LimFlow’s crossing stent diverts blood from a diseased tibial artery to a tibial vein to deliver oxygen to a patient’s ischemic foot. [Illustration courtesy of LimFlow]
LimFlow’s breakthrough system for treating chronic limb-threatening ischemia (CLTI) is the first of its kind approved by the FDA for this severe form of peripheral artery disease (PAD).
The LimFlow System for Transcatheter Arterialization of Deep Veins (TADV) is now the only option other than amputation for ceratin CLTI patients who have lost blood flow below their knee. LimFlow’s TADV system won breakthrough device designation in October 2017 and secured FDA premarket approval (PMA) in September 2023.
“A lot of technologies come out of people fiddling with technologies that already exist, and then developing unique proprietary solutions after that,” LimFlow CEO Dan Rose said in an interview with Medical Design & Outsourcing. “That was kind of our journey. … We hope to break a logjam, which is the limit of coronary technology below the knee by creating a new circuit that allows us to deliver the oxygenated blood these patients need.”
LimFlow’s minimally invasive procedure diverts blood around diseased arteries and into veins to restore blood flow into a patient’s ischemic foot.
Deep vein arterialization to relieve ischemia by using veins to oxygenate tissue (essentially turning them into arteries) is a relatively simple concept that goes back more than a century. But the risks of creating such a large surgical wound — including infection that could require amputation — have historically outweighed the benefit.
However, modern coronary and peripheral interventional medicine and the ever-growing use of catheters, wires, stents and balloons now allows surgeons to make small, precise punctures in the vasculature.
“How we actually did the first-in-man was saying, ‘How can we try to use just interventional techniques to accomplish the goal with a surgical procedure [using] off-the-shelf devices? And that was the beginning of LimFlow — using common tools to prove the principle,” Rose said.
How LimFlow’s devices restore blood flow
LimFlow’s ARC arterial catheter (pictured with needle extended) and the mesh V-Ceiver venous catheter [Image courtesy of LimFlow]
As the LimFlow team worked on the procedure to make it simpler, faster and reproducible — figuring out how to knock out vein valves to allow reverse blood flow, avoiding vein spasms and edema and the like — they learned which tools they needed to customize.
One example is LimFLow’s proprietary technology for artery-to-vein crossing. They designed their nitinol V-Ceiver venous catheter with radiopaque mesh to expand inside the tibial vein, providing a clear target with fluoroscopy so the nitinol needle on LimFlow’s ARC arterial catheter inside the tibial artery can puncture the vein and deliver a micro guidewire. The V-Ceiver’s snaring mesh captures the guidewire, which then runs out of the venous access site on the patient’s foot.
Then, an angioplasty balloon opens up the artery-vein connection. Next, the LimFlow Valvulotome cuts through vein valves at the bottom of the foot to allow the blood to flow in the opposite direction.
Self-expanding stent grafts covered with electrospun polytetrafluoroethylene (PFTE) run up the leg to keep the vein open. The last piece of the puzzle is LimFlow’s self-expanding nitinol crossing stent, which is also covered with electrospun PFTE and routes oxygenated blood from the artery into the vein, restoring a rush of blood flow to the foot. (You can watch the entire procedure in the video at the bottom of this post.)
The LimFlow Valvulotome [Image courtesy of LimFlow]
“The artery is a very different diameter than the vein and you want a stent that matches the diameter of the artery so it’s going to stay open … and the same thing in the vein, so we had to develop a conical stent graft so that we weren’t creating a mismatch of sizing,” Rose said. “We had to figure out a way to atraumatically destroy the veins endovascularly using a unique forward-cutting valvulotome because a push valvulotome didn’t exist. We invented it.”
Creating these tools wasn’t enough; they needed to be refined for speed, simplicity and dependability.
“All interventionalists have a spectrum of skills, and we have to aim for a procedure that is reproducible in the hands of the average physician. Because if you don’t, you’re building a niche technology,” Rose said.
What’s next for LimFlow
CLTI is often seen in patients with diabetes, coronary artery disease, obesity or high blood pressure. It’s estimated to affect as many as 4 million people in the U.S., causing 150,000 amputations per year in late-stage patients whose limbs can’t be saved with angioplasty or open bypass surgery.
Amputations above the ankle for vascular disease are associated with a 50% mortality rate within a year. For those who survive, losing a limb means they may never walk again.
LimFlow CEO Dan Rose [Photo courtesy of LimFlow]
After treatment with LimFlow’s system, Rose said, “we see these patients go from gangrene, dry, cold foot to completely healed in three or four months. And their foot is warm. There’s no pain. It’s not every patient, but we see lots of patients go through that.”
Now that LimFlow is able to treat the most serious cases, they’re still studying how they can expand their system to patients in less advanced stages. That includes revising their products and developing new ones. They’re already working on a new PMA submission, Rose said, though he declined to offer details.
“We’ve opened a new circuit, a new pathway,” Rose said. “We have to learn how to use that, we have to learn which patients it’s ideal for. That will take place over time. … I can’t speak openly about it, but we are and will be developing new technology solutions that make the procedure easier and faster and better as we go.”
“We’re passing through the first door,” he continued, “but there are many, many further doors to open and the only way we do that is by continuing the journey.”