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Safety of in-hospital insertable cardiac monitor procedures performed outside the traditional settings: results from the Reveal LINQ in-office 2 international study

BACKGROUND: Historically, the majority of insertable cardiac monitor (ICM) procedures were performed in the cardiac catheterization (cath) lab, electrophysiology (EP) lab, or operating room (OR). The miniaturization of ICMs allows the procedure to be relocated within the hospital without compromisin...

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Autores principales: Sanders, Prashanthan, Piorkowski, Christopher, Kragten, Johannes A., Goode, Grahame K., Raj, Satish R., Dinh, Trang, Sohail, M. Rizwan, Anand, Rishi, Moya-Mitjans, Angel, Franco, Noreli, Stromberg, Kurt, Rogers, John D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6545016/
https://www.ncbi.nlm.nih.gov/pubmed/31151383
http://dx.doi.org/10.1186/s12872-019-1106-3
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author Sanders, Prashanthan
Piorkowski, Christopher
Kragten, Johannes A.
Goode, Grahame K.
Raj, Satish R.
Dinh, Trang
Sohail, M. Rizwan
Anand, Rishi
Moya-Mitjans, Angel
Franco, Noreli
Stromberg, Kurt
Rogers, John D.
author_facet Sanders, Prashanthan
Piorkowski, Christopher
Kragten, Johannes A.
Goode, Grahame K.
Raj, Satish R.
Dinh, Trang
Sohail, M. Rizwan
Anand, Rishi
Moya-Mitjans, Angel
Franco, Noreli
Stromberg, Kurt
Rogers, John D.
author_sort Sanders, Prashanthan
collection PubMed
description BACKGROUND: Historically, the majority of insertable cardiac monitor (ICM) procedures were performed in the cardiac catheterization (cath) lab, electrophysiology (EP) lab, or operating room (OR). The miniaturization of ICMs allows the procedure to be relocated within the hospital without compromising patient safety. We sought to estimate the rate of untoward events associated with procedures performed within the hospital but outside the traditional settings and to characterize resource utilization, procedure time intervals, and physician experience. METHODS: The Reveal LINQ in-Office 2 (RIO 2) International study was a single arm, multicenter, prospective study. Patients indicated for an ICM and willing to undergo device insertion outside the cath/EP lab or OR were eligible and followed for 90 days after insertion. RESULTS: A total of 191 patients (45.5% female aged 63.8 ± 26.9 years) underwent successful Reveal LINQ ICM insertion at 17 centers in Europe, Canada and Australia. The median total visit duration was 106 min (interquartile range [IQR]: 55–61). Patient preparation and patient education accounted for 10 min (IQR: 5–20) and 10 min (IQR: 8–15) of total visit duration, respectively. Preparation and education occurred in the procedure room for 90.6 and 60.2% of patients, respectively. There were no untoward events (0.0, 95% CI: 0.0–2.1%) though four patients presented with procedure-related adverse events that did not require invasive intervention. Physicians rated procedure location as convenient or very convenient. CONCLUSIONS: The Reveal LINQ™ ICM insertion can be safely and efficiently performed in the hospital outside the cath/EP lab or OR. TRIAL REGISTRATION: ClinicalTrials.gov identifier NCT02412488; registered on April 9, 2015. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12872-019-1106-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-65450162019-06-04 Safety of in-hospital insertable cardiac monitor procedures performed outside the traditional settings: results from the Reveal LINQ in-office 2 international study Sanders, Prashanthan Piorkowski, Christopher Kragten, Johannes A. Goode, Grahame K. Raj, Satish R. Dinh, Trang Sohail, M. Rizwan Anand, Rishi Moya-Mitjans, Angel Franco, Noreli Stromberg, Kurt Rogers, John D. BMC Cardiovasc Disord Technical Advance BACKGROUND: Historically, the majority of insertable cardiac monitor (ICM) procedures were performed in the cardiac catheterization (cath) lab, electrophysiology (EP) lab, or operating room (OR). The miniaturization of ICMs allows the procedure to be relocated within the hospital without compromising patient safety. We sought to estimate the rate of untoward events associated with procedures performed within the hospital but outside the traditional settings and to characterize resource utilization, procedure time intervals, and physician experience. METHODS: The Reveal LINQ in-Office 2 (RIO 2) International study was a single arm, multicenter, prospective study. Patients indicated for an ICM and willing to undergo device insertion outside the cath/EP lab or OR were eligible and followed for 90 days after insertion. RESULTS: A total of 191 patients (45.5% female aged 63.8 ± 26.9 years) underwent successful Reveal LINQ ICM insertion at 17 centers in Europe, Canada and Australia. The median total visit duration was 106 min (interquartile range [IQR]: 55–61). Patient preparation and patient education accounted for 10 min (IQR: 5–20) and 10 min (IQR: 8–15) of total visit duration, respectively. Preparation and education occurred in the procedure room for 90.6 and 60.2% of patients, respectively. There were no untoward events (0.0, 95% CI: 0.0–2.1%) though four patients presented with procedure-related adverse events that did not require invasive intervention. Physicians rated procedure location as convenient or very convenient. CONCLUSIONS: The Reveal LINQ™ ICM insertion can be safely and efficiently performed in the hospital outside the cath/EP lab or OR. TRIAL REGISTRATION: ClinicalTrials.gov identifier NCT02412488; registered on April 9, 2015. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12872-019-1106-3) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-31 /pmc/articles/PMC6545016/ /pubmed/31151383 http://dx.doi.org/10.1186/s12872-019-1106-3 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Technical Advance
Sanders, Prashanthan
Piorkowski, Christopher
Kragten, Johannes A.
Goode, Grahame K.
Raj, Satish R.
Dinh, Trang
Sohail, M. Rizwan
Anand, Rishi
Moya-Mitjans, Angel
Franco, Noreli
Stromberg, Kurt
Rogers, John D.
Safety of in-hospital insertable cardiac monitor procedures performed outside the traditional settings: results from the Reveal LINQ in-office 2 international study
title Safety of in-hospital insertable cardiac monitor procedures performed outside the traditional settings: results from the Reveal LINQ in-office 2 international study
title_full Safety of in-hospital insertable cardiac monitor procedures performed outside the traditional settings: results from the Reveal LINQ in-office 2 international study
title_fullStr Safety of in-hospital insertable cardiac monitor procedures performed outside the traditional settings: results from the Reveal LINQ in-office 2 international study
title_full_unstemmed Safety of in-hospital insertable cardiac monitor procedures performed outside the traditional settings: results from the Reveal LINQ in-office 2 international study
title_short Safety of in-hospital insertable cardiac monitor procedures performed outside the traditional settings: results from the Reveal LINQ in-office 2 international study
title_sort safety of in-hospital insertable cardiac monitor procedures performed outside the traditional settings: results from the reveal linq in-office 2 international study
topic Technical Advance
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6545016/
https://www.ncbi.nlm.nih.gov/pubmed/31151383
http://dx.doi.org/10.1186/s12872-019-1106-3
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