青少年住院患者早、早发性精神病的治疗分析。

HCA healthcare journal of medicine Pub Date : 2024-12-01 eCollection Date: 2024-01-01 DOI:10.36518/2689-0216.1637
Acelyne Marie Summerson, Jordan Kalosieh, Sindhura Kompella, Clara Alvarez Villalba, Yukthi Kodali
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引用次数: 0

摘要

背景:美国食品和药物管理局批准了6种非典型抗精神病药物用于儿童精神分裂症的治疗。然而,很少有关于这些药物在青少年精神病急性治疗环境中的有效性的报道。由于早期精神分裂症的临床不确定性和预后不良对儿童的发育有重大影响,因此迫切需要针对这一人群的循证数据。本研究的目的是探讨各种抗精神病药物对入院的急性精神病年轻患者的影响。方法:回顾性分析住院精神科接受抗精神病药物治疗的特定精神分裂症患者的医疗记录。我们通过测量30天再入院率(是/否)、30天内再入院次数和住院时间来分析治疗效率。负二项回归和二元逻辑回归用于计算结果的离散发生并预测该结果的可能性。结果:我们分析了1117例患者的病历,根据患者是否接受阿立哌唑(31.9%)、利培酮(26.0%)、喹硫平(16.2%)和奥氮平(26.0%)进行分组。两组比较显示,与接受阿立哌唑组相比,接受利培酮组的对数天数增加了1.15(1/0.87)的发生率反应比(P < 0.05, 95% CI[0.76, 0.98])。同样,与阿立哌唑相比,喹硫平增加了1.22(1/0.82)的住院天数(P < 0.01, 95% CI[0.70, 0.94]),奥氮平增加了1.23(1/0.82)的住院天数(P < 0.001, 95% CI[0.72, 0.93])。在控制其他变量的情况下,30天入院次数与用药组之间无显著相关性(χ2 = 3.93, P = 0.270)。在控制其他变量后,用药组与再入院的可能性也无显著相关(χ2 = 5.594, P = 0.133)。结论:与奥氮平、喹硫平相比,阿立哌唑与缩短对数天数有显著相关性(χ2 = 21.82, P < 0.0001)。在再入院率方面,没有统计学证据表明用药组之间存在差异。据我们所知,这些结果提供了最大的队列描述不同的抗精神病药物对住院患者急性精神病稳定的疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Treatment Analysis of Very Early and Early Onset Psychosis in the Youth Inpatient Setting.

Background: The United States Food and Drug Administration approved 6 atypical antipsychotics for pediatric treatment of schizophrenia. However, little has been published on the effectiveness of these medications in the acute treatment setting of adolescents with psychosis. Since the clinical uncertainty and poor prognosis proceeding the early onset of schizophrenia has a significant impact on a child's development, there is a critical need for evidence-based data on this population. The aim of our study was to investigate the effect of various antipsychotics on young patients admitted to the inpatient ward presenting with acute psychosis.

Methods: A retrospective analysis was performed to review the medical records of the patients with specified schizophrenia disorders who were admitted to the inpatient psychiatric unit for treatment with antipsychotics. We analyzed the efficiency of treatment by measuring 30-day readmissions (yes/no), number of readmissions in 30 days, and the length of stay in the inpatient ward. Negative binomial regression and binary logistic regression were used to count the discrete occurrences of an outcome and predict the likelihood of that outcome.

Results: We analyzed the medical records of 1117 patients who were assigned to groups based on whether they were treated with aripiprazole (31.9%), risperidone (26.0%), quetiapine (16.2%), and olanzapine (26.0%). Pairwise comparisons revealed receiving risperidone increased the log count of days by an incidence response ratio of 1.15 (1/0.87) compared to receiving aripiprazole (P < .05, 95% CI [0.76, 0.98]). Similarly, quetiapine increased the count of hospital days by a factor of 1.22 (1/0.82) (P < .01, 95% CI [0.70, 0.94]), as well as olanzapine by a factor of 1.23 (1/0.82) compared to receiving aripiprazole (P < .001, 95% CI [0.72, 0.93]). The number of admissions in 30 days was not significantly associated with medication groups (χ2 = 3.93, P = .270) when controlling for other variables. The medication group was also not significantly associated with the likelihood of readmission (χ2 = 5.594, P = .133) when controlling for other variables.

Conclusion: Aripiprazole was significantly associated with shortening the log count of days (χ2 = 21.82, P < .0001) when compared to olanzapine and quetiapine. There was no statistical evidence to conclude a difference in readmission rates when comparing medication groups. To our knowledge, these results provide the largest cohort describing the efficacy of different antipsychotics for acute stabilization of psychosis in the inpatient setting.

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