Welcome to the new SADS site.
Click Here
to report any problems.
SADS Foundation USA
SADS Foundation Canada
SADS Foundation UK
SADS Foundation Netherlands
SADS Foundation China
SADS Foundation Hong Kong
Search for:
Log in
Supporting Families.
Saving Lives.
Sign-up for our
Enewsletter
here
.
SADS International
SADS Channel Blog
About Us
Contact Us
Library
Advocacy
Schools
Medical Professionals
Get Involved
Living with SADS
Research
Home
|
News
|
What's new for 'CHOA Cardiac Faculty' in PubMed
What's new for 'CHOA Cardiac Faculty' in PubMed
11/15/2016
Abstract
OBJECTIVES:
To identify the clinical presentation of children and adolescents affected by 1 of 4 cardiac conditions predisposing to sudden cardiac arrest: hypertrophic cardiomyopathy, long QT syndrome (LQTS), catecholaminergic polymorphic ventricular tachycardia (CPVT), and anomalous origin of the left coronary artery from the right sinus of Valsalva (ALCA-R).
STUDY DESIGN:
This was a retrospective review of newly diagnosed pediatric patients with hypertrophic cardiomyopathy, LQTS, CPVT, and ALCA-R referred for cardiac evaluation at 6 US centers from 2008 to 2014.
RESULTS:
A total of 450 patients (257 male/193 female; median age 10.1 years [3.6-13.8 years, 25th-75th percentiles]) were enrolled. Patient age was ≤13 years for 70.4% of the cohort (n = 317). Sudden cardiac arrest was the initial presentation in 7%; others were referred on the basis of abnormal or suspicious family history, personal symptoms, or physical findings. Patients with LQTS and hypertrophic cardiomyopathy were referred most commonly because of family history concerns. ALCA-R was most likely to have abnormal signs or symptoms (eg, exercise chest pain, syncope, or sudden cardiac arrest). Patients with CPVT had a high incidence of syncope and the greatest incidence of sudden cardiac arrest (45%); 77% exhibited exercise syncope or sudden cardiac arrest. This study demonstrated that suspicious or known family history plays a role in identification of many patients ultimately affected by 1 of the 3 genetic disorders (hypertrophic cardiomyopathy, LQTS, CPVT).
CONCLUSION:
Important patient and family history and physical examination findings may allow medical providers to identify many pediatric patients affected by 4 cardiac disorders predisposing to sudden cardiac arrest.
Read the entire study
HERE
.
Back To News Page
Whats New
TSA
Donate
About Us
Advocacy
International Partners
Schools
Dropbox
Medical Professionals
Get Involved
Library
Living with SADS
MatReqTest
Medical Professional Education
News
Press Room
Research
Paypal Success
Paypal Failure
Thank you for your donation!
Volunteer to Fight SADS!
Overview of SADS Conditions
Online Community
SADS Online Support Community
Share Your Story
Stories: Living & Thriving with SADS
Stories: Forever in our Hearts
Enews Archives & Sign up
Find it Fast
Family Registration & Request Materials
Find a Physician
International SADS
Risk Assessment
Genetic Testing
Our Partners
Warning Signs
Family history of unexpected, unexplained sudden death under age 40.
Fainting or seizure during exercise, excitement or startle.
Consistent or unusual chest pain &/or shortness of breath during exercise.