Super High-Flux - High Volume Dialysis in Sepsis-Induced Acute Renal Failure

BACKGROUND AND RATIONALE The combination of acute renal failure (ARF) and sepsis is associated with a very high morbidity and mortality (1). Accordingly, there have many attempts to develop better treatments for this condition. Much clinical and molecular biology research suggests that septic shock occurs because of the uncontrolled immune system's response to infection (2-13). This response involves the production of several substances (so called "humoral mediators"), which enter the blood stream and, at different times in the course of the patients' illness, cause either severe inflammation or profound depression of the immune system's ability to kill microbes. The vast majority of these substances (cytokines, complement anaphylatoxins, platelet activating factor, leukotrienes, chemokines), which are responsible for this state of "blood poisoning" are water soluble and of small to middle molecular weight (up to 40 kilodaltons). These properties make them potentially removal by artificial membranes similar to those used during continuous hemofiltration (the type of artificial kidney support used in intensive care). It is possible that using a different and more porous membrane, the removal of such cytokines would be much more efficient and the clinical benefits of blood purification would, therefore, be greater. A membrane of this kind is now available. It is a modification (moderate increase in pore size) of standard material called polyamide, which has already been used in millions of people for dialysis and hemofiltration. This larger pore polyamide membrane has now been used in preliminary studies in humans (14) and has been found to be capable of lowering the blood levels of a marker cytokine (interleukin-6, molecular weight: 26.2 kD). In laboratory studies conducted by ourselves, this new polyamide membrane achieves the highest reported cytokine and beta2-Microglobulin - as another marker of removal of middle molecules - clearances in the literature and is associated with a negligible loss of albumin (15). Recent investigations by ourselves and others, however, have made the following findings: 1. Standard membranes are of only limited effectiveness in filtering these "humoral mediators" (16) 2. Unless high volume plasma-water exchange is applied (100 ml/min), the effect of blood purification on the blood levels of these mediators are minimal (17-20) 3. High volume hemofiltration with standard membranes, results in an improvement in the state of the circulation such that the infusion of drugs used to support blood pressure (noradrenaline) can be decreased (20). 4. Even with high volume hemofiltration the removal of "humoral mediators" such as cytokines is still of limited efficiency (20) It is possible that using a different and more porous membrane, the removal of such cytokines would be much more efficient and the clinical benefits of blood purification would, therefore, be greater. A membrane of this kind is now available. It is a modification (moderate increase in pore size) of standard material called polyamide, which has already been used in millions of people for dialysis and hemofiltration. We, therefore, propose to study the effect of combining hemodialysis and this new polyamide membrane with larger pores in the treatment of patients with sepsis and acute kidney failure. We wish to compare the effect of this new therapy to that of hemodialysis with a standard membrane. The terms of comparison (outcome measures) will be: A). The effect of each therapy on the blood concentration of several cytokines (TNF-alpha, IL-1 beta, Il-6, IL-8, and IL-10). B). The effect of each therapy on the blood concentration of beta2-Microglobulin as another marker of removal of middle molecules. C). The effect of each therapy on blood pressure and the need for noradrenaline infusion and, for safety assessment D). The effect of each therapy on the blood concentration of albumin and electrolytes If this new membrane were found to have a major effect on the blood concentration of cytokines and on the patients' blood pressure, further studies would then be justified to assess its clinical effects (time in ICU, time in hospital, time on ventilator, duration of organ failure, etc) in further trial. STUDY OBJECTIVE The aim of the study is to compare the effect of hemodialysis combined with a larger pore membrane to that of hemodialysis with a standard membrane on 1. the serum concentration of several cytokines (efficacy assessment) 2. the serum concentration and clearance rates of beta2- Microglobulin (efficacy assessment) 3. blood pressure and noradrenaline requirements (efficacy assessment) 4. the serum concentration of albumin and electrolytes (safety assessment) NULL HYPOTHESIS The use of hemodialysis combined with a larger pore membrane has no effect on serum cytokine or beta2-Microglobulin levels, blood pressure and noradrenaline requirements when compared to hemodialysis with a standard membrane. STUDY DESIGN This study is a phase I/II equivalent investigation. It is a pilot, randomised, crossover, controlled study. Eligible patients will receive both treatments. However, the order of treatment (first treatment A and then B or vice versa) will be allocated in a random fashion (computer generated random numbers). After completing the first treatment, patients will then be crossed over to the alternative treatment. Treatments will consist of either: A) hemodialysis with a new polyamide (P2SH) membrane for 4 hours or B) hemodialysis with a standard polyamide membrane Blood will be sampled (serum cytokine and beta2-Microglobulin measurement) at the start of each treatment and after 4 hours of each treatment. Dialysate will also be collected for the measurement of cytokines and beta2-Microglobulin in order to calculate cytokine and beta2-Microglobulin clearance. The changes in blood pressure and noradrenaline dose will be recorded hourly as is routine in Intensive Care. Patient treatment will otherwise continue according to clinical needs and to standard ICU care. It is important to note that patients involved in the study would normally receive standard hemofiltration anyway because of their kidney failure, with all the risks and benefits associated with the procedure (insertion of double lumen catheter, extracorporeal circulation, anticoagulation). As part of the study, however, they will also receive increased intensity of treatment, 4 hours of exposure to a modified membrane and some additional blood sampling (one spoonful). It is possible that the effect of the first therapy would cross over to the second. To control for this crossover effect, statistical comparison will be undertaken according to order of treatment as well as type of treatment, as recently published. (23) STUDY POPULATION All patients who fulfil the consensus criteria for sepsis (21) and recently proposed criteria for severe ARF (1) are eligible for the study. SPECIFIC EXCLUSIONS * Patients under 18 years of age. * Patients who are pregnant or breastfeeding * Patients with a known allergy to polyamide * Patients expected to die within 24 hours * Patients in whom there are limitations on the intensity of therapy ENROLMENT Once patient eligibility is established informed consent will be sought from the next of kin. If informed consent is obtained, the patient will be enrolled in the study. The ICU research nurse will be responsible for enrolment and subsequent data collection. STUDY PROTOCOL Following enrolment and randomisation, the patient will be allocated to either treatment A or B. An extracorporeal circuit will be set up for dialysis with the Fresenius 2008 machine. The only difference will be that, one filter which is being applied, will be a larger pore polyamide filter. The other filter whic is being applied, will be a standard polyamide filter. Each treatment will be applied for 4 hours. After each treatment, the extracorporeal circuit will be flushed with Hartmann's solution and the membrane changed to the alternative material (cross over). For each treatment, the following technical settings will apply: 1. Blood flow at 200 ml/min 2. Dialysate flow at 300 ml/min 3. Anticoagulation of filter with prefilter heparin, if necessary (e.g. 1,000 IU/hr) 4. Bicarbonate-buffered dialysate After the completion of the 2 periods of 4 hours of hemodialysis, patients will revert to standard therapy (hemofiltration with AN 69 membrane at 2 L/hr of plasma water exchange) and continue their normal treatment. Randomisation and Concealment The randomisation will be based on random numbers generated by computer. The allocation to either treatment A or B as the first treatment will be placed in an opaque envelope by an independent person. Once consent is obtained, the envelope will be opened and treatment initiated. Filters will be blinded and both will have identical appearance, outlining only "Filter A" or "Filter B", respectively, on a label sticking to each filter. For reasons of patient safety, filter monitoring for membrane clotting requires that the filter be visualized at all times. EXPECTED SIZE OF TREATMENT DIFFERENCE This study is designed to detect a 30% decrease in IL-6 levels. From a previous very similar investigation (19), we also assume a standard deviation equal in size to the effect being tested for. Using non-parametric paired comparison statistics (Wilcoxon ranked sign test), a sample of 10 patients would offer a \> 80% power of detecting a 30% difference at an alpha of 0.05 (22). CLINICAL OUTCOMES AND DATA ANALYSIS Primary analysis will be performed on the basis of intention to treat. Secondary analysis will be performed on per protocol analysis. The primary outcome measure for this study is the clearance and the change in IL-6 levels The secondary outcome is the the clearance and change in the levels of other cytokines and beta2-Microglobulin. The other secondary outcome is the change in noradrenaline dose required to maintain baseline mean blood pressure (typically 70 mmHg) Treatment groups will be analysed for differences in IL-6 levels after 4 hours of treatment. It is expected from clinical observation that the criteria for normal distribution will be violated. Therefore comparison will be performed using a non-parametric test (Wilcoxon ranked sign test). Statistical significance will be set at p\<0.05. The groups will also be tested for differences in secondary outcome variables. Such secondary outcome variables are: 1. Absolute change in all serum cytokine levels for each cytokine and for beta2-Microglobulin 2. Percentage change in noradrenaline dose 3. Change in blood pressure from pre-treatment value to value after 4 hours of treatment 4. Percentage change in serum cytokine levels for each cytokine Using the primary outcome variable, this study has an 80% power of detecting a 30% difference at an alpha of \<0.05. It is expected from clinical observation that recruitment of 10 patients will take 3 months. Data Collection Data collection will be by the Intensive Care Dept. research nurse and research fellows. The following variables will be obtained: Name, gender, age and medical record number Date of admission to ICU Admission diagnosis SAPS II illness severity score on admission Time of onset of septic shock Time of onset of ARF Time of onset of hemofiltration Hemodynamic indices, temperature and biochemical indices at baseline and after 4 hours Use of inotropic drugs and dose Use of vasopressor drugs and dose Hourly urine output (if present) Time of onset of mechanical ventilation Fluid balance during each 4 hours of treatment Albumin and electrolytes at baseline and after 4 hours CONCOMITANT MEDICATIONS Concomitant medications will be administered according to standard intensive care ADVERSE EVENTS If any adverse events occur which may be related to the trial device, treatment will be stopped. The event will be immediately reported to the Ethics Committee according to institutional protocol. PROTOCOL VIOLATIONS All protocol violations will be recorded. It will then be decided whether the nature of such violations has been such that the patient should be excluded from primary data analysis. WITHDRAWAL The treating clinician will have the right to withdraw the patient from the study if he or she believes that continued participation is jeopardizing the patient's well being. Patients who require take back to theatre during the study period for a surgical emergency will be withdrawn from the trial. CONSENT TO TRIAL ENROLMENT In all patients it may be necessary to ask for consent from the next of kin. All of these patients are mechanically ventilated and too ill to give informed consent ETHICAL ISSUES The polyamide material used for the study membrane is very safe and has been used in millions of patients. Its modification is exclusively to the pore size, not to its composition. The effect of pore size on protein losses appears minimal for proteins \> 60 kD in molecular weight such as albumin. Accurate in vitro testing confirms this. 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