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- Publisher Website: 10.1111/j.1440-1681.1997.tb02734.x
- Scopus: eid_2-s2.0-0030831918
- PMID: 9406671
- WOS: WOS:A1997YJ03600018
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Conference Paper: Electrical remodelling of chronic atrial fibrillation
Title | Electrical remodelling of chronic atrial fibrillation |
---|---|
Authors | |
Keywords | Atrial fibrillation Electrophysiology Remodelling |
Issue Date | 1997 |
Publisher | Blackwell Publishing Asia. The Journal's web site is located at http://www.blackwellpublishing.com/journals/CEP |
Citation | Clinical And Experimental Pharmacology And Physiology, 1997, v. 24 n. 12, p. 982-983 How to Cite? |
Abstract | 1. It is now recognized that atrial fibrillation (AF) is not a benign condition, as it is associated with a 40% increase in mortality and a doubling of the risk of stroke. 2. The development of AF leads to mechanical, electrophysiological and cellular changes in the atria that fend to sustain AF. This process is known as atrial remodelling. 3. The three electrophysiological elements in the atria that initiate and sustain AF are: (i) shortening of the refractory period and an increase in dispersion; (ii) slowing of conduction velocity; and (iii) the presence of triggering foci. 4. As AF is a heterogeneous disorder, therapeutic strategies include the use of devices (pacemakers and atrial defibrillators), radiofrequency ablation (focal ablation or the creation of linear lines) and drug therapy that may reverse a remodelled atrium. |
Description | Proceedings of the Symposium on Cardiovascular Science and Medicine: From Bench to Bedside, Hong Kong, April 1997. |
Persistent Identifier | http://hdl.handle.net/10722/77424 |
ISSN | 2023 Impact Factor: 2.4 2023 SCImago Journal Rankings: 0.610 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lau, CP | en_HK |
dc.contributor.author | Tse, HF | en_HK |
dc.date.accessioned | 2010-09-06T07:31:45Z | - |
dc.date.available | 2010-09-06T07:31:45Z | - |
dc.date.issued | 1997 | en_HK |
dc.identifier.citation | Clinical And Experimental Pharmacology And Physiology, 1997, v. 24 n. 12, p. 982-983 | en_HK |
dc.identifier.issn | 0305-1870 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/77424 | - |
dc.description | Proceedings of the Symposium on Cardiovascular Science and Medicine: From Bench to Bedside, Hong Kong, April 1997. | - |
dc.description.abstract | 1. It is now recognized that atrial fibrillation (AF) is not a benign condition, as it is associated with a 40% increase in mortality and a doubling of the risk of stroke. 2. The development of AF leads to mechanical, electrophysiological and cellular changes in the atria that fend to sustain AF. This process is known as atrial remodelling. 3. The three electrophysiological elements in the atria that initiate and sustain AF are: (i) shortening of the refractory period and an increase in dispersion; (ii) slowing of conduction velocity; and (iii) the presence of triggering foci. 4. As AF is a heterogeneous disorder, therapeutic strategies include the use of devices (pacemakers and atrial defibrillators), radiofrequency ablation (focal ablation or the creation of linear lines) and drug therapy that may reverse a remodelled atrium. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Blackwell Publishing Asia. The Journal's web site is located at http://www.blackwellpublishing.com/journals/CEP | en_HK |
dc.relation.ispartof | Clinical and Experimental Pharmacology and Physiology | en_HK |
dc.subject | Atrial fibrillation | - |
dc.subject | Electrophysiology | - |
dc.subject | Remodelling | - |
dc.subject.mesh | Atrial Fibrillation - physiopathology | en_HK |
dc.subject.mesh | Chronic Disease | en_HK |
dc.subject.mesh | Electrophysiology | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.title | Electrical remodelling of chronic atrial fibrillation | en_HK |
dc.type | Conference_Paper | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0305-1870&volume=24&spage=982&epage=&date=1997&atitle=Electrical+Remodelling+of+Chronic+Atrial+Fibrillation | en_HK |
dc.identifier.email | Tse, HF:hftse@hkucc.hku.hk | en_HK |
dc.identifier.authority | Tse, HF=rp00428 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1111/j.1440-1681.1997.tb02734.x | - |
dc.identifier.pmid | 9406671 | - |
dc.identifier.scopus | eid_2-s2.0-0030831918 | en_HK |
dc.identifier.hkuros | 32857 | en_HK |
dc.identifier.hkuros | 28864 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0030831918&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 24 | en_HK |
dc.identifier.issue | 12 | en_HK |
dc.identifier.spage | 982 | en_HK |
dc.identifier.epage | 983 | en_HK |
dc.identifier.isi | WOS:A1997YJ03600018 | - |
dc.publisher.place | Australia | en_HK |
dc.identifier.scopusauthorid | Lau, CP=7401968501 | en_HK |
dc.identifier.scopusauthorid | Tse, HF=7006070805 | en_HK |
dc.identifier.issnl | 0305-1870 | - |