Cargando…

Multiple chronic conditions at a major urban health system: a retrospective cross-sectional analysis of frequencies, costs and comorbidity patterns

OBJECTIVE: To (1) examine the burden of multiple chronic conditions (MCC) in an urban health system, and (2) propose a methodology to identify subpopulations of interest based on diagnosis groups and costs. DESIGN: Retrospective cross-sectional study. SETTING: Mount Sinai Health System, set in all f...

Descripción completa

Detalles Bibliográficos
Autores principales:	Majumdar, Usnish B, Hunt, Christophe, Doupe, Patrick, Baum, Aaron J, Heller, David J, Levine, Erica L, Kumar, Rashi, Futterman, Robert, Hajat, Cother, Kishore, Sandeep P
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BMJ Publishing Group 2019
Materias:	Health Informatics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6797368/ https://www.ncbi.nlm.nih.gov/pubmed/31619421 http://dx.doi.org/10.1136/bmjopen-2019-029340

Ejemplares similares

The case for a global focus on multiple chronic conditions
por: Hajat, Cother, et al.
Publicado: (2018)

UMD‐Predictor: A High‐Throughput Sequencing Compliant System for Pathogenicity Prediction of any Human cDNA Substitution
por: Salgado, David, et al.
Publicado: (2016)

3515 Readability of online patient education materials on gynecologic malignancies from major medical associations
por: Samuel, David, et al.
Publicado: (2019)

Hypertension screening, prevalence, treatment, and control at a large private hospital in Kampala, Uganda: A retrospective analysis
por: Majumdar, Usnish, et al.
Publicado: (2022)

Predicting the Functional, Molecular, and Phenotypic Consequences of Amino Acid Substitutions using Hidden Markov Models
por: Shihab, Hashem A, et al.
Publicado: (2013)

Prioritization of Genetic Variants in the microRNA Regulome as Functional Candidates in Genome-Wide Association Studies
por: Bulik-Sullivan, Brendan, et al.
Publicado: (2013)

RNAsnp: Efficient Detection of Local RNA Secondary Structure Changes Induced by SNPs
por: Sabarinathan, Radhakrishnan, et al.
Publicado: (2013)

Rapid Detection of Rare Deleterious Variants by Next Generation Sequencing with Optional Microarray SNP Genotype Data
por: Watson, Christopher M., et al.
Publicado: (2015)

ProKinO: A Unified Resource for Mining the Cancer Kinome
por: McSkimming, Daniel Ian, et al.
Publicado: (2015)

Robust Diagnostic Genetic Testing Using Solution Capture Enrichment and a Novel Variant-Filtering Interface
por: Watson, Christopher M, et al.
Publicado: (2014)

Evaluating the Reliability of EHR-Generated Clinical Outcomes Reports: A Case Study
por: Kanger, Chatrian, et al.
Publicado: (2014)

The COMET Sleep Research Platform
por: Nichols, Deborah A., et al.
Publicado: (2014)

Developing a Communitywide Electronic Health Record Disease Registry in Primary Care Practices: Lessons Learned from the Western New York Beacon Community
por: Heider, Arvela R., et al.
Publicado: (2014)

Preparing Electronic Clinical Data for Quality Improvement and Comparative Effectiveness Research: The SCOAP CERTAIN Automation and Validation Project
por: Devine, Emily Beth, et al.
Publicado: (2013)

Recommendations for the Use of Operational Electronic Health Record Data in Comparative Effectiveness Research
por: Hersh, William R., et al.
Publicado: (2013)

How Patients Can Improve the Accuracy of their Medical Records
por: Dullabh, Prashila M., et al.
Publicado: (2014)

Transforming the Premier Perspective® Hospital Database into the Observational Medical Outcomes Partnership (OMOP) Common Data Model
por: Makadia, Rupa, et al.
Publicado: (2014)

Security Approaches in Using Tablet Computers for Primary Data Collection in Clinical Research
por: Wilcox, Adam B., et al.
Publicado: (2013)

Mission and Sustainability of Informatics for Integrating Biology and the Bedside (i2b2)
por: Murphy, Shawn, et al.
Publicado: (2014)

Quality Measure Performance in Small Practices Before and After Electronic Health Record Adoption
por: McCullough, Colleen M., et al.
Publicado: (2015)

Scalable Architecture for Federated Translational Inquiries Network (SAFTINet) Technology Infrastructure for a Distributed Data Network
por: Schilling, Lisa M., et al.
Publicado: (2013)

Web-based Comparative Patient-reported Outcome Feedback to Support Quality Improvement and Comparative Effectiveness Research in Total Joint Replacement
por: Zheng, Hua, et al.
Publicado: (2014)

Development and Implementation of ExPLORE Clinical Practice, a Web-accessible Comparative Outcomes Tool for California Hospitals and Physicians
por: McNair, Peter D., et al.
Publicado: (2015)

The Visit-Data Warehouse: Enabling Novel Secondary Use of Health Information Exchange Data
por: Fleischman, William, et al.
Publicado: (2014)

Development and Implementation of an Electronic Decision Support to Manage the Health of a High-Risk Population: The enhanced Electronic Medical Record Aging Brain Care Software (eMR-ABC)
por: Frame, Amie, et al.
Publicado: (2013)

Sustainability Through Technology Licensing and Commercialization: Lessons Learned from the TRIAD Project
por: Payne, Philip R.O.
Publicado: (2014)

Development of a Web Service for Analysis in a Distributed Network
por: Jiang, Xiaoqian, et al.
Publicado: (2014)

Advances in Patient-Reported Outcomes: The NIH PROMIS(®) Measures
por: Broderick, Joan E., et al.
Publicado: (2013)

The Future of Public Health Informatics: Alternative Scenarios and Recommended Strategies
por: Edmunds, Margo, et al.
Publicado: (2014)

The HMO Research Network Virtual Data Warehouse: A Public Data Model to Support Collaboration
por: Ross, Tyler R., et al.
Publicado: (2014)

In Search of a Data-in-Once, Electronic Health Record-Linked, Multicenter Registry—How Far We Have Come and How Far We Still Have to Go
por: Marsolo, Keith
Publicado: (2013)

Advancing User Experience Research to Facilitate and Enable Patient-Centered Research: Current State and Future Directions
por: Payne, Philip R.O.
Publicado: (2013)

Enhancing a Geriatric Emergency Department Care Coordination Intervention Using Automated Health Information Exchange-Based Clinical Event Notifications
por: Gutteridge, David L., et al.
Publicado: (2014)

Electronic Clinical Surveillance to Improve Outpatient Care: Diverse Applications within an Integrated Delivery System
por: Danforth, Kim N., et al.
Publicado: (2014)

Network‐Informed Gene Ranking Tackles Genetic Heterogeneity in Exome‐Sequencing Studies of Monogenic Disease
por: Dand, Nick, et al.
Publicado: (2015)

Assessing the Pathogenicity of Insertion and Deletion Variants with the Variant Effect Scoring Tool (VEST‐Indel)
por: Douville, Christopher, et al.
Publicado: (2015)

VariantValidator: Accurate validation, mapping, and formatting of sequence variation descriptions
por: Freeman, Peter J., et al.
Publicado: (2017)

Aggregation of population‐based genetic variation over protein domain homologues and its potential use in genetic diagnostics
por: Wiel, Laurens, et al.
Publicado: (2017)

hgvs: A Python package for manipulating sequence variants using HGVS nomenclature: 2018 Update
por: Wang, Meng, et al.
Publicado: (2018)

The Clinical Next‐Generation Sequencing Database: A Tool for the Unified Management of Clinical Information and Genetic Variants to Accelerate Variant Pathogenicity Classification
por: Nishio, Shin‐ya, et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_ph7rl6913dmro7joti3lgv8tos