Health literacy

What links low health literacy and risk of cardiovascular disease?

Cardiovascular disease is the most common cause of death worldwide. A big share of the world population will face at least one of the cardiovascular issues that fall under CVD in their lifetime, which include stroke and coronary heart disease among other problems. If you would like more detailed information about CVD and its causes information about CVD I recommend visiting the NHS page on the topic.

The risk someone has of getting cardiovascular disease is determined in large part by lifestyle factors, as can be found on the website I link to above. It stands to reason that for this reason, and because cardiovascular disease takes so many lives every year, getting information about the lifestyle choices and changes people can make to reduce their risk of CVD is critical. With small adjustments much suffering can be prevented.

A barrier

I hope you’re now as convinced as I am of the importance of communicating ways to improve lifestyle and with that cardiovascular health. However, as one can imagine, getting this information to absolutely everyone can be difficult. One major barrier in that sense is that some people have limited (health) literacy, which can be taken to mean someone’s ability to digest medical information and put it into practise in their life. Studies (example) have shown that there is a link between CVD and low health literacy.

Basically, if you have limited health literacy, this tends to mean that you have a higher risk profile for cardiovascular conditions. This can be attributed to other factors than just a person’s health literacy, such as socioeconomic position or general care for their health even. However, the same study I gave as an example earlier, also looked into what effect extra nurse-coordinated care has. This proved to be a significant improvement in risk profile, both in low-health literate and health-literate patients. What I think we should take away from there not being a difference between those groups is that when the patients have the information, they do all act on it. That means that it really is a lack of understanding of information that makes them more at risk, rather than other factors, I would argue

What can be done?

I think it is clear that it is very important that we figure out how to get CVD information to people with limited health literacy. But how do we go about this? I will discuss that in another post, if you’re interested.

I hope this has been an interesting read, feel free to share any thoughts below!