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EANS-Adhoc: LifeWatch announces joint development of new breakthrough test for its wireless cardiac monitoring platform (with document)
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 ad-hoc disclosure transmitted by euro adhoc with the aim of a Europe-wide
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 announcement.
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24.02.2012
The testing technology will be deployed on LifeWatch wireless cardiac monitors
 in coming months.
Neuhausen am Rheinfall/Switzerland - LifeWatch AG (SIX Swiss Exchange:LIFE), the
 leading wireless cardiac monitoring service provider in the U.S., announced
 today the joint development of additional Sympathetic and Parasympathetic
 testing with the ANSAR Group.
For the first time in the wireless cardiac monitoring industry, the treating
 physician will be able to measure individual parasympathetic and sympathetic
 responses of their patient. This information will be significant in providing
 additional clinical data for patients with Atrial Fibrillation, Syncope
 (fainting), Congestive Heart Failure, Cardiac Autonomic Neuropathy (associated
 with increased risk of mortality and morbidity) and Hypertension. These
 conditions together affect an estimated 99 million Americans1. An additional
 subset of patients who could benefit from this test includes millions of
 Americans who are currently prescribed Beta blockers.
"The Ansar test integrated with our ACT cardiac telemetry platform is a very
 important technological advance", stated Dr. Yacov Geva, Chairman and CEO of
 LifeWatch AG. "For the first time ever, a physician will be provided with
 invaluable clinical information about a patient's sympathetic and
 parasympathetic nervous system in a comprehensive arrhythmia report via an
 outpatient cardiac monitoring platform. The data generated from the Ansar test
 and LifeStar ACT cardiac monitor will assist in guiding therapy. Physicians will
 be able to diagnose vasovagal or neurocardiogenic syncope, orthostasis,
 arrhythmia or palpitations caused by surges in the parasympathetic or
 sympathetic tone with the LifeWatch ACT monitor. This has the potential to
 improve patient outcomes, reduce medication loads, hospitalizations, unnecessary
 deaths and overall healthcare costs. It is an honor for LifeWatch to be able to
 empower physicians with this capability."
The Ansar parasympathetic and sympathetic response monitoring test allows for
 the differential diagnosis of three main causes of syncope (neurogenic,
 vasovagal and cardiogenic), and other causes of dizziness (including orthostasis
 and arrhythmia). These individual measurements can be recorded preceding an
 arrhythmic event, which will provide physicians with clear and precise
 documentation of the causes of underlying syncope, dizziness, arrhythmia, chest
 pain, or sleep disordered cardiac disturbances, etc., and aid the physician in
 the differential diagnosis and guiding therapy.
The easy-to-use test utilizes a LifeStar ACT wireless cardiac monitor enabling
 real-time viewing of the ECG before the patient is sent home for continued
 arrhythmia monitoring. The Ansar test, which is reimbursable, includes
 physiological parameters equivalent to a head-up tilt table test, and has
 demonstrated higher rates of specificity and sensitivity2. This test is
 encouraged by many of the leading professional medical societies in the United
 States, including the AHA, ADA, JDFI, AAN, AAFP, NIH. Published, peer-reviewed,
 parasympathetic and sympathetic response testing data shows how to optimize
 therapy for many difficult to treat conditions, including Atrial Fibrillation,
 Heart Failure, Hypertension, Dizziness (including syncope) and sleep disorders.
 This technology will be available in the US in the following months.
Sources: 1. Circulation 2012, 125:e2-e220, 2. Am Heart J 1997;134:316-20.
About LifeWatch AG:
LifeWatch AG, headquartered in Neuhausen am Rheinfall and listed on SIX Swiss
 Exchange (LIFE), Switzerland, is the leading healthcare technology and solution
 company, specializing in advanced telehealth systems and wireless remote patient
 monitoring services. LifeWatch services cater to individuals, ranging from
 high-risk and chronically ill patients, to consumers of health and wellness
 products. LifeWatch has subsidiaries in the United States, the Netherlands,
 Japan, the United Kingdom, Switzerland and Israel. LifeWatch AG is the parent
 company of LifeWatch Services Inc., a leading US-based cardiac monitoring
 service provider, and manufacturer of telecardiology products. LifeWatch is also
 introducing a new program for Home Sleep Testing of Obstructive Sleep Apnea
 (OSA) patients under the brand name NiteWatch. For additional information,
 please visit http://www.lifewatch.com.
Sign-up for customized E-mail alerts and documentation requests is available at 
 http://production.investis.com/lifewatch/alert-service/
This press release includes forward-looking statements. All statements other
 than statements of historical facts contained in this press release, including
 statements regarding future results of operations and financial position,
 business strategy and plans and objectives for future operations, are
 forward-looking statements. The words "believe," "may," "will," "estimate,"
 "continue," "anticipate," "intend," "expect" and similar expressions are
 intended to identify forward-looking statements. LifeWatch AG has based these
 forward-looking statements largely on current expectations and projections about
 future events and financial trends that it believes may affect the financial
 condition, results of operations, business strategy, short term and long term
 business operations and objectives, and financial needs. These forward-looking
 statements are subject to a number of risks, uncertainties and assumptions. In
 light of these risks, uncertainties and assumptions, the forward-looking events
 and circumstances described may not occur and actual results could differ
 materially and adversely from those anticipated or implied in the
 forward-looking statements. All forward-looking statements are based only on
 data available to LifeWatch AG at the time of the issue of this press release.
 LifeWatch AG does not undertake any obligation to update any forward-looking
 statements contained in this press release as a result of new information,
 future events or otherwise.
THIS PRESS RELEASE IS NOT BEING ISSUED IN THE UNITED STATES OF AMERICA AND
 SHOULD NOT BE DISTRIBUTED TO UNITED STATES PERSONS OR PUBLICATIONS WITH A
 GENERAL CIRCULATION IN THE UNITED STATES. THIS PRESS RELEASE DOES NOT CONSTITUTE
 AN OFFER OF SECURITIES OF LIFEWATCH AG OR ANY OF ITS SUBSIDIARIES FOR SALE IN
 THE UNITED STATES OR AN INVITATION TO SUBSCRIBE FOR OR PURCHASE ANY SECURITIES
 OF LIFEWATCH AG OR ITS SUBSIDIARIES IN THE UNITED STATES. IN ADDITION, THE
 SECURITIES OF LIFEWATCH AG AND ITS SUBSIDIARIES HAVE NOT BEEN REGISTERED UNDER
 THE UNITED STATES SECURITIES LAWS AND MAY NOT BE OFFERED, SOLD OR DELIVERED
 WITHIN THE UNITED STATES OR TO U.S. PERSONS ABSENT REGISTRATION UNDER OR AN
 APPLICABLE EXEMPTION FROM THE REGISTRATION REQUIREMENTS OF THE UNITED STATES
 SECURITIES LAWS. ANY PUBLIC OFFERING OF SECURITIES TO BE MADE IN THE UNITED
 STATES WILL BE MADE BY MEANS OF A PROSPECTUS THAT MAY BE OBTAINED FROM LIFEWATCH
 AG OR ITS SUBSIDIARIES, AS APPLICABLE, AND WILL CONTAIN DETAILED INFORMATION
 ABOUT THE ISSUER AND ITS MANAGEMENT AS WELL AS FINANCIAL STATEMENTS OF THE
 ISSUER.
Further inquiry note:
 Sensus Investor and Public Relations GmbH, Zürich:
 Tel+41 433665511 | Fax+41 43 366 55 12|Email lifewatch@sensus.ch
 end of announcement euro adhoc 
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Attachments with Announcement:
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 http://resources.euroadhoc.com/us/9HSfZYNF
issuer: LifeWatch AG
 Rundbuckstrasse 6
 CH-8212 Neuhausen am Rheinfall
 phone: +41 52 632 00 50
 FAX: +41 52 632 00 51
 mail: users@lifewatch.com
 WWW: www.lifewatch.com
 sector: Healthcare Providers
 ISIN: CH0012815459
 indexes: SPI, SPIEX
 stockmarkets: free trade: Berlin, Open Market / XETRA: Frankfurt, Main Standard:
 SIX Swiss Exchange 
 language: English
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