The Potential Role of an Extended-Release, Abuse-Deterrent Oxycodone/Acetaminophen Fixed-Dose Combination Product for the Treatment of Acute Pain

被引:6
作者
Pergolizzi, Joseph V., Jr. [1 ,2 ,3 ,4 ]
Taylor, Robert, Jr. [5 ]
Raffa, Robert B. [6 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[2] Temple Univ, Sch Med, Dept Pharmacol, Philadelphia, PA 19122 USA
[3] Georgetown Univ, Sch Med, Dept Anesthesiol, Washington, DC USA
[4] Assoc Chron Pain Patients, Houston, TX USA
[5] NEMA Res Inc, Bonita Springs, FL 34134 USA
[6] Temple Univ, Sch Pharm, Dept Pharmaceut Sci, Philadelphia, PA 19122 USA
关键词
Acute pain control; Extended-release analgesics; Fixed-dose combination products; Oxycodone/acetaminophen (paracetamol); Postoperative pain; Xartemis (R) XR; EVIDENCE BASED RECOMMENDATIONS; EULAR-STANDING-COMMITTEE; CHRONIC NONCANCER PAIN; LONG-ACTING OPIOIDS; IMMEDIATE-RELEASE; DOUBLE-BLIND; EMERGENCY-DEPARTMENT; MITIGATION STRATEGY; RISK-EVALUATION; NATIONAL-SURVEY;
D O I
10.1007/s12325-015-0213-5
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Acute pain, prevalent as part of postoperative and traumatic pain, is often sub-optimally or inadequately treated. Fixed-dose combination analgesic products that combine a reduced amount of opioid with a nonopioid analgesic such as acetaminophen (paracetamol) in a single tablet offer potential pharmacodynamic and/or pharmacokinetic benefits, and may also result in an opioid-sparing effect. A new analgesic product (XARTEMIS (TM) XR, Mallinckrodt Brand Pharmaceuticals, Dublin, Ireland) combines oxycodone (7.5 mg) with acetaminophen (325 mg) in an immediate-release/extended-release (ER) formulation that is indicated for the treatment of acute pain. The ER formulation of this product provides stable serum drug concentrations that in this case lasts 12 h. Oxycodone/acetaminophen is a drug combination that offers safe and effective pain relief in a variety of acute pain syndromes such as postoperative pain. The combination formulation allows a smaller amount of oxycodone per tablet and the biphasic-layered matrix of the pill for ER may present obstacles to potential abusers. No opioid is totally abuse resistant, but the lower opioid content and tamper-resistant formulation of this product might discourage abuse. Clinicians must still be mindful of the acetaminophen part of this product in the patient's overall daily intake (in light of acetaminophen hepatotoxicity). The new product appears to provide an important new choice in the armamentarium against acute pain.
引用
收藏
页码:485 / 495
页数:11
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