6,160 research outputs found
Towards Evidence Based M-Health Application Design in Cancer Patient Healthy Lifestyle Interventions
Cancer is one of the most prevalent diseases in
Europe and the world. Significant correlations between dietary
habits and cancer incidence and mortality have been
confirmed by the literature. Physical activity habits are also
directly implicated in the incidence of cancer. Lifestyle
behaviour change may be benefited by using mobile technology
to deliver health behaviour interventions. M-Health offers a
promising cost-efficient approach to deliver en-masse
interventions. Smartphone apps with constructs such as
gamification and personalized have shown potential for
helping individuals lose weight and maintain healthy lifestyle
habits. However, evidence-based content and theory-based
strategies have not been incorporated by those apps
systematically yet. The aim of the current work is to put the
foundations for a methodologically rigorous exploration of
wellness/health intervention literature/app landscape towards
detailed design specifications for connected health m-apps. In
this context, both the overall work plan is described as well as
the details for the significant steps of application space and
literature space review. Both strategies for research and initial
outcomes of it are presented. The expected evidence based
design process for patient centered health and wellness
interventions is going to be the primary input in the
implementation process of upcoming patient centered
health/wellness m-health interventions.ENJECT COST-STSM-ECOST-STSM-TD1405-220216-07045
Towards a New Science of a Clinical Data Intelligence
In this paper we define Clinical Data Intelligence as the analysis of data
generated in the clinical routine with the goal of improving patient care. We
define a science of a Clinical Data Intelligence as a data analysis that
permits the derivation of scientific, i.e., generalizable and reliable results.
We argue that a science of a Clinical Data Intelligence is sensible in the
context of a Big Data analysis, i.e., with data from many patients and with
complete patient information. We discuss that Clinical Data Intelligence
requires the joint efforts of knowledge engineering, information extraction
(from textual and other unstructured data), and statistics and statistical
machine learning. We describe some of our main results as conjectures and
relate them to a recently funded research project involving two major German
university hospitals.Comment: NIPS 2013 Workshop: Machine Learning for Clinical Data Analysis and
Healthcare, 201
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Systematic associations between germ-line mutations and human cancers
YesThe revolution in Big Data has opened the gate for new research challenges in biomedical science. The aim of this study was to investigate whether germ-line gene mutations are a significant factor in 29 major primary human cancers. Using data obtained from multiple biological databases, we identified 424 genes from 8879 cancer mutation records. By integrating these gene mutation records a human cancer map was constructed from which several key results were obtained. These include the observations that missense/nonsense and regulatory mutations might play central role in connecting cancers/genes, and tend to be distributed in all chromosomes. This suggests that, of all mutation classes missense/nonsense and regulatory mutation classes are over-expressed in human genome and so are likely to have a significant impact on human cancer aetiology and pathomechanism. This offers new insights into how the distribution and interconnections of gene mutations influence the development of cancers
Engineering simulations for cancer systems biology
Computer simulation can be used to inform in vivo and in vitro experimentation, enabling rapid, low-cost hypothesis generation and directing experimental design in order to test those hypotheses. In this way, in silico models become a scientific instrument for investigation, and so should be developed to high standards, be carefully calibrated and their findings presented in such that they may be reproduced. Here, we outline a framework that supports developing simulations as scientific instruments, and we select cancer systems biology as an exemplar domain, with a particular focus on cellular signalling models. We consider the challenges of lack of data, incomplete knowledge and modelling in the context of a rapidly changing knowledge base. Our framework comprises a process to clearly separate scientific and engineering concerns in model and simulation development, and an argumentation approach to documenting models for rigorous way of recording assumptions and knowledge gaps. We propose interactive, dynamic visualisation tools to enable the biological community to interact with cellular signalling models directly for experimental design. There is a mismatch in scale between these cellular models and tissue structures that are affected by tumours, and bridging this gap requires substantial computational resource. We present concurrent programming as a technology to link scales without losing important details through model simplification. We discuss the value of combining this technology, interactive visualisation, argumentation and model separation to support development of multi-scale models that represent biologically plausible cells arranged in biologically plausible structures that model cell behaviour, interactions and response to therapeutic interventions
How to improve efficiency in cancer care: dimensions, methods, and areas of evaluation
Efficiency in healthcare is crucial since available resources are scarce, and the cost of inefficient allocation is measured in prior outcomes. This is particularly relevant for cancer. The aim of this paper is to gain a comprehensive overview of the areas and dimensions to improve efficiency, and establish the indicators, different methods, perspectives, and areas of evaluation, to provide recommendations for how to improve efficiency and measure gains in cancer care.Methods: We conducted a two-phase design. First, a comprehensive scoping literature review was conducted, searching four databases. Studies published between 2000 and 2021 were included if they described experiences and cases of efficiency in cancer care or methods to evaluate efficiency. The results of the literature review were then discussed during two rounds of online consultation with a panel of 15 external experts invited to provide insight and comments to deliberate policy recommendations.Results: 46 papers met the inclusion criteria. Based on the papers retrieved we identified six areas for achieving efficiency gains throughout the entire care pathway and, for each area of efficiency, we categorized the methods and outcomes used to measure efficiency gain.Conclusion: This is the first attempt to systemize a scattered body of literature on how to improve efficiency in cancer care and identify key areas of improvement. Policy summary: There are many opportunities to improve efficiency in cancer care. We defined seven policy recommendations on how to improve efficiency in cancer care throughout the care pathway and how to improve the measurement of efficiency gains
An Assessment of Health-Economic Burden of Obesity Trends with Population-Based Preventive Strategies in a Developed Economy
The burden of obesity varies with age, ethnicity, socio-economic status and state economies. All new projections should hence accommodate population ageing, and other population changes such as immigration, health-care system reform, or technological advances for disease treatment for a comprehensible assessment of global burden. The unfordable and expensive nature for reversing the obesity tide arises from policies developed to combat obesity. Most of these approaches aim at bringing the problem under control, rather than affecting a cure, and obviously require a multi-disciplinary and intensive regimen. Prevention is the only feasible option and is essential for all affected countries. Yet it is not simple to have population based UK-wide strategic framework for tackling obesity. Besides existence of multiple layers of governance, there are clear demarcations between targets in diet; nutrition and physical activity level between regions some of which are not realistic. Population based approaches target policies and process, aiming for a transition towards healthy population diets, activity levels and weight status. It is essential to understand these aspects differ culturally and between and within countries. There are still no clear and appropriate answers about answer when, where, why, and, how costs accrue in obese populations, further long term commitments are required for the same. Most population-based prevention policies are cost effective, largely paying for themselves through future health gains and resulting reductions in health expenditures. Therefore these prevention programs should be high on the scientific and political agendas
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Όλ¬Έ(λ°μ¬) -- μμΈλνκ΅λνμ : 곡과λν μ»΄ν¨ν°κ³΅νλΆ, 2022. 8. μμ§μ±.Evidence-based medicine, "the conscientious, explicit, and judicious use of current best evidence in healthcare and medical research" [98], is one of the most widely accepted medical paradigms of modern times. Searching, reviewing, and synthesizing reliable and high-quality scientific evidence is the key step for the paradigm. However, despite the widespread use of the EBM paradigm, challenges remain in applying Evidence-based medicine protocols to medical research. One of the barriers to applying the best scientific evidence to medical research is the severe literature and clinical data overload that causes the evidence-based tasks to be tremendous time-consuming tasks that require vast human effort. In this dissertation, we aim to employ visual analytics approaches to address the challenges of searching and reviewing massive scientific evidence in medical research. To overcome the burden and facilitate handling scientific evidence in medical research, we conducted three design studies and implemented novel visual analytics systems for laborious evidence-based tasks.
First, we designed PLOEM, a novel visual analytics system to aid evidence synthesis, an essential step in Evidence-Based medicine, and generate an Evidence Map in a standardized method. We conducted a case study with an oncologist with years of evidence-based medicine experience. In the second study, we conducted a preliminary survey with 76 medical doctors to derive the design requirements for a biomedical literature search. Based on the results, We designed EEEVis, an interactive visual analytic system for biomedical literature search tasks. The system enhances the PubMed search result with several bibliographic visualizations and PubTator annotations. We performed a user study to evaluate the designs with 24 medical doctors and presented the design guidelines and challenges for a biomedical literature search system design. The third study presents GeneVis, a visual analytics system to identify and analyze gene expression signatures across major cancer types. A task that cancer researchers utilize to discover biomarkers in precision medicine. We conducted four case studies with domain experts in oncology and genomics. The study results show that the system can facilitate the task and provide new insights from the data. Based on the three studies of this dissertation, we conclude that carefully designed visual analytics approaches can provide an enhanced understanding and support medical researchers for laborious evidence-based tasks in medical research.κ·Όκ±°μ€μ¬μν(Evidence-Based Medicine)μ΄λ "μμ μΉλ£ λ° μν μ°κ΅¬μμ νμ¬ μ‘΄μ¬νλ μ΅κ³ μ μ¦κ±°λ₯Ό μμ¬μ μ΄κ³ , λͺ
λ°±νλ©°, λΆλ³ μκ² μ΄μ©νλ λ°©λ²λ‘ "μ΄λ©° [98], νλ μνμμ κ°μ₯ λ리 λ°μλ€μ¬μ§λ μν ν¨λ¬λ€μμ΄λ€. μ λ’°ν μ μλ κ³ μμ€μ κ³Όνμ κ·Όκ±°λ₯Ό κ²μ, κ²ν , ν©μ±νλ κ²μ΄μΌ λ§λ‘ κ·Όκ±°μ€μ¬μνμ ν΅μ¬μ΄λ€. νμ§λ§, κ·Όκ±°μ€μ¬μνμ΄ μ΄λ―Έ κ΄λ²μνκ² μ¬μ©λκ³ μμμλ λΆκ΅¬νκ³ , μν μ°κ΅¬μ κ·Όκ±°μ€μ¬μνμ νλ‘ν μ½μ μ€μ²νλ λ°μλ μ¬μ ν λ§μ μ΄λ €μμ΄ λ°λ₯Έλ€. μλ£ λ¬Έν μ 보, μμ μ 보 λ° μ μ 체ν μ 보κΉμ§ μ°κ΅¬μκ° κ²ν ν΄μΌ ν κ·Όκ±°μ μμ λ°©λνλ©° κ΄λ²μνλ€. λν μνκ³Ό κΈ°μ μ λ°μ μΌλ‘ μΈν΄ μ μ°¨ λ λΉ λ₯Έ μλλ‘ λμ΄λκ³ μκΈ°μ, μ΄λ₯Ό λͺ¨λ μλ°ν κ²ν νκΈ° μν΄μλ λ§λν μμ μκ°κ³Ό μΈλ ₯μ΄ μμ΄μΌ νλ€.
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μ μμ§ μ 보 μκ°ν μΈν°νμ΄μ€μ PubTatorμ μ£Όμ μ 보λ₯Ό νμ©νμ¬ PubMed κ²μ μμ§μ κ²μ κ²°κ³Όλ₯Ό μ¦κ°νλ μμ€ν
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μ λν μ€κ³ μ§μΉ¨κ³Ό κ³Όμ λ₯Ό μ μνλ€. λ§μ§λ§μΌλ‘ μΈ λ²μ§Έ λμμΈ μ°κ΅¬μμλ μμμ μ μ μκ΅°μ μ μ μ λ°ν ν¨ν΄μ μ£Όμ μ μ νμ λ°λΌ μκ°ννκ³ λΆμν μ μλ μμ€ν
μΈ GeneVisλ₯Ό μ€κ³νμλ€. μ μ νμ λ°λ₯Έ μ μ μ λ°ν ν¨ν΄μ λΆμκ³Ό λΉκ΅λ μ μ°κ΅¬μλ€μ΄ μ λ° μνμμ μ체 μ§ν(Biomarker)λ₯Ό λ°κ²¬νκΈ° μν΄ λΉλ²ν μννλ μμ
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μν μ λ¬Έκ° λ° μ μ 체ν μ λ¬Έκ° μ΄ 4μΈμ λμμΌλ‘ μ¬λ‘ μ°κ΅¬λ₯Ό μ§ννμκ³ , κ·Έ κ²°κ³Ό GeneVisκ° ν΄λΉ μμ
μ λ μμνκ² μννλ κ²κ³Ό κΈ°μ‘΄μ λ°μ΄ν°μμ μλ‘μ΄ μ 보λ₯Ό λμΆνλ κ²μ λμμ΄ λμμμ νμΈνμλ€.
μμ μΈ λμμΈ μ°κ΅¬μ κ²°κ³Όλ₯Ό λ°νμΌλ‘, λ³Έ λ
Όλ¬Έμ μ¬μ©μ λΆμκ³Ό μμ
λΆμμ λλ°ν μκ°μ λΆμ λ°©λ²λ‘ μ΄ μν μ°κ΅¬μ κ·Όκ±° κ΄λ ¨ μμ
μ μ΄λ €μμ ν΄μνκ³ , λΆμ λ°μ΄ν°μ λν λ³΄λ€ λμ μ΄ν΄λ₯Ό μ 곡νλ κ²μ΄ κ°λ₯νλ€κ³ κ²°λ‘ λ΄λ¦°λ€.CHAPTER1 Introduction 1
1.1 Background and Motivation 1
1.2 Dissertation Outline 5
CHAPTER2 Related Work 7
2.1 Evidence Mapping: Graphical Representation for a Scientific Evidence Landscape 7
2.2 Scientific Literature Visualizations and Bibliography Visualizations 9
2.3 Visual Anlytics Systems for Genomics Data sets and Research Tasks 10
CHAPTER3 PLOEM: An Interactive Visualization Tool for Effective Evidence Mapping with Biomedical literature 12
3.1 Introduction 12
3.2 Visual Representations and Interactions of PLOEM 14
3.2.1 Overview of the PICO Criteria 14
3.2.2 Trend Visualization with the Timeline view 17
3.2.3 Representing the PICO Co-occurrence with the Relation view 20
3.2.4 Study detail view 22
3.3 Usage Scenarios: Visualizing Various Study Sizes with PLOEM 23
3.4 Conclusion 24
CHAPTER4 EEEvis: Efficacy improvement in searching MEDLINE database using a novel PubMed visual analytic system 26
4.1 Introduction 26
4.1.1 Motivation 26
4.1.2 Preliminary Survey: A Questionnaire on conventional literature search methods 28
4.1.3 Design Requirements for Biomedical Literature Search Systems 36
4.2 System and Interface Implementation of EEEVis 37
4.2.1 System Overview 37
4.2.2 Bibliography Filters 40
4.2.3 Timeline View 41
4.2.4 Co-authorship Network View 43
4.2.5 Article List and Detail View 44
4.3 User Study 46
4.3.1 Participants 46
4.3.2 Procedures 48
4.3.3 Results and Observations 50
4.4 Discussion 54
4.4.1 Design Implications 56
4.4.2 Limitations and Future Work 57
4.5 Conclusions 59
CHAPTER5 GeneVis: A Visual Analytics Systemfor Gene Signature Analysis in Cancers 68
5.1 Motivation 68
5.2 System and Interface Implementation 69
5.2.1 System Overview 69
5.2.2 Gene Expression Detail View 71
5.2.3 Gene Vector Projection View 72
5.2.4 Gene x Cancer Type Heatmap view 74
5.2.5 User Interaction in Multiple Coordinated Views 76
5.3 Case Studies 76
5.3.1 Participants 76
5.3.2 Task and Procedures 76
5.3.3 Case1: Identifying SimilarGeneSignatures with TGFB1in Hallmark Gene Sets 80
5.3.4 Case2: Identifying Cluster Patterns in the HRD data set 81
5.3.5 Results 82
5.4 Summary 85
CHAPTER6 Conclusion and future work 86
6.1 Conclusion 86
6.2 Future Work 87
Abstract (Korean) . . . . . . . . . . . . . . . . . . . . . . . . . . . . 102λ°
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