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Clinical relevance of paliperidone palmitate 3-monthly in treating schizophrenia.
Mathews, Maju; Gopal, Srihari; Nuamah, Isaac; Hargarter, Ludger; Savitz, Adam J; Kim, Edward; Tan, Wilson; Soares, Bernardo; Correll, Christoph U.
Afiliação
  • Mathews M; Department of Neuroscience, Janssen Research & Development, LLC, Raritan, NJ, USA.
  • Gopal S; Department of Neuroscience, Janssen Research & Development, LLC, Raritan, NJ, USA.
  • Nuamah I; Department of Neuroscience, Janssen Research & Development, LLC, Raritan, NJ, USA.
  • Hargarter L; Department of Neuroscience, Janssen-Cilag EMEA, Neuss, Deutschland.
  • Savitz AJ; Department of Neuroscience, Janssen Research & Development, LLC, Raritan, NJ, USA.
  • Kim E; Janssen Scientific Affairs, LLC, Hopewell, NJ, USA.
  • Tan W; Regional Medical Affairs, Janssen Pharmaceutical Companies of Johnson and Johnson, Singapore.
  • Soares B; Neuroscience Medical Affairs, Janssen-Cilag, High Wycombe, Buckinghamshire, UK.
  • Correll CU; The Zucker Hillside Hospital, Psychiatry Research, Glen Oaks, NY, USA.
Neuropsychiatr Dis Treat ; 15: 1365-1379, 2019.
Article em En | MEDLINE | ID: mdl-31190840
ABSTRACT
Antipsychotics are the mainstay in schizophrenia management, and long-acting injectable (LAI) antipsychotics contribute to the successful maintenance of treatment by improving non-adherence and preventing relapses. Paliperidone palmitate 3-monthly (PP3M) formulation is the only available LAI antipsychotic that offers an extended 3-month window of stable plasma drug concentration, enabling only four injections per year. This paper summarizes clinically relevant endpoints from available evidence for PP3M to bridge translational research gaps and provide measurable outcomes that can be interpreted in clinical practice. Low number-needed-to-treat (NNT) for relapse prevention (NNT [95% CI] 6-month estimate 4.8 [3.2; 10.0]; 12-month estimate 3.4 [2.2; 7.0]), and high number-needed-to-harm (NNH [95% CI] akathisia, 27.1 [12.3; -667.1]; tremor, 80.0 [22.5; 67.3]; dyskinesia, -132.6 [44.5; -23.2]; parkinsonism, 160.0 [28.9; -49.8]) quantify the relative benefits and low propensity for adverse events with PP3M. Symptom remission and reductions in positive and negative symptoms indicate treatment stability. Additionally, meaningful functional remission, reduced dosing frequency, and freedom from daily negotiations favorably impact patient preference and attenuate burdensome aspects of caregiving, representing important healthcare determinants that enhance prospects of treatment continuity in schizophrenia. This information can potentially improve clinicians' judgment of treatment choices, clinical response, and patient selection in routine care. Taken together, PP3M is a valuable antipsychotic treatment option, meriting consideration for a broader role in the long-term management of schizophrenia; its utility should not be limited to patients with poor adherence or when oral antipsychotics have failed.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Neuropsychiatr Dis Treat Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Neuropsychiatr Dis Treat Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos