Showing posts with label health literacy. Show all posts
Showing posts with label health literacy. Show all posts

Thursday, March 8, 2018

5 questions with health literacy expert Beccah Rothschild


Below is some valuable advice from my colleague/friend, Beccah. 


Thanks to Amino / Sophia Lee / March 6, 2018





Last week, we sat down with with Beccah Rothschild, a health and adult literacy expert with more than 20 years of experience in the field. Her passion revolves around ensuring that information is accessible and available to everyone — regardless of educational, literacy, cultural, or linguistic background. In this Q&A, we cover topics that range from tips for effectively educating people on healthcare to the role employers play in protecting their employees from financial harm.

Q1: You educate patients about the overuse of healthcare treatments. What are some commonly over prescribed treatments, and what is your advice to get people to think twice about them?
Examples of commonly overused tests, procedures, and medications include antibiotics for colds, imaging tests for low back pain and headaches, and C-sections in healthy pregnancies. These may not be the most overused treatments or tests, but they’re ones healthcare consumers frequently encounter. Another interesting overuse case is the Pap test. For a long time, the standard was to get one annually, but the latest research shows that most women — depending on their age, medical history, and risks — only need one every three to five years. When I started to write about this topic, a lot of women — especially aged 45-50 and above — pushed back saying they were taught to get it every year. It’s interesting because these women don’t actually want to get this uncomfortable test done annually (who would?), but it just goes to show how challenging it is to change the culture around medical testing.
In terms of my best advice, I’ve found that if you talk in generalities about the physical and financial harm of overuse, people are less inclined to act in their best interest. For instance, if you say: “ordering unnecessary tests makes insurance premiums go up and causes people to pay more for care,” it doesn’t resonate because it doesn’t hit you personally. But if you say: “if you get this test done, you’re going to pay $2,000 out-of-pocket for something that you don’t need — and might even harm you,” it clicks. You really need to appeal to people on a personal level.

Q2: What role do employers play in helping their employees with regard to health literacy?

The employer has a huge responsibility to ensure that the health insurance information employees receive is readable, understandable, and written in a way that’s not full of jargon. The average person doesn’t understand what a deductible, copay, or coinsurance is, so the employer has the obligation to make sure this type of information is provided in a way that employees can understand, use, and act on it.
Insurance companies play a role in this as well. Fortunately, insurance companies have really stepped up to try and make materials easier to understand — but there’s still a long ways to go. There’s been huge progress though compared to back in 2003 or 2004 when health literacy was just becoming a much wider-known issue, which is around when I was involved in starting up the California Health Literacy Initiative — the first statewide health literacy project ever. Ultimately, it must be a shared responsibility between both insurance companies and employers to make sure the healthcare they provide is easy to understand and access.
It’s also important for employees to trust the information from their employers. A good way to do this is for employers to share information that’s data-driven, evidence-based, and comes from a trusted third-party. People also need to understand that the information they’re getting from their employer isn’t going to impact their benefits. It’s common for employees to be worried about going to the HR or management and saying “I’m considering getting pregnant” or “I have a chronic condition” because they fear retribution, judgement, being passed over for a promotion, or having certain benefits taken away.

Q3: What’s your advice for chronically ill patients who frequently interact with the healthcare system?

Ask questions and take notes. A few years ago, my mom — who lives across the country from me — simultaneously had two cancers. For every single appointment, my parents conference called me in. And before every appointment, I would send them a list of questions ahead of time. You would never go into a meeting without an agenda, so why would you go to a doctor’s appointment without one?
While on the call, I would take notes verbatim while my dad asked the questions. Doctors knew that I was on the phone and taking notes, so it was very transparent — especially when I would pipe in with clarifying questions. After the appointment, I would write up the notes and distribute them to members of the family so we all knew exactly what was going on and could follow up with more questions if needed. If you don’t do this, or some version of this, you leave the appointment and forget things or perhaps misinterpret them. You can also always ask at your appointment if you can record the conversation. And if the doctor says no, find someone else to go to. Don’t forget that the healthcare provider works for you, not the other way around. I can’t stress that enough.

Q4: What are your biggest takeaways when it comes to educating people about healthcare?

I would say there are two major takeaways:
Keep it short and simple. It’s hard to do this because healthcare is so complex. I always want people to have all the information possible so they can make the best decision. But what I learned is that very few people want that — whether it’s an executive in the C-suite or someone with limited literacy skills, most people don’t have the time or capability to read through so much information.
If you tell someone what not to do, you also have to tell them what to do. It’s important to frame things in a positive way for people who are in pain, frustrated by their situations, or scared. For instance, if you say “it’s not a good idea to get treatment ABC,” you should also say “instead, I’m going to give you XYZ and it will still help you.” People need to be reassured that they have options and that they’re going to be ok.

Q5: If you could wave a magic wand and make a single change to improve the future of health literacy, what would you wish for?

I would do a major overhaul of our culture of healthcare. I wish it would change so that patients understand they are consumers and see healthcare as a consumer good. For instance, when you go to buy a car or fridge, you always ask how much it costs, how long it will last — and you negotiate on the price. But when it comes to healthcare, people don’t know that the price of filling a prescription varies widely depending on where you go. They don’t know that you can negotiate costs with a hospital if you’re paying out-of-pocket or with cash. They don’t know that the quality of care varies wildly. And it’s all because they don’t think of healthcare as a consumer good, so they don’t ask the important questions. I want to shake up the culture of healthcare and make these conversations actually happen.


Friday, May 3, 2013

Friday's Digital Health Finds: Text messages for asthmatic kids, 5 ways to use Pinterest in healthcare, and more!

Study: Text messages are effective intervention for asthmatic children [Healthcare Informatics]
According to the results of a study, researchers at the Georgia Institute of Technology, sending a child with asthma a text message that prods them on their symptoms and help them better understand the condition can improve outcomes. “It appears that text messages acted as an implicit reminder for patients to take their medicine and by the end of the study, the kids were more in tune with their illness,” Rosa Arriaga, study leader and senior research scientist in the College of Computing’s School of Interactive Computing at Georgia Tech, said in a statement.

Can making data beautiful engage patients and boost health literacy  [Med City News]
Providing consumers access to their data without overwhelming their health literacy threshold is probably the biggest challenge for companies developing patient portals to provide access to electronic health records. Too much of a focus on images can be distracting but too much text can cause eye strain or be daunting for users. And you still need to guide users through the components so there needs to be, if not breadcrumbs, an easy way for users to navigate.

Why doctors should use their real name on Twitter [KevinMd.com]
What we say on Twitter as doctors, particularly with medically related topics, carries weight. By saying we are doctors gives our tweets a greater level of authenticity that is not commonly afforded to other users. Not only do we hold power with knowledge, we are respected for the judicious use of our knowledge which has been painstakingly acquired over many years and enhanced by a responsibility for life long learning. It is incumbent upon us to not abuse this privilege.

UC San Francisco opens Center for Digital Health Innovation  [UCSF]
Institutions around the world are experiencing fundamental cultural and societal shifts brought about by the explosive use of social media, mobile technologies and cloud computing. “While health care has not experienced the full force of the social media revolution, it will shortly,” Blum says. These technologies will truly democratize health care, and UCSF must be prepared to integrate them into its infrastructure and workflows, he says. These technologies will generate an unprecedented flood of clinical and research data that UCSF will need to manage, analyze and optimize for clinical care, discovery, and education.

5 ways Pinterest can be used for patient education in healthcare [ParkerWhite]
As more and more people use the Internet to search about healthcare, Pinterest is a way to organize the information they find, also allowing for them to share content easily with others. The other potential benefit from Pinterest is to reach people when they’re in various Internet “mindsets.” It can be a way to reach the patient when they’re not necessarily concerned with a particular problem at the moment (i.e. searching for specific health information for an issue they have right now). Pinterest can provide a medium for reaching patients to remind people of the many aspects of their life in which health plays an important role.

Specialists see tools to treat pain in video games [NYT]
…TubeRunner is one of four of galaxy-themed video games created specifically for this complex, where pain specialists and game developers are piloting an approach to measuring pain. Dr. Julia Finkel hopes that using technical data from games and interactive activities to objectively identify and monitor pain can help determine how to evaluate the techniques used to treat it. Central to their effort to quantify pain, said Dr. Finkel, the chief of pain medicine here, is a squat, rectangular black box with three eyes peering up from below the screen. It was a Kinect, a motion sensor device that allows users to control games using gestures and spoken commands.