NAIT Registry

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The Neonatal Alloimmune Thrombocytopenia (NAIT) Registry was established in December 2008 at the Department of Epidemiology and Preventive Medicine. The purpose of this registry is to better define the incidence, natural history and clinical outcomes of NAIT nationally. Establishment of a register will provide valuable observational data on the range of therapeutic strategies being employed in the treatment of NAIT patients. This data will be of substantial value in the development in exploring factors influencing clinical outcomes with the goal to be able to better define the optimal management of NAIT patients. The registry will inform and inspire future research, and coordinate future national research.

Steering Committee

• Dr Helen Savoia (Chair), Royal Children's Hospital
• Dr Stephen Cole, Royal Women's Hospital
• Dr Rhonda Holdsworth, Australian Red Cross Blood Service
• Dr Louise Phillips, Monash University
• Dr Zoe McQuilten, Australian Red Cross Blood Service
• Dr Shelley Rowlands, Royal Women's Hospital
• Dr Ben Saxon, Women's and Children's Hospital
• Dr Bronwyn Williams, Royal Brisbane and Women's Hospital
• Dr Erica Wood, Australian Red Cross Blood Service
  
  

Web Data Entry

Data Dictionary

Database User Manual

Enrolling your hospital

Contact Details

Miss Nikita Schembri
Research Assistant

Dr Louise Phillips
Research Manager

NAIT Registry
Department of Epidemiology and Preventative Medicine
Monash University

Ph: +61 3 9903 0551
Fax: +61 3 9903 0576