Literature DB >> 9505923

Marfan syndrome in children and adolescents: an adjusted nomogram for screening aortic root dilatation.

L Rozendaal1, M Groenink, M S Naeff, R C Hennekam, A A Hart, E E van der Wall, B J Mulder.   

Abstract

OBJECTIVE: To construct an adjusted nomogram for the echocardiographic screening of aortic root diameter in children with possible Marfan disease.
DESIGN: In 91 children (42 boys, 49 girls, age range 3.2 to 18.4 years) undergoing Marfan screening from 1983 until 1996, the diagnosis Marfan syndrome and any other aortic pathology was definitely ruled out. These served as a control population to set appropriate reference standards.
RESULTS: Compared with a standard Dutch reference population, body surface area of the control subjects (mean (SD)) was above the 50th centile (boys 0.09 (0.20) m2, range -0.28 to 0.69 m2; girls 0.09 (0.17) m2, range -0.17 to 0.69 m2). Echocardiographically determined aortic root diameter and body surface area showed a linear relation and a greater variability of aortic root diameter in these relatively tall subjects (n = 91, R2 = 0.62) than in the standard nomogram (n = 56, R2 = 0.93). In 24% of cases (n = 22), the aortic root exceeded the upper limit of normal in the standard nomogram, by 2.2 (2.0) mm. An adjusted nomogram was constructed with a higher upper limit.
CONCLUSIONS: A Marfan screening population differs from the unselected population in body surface area and aortic root size variability. An adjusted nomogram should therefore be used to detect a truly enlarged aortic root.

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Year:  1998        PMID: 9505923      PMCID: PMC1728579          DOI: 10.1136/hrt.79.1.69

Source DB:  PubMed          Journal:  Heart        ISSN: 1355-6037            Impact factor:   5.994


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Journal:  Circulation       Date:  1978-12       Impact factor: 29.690

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3.  Predictors of Rapid Aortic Root Dilation and Referral for Aortic Surgery in Marfan Syndrome.

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5.  Automated analysis of four-dimensional magnetic resonance images of the human aorta.

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6.  Aortic root asymmetry in marfan patients; evaluation by magnetic resonance imaging and comparison with standard echocardiography.

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7.  Left ventricular diastolic dysfunction in children and young adults with Marfan syndrome.

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8.  Marfan syndrome in children and adolescents: predictive and prognostic value of aortic root growth for screening for aortic complications.

Authors:  M Groenink; L Rozendaal; M S Naeff; R C Hennekam; A A Hart; E E van der Wall; B J Mulder
Journal:  Heart       Date:  1998-08       Impact factor: 5.994

9.  The distal aorta in the Marfan syndrome.

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10.  Aortic size in children: Systolic measurements are different from diastolic measurements.

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