Volume 28, Issue s1 pp. S31-S35

A New Endocardial “Over-the-Wire” or Stylet-Driven Left Ventricular Lead:

First Clinical Experience

SUE ELLERY

SUE ELLERY

From St Peter's Hospital, Chertsey, Surrey, United Kingdom

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VINCE PAUL

VINCE PAUL

From St Peter's Hospital, Chertsey, Surrey, United Kingdom

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GUENTHER PRENNER

GUENTHER PRENNER

University Hospital Graz, Austria

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KARLHEINZ TSCHELIESSNIGG

KARLHEINZ TSCHELIESSNIGG

University Hospital Graz, Austria

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BELA MERKELY

BELA MERKELY

Semmelweis Medical University, Budapest, Hungary

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KLAUS MALINOWSKI

KLAUS MALINOWSKI

Helios Clinic, Aue, Germany

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GERD FRÖHLIG

GERD FRÖHLIG

Saarland University Clinics, Homburg/Saar, Germany

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FLORIAN HINTRINGER

FLORIAN HINTRINGER

University of Innsbruck School of Medicine, Innsbruck, Austria

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OLAF BOSSE

OLAF BOSSE

Traunstein Clinic, Traunstein, Germany

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PAOLO DIOTALLEVI

PAOLO DIOTALLEVI

Ospedale Civile SS. Antonio e Biagio, Alessandria, Italy

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ANTONIO P. RAVAZZI

ANTONIO P. RAVAZZI

Ospedale Civile SS. Antonio e Biagio, Alessandria, Italy

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HORST FLATHMANN

HORST FLATHMANN

Center for Clinical Research and Scientific Studies, Biotronik GmbH & Co. KG, Erlangen, Germany

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DEJAN DANILOVIC

DEJAN DANILOVIC

Center for Clinical Research and Scientific Studies, Biotronik GmbH & Co. KG, Erlangen, Germany

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CHRISTINA UNTERBERG-BUCHWALD

CHRISTINA UNTERBERG-BUCHWALD

Georg-August University, Göttingen, Germany

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OVID STUDY INVESTIGATORS

OVID STUDY INVESTIGATORS

From St Peter's Hospital, Chertsey, Surrey, United Kingdom

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First published: 31 January 2005
Citations: 11
Address for reprints: Sue Ellery, St Peter's Hospital, Guildford Road, Chertsey, Surrey, KP15 OPZ, United Kingdom. Fax: +44-(0)-1932-872011; e-mail: [email protected]

The study was funded by: Biotronik GmbH & Co. KG, Berlin, Germany.

Abstract

Transvenous left ventricular (LV) leads are primarily inserted “over-the-wire” (OTW). However, a stylet-driven (SD) approach may be a helpful alternative. A new polyurethane-coated, unipolar LV lead can be placed either by a stylet or a guide wire, which can be inserted into the lead body from both ends. The multicenter OVID study evaluates the clinical performance of this new steroid- and nonsteroid eluting lead. The primary endpoint is the LV lead implant success rate after identification of the coronary sinus (CS). Secondary endpoints include complication rate, short- and long-term lead characteristics, overall procedure and LV lead placement duration, total fluoroscopy time, and lead handling characteristics ratings. To date, 96 patients with heart failure (68 ± 9 years old, 76% men) are enrolled. The CS was identified in 95 patients and, in 85 (88.5%), the LV lead was successfully implanted. The final lead positioning was lateral in 41%, posterolateral in 35%, anterolateral in 18%, and great cardiac vein in 6% of patients. In 70%, the 85 successful implantations, both stylet-driven and guide-wire techniques were used, a stylet only was used in 22%, and a guide wire only in 8%. Mean overall duration of 85 successful procedures was 112 ± 40 minutes, total fluoroscopy time 28 ± 15 minutes, and the duration of LV lead placement was 35 ± 29 minutes. During a 3-month follow-up, the loss of LV capture occurred in three and phrenic nerve stimulation in six patients. The mean long-term pacing threshold is 0.8 V/0.5 ms and pacing impedance is 550 Ω. The OVID data suggest that these new leads are safe and effective. The choice of both OTW and SD techniques during lead implantation offers greater procedural flexibility.

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