Gunasekara N S, Noble S, Benfield P
Adis International Limited, Auckland, New Zealand.
Drugs. 1998 Jan;55(1):85-120. doi: 10.2165/00003495-199855010-00007.
Paroxetine is a potent and selective inhibitor of the neuronal reuptake of serotonin (5-hydroxytryptamine; 5-HT), which was previously reviewed as an antidepressant in Drugs in 1991. Since then, more comparative trials with other antidepressants have become available, and its use in the elderly and as long term maintenance therapy has been investigated. Paroxetine has also been studied in several other disorders with a presumed serotonergic component, primarily obsessive compulsive disorder (OCD) and panic disorder. In short term clinical trials in patients with depression, paroxetine produced clinical improvements that were significantly greater than those with placebo and similar to those achieved with other agents including tricyclic antidepressants (TCAs), maprotiline, nefazodone and the selective serotonin reuptake inhibitors (SSRIs) fluoxetine, fluvoxamine and sertraline. Long term data suggest that paroxetine is effective in preventing relapse or recurrence of depression in patients treated for up to 1 year. In the elderly, the overall efficacy of paroxetine was at least as good as that of comparator agents. In short term clinical trials involving patients with OCD or panic disorder, paroxetine was significantly more effective than placebo and of similar efficacy to clomipramine. Limited long term data show that paroxetine is effective in maintaining a therapeutic response over periods of 1 year (OCD) and up to 6 months (panic disorder). Preliminary data suggest that paroxetine has potential in the treatment of social phobia, premenstrual dysphoric disorder and chronic headache. Like the other SSRIs, paroxetine is better tolerated than the TCAs, causing few anticholinergic adverse effects. The most commonly reported adverse event associated with paroxetine treatment is nausea, although this is generally mild and subsides with continued use. Fewer withdrawals from treatment due to adverse effects occurred with paroxetine treatment than with TCAs. The adverse events profile of paroxetine appears to be broadly similar to that of other SSRIs, although data from comparative trials are limited. Serious adverse effects associated with paroxetine are very rare. In conclusion, paroxetine is effective and well tolerated, and suitable as first-line therapy for depression. It also appears to be a useful alternative to other available agents for the treatment of patients with OCD or panic disorder.
帕罗西汀是一种强效且具有选择性的5-羟色胺(5- HT)神经元再摄取抑制剂,该药于1991年在《药物》杂志上作为抗抑郁药被首次综述。自那时起,有了更多与其他抗抑郁药的对比试验,并且对其在老年人中的应用以及作为长期维持疗法进行了研究。帕罗西汀还在其他几种可能存在5-羟色胺能成分的疾病中进行了研究,主要是强迫症(OCD)和惊恐障碍。在抑郁症患者的短期临床试验中,帕罗西汀产生的临床改善显著大于安慰剂组,且与包括三环类抗抑郁药(TCAs)、马普替林、奈法唑酮以及选择性5-羟色胺再摄取抑制剂(SSRIs)氟西汀、氟伏沙明和舍曲林在内的其他药物所取得的效果相似。长期数据表明,帕罗西汀对于接受长达1年治疗的抑郁症患者预防复发有效。在老年人中,帕罗西汀的总体疗效至少与对照药物相当。在涉及强迫症或惊恐障碍患者的短期临床试验中,帕罗西汀比安慰剂显著更有效,且与氯米帕明疗效相似。有限的长期数据表明,帕罗西汀在长达1年(强迫症)和长达6个月(惊恐障碍)的时间段内维持治疗反应有效。初步数据表明,帕罗西汀在社交恐惧症、经前烦躁障碍和慢性头痛的治疗中具有潜力。与其他SSRIs一样,帕罗西汀的耐受性优于TCAs类药物,几乎不产生抗胆碱能不良反应。与帕罗西汀治疗相关的最常见不良事件是恶心,不过通常较为轻微,且持续用药后会消退。与TCAs类药物相比,因不良反应而停药的情况在帕罗西汀治疗中较少。尽管对比试验的数据有限,但帕罗西汀的不良事件谱似乎与其他SSRIs大致相似。与帕罗西汀相关的严重不良反应非常罕见。总之,帕罗西汀有效且耐受性良好,适合作为抑郁症的一线治疗药物。它似乎也是治疗强迫症或惊恐障碍患者的其他可用药物的有用替代药物。