among other treatments
    • Acetaminophen and NSAIDs should be considered first line treatment of acute pain, unless contraindicated
    • A multitude of other nonopioid medications are effective for acute pain including but not limited to steroids, gabapentinoids, IV ketamine, and IV lidocaine
    • Maximize use of nonpharmacologic and nonopioid pharmacologic therapies and only initiate opioids for acute pain if benefits outweigh potential risks to the patient
    • Consult an anesthesiologist or acute pain service for consideration of regional anesthesia (particularly epidural or peripheral nerve catheters)
    • A multimodal approach to acute pain management may reduce development of peripheral and central sensitization, which can increase risk of conversion to chronic pain

    Alarm Signs and Symptoms

    • Severe abdominal pain (concern for gastric ulcer due to NSAIDs)
    • New onset hypotension or anemia (concern for gastrointestinal bleed due to NSAIDs)
    • Respiratory depression, sedation (consider naloxone in setting of opioid use)
    • Acute psychosis (if secondary to ketamine infusion, then discontinue ketamine)
    • Sedation, ringing in the ears, metallic taste in the mouth (in setting of lidocaine infusion may be early signs of local anesthetic toxicity that may lead to seizure or cardiovascular collapse, in which case discontinue lidocaine)
    • New severe back pain, new lower extremity deficits not explained by the epidural medication itself, and/or loss of bowel or bladder control (concern for epidural hematoma or abscess in setting of epidural infusion)
    • Shortness of breath and/or tingling in the arms (in setting of epidural may be signs of epidural too high leading to respiratory failure, in which case discontinue epidural infusion)

    Basic Information

    Terminology

    • Pain is "an unpleasant sensory and emotional experience associated with, or resembling that associated with, actual or potential tissue damage," as defined by the International Association for the Study of Pain
    • Acute pain is typically:
      • Sudden onset
      • In response to a specific noxious stimulus
      • Self-limited, as it should stop when the underlying cause is treated or healed
      • Less than or equal to 1 month in duration
        • Subacute pain is present for 1 to 3 months

    Background Information

    • Acute pain is one of the most common reasons patients present to the emergency department or primary care physicians
    • Acute pain that does not resolve may become chronic, which is associated with significant morbidity and socioeconomic impact
    • Acute pain may have an obvious etiology such as postsurgical pain or blunt trauma but may require further workup to diagnose and provide specific treatment
    • Characterization of pain will aid in diagnosis; important elements include:
      • Location
      • Intensity
      • Quality (eg, sharp, throbbing, burning, tingling, stabbing, aching)
      • Duration
      • Associated symptoms such as weakness or numbness
    • Acute pain is most often reported using validated unidimensional assessment tools
      • May not account for the complex nature of pain and impact on function
      • The patient’s subjective report of pain is also important
      • Assessing pain at rest and during mobilization may give a more thorough clinical picture
      • Tools include (Figure 1):1
        • NRS (numeric rating scale) requires patients rate pain intensity from 0 to 10
        • VRS (verbal rating scale) prompts patients to rate pain using a verbal description ranging from none, mild, moderate, to severe
        • VAS (visual analogue scale) asks patients to indicate their pain level along a continuum from no pain to worst pain imaginable

    Treatment

    Approach to Treatment

    • For many instances of acute pain, treatment of the underlying cause is required
      • Therefore, accurate diagnosis is paramount
    • Regardless of cause, multimodal treatment is considered standard of care and includes nonpharmacologic management, drug therapy, and/or procedures2
    • Goals of acute pain management include:
      • Reduce suffering
      • Facilitate function and participation in therapies to promote healing
      • Provide treatment with minimal adverse effects
    • Some surgical procedures have associated ERAS (enhanced recovery after surgery) protocols that include specific pain management recommendations
      • Elements of these protocols may vary by institution though improved functional recovery and decreased complications are common goals
      • Colorectal surgery
        • ERAS protocols for colorectal surgery emphasize opioid-sparing analgesia using agents such as oral acetaminophen and gabapentin/pregabalin, ketamine or lidocaine infusions, or thoracic epidural analgesia or transversus abdominus plane blocks, among other options to facilitate early mobility and return of bowel function3
      • Spine surgery
        • ERAS protocols for spine surgery have shown shorter length of stay with decreased pain scores with use of acetaminophen, NSAIDs, gabapentin, and ketamine infusions4
      • Many published, procedure-specific ERAS protocols are available for review2

    Nondrug and Supportive Care

    • Nondrug and supportive care should be recommended to all patients given minimal adverse effects, few contraindications, and established efficacy across a variety of pain etiologies5
    • Apply ice and/or heat to affected areas to reduce pain
      • Do not apply for excessive length of time or while sleeping to avoid skin irritation or breakdown
    • Consult rehabilitation psychology support if available
      • Consult early, particularly in patients with significant trauma or preexisting mood disorders
    • Recommend cognitive strategies
      • Nursing, psychology consult service, or hospital-provided television programming may assist patients with utilizing these strategies
      • Examples include:
        • Guided imagery (eg, encourage patient to imagine walking through snow when experiencing a burning sensation)
        • Music therapy
        • Relaxation (eg, encourage deep breathing and meditation)
          • May be supported by mobile apps or patients’ preexisting practices
        • Distraction (eg, provide a crossword puzzle or coloring book)
        • Virtual reality
        • Hypnosis
          • May be useful for minor procedural pain and some patients may be appropriate for self-hypnosis training6
        • Aromatherapy
          • Lavender in particular may have potential for pain reduction7
    • Physical therapy should be engaged early for both outpatients and inpatients
      • Special techniques for pain reduction exist for specific conditions; examples include:
        • Mirror therapy for phantom limb pain
        • Graded motor imagery for complex regional pain syndrome
    • Encourage massage for acute musculoskeletal pain with resulting muscle spasm
      • Prescribe massage therapy for outpatients with specific muscular ailments
      • Patients can use a self-massage cane at home as an alternative to formal massage therapy
    • TENS (transcutaneous electrical nerve stimulation) has evidence for benefit in acute pain, with some studies suggesting improved pain and reduced analgesic use compared to placebo in the perioperative period5
      • Patients can purchase a low-cost device over the counter for home use without a prescription or it can be ordered in the hospital or provided during physical therapy sessions
      • The device pads should be placed over the area of pain, along an affected muscle, or on either side of a surgical incision
      • The stimulation should be increased to the maximum tolerated intensity for best effect. If it is painful or causing muscle twitching, it is set too high
      • Physical therapists can help patients optimize device settings and placement
      • TENS should be avoided in patients with:
        • Implanted electrical devices such as a pacemaker
        • Delirium
        • Extensive wounds or skin breakdown
        • Pregnancy, though TENS can be used safely with appropriate counseling regarding placement and during active labor
    • Consider spiritual care support

    Drug Therapy

    • NSAIDs and acetaminophen (Table 1)
      • Administer acetaminophen and NSAIDs as first line medications, either as a sole agent for mild pain complaints or in conjunction with other medications for more severe pain8
        • Unless contraindicated, consider scheduling acetaminophen to ensure patient timely dosing
      • Adverse effects:
        • With prolonged use, all NSAIDs may cause:
          • Gastrointestinal bleeding
          • Gastric ulcer
          • Renal dysfunction
          • Cardiac events
        • NSAIDs carry a black box warning for use after coronary artery bypass graft9
        • Studies have evaluated the effect of NSAIDs on delayed bone healing and anastomotic closure. Some surgeons may prefer NSAIDs be avoided after certain surgeries. However, prudent use of limited duration (less than 10 days) is unlikely to have a clinically significant impact5
    • Steroids (Table 2)
      • Consider systemic steroids if the patient has a significant inflammatory component to pain that is not responsive to NSAIDs; however, evidence is variable depending on indication
        • Systemic corticosteroids may improve pain more quickly due to acute radiculopathy but are likely no more effective than placebo in nonradiculitis pain10
      • Indications for steroids include but are not limited to:
        • Bursitis
        • Tendinitis
        • Severe arthritis flair
        • Acute radicular pain
        • Cancer pain
      • Adverse effects
        • Avoid use of steroids concurrently with NSAIDs to avoid gastric adverse effects
        • Steroids are associated with a multitude of other adverse effects including:
          • Elevated blood glucose
          • Elevated blood pressure
          • Increased appetite
          • Immune suppression
          • Poor sleep
          • Mood destabilization
          • Adrenal suppression with prolonged use
        • Use steroids with caution in patients with:
          • Diabetes
          • Uncontrolled blood pressure
          • Ongoing infection
          • Concern for poorly controlled mood disorder or history of mania
    • Opioids (Table 3)
      • Reference the CDC Clinical Practice Guideline for Prescribing Opioids for Pain11 as well as any opioid prescribing guidelines published by your state to ensure compliance with the most recent recommendations and rules
      • Opioids are effective for moderate to severe acute pain
        • Maximize use of nonpharmacologic and nonopioid pharmacologic therapies and only initiate opioids for acute pain if benefits outweigh potential risks to the patient12
        • Prescribe the lowest effective dose
        • Adverse effects
          • Prescribe the lowest effective dose to minimize adverse effects including:
            • Respiratory depression
            • Sedation
            • Nausea and vomiting
            • Constipation
            • Pruritis
            • Urinary retention
            • Altered mental status
        • Cautions
          • Monitor patients at risk for respiratory effects such as those with chronic obstructive pulmonary disease or obstructive sleep apnea
          • Minimize concurrent use of other sedating medications such as benzodiazepines and Z-drugs
          • For patients chronically prescribed these medications, consider halving or holding home dosages until the effect of opioids is clear
          • Do not use long-acting oral opioids for acute pain due to safety concerns and inability to titrate doses easily
            • The fentanyl patch carries a black box warning for use in acute pain
        • Administration
          • Oral routes of opioids are preferred over IV due to longer duration of action with similar analgesic effects
          • Consider PCA (patient-controlled analgesia) when parenteral route is required
            • Do not use basal infusions in opioid-naïve adults due to increased risk of adverse effects without proven analgesic benefit
            • Minimize basal infusions in opioid-tolerant patients
    • Anticonvulsants/membrane stabilizers (Table 4)
      • Medications such as gabapentin and pregabalin are commonly used as part of a multimodal pain strategy, particularly during the perioperative period5
        • Multiple dosing strategies have been studied with no clear best regimen13
          • Medication can be prescribed 2 to 3 times daily until acute pain has subsided or given as a single periprocedural dose
      • Gabapentin/pregabalin are particularly beneficial in spine surgery, thoracotomy, amputation, and joint replacement. Adverse effects include:
        • Sedation
          • Reduce dose in renal dysfunction (though drugs themselves are not nephrotoxic) and in geriatric population
        • Peripheral edema
        • Dizziness
        • Tremor
      • Cautions
        • In 2019 the FDA issued a statement warning that breathing difficulties may occur in patients using gabapentin and pregabalin who have respiratory risk factors such as concurrent use of opioids or other central nervous system depressants, COPD, or are older aged
        • Taper anticonvulsants over 1 week or more in patients predisposed to seizures rather than abruptly discontinuing
        • For patients already taking anticonvulsants for other indications such as topiramate for migraine headache or lamotrigine for mood stabilization, the addition of gabapentin or pregabalin is likely low yield for pain reduction
    • Specialized infusions (Table 5)
      • Consult appropriate hospital resources (acute pain service, anesthesiology, ICU) for consideration of specialized infusions for acute pain. Ketamine infusions for acute pain (low dose) can be safely administered on regular inpatient hospital floors, though may require oversight by acute pain services or anesthesiology per local hospital policies5
        • Consider requesting evaluation for ketamine when pain continues to be difficult to manage despite multimodal analgesia
        • Indications
          • Ketamine is particularly useful in patients with opioid tolerance
          • Shown to be beneficial in spine surgery, thoracotomy, and many other surgeries
        • Adverse effects
          • Hallucinations, nightmares, nystagmus, increased salivation, increased sympathetic activity
          • Adverse effects more likely to occur at higher doses; low-dose infusions tend to be well tolerated
        • Contraindications
          • Although not absolutely contraindicated, use caution in those with poorly controlled psychiatric comorbidities such as psychosis, mania, and posttraumatic stress disorder
          • Avoid in patients with significant intracranial pathology as it may increase intracranial pressure at higher doses
          • Avoid in unstable coronary artery disease due to increased sympathetic activity
      • Lidocaine infusions for acute pain are typically administered on regular inpatient hospital floors, though similar to ketamine may require oversight by acute pain services or anesthesiology per local hospital policies5
        • Indications
          • Postoperative pain (particularly beneficial for intraabdominal surgery and spine surgery)
          • Potentially useful in migraine headache, acute radiculopathy, renal colic
        • Adverse effects
          • Dizziness, tinnitus, perioral numbness, seizures, conduction delay, bradycardia
        • Contraindications
          • Absolutely contraindicated in Wolff-Parkinson-White syndrome and severe sinoatrial, atrioventricular, or intraventricular heart block
          • Use caution or avoid in patients with significant hepatic dysfunction as reduced clearance increases risk of local anesthetic toxicity
          • Avoid in patients with history of seizures, those unable to self-report adverse effects, or those taking medications that inhibit CYP1A2 and CYP3A4
          • Consult cardiology to assess risks for patients on additional antiarrhythmic agents, β-blockers, or α-2 agonists
      • Dexmedetomidine infusions most often require continuous monitoring in the ICU as they can be sedating and cause hemodynamic changes14
        • Due to monitoring requirements, dexmedetomidine is usually reserved for cases when pain has not been sufficiently treated by other means
        • Indications
          • Postoperative pain
        • Adverse effects
          • Sedation, severe hypotension, bradycardia
          • May cause hypertension when stopped
        • Contraindications
          • Avoid if adequate monitoring not available (ICU) or concern for oversedation
      • Magnesium is a less commonly used infusion15
        • Indications
          • Not a primary analgesic but may enhance role of other analgesics used in perioperative period
          • May be given as part of intraoperative analgesia
        • Contraindications
          • Will enhance effects of nondepolarizing muscle relaxants used in operating room
      • Be aware that much of the literature supporting use of specialized infusion therapies comes from studies in perioperative management and there is little guidance for optimal postoperative dosing strategies
    • Adjunct agents
      • Other agents that may have some utility in acute pain include:
        • Clonidine16
          • Typical dose 0.2 to 0.3 mg PO twice daily
          • May cause hypotension and rebound hypertension when discontinued
          • Avoid concurrent use with other antihypertensives
        • Dextromethorphan17
          • Typical dose 30 mg PO every 6 hours PRN pain
          • Can be considered an oral option of an NMDA (N-methyl-D-aspartate) receptor antagonist. However, supporting data in comparison to ketamine IV are extremely limited so it should be considered an end-of-the-line option
          • Can cause sedation
    • Muscle relaxants (Table 6)
      • Evidence for use of muscle relaxants in acute pain is mixed and therefore not generally recommended in practice guidelines18
      • If other analgesics have been insufficient or a patient endorses prior benefit, they can be trialed
      • Given no one agent is known to be superior for acute pain, choose based on adverse-effect profile18
    • Topical agents (Table 7)
      • Topical application of medications should be considered for acute pain and present less concern for systemic adverse effects
    • Table 1. Common dosing of acetaminophen and common NSAIDs.19COX-2, cyclooxygenase 2; GERD, gastroesophageal reflux disease.Data from Young A et al. Nonsteroidal anti-inflammatory drugs and acetaminophen. In: Ballantyne JC et al, eds. Bonica’s Management of Pain. 5th ed. Lippincott Williams & Wilkins; 2019: 1315-1323.
      DrugDoseComments
      AcetaminophenOral/IV: 325-1000 mg every 4-6 hours19



      Maximum: 4 g/day in typical adult. Consider dose reduction to 2-3 g/day in older adults20 and patients with significant hepatic dysfunction20
      May cause hepatotoxicity
      IbuprofenOral: 400 mg every 4-6 hours



      Reduce dose to 200-400 mg in older adults
      In patients with history of GERD or gastric ulcer, may add proton pump inhibitor as prophylaxis
      KetorolacIV: 15-30 mg every 6-8 hours



      Reduce dose to 7.5 mg in older adults
      Recommend limiting duration to 5 days to reduce incidence of adverse effects
      CelecoxibOral: 100-200 mg twice daily



      Maximum: 400 mg/day
      Reduced risk of bleeding due to selective COX-2 inhibition
      NaproxenOral: 250-500 mg twice daily

      Higher doses of 750 mg can be given as a first dose for acute gout,21 bursitis, tendinitis, or other acute pain. Total daily dose should not exceed 1250 mg
      If an NSAID must be used in a patient with preexisting cardiac disease, naproxen is likely the safest option
    • Table 2. Sample dosing strategies of commonly used steroids for acute pain.
      DrugDoseIndication
      Prednisone40-60 mg PO daily, tapered over 3 weeks22Herpes zoster

      Note: Although this is commonly done, evidence is limited
      Prednisolone35 mg PO daily for 5 days23Acute gout
      Methylprednisolone24 mg PO for 1 day, 20 mg PO for 1 day, 16 mg PO for 1 day, 12 mg PO for 1 day, 8 mg PO for 1 day, 4 mg PO for 1 day24Sports-related injury, bursitis, tendonitis
      Dexamethasone0.1-0.2 mg/kg IV once25May be given preoperatively as adjunct to postoperative pain management
    • Table 3. Commonly used opioid medications with suggested starting dose.26SL, sublingual; SNRI, serotonin-norepinephrine reuptake inhibitor; SSRI, selective serotonin reuptake inhibitor; TCA, tricyclic antidepressant.Data from Inturrisi C et al. Opioid analgesics. In: Ballentyne JC et al, eds. Bonica’s Management of Pain. 5th ed. Lippincott Williams & Wilkins; 2019:1334-1342.
      RouteDrugStarting doseComments
      OralOxycodone5-10 mg every 4 hours PRN

      Reduce to 2.5 mg in geriatric patients
      Hydromorphone2-4 mg every 4 hours PRN
      Morphine7.5-15 mg every 4 hours PRNAvoid in geriatric patients and patients with renal impairment
      Hydrocodone-acetaminophen5-325 mg every 4 hours PRNEnsure patient does not exceed maximum dose of acetaminophen per 24 hours

      Hydrocodone paired with 325 mg acetaminophen is known as Norco. When paired with 500 mg it was known as Vicodin and is no longer available
      Tramadol50-100 mg every 4 hours PRN

      Do not exceed 400 mg in 24 hours

      Do not exceed 300 mg in 24 hours in patients older than 75 years
      Has relatively low potency compared to other opioids so may be useful in patients sensitive to opioid-related adverse effects. However, can still cause somnolence and dizziness

      Use with caution in patients on SNRIs/SSRIs, TCAs, or similar agents due to risk of serotonin syndrome
      IVHydromorphone0.2-0.4 mg IV every 4 hours PRN

      PCA: demand dose 0.2 mg, lockout 10 minutes. Reduce demand dose to 0.1 mg in geriatric patients. May increase to 0.3 mg in opioid-tolerant27
      When using PCA, a loading dose may be required to bring a patient to a therapeutic window that is then maintained by the patient (eg, consider a loading dose that is twice the patient demand dose every 10 minutes × 3 doses)
      Morphine1-2 mg IV every 4 hours PRN

      PCA: demand dose 1 mg, lockout 12 minutes. May increase to 1.5 mg in opioid-tolerant27
      Avoid in geriatric patients and patients with renal impairment
      Fentanyl25-50 mcg IV every 4 hours PRNDue to short duration of analgesia of 30-60 minutes, best reserved for specific painful procedure or wound care

      Hospitals may have specific policies regarding where fentanyl can by administered
      Meperidine50-150 mg IV every 4 hours PRN

      Maximum 600 mg in 24 hours
      Generally not recommended for pain management due to risk of neurotoxicity (particularly seizure) and available safer alternatives

      Concomitant use of cytochrome P450 3A4 inhibitors or monoamine oxidase inhibitors, or discontinuation of P450 inducers may result in fatal reactions
      Nalbuphine5-10 mg IV every 4 hours PRNAs a lower potency opioid agonist-antagonist, may be useful in geriatric or frail patients

      5 mg IV is given routinely as an effective treatment for opioid-induced itching
      OtherFentanyl lozenge200 mcg transmucosal dailyAllows patient to self-administer medication by rubbing on inside cheek

      Only FDA-approved for management of breakthrough pain in opioid-tolerant patients with cancer
      Buprenorphine-naloxoneSample dose: ¼ of buprenorphine-naloxone 2 mg-0.5 film SL 4 times daily PRN for pain (equivalent of 0.5 mg buprenorphine per dose)Off-label use of suboxone

      Dosage for pain is significantly lower than that used for opioid use disorder

      Buprenorphine 0.5 mg SL is not expected to precipitate withdrawal, regardless of prior opioid administration. This dose is commonly used for microinduction of buprenorphine28
    • Table 4. Anticonvulsant dosing strategies.5,13Data from . Chou R et al. Management of postoperative pain: a clinical practice guideline from the American Pain Society, the American Society of Regional Anesthesia and Pain Medicine, and the American Society of Anesthesiologists’ Committee on Regional Anesthesia, Executive Committee, and Administrative Council. J Pain. 2016;17(2):131-157; and Verret M et al; Canadian Perioperative Anesthesia Clinical Trials (PACT) Group. Perioperative use of gabapentinoids for the management of postoperative acute pain: a systematic review and meta-analysis. Anesthesiology. 2020;133(2):265-279.
      DrugDose
      GabapentinOral: 600-1200 mg 1-2 hours preoperatively, 600 mg postoperatively (single or multiple doses)

      Can consider continuing 600-900 mg 2-3 times daily in subacute phase though supportive evidence of this practice is inconsistent

      Renal dysfunction/geriatric patients: Reduce dose to 100-300 mg. Consider dosing immediately following dialysis29
      PregabalinOral: 150-300 mg preoperatively followed by same dose 12 hours later

      Can consider continuing 75-150 mg 2-3 times daily in subacute phase though supportive evidence of this practice is inconsistent

      Renal dysfunction/geriatric patients: Reduce dose to 25-50 mg 2 times daily30
    • Table 5. IV infusions for pain.
      DrugDose
      Ketamine5,31IV bolus: 0.3-0.5 mg/kg

      Infusion: 0.1-0.2 mg/kg/hour
      Lidocaine5IV bolus: 1.5 mg/kg

      Infusion: 1-2 mg/kg/hour
      Dexmedetomidine14IV bolus: 0.25-1 mg/kg over 10 minutes

      Infusion 0.2-1 mg/kg/hour
      Magnesium15IV bolus: 30-50 mg/kg

      Infusion: 6-20 mg/kg/hr
    • Table 6. Example muscle relaxant dosing and adverse effects.
      DrugDoseAdverse effects/comments
      Cyclobenzaprine325-10 mg PO every 8 hours PRNSedation, associated with anticholinergic effects, avoid in patients at risk for arrhythmia or seizure, monitor for serotonin syndrome if used with other serotonergic agents; pregnancy category B
      Methocarbamol33500-1500 mg PO every 6 hours PRNSedation, though low dosage may be associated with less sedation

      May cause black/green urine
      Tizanidine342-4 mg PO every 6 hours PRNHypotension, hepatotoxicity, sedation, interacts with CYP1A2 pathway (concomitant use with ciprofloxacin or fluvoxamine is contraindicated), use with other strong 1A2 inhibitors or oral contraceptives should be avoided (if clinically indicated start tizanidine at low dose and monitor closely for adverse effects)
      Carisoprodol35350 mg PO every 8 hours PRNDue to potential for addiction with lack of clear benefit, initiating carisoprodol is not recommended. Given potential for withdrawal syndrome, it is acceptable to continue in an acute setting, though consider reducing dose if patient is receiving other sedating agents
      Diazepam362-4 mg PO every 6 hours PRNGenerally avoided due to concern for respiratory depression when combined with other sedating agents in acute setting as well as potential for dependency and abuse. May be a role for use in spasticity
      Baclofen375 mg PO every 8 hours for 3 days, followed by 10 mg PO every 8 hours. May be titrated to 40-80 mg daily when used for spasticityAs an antispasticity agent, baclofen is considered off-label for use in skeletal muscle spasm. It is associated with a life-threatening withdrawal syndrome, especially at higher doses—caution should be used in patients with poor medication compliance
    • Table 7. Selection of topical agents and uses.38,39Data from Derry S et al. Topical analgesics for acute and chronic pain in adults--an overview of Cochrane Reviews. Cochrane Database Syst Rev. 2017;5(5):CD008609; and Qaseem A et al. Nonpharmacologic and pharmacologic management of acute pain from non-low back, musculoskeletal injuries in adults: a clinical guideline from the American College of Physicians and American Academy of Family Physicians. Ann Intern Med. 2020;173(9):739-748.
      MedicationUse
      Lidocaine patchTo be applied over painful area. Intended to be used for superficial pain such as that associated with postherpetic neuralgia. Can be used around a surgical incision or drain. Available in OTC and prescription strength
      Lidocaine gel/creamMost useful for superficial pain. Can be used prior to procedures such as IV line placement in patients sensitive to needles. Available in OTC and prescription strength
      Viscous lidocaineConsider for use in wound care. For example, may soak burn wounds prior to dressing changes. Alternatively, can be used as a swish-and-swallow agent for patients with sores in mouth or sore throat (use caution in patients with aspiration risk). Typically used inpatient or in emergency department
      Menthol creamParticularly beneficial for musculoskeletal and joint pain. May combine with massage for acute massage spasm. Available OTC
      Diclofenac gelParticularly beneficial for musculoskeletal and joint pain with inflammatory component. This medication is intended to be used regularly 4 times per day rather than as needed. Available OTC
      Capsaicin creamIntended to be used for superficial neuropathic pain. If patient finds application painful, the area can be pretreated with lidocaine gel/cream. Available OTC

    Treatment Procedures

    • Neuraxial or peripheral regional anesthesia can be performed in conjunction with the nonpharmacologic and pharmacologic modalities listed above to enhance pain relief and potentially minimize opioid use40
      • Consultation with anesthesiology, acute pain service, interventional radiology, or appropriately trained clinician or consult service is appropriate for consideration and placement of nerve blocks
    • Neuraxial blocks (epidural, spinal, or combined spinal/epidural)
      • Provide effective analgesia in the chest, abdomen, pelvis, or lower extremities depending on level of placement
      • May be used as part of a surgical anesthetic and/or for ongoing pain relief outside of surgery (eg, pain control for rib fractures)
        • Spinal injections allow direct administration of local anesthetic with or without opioid to the central nervous system
          • Most appropriate for a surgical anesthetic and not solely pain relief
        • Epidural anesthesia involves placement of a catheter to allow continuous administration of local anesthetic with or without opioid
          • May provide ongoing pain relief
        • Combined spinal epidural analgesia is used if both rapid onset of surgical anesthesia and prolonged pain relief are desired
      • The area covered by an epidural is dependent on:
        • Level of placement
        • Rate and volume of medication being infused
        • Position of the patient
        • Height of the patient
      • The density of the block or perceived numbness by the patient is dependent on the concentration of local anesthetic ordered and volume
        • When using an epidural for pain control, lower concentrations are used to prevent motor block, which may otherwise present fall risk for a patient
          • Thorough neurologic examination of patients with lumbar epidurals should be done before allowing ambulation
          • Thoracic epidurals are not typically associated with weakness in the legs and should not preclude ambulation (also referred to as "walking epidurals")
            • However, if the spread of an epidural is too high, the patient may get numbness in the arms
            • Depending on local anesthetic concentration the patient may also experience weakness of the upper extremities or intercostal muscles and become short of breath
      • Adverse effects
        • Expected adverse effects such as hypotension may also limit the dose of local anesthetic that can be used
        • Urinary retention is common with lumbar epidurals, though some patients may be able to urinate with the lower concentrations of local anesthetic often used for pain
        • Thoracic epidurals are less likely to be associated with urinary retention and use of a Foley catheter is not required
      • Epidurals may have a simple continuous infusion rate or a defined intermittent bolus dose, or be programmed to have PCEA (patient-controlled epidural analgesia) allowing the patient to push a button to administer themselves a small bolus of medication through the epidural at a defined interval
        • If the patient has PCEA with opioid in their epidural, generally it is safest to avoid administering additional opioids through other routes
          • If pain control is not sufficient, opioid should be removed from the epidural and patient may receive additional opioids PO or IV
        • IV lidocaine infusions should not be given to patients receiving neuraxial anesthesia due to risk of local anesthetic toxicity
      • Contraindications to neuraxial anesthesia include:
        • Patient refusal
        • Coagulopathy
          • Strict anticoagulation guidelines exist to minimize risk of epidural hematoma, which can result in paraplegia if not identified and treated rapidly41,42
        • Infection, either systemic or at site of insertion
        • Hemodynamic instability
          • Sympathectomy from epidural will predispose to hypotension
        • Transverse process, spine fractures, or other anatomic anomalies that impact ability to reliably predict the level of the spinal cord or access of epidural space based on tactile feedback using the loss of resistance technique
      • Cautions
        • Monitor patients with epidural catheters for new severe back pain, changes in neurologic examination not explained by medications being infused through epidural, and redness or swelling at the epidural catheter insertion site
          • Patients who are unable to self-report or easily be monitored for symptoms related to epidural complications may not be appropriate for this treatment modality
    • Peripheral nerve blocks
      • Ideal in management of a focal area of pain as they involve injecting local anesthetic either perineurally or in a plane where nerves are expected to be in order to reduce sensation in a specific distribution
      • Peripheral nerve blocks achieve different goals by using different concentrations and doses of local anesthetics
        • A very dilute local anesthetic may just "take the edge" off of pain where a dense local anesthetic can achieve a complete numbness with motor block for a period of time (typically intended for surgical anesthesia rather than pain)
      • Duration of a peripheral nerve block can be extended by:
        • Increasing the dose of local anesthetic (volume and/or concentration)
        • Inserting an indwelling catheter
          • Some institutions may have an option to send a patient home with an ambulatory infusion pump to continue using a catheter for several days
        • Adding pharmacologic adjuncts to the local anesthetic injected such as clonidine, dexmedetomidine, dexamethasone, or magnesium
          • Though these are usually given perineurally, there may still be some systemic absorption that could cause adverse effects such as hypotension or elevated blood glucose
        • Use of novel products such as liposomal bupivacaine, though evidence varies for different indications
      • Contraindications include:
        • Patient refusal
        • Coagulopathy
          • Low-risk peripheral nerve blocks can still be performed if site is compressible and risks are outweighed by potential benefits41,42
        • Infection, either systemic or at site of insertion
        • Special considerations for specific blocks
          • Interscalene block causes hemidiaphragmatic paresis leading to possible desaturation in patients with impaired lung function
          • Concern for fall risk with sciatic or femoral nerve block (generally not appropriate to perform bilaterally in an ambulatory patient)
            • Recommend use of crutches
          • Mild hypotension following paravertebral blocks

    Persistent or Recurrent Disease

    • Acute pain that persists beyond 3 months is considered chronic pain
    • Persistent postsurgical pain is common with estimates ranging from 10% to 50%43
      • Procedures associated with a greater risk of persistent postsurgical pain include:
        • Thoracotomy
        • Cardiac surgery
        • Sternotomy
        • Breast surgery
        • Limb amputation
        • Hernia repair
      • Risk factors include:
        • Preoperative anxiety and/or depression
        • High level of catastrophizing
        • Preexisting pain before surgery
        • Significant acute pain in the first 3 to 4 postoperative days
        • Surgery involving division or prolonged retraction of nerves
        • Younger age
        • Female sex
        • Genetic susceptibility
    • The conversion of acute to chronic pain is a complex process involving both peripheral and central sensitization
      • Identifying risk factors and employing a multimodal approach early on can help combat sensitization44,45
      • Perioperative psychological interventions can be effective in reducing conversion to subacute and chronic pain

    Admission Criteria

    • Inpatient admission for pain should be predicated on the underlying etiology and whether hospital admission is needed for treatment or additional workup
    • A select few patients may require inpatient admission if they are unable to achieve adequate relief with oral pain medications or there is concern for safety due to medication adverse effects

    Special Considerations

    Older Adults

    • Use the ADD protocol (assessment of discomfort in dementia) (Figure 2)46 or other special assessment tools for patients with dementia
    • Older adults are more susceptible to adverse effects particularly from opioids, gabapentinoids, and NSAIDs
      • Consider use of low potency opioids such as hydrocodone-acetaminophen as an oral agent or nalbuphine as an IV agent
      • Avoid use of morphine due to reduced renal clearance in older patients
      • Consider dose reductions of pain medications
    • Note that both pain itself and pain medications can contribute to delirium

    Patients With Chronic Pain

    • When treating acute pain in patients with preexisting pain, determine the patient’s baseline pain level and functional status; it is unlikely you will be able to improve upon this during an acute pain situation
    • Ensure patients receive their home pain medications, including long-acting opioids
      • Confirm with patient when they last took their medication before ordering
      • For controlled substances, check the state prescription drug monitoring program and pharmacy records to confirm the patient’s prescription and compliance
      • For patients taking multiple doses of tramadol daily, abruptly stopping may feel similar to withdrawal from an SSRI (selective serotonin reuptake inhibitor)47
        • In this instance, tramadol can be scheduled and treated similarly to a long-acting opioid
      • Buprenorphine products should be continued similarly to any other long-acting opioid, unless there has been a significant disruption in receiving it (48-72 hours)
        • If there has been a significant disruption, reinduction or a microinduction may be required to restart the medication and pain specialist consultation is appropriate
        • Full agonist opioids can be given to treat pain in a patient taking buprenorphine with good effect, contrary to prior understanding of buprenorphine48
      • For patients prescribed fentanyl or buprenorphine patches chronically, consider replacing the patch if it is unclear when it was last changed or if it may have been exposed to extreme temperatures affecting absorption (such as under a heated blanket in the operating room)
      • Long-acting opioids should not be used for treatment of acute pain11

    Patients With Substance Use Disorder

    • Methadone
      • Patients taking methadone for opioid use disorder should have methadone resumed after the dose has been confirmed with their clinic
        • Confirm with patient the last time they took methadone
        • If the dose is unable to be confirmed due to clinic hours, it is reasonable to start 30 mg PO daily, as this is a common starting dose for methadone49
        • For inpatients, methadone can be given as a single daily dose or divided into every-6-hour or every-8-hour doses
          • Divided dosing may give some advantage in treatment of pain due to methadone’s 6-hour analgesic window and also allows for additional safety by allowing doses to be held in patients that are critically ill50
          • Some patients may prefer once-daily dosing
        • The patient may need an increased dose of opioid for treatment of acute pain given opioid tolerance
    • Buprenorphine-naltrexone SL (sublingual)
      • Patients taking buprenorphine-naltrexone SL for opioid use disorder should have the medication continued to prevent destabilization of addiction51
        • Buprenorphine-naltrexone prescriptions should be confirmed using the state prescription monitoring program and pharmacy records
        • Confirm with the patient when they last took their medication
          • If more than 48 to 72 hours has passed since the last dose and other full agonist opioids have been administered, resumption of moderate-high doses of buprenorphine can precipitate withdrawal; in this case, the patient will need to undergo another full induction or microinduction if receiving full agonist opioids
          • For patients on higher doses of buprenorphine and with history of difficult-to-control postoperative pain while taking buprenorphine, consider reducing the dose to 16 mg per day or less to optimize µ opioid receptor availability
        • Similar to methadone, dividing buprenorphine-naloxone into every-6-hour or every-8-hour dosing will take better advantage of the medication’s analgesic window
          • However, patients will still have analgesic benefit when the medication is at a steady state if dosed daily or twice daily (the typical dosing schedule for addiction management); patient preference should be considered
        • Pain can be adequately treated in patients taking buprenorphine despite prior assumptions that it cannot48
          • A multimodal approach should be used as with any patient
          • Full agonist opioids can be successfully used to treat pain
            • Start at typical doses and increase based on effect, similar to any opioid tolerant patient
          • In very-high-risk patients consider additional buprenorphine-naloxone SL as an alternative to full agonist opioids
    • Patients with active opioid use disorder and not engaged in treatment
      • Consider offering to start medication-assisted therapy
      • Starting dose of methadone is typically 30 mg PO daily (methadone solution)
        • Give all at once if patient is acutely experiencing withdrawal; otherwise can give in divided doses such as 10 mg PO every 8 hours52
        • Some hospital systems may be able to help facilitate intake appointments at methadone clinics after discharge
          • If the patient is unable to be established at a methadone clinic after discharge, do not prescribe methadone tablets
            • Prescribing methadone for MOUD (medication for opioid use disorder) outside a treatment center is against the law
          • If the patient will not be able to access a methadone clinic after discharge, buprenorphine may be a better option for MOUD as it may be prescribed and dispensed from a regular pharmacy
      • Buprenorphine products can be initiated through traditional induction if the patient experiences withdrawal or microinduction if receiving other opioid for acute pain
        • As a patient’s dose of buprenorphine increases, their use of full agonist opioids for acute pain should reduce
    • Naltrexone
      • Given the interaction between naltrexone and opioids, patients taking naltrexone for alcohol use disorder or opioid use disorder should pause this medicine while requiring opioid medications for acute pain and discuss when to resume it with their prescriber53
    • Methamphetamine use disorder
      • Patients that regularly use methamphetamines can be challenging to treat while experiencing methamphetamine withdrawal
      • Reduced doses of pain medications may be required due to sedation

    Pregnant Patients

    • Acetaminophen should be considered a first line agent
    • NSAIDs can be used in the first and early second trimester of pregnancy but should be avoided after 20 weeks due to risk of kidney problems resulting in low amniotic fluid54
    • Limited short-term use of opioids is acceptable, though it can cause respiratory depression
    • IV ketamine is contraindicated in treatment of acute pain in pregnancy, though it can be used as part of an anesthetic during delivery55
    • The safety of IV lidocaine in pregnancy is unclear due to limited studies in the population56
    • Regional anesthesia techniques are safe and often preferable to systemic therapies57
    • Nonpharmacologic therapies should be encouraged such as:
      • Acupuncture
      • Massage
      • Physical therapy (including pelvic floor physical therapy)
      • Hot and cold packs
      • Meditation/mindfulness

    Breastfeeding Patients

    • Acetaminophen and NSAIDs should be considered as first line agents
    • Use of opioids while breastfeeding can cause infant drowsiness and central nervous system depression
      • Low-dose morphine may be preferable to other opioids58
    • Avoid meperidine59
      • Infants have an impaired metabolism and higher oral bioavailability than adults
      • The active metabolite normeperidine causes more central nervous depression in newborns than in adults
    • Avoid tramadol60
      • Ultrarapid metabolism to M1 (O-desmethyltramadol) can cause life-threatening respiratory depression in the infant
    • Avoid codeine60
      • Ultrarapid metabolism to morphine can cause life-threatening respiratory depression in the infant
    • Nonpharmacologic therapies should be encouraged such as:
      • Acupuncture
      • Massage
      • Physical therapy (including pelvic floor physical therapy)
      • Hot and cold packs
      • Meditation/mindfulness

    Critically Ill Patients

    • Communication barriers such as sedation, delirium, or presence of airway devices make assessment of pain challenging in critically ill patients
      • CPOT (Critical-Care Pain Observation Tool) uses observations of facial expressions and body movement to extrapolate a level of pain (Table 8)61
    • Difficulty in assessment of adverse effects of treatment in intubated/sedated patients will impact treatment options
      • Peripheral nerve blocks such as erector spinae or serratus anterior have a lower risk profile than epidural analgesia
      • Symptoms of local anesthetic toxicity may not be detected early on during lidocaine infusion
      • Opioids may be given more liberally while a patient is intubated as the airway is protected
        • Explore other options when nearing extubation
      • Careful consideration of risks versus benefits should be given on a case-by-case basis
    • Table 8. CPOT.CPOT, Critical-Care Pain Observation Tool.Adapted from Gelinas C et al. Validation of the critical-care pain observation tool in adult patients. Am J Crit Care. 2006;15(4):420-427.
      IndicatorDescriptionScore
      Facial expressionNo muscular tension observedRelaxed, neutral0
      Presence of frowning, brow lowering, orbit tightening, and levator contractionTense1
      All of the above facial movements plus eyelid tightly closedGrimacing2
      Body movementsDoes not move at allAbsence of movements0
      Slow, cautious movements; touching or rubbing the pain site; seeking attention through movementsProtection1
      Pulling tube, attempting to sit up, moving limbs/thrashing, not following commands, striking at staff, trying to climb out of bedRestlessness2
      Muscle tension

      Evaluation by passive flexion and extension of upper extremities
      No resistance to passive movementsRelaxed0
      Resistance to passive movementsTense, rigid1
      Strong resistance to passive movements, inability to complete themVery tense or rigid2
      Compliance with the ventilator (intubated patients)

      OR

      Vocalization (extubated patients)
      Alarms not activated, easy ventilationTolerating ventilator or movement0
      Alarms stop spontaneouslyCoughing but tolerating1
      Asynchrony: block ventilation, alarms frequently activatedFighting ventilator2
      Talking in normal tone or no soundTalking in normal tone or no sound0
      Sighing, moaningSighing, moaning1
      Crying out, sobbingCrying out, sobbing2
      Total, range0-8

    Follow-Up

    Monitoring

    • Vital sign monitoring
      • Elevated heart rate and blood pressure are consistent with a stress response during acute pain
        • However, it is important to not assume these elevations are due to pain
        • Also note that pain can be present without these
    • Monitoring for resolution of acute pain can be tracked by:
      • Participation in therapies
      • Duration and quality of sleep
      • Trending pain scores
      • Change in usage of PRN pain medications

    Complications

    • Poorly controlled acute pain increases risk of:
      • Development of chronic pain62
      • Delay in recovery or hospital discharge63
      • Delirium64

    Prognosis

    • Expected course of acute pain is dependent on etiology
    • Acute low back pain
      • Meta-analysis of acute low back pain revealed significant improvement within the first 6 weeks followed by slower improvement65
    • Surgical procedures can be categorized into:66
      • Expected rapid recovery
        • NSAIDs and/or acetaminophen and nonpharmacologic therapies may be sufficient
        • If opioids are required, 3 days or less are recommended
        • Examples include oral surgery, laparoscopic appendectomy, inguinal hernia repair, carpal tunnel release, thyroidectomy, breast biopsy/lumpectomy, meniscectomy, vaginal hysterectomy, among others
      • Expected medium-term recovery
        • NSAIDs and/or acetaminophen and nonpharmacologic therapies are first line
        • Opioids should be prescribed for 7 days or less for severe pain
          • Exceptional cases may warrant greater than 7 days of opioid treatment, though patients should be reevaluated by surgeons in the weeks following surgery and taper off within 6 weeks after surgery
        • Examples include anterior cruciate ligament repair, rotator cuff repair, laminectomy, open or laparoscopic colectomy, open small bowel resection, laparoscopic hysterectomy, simple mastectomy, cesarean section, among others
      • Expected longer-term recovery
        • NSAIDs and/or acetaminophen and nonpharmacologic therapies are first line
        • Opioids should be prescribed 14 days or less for severe pain
          • Exceptional cases may warrant greater than 14 days of opioid treatment, though patients should be reevaluated by surgeons prior to refilling opioids and taper off within 6 weeks after surgery
        • Examples include lumbar fusion, knee/hip replacement, abdominal hysterectomy, modified radical mastectomy, ileostomy/colostomy creation or closure, thoracotomy, among others

    Referral

    • Consult anesthesiology or a specialized pain service for:
      • Inadequately controlled pain
      • High risk of inadequately controlled pain67
        • History of long-term opioid therapy
        • History of substance use disorder
      • Consideration of regional anesthesia
      • Management of specialized medications such as IV ketamine or IV lidocaine
    • Consider referral to a chronic pain specialist when:
      • Acute pain is not resolving within the expected time course despite resolution of underlying etiology
      • Concern for development of CRPS (complex regional pain syndrome)
        • Classically this includes pain out of proportion to the inciting event and no other diagnosis better explains the signs and symptoms
        • Symptoms may include:
          • Hyperesthesia or allodynia
          • Asymmetry in temperature or sweat patterns
          • Decreased range of motion and/or motor dysfunction
          • Edema
          • Trophic changes of hair/nails/skin
        • Early treatment of CRPS will improve prognosis68
    • Consider referral to an addiction medicine specialist if there is concern for opioid misuse or dependency

    Author Affiliations

    Katherin Peperzak, MD
    Assistant Professor, Medical Director Center for Pain Relief at UWMC-Roosevelt
    Anesthesiology & Pain Medicine
    University of Washington

    Breivik H et al. Assessment of pain. Br J Anaesth. 2008;101(1):17-24.18487245https://doi.org/10.1093/bja/aen103Ljungqvist O et al. Enhanced Recovery After Surgery: a review. JAMA Surg. 2017;152(3):292-298.28097305https://doi.org/10.1001/jamasurg.2016.4952Simpson JC et al. Pain management in Enhanced Recovery After Surgery (ERAS) protocols. Clin Colon Rectal Surg. 2019;32(2):121-128.30833861https://doi.org/10.1055/s-0038-1676477Dietz N et al. Enhanced Recovery After Surgery (ERAS) for spine surgery: a systematic review. World Neurosurg. 2019;130:415-426.31276851https://doi.org/10.1016/j.wneu.2019.06.181Chou R et al. Management of postoperative pain: a clinical practice guideline from the American Pain Society, the American Society of Regional Anesthesia and Pain Medicine, and the American Society of Anesthesiologists’ Committee on Regional Anesthesia, Executive Committee, and Administrative Council. J Pain. 2016;17(2):131-157.26827847https://doi.org/10.1016/j.jpain.2015.12.008Kendrick C et al. Hypnosis for acute procedural pain: a critical review. Int J Clin Exp Hypn. 2016;64(1):75-115.26599994https://doi.org/10.1080/00207144.2015.1099405Tabatabaeichehr M et al. The effectiveness of aromatherapy in the management of labor pain and anxiety: a systematic review. Ethiop J Health Sci. 2020;30(3):449-458.32874088https://doi.org/10.4314/ejhs.v30i3.16Chou R et al. Treatments for acute pain: a systematic review. AHRQ Comparative Effectiveness Reviews. Agency for Healthcare Research and Quality (US); 2020.https://www.ncbi.nlm.nih.gov/books/NBK566506/Kulik A et al. Non-steroidal anti-inflammatory drug administration after coronary artery bypass surgery: utilization persists despite the boxed warning. Pharmacoepidemiol Drug Saf. 2015;24(6):647-653.25907164https://doi.org/10.1002/pds.3788Chou R et al. Systemic corticosteroids for radicular and non-radicular low back pain. Cochrane Database Syst Rev. 2022;10(10):CD012450.36269125https://doi.org/10.1002/14651858.CD012450.pub2Dowell D et al. CDC clinical practice guideline for prescribing opioids for pain--United States, 2022. MMWR Recomm Rep. 2022;71(RR-3):1-95.36327391https://doi.org/10.15585/mmwr.rr7103a1Pain management best practices inter-agency task force report. U.S. Department of Health and Human Services. Last reviewed December 16, 2022. Accessed March 14, 2024.https://www.hhs.gov/opioids/prevention/pain-management-options/index.htmlVerret M et al; Canadian Perioperative Anesthesia Clinical Trials (PACT) Group. Perioperative use of gabapentinoids for the management of postoperative acute pain: a systematic review and meta-analysis. Anesthesiology. 2020;133(2):265-279.32667154https://doi.org/10.1097/ALN.0000000000003428Kaye AD et al. Dexmedetomidine in Enhanced Recovery After Surgery (ERAS) protocols for postoperative pain. Curr Pain Headache Rep. 2020;24(5):21.32240402https://doi.org/10.1007/s11916-020-00853-zAlbrecht E et al. Peri-operative intravenous administration of magnesium sulphate and postoperative pain: a meta-analysis. Anaesthesia. 2013;68(1):79-90.23121612https://doi.org/10.1111/j.1365-2044.2012.07335.xBlaudszun G et al. Effect of perioperative systemic α2 agonists on postoperative morphine consumption and pain intensity: systematic review and meta-analysis of randomized controlled trials. Anesthesiology. 2012;116(6):1312-22.22546966https://doi.org/10.1097/ALN.0b013e31825681cbWeinbroum AA et al. Dextromethorphan and dexmedetomidine: new agents for the control of perioperative pain. Eur J Surg. 2001;167(8):563-569.11716440https://doi.org/10.1080/110241501753171146Chang WJ. Muscle relaxants for acute and chronic pain. Phys Med Rehabil Clin N Am. 2020;31(2):245-254.32279727https://doi.org/10.1016/j.pmr.2020.01.005Young A et al. Nonsteroidal anti-inflammatory drugs and acetaminophen. In: Ballantyne JC et al, eds. Bonica’s Management of Pain. 5th ed. Lippincott Williams & Wilkins; 2019: 1315-1323.Hayward KL et al. Can paracetamol (acetaminophen) be administered to patients with liver impairment? Br J Clin Pharmacol. 2016;81(2):210-222.26460177https://doi.org/10.1111/bcp.12802Roddy E et al. Open-label randomised pragmatic trial (CONTACT) comparing naproxen and low-dose colchicine for the treatment of gout flares in primary care. Ann Rheum Dis. 2020;79(2):276-284.31666237https://doi.org/10.1136/annrheumdis-2019-216154Chen N et al. Corticosteroids for preventing postherpetic neuralgia. Cochrane Database Syst Rev. 2010;(12):CD005582.21154361https://doi.org/10.1002/14651858.CD005582.pub3Qaseem A et al; Clinical Guidelines Committee of the American College of Physicians. Management of acute and recurrent gout: a clinical practice guideline from the American College of Physicians. Ann Intern Med. 2017;166(1):58-68.27802508https://doi.org/10.7326/M16-0570Langer P et al. Survey of orthopaedic and sports medicine physicians regarding use of medrol dosepak for sports injuries. Arthroscopy. 2006;22(12):1263-1269.e2.17157723https://doi.org/10.1016/j.arthro.2006.08.020De Oliveira GS Jr et al. Perioperative single dose systemic dexamethasone for postoperative pain: a meta-analysis of randomized controlled trials. Anesthesiology. 2011;115(3):575-588.21799397https://doi.org/10.1097/ALN.0b013e31822a24c2Inturrisi C et al. Opioid analgesics. In: Ballentyne JC et al, eds. Bonica’s Management of Pain. 5th ed. Lippincott Williams & Wilkins; 2019:1334-1342.Grass JA. Patient-controlled analgesia. Anesth Analg. 2005;101(5 Suppl):S44-S61.16334492https://doi.org/10.1213/01.ANE.0000177102.11682.20Ahmed S et al. Microinduction of buprenorphine/naloxone: a review of the literature. Am J Addict. 2021;30(4):305-315.33378137https://doi.org/10.1111/ajad.13135Gabapentin capsule. Prescribing information. ACI Healthcare USA Inc; 2023. Accessed March 14, 2024.https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f2d9c3de-4749-4265-a26e-50026ab46ee4Pregabalin capsule. Prescribing information. Actavis Pharma Inc; 2021. Accessed March 14, 2024.https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f0a41ead-e56a-4338-91f0-b084b938ee80Guo J et al. Low-dose ketamine versus morphine in the treatment of acute pain in the emergency department: a meta-analysis of 15 randomized controlled trials. Am J Emerg Med. 2024;76:140-149.38071883https://doi.org/10.1016/j.ajem.2023.11.056Cyclobenzaprine—cyclobenzaprine hydrochloride tablet, film coated. Prescribing information. Rising Health LLC; 2019. Accessed March 14, 2024.https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b12fb4ea-182e-462b-b6ed-cfd2f6bb71e8Methocarbamol—methocarbamol tablet. Prescribing information. Camber Pharmaceuticals Inc; 2021. Accessed March 14, 2024.https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=43af0c41-9990-4902-9384-75de5ea08283Tizanidine hydrochloride capsule. Prescribing information. Advagen Pharma Limited; 2020. Accessed March 14, 2024.https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7f39499a-98cf-4d13-9b07-ccb5c22e43c8Carisoprodol—carisoprodol tablet. Prescribing information. Nostrum Laboratories Inc; 2021. Accessed March 14, 2024.https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ab22f1be-16c8-45b6-adaf-09e08bf7a545Diazepam tablet. Prescribing information. Aurobindo Pharma Limited; 2023. Accessed March 14, 2024.https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2f799120-0d08-47cd-8183-a98f0267c845Baclofen tablet. Prescribing information. Advagen Pharma Limited; 2023. Accessed March 14, 2024.https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=04dac0f6-cc6c-4959-9bca-a6e4a99690f3Derry S et al. Topical analgesics for acute and chronic pain in adults--an overview of Cochrane Reviews. Cochrane Database Syst Rev. 2017;5(5):CD008609.28497473https://doi.org/10.1002/14651858.CD008609.pub2Qaseem A et al. Nonpharmacologic and pharmacologic management of acute pain from non-low back, musculoskeletal injuries in adults: a clinical guideline from the American College of Physicians and American Academy of Family Physicians. Ann Intern Med. 2020;173(9):739-748.32805126https://doi.org/10.7326/M19-3602Wardhan R et al. Recent advances in acute pain management: understanding the mechanisms of acute pain, the prescription of opioids, and the role of multimodal pain therapy. F1000Res. 2017;6:2065.29225793https://doi.org/10.12688/f1000research.12286.1Narouze S et al. Interventional spine and pain procedures in patients on antiplatelet and anticoagulant medications (Second Edition): guidelines from the American Society of Regional Anesthesia and Pain Medicine, the European Society of Regional Anaesthesia and Pain Therapy, the American Academy of Pain Medicine, the International Neuromodulation Society, the North American Neuromodulation Society, and the World Institute of Pain. Reg Anesth Pain Med. 2018;43(3):225-262.29278603https://doi.org/10.1097/AAP.0000000000000700Horlocker T et al. Regional anesthesia in the patient receiving antithrombotic or thrombolytic therapy. Reg Anesth Pain Med. 2018;43:263-309.Kehlet H et al. Persistent postsurgical pain: risk factors and prevention. Lancet. 2006;367(9522):1618-1625.16698416https://doi.org/10.1016/S0140-6736(06)68700-XNadinda PG et al. Can perioperative psychological interventions decrease the risk of postsurgical pain and disability? A systematic review and meta-analysis of randomized controlled trials. Pain. 2022;163(7):1254-1273.34711760https://doi.org/10.1097/j.pain.0000000000002521Katz J et al. Chronic postsurgical pain: from risk factor identification to multidisciplinary management at the Toronto General Hospital Transitional Pain Service. Can J Pain. 2019;3(2):49-58.35005419https://doi.org/10.1080/24740527.2019.1574537Kovach CR et al. The assessment of discomfort in dementia protocol. Pain Manag Nurs. 2002;3(1):16-27.11893998https://doi.org/10.1053/jpmn.2002.30389Senay E et al. Physical dependence on Ultram (tramadol hydrochloride): both opioid-like and atypical withdrawal symptoms occur. Drug Alcohol Depend. 2003;69(3):233-241.12633909https://doi.org/10.1016/s0376-8716(02)00321-6Buresh M et al. Treating perioperative and acute pain in patients on buprenorphine: narrative literature review and practice recommendations. J Gen Intern Med. 2020;35(12):3635-3643.32827109https://doi.org/10.1007/s11606-020-06115-3Annex 12, Prescribing guidelines. In: Guidelines for the psychosocially assisted pharmacological treatment of opioid dependence. World Health Organization; 2009. Accessed March 14, 2024.https://www.ncbi.nlm.nih.gov/books/NBK143167/Dale RC et al. An acute pain service experience initiating methadone for opioid use disorder in hospitalized patients with acute pain. J Opioid Manag. 2019;15(4): 275-283.31637680https://doi.org/10.5055/jom.2019.0513Kohan L et al. Buprenorphine management in the perioperative period: educational review and recommendations from a multisociety expert panel. Reg Anesth Pain Med. 2021;46(10): 840-859.34385292https://doi.org/10.1136/rapm-2021-103007Dale RC et al. An Acute Pain Service experience initiating methadone for opioid use disorder in hospitalized patients with acute pain. J Opioid Manag. 2019;15(4):275-283.31637680https://doi.org/10.5055/jom.2019.0513Ward EN et al. Opioid use disorders: perioperative management of a special population. Anesth Analg. 2018;127(2):539-547.29847389https://doi.org/10.1213/ANE.0000000000003477FDA recommends avoiding use of NSAIDs in pregnancy at 20 weeks or later because they can result in low amniotic fluid. US Food and Drug Administration. Last updated September 1, 2022. Accessed March 14, 2024.https://www.fda.gov/media/142967/download?attachmentSchwenk ES et al. Consensus guidelines on the use of intravenous ketamine infusions for acute pain management from the American Society of Regional Anesthesia and Pain Medicine, the American Academy of Pain Medicine, and the American Society of Anesthesiologists. Reg Anesth Pain Med. 2018;43(5):456-466.29870457https://doi.org/10.1097/AAP.0000000000000806Weibel S et al. Continuous intravenous perioperative lidocaine infusion for postoperative pain and recovery in adults. Cochrane Database Syst Rev. 2018;6(6):CD009642.29864216https://doi.org/10.1002/14651858.CD009642.pub3Upadya M et al. Anaesthesia for non-obstetric surgery during pregnancy. Indian J Anaesth. 2016;60(4):234-41.27141105https://doi.org/10.4103/0019-5049.179445Morphine. Drugs and Lactation Database (LactMed) [Internet]. National Institute of Child Health and Human Development; 2006-. Updated December 15, 2023. Accessed March 14, 2024.https://www.ncbi.nlm.nih.gov/books/NBK501237/Meperidine. Drugs and Lactation Database (LactMed) [Internet]. National Institute of Child Health and Human Development; 2006-. Updated December 15, 2023. Accessed March 14, 2024.https://www.ncbi.nlm.nih.gov/books/NBK501232/Use of codeine and tramadol products in breastfeeding women--questions and answers. US Food and Drug Administration. Updated August 1, 2019. Accessed March 14, 2024.https://www.fda.gov/drugs/postmarket-drug-safety-information-patients-and-providers/use-codeine-and-tramadol-products-breastfeeding-women-questions-and-answersGélinas C et al. Validation of the critical-care pain observation tool in adult patients. Am J Crit Care. 2006;15(4):420-427.16823021Sinatra R. Causes and consequences of inadequate management of acute pain. Pain Med. 2010;11(12):1859-1871.21040438https://doi.org/10.1111/j.1526-4637.2010.00983.xGan TJ et al. Practice patterns and treatment challenges in acute postoperative pain management: a survey of practicing physicians. Pain Ther. 2018;7(2):205-216.30367388https://doi.org/10.1007/s40122-018-0106-9Daoust R et al. Relationship between pain, opioid treatment, and delirium in older emergency department patients. Acad Emerg Med. 2020;27(8):708-716.32441414https://doi.org/10.1111/acem.14033da C Menezes Costa L et al. The prognosis of acute and persistent low-back pain: a meta-analysis. CMAJ 2012;184(11):E613-E624.22586331https://doi.org/10.1503/cmaj.111271Bree Collaborative; Agency Medical Directors’ Group. Prescribing Opioids for Postoperative Pain-Supplemental Guidance. Foundation for Health Care Quality. Published July 2018. Accessed March 14, 2024.https://www.qualityhealth.org/bree/wp-content/uploads/sites/8/2018/09/Final-Supplemental-Bree-AMDG-Postop-pain-091318-wcover.pdfMariano ER et al. A multisociety organizational consensus process to define guiding principles for acute perioperative pain management. Reg Anesth Pain Med. 2022;47(2):118-127.34552003https://doi.org/10.1136/rapm-2021-103083Complex regional pain syndrome. National Institute of Neurological Disorders and Stroke. Last reviewed January 31, 2024. Accessed March 14, 2024.https://www.ninds.nih.gov/health-information/disorders/complex-regional-pain-syndrome
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