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Volume 46, Issue 3, Pages 421-426 (September 2007)


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Spinal cord ischemia may be reduced via a novel technique of intercostal artery revascularization during open thoracoabdominal aneurysm repair

Presented at the Thirty-fifth Annual Society for Clinical Vascular Surgery Meeting in March 21-24, 2007.

Edward Y. Woo, MDaCorresponding Author Informationemail address, Michael Mcgarvey, MDc, Benjamin M. Jackson, MDa, Joseph E. Bavaria, MDb, Ronald M. Fairman, MDa, Albert Pochettino, MDb

Received 13 March 2007; accepted 17 April 2007. published online 03 August 2007.

Objective

To describe a novel technique for maximal reimplantation of intercostal arteries during thoracoabdominal aortic aneurysm repair.

Methods

Eight patients underwent thoracoabdominal aortic aneurysm (TAAA) repair with this new technique from 2005 to 2006. Follow-up ranged from 6 to 14 months. All patients had a previous type B dissection with subsequent aneurysmal degeneration into an extent I TAAA. Aneurysm repair was performed through a thoracoabdominal incision and circulatory arrest in seven and left atrial-left femoral (LA-FA) bypass in one. The grafts extended from the distal arch at the subclavian artery to the visceral and renal arteries. An 8 mm graft was then extended from the proximal to the distal graft with a spatulation of the graft allowing a side-to-side anastomosis of the graft to the posterior aortic wall incorporating multiple pairs of intercostal arteries. Intraoperative electroencephalogram (EEG) and somatosensory evoked potentials (SSEP) were monitored during each operation.

Results

All patients were ambulatory at the time of admission. One patient had suffered a previous spinal cord infarction from the original dissection and had residual unilateral leg weakness prior to the TAAA repair. There was an average of seven pairs of patent intercostal arteries upon opening the aorta. We reimplanted an average of five pairs of vessels. There were no perioperative complications. No patients sustained transient or permanent paraplegia in the postoperative or follow-up period. The one patient with preoperative leg weakness had reported subjective increased strength in the affected leg after the operation. In four cases, normalization of SSEP waveforms did not occur until after reimplantation of the intercostal arteries despite full return of EEG waveforms, restoration of lower extremity perfusion, and rewarming of the patient. Follow-up CT scan angiogram demonstrated that all reconstructions were patent through the follow-up period.

Conclusions

Paraplegia is an extremely morbid complication associated with TAAA repair. We describe a technique that allows reimplantation of almost all intercostal arteries as one patch circumventing the need for selective reimplantation. Furthermore, our technique ensures continued patency of this patch graft as the outflow resistance is decreased by creating a continuous flow loop. Although this is a small case series, we had no incidence of acute or delayed paraplegia in this high risk group. Our technique of intercostal reimplantation is applicable to all open TAAA repair at high-risk for paraplegia and may be an important adjunct in preventing spinal cord ischemia.

Article Outline

Abstract

Methods

Results

Discussion

Conclusion

Author contributions

Acknowledgment

References

Copyright

Thoracoabdominal aortic aneurysms (TAAA) have been classified by their anatomic extent. With the exception of experimental branched-graft devices, repair has been via open operation.1, 2 Indications for repair have generally included rupture, symptoms, rapid growth, or absolute size. Unfortunately, due to the extent of the operation, morbidity and mortality can be quite significant.3, 4, 5, 6, 7, 8 Major complications can include myocardial infarction (MI), renal failure, respiratory failure, visceral ischemia, stroke, and paraplegia.

Paraplegia is a devastating complication in this patient group and leads to significant morbidity and mortality. As a result, there has been much interest in improving techniques to minimize this complication. Intraoperative maneuvers such as distal aortic perfusion, cerebrospinal fluid drainage, and elevation of mean arterial pressures have been successful.6, 9, 10 Furthermore, intraoperative monitoring of somatosensory or motor evoked potentials (SSEP/MEP) has been beneficial in identifying and potentially reducing the incidence of intraoperative spinal cord ischemia.11, 12, 13, 14 Unfortunately, attempts at preoperatively or intraoperatively identifying one or two critical spinal arteries (artery of Adamkiewicz or great radicular artery) and subsequent revascularization have not yielded improved results.15, 16, 17

On the other hand, patent intercostal arteries, especially in the T6-T12 region are still likely important for spinal cord perfusion. Although, many of these arteries are occluded in atherosclerotic aneurysms, the majority are patent in aneurysms secondary to aortic dissections. Furthermore, these intercostal arteries may be important in providing continued spinal perfusion. As a result, we have developed a novel technique to reimplant these arteries as one patch. Furthermore, our technique allows a continuous flow loop to ensure persistent patency of our reconstruction. Although we have applied this technique to a specific patient population (aneurysms secondary to aortic dissections), it certainly is applicable to all thoracoabdominal aneurysm reconstruction.

Methods 

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We retrospectively reviewed our records for patients having received this procedure. Overall, eight patients were repaired under this manner in the course of one year (2005-2006). Patient ages ranged from 46 to 70 with a mean of 56 years of age. All patients had a previous aortic dissection with aneurysmal degeneration from the left subclavian artery to the visceral segment (type I TAAA). Indications for repair included symptomatic pain, rupture, rapid enlargement, or size greater than 6.5 cm.

All operations were approached from a left thoracoabdominal incision. Cerebrospinal fluid drainage was utilized in all cases. With the exception of one case, all were performed under deep hypothermic circulatory arrest (DHCA) due to lack of a proximal clamp site and a difficult proximal reconstruction. A standard Dacron graft was used to replace the aorta as an end-end anastomosis proximally and a beveled anastomosis distally. The aorta was replaced from the distal arch to the visceral vessels. An 8 mm limb was sewn end-side to the proximal graft prior to opening the aorta. Under circulatory arrest or partial bypass the aorta was opened and the proximal and distal anastomoses were performed. While rewarming the patient, the 8 mm limb was opened longitudinally and then sutured to multiple intercostal artery pairs in a side-side manner. The distal end of the 8 mm limb was then sutured to the distal graft in an end-side manner with a side-biting clamp on the aortic graft to allow continuous aortic perfusion (Fig 1, Fig 2). Intraoperative electroencephalograms (EEG) and upper and lower somatosensory evoked potentials (SSEP) were monitored throughout the procedure. In cases employing deep hypothermic circulatory arrest, patients were cooled on cardiopulmonary bypass and 10-channel EEG was used to confirm electrocerebral silence prior to the initiation of circulatory arrest at an average nasopharyngeal temperature of 14 degrees Celsius.


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Fig 1. A graphic representation of the intercostal patch graft.



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Fig 2. An intraoperative photograph of the intercostal patch graft.


Patients were followed by history and physical exam at 1 month postprocedure. They were subsequently followed at 6-month intervals with a history, physical exam, and a CT scan. Follow-up ranged from 6 to 14 months.

Results 

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All patients were ambulatory at the time of admission although one patient reported mild unilateral leg weakness from a previous spinal cord infarction from a type A dissection. The average aneurysm size was 7.5 cm. Four patients were symptomatic upon presentation.

Seven operations were performed with deep hypothermic circulatory arrest. One case was performed under left atrial-left femoral artery bypass. Upon opening the aorta, there was an average of seven pairs of patent intercostal arteries. We reimplanted an average of five pairs of intercostal arteries extending to the T10-T11 level. The remainder of the patent intercostal arteries was over sewn.

In all seven cases involving DHCA, the typical pattern of burst-suppression of the EEG was followed by electrocerebral silence with cooling. There was also the typical pattern of loss of the cortical evoked potentials from both the arms and legs. In four cases recovery of continuous, symmetrical EEG and cortical SSEP was seen following rewarming after circulatory arrest. In three cases of DHCA spinal SSEP did not recover with rewarming and in the one LA-FA case, SSEP were lost with aortic clamping These changes in the spinal SSEP were consistent with spinal ischemia. Prompt reimplantion of intercostal arteries with the described technique was undertaken. Following reimplantation, there was a return of lower extremity spinal SSEP to baseline. These patients had a normal postoperative exam.

There were no perioperative complications. No patients suffered any significant hemodynamic changes postoperatively. No patients were taken back to the operating room for bleeding. No patients suffered transient or permanent paraplegia during the postoperative or follow-up periods. All patients were discharged ambulating. The one patient who had unilateral leg weakness reported subjective improvement in strength of the affected leg.

Follow-up ranged from 6 months to 14 months. All patients remained ambulatory throughout the follow-up period. There was no evidence of pseudoaneurysm formation or patch aneurysm formation. All intercostal reconstructions remained patent through follow-up as demonstrated by CT (Fig 3, Fig 4, Table). Furthermore, follow-up CTA demonstrated persistent flow into intercostal arteries from the graft (Fig 5, Table).


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Fig 3. CT angiogram demonstrating an aortic graft with a patent intercostal patch graft.



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Fig 4. Three-dimensional reconstruction demonstrating patency in the follow-up period.


Table.

Latest follow-up imaging study after the procedure

PatientFollow-up studyGraftPatent intercostals
112moCTApatent5
23moCTpatentN/A
314moCTApatent4
46moCTpatentN/A
53moCTpatentN/A
66moCTApatent7
712moCTApatent5
83moCTApatent5

Either a traditional CT scan or CT angiogram was performed. Intercostal patency was only able to be reliably assessed on the CT angiograms.


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Fig 5. CT angiogram demonstrating patent intercostal arteries off the patch graft.


Discussion 

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Repair of thoracoabdominal aortic aneurysms has been associated with substantial morbidity. Due to the anatomic location and extent of disease, paraplegia is a considerable risk. Despite maneuvers to reduce this risk, such as distal aortic perfusion, cerebrospinal fluid drainage, elevation of mean arterial pressure, and intraoperative neuromonitoring, the risk of paraplegia remains significant.6, 9, 10, 11, 12, 13, 14, 18 As a result, we have devised a novel technique to improve spinal perfusion during TAAA repair.

We applied this technique to patients who had previous aortic dissections and subsequent aneurysmal degeneration. Traditionally, patients with previous abdominal aortic repairs and patients requiring full aortic replacement (type II TAAA) have been at highest risk for paraplegia.5, 19 Although, some studies have not demonstrated chronic dissection as a risk factor for paraplegia, it is our experience, and that of others, that these patients with previous aortic dissections seem to be at increased risk.20, 21 This may be due to decreased thrombus formation within the aneurysm sac. This is likely due to a combination of flow dynamics within the true and false lumen as well as rapid aneurysmal enlargement which decreases the amount of time for static flow and thrombus formation. As a result, there are often more patent intercostal arteries.15 This may result in a less mature or well-formed collateral circulation pathway to the spinal cord and increased dependence upon direct perfusion of the intercostal arteries.

In order to maximize adequate spinal cord perfusion during and after repair, attempts have been made to identify the artery of Adamkiewicz or the great radicular artery via multiple imaging techniques.22, 23 Nevertheless, reimplantation of these vessels has not yielded markedly reduced rates of paraplegia.15, 16, 17 In addition, exclusion of the Adamkiewicz artery does not necessarily correlate with spinal cord dysfunction.24 Rather, reimplantation of as many intercostal arteries as possible, whether or not they feed the Adamkiewicz or great radicular artery, may be critical. Furthermore, in cases of aortic dissection and subsequent aneurysmal degeneration, there can often be many patent intercostal arteries. Creating separate bypass grafts to each vessel or vessel pair would be cumbersome and not feasible. As a result, reimplanting multiple branches as one patch would seem most beneficial in terms of reperfusing the spinal cord and minimizing ischemic times. In general, we sought to reimplant as many intercostals as possible at the T6-T11 level. This also served to potentially revascularize the Artery of Adamkiewicz, which is most often found in this location.25 Because of the potential increased outflow resistance due to the small caliber of these vessels and subsequent potential for thrombosis, we reconnected the distal aspect of the side-limb to the main tube graft. As a result, the outflow for the side-limb becomes that of the tube graft (the entire lower body). Based upon the conservation of the principles of inertia and energy, antegrade flow is maintained within the side-limb allowing for a continuous flow loop and continuous flow to the intercostal arteries. Also, by avoiding a direct anastomosis of the main tube graft to the intercostals, aortic ischemia is minimized. Aortic perfusion is restored immediately after the distal aortic anastomosis is completed. While reimplanting the intercostal arteries, there is continuous aortic perfusion through the main tube graft. In addition, the distal end-side anastomosis of the side-limb is performed with a side-biting clamp which does not interrupt aortic flow. As a result, continued perfusion through spinal collaterals (internal iliacs, viscerals, vertebrals) is maintained.

We found that this technique was able to be performed with technical success. The reconstructions did not lengthen the case as they were performed during patient rewarming. Postoperatively, no patients required replacement of spinal drains after their removal. Furthermore, no patients required blood pressure augmentation due to lower extremity weakness. All reconstructions remained patent throughout the follow-up period. All patients also had full preservation of lower extremity strength and sensation.

The importance of reimplanting multiple intercostal vessels was recognized in this study. Persistent loss of spinal SSEP from the legs has been shown to be predictive of lower extremity neurologic dysfunction.12 In our cohort, four patients had evidence of a persistent intraoperative injury on lower extremity SSEP during the aortic repair. This change is the typical finding of ischemia and dysfunction of the spinal sensory pathways from the legs. Shortly following reimplantation of intercostal arteries there was return of the lower extremity SSEP to baseline. It is our experience and others that patients developing persistent or transient spinal SSEP changes are typically at high risk for developing postoperative spinal ischemia.12 These patients had no evidence of spinal cord ischemia upon arousal from anesthesia nor did the patients develop an episode of postoperative spinal cord ischemia. It is possible that reimplantation not only reversed these patients’ intraoperative ischemia but also added an additional level of postoperative protection. It is certainly possible and likely that these patients would have had significant neurologic dysfunction without reimplantation.

Conclusion 

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Paraplegia is a devastating complication of TAAA repair. Moreover, certain types of TAAA are at increased risk for paraplegia when repaired. Many techniques have been devised for eliminating spinal cord injury. While these techniques have decreased the incidence, spinal cord ischemia still occurs at an unacceptably high rate. We report a technique which improves spinal cord perfusion and may help reduce this incidence.

Author contributions 

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Conception and design: EW, JB, RF, AP

Analysis and interpretation: EW, MM, BJ, AP

Data collection: EW, MM

Writing the article: EW, MM, BJ, AP

Critical revision of the article: EW, MM, BJ, JB, RF, AP

Final approval of the article: EW, MM, BJ, JB, RF, AP

Statistical analysis: Not applicable

Obtained funding: Not applicable

Overall responsibility: EW, AP

 

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The authors would like to acknowledge Dr Frank Bowen for his detailed drawing of the patch graft used in this manuscript.

References 

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1. 1Chuter TA, Gordon RL, Reilly LM, Goodman JD, Messina LM. An endovascular system for thoracoabdominal aortic aneurysm repair. J Endovasc Ther. 2001;8:25–33. MEDLINE | CrossRef

2. 2Safi HJ. How I do it: thoracoabdominal aortic aneurysm graft replacement. Cardiovasc Surg. 1999;7:607–613. MEDLINE | CrossRef

3. 3Lombardi JV, Carpenter JP, Pochettino A, Sonnad SS, Bavaria JE. Thoracoabdominal aortic aneurysm repair after prior aortic surgery. J Vasc Surg. 2003;38:1185–1190. Abstract | Full Text | Full-Text PDF (107 KB) | CrossRef

4. 4Cambria RP, Clouse WD, Davison JK, Dunn PF, Corey M, Dorer D. Thoracoabdominal aneurysm repair: results with 337 operations performed over a 15-year interval. Ann Surg. 2002;236:471–479discussion 479. MEDLINE | CrossRef

5. 5Coselli JS, LeMaire SA, Miller CC, Schmittling ZC, Koksoy C, Pagan J, et al. Mortality and paraplegia after thoracoabdominal aortic aneurysm repair: a risk factor analysis. Ann Thorac Surg. 2000;69:409–414. MEDLINE | CrossRef

6. 6Coselli JS, LeMaire SA, Conklin LD, Koksoy C, Schmittling ZC. Morbidity and mortality after extent II thoracoabdominal aortic aneurysm repair. Ann Thorac Surg. 2002;73:1107–1115discussion 1115-6. MEDLINE | CrossRef

7. 7Chiesa R, Melissano G, Civilini E, de Moura ML, Carozzo A, Zangrillo A. Ten years experience of thoracic and thoracoabdominal aortic aneurysm surgical repair: lessons learned. Ann Vasc Surg. 2004;18:514–520. Abstract | Full Text | Full-Text PDF (641 KB) | CrossRef

8. 8Rigberg DA, Zingmond DS, McGory ML, Maggard MA, Agustin M, Lawrence PF, et al. Age stratified, perioperative, and one-year mortality after abdominal aortic aneurysm repair: a statewide experience. J Vasc Surg. 2006;43:224–229. Abstract | Full Text | Full-Text PDF (131 KB) | CrossRef

9. 9Cina CS, Abouzahr L, Arena GO, Lagana A, Devereaux PJ, Farrokhyar F. Cerebrospinal fluid drainage to prevent paraplegia during thoracic and thoracoabdominal aortic aneurysm surgery: a systematic review and meta-analysis. J Vasc Surg. 2004;40:36–44. Abstract | Full Text | Full-Text PDF (309 KB) | CrossRef

10. 10Kuniyoshi Y, Koja K, Miyagi K, Shimoji M, Uezu T, Arakaki K, et al. Prevention of postoperative paraplegia during thoracoabdominal aortic surgery. Ann Thorac Surg. 2003;76:1477–1484. MEDLINE | CrossRef

11. 11Galla JD, Ergin MA, Lansman SL, McCullough JN, Nguyen KH, Spielvogel D, et al. Use of somatosensory evoked potentials for thoracic and thoracoabdominal aortic resections. Ann Thorac Surg. 1999;67:1947–1952discussion 1953-8. MEDLINE | CrossRef

12. 12Wada T, Yao H, Miyamoto T, Mukai S, Yamamura M. Prevention and detection of spinal cord injury during thoracic and thoracoabdominal aortic repairs. Ann Thorac Surg. 2001;72:80–84discussion 85. MEDLINE | CrossRef

13. 13Jacobs MJ, Elenbaas TW, Schurink GW, Mess WH, Mochtar B. Assessment of spinal cord integrity during thoracoabdominal aortic aneurysm repair. Ann Thorac Surg. 2002;74:S1864–S1866discussion S1892-8. MEDLINE | CrossRef

14. 14Jacobs MJ, Mess WH. The role of evoked potential monitoring in operative management of type I and type II thoracoabdominal aortic aneurysms. Semin Thorac Cardiovasc Surg. 2003;15:353–364. Abstract | Full Text | Full-Text PDF (549 KB)

15. 15Williams GM, Roseborough GS, Webb TH, Perler BA, Krosnick T. Preoperative selective intercostal angiography in patients undergoing thoracoabdominal aneurysm repair. J Vasc Surg. 2004;39:314–321. Abstract | Full Text | Full-Text PDF (188 KB) | CrossRef

16. 16Minatoya K, Karck M, Hagl C, Meyer A, Brassel F, Harringer W, et al. The impact of spinal angiography on the neurological outcome after surgery on the descending thoracic and thoracoabdominal aorta. Ann Thorac Surg. 2002;74:S1870–S1872discussion S1892-8. MEDLINE | CrossRef

17. 17Griepp RB, Ergin MA, Galla JD, Lansman S, Khan N, Quintana C, et al. Looking for the artery of Adamkiewicz: a quest to minimize paraplegia after operations for aneurysms of the descending thoracic and thoracoabdominal aorta. J Thorac Cardiovasc Surg. 1996;112:1202–1213discussion 1213-5. Abstract | Full Text | Full-Text PDF (1563 KB) | CrossRef

18. 18Estrera AL, Miller CC, Huynh TT, Porat E, Safi HJ. Neurologic outcome after thoracic and thoracoabdominal aortic aneurysm repair. Ann Thorac Surg. 2001;72:1225–1230discussion 1230-1. MEDLINE | CrossRef

19. 19Kawaharada N, Morishita K, Fukada J, Watanabe T, Abe T. Surgical treatment of thoracoabdominal aortic aneurysm after repairs of descending thoracic or infrarenal abdominal aortic aneurysm. Eur J Cardiothorac Surg. 2001;20:520–526. Abstract | Full Text | Full-Text PDF (95 KB) | CrossRef

20. 20Coselli JS, LeMaire SA, de Figueiredo LP, Kirby RP. Paraplegia after thoracoabdominal aortic aneurysm repair: is dissection a risk factor?. Ann Thorac Surg. 1997;63:28–35discussion 35-6. MEDLINE | CrossRef

21. 21Dudra J, Shiiya N, Matsui Y, Sakuma M, Ishii K, Asada M, et al. Operative results of thoracoabdominal repair for chronic type B aortic dissection. J Cardiovasc Surg. 1997;38:147–151(Torino).

22. 22Yoshioka K, Niinuma H, Ohira A, Nasu K, Kawakami T, Sasaki M, et al. MR angiography and CT angiography of the artery of Adamkiewicz: noninvasive preoperative assessment of thoracoabdominal aortic aneurysm. Radiographics. 2003;23:1215–1225. CrossRef

23. 23Savader SJ, Williams GM, Trerotola SO, Perler BA, Wang MC, Venbrux AC, et al. Preoperative spinal artery localization and its relationship to postoperative neurologic complications. Radiology. 1993;189:165–171. MEDLINE

24. 24Nijenhuis RJ, Jacobs MJ, Schurink GW, Kessels AG, van Engelshoven JM, Backes WH. Magnetic resonance angiography and neuromonitoring to assess spinal cord blood supply in thoracic and thoracoabdominal aortic aneurysm surgery. J Vasc Surg. 2007;45:71–77discussion 77-8. Abstract | Full Text | Full-Text PDF (336 KB) | CrossRef

25. 25Koshino T, Murakami G, Morishita K, Mawatari T, Abe T. Does the Adamkiewicz artery originate from the larger segmental arteries?. J Thorac Cardiovasc Surg. 1999;117:898–905. Abstract | Full Text | Full-Text PDF (96 KB) | CrossRef

a Division of Vascular Surgery, University of Pennsylvania Medical Center, Philadelphia, Pa

b Division of Cardiothoracic Surgery, University of Pennsylvania Medical Center, Philadelphia, Pa

c Department of Surgery, and the Division of Neurology, Department of Medicine, University of Pennsylvania Medical Center, Philadelphia, Pa.

Corresponding Author InformationCorrespondence: Edward Y. Woo, MD, University of Pennsylvania Medical Center, 4 Silverstein, 3400 Spruce Street, Philadelphia, PA 19104.

 Competition of interest: none.

PII: S0741-5214(07)00732-X

doi:10.1016/j.jvs.2007.04.048


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