A Framework for Generating Summaries from Temporal Personal Health Data

2021 ◽  
Vol 2 (3) ◽  
pp. 1-43
Author(s):  
Jonathan J. Harris ◽  
Ching-Hua Chen ◽  
Mohammed J. Zaki

Although it has become easier for individuals to track their personal health data (e.g., heart rate, step count, and nutrient intake data), there is still a wide chasm between the collection of data and the generation of meaningful summaries to help users better understand what their data means to them. With an increased comprehension of their data, users will be able to act upon the newfound information and work toward striving closer to their health goals. We aim to bridge the gap between data collection and summary generation by mining the data for interesting behavioral findings that may provide hints about a user’s tendencies. Our focus is on improving the explainability of temporal personal health data via a set of informative summary templates, or “protoforms.” These protoforms span both evaluation-based summaries that help users evaluate their health goals and pattern-based summaries that explain their implicit behaviors. In addition to individual-level summaries, the protoforms we use are also designed for population-level summaries. We apply our approach to generate summaries (both univariate and multivariate) from real user health data and show that the summaries our system generates are both interesting and useful.

2018 ◽  
Author(s):  
Alan Rozet ◽  
Ian M Kronish ◽  
Joseph E Schwartz ◽  
Karina W Davidson

BACKGROUND Investigations into person-specific predictors of stress have typically taken either a population-level nomothetic approach or an individualized ideographic approach. Nomothetic approaches can quickly identify predictors but can be hindered by the heterogeneity of these predictors across individuals and time. Ideographic approaches may result in more predictive models at the individual level but require a longer period of data collection to identify robust predictors. OBJECTIVE Our objectives were to compare predictors of stress identified through nomothetic and ideographic models and to assess whether sequentially combining nomothetic and ideographic models could yield more accurate and actionable predictions of stress than relying on either model. At the same time, we sought to maintain the interpretability necessary to retrieve individual predictors of stress despite using nomothetic models. METHODS Data collected in a 1-year observational study of 79 participants performing low levels of exercise were used. Physical activity was continuously and objectively monitored by actigraphy. Perceived stress was recorded by participants via daily ecological momentary assessments on a mobile app. Environmental variables including daylight time, temperature, and precipitation were retrieved from the public archives. Using these environmental, actigraphy, and mobile assessment data, we built machine learning models to predict individual stress ratings using linear, decision tree, and neural network techniques employing nomothetic and ideographic approaches. The accuracy of the approaches for predicting individual stress ratings was compared based on classification errors. RESULTS Across the group of patients, an individual’s recent history of stress ratings was most heavily weighted in predicting a future stress rating in the nomothetic recurrent neural network model, whereas environmental factors such as temperature and daylight, as well as duration and frequency of bouts of exercise, were more heavily weighted in the ideographic models. The nomothetic recurrent neural network model was the highest performing nomothetic model and yielded 72% accuracy for an 80%/20% train/test split. Using the same 80/20 split, the ideographic models yielded 75% accuracy. However, restricting ideographic models to participants with more than 50 valid days in the training set, with the same 80/20 split, yielded 85% accuracy. CONCLUSIONS We conclude that for some applications, nomothetic models may be useful for yielding higher initial performance while still surfacing personalized predictors of stress, before switching to ideographic models upon sufficient data collection.


Author(s):  
Michael Toze ◽  
Julie Fish ◽  
Trish Hafford-Letchfield ◽  
Kathryn Almack

Internationally, there is increasing recognition that lesbian, gay, bisexual and trans (LGBT) populations experience substantial public health inequalities and require interventions to address these inequalities, yet data on this population is often not routinely collected. This paper considers the case study of the UK, where there are proposals to improve government and health data collection on LGBT populations, but also a degree of apparent uncertainty over the purpose and relevance of information about LGBT status in healthcare. This paper applies a health capabilities framework, arguing that the value of health information about LGBT status should be assessed according to whether it improves LGBT people’s capability to achieve good health. We draw upon 36 older LGBT people’s qualitative accounts of disclosing LGBT status within UK general practice healthcare. Participants’ accounts of the benefits and risks of disclosure could be mapped against multiple domains of capability, including those that closely align with biomedical accounts (e.g., longevity and physical health), but also more holistic considerations (e.g., emotion and affiliation). However, across all domains, individuals tend to assess capabilities at an individual level, with relatively little reference to population-level impact of disclosure. Clearer articulation of the benefits of disclosure and data collection for the collective capabilities of LGBT populations may be a beneficial strategy for improving the quality of information on LGBT populations.


2017 ◽  
Vol 9 (1) ◽  
Author(s):  
Sameul Patnoe ◽  
Martin LaVenture ◽  
Rebecca E. Johnson ◽  
Jennifer Fritz ◽  
Barbara Frohnert ◽  
...  

ObjectiveTo create an informatics framework and provide guidanceto help Minnesota’s public health surveillance systems achieveinteroperability and transition to standards-based electronicinformation exchange with external health care providers using thestate’s birth defects registry as an initial pilot program.IntroductionThe Minnesota Department of Health (MDH) needs to be ableto collect, use, and share clinical, individual-level health dataelectronically in secure and standardized ways in order to optimizesurveillance capabilities, support public health goals, and ensureproper follow-up and action to public health threats. MDH programs,public health departments, and health care providers across the stateare facing increasing demands to receive and submit electronic healthdata through approaches that are secure, coordinated, and efficient;use appropriate data standards; meet state and federal privacy laws;and align with best practices. This framework builds upon existinginformatics models and two past studies assessing health informationexchange (HIE) conducted by the MDH Office of Health InformationTechnology (OHIT) to provide MDH surveillance systems with anoutline of the key elements and considerations for transitioning tomore secure, standards-based, electronic data exchange.MethodsDevelopment of the informatics framework incorporatesinformation gathered in several phases. The first phase involvesadditional analysis of data collected from the MDH InformaticsAssessment of Interoperability and HIE1that was conducted in 2015to evaluate the current state of interoperability and HIE readinessacross the agency. The second phase involves a comprehensiveenvironmental scan and literature review of existing standards,practices, models, toolkits, and other resources related to electronicHIE and interoperability. The third phase involves gathering additionalinformation on programmatic needs, workflows, and capabilitiesthrough key informant interviews. Key informants include programmanagers, staff, and content-area experts from select MDH programs,the state’s central information technology organization (MN.IT), andexternal health care provider organizations including hospitals.Minnesota’s birth defects registry, the Birth Defects InformationSystem (BDIS), was selected as the pilot program because it wasidentified in the 2015 MDH Informatics Assessment as having a highlevel of interest in implementing an interoperable and standards-driven approach to electronic health data exchange. The BDIS is alsoexploring options for being designated as an eligible public healthregistry for Meaningful Use. As a pilot program for this project,the BDIS assists in the development and implementation of theinformatics framework.ResultsThe 2015 MDH Informatics Assessment identified and evaluated21 MDH programs with information systems that accept and manageclinical, individual-level health information. Among these 21 MDHprograms, wide variations exist regarding information system size(range, 400 to 10,000,000 individuals), staffing numbers (range, 0.2 to21 FTEs), budgets (range, $20,000 to $1,876,000), and other keycharacteristics. Despite these variations, programs identified similarbarriers and needs related to achieving interoperability and electronicHIE. Areas of need include management and information technologysupport to make interoperability a priority; policies and governance;additional application functionality to support HIE; and additionalskills for the workforce. Results from the environmental scan and keyinformant interviews will be incorporated with additional analyses ofthe 2015 MDH Informatics Assessment to inform the development ofan agency-wide informatics framework to support MDH programs inachieving interoperability.ConclusionsMDH surveillance systems are calling for practical guidance tohelp implement and maintain a more efficient and effective wayto electronically collect, use, and share health data with externaland internal stakeholders. This informatics framework provides anoutline of the key elements and considerations for achieving greaterinteroperability across MDH surveillance systems. Additionalresearch is required to assess how system interoperability and HIEcan improve data quality and advance population health goals.


2021 ◽  
Vol 2021 ◽  
pp. 1-10
Author(s):  
Li Ai

Most of the current health management products are used in medical institutions and generally do not pay enough attention to the student population. Based on this, this paper designs a student-oriented and functional autonomous health management system. This paper proposes a personal health management system based on a multidimensional data model based on the main social characteristics of the population with chronic diseases and the actual needs of personal health management for chronic diseases. The value of various health data for health management is deeply analyzed and mined, and a multidimensional model data warehouse is constructed according to relevant national health data standards to create a standard data platform for intelligent health warning and disease risk assessment. This paper researches and designs a closed-loop personal health management method based on the Plan-Do-Check-Action (PDCA) cycle management model, with detailed functional design in four aspects: health data collection and recording, health assessment, health planning, and tracking and execution. This paper researches health data collection, processing, and storage technologies and adopts HDFS data storage technology, html, css, Java Script, java, and other software development technologies, combined with j Query, UEditor, Date Range Picker, and other plug-ins, as well as SMS email generation interface, wireless Bluetooth transmission interface, etc. This system web and mobile application platforms are designed and developed. Relational database is used as the system database, and a snowflake-type multidimensional data model is designed. Finally, the functions and performance of this system were tested, and the development and trial run of the basic version have been completed.


Author(s):  
Kevin J. Konty ◽  
Benjamin Bradshaw ◽  
Ernesto Ramirez ◽  
Wei-Nchih Lee ◽  
Alessio Signorini ◽  
...  

ObjectiveTo describe population-level response to influenza-like illness (ILI) as measured by wearable mobile health (mHealth) devices across multiple dimensions including steps, heart rate, and sleep duration and to assess the potential for using large networks of mHealth devices for influenza surveillance.IntroductionInfluenza surveillance has been a major focus of Data Science efforts to use novel data sources in population and public health [1]. This interest reflects the public health utility of timely identification of flu outbreaks and characterization of their severity and dynamics. Such information can inform mitigation efforts including the targeting of interventions and public health messaging. The key requirement for influenza surveillance systems based on novel data streams is establishing their relationship with underlying influenza patterns [2]. We assess the potential utility of wearable mHealth devices by establishing the aggregate responses to ILI along three dimensions: steps, sleep, and heart rate. Surveillance based on mHealth devices may have several desirable characteristics including 1) high resolution individual-level responses that can be prospectively analyzed in near real-time, 2) indications of physiological responses to flu that should be resistant to feedback loops, changes in health seeking behavior, and changes in technology use, 3) a growing user-base often organized into networks by providers or payers with increasing data quality and completeness, 4) the ability to query individual users underlying aggregate signals, and 5) demographic and geographic information enabling detailed characterization. These features suggest the potential of mHealth data to deliver “faster, more locally relevant” surveillance systems [3].MethodsDuring the 2017/2018 influenza season, surveys were conducted within the Achievement platform, a health app that integrates with a variety of wearable trackers and consumer health applications [4]. The Achievement population has given consent agreeing to participation in studies like the one presented here and permitting access to their data. Surveys queried users as to whether they had experienced flu-like (ILI) symptoms in the preceding 14 days. Respondents who had experienced symptoms were then asked to identify symptom days. Those who had not experienced symptoms were queried again two weeks later. Positive responses were re-indexed to align by date of symptom onset. Individual respondent’s measures were standardized on a per-individual level in the 6 week period centered on the index date. Population-level mean signals were directly computed across several dimensions including steps, sleep, and heart rate. Uncertainty was quantified using resampling.ResultsBeginning February 17th, 2018, surveys were distributed to Achievement users. Within the first week 31,934 users had responded to the survey. Over a 12-week period, 124,892 individuals completed the survey with 25,512 reporting flu-like symptoms in a two week period prior to the survey. Of these, 9,495 had wearable device data in the 90-day window surrounding their symptom dates and 3,362 respondents had “dense” data defined as no more than 4 consecutive missing days in the 6-week period surrounding the index date.Population-level signals to ILI were clearly evident for five measures across the three dimensions. Step count [fig. 1] and time spent active [fig. 2] decreased 1 day prior to reported symptom onset date (index date), with a minimum at day 2 of -.24 std. dev. for step count and -.25 std. dev for time spent active, and a return to baseline at day 8. Sleeplessness [fig.3] and time spent in bed [fig. 4] increased one day prior to index, peaking 4 days after index at a mean increase of .16 std. dev. for sleeplessness and .13 std. dev. for time spent in bed, and returning to baseline at 7 days. Heart rate was elevated from 1 day before index to day 6 with a peak increase of .18 std. dev. on days 2 and 3 after index.ConclusionsThe potential of mHealth devices to register illness has been recognized [5]. This study is the first to present population-level influenza signals in a large network of mHealth users. Mobile health device data linked to ILI-specific survey responses taken during the 2017/18 flu season demonstrate clear aggregate patterns across several dimensions including sleep, steps, and heart rate. These signals suggest the potential for systems to rapidly process individual-level responses to classify ILI and to use such classifiers for ILI surveillance. The data described here, high resolution individual-level behavioral and physiological data linked to timely survey responses, suggests the potential to further enhance outbreak detection and improve characterization of ILI patterns. The setting of our study, a very large network of mobile health device users who have consented to the prospective use of their data and to being queried about their health status, could provide a framework for automated prospective influenza surveillance using “real world evidence” [6]. Employed over a population-representative sample, this approach could provide adjunct to standard clinically-based sentinel systems.References[1] Althouse, Benjamin M., et al. "Enhancing disease surveillance with novel data streams: challenges and opportunities." EPJ Data Science 4.1 (2015): 17.[2] Henning KJ. What is syndromic surveillance?. Morbidity and Mortality Weekly Report. 2004 Sep 24:7-11[3] Simonsen L, Gog JR, Olson D, Viboud C. Infectious disease surveillance in the big data era: towards faster and locally relevant systems. The Journal of infectious diseases. 2016 Nov 14;214(suppl_4):S380-5.[4] https://www.myachievement.com/[5] Li, Xiao, et al. "Digital health: tracking physiomes and activity using wearable biosensors reveals useful health-related information." PLoS biology 15.1 (2017): e2001402.[6]https://www.fda.gov/scienceresearch/specialtopics/realworldevidence/default.htm


EP Europace ◽  
2021 ◽  
Vol 23 (Supplement_3) ◽  
Author(s):  
HAK Hillmann ◽  
J Eiringhaus ◽  
S Hohmann ◽  
JL Mueller-Leisse ◽  
C Zormpas ◽  
...  

Abstract Funding Acknowledgements Type of funding sources: None. Background The wearable cardioverter-defibrillator (WCD) can be prescribed in patients with newly diagnosed heart failure. The WCD provides additional heart failure parameters, like heart rate, step count and body position, accessible via remote monitoring. The purpose of this study was to evaluate clinical relevance of additionally recorded data in patients using the WCD. Methods Patients with newly diagnosed heart failure and WCD, an average wear time with at least 20 hours per day and available heart failure parameters were included. The heart failure parameters were provided in 5-minute data intervals. An approximate for the heart rate variability was calculated via the standard deviation of the cycle length of the given heart rate per 5-minute data interval (HRV5). Results 276 patients (68% male) were included between 04/2013 and 12/2017. Mean age was 57.4 ± 15.3 years. 174 patients (63%) suffered from non-ischemic and 102 patients (37%) from ischemic cardiomyopathy. Mean NYHA functional class at prescription was 2.6 ± 0.8. Mean left ventricular ejection fraction (LVEF) was 25.3 ± 8.5%. Mean wear time of the WCD was 111.8 ± 74.5 days. Recorded median heart rate using the WCD was 70.8 (IQR 63.1 - 78.7) beats per minute on the first wear day and 64.5 (IQR 59.7 - 71.3) on the last wear day. Median step count amounted to 4294 (IQR 2283 - 7092) steps on the first wear day compared to 5688 (IQR 3153 - 8263) steps on the last wear day. Median HRV5 was 85.4 (IQR 60.1 - 109.8) ms on the first wear day and 110.4 (IQR 78.6 - 134.9) ms on the last wear day.  Between the first and last seven days of usage, median heart rate was significantly reduced (69.5 (IQR 62.0 - 76.8) to 65.9 (IQR 60.4 - 72.2) beats per minute; p < 0.001), while median step counts per day (4657 (IQR 2778 – 6918) to 5562 (IQR 3890 – 8446) steps; p < 0.001) and HRV5 (89.0 (IQR 64.8 - 110.7) to 111.0 (IQR 83.7 - 134.7) ms; p < 0.001) were significantly elevated. A higher delta of heart rate correlated with a higher delta of HRV5A (p < 0,001; rs = 0.488) between the first and last seven days of usage. A higher delta of step counts per day in the first and last seven days correlated with a higher HRV5 (p < 0.001; rs = 0.320). Patients with a higher delta of step count per day (p = 0,005; rs = 0,189) and patients with a higher delta of HRV5 (p = < 0.001; rs = 0.255) showed a higher delta of LVEF measured at prescription and three months follow-up. Conclusion The WCD provides heart failure monitoring using additional heart failure parameters. Patients with newly diagnosed heart failure show a significant difference in heart rate, step count per day and heart rate variability approximate between beginning and end of prescription time. Step count and heart rate variability correlate with LVEF reverse remodeling. Remote monitoring for parameters regarding heart failure might be helpful for close monitoring and further heart failure therapy optimization during WCD wearing.


2021 ◽  
Vol 31 (3) ◽  
pp. 411-416
Author(s):  
Jana Uher

Given persistent problems (e.g., replicability), psychological research is increasingly scrutinised. Arocha (2021) critically analyses epistemological problems of positivism and the common population-level statistics, which follow Galtonian instead of Wundtian nomothetic methodologies and therefore cannot explore individual-level structures and processes. Like most critics, however, he focuses on only data analyses. But the challenges of psychological data generation are still hardly explored—especially the necessity to distinguish the study phenomena from the means to explore them (e.g., concepts, terms, methods). Widespread fallacies and insufficient consideration of the epistemological, theoretical, and methodological foundations of data generation—institutionalised in psychological jargon and the popular rating scale methods—entail serious problems in data analysis that are still largely overlooked, even in most proposals for improvements.


2018 ◽  
Author(s):  
Ram Dixit ◽  
Sahiti Myneni

BACKGROUND Connected Health technologies are a promising solution for chronic disease management. However, the scope of connected health systems makes it difficult to employ user-centered design in their development, and poorly designed systems can compound the challenges of information management in chronic care. The Digilego Framework addresses this problem with informatics methods that complement quantitative and qualitative methods in system design, development, and architecture. OBJECTIVE To determine the accuracy and validity of the Digilego information architecture of personal health data in meeting cancer survivors’ information needs. METHODS We conducted a card sort study with 9 cancer survivors (patients and caregivers) to analyze correspondence between the Digilego information architecture and cancer survivors’ mental models. We also analyzed participants’ card sort groups qualitatively to understand their conceptual relations. RESULTS We observed significant correlation between the Digilego information architecture and cancer survivors’ mental models of personal health data. Heuristic analysis of groups also indicated informative discordances and the need for patient-centric categories relating health tracking and social support in the information architecture. CONCLUSIONS Our pilot study shows that the Digilego Framework can capture cancer survivors’ information needs accurately; we also recognize the need for larger studies to conclusively validate Digilego information architectures. More broadly, our results highlight the importance of complementing traditional user-centered design methods and innovative informatics methods to create patient-centered connected health systems.


1976 ◽  
Author(s):  
N. Phillip Ross ◽  
Meyer Katzper
Keyword(s):  

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