Title: Dimitrios G. Katehakis
1Nordic Workshop Copenhagen, March 13, 2003
The Shared Record Service Web-access to patient
data from different record systems
- Dimitrios G. Katehakis
- Senior Telecommunications Engineer
- Center of Medical Informatics and Health
Telematics Applications
2Institute of Computer Science
- one of the largest research centers of Greece
- distributed national research center (seven
institutes)
FOR MORE INFO...
3CMI/ HTA
Innovative RD and its application in the domain
of medical informatics and health telematics
CRETE Health Telematics Center
HEALTHNET
I.H.I.S.
4What is the EHR?
- an electronic longitudinal collection of personal
health information usually based on the
individual, entered or accepted by health care
providers, which can be distributed over a number
of sites or aggregated at a particular source.
The information is organised primarily to support
continuing, efficient and quality health care.
The record is under the control of the consumer
and is stored and secured securely. (HINA) - a longitudinal collection of personal health
information of a single individual, entered or
accepted by health care providers, and stored
electronically. The record may be made available
at any time to providers, who have been
authorized by the individual, as a tool in the
provision of health care services. The individual
has access to the record and can request changes
to its contents. The transmission and storage of
the record is under strict security. (OHIH) - a collection of data and information gathered or
generated to record clinical care rendered to an
individual. (ASTM) - a healthcare record in computer readable format
(CEN)
- a comprehensive, structured set of clinical,
demographic, environmental, social, and financial
data and information in electronic form,
documenting the health care given to a single
individual. (ASTM) - an electronic patient record that resides in a
system designed to support users through
availability of complete and accurate data,
practitioner reminders and alerts, clinical
decision support systems, links to bodies of
medical knowledge, and other aids. (IOM) - a virtual compilation of non-redundant health
data about a person across a lifetime, including
facts, observations, interpretations, plans,
actions, and outcomes. Health data include
information on allergies, history of illness and
injury, functional status, diagnostic studies,
assessments, orders, consultation reports,
treatment records, etc. Health data also include
wellness data such as immunization history,
behavioral data, environmental information,
demographics, administrative data for care
delivery processes, health insurance, and legal
data such as consents. (CPRI)
ISO/ TC 215 Ad Hoc Group Report, Standards
Requirements for the Electronic Health Record
Discharge/ Referral Plans, Final Report, July 26,
2002.
5The Shared Records Service
- An IT Service for professionals or citizens who
need a uniform way to access parts of patient
record data that are physically located in
different clinical information systems. - Provides fast, secure and authorized access to
distributed patient record information from
multiple disparate sources.
- This service should not be confused with
- Autonomous Clinical Information Systems (CIS)
- Message based communication of EHR data
- Centralized Clinical Data Repositories (CDR), or
- Monolithic information systems that have embedded
in their structure mechanisms for accessing
directly host systems.
6The Concept in Space
Medical Encounter
Health Record Segment
Fast Virtual Link
Slow Virtual Link
Temporarily Available Virtual Link
7The Concept in Time
8Shared Records Why?
- Vital health information available and accessible
24 hours a day, seven days a week. - Healthcare practitioners better positioned to
offer more effective and efficient treatment, and
could spend more quality time with the patient. - Access to information on previous medical or lab
tests would reduce the number of redundant
procedures and result in greater cost savings. - Empowered individuals make informed choices about
options available to them and exercise greater
control over their own health. - Improved quality of care, based on an enhanced
ability of health planners and administrators to
develop relevant healthcare policies for the
future.
- Medical errors are of growing concern
- Approximately 100,000 Americans die each year
from preventable errors in hospitals1 - More than combined number of deaths from breast
cancer, AIDS motor vehicles2
1 J. Corrigan, et al (Eds) To Err is Human
Building a safer health system, Committee on
Quality of Healthcare in America, Washington,
Institute of Medicine, 1999 2 Reducing medical
errors and improving patient safety The National
Coalition of Healthcare and the Institute for
Healthcare Improvements, Feb. 2000
9Current International Efforts
- EU Projects
- GEHR
- Synapses
- InterCare
- SynEx
- Open Source Software
- OpenEMed
- Los Alamos, NM, USA
- Australia Initiatives
- GEHR
- OpenEHR
- Standards
- CEN/ TC 251
- WGI, Information Models
- WGIV, Technology for Interoperability
- ISO TC 215
- WG1, Health Records and Modeling Coordination
- ASTM
- E31, Health Informatics
- HL7
- CDA, RIM
- OMG
- Healthcare DTF
10in the US
- along with the Health Insurance Portability and
Accountability Act of 1996 (HIPAA) financial and
administrative transaction standards, a
comprehensive set of Patient Medical Record
Information (PMRI) standards can move the Nation
closer to a healthcare environment where
clinically specific data can be captured once at
the point of care with derivatives of this data
available for meeting the needs of payers,
healthcare administrators, clinical research, and
public health. This environment could
significantly reduce the administrative and data
capture burden on clinicians dramatically
shorten the time for clinical data to be
available for public health emergencies and for
traditional health purposes profoundly reduce
the cost for communicating, duplicating and
processing healthcare information and, last but
not least, greatly improve the quality of care
and safety for all patients
Report and Recommendations From the National
Committee on Vital and Health Statistics
Information for Health, Report and
Recommendations from the National Committee on
Vital and Health Statistics, U.S. Department of
Health and Human Services, Washington, D.C.,
November 15, 2001
11Standards for the EHR
ISO/ TC 215 Ad Hoc Group Report, Standards
Requirements for the Electronic Health Record
Discharge/ Referral Plans, Final Report, July 26,
2002.
12Inter-enterprise Integration
Collaboration (consultation, telemedicine)
Integrating patient data (i-EHR)
Patient validation
Messaging
PICNIC services
SRS
COLS
CDA
PIDS
...
interfaces based on World Wide Web Consortium
standards
13The Unified Process
14Enabling Components
- Clinical Observations Access Service
- Collaboration Service
- Message Broker
- Patient Identification Service
- Resource Service
- Shared Records Indexing Service
- Shared Records Update Broker
- Terminology Service
- User Profile Service
15Security Services
- Access Control
- Auditing
- Certification
- Client Authentication
- Client Impersonation and Delegation
- Consent Management
- Cryptography
- Smart Cards
16Component Orchestration
PIDS
CIS
COAS
GUI
4
Generic Components
3
1
AUDS
2
CIS
COAS
UB
AUTS
ENCS
RESS
IS
Access to Patient Data
TERS
UPS
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20Sequence diagram
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24Federated Approach
Federated Schema Or Schemata
- Reference Model
- Contains generic data structures (RIM, CEN 13606)
Mapping
Mapping
schema integration/ translation effort depends on
the richness of the federated model
Export Schema or Schemata
Export Schema or Schemata
Local Schema
Local Schema
Independent, heterogeneous local schemata
25PICNIC Prototype for Crete
- Involves
- two hospitals
- Sitia
- Rethymno
- five vendors
- FORTH (?)
- ?????f????? ????da? (?)
- Computer Team (?)
- Unisoft (?)
- CCS (?)
- nine clinical information systems
- PHCCIS (?)
- PATHIS (?)
- XRFDC (?)
- CARDIS (?)
- NIS (? ? )
- LIS (? ?)
- Administrative (? ?)
- Financial (? ?)
- Pharmacy (?)
26PICNIC Prototype for SEBT
Allergy Referral Medication Event Consultation
27Dependencies
- Existence of Reliable and Useful Information
- Patient Identification
- Availability of Information
- Use of Coding Schemes
- Systems Interoperability
- Patient Consent on Sharing Personal Information
- Organizational Commitment
- Legal Framework
28Lessons Learned Conclusions
- The needs for stability, manageability,
maintainability and most importantly ability to
evolve are of paramount importance - the multitude of complex issues arising in
developing a longitudinal SRS was successfully
solved through - evolving technical infrastructure
- a component based architecture
- consistent use of widely available standards and
technical frameworks - Whatever the technical platform is in real life,
its selection is only part of the solution.