Effects of low-dose intranasal (S)-ketamine in patients with neuropathic pain
Background: NMDA receptors are involved in the development and maintenance of neuropathic pain. We evaluated the efficacy and safety of intranasal (S)-ketamine, one of the most potent clinically available NMDA receptor antagonists. Methods: Sixteen patients with neuropathic pain of various origins w...
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| Hauptverfasser: | , , , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
[April 2010]
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| In: |
European journal of pain
Year: 2010, Jahrgang: 14, Heft: 4, Pages: 387-394 |
| ISSN: | 1090-3801 |
| DOI: | 10.1016/j.ejpain.2009.08.002 |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.ejpain.2009.08.002 Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1016/j.ejpain.2009.08.002 
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| Verfasserangaben: | Volker Huge, Meike Lauchart, Walter Magerl, Gustav Schelling, Antje Beyer, Detlef Thieme, Shahnaz C. Azad |
| Zusammenfassung: | Background: NMDA receptors are involved in the development and maintenance of neuropathic pain. We evaluated the efficacy and safety of intranasal (S)-ketamine, one of the most potent clinically available NMDA receptor antagonists. Methods: Sixteen patients with neuropathic pain of various origins were randomized into two treatment groups: (S)-ketamine 0.2mg/kg (group 1); (S)-ketamine 0.4mg/kg (group 2). Plasma concentrations of (S)-ketamine and (S)-norketamine were measured over 6h by High Performance Liquid Chromatography combined with mass spectrometry. Quantitative sensory testing (QST) was conducted before, during and after treatment. Side effects and amount of pain reduction were recorded. Results: Intranasal (S)-ketamine administration lead to peak plasma concentrations of 27.7±5.9ng/ml at 10±6.3min (group 1) and 34.3±22.2ng/ml at 13.8±4.8min after application (group 2). Maximal plasma concentrations of (S)-norketamine were 18.3±14.9ng/ml at 81±59min (group 1) and 34.3±5.5ng/ml at 75±40min (group 2). Pain scores decreased significantly in both groups with minimal pain at 60min after drug administration (70±10% and 61±13% of initial pain in groups 1 and 2). The time course of pain decrease was significantly correlated with plasma concentrations of (S)-ketamine and (S)-norketamine (partial correlations: (S)-norketamine: −0.90 and −0.86; (S)-ketamine: −0.72 and −0.71 for group 1 and group 2, respectively). Higher dosing elicited significantly more side effects. Intranasal (S)-ketamine had no significant impact on thermal or mechanical detection and pain thresholds in normal or symptomatic skin areas. Conclusions: Intranasal administration of low dose (S)-ketamine rapidly induces adequate plasma concentrations of (S)-ketamine and subsequently of its metabolite (S)-norketamine. The time course of analgesia correlated with plasma concentrations. |
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| Beschreibung: | Available online: 3 September 2009, Frontdoor: first published: 09 January 2012 Gesehen am 01.06.2023 |
| Beschreibung: | Online Resource |
| ISSN: | 1090-3801 |
| DOI: | 10.1016/j.ejpain.2009.08.002 |