Standardization of Research-Quality Anthropometric Measurement of Infants and Implementation in a Multicenter Study

Christine Coburn-Miller1, Susan Casey2, Quynh Luong3

  • 1Women and Children's Hospital of Buffalo, Buffalo, New York, USA.

Insights

Accurate infant growth measurements are crucial for cystic fibrosis (CF) research. Standardized methods ensure reliable data for understanding CF

Area of Science:

  • Pediatric Nutrition
  • Cystic Fibrosis Research
  • Anthropometry

Background:

  • Malnutrition is an early clinical sign in cystic fibrosis (CF).
  • Poor nutrition in infancy correlates with adverse pulmonary, cognitive, and survival outcomes.
  • Infant growth metrics are vital for clinical research in pediatric CF populations.

Purpose of the Study:

  • To standardize anthropometric measurement techniques for infants with CF.
  • To implement research-quality growth assessments in a multicenter trial.
  • To establish reliable growth data for early intervention and research in CF.

Main Methods:

  • Development of standardized protocols for anthropometric measurements.
  • Training of research personnel across multiple study sites.
  • Implementation of these methods within the Baby Observational Nutrition Study (BONuS) trial.

Main Results:

  • Established standardized, research-quality anthropometric measurement protocols.
  • Successfully implemented these methods in a multicenter infant CF study.
  • Generated reliable growth data for the studied infant population.

Conclusions:

  • Standardized anthropometry is feasible and essential for CF infant research.
  • Accurate growth monitoring provides a responsive measure for clinical studies.
  • This methodology supports better understanding and management of pediatric CF.

Related Concept Videos