精神分裂症患者的氯丙嗪剂量
Información
- DOI:
- https://doi.org/10.1002/14651858.CD007778.pub2Copiar DOI
- Base de datos:
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- Cochrane Database of Systematic Reviews
- Versión publicada:
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- 13 abril 2017see what's new
- Tipo:
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- Intervention
- Etapa:
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- Review
- Grupo Editorial Cochrane:
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Grupo Cochrane de Esquizofrenia
- Copyright:
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- Copyright © 2017 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
Cifras del artículo
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Autores
Contributions of authors
Katharine Dudley ‐ data re‐extraction, 'Risk of bias' tables, 'Summary of findings' tables, analyses, re‐writing the report (2014, 2016 searches).
Saskia de Haan ‐ development of the protocol, data extraction, analyses, writing the report (2009 search).
Xiaomeng Liu ‐ development of the protocol, data extraction, analyses, writing the report (2009 search).
Sources of support
Internal sources
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University of Nottingham, UK.
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Utrecht University, Netherlands.
External sources
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No sources of support supplied
Declarations of interest
None known.
Acknowledgements
We would like to thank the staff at the Cochrane Schizophrenia Group for their help and assistance, in particular Hirsto Girgorov for translating a Russian paper, Jun Xia for her help with Chinese papers and Farhad Shokraneh the Information Scientist. Special thanks to Professor Clive Adams for his guidance and support. We have used the generic text supplied by the Cochrane Schizophrenia Group for the Methods section and adapted it to our needs.
We would like to thank Lorna Lawrence for peer reviewing this review.
Version history
Published | Title | Stage | Authors | Version |
2017 Apr 13 | Chlorpromazine dose for people with schizophrenia | Review | Katharine Dudley, Xiaomeng Liu, Saskia De Haan | |
2009 Apr 15 | Chlorpromazine dose for people with schizophrenia | Review | Xiaomeng Liu, Saskia De Haan | |
Differences between protocol and review
For the 2014 update, we included data from Wode‐Helgodt 1978 for extrapyramidal adverse effects that had been reported using a modification of a previously published scale (Simpson 1970). We realise that this is not entirely in keeping with our previous methods where we stated that we should not use any modified scales ‐ citing Marshall 2000. However, we felt these outcomes to be important although they must carry high risk of bias.
We have moved the outcome of leaving the study early to below global and mental state, moved 'death' to adverse effects.