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Evaluating Healthcare Simulation Escape Rooms as an Educational Tool in Nursing Continuing Education: A Fellowship Journey

Posted on December 16, 2024 by admin

By: Brennah Holley

Fellowship Overview

Brennah Holley, Clinical Nurse Educator at CHEO in Ottawa (and former Co-Chair of the POGO Nursing Committee), recently completed an Advanced Clinical Practice Fellowship (ACPF) through the Registered Nurses Association of Ontario and is now conducting an exciting research project (directly related to her fellowship) to explore the potential of Healthcare Simulation Escape Rooms (HSER) as an innovative educational tool in nursing. With the nursing profession facing pressing challenges such as staffing shortages and varied learning needs, her research aims to assess whether HSERs can enhance knowledge acquisition among nursing staff.

“HSERs merge gamification with traditional learning, creating engaging team-based experiences,” Brennah explains. As defined by Anderson et al. (2020), HSERs infuse healthcare themes into interactive escape room settings, offering a fresh platform for education and assessment.

Research Objective and Methodology

At the heart of Brennah’s research is the objective to evaluate HSERs’ effectiveness in nursing education. The study, which began in early 2024, will investigate whether engaging in an HSER focused on anaphylaxis leads to better knowledge retention and application compared to traditional lecture formats.

In a randomized controlled trial, nurses at CHEO will be divided into two groups: Group A will receive a lecture, while Group B will experience both the lecture and the HSER. “This approach allows us to gather vital data on the impact of immersive learning,” she notes.

Learning Experience and Skill Development

Brennah’s journey through the fellowship has been rich with learning. She acquired essential skills in research design, ethics submissions, and statistical analysis. Working alongside the Clinical Research Unit (CRU) at CHEO, she navigated the complexities of ethics applications, completing necessary training and developing vital documentation like consent forms.

Addressing knowledge gaps in statistical analysis was a significant focus for Brennah. By collaborating with a co-investigator from CHEO’s CRU, she enhanced her research capacity. “This partnership has been instrumental in refining my project,” she emphasizes.

Brennah also developed her skills in survey design and literature reviews, both critical for creating effective educational tools.

Some of Brennah’s students showing off their excellent escape room skills in the nursing lab.

Outcomes and Future Directions

Data collection for her research will extend until early 2025, with plans to draft a manuscript by fall 2025. The implications of Brennah’s research could be profound, providing evidence to support the integration of HSERs into nursing curricula and continuing education programs. “Ultimately, we want to enhance patient care through improved educational strategies,” she states.

Reflections

Reflecting on her ACPF experience, Brennah describes it as transformative, filled with opportunities for professional growth. Presenting at international conferences and collaborating with nurse educators worldwide have enriched her journey. As she begins her master’s in Nursing, she is eager to further explore innovative educational methodologies, with HSERs leading her efforts to improve nursing practice.

In summary, Brennah Holley’s fellowship at CHEO highlights the promise of innovative educational approaches in nursing, paving the way for advancements in continuing education and enhanced patient care.

“We are on the brink of a new era in nursing education,” she concludes, optimistic about the future.

To learn more about Brennah’s fellowship experience or research endeavours, feel free to reach out to her.

Posted in Nursing Newsletter | Tagged Nurses, nursing, nursing newsletter, pediatric oncology nursing

Premier Ford and Minister Jones join POGO to launch new roadmap to strengthen Ontario’s world-class childhood cancer care system

Posted on September 23, 2024 by admin

Ontario’s new five-year Childhood Cancer Care Plan, produced by the Pediatric Oncology Group of Ontario (POGO) and its partners, builds on strong, province-wide coordination to deliver wrap-around care and support for children, youth, survivors and families at every step of the childhood cancer journey.

September 23, 2024, Toronto, ON – Premier Doug Ford and Minister of Health Sylvia Jones recently joined POGO to launch the Childhood Cancer Care Plan: A Roadmap for Ontario 2024-2029. Published by POGO and its partners, the Plan leverages strong collaboration and coordination across the province to ensure wrap-around care and support for children and youth with cancer, survivors and families at every step of the childhood cancer journey.  With support from the Government of Ontario, this new roadmap will continue to strengthen the province’s world-class childhood cancer system.

“Unfortunately, too many families here in Ontario are faced with the harsh reality of childhood cancers,” says Premier Doug Ford. “It’s a terrible disease that impacts not just the children, but their entire family. We’re incredibly grateful for the outstanding work that POGO does to support these families, ensuring they have access to the care they need, when and where they need it.”

“We thank POGO for your dedication, for your leadership and collaboration, for everything you do to support children and their families facing a cancer diagnosis,” says Health Minister Sylvia Jones. “I look forward to our continued work to ensure families have access to the best possible treatment and care throughout their journey.”

POGO works to ensure that everyone affected by childhood cancer has access to the best care and support. Informed by diverse voices from across the childhood cancer community, the Plan has priorities which focus on bringing care closer to home, ensuring survivor well-being, harnessing data, improving access to drugs and therapies, and enhancing the availability of mental health and financial supports for families.

Sam Taylor’s daughter, Ellie, was diagnosed with rhabdomyosarcoma, a soft tissue cancer, at age 10.  “Shortly after Ellie’s diagnosis, we were connected with a POGO Interlink Nurse, an invaluable resource who guided us through the hospital system and helped us understand the unfamiliar world of childhood cancer,” says Sam Taylor. “Through her visits to our home and Ellie’s school, we knew we were in good hands. And when the time was right, the nurse helped us with the transition to care closer to home at the POGO Satellite Clinic at our local community hospital. This meant more time for Ellie with her friends and brother and a lot less time on the road. The POGO Satellite quickly became a second home for our family—an inviting place with an incredible staff where Ellie felt safe and relaxed, and where we, as her parents, felt reassured that she was receiving the best possible care.”

“Ontario’s childhood cancer care system is considered one of the best in the world, and we have the opportunity to make it even better by addressing current challenges and thinking ahead to navigate future demands,” says James Scongack, Chair of the POGO Board of Directors. “On behalf of POGO and our partners, I want to thank the Government of Ontario for its support, and its commitment to improving the lives of thousands of kids and families across Ontario dealing with this devastating disease.”

“There is exceptional pride in the quality and accessibility of Ontario’s childhood cancer care system. This is made possible by a shared vision of excellence across our incredible community,” says Lauren Ettin, Chief Executive Officer of POGO. “Working together, we can continue building on our collective success, so that children and youth with cancer, survivors and families can count on having the treatments, resources and supports they need, now – and for life.”

Download and share the Childhood Cancer Care Plan: A Roadmap for Ontario 2024-2029.

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About Pediatric Oncology Group of Ontario (POGO)

Pediatric Oncology Group of Ontario (POGO) works to ensure that everyone affected by childhood cancer has access to the best care and support. We partner to achieve an excellent childhood cancer care system for children, youth, survivors, and their families and healthcare teams, in Ontario and beyond. POGO champions childhood cancer care, and as the collective voice of this community, is the official advisor to Ontario’s Ministry of Health on children’s cancer control and treatment. POGO is a non-profit organization with charitable status, here for kids with cancer, for now, for life.

Media Contact
Jacqui DeBique
Senior Manager, Communications
Pediatric Oncology Group of Ontario (POGO)
416-592-1232 ext. 266

Posted in In the News | Tagged Cancer Plan, childhood cancer care plan, Doug Ford, Government of Ontario, press release, Southlake Regional Health Centre

Childhood Cancer is a Lifelong Journey

Posted on September 17, 2024 by admin

Appearing in Metroland publications, September 17, 2024

While more kids are being diagnosed with cancer, more are surviving. Ontario’s childhood cancer survival rate is now 85 per cent — up from about 70 per cent in the mid-1980s. And while surviving cancer is certainly the goal, the impacts of childhood cancer can last a lifetime.

Richard Lautens Toronto Star file photo


By Lauren Ettin and Dr. David Hodgson

Lauren Ettin is the chief executive officer of the Pediatric Oncology Group of Ontario. Dr. David Hodgson  is the medical director and chair in childhood cancer control for the Pediatric Oncology Group of Ontario, a radiation oncologist and clinician scientist at the Princess Margaret Cancer Centre, and associate staff at The Hospital for Sick Children.

Life for the Pugliese family changed forever when six-year-old Giacomo was diagnosed with acute lymphoblastic leukemia. For three years, they made countless trips to McMaster Children’s Hospital, watching their once-energetic little boy endure the challenges of cancer treatment, with interruptions to school and play dates.

Now 17, Giacomo’s treatment is behind him, but he is monitored regularly at the Pediatric Oncology Group of Ontario (POGO) AfterCare Clinic at McMaster Children’s Hospital for secondary cancers and heart issues — risks from his cancer and treatment. The clinic staff also emphasize the importance of a healthy, active lifestyle. His family is reassured that Giacomo will receive this crucial care for the rest of his life.

POGO’s network of clinics across Ontario play a vital role in the ongoing care of childhood cancer survivors, becoming an essential part of their lifelong health journey.

September is Childhood Cancer Awareness Month, a time to spotlight stories like Giacomo’s, which are increasingly common in Ontario.

While more kids are being diagnosed with cancer, more are surviving. Ontario’s childhood cancer survival rate is now 85 per cent — up from about 70 per cent in the mid-1980s. This is thanks to decades of clinical innovation, improvements in diagnostics and treatments, and approaches to addressing some of the related side effects.

While surviving cancer is certainly the goal, it is not where the journey ends. The impacts of childhood cancer can last a lifetime.

Childhood cancers are distinct from adult cancers in significant ways. For one thing, these cancers don’t result from lifestyle or diet. They come suddenly — and some are more likely to strike at a specific age. Typically, childhood cancers require intensive treatments, at major teaching hospitals, with highly specialized protocols. Consequently, care teams may be larger and include parents and caregivers as key decision makers.

A childhood cancer diagnosis impacts the whole family. One parent is often forced to give up work to manage the daily practicalities of their child’s care. Often, extensive travel or temporary relocation is required, uprooting families for months or sometimes years. This disruption reverberates, impacting extended family members, friends, teachers, classmates, work colleagues and communities.

Childhood cancers strike during a critical phase of development, when children and adolescents are marking key physical, mental and social milestones. As a result, two of every three survivors are at increased risk of at least one long-term side effect resulting from their cancer or its treatment, including heart disease, second cancers and cognitive challenges.

To address the unique complexities, ripple effects and long-term impacts of childhood cancer, POGO and its partners have built a system that provides wraparound care and support for children and families at every stage of the journey. Considered among the best in the world, Ontario’s childhood cancer system goes beyond diagnosis and treatment. Families are paired with nurses who help navigate the transition from hospital to home, and they can also access mental health services, financial supports, and programs that help survivors thrive into adulthood.

During Childhood Cancer Awareness Month, it’s important to recognize the tremendous progress made in childhood cancer care. But there is more we can do to ensure kids not only survive, but thrive.

It is vital that children with cancer and their families have access to the best evidence-based treatments and supports, closer to home. This requires strong, ongoing collaboration between care teams, hospitals, nonprofits, government, regulatory bodies, industry and others.

Over the past decade, we have also seen an increasing need for mental health services, a need that is urgently felt among the many who are impacted by a childhood cancer diagnosis. These priorities and others will be key components of Ontario’s Childhood Cancer Care Plan 2024-2029, a road map developed by POGO and its partners to be published later this month.

Ontario must continue strengthening its world-class childhood cancer system so that survivors like Giacomo can count on having the treatments, resources and supports they need today — and for life.

Posted in In the News | Tagged CCAM, CEO, Chief Executive Officer, childhood cancer awareness month, Childhood Cancer Survivor, Medical Director, patient care, Survivor Care, survivorship

POGO CEO Lauren Ettin Makes the Rounds

Posted on September 9, 2024 by admin

Since Lauren Ettin joined POGO as Chief Executive Officer in April 2024, she has been making the rounds, becoming familiar with the inner workings of POGO programs and services at our partner hospitals, and the unique nature of childhood cancer care and Ontario’s childhood cancer care system. Here’s what she shared.

Q: How has your experience and background prepared you for your new role at POGO?

Lauren: My career has been in health care across all sectors: public, private and not-for-profit, with the same vision of always improving the delivery of care for all Ontarians. I’ve worked in the Ontario government, consulting, in an association and led a not-for-profit.

My last role was my first in pediatrics and I was really struck that children are not little adults; delivering care for kids is distinct and unique. In Ontario, we have a remarkable childhood cancer care system—an actual cohesive system—established by visionary leaders and recognized as a national, if not international, leader in the healthcare field.


Q: In the last four months, you have spent a lot of time getting to know POGO’s partners and our various stakeholders. Why was it important to spend so much time in the community?

Lauren: In pediatric cancer, there are so many different lenses and perspectives. It was really important for me to spend time meeting our partners, building relationships with people and understanding their experience and vision for the system; where they see our collective strengths and opportunities—and then bringing that all back to inform POGO’s work and priorities.

There is exceptional pride in the quality and accessibility of Ontario’s childhood cancer care system. At POGO, we have an opportunity to build on our ability to bring people together to learn from each other, and plan, execute and spread in scale together—not only to other parts of Ontario’s healthcare system, but around the world.

Q: Describe what has stood out for you in your short time at POGO.

Lauren: What stands out most is how we put children and family at the centre of care, knowing a childhood cancer diagnosis impacts the child but reverberates more broadly. And the interprofessional healthcare teams are experts in supporting individual patients from diagnosis and treatment to survivorship, and sometimes, unfortunately, to end of life. POGO’s programs address their physical medical needs, but also their mental health and personal needs.

POGO also collects data on every child diagnosed to inform system planning. The research we do and the clinical practice guidelines we develop translate into better care and improved outcomes.

What’s more, we have incredibly supportive donors who share our vision for children’s cancer care in the province.

This all makes POGO incredibly unique.

Q: September is Childhood Cancer Awareness Month. What do you want people to know or understand about childhood cancer in Ontario?

Lauren: Over the past 50 years, there have been dramatic improvements in childhood cancer care and fewer kids are dying of cancer. Today we expect approximately 85% of children who are diagnosed to be long-term survivors due to things like research and clinical trials. Still, with all this good news about increase in survivorship, cancer is still the most common disease-related cause of death in children over the age of 1 year.

Also, it is important to note that two of every three childhood cancer survivors are at risk of a late effect due to their cancer or its treatment, like second cancers or cognitive challenges. While surviving cancer is certainly the goal, it is not where the journey ends. The impacts of childhood cancer can last a lifetime.

Q: POGO will soon release a new Childhood Cancer Care Plan, developed in consultation with a wide range of stakeholders. What are two or three things that made a strong impression on you as you stepped into your role and worked to bring the Plan to completion?

Lauren: To address the unique complexities, ripple effects and long-term impacts of childhood cancer, POGO and its partners have built a system that provides wrap-around care and support for children and families at every stage of the journey. One of the things we heard from the consultations is that we’re on the right path with opportunity for improvements, and the way to execute on the Childhood Cancer Care Plan is for all our partners, within their different roles, to work together to move the Plan’s goals and objectives forward.

Q: With all that you’ve seen and heard through your rounds what are you most excited about?

Lauren: I’m excited to build on POGO’s collaboration with current and new partners; to convene leaders and focus our attention on making tangible improvements in care that are aligned to the goals and objectives in the next Childhood Cancer Care Plan. I feel strongly that our intentional efforts are sure to reap great rewards. Ontario can continue to strengthen its world-class childhood cancer system so that patients and survivors can count on having the treatments, resources and supports they need today – and for life.

Related Content

POGO Welcomes New CEO, Lauren Ettin

Posted in In the News | Tagged CEO, childhood cancer awareness month, Interview, Lauren Ettin, POGO CEO, Q&A

Study Examines Late Effects and Treatment Protocols for Hodgkin Lymphoma in Children 

Posted on April 3, 2024 by admin

Childhood cancer and its treatment come at a risk of late effects for survivors. In fact, the evidence shows that two of every three childhood cancer survivors are at increased risk of at least one late effect due to their cancer or its treatment, including heart disease, second cancers and cognitive challenges.  

A recent study published in JAMA (The Journal of the American Medical Association) looks at the treatment of Hodgkin lymphoma in children and the resulting risk of cardiac disease to survivors.  

POGO Medical Director, Dr. David Hodgson, is the lead author of the study titled Late Cardiac Toxic Effects and Treatment Protocols for Hodgkin Lymphoma in Children. 

“Cardiac disease as a late effect of treating Hodgkin lymphoma is a serious risk that is well documented,” he says. “One of the challenges of improving treatment is that we don’t want to wait for over 20 years to observe the late effects of treatments we’re currently giving today. The goal of this study was to estimate the risk of late effects of current treatment to better understand how to advise current patients and families, and also explore what changes to treatment would have the greatest benefit to reduce these risks.” 

Understanding the extent to which treatment can be modified for improved health outcomes is critical for several reasons. 

  • Reducing treatment intensity is a trade-off against the risk of relapse. 
  • Understanding which components of treatment can be adjusted, and to what extent, can lead to better decisions about treatment modifications. 
  • Care for survivors is based on their treatment exposure making the burden of follow-up care an important consideration. 

The study evaluated the treatment of 2,563 patients with Hodgkin lymphoma treated in four consecutive Children’s Oncology Group clinical trials between 2002 and 2022. Patients were treated with different doses of radiation therapy and doxorubicin chemotherapy – both of which are known to increase the risk of cardiac late effects.  Based on the doses of these treatments, the 30-year cumulative incidence of severe or life-threatening heart disease was estimated to decrease from 10% in the first trial to 6% in the last trial. The findings were favourable, suggesting that evolutions in treating Hodgkin lymphoma will lead to a net reduction in late cardiac disease. Moreover, findings suggest that for adolescent and young adult patients, increasing the use of “cardioprotective” medications during treatment would be one of the best ways to reduce this risk further, without compromising cure rates. 

“While there is still work to be done to monitor the long-term gains in reducing cardiac toxic effects, this is encouraging news that bodes well for the quality of life of childhood cancer survivors,” says Dr. Hodgson. “And, as with every study, we need to ensure that the guidelines for follow-up care of survivors, particularly in POGO AfterCare Clinics, are updated to reflect the latest evidence.” 

Read the study here.

Related Content

Survivor Care – POGO
Childhood Cancer Care Plan


Posted in Research | Tagged Cardiac Disease, Childhood Cancer Survivor, Hodgkin Lymphoma, POGO Research

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