national registry
Recently Published Documents


TOTAL DOCUMENTS

1771
(FIVE YEARS 653)

H-INDEX

73
(FIVE YEARS 9)

2022 ◽  
Vol 17 (1) ◽  
Author(s):  
Elisa Raulino Silva ◽  
Nicola Maffulli ◽  
Filippo Migliorini ◽  
Gilmar Moraes Santos ◽  
Fábio Sprada de Menezes ◽  
...  

Abstract Background The shoulder joint is the most commonly injured joint in CrossFit practitioners, because of the high intensity and loads associated with this sport. Despite the large number of clinical cases, there is a shortage of studies that investigate influence of biomechanical aspects of upper limbs' injuries on CrossFit practitioners. This study hypothesized that there would be a difference in function, strength, and muscle activation between Crossfit practitioners with and without shoulder pain. Methods We divided 79 Crossfit practitioners into two groups according to whether they reported pain (n = 29) or no pain (n = 50) in the shoulder during Crossfit training. Muscle function, strength, and activation were assessed using the Disability Arm, Shoulder and Hand function questionnaire, Upper Quarter Y Balance Test and Closed Kinetic Chain Upper Extremity Stability Test shoulder tests, isometric muscle strength assessment by manual dynamometry and muscle activation by surface electromyography and pain report. Results The function based on questionnaire was associated with pain (p = 0.004). We observed a statistically significant difference between the two groups only in the surface electromyography activity of the lower trapezius, and in the variables of shoulder pain and function (p = 0.038). Conclusion Crossfit practitioners with shoulder pain occurring during training showed good function and stability of the shoulder joint, but there was a reduction in the activation of stabilizing muscles, especially the lower trapezius. Trial registration Registro Brasileiro de Ensaios Clinico (Brasilian National Registry) with the ID: RBR-2gycyv.


Vox Sanguinis ◽  
2022 ◽  
Author(s):  
Gagan Mathur ◽  
Matthew B. Wilkinson ◽  
Eddie R. Island ◽  
Jay E. Menitove ◽  
Lowell Tilzer

2022 ◽  
Author(s):  
Madison K. Krischak ◽  
Sandra Au ◽  
Samantha E. Halpern ◽  
Danae G. Olaso ◽  
Dimitrios Moris ◽  
...  

JAMIA Open ◽  
2022 ◽  
Vol 5 (1) ◽  
Author(s):  
Sophia Z Shalhout ◽  
Farees Saqlain ◽  
Kayla Wright ◽  
Oladayo Akinyemi ◽  
David M Miller

Abstract Objective To develop a clinical informatics pipeline designed to capture large-scale structured Electronic Health Record (EHR) data for a national patient registry. Materials and Methods The EHR-R-REDCap pipeline is implemented using R statistical software to remap and import structured EHR data into the Research Electronic Data Capture (REDCap)-based multi-institutional Merkel Cell Carcinoma (MCC) Patient Registry using an adaptable data dictionary. Results Clinical laboratory data were extracted from EPIC Clarity across several participating institutions. Laboratory values (Labs) were transformed, remapped, and imported into the MCC registry using the EHR labs abstraction (eLAB) pipeline. Forty-nine clinical tests encompassing 482 450 results were imported into the registry for 1109 enrolled MCC patients. Data-quality assessment revealed highly accurate, valid labs. Univariate modeling was performed for labs at baseline on overall survival (N = 176) using this clinical informatics pipeline. Conclusion We demonstrate feasibility of the facile eLAB workflow. EHR data are successfully transformed and bulk-loaded/imported into a REDCap-based national registry to execute real-world data analysis and interoperability.


Author(s):  
Yannick J.J.M. Hazen ◽  
Peter G. Noordzij ◽  
Bastiaan M. Gerritse ◽  
Thierry V. Scohy ◽  
Saskia Houterman ◽  
...  

2021 ◽  
Vol 79 (12) ◽  
pp. 1320-1327
Author(s):  
Karol Sabatowski ◽  
Krzysztof P Malinowski ◽  
Zbigniew Siudak ◽  
Krzysztof Reczuch ◽  
Sławomir Dobrzycki ◽  
...  

Angiology ◽  
2021 ◽  
pp. 000331972110313
Author(s):  
Jing Wen Yong ◽  
Yue Yan Xing ◽  
Meng Ge Zhou ◽  
Na Yang ◽  
Yong Chen Hao ◽  
...  

Previous studies reported regional variations in in-hospital acute coronary syndrome (ACS) mortality, but the reasons for that were not clearly defined. We explored whether differences in patient characteristics could explain regional variation. The Improving Care for Cardiovascular Disease in China (CCC)-ACS project is an ongoing national registry and quality improvement project, involving 150 tertiary hospitals from 30 provinces across China. We applied a prediction model that included patient-specific variables to calculate the expected in-hospital mortality. For each province, we reported the observed, expected in-hospital mortality and the risk-adjusted ratio which is based on the observed divided by the expected mortality. From 2014 to 2018, 79 585 ACS patients were enrolled. The average in-hospital mortality was 1.8%. There was a wide variation in the in-hospital mortality among different provinces (0.2-3.9%). Patient characteristics explained part of this variation because of differences in the expected in-hospital mortality (0.7-2.8%). There was a substantial variation in the risk-adjusted ratio among provinces (0.2-3.5), which suggests that the variations in the mortality cannot be completely explained by the differences in patient characteristics. In conclusion, we observed a wide regional variation in mortality for ACS, part of which could be explained by the difference in patient characteristics.


2021 ◽  
Author(s):  
Lorene M. Nelson ◽  
Barbara Topol ◽  
Wendy Kaye ◽  
Jaime Raymond ◽  
D. Kevin Horton ◽  
...  

Introduction: The Centers for Disease Control and Prevention (CDC) National Amyotrophic Lateral Sclerosis (ALS) Registry is the first national registry for a chronic neurologic disease in the U.S. and uses a combination of case-finding methods including administrative healthcare data and patient self-registration. Methods: We applied capture-recapture methodology to estimate the completeness of the Registry for ascertaining patients with ALS for the first full year and the fourth years of the Registry (2011, 2014). The Registry uses the combination of two national administrative claims databases (Medicare and Veterans Affairs) with a self-register option at the registry portal. We conducted descriptive analyses of the demographic and clinical characteristics of the ALS cases identified by each of the sources and estimated the completeness of case ascertainment for each of the three ALS Registry sources individually, pairwise, and in all combinations. Results: Case-finding completeness was 54% in 2011 and improved to 56% in 2014. A smaller proportion of ALS patients under age 65 were ascertained than those 65 or older and ascertainment was also lower for non-White than White patients. The uncorrected ALS prevalence was 4.3/100,000 in 2011 (in 2014 5.0/100,000), but after correction for under-ascertainment, annual prevalence in 2011 was 7.9/100,000 (95% CI 7.6-8.2) (in 2014 was 8.9/100,000 (95% CI 8.7-9.2)). Discussion/Conclusion: Our findings indicate that administrative healthcare databases are a very efficient method for identifying the majority of ALS prevalent cases in the National ALS Registry and that the inclusion of a web registry portal for patients to self-register is important to ensure a more representative population for estimating ALS prevalence. Nonetheless, more than 40% of ALS cases were not ascertained by the Registry, with individuals younger than age 65 and people of color underrepresented. Recommendations are provided for additional methods that can be considered to improve the completeness of case ascertainment.


2021 ◽  
pp. jech-2020-215716
Author(s):  
Ondřej Mikeš ◽  
Anne Lise Brantsæter ◽  
Helle Katrine Knutsen ◽  
Liv Elin Torheim ◽  
Julie Bienertová Vašků ◽  
...  

ObjectivesThe aim of this study was to identify dietary patterns in a Czech pregnancy cohort established in the early postcommunist era and investigate associations between dietary patterns, maternal characteristics and birth outcomes.MethodsPregnant women were recruited for the Czech part of the European Longitudinal Study of Pregnancy and Childhood. A self-reported questionnaire answered in late pregnancy was used to assess information about the weekly intake of 43 food items. Information about birth outcomes (birth weight, height, ponderal index, head circumference, cephalisation index, gestational length and Apgar score) was obtained from the National Registry of Newborns. Complete details on diet and birth outcomes were available for 4320 mother–infant pairs.Results and conclusionThe food items were aggregated into 28 variables and used for extraction of two dietary patterns by principal component factor analysis. The patterns were denoted ‘unhealthy’ and ‘healthy/traditional’ based on the food items with the highest factor loadings on each pattern. The ‘unhealthy’ pattern had high positive loadings on meat, processed food and confectionaries. In contrast, the ‘healthy/traditional’ pattern had high positive loadings on vegetables, dairy, fruits and wholemeal bread. Following adjustment for covariates, we found that high adherence to the unhealthy pattern (expressed as beta for 1 unit increase in pattern score), that is, the higher consumption of less healthy foods, was associated with lower birth weight: −23.8 g (95% CI −44.4 to −3.2) and length: −0.10 cm (95% CI −0.19 to −0.01) and increased cephalisation index: 0.91 μm/g (95% CI 0.23 to 1.60). The ‘healthy/traditional’ pattern was not associated with any birth outcomes. This study supports the recommendation to eat a healthy and balanced diet during pregnancy.


Sign in / Sign up

Export Citation Format

Share Document