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Gepubliceerd in:

01-07-2008 | case report

Pulmonary hypertension: the role of the electrocardiogram

Auteurs: I. R. Henkens, R. W. C. Scherptong, K. W. van Kralingen, S. A. M. Said, H. W. Vliegen

Gepubliceerd in: Netherlands Heart Journal | Uitgave 7/2008

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Extract

In August 2005, a 54-year-old female was referred to our centre for additional evaluation into the aetiology of recently established severe pulmonary arterial hypertension (PAH). The patient had first experienced exertional dyspnoea six months prior to presentation to the referring cardiologist. There was no history of cardiac or pulmonary disease, but this patient had undergone an extensive cardiac evaluation seven years before, after a single episode of syncope. At that time, the ECG showed a sinus rhythm, a QRS axis of 36°, normal P waves, conduction intervals within normal limits, and inverted T waves in leads II, III, aVF and V1 to V6 (figure 1A). Because of the observed repolarisation abnormalities, a series of additional tests was performed. Apart from severe hyperthyroidism, there were no cardiac or pulmonary abnormalities found at echocardiography (tricuspid and pulmonary valve regurgitation gradients were within normal limits, there was no right atrial or ventricular dilatation, right ventricular hypertrophy, or paradoxical septal bowing), left heart and coronary catheterisation, or pulmonary function tests. At renewed presentation, the ECG now showed a QRS axis of 90°, the R wave in lead V1 measured 6 mm in the absence of an S wave, and there were diffuse repolarisation abnormalities, all in agreement with an increased right heart load (figure 1B).
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Metagegevens
Titel
Pulmonary hypertension: the role of the electrocardiogram
Auteurs
I. R. Henkens
R. W. C. Scherptong
K. W. van Kralingen
S. A. M. Said
H. W. Vliegen
Publicatiedatum
01-07-2008
Uitgeverij
Bohn Stafleu van Loghum
Gepubliceerd in
Netherlands Heart Journal / Uitgave 7/2008
Print ISSN: 1568-5888
Elektronisch ISSN: 1876-6250
DOI
https://doi.org/10.1007/BF03086156