Dose-response of pregabalin for diabetic peripheral neuropathy, postherpetic neuralgia, and fibromyalgia

被引:21
|
作者
Arnold, Lesley M. [1 ]
McCarberg, Bill H. [2 ]
Clair, Andrew G. [3 ]
Whalen, Ed [4 ]
Thomas, Neal [3 ,5 ]
Jorga, Anamaria [3 ]
Pauer, Lynne [6 ]
Vissing, Richard [7 ]
Park, Peter W. [8 ]
机构
[1] Univ Cincinnati, Coll Med, Dept Psychiat & Behav Neurosci, Cincinnati, OH USA
[2] Univ Calif San Diego, Sch Med, Dept Family Med, San Diego, CA 92103 USA
[3] Pfizer, US Med Affairs, New York, NY USA
[4] Pfizer, Stat, New York, NY USA
[5] Pfizer, Stat, Groton, CT USA
[6] Pfizer, Global Prod Dev Clin Sci & Operat, Groton, CT USA
[7] Pfizer Inc, Neurosci & Pain Div, Louisville, KY USA
[8] Pfizer Inc, North Amer Med Affairs, New York, NY 10017 USA
关键词
Pregabalin; dose-response; diabetic peripheral neuropathy; postherpetic neuralgia; fibromyalgia; PHASE-III TRIAL; DOUBLE-BLIND; PLACEBO; PAIN; EFFICACY; SAFETY; TOLERABILITY; PATTERNS; METAANALYSIS; MULTICENTER;
D O I
10.1080/00325481.2017.1384691
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: The pregabalin dose-response for pain, Patient Global Impression of Change (PGIC), and sleep quality measures in painful diabetic peripheral neuropathy (pDPN), postherpetic neuralgia (PHN), and fibromyalgia (FM) is relevant for physicians treating these patients. This analysis aimed to demonstrate the dose-response of pregabalin for each indication and describe the onset (incidence), onset/continuation (prevalence), and resolution of adverse events (AEs) occurring during treatment. Methods: Data from 14 placebo-controlled, fixed-dose pregabalin trials in pDPN, PHN, and FM were pooled within each indication. Patients had mean baseline pain scores 6 on an 11-point numeric rating scale. A hyperbolic E-max dose-response model examined the dose-response of pregabalin for pain, PGIC, and sleep quality. Safety assessments included onset and prevalence of common AEs each week, and resolution in the first 2months of treatment. Results: In all indications, the likelihood of patients experiencing pain relief and improvements in PGIC and sleep quality increased in a dose-dependent manner with increasing doses. In all indications, new incidences of dizziness and somnolence were highest after 1week of treatment, with few subsequent new reports at a given dose. Prevalence rates decreased steadily after 1week of treatment. In FM, new onset weight gain emerged 6-8weeks following treatment; prevalence rates generally increased then remained steady over time. With the exception of weight gain, many AEs resolved in month 1. Conclusion: The dose-response of pregabalin for pain, PGIC, and sleep quality was demonstrated, highlighting the benefit of achieving the maximum recommended dose of 300mg/day for pDPN, 300-600mg/day for PHN, and 300-450mg/day for FM. Common AEs are generally seen within 1week of starting treatment, with few subsequent new reports at a given dose. New onset weight gain occurs after 6weeks of treatment, reinforcing the need for regular monitoring of weight.
引用
收藏
页码:921 / 933
页数:13
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