International Journal of Neonatology

International Journal of Neonatology

International Journal of Neonatology – Instructions For Author

Open Access & Peer-Reviewed

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Instructions for Authors

Comprehensive guidance for neonatal research manuscript preparation.

Author Guidelines

The International Journal of Neonatology publishes original research advancing care for newborn infants. These guidelines ensure your manuscript meets our standards for scientific rigor, clinical relevance, and ethical compliance.

Manuscript Types
RESEARCH

Original Article

  • Word limit: 4,500 words
  • Abstract: 250 words structured
  • Figures/Tables: Up to 6 total
  • References: 40 maximum
  • Full methods required
BRIEF

Case Report

  • Word limit: 2,000 words
  • Abstract: 150 words
  • Figures/Tables: Up to 3
  • References: 15 maximum
  • Rapid pathway
Manuscript Structure

IMRAD Format: Original research should follow Introduction, Methods, Results, and Discussion structure with clear Conclusions summarizing neonatal care implications.

  • Title Page: Full title, all authors with ORCID, affiliations, corresponding author, word count, funding sources
  • Abstract: Structured with Background, Methods, Results, Conclusions; 5-7 keywords
  • Introduction: Context, knowledge gap, objectives; cite foundational neonatal literature
  • Methods: Detailed protocols, statistical approaches, ethical approvals, CONSORT/STROBE adherence
  • Results: Clear presentation with statistics, gestational age stratification where appropriate
  • Discussion: Interpretation, limitations, clinical implications, future research directions
Neonatal-Specific Requirements

Population Details

Specify gestational age, birth weight, and inclusion/exclusion criteria. Report corrected age for developmental outcomes.

Ethical Approval

IRB approval required. Parental consent must be documented. Report ethics committee protocol numbers.

Outcome Definitions

Use Vermont Oxford Network or other standard definitions for common neonatal outcomes.

Statistical Reporting

Report confidence intervals, effect sizes, and multiple comparison corrections. Power analyses for RCTs.

Figures and Tables
  • Submit figures as separate high-resolution files (300 dpi minimum)
  • Clinical images must have parental consent documented
  • Patient identifiers must be removed from all images
  • Tables should be editable with clear headers and units
  • Supplementary materials for additional data or protocols
Clinical Trial Reporting

RCT Standards

Randomized controlled trials must follow CONSORT guidelines. Submit completed CONSORT checklist with flow diagram showing participant progression.

Observational Studies

Cohort and case-control studies must follow STROBE guidelines. Cross-sectional studies require appropriate adjustments.

Quality Improvement

QI studies should follow SQUIRE 2.0 guidelines. Describe intervention, context, and sustainability considerations.

Systematic Reviews

Follow PRISMA guidelines with registered protocol. Include risk of bias assessment and certainty of evidence grading.

Data Sharing Requirements

IJNE encourages data sharing where ethically and legally permissible. Include data availability statement describing access conditions. For patient data, aggregate or de-identified datasets are acceptable. Register protocols in PROSPERO for systematic reviews.

Authorship Criteria

All authors must meet ICMJE criteria: substantial contributions to conception/design, data acquisition/analysis, manuscript drafting/revision, and final approval. Contributors not meeting criteria should be acknowledged. Corresponding author responsibilities include ensuring all authors meet criteria and managing revisions.

Conflict of Interest

All authors must disclose potential conflicts including financial relationships, consulting arrangements, and industry support. Describe the role of funders in study design, data collection, analysis, and manuscript preparation. Complete ICMJE disclosure forms are required.

Reference Format

Use Vancouver (numbered) citation style. Include DOIs. Cite neonatal-specific guidelines including AAP, Vermont Oxford, and WHO recommendations where relevant.

Trial Registration

Clinical trials must be registered in a recognized registry (ClinicalTrials.gov, ISRCTN, or equivalent) before enrollment begins. Include registration number in abstract.

Ethical Considerations

Research involving neonates requires highest ethical standards. Obtain informed parental consent before study enrollment. Document consent processes clearly in methods. For retrospective studies using medical records, describe institutional review board approval and waiver of consent if applicable. Report any serious adverse events. Follow Declaration of Helsinki principles for all human subjects research.

Image and Media Guidelines

Clinical photographs must have documented parental consent for publication. Remove all identifying information including dates, names, and medical record numbers. Include scale bars where appropriate. Video submissions should be compressed appropriately with clear captions describing content.

Peer Review Process

All submissions undergo rigorous double-blind peer review by 2-3 neonatal medicine experts. Reviewers evaluate scientific validity, methodological rigor, clinical applicability, and potential impact on newborn care. Authors receive detailed feedback within our target 21-day first decision timeline. Revisions typically address methodology clarifications, statistical approaches, or clinical interpretation. We are committed to supportive, constructive feedback that strengthens manuscripts.

Language Requirements

Manuscripts must be written in clear, grammatical English suitable for international readers. Authors whose first language is not English should consider professional language editing services. Use SI units throughout. Define abbreviations at first use including gestational age (GA), birth weight (BW), and other neonatal-specific terms. Spell out numbers below 10 except with units.

Supplementary Materials

Extended data tables, additional figures, video content, and detailed protocols may be submitted as supplementary materials. Supplementary files should be clearly labeled and referenced in the main text. Large datasets should be deposited in appropriate repositories with access information provided.

Submission Process

Submit through ManuscriptZone for full tracking, or use Simple Submission for initial contact. Include cover letter explaining significance. Suggest 3-5 expert neonatal reviewers.

Questions? Contact [email protected] for guidance specific to your research area.

Submit Your Neonatal Research

Advance care for newborns through rigorous science publication and evidence-based research.