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Erschienen in: HSS Journal ® 1/2018

06.11.2017 | Original Article

Pregabalin Did Not Improve Pain Management After Spinal Fusions

verfasst von: Michael K. Urban, MD, PhD, Kristy M. Labib, MD, Shane C. Reid, MBS, BA, Amanda K. Goon, BA, Valeria Rotundo, Frank P. Cammisa Jr., MD, Federico P. Girardi, MD

Erschienen in: HSS Journal ® | Ausgabe 1/2018

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Abstract

Background

The treatment of postoperative pain is a challenge after posterior spinal fusions. Pain management using predominantly opioids is often associated with multiple adverse effects, while multimodal postoperative analgesia may provide adequate pain relief with fewer opioid side effects.

Questions/Purposes

The purpose of this review is to determine whether addition of 150 mg pregabalin daily would reduce narcotic requirements and improve outcomes after posterior lumbar fusion (PLF).

Methods

The method used is a randomized, controlled trial of elective PLF patients who received pregabalin or placebo. With institutional review board (IRB) approval, 86 patients undergoing elective posterior lumbar fusion, ASA I–III, were randomized to receive either a placebo or pregabalin after obtaining written informed consent. Both arms, i.e., placebo and pregabalin, consisted of 43 patients each.
The 86 patients for elective PLF were randomly assigned to receive 150 mg of pregabalin 1 h before surgery and then 150 mg daily, or a placebo tablet. All patients received a similar general anesthetic and in the post-anesthesia care unit (PACU), started on intravenous (IV) patient-controlled analgesia (PCA) of hydromorphone (0.2 mg/ml). Postoperative pain was assessed daily until discharge using a Numerical Rating Scale (NRS) at rest and with physical therapy (PT). Patients were also assessed twice daily for level of sedation and nausea and/or vomiting and expected PT milestones. All narcotics (IV, oral) were documented.

Results

Demographics and operative time between groups were similar. PCA hydromorphone administration and oral narcotic intake were not statistically different between the two groups. However, an increased incidence of nausea and vomiting in the placebo group reached statistical significance (p < 0.05). In addition, there was no statistical difference between groups with respect to achieving PT milestones and hospital discharge day.

Conclusion

After PLF, patients receiving pregabalin 150 mg/day did not have reduced IV narcotic usage, improved PT milestones, or reduced length of hospital stay. We were unable to demonstrate an analgesic advantage to prescribing pregabalin to patients undergoing lumbar spinal fusions.
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Metadaten
Titel
Pregabalin Did Not Improve Pain Management After Spinal Fusions
verfasst von
Michael K. Urban, MD, PhD
Kristy M. Labib, MD
Shane C. Reid, MBS, BA
Amanda K. Goon, BA
Valeria Rotundo
Frank P. Cammisa Jr., MD
Federico P. Girardi, MD
Publikationsdatum
06.11.2017
Verlag
Springer US
Erschienen in
HSS Journal ® / Ausgabe 1/2018
Print ISSN: 1556-3316
Elektronische ISSN: 1556-3324
DOI
https://doi.org/10.1007/s11420-017-9584-2

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