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Comparative study of the effectiveness of zuclopenthixol acetate and haloperidol in acutely disturbed psychotic patients.
Author: KuasirikulSurachai, TaymeeyapraditUnchulee
Original Abstract of the Article :
OBJECTIVES: To study the effectiveness, frequency of administration and side effects of zuclopenthixol acetate (ZPTA) and haloperidol (HAL) in the treatment of acute psychotic disturbance with aggression. METHOD: Purposive sampling method was employed in a group of psychotic patients with aggressio...See full text at original site
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引用元:
https://pubmed.ncbi.nlm.nih.gov/12678168
データ提供:米国国立医学図書館(NLM)
Zuclopenthixol Acetate vs. Haloperidol: Navigating the Desert of Psychosis
Psychosis is a complex mental health condition that can lead to significant distress and impairment. This research compares the effectiveness of two antipsychotic medications, zuclopenthixol acetate (ZPTA) and haloperidol (HAL), in managing acute psychotic disturbance with aggression. It's like comparing two different desert routes, searching for the most effective path to relief.
Finding the Right Path to Relief
The study found that both ZPTA and HAL were effective in reducing symptoms of psychosis and aggression, but ZPTA required less frequent administration. It's like discovering a shortcut through a desert, reaching the desired destination with less effort. This finding may be beneficial for patients who prefer less frequent medication administration.
Managing Psychosis with Targeted Therapies
This research highlights the importance of personalized treatment approaches for psychosis. It's a reminder that the desert of mental health is vast and diverse, requiring careful consideration of each individual's needs and preferences.
Dr.Camel's Conclusion
This research contributes to our understanding of the effectiveness of different antipsychotic medications in managing psychosis. By exploring alternative treatment options and considering individual needs, we can create a more personalized and effective approach to navigating the desert of mental illness.
Date :
- Date Completed 2003-04-25
- Date Revised 2013-11-21
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English
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