Naveed Rajper MD

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Naveed Rajper MD

Naveed Rajper MD

@naviyd

heart + vascular + tech

Charlotte, NC Katılım Nisan 2010
787 Takip Edilen1K Takipçiler
Peter Steinberger 🦞
@keenon Because software is hard? We're on it. Use an older version or install dependencies manually or use hackable install.
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keenon
keenon@keenon·
You reply to everybody but now you’re afk huh? I updated to 4.29 by clicking “update” button in web ui and broke everything . Why? @steipete why would you do this?
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Peter Steinberger 🦞
Peter Steinberger 🦞@steipete·
Built clawsweeper, which runs 50 codex in parallel around the clock, scans issues/prs deep and closes what is already implemented or what makes no sense. Closed around 4000 issues today, a few thousand are in the pipeline. (rate limits are rough) github.com/openclaw/claws…
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Naveed Rajper MD
Naveed Rajper MD@naviyd·
@TWilsonMD @Hragy What do you treat the latter two with? I’ve had more luck with lifestyle modification and sometimes GLP1a than anything else.
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Tom Wilson
Tom Wilson@TWilsonMD·
@Hragy My brother and I have done >25 Coroflow/vasospastic cases over last 6m. We have seen plenty of spasm, endothelial dysfxn, and microvascular disease. Only lab in 500mi doing this work.
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Hany Ragy
Hany Ragy@Hragy·
What is important is ischemia with normal coronary arteries, angina alone may not be ischemic, there is a lot of etiologies, and there is still a subset of patients with non coronary chest pain that may not fall under any category, and is not INOCA , is ANOCA
INOCA INTERNATIONAL@InocaInternati1

Still seeing angina in patients with “normal” coronary arteries? 🫀 Join me on 29 April for a @JCM webinar created by Professor Atilla Kardos, including a truly outstanding expert panel! Advancement in diagnosis of INOCA and ANOCA Free to attend: brnw.ch/21x1qOr

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Naveed Rajper MD
Naveed Rajper MD@naviyd·
@Hragy Given the recent trials, I’m curious what level of recommendation the American guidelines will give for LAAO. I predict the recommendation will be higher than other international guidelines.
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Hany Ragy
Hany Ragy@Hragy·
I was having a coffee with the person who does more LAAO than anyone on this planet, I asked: what are the indications in this patient? They replied:they don’t want to take a daily pill for the rest of their lives. I said: what about the guidelines? They replied: the GL 4 others!
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Naveed Rajper MD
Naveed Rajper MD@naviyd·
@farkomd That’s just a start - later on get your cases out of their (PE/hospital owned) cath lab and into our (physician owned) cath lab.
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Naveed Rajper MD
Naveed Rajper MD@naviyd·
A candid conversation with hip hop artists to improve underserved access to healthcare
Naveed Rajper MD tweet media
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Naveed Rajper MD
Naveed Rajper MD@naviyd·
@BaoGTran @anish_koka The hospital or health system makes a vast majority of the money for CTCA from CT-FFR. Calling a lesion potentially significant allows for CT-FFR to be performed.
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Bao Tran, MD
Bao Tran, MD@BaoGTran·
@naviyd @anish_koka Who’s receiving the financial incentive? Physicians are not getting any reimbursement for ordering the test. And the professional fees for reading the CTA are relatively modest.
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Naveed Rajper MD
Naveed Rajper MD@naviyd·
Thrilled PHVI is one of the first outpatient sites in North Carolina to use IVL for PAD! @ShockwaveIVL
Naveed Rajper MD tweet mediaNaveed Rajper MD tweet media
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Naveed Rajper MD
Naveed Rajper MD@naviyd·
Beyond optimizing daily choices, he could rationally choose - no meds (opts out despite consensus data) - LDL < 70 (opts in based on current consensus data) - LDL < 50 or lower (dives in based on high probability trends in data) Informed decision making is key! …as he awaits data on Lp(a) or other tech advancements.
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Naveed Rajper MD
Naveed Rajper MD@naviyd·
Some of my thoughts - the future for cardiovascular prevention is very bright, as revolutions in medical imaging, therapeutics, and genomics all synergize and accelerate with compute.
Naveed Rajper MD@naviyd

piedmonthealthcare.com/the-future-of-… The Hidden Threat of Cardiovascular Disease in Midlife In our 40s and 50s, cardiovascular disease emerges as the leading cause of harm and death, surpassing cancer and lung disease. Yet, when we examine a seemingly healthy population of adults around this age using noninvasive imaging, we often uncover the root cause—atherosclerosis—long before symptoms appear in most people. Unfortunately, many patients receive a diagnosis and treatment only later in life, often after developing obvious symptoms or even suffering a heart attack or stroke. A Surprising Pattern in Atherosclerosis Development Contrary to popular belief, and according to seminal research by Dr. Valentin Fuster and others, atherosclerosis doesn’t first target the heart, as one might assume. In studies such as the Progression of Early Subclinical Atherosclerosis (PESA), which followed aging cohorts with serial noninvasive imaging, plaque buildup tends to appear in the legs (the common and superficial femoral arteries) first, the neck (the carotid arteries) second, and the heart (the coronary arteries) last. This suggests we are often searching for the causes of cardiovascular events—primarily atherosclerosis—in the wrong parts of the body and at the wrong time of life. The Era of Rapid Medical Innovation We are witnessing unprecedented technological acceleration, in which the next decade’s innovations may surpass the gains of the past century. Medical imaging now allows visualization of disease well before symptoms arise. At the same time, pharmacologic advancements target lipids, platelets, coagulation, inflammation, and metabolism more effectively. In the 1980s, endocrinologist Gerald Reaven described a cluster of high-risk features in Americans—closely linked to obesity—as the enigmatic “Syndrome X.” Decades later, our understanding, recognition, and management of what we now call metabolic syndrome have vastly improved and continue to evolve. This syndrome is strongly tied to excess visceral fat and insulin resistance, as well as increased risks for sleep apnea, heart rhythm disorders, hypertension, hyperlipidemia, atherosclerosis, fluid retention, kidney disease, and overall diminished mobility and wellness. By 2026, treatments have evolved dramatically and include disease-modifying agents that address metabolic syndrome head-on. These therapies are safer and more effective than ever and often work synergistically to reduce risk and extend both quality of life and lifespan. What’s Next: Beyond Early Detection of Disease — The Genetic Revolution Today, we can detect disease far earlier—often between ages 25 and 50—well before symptoms emerge—and treat it more effectively than before. So, what’s on the horizon? Lipoprotein(a), discovered in 1963, may ignite the genetic revolution in healthcare. This highly atherogenic, disease-causing lipid particle is inherited and present at birth, affecting 20–30% of the population. If ongoing clinical trials demonstrate that therapies lowering lipoprotein(a) are safe and reduce cardiovascular events or mortality, humanity could take a giant leap forward in the prevention of disease. In the next decade, genome-based risk assessment and targeted therapies will likely become widely available. As this genetic revolution accelerates—synergistically alongside those of imaging and therapeutics—risk stratification, and potentially even therapies, could begin around birth or early in life. The sum of these technological advancements may lead to remarkable increases in average human lifespan in the coming years.

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Naveed Rajper MD
Naveed Rajper MD@naviyd·
piedmonthealthcare.com/the-future-of-… The Hidden Threat of Cardiovascular Disease in Midlife In our 40s and 50s, cardiovascular disease emerges as the leading cause of harm and death, surpassing cancer and lung disease. Yet, when we examine a seemingly healthy population of adults around this age using noninvasive imaging, we often uncover the root cause—atherosclerosis—long before symptoms appear in most people. Unfortunately, many patients receive a diagnosis and treatment only later in life, often after developing obvious symptoms or even suffering a heart attack or stroke. A Surprising Pattern in Atherosclerosis Development Contrary to popular belief, and according to seminal research by Dr. Valentin Fuster and others, atherosclerosis doesn’t first target the heart, as one might assume. In studies such as the Progression of Early Subclinical Atherosclerosis (PESA), which followed aging cohorts with serial noninvasive imaging, plaque buildup tends to appear in the legs (the common and superficial femoral arteries) first, the neck (the carotid arteries) second, and the heart (the coronary arteries) last. This suggests we are often searching for the causes of cardiovascular events—primarily atherosclerosis—in the wrong parts of the body and at the wrong time of life. The Era of Rapid Medical Innovation We are witnessing unprecedented technological acceleration, in which the next decade’s innovations may surpass the gains of the past century. Medical imaging now allows visualization of disease well before symptoms arise. At the same time, pharmacologic advancements target lipids, platelets, coagulation, inflammation, and metabolism more effectively. In the 1980s, endocrinologist Gerald Reaven described a cluster of high-risk features in Americans—closely linked to obesity—as the enigmatic “Syndrome X.” Decades later, our understanding, recognition, and management of what we now call metabolic syndrome have vastly improved and continue to evolve. This syndrome is strongly tied to excess visceral fat and insulin resistance, as well as increased risks for sleep apnea, heart rhythm disorders, hypertension, hyperlipidemia, atherosclerosis, fluid retention, kidney disease, and overall diminished mobility and wellness. By 2026, treatments have evolved dramatically and include disease-modifying agents that address metabolic syndrome head-on. These therapies are safer and more effective than ever and often work synergistically to reduce risk and extend both quality of life and lifespan. What’s Next: Beyond Early Detection of Disease — The Genetic Revolution Today, we can detect disease far earlier—often between ages 25 and 50—well before symptoms emerge—and treat it more effectively than before. So, what’s on the horizon? Lipoprotein(a), discovered in 1963, may ignite the genetic revolution in healthcare. This highly atherogenic, disease-causing lipid particle is inherited and present at birth, affecting 20–30% of the population. If ongoing clinical trials demonstrate that therapies lowering lipoprotein(a) are safe and reduce cardiovascular events or mortality, humanity could take a giant leap forward in the prevention of disease. In the next decade, genome-based risk assessment and targeted therapies will likely become widely available. As this genetic revolution accelerates—synergistically alongside those of imaging and therapeutics—risk stratification, and potentially even therapies, could begin around birth or early in life. The sum of these technological advancements may lead to remarkable increases in average human lifespan in the coming years.
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Naveed Rajper MD
Naveed Rajper MD@naviyd·
Statin intolerant patient with paradoxic substantial increase of ApoB on incliseran. I am going to switch to evolocumab and do genetic testing. Have you seen this? I suspect PSCK9 or LDLR gene defect. @Drlipid @lipiddoc @nationallipid
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