有没有制药公司炒作社交焦虑症来增加销量?是的:营销阻碍了长期解决方案的发现。

D. Healy
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引用次数: 8

摘要

社交恐惧症,也被称为社交焦虑症,会导致酗酒、吸毒、失业,甚至自杀。与被视为最常见的神经性疾病的东方相比,它在西方相对不为人所知葛兰素史克(GlaxoSmithKline)最近获准推广使用帕罗西汀(paroxetine)治疗社交恐惧症,这似乎肯定会提高人们对这种潜在严重疾病的认识。这种双赢的局面有什么不好呢?第一个问题在于解释许可证的含义。许可证并不是食品和药物管理局对帕罗西汀治疗社交恐惧症有效的声明。如果一种治疗方法可以证明对某种疾病有所帮助,那么从法律上讲,许可证不能被拒绝,但它们不能保证这种治疗是值得的。虽然简单地提高对社交恐惧症的认识可能会减少患者的孤立感,但除非患者得到有效的治疗,使他们的生活发生实质性的变化,否则这种治疗可能不值得冒险。风险是什么?从SmithKline公司在20世纪80年代进行的研究中可以清楚地看出,即使短暂接触帕罗西汀也会导致许多服药者在身体上产生依赖试验还表明,选择性5 -羟色胺再摄取抑制剂(SSRIs)的使用会使患者产生自杀倾向,并且这些药物会导致性功能障碍和神经系统障碍尽管ssri类药物在市场上被宣传为比旧药物更无副作用,但反映这种自由的生活质量量表的结果尚未发表,该结果已在多达100个临床试验中使用这强烈表明,对许多人来说,SSRIs可能是错误的药物。如果SmithKline公司像推销病情一样努力推销治疗的危害,那么所有这些危害都可以被最小化。与最近被公司推销的强迫症不同,社交恐惧症更像是抑郁症——一种可能由多种情况引起的综合症。在某些情况下,它可能是精神障碍的前驱症状。尽管一些患者使用帕罗西汀可能会有所好转,但我们清醒地认识到,第一批抗抑郁药物的发现是因为它们使一些患者变得精神错乱。在用ssri类药物治疗抑郁症的试验中,很大一部分本来没有精神病的患者变成了精神病患者。社交恐惧症也是如此。患有这种可能使人衰弱的疾病的人需要的是研究,以理解为什么会出现这种情况,而不是推销一种可能对少数患者有益,但对同样大的群体有害的药物。毫无疑问,一些社交恐惧症患者在服用帕罗西汀后不会产生自杀倾向、依赖性或精神病,他们的生活质量也不会差。然而,即使是这些病人也有需要担心的事情。当像社交恐惧症这样的疾病成为制药公司营销的“遮羞布”时,我们都输了,因为临床试验的结果被封住了——没有发表,也无法获得——业内领军人物的名字被写在了代写的文章上,以及对制药公司资助发展的依赖将社交恐惧症重新命名为社交焦虑症象征着可能发生的事情。找到真正具有突破性的药物,就像找到打开囚禁我们的疾病地牢的钥匙一样。现代制药公司的营销影响力是如此之大,以至于它们可以塑造和塑造钥匙必须适合的锁。营销帕罗西汀治疗社交恐惧症是一种转移注意力的方式,可能会阻碍长期解决方案的发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Have drug companies hyped social anxiety disorder to increase sales. Yes: marketing hinders discovery of long-term solutions.
Social phobia, also called social anxiety disorder, can lead to alcoholism, drug abuse, job loss, and even suicide. It has been relatively unrecognized in the West compared with in the East, where it is seen as the most common neurotic condition.1 GlaxoSmithKline's recent license to promote the use of paroxetine to treat social phobia looks certain to increase the recognition of this potentially serious condition. What could be wrong with this win-win situation? The first problem lies in interpreting what a license means. A license is not a statement by the Food and Drug Administration that paroxetine will be effective for treating social phobia. Licenses legally cannot be denied if a treatment can be shown to do something for a condition, but they are no guarantee that this treatment is worth-while. Although simply increasing the recognition of social phobia may reduce the isolation of sufferers, unless sufferers receive an effective treatment that makes a substantial difference in their lives, the treatment may not be worth the risks. What are the risks? It is clear from studies undertaken by SmithKline in the 1980s that even a brief exposure to paroxetine can lead many takers to become physically dependent.2 Trials have also shown that the use of selective serotonin reuptake inhibitors (SSRIs) can precipitate suicidality in patients and that these agents can cause sexual dysfunction and neurologic disorders.3 Although the SSRIs have been marketed as being freer of side effects than older agents, results on the quality-of-life scales that should reflect this freedom, which have been used in up to 100 clinical trials, have been left unpublished.4 This strongly suggests that SSRIs may be the wrong drugs for many people. All of these hazards could be minimized if SmithKline marketed the hazards of treatment as assiduously as they market the condition. Unlike obsessive-compulsive disorder, which was recently marketed by companies, social phobia is more like depression—a syndrome that may result from a variety of conditions. In some instances, it may be a prodrome for a psychotic disorder. Whereas some patients may get better with the use of paroxetine, it is sobering to realize that the discovery of the first antidepressant agents came about because they made some patients psychotic. In trials of SSRIs to treat depression, a significant proportion of patients not already having psychosis became psychotic. The same can be expected for social phobia. What people with this potentially debilitating condition need is research to understand why this is the case, rather than the marketing of a drug that may be beneficial for a few sufferers but hazardous for an equally large group. Undoubtedly some patients with social phobia will not become suicidal, dependent, or psychotic while taking paroxetine, and their quality of life will not be poor. Even these patients have something to worry about, however. When a condition like social phobia becomes a marketing “fig leaf” for a pharmaceutical company, we all lose because the results of clinical trials get sealed—left unpublished and inaccessible—the names of leading figures in the profession get put on ghost-written articles, and a dependence on pharmaceutical company funding develops.5 The renaming of social phobia as social anxiety disorder is symbolic of what can happen. Finding genuinely breakthrough drugs is a case of finding the right key to unlock the dungeons of illness that imprison us. The marketing clout of modern pharmaceutical companies is such that they can mould and shape the lock in which keys must fit. Marketing paroxetine for social phobia is the kind of diversion likely to inhibit the discovery of long-term solutions.
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