Results 111 to 120 of about 29,787,584 (247)

Planning services for people with disabilities: a guide to the Intellectual Disability Database.

open access: yes, 2001
To monitor current service provision To predict future service requirements for research A summary of the current level of service provision is provided each year in the Annual Report of the National Intellectual Disability Database Committee.
National Intellectual Disability Database Committee   +2 more
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Obesity and injury in the National Hospital Morbidity Database [PDF]

open access: yes, 2013
This report studies the feasibility of using the National Hospital Morbidity Database (NHMD) to investigate the relationship between obesity and hospitalised injury in Australia.It concludes that the NHMD does not currently provide a reliable basis for

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Requirements for hospitals in Japan to have low operative mortality and failure‐to‐rescue rates

open access: yesAnnals of Gastroenterological Surgery
Aim We explored institutional factors in Japan associated with lower operative mortality and failure‐to‐rescue (FTR) rates for eight major gastrointestinal procedures. Methods A 22‐item online questionnaire was sent to 2119 institutional departments (IDs)
Itaru Endo   +9 more
doaj   +1 more source

Establishing a national linked database for Fetal Alcohol Spectrum Disorder (FASD) in the UK: multi-method public and professional involvement to determine acceptability and feasibility

open access: yesInternational Journal of Population Data Science
Introduction Fetal Alcohol Spectrum Disorder (FASD) is one of the leading non-genetic causes of developmental disability worldwide and is thought to be particularly common in the UK. Despite this, there is a lack of data on FASD in the UK.
Sarah Harding   +7 more
doaj   +1 more source

Comprehensive Characterization of 98 Chinese Cases of Genetic Creutzfeldt‐Jakob Disease With T188K Mutation

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To characterize the demographic, clinical, and laboratory features of the Chinese patients of genetic Creutzfeldt‐Jakob disease with T188K variant (T188K‐gCJD), the most common subtype of genetic prion diseases (gPrDs) in China. Methods In this nationwide retrospective study, data from 98 genetically confirmed T188K‐gCJD patients ...
Chun‐Jie Li   +11 more
wiley   +1 more source

National Major Trauma Audit National Report 2014-2015.

open access: yes, 2016
Major Trauma Audit (MTA) was established in the National Office of Clinical Audit (NOCA) in 2013. It specifically focuses on the care provided to the more severely injured patients in our healthcare system.
National Office of Clinical Audit
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Plasma EV Proteomics Identifies ECM Remodeling and Inflammatory Proteins LUM and C7 as Candidate Biomarkers in FSHD

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Facioscapulohumeral muscular dystrophy (FSHD) is one of the most debilitating and common muscular dystrophies. Despite its severity, no approved therapy exists for FSHD patients. However, several therapeutic candidates are currently under development, and some have recently entered clinical trials, marking the need for reliable ...
Mustafa Bilal Bayazit   +11 more
wiley   +1 more source

Best available evidence on artificial airway suctioning in critically ill older adults: An evidence-based synthesis

open access: yesExperimental Gerontology
Objective: This study aims to identify and synthesize the best available evidence on the suctioning process for artificial airways in critically ill elderly patients, including suctioning indications, preparation before suctioning, suctioning methods ...
Jun Tang   +4 more
doaj   +1 more source

White Matter Microstructural Abnormalities in Neonatal Onset Genetic Epilepsy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Recent evidence indicates that epilepsy is associated with abnormal white matter. If seizures alter white matter, then the impact upon network function, epileptogenesis, and cognition could be pronounced in neonates undergoing rapid developmental myelination. Neonates with epilepsy due to nonstructural genetic causes provide a unique
Amanda G. Sandoval Karamian   +8 more
wiley   +1 more source

Irish Maternity Early Warning System (IMEWS) V2 National Clinical Guideline No. 4 [PDF]

open access: yes, 2019
Providing standardised clinical care to patients in healthcare is challenging. This is due to a number of factors, among them diversity in environments of care and complex patient presentations.
HSE National Clinical Programme for Obstetrics and Gynaecology
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