The survey found that care coordinators need more support and resources to help patients. Nearly 70% rely on colleagues and 60% use personally collected materials for referrals. 98% want additional support like online referral resources and networking. Over half preferred online referral resources. The survey identified needs for improved training, current information, and abilities to understand learning styles and listen to patients. Care coordinators help with various needs including education, appointments, insurance, and translation. More support is needed for their important role in improving health outcomes.
PIHCI programmatic grants webinar (en) for circulationAlexandra Enns
These are the slides from CIHR’s webinar providing information for the upcoming PIHCI Network Programmatic Grant funding opportunity.
The complete instructions are on ResearchNet: https://www.researchnet-recherchenet.ca/rnr16/vwOpprtntyDtls.do?prog=2734&view=currentOpps&org=CIHR&type=EXACT&resultCount=25&sort=program&next=1&all=1&masterList=true
Patients and their loved ones often hold critical knowledge that informs diagnosis. This toolkit from the Institute of Medicine offers patients, families and clinicians guidance on how they can collaborate to improve diagnosis.
Patient Engagement Presentation - MPN Network Forum April 18, 2017Alexandra Enns
April 18, 2017
In April we held a Network Forum on engaging policymakers and patients/public effectively and appropriately. We would like to give a warm thanks to both Carolyn Shimmin, Patient Engagement expert of CHI's Knowledge Translation team, and Marcia Thomson, Assistant Deputy Minister of Manitoba Health, Seniors and Active Living for their presentations. Below you can see Carolyn's presentation - to see more of her work on patient engagement and to learn more about knowledge translation at CHI, please check out the blog Knowledge Nudge here. If you would like more information, helpful tools or advice about patient/public engagement in research, please contact Carolyn Shimmin at cshimmin@exchange.hsc.mb.ca
Safety is Personal: Partnering with Patients and Families for the Safest CareEngagingPatients
The work of NPSF"s Lucian Leape Institute's Roundtable on Consumer Engagement, "Safety Is Personal: Partnering with Patients and Families for the Safest Care" is a call to action for health leaders, clinicians, and policy makers to take the necessary steps to ensure patient and family engagement at all levels of health care.The report identifies specific action items for health leaders, clinicians, and policy makers to pursue in making patient and family engagement a core value in the provision of health. care.
The cervical screening culturally and linguistically diverse (CALD) Engagement Strategy was implemented by Cancer Institute NSW in 2014 – 2015 to address cervical screening rates in three priority populations in NSW, including Arabic-speaking, Cantonese-speaking and Mandarin-speaking women. Each of these populations were identified as having significant numbers who had never attended cervical screening.
PIHCI programmatic grants webinar (en) for circulationAlexandra Enns
These are the slides from CIHR’s webinar providing information for the upcoming PIHCI Network Programmatic Grant funding opportunity.
The complete instructions are on ResearchNet: https://www.researchnet-recherchenet.ca/rnr16/vwOpprtntyDtls.do?prog=2734&view=currentOpps&org=CIHR&type=EXACT&resultCount=25&sort=program&next=1&all=1&masterList=true
Patients and their loved ones often hold critical knowledge that informs diagnosis. This toolkit from the Institute of Medicine offers patients, families and clinicians guidance on how they can collaborate to improve diagnosis.
Patient Engagement Presentation - MPN Network Forum April 18, 2017Alexandra Enns
April 18, 2017
In April we held a Network Forum on engaging policymakers and patients/public effectively and appropriately. We would like to give a warm thanks to both Carolyn Shimmin, Patient Engagement expert of CHI's Knowledge Translation team, and Marcia Thomson, Assistant Deputy Minister of Manitoba Health, Seniors and Active Living for their presentations. Below you can see Carolyn's presentation - to see more of her work on patient engagement and to learn more about knowledge translation at CHI, please check out the blog Knowledge Nudge here. If you would like more information, helpful tools or advice about patient/public engagement in research, please contact Carolyn Shimmin at cshimmin@exchange.hsc.mb.ca
Safety is Personal: Partnering with Patients and Families for the Safest CareEngagingPatients
The work of NPSF"s Lucian Leape Institute's Roundtable on Consumer Engagement, "Safety Is Personal: Partnering with Patients and Families for the Safest Care" is a call to action for health leaders, clinicians, and policy makers to take the necessary steps to ensure patient and family engagement at all levels of health care.The report identifies specific action items for health leaders, clinicians, and policy makers to pursue in making patient and family engagement a core value in the provision of health. care.
The cervical screening culturally and linguistically diverse (CALD) Engagement Strategy was implemented by Cancer Institute NSW in 2014 – 2015 to address cervical screening rates in three priority populations in NSW, including Arabic-speaking, Cantonese-speaking and Mandarin-speaking women. Each of these populations were identified as having significant numbers who had never attended cervical screening.
Presented at the 2015 IHI International Forum byThe Royal Melbourne Hospital of Victoria,Australia, this poster,speaks to the power of Shadowing to engage patients and families in decisions of care, specifically the post-discharge planning process.
June 27/2017 - SPOR-PIHCI Network presentations from the pre-CAHSPR conference day in Toronto, Ontario
Sharing Practical Advances in Research Knowledge-
Translating Findings to Action from PIHCIN Research
Clinical Workforce Development NCA Informational WebinarCHC Connecticut
Learn more about training and technical assistance offered through Community Health Center Inc.'s National Cooperative Agreement (NCA) on Clinical Workforce Development. Hear more about FREE Learning Collaboratives opportunities to enhance or implement a model of Team-Based Care at your Health Center, and how to implement a Post-Graduate Residency program for Nurse Practitioners and Post-Doc Clinical Psychologists.
Meaningful Approaches to Patient EngagementCISCRP Page
This presentation is for a webinar held by CISCRP’s Jill McNair and Annick Anderson on March 27, 2017. The purpose of this webinar was explore various methods and tools that can be utilized to drive patient engagement strategies. Examples include CISCRP’s Patient Advisory Boards, Patient Journey Roadmaps, and Lay Language Summaries. Learn more at www.ciscrp.org or via email at jmatthews@ciscrp.org.
Weitzman 2013 Relative patient benefits of a hospital-PCMH collaboration with...CHC Connecticut
Anuj K Dalal presents information on a PCORI research grant: Relative patient benefits of a hospital-PCMH collaboration within an ACO to improve care transitions.
Dr. Edward Wagner, Director (Emeritus) MacColl Center, Senior Investigator, Group Health Research Institute addresses the 2014 Weitzman Symposium on The Future of Primary Care
Primary Health Care Strategy:
Key Directions for the Information Environment. Case study report and composite success model.
Steve Creed & Philip Gander
Presented at the 2015 IHI International Forum byThe Royal Melbourne Hospital of Victoria,Australia, this poster,speaks to the power of Shadowing to engage patients and families in decisions of care, specifically the post-discharge planning process.
June 27/2017 - SPOR-PIHCI Network presentations from the pre-CAHSPR conference day in Toronto, Ontario
Sharing Practical Advances in Research Knowledge-
Translating Findings to Action from PIHCIN Research
Clinical Workforce Development NCA Informational WebinarCHC Connecticut
Learn more about training and technical assistance offered through Community Health Center Inc.'s National Cooperative Agreement (NCA) on Clinical Workforce Development. Hear more about FREE Learning Collaboratives opportunities to enhance or implement a model of Team-Based Care at your Health Center, and how to implement a Post-Graduate Residency program for Nurse Practitioners and Post-Doc Clinical Psychologists.
Meaningful Approaches to Patient EngagementCISCRP Page
This presentation is for a webinar held by CISCRP’s Jill McNair and Annick Anderson on March 27, 2017. The purpose of this webinar was explore various methods and tools that can be utilized to drive patient engagement strategies. Examples include CISCRP’s Patient Advisory Boards, Patient Journey Roadmaps, and Lay Language Summaries. Learn more at www.ciscrp.org or via email at jmatthews@ciscrp.org.
Weitzman 2013 Relative patient benefits of a hospital-PCMH collaboration with...CHC Connecticut
Anuj K Dalal presents information on a PCORI research grant: Relative patient benefits of a hospital-PCMH collaboration within an ACO to improve care transitions.
Dr. Edward Wagner, Director (Emeritus) MacColl Center, Senior Investigator, Group Health Research Institute addresses the 2014 Weitzman Symposium on The Future of Primary Care
Primary Health Care Strategy:
Key Directions for the Information Environment. Case study report and composite success model.
Steve Creed & Philip Gander
As new payment models emerge that emphasize value over volume, providers are being compelled to look more closely at how to motivate patients—especially those with multiple chronic conditions—to actively manage their care, make better decisions and change behaviors. This editorial webinar will explore the relationships between engagement and improved health outcomes, greater patient satisfaction and better resource utilization. Our panel of experts will share proven strategies for building patients' confidence, disseminating self-management tools and making the best use of your care team.
Patient Engagement in Healthcare Improves Health and Reduces CostsM2SYS Technology
It’s been said that patient engagement develops naturally when there is a regular, focused communication between patient and provider and it leads to behaviors that meet or more closely approach treatment guidelines. It is also believed that patients engaged in their own care make fewer demands on the health care system and more importantly, they experience improved health. Patients who are educated about both their condition and their care are also patients who are most likely to get and stay healthy. In fact, many believe that empowering patients to actively process information, decide how that information fits into their lives, and act on those decisions is a key driver to improving care and reducing costs.
Research shows that informed and engaged patients take a more active role in their own care and furthermore, health care organizations are slowly discovering how patient engagement contributes to their financial and quality objectives. Patient engagement essentially revolves around the theory that if patients understand their condition, know the symptoms to watch for, know why they’re taking medication for example and how to implement the necessary lifestyle changes, the chances of them getting and staying healthy are significantly improved and when you proactively engage patients in their care, the quality of that care improves.
Listen in to our latest podcast with Brad Tritle, Director of Business Development for Vitaphone Health Solutions, chair of the HIMSS Social Media Task Force and contributing editor of the HIMSS book Engage! Transforming Healthcare through Digital Patient Engagement as we discuss the current state of patient engagement in healthcare, how it is defined, whether it really does have a significant impact on improving health and reducing the cost of care, what engagement initiatives are providers using and what the future of patient engagement may look like.
Evaluating the Effectiveness of Communityand Hospital MedicaBetseyCalderon89
Evaluating the Effectiveness of Community
and Hospital Medical Record Integration
on Management of Behavioral Health
in the Emergency Department
Stephanie Ngo, MD
Mohammad Shahsahebi, MD, MBA
Sean Schreiber, MSED, LPC
Fred Johnson, MBA
Mina Silberberg, PhD
Abstract
This study evaluated the correlation of an emergency department embedded care coordinator
with access to community and medical records in decreasing hospital and emergency
department use in patients with behavioral health issues. This retrospective cohort study
presents a 6-month pre-post analysis on patients seen by the care coordinator (n=524). Looking
at all-cause healthcare utilization, care coordination was associated with a significant median
decrease of one emergency department visit per patient (p G 0.001) and a decrease of 9.5 h in
emergency department length of stay per average visit per patient (pG0.001). There was no
significant effect on the number of hospitalizations or hospital length of stay. This intervention
demonstrated a correlation with reducing emergency department use in patients with behavioral
health issues, but no correlation with reducing hospital utilization. This under-researched
approach of integrating medical records at point-of-care could serve as a model for better
emergency department management of behavioral health patients.
Address correspondence to Mohammad Shahsahebi, MD, MBA, Department of Community and Family Medicine, Duke
University, Durham, NC, USA. Phone: (919) 342-8845; Email: [email protected]
Stephanie Ngo, MD, Department of Community and Family Medicine, Duke University, Durham, NC, USA.
Fred Johnson, MBA, Department of Community and Family Medicine, Duke University, Durham, NC, USA.
Mina Silberberg, PhD, Department of Community and Family Medicine, Duke University, Durham, NC, USA.
Mohammad Shahsahebi, MD, MBA, Northern Piedmont Community Care, Durham, NC, USA. Phone: (919) 342-8845;
Email: [email protected]
Fred Johnson, MBA, Northern Piedmont Community Care, Durham, NC, USA.
Sean Schreiber, MSED, LPC, Alliance Behavioral Health, Raleigh, NC, USA.
Journal of Behavioral Health Services & Research, 2017. 651–658. c)2017 National Council for Behavioral Health. DOI
10.1007/s11414-017-9574-7
Evaluating the effectiveness of community NGO ET AL. 651
Introduction
Background
Patients with behavioral health issues often require more resource-intensive care and are more
likely to be frequent users of health services.1–7 Brennan et al. found that patients with at least one
primary psychiatric visit to the emergency department (ED) were 4.6 times more likely than those
without a primary psychiatric visit to be classified as high utilizers of health services overall, and
that on average, high utilizers with a primary psychiatric visit had a significantly higher number of
ED visits than non-psychiatric high utilizers.7
Furthermore, Bboarding^ of patients with behavioral health issues has become a serious problem
for patients who requi ...
1. Care Coordinator Needs Assessment Survey
A recent study conducted by The Center for Workforce Studies that Care Coordination is viewed
“by case study participants as a valuable tool to improve both individual and population health”
and “an important strategy to improve health outcomes because it provides patients with
appropriate access to health services and permits them to participate in improving their health
status and enjoy healthier lives.” With this important Care Coordination need in mind, Healthy
Capital District Initiative (HCDI)of Albany, NY seeks to identify ways to support Care Coordinators
in their profession to assist with better health outcomes for patients.
Survey participants
The survey was conducted by HCDI in summer, 2015 and participants included a variety of
nurses, special needs providers, care coordinators, community health workers, home care
providers and others. Ninety-five percent of the participants were from the Albany, NY capital
district area. Prior to the survey, primary information was gathered from local health
organization leadership, acting as key informants, with detailed qualitative interviews being
conducted.
Key Results
From the data, it was determined that nearly seventy percent of respondents indicated that they
have to rely on other professionals within their organization for informational and referral
resources needed to identity means for patient care support. Sixty percent of those surveyed
rely on materials that they had to personally collect in order to provide patient care support.
(Example 1) This could be an indication that many care providers and coordinators themselves
are in need of additional support from the community.
Results confirm that there is a clear need for support in that 98% of respondents chose some
form of additional support needed to help them be successful in their jobs. Of the 98% two-
thirds chose regional online information referral resources and local networking opportunities.
(Example 2) When asked about preferred means of obtaining referral resources, over half of
survey participants indicated online referral resources as a source and an additional one third
would prefer online forums. (Example 3)
Qualitative interviews also indicated that current training for care providers had some
deficiencies in that there was a “need to run the training for a longer period” or that “some sort
of repeat/refresh situation would be helpful.” It was also indicated that there is a need for “a
forum resource for continuous training/knowledge upkeep”. Interviews also disclosed
deficiencies found in many currently available resources were indicated to be a lack of current
data with “no real alerts to changes”.
2. Example 1
What informational and referral resources do you use to identity means for patient care support?
Answer Options Response Percent
Other professionals in my organization 67.6%
Personally collected material 59.5%
In house directory of regional referral sources 48.6%
Insurance providers 40.5%
Organizational protocol or procedures 45.9%
Professional organizations 43.2%
Health related webpages 37.8%
United Way 2-1-1 Northeast Region 18.9%
Please specify other referral guidance from local organizations. 10.8%
Empirical research journals 8.1%
Example 2
What other referral resource(s) would help you to be successful in your job?
Answer Options Response Percent
Regional online information & referral resources 33.3%
Local networking opportunities 33.3%
Local speaker series 16.7%
Regional list of training opportunities 11.1%
Regional online forums for sharing 2.8%
Other(s) (please specify) 2.8%
3. Example 3
Meeting the Needs
Survey data gathered provides a snapshot of services and support provided to chronically ill and
other patients in the Capital District area. Approximately,two thirds are providing patients with
health education and assistance with health insurance coverage. Half of those surveyed are
arranging appointments and behavior health needs; while many are assisting with language
barriers, transportation, nutrition and other critical needs. (Example 4)
Additional outreach to local care provider leadership indicated that Care Coordinators need
abilities in “identifying patient’s mode or style of learning (ex. Visual learners), ability to read
social ques and listen (very important) and to be non-judgmental; as patients can be intimidated.
The required level of critical thought skills needed for those in care coordination is elevated.
Example 4
What are the primary service needs that you are helping patients to secure?
Answer Options Response Percent
Health education 66.7%
Ensuring health Insurance coverage 61.1%
Arranging appointments 55.6%
Arranging social support services needed 52.8%
Arranging for behavior health needs 52.8%
Communication and translation for non-English speaking
patients
41.7%
0.0%
10.0%
20.0%
30.0%
40.0%
50.0%
60.0%
Online referral
resources
Conferences Online Forums Webinars Other
How would you ideally access referralresources
that may be available to you?
4. Arranging transportation 38.9%
Arranging for nutritional needs 38.9%
Arranging for Physical or Occupational Therapy needs 36.1%
Counseling or training family caregivers 36.1%
Coordinating prescription/medicine needs 30.6%
Accompanying patient to appointments 22.2%
Ensuring emergency room follow up appointments 11.1%
Arranging for Hospice or Palliative Care 11.1%
Arranging patient legal counsel 8.3%
Preliminary Research
Care Coordination
Care coordination is the deliberate organization of patient care activities between two or more
participants (including the patient) involved in a patient’s care to facilitate the appropriate
delivery of health care services. Organizing care involves the marshaling of personnel and other
resources needed to carry out all required patient care activities, and is often managed by the
exchange of information among participants responsible for different aspects of care.
Services provided
Establishing accountability and agreeing on responsibility
Communicating/sharing knowledge
Helping with transitions of care
Assessing patient needs and goals
Creating a proactive care plan
Monitoring and follow up, including responding to changes in patients' needs
Supporting patients' self-management goals
Linking to community resources
Working to align resources with patient and population needs
Care Management
Care Management is an emerging concept that refers to a set of evidence-based, integrated
clinical care activities that are tailored to the individual patient, and that ensure each patient has
his or her own coordinated plan of care and services.
Case management refers to the case (ie diagnosis) and how to best meet the guideline criteria
for this particular case, e.g., by involving case managers (most often: nurses or nurse
practitioners) who could steer the process;
5. Services provided
Coordination activities
Making appointments
Calling patients to check-up on them
Helping arrange for services or connecting patients to community resources
Finding a nursing home and getting the patient accepted to it
Systematic assessment of the patient’s medical, functional, and psychosocial needs
System-based approaches to ensure timely receipt of all recommended preventive care
services
Medication reconciliation with review of adherence and potential interactions
Oversight of patient self-management of medications.
Resources
1. The Center for Health Workforce Studies. Care Coordination Case Study Preliminary
Findings. N.p., Apr. 2014. Web. Aug. 2015.
2. Rieve, Julia A. “Asthma Case Management Outcomes.” The Case Manager. 26-27. Print
3. Closing the Quality Gap: A Critical Analysis of Quality Improvement Strategies: Volume
7—Care Coordination. Publication No. 04(07)-0051-7, June 2007.
4. Agency for Healthcare Research and Quality, Rockville, MD. Available
at: http://www.ahrq.gov/clinic/tp/caregaptp.htm. Accessed October 17, 2012.