Richter R, Reisinger I, Mahlke E, Thal W
Klinik für Kinderheilkunde, Medizinischen Akademie Magdeburg.
Z Erkr Atmungsorgane. 1988;171(2):156-62.
Pulmonary hypertension with right ventricular hypertrophy (Cor pulmonale) is a critical complication in cystic fibrosis patients. Early detection and therapy might decrease mortality. Noninvasive diagnostic methods as vector-ECG, m-mode echocardiography and thallium myocardial scintigraphy were performed in 50 children with cystic fibrosis to determine the degree of right ventricular hypertrophy.