心房颤动:我们到底知道多少?

来源 :中华心律失常学杂志 | 被引量 : 0次 | 上传用户:wangheng1991
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Atrial fibrillation (AF) is one of the most emphasized issues in the past two decades. But till now, we really know little about its mechanisms. The three classical theories about AF mechanism could not totally eluci-date the occurrence and development of AF. The remodeling theory including structural and electrical remodeling was used to interpret the pathological course. Based on patch-clamp studies, kinetics of a lot of ion channels such as potassium, calcium, sodium channel were involved in the development of AF. But the change of single channel can not explain the whole aspects of electrical remodeling and also can not explain the interaction of multichannels and microcosmic circumstance. Autonomic nervous system seems to play an important role in AF, but its real effects were still controversial. Gene research of familial AF and gene therapy of AF were emerged in recent years. More efforts will be put on the mutated gene and provide candidates for gene therapy. One paper on this issue writ-ten by HUANG Cong-xin, ZHANG Shu, MA Chang-sheng et al, on behalf of the working group of Chinese society of pacing and Electrophysiology, is worthy to read carefully[1]. The highlights of AF therapeutics were focus on non-drug therapies, especially on radiofrequency catheter ablation (RFCA). RFCA may be the most promise therapy to cure AF. Now, there are several kinds of RFCA including CPVI, SPVI, CFAE ablation, Ganglion plex ablation and stepwise ablation[15-20]. The most accepted methods is CPVI with or without extension. The success rates of RF-CA is still not satisfied[1,15,17-18,20-21]. The other question we encountered in RFCA is how to improve and optimize procedures and techniques[1,15,17-18,20-21]. Also, a lot of attention is paid to drug therapy of AF[1]. Dronedarone was supposed to replace anmiodarone with less side-effects and more efficient. Unfortunately, the clinical data did not support the hypothesis. The investigation of new anti-coagulant meets the same embarrassment. Ximelagatran could not get into market because of its hepatic toxicity[1]. In conclusion, there are only a little achievements regarding AF. There are still many hard tasks to be deal with in AF area.
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