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NxStage: NIH Study Published in New England Journal of Medicine Adds to Growing Body of Evidence in Support of More Frequent Hemodialysis
Date:9/23/2011

ure that all patients have access to more frequent hemodialysis."

Among its published findings, the study showed that the long (2-day) interdialytic interval is a time of heightened risk among patients receiving conventional dialysis for all-cause mortality, mortality from cardiac causes and cardiac arrest, infection related mortality, mortality from myocardial infarction, and hospital admissions for complications including myocardial infarction, congestive heart failure, stroke, dysrhythmia, and any cardiovascular events.

Study results were published in the New England Journal of Medicine http://www.nejm.org/doi/full/10.1056/NEJMoa1103313?query=featured_home& on September 22, 2011.

About the NxStage System One

The NxStage System One is the first and only truly portable hemodialysis system cleared for home use by the U.S. Food & Drug Administration (FDA). Its simplicity and revolutionary size (just over a foot tall) are intended to allow convenient use in patients' homes and give patients the freedom to travel with their therapy.   When combined with the NxStage Pureflow SL Dialysis Preparation System, patients are able to further simplify, using ordinary tap water to create dialysis fluid on demand.  Unlike conventional hemodialysis systems, the System One requires no special infrastructure to operate. Under the guidance of their physician, patients can use the NxStage System One, with their trained partners, where, how and when it best meets their needs, at home or on vacation.

About NxStage Medical

NxStage Medical, Inc. (Nasdaq: NXTM) is a medical device company, headquartered in Lawrence, Massachusetts, USA, that develops, manufactures and markets innovative systems for the treatment of end-stage renal disease, o
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SOURCE NxStage Medical, Inc.
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