| Literature DB >> 27828892 |
Denise Sullivan1, Mary Lyons, Robert Montgomery, Ann Quinlan-Colwell.
Abstract
Challenges with opioids (e.g., adverse events, misuse and abuse with long-term administration) have led to a renewed emphasis on opioid-sparing multimodal management of trauma pain. To assess the extent to which currently available evidence supports the efficacy and safety of various nonopioid analgesics and techniques to manage trauma pain, a literature search of recently published references was performed. Additional citations were included on the basis of authors' knowledge of the literature. Effective options for opioid-sparing analgesics include oral and intravenous (IV) acetaminophen; nonsteroidal anti-inflammatory drugs available via multiple routes; and anticonvulsants, which are especially effective for neuropathic pain associated with trauma. Intravenous routes (e.g., IV acetaminophen, IV ketorolac) may be associated with a faster onset of action than oral routes. Additional adjuvants for the treatment of trauma pain are muscle relaxants and alpha-2 adrenergic agonists. Ketamine and regional techniques play an important role in multimodal therapy but require medical and nursing support. Nonpharmacologic treatments (e.g., cryotherapy, distraction techniques, breathing and relaxation, acupuncture) supplement pharmacologic analgesics and can be safe and easy to implement. In conclusion, opioid-sparing multimodal analgesia addresses concerns associated with high doses of opioids, and many pharmacologic and nonpharmacologic options are available to implement this strategy. Nurses play key roles in comprehensive patient assessment; administration of patient-focused, opioid-sparing, multimodal analgesia in trauma; and monitoring for safety concerns.Entities:
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Year: 2016 PMID: 27828892 PMCID: PMC5123624 DOI: 10.1097/JTN.0000000000000250
Source DB: PubMed Journal: J Trauma Nurs ISSN: 1078-7496 Impact factor: 1.010
Figure 1.Potential advantages of opioid-sparing multimodal therapy.
Figure 2.Diagram showing the location of action in the nervous system for analgesics used in multimodal therapy (De Kock & Lavand'homme, 2007; D'Mello & Dickenson, 2008; Gottschalk & Smith, 2001; Kehlet & Dahl, 1993; Ossipov, Dussor, & Porreca, 2010; Smith, 2009; Warner & Mitchell, 2004). COX-2 = cyclooxygenase-2; NMDA = N-methyl-d-aspartate; NSAID = nonsteroidal anti-inflammatory drug. From “The Value of ‘Multimodal' or ‘Balanced Analgesia' in Postoperative Pain Treatment,” by H. Kehlet and J. B. Dahl, 1993, Anesthesia and Analgesia, Vol. 77(5), pp. 1048–1056. Copyright Wolters Kluwer Health. Adapted with permission.
Figure 3.Hierarchy of pain assessment techniques, including assessment tools discussed in this review within the relevant steps. BPS = Behavioral Pain Scale; CHEOPS = Children's Hospital of Eastern Ontario Pain Scale; CPOT = Critical-Care Pain Observation Tool; FLACC = Face, Legs, Arms, Cry, and Consolability; N-PASS = Neonatal Pain, Agitation, and Sedation Scale; NRS = numeric rating scale; VAS = visual analog scale. From Pain Assessment and Pharmacologic Management by C. Pasero and M. McCaffery, Eds., 2011, St. Louis, MO: Elsevier. Copyright Elsevier. Adapted with permission.
Figure 4.Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) diagram of the literature search process for obtaining articles on medications and techniques for pain relief.
Summary of the Key Advantages and Disadvantages Associated With Each Type of Analgesic Discussed in the Review
| Analgesic Type | Key Clinical Advantages | Key Clinical Disadvantages |
|---|---|---|
| Acetaminophen | Long history of safety and efficacy in oral and IV routes; IV route may be opioid sparing and have faster onset of action and less hepatotoxicity than oral route | Can be hepatotoxic at high doses or in at-risk populations |
| NSAIDs | Effective across multiple routes (e.g., oral, IM, IV) | Nonsystemic administration is associated with local AEs |
| Topical local anesthetics | May be locally effective for neuropathic pain associated with trauma | Several studies did not show significant pain relief for various types of trauma pain |
| Gabapentinoids | Some evidence for efficacy for neuropathic pain associated with trauma; opioid sparing | Not all studies support efficacy for trauma pain |
| Muscle relaxants | Can reduce painful muscle spasms | Caution is warranted because of AEs such as dizziness and drowsiness |
| Alpha-2 adrenergic agonists | Sedative and anxiolytic properties; opioid sparing | Should be used with caution in hemodynamically unstable patients |
| Ketamine | May decrease incidence of pain hypersensitivity and opioid tolerance; opioid sparing | Requires provider training and patient monitoring |
| Regional techniques | A variety of effective techniques are available to target pain at various locations; opioid sparing | Require provider training; caution should be exercised if the patient is receiving anticoagulation therapy |
| Nonpharmacologic options | May be safe and simple to implement; opioid sparing | Are considered complementary to and not a substitute for analgesics; studies supporting their efficacy are typically not double-blind |
Abbreviations: AE, adverse event; IM, intramuscular; IV, intravenous; NSAID, nonsteroidal anti-inflammatory drug.