Additional Resources

Several things go into high quality care. The first is safety. We want our care to be safe and we don’t want to do any harm in the care that we provide. We want care to be effective. We want to be using the best care, according to the guidelines to achieve the best outcomes for patients. We want care to be efficient. We don’t want waste in our healthcare system. We want care to be equitable. So we want to make sure that we’re providing care to patients regardless of where they live or their resources. We want to make sure that care is patient-centered so that patients are at the center of their care and their care teams – guiding decisions according to what’s best for them. And we want care to be timely so that people are getting access to care at the right time for the right reasons with the right provider.

There are a number of factors. Doctors first ensure they have the correct diagnosis. This may be established via blood tests, physical exams and hearing the patient’s story. Doctors then evaluate the evidence and best guidance and make treatment recommendations. Patient preference for treatment, as well as other health factors and stage of life are also considered. Arthritis treatment decisions are shared decisions between doctor and patient.

Yes, it’s critical that the patient’s perspective is taken into consideration when developing recommendations. Patients are the ones living with arthritis and making a recommendation is all about balancing risks and benefits of treatment. Preference sensitive recommendations, sometimes called conditional recommendations, are recommendations where there isn’t one best treatment for all patients. One treatment may be appropriate for one patient and another treatment may be more appropriate for someone else. It really comes down to the physician and patient discussing risks and benefits and choosing a treatment that works best for the individual patient. This is what shared decision-making is all about.

Arthritis care teams can include a family physician, rheumatologist, physiotherapist, occupational therapist, social worker, pharmacist, etc. Each patient is at the centre of his/her care team and should be the one directing it and deciding who needs to be on the team.

Arthritis is over 100 diseases, so finding cures is no simple task. It’s important that in the meantime, we’re also doing research that allows us to improve the quality of life for people who are living with these serious diseases until the time when there are cures.

Unfortunately, many patients across Canada may not have timely access to care. The reasons for this are varied. It may be that people aren’t aware that their symptoms require a visit to a family doctor. And in some cases, the family doctor may not have the skill set to identify symptoms as requiring urgent attention. Many regions across Canada also lack access to rheumatologists. While the country has a large number of rheumatologists, they tend to be centred in more urban areas in the south. Individuals living in northern parts of many provinces and territories may not have the same access to rheumatologists and/or rheumatology specialty care.

Physicians in Canada are licensed and, to maintain that license, are required to do maintenance and certification. This means doctors have to prove to their licensing bodies that they are staying up to date in a variety of ways. Maintenance can include self-improvement projects through evaluations, research, attending conferences, reading journal articles, guidelines and discussing difficult cases with colleagues to enhance learning. It’s a continuous process to ensure physicians are applying the best evidence in every clinical situation.

Patients should always be the centre of their care teams – communicating their needs, how they’re feeling, and the information that they need to make the best healthcare decisions for them. Patients should find healthcare providers that can listen effectively and work with them as a team.

How can we get patients access to care in a timely fashion? How can we get them the best treatments? How can we support them through their journey? How can we get the best outcomes for patients? Physician, healthcare system and patient factors all come into play when asking these types of questions.

Healthcare guidelines are documents that outline best practices for a certain health condition. They can include recommendations about what treatments patients should receive, what tests should be ordered, how closely people should be followed up with and a number of other recommendations.

Guidelines help standardize practice between different physicians. This doesn’t mean all patients will receive the same treatment, but rather that the discussion that physicians have with their patients should be similar regardless of where they live in Canada. Guidelines can also be a way for physicians to stay up to date on the latest evidence. And they are a great resource for patients to learn about their health condition and the different treatments that are available to them. Ultimately, guidelines help ensure quality of care for patients.

Once a topic is judged to be important, a guideline panel is assembled. This includes physicians, researchers, patients with arthritis and other healthcare providers, physiotherapists, occupational therapists, pharmacists, etc. Guidelines are typically published by physician and healthcare societies. The Canadian Rheumatology Association publishes several guidelines on its website.

An example of guidelines would be the “CRA Recommendation on COVID-19 Vaccination in Persons with Autoimmune Rheumatic Disease.” To view these guidelines, please click here.

This depends on the guidelines that are being addressed. For example, we know that exercise is beneficial for knee and hip osteoarthritis. For other conditions, the evidence is still evolving. So those recommendations will change more frequently and will be informed by ongoing research at Arthritis Research Canada. Guidelines are usually updated when new treatments are available or new evidence about a particular condition emerges.

A living guideline is updated as soon as new evidence emerges. The typical period of time for updating a guideline is around two to three years. Living guidelines reduce this time period to several months.

Availability of treatments, costs and patient preference also play a role in treatment decisions. 

Guidelines can vary from country to country. For some situations, it’s very clear that one treatment is best. And in these situations you’ll typically see international guidelines agree. In other situations, there may be different treatments that are available in one country or varying treatment practices that influence recommendations. For this reason, it’s really important that guidelines are contextualized to the country that they’re being applied to. Even within Canada, guidelines can vary by province. There may be different access to different medications or other types of treatment, and this can impact what recommendations are made.

The most important tool and resource patients have is their healthcare team, including physician, pharmacist, physiotherapist, or occupational therapist, depending on the decision. There are also tools called decision aids. These are resources that are either paper-based or online and help patients make decisions about their care that are in line with their preferences and values. Of course, decision aids should not replace the patient-physician discussion, but should be used to supplement it.