Introduction
Over the last
decade, patient engagement has been considered critical to improving the
quality of care provided by the healthcare system. Patient engagement can be defined as involvement
of patient, their family and representatives, in working actively with health
professionals at various levels across the health care system to improve health
and health care services. It is the active involvement of the patient in
planning, delivery, monitoring and evaluation of their own care. A patient is
an individual receiving healthcare care services from an organization providing
healthcare.
The scientific studies
suggests that patient engagement has become a cornerstone for quality of care
improvement and is also a frequently stated goal for healthcare organizations
level, there are growing efforts to integrate patients in many area to improve
or redesign service delivery, by incorporating their experiences and
experiential knowledge, not only concerning chronic diseases but also the
services delivered by the system and the healthcare organization.
Patient’s perspective is unique. Given the
first-hand experience of every stage of the care pathway, they are legitimately
positioned to evaluate the care and services received, in terms of whatever
their needs and perspectives which were remarkably different, were not usually
well understood.
Patient-As-Partner:
For
20 years, paternalistic healthcare approaches have gradually given way to
patient-oriented approaches that take into account patients’ differences,
values, and experiences. Healthcare organizations, institutions, and
universities around the world are increasing their efforts to involve patients
and make their participation active using different forms of engagement and
various means of motivation. However, recent initiatives such as shared
decision-making and some therapeutic education approaches, maintain the
healthcare provider’s monopoly on determining the course and outcomes of
treatment.
Patients
can be partners in many ways.
For example, in healthcare
patients-as-partners interact and share the knowledge, acquired by their
experience of living with the disease and its impact on their lifestyle, with
multidisciplinary teams. They also wish to share their experience with
other patients to help them get through their episode of care. Such patients
are here called resource patients; they are willing to use their experience to
improve the organization of the health system.
Partnership
in Care Program:
To
implement this new paradigm, a unit for patient collaboration and partnership
(Direction collaboration partenariat patient - DCPP) was created in the context
of these healthcare service activities developed by the DCPP, the ‘Partnership
in Care Program’ (PCP) aims to develop a continuous quality improvement process
through the implementation of interdisciplinary committees for continuous
quality improvement (CQI), each including professionals and at least two
resource patients. CIC means Continuous Improvement Committee.
The PCP consists of five phases that occur in sequence :
Phase A : Preparation of Health Institutions
During
this phase, the PCP is submitted to the Executive Committee of each institution
to obtain a commitment from senior management. In addition, members of the CIC
are selected and a doctor–nurse team is identified to coordinate the CIC. Team
members consist of professionals and patients.
Professionals
are representatives of different professions (physicians, nurses,
physiotherapists, social workers, etc.) who have been chosen on a voluntary
basis. Patient participants are selected by the DCPP from a list of names
suggested by their departments, according to special criteria applied to
patients with chronic illness.
Phase B:
Team diagnosis for collaborative practices in
patient partnership
The
DCPP drafts a report on the department where the CIC is implemented, using standardized
tools to identify strengths and opportunities for clinical teams in regard to
quality of care and ‘partnership-oriented’ practices.
Phase C: Definition of goals for
quality Improvement
During
the CQI second meeting, members comment on the report, make recommendations,
and are invited to submit their suggestions for improvement based on their
experience within the team and on principles of healthcare partnership.
Phase D:
Implementation of action
The
CQI carries out the processing activities described in the action plan. A third
meeting is held six to eight weeks after the second meeting of the Committee,
to ensure monitoring and follow-up of activities. The specific topics covered
include: input from a resource patient, distribution of tasks, work progress,
inclusion of healthcare partnership dimensions, and coordination between
members.
Phase E:
Assessment of the impact of actions and preparation
of a new cycle of improvement
In
a time frame of eight to ten weeks following the CIC's third meeting, the team
pursues and completes its transformation activities. Four months after the
first meeting (phase B), a fourth meeting of the committee is held to assess
achievement of goals and share members’ comments on their experience in the
committee, in a focus group format. Topics covered during this assessment
include: facilitating factors (conditions promoting strong inclusion of
patients in the committee); obstacles encountered during this cycle and how they
have been addressed; learning acquired; direct and indirect impacts of the
project; participants’ satisfaction and opportunities for improvement. At the
end of the cycle, an official certificate of acknowledgment of the team’s
achievement is handed out in recognition of members’ work and as an incentive
to continue with improvement cycles. In addition, preparation for the following
cycle is initiated.
Contribution of patients to the teams
All
the patients perceived CIC as a structured entity that was not demanding and
was centered on the search for practical solutions, mainly to improve
communication with healthcare professionals through the development of simple
and effective tools. They also found that the participation of professionals in
this process of continuous quality improvement led to a better understanding of
patients’ expectations and highlighted the interdependence of various
professionals within a given situation. The most valuable thing that patients
got from participating in the CIC was sharing their vision and experiences
regarding the care process and having them taken into account in various ways.
Learning Acquired by Patients
The
main learning acquired by patients concerned their personality and behavior, in
addition to learning about their disease and care procedures employed. Their
participation also allowed them to improve their communication with
professionals.
Challenges of participation
The
main barrier to participation noted by all patients was the time factor.
Indeed, they commented not only on the difficulty in finding time for the
activities but also on the slowness of decision-making in healthcare
facilities.
Outcomes of quality care through patient participation
The
outcomes related to quality care include a reduction in Mortality rate,
Readmission rate, Length of stay, Hospital acquired infection rate; improved
adherence to treatment regimes; decreased adverse events; reduced operating
costs and decreased malpractice claims. It also optimizes self-management of
patients with chronic illness and improve patient adherence to health care
practices.
Conclusion
The
aim of this study is to gain an understanding of patients’ experience as
partners in quality improvement committees, by presenting their perceptions of
their contribution to quality teams, of their learning, and of the challenges
encountered during the process.
It
is interesting to note that, although patients had different healthcare
experiences and came from different health facilities, there were no
significant differences in their perceptions, which led to reaching theoretical
saturation quickly. However, a limitation of this study is that it focuses only
on patients' perceptions.
Written by:
Shipra
Damir
Senior Advisory of Ingenious Healthcare Consultants Pvt. Ltd.
Director
of Society for Hospital Administrators
B.
Pharm, MBA in Pharmacy Business Management, Industry Integrated Diploma in
Pharma Management, MBA in Hospital Administration, B.Ed
That's so true!
ReplyDeleteThank you so much for sharing this with everyone
I really appreciate you making time and guiding everyone in the right direction
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