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. 2006 Feb 17;92(9):1238–1243. doi: 10.1136/hrt.2005.081638

Table 1 Baseline characteristics of 268 patients with Marfan's syndrome.

No dissection or aortic repair (n = 189) Elective aortic repair (n = 53) Dissection (type B: n = 2) (n = 26) p Value*
Age (years) 30 (11) 36 (13) 35 (10)
Women (n = 139) 60% 32% 39%
Ever pregnant (n/m)** 48% (53/110) 31% (5/16) 44% (4/9)
Mutations
 Yes 52 12 8
 No 60 19 5
 Unknown 74 21 13
Mitral valve intervention 3 (2%) 6 (11%) 1 (4%)
Arrhythmias 17 (9%)) 6 (11%) 5 (19%)
β blockers 94 (50%) 28 (53%) 16 (62%)
Aortic diameter (mm)
 Root n = 182† 40 (36–45) NA
 Arch n = 112,18,13† 24 (22–27) 26 (24–30)‡ 27 (23–41)§ 0.014
 Descending n = 83,15,11† 20 (18–22) 25 (20–28)‡ 30 (26–42)§ 0.003
 Abdominal n = 76,21,11† 17 (15–19) 20 (18–23)‡ 30 (27–40)§ 0.003

Age is reported as mean (SD); aortic dimensions as medians (interquartile range).

*Patients without dissection or aortic repair compared with patients with an elective aortic repair; †numbers of patients in each of the groups for whom data were available, enumerated in the same order as the columns of the table: no dissection, elective surgery, dissection; ‡patients who had undergone an aortic intervention in another part than the root (n = 6) were excluded in calculating these averages; §one patient who had undergone surgery of the distal aorta was excluded; **The denominator “m” refers to the numbers of patients for whom data on pregnancy were available.