Szumowski Lukasz, Bodalski Robert, Jedynak Zbigniew, Szufladowicz Ewa, Kepski Roman, Derejko Paweł, Urbanek Piotr, Michalak Ewa, Orczykowski Michał, Zakrzewska Joanna, Przybylski Andrzej, Walczak Franciszek
Institute of Cardiology, Warszawa Anin, Poland.
Cardiol J. 2008;15(4):365-70.
Pseudo-Mahaim (AP-M) fibers are a rare variant of atrioventricular (AV) accessory pathways. Atriofascicular and atrioventricular accessory connections are characterized by slow conduction and decremental properties. Dual physiological AV node pathways, slow and fast, are observed in a large number of patients with AP-M. Therefore, there is substrate for AV nodal reentrant tachycardia (AVNRT) in addition to antidromic AV reentrant tachycardia (AVRT) with left bundle branch block (LBBB)-like morphology. Other arrhythmia such as atrial fibrillation (AF) or atrial flutter (AFL) and ventricular fibrillation (VF) are also observed. We analysed the occurrence of arrhythmias in a group of patients with AP-M treated in our department.
We evaluated 27 patients (12 women) aged 14-53 years (mean age 25.6 years) with AP-M. The clinical course in these patients, in particular with regard to the occurrence of arrhythmias, was analysed. Patients with dual AV node properties were compared to patients without such findings.
We found dual AV node properties in 18 patients (Group 1), while 9 patients had fast pathway only (Group 2). Twenty-six patients presented with AVRT, 2 patients with AVNRT, 3 patients with AF, 1 patient with AT, 2 patients with AFL, and 3 patients with VF. In 2 patients, AP-M were seen in an atypical area. In one patient, the pathway connected the right atrium with the left ventricle (septal region), and in the other patient it connected the left atrium with the left ventricle (left anterior region).
The majority of AP-M was right-sided. Two thirds of patients with AP-M had anatomical substrate for AVNRT (fast/slow pathway AV node). VF or asystole occurred in 10% of patients.
伪Mahaim(AP-M)纤维是房室(AV)旁路的一种罕见变异类型。房室束旁和房室旁路连接的特点是传导缓慢且具有递减特性。在大量AP-M患者中可观察到双生理房室结路径,即慢径和快径。因此,除了具有左束支传导阻滞(LBBB)样形态的逆向房室折返性心动过速(AVRT)外,还存在房室结折返性心动过速(AVNRT)的基质。还观察到其他心律失常,如心房颤动(AF)或心房扑动(AFL)以及心室颤动(VF)。我们分析了在我科接受治疗的一组AP-M患者的心律失常发生情况。
我们评估了27例年龄在14至53岁(平均年龄25.6岁)的AP-M患者(12例女性)。分析了这些患者的临床病程,特别是心律失常的发生情况。将具有双房室结特性的患者与未发现此类情况的患者进行比较。
我们发现18例患者(第1组)具有双房室结特性,而9例患者仅具有快径(第2组)。26例患者出现AVRT,2例患者出现AVNRT,3例患者出现AF,1例患者出现房性心动过速(AT),2例患者出现AFL,3例患者出现VF。在2例患者中,AP-M出现在非典型区域。1例患者中,旁路连接右心房与左心室(间隔区域),另1例患者中,旁路连接左心房与左心室(左前区域)。
大多数AP-M位于右侧。三分之二的AP-M患者具有AVNRT(快/慢径房室结)的解剖学基质。10%的患者发生VF或心搏停止。