Hynes Caroline, McWilliams Stephen, Clarke Mark, Fitzgerald Ita, Feeney Larkin, Taylor Mark, Boland Fiona, Keating Dolores
Saint John of God Hospitaller Services, Stillorgan, Dublin, DL1 1RW, Ireland.
Saint John of God Hospitaller Services, Dublin, Ireland.
Ther Adv Psychopharmacol. 2020 Sep 25;10:2045125320957119. doi: 10.1177/2045125320957119. eCollection 2020.
Antipsychotics are associated with a range of side-effects that can influence patients' subjective well-being negatively resulting in poor adherence. In order to limit the negative consequences of side-effects, they should be regularly systematically assessed. The aim of this study was to systematically assess antipsychotic side-effects in an inpatient cohort using validated rating scales.
Eligible individuals prescribed an antipsychotic for at least 2 weeks were invited to have their side-effects assessed systematically.
A total of 208 individuals were assessed systematically for antipsychotic side-effects; 71.5% ( = 138) stated that they had not reported side-effects to their clinician prior to the assessment. The most commonly reported side-effects were daytime drowsiness (75%), dry mouth (58.2%) and weight gain (50.0%), while the most distressing side-effects reported were erectile dysfunction (35.0%), sexual dysfunction (26.3%) and amenorrhoea (26.3%). There was no evidence of an association between side-effect severity/number of side-effects reported/distress caused by those taking high dose/combination antipsychotics standard dose monotherapy.
Side-effects must be regularly and systematically assessed using a validated rating scale. As distress caused by side-effects plays a major role in non-adherence, assessment should examine distress and data on distressing side-effects should be available to those choosing an antipsychotic. Given the lack of correlation between high dose/combination antipsychotics and side-effects, treatment should be tailored to the individual based on response/tolerance and dose reduction/avoidance of polypharmacy should not be recommended to minimise side-effects.
抗精神病药物会引发一系列副作用,这些副作用会对患者的主观幸福感产生负面影响,进而导致依从性差。为了限制副作用的负面影响,应对其进行定期系统评估。本研究的目的是使用经过验证的评定量表对住院患者队列中的抗精神病药物副作用进行系统评估。
邀请至少服用抗精神病药物2周的符合条件的个体进行副作用系统评估。
共对208名个体进行了抗精神病药物副作用的系统评估;71.5%(n = 138)表示在评估前未向临床医生报告过副作用。最常报告的副作用是日间嗜睡(75%)、口干(58.2%)和体重增加(50.0%),而报告的最困扰的副作用是勃起功能障碍(35.0%)、性功能障碍(26.3%)和闭经(26.3%)。没有证据表明服用高剂量/联合抗精神病药物与标准剂量单一疗法的副作用严重程度/报告的副作用数量/所引起的困扰之间存在关联。
必须使用经过验证的评定量表定期系统地评估副作用。由于副作用引起的困扰在不依从性中起主要作用,评估应检查困扰情况,并且选择抗精神病药物的人员应可获得有关困扰性副作用的数据。鉴于高剂量/联合抗精神病药物与副作用之间缺乏相关性,应根据个体反应/耐受性进行个体化治疗,并且不建议为尽量减少副作用而减少剂量/避免联合用药。