Technology

AngioScore Inc. announced the launch of its new 100 mm length AngioSculpt PTA Scoring Balloon Catheters for the treatment of peripheral artery disease (PAD) below the knee (BTK).

Home January 28, 2013
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Technology

Fujifilm Medical Systems U.S.A. Inc. brought a broad portfolio of diagnostic and informatic solutions to the 2012 meeting of the Radiological Society of North America (RSNA). The company showcased its advanced Cardiovascular product, Synapse Cardiovascular 5.0.

Home January 28, 2013
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Feature

January 25, 2013 — Mobile drug reference app provider Epocrates recently conducted its annual survey of cardiologists to uncover the biggest trends and challenges facing them today. The survey explores their perspectives on a range of issues related to patient care, healthcare technology usage/adoption and practice concerns. Following are some highlights from the survey findings.

Home January 25, 2013
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News

The American College of Cardiology (ACC) has released the late-breaking clinical trials that will be highlighted as the cutting edge of cardiology at the ACC.13 annual meeting March 9-11 in San Francisco.

Home January 25, 2013
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BRIT Systems announced new capabilities for their digital imaging and communications in medicine (DICOM) routers that can pre-fetch studies from multiple servers and/or facilities based on select criteria that do not need to include the patient ID. The router morphs the patient ID in a pre-fetched study into the original or trigger ID, storing the pre-fetched IDs into alternate ID fields in both the database and the DICOM header. The new morphing router facilitates the creation of a single patient record and enables clinicians to view all studies on a single timeline. With this capability, clinicians will have access to a complete, cross-facility patient record that can be used to reduce unnecessary or duplicate imaging studies. The new capabilities were highlighted at the Radiological Society of North America (RSNA) annual meeting.

Home January 24, 2013
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AirStrip Technologies Inc. announced that it has entered into a long-term strategic partnership with Vanguard Health Systems Inc.

Home January 24, 2013
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Spectranetics Peripheral Artery Disease Laser Atherectomy
Feature

The Spectranetics Corporation announced final results from the PATENT (Photo-Ablation using the TURBO-Booster(R) and Excimer Laser for In-Stent Restenosis Treatment) study evaluating the safety and efficacy of the Spectranetics peripheral laser atherectomy catheters for the treatment of in-stent restenosis (ISR) in the femoropopliteal artery in the leg. ISR occurs as a result of narrowing of the artery in patients who have undergone stenting for the treatment of peripheral arterial disease (PAD). There is currently no U.S. Food and Drug Administration (FDA)-cleared or approved device to treat peripheral in-stent restenosis, which remains a major unsolved medical problem.

Home January 24, 2013
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According to Millennium Research Group (MRG), the segment of the U.S. nonvascular interventional radiology device market with the fastest growth and greatest potential is ablation devices, comprising radiofrequency (RF) ablation, cryoablation and microwave ablation devices. The overall market will grow moderately to $295 million by 2017.

Home January 23, 2013
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Bathing dangerous blood clots in special medication, breaking them up with jets of saline and vacuuming them out of the body is a fast, effective method of treating deep vein thrombosis (DVT), suggests data being presented at the 25th annual International Symposium on Endovascular Therapy (ISET).

Home January 23, 2013
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St. Jude Medical Inc. announced European CE mark approval of its ViewFlex Xtra Intracardiac Echocardiography (ICE) Catheter. Designed for control and maneuverability during complex cardiac ablation procedures, the technology will be on display at the eighteenth annual Boston AF Symposium.

Home January 23, 2013
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Peri-natal systems real-time clinical decision support company PeriGen Inc. announced the results of an independent validation study on fetal ECG strip interpretation favorably comparing PeriGen PeriCALM Patterns software with the findings of three experts from the National Institute of Health (NIH). The U.S. Food and Drug Administration (FDA)-cleared fetal strip interpretation technology is a component of the company's perinatal central surveillance offering.

Home January 22, 2013
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C-section Hysterectomy Clinical trial Interventional Radiology Balloon Catheter
Feature

Using tiny balloons to temporarily block blood flow to the uterus during a high-risk Caesarean-section delivery can save the life of the mother while preventing hysterectomy and preserving fertility, suggests research being presented at the 25th annual International Symposium on Endovascular Therapy (ISET).

Home January 22, 2013
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Case Study

Cordis Corporation announced the presentation of the two-year STROLL study results at the Abstracts and Late Breaking Clinical Trials session at ISET 2013.

Home January 22, 2013
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News

Biotronik announced that the U.S. Food and Drug Administration (FDA) has approved, with conditions, the ProMRI clinical trial via an Investigational Device Exemption. Biotronik is sponsoring the trial (NCT01761162) and has already initiated U.S. site recruitment. The ProMRI clinical trial is designed to recruit 245 subjects implanted with one of Biotronik’s cardiac devices that include ProMRI technology at 30 U.S. investigational centers.

Home January 22, 2013
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Technology

GNAX Health announced the availability of GNAX SDEX Secure digital imaging and communications in medicine (DICOM) Exchange, allowing hospitals, ACOs and HIEs the ability to transfer medical images securely. The announcement was made by Jeff Hinkle, CEO, GNAX, at the Radiological Society of North America's 98th Scientific Assembly and Annual Meeting in Chicago, Ill.

Home January 21, 2013
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