| Literature DB >> 33040015 |
Rui Yang1, Yao Zhang2, Hua Wang3, Xinfen Xu4,5.
Abstract
INTRODUCTION: Due to immature brain development, preterm infants are more likely to develop neurological developmental defects compared with full-term infants. Most preterm infants without neurodevelopmental damage can eventually reach the same scholastic level as their same-age peers; however, some show persistent impairment. Breast feeding (BF), which is an important public health measure, is of great significance for preterm infants. Various active substances in breast milk promote the development of the brain and central nervous system in premature infants. We present a protocol for a prospective longitudinal cohort study to explore the effect of in-hospital BF on brain development in preterm infants and possible influencing factors. METHODS AND ANALYSIS: This study will enrol 247 Chinese preterm infants (gestational age: 30-34 weeks) delivered in Women's Hospital School of Medicine, Zhejiang University, and transferred to the neonatal intensive care unit. Demographic, clinical and in-hospital BF data will be collected through electronic medical records. Moreover, follow-up data will be obtained by telephone, interview or online. Measurements will be obtained using the Breastfeeding Self-Efficacy Scale-Short Form, neuroimaging with functional near-infrared spectroscopy, extrauterine growth restriction and the Ages and Stages Questionnaire. Follow-up will be performed at 3, 6 and 12 months after birth. ETHICS AND DISSEMINATION: This study has been approved by the Women's Hospital School of Medicine Zhejiang University Medical Ethics Committee (2019-058). The study results are expected to be published in peer-reviewed journals and reported at relevant national and international conferences. TRIAL REGISTRATION NUMBER: ChiCTR1900027648; Pre-results. © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: developmental neurology & neurodisability; neonatal intensive & critical care; nutrition & dietetics
Mesh:
Year: 2020 PMID: 33040015 PMCID: PMC7549488 DOI: 10.1136/bmjopen-2020-038879
Source DB: PubMed Journal: BMJ Open ISSN: 2044-6055 Impact factor: 2.692
Figure 1Study flowchart. ASQ, Ages and Stages Questionnaire; BESE-SF, Breastfeeding Self-Efficacy Scale Short Form; EUGR, extrauterine growth restriction.
Schedule overview of participants
| Measures | Time points | ||||
| t1 | t2 | t3 | t4 | t5 | |
| Enrolment | |||||
| Eligibility screen | X | ||||
| Informed consent | X | ||||
| Data collection | |||||
| Demographic information of preterm infants and mothers | X | ||||
| Daily nutrition intake collection | X | ||||
| Head circumference | X | X | X | X | X |
| fNIRS scan | X | ||||
| EUGR | X | ||||
| ASQ | X | X | X | ||
| Breastfeeding type information collection | X | X | X | ||
| BSES-SF | X | X | X | ||
t1=during hospitalisation, t2=the day of discharge or the day before, t3=3 months after discharge, t4=6 months after discharge and t5=12 months after discharge.
ASQ, ages and stages questionnaire; BESE-SF, breastfeeding self-efficacy scale short form; EUGR, extrauterine growth restriction; fNIRS, functional near-infrared spectroscopy.
Definition of BF type
| Categories | Proportions* | |||
| 100 | 80 | 20 | 0 | |
| Full BF | ||||
| Exclusive BF | = | |||
| Almost exclusive BF† | ≈ | |||
| Partial BF | ||||
| High proportion BF | < | ≥ | ||
| Medium proportion BF | < | ≥ | ||
| Low proportion BF | < | > | ||
| Token BF‡ | ≈ | |||
*Breast milk as a percentage of total infant food intake.
†Infants are also given vitamins, water and juice for no more than one to two times a day and no more than one to two mouthfuls each time in addition to breast milk.
‡Breast milk intake that provides almost no calories.
BF, breast feeding.