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Preop Hemodialysis or Intraop Ultrafiltration for Patients With Severe Renal Dysfunction Undergoing Open Heart Surgery (SeRenaD-CPB)

Primary Purpose

Non-Dialysis Dependent Severe Renal Dysfunction, Cardiovascular Disease

Status
Unknown status
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
Open Heart Surgery (OHS)
Intraoperative Modified Ultrafiltration (MUF)
Hemodialysis (HD)
Sponsored by
University Hospital, Geneva
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Non-Dialysis Dependent Severe Renal Dysfunction focused on measuring Renal dysfunction, Hemodialysis, Modified ultrafiltration, Open heart surgery

Eligibility Criteria

18 Years - 95 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18 years or older
  • Diagnosis of SCr > 180 µmol/L or 2.0 mg/dL, and/or a GFR < 30 mL/min/1.73 m2.
  • Indication for elective open heart surgery under CPB.

Exclusion Criteria:

  • History of chronic or recent HD.
  • Emergency status.
  • Off-pump surgery.
  • Failure to obtain patient consent documented by a signed consent form.

Sites / Locations

  • University of Lyon, Hopital Cardiothoracique Louis Pradel
  • German Heart Institute Berlin
  • Hospital Clinico, University of Barcelona, Department of Cardiovascular Surgery
  • University Hospital of Geneva, Service for Cardiovascular Surgery
  • Ankara University, Department of Cardiovascular Surgery
  • Pamukkale University, Department of Cardiovascular Surgery
  • Gaziantep University, Department of Cardiovascular Surgery

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Experimental

Experimental

Arm Label

1

2

3

Arm Description

Control Group (Open heart surgery alone)

Intraoperative Modified Ultrafiltration (MUF) Group (Open heart surgery with intraoperative MUF)

Preoperative Hemodialysis Group (Open Heart Surgery after preoperative hemodialysis)

Outcomes

Primary Outcome Measures

Operative mortality, defined as any death occurring within 30 days after the operation or any death occurring before discharge during the same hospitalization (in percentage).

Secondary Outcome Measures

Survival at one year after surgery (in percentage).
Postoperative low cardiac output (in percentage).
Postoperative permanent neurological deficit (in percentage).
Postoperative transient neurological deficit (in percentage).
Postoperative acute renal dysfunction (in percentage).
Postoperative persistent renal dysfunction requiring hemodialysis (in percentage).
Postoperative gastrointestinal complication (in percentage).
Postoperative respiratory failure (in percentage).
Postoperative systemic infection (in percentage).
Postoperative local infection (in percentage).
Postoperative new-onset arrythmia (in percentage).
Postoperative surgical drainage (in mL).
Postoperative need for transfusion of blood products (in unit packs).
Postoperative length of ICU stay (in days)
Postoperative length of hospital stay (in days)
Total hospital costs for the admission of operation (in Euros)

Full Information

First Posted
July 21, 2008
Last Updated
July 22, 2008
Sponsor
University Hospital, Geneva
Collaborators
University of Gaziantep, Ankara University, Pamukkale University, German Heart Institute, Hospices Civils de Lyon, Hospital Clinic of Barcelona
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1. Study Identification

Unique Protocol Identification Number
NCT00720967
Brief Title
Preop Hemodialysis or Intraop Ultrafiltration for Patients With Severe Renal Dysfunction Undergoing Open Heart Surgery
Acronym
SeRenaD-CPB
Official Title
Influence of Preoperative Hemodialysis or Intraoperative Modified Ultrafiltration on Postoperative Outcome for Patients With Severe Renal Dysfunction Undergoing Open Heart Surgery: Randomized, Controlled, Multicenter Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2008
Overall Recruitment Status
Unknown status
Study Start Date
November 2008 (undefined)
Primary Completion Date
November 2011 (Anticipated)
Study Completion Date
November 2012 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
University Hospital, Geneva
Collaborators
University of Gaziantep, Ankara University, Pamukkale University, German Heart Institute, Hospices Civils de Lyon, Hospital Clinic of Barcelona

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine whether preoperative hemodialysis or intraoperative modified ultrafiltration are effective for patients with non-dialysis dependent severe renal dysfunction undergoing open heart surgery.
Detailed Description
1. BACKGROUND 1.1. RENAL DYSFUNCTION AND OPEN HEART SURGERY: The incidences of both cardiovascular disease (CVD) and chronic renal dysfunction (RD) are increasing with the aging population in the western world (1). The intense relationship between the pathogenesis of CVD and chronic RD has recently been reviewed by Schiffrin et al, in detail (2). They both have common risk factors such as diabetes, hypertension, activation of renin-angiotensin system, endothelial dysfunction, oxydative stress, etc. Besides, each has an impact on the other's outcome. On the one hand, CVD is the most frequent cause of death in chronic RD patients (3). On the other hand, even mild chronic RD is one of the major risk factors of postoperative mortality and morbidity after cardiac operations (4, 5). The mechanism is not clear yet, however, volume overload, electrolyte imbalance and inflammatory state created by cardiopulmonary bypass (CPB) may have an impact. Zakeri et al showed that in-hospital mortality after isolated primary coronary artery bypass grafting (CABG) increases exponentially with increasing levels of renal dysfunction (6). They reported an in-hospital mortality of 2.2%, 4.3%, 9.3% and 14.8% in patients who have a preoperative serum creatinine level (SCr) of <130 µmol/L, 130-149 µmol/L, 150-179 µmol/L and 180-199 µmol/L, respectively. These results were similar to the study published previously by Weerasinghe et al with the same cut-off levels of SCr (7). Using the Glomerular Filtration Rate (GFR) instead of SCr, Cooper et al. came to the same conclusion after analysing 483,914 patients receiving isolated CABG in the Society of Thoracic Surgeons (STS) National Adult Cardiac Database (5). They reported that operative mortality rose inversely with declining renal function, from 1.3% for those with normal renal function to 1.8%, 4.3% and 9.3% for patients with mild, moderate and severe RD, respectively. Another study regarding the effect of preoperative RD on mortality after valve surgery was also published with a relatively smaller patient population (8). Although the RD group had significantly worse outcomes with regard to postoperative ventilation time, re-operation, blood transfusion and length of hospital stay, operative mortality was not statistically different between the two groups (3.4% for RD group vs. 2.3% for the control group), probably because of small sample size. However, Filsoufi et al. reported an increased mortality for patients having SCr of >2.5 mg/dL after single valve replacement (25.0% vs. 2.4%),multiple valve replacement (26.7% vs. 3.4%), and combined valve replacement with CABG (28.0% vs. 4.6%) in a large, single-center cohort (9). Regarding long-term survival, Devbhandari reported 1-, 3- and 5-year survival rates following on-pump coronary bypass surgery as 90.3%, 83.2% and 71.4% for non-dialysis dependent renal dysfunction (NDDRD) patients, and 97.4%, 94.6% and 91.0% for patients with no history of RD, respectively (10). Chronic RD affects not only the operative mortality, but also the morbidity after open heart surgery. It has been shown that preoperative RD is an independent predictor of postoperative acute RD and hemodialysis (HD) (5, 7, 9-12) as well as gastrointestinal (GI) (4, 9), respiratory (5, 9), infectious (5) and neurological (5) complications. 1.2. HEMODIALYSIS: HD is the most common renal replacement therapy for decades, for those who have end-stage RD and have not received renal transplantation. Intermittent HD is a very efficient method to decrease blood urea and creatinine as well as to treat volume overload. Intermittent HD can be performed temporarily in the setting of acute RD or permanently in the setting of chronic RD. In chronic RD, 3 sessions of 4 hours are usually prescribed to adequately substitute the renal function. A good vascular access is essential to perform HD. A temporary dual- or tri-lumen dialysis catheter has to be inserted into a central vein such as the internal jugular, the subclavian or the femoral vein. 1.3. ULTRAFILTRATION: Intraoperative ultrafiltration has been used widely in pediatric open heart surgery for decades, reducing total body water, increasing hematocrit (Htc) levels, removing inflammatory mediators, thus improving the operative outcome (13). In the 90's, Naik et al. modified the technique (14), and reported better outcomes with modified ultrafiltration (MUF) in pediatric population (15). However, use of MUF has been limited to end-stage RD patients with volume overload undergoing open heart surgery, as an adjunct to pre- and postoperative HD in the adult population. The Verona group reported fewer respiratory, neurological, GI complications, and less blood product transfusion in the group of patients who received MUF after CPB, however mortality, overall morbidity, length of Intensive Care Unit (ICU) stay and length of hospital stay were comparable between MUF and control groups including 573 consecutive patients (16). A meta-analysis evaluating the effects of ultrafiltration on postoperative blood product use and perioperative bleeding in adult patients revealed fewer bleeding complications and reduced blood product use after intraoperative ultrafiltration (17). Boga et al reported improved cardiac performance after CABG surgery with MUF. However, they could not find any difference in Interleukin-6, Interleukin-8 and Neopterin levels. They attributed this effect to prevention of hemodilution and hypervolemia (18). In summary, no clear evidence is available at the present regarding the impact of intraoperative MUF on the operative outcome of NDDRD patients undergoing open heart surgery. Capuano et al. recently (19) reported successful results in a NDDRD patient who required urgent coronary revascularisation. Nevertheless, the impact of intraoperative MUF on the outcome of NDDRD patients undergoing open heart surgery remains unclear, and is worth investigation. 1.4. PREVIOUS STUDIES: The quest to improve the outcome of NDDRD patients undergoing open heart surgery has been in the agenda of some groups to date. Two pioneering studies were recently published from Turkey (20, 21). The target patient population was NDDRD patients undergoing elective isolated primary CABG surgery. Patients were randomized into two groups prospectively, one group received 2 doses of prophylactic HD just before surgery whereas the other did not, and served as control. Both studies reported reduced operative mortality rates, reduced postoperative need for HD, and shorter length of stay in the prophylactic HD groups. However, these two studies had very limited number of patients with a short period of follow-up, excluded valve surgery, and did not analyse cost-effectiveness. Furthermore, intraoperative ultrafiltration was not studied. 1.5. ASSESSMENT OF RENAL FUNCTION: GFR is the best measure of overall kidney function (22). The Cockroft-Gault formula is a commonly used way to predict GFR (23). GFR <30 mL/min/1.73 m2 is accepted as "severe RD" (22). SCr is a simple and practical universal biologic marker used for estimating glomerular filtration. Although SCr does not have a linear association with GFR, it has also been reported to be a powerful predictor of operative mortality (6). Thus, SCr and GFR were both accepted as preoperative indicators of RD with the cut-off levels of 180 µmol/L (or 2.0 mg/dL) and 30 mL/min/1.73 m2, respectively. 1.6. CONCLUSION: In summary, this data mandates us a well defined strategy for patients with NDDRD in order to obtain better operative outcome. Under the guidance of the current literature, a randomized controlled trial (RCT) with a larger number of patients undergoing open heart surgery will provide precise answers for these questions. Comparison of hospital costs may add an extra value for the assessment of cost-effectiveness as well.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non-Dialysis Dependent Severe Renal Dysfunction, Cardiovascular Disease
Keywords
Renal dysfunction, Hemodialysis, Modified ultrafiltration, Open heart surgery

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
450 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
Control Group (Open heart surgery alone)
Arm Title
2
Arm Type
Experimental
Arm Description
Intraoperative Modified Ultrafiltration (MUF) Group (Open heart surgery with intraoperative MUF)
Arm Title
3
Arm Type
Experimental
Arm Description
Preoperative Hemodialysis Group (Open Heart Surgery after preoperative hemodialysis)
Intervention Type
Procedure
Intervention Name(s)
Open Heart Surgery (OHS)
Intervention Description
General anesthesia, use of iodine impregnated adhesive dressing, median sternotomy and/or thoracotomy incision, full heparinization (300-400 ui/kg), arterial and venous cannulation, initialization of CPB with or without aortic cross-clamping and high-potassium cold cardioplegia, surgical repair under mild-moderate hypothermia. De-clamping (if cross clamp was applied), neutralization of heparin by protamin, de-cannulation and hemostasis after surgical repair. Insertion of drain(s) and pacing wire(s). Closure of all layers in anatomical plan.
Intervention Type
Procedure
Intervention Name(s)
Intraoperative Modified Ultrafiltration (MUF)
Intervention Description
Once the surgical repair is finished, and CPB will be stopped after aortic declamping. The arterial and venous cannulae will be connected to each other using 3-way connectors and a cardioplegia line. When hemodynamic stability is established (MAP >75 mmHg, CVP > 12 mmHg, Htc > 25%), blood will be drained from the arterial cannula using a roller pump, driven to the ultrafilter, and eventually to the venous cannula. The blood flow will be maintained at ~150 mL/min, and suction will be applied to the filtrate port to achieve an ultrafiltration of 100-120 mL/min. Heat exchanger and bubble trap of the cardioplegia line will be used to maintain the filtered blood at body temperature and to prevent air embolism, respectively. MUF will continue 20 minutes. The filtered volume will be collected.
Intervention Type
Procedure
Intervention Name(s)
Hemodialysis (HD)
Intervention Description
Two HD sessions will be performed at 3 days and 1 day prior to surgery. Each session will last 3 hours if the patient weighs < 75 kg, and 4 hours if > 75 kg. Conventional HD will be carried out using a volume-controlled dialysis machine. A bicarbonate dialysate containing K (3 mmol/L), Ca (1.5 mmol/L) and HCO3 (31 mmol/L) will be used. Sodium conductivity will be set at 138 mmol/L. Medium-flow filters will be used as artificial kidney devices. Dialysate temperature will be set at 36oC. Dialysate and blood flow rate will be set at 500 mL/min and 250-300 ml/min, respectively. Intradialytic ultrafiltration will not be used routinely unless the patient has volume overload. The decision to use intradialytic ultrafiltration will be taken with the anaesthesiologist and the cardiac surgeon. If intradialytic ultrafiltration is indicated, maximal rate of ultrafiltration will be 10 ml/kg/hour. These patients will undergo open heart surgery after two sessions of HD.
Primary Outcome Measure Information:
Title
Operative mortality, defined as any death occurring within 30 days after the operation or any death occurring before discharge during the same hospitalization (in percentage).
Time Frame
within the first 30 days after surgery or before the discharge after surgery
Secondary Outcome Measure Information:
Title
Survival at one year after surgery (in percentage).
Time Frame
one year after surgery
Title
Postoperative low cardiac output (in percentage).
Time Frame
within the first 30 days after surgery or before the discharge after surgery
Title
Postoperative permanent neurological deficit (in percentage).
Time Frame
within the first 30 days after surgery or before the discharge after surgery
Title
Postoperative transient neurological deficit (in percentage).
Time Frame
within the first 30 days after surgery or before the discharge after surgery
Title
Postoperative acute renal dysfunction (in percentage).
Time Frame
within the first 30 days after surgery or before the discharge after surgery
Title
Postoperative persistent renal dysfunction requiring hemodialysis (in percentage).
Time Frame
within the first 30 days after surgery or before the discharge after surgery
Title
Postoperative gastrointestinal complication (in percentage).
Time Frame
within the first 30 days after surgery or before the discharge after surgery
Title
Postoperative respiratory failure (in percentage).
Time Frame
within the first 30 days after surgery or before the discharge after surgery
Title
Postoperative systemic infection (in percentage).
Time Frame
within the first 30 days after surgery or before the discharge after surgery
Title
Postoperative local infection (in percentage).
Time Frame
within the first 30 days after surgery or before the discharge after surgery
Title
Postoperative new-onset arrythmia (in percentage).
Time Frame
within the first 30 days after surgery or before the discharge after surgery
Title
Postoperative surgical drainage (in mL).
Time Frame
within the first 72 hours after surgery
Title
Postoperative need for transfusion of blood products (in unit packs).
Time Frame
within the first 72 hours after surgery
Title
Postoperative length of ICU stay (in days)
Time Frame
within the first 30 days after surgery or before the discharge after surgery
Title
Postoperative length of hospital stay (in days)
Time Frame
within the first 30 days after surgery or before the discharge after surgery
Title
Total hospital costs for the admission of operation (in Euros)
Time Frame
From the day of admission to hospital until the day of discharge after surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
95 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18 years or older Diagnosis of SCr > 180 µmol/L or 2.0 mg/dL, and/or a GFR < 30 mL/min/1.73 m2. Indication for elective open heart surgery under CPB. Exclusion Criteria: History of chronic or recent HD. Emergency status. Off-pump surgery. Failure to obtain patient consent documented by a signed consent form.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Erman Pektok, MD
Phone
+41.76.3169990
Email
epektok@hotmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Patrick O. Myers, MD
Phone
+41.22.3727630
Email
patrick.myers@hcuge.ch
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Erman Pektok, MD
Organizational Affiliation
University Hospital of Geneva, Service for Cardiovascular Surgery
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Patrick O Myers, MD
Organizational Affiliation
University Hospital of Geneva, Service for Cardiovascular Surgery
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Thomas Perneger, MD, PhD
Organizational Affiliation
University Hospital of Geneva, Center of Clinical Research
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Afksendiyos Kalangos, MD, PhD
Organizational Affiliation
University Hospital of Geneva, Service for Cardiovascular Surgery
Official's Role
Study Chair
Facility Information:
Facility Name
University of Lyon, Hopital Cardiothoracique Louis Pradel
City
Lyon
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jean-Francois I. Obadia, MD, PhD
Phone
+33.4.75357546
Email
jean-francois.obadia@chu-lyon.fr
First Name & Middle Initial & Last Name & Degree
Jean-Francois I. Obadia, MD, PhD
Facility Name
German Heart Institute Berlin
City
Berlin
ZIP/Postal Code
D-13353
Country
Germany
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Roland Hetzer, MD
Phone
+49.30.45932000
Email
hetzer@dhzb.de
First Name & Middle Initial & Last Name & Degree
Roland Hezter, MD
First Name & Middle Initial & Last Name & Degree
Boris Nasseri, MD
First Name & Middle Initial & Last Name & Degree
Sabine Huebler, MD
First Name & Middle Initial & Last Name & Degree
Semih Buz, MD
Facility Name
Hospital Clinico, University of Barcelona, Department of Cardiovascular Surgery
City
Barcelona
Country
Spain
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Carlos A. Mestres, MD, PhD
Phone
+34.93.2275515
Email
cmestres@clinic.ub.es
First Name & Middle Initial & Last Name & Degree
Carlos A. Mestres, MD, PhD
Facility Name
University Hospital of Geneva, Service for Cardiovascular Surgery
City
Geneva
ZIP/Postal Code
1211
Country
Switzerland
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Erman Pektok, MD
Phone
+41.76.3169990
Email
epektok@hotmail.com
First Name & Middle Initial & Last Name & Degree
Patrick O. Myers, MD
Phone
+41.22.3727630
Email
patrick.myers@hcuge.ch
First Name & Middle Initial & Last Name & Degree
Erman Pektok, MD
First Name & Middle Initial & Last Name & Degree
Patrick O. Myers, MD
First Name & Middle Initial & Last Name & Degree
Ebrahim Khabiri, MD
First Name & Middle Initial & Last Name & Degree
Mustafa Cikirikcioglu, MD, PhD
First Name & Middle Initial & Last Name & Degree
Pierre-Yves Martin, MD, PhD
First Name & Middle Initial & Last Name & Degree
Afksendiyos Kalangos, MD, PhD
Facility Name
Ankara University, Department of Cardiovascular Surgery
City
Ankara
ZIP/Postal Code
06340
Country
Turkey
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ruchan Akar, MD
Phone
+90.312.5082202
Email
akarruchan@gmail.com
First Name & Middle Initial & Last Name & Degree
Ruchan Akar, MD
First Name & Middle Initial & Last Name & Degree
Serkan Durdu, MD
First Name & Middle Initial & Last Name & Degree
Levent Yazicioglu, MD
First Name & Middle Initial & Last Name & Degree
Sim Kutlay, MD
First Name & Middle Initial & Last Name & Degree
Sadik Eryilmaz, MD
First Name & Middle Initial & Last Name & Degree
Mustafa Sirlak, MD
Facility Name
Pamukkale University, Department of Cardiovascular Surgery
City
Denizli
ZIP/Postal Code
20070
Country
Turkey
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gokhan Onem, MD
Phone
+90.258.4440728
Ext
2294
Email
gonem@pau.edu.tr
First Name & Middle Initial & Last Name & Degree
Gokhan Onem, MD
First Name & Middle Initial & Last Name & Degree
Mustafa Sacar, MD
First Name & Middle Initial & Last Name & Degree
Belda Dursun, MD
Facility Name
Gaziantep University, Department of Cardiovascular Surgery
City
Gaziantep
ZIP/Postal Code
27310
Country
Turkey
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hasim Ustunsoy, MD
Phone
+90.342.3603910
Email
hustunsoy@yahoo.com
First Name & Middle Initial & Last Name & Degree
Hasim Ustunsoy, MD
First Name & Middle Initial & Last Name & Degree
Celaleddin Usalan, MD
First Name & Middle Initial & Last Name & Degree
Oktay Burma, MD

12. IPD Sharing Statement

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Preop Hemodialysis or Intraop Ultrafiltration for Patients With Severe Renal Dysfunction Undergoing Open Heart Surgery

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