Department of Psychosis Studies, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.
MRC London Institute of Medical Sciences, Hammersmith Hospital, London, UK.
Acta Psychiatr Scand. 2018 Jan;137(1):39-46. doi: 10.1111/acps.12825. Epub 2017 Oct 26.
Treatment resistance is a challenge for the management of schizophrenia. It is not always clear whether inadequate response is secondary to medication ineffectiveness, as opposed to medication underexposure due to non-adherence or pharmacokinetic factors. We investigated the prevalence of subtherapeutic antipsychotic plasma levels in patients identified as treatment-resistant by their treating clinician.
Between January 2012 and April 2017, antipsychotic plasma levels were measured in 99 individuals provisionally diagnosed with treatment-resistant schizophrenia by their treating clinicians, but not prescribed clozapine. Patients were followed up to determine whether they were subsequently admitted to hospital.
Thirty-five per cent of plasma levels were subtherapeutic, and of these, 34% were undetectable. Black ethnicity (P = 0.006) and lower dose (P < 0.001) were significantly associated with subtherapeutic/undetectable plasma levels. Individuals with subtherapeutic/undetectable levels were significantly more likely to be admitted to hospital (P = 0.02).
A significant proportion of patients considered treatment-resistant have subtherapeutic antipsychotic plasma levels, and this is associated with subsequent admission. The presence of subtherapeutic plasma levels may suggest a need to address adherence or pharmacokinetic factors as opposed to commencing clozapine treatment. While antipsychotic levels are not recommended for the routine adjustment of dosing, they may assist with the assessment of potential treatment resistance in schizophrenia.
治疗抵抗是精神分裂症治疗的一个挑战。对于治疗反应不佳,究竟是药物无效所致,还是由于不遵医嘱或药代动力学因素导致药物暴露不足,并不总是明确的。我们调查了治疗师诊断为治疗抵抗的患者中治疗性抗精神病药血浆水平低的发生率。
2012 年 1 月至 2017 年 4 月,对 99 名由治疗医生初步诊断为治疗抵抗的精神分裂症患者进行了抗精神病药血浆水平检测,但未开具氯氮平。对患者进行随访以确定他们是否随后住院。
35%的血浆水平为治疗性低,其中 34%为未检出。黑种人(P=0.006)和较低剂量(P<0.001)与治疗性/未检出的血浆水平显著相关。治疗性/未检出水平的个体更有可能住院(P=0.02)。
相当一部分被认为是治疗抵抗的患者存在治疗性低的抗精神病药血浆水平,这与随后的住院有关。治疗性血浆水平低可能提示需要解决依从性或药代动力学因素,而不是开始氯氮平治疗。虽然不建议常规调整剂量来监测抗精神病药水平,但它们可能有助于评估精神分裂症潜在的治疗抵抗。