Literature DB >> 17460129

A self-scaling, distributed information architecture for public health, research, and clinical care.

Andrew J McMurry1, Clint A Gilbert, Ben Y Reis, Henry C Chueh, Isaac S Kohane, Kenneth D Mandl.   

Abstract

OBJECTIVE: This study sought to define a scalable architecture to support the National Health Information Network (NHIN). This architecture must concurrently support a wide range of public health, research, and clinical care activities. STUDY
DESIGN: The architecture fulfils five desiderata: (1) adopt a distributed approach to data storage to protect privacy, (2) enable strong institutional autonomy to engender participation, (3) provide oversight and transparency to ensure patient trust, (4) allow variable levels of access according to investigator needs and institutional policies, (5) define a self-scaling architecture that encourages voluntary regional collaborations that coalesce to form a nationwide network.
RESULTS: Our model has been validated by a large-scale, multi-institution study involving seven medical centers for cancer research. It is the basis of one of four open architectures developed under funding from the Office of the National Coordinator of Health Information Technology, fulfilling the biosurveillance use case defined by the American Health Information Community. The model supports broad applicability for regional and national clinical information exchanges.
CONCLUSIONS: This model shows the feasibility of an architecture wherein the requirements of care providers, investigators, and public health authorities are served by a distributed model that grants autonomy, protects privacy, and promotes participation.

Entities:  

Mesh:

Year:  2007        PMID: 17460129      PMCID: PMC2244902          DOI: 10.1197/jamia.M2371

Source DB:  PubMed          Journal:  J Am Med Inform Assoc        ISSN: 1067-5027            Impact factor:   4.497


  27 in total

1.  Integrating syndromic surveillance data across multiple locations: effects on outbreak detection performance.

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2.  A submission model for use in the indexing, searching, and retrieval of distributed pathology case and tissue specimens.

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3.  Communities' readiness for health information exchange: the National Landscape in 2004.

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4.  The PING personally controlled electronic medical record system: technical architecture.

Authors:  William W Simons; Kenneth D Mandl; Isaac S Kohane
Journal:  J Am Med Inform Assoc       Date:  2004-10-18       Impact factor: 4.497

Review 5.  Pathology data integration with eXtensible Markup Language.

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Journal:  Hum Pathol       Date:  2005-02       Impact factor: 3.466

6.  No place to hide--reverse identification of patients from published maps.

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7.  Federal policy for the protection of human subjects. Final rule.

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8.  Implementing syndromic surveillance: a practical guide informed by the early experience.

Authors:  Kenneth D Mandl; J Marc Overhage; Michael M Wagner; William B Lober; Paola Sebastiani; Farzad Mostashari; Julie A Pavlin; Per H Gesteland; Tracee Treadwell; Eileen Koski; Lori Hutwagner; David L Buckeridge; Raymond D Aller; Shaun Grannis
Journal:  J Am Med Inform Assoc       Date:  2003-11-21       Impact factor: 4.497

9.  GenePING: secure, scalable management of personal genomic data.

Authors:  Ben Adida; Isaac S Kohane
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10.  Technical description of RODS: a real-time public health surveillance system.

Authors:  Fu-Chiang Tsui; Jeremy U Espino; Virginia M Dato; Per H Gesteland; Judith Hutman; Michael M Wagner
Journal:  J Am Med Inform Assoc       Date:  2003-06-04       Impact factor: 4.497

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  18 in total

1.  AEGIS: a robust and scalable real-time public health surveillance system.

Authors:  Ben Y Reis; Chaim Kirby; Lucy E Hadden; Karen Olson; Andrew J McMurry; James B Daniel; Kenneth D Mandl
Journal:  J Am Med Inform Assoc       Date:  2007-06-28       Impact factor: 4.497

2.  The Shared Health Research Information Network (SHRINE): a prototype federated query tool for clinical data repositories.

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Review 3.  Clinical research data warehouse governance for distributed research networks in the USA: a systematic review of the literature.

Authors:  John H Holmes; Thomas E Elliott; Jeffrey S Brown; Marsha A Raebel; Arthur Davidson; Andrew F Nelson; Annie Chung; Pierre La Chance; John F Steiner
Journal:  J Am Med Inform Assoc       Date:  2014-03-28       Impact factor: 4.497

4.  Federalist principles for healthcare data networks.

Authors:  Kenneth D Mandl; Isaac S Kohane
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5.  Using global unique identifiers to link autism collections.

Authors:  Stephen B Johnson; Glen Whitney; Matthew McAuliffe; Hailong Wang; Evan McCreedy; Leon Rozenblit; Clark C Evans
Journal:  J Am Med Inform Assoc       Date:  2010 Nov-Dec       Impact factor: 4.497

6.  A pragmatic framework for single-site and multisite data quality assessment in electronic health record-based clinical research.

Authors:  Michael G Kahn; Marsha A Raebel; Jason M Glanz; Karen Riedlinger; John F Steiner
Journal:  Med Care       Date:  2012-07       Impact factor: 2.983

7.  Patient-controlled sharing of medical imaging data across unaffiliated healthcare organizations.

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8.  Federated queries of clinical data repositories: the sum of the parts does not equal the whole.

Authors:  Griffin M Weber
Journal:  J Am Med Inform Assoc       Date:  2013-01-24       Impact factor: 4.497

9.  Health information technology will shift the medical care paradigm.

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Review 10.  A Federated Network for Translational Cancer Research Using Clinical Data and Biospecimens.

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Journal:  Cancer Res       Date:  2015-12-15       Impact factor: 12.701

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