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1.
Gesundheitswesen ; 82(S 02): S131-S138, 2020 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-31822021

RESUMO

BACKGROUND: The evaluation of population-based screening programs, like the German Mammography Screening Program (MSP), requires collection and linking data from population-based cancer registries and other sources of the healthcare system on a case- specific level. To link such sensitive data, we developed a method that is compliant with German data protection regulations and does not require written individual consent. METHODS: Our method combines a probabilistic record linkage on encrypted identifying data with 'blinded anonymisation'. It ensures that all data either are encrypted or have a defined and measurable degree of anonymity. The data sources use a software to transform plain-text identifying data into a set of irreversibly encrypted person cryptograms, while the evaluation attributes are aggregated in multiple stages and are reversibly encrypted. A pseudonymisation service encrypts the person cryptograms into record assignment numbers and a downstream data-collecting centre uses them to perform the probabilistic record linkage. The blinded anonymisation solves the problem of quasi-identifiers within the evaluation data. It allows selecting a specific set of the encrypted aggregations to produce data export with ensured k-anonymity, without any plain-text information. These data are finally transferred to an evaluation centre where they are decrypted and analysed. Our approach allows creating several such generalisations, with different resulting suppression rates allowing dynamic balance information depth with privacy protection and also highlights how this affects data analysability. RESULTS: German data protection authorities approved our concept for the evaluation of the impact of the German MSP on breast cancer mortality. We implemented a prototype and tested it with 1.5 million simulated records, containing realistically distributed identifying data, calculated different generalisations and the respective suppression rates. Here, we also discuss limitations for large data sets in the cancer registry domain, as well as approaches for further improvements like l-diversity and how to reduce the amount of manual post-processing. CONCLUSION: Our approach enables secure linking of data from population-based cancer registries and other sources of the healthcare system. Despite some limitations, it enables evaluation of the German MSP program and can be generalised to be applicable to other projects.


Assuntos
Detecção Precoce de Câncer , Registro Médico Coordenado , Sistema de Registros , Alemanha , Humanos , Mamografia
2.
Stud Health Technol Inform ; 169: 644-8, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21893827

RESUMO

Biomedical research requires large numbers of well annotated, quality-assessed samples which often cannot be provided by a single biobank. Connecting biobanks, researchers and service providers raises numerous challenges including trust among partners and towards the infrastructure as well as interoperability problems. Therefore we develop a holistic, open-source and easy-to-use IT infrastructure. Our federated approach allows partners to reflect their organizational structures and protect their data sovereignty. The search service and the contact arrangement processes increase data sovereignty without stigmatizing for rejecting a specific cooperation. The infrastructure supports daily processes with an integrated basic sample manager and user-definable electronic case report forms. Interfaces for existing IT systems avoid re-entering of data. Moreover, resource virtualization is supported to make underutilized resources of some partners accessible to those with insufficient equipment for mutual benefit. The functionality of the resulting infrastructure is outlined in a use-case to demonstrate collaboration within a translational research network. Compared to other existing or upcoming infrastructures, our approach has ultimately the same goals, but relies on gentle incentives rather than top-down imposed progress.


Assuntos
Pesquisa Biomédica/tendências , Biologia Computacional/métodos , Sistemas de Informação/organização & administração , Informática Médica/organização & administração , Bancos de Tecidos , Redes de Comunicação de Computadores , Segurança Computacional , Comportamento Cooperativo , Coleta de Dados , Humanos , Comunicação Interdisciplinar , Modelos Organizacionais , Software , Integração de Sistemas
3.
Stud Health Technol Inform ; 210: 424-8, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-25991179

RESUMO

Evaluating cancer prevention programs requires collecting and linking data on a case specific level from multiple sources of the healthcare system. Therefore, one has to comply with data protection regulations which are restrictive in Germany and will likely become stricter in Europe in general. To facilitate the mortality evaluation of the German mammography screening program, with more than 10 Million eligible women, we developed a method that does not require written individual consent and is compliant to existing privacy regulations. Our setup is composed of different data owners, a data collection center (DCC) and an evaluation center (EC). Each data owner uses a dedicated software that preprocesses plain-text personal identifiers (IDAT) and plaintext evaluation data (EDAT) in such a way that only irreversibly encrypted record assignment numbers (RAN) and pre-aggregated, reversibly encrypted EDAT are transmitted to the DCC. The DCC uses the RANs to perform a probabilistic record linkage which is based on an established and evaluated algorithm. For potentially identifying attributes within the EDAT ('quasi-identifiers'), we developed a novel process, named 'blinded anonymization'. It allows selecting a specific generalization from the pre-processed and encrypted attribute aggregations, to create a new data set with assured k-anonymity, without using any plain-text information. The anonymized data is transferred to the EC where the EDAT is decrypted and used for evaluation. Our concept was approved by German data protection authorities. We implemented a prototype and tested it with more than 1.5 Million simulated records, containing realistically distributed IDAT. The core processes worked well with regard to performance parameters. We created different generalizations and calculated the respective suppression rates. We discuss modalities, implications and limitations for large data sets in the cancer registry domain, as well as approaches for further improvements like l-diversity and automatic computation of 'optimal' generalizations.


Assuntos
Neoplasias da Mama/prevenção & controle , Confidencialidade/legislação & jurisprudência , Anonimização de Dados/legislação & jurisprudência , Mineração de Dados/métodos , Registros Eletrônicos de Saúde/legislação & jurisprudência , Neoplasias da Mama/epidemiologia , Feminino , Alemanha , Regulamentação Governamental , Humanos , Registro Médico Coordenado/métodos , Avaliação de Programas e Projetos de Saúde/métodos
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