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Long-Acting Injectable Second-Generation Antipsychotics Improve Negative Symptoms and Suicidal Ideation in Recent Diagnosed Schizophrenia Patients: A 1-Year Follow-up Pilot Study
被引:19
|作者:
Corigliano, Valentina
[1
]
Comparelli, Anna
[1
]
Mancinelli, Iginia
[1
]
Montalbani, Benedetta
[1
]
Lamis, Dorian A.
[2
]
De Carolis, Antonella
[3
]
Erbuto, Denise
[1
]
Girardi, Paolo
[1
]
Pompili, Maurizio
[1
]
机构:
[1] Sapienza Univ Rome, Unit Psychiat, Dept Neurosci, Sch Med & Psychol, Via Grottarossa 1035-39, I-00198 Rome, Italy
[2] Grady Hosp, Emory Sch Med, Dept Psychiat & Behav Sci, Atlanta, GA USA
[3] Sapienza Univ Rome, Sch Med & Psychol, Unit Neurol, Dept Neurosci, Via Grottarossa 1035-39, I-00198 Rome, Italy
关键词:
D O I:
10.1155/2018/4834135
中图分类号:
R749 [精神病学];
学科分类号:
100205 ;
摘要:
Long-acting injectable second-generation antipsychotics (LAI-SGA) are typically used to maintain treatment adherence in patients with chronic schizophrenia. Recent research suggests that they may also provide an effective treatment strategy for patients with early-phase disease. The aim of this study is to evaluate clinical and psychosocial outcomes among recent and long-term diagnosed schizophrenia outpatients treated with LAI-SGA during a follow-up period of 12 months. Stable schizophrenia patients receiving LAI-SGA with 5 or less years of illness duration (n = 10) were compared to those with more than 5 years of illness duration (n = 15). Clinical data was assessed through the Positive and Negative Syndrome Scale (PANSS), the Global Assessment of Functioning (GAF), the Columbia Suicide Severity Rating Scale (C-SSRS), the Recovery Style Questionnaire (RSQ), and the Mayer-Salovey-Caruso Emotional Intelligence Test (MSCEIT) Managing Emotion branch. Recently diagnosed patients showed greater improvement versus patients diagnosed for more than 5 years in adjusted mean GAF score, in PANSS factor score for negative and depressive symptoms, and in severity and intensity of suicidal ideation. Our preliminary findings support the hypothesis that LAI-SGA may influence the course of the illness if administered at the early phase of the illness. However, replicate studies are needed, possibly with larger samples.
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