Next Article in Journal
Long-Term Results of Complex Abdominal Aortic Aneurysm Open Repair
Next Article in Special Issue
The Cardiac Power Index during Abdominal Open Aortic Surgery: Intraoperative Insights into the Cardiac Performance—A Retrospective Observational Analysis
Previous Article in Journal
Implementation of Routine Endoscopy with Narrow Band Imaging in the Evaluation of Oral and Upper Airways Lesions in Oral Chronic Graft-Versus-Host Disease: A Preliminary Study
Previous Article in Special Issue
Characteristics of Patients with Unrecognized Sleep Apnea Requiring Postoperative Oxygen Therapy
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
JPM
Volume 12
Issue 10
10.3390/jpm12101629
jpm-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Prevention of Spinal Cord Injury during Thoracoabdominal Aortic Aneurysms Repair: What the Anaesthesiologist Should Know

by
Federico Marturano
1,
Fulvio Nisi
2,*,
Enrico Giustiniano
2,
Francesco Benedetto
2,3,
Federico Piccioni
2 and
Umberto Ripani
4
1
Department of Anaesthesia, Analgesia and Intensive Care, Vito Fazzi Hospital, 73100 Lecce, Italy
2
Department of Anaesthesia and Intensive Care Unit, IRCCS Humanitas Research Hospital, 20089 Milan, Italy
3
Department of Biomedical Sciences, Humanitas University, 20090 Milan, Italy
4
Division of Clinic Anaesthesia, Department of Emergency Hospital Riuniti, Conca Street 71, 60126 Ancona, Italy
*
Author to whom correspondence should be addressed.
J. Pers. Med. 2022, 12(10), 1629; https://doi.org/10.3390/jpm12101629
Submission received: 20 August 2022 / Revised: 20 September 2022 / Accepted: 21 September 2022 / Published: 1 October 2022
(This article belongs to the Special Issue Individual Evaluation, Management and Outcome in Perioperative Medicine)
Browse Figure
Versions Notes

Abstract

:
Thoraco-abdominal aortic repair is a high-risk surgery for both mortality and morbidity. A major complication is paraplegia-paralysis due to spinal cord injury. Modern thoracic and abdominal aortic aneurysm repair techniques involve multiple strategies to reduce the risk of spinal cord ischemia during and after surgery. These include both surgical and anaesthesiologic approaches to optimize spinal cord perfusion by staging the procedure, guaranteeing perfusion of the distal aorta through various techniques (left atrium–left femoral artery by-pass) by pharmacological and monitoring interventions or by maximizing oxygen delivery and inducing spinal cord hypothermia. Lumbar CSF drainage alone or in combination with other techniques remains one of the most used and effective strategies. This narrative review overviews the current techniques to prevent or avoid spinal cord injury during thoracoabdominal aortic aneurysms repair.

Graphical Abstract

1. Introduction

Thoracic endovascular aortic repair (TEVAR) is a minimally invasive option for the management of the pathology of the descending thoracic aorta compared to open surgical repair (OPEN). Mortality of OPEN surgery for thoracic aortic aneurysm (TAA) is between 3 and 28%, while for endovascular correction it is between 0 and 16.9% [1]. TEVAR reduces the morbidity and mortality rates compared to the OPEN procedure but is associated with a significant risk of spinal cord ischemia (SCI) and consequently paraplegia (22% open versus 19% endovascular) [2]. This risk is similar between the two procedures [3]. Spinal cord blood flow depends on a single anterior longitudinal spinal artery and two posterolateral spinal arteries, which form a plexus running along the medulla. Anterior and posterior spinal arteries originate from vertebral arteries and receive a contribution from segmental arteries, collateral vessels emerging directly from the aorta or left subclavian artery [4]. In the thoracic region, arterial blood flow is supplied directly by the aorta through intercostal arteries; the Adamkiewicz artery, also known as arteria radicularis magna, is a large radicular artery that originates between T8 and T12 and is the most important collateral artery at the thoracic level [5]. At the lumbar and sacral level, collateral circles are provided by lumbar arteries (parietal branches of the abdominal aorta) and by the lateral sacral arteries (parietal branches of the internal iliac artery).

2. Pathophysiology of Spinal Cord Ischemia

The pathogenesis of spinal cord ischemia after TEVAR is multifactorial and is not completely elucidated. In the past, Adamkiewicz artery’s occlusion was supposed to be a main contributor of spinal cord ischemia after aortic aneurysm repair [6], but current data show alterations of collateral circulation have greater relevance in the development of SCI [7]. Two theories have been developed in this regard: the first is based on the inadequate remodelling of collateral vessels’ network; the latter involves micro embolism originated from aortic plaques in segmental arteries. Collateral circulations are a network of blood vessels interconnecting the anterior spinal artery with vessels that supply blood to the adjacent muscles of the back [4]. These interconnections act as an important alternative supply of blood when the main sources are excluded, such as during aortic clamping in open repair or exclusion of segmental arteries after release of the thoracic stent [8]. These features interact with the hydrodynamics of the cerebrospinal fluid. In OPEN repair of TAA, aortic clamping causes systemic arterial hypertension proximal to clamping and hypotension distal to the clamp and increased splanchnic and central venous pressure [9] raising intracranial pressure (PIC) and cerebrospinal fluid (CSF) pressure [10]. Distal systemic arterial hypotension causes renal, intestinal, and lower limb ischemia and reduces spine cord perfusion pressure (SCPP) if we consider the main vessels which guarantee the blood perfusion supply, according to the following relationship [11]:
SCPP = MAPd (mean arterial pressure distal to clamp) − CSF pressure
Furthermore, after aortic unclamping, reperfusion may contribute to spinal cord injury as well, through inflammatory response, hypercarbia, which increases CSF pressure, and systemic hypotension which decreases spinal perfusion pressure. Metabolic acidosis can increase cerebral blood flow, intracranial pressure, and CSF pressure upon unclamping. Moreover, anaerobic metabolites are responsible for a reduction in peripheral vascular resistance and therefore for severe hypotension. Spinal cord oedema caused by reperfusion injury can also increase CSF pressure [12]. During TEVAR, the remodeling of the collateral network plays a fundamental role in maintaining spinal perfusion through changes in distribution of blood flow between intraspinous and paraspinous collateral network after the exclusion of segmental arteries [13]. These changes occur between the second and fifth day after surgery [13]. Furthermore, non-occluded segmental arteries can ensure perfusion to ischemic spinal segments by reversing the direction of blood flow in the anterior spinal artery through proximal and distal segmental arteries. SCI may arise if all these compensatory mechanisms fail or if supplying vessels are obstructed by thrombo-embolic formations or by flow alterations due to the stent [14]. Collateral circles that supply blood to the spine are the left subclavian artery, intercostal, lumbar, and hypogastric arteries. There is a close correlation between the coverage of two or more collateral circles and the development of symptomatic medullary ischemia, especially when associated with prolonged perioperative hypotension. The left subclavian artery is one of the most important tributary arteries of collateral circulation to the spine. Indeed, it ensures blood flow both to the brain and spinal cord through the left vertebral artery, which divides into the basilar artery, perfusing the posterior part of the circle of Willis and into the anterior spinal artery directed to the spinal cord. In addition, the thyrocervical trunk arising from the left subclavian artery supplies blood to the spine through anterior and posterior radicular arteries. Unfortunately, more than 40% of patients undergoing TEVAR require intentional coverage of the left subclavian due to the proximity of thoracic aortic disease [15]. This increases the risk of spinal cord injury. The internal iliac artery, also known as hypogastric, supplies blood to the spine through lumbosacral radicular arteries [15]. During TEVAR, impaired hypogastric blood flow may occur when an iliac artery graft is used as a vascular access in patients with severe atherosclerosis of the ileo-femoral arteries. This was associated with a high risk of spinal cord ischemia (4.3%) [16]. The extension of the aortic coverage by stents is one of the most important surgical risk factors which increase the risk of SCI by 30% every 2 cm of additional aortic coverage [17].

3. Clinical Presentation

The clinical presentation of SCI varies from limb paresis to complete paraplegia with or without autonomic dysfunction. These manifestations can be transient with partial or complete recovery or permanent [18]. SCI can manifest immediately after surgery, the patient showing focal neurological deficits upon awakening from anaesthesia or more often with a delayed onset, 24–48 h after surgery [5,19]. Early onset SCI is associated with a negative prognosis since it is not possible to determine whether the onset of ischemia and spine cord infarction has already begun. On the other hand, delayed onset SCI, when promptly detected and treated, has a relatively good prognosis [20,21]. Immediate paralysis occurs more frequently after OPEN repair, whilst delayed onset paralysis occurs generally after TEVAR. The different clinical presentation during OPEN repair is due to clamping that quickly avoids perfusion to intercostal arteries suppling blood to anterior part of spinal cord. After unclamping, the blood flow to these arteries is restored. The ischemia-reperfusion damage caused by clamping–unclamping contributes to immediate SCI. On the other hand, during TEVAR the stent permanently covers the intercostal arteries branches with a constant reduction of blow flow and the development of compensatory circulations. This avoids the risks of reperfusion damage but induces long-term effects of impaired spinal blood flow compared to the shorter period of aortic clamping during OPEN repair [22]. Tthe ideal preventive and treatment measures for spinal cord ischemia after TEVAR are still a matter of debate, but most strategies are aimed either at increasing mean arterial pressure or at reducing the cerebrospinal fluid pressure through CSF drainage to optimize medullary perfusion. Current guidelines [23] recommend CSF drainage for spinal cord protection in both open and endovascular surgery in patients at high risk of SCI. Risk factors for development of SCI after thoracic aortic repair are both related to the patient and associated with the surgical procedure. They are listed in Table 1.

4. Neuroprotective Strategies for Spinal Cord during TEVAR

Avoiding SCI during thoracic aortic aneurysms repair is essential. Several strategies can be implemented to prevent SCI, both surgical and anaesthetic (Table 2).

4.1. Surgical Strategies

In cases where an extensive coverage of the aorta is planned (e.g., >30 cm), a two-stage procedure can be considered to reduce risk of SCI [24]. A two-stage approach includes firstly implanting a thoracic proximal endograft above emerging vessels. After two to three months, a distal stent will be placed [25]. Furthermore, surgical options to ensure flow to the left subclavian artery are revascularization or endovascular techniques are used. Revascularization procedures include the transposition of the subclavian on the left common carotid artery or insertion of a small bypass [26]. Endovascular techniques involve the use of fenestrated/branched stents, chimney and periscope graft, sandwich techniques, and fenestration techniques in situ [27]. Current guidelines [28] suggest previous revascularization of the left subclavian artery in patients undergoing TEVAR if proximal stent seal covers the artery emergence. Selective revascularization is absolutely indicated in patients with coronary artery bypass grafted with internal mammary artery in the presence of an arteriovenous fistula on the left arm and in left-handed patients. Relative indications include dominance of the left vertebral artery, extensive aortic coverage, previous AAA repair, and occlusion of the hypogastric artery. Post-operative indications to revascularization concern upper limb ischemia or onset of vertebrobasilar insufficiency [29]. Minimally invasive segmental artery coil embolization (MISACE) is a novel technique preconditioning to ischemia, inducing neo-angiogenesis, and improving vascularization of spinal cord before TEVAR. Despite encouraging prospects, reproducibility of this technique in patients with tortuous vessels or with thrombi localized in the aneurysm sac is not easy [30], and there are also concerns because the procedure itself can cause SCI. Temporary aneurysm sac perfusion (TASP) is a technique involving a two-stage procedure: the first step consists of the creation of an endoleak in the lateral branch of the endoprosthesis which perfuses the main splanchnic vessels, and one to three months later, a stent deployment will close the endoleak [31]. The use of branched or fenestrated stents is associated with a lower risk of the onset of SCI [32].

4.2. Anaesthesiologic Strategies

The anaesthetic approach to perioperative management of thoracic aortic aneurysms repair is fundamental and contributes to the prevention and management of complications. A goal-directed hemodynamic strategy is mandatory to achieve adequate spinal cord oxygenation and perfusion by a correct and adequate management of cardiac index (>2.5 L/min/m2) and serum hemoglobinemia concentration [18]. As stated before, spinal cord perfusion pressure is the difference between mean arterial pressure (MAP) and CSF pressure [10]. Optimizing systemic arterial blood pressure (MAP > 90 mmHg) and CSF pressure (<10 mmHg) allows to achieve an adequate spinal cord perfusion pressure (>80 mmHg) [33]. Data reported in literature [18] demonstrates that maintenance of spinal cord perfusion pressure >80 mmHg through MAP increase and CSF drainage after placement of the aortic stent can prevent and reverse SCI and paralysis. In patients developing postoperative ischaemia, MAP > 90 mmHg should be the first step of treatment (vasoactive drugs). Vasopressors should be gradually reduced over the next 24–48 h after the improvement of symptoms [34]. Neurophysiological monitoring is useful to detect spinal cord ischemia during both open and endovascular surgery [22,33]. Motor evoked potentials (MEPs) can evaluate descending spinal pathways, while somatosensory evoked potentials (SSEP) are used for ascending pathways. One limitation to their application is the inability to differentiate medium from severe SCI. They are also affected by lower limb ischemia caused by vascular introducers [35]. Furthermore, volatile anaesthetics alter cortical waves, increasing latency and reducing the amplitude of SSEP; then, they should be administered at no more than 0.5 MAC [36,37]. For these reasons, intravenous anaesthesia is recommended when evoked potentials are monitored (e.g., propofol and remifentanil infusions and, if necessary, low concentrations of volatile anaesthetic) [38]. Administration of neuromuscular blockers must also be carefully monitored to ensure muscle relaxation and an adequate MEP response. Near infrared spectroscopy (NIRS) is another useful monitoring used during TEVAR for diagnosis of SCI. Electrodes are placed on the surface of paraspinous muscles at the thoracic and lumbar level. NIRS provides measurement of blood oxygen saturation in paraspinous circulations, close to spinal cord microcirculation, reflecting indirectly its oxygenation and blood perfusion [39]. However, this promising technique has yet to be clinically validated [40], and its routinary use is not yet recommended [41]. Moderate hypothermia (32–35 °C) may play a role in spinal cord neuroprotection [42]. Hypothermia may be used to provide some degree of acute tolerance of spinal cord to perfusion disruption during surgery, especially OPEN. It can be achieved systemically through cardiopulmonary bypass or by infusion of cold fluids into epidural space [41]. However, systemic hypothermia is associated with several risks, such as dysrhythmias, coagulopathy, and metabolic alterations, while selective spinal cord hypothermia through epidural cooling is an invasive procedure, applicable for a limited duration with high risk of contamination and spinal cord rebound oedema [43]. However, this practice is poorly used in TEVAR as it requires a very invasive approach compared to the procedure which is minimally invasive [44], and in vitro studies showed hypothermia can alter the structure of grafts, causing deformation, migration, and endoleak [45]. The pharmacological protective strategy can also reduce spinal cord metabolic demands and inflammatory-neurochemical response to ischemia and reperfusion, especially when combined with other preventive strategies, such as CSF drainage. High dose of methylprednisolone (30 mg/kg) before aortic clamping [46] or intrathecal papaverine to improve spinal cord perfusion [47] or naloxone infused at a rate of 1 mcg/kg/h, starting before induction up to 48 h after surgery [48], are the most adopted strategies. SCI-induced neuronal cell death is triggered by the presence of redundant excitatory neurotransmitters, especially glutamate, glycerine, and aspartate that cause an excessive influx of calcium [49]. In experimental settings, naloxone reduces CSF glutamate and aspartate concentrations but not glycerine [50]. However, today there are no definite recommendations on routine use of these drugs to avoid SCI. CSF drainage is the most effective procedure in preventing SCI after aortic repair because acute changes due to ischemia and reperfusion result in spinal cord oedema and increased CSF pressure and finally SCPP reduces. Current guidelines [22] recommend CSF drainage for both open and endovascular TAA repair in patients at high risk of SCI. Specific indications to CSF drainage in patient undergoing TEVAR were recently identified (Table 3), although further validation needs [21].
Postoperative CSF drainage is indicated in patients with delayed paralysis following TEVAR within two hours of symptom onset. Although recent works [18] do not recommend this practice since the mechanisms of delayed paraplegia are not fully understood yet, CSF drainage can be performed on the day before surgery to recognize early any sort of complications [51] or can be scheduled on the day of surgery [40]. In any case, the timing of CSF drain placement does not have an impact on the post-discharge functional impairment or long-term mortality [52]. Hemodynamic optimization plus CSF drainage is currently recommended as the best strategy to avoid or reduce risks of SCI during TEVAR [40]. For this purpose, a silicon drainage catheter is inserted approximately 8–10 cm into the subarachnoid space at the lumbar level, allowing measurement of CSF pressure and CSF drainage [53]. Current recommendations [22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55] suggest continuous monitoring of CSF pressure to monitor the ICP wave and prevent catheter obstruction. Intermittent rather than continuous CSF drainage reduce the risks of the development subarachnoid haemorrhage due to excessive loss of CSF in a short time [56,57,58]. The rate of complications after lumbar drainage placement is 0.3–1.0% [59]. The most frequent is localized infection (11.1%), post-dural puncture headache (3.3%), puncture site bleeding (2.1%), persistent CSF loss (1.3%), subdural hematoma with no clinical evidence, abducens nerve palsy, catheter displacement-occlusion (0.1%), or fracture (0.15%). More severe complications are meningitis (0.1%), subdural hematoma (1.7%), and intracranial haemorrhage (1.8%) [60]. The latter may be associated with excessive CSF drainage stretching and tearing of the dural veins. To minimize the risks of subdural hematoma, a CSF pressure ≥10 mmHg is recommended in the absence of ischaemia or to perform an intermittent drainage of 10–20 mL/h with continuous blood pressure monitoring. Patients with cerebral atrophy, arteriovenous malformations, brain aneurysms, and history of previous subdural hematoma are particularly disposed to develop cerebral haemorrhage [57]. Normal haemostatic panel and platelet count is also recommended before the procedure and withdrawal time of any anticoagulant and antiaggregant drugs must be properly respected [61]. The catheter should be kept in place for at least three days. In fact, delayed paralysis occurs after 1.8 days and is frequently associated with hypotension or catheter malfunction. CSF aspiration of 10–20 mL/h is recommended if PIC > 10 mmHg, while fluid or vasopressor infusion can support the hemodynamics [62].
In addition to this, CSF drainage system may be useful to measure the lactate concentration in the cerebrospinal fluid [63]. During descending aorta surgery, CSF lactate has been proposed as a marker of neuronal anaerobic metabolism due to spinal ischemia related to aortic clamping proximal to the Adamkiewicz arteria or to the exclusion of the main spinal arteries from the blood flow because of the endovascular prosthesis, and its increase occurs earlier than other markers, such as S-100 protein [64,65]. Noteworthy, in neurosurgical patients, point-of-care measurements of cerebrospinal fluid lactate could aid in detecting infections of the central nervous system and surrounding structures [66]. This implies that CSF-lactate levels may even increase for reasons different from spinal cord ischemia [67]. Nevertheless, Casiraghi et al. demonstrated that preoperative baseline CSF lactate levels were somehow higher in patients with spinal cord injury compared with those with no injury [68]. Normal values of spinal fluid lactate concentration are debated. According to some authors, normal concentration is age-related and ranges from 0.6 to 3.1 mmol/L, with increasing levels which also depend on the duration of the low-flow state when spinal ischemia occurs [63].

Type of Anaesthesia

General anaesthesia is mandatory for open thoracic aortic surgery, and it is often performed for TEVAR. This allows a safe control of the airways in case of haemorrhagic shock or rapid conversion to open surgery, the possibility for intraoperative monitoring with trans-esophageal echocardiography, avoids involuntary movements of the surgical field related to the patient’s respiratory pattern, and ensures the pacemaker’s heart rate control. Nevertheless, neuraxial and locoregional anaesthesia are emerging techniques in TEVAR [69]. Neuraxial anaesthesia can provide adequate pain relief on large bore of vascular access sites and relieve discomfort related to the prolonged fixed position. Moreover, it allows continuous monitoring of clinical signs of cerebral ischemia. On the other hands, spinal anaesthesia is associated with haemodynamic instability and with the risk of spinal hematoma. Local anaesthetic infiltration of femoral access sites, combined with slight sedation (also known as monitored anaesthesia care), is an alternative technique preserving patient’s consciousness and ability to obey orders without pain and haemodynamic stability and finally allowing to directly monitor the spinal cord function. In these cases, patient cooperation is crucial as spontaneous movements are possible during critical surgical manoeuvres, and pain and stress are less manageable. Currently, there are insufficient scientific data to recommend any of these techniques as a first choice in the management of TEVAR; still evidences in endovascular abdominal aneurysm repair (EVAR) show less postoperative pulmonary complications [70], shorter in-hospital length of stay, and lower mortality [71] in patients undergoing regional/local anaesthesia.

4.3. Special Consideration for Aortic Dissection Repair

Aortic dissection is a life-threatening condition caused by tears of the aortic inner layer through which blood enters and flows. The resulting false lumen can lead to occlusion of aortic branches and consequent ischemia. The Stanford classification divides aortic dissections into type-A with involvement of the ascending aorta and type-B, originating distal to the left subclavian artery. Emergency surgery is mandatory for treatment of type-A dissections. Total arch replacement is obtained by a Dacron prosthesis (frozen elephant trunk) that provides an anchoring platform for following distal endograft.
Spinal cord injury is a well-known complication following this procedure (8.9%) [72].
Risk factors associated with SCI are stent extent greater than 15 cm, a coverage at or distal to T8, and length of circulation arrest [73]. Ensuring blood flow to the left subclavian and femoral artery via extracorporeal circulation during circulation arrest and guaranteeing hypothermia are techniques used to prevent SCI during aortic arch repair [74]. Intraoperative CSF drainage is not currently recommended due to emergency surgery, but it can be useful postoperatively to treat sudden paraplegia, according to data of aortic aneurysm repair [75]. Not-complicated type-B dissection requires a first step conservative treatment with medical therapy and rest. Then, endovascular surgery can be planned. Urgent TEVAR is indicated in the type-B dissection presenting with persistent pain, uncontrolled hypertension, early aortic expansion, signs of malperfusion, or rupture [76]. In all these cases, recommendations similar to those postulated for aneurysm repair can be applied for the prevention of SCI.

5. Conclusions

Thoracic aneurysm repair is associated with high risks of perioperative complications. Spinal cord ischemia injury is the most frequent complication causing paraplegia. Each case scheduled for surgery must be discussed between surgeons and anaesthesiologists to consider case-by-case benefits and risks related to thoracic aneurysm repair. Several strategies can be implemented to avoid or reduce the risk of SCI. Anaesthesiologists should guarantee adequate spinal cord perfusion by increasing MAP to ensure collateral circulation and decreasing CSF pressure through CSF drainage. All the other interventions still need a prospective validation, and their uses should be tailored individually on to the patient.

Author Contributions

Conceptualization, F.M. and F.N.; methodology, F.B.; validation, E.G. and U.R.; investigation, F.B.; writing—original draft preparation, F.M.; writing—review and editing, F.N.; supervision, E.G. and F.P.; project administration, U.R. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Adnan, Z.; Rizvi, M.D. Incidence, prevention and management in spinal cord protection during TEVAR. J. Vasc. Surg. 2010, 52, 86–90. [Google Scholar]
  2. Okita, Y. Fighting spinal cord complication during surgery for thoracoabdominal aortic diseas. Gen. Thorac. Cardiovasc. Surg. 2011, 59, 79–90. [Google Scholar] [CrossRef]
  3. Cheung, A.T.; Weiss, S.J.; McGarvey, M.L.; Stecker, M.M.; Hogan, M.S.; Escherich, A.; Bavaria, J.E. Interventions for reversing delayed onset postoperative paraplegia after thoracic aortic reconstruction. Ann. Thorac. Surg. 2002, 74, 413–421. [Google Scholar] [CrossRef]
  4. Melissano, G.; Bertoglio, L.; Rinaldi, E.; Leopardi, M.; Chiesa, R. An anatomical rewiew of spinal cord blood supply. J. Cardiovasc. Surg. 2015, 56, 699–706. [Google Scholar]
  5. Cheung, A.T.; Pochettino, A.; McGarvey, M.L.; Appoo, J.J.; Fairman, R.M.; Carpenter, J.P.; Moser, W.G.; Woo, E.Y.; Bavaria, J.E. Strategies to manage paraplegia risk after endovascular stent repair of descending thoracic aortic aneurysms. Ann. Thorac. Surg. 2005, 80, 1280–1289. [Google Scholar] [CrossRef]
  6. Mehrez, I.O.; Nabseth, D.C.; Hogan, E.L.; Deterling, R.A., Jr. Paraplegia following resection of abdominal aortic aneurysm. Ann. Surg. 1962, 156, 890–898. [Google Scholar] [CrossRef]
  7. Griepp, R.B.; Griepp, E.B. Spinal cord protection in surgical andendovascular repair of thoracoabdominal aortic disease. J. Thorac. Cardiovasc. Surg. 2015, 149 (Suppl. 2), S86–S90. [Google Scholar] [CrossRef] [Green Version]
  8. Leyvi, G.; Ramachandran, S.; Wasnick, J.D.; Plestis, K.; Cheung, A.T.; Drenger, B. Risk and benefits of cerebrospinal fluid drainage during thoracoabdominal aortic aneurysm surgery. J. Cardiothorac. Vasc. Anesth. 2005, 19, 392–399. [Google Scholar] [CrossRef]
  9. D’Ambra, M.N.; Dewhirst, W.; Jacobs, M.; Bergus, B.; Borges, L.; Hilgenberg, A. Cross-clamping the thoracic aorta. Effect on intracranial pressure. Circulation 1988, 78 Pt 2, 198–202. [Google Scholar]
  10. Carroccio, A.; Marin, M.L.; Ellozy, S.; Hollier, L.H. Pathophysiology of paraplegia following endovascular thoracic aortic aneurysm repair. J. Card. Surg. 2003, 18, 359–366. [Google Scholar] [CrossRef]
  11. Gelman, S. The pathophysiology of aortic cross-clamping and unclamping. Anesthesiology 1995, 82, 1026–1057. [Google Scholar] [CrossRef]
  12. Etz, C.D.; Kari, F.A.; Mueller, C.S.; Silovitz, D.; Brenner, R.M.; Lin, H.-M.; Griepp, R.B. The collateral network concept: A reassessment of the anatomy of spinal cord perfusion. J. Thorac. Cardiovasc. Surg. 2011, 141, 1020–1028. [Google Scholar] [CrossRef] [Green Version]
  13. Stokum, J.A.; Gerzanich, V.; Simard, J.M. Molecular pathophysiology of cerebral edema. J. Cereb. Blood Flow Metab. 2016, 36, 513–538. [Google Scholar] [CrossRef] [Green Version]
  14. Martirosyan, N.L.; Feuerstein, J.S.; Theodore, N.; Cavalcanti, D.D.; Spetzler, R.F.; Preul, M.C. Blood supply and vascular reactivity of the spinal cord under normal and pathological conditions. J. Neurosurg. Spine 2011, 15, 238–251. [Google Scholar] [CrossRef] [Green Version]
  15. Khoynezhad, A.; Donayre, C.E.; Bui, H.; Kopchok, G.E.; Walot, I.; White, R.A. Risk factors of neurologic deficit after thoracic aortic endografting. Ann. Thorac. Surg. 2007, 83, S882–S889. [Google Scholar] [CrossRef]
  16. Feezor, R.J.; Martin, T.D.; Hess, P.J., Jr.; Daniels, M.J.; Beaver, T.M.; Klodell, C.T.; Lee, W.A. Extent of aortic coverage and incidence of spinal cord ischemia after thoracic endovascular aneurysm repair. Ann. Thorac. Surg. 2008, 86, 1809–1814. [Google Scholar] [CrossRef]
  17. Mehmedagic, I.; Resch, T.; Acosta, S. Complications to cerebrospinal fluid drainage and predictors of spinal cord ischemia in patients with aortic disease undergoing advanced endovascular therapy. Vasc. Endovasc. Surg. 2013, 47, 415–422. [Google Scholar] [CrossRef]
  18. Kakinohana, M. What should we do against delayed onset paraplegia following TEVAR? J. Anesth. 2014, 28, 1–3. [Google Scholar] [CrossRef] [Green Version]
  19. Ullery, B.W.; Cheung, A.T.; Fairman, R.M.; Jackson, B.M.; Woo, E.Y.; Bavaria, J.; Pochettino, A.; Wang, G.J. Risk factors, outcomes, and clinical manifestations of spinal cord ischemia following thoracic endovascular aortic repair. J. Vasc. Surg. 2011, 54, 677–684. [Google Scholar] [CrossRef] [Green Version]
  20. Keith, C.J., Jr.; Passman, M.A.; Carignan, M.J.; Parmar, G.M.; Nagre, S.B.; Patterson, M.A.; Taylor, S.M.; Jordan, W.D., Jr. Protocol implementation of selective postoperative lumbar spinal drainage after thoracic aortic endograft. J. Vasc. Surg. 2012, 55, 1–8. [Google Scholar] [CrossRef] [Green Version]
  21. Davidovic, L.; Ilic, N. Spinal cord ischemia after aortic surgery. J. Cardiovasc. Surg. 2014, 55, 741–757. [Google Scholar]
  22. Hiratzka, L.F.; Bakris, G.L.; Beckman, J.A.; Bersin, R.M.; Carr, V.F.; Casey, D.E., Jr.; Eagle, K.A.; Hermann, L.K.; Isselbacher, E.M.; Kazerooni, E.A.; et al. 2010 ACCF/AHA/AATS/ACR/ASA/ SCA/SCAI/SIR/ STS/ SVM guidelines for the diagnosis and management of patients with Thoracic Aortic Disease: A report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines, American Association for Thoracic Surgery, American College of Radiology, American Stroke Association, Society of Cardiovascular Anesthesiologists, Society for Cardiovascular Angiography and Interventions, Society of Interventional Radiology, Society of Thoracic Surgeons, and Society for Vascular Medicine. Circulation 2010, 121, 266–369. [Google Scholar]
  23. Uchida, N. How to prevent spinal cord injury during endovascular repair of thoracic aortic disease. Gen. Thorac. Cardiovasc. Surg. 2014, 62, 391–397. [Google Scholar] [CrossRef]
  24. O’Callaghan, A.; Mastracci, T.M.; Eagleton, M.J. Staged endovascular repair of thoracoabdominal aortic aneurysms limits incidence and severity of spinal cord ischemia. J. Vasc. Surg. 2015, 61, 347–354. [Google Scholar] [CrossRef] [Green Version]
  25. Saouti, N.; Hindori, V.; Morshuis, W.J.; Heijmen, R.H. Left subclavian artery revascularization as part of thoracic stent grafting. Eur. J. Cardiothorac. Surg. 2015, 47, 120–125. [Google Scholar] [CrossRef] [Green Version]
  26. Dias, N.; Sonesson, B. Revascularization options for left subclavian salvage during TEVAR. J. Cardiovasc. Surg. 2014, 55, 497–503. [Google Scholar]
  27. Matsumura, J.S.; Lee, W.A.; Mitchell, R.S.; Farber, M.A.; Murad, M.H.; Lumsden, A.B.; Greenberg, R.K.; Safi, H.J.; Fairman, R.M. The Society for Vascular Surgery Practice Guidelines: Management of the left subclavian artery with thoracic endovascular aortic repair. J. Vasc. Surg. 2009, 50, 1155–1158. [Google Scholar] [CrossRef] [Green Version]
  28. Rizvi, A.Z.; Murad, M.H.; Fairman, R.M.; Erwin, P.J.; Montori, V.M. The effect of left subclavian artery coverage on morbidity and mortality in patients undergoing endovascular thoracic aortic interventions: A systematic review and meta-analysis. J. Vasc. Surg. 2009, 50, 1159–1169. [Google Scholar] [CrossRef] [Green Version]
  29. Wheatley, G.H., 3rd. Setting the stage: Thoracoabdominal aortic aneurysm repair in 2 acts. J. Thorac. Cardiovasc. Surg. 2015, 149, 1079–1080. [Google Scholar]
  30. Kasprzak, P.M.; Gallis, K.; Cucuruz, B.; Pfister, K.; Janotta, M.; Kopp, R. Editor’s choice–Temporary aneurysm sac perfusion as an adjunct for prevention of spinal cord ischemia after branched endovascular repair of thoracoabdominal aneurysms. Eur. J. Vasc. Endovasc. Surg. 2014, 48, 258–265. [Google Scholar] [CrossRef] [Green Version]
  31. Maurel, B.; Delclaux, N.; Sobocinski, J.; Hertault, A.; Martin-Gonzalez, T.; Moussa, M.; Spear, R.; Le Roux, M.; Azzaoui, R.; Tyrrell, M.; et al. The impact of early pelvic and lower limb reper-fusion and attentive peri-operative management on the incidence of spinal cord ischemia during thoracoabdominal aortic aneurysm endovascular repair. Eur. J. Vasc. Endovasc. Surg. 2015, 49, 248–254. [Google Scholar] [CrossRef] [Green Version]
  32. Weigang, E.; Hartert, M.; Siegenthaler, M.P.; Beckmann, N.A.; Sircar, R.; Szabò, G.; Etz, C.D.; Luehr, M.; von Samson, P.; Beyersdorf, F. Perioperative management to improve neurologic outcome in thoracic or thoracoabdominal aortic stent-grafting. Ann. Thorac. Surg. 2006, 82, 1679–1687. [Google Scholar] [CrossRef]
  33. Kemp, C.M.; Feng, Z.; Aftab, M.; Reece, T.B. Preventing spinal cord injury following thoracoabdominal aortic aneurysm repair: The battle to eliminate paraplegia. JTCVS Tech. 2021, 8, 11–15. [Google Scholar] [CrossRef]
  34. Sloan, T.B.; Edmonds, H.L., Jr.; Koht, A. Intraoperative electrophysiologic monitoring in aortic surgery. J. Cardiothorac. Vasc. Anesth. 2013, 27, 1364–1373. [Google Scholar] [CrossRef]
  35. Haghighi, S.S.; Sirintrapun, S.J.; Johnson, J.C.; Keller, B.P.; Oro, J.J. Suppression of spinal and cortical somatosensory evoked potentials by desflurane anesthesia. J. Neurosurg. Anesthesiol. 1996, 8, 148–153. [Google Scholar] [CrossRef]
  36. Malcharek, M.J.; Loeffler, S.; Schiefer, D.; Manceur, M.; Sablotzki, A.; Gille, J.; Pilge, S.; Schneider, G. Transcranial motor evoked potentials during anesthesia with desflurane versus propofol—A prospective randomized trial. Clin. Neurophysiol. 2015, 126, 1825–1832. [Google Scholar] [CrossRef]
  37. Husain, A.M.; Swaminathan, M.; McCann, R.L.; Hughes, G.C. Neurophysiologic intraoperative monitoring during endovascular stent graft repair of the descending thoracic aorta. J. Clin. Neurophysiol. 2007, 24, 328–335. [Google Scholar] [CrossRef]
  38. von Aspern, K.; Haunschild, J.; Hoyer, A.; Luehr, M.; Bakhtiary, F.; Misfeld, M.; Mohr, F.W.; Etz, C.D. Non-invasive spinal cord oxygenation monitoring: Validating collateral network near-infrared spectroscopy for thoracoabdominal aortic aneurysm repair. Eur. J. Cardiothorac. Surg. 2016, 50, 675–683. [Google Scholar] [CrossRef] [Green Version]
  39. Giustiniano, E.; Battistini, G.M.; Piccirillo, F.; Poletto, G.L.; Popovich, A.; Civilini, E.; Cecconi, M. May near infra-red spectroscopy and rap-id perfusion pressure recovering be enough to rule out post-operative spinal cord injury? Two compared case-reports. J. Clin. Monit. Comput. 2020, 34, 955–959. [Google Scholar] [CrossRef]
  40. Bobadilla, J.L.; Wynn, M.; Tefera, G.; Acher, C.W. Low incidence of paraplegia after thoracic endovascular aneurysm repair with proactive spinal cord protective protocols. J. Vasc. Surg. 2013, 57, 1537–1542. [Google Scholar] [CrossRef] [Green Version]
  41. Luehr, M.; Bachet, J.; Mohr, F.W.; Etz, C.D. Modern temperature management in aortic arch surgery: The dilemma of moderate hypothermia. Eur. J. Cardiothorac. Surg. 2014, 45, 27–39. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  42. Shimizu, H.; Mori, A.; Yoshitake, A.; Yamada, T.; Morisaki, H.; Okano, H.; Yozu, R. Thoracic and thoracoabdominal aortic repair under regional spinal cord hypothermia. Eur. J. Cardiothorac. Surg. 2014, 46, 40–43. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  43. Cambria, R.P.; Davison, J.K.; Carter, C.; Brewster, D.C.; Chang, Y.; Clark, K.A.; Atamian, S. Epidural cooling for spinal cord protection during thoracoabdominal aneurysm repair: A five-year experience. J. Vasc. Surg. 2000, 31, 1093–1102. [Google Scholar] [CrossRef] [PubMed]
  44. Kulik, A.; Castner, C.F.; Kouchoukos, N.T. Outcomes after thoracoabdominal aortic aneurysm repair with hypothermic circulatory arrest. J. Thorac. Cardiovasc. Surg. 2011, 141, 953–960. [Google Scholar] [CrossRef] [Green Version]
  45. Robich, M.P.; Hagberg, R.; Schermerhorn, M.L.; Pomposelli, F.B.; Nilson, M.C.; Gendron, M.L.; Sellke, F.W.; Rodriguez, R. Hypothermia severely effects performance of nitinol-based endovascular grafts in vitro. Ann. Thorac. Surg. 2012, 93, 1223–1227. [Google Scholar] [CrossRef] [Green Version]
  46. Laschinger, J.C.; Cunningham, J.N., Jr.; Cooper, M.M.; Krieger, K.; Nathan, I.M.; Spencer, F.C. Prevention of ischemic spinal cord injury following aortic cross-clamping: Use of corticosteroids. Ann. Thorac. Surg. 1984, 38, 500–507. [Google Scholar] [CrossRef]
  47. Svensson, L.G.; Stewart, R.W.; Cosgrove, D.M.; Lytle, B.W.; Beven, E.G.; Furlan, A.J.; Gottlieb, A.J.; Grum, D.F.; Lewis, B.S.; Salgado, A. Preliminary results and rationale for the use of intrathecal papaverine for the prevention of paraplegia after aortic surgery. S. Afr. J. Surg. 1988, 26, 153–160. [Google Scholar]
  48. Kunihara, T.; Matsuzaki, K.; Shiiya, N.; Saijo, Y.; Yasuda, K. Naloxone lowers cerebrospinal fluid levels of excitatory amino acids after thoracoabdominal aortic surgery. J. Vasc. Surg. 2004, 40, 681–690. [Google Scholar] [CrossRef] [Green Version]
  49. Acher, C.W.; Wynn, M.M.; Hoch, J.R.; Popic, P.; Archibald, J.; Turnipseed, W.E. Combined use of cerebral spinal fluid drainage and naloxone reduces the risk of paraplegia in thoracoabdominal aneurysm. J. Vasc. Surg. 1994, 19, 236–249. [Google Scholar] [CrossRef] [Green Version]
  50. Obrenovitch, T.P.; Richards, D.A. Extracellular neurotransmitter changes in cerebral ischaemia. Cerebrovasc. Brain Metab. Rev. 1995, 7, 1–54. [Google Scholar]
  51. Arnaoutakis, D.J.; Arnaoutakis, G.J.; Beaulieu, R.J.; Abularrage, C.J.; Lum, Y.W.; Black, J.H., 3rd. Results of adjunctive spinal drainage and/or left subclavian artery bypass in thoracic endovascular aortic repair. Ann. Vasc. Surg. 2014, 28, 65–73. [Google Scholar] [CrossRef] [PubMed]
  52. DeSart, K.; Scali, S.T.; Feezor, R.J.; Hong, M.; Hess, P.J.; Beaver, T.M.; Huber, T.S.; Beck, A. Fate of patients with spinal cord ischemia complicating thoracic endovascular aortic repair. J. Vasc. Surg. 2013, 58, 635–642. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  53. Estrera, A.L.; Sheinbaum, R.; Miller, C.C.; Azizzadeh, A.; Walkes, J.C.; Lee, T.Y.; Kaiser, L.; Safi, H.J. Cerebrospinal fluid drainage during thoracic aortic repair: Safety and current management. Ann. Thorac. Surg. 2009, 88, 9–15. [Google Scholar] [CrossRef] [PubMed]
  54. Pokhrel, B.; Hasegawa, T.; Izumi, S.; Ohmura, A.; Munakata, H.; Okita, Y.; Okada, K. Excessively high systemic blood pressure in the early phase of reperfusion exacerbates early-onset paraplegia in rabbit aortic surgery. J. Thorac. Cardiovasc. Surg. 2010, 140, 400–407. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  55. Fedorow, C.A.; Moon, M.C.; Mutch, W.A.; Grocott, H.P. Lumbar cerebrospinal fluid drainage for thoracoabdominal aortic surgery: Rationale and practical considerations for management. Anesth. Analg. 2010, 111, 46–58. [Google Scholar] [CrossRef] [PubMed]
  56. Puchakalaya, M.R.; Tremper, K.K. Brown-Sequard syndrome following removal of a cerebrospinal fluid drainage catheter after thoracic aortic surgery. Anesth. Analg. 2005, 101, 322–324. [Google Scholar] [CrossRef]
  57. Weaver, K.D.; Wiseman, D.B.; Farber, M.; Ewend, M.G.; Marston, W.; Keagy, B.A. Complications of lumbar drainage after thoracoabdominal aortic aneurysm repair. J. Vasc. Surg. 2001, 34, 623–627. [Google Scholar] [CrossRef] [Green Version]
  58. Dardik, A.; Perler, B.A.; Roseborough, G.S.; Williams, G.M. Subdural hematoma after thoracoabdominal aortic aneurysm repair: An underreported complication of spinal fluid drainage? J. Vasc. Surg. 2002, 36, 47–50. [Google Scholar] [CrossRef] [Green Version]
  59. Wynn, M.M.; Mell, M.W.; Tefera, G.; Hoch, J.R.; Acher, C.W. Complications of spinal fluid drainage in thoracoabdominal aorticaneurysm repair: A report of 486 patient streated from 1987 to 2008. J. Vasc. Surg. 2009, 49, 29–35. [Google Scholar] [CrossRef] [Green Version]
  60. Hanna, J.M.; Andersen, N.D.; Aziz, H.; Shah, A.A.; McCann, R.L.; Hughes, G.C. Results with selective preoperative lumbar drain placement for thoracic endovascular aortic repair. Ann. Thorac. Surg. 2013, 95, 1968–1974. [Google Scholar] [CrossRef]
  61. Narouze, S.; Benzon, H.T.; Provenzano, D.; Buvanendran, A.; De Andres, J.; Deer, T.; Rauck, R.; Huntoon, M.A. Interventional spine and pain procedures in patients on antiplatelet and anticoagulant medications: Guidelines from the American Society of Regional Anesthesia and Pain Medicine, the Society of Regional Anaesthesia and Pain Therapy, the American Academy of Pain Medicine, the International Neuromodulation Society, the North American Neuromodulation Society, and the World Institute of Pain. Reg. Anesth. Pain Med. 2015, 40, 182–212. [Google Scholar]
  62. Azizzadeh, A.; Huynh, T.T.; Miller, C.C.; Estrera, A.L.; Porat, E.E.; Sheinbaum, R.; Safi, H.J. Postoperative risk factors for delayed neurologic deficit after thoracic and thoracoabdominal aortic aneurysm repair: A case-control study. J. Vasc. Surg. 2003, 37, 750–754. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  63. Giustiniano, E.; Ruggieri, N. Is intrathecal lactate concentration monitoring helpful for postoperative paraplegia after descending aorta surgery? J. Clin. Anesth. 2014, 26, 506–508. [Google Scholar] [CrossRef] [PubMed]
  64. Giustiniano, E.; Malossini, S.E.; Pellegrino, F.; Cancellieri, F. Subarachnoid fluid lactate and paraplegia after descending aorta aneurismectomy: Two compared case reports. Case Rep. Anesthesiol. 2013, 2013, 925739. [Google Scholar]
  65. Kahaladj, N.; Teebken, O.E.; Hagl, C.; Wilhelmi, M.; Tschan, C.; Weissenborn, K.; Lichtinghagen, R.; Hoy, L.; Haverich, A.; Pichlmaier, M. The role of cerebrospinal fluid S100 and lactate to predict clinically evident spinal cord ischaemia in thoracoabdominal aortic surgery. Eur. J. Vasc. Endovasc. Surg. 2008, 36, 11–19. [Google Scholar]
  66. Stephani, C.; Choi, A.H.K.; Moerer, O. Point-of-care detection of lactate in cerebrospinal fluid. Intensiv. Care Med. Exp. 2021, 9, 18. [Google Scholar] [CrossRef]
  67. Anderson, R.E.; Winnerkvist, A.; Hansson, L.O.; Nilsson, O.; Rosengren, L.; Settergren, G.; Vaage, J. Biochemical marker of cerebrospinal ischemia after repair of aneurysms of the descending and thoracoabdominal aorta. J. Cardiothorac. Vasc. Anesth. 2003, 17, 598–603. [Google Scholar] [CrossRef]
  68. Casiraghi, G.; Poli, D.; Landoni, G.; Buratti, L.; Imberti, R.; Plumari, V.; Turi, S.; Mennella, R.; Messina, M.; Covello, R.D.; et al. Intrathecal lactate concentration and spinal cord injury in thoracoabdominal aortic surgery. J. Cardiothorac. Vasc. Anesth. 2011, 25, 120–126. [Google Scholar] [CrossRef]
  69. van Dorp, M.; Gilbers, M.; Lauwers, P.; Van Schil, P.E.; Hendriks, J.M. Local Anesthesia for Percutaneous Thoracic Endovascular Aortic Repair. Aorta 2016, 4, 78–82. [Google Scholar] [CrossRef] [Green Version]
  70. Bettex, D.; Lachat, M.; Pfammatter, T.; Schmidlin, D.; Turina, M.; Schmid, E. To compare general, epidural and local anaesthesia for endovascular aneurysm repair (EVAR). Eur. J. Vasc. Endovasc. Surg. 2001, 21, 179–184. [Google Scholar]
  71. Walschot, L.H.; Laheij, R.J.; Verbeek, A.L. Outcome after endovascular abdominal aortic aneurysm repair: A meta-analysis. J. Endovasc. Ther. 2002, 9, 82–89. [Google Scholar] [CrossRef] [PubMed]
  72. Pacini, D.; Tsagakis, K.; Jakob, H.; Mestres, C.-A.; Armaro, A.; Weiss, G.; Grabenwoger, M.; Borger, M.A.; Mohr, F.W.; Bonser, R.S.; et al. The frozen elephant trunk for the treatment of chronic dissection of the thoracic aorta: A multicenter experience. Ann. Thorac. Surg. 2011, 92, 1663–1670. [Google Scholar] [CrossRef] [PubMed]
  73. Preventza, O.; Liao, J.L.; Olive, J.K.; Simpson, K.; Critsinelis, A.C.; Price , M.D.; Galati, M.; Cornwell, L.D.; Orozco-Sevilla, V.; Omer, S.; et al. Neurologic complications after the frozen elephant trunk procedure: A meta-analysis of more than 3000 patients. J. Thorac. Cardiovasc. Surg. 2020, 160, 20–33.e4. [Google Scholar] [CrossRef] [Green Version]
  74. Hohri, Y.; Yamasaki, T.; Matsuzaki, Y.; Hiramatsu, T. Early and mid-term outcome of frozen elephant trunk using spinal cord protective perfusion strategy for acute type A aortic dissection. Gen. Thorac. Cardiovasc. Surg. 2020, 68, 1119–1127. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  75. Elshony, H.; Idris, A.; Ahmed, A.; Almaghrabi, M.; Ahmed, W.; Fallatah, S. Spinal Cord Ischemia Secondary to Aortic Dissection: Case Report with Literature Review for Different Clinical Presentations, Risk Factors, Radiological Findings, Therapeutic Modalities, and Outcome. Case Rep. Neurol. 2021, 13, 634–655. [Google Scholar] [CrossRef] [PubMed]
  76. Erbel, R.; Aboyans, V.; Boileau, C.; Bossone, E.; Di Bartolomeo, R.; Eggebrecht, H.; Evangelista, A.; Falk, V.; Frank, H.; Gaemperli, O.; et al. 2014 ESC Guidelines on the diagnosis and treatment of aortic diseases: Document covering acute and chronic aortic diseases of the thoracic and abdominal aorta of the adult. The Task Force for the Diagnosis and Treatment of Aortic Diseases of the European Society of Cardiology (ESC). Eur. Heart J. 2014, 35, 2873–2926. [Google Scholar] [PubMed] [Green Version]
Table
Table 1. Risk factors for susceptibility of spine cord ischemia after thoracic aortic repair 1.
Table 1. Risk factors for susceptibility of spine cord ischemia after thoracic aortic repair 1.
Patient Risk FactorsSurgical Risk Factors
1-Advanced age (>70 yrs.)1-Total aortic coverage > 205 mm
2-Perioperative hypotension (MAP < 70 mmHg)2-Concomitant abdominal aortic aneurysm or prior abdominal aortic aneurysm surgical repair
3-Renal insufficiency (Creatinine > 132 μMol/L)3-Coverage of ≥2 vascular territories
4-COPD4-Left subclavian artery coverage
5-Hypertension5-Urgent procedure
6-Degenerative aneurysm6-Coverage of hypogastric artery
7-Adjunct procedure (Iliac conduit)
8-Use of ≥3 stents
9-Longer duration of the procedure
10- Excessive blood loss
1 Adapted from [22] Hiratzka LF, Bakris GL, Beckman JA, et al. 2010 ACCF/AHA/AATS/ACR/ASA/ SCA/SCAI/SIR/ STS/ SVM guidelines for the diagnosis and management of patients with thoracic aortic disease: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines, American Association for Thoracic Surgery, American College of Radiology, American Stroke Association, Society of Cardiovascular Anesthesiologists, Society for Cardiovascular Angiography and Interventions, Society of Interventional Radiology, Society of Thoracic Surgeons, and Society for Vascular Medicine. Circulation 2010, 121, 266–369.
Table
Table 2. Anaesthetic and surgical strategies to prevent and treat spine cord ischemia.
Table 2. Anaesthetic and surgical strategies to prevent and treat spine cord ischemia.
Anaesthetic ApproachesSurgical Techniques
1-Maximize oxygen delivery (increase Cardiac Index > 2.5 L/min/m2 or optimize haemoglobin)1-Staging the procedure
2-Mild hypothermia (32–35 °C)2-Left subclavian artery revascularization
3-Maintain CSF pressure (≤10 mmHg)3-Minimally invasive segmental artery coil embolization (MISACE)
4-Maintain spinal cord perfusion pressure (≥80 mmHg)4-Temporary aneurysm sac perfusion (TASP)
5-Neuromonitoring (e.g., motor/sensory evoked potentials, NIRS)5-New implantation sequence for branched/fenestrated stents
6-Monitor CSF lactate
Table
Table 3. Indications for positioning CSF drainage in patient undergoing TEVAR 1.
Table 3. Indications for positioning CSF drainage in patient undergoing TEVAR 1.
Indications for the Use of CSF Drain in TEVAR
1. Anticipated endograft coverage of T8-L1 (especially intercostal/lumbar arteries that supply Adamkiewicz artery identified by preoperative CT/MRI angiography).
2. Coverage of a long segment of thoracic aorta (>30 cm).
3. Compromised collateral pathways (e.g., previous infrarenal aortic aneurysm repair, occluded hypogastric arteries, coverage of the left subclavian artery without revascularization).
4. Symptomatic spinal ischemia in a patient who did not have a drain placed preoperatively.
1 Adapted from [23] Uchida N. How to prevent spinal cord injury during endovascular repair of thoracic aortic disease. Gen Thorac Cardiovasc Surg 2014, 62, 391–397.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Marturano, F.; Nisi, F.; Giustiniano, E.; Benedetto, F.; Piccioni, F.; Ripani, U. Prevention of Spinal Cord Injury during Thoracoabdominal Aortic Aneurysms Repair: What the Anaesthesiologist Should Know. J. Pers. Med. 2022, 12, 1629. https://doi.org/10.3390/jpm12101629

AMA Style

Marturano F, Nisi F, Giustiniano E, Benedetto F, Piccioni F, Ripani U. Prevention of Spinal Cord Injury during Thoracoabdominal Aortic Aneurysms Repair: What the Anaesthesiologist Should Know. Journal of Personalized Medicine. 2022; 12(10):1629. https://doi.org/10.3390/jpm12101629

Chicago/Turabian Style

Marturano, Federico, Fulvio Nisi, Enrico Giustiniano, Francesco Benedetto, Federico Piccioni, and Umberto Ripani. 2022. "Prevention of Spinal Cord Injury during Thoracoabdominal Aortic Aneurysms Repair: What the Anaesthesiologist Should Know" Journal of Personalized Medicine 12, no. 10: 1629. https://doi.org/10.3390/jpm12101629

APA Style

Marturano, F., Nisi, F., Giustiniano, E., Benedetto, F., Piccioni, F., & Ripani, U. (2022). Prevention of Spinal Cord Injury during Thoracoabdominal Aortic Aneurysms Repair: What the Anaesthesiologist Should Know. Journal of Personalized Medicine, 12(10), 1629. https://doi.org/10.3390/jpm12101629

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop