Inyección de glucocorticoides guiada por imágenes o a ciegas para el dolor del hombro
Información
- DOI:
- https://doi.org/10.1002/14651858.CD009147.pub2Copiar DOI
- Base de datos:
-
- Cochrane Database of Systematic Reviews
- Versión publicada:
-
- 15 agosto 2012see what's new
- Tipo:
-
- Intervention
- Etapa:
-
- Review
- Grupo Editorial Cochrane:
-
Grupo Cochrane de Salud musculoesquelética
- Copyright:
-
- Copyright © 2012 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
Cifras del artículo
Altmetric:
Citado por:
Autores
Contributions of authors
All authors contributed to the writing of the review.
Sources of support
Internal sources
-
Department of Epidemiology and Preventive Medicine, School of Public Health and Preventive Medicine, Monash University, Australia.
In kind support
-
Cabrini Institute, Cabrini Hospital, Malvern, Victoria, Australia.
In kind support
External sources
-
No sources of support supplied
Declarations of interest
None known.
Acknowledgements
We would like to thank Louise Falzon, Search Specialist for the Cochrane Musculoskeletal Group, for designing the search strategy, and performing the search. We would like to thank Dr Juliana Roos who contributed to the drafting of the protocol. We would also like to thank Drs Ekeberg and Naredo who responded to our requests for further details with additional information about their trials.
Version history
| Published | Title | Stage | Authors | Version |
| 2021 Aug 26 | Image‐guided glucocorticoid injection versus injection without image guidance for shoulder pain | Review | Joshua Zadro, Adam Rischin, Renea V Johnston, Rachelle Buchbinder | |
| 2012 Aug 15 | Image‐guided versus blind glucocorticoid injection for shoulder pain | Review | Jason E Bloom, Adam Rischin, Renea V Johnston, Rachelle Buchbinder | |
| 2011 May 11 | Image‐guided versus blind corticosteroid injection for shoulder pain | Protocol | Juliana F Roos, Renea V Johnston, Rachelle Buchbinder | |
Differences between protocol and review
We have clarified that included trials could include comparators of anatomic landmark guided injection or intramuscular injection.
We planned a sub‐group analysis based on three time points (≤ 6 weeks; >6 weeks to 6 months; > 6 months), but included studies only measured outcomes to 6 weeks. For the purpose of pooling data we combined 1‐2 weeks in one analysis and 6 weeks in another analysis.
We also planned to perform sensitivity analysis to investigate the effect of imputation of missing data (e.g., imputation of standard deviation) if data were available but this was not performed.
