File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1001/archinternmed.2011.1681
- Scopus: eid_2-s2.0-84858956030
- PMID: 22450940
- WOS: WOS:000301953800014
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Fatal lung toxic effects related to dronedarone use
Title | Fatal lung toxic effects related to dronedarone use |
---|---|
Authors | |
Keywords | Antibiotic agent Dronedarone Methylprednisolone |
Issue Date | 2012 |
Publisher | American Medical Association. The Journal's web site is located at http://www.archinternmed.com |
Citation | Archives of Internal Medicine, 2012, v. 172 n. 6, p. 516-517 How to Cite? |
Abstract | Dronedarone is a derivative of amiodarone that aimed to reduce the extracardiac adverse effects while preserving its antiarrhythmic effects for treatment of atrial fibrillation (AF).1 In the ATHENA trial (A Placebo-Controlled, Double-Blind, Parallel Arm Trial to Assess the Efficacy of Dronedarone 400 mg bid for the Prevention of Cardiovascular Hospitalization or Death from Any Cause in Patients with Atrial Fibrillation/Atrial Flutter),2 dronedarone reduced cardiovascular hospitalization and death in patients with nonpermanent atrial fibrillation (AF) with other cardiovascular risk factors. However, an experimental study3 suggested that dronedarone might have toxic effects on the lung greater than or equal to amiodarone. We describe 2 cases of fatal and near-fatal lung toxic effects associated with dronedarone use. Abstract by, American Medical Association. |
Description | Research letters |
Persistent Identifier | http://hdl.handle.net/10722/159614 |
ISSN | 2014 Impact Factor: 17.333 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Siu, CW | en_US |
dc.contributor.author | Wong, MP | en_US |
dc.contributor.author | Ho, CM | en_US |
dc.contributor.author | Lam, CLD | en_US |
dc.contributor.author | Tse, HF | en_US |
dc.date.accessioned | 2012-08-16T05:53:24Z | - |
dc.date.available | 2012-08-16T05:53:24Z | - |
dc.date.issued | 2012 | en_US |
dc.identifier.citation | Archives of Internal Medicine, 2012, v. 172 n. 6, p. 516-517 | en_US |
dc.identifier.issn | 0003-9926 | - |
dc.identifier.uri | http://hdl.handle.net/10722/159614 | - |
dc.description | Research letters | - |
dc.description.abstract | Dronedarone is a derivative of amiodarone that aimed to reduce the extracardiac adverse effects while preserving its antiarrhythmic effects for treatment of atrial fibrillation (AF).1 In the ATHENA trial (A Placebo-Controlled, Double-Blind, Parallel Arm Trial to Assess the Efficacy of Dronedarone 400 mg bid for the Prevention of Cardiovascular Hospitalization or Death from Any Cause in Patients with Atrial Fibrillation/Atrial Flutter),2 dronedarone reduced cardiovascular hospitalization and death in patients with nonpermanent atrial fibrillation (AF) with other cardiovascular risk factors. However, an experimental study3 suggested that dronedarone might have toxic effects on the lung greater than or equal to amiodarone. We describe 2 cases of fatal and near-fatal lung toxic effects associated with dronedarone use. Abstract by, American Medical Association. | - |
dc.language | eng | en_US |
dc.publisher | American Medical Association. The Journal's web site is located at http://www.archinternmed.com | - |
dc.relation.ispartof | Archives of Internal Medicine | en_US |
dc.subject | Antibiotic agent | - |
dc.subject | Dronedarone | - |
dc.subject | Methylprednisolone | - |
dc.subject.mesh | Aged | - |
dc.subject.mesh | Amiodarone - adverse effects - analogs and derivatives | - |
dc.subject.mesh | Fatal Outcome | - |
dc.subject.mesh | Lung Diseases - chemically induced | - |
dc.subject.mesh | Male | - |
dc.subject.mesh | Aged, 80 and over | - |
dc.subject.mesh | Female | - |
dc.subject.mesh | Humans | - |
dc.title | Fatal lung toxic effects related to dronedarone use | en_US |
dc.type | Article | en_US |
dc.identifier.email | Siu, CW: cwdsiu@hkucc.hku.hk | en_US |
dc.identifier.email | Wong, MP: mwpik@hkucc.hku.hk | en_US |
dc.identifier.email | Ho, CM: jhocm@hku.hk | en_US |
dc.identifier.email | Lam, CL: dcllam@hku.hk | en_US |
dc.identifier.email | Tse, HF: hftse@hku.hk | en_US |
dc.identifier.authority | Siu, CW=rp00534 | en_US |
dc.identifier.authority | Wong, MP=rp00348 | en_US |
dc.identifier.authority | Ho, CM=rp00258 | en_US |
dc.identifier.authority | Lam, CL=rp01345 | en_US |
dc.identifier.authority | Tse, HF=rp00428 | en_US |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1001/archinternmed.2011.1681 | - |
dc.identifier.pmid | 22450940 | - |
dc.identifier.scopus | eid_2-s2.0-84858956030 | - |
dc.identifier.hkuros | 202200 | en_US |
dc.identifier.hkuros | 201297 | - |
dc.identifier.volume | 172 | en_US |
dc.identifier.issue | 6 | en_US |
dc.identifier.spage | 516 | en_US |
dc.identifier.epage | 517 | en_US |
dc.identifier.eissn | 2168-6114 | - |
dc.identifier.isi | WOS:000301953800014 | - |
dc.publisher.place | United States | - |