Emerging treatment modalities: balancing efficacy and safety

Am J Health Syst Pharm. 2007 Mar 15;64(6 Suppl 4):S6-S11. doi: 10.2146/ajhp060680.

Abstract

Purpose: The advantages and disadvantages of intravenous patient-controlled analgesia (i.v. PCA) and epidural analgesia are discussed. New approaches to the management of patients with acute post-operative pain are described. The results of controlled clinical trials with these modalities are presented.

Summary: Intravenous patient-controlled analgesia, while effective, is a burdensome technology requiring approximately 125 steps and at least 6 staff members. Furthermore, medication and pump programming errors may lead to patient injury. Epidural analgesia via catheter has a high reported failure rate, causing analgesic gaps and requiring a high level of staff intervention. In a clinical trial involving hip arthroplasty, extended-release epidural morphine demonstrated a 48-hour duration of action with a marked reduction in need for supplemental analgesia. The fentanyl Iontophoretic Transdermal System has demonstrated therapeutic equivalence with morphine intravenous patient-controlled analgesia and similar safety. Selective opioid antagonists are under development that may selectively block gastrointestinal opioid receptors while preserving analgesia.

Conclusion: Recently approved agents and those in development may address a variety of unmet needs in the management of patients with post-operative pain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Cutaneous
  • Analgesia, Epidural*
  • Analgesia, Patient-Controlled*
  • Analgesics, Opioid / adverse effects
  • Analgesics, Opioid / therapeutic use*
  • Drugs, Investigational / pharmacology
  • Drugs, Investigational / therapeutic use
  • Fentanyl / therapeutic use
  • Humans
  • Medication Errors
  • Morphine / therapeutic use
  • Narcotic Antagonists / pharmacology
  • Narcotic Antagonists / therapeutic use
  • Postoperative Pain / drug therapy*

Substances

  • Analgesics, Opioid
  • Drugs, Investigational
  • Narcotic Antagonists
  • Morphine
  • Fentanyl