Your browser doesn't support javascript.
loading
Postnatal gestational age estimation using newborn screening blood spots: a proposed validation protocol.
Murphy, Malia S Q; Hawken, Steven; Atkinson, Katherine M; Milburn, Jennifer; Pervin, Jesmin; Gravett, Courtney; Stringer, Jeffrey S A; Rahman, Anisur; Lackritz, Eve; Chakraborty, Pranesh; Wilson, Kumanan.
Affiliation
  • Murphy MSQ; Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Canada.
  • Hawken S; Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Canada.
  • Atkinson KM; Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Canada.
  • Milburn J; Newborn Screening Ontario, Children's Hospital of Eastern Ontario, Ottawa, Canada.
  • Pervin J; Maternal and Child Health Division, International Centre for Diarrhoeal Disease Research, Dhaka, Bangladesh.
  • Gravett C; Global Alliance to Prevent Prematurity and Stillbirth, Seattle, USA.
  • Stringer JSA; Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, USA.
  • Rahman A; Matlab Health Research Centre, International Centre for Diarrhoeal Disease Research, Dhaka, Bangladesh.
  • Lackritz E; Global Alliance to Prevent Prematurity and Stillbirth, Seattle, USA.
  • Chakraborty P; Newborn Screening Ontario, Children's Hospital of Eastern Ontario, Ottawa, Canada.
  • Wilson K; Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Canada.
BMJ Glob Health ; 2(2): e000365, 2017.
Article in En | MEDLINE | ID: mdl-29104765
ABSTRACT

BACKGROUND:

Knowledge of gestational age (GA) is critical for guiding neonatal care and quantifying regional burdens of preterm birth. In settings where access to ultrasound dating is limited, postnatal estimates are frequently used despite the issues of accuracy associated with postnatal approaches. Newborn metabolic profiles are known to vary by severity of preterm birth. Recent work by our group and others has highlighted the accuracy of postnatal GA estimation algorithms derived from routinely collected newborn screening profiles. This protocol outlines the validation of a GA model originally developed in a North American cohort among international newborn cohorts.

METHODS:

Our primary objective is to use blood spot samples collected from infants born in Zambia and Bangladesh to evaluate our algorithm's capacity to correctly classify GA within 1, 2, 3 and 4 weeks. Secondary objectives are to 1) determine the algorithm's accuracy in small-for-gestational-age and large-for-gestational-age infants, 2) determine its ability to correctly discriminate GA of newborns across dichotomous thresholds of preterm birth (≤34 weeks, <37 weeks GA) and 3) compare the relative performance of algorithms derived from newborn screening panels including all available analytes and those restricted to analyte subsets. The study population will consist of infants born to mothers already enrolled in one of two preterm birth cohorts in Lusaka, Zambia, and Matlab, Bangladesh. Dried blood spot samples will be collected and sent for analysis in Ontario, Canada, for model validation.

DISCUSSION:

This study will determine the validity of a GA estimation algorithm across ethnically diverse infant populations and assess population specific variations in newborn metabolic profiles.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies / Screening_studies Language: En Journal: BMJ Glob Health Year: 2017 Document type: Article Affiliation country: Canada

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies / Screening_studies Language: En Journal: BMJ Glob Health Year: 2017 Document type: Article Affiliation country: Canada