Controlled-release pregabalin in the treatment of fibromyalgia

被引:11
作者
Alciati, Alessandra [1 ,2 ]
Atzeni, Fabiola [3 ]
Masala, Ignazio Francesco [4 ]
Cirillo, Mariateresa [2 ]
Sciortino, Davide [2 ]
Perna, Giampaolo [1 ,5 ,6 ,7 ]
Sarzi-Puttini, Piercarlo [8 ]
机构
[1] Hermanas Hosp, Dept Clin Neurosci, Villa San Benedetto Menni, FoRiPsi, Como, Italy
[2] Humanitas Clin & Res Ctr, Milan, Italy
[3] Univ Messina, Dept Clin & Expt Med, Rheumatol Unit, Messina, Italy
[4] Santissima Trinita Hosp, Trauma & Orthoped Unit, Cagliari, Italy
[5] Maastricht Univ, Fac Hlth Med & Life Sci, Res Inst Mental Hlth & Neurosci, Maastricht, Netherlands
[6] Maastricht Univ, Fac Hlth Med & Life Sci, Dept Psychiat & Neuropsychol, Maastricht, Netherlands
[7] Univ Miami, Leonard Miller Sch Med, Dept Psychiat & Behav Sci, Miami, FL USA
[8] ASST Fatebenefratelli Sacco, Dept Rheumatol, Milan, Italy
关键词
Fibromyalgia; pharmacological treatment; pregabalin; controlled-release pregabalin; HEALTH-CARE COSTS; PLACEBO-CONTROLLED TRIAL; OF-RHEUMATOLOGY; 1990; PHASE-III TRIAL; DOUBLE-BLIND; MEDICATION ADHERENCE; DIAGNOSTIC-CRITERIA; DULOXETINE; PHARMACOKINETICS; METAANALYSIS;
D O I
10.1080/14737175.2018.1508344
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Fibromyalgia (FM) is a chronic disorder whose symptoms of musculo-skeletal pain, fatigue, sleep disturbances, and cognitive impairment pervade the personal, occupational, and social aspects of a patient's life. Together with the antidepressants duloxetine and milnacipran, the anticonvulsant pregabalin (PGB) is one of the three drugs approved by the Food and Drug Administration for the treatment of FM. The aim of this narrative review is to summarize the data relating to the efficacy and safety of the controlled-release formulation of PGB (PGB-CR) in patients with FM. Areas covered: Efforts by the pharmaceutical industry have led to the introduction of new formulations of already approved drugs to enhance treatment convenience and adherence. Expert opinion: Although there are no published studies specifically comparing PGB-CR and PGB-IR formulations in FM patients, the efficacy and safety profiles of PGB-CR seem to be similar to those of the IR formulation, and the convenience of once-daily dosing potentially enhances patient compliance. However, the amount of evidence is not sufficient to draw any definite conclusions, and further studies of larger patient samples are needed.
引用
收藏
页码:617 / 623
页数:7
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