scholarly journals High‐risk features and predictors of unexplained syncope in the young SCD‐SOS cohort

2021 ◽  
Author(s):  
Mafalda Carrington ◽  
João Pais ◽  
Diogo Brás ◽  
Antonio Creta ◽  
Rogério Teixeira ◽  
...  
Keyword(s):  
High Risk ◽  
Unexplained Syncope

scholarly journals High-risk features and predictors of unexplained syncope in the young SCD-SOS cohort

2020 ◽  
Author(s):  
Mafalda Carrington ◽  
João Pais ◽  
Diogo Brás ◽  
Antonio Creta ◽  
Rogério Teixeira ◽  
...  
Keyword(s):  
High Risk ◽  
Unexplained Syncope

Unexplained syncope in patients with high risk of sudden cardiac death

ESC CardioMed ◽  
2018 ◽  
pp. 2037-2040
Author(s):  
Vincent Probst ◽  
Jean-Baptiste Gourraud
Keyword(s):  
High Risk ◽  
Sudden Cardiac Death ◽  
Cardiac Death ◽  
Vasovagal Syncope ◽  
Left Ventricular ◽  
Precise Definition ◽  
Inherited Diseases ◽  
Unexplained Syncope ◽  
Definition Of ◽  
European Society Of Cardiology

The occurrence of syncope is a frequent event in patients affected by diseases at high risk of sudden death. This should be evaluated with great attention because it may represent a turning point in the risk assessment of the disease. When the patient already has a defibrillator implantation indication (e.g. in patients with left ventricular function <35%), the occurrence of syncope is an opportunity to move towards the implantation. However, in many cases, it is the syncope by itself that will guide the therapeutic management. It is therefore particularly important to pay attention to its evaluation since the question to determine if the syncope is related to life-threatening arrhythmia or whether it is just a simple vasovagal syncope will determine entirely the way to treat the patient. Unfortunately, in many patients with structural cardiac or inherited diseases, the diagnosis remains unexplained at the end of a complete work-up. Most studies in the literature lack a precise definition of unexplained syncope. The contribution of the 2018 European Society of Cardiology Guidelines on syncope is to provide a more precise definition of unexplained syncope which is of help in identifying patients at high risk of sudden cardiac death. For this chapter, unexplained syncope is defined as syncope that does not meet any class I diagnostic criterion of those guidelines. In the presence of clinical features of structural cardiac or inherited diseases described in this chapter, unexplained syncope is considered a suspected arrhythmic syncope.

A Community Based High Risk Register for Hearing Loss

1982 ◽  
Vol 47 (4) ◽  
pp. 373-375 ◽  
Author(s):  
James L. Fitch ◽  
Thomas F. Williams ◽  
Josephine E. Etienne
Keyword(s):  
Hearing Loss ◽  
System Identification ◽  
High Risk ◽  
Language Learning ◽  
Education Program ◽  
Communication System ◽  
Auditory Signal ◽  
Early Age ◽  
Community Based ◽  
Children With Hearing Loss

The critical need to identify children with hearing loss and provide treatment at the earliest possible age has become increasingly apparent in recent years (Northern & Downs, 1978). Reduction of the auditory signal during the critical language-learning period can severely limit the child's potential for developing a complete, effective communication system. Identification and treatment of children having handicapping conditions at an early age has gained impetus through the Handicapped Children's Early Education Program (HCEEP) projects funded by the Bureau of Education for the Handicapped (BEH).

A Community Based High Risk Register for Hearing Loss

1983 ◽  
Vol 48 (1) ◽  
pp. 110-110
Keyword(s):  
Hearing Loss ◽  
High Risk ◽  
Community Based

For the November 1982 JSHD article, "A Community Based High Risk Register for Hearing Loss," the author would like to acknowledge three additional individuals who made valuable contributions to the study. They are Marie Carrier, Gene Lyon, and Bobbie Robertson.

The development of allergy in high-risk children

1997 ◽  
Vol 27 (11) ◽  
pp. 1247-1253 ◽  
Author(s):  
M. L. BURR ◽  
T. G. MERRETT ◽  
F. D. J. DUNSTAN ◽  
M. J. MAGUIRE
Keyword(s):  
High Risk ◽  
High Risk Children

I1307K APC gene variant has no clinical implication in Israeli jews at average or high risk for colorectal neoplasia

2001 ◽  
Vol 120 (5) ◽  
pp. A120-A121
Author(s):  
H STRUL ◽  
E BIRENBAUM ◽  
B STERN ◽  
D KAZANOV ◽  
L THEODOR ◽  
...  
Keyword(s):  
High Risk ◽  
Clinical Implication ◽  
Colorectal Neoplasia ◽  
Apc Gene ◽  
Gene Variant
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