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Department of Cardiovascular Surgery, Nagoya Daini Red Cross Hospital, Nagoya, Japan
Accepted for publication July 27, 2009.
* Address correspondence to Dr Takami, Department of Cardiovascular Surgery, Nagoya Daini Red Cross Hospital, 2-9 Myouken-cho, Showa-ku, Nagoya, 466-8650, Japan (Email: takami{at}nagoya2.jrc.or.jp).
| Abstract |
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Methods: A retrospective analysis of 245 HD patients who underwent cardiac surgery between 1994 and 2007 was conducted. The basic management strategies were (1) low-potassium HD for 2 days before surgery, (2) only hemofiltration during cardiopulmonary bypass, and (3) start of regular intermittent HD on the first postoperative day. Continuous venovenous hemodiafiltration was applied only for patients with hemodynamic instability.
Results: The causes of renal failure included diabetic (n = 89, 36%), glomerulonephritis (n = 49, 20%), and unknown (n = 75, 31%). The history of HD was 9.7 ± 7.6 years. The operative procedures included coronary (n = 135), valve (n = 103), and others. The amount of intraoperative ultrafiltration was 6,123 ± 324 mL during cardiopulmonary bypass for 197 ± 67 minutes. Two hundred eight patients (85%) were managed with only intermittent HD, whereas 36 patients (15%) needed continuous venovenous hemodiafiltration. The use of continuous venovenous hemodiafiltration significantly declined during the year (26% before 2003 and 3% after 2003; p < 0.001). The amount of fluid removal on the first postoperative day was 1,297 ± 81 mL. The hospital mortality was 9.7% with the causes including infection (n = 11), cardiac events (n = 6), gastrointestinal events (n = 5), and stroke (n = 2). A multivariate logistic regression analysis revealed that selection of intermittent HD or continuous venovenous hemodiafiltration was not related to the hospital mortality.
Conclusions: Simplified management only with intermittent HD can be safely performed in most HD-dependent patients undergoing cardiac surgery.
| Introduction |
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| Patients and Methods |
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The preoperative HD on the consecutive 2 days before surgery was performed using a low-potassium dialysate containing 1.5 mEq/L of potassium, in contrast to a potassium concentration of 2.0 mEq/L in the standard dialysate, to obtain a serum potassium of 3.0 mEq/L. All surgical procedures were performed through a median sternotomy, except left anterior minithoracotomy for off-pump coronary artery bypass grafting (CABG) in 3 patients, by using standard anesthetic and surgical techniques. Under cardiac arrest, cardioplegia with high-potassium (20 mEq/L) cold blood was administered in an antegrade fashion, a retrograde fashion, or both for myocardial protection. As reported previously [7], when the ascending aorta was unable to be clamped because of severe atherosclerosis, we applied a technique of safer cross-clamping after inspection and debridement inside the aorta using the Cavitron Ultrasonic Surgical Aspirator (CUSA; Tyco Healthcare, Mansfield, MA) under short-time moderate hypothermic circulatory arrest at an esophageal temperature of approximately 30°C. During CPB, we performed only hemofiltration, as well as in non-HD patients, using a hemoconcentrator (CX-HC11L; Terumo Co, Tokyo, Japan) incorporated into the CPB circuit. Blood from the venous drainage line of the CPB circuit was pumped into the hemoconcentrator, and then the hemoconcentrated blood was returned into the venous reservoir. A standard dialysis fluid (Sublood-B; Fuso Pharmaceutical, Ltd, Osaka, Japan) was used for fluid replacement. Our goal for discontinuation of CPB was to obtain a hemoglobin greater than 10.0 g/dL, a hematocrit greater than 30%, and serum potassium value less than 4.0 mEq/L by blood transfusion and increased hemofiltration. In patients undergoing off-pump CABG, we did not perform any hemofiltration during the surgery.
The first postoperative HD was carried out on the first day after surgery in the intensive care unit (ICU) using a standard HD device (DBG-O1 or DBB-22B; Nikkiso Co, Tokyo, Japan) and tubing lines through the shunt vessel of the patient. We did not insert any additional catheters as a vascular access for intermittent HD. A low-flux polysulphone HD membrane (FDY-180GW; Nikkiso Co) with an active surface area of 1.3 m2 was used. Anticoagulation of the extracorporeal circuit was achieved using a dose of 25 mg/h of nafamostat mesylate (Futhan; Torii Pharmaceutical Co, Osaka, Japan), followed by patient-adjusted regimen based on the activated clotting time (150 to 180 seconds). Blood flow was 200 mL/min and ultrafiltration rate was 250 to 500 mL/h to achieve a negative fluid balance for 4 hours. A bicarbonate-buffered dialysate (Kindary AF; Fuso Pharmaceutical, Ltd) was used during the HD. Approximately 4 hours of HD was performed to obtain the potassium value less than 4.5 mEq/L. The second postoperative HD was carried out on the third postoperative day by the usual standard methods using heparin in the HD unit when the patient's condition was uneventful.
When the patient was hemodynamically unstable after surgery, we conducted CVVH using a high-flux polyacrylonitrile hemofilter with a surface area of 0.6 m2 (Panflo APF-06S; Asahi Kasei Kuraray Medical Co, Tokyo, Japan) through a 12F dual-lumen catheter (Naiagara Slim-Cath; C.R. Bird, Inc, Salt Lake City, UT) newly inserted into the femoral vein. Blood from the femoral vein entering through the side ostium of the catheter was pumped into the dialyzer attached to the CVVH machine (ACH-10; Asahi Kasei Kuraray Medical Co) and returned to the patient through the ostium tip of the catheter. As used for HD in the ICU, nafamostat mesylate was used for anticoagulation. Hemodiafiltration was initially accomplished by using a blood flow rate of 100 mL/min, a dialysate flow rate of 500 mL/h, a fluid replacement rate of 500 mL/hr, and an ultrafiltration rate of 1 L/hr, resulting in no net fluid removal. A bicarbonate-buffered fluid (Sublood-BS; Fuso Pharmaceutical, Ltd) was replaced continuously. After the hemodynamics became stable, the filtration rate and dialysate flow were adjusted to remove the fluid excess. When the patient's condition was considered to be stable enough for HD, the patient was weaned from CVVH and the dual-lumen catheter was removed, followed by institution of intermittent regular HD using the usual methods.
Statistical Analysis
Continuous data were expressed as mean ± standard deviations and compared using the Mann-Whitney U test for analysis. Category variables were expressed as percentages and compared using Fisher's exact test for analysis. In addition, a multivariate logistic regression analysis was performed examining the outcome of hospital mortality. A probability value of less than 0.05 was considered statistically significant. The statistical analyses were performed with StatView 5.0 (Abacus Concepts Inc, Berkeley, CA).
| Results |
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The operative procedures in the study patients were listed in Table 2. Fourteen (5.7%) and 11 patients (4.5%) underwent emergency and urgent operations, respectively. The HD patients undergoing isolated CABG (n = 135) received 2.7 ± 1.0 graft anastomoses using the left internal thoracic artery (n = 126), right internal thoracic artery (n = 41), right gastroepiploic artery (n = 28), and saphenous veins (n = 178). Among them, 39 patients (29%) underwent all in situ arterial grafting using left internal thoracic artery, right internal thoracic artery, or right gastroepiploic artery. In the patients undergoing aortic valve replacement (n = 83), a mechanical valve was used in 54 patients (65%) and a bioprosthesis was used in 29 patients (35%). The mechanical valves implanted included ATS (ATS Medical Inc, Minneapolis, MN; n = 17), CarboMedicus (CarboMedicus Inc, Austin, TX; n = 14), Sorin Bicarbon (Sorin Biomedica, Saluggia, Italy; n = 10), OnX (On-X Life Technologies, Inc, Austin, TX; n = 8), and SJM (St. Jude Medical Inc, St. Paul, MN; n = 6). The tissue valves implanted were Carpentier-Edwards Pericardial (CEP, Baxter Healthcare Corp, Newport Beach, CA; n = 24), Mosaic (Medtronic Inc, Minneapolis, MN; n = 4), and Hancock (Medtronic Inc; n = 1). Six patients (7.4%) among the aortic valve replacement patients required annular enlargement with a commercially available bovine or equine pericardium to obtain an effective orifice area greater than 0.85 cm2/m2.
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Perioperative Renal Replacement Therapy
Intraoperative hemofiltration during CPB removed fluid of 6,123 ± 3,024 mL (range, 710 to 20,900 mL). The intraoperative fluid balance was +2,847 ± 1,842 mL (range, –230 to +11,864 mL) in all patients, including off-pump patients.
Postoperative renal replacement therapy was performed using only intermittent HD in 208 patients (85%). Thirty-six patients (15%) needed CVVH owing to hemodynamic instability after surgery. Only 1 patient underwent continuous ambulatory peritoneal dialysis, as performed preoperatively. The prevalence of patients who were managed with only intermittent HD increased during the year. The prevalence after 2003 was significantly higher (97%, 117 of 121 patients) than that before 2003 (74%, 91 of 124 patients; p < 0.001). The mean volume of removed fluid on the first day after surgery was 1,297 ± 810 mL (range, 0 to 3,700 mL). The perioperative changes in values of serum potassium, creatinine, and blood urea nitrogen are presented in Table 3. The value of serum potassium just before surgery was significantly decreased from the value on admission. The postoperative values of serum potassium gradually increased, although they mostly remained less than 5.0 mEq/L. Both values of serum creatinine and blood urea nitrogen were controlled perioperatively at significantly lower levels than those on admission, regardless of the manner of renal replacement therapy, intermittent HD or CVVH.
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| Comment |
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The first key point of our management strategies is to apply low-potassium HD for 2 days before surgery. The main goal is to remove excessively accumulated potassium and to make room for an intraoperative potassium load resulting from potassium-rich cardioplegia, blood transfusion, and impaired cellular potassium uptake in metabolic acidosis. With low-potassium HD, we must be careful of potential hemodynamic effects, especially rebound hypertension. Although reduced dialysis efficiency may also be a concern with low-potassium HD, a recent study revealed that high potassium removal has no influence on urea elimination [8].
The second key point of our management strategies is to apply only hemofiltration, not HD, during CPB. Previous reports advocated intraoperative HD during CPB to avoid marked hyperkalemia, especially owing to potassium-rich cardioplegia [3, 4]. Certainly, intraoperative HD has the benefit of normalizing the acid–base status, controlling postoperative levels of blood urea nitrogen and other toxins, and removing extra fluid administered during CPB. However, our results demonstrated that intraoperative HD, which is costly and complicated, is not necessary and that intraoperative hemofiltration, which is routinely incorporated into the CPB circuit for non-HD patients, is enough to avoid hyperkalemia.
The third key point of our management strategies is the routine use of intermittent HD, not CVVH, after surgery. Recently, the use of continuous renal replacement techniques, including CVVH, with several modifications has emerged as an alternative dialytic modality for critically ill patients with severe acute renal failure [5, 6, 9, 10]. The theoretical advantages of CVVH include improved hemodynamic stability, easier removal of fluid and electrolytes, and steady control of azotemia. In contrast, the CVVH exhibits potential drawbacks such as access-related complications and increased manpower or financial investments when highly sophisticated devices are used. There have been controversies about whether CVVH improves the outcomes of critically ill patients with acute renal failure in ICU settings when compared with intermittent HD [9–16]. From technological aspects, CVVH not only enables a significantly higher dialysis dose to be delivered when compared with intermittent HD, more mass of urea is also removed in CVVH at a similar dialysis dose (calculated from clearance, time, and the volume distribution of urea). The nonlinearity of diffusion-based solution removal, compartmentalization phenomena, and flow-related disequilibrium are also concerns in the use of intermittent HD [11, 12]. However, several randomized controlled trials showed no evidence of a survival benefit of CVVH compared with intermittent HD [13–16]. These evidences in the ICU settings may support our management strategies in HD patients undergoing cardiac surgery.
Our management with these key points proved to be simple and effective in the present study. As a limitation, however, the present study is a retrospective observational study, and therefore any conclusions are limited in their interpretation. The overall hospital mortality was 9.8% in our report. It is superior to the mortality rates reported in the review in 2000 (12.5%) [17] and in the report from a large-volume single center (12.7%) [18]. Although the patient demographics are different, the improved mortality in our patients may justify our simplified management strategy with only intermittent HD. The causes of death can be categorized into four types in our study. The first cause was infection, including sternal mediastinitis. The second was a cardiac event, the third was a gastrointestinal adverse event, and the fourth cause was a cerebral event. These causes were closely associated with basic pathophysiology of the HD patients, including compromised immune conditions, poor nutrition, and advanced atherosclerosis. Our results revealed that diabetes mellitus is the only independent predictor of hospital mortality, but selection of intermittent HD or CVVH was not significantly related to mortality. In our institution, the mortality rate of HD patients gradually decreased with time. Although we did not reveal which aspects of our renal replacement protocol reduced mortality, this improvement may be associated with advances in infection control. We also think that it is important not to remove too much of the excessive fluid immediately after surgery to make intermittent HD safer and to prevent ischemic events in HD patients.
In conclusion, our simplified management with only intermittent HD can be safely performed, whereas the frequency of CVVH use is low, in most HD-dependent patients who underwent cardiac surgery. Our strategy may be useful to reduce the complexity and manpower in routine managements.
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