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Refractory Supraventricular Tachycardias [PDF]

open access: yesCirculation, 1973
This essay is designed to review some of the basic and more recent contributions to our understanding of supraventricular tachyarrhythmias, their mechanisms, pertinent points in diagnosis, and treatment. Supraventricular tachycardia is discussed under the concept of reentrant mechanisms versus accelerated ectopic pacemakers.
A R, Ticzon, R W, Whalen
exaly   +3 more sources

Supraventricular tachycardia in pregnancy [PDF]

open access: yesBritish Journal of Anaesthesia, 2004
We present four cases of supraventricular tachycardia in pregnancy of varied aetiology. Risk factors for the development of supraventricular tachycardia and options for obstetric anaesthetic management, during pregnancy, labour, and at Caesarean section are discussed. We recommend the use of adenosine as first line therapy.
K, Robins, G, Lyons
exaly   +3 more sources

Neonatal supraventricular tachycardia

open access: yesIndian Pacing and Electrophysiology Journal, 2019
Supraventricular tachycardia (SVT) is one of the most common conditions requiring emergency cardiac care in neonates. Atrioventricular reentrant tachycardia utilizing an atrioventricular bypass tract is the most common form of SVT presenting in the neonatal period.
Chandra Srinivasan
exaly   +4 more sources

Supraventricular Tachycardia [PDF]

open access: yesArchives of Pediatrics & Adolescent Medicine, 2009
Supraventricular tachycardia is the most common rhythm disturbance in children. We reviewed the spectrum of this common rhythm disorder from symptom recognition and epidemiology to management, with special attention to advancements in the available treatment options.
Jack C, Salerno, Stephen P, Seslar
  +6 more sources

The Mechanism of Supraventricular Tachycardia [PDF]

open access: yesCirculation, 1970
In six successive patients, none of whom had the Wolff-Parkinson-White syndrome, recurrent episodes of paroxysmal supraventricular tachycardia (SVT) were analyzed to determine the mechanism by which this arrhythmia is initiated and sustained. In each patient, simultaneous intracavitary atrial electrograms and surface electrocardiograms were recorded ...
J T, Bigger, B N, Goldreyer
openaire   +2 more sources

Syncope and Supraventricular Tachycardia [PDF]

open access: yesCirculation, 2001
A 41-year-old man was referred for electrophysiological evaluation after recurrent syncope that occurred frequently during vigorous exercise. The patient had a complete, normal cardiological work up, including a resting ECG, an exercise stress test, and an echocardiogram.
V, Kühlkamp, R, Bosch, C, Mewis
openaire   +2 more sources

Paroxysmal Supraventricular Tachycardia [PDF]

open access: yesCureus, 2019
Supraventricular tachycardia is a common emergency department (ED) pathology that frequently leads to hospital admission, but this may not be necessary in all cases. Here, we present a supraventricular tachycardia patient who was discharged from the ED after vagal maneuvers.
Arnold, Casey   +1 more
openaire   +2 more sources

Dermatomyositis and supraventricular tachycardia

open access: yesInternational Archives of Medicine, 2008
Dermatomyositis is an idiopathic inflammatory myopathy, often associated with an underlying malignancy. Its prevalence rate is approximately one per 100,000 in the general population, and is even rarer without evidence of a cancer. Dermatomyositis rarely involves myocardial muscle fibers, but has shown to be associated with cardiac arrhythmias.We ...
Dhoble, Abhijeet   +2 more
openaire   +2 more sources

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12‐Related Developmental Disorders

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken   +4 more
wiley   +1 more source

Atypical Clinical Course of Griscelli Syndrome Type 2 With Primarily Neurologic Presentation and Adult‐Onset in a 46‐Year‐Old Male

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Griscelli Syndrome Type 2 (GS2) is a rare autosomal recessive disorder caused by pathogenic mutations in the RAB27A gene. Typically, it is characterized by cutaneous hypopigmentation, immunodeficiency, with or without neurological abnormalities secondary to hemophagocytic lymphohistiocytosis (HLH). Without treatment, GS2 often results in fatal
Dzhoy Papingi   +6 more
wiley   +1 more source

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