نتایج جستجو برای: hospital registries
تعداد نتایج: 408372 فیلتر نتایج به سال:
C ommunity-based registries are considered the best source of information on stroke incidence, risk factors, characteristics , and outcome. They can be used for developing adequate strategies for stroke care and prevention. Criteria to perform an ideal stroke incidence study had been defined and refined in the past 2 decades and include standards for definitions, methods , and data presentation...
Before these two studies the published data on penile implant surgery consisted mostly of single-surgeon small series and retrospective experiences, rather than prospective, large, multicenter data collection [3-7]. Accordingly, it has been advocated the creation of prospective databases i.e. clinical data registries also to monitor more accurately the results of surgery, and to have solid grou...
Federating metadata registries introduces a range of problems to address, from identifying the commonality in data models across registries, to agreeing on a well-defined data dictionary. As more and more registries participate in the federation, the number of problems to solve can potentially rise to unmanageable levels. While solutions to these issues are researched, generic federation system...
The risk of major malformations in the offspring of mothers with epilepsy receiving antiepileptic drugs is 4--8% compared to 2--4% in the general population. Risk factors include daily dose and polytherapy. Selected drugs have been found to be associated with a higher risk of specific malformations (congenital heart defects and cleft palate with phenytoin and barbiturates; neural tube defects w...
BACKGROUND Government legislators and research ethics boards in some jurisdictions require all patients to give written informed consent before enrollment in clinical registries. However, the effect of such a requirement on the use of clinical registries and the extent to which registry data can be generalized remain uncertain. METHODS We examined the effectiveness of a comprehensive attempt ...
BACKGROUND Electronic-health (e-health) provides opportunities for quality improvement of healthcare, but implementation in low and middle income countries is still limited. Our aim was to describe the implementation of a registration (case record form; CRF) for obstetric interventions and childbirth events using e-health in a prospective birth cohort study in Palestine. We also report the comp...
UNLABELLED Cancer registries must provide complete and reliable incidence information with the shortest possible delay for use in studies such as comparability, clustering, cancer in the elderly and adequacy of cancer surveillance. Methods of varying complexity are available to registries for monitoring completeness and timeliness. We wished to know which methods are currently in use among canc...
BACKGROUND Accurate case ascertainment is essential for clinical registries to be valid and representative. We assessed case ascertainment in the Michigan Stroke Registry by linking to a statewide hospital discharge database (Michigan Inpatient Database [MIDB]). METHODS AND RESULTS In 2009, all ischemic stroke cases submitted by 30 registry hospitals were linked to ischemic stroke discharges ...
OBJECTIVE To develop and validate a set of practical prediction tools that reliably estimate the outcome of subarachnoid haemorrhage from ruptured intracranial aneurysms (SAH). DESIGN Cohort study with logistic regression analysis to combine predictors and treatment modality. SETTING Subarachnoid Haemorrhage International Trialists' (SAHIT) data repository, including randomised clinical tri...
Patient registries are an essential tool to increase current knowledge regarding rare diseases. Understanding these data is a vital step to improve patient treatments and to create the most adequate tools for personalized medicine. However, the growing number of disease-specific patient registries brings also new technical challenges. Usually, these systems are developed as closed data silos, w...
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