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Biomedical subjects

E Wiebringhaus

Publications and source records attributed to E Wiebringhaus.

16 recordsLinked to original sources

Effect of propafenone in the Wolff-Parkinson-White syndrome: electrophysiologic findings and long-term follow-up.

The electrophysiologic and long-term efficacy of propafenone, a relatively new antiarrhythmic agent, was assessed in 47 patients with accessory pathways. In 23 patients (group I), the electrophysiologic effects were assessed initially. In 19 patients in this group and in 24 additional patients (group II), long-term therapy with oral propafenone was initiated. The mean age of the patients was 38 years in group I and 41 years in group II. The duration of a history of tachycardia in both groups was 12 years (mean); 14 patients previously had had attacks of syncope. During the electrophysiologic study in group I, propafenone did not change the spontaneous sinus rate. Corrected sinus node recovery time as well as the AH interval, HV time, QRS duration and effective refractory periods of the atria and ventricles was significantly prolonged. The effective refractory period of the accessory pathway increased from 238 to 322 ms (p less than 0.02). The 1:1 conduction capacity of the accessory pathway decreased from 231 to 176 beats/min (mean; p less than 0.01). Complete block in the anterograde direction occurred in 6 patients. The shortest RR interval during atrial fibrillation increased from 232 to 303 ms (p less than 0.05). The retrograde refractory period of the accessory pathway was prolonged from 245 to 295 ms (p less than 0.01). Complete or 2:1 retrograde block during basic drive occurred in 3 patients and 1 patient, respectively. In 6 of 15 patients, propafenone made sustained supraventricular tachycardia (SVT) either no longer inducible or nonsustained. The cycle length of induced SVT increased from 324 to 395 ms (p less than 0.01). During long-term administration (follow-up duration 2 to 3 years), 17 of 43 patients did not report any episode of symptomatic tachycardia. In another 18 patients, tachycardia was rare, slower and self-terminating. In only 3 patients, the frequency and severity of attacks had not changed. One patient with dilated cardiomyopathy died suddenly. Side effects necessitating discontinuation of medication were observed in only 2 patients. The remaining side effects, if present, were tolerated, and dosage dependent. In conclusion, propafenone is an effective and well-tolerated antiarrhythmic agent in the long-term management of patients with the Wolff-Parkinson-White syndrome.

Adolescent↗

[The electrophysiological effects of the Ca-antagonists gallopamil (D 600), dimeditiapramine (Ro 11-1781) and verapamil in man (author's transl)].

The electrophysiological effects of D 600 (D) (0.03 mg/kg i.v., 10 pts) and Ro 11-1781 (Ro) (1.0 mg kg i.v., 10 pts) were compared with those of verapamil (V) (0.1 mg/kg i.v., 20 pts). All three Ca-antagonists caused a slight shortening of the cycle length which was only significant after verapamil. There was practically no change in SNRT. As a consequence, the SNRT corrected for heart rate (CNSRT) increased insignificantly in all three groups (control C): 359.7 +/- 174.8 ms, V: 397.1 +/- 204.6 ms; C: 362.5 +/- 125.2 ms, Ro: 420.8 +/- 179.0 ms; C: 339.5 +/- 93.6 ms, D: 407.7 +/- 272.0 ms). In addition, the calculated "sinoatrial conduction time" increased insignificantly (C: 84.3 +/- 23.0 ms, V: 101.3 +/- 39.4 ms; C: 105.2 +/- 35.1 ms, Ro: 114.8 +/- 31.9 ms) or did not change (C: 105.9 +/- +/- 20.6 ms, D: 101.6 +/- 32.2 ms). The conduction time from high-to-low right atrium (HRA-A) as well as the His-ventricle time (HV) and the conduction interval from the septum to the right ventricular apex (V RVA) did not change. In contrast, the conduction time through the AV node (A-H) was significantly prolonged by all three drugs (C: 78.1 +/- 16.0 ms, V: 88,4 +/- 19.5 ms; C: 92.9 +/- 16.2 ms, Ro: 104.3 +/- 19.1 ms; C: 88.5 +/- 20.0 ms, D: 102.5 +/- 22.6 ms). The effective refractory period of the AV node (ERP AVN) was significantly prolonged by verapamil (C: 290.0 +/- 77.6 ms, V: 360.5 +/- 93.3 ms) and by D 600 (C: 266.7 +/- 72.6ms, D: 380.0 +/- 112.7 ms). Ro 11-1781 did not show any effect on this parameter. As a consequence, the Wenckebach point during high rate atrial pacing was significantly lowered by Verapamil and D 600, but only insignificantly by Ro 11-1781. The refractoriness of the right atrium and ventricle was not altered by any of the drugs. The results show that all three Ca-antagonists have similar electrophysiological effects in man after acute i.v. application. In the dose given, D 600 and verapamil are equipotent, whereas Ro 11-1781 is less effective.

Blood Pressure↗

[Long-term treatment with the new antiarrhythmic drug propafenone in correlation to plasma levels (author's transl)].

The results of long term oral therapy of cardiac arrhythmias in 43 patients successfully treated with propafenone are reported. The patients were treated for periods ranging between 1 month and 34 months with a mean of 13.4 months. The administered dose varied between 150 mg tds and 300 mg qds with an average daily dose of between 600 and 750 mg. The doses were decided on a body-weight basis with range of 6 to 17 mg/kg and an average of 12 mg/kg. Altogether 30 patients were successfully treated over a long period, sometimes in combination with other antiarrhythmic agents, particularly beta-blockers. 2 patients did not appear after some first controls. In 7 patients the drug was not effective, even when used in combination with others. 4 patients stopped the treatment due to side-effects. Further 18 patients complained temporarily of gastrointestinal and cerebral side-effects. Some Ecg changes were noted, particularly A-V conduction delays and spreading of the QRS-complex. We suggest that the clinically most important parameters for monitoring an antiarrhythmic regimen of propafenone are the patients's own history and Ecg-examination noting the PQ interval and particularly the width of the QRS-complex and long-term monitoring.

Adrenergic beta-Antagonists↗

[Cardiodepressive effect of alcohol in low doses in normal persons and patients with coronary disease].

To study the effect of small amounts of ethanol 1 ml whisky (43 vol. %) per kg body weight was given to normal subjects (n = 11) and patients with coronary heart disease (n = 11) and the systolic time intervals (STI) PEP (preejection period), LVET (left ventricular ejection time), QS2 (total electromechanical systole) and PEP/LVET were measured. A control group consisted of five patients with coronary heart disease. The following results were obtained: Already at rest PEP/LVET was significantly higher in patients with coronary heart disease. After the ingestion of alcohol, significant changes of the STI were observed; mainly an increase of PEP and PEP-LVET was found. In patients with coronary heart disease the effect began earlier, was significantly higher and lasted significantly longer than in normal subjects. According to invasive correlation-studies of different authors, these results indicate an impairment of left ventricular function, especially of ejection fraction and contractility. These alterations seem to be more pronounced in patients with coronary heart disease. The results of this study should be considered in advising patients with coronary heart disease.

Adult↗