Advertisement






Click here for more guidelines.
CME Topic Collections Past Issues Search Current Issue Home
     

J Am Coll Cardiol, 2003; 41:315-321
© 2003 by the American College of Cardiology Foundation
This Article
Right arrow Figures Only
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Olivotto, I.
Right arrow Articles by Cecchi, F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Olivotto, I.
Right arrow Articles by Cecchi, F.

CLINICAL STUDY: PRIMARY MYOCARDIAL DISEASE

Maximum left ventricular thickness and risk of sudden death in patients with hypertrophic cardiomyopathy

Iacopo Olivotto, MD*,*, Roberto Gistri, MD*, Pasquale Petrone, MD*, Elena Pedemonte, MD*, Daniela Vargiu, RN* and Franco Cecchi, MD*

* Cardiologia S. Luca, Azienda Ospedaliera Careggi, Florence, Italy

Manuscript received February 19, 2002; revised manuscript received July 16, 2002, accepted August 26, 2002.

* Reprint requests and correspondence: Dr. Iacopo Olivotto, Studio Medico, Via Jacopo Nardi 30, Firenze, 50132, Italy.
iacopo.olivotto{at}virgilio.it

OBJECTIVES: We sought to assess the relationship between maximum left ventricular (LV) wall thickness and outcome in patients with hypertrophic cardiomyopathy (HCM).

BACKGROUND: An association between maximum LV wall thickness and risk of sudden death was suggested in HCM. This finding requires further investigation, given the important implications for risk stratification and treatment.

METHODS: We analyzed the mortality and risk profile of 237 patients (age 41 ± 17 years; 63% male) classified into five groups based on echocardiographic maximum LV thickness.

RESULTS: During follow-up (12 ± 7 years), 36 patients died of cardiovascular causes, including 16 sudden deaths. Maximum LV thickness was not associated with a risk of sudden death (p = 0.37) nor with overall cardiovascular mortality (p = 0.7). With the exception of the small subset with thickness values ≤15 mm, with a consistently benign clinical course, the distribution of sudden death and overall cardiovascular mortality was not significantly different among the other four classes, ranging from 16 to 19 mm to ≥30 mm. Among 30 patients with extreme LV thickness (≥30 mm), only one sudden event occurred among six patients diagnosed at <18 years of age (17%) and none among 24 diagnosed at ≥18 years of age. The prevalence of nonsustained ventricular tachycardia, syncope, an abnormal blood pressure response to exercise, and atrial fibrillation was similar among the five thickness classes.

CONCLUSIONS: During 12-year follow-up, we observed no association between maximum LV thickness and cardiovascular mortality in a community-based population with HCM. The degree of maximum LV wall thickness should be considered in the context of a multifactorial approach to risk stratification, rather than as an isolated risk factor. Only in those patients diagnosed at a very young age might the presence of extreme LV wall thickness represent, per se, a potential marker of risk of sudden death.

Abbreviations and Acronyms
  HCM
  hypertrophic cardiomyopathy
  HF
  heart failure
  LV
  left ventricular




This article has been cited by other articles:


Home page
J. Clin. Pathol.Home page
G S Soor, A Luk, E Ahn, J R Abraham, A Woo, A Ralph-Edwards, and J Butany
Hypertrophic cardiomyopathy: current understanding and treatment objectives
J. Clin. Pathol., March 1, 2009; 62(3): 226 - 235.
[Abstract] [Full Text] [PDF]


Home page
J Am Coll CardiolHome page
Z.-Z. Song
Left ventricular mass and the outcome of patients with hypertrophic cardiomyopathy.
J. Am. Coll. Cardiol., January 27, 2009; 53(4): 399 - 399.
[Full Text] [PDF]


Home page
J Am Coll CardiolHome page
I. Olivotto, M. S. Maron, F. Cecchi, and B. J. Maron
Reply.
J. Am. Coll. Cardiol., January 27, 2009; 53(4): 399 - 399.
[Full Text] [PDF]


Home page
HeartHome page
P Elliott and P Spirito
Prevention of hypertrophic cardiomyopathy-related deaths: theory and practice
Heart, October 1, 2008; 94(10): 1269 - 1275.
[Abstract] [Full Text] [PDF]


Home page
J Am Coll CardiolHome page
I. Olivotto, M. S. Maron, C. Autore, J. R. Lesser, L. Rega, G. Casolo, M. De Santis, G. Quarta, S. Nistri, F. Cecchi, et al.
Assessment and Significance of Left Ventricular Mass by Cardiovascular Magnetic Resonance in Hypertrophic Cardiomyopathy
J. Am. Coll. Cardiol., August 12, 2008; 52(7): 559 - 566.
[Abstract] [Full Text] [PDF]


Home page
Eur Heart JHome page
C. J. McLeod, S. R. Ommen, M. J. Ackerman, P. L. Weivoda, W. K. Shen, J. A. Dearani, H. V. Schaff, A. J. Tajik, and B. J. Gersh
Surgical septal myectomy decreases the risk for appropriate implantable cardioverter defibrillator discharge in obstructive hypertrophic cardiomyopathy
Eur. Heart J., November 1, 2007; 28(21): 2583 - 2588.
[Abstract] [Full Text] [PDF]


Home page
HeartHome page
A. Nasermoaddeli, K. Miura, A. Matsumori, Y. Soyama, Y. Morikawa, A. Kitabatake, Y. Inaba, and H. Nakagawa
Prognosis and prognostic factors in patients with hypertrophic cardiomyopathy in Japan: results from a nationwide study
Heart, June 1, 2007; 93(6): 711 - 715.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
A. W. Nugent, P. E.F. Daubeney, P. Chondros, J. B. Carlin, S. D. Colan, M. Cheung, A. M. Davis, C.W. Chow, R. G. Weintraub, and for the National Australian Childhood Cardiomyopat
Clinical Features and Outcomes of Childhood Hypertrophic Cardiomyopathy: Results From a National Population-Based Study
Circulation, August 30, 2005; 112(9): 1332 - 1338.
[Abstract] [Full Text] [PDF]


Home page
JNMHome page
P. A. Kaufmann and P. G. Camici
Myocardial Blood Flow Measurement by PET: Technical Aspects and Clinical Applications
J. Nucl. Med., January 1, 2005; 46(1): 75 - 88.
[Full Text] [PDF]


Home page
NEJMHome page
F. Cecchi, I. Olivotto, R. Gistri, R. Lorenzoni, G. Chiriatti, and P. G. Camici
Coronary Microvascular Dysfunction and Prognosis in Hypertrophic Cardiomyopathy
N. Engl. J. Med., September 11, 2003; 349(11): 1027 - 1035.
[Abstract] [Full Text] [PDF]



 
  CME Topic Collections Past Issues Search Current Issue Home

Advertisement