Research

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BPSU - International activities

The BPSU is a founding member of the International Network of Paediatric Surveillance Units (INoPSU). INoPSU's mission is the advancement of knowledge of uncommon childhood infections and disorders and the participation of paediatricians in surveillance on a national and international basis.

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BPSU - Patient and public involvement

The BPSU is committed to ensuring that patient and public involvement (PPI) is embedded in its work in every way possible. The unit works with investigators to encourage and support public and patient involvement in their research. The information provided here is designed to support, not replac...

BPSU

Conditions

Rare disease

Engaging children and young people

Children and young people's voice

Patient information

Patient involvement

Research

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BPSU - Research using health records

BPSU studies collect information about rare conditions. It is important not to miss counting or collecting information about children with such conditions.

BPSU

Research

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BPSU Sir Peter Tizard research bursary

Each year we invite trainee paediatricians and newly qualified consultants planning a surveillance study through the British Paediatric Surveillance Unit (BPSU) to apply for this bursary. The successful applicant receives a free slot on the BPSU Orange Card and a stipend towards their training needs...

BPSU

Rare disease

Fellowships, awards and prizes

Research

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UK Child Health Research Collaboration

The UKCHRC is a growing partnership among funders of child health research. Through increasing and strengthening research, it aims to advance paediatric research and improve the health and wellbeing of children.

Research

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BPSU impact - case studies

The BPSU has facilitated research into over 100 rare conditions. In many instances, the findings have had an immense influence over decisions relating to the condition and patient. Read case studies on the impact of BPSU's research below.

BPSU

Rare disease

Research

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Patient Reported Experience Measure (PREM) for urgent and emergency care

These tools measure the experience of patients aged 0-16 years, or their parents, in urgent and emergency care (U&EC) settings. You can download surveys for ambulance services, GPs and emergency departments/walk-in centres. Our research report explains how they were developed, and we also have guida...

Ambulance services

Primary care

Children and young people's voice

Quality improvement

Research

Document

Research Charter - case studies

We asked healthcare professionals, researchers and patient public involvement leads how they use the Charter in their work settings. Here we bring together case studies on how the Charter has been used to raise awareness of the importance of child health research.

Patient involvement

Research

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Understanding parents' information needs and experiences about non-accidental injury - research report

The responsibilities of paediatricians in relation to the recognition of child abuse place them in difficult diagnostic situations which require a sensitive approach. This research set out to explore parents' experiences of situations where concerns of non-accidental injury (NAI) were raised, with a...

Research

Safeguarding

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Training in research for the benefit of children - guide

All trainees have to attain research competencies. And, trainees who train in research are afforded unique opportunities to develop academic skills and undertake original research and, for some, develop an academic career. All of this can be achieved while maintaining and excelling in clinical train...

Research