Monitoring adverse events of low-dose glucocorticoid therapy: EULAR recommendations for clinical trials and daily practice.

@article{Goes2010MonitoringAE,
  title={Monitoring adverse events of low-dose glucocorticoid therapy: EULAR recommendations for clinical trials and daily practice.},
  author={Marlies C van der Goes and Johannes Wilhelmus Gerardus Jacobs and Maarten Boers and Tanya Andrews and M A M Blom-Bakkers and Frank Buttgereit and Nele Caeyers and Maurizio Cutolo and Jos{\'e} Ant{\'o}nio Pereira da Silva and L{\"o}ic Guillevin and John R Kirwan and Josef Rovensky and Guy Severijns and S Webber and Ren{\'e} Westhovens and Johannes W J Bijlsma Bijlsma},
  journal={Annals of the rheumatic diseases},
  year={2010},
  volume={69 11},
  pages={1913-9}
}
OBJECTIVE To develop recommendations on monitoring for adverse events (AEs) of low-dose glucocorticoid (GC) therapy (≤7.5 mg prednisone or equivalent daily) in clinical trials and daily practice. METHODS Literature was searched for articles containing information on incidence and monitoring of GC-related AEs using PubMed, EMBASE and Cochrane databases. Second, the authors searched for broad accepted guidelines on the monitoring of certain AEs (eg, WHO guidelines on screening for diabetes… CONTINUE READING
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