Davidson Michael
UniSackler School of Medicine, Tel Aviv, Israel; Nicosia Medical School, Nicosia, Cyprus.
Dialogues Clin Neurosci. 2018 Sep;20(3):215-221. doi: 10.31887/DCNS.2018.20.3/mdavidson.
Several large meta-analyses of maintenance trials have confirmed that patients who suffer from chronic schizophrenia, randomized to placebo, are likely to experience earlier symptomatic worsening than patients randomized to a dopamine (DA)-blocking drug. These findings led expert groups to issue treatment guidelines, which recommend treatment with DA-blocking drugs for periods ranging from several years to indefinitely. The recommendations were accepted by the majority of, but not all, the experts, some of whom proposed a targeted or intermittent therapy approach by which DA-blocking drugs are discontinued upon symptomatic remission, to be renewed in case of symptom re-emergence. The debate between continued and targeted treatment approaches arises from disagreements regarding scientific and ethical questions. Scientifically, the discussion focuses on the quality and interpretation of the supporting or detracting evidence regarding each treatment option. For example, what is the percentage of individuals who can maintain stability off drugs? What is the rate of individuals who exacerbate despite maintenance treatment? What is the percentage of individuals who experience drug-related adverse effects? How can we interpret results of open-label, nonrandomized targeted trials? Regarding ethical questions, the debating sides disagree on how to weigh the impact of the decreased risk for exacerbation versus the certainty of adverse effects on the patients quality of life, and how to reach a patient-therapist shared decision within the constraints of mental illness.
多项针对维持治疗试验的大型荟萃分析证实,患有慢性精神分裂症且被随机分配到安慰剂组的患者,比被随机分配到多巴胺(DA)阻断药物组的患者,更有可能更早出现症状恶化。这些发现促使专家小组发布治疗指南,建议使用DA阻断药物进行数年至无限期的治疗。大多数但并非所有专家都接受了这些建议,其中一些专家提出了一种有针对性的或间歇性的治疗方法,即症状缓解后停用DA阻断药物,症状再次出现时再重新使用。持续治疗方法和有针对性治疗方法之间的争论源于对科学和伦理问题的分歧。在科学方面,讨论集中在关于每种治疗选择的支持或反对证据的质量和解释上。例如,能够在不使用药物的情况下维持病情稳定的个体比例是多少?尽管进行了维持治疗仍病情加重的个体比例是多少?经历药物相关不良反应 的个体比例是多少?我们如何解释开放标签、非随机的有针对性试验的结果?关于伦理问题,争论双方在如何权衡病情加重风险降低的影响与不良反应对患者生活质量的确定性影响,以及如何在精神疾病的限制范围内达成患者与治疗师共同的决定方面存在分歧。