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CLINICAL NEWS JACC in a FLASH stroke during follow-up with number of events increasing with worsening renal function. The researchers observed a lower risk of MI after 3 years with ACE inhibitors. In patients with de novo ACE inhibitor/ARB, they observed an even lower risk of MI regardless of renal function. There was not a lower risk of stroke in patients treated with an ACE inhibitor or ARB. In an accompanying editorial, Jay N. Cohn, MD, notes that these findings reaffirm the continued use of ACE inhibitors and ARBs even if patients experience modest increases in creatinine levels and that these drugs should be standard therapy for patients suffering from atherosclerotic disease. “Since renal dysfunction may serve as a signal for more severe vascular disease, its presence should if anything, enhance the message,” he writes. with the higher risk, CAC of 4-12, 56% had high risk BAC, 17% had 1-3 BAC and 27% had 0 BAC. The researchers also found that BAC was superior to conventional risk factors. The agreements of Framingham Risk Scores in the population were only 57% for CAC and 55% for BAC. The agreement of pooled cohort equation risk categories were 47% for CAC and 54% for BAC. According to the authors, these findings strongly suggest that BAC should be studied further. It may be reasonable to recommend that BAC positive women receive further Orenitram is indicated for the treatment of pulmonary arterial hypertension (PAH) (WHO Group 1) to improve exercise capacity FOR pulmonary arterial hypertension ORENITRAM DOSING ADAPTS Evan M, Carrero JJ, Szummer K, et al. J Am Coll Cardiol. 2016;doi:10.1016/j. jacc.2016.01.050. Can a Mammogram Detect CV Risk? Breast arterial calcification (BAC), seen on a digital mammography, is strongly associated with coronary artery calcium (CAC), an early sign of heart disease, according to a study published March 24 in JACC: Cardiovascular Imaging and presented at the ACC’s 65th Annual Scientific Session in Chicago, IL. BAC was found in 42.5% of the 292 women included in the study while CAC was found in 47.6% of the cohort. The mean BAC score was 2.2 ± 2.9 and the mean CAC score was 1.6 ± 2.5. The frequency of BAC and CAC increased as the age of the patients increased. The positive predictive value of BAC > 0 increased from 53% to 86% and the negative predictive value decreased from 81% to 36% with increasing age. There was an increasing frequency of both BAC and CAC with increasing age as well as increasing percentages of higher CAC in those with BAC. In 76% of patients with 0 CAC also had 0 BAC, and 10% had 1-3 BAC and 14% had 4-12 BAC. In the 1-3 CAC group, the BAC was evenly distributed. In those 16 risk assessment for heart disease, preferably with a CAC scan. It is also important to note that the absence of BAC does not assure low cardiovascular risk. In an accompanying editorial comment, Khurram Nasir, MD, MPH and John W. McEvoy, MB BCH BAO, Introduce prostacyclin treatment early with Orenitram, which enables you to adjust dose based on tolerability and clinical response. The only prostacyclin analogue in a tablet: For PAH, a progressive disease1-3 Early use in FC II and III1 Ability to transition from treprostinil parenteral therapy1* Orenitram allows you to initiate treatment with 0.125 mg TID (~8 hrs apart) or 0.25 mg BID (~12 hrs apart), then titrate up or down every 3 to 4 days as needed per Full Prescribing Information (PI). In the pivotal trial, dose was titrated based on clinical response and tolerability. If not tolerated, titrate slower or decrease dose by 0.25 mg. Avoid abrupt discontinuation. Orenitram tablets should be taken whole and with food. If a dose is missed, please refer to the PI. Orenitram should not be used in patients with moderate hepatic impairment. Dose adjustments required for mild hepatic impairment. *In a 24-week, multicenter, open-label study to establish safety and tolerability of transition, WHO Group 1 patients (FC I or II) on stable doses of IV/SC treprostinil as well as a PDE-5i and/or ERA were evaluated. request aN ORENITRAM representative or VISIT orenitram.com © 2016 Unit ed Therapeutics Corporation. All rights reserved. US/ORE/DEC15/146a Printed in USA. CardioSource WorldNews 7618-7_FullSpreadResize_CardioSourceWorldNews_M1.indd 1