Few axSpA patients infected with COVID-19 – Survey shows

Despite concerns of possible risk factors, very few patients with axial spondyloarthritis have been infected with the coronavirus so far.

This is very good news. It looks like the axSpA-patients have been protecting themselves, adhering to the advice of the health authorities and taking the risk of infection seriously,” ASIF-president Zhivko Yankov says.

By Trine Dahl-Johansen

COVID-19 has caused global disruptions in the management of chronic illnesses like axial spondyloarthritis (axSpA). The extent to which patients with axSpA have been affected by the coronavirus needed to be established, and Axial Spondyloarthritis International Federation (ASIF), The Spondylitis Association of America and survey company Any-3, developed the international COVID-19 axSpA-survey, which opened in April.

The preliminary results show some of the effects of the pandemic for this patient group and are based on answers through the questionnaire for the period of 3rd April to 31st October 2020. There are 4900 patients across 72 countries who have answered the patient survey. 93 % have completed all the questions.

The good news

Easy interventions like keeping distance, isolating from other people, washing hands, using antibacterial liquid and face masks etc. in public are essential to avoid infections like the coronavirus. Only 4 % of the total survey population report they have had the coronavirus. This is good news, but many of the respondents have not been tested to confirm it and are self-diagnosed. A lot of the symptoms of COVID-19 are very similar to those of an ordinary cold or flu, like fever, fatigue, sore throat and continuous cough. Therefore, it is almost impossible to know for sure if you have Covid-19 without being tested.

Despite the low COVID-19 testing, the low numbers in coronavirus patients amongst the axSpA-group is probably due to many taking the risk of viral infection seriously and doing what they can to protect themselves from such an infection. As chronically ill, many axSpA patients are used to taking illness seriously and making changes when life presents challenges. The ability to adapt to fluctuations in the disease throughout life probably leads to people coping with such a pandemic situation better than many feared.

It is still amazing that so few with rheumatic diseases are infected with COVID-19 during this period,” Zhivko says.

Adapting to the situation

Many might also easily adapt to the rules of isolation and less social activity because they already are limited due to their health challenges in everyday life. For example, those who live with a lot of pain, fatigue and impaired mobility are accustomed to pacing their activities, and many already have a limited level of activity and social life. For many people with axSpA activity regulation is important, so they are able to accomplish the most necessary things.

Our members are used to accepting periods where you cannot do everything you want. Many have probably adapted well to the pandemic restrictions and have good skills when it comes to taking care of their own health,” Zhivko elaborates.

Response to the global coronavirus pandemic has resulted in major changes to how people go about their daily lives. A study presented at ACR 2020 shows that individuals with axSpA with higher levels of stress and anxiety, had significantly higher disease activity levels. [1]

Good recovery status

The low frequency of testing for the coronavirus is a well-known situation internationally, due to variable test capacity worldwide, which leads to a very different situations for each country represented.

Although patient-reported outcomes have limitations, especially regarding the accuracy of self-diagnosis of COVID-19, the current results from the survey may add to more knowledge on potential risk factors and the course of this coronavirus infection in axSpA-patients.

Several international data show there are very few patients with rheumatic diseases who have contracted the virus, and few have been hospitalized or died because of infection. This is the same trend as the axSpA-survey.

Now it is crucial to get more responders to answer the axSpA-survey, especially those who have been tested for COVID-19, regardless of whether they have a positive or negative test result. It will provide the survey with better data and higher credibility.

I encourage all ASIF-member organizations to invite more people to respond to the survey,” Zhivko says.

The following link allows new participants to self-register: https://covid19-axspa.any-survey.com/go/

Similar risk factors

The risk factors for people with autoimmune diseases are the same as for the general population. Those who also have cardiovascular disease and get infected with the coronavirus often have a tougher course, and are at higher risk of death, but they are not at a higher risk of getting infected overall compared to the normal population, according to The COVID-19 Rheumatology Alliance. [2]

This is supported by more studies released during the digital EULAR-congress in June.

The study shows that most patients with rheumatological conditions recover from COVID-19, independent of the medication they receive,” professor Dr. John Isaacs, Chair of the EULAR Scientific Committee stated in a press release. [3]

Some concerns

The preliminary results of the axSpA-survey also enhance some worries regarding some patients discontinuing their medications during these months, often without consulting their rheumatologist. Amongst the patients with more severe disease measured by BASDAI the percentage of those discontinuing their medications also increases. The data show that amongst those who measured between 6 and 10 on the BASDAI-scale from 1 to 10, 19-28 % had changed their medication in fear of COVID-19. This is a big concern because this might lead to flare-ups that requires a doctor’s appointment in a health system already overloaded.

In total 17 % of the 4900 respondents report they have changed their medications due to the concern of COVID-19. In the age groups 20-29, 30-39 and 40-49 more than 20 % have done this. Type of spondyloarthritis diagnosis does not seem to influence this decision. Neither do other diagnoses believed to affect the coronavirus, like high blood pressure, chronic lung disease, diabetes, heart disease and heart failure, systemic lupus or cancer.

The answers about changing medication reflect the huge worry many with axSpA faced when the pandemic was a fact in the beginning of 2020 and when there was little information about immunosuppressive medications and the risk of contracting the new virus. Both rheumatologists and patients were in doubt of what to do regarding medications, and this continued for several months.

An American based survey, answered by rheumatologists, was presented at the ACR Convergence congress in November 2020. A third of the respondents indicated that at least 10 % of their patients had self-discontinued or reduced at least one immunosuppressive medication to mitigate their risk of COVID-19. [4]

In the early months of the COVID-19 pandemic, patients with RA, PsA, AS, and SLE frequently avoided office visits and laboratory testing. (…) Participants often stopped medications without the advice of a physician, and medication interruptions were more common in participants without access to telehealth”, another ACR-abstract reveals. [5]

Knowledge is key

Even some rheumatologists were uncertain if patients should sustain their treatment because there were no recommendations due to the brand-new virus.

There is considerable uncertainty about the drug management in the context of rheumatic conditions,” EULAR-president professor Dr. Iain B. McInnes explained in a press release in June.

According to another poster session at ACR a national American sample of rheumatologists answered a survey in the period of April to August this year. It revealed there are still variations regarding perceptions of patients’ risk of COVID-19, and how to manage medications such as NSAIDs, biologics and steroids during the pandemic. [6]

After many months and several studies, it is now well established there is currently no evidence to suggest that there are grounds for stopping or slowing down ongoing immunosuppressive therapy, i.e., treatment that suppresses the immune system, including disease-modifying medications (DMARDs) such as methotrexate and TNF-inhibitors. [7] [8]

In hindsight studies show that both the HLA-B27 gene and the use of some biological medications (bDMARD) might in fact be protecting axSpA-patients from contracting the virus and lead to a less difficult course of the disease for those who do become infected. The majority of patients do not require hospitalization, even if they use immunosuppressive drugs.

It is reasonable that patients with inflammatory diseases treated with b/tsDMARD (biologic, targeted disease modifying anti-rheumatic drugs) continue their treatment during the COVID-19 epidemic. The different rates of hospitalization based on the diagnosis or DMARD may be due to comorbidity, confounding by indication and other bias,” one ACR-abstract concludes. [9]

If you do get infected with COVID-19, standard procedures for other types of infections apply. You should discontinue or postpone the medication until you recover from COVID-19, consistent with guidelines on the management of patients with active infections on biologic therapy. [10]

The SAA’s initial findings from the survey data can be found on the SAA Website

 

[1] https://acrabstracts.org/abstract/disease-activity-in-an-axial-spondyloarthritis-cohort-during-the-covid-19-pandemic/

[2] https://rheum-covid.org/epidemiology-and-outcomes-of-novel-coronavirus-2019-in-patients-with-immune-mediated-inflammatory-diseases/

[3] https://www.eular.org/sysModules/obxContent/files/www.eular.2015/1_42291DEB-50E5-49AE-5726D0FAAA83A7D4/eular_press_release_covid_registry_final.pdf

[4]  https://acrabstracts.org/abstract/geographical-variations-in-covid-19-perceptions-and-patient-management-a-national-survey-of-rheumatologists/

[5] https://acrabstracts.org/abstract/concerns-and-behaviors-of-patients-with-common-autoimmune-rheumatic-diseases-in-the-united-states-early-in-the-covid-19-pandemic/

[6] https://acrabstracts.org/abstract/geographical-variations-in-covid-19-perceptions-and-patient-management-a-national-survey-of-rheumatologists/

[7]  https://diakonhjemmetsykehus.no/nyheter/korona-informasjon-til-pasienter-med-inflammatorisk-revmatisk-sykdom#er-det-spesielle-forholdsregler-hvis-du-far-infusjonspreparater

[8]  https://spondylitis.org/research-new/covid-19-and-spondyloarthritis-your-questions-answered/

[9] https://acrabstracts.org/abstract/use-of-biologic-treatment-and-risk-to-be-admitted-for-covid-19-infection/

[10] https://www.jaad.org/article/S0190-9622(18)33001-9/fulltext

IMAS is expanding – News Update


The International Map of Axial Spondyloarthritis (IMAS), a patient experience survey, continues to be a hugely important project for everyone involved in the axSpA community.

The project has produced a wealth of information, which is being used globally to raise awareness, support our advocacy efforts and, ultimately improve the lives of people living with axSpA. The IMAS team have been working hard on disseminating information on the issues identified through the data. They have so far produced a variety of reports and papers on issues ranging from psychological distress; the impact on work and social life; how people manage their disease and, of course, why it takes so long to diagnose axSpA.

Whilst the project was running in Europe (EMAS), 2840 patients from 13 countries completed the survey. We eagerly await the full report of EMAS, which is due to be published early next year.

 

As well as the European countries, the survey has also now closed in Canada, Taiwan and South Korea – with responses from a further 800 patients.

 

And IMAS continues to grow! The survey is currently open in Turkey and four Latin American countries; Mexico, Colombia, Argentina and Costa Rica. We are working hard to maximise the number of people who complete the survey in these countries; and are looking to make sure as many axSpA patients as possible know about IMAS.

 

On top of these countries, IMAS is expanding further into six new countries; USA, Philippines, India, South Africa, Algeria and Lithuania – ensuring that this is truly an international project that delivers robust global data to everyone involved in the fight against axSpA.

 

Patients in these six new countries will be invited to complete the survey from early 2021. IMAS will also be relaunched early next year in the UK, where the aim is to significantly improve on the number of respondents from the first round of the survey.

Alongside the survey itself, the IMAS team continue to work hard on disseminating information gained from the data. Early in 2021, we will invite all the Patient Organisations involved in IMAS to a meeting to discuss how we can best use the data to support their work and what work we can do that will be of most value to ASIF’s members. With this in mind, we are already beginning some IMAS sub-projects; one is to identify the most powerful public affairs messages, so that we can support our members with information and statistics to lobby and approach policymakers. Another project will bring to life some of the IMAS data through patient videos; we will ask patients to talk about their personal experiences of axSpA, viewed through a particular lens – such as how the disease has affected their career or how they coped with their diagnosis.

For more information on IMAS, you can visit the IMAS page on the ASIF website or you can contact Jo Lowe, ASIF Project Manager.

Delay to Diagnosis Project – News Update

 

 

ASIF’s Delay to Diagnosis project focusses on the unacceptable delay in receiving a diagnosis that most patients with axSpA must endure. Through the project, we aim to better understand why the delay to diagnosis occurs; how this affects patients, their families and friends and healthcare systems. Crucially, we must decide collectively what ASIF can do raise awareness and to support our members globally in tackling this burden that axSpA patients face.

 

The project, which launched early in summer this year, has achieved a lot in a short space of time. Most notably, we hosted two international Global Forum events in the autumn, which were a huge success, and we are very pleased to have received positive feedback from everyone involved. The events brought together patients, researchers, rheumatologists, physiotherapists and other healthcare professionals to discuss the delay to diagnosis around the world. We were delighted to have participants from Argentina to Australia – and many countries in between! In total, we welcomed 48 delegates from 23 countries across five continents. We thank, in particular our Asian and Australian representatives who had to stay up very late!

 

Dr Dale Webb, CEO of NASS (the UK patient group) gave a presentation on the existing research evidence and what it tells us about the delay to diagnosis. Included in this is data from the IMAS project, evidence collected directly from patients about living with axSpA. We held break-out discussions during which we collectively explored the reasons that the delay to diagnosis occurs – almost without exception – around the world. In understanding the reasons for the delay, we can start to identify ways to tackle it. We heard time and again from patients of the suffering they had endured in waiting for their diagnosis. But, we also heard about some positive steps taken in certain parts of the world where small projects or schemes had led to some success in reducing the delay.

Dr Dale Webb presents at the ASIF axSpA Global Forum event on 13 October 2020

We will launch dedicated webpages on the ASIF website very soon, where you can read in more detail about the project and keep up to date with developments. There you will also find resources on the delay to diagnosis, including links to the existing research, videos and infographics that can be tailored to your requirements.

 

During this initial phase of the project, we have also asked our member organisations to tell us more about the delay to diagnosis in their country and have collated and reviewed the existing research. We are now producing our final report from this stage of the Delay to Diagnosis project; this will be the definitive report on the impact of axSpA globally. We will highlight – most importantly – the burden on patients who wait too long for their diagnosis. This burden statement will be launched in spring of 2021 and we will use the knowledge gathered during this phase of the project to agree what work is most needed in the next phases of the Delay to Diagnosis project.

 

Stemming from ideas and discussions at the Global Forums and from existing research, we will explore ideas on how to take forward the project. We could look at how to support our members with better messaging to policymakers; we might develop a toolkit that can be tailored by countries to international or regional campaigns; we could help by making videos about the disease symptoms to raise awareness in the general public and alert people to the possibility that they have axSpA.

 

We will consider a range of ideas and explore how we build a project or programme of work around them. Most importantly, we will consult with our members to find out what would be most useful and how they can get involved in the ongoing project. For now, ASIF would like to say a huge thank you to everyone that has been involved so far and we look forward to continuing this essential work. Together, we can – and must – create a better experience for axSpA patients. 

 

We have heard throughout the Global Forums how many barriers we face in reducing the delay to diagnosis. Here at ASIF, we understand that this project should develop and grow to support our members in tackling these obstacles. We thank you again for your participation and look forward to working with you to achieve our goal.