Kane J M, Aguglia E, Altamura A C, Ayuso Gutierrez J L, Brunello N, Fleischhacker W W, Gaebel W, Gerlach J, Guelfi J D, Kissling W, Lapierre Y D, Lindström E, Mendlewicz J, Racagni G, Carulla L S, Schooler N R
Department of Psychiatry, Hillside Hospital, Division of Long Island Jewish Medical Center, Glen Oaks, NY 11004, USA.
Eur Neuropsychopharmacol. 1998 Feb;8(1):55-66. doi: 10.1016/s0924-977x(97)00045-x.
These guidelines for depot antipsychotic treatment in schizophrenia were developed during a two-day consensus conference held on July 29 and 30, 1995 in Siena, Italy. Depot antipsychotic medications were developed in the 1960s as an attempt to improve the long-term treatment of schizophrenia (and potentially other disorders benefiting from long-term antipsychotic medication). Depot drugs as distinguishable from shorter acting intramuscularly administered agents can provide a therapeutic concentration of at least a seven day duration in one parenteral dose. The prevention of relapse in schizophrenia remains an enormous public health challenge worldwide and improvements in this area can have tremendous impact on morbidity, mortality and quality of life, as well as direct and indirect health care costs. Though there has been debate as to what extent depot (long-acting injectable) antipsychotics are associated with significantly fewer relapses and rehospitalizations, in our view when all of the data from individual trials and metaanalyses are taken together, the findings are extremely compelling in favor of depot drugs. However in many countries throughout the world fewer than 20% of individuals with schizophrenia receive these medications. The major advantage of depot antipsychotics over oral medication is facilitation of compliance in medication taking. Non-compliance is very common among patients with schizophrenia and is a frequent cause of relapse. In terms of adverse effects, there are not convincing data that depot drugs are associated with a significantly higher incidence of adverse effects than oral drugs. Therefore in our opinion any patient for whom long-term antipsychotic treatment is indicated should be considered for depot drugs. In choosing which drug the clinician should consider previous experience, personal patient preference, patients history of response (both therapeutic and adverse effects) and pharmacokinetic properties. In conclusion the use of depot antipsychotics has important advantages in facilitating relapse prevention. Certainly pharmacotherapy must be combined with other treatment modalities as needed, but the consistent administration of the former is often what enables the latter.
这些精神分裂症长效抗精神病药物治疗指南是在1995年7月29日至30日于意大利锡耶纳举行的为期两天的共识会议期间制定的。长效抗精神病药物于20世纪60年代研发出来,旨在改善精神分裂症的长期治疗(以及可能受益于长期抗精神病药物治疗的其他疾病)。与作用时间较短的肌肉注射药物不同,长效药物一次注射剂量可提供至少持续七天的治疗浓度。在全球范围内,预防精神分裂症复发仍然是一项巨大的公共卫生挑战,该领域的改善对发病率、死亡率和生活质量以及直接和间接医疗保健成本都可能产生巨大影响。尽管对于长效(长效注射)抗精神病药物在多大程度上与显著减少复发和再住院相关存在争议,但我们认为,综合各个试验和荟萃分析的所有数据来看,结果非常有力地支持长效药物。然而,在世界上许多国家,接受这些药物治疗的精神分裂症患者不到20%。长效抗精神病药物相对于口服药物的主要优势在于便于服药依从性。不依从在精神分裂症患者中非常普遍,且是复发的常见原因。在不良反应方面,没有令人信服的数据表明长效药物的不良反应发生率比口服药物显著更高。因此,我们认为,任何需要长期抗精神病治疗的患者都应考虑使用长效药物。在选择药物时,临床医生应考虑既往经验、患者个人偏好、患者的反应史(包括治疗反应和不良反应)以及药代动力学特性。总之,使用长效抗精神病药物在促进预防复发方面具有重要优势。当然,药物治疗必须根据需要与其他治疗方式相结合,但前者的持续给药往往是后者得以实现的条件。