|
|
||||||||
Ann Thorac Surg 2000;69:1288-1294
© 2000 The Society of Thoracic Surgeons
a Department of Cardiac Surgery, University of Milan, Milan, Italy
b Department of Cardiac Surgery, University of Parma, Parma, Italy
Address reprint requests to Dr Parolari, Department of Cardiac Surgery, University of Milan, Centro Cardiologico, Fondazione I Monzino IRCCS, Via Parea, 4, 20138, Milan, Italy
e-mail: aparolari{at}cardiologicomonzino.it
| Abstract |
|---|
|
|
|---|
| Introduction |
|---|
|
|
|---|
| Historical note |
|---|
|
|
|---|
The use of the RA as coronary graft was proposed again in 1992 by Acar and colleagues [9], after the casual finding that some of the grafts implanted in 1972 were still patent 15 years later. Encouraging early patency rates were obtained during this new era, and were ascribed to an improved harvesting technique, together with the use of calcium channel blockers or other vasodilators to prevent perioperative spasm of the graft [1012]. These reports led many other groups to reassess the role of this conduit in coronary bypass procedures.
| Anatomy, suitability for harvest, and pathology of the RA |
|---|
|
|
|---|
The proximal RA courses underneath the muscle belly of the brachioradialis muscle, and then progressively leaves the lower surface of the muscle, running beneath the antebrachial fascia, between the brachioradialis muscle and the flexor carpi radialis muscle or the flexor carpi radialis tendon. In this area, care has to be taken to spare the lateral antebrachial cutaneous nerve, a branch of muscolocutaneous nerve which lies over the belly of the brachioradial muscle, to avoid postoperative paresthesias to the radial aspect of the volar forearm [13].
The intermediate portion of the RA lies close to the superficial branch of the radial nerve, which lies under the brachioradialis muscle. This nerve must be spared in order to avoid postoperative paresthesias to the thumb and the dorsum of the hand [13]. Near the wrist, the RA becomes superficial, lying anterior to the radius and pronator quadratus muscle, between the tendons of the brachoradialis and the flexor carp radialis muscles.
From its more distal portion, the RA has many branches, which anastomose with similar branches of the ulnar artery, providing the vascularization of the hand: (1) the carpal palmar branch anastomoses with a similar branch of the ulnar artery [14]; (2) the superficial palmar branch, together with the main trunk of the ulnar artery, forms the superficial palmar arch, which gives four common digital palmar arteries that bifurcate in proper digital palmar arteries. This arch has a dominant ulnar supply and a small radial end that may be absent in some cases [14]; (3) the dorsal carpal branch, with a similar ulnar branch, forms the dorsal carpal arch, and from this arch, the dorsal metacarpal arteries that anastomose with the deep palmar arch and the corresponding palmar metacarpal arteries arise by perforating branches. Subsequently the dorsal metacarpal arteries bifurcate in the dorsal digital arteries [14]; and (4) the termination of the RA itself anastomoses with the deep palmar branch of the ulnar artery to form the deep palmar arch. This arch has a dominant radial supply, and is slightly more proximal than the superficial arch, lying just beyond the basis of the metacarpals. From its convexity arise the palmar metacarpal arteries that anastomose with the corresponding common digital palmar arteries (superficial arch), and with dorsal metacarpal arteries (dorsal carpal arch) [14].
The rich intercommunication among the branches of the deep, superficial, and dorsal carpal arches allows the vascularization of the hand, in case of RA harvest at the forearm. Various reports on surgical management of forearm vascular trauma suggest that one functional artery, distal to the elbow, is enough for limb viability and vascular function [15, 16].
In fact, the harvest of the RA, which usually begins proximally after the radial recurrent branch, and terminates distally before the origin of the superficial palmar branch, in order to preserve as much collateral circulation as possible [17], is rarely a cause of hand ischemia. This is because the numerous anastomoses between the superficial and deep palmar arches, and dorsal carpal arch, can supplement small or missing branches of the others.
Only the absence, hypoplasia, or atrophy of the ulnar artery, which are rare findings [14, 18], contraindicate RA harvest, even if in these cases, a persistent median or a common interosseous or anterior interosseous artery may supplement or replace the ulnar artery, and may originate the palmar superficial arch or the digital arteries.
It is however, mandatory to assess the adequacy of the ulnar collateral circulation to the hand, before RA harvest. The up-to-date methods employed, include the Allen test [19] and modifications [20, 21], static and dynamic Doppler testing [22], direct digit pressure measurement during RA compression [23], and oxymetric plethysmography, together with the computation of a perfusion index [24]. Concerns with the adequacy of forearm collateral circulation, raised by the preoperative testing method, have excluded RA harvest unilaterally in 5% [12] to 11.6% [20], and bilaterally in 5% [20] to 6.4% [24] of patients who are candidates for RA harvest.
In addition, sometimes the Allen test can be falsely normal, due to the presence of a high origin of the superficial palmar branch, or of an anomalous anterior interosseous artery. In these cases, it is cautious to perform an intraoperative Allen test, with the occlusion of these branches before ligating them [25].
Another anatomical feature, which must be considered when harvesting the RA, is that in about 15% of extremities, the RA may show a high origin, between the axilla and the elbow [18]. In these cases, RA course in the forearm can be more superficial, between the forearm muscles or in the subcutaneous tissue [14], and there is the chance of damage to the median nerve, which in case of origin of the RA directly from the axillary artery, can be immediately deep to the RA in the cubital fossa [18].
With regard to the anatomopathological features, the average RA length suitable for bypass varies between 18 and 22 cm, and its inner diameter varies between 2 and 3 mm [2628]. The RA is a thick-walled muscular artery. The intima has one layer of endothelial cells beneath, where multiple layers of subendothelial cells, and small amount of myocytes, are present. The internal elastica lamina has multiple fenestrations, and the media is constituted by many leiomyocytes, elastic and collagen fibers, fibroblasts, and rare macrophages. The external elastic lamina is less individualized than the internal lamina. Some evidence suggests that the vasa vasorum, nerves, and lymphatic vessels are confined to the adventitia, and do not join the medial layer within the structure of the adventitia [29], while others describe vasa vasorum penetration into RA media. This may theoretically cause some degree of hypoxia after the RA harvest [30].
With respect to the internal thoracic artery, the RA is a greater in size, has a thicker wall, and a higher density of muscle cells with the same amount of elastic tissue in its media [27]. Moreover, in the RA, the myocytes are organized in to multiple tight layers, while in the internal thoracic artery, the muscle cells are less organized and irregular in shape, and this, together with the wider thickness of the media, may at least in part explain the propensity of the RA to spasm [29].
Finally, it has been reported that the RA has a low prevalence of atherosclerosis [31]. However, comparative studies among arterial conduits used in myocardial revascularization have shown that the RA has a slightly higher degree of atherosclerosis than the internal thoracic artery, which also seems to be more resistant to the development of atherosclerosis, in the presence of vascular disease risk factors [29, 32, 33]. This slightly higher propensity of the RA to atherosclerosis usually does not impair RA flow, because of its relatively large diameter. Moreover, the RA is more subject to the chance of previous iatrogenous vascular trauma. The inability to use the RA because of severe calcification of this artery, or chronic dissection of the RA from prior cannulation, is a relatively rare event, occuring in only about 1% to 2% of candidates for RA harvest [34].
| Biology and spasm of the RA |
|---|
|
|
|---|
Early reports emphasized the high propensity of the RA to spasm [35], even though this phenomenon has also been reported in other arterial grafts, and the real incidence in the various conduits is still debated [36, 37]. Spasm has also been described in greater saphenous veins as well [38]. There are different hypotheses regarding the mechanisms underlying arterial graft and RA spasm, varying from endothelial trauma related to harvest [39], impaired vasomotor function due to coexistent systemic disease [39], and differing arterial graft endothelial function properties [40]. The advent of less traumatic RA harvesting techniques has significantly reduced the chance of endothelial trauma to this graft. It is commonly agreed upon that RA harvest must be performed with gentle mobilization of the RA, with light tractions, minimal touch, and minimal diathermy. Mechanical or hydrostatical dilation of the graft should be avoided, and the RA should only be flushed with a mixture of heparinized blood and papaverine [13, 24, 25].
The propensity of the RA to spasm has greatly been reduced using both topically and systemically different categories of vasodilators, including calcium channel blockers [9, 13, 41], papaverine [42], the phosphodiesterase inhibitor milrinone [25], and drug mixtures such as verapamil and nitroglycerin [43], or verapamil and papaverine [28]. Recent experimental evidence suggests that diltiazem and verapamil may have little effect in preventing both receptor-dependent and receptor-independent RA contractions, while organic nitrates and nifedipine seem to be more effective in inhibiting and reversing RA contractions [44]. Table 1 reports some of the intravenous antispasmodic drug administration protocols currently adopted.
|
Concern still exists however, for the theoretical possibility of RA spasm, and for that reason various studies have focused on the biological properties of this conduit in order to investigate the basis of this phenomenon.
It has been shown that the endothelial function of the RA, as it releases endothelium-derived relaxing factors in response to endogenous and exogenous agents, is similar to that of other arteries. Significant basal and stimulated nitric oxide release have been reported in vivo [45], as well as maximal relaxation of the RA after acetylcholine administration [46]. Some comparative studies have shown that both endothelium-dependent and endothelium-independent vasorelaxation were similar to that of the internal thoracic artery [47], and that sensitivity to vasoconstricting agents like norepinephrine and serotonin was also similar [36].
On the other hand, it has been shown that, despite similar endothelial function, the RA can develop significantly higher maximal contractile force to vasoconstricting agents such as norepinephrine, serotonin, endothelin-I, and angiotensin II [36, 47], or to depolarizing agents such as potassium, with respect to the internal thoracic artery. This can be explained by the more muscular nature of this graft, which has a considerably thicker media, with respect to internal thoracic, gastroepiploic, and epigastric arteries, which are the usual conduits for arterial myocardial revascularization [29].
From the aforementioned data, it is suggested that the differences between the RA and internal thoracic artery are mainly related to histological features, and in particular, to the muscle cell population of the media and intima. This may affect the contractile properties of the graft, while the endothelial function seems to be very similar to that of the internal thoracic artery, and could be the basis for a more than satisfactory long-term patency. Because of these features, modulation of the RA graft with antispasmodic drugs of the RA graft contractile properties seems to be mandatory, especially in the early perioperative period, in order to avoid perioperative spasm, and possible failure of the graft.
| Review of recent clinical experience concerning the use of the RA as a bypass graft |
|---|
|
|
|---|
Operative strategies
The current indication in the use of the RA as a coronary graft is to supplement the internal thoracic artery in achieving complete arterial coronary revascularization [24], and, for that reason, the usual targets for this conduit are the right and circumflex arteries, and their branches (Table 2). Less frequently, the RA is used to revascularize some diagonal branches or the ramus intermedius. Finally, only when the mammary arteries are not suitable, the RA is anastomosed to the left anterior descending coronary artery [3, 4, 24, 34].
|
Sometimes a RA of adequate length can be divided into two segments, in order to obtain two separate grafts [9, 20, 24], or it can be used to perform multiple distal anastomoses in a sequential fashion [11, 50].
There is still some debate on how to locate the proximal anastomosis of the RA, even if, in most cases, the majority of the groups prefer to anastomose the RA to the ascending aorta [9, 11, 34, 42, 52]. There is a consistent group of surgeons who suggest that the optimal method for proximal anastomosis is to perform a composite arterial graft with the RA coming off the left internal thoracic artery [12, 17, 50, 53, 54]. However, as reported patency rates are similar in both cases, it is suggested that performing proximal anastomosis on the ascending aorta should be the preferred method, because it is less technically demanding with respect to composite arterial grafting. In some selected cases, the RA can also be proximally anastomosed to a saphenous vein graft [12, 28, 53, 54], to the right internal thoracic artery [12, 17, 53, 54], to another radial artery graft [34], to the innominate artery [52], or to another coronary artery, as a coronary to coronary bypass graft [58, 59].
| Early results |
|---|
|
|
|---|
|
|
Complications related to RA harvest are usually very low, and postoperative acute hand ischemia after RA harvest is a rare event whichever method is used for the assessment of collateral circulation. In fact, most of the previous reports could not document a postoperative case of hand ischemia, and only 1 case of acute hand ischemia, due to congenital absence of the ulnar artery, has been described after harvest of the RA [60], to our knowledge.
In this surgical series, no cases of compartment syndrome were reported, and only 1 case of upper limb motor loss, due to surgical lesion of a forearm peripheral nerve, was reported [34]. The incidence of dysesthesias of the forearm and the hand, the most frequent upper limb complications, was under 10% [11, 17, 24, 48, 52] and, in most cases, these sensitive symptoms disappeared completely within days or weeks. The occurrence of forearm surgical wound infection was a rare event [42], as well as the development of forearm hematoma, which happened in less than 4% of patients [34, 42, 48, 50].
| Follow-up studies |
|---|
|
|
|---|
|
| Comment |
|---|
|
|
|---|
The collateral flow to the hand which is almost constantly furnished by the ulnar artery through the palmar arches, and the low incidence of atherosclerosis on the native vessel, support RA grafting within a large spectrum of age. Correct preoperative assessment of the adequacy of the ulnar collateral circulation is critical in avoiding ischemic complications to the forearm and the hand.
The use of the RA can help to expand complete arterial myocardial revascularizations, and moreover, its morphometric features allow it to reach virtually any coronary artery, to perform multiple distal anastomoses in sequential fashion, and sometimes to obtain two separate grafts by dividing one RA of adequate length. It has also been shown that it is possible to construct composite arterial conduits by proximally anastomosing the RA to the internal thoracic arteries.
The recent evidence regarding 5-years patency rates, supports the use of the RA as the second arterial graft, after the internal thoracic arteries, and we can expect that in future years further data will add strength to the use of the RA graft.
| Acknowledgments |
|---|
| References |
|---|
|
|
|---|
This article has been cited by other articles:
![]() |
D. G. Nezic, A. M. Knezevic, P. S. Milojevic, B. P. Dukanovic, M. D. Jovic, M. D. Borzanovic, and A. N. Neskovic The fate of the radial artery conduit in coronary artery bypass grafting surgery. Eur. J. Cardiothorac. Surg., August 1, 2006; 30(2): 341 - 346. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Reyes, A. Traba, L. Lopez, A. Pinto, J. Duarte, and J. L. Vallejo Neurological damage after radial artery harvesting in coronary surgery: a direct measure Interactive CardioVascular and Thoracic Surgery, August 1, 2006; 5(4): 433 - 438. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Agrifoglio, L. Dainese, S. Pasotti, A. Galanti, A. Cannata, M. Roberto, A. Parolari, and P. Biglioli Preoperative Assessment of the Radial Artery for Coronary Artery Bypass Grafting: Is the Clinical Allen Test Adequate? Ann. Thorac. Surg., February 1, 2005; 79(2): 570 - 572. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. D. Desai, E. A. Cohen, C. D. Naylor, S. E. Fremes, and the Radial Artery Patency Study Investigators A Randomized Comparison of Radial-Artery and Saphenous-Vein Coronary Bypass Grafts N. Engl. J. Med., November 25, 2004; 351(22): 2302 - 2309. [Abstract] [Full Text] [PDF] |
||||
![]() |
F.P. Casselman, M. La Meir, G. Cammu, F. Wellens, R. De Geest, I. Degrieck, F. Van Praet, Y. Vermeulen, and H. Vanermen Initial experience with an endoscopic radial artery harvesting technique J. Thorac. Cardiovasc. Surg., September 1, 2004; 128(3): 463 - 466. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Verma, P. E. Szmitko, R. D. Weisel, D. Bonneau, D. Latter, L. Errett, Y. LeClerc, and S. E. Fremes Should Radial Arteries Be Used Routinely for Coronary Artery Bypass Grafting? Circulation, August 3, 2004; 110(5): e40 - e46. [Full Text] [PDF] |
||||
![]() |
H. Kamiya, G. Watanabe, H. Takemura, S. Tomita, H. Nagamine, and T. Kanamori Total arterial revascularization with composite skeletonized gastroepiploic artery graft in off-pump coronary artery bypass grafting J. Thorac. Cardiovasc. Surg., April 1, 2004; 127(4): 1151 - 1157. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Tatoulis, B. F. Buxton, and J. A. Fuller Patencies of 2,127 arterial to coronary conduits over 15 years Ann. Thorac. Surg., January 1, 2004; 77(1): 93 - 101. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Kamiya, T. Ushijima, T. Kanamori, C. Ikeda, C. Nakagaki, K. Ueyama, and G. Watanabe Use of the radial artery graft after transradial catheterization: is it suitable as a bypass conduit? Ann. Thorac. Surg., November 1, 2003; 76(5): 1505 - 1509. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Caputo, B. Reeves, G. Marchetto, B. Mahesh, K. Lim, and G. D. Angelini Radial versus right internal thoracic artery as a second arterial conduit for coronary surgery: early and midterm outcomes J. Thorac. Cardiovasc. Surg., July 1, 2003; 126(1): 39 - 47. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Wakeyama, H. Ogawa, H. Iida, A. Takaki, T. Iwami, M. Mochizuki, and T. Tanaka Intima-media thickening of the radial artery after transradial intervention: An intravascular ultrasound study J. Am. Coll. Cardiol., April 2, 2003; 41(7): 1109 - 1114. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. V. Riekkinen, K. O. Karkola, and A. Kankainen The radial artery is larger than the ulnar Ann. Thorac. Surg., March 1, 2003; 75(3): 882 - 884. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. E. Drossos, I. K. Toumpoulis, D. G. Katritsis, J. P. A. Ioannidis, P. Kontogiorgi, E. Svarna, and C. E. Anagnostopoulos Is vitamin C superior to diltiazem for radial artery vasodilation in patients awaiting coronary artery bypass grafting? J. Thorac. Cardiovasc. Surg., February 1, 2003; 125(2): 330 - 335. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Beghi, F. Nicolini, A. M. Budillon, B. Borrello, L. Ballore, C. Reverberi, and T. Gherli Midterm Clinical Results in Myocardial Revascularization Using the Radial Artery Chest, December 1, 2002; 122(6): 2075 - 2079. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Amano, A. Takahashi, and H. Hirose Skeletonized radial artery grafting: improved angiographic results Ann. Thorac. Surg., June 1, 2002; 73(6): 1880 - 1887. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. L. Quigley, S. J. Weiss, R. Y. Highbloom, and J. Pym Creative arterial bypass grafting can be performed on the beating heart Ann. Thorac. Surg., September 1, 2001; 72(3): 793 - 797. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Amano, H. Hirose, A. Takahashi, and N. Nagano Coronary artery bypass grafting using the radial artery: midterm results in a Japanese institute Ann. Thorac. Surg., July 1, 2001; 72(1): 120 - 125. [Abstract] [Full Text] [PDF] |
||||
![]() |
|