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innovation dot com.

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Worldwide, cardiovascular

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disease affects the lives of hundreds of millions,

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Dedicated cardio nerds everywhere. Are working hard to

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fight this global epidemic. These are their stories.

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Hi, everyone. Dan M here. On behalf of

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all of us at coordinators, we are thrilled

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to bring you our decipher for the guideline

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syringe for the 20 20 2AHA

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guideline for the management of heart failure, get

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ready for short and bite sized, high impact

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critical did yet based questions designed to highlight

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core concepts based on cutting edge evidence that

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are relevant to your practice. The cases we

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use are hypothetical and for educational purposes only.

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This series was developed by car and created

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in collaboration with the American

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association and the Heart failure Society of America.

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It was created by 30 trainees spanning college

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students through advanced fellowship with mentorship doctor Anu

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la, Doctor. Robert Men and Doctor. Nancy Sc,

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we thank Doctor. Judy And doctor Elliot Amin

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for their guidance. So join us as we

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get to learn about the guidelines and beyond

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from 16 leading faculty experts. With that said,

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it's time to get nerdy.

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The following question refers to section 5.1 of

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the 2022

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a

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acc, H guidelines for the management of heart

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failure.

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The question is asked by ke School of

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Medicine and Usc Medical student and cardio earth's

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intern, First El,

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answered first by recent advanced heart failure and

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transplant fellowship graduate and our faculty at the

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University of Chicago and c chair for the

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Cardio critical care cardiology series, Doctor Mark Be,

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and then by expert faculty, Doctor Vi Bo.

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Doctor. Ba is the Marion Gordon Keen sc,

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professor of Medicine,

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director of the Winter center for heart failure

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research and an advanced heart failure and transplant

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cardiologist

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at Baylor College of Medicine in Houston, Texas.

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She the former president of H,

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former senior associate editor for circulation, and the

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current editor and chief of Jack Heart failure.

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Doctor Bo was the Vice chair of the

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writing committee for the 2002 heart failure guidelines.

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Doctor Bo is an honor to have you

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with us. A great pleasure for me to

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be with you at the cardio nerds. It's

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a fantastic platform for timely and insightful

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conversations in cardiology and heart failure.

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Thank you for inviting me.

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Jason, thank you so much for the intro.

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And Mark, my question for you today is

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about a 63 year old patient with the

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past medical history of hypertension. And type 2

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diabetes

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who presents for routine follow up.

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Your reports feeling in general Good health and

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enjoys 2 mile walks daily

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Review of symptoms is negative for any symptoms.

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Which of the following laboratory studies may be

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beneficial for screening.

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Option a is Nt prob b p,

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option b, ck k mb.

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Option c, troponin,

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option d,

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Crp

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and option e, none of the above. And,

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Mark, oh, yeah, I love your help figuring

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out what the next step should be for

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this patient. Thanks Harsh. That's a great question

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and comes up frequently clinic.

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Correct answers is a, nt prob p. The

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patient's at risk for heart failure or stage

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a, given the presence of risk factors of

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hypertension and type 2 diabetes, but absence of

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signs of symptoms of heart failure.

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Patients at risk for heart failure screened with

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B p or anti nt prob

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followed by collaborative care, diagnostic

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evaluation and treatment in those elevated levels can

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reduce combined rates of L systolic dysfunction, diastolic

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dysfunction and heart failure.

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The stop H trial, which was the saint

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vincent screening to prevent heart failure study, is

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a large single center trial of patients at

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risk for heart failure. That showed B based

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screening reduce the composite endpoint of incident

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asymptomatic L dysfunction with or without newly diagnosed

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heart failure.

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Therefore, for patients at risk of developing heart

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failure,

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peptide biomarker a based screening followed by team

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based care, including a cardiovascular specialist optimizing guidelines

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directed medical therapy can be useful to prevent

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the development of l dysfunction, whether assist systolic

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diastolic or and heart failure. Find Is that

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class 2a a recommendation with the level evidence

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b from a randomized control trial. There is

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no indication for measuring troponin, Ck b or

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Cr at this time. The main takeaway here

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is in patients at risk for heart failure,

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screening for pre heart failure using peptide testing

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followed by team based care may be helpful

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for preventing disease progression.

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So about Actually in in my short time

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now is faculty have seen us a few

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times in clinic. The guidelines are pretty clear

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in 1 to screen of peptides, but how

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often do you repeat the testing after your

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initial screen?

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It's a great question. And the examine what

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was done in this stop H f trial,

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which, this recommendation was formulated

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from, they screen on an annual basis.

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The approach was very well structured, and a

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randomized to the B screening versus own screening.

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And if

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Amongst the screen ones on an annual basis,

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B levels exceeded that of 50.

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Per liter is actually a relatively

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low value.

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If the level exceeded that of 50, they

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down refer to this multi disciplinary chair coordination

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that included a cardiovascular specialist, As to 1

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wonders what did they exactly do because these

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individuals were with hypertension diabetes, coronary artery disease,

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but without

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established heart failure. So what they did was,

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they actually

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image

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and treated the risk factors very effectively.

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And when they

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enhanced this risk treatment strategies,

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the endpoint was very striking in the sense

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that both the future development of heart failure,

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mace events, and future development of diastolic or

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systolic

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dysfunction was prevented. So a very important trial

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and that gives a glimpse into what this

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structure of the screening could be. So back

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to your question, top H trial

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screened on an annual basis.

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Perhaps 1 approach could be

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the risk.

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If the risk is high, annual screening makes

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sense. If the risk is low, like that

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23 year old, 1 and probably reduce the

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frequency of screening to several years apart. And

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maybe only do it when there is a

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change either in the profile and or in

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the risk category. So the population based screening

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levels

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rely on cost effectiveness and the pre test

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likelihood.

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And the stop H trial actually was further

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analyzed and the B based screening was found

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to be cost effective, and thus it is

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likely gonna be in rated in our practice,

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especially for the patient, like, the 1 that

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you just presented, who truly would benefit from

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a screening and optimization of treatment strategies that

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are targeted towards heart failure. And it should

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be kept in mind that in the Stop

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H trial,

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there was a multi

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disciplinary team. In the

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recommendations that we formulated,

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we recommend or patients at risk or development

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of heart failure,

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nat peptide

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by a marker based screening followed by

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team based care, including a cardiovascular

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specialist,

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optimizing the guideline directed therapy can be useful

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to prevent

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feature the development of L dysfunction,

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as well as new ones onset heart failure.

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The only challenge right now is The

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recognition for screening is there among specialists.

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It's not widely known by primary care providers,

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and it's not widely adopted by the healthcare

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systems

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and not covered by the payers.

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So the importance of this

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recognition is critical

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or our patients to be provided timely care

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This is very similar to screening for cancer

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because we now in heart failure as we

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discussed earlier that there are specific

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treatment strategies that prevents heart failure. And in

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individuals who are at higher risk for heart

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failure,

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treatment with These specific agents such as a

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2 inhibitors amongst patients with diabetes

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can prevent forte by about 30 percent.

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Thus screening is critical

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to prevent future risk for development of heart

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failure. And I think that's gonna be an

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important concept

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as we of as healthcare care clinicians

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advocate for our patients, for appropriate coverage and

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timely care. A fantastic Doctor. Ba I think

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that's a key point about the recommendations and

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updated guidelines being there and then that translating

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into

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education for clinicians specifically outside of advanced heart

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failure and cardiology and then and the payers.

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A follow question I had in terms of

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screening, for

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yearly screening and let's say a high risk

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patient, who many of our patients happen to

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have hypertension diabetes that may also be obese.

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And we know that Bm tends to be

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falsely low in patients with obesity? How would

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you interpret B p screening in this type

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of situation? 2 answers. In the selling of

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mobile obesity, we do know that the peptide

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levels will be low. And there are other

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modalities by which 1 can examine the heart

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and the filling pressures, including

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echo c

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and other imaging. In the context of a

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morbid obese individuals who may even have symptoms

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because most of our patients actually do have

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symptoms of d, it would be prudent to

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of contain imaging in those patients to look

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at the left atrial size, the mitral inflow,

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at the wall thickness, the structure of the

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heart in terms of overall ejection fraction as

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well as variables that may suggest diastolic is

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dysfunction or even elevated filling pressure. So the

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concept of screening,

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I believe is gonna evolve as the field

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has more evidence

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supporting these strategies. There are currently large scale

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echo

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data, demonstrating very similar,

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role for echo screening. As you... We are

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all aware, we have now, a very practical

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focus point of care ultrasound as well as

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other

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imaging modalities that are being widely available.

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And I think this paradigm is gonna evolve

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with even digital technologies that may look at

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the cardiac structure in a non amazing manner

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and the ability to detect cardiac structural.

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May not need to solely rely on biomarkers

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markers in essence, nat peptides are an indirect

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way of demonstrating

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increased filling pressures or myocardial stretch.

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Maybe if we were to have affordable, widely

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available,

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practical

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imaging, they could complement biomarker a screening or

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in the setting of obesity as you alluded

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to add specificity.

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And sensitivity.

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It's very helpful clarification, and look forward to

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further screening patients and being able to combat

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heart failure.

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With the new guidelines.

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Thank you. These were excellent cases, and thanks

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for the discussion, and the opportunity to provide

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the perspective we'll how the recommendations were formulated

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in the guidelines with evidence from the clinical

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trials. Thank you so much, Doctor. Ba and

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marked for that really wonderful discussion.

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Thank you. It was a true pleasure.