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Eur J Cardiothorac Surg 1999;16:607-612
© 1999 Elsevier Science NL
Department of Cardiothoracic Surgery, St. Antonius Hospital, Koekoekslaan 1, NL-3435 CM Nieuwegein, The Netherlands
Corresponding author. Tel.: +31-30-609-2047; fax: +31-30-609-2120
e-mail: dossche{at}planet.nl
| Abstract |
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Key Words: Reoperations Ascending aorta Aortic root
| 1. Introduction |
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Degeneration of aortic valve substitutes, prosthetic valve endocarditis, vascular graft infection, true or false aneurysm formation are late complications that can cause substantial mortality and morbidity. All form indications for reoperation. In this report, we present our entire experience with reoperations on the ascending aorta and/or aortic root over a 24-year period.
| 2. Materials and methods |
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Cardiopulmonary bypass (CPB) was instituted routinely after resternotomy with an oscillating saw (43 patients, 77%). In these patients, the common femoral artery (30 patients) or the distal ascending aorta or aortic arch (13 patients) were used for arterial inflow, and the right atrium or femoral vein for venous return. In only ten patients, CPB was started before the sternotomy. Five patients were emergency procedures, in another five patients, there was close contact between the sternum and the aortic aneurysm. Under these circumstances, the common femoral artery was used for arterial inflow and the common femoral vein for venous return (long venous 31F or 33F cannula positioned in the right atrium). CPB was not discontinued in any of these patients after division of the sternum. In the entire series, there was no need for alternative arterial cannualtion sites. In three patients, there was no need for CPB as they had a small false aneurysm at an easily accessible localization. In all three patients, the leaking false aneurysm was temporarily occluded by percutaneous insertion of a balloon catheter into the mouth of the false aneurysm [10]. Cold, low sodium, normopotassic cardioplegia was used in 50 (90.0%) patients, in six other patients there was no need for cardioplegic arrest. Details of operative procedures are listed in Table 2. In 12 (21.5%) patients, deep hypothermic circulatory arrest (DHCA) with a mean duration of 18±7 min (range, 530 min) was required. Moderate hypothermic circulatory arrest and antegrade selective cerebral perfusion (ASCP) for brain protection was used in 13 (23.2%) patients with a mean duration of 56±14 min (range, 3988 min). New saphenous vein grafts were sutured to the innominate artery or to the new aortic graft. The mean duration of CPB (for 56 patients) was 192±72 min; mean myocardial ischemic time (for 50 patients) was 127±48 min. Aprotinin or other hemostatic agents were not used routinely.
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2 or two-tailed Fisher's exact test as appropriate. Patients who underwent more than one reoperation were only included once. End points examined were hospital mortality, late mortality, subsequent reoperation on the ascending aorta and/or aortic root and incidence of prosthetic endocarditis, graft infection, anticoagulant-related or thromboembolic complications. KaplanMeier survival curves were used for analysis of survival times, and log-rank test for comparisons between survival curves. The patient- and operation- related variables are listed in the appendix. A P-value of less than 0.05 was considered significant. All computations were performed with SPSS statistical software packages (SPSS 8.0 for Windows, SPSS Inc., Chicago, IL). | 3. Results |
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3.2. Hospital mortality
Hospital mortality was 5.4% (n=3; 70% CL: 2.48.4%). Two of these patients had active endocarditis (2/8, 25%), the third patient had healed endocarditis (1/48, 2.1%) (P=0.05). All had undergone replacement of the aortic root (two patients) or the ascending aorta (one patient) with aortic allograft tissue. Cause of death was low cardiac output in two patients and rupture of the aorta at the distal suture line in one patient. In the univariate analysis, two or more previous operations (P=0.038) and the interval between initial operation and reoperation for complication of less than 8 months (P=0.005) were risk factors for hospital death. Neither the type of previous operation, i.e. ARR vs. AAR (P=0.592), nor the type of the actual intervention i.e. AAR or ARR vs. repair of false aneurysm (P=0.565) had influence on overall hospital mortality. Multivariate analysis indicated operation for active endocarditis or vascular graft infection as an independent risk factor for hospital mortality (P=0.038, odds 14.6).
3.3. Hospital morbidity
Nine (16.0%; 70% CL: 10.721.3%) patients underwent early (<48 h) reoperation: three for excessive bleeding, five for removal of gauzes left in place for hemostatic purposes and one for cardiac arrest in the intensive care unit. Reintervention rate was not influenced by the type of procedure performed, i.e. AAR or ARR vs. repair of false aneurysm (P=0.16). Seven (12.5%; 70% CL: 8.116.9%) patients required mechanical ventilation for more than 5 days, four of them needed a tracheotomy. Five (9.0%; 70% CL: 5.212.8%) patients experienced renal insufficiency necessitating temporary hemodialysis. One of them died, four others recovered uneventfully. Other complications included myocardial damage in one patient, requiring prolonged postoperative inotropic support and a central neurologic deficit in one patient due to massive air embolism (proven by intraoperative transcranial doppler); he recovered completely. There were no total AV blocks reported caused by the redo procedures.
3.4. Late mortality and morbidity
Follow-up of the 53 hospital survivors was complete with a total of 201.2 patient-years. There have been nine late deaths (16.9%; 70% CL: 11.7-22.1%) during follow-up, which extends to 13.5 years (median follow-up 3.1 years). Three patients died of intracerebral hemorrhage, all were patients on anticoagulation for mechanical aortic valves. Two other patients died of rupture of a distant aneurysm, four patients died of unknown causes. Among the survivors, the 1-, 5- and 10-year survival rates for the entire group were 91.2±4.2%, 84.0±6.3% and 76.4±9.2% (Fig. 1). The survival rates did not differ significantly between patients having AAR or ARR and those having repair of a false aneurysm (log-rank P=0.69) (Fig. 2). Due to the small numbers, Cox regression analysis failed to recognize risk factors for late death.
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| 4. Discussion |
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A key element to successful reoperation on the ascending aorta or aortic root is a safe re-entry into the chest. In all operations on the aortic root or ascending aorta, we close the pericardium with or without the use of prosthetic material, if tolerated hemodynamically. We believe that a closed pericardium reduces the risk of damage to the right ventricle if a reoperation is required. A proper preparation and assessment of the risk of each step can decrease the incidence of severe problems. We advise a preoperative CT scan of the chest in every patient since this will allow the accurate delineation of the relation between the aorta, aneurysm or conduit and the bony structures of the chest wall. In five patients of our series, femorofemoral partial cardiopulmonary bypass was started before reopening the chest because of doubts about the safety of re-entry. Mostly, in case of laceration of major structures and important blood loss, the pump suckers can return the blood to the oxygenator, thus preventing severe hypotension. The indications for reoperation were different in patients operated on previously for acute type A dissection and patients operated on for degenerative aneurysm or annuloaortic ectasia. The incidence of reoperation for progressive aortic root dilatation and/or dilatation of the residual ascending aorta in patients who underwent surgery for acute type A dissection might be reduced by a more aggressive surgical approach at the first operation. All of the patients with aortic root dilatation had undergone resuspension of the commissures at the first operation, using Teflon felt or glutaraldehyderesorcine formaldehyde glue. This was probably not sufficient to prevent the sinuses of Valsalva from dilating during follow-up. With the newer type of aortic valve-sparing operations, where the sinuses are completely excised, this problem may be avoided in the future [5,6]. Concerning the dilatation of the residual ascending aorta, this may be due to a repair too limited at first operation or due to trauma of the dissected aorta at the clamping site. We now perform an open distal anastomosis in every patient, and cross-clamping of the dissected aorta is avoided. If a tear is found in the aortic arch, we do not hesitate to perform a hemiarch or total aortic arch replacement. In case of a time-consuming distal ascending aortic repair or involvement of the aortic arch, ASCP has been very useful. Advantages include cooling of the body to only 25°C and a longer safe period of brain protection as compared to DHCA. This gives the surgeon time for a more complete repair at the initial operation.
False aneurysm formation at the various suture lines with the original Bentall technique has been reported repeatedly [4,15]. The reported incidence varies from 7 to 25%, although the true incidence is probably higher [15,16]. The open technique seems to overcome the problem of false aneurysm formation, although in our series, two patients with the open technique required reintervention for false aneurysm formation at the left coronary ostial suture [4,17]. Although some continue to use the inclusion technique for hemostatic purposes, we think that the open technique is the technique of choice in every situation. As we have used the Cabrol II technique only in one patient, we can not make any conclusions on the long-term results with this technique.
The need for continued long-term cardiovascular surveillance is accentuated by the fact that eight patients needed a reintervention more than 10 years after AAR or ARR. The median interval of 51 months illustrates that patients remain at risk for later development of complications that require new repair, even if the first repair was a radical one. This warrants for annual examination by the cardiologist and/or cardiovascular surgeon including echocardiography, CT scan or MRI.
| Appendix A |
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A.1. Patient variables
Sex, male (n=40), female (n=16); age,
65 years (n=46), >65 years (n=10); Marfan's syndrome, yes (n=8), no (n=48); previous cardiac intervention, one (n=49), two (n=5), three (n=2); functional class, NYHA I or II (n=29), NYHA III or IV (n=27); aortic regurgitation (AR), no AR (n=28), AR grade IIV (n=28); serum creatinine (µmol/l),
150 µmol/l (n=52), >150 µmol/l (n=4); indication for operation, false aneurysm (n=25), true aneurysm (n=18), prosthetic valve endocarditis (n=5), vascular graft infection (n=3), failure of aortic valve substitute (n=4), other (n=1); interval between operations: <8 months (n=18),
8 months (n=38).
A.2. Operative variables
Timing, elective (n=51), urgent (n=5); pericardium (at previous operation), open (n=8), closed (n=48); CPB time (min),
180 (n=17), >180 (n=36), no CPB (n=3); myocardial ischemic time (min),
120 (n=22), >120 (n=28), no cardiac arrest (n=6); type of procedure, ARR (n=30), AAR (n=10), repair false aneurysm (n=14), aortic valve replacement (n=2); concomitant procedures, none (n=36), aortic arch replacement (n=14), CABG (n=2), aortic arch replacement and CABG (n=4); deep hypothermic circulatory arrest, yes (n=12), no (n=44); antegrade selective cerebral perfusion, yes (n=13), no (n=43).
| References |
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