Alterations of Blood Clotting With the Use of Sequential Compression Devices on the Lower Limbs (TEGLeg)
Primary Purpose
Coagulation, Blood, Compression Devices, Intermittent Pneumatic, Postoperative Complications
Status
Terminated
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Sequential compression device therapy
Dalteparin
TEG
Sponsored by
About this trial
This is an interventional diagnostic trial for Coagulation, Blood focused on measuring Disorders, Blood coagulation, Deep Vein Thrombosis, Perioperative Care, Digestive System Surgical Procedures
Eligibility Criteria
Inclusion Criteria:
- Elective major abdominal surgery for neoplasm
Planned admission to postsurgical ICU due to the patient's meeting one or more of the following:
- ASA Physical Status Class 4
- Surgery of modified Johns-Hopkins class ≥IV
- ASA 3 with modified Johns-Hopkins class 3 surgery
- Expected duration of surgery ≥8 h
Exclusion Criteria:
- History of coagulation abnormalities, either congenital or acquired
- Ongoing treatment with anticoagulants/antiplatelet agents other than LMWH or hormones
- Massive edema of the legs
- Severe peripheral arteriopathy or neuropathy
- Malformations or recent surgery/trauma to the lower extremities
Sites / Locations
- University Hospital / Azienda Ospedaliero-Universitaria
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
SCD + LMWH
LMWH only
Arm Description
This group will receive sequential compression device therapy to the lower limbs from their ICU admission until the morning after surgery.
Patients in this group will receive only standard LMWH therapy during their ICU stay.
Outcomes
Primary Outcome Measures
Reduction in the area under the curve of maximum amplitude (MA) TEG value over time
Secondary Outcome Measures
Reduction in the area under the curve of the r time TEG value over time
Reduction in the area under the curve of the alpha angle TEG value over time
Incidence of hypotension (mean arterial pressure ≤60 mmHg)
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00726570
Brief Title
Alterations of Blood Clotting With the Use of Sequential Compression Devices on the Lower Limbs
Acronym
TEGLeg
Official Title
Effects of Sequential Compression Devices on Coagulation Parameters Assessed by TEG® in Patients Undergoing Major Abdominal Surgery
Study Type
Interventional
2. Study Status
Record Verification Date
November 2013
Overall Recruitment Status
Terminated
Why Stopped
Failed to reach the expected enrollment rates by the end of 2010
Study Start Date
August 2008 (undefined)
Primary Completion Date
November 2010 (Actual)
Study Completion Date
November 2010 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Parma
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study aims to assess possible alteration in coagulation (blood clotting) following treatment with sequential compression devices (SCD) plus low-molecular weight heparin (LMWH) as opposed to LMWH alone.
The investigators will examine coagulation in the early postoperative period of patients undergoing major abdominal surgery during their stay in our Intensive Care Unit.
In addition to common laboratory tests, the investigators will examine coagulation using TEG®, a device which allows a semi-quantitative examination of all phases of coagulation.
Detailed Description
Low molecular weight heparins (LMWH) are routinely used in perioperative prophylaxis of thromboembolic complications [(chiefly deep vein thrombosis (DVT)]. LMWHs have been proved to be safe and equipotent or superior when compared with unfractionated heparin.
Sequential compressing devices (SCD) are relatively novel pneumatic stockings with several air chambers. A computerized pump applies a gradient of pressure which decreases from the foot cranially. Pressure is also applied intermittently according to predetermined schedules. This devices are being employed for DVT prophylaxis in patients for whom anticoagulation therapy is contraindicated, or in those who have a low risk of DVT. They have also been employed to complement anticoagulant therapy in patients at high risk of DVT, such as those undergoing orthopedic surgery (Fordyce, 1992; Handoll, 2002; Warwick, 2002; Pitto, 2004).
The mechanism of action of SCD seems to be primarily mechanical, through a displacement of a column of blood through the venous system and towards the heart; they act as a surrogate of the muscular pump in immobilized patients (Killewich, 1995).
There is also some evidence that SCD activity may influence the coagulation/fibrinolysis system towards hypocoagulability (Dai, 2000; Kohro, 2003); Kohro and colleagues have also hypothesized that the shear forces generated by SCD may alter platelet adhesion by a direct effect on platelets and/or by increasing the release of factors from the venous endothelium (Kohro, 2005).
The investigators aim to assess the effects on coagulation when SCD are applied to patients at high risk of DVT in addition to standard LMWH therapy.The investigators chose to study a population in whom SCD may be useful in reducing the incidence of DVT, such as patients undergoing postoperative monitoring in the intensive care unit (ICU) after major abdominal surgery for cancer.
In addition to standard laboratory tests, the investigators will use thrombelastography (TEG®) to assess all phases of coagulation. A TEG parameter, maximum amplitude (MA), has been linked to an increase of thrombotic complications in a postoperative population (McCrath, 2005).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coagulation, Blood, Compression Devices, Intermittent Pneumatic, Postoperative Complications, Thrombelastography
Keywords
Disorders, Blood coagulation, Deep Vein Thrombosis, Perioperative Care, Digestive System Surgical Procedures
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Actual)
8. Arms, Groups, and Interventions
Arm Title
SCD + LMWH
Arm Type
Experimental
Arm Description
This group will receive sequential compression device therapy to the lower limbs from their ICU admission until the morning after surgery.
Arm Title
LMWH only
Arm Type
Active Comparator
Arm Description
Patients in this group will receive only standard LMWH therapy during their ICU stay.
Intervention Type
Device
Intervention Name(s)
Sequential compression device therapy
Other Intervention Name(s)
SCD EXPRESS, Foot pump
Intervention Description
Pneumatic stockings will be applied to patients.
Pressures ranging from 12 to 40 mmHg will be applied at different levels of the lower limb for 40-second cycles at 2-minute intervals. Therapy will continue until the morning after surgery.
Intervention Type
Drug
Intervention Name(s)
Dalteparin
Other Intervention Name(s)
low molecular weight heparin, Fragmin, heparin, thromboprophylaxis, anticoagulant, LMWH
Intervention Description
2500 UI qd if ≤ 50 kg body weight
5000 UI qd if > 50 kg
Intervention Type
Procedure
Intervention Name(s)
TEG
Other Intervention Name(s)
thrombelastography, TEG®, thrombelastogram
Intervention Description
A 2-ml blood sample will be used for each exam. A full analysis will be run both with and without heparinase at each time point.
TEG analyses will be run at:
Patient admission (before SCD start)
40-60 min after admission
Morning after surgery
Primary Outcome Measure Information:
Title
Reduction in the area under the curve of maximum amplitude (MA) TEG value over time
Time Frame
24 hours from application of SCD
Secondary Outcome Measure Information:
Title
Reduction in the area under the curve of the r time TEG value over time
Time Frame
24 h after application of SCD
Title
Reduction in the area under the curve of the alpha angle TEG value over time
Time Frame
24 h after application of SCD
Title
Incidence of hypotension (mean arterial pressure ≤60 mmHg)
Time Frame
≤24 h after application of SCD
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Elective major abdominal surgery for neoplasm
Planned admission to postsurgical ICU due to the patient's meeting one or more of the following:
ASA Physical Status Class 4
Surgery of modified Johns-Hopkins class ≥IV
ASA 3 with modified Johns-Hopkins class 3 surgery
Expected duration of surgery ≥8 h
Exclusion Criteria:
History of coagulation abnormalities, either congenital or acquired
Ongoing treatment with anticoagulants/antiplatelet agents other than LMWH or hormones
Massive edema of the legs
Severe peripheral arteriopathy or neuropathy
Malformations or recent surgery/trauma to the lower extremities
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Guido Fanelli, MD
Organizational Affiliation
University of Parma
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Maria Barbagallo, MD
Organizational Affiliation
UO II Anestesia e Rianimazione, Azienda Ospedaliero-Universitaria di Parma
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital / Azienda Ospedaliero-Universitaria
City
Parma
State/Province
PR
ZIP/Postal Code
43100
Country
Italy
12. IPD Sharing Statement
Citations:
PubMed Identifier
1732264
Citation
Fordyce MJ, Ling RS. A venous foot pump reduces thrombosis after total hip replacement. J Bone Joint Surg Br. 1992 Jan;74(1):45-9. doi: 10.1302/0301-620X.74B1.1732264.
Results Reference
background
PubMed Identifier
12519540
Citation
Handoll HH, Farrar MJ, McBirnie J, Tytherleigh-Strong G, Milne AA, Gillespie WJ. Heparin, low molecular weight heparin and physical methods for preventing deep vein thrombosis and pulmonary embolism following surgery for hip fractures. Cochrane Database Syst Rev. 2002;(4):CD000305. doi: 10.1002/14651858.CD000305.
Results Reference
background
PubMed Identifier
12002490
Citation
Warwick D, Harrison J, Whitehouse S, Mitchelmore A, Thornton M. A randomised comparison of a foot pump and low-molecular-weight heparin in the prevention of deep-vein thrombosis after total knee replacement. J Bone Joint Surg Br. 2002 Apr;84(3):344-50. doi: 10.1302/0301-620x.84b3.12372.
Results Reference
background
PubMed Identifier
15274256
Citation
Pitto RP, Hamer H, Heiss-Dunlop W, Kuehle J. Mechanical prophylaxis of deep-vein thrombosis after total hip replacement a randomised clinical trial. J Bone Joint Surg Br. 2004 Jul;86(5):639-42. doi: 10.1302/0301-620x.86b5.14763.
Results Reference
background
PubMed Identifier
7494362
Citation
Killewich LA, Sandager GP, Nguyen AH, Lilly MP, Flinn WR. Venous hemodynamics during impulse foot pumping. J Vasc Surg. 1995 Nov;22(5):598-605. doi: 10.1016/s0741-5214(95)70046-3. Erratum In: J Vasc Surg 1996 Feb;23(2):240.
Results Reference
background
PubMed Identifier
11054230
Citation
Dai G, Tsukurov O, Orkin RW, Abbott WM, Kamm RD, Gertler JP. An in vitro cell culture system to study the influence of external pneumatic compression on endothelial function. J Vasc Surg. 2000 Nov;32(5):977-87. doi: 10.1067/mva.2000.110357.
Results Reference
background
PubMed Identifier
12911214
Citation
Kohro S, Yamakage M, Takahashi T, Ota K, Kondo M, Namiki A. Effects of intermittent pneumatic foot compression on blood coagulability and fibrinolysis assessed by a whole blood viscometer Sonoclot. J Anesth. 2003;17(3):208-10. doi: 10.1007/s00540-003-0180-x. No abstract available.
Results Reference
background
PubMed Identifier
15836680
Citation
Kohro S, Yamakage M, Sato K, Sato JI, Namiki A. Intermittent pneumatic foot compression can activate blood fibrinolysis without changes in blood coagulability and platelet activation. Acta Anaesthesiol Scand. 2005 May;49(5):660-4. doi: 10.1111/j.1399-6576.2005.00661.x.
Results Reference
background
PubMed Identifier
15920177
Citation
McCrath DJ, Cerboni E, Frumento RJ, Hirsh AL, Bennett-Guerrero E. Thromboelastography maximum amplitude predicts postoperative thrombotic complications including myocardial infarction. Anesth Analg. 2005 Jun;100(6):1576-1583. doi: 10.1213/01.ANE.0000155290.86795.12.
Results Reference
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Alterations of Blood Clotting With the Use of Sequential Compression Devices on the Lower Limbs
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