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1.
Curr Med Res Opin ; 35(2): 189-202, 2019 02.
Article in English | MEDLINE | ID: mdl-29569951

ABSTRACT

OBJECTIVE: Dexketoprofen trometamol is a modified non-selective COX inhibitor with a rapid onset of action that is available as both oral and parenteral formulations. The aim of this narrative review was to assess the efficacy and tolerability/safety of dexketoprofen trometamol in acute pain states using the best available published scientific evidence (randomized controlled clinical trials and systematic reviews/meta-analyses). METHODS: Literature retrieval was performed via Medline, Embase and the Cochrane Library (from inception up to March 2017) using combinations of the terms "randomized controlled trials", "dexketoprofen", "celecoxib", "etoricoxib", "parecoxib" and "acute pain". RESULTS: Single-dose dexketoprofen trometamol provides effective analgesia in the treatment of acute pain, such as postoperative pain (dental and non-dental surgery), renal colic, acute musculoskeletal disorders and dysmenorrhea, and reduces opioid consumption in the postoperative setting. It has a rapid onset of action (within 30 minutes) and is well tolerated during short-term treatment. Direct comparisons with COX-2 inhibitors are lacking; however, the efficacy and tolerability of single-dose dexketoprofen trometamol appears to be consistent with that seen with celecoxib, etoricoxib and parecoxib in the acute pain setting. CONCLUSION: In conclusion, dexketoprofen trometamol appears to provide similar analgesic efficacy to COX-2 inhibitors when used to treat acute pain, has a rapid onset of action, is well tolerated, and has an opioid-sparing effect when used as part of a multimodal regimen in the acute pain setting.


Subject(s)
Acute Pain/drug therapy , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Ketoprofen/analogs & derivatives , Tromethamine/therapeutic use , Analgesics, Opioid/therapeutic use , Cyclooxygenase 2 Inhibitors/therapeutic use , Humans , Ketoprofen/therapeutic use , Pain, Postoperative/drug therapy , Randomized Controlled Trials as Topic
2.
Anesthesiology ; 113(3): 666-71, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20693880

ABSTRACT

BACKGROUND: The hanging drop technique is used for identifying the cervical epidural space, using its negative pressure. However, it is doubtful whether the epidural space intrinsically exhibits a negative pressure. We designed this study to test the hypothesis that the cervical epidural pressure (CEP) is significantly higher in the prone position than in the sitting position. To evaluate this hypothesis, we measured and compared 30 CEP values in the prone and sitting positions. METHODS: We measured and compared 15 CEPs in the prone group and 15 in the sitting group using a closed pressure measurement system under fluoroscopic guidance. RESULTS: All CEPs in the prone group were consistently positive (median, 10 mmHg; range, 4.8-18.7; mean+/-SD, 10.5+/-4.4) in contrast to the sitting group (median, -0.3 mmHg; range, -2.4-7.9; mean+/-SD, 0.5+/-2.8). CEPs in the prone group were significantly higher than in the sitting group (P<0.001). CONCLUSION: CEP was found to be significantly higher in the prone position than in the sitting position. Furthermore, CEPs were not consistently negative even in the sitting position. These results suggest that the hanging drop technique is inappropriate for identifying the cervical epidural space in either the prone or sitting positions. Clinical Trials Ref: NCT01009385.


Subject(s)
Cervical Vertebrae/physiology , Epidural Space/physiology , Pressure , Prone Position/physiology , Adult , Aged , Aged, 80 and over , Female , Humans , Injections, Epidural , Male , Middle Aged , Posture/physiology
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