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Rianne Oostenbrink (ErasmusMC-Sophia Rotterdam, REPEM), Luis Garcia-Castrillo Riesgo (EUSEM), Michael Rigby (Imperial College London, MOCCHA), Frederik Ehler
(HUG), Lembit Pirn ( Health and Welfare Information Systems Center, Estonia), Catherine Chronaki (HL7 Foundation)
.
Towards integrated pediatric care; solutions, effectiveness and safety considerations
AIM
to study if the International Patient
Summary (IPS) standard comprising
a minimal and non-exhaustive
specialty-agnostic, condition-
independent, but clinically-relevant
collection of clinical and contextual
information, can be used to integrate
health data for children
Methods
We described pathways identifying
main components or care covering
preventive, family, supportive, and
acute care. Data were retrieved from
large collaborative studies and
guidelines.
Conclusions
IPS could link health data at
transition points for prompt feedback.
Needs
rules on what data to use and how to
present them across the pathway
to empower patients to access and
amend IPS data
Results
Electronic health record (EHRs) exist
at focal points but lack information
transfer. Resources are accessible to
health policy makers or researchers
mostly. Data are influenced by
variability of health care structures.
International
Patient Summary
(IPS)

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Towards integrated pediatric care; solutions, effectiveness and safety considerations

  • 1. Rianne Oostenbrink (ErasmusMC-Sophia Rotterdam, REPEM), Luis Garcia-Castrillo Riesgo (EUSEM), Michael Rigby (Imperial College London, MOCCHA), Frederik Ehler (HUG), Lembit Pirn ( Health and Welfare Information Systems Center, Estonia), Catherine Chronaki (HL7 Foundation) . Towards integrated pediatric care; solutions, effectiveness and safety considerations AIM to study if the International Patient Summary (IPS) standard comprising a minimal and non-exhaustive specialty-agnostic, condition- independent, but clinically-relevant collection of clinical and contextual information, can be used to integrate health data for children Methods We described pathways identifying main components or care covering preventive, family, supportive, and acute care. Data were retrieved from large collaborative studies and guidelines. Conclusions IPS could link health data at transition points for prompt feedback. Needs rules on what data to use and how to present them across the pathway to empower patients to access and amend IPS data Results Electronic health record (EHRs) exist at focal points but lack information transfer. Resources are accessible to health policy makers or researchers mostly. Data are influenced by variability of health care structures. International Patient Summary (IPS)