University of Washington

Department of Rehabilitation Medicine

http://rehab.washington.edu/research/articles/showref.asp?id=4425


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Title:

Early pain reduction can predict treatment response: results of integrated efficacy analyses of a once-daily gastroretentive formulation of gabapentin in patients with postherpetic neuralgia.

Author(s):

Jensen MP, Hsu PH, Vanhove GF

Year:

2012

Publication Info:

Pain Medicine, 13(8):1059-1066

Abstract:

OBJECTIVE: The objectives of this study were to identify and determine the validity of early decision criteria following once-daily gastroretentive gabapentin (G-GR) treatment in patients with postherpetic neuralgia (PHN).
DESIGN: In two placebo-controlled studies, 279 patients were randomized to 1,800 mg G-GR and 270 to placebo with the evening meal; patients underwent a 2-week dose titration, followed by 8 weeks of stable dosing, and 1 week of dose tapering. Patients. Adults with PHN for =6 months and an average baseline Numerical Pain Rating Scale (NPRS) score of =4 were included in the study.
OUTCOME MEASURES: Percent change from baseline to week 10 in NPRS scores and the percentage of responders (defined as =30% reduction in NPRS scores from baseline to week 10) were determined.
METHODS: Patients randomized to G-GR were categorized at each week based on their percent pain reduction up to that week, and for each category, the percentage of week 10 responders was computed. For several early-improvement criteria, the percentage of week 10 responders, odds ratios for achieving week 10 treatment response, sensitivity, and specificity were calculated.
RESULTS: There was a significant positive association between early pain reduction and week 10 treatment response. Pain reduction of <10% at week 5 of G-GR treatment was the best early predictor of lack of endpoint response, with only 8% of these patients moving on to become week 10 treatment responders.
CONCLUSIONS: Early response was a reliable predictor of final response. This approach holds promise for aiding clinicians in decision making regarding the need for alternative or supplemental treatment during G-GR therapy for PHN.

Link to Article:

http://www.ncbi.nlm.nih.gov/pubmed/22757655


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