A systematic mapping review identifying key features of restraint research in inpatient pediatric psychiatry: A human

Elvira Pértega1, Christopher Holmberg2

  • 1Faculty of Law, University of Technology Sydney, Sydney, Australia; Child and Adolescens Mental Health Department, Hospital Lucus augusti, Lugo, Spain.

Insights

Research on pediatric restraints is increasing but lacks consistency, hindering understanding and human rights alignment. Studies often omit contextual factors and stakeholder perspectives, failing to fully incorporate the Convention on the Rights of the Child and the Convention on the Rights of Persons with Disabilities.

Area of Science:

  • Child and Adolescent Psychiatry
  • Human Rights Law
  • Health Services Research

Background:

  • Restraints in pediatric psychiatry are highly regulated yet contentious, with significant negative impacts on children.
  • International human rights standards (CRC, CRPD) promote reducing restraint use, but inconsistent definitions and quality indicators impede progress.

Approach:

  • A systematic mapping review adhering to PRISMA guidelines was conducted.
  • Six databases were searched for empirical studies and literature reviews on pediatric restraints in inpatient psychiatric settings.
  • The review adopted a descriptive-configurative approach to identify research gaps and trends.

Key Points:

  • 114 publications were analyzed, predominantly quantitative studies (76%) using institutional records.
  • Research often lacks contextual details, adequate stakeholder representation (patients, families, professionals), and consistent terminology.
  • Studies primarily focus on intrinsic child factors, neglecting contextual elements and human rights considerations, with limited exploration of legal/ethical aspects.

Conclusions:

  • Increasing research on pediatric restraints is hampered by inconsistent reporting, obscuring meaning and frequency.
  • Inadequate inclusion of environmental, facility, and family factors suggests poor alignment with the CRPD.
  • The scarcity of qualitative studies and focus on patient-only factors indicates the social model of disability has not fully influenced research, neglecting child/adolescent perspectives and CRC principles.
Abstract