2004
DOI: 10.1007/s00213-003-1685-6
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Fine-tuning risperidone dosage for acutely exacerbated schizophrenia: clinical determinants

Abstract: These findings suggest that dosage adjustment to diminish side effects does not compromise risperidone response and that disorganized patients and perhaps patients with longer illness duration are prone to receive larger doses.

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Cited by 13 publications
(4 citation statements)
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“…After hospital admission, the duration of the placebo lead-in period and the risperidone doses during the trial were also similar among the groups (Table 1). The symptom severity of the patients was similar to that in the clinical trials 25,26 of schizophrenia with acute exacerbation.…”
Section: Resultssupporting
confidence: 74%
See 1 more Smart Citation
“…After hospital admission, the duration of the placebo lead-in period and the risperidone doses during the trial were also similar among the groups (Table 1). The symptom severity of the patients was similar to that in the clinical trials 25,26 of schizophrenia with acute exacerbation.…”
Section: Resultssupporting
confidence: 74%
“…25,26 For acutely exacerbated individuals, the mean end-point dosages in most studies [27][28][29][30][31] were 8 to 12 mg/d; another study 32 used a fixed dose of 6 mg/d. However, in previous studies 25,26 in a similar population we found that the dosing strategy to minimize adverse effects can still yield favorable efficacy. Therefore, we applied the same dosing strategy to obtain the optimal response to risperidone treatment in this study.…”
Section: Study Design and Interventionmentioning
confidence: 99%
“…Risperidone has been known to be effective to 60-80% of acutely exacerbated schizophrenia patients (Lane et al, 2000(Lane et al, , 2004. In this study, 17 patients (17%) showed no change or worsening of symptoms (i.e., they scored 4 or more on the CGI-I) after 4 weeks of risperidone treatment, and these patients were thus categorized as nonresponders.…”
Section: Comparison Between Responders and Nonrespondersmentioning
confidence: 98%
“…According to the consensus guideline for switching from oral antipsychotics to RLAI [13], the original oral risperidone dose was maintained for the first 3 weeks, after which time it was either stopped or tapered off within 3 days because of the time required to achieve therapeutic serum levels of RLAI. The consensus guideline also suggested that 25 mg dose of RLAI is adequate for most patients [13], and the average oral dose of risperidone for schizophrenic patients in Taiwan was less than 4 mg/day [15,19]. Therefore, we defined the dose switching equivalency as 25 mg RLAI for an original risperidone dose less or equal to 4 mg/day, 37.5 mg RLAI for an original risperidone dose of more than 4 and less or equal 6 mg/day, and 50 mg RLAI for an original risperidone dose of more than 6 mg/day.…”
Section: Trial Medicationmentioning
confidence: 99%