Suchergebnisse

RESUMO Este artigo analisa a série histórica de um conjunto de indicadores, de 2002 a 2014, relacionados ao Sistema Único de Saúde do Brasil, embasado na metodologia da Proposta de Avaliação de Desempenho do Sistema de Saúde. Os resultados mostram que houve uma sensível melhoria nos indicadores de dimensão socioeconômica e nos da dimensão condições de saúde. A melhoria dos indicadores de condições de saúde pode estar relacionada ao incremento de suporte financeiro; ao incremento de recursos humanos; ao aumento do acesso às consultas médicas e aos serviços de alta complexidade; e a uma maior disponibilização de horas de profissionais de saúde para a população residente.

Avaliou-se o preenchimento da variável raça/cor em oito sistemas/módulos nacionais de informação em saúde, bem como a viabilidade de cálculo e uso de indicadores segundo esse quesito na avalição do Sistema Único de Saúde. Somente três sistemas/módulos estavam adequados para validar três dos 24 indicadores usados pelo Índice de Desempenho do SUS. Apesar dos avanços nas estratégias para saúde de grupos étnico-raciais, o aprimoramento do preenchimento da variável permitirá melhor avaliação da situação de saúde da população negra. Recomenda-se monitoramento dessa variável por meio da qualificação da coleta e alimentação dos dados. É importante socializar o debate sobre equidade étnico-racial em saúde, utilizando-se o referido índice de desempenho para acompanhamento da atenção à saúde da população negra pelos governos e movimentos sociais.

ABSTRACTObjectivesOur objectives were unify and deduplicate databases' of patients registration information coming from Information Systems of SUS in Brazil: Hospital, Outpatient, Births, Notifications and Mortalities, between the years 2008-2015, to get an individualize data and plot patients' lines of care during the period, enabling pharmacoeconomic and epidemiological studies that parameterize effectiveness and efficiency of public policies and embedded technologies.
MethodsSemantic analysis of data was performed to describe and understand different meanings of different fields existing in the studied bases. In addition, there were four main procedures, executed with database operations tools and PLSQL programming language: cleaning and standardization of databases(document's numbers was checked in the brazilian national people's database, with a string approximator algorithm to decide if the document's number belonged or no the register); registration information extraction, deterministic and probabilistic deduplication thereof. The procedures were first performed on each database separately and after the unification of the records, was held again a deterministic deduplication. Except the probabilistic deduplication which was performed only on the final deterministic deduplicated's database.
Performed procedures allowed a decision-making to chose fields used in data model for the unified database creation. Nine database's representative fields related to patients were selected: patient's name; patient mother's name; sex; birth date; state; city; zip code; cpf and cns(brazilian documents).
ResultsInitially, the unified registration database resulted in 705.599.785 records, after deterministic deduplication there was a reduction culminating in 198.400.762 records. This reduction is explained because these databases are not fully integrated. Moreover, there is not always agreement between systems' semantics and in some cases changes occur in the data format over the period within the same system. After probabilistic deduplication, the number of unique records decreased to 124.545.186 which is explained by non-linked pairs by deterministic process. This result is guaranteed with a estimate error of at most 3.3% of false positive and at most 12.3% of false negative pairs.
ConclusionThe results show that data deduplication is necessary and should be carried out thoroughly. Where the databases had limited patients' registration information, the technique enabled to capture, in more complete basis, additional information. Futhermore, it allowed to identify and assist in the understanding of positive and negative aspects within systems and trace clinical condition of patients, enabling pharmacoeconomic and epidemiological studies that define effectiveness and efficiency of public policies and embedded technologies. As future work, is important ensure the univocity of records and link this database with past period.

IntroductionIn Brazil, the National Health System (SUS) provides healthcare to the public. The system hasmultiple administrative databases; the major databases record hospital (SIH) and outpatient (SIA)procedures. Epidemiological information is collected for all populations in subsystems, such as mor-tality (SIM), live births (SINASC) and diseases of compulsory declaration (SINAN). Each subsystemhas its own information system, which is able to provide information about consultations, clinicalinformation and medicines dispensed. However, these systems are not linked, thereby preventingindividual-centred analysis.
ObjectiveTo describe the methods and results of parameter setting that are needed to execute the probabilisticdeduplication of large administrative and epidemiological databases in Brazil and to create a NationalHealth Database Centred on the individual.
MethodsThis paper shows the results of a record linkage model to integrate data from SIH, SIA, SIM, andSINAN, which have different formats and attributes between them and over time. These data consistof 1.3 billion records from 2000-2015. Probabilistic and deterministic record linkages were used todeduplicate these data. The Kappa statistic and clerical review were used to ensure the quality ofthe linkage. The graph algorithm and depth-first search were used to generate the identifiers.
ResultsThe deterministic deduplication process resulted in a database with 403,113,527 possible uniqueindividuals. After the probabilistic deduplication process of the former database was performed,159,703,805 unique individuals were identified. This result had an estimated a false positive errorrate of 3.3%, and the false negative error was estimated at 12.3%.
ConclusionsThe National Health Database centred on the individual was generated and will allow researchersto use real-world evidence to conduct clinical, epidemiological, economic and other studies. Thisdatabase represents a significant cohort, spanning 15 years of historical data and preserving patientprivacy. The success of the process described will allow repeating and appending the data for futureyears and enable important studies to promote SUS efficiency and provide better treatments forpatients.
KeywordsData linkage, record linkage, Brazilian health database, SUS deduplication