Use of an implantable loop recorder to increase the diagnostic yield in unexplained syncope: results from the PICTURE registry

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023001%3A_____%2F11%3A00055984" target="_blank" >RIV/00023001:_____/11:00055984 - isvavai.cz</a>

Výsledek na webu

<a href="http://europace.oxfordjournals.org/content/14/6/898.full.pdf+html" target="_blank" >http://europace.oxfordjournals.org/content/14/6/898.full.pdf+html</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1093/europace/euq418" target="_blank" >10.1093/europace/euq418</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Use of an implantable loop recorder to increase the diagnostic yield in unexplained syncope: results from the PICTURE registry

Popis výsledku v původním jazyce

Aims To collect information on the use of the Reveal implantable loop recorder (ILR) in the patient care pathway and to investigate its effectiveness in the diagnosis of unexplained recurrent syncope in everyday clinical practice. Methods and results Prospective, multicentre, observational study conducted in 2006-2009 in 10 European countries and Israel. Eligible patients had recurrent unexplained syncope or pre-syncope. Subjects received a Reveal Plus, DX or XT. Follow up was until the first recurrenceof a syncopal event leading to a diagnosis or for >= 1 year. In the course of the study, patients were evaluated by an average of three different specialists for management of their syncope and underwent a median of 13 tests (range 9-20). Significant physical trauma had been experienced in association with a syncopal episode by 36% of patients. Average follow-up time after ILR implant was 10 +/- 6 months. Follow-up visit data were available for 570 subjects. The percentages of patients

Název v anglickém jazyce

Use of an implantable loop recorder to increase the diagnostic yield in unexplained syncope: results from the PICTURE registry

Popis výsledku anglicky

Aims To collect information on the use of the Reveal implantable loop recorder (ILR) in the patient care pathway and to investigate its effectiveness in the diagnosis of unexplained recurrent syncope in everyday clinical practice. Methods and results Prospective, multicentre, observational study conducted in 2006-2009 in 10 European countries and Israel. Eligible patients had recurrent unexplained syncope or pre-syncope. Subjects received a Reveal Plus, DX or XT. Follow up was until the first recurrenceof a syncopal event leading to a diagnosis or for >= 1 year. In the course of the study, patients were evaluated by an average of three different specialists for management of their syncope and underwent a median of 13 tests (range 9-20). Significant physical trauma had been experienced in association with a syncopal episode by 36% of patients. Average follow-up time after ILR implant was 10 +/- 6 months. Follow-up visit data were available for 570 subjects. The percentages of patients

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

FA - Kardiovaskulární nemoci včetně kardiochirurgie

OECD FORD obor

—

Projekt

—

Návaznosti

N - Vyzkumna aktivita podporovana z neverejnych zdroju

Rok uplatnění

2011

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Europace

ISSN

1099-5129

e-ISSN

—

Svazek periodika

13

Číslo periodika v rámci svazku

2

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

8

Strana od-do

262-269

Kód UT WoS článku

000286466400021

EID výsledku v databázi Scopus

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