Dokument: Medikamentöse Therapieoptionen bei post-operativem de novo Vorhofflimmern

Titel:Medikamentöse Therapieoptionen bei post-operativem de novo Vorhofflimmern
URL für Lesezeichen:https://docserv.uni-duesseldorf.de/servlets/DocumentServlet?id=48031
URN (NBN):urn:nbn:de:hbz:061-20181217-093838-1
Kollektion:Dissertationen
Sprache:Deutsch
Dokumententyp:Wissenschaftliche Abschlussarbeiten » Dissertation
Medientyp:Text
Autor: Behlau, Corinna [Autor]
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Dateien vom 11.12.2018 / geändert 11.12.2018
Beitragende:Prof. Dr. Korbmacher, Bernhard [Gutachter]
PD Dr. Kindgen-Milles, Detlef [Gutachter]
Stichwörter:Vorhofflimmern, Vernakalant, Herzchirurgie
Dewey Dezimal-Klassifikation:600 Technik, Medizin, angewandte Wissenschaften » 610 Medizin und Gesundheit
Beschreibungen:Postoperatives Vorhofflimmern (POAF) tritt in 30-50% der Fälle nach kardiochirurgi-schen Eingriffen auf. Es geht mit erhöhten Morbiditäts- und Mortalitätsraten einher, führt zu längeren Krankenhausaufenthalten und verursacht Mehrkosten für die Gesund-heitssysteme. Obwohl es häufig transient ist, steigt das Thrombembolierisiko für diesen Zeitraum stark an. Für manche Patienten ist es enorm wichtig, eine schnelle Konversion zu erreichen, um Thrombembolien und Umbauprozesse des Herzens zu vermeiden oder Symptome zu lindern. Elektrische Kardioversion ist effektiv, aber oft nicht beständig. Außerdem erfordert es eine Sedierung des Patienten. Bisher verfügbare Antiarrhythmika sind aufgrund von Kontraindikationen, multiplen Nebenwirkungen oder langen Konver-sionszeiten unzureichend. Vernakalant ist ein seit 2010 zugelassenes Medikament zur Konversion von Vorhofflimmern in den Sinusrhythmus. Es erreicht atriale Selektivität über die multiple Blockade von Kalium- und Natriumkanälen, welche es teilweise fre-quenz- und spannungsabhängig besetzt und damit die Refraktärzeit in den Vorhöfen verlängert. Die Datenlage zur Anwendung bei herzchirurgischen Patienten ist derzeit dünn.
Wir identifizierten 75 Patienten, die im Zeitraum von 10/2011 bis 02/2014 im Anschluss an eine Herzoperation Vorhofflimmern bekamen und mit Vernakalant behandelt wur-den. Ermittelt wurden die unmittelbaren Konversionsraten, sowie die nach 120 Minuten, 10 Tagen und 6 Monaten. Hierzu gab es ein Follow up und den Kontakt zu Hausärzten, Kardiologen und Rehakliniken. Patientencharakteristika, peri- und postoperative Variab-len wurden auf Risikofaktoren für POAF, Prädiktoren für eine erfolgreiche Konversion und Nebenwirkungen hin untersucht.
Die Konversion konnte bei 77% (n=57) der Patienten erreicht werden. 89,2% aller Pati-enten wiesen POAF von ultra-kurzer Dauer (< 24 Stunden) auf. Die mediane Konversi-onszeit lag bei 18 Minuten. Nach 120 Minuten, 10 Tagen und 6 Monaten konnte bei 70,3%, 87,8% und 86% ein Sinusrhythmus nachgewiesen werden. Einzig signifikanter Prädiktor war das jüngere Alter (p = 0,0005). Bei einem Patienten trat ein intermittie-rendes Blockbild auf. Ventrikuläre Arrythmien, lebensbedrohliche Hypotensionen oder Todesfälle wurden nicht beobachtet.
Vernakalant ist effektiv – besonders bei ultra-kurzem (< 24 Stunden) Vorhofflimmern kardiochirurgischer Patienten. Prädiktiv für ein gutes Ansprechen zeigte sich das jüngere Alter. Die Ergebnisse sind als explorative Analyse zu verstehen. Für Aussagen über eine sichere Anwendung müssen weitere, größere, randomisierte und kontrollierte Studien folgen.

Postoperative atrial fibrillation occurs in 30-50% of cases after cardiac surgery. It is ac-companied by increased morbidity and rates of mortality, leads to longer hospital stays and brings about cost overruns for the health care system. Although often transient, the risk of thromboembolism in this time frame greatly increases. For some patients it can be important to obtain a speedy conversion, in order to avoid thromboembolism and re-modeling of the heart, or to alleviate symptoms. Electric cardioversion is effective, but often not enduring. Moreover, it requires sedation of the patient. Until now available antiarrhythmic drugs have been inadequate due to contraindications, multiple side effects or long conversions. Since 2010, Vernakalant has been an approved drug for the conversion from atrial fibrillation back to sinus rhythm. It achieves atrial selectivity through blockade of sodium and potassium channels, which it partly targets, depending upon rate and voltage and thereby prolongs the refractory period in the atria. The availa-bility of data of usage in cardiac patients is currently sparse.
We identified 75 patients, of whom subsequent to cardiac surgery suffered atrial fibrilla-tion and were treated with Vernakalant from 10/2011 until 02/2014. The immediate conversion rates, as well as those after 120 minutes, 10 days and 6 months were ascertained. For this purpose, there was a Follow up and contact to general practitioners, cardiologists and rehabilitation clinics. Patient characteristics, peri- und postoperative variables were screened for risk factors of POAF, indicators of a successful conversion and serious adverse events.
The conversion could be achieved in 77% (n=57) of patients. 89,2% of all patients had POAF for an extremely short period (< 24 hours). The median conversion period was around 18 minutes. After 120 minutes, 10 days and 6 months, a sinus rhythm of 70,3%, 87,8% and 86% could be ascertained. The only significant predictor was younger age (p=0,029). In the case of one patient a bundle branch block occured. Ventricular ar-rhythmia, life-threatening hypotension or death were not observed.
Vernakalant ist effective in treating - exceptionally short - atrial fibrillation of cardio-surgical patients. Younger age is a predictive marker of a good response. The findings should be interpreted as an explorative analysis. For assertations regarding a reliable ap-plication, further, larger, randomized controlled trials must follow up.
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Dokument erstellt am:17.12.2018
Dateien geändert am:17.12.2018
Promotionsantrag am:14.05.2018
Datum der Promotion:11.12.2018
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