SPMS Patients Have Higher Illness Burden than RRMS Patients, Kantar Health Study Shows

Written by Iqra Mumal, MSc |

SPMS study

Patients with secondary progressive multiple sclerosis (SPMS) have a higher burden of illness than patients with relapsing-remitting multiple sclerosis, a new study showed.

The study, “Characteristics, burden of illness, and physical functioning of patients with relapsing-remitting and secondary progressive multiple sclerosis: a cross-sectional US survey,” appeared  in the journal Neuropsychiatric Disease and Treatment.

Most multiple sclerosis (MS) patients experience RRMS, a form of the disease characterized by relapses and remission of symptoms. A subset of MS patients have another form of the disease — primary progressive MS (PPMS), which is when the illness progresses continuously without any remission. Patients who initially have RRMS followed by a progressive phase are diagnosed with SPMS.

The progression from RRMS to SPMS is fairly common in the absence of treatment. In fact, SPMS occurs in half of all RRMS patients within 10 years, and in up to 90 percent of patients within 25 years. While drugs may help stall the process, no one has studied this in depth.

Patients with SPMS have a poorer prognosis, since SPMS is associated with severe and irreversible disability. Even so, more studies have investigated RRMS than SPMS, limiting knowledge about the burden of illness and demographic data regarding SPMS patients.

Furthermore, while therapeutic options for RRMS patients have increased over the years, they have not for SPMS patients — leading researchers at New York-based Kantar Health to undertake a study to determine the characteristics of people with SPMS and their burden of illness relative to RRMS.

They used patient responses from the 2012 and 2013 U.S. National Health and Wellness Survey to determine differences in severity of disease, symptoms, healthcare resources, use of disease-modifying drugs and demographics between SPMS and RRMS patients. They also analyzed a 36-question form about work productivity and activity impairment.

SPMS patients were older (55.7 years old on average) than RRMS patients (48.9 years), results showed. Furthermore, a higher ratio of SPMS patients were likely to be males (43.8 percent) than RRMS patients (28.4 percent). In addition, 20 percent of SPMS patients were employed, versus 39.7 percent of RRMS patients.

SPMS patients also described their disease as more severe, and reported neurological symptoms more frequently. They also had higher hospitalization rates than RRMS patients, used disease-modifying drugs less frequently, and suffered higher activity impairment than their counterparts with RRMS. Physical functioning in general was lower in SPMS patients than in RRMS patients.

Taken together, this study’s results show that SPMS patients have a greater burden of illness, worse disease severity, more neurological symptoms, a higher hospitalization rate, greater work and activity impairment and significantly worse physical functioning than RRMS patients. This underscores the importance of  treating RRMS patients early before their disability progresses.

Kym avatar

Kym

No Kidding! I could have told them that!

Reply
daan avatar

daan

yes Kim, well spent money, awesome study!

Reply
Dora Jack avatar

Dora Jack

Well duh!! Like this should surprise anyone?? NOW HOW ABOUT GETTING SOMETHING THAT WILL HELP THE PRIMARY PROGRESSIVE FOLKS REGAIN SOME OF THE GROUND THEY'VE LOST WHILE YOU SPENT COPIOUS AMOUNTS OF MONEY ON RRMS!!!!!!!!

Reply
Heracles avatar

Heracles

If the money spent on this study would have instead been contributed to a MS patient's stem-cell procedure, it would have been better spent.

Reply
Jackie Krier avatar

Jackie Krier

I was not diagnosed for at least 10 years of having MS. I went to so many specialist for 5 years and finally gave up and just thought it was all in my head and I must be a hypochondriac. By the time I was diagnosed incessant SPMS and now there's nothing that can be done. Then doing research to get help have found there is no one really studying or doing anything to help people with this disease even though it's the health care system letting us down and causing treatable patients to become untreatable. Not sure what I have to do to get help and get the word out to providers Drs and patients. I'm so disappointed and angry about this. I'm so disappointed and angry with our
medical system!

Reply

Leave a comment

Fill in the required fields to post. Your email address will not be published.