Tag Archive for: endometrial cancer care

What Are Barriers to Endometrial Cancer Care Access?

What Are Barriers to Endometrial Cancer Care Access? from Patient Empowerment Network on Vimeo.

How can endometrial cancer care access be obstructed by barriers? Expert Dr. Charlotte Gamble from MedStar Health discusses common barriers to care and patient advice to overcome some barriers.

[ACT]IVATION TIP

“…rely on the support that you have in your own lives to make sure that all the barriers that are in your control you can properly address and sometimes that takes a village and to really make sure that you have an advocate either a family friend, or a family member who could help get you and navigate you through this cumbersome process.”

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See More from [ACT]IVATED Endometrial Cancer

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Advancements in Endometrial Cancer Trials: Insights and Opportunities

Advancements in Endometrial Cancer Trials | Insights and Opportunities

Should Some Gynecologic Cancer Patients Seek a Specialist?

Should Some Gynecologic Cancer Patients Seek a Specialist?

Are Beauty Products a Risk Factor for Endometrial Cancer?

Are Beauty Products a Risk Factor for Endometrial Cancer?

Transcript:

Lisa Hatfield:

Dr. Gamble, can you speak to barriers to accessing care in endometrial cancer? 

Dr. Charlotte Gamble:

Absolutely. What I’ve seen from some of my research, both with myself as well as with Kemi Doll, when we talk to patients and speak to them about what are the issues they face into getting timely gynecologic oncology care, it’s a myriad of factors. So there are some barriers at different levels. So patients themselves face barriers in their own lives where they might not understand the symptoms of endometrial cancer, which oftentimes are a postmenopausal bleeding, or sometimes bloating, or pelvic fullness, and sometimes are really busy doing other things in their lives that they can’t prioritize their own health and kind of ignore some of the symptoms.

And so knowledge gaps are a barrier. And the logistics sometimes of making it to a doctor’s office or their provider’s office can oftentimes be challenges that patients might face in their own lives. However, a lot of my concern also comes to the provider level barriers where sometimes when patients are legitimately concerned, rightfully so, with symptoms they might be having, oftentimes the health system might ignore their symptoms.

And so they might run into barriers when they actually try to call and schedule an appointment with their gynecologist or with their primary care doctor discussing symptoms, and they might be told that this doctor doesn’t have availability for the next three to four months, come and see us in August, which presents a whole set of delays that the patients face. And this might be somebody that’s an administrator for the office, the front desk staff that just might not have the insight to be able to escalate that concern upwards.

Additionally, what we see is that sometimes when patients come to their providers with these concerns, the providers themselves might not have the knowledge area or the level of concern to meet that need that patients have. And so sometimes can misdiagnose patients or not get a timely workup in place. And that’s something that the health community I think, needs to work on as well. And lastly, the health system is messy. We have a messy health system in the United States and lots of fragmentation and care.

And so the process, even when somebody appropriately raises a concern to their primary provider, gets the appropriate workup, gets a diagnosis, sometimes it’s actually very difficult for them to get that referral and make it to the oncologist or the subspecialist’s office in a timely fashion. And some of that, you know, some of my research right now goes into how can the health system be better about coordinating and helping patients navigate what is a very burdensome and cumbersome health system. So barriers are at several levels. They’re at the patient level, they’re at the organizational level, they’re at the health system level. Ranging all the way from, I didn’t know that this could be a problem, this symptom I’m experiencing, to, I don’t have the correct type of health insurance to be able to cover the subspecialty care that I now need.

 
And so all of these range and pose like challenges for us to address as health system advocates and patient advocates as we kind of try to address these barriers. My activation tip for this question is to really rely on the support that you have in your own lives to make sure that all the barriers that are in your control you can properly address and sometimes that takes a village and to really make sure that you have an advocate either a family friend, or a family member who could help get you and navigate you through this cumbersome process.

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Innovative Approaches to Endometrial Cancer Care in Underrepresented Communities

Innovative Approaches to Endometrial Cancer Care in Underrepresented Communities from Patient Empowerment Network on Vimeo.

How can endometrial cancer care use innovative approaches in underrepresented communities? Expert Dr. Emily Hinchcliff from Northwestern Medicine discusses diagnostic testing tools and support in navigating clinical trials.

[ACT]IVATION TIP

“… doing your own research and your own reading is really important, being your own advocate. But I think that your physician can serve as an excellent, almost medical translator to understand what is right for you and which of the many, many novel things that we are discovering every day is applicable to you and which might be good for you and which don’t actually apply or which are not potentially your best option in that side.”

Download Guide | Descargar Guía en Español

See More from [ACT]IVATED Endometrial Cancer

Related Resources:

Overcoming Geographical Barriers in Endometrial Cancer Care

Overcoming Geographical Barriers in Endometrial Cancer Care

Overcoming Barriers: Empowering Underrepresented Groups With Endometrial Cancer

Overcoming Barriers: Empowering Underrepresented Groups With Endometrial Cancer

Endometrial Cancer Care Disparities | The Impact of Rural Residence

Endometrial Cancer Care Disparities: The Impact of Rural Residence

Transcript:

Lisa:

Dr. Hinchcliff, are there any innovative approaches or technologies that you and your team are exploring to improve endometrial detection, treatment, or support services, especially for your underrepresented communities with limited access to healthcare resources?

Dr. Emily Hinchcliff:  

Yeah, so there are many, many different things that we’re doing here that we’re very excited about. I think I’ll probably highlight two. So one of the ones that I have been working on closely is there is an ever-increasing number of diagnostic testing tools that we have within our kind of armamentarium. And so one particular test that patients may have read about or heard about is something called circulating tumor DNA. And this is a pretty novel test that I will be completely open and honest that we don’t totally know how to use or how to incorporate in our cancer surveillance, meaning so once someone is diagnosed,  is this a test that can help us to watch to see if treatments are working or watch to see if a cancer may have come back? Similarly, can it be used as a screening tool? We just don’t know that, and so that’s an area that I am actively working in.

The other thing that one of my colleagues here is working on is trying to really create access for women who have limited access to healthcare. So we have developed a clinical trial platform to allow the women, specifically of Chicago, to better understand their options for clinical trials across the institutions in Chicago. So we have at Northwestern multiple cutting-edge endometrial cancer trials trying to bring these novel therapeutics to the forefront and to patients and also to thoughtfully triage patients to kind of treatments that we think are going to maximize their effectiveness and minimize toxicity.

But similar to us, the other institutions around Chicago have a different panel of clinical trials. And so for patients, it can be really overwhelming to know which trial, which institution, how do I know, how do I access all of that? And so we’re working to create a platform for patients and to have clinical navigators associated to help them to understand their options.

Lisa:

And do you have an activation tip?

Dr. Emily Hinchcliff:  

So I think that when patients are thinking about innovation and how can they make sure that they are at the cutting edge, I think that your physician is really your access point. So obviously, doing your own research and your own reading is really important, being your own advocate. But I think that your physician can serve as an excellent, almost medical translator to understand what is right for you and which of the many, many novel things that we are discovering every day is applicable to you and which might be good for you and which don’t actually apply or which are not potentially your best option in that side.


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Overcoming Geographical Barriers in Endometrial Cancer Care

Overcoming Geographical Barriers in Endometrial Cancer Care from Patient Empowerment Network on Vimeo.

How can endometrial cancer care barriers be overcome in regards to geographic location? Expert Dr. Emily Hinchcliff from Northwestern Medicine discusses geographic care barriers, solutions, and patient advice to be proactive in their care.

[ACT]IVATION TIP

“…understanding that post-menopausal bleeding is never normal and that you need to see a physician for that…regarding the fact that accessing care can be, as you mentioned, done in many, many different ways these days. And so understanding what your options are, whether that’s telehealth, whether that’s a consult visit and then receiving the majority of the subsequent care closer to home, you have a lot of options.”

Download Guide | Descargar Guía en Español

See More from [ACT]IVATED Endometrial Cancer

Related Resources:

Which Endometrial Cancer Clinical Trials Are Showing Promise

Which Endometrial Cancer Clinical Trials Are Showing Promise?

Understanding Endometrial Cancer Risk: Factors Influencing Incidence and Mortality

Understanding Endometrial Cancer Risk: Factors Influencing Incidence and Mortality

Endometrial Cancer Care Disparities | The Impact of Rural Residence

Endometrial Cancer Care Disparities: The Impact of Rural Residence

Transcript:

Lisa:

If a woman goes in and is diagnosed at her local cancer center and has endometrial cancer, should she see some type of subspecialist, would it be of benefit to that patient maybe to even do a consult, a telemedicine consult at least upon diagnosis? Or how can a person who is more remote geographically access a subspecialist care or expertise?

Dr. Emily Hinchcliff: 

Yeah, absolutely. So I think that telehealth has really changed medicine in general and provides some really great opportunities for access. There is a big kind of dichotomy in endometrial cancer where early stage disease is often caught because it has a symptom, vaginal bleeding is a symptom. And so early stage disease can often be treated with surgery alone.

And so that surgical management, again, can potentially be done by a GYN oncologist at a one single time point. The subsequent care, so I’ll just use myself as an example. I will often see women for sort of that initial visit, treatment decision, sometimes surgery, but then if they need additional adjuvant therapy, such as chemotherapy, they’ll go closer to home to receive some of those therapies. And then I will serve as a bit of a consultant to their providers closer to home to discuss what treatment options, what regimens and how to manage toxicities might be good in their case.

Lisa:

And do you have an activation tip for patients for that question?

Dr. Emily Hinchcliff:  

Yeah, so I think that my activation tip here regarding barriers to endometrial cancer care is first and foremost addressing the knowledge gap, understanding that post-menopausal bleeding is never normal and that you need to see a physician for that, I think is the first key tip. The second tip, I guess, if I could give a second activation tip, is regarding the fact that accessing care can be, as you mentioned, done in many, many different ways these days. And so understanding what your options are, whether that’s telehealth, whether that’s a consult visit and then receiving the majority of the subsequent care closer to home, you have a lot of options. And we as a field in GYN oncology are really collaborative. And I think most of us would feel very positively towards creating a team to help you get the care you need.


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