Survival and complication free survival in Marfan's syndrome: implications of current guidelines

被引:123
作者
Groenink, M
Lohuis, TAJ
Tijssen, JGP
Naeff, MSJ
Hennekam, RCM
van der Wall, EE
Mulder, BJM
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Cardiol, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Dept Epidemiol & Biostat, NL-1105 AZ Amsterdam, Netherlands
[3] Univ Amsterdam, Acad Med Ctr, Dept Paediat Cardiol, NL-1105 AZ Amsterdam, Netherlands
[4] Univ Amsterdam, Acad Med Ctr, Dept Paediat, NL-1105 AZ Amsterdam, Netherlands
[5] Univ Amsterdam, Acad Med Ctr, Inst Human Genet, NL-1105 AZ Amsterdam, Netherlands
[6] Leiden Univ, Med Ctr, Dept Cardiol, Leiden, Netherlands
关键词
Marfan's syndrome; aortic root dissection; survival;
D O I
10.1136/hrt.82.4.499
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective-To evaluate survival and complication free survival in patients with Marfan's syndrome and to assess the possible influence of recently revised guidelines for prophylactic aortic root replacement in these patients. Methods-130 patients who had been attending one institution over 14 years were evaluated. Kaplan-Meier analysis was performed in 125 patients who did not present with aortic root dissection as the first sign of Marfan's syndrome, with the end points: death, aortic root dissection, and prophylactic aortic root replacement after diagnosis. In the patients developing aortic root dissection, current guidelines for prophylactic aortic root replacement were retrospectively applied to investigate the number of dissections that could theoretically have been prevented. The guidelines were: (1) aortic root diameter greater than or equal to 55 mm, (2) positive family history of aortic disisections and aortic root diameter greater than or equal to 50 mm, and (3) aortic root growth 62 mm/year. Outcomes following emergency surgery (15 patients) and prophylactic surgery of the aortic root (30 patients) were compared. Results-Five and 10 year survival after diagnosis was 95% and 88%, and the five and 10 year complication free survival was 78% and 66%, respectively. Thirteen patients developed dissection, 30 underwent prophylactic repair, and 82 had an uncomplicated course. Eleven dissections could theoretically have been prevented by application of the current guidelines. Five year survival following emergency and prophylactic repair of the aortic root was 51%, and 97%, respectively. Conclusions-Survival in the Marfan's syndrome in the past 14 years seems satisfactory; with application of current guidelines, it has probably even improved. However, because of the high fatality rate in Marfan patients developing aortic root dissection, more extensive screening for Marfan's syndrome and a search for additional risk factors are desirable.
引用
收藏
页码:499 / 504
页数:6
相关论文
共 39 条
  • [1] REPEATED SURGERY FOR RECURRENT DISSECTION OF THE AORTA
    BACHET, J
    BRIZARD, C
    GOUDOT, B
    DREYFUS, G
    TEODORI, G
    BRODATY, D
    DUBOIS, C
    DELENTDEKER, P
    GUILMET, D
    [J]. EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY, 1990, 4 (05) : 238 - 244
  • [2] BEIGHTON P, 1986, AM J MED GENET, V29, P581
  • [3] A TECHNIQUE FOR COMPLETE REPLACEMENT OF ASCENDING AORTA
    BENTALL, H
    DEBONO, A
    [J]. THORAX, 1968, 23 (04) : 338 - &
  • [4] Chassignolle JF, 1997, ARCH MAL COEUR VAISS, V90, P1713
  • [5] CILD AH, 1997, J CARDIAC SURG, V12, P131
  • [6] DePaepe A, 1996, AM J MED GENET, V62, P417, DOI 10.1002/(SICI)1096-8628(19960424)62:4<417::AID-AJMG15>3.0.CO
  • [7] 2-R
  • [8] CARDIOVASCULAR MANIFESTATIONS OF MARFAN-SYNDROME IN THE YOUNG
    ELHABBAL, MH
    [J]. AMERICAN HEART JOURNAL, 1992, 123 (03) : 752 - 757
  • [9] MARFAN-SYNDROME - LONG-TERM SURVIVAL AND COMPLICATIONS AFTER AORTIC-ANEURYSM REPAIR
    FINKBOHNER, R
    JOHNSTON, D
    CRAWFORD, ES
    COSELLI, J
    MILEWICZ, DM
    [J]. CIRCULATION, 1995, 91 (03) : 728 - 733
  • [10] COMPOSITE GRAFT REPAIR OF MARFAN ANEURYSM OF THE ASCENDING AORTA - RESULTS IN 100 PATIENTS
    GOTT, VL
    PYERITZ, RE
    CAMERON, DE
    GREENE, PS
    MCKUSICK, VA
    [J]. ANNALS OF THORACIC SURGERY, 1991, 52 (01) : 38 - 45