| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
|
|
|
|||||||
|
|||||||||
J Thorac Cardiovasc Surg 1997;114:261-269
© 1997 Mosby, Inc.
CARDIOPULMONARY BYPASS, |
Presented at the Sixty-ninth Scientific Sessions of the American Heart Association, New Orleans, La., Nov. 13, 1996.
Received for publication Oct. 21, 1996 Revisions requested Nov. 26, 1996; revisions received Jan. 11, 1997 Accepted for publication Feb. 21, 1997. Address for reprints: Nobuhiko Hayashida, MD, The Second Department of Surgery, Kurume University Hospital, 67 Asahi-machi, Kurume, Fukuoka, 830 Japan.
Abstract
Objective: To evaluate the effects of minimal-dose aprotinin in patients undergoing coronary artery bypass grafting, we conducted a prospective randomized study. Methods: A total of 167 patients were randomized to receive no aprotinin treatment (control, n = 57), minimal-dose aprotinin (1.0 x 106 KIU; n = 55), or low-dose aprotinin (2.7 ± 0.5 x 106 KIU; n = 55). Blood loss and transfusion requirements, parameters of clotting and fibrinolysis, renal function, and early graft patency rates were assessed. Results: Postoperative blood loss and transfusion requirements were significantly (p = 0.01) lower in both the minimal-dose and low-dose groups than in the control group. The increase in D-dimer level after cardiopulmonary bypass was significantly (p < 0.05) less marked in the low-dose group than in the control group. The 
2-plasmin inhibitor and plasminogen activator inhibitor–1 levels were significantly (p < 0.05) greater in the minimal-dose and low-dose groups than in the control group after bypass, suggesting the prevention of fibrinolysis by both aprotinin doses. No statistically significant differences in postoperative renal function and early vein graft patency rates were noted (control group, 93.8%; minimal-dose group, 98.5%; low-dose group, 92.3%; p = 0.25). Conclusions: Aprotinin was not associated with a significant increase in the prevalence of renal dysfunction or early vein graft occlusion. Minimal-dose aprotinin inhibited enhanced fibrinolytic activity and reduced blood loss and transfusion requirements after bypass equivalently to low-dose aprotinin. The dose of 1 x 106 KIU added to the pump prime may be acceptably effective in reducing blood loss in patients undergoing primary coronary operations. J Thorac Cardiovasc Surg 1997;114:261-9
Aprotinin has been reported to decrease postoperative blood loss and transfusion requirements in patients undergoing cardiac operations.
1-4 The mechanisms of action of aprotinin in reducing blood loss are still controversial, although the drug has been shown to preserve platelet membrane receptor glycoprotein Ib, 5 to inhibit the intrinsic clotting system, 6 and to prevent fibrinolysis. 3-5,7,8 Although aprotinin markedly improved hemostasis, concerns about the side effects of high-dose aprotinin such as early vein graft thrombosis and renal dysfunction have been raised. 9-11 The possibility exists, therefore, that any reduced dose with hemostatic efficacy comparable with that of high-dose aprotinin could reduce the prevalence of the adverse side effects. Recently, half of the standard high dose of aprotinin reported by Royston and associates 1 was reported to be effective. 7,8 However, an acceptable minimal-dose regimen that would provide the best risk/benefit balance has not yet been suggested.
The purpose of this study was to evaluate the effects of minimal-dose (1 x 106 KIU) aprotinin on blood loss and transfusion requirements, clotting and fibrinolysis, renal function, and early graft patency in patients undergoing coronary artery bypass grafting (CABG).
Methods
Patient population, aprotinin administration, and surgical techniques
A prospective randomized study was performed on 167 patients undergoing primary isolated CABG by one surgeon (T.I.). Seventy-eight patients were receiving aspirin or a nonsteroidal antiinflammatory drug before the operation. Administration of these platelet-active drugs was discontinued at least 10 days before the operation in all patients. The patients were randomized into three groups according to the dose of aprotinin (1.4 mg of aprotinin, or 10,000 kallikrein inactivator units per milliliter; Bayer Yakuhin Ltd., Osaka, Japan) by means of a computer-generated randomization table. The control group received no aprotinin treatment (n = 57); the minimal-dose group received 1 x 106KIU aprotinin only in the cardiopulmonary bypass (CPB) priming solution (n = 55); and the low-dose group received 3 x 104 KIU/kg aprotinin in the priming solution and continuous infusion of aprotinin at a rate of 0.75 x 104 KIU/kg every hour during CPB 7 (n = 55). The mean dose of aprotinin in the low-dose group was 2.7 ± 0.1 x 106 KIU (range 1.4 x 106 to 4.0 x 106 KIU). So that the investigators would remain blinded to the protocol, only the perfusionists were informed regarding the administration of the regimen; surgeons and others participating in patient care were not. Before CPB was initiated, heparin sodium was administered at an initial dose of 300 IU/kg. Additional heparin was administered if the celite-activated clotting time (Hemochron 401, International Technidyne Corporation, Edison, N.J.) became less than 400 seconds. CPB was constructed with single two-staged right atrial cannulation and ascending aortic cannulation. The systemic temperature was allowed to drift to 33° ± 1° C and perfusion flow during CPB was maintained at 2.5 to 2.6 L/min. Blood cardioplegic solution at 30° ± 1° C was delivered through the aortic root and completed vein grafts in an intermittent antegrade fashion. All patients signed a consent form approved by the Human Experimental Committee of Kurume University Hospital.
Postoperative blood loss and transfusion requirements
Before closure of the sternotomy, chest tubes were inserted and the volume of blood loss drained from the tubes was measured 3, 6, 12, and 24 hours after CPB. The use of homologous blood products was carefully controlled according to the hemoglobin level, which was measured at regular intervals. Red blood cells or whole blood was administered only if the hemoglobin level fell below 8.0 gm/dl. 12 The volume (milliliters) and number of units of all blood products including packed red cells, whole blood, platelets, fresh frozen plasma, and cryoprecipitate administered to each patient in the first 24 hours after CPB were recorded.
Blood samples
Blood samples were taken before administration of heparin, 15 minutes after protamine administration, and 12 hours after cessation of CPB. Blood samples were drawn in precooled tubes containing 1.8 ml of 0.13 mol/L trisodium citrate (SRL, Tokyo, Japan). The samples were centrifuged within 30 minutes at 2000g at 4° C. An aliquot of the plasma was snap frozen and stored at –80° C until analysis.
Laboratory assessments
Chromogenic peptide substrates and test specifications from Kabivitrum AB, Stockholm, Sweden, were used for the following functional assays, with reference ranges in parentheses: antithrombin III (S-2238, 80% to 130%) and 2-plasmin inhibitor (S-2251, 80% to 130%). 13,14 Antithrombin III and 2-plasmin inhibitor were measured with a Hitachi model 101 spectrophotometer (Hitachi Medical Corp., Tokyo, Japan). Plasma fibrinogen was measured with the Clauss method. 15 The international standard 89/644 NIBSC (National Institute for Biological Standards and Control) was used for calibration. Thrombin-antithrombin III complexes were determined by an enzyme immunoassay, and plasminogen activator inhibitor-1 levels were determined by an enzyme-linked immunosorbent assay purchased from Behringwerke AG, Marburg, Germany. 16,17 D-dimer plasma concentrations were determined by the enzyme-linked immunosorbent assay purchased from Boehringer Mannheim GmbH, Mannheim, Germany. 18
Renal function
Blood and urine specimens for the measurements of renal function were obtained before the operation and 12 and 36 hours after CPB. The urinary output after CPB was recorded. Creatinine, osmolar, and free water clearances were calculated by standard formulas. Fractional sodium excretion (%NaExc) and fractional potassium excretion (%KExc) in percent were calculated as follows:
%NaExc = ([Nau/Nap])/[Cru/Crp]) x 100
%KExc = ([Ku/Kp]/[Cru/Crp]) x 100
where Nau is the concentration of urinary sodium, Nap is the concentration of serum sodium, Cru is the concentration of urinary creatinine, Crp is the concentration of serum creatinine, Ku is the concentration of urinary potassium, and Kp is the concentration of serum potassium.
Graft patency assessment
Graft angiography was performed on 120 patients (control group, n = 38; minimal-dose group, n = 41; low-dose group, n = 41) 7 to 47 days after the operation (median 25 days). Forty-seven of 167 patients enrolled in this study were excluded from the postoperative angiographic study because of the following reasons: patient refusal (n = 28: control group, n = 9; minimal-dose group, n = 11; low-dose group, n = 8), technical difficulty for either vein or arterial graft access (n = 12: control group, n = 5; minimal-dose group, n = 3; low-dose group, n = 4), patient illness (n = 4: control group, n = 3; low-dose group, n = 1), and patient death (n = 3: control group, n = 2; low-dose group, n = 1). Selective injection of contrast material in all vein, internal thoracic artery, or right gastroepiploic artery grafts was carried out. A graft and a distal anastomosis were defined as patent if contrast material was seen to flow through the graft into the distal native coronary artery.
Statistical analysis
The sample size calculation was based on estimates of blood loss determined in patients undergoing primary CABG at Kurume university Hospital. The calculations indicated that it would be possible to show a difference greater than or equal to 1.2 standard deviations with a power of 90% and a significance level of 5% if 55 patients were evaluated at each treatment group. All results were expressed as mean ± standard error of the mean for continuous variables. Categoric values were analyzed by means of the 
2 test. The Kruskal-Wallis test was used to evaluate the differences of blood loss and transfusion requirements among the groups. Where the overall test indicated significant between-group differences, pairwise comparisons among the three treatment groups were made. Because of the increased risk of type I error caused by multiple comparisons, a p value less than 0.01 was considered significant for these pairwise comparisons. A two-way repeated-measures analysis of variance was used to test the effect of study groups and sampling time points on parameters of clotting and fibrinolysis and on renal function. When the two-way repeated-measures analysis of variance indicated a significant effect of group or time (p < 0.05), the differences were specified with one-way analysis of variance and Duncan's multiple range test. A p value less than 0.05 was considered significant.
Results
Clinical and operative data of the three patient groups are shown in Table I. No significant differences were noted in age, sex, body surface area, ejection fraction, New York Heart Association functional class, autologous blood volume donated before the operation, preoperative aspirin use, crossclamp time, CPB time, number of distal anastomoses, and number of arterial grafts.
|
Table II). Postoperative blood loss and transfusions of packed red cells and all blood products during the first 24 hours after CPB were significantly (p = 0.001) lower in minimal-dose and low-dose groups than in the control group (Table III). The numbers of patients who required transfusion of any donor blood products were 46 (80.7%) in the control group, 31 (56.4%) in the minimal-dose group, and 35 (63.6%) in the low-dose group (p = 0.02). No statistically significant differences in postoperative blood loss and transfusion requirements were seen between patients in the minimal-dose and low-dose groups.
|
|
2–plasmin inhibitor was significantly (p < 0.05) decreased after CPB in the control group, whereas it increased significantly (p < 0.05) after CPB in the minimal-dose and low-dose groups. The 2-plasmin inhibitor level after CPB was significantly greater in the minimal- and low-dose groups than in the control group (p < 0.05). A marked increase (p < 0.05) in D-dimer levels was found in the control group after CPB, and the increase persisted until 12 hours after CPB. In contrast, D-dimer levels remained essentially constant in the low-dose group. The D-dimer level was significantly greater in the control group than in the low-dose group immediately after CPB and 12 hours after CPB.
|
|
Table IV). Fractional sodium and potassium excretions also increased after the operation in all groups; however, no statistically significant differences were found among the groups at any time.
|
Table V).
|
Discussion
Many studies have examined the hemostatic efficacy of aprotinin and have demonstrated significant reductions in postoperative blood loss and transfusion requirements in patients undergoing cardiac operations. 1-10 The efficacy of aprotinin as a hemostatic agent is unquestionable, but concerns about the side effects of aprotinin have been raised. A higher prevalence of postoperative renal dysfunction and early vein graft occlusion has been reported in patients receiving high-dose aprotinin. 9-11 In previous reports, high-dose aprotinin has been shown to cause a transient decrease in tubular sodium reabsorption. 19,20 It has been suggested that these side effects of aprotinin may be dose dependent. 21 In recent studies comparing low-dose aprotinin with placebo, low-dose aprotinin has been shown to prevent enhanced fibrinolysis and reduce postoperative blood loss. 7,8 Furthermore, low-dose aprotinin was reported to be as effective as high-dose aprotinin in preserving glycoprotein Ib receptors and reducing blood loss. 5 It seems reasonable, therefore, that the dose might be minimized to reduce the prevalence of side effects and the costs. However, minimal-dose aprotinin with hemostatic efficacy comparable with that of high-dose aprotinin and without any side effects has not yet been recommended.
Hemostatic efficacy
Covino and colleagues 22 reported that low-dose aprotinin (1 x 106 KIU in the priming solution and 0.5 x 106 KIU/hr during the operation) was effective in reducing blood loss and transfusion requirements, but quarter-dose aprotinin (0.5 x 106 KIU in the pump prime and 0.25 x 106 KIU/hr during the operation) was not. Van Oeveren and colleagues 5 reported that low-dose aprotinin (2 x 106 KIU aprotinin only in the pump prime) preserved glycoprotein Ib receptor and reduced blood loss and transfusion requirements similarly to high-dose aprotinin (bolus infusion of 2 x 106 KIU aprotinin during induction of anesthesia followed by a continuous infusion of 0.5 x 106 KIU/hr and additional bolus of 2 x 106 KIU aprotinin in the pump prime). They concluded that the protection of the platelet adhesive capacity through the platelet glycoprotein Ib receptor was obtained when aprotinin was present in sufficient amounts (2 x 106 KIU in the pump prime) at the first pass of blood through a circuit containing a membrane oxygenator. In the present study, the minimal-dose aprotinin regimen reduced the postoperative blood loss and transfusion requirements similarly to the low-dose regimen. Therefore, the dose of 1 x 106 KIU added only in the pump prime may be the acceptable minimum dose for the reduction of postoperative blood loss, whereas the dose of 0.5 x 106 KIU may be insufficient to be effective.
In previous reports, high-dose aprotinin has been shown to inhibit enhanced fibrinolytic activity during CPB and reduce postoperative blood loss. 3,19 Recently, low-dose aprotinin was also reported to have an inhibitory effect on enhanced fibrinolytic activity by increasing 2-antiplasmin and by decreasing fibrin(ogen) degradation products. 7,8 In the present study, we also found that low-dose aprotinin increased 2-plasmin inhibitor, plasminogen activator inhibitor-1, and decreased D-dimer levels during CPB compared with levels found in the control group. Although minimal-dose aprotinin did not decrease D-dimer levels after CPB as the low-dose aprotinin did, it significantly increased the levels of the 2-plasmin inhibitor and the plasminogen activator inhibitor-1 compared with those of the control group. These results suggest that minimal-dose aprotinin also has an inhibitory effect on enhanced fibrinolytic activity after CPB, which is sufficient for the preservation of hemostatic efficacy. Our study also demonstrated that the marked reduction of antithrombin III and fibrinogen and the increase of the thrombin-antithrombin III complexes after CPB in both aprotinin groups were comparable with those in the control group. The results were similar to previous reports that describe the hemostatic mechanism of aprotinin. 3,7,8 The similar changes between the control group and the aprotinin groups in regard to those clotting parameters suggest few additional inhibitory effects on the activation of the clotting system by the doses used in this study. However, aprotinin has been reported to prolong the activated clotting time synergetically through the intrinsic clotting pathway by inhibiting kallikrein in a dose-related manner. 6,23 Therefore high-dose aprotinin may have an inhibitory effect on the activation of the intrinsic clotting system, whereas lower doses may not. Thus there is a risk of underheparinization if the activated clotting time is used as a monitor of adequacy of heparinization when aprotinin is present. As suggested in a previous study, 24 the activated clotting time of greater than 400 seconds used in this study may have been inadequate in patients receiving aprotinin.
Renal function
Blauhut and colleagues 19 reported the increase of fractional sodium excretion during late intraoperative and early postoperative stages, which might reflect incipient renal tubular failure. However, they also found that renal function was unremarkable 24 hours after the operation. In the present study, fractional sodium excretion was slightly (p = 0.08) greater in aprotinin-treated patients during the first 12 hours after CPB. The result, as other investigators suggested, 19,20 might reflect a transient reduction of sodium reabsorption caused by renal tubular insufficiency. However, fractional sodium excretions in all groups became virtually identical (p = 0.87) by 36 hours after CPB. Furthermore, creatinine, osmolar, and free water clearances were above normal during the early postoperative period in all groups, and no significant differences were detected among the groups. The results suggested that aprotinin use was not associated with a significant increase in the prevalence of renal dysfunction. Sundt and colleagues 10 reported that aprotinin was associated with an increased risk of renal dysfunction in patients undergoing procedures on the thoracic or thoracoabdominal aorta in which hypothermic circulatory arrest was used. Other investigators suggested that adverse effects on renal function could be temperature dependent. 21 Because the systemic temperature in our patients was not cooled below 30° C (mean systemic temperature, 33° ± 1° C), the effect of aprotinin use on renal function was not investigated under hypothermic conditions. Therefore further investigations regarding the effect of aprotinin on renal function should be performed in patients undergoing hypothermic CPB and in patients with preexisting renal impairment.
Graft patency
Cosgrove and colleagues 9 have shown a trend toward an increased incidence of myocardial infarction in aprotinin-treated patients. Postmortem findings in their study demonstrated acute vein occlusions and widespread thrombosis in the kidney, native coronary vessels, and cerebral vessels in isolated patients. The early formation of thrombi on pulmonary artery catheters in patients receiving high-dose aprotinin has also been reported. 25,26 Because of these reports, concerns of early vein graft occlusion in patients undergoing CABG have been raised. 11 In contrast, several investigators have demonstrated that aprotinin did not influence early vein graft patency. 27-29 A multicenter study also has demonstrated that aprotinin was not associated with an increased risk of myocardial infarction in patients undergoing repeated CABG. 30 Using coronary arteriography in 120 patients, we also demonstrated that neither minimal-dose nor low-dose aprotinin contributed to the early vein graft occlusion and the prevalence of perioperative myocardial infarction. The results of our study and previous studies 27-30 suggest that aprotinin has no adverse effect on early vein graft patency. However, inasmuch as 47 of 167 patients (28%) were excluded from the postoperative angiographic study, patient selection might have been biased. Moreover, because the number of patients involved in the study was relatively small to detect a difference in low-incidence events such as graft occlusion or renal dysfunction, the potential for a type II statistical error exists. Therefore further investigations involving more patients are required to assert the conclusions regarding the incidence of complications in association with aprotinin.
So that the adverse side effects of systemic aprotinin can be avoided, effects of topical application of low-dose aprotinin into the pericardial cavity have been investigated. 31-33 The technique has been reported to reduce postoperative blood loss and transfusion requirements without significant side effects. 31-33 The technique therefore may provide a potential to amplify the hemostatic efficacy and consequently minimize the systemic use of the regimen. However, because the mechanism of topical aprotinin action is still unclear, further investigations are required for its routine use.
In summary, neither minimal-dose nor low-dose aprotinin was associated with a significant increase in the prevalence of renal dysfunction and early vein graft occlusion. Inhibition of fibrinolysis and significant reductions of blood loss and transfusion requirements were demonstrated in patients receiving minimal-dose aprotinin, as well as in patients receiving low-dose aprotinin. The results suggested that the dose of 1 x 106 KIU added to the pump prime was acceptably effective in reducing blood loss for primary CABG without significant side effects. Minimal-dose aprotinin may provide the optimal risk/benefit balance.
Footnotes
Copyright © 1997 by Mosby–Year Book, Inc. 
References
This article has been cited by other articles:
|
|
 |
|
  X. Wang, Z. Zheng, H. Ao, S. Zhang, Y. Wang, H. Zhang, L. Li, and S. Hu A comparison before and after aprotinin was suspended in cardiac surgery: Different results in the real world from a single cardiac center in China J. Thorac. Cardiovasc. Surg., October 1, 2009; 138(4): 897 - 903. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 J. R. Brown, N. J.O. Birkmeyer, and G. T. O'Connor Meta-Analysis Comparing the Effectiveness and Adverse Outcomes of Antifibrinolytic Agents in Cardiac Surgery Circulation, June 5, 2007; 115(22): 2801 - 2813. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 The Society of Thoracic Surgeons Blood Conservatio, V. A. Ferraris, S. P. Ferraris, S. P. Saha, E. A. Hessel II, C. K. Haan, B. D. Royston, C. R. Bridges, R. S.D. Higgins, G. Despotis, et al. Perioperative Blood Transfusion and Blood Conservation in Cardiac Surgery: The Society of Thoracic Surgeons and The Society of Cardiovascular Anesthesiologists Clinical Practice Guideline Ann. Thorac. Surg., May 1, 2007; 83(5_Supplement): S27 - S86. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 S. W Sutton, M. A Duncan, V. A Chase, R. J Marcel, T. P Meyers, and R. E Wood Cardiopulmonary bypass and mitral valve replacement during pregnancy Perfusion, December 1, 2005; 20(6): 359 - 368. [Abstract] [PDF]
|
|
|
|
 |
|
 D. Fergusson, K. C. Glass, B. Hutton, and S. Shapiro Randomized controlled trials of aprotinin in cardiac surgery: could clinical equipoise have stopped the bleeding? Clinical Trials, June 1, 2005; 2(3): 218 - 232. [Abstract] [PDF]
|
|
|
|
 |
|
 A. M. Mahdy and N. R. Webster Perioperative systemic haemostatic agents Br. J. Anaesth., December 1, 2004; 93(6): 842 - 858. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
A. Sedrakyan, T. Treasure, and J. A. Elefteriades Effect of aprotinin on clinical outcomes in coronary artery bypass graft surgery: A systematic review and meta-analysis of randomized clinical trials J. Thorac. Cardiovasc. Surg., September 1, 2004; 128(3): 442 - 448. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
Y. Kaminishi, Y. Hiramatsu, Y. Watanabe, Y. Yoshimura, and Y. Sakakibara Effects of nafamostat mesilate and minimal-dose aprotinin on blood-foreign surface interactions in cardiopulmonary bypass Ann. Thorac. Surg., February 1, 2004; 77(2): 644 - 650. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 J. M. Karski and J. T. Balatbat Blood Conservation Strategies in Cardiac Surgery Seminars in Cardiothoracic and Vascular Anesthesia, June 1, 2003; 7(2): 175 - 188. [Abstract] [PDF]
|
|
|
|
|
|
L. Englberger, B. Kipfer, P. A. Berdat, U. E. Nydegger, and T. P. Carrel Aprotinin in coronary operation with cardiopulmonary bypass: does "low-dose" aprotinin inhibit the inflammatory response? Ann. Thorac. Surg., June 1, 2002; 73(6): 1897 - 1904. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
R. C. Landis, G. Asimakopoulos, M. Poullis, D. O. Haskard, and K. M. Taylor The antithrombotic and antiinflammatory mechanisms of action of aprotinin Ann. Thorac. Surg., December 1, 2001; 72(6): 2169 - 2175. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
R. C. Landis, D. O. Haskard, and K. M. Taylor New antiinflammatory and platelet-preserving effects of aprotinin Ann. Thorac. Surg., November 1, 2001; 72(5): S1808 - 1813. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
R. J. Dignan, D. W. Law, P. W. Seah, C. W. Manganas, D. C. Newman, P. W. Grant, and H. D. Wolfenden Ultra-low dose aprotinin decreases transfusion requirements and is cost effective in coronary operations Ann. Thorac. Surg., January 1, 2001; 71(1): 158 - 164. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
F. Forestier, S. Belisle, D. Robitaille, R. Martineau, L. P. Perrault, and J.-F. Hardy Low-dose aprotinin is ineffective to treat excessive bleeding after cardiopulmonary bypass Ann. Thorac. Surg., February 1, 2000; 69(2): 452 - 456. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
N. Hayashida, H. Tomoeda, T. Oda, E. Tayama, S. Chihara, T. Kawara, and S. Aoyagi Inhibitory effect of milrinone on cytokine production after cardiopulmonary bypass Ann. Thorac. Surg., November 1, 1999; 68(5): 1661 - 1667. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 V. Mooser, F. Tinguely, P. Fontana, V. Lenain, M. Vaglio, P. Ruchat, L. K. von Segesser, S. M. Marcovina, M. Markert, R. Darioli, et al. Effect of Cardiopulmonary Bypass and Heparin on Plasma Levels of Lp(a) and Apo(a) Fragments Arterioscler Thromb Vasc Biol, April 1, 1999; 19(4): 1060 - 1065. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
A. Alonso, C. W. Whitten, and G. E. Hill Pump prime only aprotinin inhibits cardiopulmonary bypass-induced neutrophil CD11b up-regulation Ann. Thorac. Surg., February 1, 1999; 67(2): 392 - 395. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
F. Bizzarri, E. Carone, G. Capannini, G. Davoli, G. Lisi, M. Maccherini, G. Sani, and M. Toscano Bleeding reduction in cardiac surgery: A combined approach J. Thorac. Cardiovasc. Surg., May 1, 1998; 115(5): 1227 - 1227. [Full Text] [PDF]
|
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| ANN THORAC SURG | ASIAN CARDIOVASC THORAC ANN | EUR J CARDIOTHORAC SURG |
| J THORAC CARDIOVASC SURG | ICVTS | ALL CTSNet JOURNALS |
