Skip to main content
. 2019 Feb 20;5(1):2055217318820888. doi: 10.1177/2055217318820888

Table 7.

Comparison of use of disease-modifying therapies (DMTs) by Slifka study participants at the time of their interviews in 2000 and 2009.a

Rates of use, %b
Change in percentage points
 Characteristics 2000c 2009
Sample 55.3 (1193/2156) 61.5 (1451/2361) +6.2
Course
Relapsing-remitting MS 63.5 (834/1314) 68.7 (1048/1525) +5.2
Secondary progressive MSd 47.2 (220/466) 51.5 (272/528) +4.3
Primary progressive MSe 36.4 (90/247) 34.3 (69/201) –2.1
Progressive-relapsing MS 42.7 (38/89) 62.2 (51/82) +19.5
Duration since diagnosis, years
<5 75.5 (627/830) 75.7 (340/449) +0.2
6–15 50.6 (408/807) 71.3 (669/938) +20.7
>16 30.4 (158/519) 45.3 (441/973) +14.9
Disability status f
No MS symptoms NA 55.0 (133/242) NA
Mild MS symptoms with no limitations on activity on lifestyle 58.6 (259/442) 67.2 (248/369) +8.6
Non-ambulatory symptoms 60.9 (349/573) 71.6 (399/557) +10.7
Trouble walking but no aid used 58.4 (136/233) 67.2 (129/192) +8.8
Can walk 25 feet without a cane 61.9 (122/197) 65.0 (152/234) +3.1
Cannot walk 25 feet without a cane 55.0 (169/307) 60.6 (175/289) +5.6
Cannot walk 25 feet without bilateral support 49.6 (61/123) 58.5 (110/188) +8.9
Requires wheelchair or scooter 34.8 (94/270) 35.8 (101/282) +1.0
Completely bedridden 0.0 (0/7) 50.0 (4/8) +50.0
Age, years
18–54 63.6 (959/1509) 70.8 (837/1183) +7.2
>54 36.3 (234/644) 52.1 (612/1175) +15.8

a2000 analyses: DMTs include interferon beta-1a (Avonex®), interferon beta-1b (Betaseron®), glatiramer acetate (Copaxone®). 2009 analyses: DMTs include the above plus interferon beta-1a (Rebif®), natalizumab (Tysabri®). Denominators do not exclude two subjects with missing data (as in Table 2).

bUnweighted percentage of users in sample or subgroup (number of users/number in sample or subgroup). Numerators are the number of users at time of interview (not over recall period as in Table 2).

cSource: Minden et al.19

dOf the 528 patients in 2009 who reported a course of secondary progressive MS, 333 (63.1%) reported zero relapses and 195 (36.9%) reported one or more relapses in the preceding year.

eOf the 201 patients in 2009 who reported a course of primary progressive MS, 39 (19.4%) reported one or more relapses in the preceding year.

fSource: Hohol et al.21 Based on free text responses from previous waves of Slifka study interviews, ‘no MS symptoms’ and ‘completely bedridden’ were added. ‘Non-ambulatory symptoms’ include ‘sensory abnormalities’, ‘bladder impairment’, ‘incoordination’, ‘weakness’, or ‘fatigue’ of any severity.

NA: category not included in 2000 interview.