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Table 1 Sample characteristics

From: Delay in diagnosis of muscle disorders depends on the subspecialty of the initially consulted physician

  

Entire sample

(N = 101)

Men

(n = 57)

Women

(n = 44)

p

Age (yrs); mean ± SD

 

48.9 ± 14.5

49.2 ± 14.6

48.6 ± 14.8

0.854

Education level

Low

7 (7.1%)

3 (5.4%)

4 (9.3%)

0.614

 

Medium

46 (46.5%)

28 (50.0%)

18 (41.9%)

 
 

High

46 (46.5%)

25 (44.6%)

21 (48.8%)

 

Age group at onset

Childhood

/adolescence

36 (35.6%)

19 (33.3%)

17 (38.6%)

0.581

 

Adulthood

65 (64.4%)

66.7 (67%)

27 (61.4%)

 

Diagnoses

Inherited muscle

diseases*

56 (55.4%)

31 (54.4%)

25 (56.8%)

0.807

 

Acquired muscle

diseases**

22 (21.8%)

10 (17.5%)

12 (27.3%)

0.240

 

SMA III and IV***

14 (13.9%)

8 (14%)

6 (13.6%)

0.954

Time from first

consultation to

diagnosis (yrs);

mean (median)

 

4.3 (1.0)

2.9 (1.0)

6.1 (3.0)

0.014

First consultation

Neurologists

15 (14.9%)

9 (15.8%)

6 (13.6%)

0.763

 

General

practitioners

38 (37.6%)

24 (42.1%)

14 (31.8%)

0.29

 

Non-neurological

specialists

48 (47.5%)

24 (42.1%)

24 (54.5%)

0.214

  1. Note. SD = standard deviation
  2. *limb-girdle muscular dystrophies (MD), facioscapulohumeral MD, AD Emery Dreifuss MD, congenital myopathies, metabolic myopathies, channelopathies, no patients with Duchenne MD are included
  3. **inclusion body myositis, polymyositis
  4. ***spinal muscle atrophy