Digital and digital non-clinical solutions

➡️What will be the digital and digital non-clinical solutions for people with cancer in the future 🧐
This post aims to consider some possible digital solutions to bring medical resources and information to patients in the future.

➡️📱Mobile Apps: Mobile cancer apps can play a crucial role in patient education, symptom management and treatment monitoring.
These apps could provide information about cancer, medications, side effects, proper diets, as well as reminders for medications and medical appointments.

➡️⌨️Connected objects and wearables:
Wearable devices such as smart watches, bracelets and monitoring sensors could be used to monitor the vital signs of cancer patients in real time.

➡️Artificial Intelligence
(Al) and Data
Analytics: Al can be used to analyze large amounts of medical data and help identify patterns, correlations and predictions. This could contribute to a better understanding of risk factors,
treatment responses and patient
outcomes.

➡️Virtual Reality (VR):
Virtual reality can be used to help cancer
patients manage pain, anxiety and stress. Calming and interactive virtual environments can be created to distract patients during medical treatments or to help them relax during difficult times

For more just read: E-Health4Cancer : Sharing good practices in the use of nonclinical e-health solutions for cancer patients and their caregivers in Europe. Non-profit Organizations

https://www.linkedin.com/company/ehealth4cancer/

WHO/Europe explores collaborations to improve quality of health information online

The WHO Office on Quality of Care and Patient Safety in Athens recently joined forces with YouTube Health to host a workshop in Berlin to enhance the quality of health information online and support Member States’ efforts in this area. This collaborative endeavour lays the groundwork to promote health literacy and make high-quality health information universally accessible.

“We are very much looking forward to working together for a world where people can access the health information they need online without having to guess its accuracy,” noted Dr Natasha Azzopardi-Muscat, Director of WHO/Europe’s Division of Country Health Policies and Systems, at the workshop.

The role of digital platforms in health

The COVID-19 pandemic brought into the spotlight the prominent role of digital platforms in disseminating health-related information and the importance of reliable information, while also exposing the potential perils of misinformation and disinformation. Data indicates that, in the WHO European Region, a large share of consultations now take place online, as people’s initial approach is to search for symptoms and medical advice online. Health-related searches make up 7% of daily online searches, with approximately 4 billion results related to COVID-19.

In 2021, YouTube had over 110 billion views of health condition videos globally and is working on raising high-quality health content to make it easier for people to identify credible information that can help answer their questions. Commenting on the platform’s impact in the online space, Dr Nira Goren, Clinical Lead at YouTube Health, said, “People use platforms like YouTube to seek answers to questions, such as how do I live with breast cancer or how do I take care of myself.” An increasing number of individuals are also turning to online platforms to share personal stories, alleviate acute distress, and build a community to help decrease feelings of isolation.

However, online health information that is inaccurate or misleading can pose a significant risk to one’s health. A recent WHO review showed that infodemics and misinformation negatively affect people’s health behaviours. The distorted understanding of health hazards, such as smoking, alcohol intake, unhealthy eating habits, or physical inactivity, can result in various life-altering and potentially fatal noncommunicable diseases (NCDs), such as cancer or diabetes.

Empowering health through high-quality health information online

High-quality health information can empower individuals to take control of their health, make informed decisions about their treatment options, and improve their overall well-being and quality of life. With more and more people relying on the internet for medical advice, it is essential that the information available is reliable, accurate, easy to understand, and up-to-date. Collaboration with health care stakeholders in Member States across the Region is needed to ensure this. It also requires fostering inclusive partnerships that bring together patients, health care professionals, ministries, nongovernmental organizations, and major social media platforms.

“Social media platforms are crucial tools to improve and disseminate high-quality health information online and we should work on that together, involving everyone in this process. Our primary focus should be to actively listen to community concerns, promote understanding of risk and health expert advice, engage and empower communities to take positive action, and support health professionals and

Moreover, fostering trust in authoritative online health information sources at the population level entails working with academia and other partners to create further scientific evidence on the impact of misinformation on quality of care, acting as a lighthouse in consolidating the creation of scientific evidence.

“Empowering communities with education is essential to helping people live healthier lives. YouTube Health is delighted to interact with WHO and authoritative health sources across Europe to increase access to evidence-based, equitable and engaging health information,” noted Dr Garth Graham, Director and Global Head, Healthcare and Public Health, YouTube.

Πηγή: who.int

How A.I. Could Help Medical Professionals Spend Less Time on Admin Work and More Time on Care

Some entrepreneurs are betting that generative A.I. tech like ChatGPT can provide a solution to the medical industry’s burnout crisis.

A survey of 1,000 Americans and 500 health care professionals conducted by Tebra–an all-in-one digital platform used by medical providers to manage their practices–showed that one in 10 providers is currently using A.I., while 50 percent of surveyed respondents signaled an intention to adopt the tech in the future, particularly in use cases involving data entry, appointment scheduling, and medical research.

Luke Kervin, Tebra’s founder, says that if A.I. can help providers to stave off burnout by increasing efficiency, saving costs, and allowing them to spend less time on admin work and more time helping people, it will likely see mass adoption by the industry. “When we talk to our providers about what keeps them up at night, it’s always burnout,” adds Kervin, “and a lot of that burnout comes from having so much admin work to do.”

Ironically, the advent of electronic medical records (EMRs) was meant to help physicians save time that had previously been spent maintaining analog health charts, but some practitioners are now spending an increasing amount of time behind the computer. Indeed, a 2017 study published in the Annals of Family Medicine found that in an 11.4-hour workday, physicians spent an average of nearly six hours on tasks related to administrative tasks, like data entry and inbox management, which contributed to their burnout.
Some solutions are already available, such as from Microsoft-owned A.I. business solutions provider Nuance. According to a case study, physicians at the Nebraska Medicine health system were frustrated with the time and effort required to complete patient notes, so Nuance provided an A.I.-powered voice recognition solution, allowing providers to fill out notes using just their voice. The change was a success, with 94.2 percent of surveyed physicians saying that the tech helped them to save time and do their job better.

Another company working on A.I.-powered solutions for both providers and patients is New York-based mental health employee benefits company Spring Health, which has raised nearly $400 million and attained a $2.5 billion valuation since its 2016 founding. Once a client has signed up for the service, they fill out a short assessment containing a series of questions about both their medical history and the current state of their mental health. The company’s machine-learning algorithm then crafts a personalized care plan that includes both wellness recommendations like daily routines, and specific recommendations for nearby mental health care providers.

Spring Health co-founder Adam Chekroud says that they’ve barely begun to scratch the surface of how automation could improve business for health care providers, adding that the company recently rolled out a new functionality that enables providers to “translate” their shorthand notes from patient meetings into full sentences with the use of a large language learning model.

Chekroud is also excited about the possibility of integrating chatbots as a way of helping people find providers who are a perfect fit for them, and described one prototype in development. “Our chatbot could ask, ‘Is there anything you want us to know that would help us find you a provider?’” According to Chekroud, the patient could answer with something like, “I’m very religious and I want a provider who could do faith-based treatment” or “I’m going through some gender identity issues and I want to have a provider that understands that.” The chatbot would then scan through the Spring Health network to surface providers with those desired traits.

A small number of providers are even beginning to use A.I. to help them make diagnoses by using tools such as Med-PaLM, Google’s large language model for medical information. But when it comes to using chatbots as virtual therapists, Chekroud is much less convinced. He concedes that generative A.I. is surprisingly capable of imitating empathy, “but we still have this fundamental problem that you’re talking to a robot. A robot can’t know what you’re going through. Nothing can replace that human connection.”

Πηγή: inc.com

The Economics of Health for All and the Transformative Power of the Arts

In the first-ever report of its kind, the WHO Council on the Economics of Health for All has outlined a bold new path to reorient economies to deliver what matters – health for all.

The Council has put forward a bold new narrative grounded in new economic wisdom to reorient economies to deliver health for all across four interrelated themes:

  1. Value – valuing and measuring what matters through new economic metrics;
  2. Finance – how to finance health for all as a long-term investment, not a short-term cost;
  3. Innovation – how to advance health innovation for the common good;
  4. Capacity – how to strengthen dynamic public sector capacity to achieve health for all.

Meet the new WHO Goodwill Ambassadors for Arts and Health

The appointments of Fleming and Yende underscore the profound link between arts and health. Engagement in creative activities, such as music, art, and dance, positively impacts physical, mental health, social well-being, and overall quality of life.

Through their roles as Goodwill Ambassadors, Fleming and Yende will promote the integration of arts into healthcare systems, advocate for access to creative arts therapies, and champion the importance of artistic expression in improving health outcomes globally.

Health for All Film Festival

A shortlist of 93 films has been selected for the 4th Health for All Film Festival out of more than 780 entries received.

Watch the shortlisted films here. Winners will be announced on 6 June.

Key highlights from the Seventy-sixth World Health Assembly

As the world faces ongoing health and humanitarian emergencies, the Seventy-sixth World Health Assembly focuses on driving forward health for all. This year’s session of the World Health Assembly determines the immediate and longer-term future of WHO, starting with the program budget for the next two years, key decisions about the sustainable financing of the Organization and changes put in place to improve WHO’s processes and accountability. Delegates also deliberate about the critical role that WHO has in the Global Health Emergency Architecture.
Read more :

World Health Organization

Women Less Satisfied With Cancer Care

WHEN STEPHANIE RIVERA’S DOCTOR DISCOVERED THYROID NODULES during a routine exam in 2019, she began getting yearly thyroid ultrasound monitoring. She was told that 95% of the time these nodules are benign, but that she should watch for symptoms. “My doctor said if anything changes—if my voice changes or if I have trouble swallowing—I should come in sooner than my annual check-up,” says Rivera, 54, CEO of the Lazarex Cancer Foundation, which focuses on breaking barriers to health care for marginalized communities.

In April 2022, when Rivera began to experience unusual hoarseness five months before her scheduled annual thyroid ultrasound, she called her doctor as directed. But instead of getting an expedited appointment, “I was told, ‘Everything is fine. Just come back in August when you’re supposed to,’” Rivera says. When her hoarseness continued, Rivera called her doctor’s office again, and the medical staff relayed the same message: “Just come back in August.”

After that August check-up, however, Rivera was diagnosed with thyroid cancer that had spread to her lymph nodes. Rivera felt validated but remorseful. “Statistically, I wasn’t supposed to have thyroid cancer that has metastasized, but I knew my body. I should have called a third time and said, ‘This hoarseness is different. I need to come in now just to make sure everything is OK,’” she says.

Rivera is far from alone in having her cancer symptoms dismissed. According to a recent American Cancer Society Cancer Action Network (ACS CAN) survey involving 1,236 patients with cancer and survivors who have been diagnosed or treated within the past seven years, women were twice as likely as men (6% vs. 3%) to have reported symptoms five or more times before getting a diagnosis. For patients diagnosed after experiencing symptoms (as opposed to those diagnosed after screening), women were less likely than men to report that their symptoms were taken very seriously (31% vs. 21%) or taken seriously “at all” (8% vs. 1%).

“These small survey numbers echo a bigger trend women may be experiencing throughout their cancer journey: that physicians are not listening to them,” says Sarah Long, ACS CAN project manager for survey administration and analysis. “The fact that women, in particular, were going to physicians repeatedly and saying repeatedly, ‘I have these symptoms,’ and those symptoms were not taken seriously is an issue.”

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Having initial cancer symptoms dismissed may especially be a problem for younger, healthy-looking women who don’t fit the profile of what doctors believe to be a typical cancer patient, Long says. According to ACS CAN survey respondents, physicians are apt to chalk up younger patients’ symptoms, such as feeling tired, to having a stressful job or a too-busy life, when, in fact, after pushing for follow-up appointments and additional testing, many of these women are eventually diagnosed with cancer.

Women are having to say, ‘No, this isn’t normal for me’ over and over again,” says Kirsten Sloan, managing director of public policy at ACS CAN. “What we’re concerned about are those women who don’t say it over again, who just accept what their doctor says, rather than pushing for more testing. If it is cancer, they later find out it could have been diagnosed and treated sooner, with potentially a more favorable prognosis.”

Who is to blame? “It’s not the fault of the doctor. It’s the high-pressure system doctors find themselves in. The models of care are not as patient centered as they need to be,” Sloan says. “If you’ve only got a 15-minute visit, you don’t have much time to figure out which symptoms don’t make sense for the patient’s life.”

If You Feel Something, Say Something Again and Again

Still, there is no time to wait for the system to change, if it ever does. “As health care consumers, we need to educate ourselves about the symptoms to look for, make sure we’re doing our routine screenings so things are caught early, and be really good advocates for ourselves,” says Sloan. “We also need to find a doctor who listens in the way we need to be listened to.”

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Rivera, who has worked directly with doctors on various levels at major health care networks for more than 30 years, has learned a lot about herself from her experience being diagnosed with thyroid cancer. “If this can happen to me, it can happen to anyone,” she says. “I trusted my doctor. And, apparently, I trusted him very much. What I didn’t trust was myself enough to say: ‘I know my body, and something is different. I need to be seen now for peace of mind.’”

Rivera says pushing back is not in her comfort zone. Insisting on being heard by your doctor or your clinical care team can feel like talking back to the teacher or your boss. Still, when something doesn’t feel right, your life can depend on it. “The lesson I learned is that my voice about my body is a top priority,” Rivera says.

Women Less Satisfied With Cancer Care