Skip to Main Content

Research Data Management: 2019 Research Data Management Symposium

Learn how to write a successful data management plan according to funding agency requirements.

Page Contents

Thank you to all who participated in the Augusta University Research Data Symposium on Tuesday, March 19, 2019. Below you will find links to the following:

Continuing Education Statements 

Poster Presentation Abstracts

Presentations from Symposium

Speaker Biographies

Symposium Pictures

Presentations from Symposium

Note: This will be updated as presenters provide their presentation slides, posters, and exhibit table material.

Materials are deposited in Scholarly Commons, Augusta University's Institutional Repository. The direct links are listed below in order of Symposium schedule.

Trends in Research Data Management Amy Nurnberger, MS (Keynote)

Notes on Data + Information Design Holly Goodson Rubio, MS (Research Data Visualization)

 

Data Storage, Access, and Security  James Smith, DBA 

 

Data Repositories for Research Reproducibility: Kathy Davies, MS, Jennifer Putnam Davis, MA, MLIS: 

Organizing, Describing, and Sharing Research Data  Brianna Marshall, MLIS 

AU IT Data Management Services and Challenges Tony Buenger, MA, MMAS (Institutional Panel)

 

Posters (see below for abstract information):

                                         

Symposium Pictures (Photography: Si-Long Chen)

Attendees listening to Dr. James Smith's (School of Computer and Cyber Sciences) presentation: Data Storage, Access, and Security.

Attendees discuss open data during the breakout session, Repositories for Data Reproduciblity, presented by Kathy Davies and Jennifer Davis (University Libraries). 

Assistant Professor Thomas Joshua (College of Nursing) presents his poster research, SF12v2 Health Scores for African Americans in a Cluster Randomized Community Trial. Co-authored with J. T. Gavin, L. Marion, and L B. Williams. 

Institutional Panel featuring Lesleyann Hawthorn, PhD (Georgia Cancer Center), Jennifer Waller, PhD (Division of Biostatistics and Data Science), Tony BuengerMMAS (Information Technology), and Kathy Davies, MLS (University Libraries).

Assistant Professor Dr. Terri Marin (College of Nursing) presents her poster research, Non-invasive Biomarkers to Detect Acute Kidney Injury in Premature InfantsCo-authored with B. Williams, J. Bhatia, A. Sharma, W. Zhi, C. Mundy, & C. Cockfield. See abstract below.

University Libraries volunteers, from left to right, Fay Verburg, Gail Kouame, Melissa Johnson, and Peter Shipman with Symposium organizers, Steph Hendren, Jennifer Davis, Kathy Davies, and Dr. Julie Zadinsky.  

Symposium Organizers, from left to right, Steph Hendren, Jennifer Davis, Kathy Davies, and Dr. Julie Zadinsky. (Not pictured Dr. Brenda Seago). 

Attendees in the breakout session, Organizing, Describing, and Sharing Research Data, presented by Brianna Marshall, MLS, Director of Research Services, UCR Library, University of California, Riverside.  

KeyNote Speaker Amy Nurnberger, MS, Program Head, Data Management Services, Massachusetts Institute of Technology, discusses Research Data Management Trends. 

Bob Schatz, MLS, Director of Institutional Engagement, Springer Nature Publishing, speaks on the intersection of data and publishing. 

Holly Goodson Rubio, MS, Director of Institutional Research, Augusta University, presents on data visualization. 
 

Research Data Management Symposium

Poster Presentation Abstracts

Georgia Cancer Center High Performance Computing (HPC) Server

Chang-Sheng (Sam) Chang, PhD

Director of the Bioinformatics Resource

Augusta University

 

Georgia Cancer Center at Augusta University is home to a High Performance Computing (HPC) Server. One  goal of the HPC server is to host the new Biorepository software, LabVantage.  This software is a web-based laboratory information management system, which tracks samples throughout their lifespan.  All specimens that the Georgia Cancer Center Biorepository receives is entered into LabVantage, which generates a unique barcode number for each sample. Chain of custody is recorded throughout the sample’s lifespan, from inception to eventual withdrawal. LabVantage organizes data such as patient demographics, diagnosis, organ site, and linked pathology reports. 
LabVantage is compliant with all regulations relevant to patient privacy and satisfies all regulations set forth by The College of American Pathologists (CAP). All Biorepository personnel are trained to maintain confidentiality of patient information according to HIPAA regulations.

 

The HPC Server is also used for the analysis of complex data including Next-Generation Sequencing data (NGS). It is currently used to perform data analysis on datasets such as those obtained from The Cancer Genome Atlas (TCGA). The analyses that used to take several weeks can now be performed in a matter of days.  Georgia Cancer Center HPC Server is composed of 544 total compute cores and an aggregated memory of 2.9TB. The system is composed of (15) PowerEdge R430 1U systems (128 GB RAM each), (1) PowerEdge R830 (1024 GB RAM) and a high-speed 10GbE interconnect for intra-node communication.  The HPCC also houses 633 TB RAW storage capacity.  We will also be integrating existing Cancer Center servers including our Illumina Compute system that collects data directly from the Sequencer housed in the Georgia Cancer Center Integrated Genomics Shared Resource and the existing Bioinformatics HPC (see configuration diagram below).  Access to the server is available to all Augusta University employees. There is a nominal fee associated with usage and users are required to undergo training.

 

DNP Quality Improvement Toolkit for Best Practice Use of Active Secondary Data

Courtney Omary, MSN, RN-BC                                                                                                                         

DNP, Emory University, Nell Hodgson Woodruff School of Nursing

Purpose

The purpose of this project is to describe a project for the development of an educational intervention focused on secondary EHR data in nursing quality improvement (QI) research.

Background

In Advancing Healthcare Transformation: A New Era for Academic Nursing, the American Association of Colleges of Nursing (AACN, 2016) make five recommendations based on their findings that academic nursing is not positioned as a partner in healthcare transformation. Their recommendation for academic nursing to invest in nursing research programs and better integrate research into clinical practice clearly intersects with the promise of big data (AACN, 2016). Big data and translation science were two emerging and priority areas identified by the Council for the Advancement of Nursing Science (Henly et al., 2015). Strengths of big data include availability from several sources to inform intervention research. Data sharing, faculty expertise and understanding of data science are barriers to using big data (Henly et al., 2015). Opportunities in translation science include collaboration between research and quality doctorates with clinical expertise, however a lack of commitment to dissemination, little opportunity for interdisciplinary collaboration and level of faculty expertise in methods of translation and implementation are threats (Henly et al., 2015).

Doctoral programs in nursing are designed to prepare nurse scientists and scholars, and Doctor of Nursing Practice (DNP) graduates must demonstrate the ability to translate knowledge to practice (AACN, 2006). Nursing participation, through collaboration, research and dissemination of data driven interventions, is important to representation and relevance of nursing knowledge and expertise in healthcare policy (Gephart, Davis, & Shea, 2018).

Recommendations from healthcare system leaders like Institute of Medicine (IOM), Centers for Medicare and Medicaid Services (CMS) and National Institutes of Health (NIH) all point to further development of continuous learning and translation of evidence into practice (Smith, 2012; CMS, 2018; NIH, 2017). Gaps in knowledge exist in best practice to achieve translation of data-driven evidence both to and from practice, and EHR data is a fundamental part of that translation (Frink, 2016). Based on an evaluation of health science students’ research skills, Kingsley and Kingsley (2009) make a strong suggestion to design and incorporate information literacy into graduate-level curricula. AACN’s Essentials of Doctoral Education for Advanced Nursing Practice (2006) established an essential competency for advance practice nursing to “utilize information systems to evaluate programs of care, outcomes of care and care systems.”

Methods

DNP students will receive an educational intervention in the form of a toolkit. The DNP QI Toolkit will include training on local policy for clinical research, data use agreements, best practice for accessing secondary data and foundational skills for clinical research. A toolkit is defined by the Agency for Healthcare Research and Quality (AHRQ, 2018) as a “collection of information, resources or tools to guide users to develop a plan or organize efforts to follow evidence-based recommendations or meet evidence-based specific practice standards.” In other words, a toolkit is an action-oriented technique of promoting the translation of research findings into policy and practice (AHRQ, 2018).

 

Non-invasive Biomarkers to Detect Acute Kidney Injury in Premature Infants

Terri Marin, PhD, NNP-BC, FAANP, Assistant Professor, College of Nursing, Augusta University

Bryan Williams, PhD, Professor, College of Nursing, Augusta University

Jatinda Bhatia, MD, FAAP, Section Chief, Department of Pediatrics: Neonatology, Augusta University

Ashok Sharma, PhD, Assistant Professor, Department of Population Health Science, Augusta University

Wenbo Zhi, PhD, Assistant Professor, Department of Obstetrics and Gynecology, Augusta University

Cynthia Mundy, DNP, NNP-BC, Assistant Professor, College of Nursing, Augusta University

Christy Cockfield, DNP, NNP-BC, Nurse Practitioner, Children’s Hospital of Georgia Neonatal Intensive Care Unit (NICU), Augusta University Health

Background: Acute kidney injury (AKI) occurs in approximately 40% of preterm infants born ≤ 34 weeks’ gestational age (GA), many of whom become hypotensive. This condition can injure the kidney and is both difficult to detect and treat. The immature kidney only receives 3-4% of total cardiac output under optimal conditions (vs. 20% in term infants); hence, mild reductions in perfusion secondary to hypotension may quickly result in renal ischemia. Once AKI develops, mortality rates increase to >50%. Current diagnostic criteria (serial serum creatinine measures) does not detect early, subclinical injury, as up to 50% of renal function is lost by the time this method detects AKI. 

Purpose:  We sought to determine the feasibility of non-invasive physiologic biomarkers to detect early, subclinical AKI in premature infants ≤ 34 weeks’ gestation during the first 14 days of life (DOL). We hypothesized that an inverse relationship exists between renal hypoxia and urinary biomarkers when ischemic renal injury is present.

Methods: We continuously observed regional renal oxygen saturation (rSO2) using near infrared spectroscopy (NIRS) technology among 21 infants ≤ 34 weeks’ GA during the first 14 DOL. We also collected urinary AKI biomarker samples that indicate renal damage on DOL 3, 7, 10 and 14. Using non-parametric test statistics we estimated the extent to which rSO2 slope changes were associated with that of each of the urinary biomarkers. 

Results: The rate of change in rSO2 slope was positively associated with that observed in levels of osteopontin (r= -0.53) and Cystatin C (r= -0.53) urinary biomarkers (p ≤ 0.05).  There was no correlation between rSO2 slope change and serum creatinine levels (r= -0.13; p=0.16).

Conclusions:  Renal oxygenation and urinary biomarker levels in infants experiencing hypoperfusion are inversely related and identify subclinical renal ischemia, prior to changes in serum creatinine.  Combining NIRS technology with urinary biomarker measurements may better predict and aid early diagnosis of subclinical AKI than serum creatinine measures in infants ≤ 34 weeks’ gestation during the first 14 DOL.

 

Opioid Crisis Trends in Georgia: Using Data Management Systems to Better Inform Public Policy

Authors: Nafiz Sheikh, Liniya Tauhidul

Introduction: The nationwide opioid epidemic is arguably the most consequential public health crisis of the new millennium. Unfortunately, a dearth of medical literature exists analyzing the scope of the epidemic in Georgia. This presentation will investigate trends in fatal opioid overdoses in Georgia using a robust healthcare data management system: Center for Disease Control’s (CDC) WONDER.

Methods: Using CDC WONDER, a cohort of all fatal opioid overdoses in Georgia from 1999 – 2017 was obtained (N=10,070). The group was then stratified by race, sex, age group, and overdosed opioid type. Time series analyses were used to determine trends, two-sided Chi-square tests with statistical significance set to p<0.05 used to compare opioid mortality proportions from different years and mortalities between age groups. Lastly findings were correlated to geography to ascertain if urbanization correlated to opioid mortality.

Results: Approximately 1056 fatal opioid overdoses occurred in 2017, up 192% from 550 deaths in 2010. Fatal overdoses from heroin and synthetic accounted for only 2% and 17% of total deaths in 2010 but magnified to 20% and 32% by 2017 (p<0.05). Beginning 2013, heroin and synthetic opioids such as fentanyl together drove Georgia opioid mortality sharply higher. Among different age groups, Georgians aged 25-34yrs experienced the highest mortalities compared to other females within the same age group (p<0.05) and to males and female in the 35-44yrs and 45-54yrs groups (p<0.05). Correlating fatalities to geography found urban areas in Atlanta, Augusta, and Columbus to have the highest mortality rates.

Conclusion: Georgians have experienced an unprecedented surge in mortality from opioid-related overdoses in recent years. With robust healthcare data management systems, however, new research endeavors are poised to generate more thorough epidemiological reports that will better inform local and state health policy.

SF12v2 Health Scores for African Americans in a Cluster-randomized Community Trial

Thomas V. Joshua1; Jane T. Garvin2; Lucy Marion1; Lovoria B. Williams3.

1Augusta University, College of Nursing, 2University of St. Augustine for Health Sciences, 3University of Kentucky

Background: Self-administered health survey short form (SF12v2) is commonly used to assess the health related quality of life (HRQOL) among populations. However, there is lack of data regarding its effectiveness among African Americans (AAs).

Design: Secondary data analysis of a prospective cohort study.

Aim: To assess the quality of life among AAs enrolled in a faith-based diabetes prevention program, Fit Body and Soul (FBAS) compared to a health education (HE).

Methods: Data were collected at three time points; baseline, 12 weeks, and 52 weeks. SASv9.4 was used to score the data. The SF12v2 data calculate two summary component scores, Physical Component Summary Score (PCS) and Mental Health Component Summary Score (MCS) with eight sub-domains. Scores range from 0 to 100, where a zero score indicates the lowest level of health and 100 indicates the highest level of health. Both PCS and MCS combine the 12 items in such a way that they compare to a national norm with a mean score of 50.0 and a standard deviation of 10.

Results: Total of 604 people were enrolled. FBAS included 317(mean age=46.59±10.9) and 287 (mean age=46.39±10.9) were in the HE. General health was reported good or better for 85% of the sample in both groups at baseline. Overall PCS for FBAS was 49 at baseline, 51 at week 12, and 50 at week 52 and for HE was 48 at baseline, 49 at week 12 and 49 at week 52. Overall, MCS for FBAS was 51 at baseline, 53 at week 12, and 52 at week 52 and for HE was 51 at baseline, 52 at week 12 and 51 at week 52.

Conclusion: Quality of life among participants at week 12 was improved from baseline but not maintained at week 52. The SF-12v2 appears to be a valid survey tool for the assessment of HRQOL among AAs.

Authors:

V. Migdal MD, N. Haqqani MD, K. Harper MD, B. Janiak MD

Affiliations:

All Authors: Department of Emergency Medicine, Augusta University; Augusta University Medical Center

 

ABSTRACT

Purpose: To determine the time to obtain answers to five-preselected ED nursing triage/assessment questions and convert this time to the monetary cost to the emergency department.

Methods: A prospective observational study of ED Registered Nurses performing triage assessments on 200 adults presenting to the ED for medical care.  During the triage assessment, the nurse was timed by one of the study authors while the RN asked five pre-selected questions included in their current triage protocol.  The time cost of each question was determined by multiplying the time spent asking the question each year by the average hourly wage of our ED RNs. (T x V x S)/3600; where T= average time per question (in seconds), V=annual patient volume, S=average hourly RN wage

Results: A total of 200 triage assessments were observed. During these assessments, 130 patients were asked about pneumococcal vaccine status, 161 asked about tetanus vaccine status, 184 asked about medication allergies, 172 about influenza vaccine, and 73 about recent travel. The average time spent per question ranged from 4.4-6.3 seconds. The estimated annual time used to ask these 5 questions in the AUMC ED is 633.98 hrs, which equates to $22189.3 in nursing costs per year.

Conclusions: This is a cursory look at the potential monetary and time costs of standardized screening questions in the ED. These values directly affect time and cost efficiency in the ED process and could potentially be redirected to more pertinent patient care. The required screening questions are often unrelated to the patient’s chief complaint and have no impact on the medical management in the ED. Further studies are needed to determine cost effectiveness of required ED screenings.

Symposium Schedule

7:15 - 8:15 a.m. Attendee Registration and Refreshments Library Entrance
8:15 - 8:30 a.m.

Augusta University Research Data Symposium Welcome

Alvin Terry, PhD
Associate VP for Basic Science Research
Augusta University

Room 1005
8:30 - 9:30 a.m.

Research Data Management Trends Keynote Speaker

Amy Nurnberger, MS
Program Head, Data Management Services 
Massachusetts Institute of Technology

Room 1005
9:30 - 10:00 a.m. Exhibit and Poster Viewing Break

Information Desk 

Open Area

10:00 - 10:45 a.m.

Research Data Visualization

Holly Goodson Rubio, MS
Director, Institutional Research
Augusta University

Room 1005
10:45 - 11:30 a.m.

Data Storage, Access, and Security

James Smith, DBA
School of Computer and Cyber Sciences
Augusta University

Room 1005
11:30 a.m. - 1:00 p.m.

Lunch Break

Exhibit and Posters Session

Information Desk  

Open Area

1:00 - 2:30 p.m.

Breakout Session A

Intersection of Data and Publishing

Bob Schatz, MLS 
Director of Institutional Engagement 
Springer Publishing 

Room 1005
1:00 - 2:30 p.m.

Breakout Session B

Organizing, Describing, and Sharing Research Data 

Brianna Marshall, MLS
Director of Research Services
UCR Library
University of California, Riverside  

Room 2113

Historical Collections and Archives

1:00 - 2:30 p.m.

Breakout Session C

Data Repositories for Research Reproducibility  

Kathy Davies, MLS 
Interim Director of Libraries
Greenblatt Library
Augusta University 

Jennifer Davis, MA, MLS
Scholarship and Data Librarian 
Greenblatt Library
Augusta University 

Room 2109
2:30 - 2:45 p.m. Exhibit and Poster Viewing Break

Information Desk  

Open Area

2:45 - 4:00 p.m.

Institutional Panel Discussion

Augusta University Research Data Management Services

Moderator: Kathy Davies, MLS 
Interim Director of Libraries

Anthony Buenger, MA, MMAS
Chief Information Security Officer 

Lesleyann Hawthorn, PhD
Director, Georgia Cancer Center Shared Resources 

Jennifer Waller, PhD
Director, Research Support Center

Room 1005

 

Purpose

The symposium will provide education on key topic areas of research data management to university health professionals, librarians, basic science researchers, research coordinators and research administrators. Attendees will learn research data management skills and discover research services provided by Augusta University.

Questions?

For general questions:

Kathy Davies                              Associate Director  Greenblatt Library  kadavies@augusta.edu

 

For exhibitor questions:

Jennifer Davis                    Scholarship and Data Librarian  jdavis14@augusta.edu

Earn Continuing Education Credit

Accreditation

The Medical College of Georgia at Augusta University is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.

 

Designation

The Medical College of Georgia at Augusta University designates this live activity for a maximum of 4.00 AMA PRA Category 1 Credits™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.

 

For Nurses: The Augusta University Division of Professional and Community Education is an approved provider of continuing nursing education by the South Carolina Nurses Association, an accredited approver by the American Nurses Credentialing Centers Commission on Accreditation.

4.00 Contact hours.

                               

CEUs

This activity includes 4.00 hours of instruction and attendance at the entire activity is approved by Augusta University for .40 Continuing Education Unit. One Continuing Education Unit (CEU) equals ten contact hours of participation in organized continuing education classes and/or training conducted by a qualified instructor.