14 Bilder zum Thema "long qt" bei ClipDealer

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A 4-year-old boy with a clinical diagnosis of long QT syndrome. No genetic testing was done during hospitalization. The child died suddenly during follow-up.
3D illustration of an electrocardiogram (ECG) showing prolonged QT interval with broad-based T-waves, characteristic of type 1 long QT syndrome.
Bidirectional ventricular tachycardia is a kind of malignant arrhythmia. The polarity of QRS main wave alternates from beat to beat, and it is easy to degenerate into ventricular fibrillation.
Male, 75 years old, clinically diagnosed as acute anterior septal and high lateral myocardial infarction.The culprit vessel was located in the LAD proximal segment.Prolonged QT interval with TDP.
Ventricular tachyarrhythmia includes many clinical types, some benign and some malignant. For malignant ventricular arrhythmias, patients are at risk of death.
Tunnel drive to light qt the end
Early afterdepolarization is an arrhythmogenic mechanism that triggers activity, occurring before the end of the T wave and commonly seen in QT interval prolongation.
In the spatial anatomy of the heart, the axis from the base of the heart to the apex of the heart is called the long axis, that is, the upper right side faces the lower left side.
A 4-year-old boy with a clinical diagnosis of long QT syndrome. No genetic testing was done during hospitalization. The child died suddenly during follow-up.
Torsade de pointes refers to the pleomorphic ventricular tachycardia that occurs in the background of long QT interval, and the polarity of QRS wave twists around the equipotential line.
Clockwise rotation electrocardiogram refers to the transition of the rS waveform of the chest lead to the left chest lead, with the transition lead exceeding the V4 lead.
Clockwise and counterclockwise rotation are common electrocardiographic phenomena, mainly used to describe the evolution of R-wave amplitude in chest leads.
A 4-year-old boy with a clinical diagnosis of long QT syndrome. No genetic testing was done during hospitalization. The child died suddenly during follow-up.
A 4-year-old boy with a clinical diagnosis of long QT syndrome. No genetic testing was done during hospitalization. The child died suddenly during follow-up.

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