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. 2022 Aug 4;13:20406223221108391. doi: 10.1177/20406223221108391

Table 1.

Sociodemographic, clinical and pharmaceutical data of MS patients with and without pDDIs.

Parameter All patients (N = 627) Patients with ⩾1 pDDI (N = 408) Patients with no pDDI (N = 219) p-value
Sociodemographic data
 Sex 0.927 a
  Female 441 (70.3%) 286 (70.1%) 155 (70.8%)
  Male 186 (29.7%) 122 (29.9%) 64 (29.2%)
 Age (years) 19–86 b 48.6 (13.3) c 21–86 b 51.9 (12.6) c 19–75 b 42.5 (12.5) c <0.001 d
 School years 6–18 b 10.5 (1.3) c 6–18 b 10.3 (1.2) c 8–14 b 10.8 (1.3) c <0.001 d
 Educational level <0.001 e
  No training 19 (3.0%) 12 (2.9%) 7 (3.2%)
  Skilled worker 398 (63.5%) 280 (68.6%) 118 (53.9%)
  Technical college 89 (14.2%) 56 (13.7%) 33 (15.1%)
  University 121 (19.3%) 60 (14.7%) 61 (27.9%)
 Employment status <0.001 e
  In training 7 (1.1%) 2 (0.5%) 5 (2.3%)
  In studies 6 (1.0%) 1 (0.2%) 5 (2.3%)
  Employed 269 (42.9%) 130 (31.9%) 139 (63.5%)
  Unemployed 25 (4.0%) 13 (3.2%) 12 (5.5%)
  Retired 304 (48.5%) 253 (62.0%) 51 (23.3%)
  Others 16 (2.6%) 9 (2.2%) 7 (3.2%)
 Partnership 0.702 a
  No 162 (25.8%) 103 (25.2%) 59 (26.9%)
  Yes 465 (74.2%) 305 (74.8%) 160 (73.1%)
 Place of residence 0.040 e
  Rural community 224 (35.7%) 150 (36.8%) 74 (33.8%)
  Provincial town 108 (17.2%) 77 (18.9%) 31 (14.2%)
  Medium-sized town 112 (17.9%) 77 (18.9%) 35 (16.0%)
  City 183 (29.3%) 104 (25.5%) 79 (36.1%)
 Number of children 0–4 b 1 f 0–4 b 1 f 0–4 b 1 f 0.003 g
  0 169 (27.0%) 91 (22.3%) 78 (35.6%)
  1 170 (27.1%) 118 (28.9%) 52 (23.7%)
  ⩾2 288 (45.9%) 199 (48.8%) 89 (40.6%)
 Number of siblings 0–13 b 1 f 0–13 b 1 f 0–11 b 1 f 0.035 g
  0 71 (11.3%) 40 (9.8%) 31 (14.2%)
  1 305 (48.6%) 194 (47.5%) 111 (50.7%)
  ⩾2 251 (40.0%) 174 (42.6%) 77 (35.2%)
Clinical data
 EDSS score 0–9.0 b 3.5 f 0–9.0 b 4.0 f 0–7.5 b 2.0 f <0.001 g
 Disease duration (years) 0–52 b 10 f 0–50 b 12 f 0–52 b 9 f <0.001 g
 Disease course <0.001 e
  CIS/RRMS 415 (66.2%) 223 (54.7%) 192 (87.7%)
  SPMS 154 (24.6%) 136 (33.3%) 18 (8.2%)
  PPMS 58 (9.3%) 49 (12.0%) 9 (4.1%)
 Comorbidities 0–9 b 1 f 0–9 b 1 f 0–7 b 0 f <0.001 g
  No 184 (29.3%) 68 (16.7%) 116 (53.0%)
  Yes 443 (70.7%) 340 (83.3%) 103 (47.0%)
 Polypharmacy <0.001 a
  No 293 (46.7%) 97 (23.8%) 196 (89.5%)
  Yes 334 (53.3%) 311 (76.2%) 23 (10.5%)
Pharmaceutical data
 Number of drugs taken 0–19 b 5 f 2–19 b 6 f 0–9 b 2 f <0.001 g
  0 7 (1.1%) 0 (0.0%) 7 (3.2%)
  1–4 286 (45.6%) 97 (23.8%) 189 (86.3%)
  5–9 261 (41.6%) 238 (58.3%) 23 (10.5%)
   ⩾ 10 73 (11.6%) 73 (17.9%) 0 (0.0%)
Drugs divided by
 Period of drug intake
  Long-term drugs 0–16 b 4.6 (3.1) h 1–16 b 5.8 (3.0) h 0–9 b 2.2 (1.5) h <0.001 g
  PRN drugs 0–7 b 0.8 (1.2) h 0–7 b 1.0 (1.3) h 0–5 b 0.4 (0.8) h <0.001 g
 Access
  Rx drugs 0–18 b 4.2 (3.0) h 1–18 b 5.4 (3.0) h 0–6 b 1.9 (1.2) h <0.001 g
  OTC drugs 0–8 b 1.1 (1.3) h 0–8 b 1.4 (1.3) h 0–7 b 0.7 (1.1) h <0.001 g
 Therapy goal
  DMDs 0–2 b 0.9 (0.4) h 0–2 b 0.9 (0.4) h 0–1 b 0.7 (0.4) h <0.001 g
  Symptomatic drugs 0–9 b 2.0 (2.0) h 0–9 b 2.6 (2.0) h 0–8 b 0.8 (1.1) h <0.001 g
  Comorbidity drugs 0–14 b 2.5 (2.4) h 0–14 b 3.3 (2.6) h 0–6 b 1.0 (1.1) h <0.001 g

p-value for comparing patients with and without pDDIs (significant differences are indicated in bold). CIS, clinically isolated syndrome; DMD, disease-modifying drug; EDSS, Expanded Disability Status Scale; MS, multiple sclerosis; N, number of patients; OTC, over-the-counter; pDDI, potential drug–drug interaction, PPMS, primary progressive MS; PRN, pro re nata; RRMS, relapsing-remitting MS; Rx, prescription; SPMS, secondary progressive MS.

a

Fisher’s exact test.

b

Range.

c

Mean value (standard deviation).

d

Two-sample two-tailed t test.

e

Chi-squared test.

f

Median.

g

Mann–Whitney U test.

h

Average number of drugs taken per patient (standard deviation).