Tag: chronic mesenteric ischemia

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chronic mesenteric ischemia MALS median arcuate ligament syndrome Takayasu's Arteritis techniques

Takayasu’s Arteritis Driven Median Arcuate Ligament Syndrome: Unusual Symptoms Demand Unusual Solutions

precta_4

The patient is a young woman from overseas who was referred to the clinic for abdominal and chest pain that persisted after diagnosis and treatment of Takayasu’s Arteritis affecting her visceral (middle) aorta. A year prior to presentation, she had been having severe abdominal pain, 30 pound weight loss, and weakness. Laboratory findings included elevated inflammatory markers. CT scan showed inflammation around her celiac axis and superior mesenteric artery. She was treated with prednisone but only responded ultimately to immunosuppressives. Her pain remitted for a while and she regained weight and strength, but eventually in the months prior to consultation, symptoms of postprandial abdominal pain and nausea set in with concomitant constant midsternal chest pain which at times was incapacitating.

Examination was remarkable for a well nourished young woman in distress with epigastric tenderness. Inflammatory markers were normal and she was on methotrexate and tocilizumab. CTA (above) and duplex showed severe stenoses affecting the origins of the celiac axis and superior mesenteric artery. A composite of the centerlines through these showed the arteries to be critically narrowed at their origins (below), along with a mild to moderate stenosis of the aorta (above). No active inflammation could be seen.

precenterlineCA and SMA.png

The anterior view of the 3DVR images of her CT showed an absence of collateralization via the inferior mesenteric artery and Arc of Riolan.

preCTA_3.jpg

This could account for her postprandial abdominal pain which was midabdominal, but the midsternal chest pain was difficult to explain. A cardiac cause had been ruled out at her home institution. It was on the lower part of the sternum and bordered the epigastrium. Through my work with median arcuate ligament syndrome, it was not unusual to have chest pain be part of the pain syndrome which comes about through the compression of the celiac plexus by the median arcuate ligament (reference), and treated effectively with the division of the median arcuate ligament and celiac plexus neurolysis.

I did feel that revascularizing the SMA was likely to improve her postprandial symptoms, given the paucity of circulation to the gut. I had a discussion about her chest pain and the thought that this was a celiac plexus neuropathy as the result of compression of the celiac plexus by her Takayasu’s disease. Typically, for younger people, I perform a bifurcated graft to the celiac axis and SMA from the distal descending thoracic aorta for younger patients, but I had no intention of replacing her aorta at this time, and wanted to reserve any definitive revascularization of her visceral vessels for a later time if it became necessary. Her pulses were full in the legs and she had no hypertension, renal insufficiency, or claudication. I therefore planned a ilio-mesenteric bypass, as it would preserve planes for a later more definitive operation if necessary, and would address her mesenteric ischemia.

I also proposed taking down the median arcuate ligament and lysing her celiac plexus to treat her chest pain symptoms. While I knew this would be fraught with some hazard because of the inflammation that had been there, it would be the best chance at treating this symptom that was debilitating her. I did not think the constant chest/epigastric pain had a vascular etiology. Normally, I would test this with a celiac plexus block, but given the likely inflammation involved, a failed block would not be helpful, and a positive one achieved with some difficulty.

The patient thought this was reasonable and agreed. She underwent a midline laparotomy and I exposed both the SMA and right common iliac artery in the retroperitoneum and tunneled a PTFE graft in a C-pattern in the retroperitoneum. The SMA was diseased proximally under the pancreas and affected by inflammatory scar tissue, and the vessel was thickened as well. The iliac pulse was normal and full and provided excellent inflow.

Going into the lesser sac, the crurae of the diaphragm were heavily scarred near the celiac axis. Division of these fiber was taken slowly and with the aid of both loupe magnification and a hook cautery (borrowed from laparoscopic surgery). The aorta was cleared of tissue first -it was also encased in scar tissue. The dissection going distally was made difficult by inflammatory scar tissue as well, but several large nerve trunks were encountered and divided. The celiac axis was atretic and small within this scar tissue, but was released down to the trifurcation.

The recovery was notable for remission of her chest pain and her ability to resume eating without pain or nausea. A CTA done before discharge showed a patent bypass.

post-cta_1

Followup communication has revealed continued remission of her presenting symptoms months after her operation.

We are working on presenting a followup to our recent paper on MALS. Increasingly, it is apparent that consideration of celiac plexus compression as an etiology of epigastric abdominal pain unexplained by more common gastrointestinal causes provides solutions for patients given no explanation for their debilitating pain. This pain can also affect the chest, and flanks and back in the distal thoracic dermatomes, and mimic the some of the symptoms of mesenteric ischemia. In those with recurrent MALS after a successful ligament release and interval of symptom remission, even in the absence of celiac axis compression, a positive response to a celiac plexus block points to the presence of either remnant plexus fibers or compression by scar tissue of the cut nerve endings (neuromata) and reoperation has been successful. Extrapolating this experience to this patient with inflammatory compression of the celiac plexus secondary to Takayasu’s Arteritis made sense and celiac neurolysis appears effective.

Reference

Weber JM, Boules M, Fong K, Abraham B, Bena J, El-Hayek K, Kroh M, Park WM. Median arcuate ligament syndrome is not a vascular disease. Ann Vasc Surg. 2016 Jan;30:22-7.

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acute mesenteric ischemia AIOD aortoiliac occlusive disease (AIOD) chronic mesenteric ischemia CTA PAD techniques visceral malperfusion

When good enough is better than perfect: a case of end stage visceral segment aortic occlusive disease

The patient is a woman in her 60’s who self referred for complaint of abdominal pain, weight loss, and rest pain of the lower extremities. She is a 40 pack year smoker and had severe COPD, hypertension, congestive heart failure with mitral regurgitation, chronic kidney disease stage IV, and ischemic rest pain of the legs. She had a 30 pound weight loss due to severe postprandial abdominal pain. She had bloody stools. Her kidney function was worsening, and dialysis was being planned for likely renal failure but she was against dialysis. She had consulted several regional centers but was felt to be too high risk for surgery and with her refusal of dialysis, would be a high risk for renal failure and death with intervention. Physical examination revealed weakened upper extremity pulses, and nonpalpable lower extremity pulses and a tender abdomen. In clinic, she developed hypoxia and dyspnea and was admitted directly to the ICU.

preop-cta

CTA (above) revealed severely calcified atherosclerotic plaque of her visceral segment aorta occluding flow to her mesenteric and renal arteries and to her leg. The right kidney was atrophic. The left kidney had a prior stent which looked crushed. The infrarenal aorta was severely diseased but patent and there were patent aortic and bilateral iliac stents.

Echocardiography revealed a normal ejection fraction of 60%, diastolic failure,  +2 to+3 mitral regurgitation, and pulmonary artery hypertension. She did respond to diuresis and stabilized in the ICU. Intervention was planned.

Options that I considered were an extranatomic bypass to her legs and revascularization from below. I have come across reports of axillo-mesenteric bypass, and I have performed ascending and descending thoracic aorta to distal bypass for severe disease, but concluded, as did the outside centers, that she was a formidable operative risk. Also, there was a high likelihood of great vessel occlusive disease. Looking at her CTA, I felt that she needed just a little improvement in flow -not perfect but good enough. The analogy is like drilling an airline through a cave-in. Also, her left kidney gave a clue -it was normal sized and survived the stress test of a contrast bolus for the CTA without dying. A discussion with the patient green lighted an attempt -she understood the cost of failure but did not wish to linger with this abdominal pain.

Access for intervention was via the left brachial artery. Aortography showed the severe stenosis at the origin of the SMA and the nearly occlusive plaque in the visceral segment aorta.

preintervention-aortogram

The plaque was typical of the coral reef type, and had an eccentric channel that allowed passage of a Glidewire. Access into the left renal artery was achieved. Its stent was patent but proximally and distally there were stenoses; this was treated with a balloon expandable stent. The path to it was opened with a balloon expandable stent to 8 mm from femoral access. This was the improvement the renal needed. A large nitinol stent was placed from this access in the infrarenal aorta when severe disease above the iliac stents was encountered.  The SMA was then accessed and treated with a bare metal stent.

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Renal stent was reaccessed and ballooned in this pentultimate angiogram

Her creatinine improved, as did her intestinal angina. She was discharged home. She later returned a month after the procedure with complaints of nausea and vomiting and right lower quadrant abdominal pain and was discovered to have an ischemic stricture of her small bowel. This was removed laparoscopically and she recovered well. She recovered her lost weight and now a year and a half later, remains patent and symptom free.

Discussion: Dr. Jack Wiley includes in the preface to his atlas of vascular surgery the words of Dr. Joao Cid Dos Santos, the pioneer of endarterectomy techniques, “Vascular surgery is the surgery of ruins.” And in that context, good enough is sufficient.

 

Categories
acute mesenteric ischemia chronic mesenteric ischemia techniques

The inferior mesenteric artery is a poor target for revascularization in chronic mesenteric ischemia

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The patient was referred to me after having undergone an intervention for chronic mesenteric ischemia. She is over 70 years of age and had lost over thirty pounds in 3 months due to severe abdominal pain with eating. A month prior to seeing me, she had undergone arteriography at an outside hospital and was found to have occlusion of her celiac axis (CA) and superior mesenteric artery (SMA) with a small but patent inferior mesenteric artery. Attempt at recanalization, done from left brachial access, of the SMA was abandoned after the patient started having pain, and the inferior mesenteric artery was accessed and stented with a balloon expandable stent. Despite the stent, the pain persisted. On examination, she was cachectic, weighing about a hundred pounds, and had moderate to severe pain with abdominal palpation. CT angiography (shown above) showed a chronically occluded CA and SMA and a patent stent to the IMA.

After discussion with the patient about the possibility of a bypass, we decided to proceed with diagnostic arteriography and an attempt at recanalization. When planning these, I always try to come from the groin first as most of the time I am able to revascularize from below. I try to avoid 6F sheaths in the arms of thin cachectic patients -women especially where the brachial artery is likely the same diameter as a 6F sheath. The only downside about coming from below is that it is technically challenging and the stent comes off at a higher angle than the SMA typically has in situ.

The image below shows the procedure:

SMA intervention.jpg

The series of images shows the initial aortogram and access. The superior mesenteric artery has a stenosis at the origin, with an area of post stenotic dilatation or small aneurysm, which occludes beyond the first three branches of the SMA. The IMA fails to feed the bowel -the later phases not shown shows filling from the SMA segment to the CA and ileal branches.

The key step to this procedure is in getting “deep” access with a wire -in this case a floppy Glidewire, which I used to cross the occluded SMA. There is feedback from the tip which occurs if you spin it without a torque device. The wire has the quality, a feature really, of being tacky when dry, allowing for a great deal of coaxial spin with your first two fingers and your thumb. The tip transmits information about what it is crossing as you spin it -this is something that is hard to teach at first, but is gained largely through experience, but I learned it from Dan Clair over a decade ago when he barked at me to get rid of the torque device (“a tool for babies!”). The tip will go where it should if you spin, not push.

Once the wire is buried, a suitable catheter that tracks well is brought across the occlusion. Again, while there are many catheters that can do this, the Glide Catheter is suitable again from spinning across an occlusion over the wire that would push out the lowest profile and equally hyrdophillic catheters. Once the catheter is buried, a suitably stiff wire (in this case a Rosen wire) should be brought across -this widens the arc created by the wire as it goes up and over the SMA origin and allows for delivery balloons and stents. Using the balloon-piton technique (a requisite for FEVAR), the sheath is brought into the SMA, securing access into it.

The occlusion in the mid-SMA ballooned nicely and did not require a stent -a nonocclusive dissection is seen but I chose not to treat this as placing a stent is likely to cause as many problems as solve and the dissection is in line with flow. The origin was stented with a balloon expandable stent -having the patient awake is useful in determining if the stent is “big enough.” Final arteriography in two planes is shows below.

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Gratifyingly, the entire mesenteric system in the CA (foregut) and SMA (midgut) lit up. I admitted her for observation as I have seen patients develop bowel infarction with reperfusion which may be due to embolization but I think just as likely due to edema. Food needs to be reintroduced slowly as there maybe metabolic consequences to rapid refeeding. Her baseline lactate was 2.6mMol/L but came down to 0.8mMol/L the next day. Her other labs were normal. Her pain remitted and she was able to tolerate a regular diet by postoperative day 2.

Discussion: 

Mesenteric ischemia is a particularly morbid condition. When it presents acutely, there is a high mortality rate (ref 1). Revascularization in good risk individuals is still bypass surgery (ref 2,3). The inferior mesenteric artery offers a dismal revascularization target for this reason -while the artery will remodel and dilated in the setting of mesenteric ischemia, its orifice from the aorta does not and is usually no more than 1-2mm from birth to adulthood. Also, while the large bowel will get perfusion from the IMA, and the foregut may get collateral flow from collaterals fed from the middle colic via the Arc of Riolan, the midgut does not get sufficient flow from from the IMA because it requires the longest path to fill the ileal and jejunal branches. The development of atherosclerosis in the aorta further complicates attempts at stenting. Despite this, it is still attempted (ref 4) and in 4 patients was successful at relieving pain for short periods of time, with one patient requiring eventual bypass despite characterization as “high risk.” It is a reflection of how poorly this vessel does with intervention that this 4 case series is the largest in the literature.

The analogy to IMA stenting in the legs is stenting of a heavily diseased profunda femoral artery in the setting of critical limb ischemia with femoropopliteal occlusive disease. It is occasionally successful in the short term, but will only delay the inevitable operation. There are no low risk patients with severe weight loss due to mesenteric ischemia. Aggressive intervention offers a path of survival for these patients, and but long term results are only possible with bypass.

References

  1. Park WM, Gloviczki P, Cherry KJ Jr, Bower TC, Panneton JM, Schleck C, Ilstrup D, Harmsen WS, Noel AA. Contemporary management of acute mesenteric ischemia: factors associated with survival. J Vasc Surg. 2002;35(3);445-452.
  2. Park WM, Cherry KJ, Jr, Chua HK, Clark RC, Jenkins G, Harmsen WS, et al. Current results of open revascularization for chronic mesenteric ischemia: a standard for comparison. J Vasc Surg. 2002;35(5):853–859.
  3. Kasirajan K, O’Hara PJ, Gray BH, Hertzer NR, Clair DG, Greenberg RK, et al. Chronic mesenteric ischemia: open surgery versus percutaneous angioplasty and stenting. J Vasc Surg. 2001;33:63–71.
  4. Wohlauer M, Kobeiter H, Desgranges P, Becquemin JP, Cochennec F. Inferior Mesenteric Artery Stenting as a Novel Treatment for Chronic Mesenteric Ischemia in Patients with an Occluded Superior Mesenteric Artery and Celiac Trunk. Eur J Vasc Endovasc Surg. 2014;27(3):e21-e23.