276 Trans-Atlantic Debate Part Two: Against the Motion. An Endovascular First Strategy is not the Optimal Approach for Treating Acute Mesenteric Ischemia N.T. Orr, E.D. Endean * Department of Surgery, University of Kentucky, Lexington, KY 40536, USA There are a number of pathologic conditions that can result in acute mesenteric ischemia (AMI). These include embolus to a mesenteric vessel (usually the superior mesenteric artery [SMA]); thrombosis of underlying atherosclerotic disease; nonocclusive mesenteric ischemia; interruption of the inferior mesenteric artery blood supply, as seen after abdominal aortic aneurysm repair; mesenteric venous thrombosis; and mechanical causes such as volvulus, intussusception, torsion around adhesions, or internal hernia. For the purposes of this discussion, the focus will be on mesenteric ischemia as caused by either embolic disease or thrombosis of underlying atherosclerosis. Since Klass first reported a successful operation to restore the midgut blood supply, AMI has remained an uncommon disease that is primarily addressed surgically.1 The presentation of AMI often presents a diagnostic challenge for a number of reasons. Symptoms are often nonspecific and, outside of imaging studies, there are no tests that reliably make or exclude the diagnosis of AMI. This can lead to a delay in diagnosis, which, in turn, can have catastrophic consequences. Delay in diagnosis is the biggest factor that contributes to a continued mortality rate as high as 30e 70% despite >50 years of operative intervention, as documented in contemporary reports.2e4 Despite the low incidence of this disease, as the mean age of the population increases, the incidence of AMI will predictably rise. With continued evolution of endovascular therapies, the vascular surgeon is faced with the question of which is the best technique to address AMI. Multiple recent studies have attempted to clarify the optimal approach to treat AMI; however, no definitive consensus has been reached.5e7 Therefore, the objective of this debate is to evaluate the available literature and present an argument that an open operative approach, as opposed to endovascular therapy, should be the first-line and optimal treatment of AMI. The thrust of the argument is that an open approach is best because (1) it provides the ability to assess bowel viability directly; (2) it decreases delay in restoring mesenteric blood flow; (3) it eliminates the variables in physician expertise; and (4) there is no proven mortality advantage with an endovascular approach. Each of these four points will be discussed in turn. The goal of surgical intervention for AMI is threefold: reestablish blood supply to the ischemic bowel, resect all nonviable bowel, and preserve as much bowel length as possible. Bowel viability is the most important factor that affects outcome in patients with AMI. Nonviable bowel, if unrecognized, results in multisystem organ failure and death. Massive bowel infarction is a nonsurvivable condition. In the authors’ practice, when massive mid-gut necrosis is found, the patient is closed and comfort care measures are instituted, with no attempt to revascularize. While this situation is extreme, the only way to determine definitively the extent of bowel infarction is to visualize the bowel. In other less extreme cases, failure to recognize even localized segments of bowel infarction can be catastrophic. The key to the long-term welfare of patients is the preservation of as much viable bowel as possible in order to avoid short gut syndrome. Therefore, the early diagnosis of mesenteric ischemia is essential for the preservation of bowel and avoidance of the associated high morbidity and mortality.8 Recent studies have shown that bowel resection is required in 31e93% of AMI cases.6,9e12 These rates of bowel resection mandate that a reliable assessment of bowel viability be required regardless of the technique employed to reestablish blood flow. The proponents for an endovascular approach for AMI argue that assessment of the bowel can be determined by the patient’s clinical status and physical examination. It can be argued that such an approach is risky for the patient. Most patients with AMI are elderly, with multiple comorbid conditions. These patients are often receiving pain medication and have unreliable physical examinations. While imaging studies can identify occlusion of a mesenteric vessel with a high degree of accuracy, there are no radiologic or laboratory studies that are sufficiently accurate to identify the presence, or absence, of infarcted bowel. As a result, the first sign of bowel infarction may be that the clinical status of the patient worsens. Given the medical condition of these elderly patients, their clinical status can quickly degenerate and, with limited metabolic reserve, their chance of survival in such circumstances is poor. In a retrospective study, Arthurs et al. described that the cohort of patients treated with an endovascular intervention was monitored in an intensive care unit.5 Abdominal exploration was reserved for those who developed peritoneal findings on abdominal examination or had clinical deterioration. They reported that a third (31%) of patients treated with endovascular therapy avoided laparotomy.5 Conversely, almost 70% of patients required laparotomy, and although the findings at the time of operation were not documented, Arthurs et al. state that “necrotic bowel requiring resection.negatively affected overall mortality”.5 Certainly, the avoidance of the complications associated with abdominal exploration is commendable, but it can be suggested that the risks associated with a delay in resecting infracted bowel far outweigh the risk of a laparotomy. In order for this method of clinical assessment to be effective, European Journal of Vascular and Endovascular Surgery Volume 50 Issue 3 p. 273e280 September/2015 serial monitoring of the patient by a provider skilled in the diagnosis of peritonitis with the clinical acumen to suspect bowel ischemia is mandatory. While this might be reproducible in a large academic center, smaller community centers may not have the personnel to achieve such close scrutiny with concern that the diagnosis of peritonitis would be delayed. Also, many of these patients are very sick and require intubation, which complicates the reliability of the physical examination as the major determinant of bowel ischemia. Others may argue that superior imaging technology can now adequately identify patients with bowel ischemia and thereby predict who should undergo laparotomy. It is true that multidetector computed tomography (CT) angiography, as well as magnetic resonance angiography, have developed rapidly over the last two decades. Additionally, the widespread availability of such technology often ensures that most patients will undergo radiologic evaluation prior to any surgical intervention. The presence of SMA occlusion due to thrombosis or embolus can be accurately identified on most CT angiography studies.13,14 However, multiple examples have shown CT imaging to have low rates of ruling out associated bowel ischemia.15,16 Indeed, Bani Hani et al. found that in patients with bowel ischemia or necrosis only 34% had pneumatosis and portal venous gas.16 Therefore, even the most sophisticated imaging techniques will have difficulty reliably identifying patients with bowel ischemia. It is also noteworthy that profound radiographic changes are not predictive of infracted bowel versus ischemic bowel (Fig. 1). It is well established that the need to reduce treatment delays for AMI remains the greatest challenge, as well as the greatest opportunity, for reducing the morbidity and mortality associated with this disease.12 The diagnosis of AMI continues to be elusive in the early stages of the disease process. The most common presenting symptom is acute-onset of vague abdominal pain.8,12 AMI can easily be mistaken for more common intra-abdominal pathologies, including pancreatitis, cholecystitis, diverticulitis, or bowel obstruction. Therefore, it is common that significant time delays have occurred by the time the diagnosis of AMI has been made. It becomes imperative that restoration of blood flow be accomplished quickly. There is a direct relationship between prolonged times to treatment and bowel viability. Small studies have shown that patients with symptoms lasting < 12 h can undergo revascularization without requiring bowel resection.17,18 In one large, retrospective study of open versus endovascular intervention by Arthurs et al.,5 the authors argued that a delay in definitive treatment did not affect outcomes. As proof, Arthurs et al. found that patients receiving endovascular treatment in their study presented with a median of 62 h of symptoms, while patients in the open repair group presented with a much shorter duration of symptoms (26 h).5 It seems likely that the reason for these findings is that patients with AMI who present with > 60 h of pain are essentially “self-selecting” to a lower risk stratification and it can be assumed that these patients either had a partially 277 Figure 1. Computed tomography scan of a patient who had acute mesenteric artery occlusion and significant portal venous gas (arrows). After restoration of flow, no bowel resection was required and the patient had a rapid recovery. occlusive process or had well-developed mesenteric collateral vessels that maintained bowel viability. Indeed, in the study by Arthurs et al.,5 an embolic cause of AMI was present in 64% of patients treated with open operation compared with 28% treated with an endovascular approach. It is likely that the severity of pain and other associated factors in patients with a mesenteric embolus mandated an open approach, while patients with thrombosis of underlying occlusive disease had already developed collateral flow. As is inherent in any retrospective analysis, these types of selection biases cloud the true meaning of the results. The same study also found that about half (48%) of the endovascular cohort was initially treated with chemical thrombolysis. The duration of thrombolysis lasted from 1 day (58%) up to 3 days (5%). Although the chemical thrombolysis may have allowed at least partial restoration of blood flow early in its course, the fact that these patients tolerated multiple days of thrombolysis again points to the high degree of selection bias that is prevalent in all the published reports comparing endovascular with open treatment. The patient response to intra-arterial treatment is highly variable. Simó et al. demonstrated that two patients with symptoms lasting > 18 h had a favorable response to chemical thrombolysis, while the same therapy failed in another two patients who had symptoms for only 6 h prior to treatment.19 In evaluating the feasibility of percutaneous stent placement in AMI, Wyers et al. found that the mean operative time was 329 46 minutes.20 This is substantially different than the procedure duration reported by Arthurs et al. of 120 minutes and highlights the enormous variability that exists between reported outcomes.5 The time necessary to access and stent potentially occluded vessels, or the time required to deliver tissue plasminogen activator for 278 adequate treatment creates a substantial potential for delay in definitive revascularization. Additionally, there is the potential that the patient will not respond to thrombolysis or that the occlusive disease cannot be crossed, further contributing to delay in revascularization. Successful revascularization using an endovascular approach requires advanced catheter skills. While it is true that recent graduates from vascular training programs should have a wide range of catheter-based skills, these skills are not uniform across the country. Additionally, good imaging is required for cannulation of mesenteric arteries. Many smaller hospitals rely on portable fluoroscopy units with poorer imaging quality. Even in the best hands, there is a certain percentage of patients in whom the endovascular approach is unsuccessful. In one report the failure rate of the initial endovascular treatment was approximately 9%, with an overall technical success rate for endovascular therapy of 87%.5 The failures are largely related to the inability to cross an occluded lesion. These results were published by an academic institution with highly skilled interventionists who are exposed to large volumes of AMI cases. It would be expected that in smaller facilities with less exposure to complex endovascular cases, and specifically AMI, the failure rate would be higher. This inherently adds to delay. Another potential concern with limited experience by physicians is that an attempt at endovascular treatment could result in worsening of the condition. Endovascular procedures have known complications, including dissection of the vessel. Attempts to access an occluded vessel or highly stenotic vessel could result in mesenteric dissection. Should there be a need to covert to open revascularization, such complications will potentially make on open repair more difficult. Another potential complication with an endovascular approach is distal embolization. The result of the main trunk could be technically excellent, but a distal embolus could result in unrecognized bowel infarction. Likewise, use of a covered stent could occlude branch vessels, exacerbating the ischemia. There are few studies that directly compare endovascular with open surgical repair for AMI, and the author’s of this debate are unaware of any randomized trials. All studies to date have inherent selection bias that dictates which approach is chosen for treatment of an individual patient. Included in such bias are the patient’s presenting findings, comorbid conditions, physical examination findings, and the expertise of the treating physicians. It would seem that in studies comparing the open and endovascular approach for AMI, open repair is preferentially chosen for patients who, based on presentation, have infracted bowel. In this patient population, these are patients who are likely to be more critically ill at the time of presentation. As such, it would be expected that they should fare worse than the patient who would seem to tolerate the additional time required to reestablish flow with endovascular approaches. Yet, the small studies that are available show no difference in outcome and specifically fail to demonstrate improved outcome with patients treated with an endovascular approach. Trans-Atlantic Debate Endovascular treatment has made significant advances. It is now possible to use such techniques for the treatment of AMI. However, the question is not if it can be done, but should it be done? While some selected patients will do well with an endovascular mesenteric revascularization, in general, it is concluded herein that there is no proven benefit to an endovascular approach for patients with AMI and, in fact, it is suggested that such an approach may actually place patients at risk for increased morbidity and mortality. Until there is an accurate way to assess for the presence of bowel infarction, it would seem that the safest approach in the care for these critically ill patients is definitive open revascularization with an assessment of bowel viability. Liberal use of second-look laparotomy for questionable bowel should be encouraged in order to preserve bowel length and avoid the complications of short gut and to identify infracted bowel before perforation and contamination occurs. REFERENCES 1 Klass AA. Embolectomy in acute mesenteric occlusion. Ann Surg 1951;134:913e7. 2 Bradbury AW, Brittenden J, McBride K, Ruckley CV. Mesenteric ischaemia: a multidisciplinary approach. Br J Surg 1995;82: 1446e59. 3 Mamode N, Pickford I, Leiberman P. Failure to improve outcome in acute mesenteric ischaemia: seven-year review. Eur J Surg 1999;16:203e8. 4 Kassahun WT, Schulz T, Richter O, Hauss J. Unchanged high mortality rates from acute occlusive intestinal ischemia: six year review. Langenbecks Arch Surg 2008;393:163e71. 5 Arthurs ZM, Titus J, Bannazadeh M, Eagleton MJ, Srivastava S, Sarac TP, et al. A comparison of endovascular revascularization with traditional therapy for the treatment of acute mesenteric ischemia. J Vasc Surg 2011;53:698e705. 6 Beaulieu RJ, Arnaoutakis KD, Abularrage CJ, Efron DT, Schneider E, Black 3rd JH. Comparison of open and endovascular treatment of acute mesenteric ischemia. J Vasc Surg 2014;59:159e64. 7 Resch TA, Acosta S, Sonesson B. Endovascular techniques in acute arterial mesenteric ischemia. Semin Vasc Surg 2010;23: 29e35. 8 Park WM, Gloviczki P, Cherry Jr KJ, Hallett JW, Bower TC, Panneton JM, et al. Contemporary management of acute mesenteric ischemia: factors associated with survival. J Vasc Surg 2002;35:445e52. 9 Yun WS, KKm Lee, Cho J, Kim HK, Huh S. Treatment outcome in patients with acute superior mesenteric artery embolism. Ann Vasc Surg 2013;27:613e20. 10 Alhan E, Usta A, Cekic A, Saglam K, Türkyilmaz S, Cinel A. A study on 107 patients with acute mesenteric ischemia over 30 years. Int J Surg 2012;10:510e3. 11 Ryer EJ, Kalra M, Oderich GS, Duncan AA, Gloviczki P, Cha S, et al. Revascularization for acute mesenteric ischemia. J Vasc Surg 2012;55:1682e9. 12 Kougias P, Lau D, El Sayed HF, Zhou W, Huynh TT, Lin PH. Determinants of mortality and treatment outcome following surgical interventions for acute mesenteric ischemia. J Vasc Surg 2007;46:467e74. 13 Debus ES, Müller-Hülsbeck S, Kölbel T, Larena-Avellaneda A. Intestinal ischemia. Int J Colorectal Dis 2011;26:1087e97. European Journal of Vascular and Endovascular Surgery Volume 50 Issue 3 p. 273e280 September/2015 14 Aschoff AJ, Stuber G, Becker BW, Hoffmann MH, Schmitz BL, Schelzig H, et al. Evaluation of acute mesenteric ischemia: accuracy of biphasic mesenteric multi-detector CT angiography. Abdom Imaging 2009;34:345e57. 15 Milone M, Di Minno MN, Musella M, Maietta P, Iaccarino V, Barone G, et al. Computed tomography findings of pneumatosis and portomesenteric venous gas in acute bowel ischemia. World J Gastroenterol 2013;19:6579e84. 16 Bani Hani M, Kamangar F, Goldberg S, Greenspon J, Shah P, Volpe C, et al. Pneumatosis and portal venous gas: do CT findings reassure? J Surg Res 2013;185:581e6. 279 17 Lobo ME, Meroño CE, Sacco O, Martinez ME. Embolectomy in mesenteric ischemia. Rev Esp Enferm Dig 1993;83:351e4 (in Spanish). 18 Wadman M, Syk I, Elmstahl S. Survival after operations for ischaemic bowel disease. Eur J Surg 2000;166:872e7. 19 Simó G, Echenagusia AJ, Camúñez F, Turégano F, Cabrera A, Urbano J. Superior mesenteric arterial embolism: local fibrinolytic treatment with urokinase. Radiology 1997;204:775e9. 20 Wyers MC, Powell RJ, Nolan BW, Cronenwett JL. Retrograde mesenteric stenting during laparotomy for acute occlusive mesenteric ischemia. J Vasc Surg 2007;45:269e75. * Corresponding author. Email-address: [email protected] (E.D. Endean) 1078-5884/$ e see front matter Ó 2015 Published by Elsevier Ltd on behalf of European Society for Vascular Surgery. http://dx.doi.org/10.1016/j.ejvs.2015.04.026 EDITORS’ COMMENT Trans-Atlantic Debate: Is an “Endovascular First” Strategy the Optimal Approach for Treating Acute Mesenteric Ischemia? A.R. Naylor, Editor-in-Chief, European Journal of Vascular and Endovascular Surgery * Vascular Research Group, Division of Cardiovascular Sciences, Clinical Sciences Building, Leicester Royal Infirmary, Leicester LE2 7LX, UK T.L. Forbes, Associate Editor, Journal of Vascular Surgery Division of Vascular Surgery, University of Toronto, Toronto, ON, Canada Notwithstanding the headline debate about whether an “endovascular first” or an “open surgery first” strategy is preferable or safer, the most important issue raised by our debaters (and one which should concern all of us) is that a diagnosis of acute mesenteric ischemia (AMI) is still invariably delayed and usually only considered once the patient has become too ill to undergo any form of meaningful intervention. The data from the US National Inpatient Sample, which showed that only 15% of patients with AMI were actually treated and that only 3% had the chance to benefit from endovascular or open revascularization, makes extremely depressing reading. Put another way: almost nine out of every 10 patients with a diagnosis of suspected AMI will undergo no active treatment. Such bleak statistics demand that medical professionals (of all disciplines) be made more aware of the importance of at least considering a diagnosis of AMI in patients. Returning to the “meat” of the debate, the contributors have provided positive and negative data regarding their respective positions. That is not surprising, given the nature of a debate. We suspect, however, that a significant proportion of our surgical readers will rarely (or never) consider an “endovascular first” strategy for the treatment of patients with AMI (unlike patients with chronic mesenteric ischemia), largely because of an intuitively held belief (espoused by Drs. Orr and Endean) that endovascular strategies have little to offer in these acute, life-threatening situations, and that emergency laparotomy is mandatory in order to gauge the severity of ischemia, enable revascularization, and allow the resection of compromised bowel before it worsens and precipitates multiorgan failure. However, Martin Björck has also shown that surgeons may have been wrong to uncritically dismiss a role for an “endovascular first” strategy. This is supported by international registries reporting that up to 50% of contemporary arterial revascularizations for AMI now follow an “endovascular first” strategy, with bailout surgical bypass being possible in up to half of those cases where an endovascular intervention failed to recanalize the superior mesenteric artery. One would not expect to have observed such an increase in the proportion of interventional therapies if an “endovascular first” strategy was associated with poorer outcomes compared with the traditional open surgical approach. There are obvious advantages to either strategy. Endovascular therapy is less invasive, can be done under local anesthesia, avoids a major laparotomy in compromised individuals, and (perhaps most importantly) finishes with completion angiography in order to identify and treat residual thrombus/defects, thereby optimizing the overall quality of the revascularization. The “Achilles’ heel” of an “endovascular first” strategy, however, is determining exactly when someone needs a second-look laparotomy to identify the patient with persisting focal bowel ischemia before it perforates. Martin Björck advocates a liberal approach to second-look laparotomy, but it is not always apparent when one is required. The “open surgery first” approach, as stated
© Copyright 2026 Paperzz