Roneyee Capstone Final
Roneyee Capstone Final
Roneyee Capstone Final
Abstract
The current baseline of timely issuance of Durable Medical Equipment (DME) to patients
at a prison facility located in southern California is far below the institution’s target goal of 95%.
The current process is prone to errors, wasted resources, and unnecessary staff rework. By using
Lean Six Sigma methodologies, this process improvement proposal aims to streamline the
workflow, eliminate out of compliance DME issuance, free up wasted resources, and make the
institution compliant with patient safety standards, Americans With Disability (ADA) laws, and
policy directives. The goal of this proposal is to provide this facility with high-level workflow
Introduction
Durable medical equipment (DME) is any equipment that offers therapeutic benefits to a
patient in need due to a particular medical condition and consists of items that are primarily:
ordered by a physician, used to serve a medical purpose, and are reusable (BlueCross, 2018). In
healthcare, DME is typically prescribed by a physician for a patient to safely and appropriately
use in their home. Unfortunately, many patients in the United States face institutional barriers to
DME access. Although universal access to healthcare for incarcerated persons is mandated by
the Eighth Amendment of the U.S. Constitution, many prison inmates are subjected to delayed
assessment of DME necessity, prescribing, and procurement due to constraints of the prison
system and its typically limited resources (Shalit & Lewin, 2004). A prison facility located in
southern California is facing potential negative patient outcomes due to delayed DME issuance
as a result of a poorly designed workflow process. The facility has no effective tracking process
to ensure each individual inmate has necessary DME in their possession and many inmates have
not been issued critical DME such as wheelchairs, walkers, braces, monitors, and protective
vests.
unnecessary staff rework, delays in treatment, and negative patient health outcomes at this
correctional facility by using Lean Six Sigma methodologies to streamline the DME distribution
and tracking process. Analysis of the current DME workflow will reveal nonvalue added (NVA)
and value added (VA) steps and identify gaps and inefficiencies in the process. This information
will be applied to the process improvement proposal, presented in the form of a future state
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workflow with projected benefits. The objective of the proposal is to aid this facility in meeting
its 95% DME compliance goal and reduce negative DME-related patient outcomes.
Problem
Timely issuance of DME was identified as a problem at this institution through the high
volume of healthcare grievances and healthcare requests for services submitted by patients.
Within this correctional facility, effective coordination between care teams and patients is
required to dispense DME within required timeframes. Unfortunately, the current work flow for
DME. Without a streamlined approach, the current process is prone to errors and negative patient
outcomes. Not only is timely issuance of DME imperative to ensuring patient safety, but it is also
Outdated electronic health records (EHR) systems, policies, and lack of human resources
result in communication breakdown which ultimately compromises patient safety. Inmates with
debilitating medical conditions are not receiving critical DME in a timely manner or are issued
incorrect DME altogether due to mistakes made during the ordering process. When ordering
DME, physicians are placing orders under incorrect categories or inappropriate levels of need.
Clinical and procurement staff are often unable to provide requested DME in the requested time
frame due to unclear DME descriptions or lack of availability, resulting in non-compliance. The
current distribution process at this facility includes a flawed receipt-based system, which further
delays delivery of DME. While the receipt process is intended to serve as a supplementary
tracking system to the EHR, it has instead created inaccurate noncompliance data as correctly
issued DME are not always reflected in these receipts. These errors in turn result in staff rework
and wasted resources as staff are consistently working to absolve these DME-related issues.
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Historical data at this facility showed a baseline of performance far below their goal of 95% for
Literature Review
Romanoski and Swope (2018) described that for individuals with a disability, DME can
functional mobility and activities of daily living (ADLs). Durable medical equipment greatly
helps patients live healthier lives and it can therefore be considered insufficient treatment if
DME is not appropriately incorporated in patient treatment plans (Antod, 2012). By determining
appropriate equipment needs, individuals who were once dependent on others may regain
independence in hopes of returning to their prior level of function and enhance their
Studies have also shown that new medical devices are getting to patients too slowly,
delaying treatment and leading to adverse events (Blanding, 2015). This can be attributed to
lengthy delays to the medical device approval process as well as clinicians’ attitudes toward
medical devices in healthcare delivery. According to a systematic review by Zhang, Bariball, and
While (2014), clinicians associated the use of medical devices with increased personal stress,
decreased autonomy, and increased administrative time. Because DMEs improve safety and
decrease the need for caregiver assistance, clinicians should not only issue DME in a timely
manner, but also understand the importance of DME in contributing to better patient outcomes.
health conditions. The accessibility and maximum use of medical equipment is essential in
improving the quality of health services. Problems with the timely issue of medical equipment
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and materials disrupt care and waste the health specialists’ workdays. Besides, the patients and
Many health centers do not give attention to ensure there is a timely supply of all types of
medical equipment that meet the needs of all patients. As a result, clinicians have no option but
to leave the patients bedsides and unattended to look for equipment or materials delaying care.
The unattended patient in many cases feels devastated because the health specialists who are
supposed to help are paying little or no attention (Guédon et al., 2016). The privileged families
may be able to purchase or hire the necessary resources, but the unprivileged are left unattended,
which may lead to their death. This is common especially to patients who do not have or cannot
and delays in the operating room, which can elicit extra risks to patients (Moyimane, Matlala, &
Kekan, 2017). Stress reduces the level of human performance, which increases the probability of
errors in the operating room. Besides, delays in the operating room can worsen the condition of
the patient or cause death. Therefore, hospitals should ensure there is a timely supply of medical
equipment to avoid delays and stress among clinicians and patients. Timely supply will increase
This proposal aims to improve patient care by eliminating out of compliance DME
issuance and free up wasted resources that result from the current DME process. In Lean
methodology, inefficiencies are called “waste” (Qualis Health, 2011). In this proposal, workflow
analysis and process mapping will be used to analyze the system of steps, expose waste, and
guide a more efficient design. A value stream map will be provided identify which parts of the
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workflow are causing the most waste and inform how the future state process map should look.
Streamlining the process should directly result in improved timely issuance of DME and
compliance rates. DME includes but is not limited to improve the timely issuance of following
items: wheelchairs, wheelchair cushions, walkers, C PAP machines, pillows wedges, reading and
sunglasses. A more efficient design should reduce confusion for all teams involved in the process
and provide easier tracking of DME. By eliminating NVA steps, which only cause unnecessary
workflow complications, staff should better be able to track DME once ordered for an inmate.
The goal for this process improvement proposal if implemented is that the institution will
achieve its target DME compliance of 95% across all DME categories (Same-Day, 5-Day, 14-
increasing the efficiency and speed in which the inmates receive critical DME, the institution
(Romanoski & Swope, 2018). As described, the inmates have reported several grievances and
requests for care related to lacking DME equipment. This process improvement will ensure that
these inmates receive appropriate DME in order to receive therapeutic benefit and to prevent
further associated complications. Patients with debilitating conditions should no longer wait for
extended periods to receive their DME due to inadequate organizational processes. A decrease in
these healthcare grievances reported by inmates should therefore follow process improvement
implementation.
The scope of this proposal will only include DME orders placed by the physicians in the
institution. Orders for medications, therapy, and other treatments will not be addressed as they
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follow different workflow processes. Durable medical equipment supplies (wheelchair gloves,
seat cushions), accessories (distilled water for C-Pap/Bi-Pap machines, test strips for
glucometers) and other materials (bandages, incontinence supplies), will also be excluded from
this proposal since these supplies are available onsite and do not require the same acquisition
process as DME.
This project will initiate with the workflow analysis of the DME process. The Chief
Support Executive (CSE) will function as a liaison to the project and help identify process steps,
length of each step, and which departments are responsible. The institution’s EHR will also be
used to analyze documentation and research the flow of the DME ordering process.
To focus the project, a defect analysis must first be conducted to identify what type of
DME errors are occurring most frequently. Once this is established, the proposal will be focused
on targeting these specific sections of the workflow. With information provided from the CSE,
an initial work flow process map will be developed. Once the process has been mapped out,
additional research will be conducted to create a VA vs. NVA steps table to analyze the current
DME process. This additional research will include interviewing the CSE, analyzing DME
documentation within the EHR, and performing audits on the many data points provided by the
institution. The VA vs. NVA table will function as a gap analysis to aid in pinpointing which
steps are causing the most delays and restraints. These wastes will be then revised to create the
future state process map, which will encompass this project’s process improvement proposal.
The hope for this project is that it will ultimately involve many departments within the
institution as their input is required to confirm effectiveness of the proposed solution and
implement if so desired. For the purposes of the proposal itself, the developing team is
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comprised of healthcare informaticists (see Figure 1). Working closely with the CSE, these
informaticists are tasked with utilizing the EHR to collect data entered by clinical staff and audit
the information to find waste. These NVA steps are to be reported to and confirmed with the
CSE throughout the research process and prior to creation of the current state process and value
stream maps.
The completed process improvement proposal, including the future state process map,
will be submitted to the CSE. Should the proposal be reported to and approved by the executive
sponsor as an effective and valid DME workflow, the proposal may be implemented for the
institution. A project manager would be needed to implement the new process for the
organization to delegate change tasks and training as necessary to the appropriate departments. If
successful, this new process has the potential to be applied to associated facilities statewide.
Deliverables
In order to perform a structured workflow analysis, each individual step within the initial
process was categorized into the VA vs. NVA table (see Figure 2). By separating the VA-only
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steps, this table eliminated all remaining workflow waste and staff re-work loops and identified
which steps would be included in the final future process map (see Figure 3).
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Conclusion/Next Steps
Next steps, possible outcomes and future opportunities involve numerous meetings with
the Chief Support Executive (CSE) and her team to discuss: potential financial benefits for
financial benefits are best supported annual soft savings which displays staff rework by cost
per defects; defects total to the amount of project savings $1,326,239.14 (see Figure 4).
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Moreover, project savings will contribute to feasibility of the proposal along with working
with stakeholders in headquarters. Implementation strategies will include the removal of the
7536, implemented in process map above, and optimization of the EHR; which will capture
all data in one area. Following steps will be to proceed working with multi departments to
References
Antod, J. (2012). Why every chiropractor should be a DME (durable medical equipment)
http://theamericanchiropractor.com/why-every-chiropractor-should-be-a-dme-durable-
medical-equipment-supplier/
Blanding, M. (2015). New medical devices get to patients too slowly. Forbes HBS Working
https://www.forbes.com/sites/hbsworkingknowledge/2015/08/11/new-medical-devices-
get-to-patients-too-slowly/
https://www.bluecrossnc.com/sites/default/files/document/attachment/services/public/pdf
s/medicalpolicy/durable_medical_equipment_%28dme%29.pdf
Centers for Medicare & Medicaid Services. (2017). Durable Medical Equipment (DME) Center.
dme-center.html
Guédon, A. C., Wauben, L. S., van der Eijk, A. C., Vernooij, A. S., Meeuwsen, F. C., van der
Elst, M., & van den Dobbelsteen, J. J. (2016). Where are my instruments? Hazards in
Moyimane, M. B., Matlala, S. F., & Kekan, M. P. (2017). Experiences of nurses on the critical
Romanoski, N. L., & Swope, K. (2018, Sept.). Durable medical equipment that supports
from https://now.aapmr.org/durable-medical-equipment-that-supports-activities-of-daily-
living-transfers-and-ambulation/
basics/workflow-analysis
Shalit, M., & Lewin, M. R. (2004). Medical care of prisoners in the USA. Medicine, Crime, and
Zhang, W., Barriball, K. L., & While, A. E. (2014). Nurses’ attitudes towards medical devices in
doi:10.1111/jocn.12601
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The Health Science Knowledge and Skills Outcome reflects the human-computer
health care delivery system, models of care, health care provider roles, and impact on
populations that access them. The HCI will establish and sustain feasible operations and improve
through the strategic planning completion process of streamline auditing of Durable Medical
Moreover, competencies will address ethical leadership principles to solving complex human
Systems Design and Management Outcome reflects HCI program competencies with the
deliverance of a current and future state process map to reach a DME timely issuance of 95%.
Process map aims to improve DME tracking process and documentation utilizing while reducing
Data and Knowledge Management Outcome reflects HCI program competencies of this
project by the integration of systems and technologies into the long-term information
management needs and plans of the prison. In addition, Microsoft Office and Powerchart will
Quality and Regulatory Outcome reflects HCI program competencies of this project by
improving policy and privacy through management of electronic health services. In an effective
streamline process, good regulatory outcomes should measure patient quality to prevent medical
Social Justice - to demonstrate and promote diversity and equality effectively to improve
the opportunity to sustain community flourish and social well-being. Social justice reflects HCI
program competencies of this project by creating a system that delivers timely issuance of DME.
A system that contributes to improve equality for all inmates, reassuring them that their medical