Track topics on Twitter Track topics that are important to you
USF Hemostasis - USage of HemCon for Femoral Hemostasis after Percutaneous Procedures. A Comparative Open Label Study The purpose of this trial is to test HemCon pad after diagnostic percutaneous coronary angiography as an adjunct to manual compression to better control vascular access site bleeding and reduce time-to-hemostasis.
We hypothesize that the use of HemCon bandage (containing a carbohydrate called chitosan, found in the shells of shrimp, lobster and beetles) will shorten the time needed to achieve hemostasis, time to patient's ambulation, and patient's satisfaction without increasing vascular complications.
278 patients undergoing diagnostic coronary angiography receiving 2500 u intravenous Heparin will be studied and randomized for manual homeostasis with either a HemCon or a regular pad. Primary efficacy endpoint will be time to hemostasis. Secondary endpoints will be safety (complication rate) and satisfaction of patients regarding time to sitting incline and time to ambulation. 25% of patients from each arm will be randomized for Duplex examination of the femoral artery at the access site.
USF Hemostasis USage of HemCon for Femoral Hemostasis after Percutaneous Procedures A Comparative Open Label Study Introduction After completion of angiography performed via the femoral artery, hemostasis is achieved by applying local pressure either manually or by mechanical devices for 10-20 minutes. This is time consuming for the physician, uncomfortable for the patient and occasionally complicated with vascular events that increase morbidity and hospital duration and reduce patient satisfaction. Closure devices have been developed to shorten pressure time but they are costly.
The HemCon pad is composed of a bandage containing a carbohydrate called chitosan, found in the shells of shrimp, lobster and beetles. Its molecules are positively charged and attract the negatively charged blood cells and platelets, and thus promote clotting. Chitosan hemorrhage control dressings have been shown to be effective in animal models of severe hemorrhage (1-4). Bandage. U.S. military personnel in the Iraquean and Afghanistan conflicts have used the HemCon Bandage to successfully stop arterial hemorrhage not controlled by conventional bandages in more then 64 patients without adverse effects (3,5). The HemCon bandage is also an FDA-cleared hemostatic dressing suitable for use in hemodialysis access puncture (2).
The purpose of this trial is to test HemCon pad after diagnostic percutaneous coronary angiography as an adjunct to manual compression to better control vascular access site bleeding and reduce time-to-hemostasis.
We hypothesize that the use of HemCon bandage will shorten the time needed to achieve hemostasis, time to patient's ambulation, and patient's satisfaction without increasing vascular complications.
Endpoints Primary endpoint
- Compare efficacy (time to hemostasis) of HemCon to regular pads Secondary endpoints
- Compare efficacy (time to ambulation) of HemCon to regular pads
- Compare safety (complication rate) of HemCon to regular pads using a protocol of shorter time to ambulation with the HemCon pad.
- Compare satisfaction of patients regarding time to sitting incline and time to ambulation.
Patients 278 patients undergoing diagnostic coronary angiography receiving 2500 u intravenous Heparin will be studied and randomized as written hereinafter.
- Age 18-80 years old
- Signing an informed consent
- Percutaneous coronary angiography with a 6 french sheath via the femoral artery
- Post catheterization non-invasive systolic blood pressure 150 mm Hg
- Patients who received IIb-IIIa antagonists before or during angiography.
- Patients who received more than 2500u IV Heparin or more than 0.5 mg/kg LMWH within 8 hours before the procedure.
- Known bleeding tendency, disturbed clotting system or platelet function
- Evidence of bleeding or hematoma at the access site prior to sheath removal.
All patients will receive IV 2500 u Heparin immediately after introducing the femoral sheath.
- Procedure duration:
Procedure duration will be recorded in minutes.
A 1:1 randomization of HemCon and regular pad will be performed after completion of the procedure. Envelopes marked with consecutive numbers will contain a note written: "HemCon pad" or "Regular pad ". Notes content will be randomized by a computer program.
After the procedure is completed and a decision is taken to withdraw the sheath the next consecutive envelope will be opened to determine the sheath removal technique to be used.
- Arterial sheath removal:
1. The femoral sheath will be removed at the patient's bed (and not on the angiography table). One ml of blood will be allowed to flow from the access site. A HemCon or a regular pad (according to randomization) will be applied manually with occlusive pressure for 5 minutes.
2. After 5 minutes the operator will release the pressure. If bleeding continues, application of local pressure will be resumed. After this stage, the operator is allowed to release the pressure after every 5 minutes or longer at the operator's discretion. The total numbers of pressure release and the total time to hemostasis will be recorded.
3. After achieving hemostasis a pressure bandage will be applied at the access site for 3 hours.
1. Minimal bed rest duration will be 2 hours. Longer bed rest duration in increments of 30 minutes will be decided at the operator's discretion according to hemostasis. Total bed rest time will be recorded.
2. During bed rest the operator may allow the patient to sit up in 450 incline after 1 hour. Time to sitting up will be recorded.
3. If hematoma occurs, it will be evaluated by palpation and diameter measurement will be recorded.
After bed rest, ambulation is allowed providing no confounding events such as blood pressure abnormalities and hematoma have developed.
- In hospital follow-up:
1. A duplex examination of the femoral artery at the access site will be performed at the operator's discretion.
2. One day after the procedure patient's complaints and physical findings will be recorded.
3. Blood count will be taken from all patients on the day after the procedure. Earlier blood count and other blood examinations may be taken at the operator's discretion and will be recorded.
The patient will be discharged at the operator's discretion. Complications or adverse events will be noted and recorded upon discharge.
• Out of hospital and patient's satisfaction follow up: One day after discharge the patient will be contacted by phone and asked for any procedural complications (groin pain, hematoma) that appeared after discharge. If needed, the patient will be invited to the hospital for further investigation.
During the phone call the patient will be asked of his / her satisfaction of the ambulation procedure at a scale of 1-10 (10 mostly satisfactory).
The following data will be compared between the 2 groups using t-test:
- Time to hemostasis
- Duration of bed rest (total, supine position and incline sit-up position)
- Incidence of minor and major hematoma
- Hematoma size
- Post procedural stay at the hospital
- Level of satisfaction evidenced in post-procedure satisfaction surveys. The number of patients to be studied (278) was calculated with the assumption that the HemCon will achieve a decrease of 30% in hemostasis time (the primary endpoint), with alpha value of 0.05 and power of 0.8.
1. Pausateri AE, McCarthy SG, et al. Effect of chitosan-based hemostatic dressing on blood loss and survival in a model of severe venous hemorrhage and hepatic injury in swine. J Trauma. 2003;54:177-182.
2. Gustafson SB, Fulkerson P, et al. Chitosan dressing provides hemostasis in swine femoral arterial injury model. Prehospital emergency care. 2007;11: 172-178.
3. Wedmore I, McManus JG, et al. A special report on chitosan based hemostatic dressing: Experience in current combat operations. J Trauma. 2006;60:655- 658 .
Allocation: Randomized, Control: Placebo Control, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care
Meir Medical Center
Meir Medical Center
Published on BioPortfolio: 2014-08-27T03:29:03-0400
Patients planned for elective conventional coronary angiography will undergo CT coronary angiography (Dual Source CT) in order to assess the correlation of stenosis detection and therapeut...
The purpose of this study is to test the ability of a new X-ray technique called CT angiography to identify significant narrowing of the coronary arteries compared to traditional coronary ...
The purpose of this study is to determine if the HemCon Dental Dressing is effective in stopping bleeding during dental surgeries in patients taking anticoagulant medications.
The purpose of this study is to evaluate the radiation exposure in patients undergoing coronary angiography, and to identify reference values for the main radiation doses parameters.
The purpose of this study is to evaluate whether 64-slice CT coronary angiography is useful for rapid diagnosis or exclusion of significant coronary artery disease in patients who present ...
Heavy coronary artery calcification (CAC) impairs diagnostic accuracy of coronary computed tomography angiography (cCTA) and is considered to be a major limitation.
Invasive coronary angiography (ICA) with fractional flow reserve (FFR) assessment is the reference standard for the detection of hemodynamically relevant coronary lesions. We have investigated whether...
To prospectively evaluate the diagnostic performance of coronary CT angiography (CCTA) for the assessment of coronary stenosis in a calcified plaque, by using conventional coronary angiography (CAG) a...
CT Angiography for the Prediction of Hemodynamic Significance in Intermediate and Severe Lesions: Head-to-Head Comparison With Quantitative Coronary Angiography Using Fractional Flow Reserve as the Reference Standard.
The goal of this study was to compare the diagnostic performance of coronary computed tomography angiography (CTA) versus quantitative coronary angiography (QCA) for the detection of lesion-specific i...
Purpose To evaluate the diagnostic performance of self-navigated whole-heart coronary 3-T magnetic resonance (MR) angiography by using conventional invasive coronary angiography (ICA) as the reference...
Radiography of the vascular system of the heart muscle after injection of a contrast medium.
Abnormal balloon- or sac-like dilatation in the wall of CORONARY VESSELS. Most coronary aneurysms are due to CORONARY ATHEROSCLEROSIS, and the rest are due to inflammatory diseases, such as KAWASAKI DISEASE.
Malformations of CORONARY VESSELS, either arteries or veins. Included are anomalous origins of coronary arteries; ARTERIOVENOUS FISTULA; CORONARY ANEURYSM; MYOCARDIAL BRIDGING; and others.
Complete blockage of blood flow through one of the CORONARY ARTERIES, usually from CORONARY ATHEROSCLEROSIS.
Non-invasive method of vascular imaging and determination of internal anatomy without injection of contrast media or radiation exposure. The technique is used especially in CEREBRAL ANGIOGRAPHY as well as for studies of other vascular structures.
Radiology is the branch of medicine that studies imaging of the body; X-ray (basic, angiography, barium swallows), ultrasound, MRI, CT and PET. These imaging techniques can be used to diagnose, but also to treat a range of conditions, by allowing visuali...
Blood is a specialized bodily fluid that delivers necessary substances to the body's cells (in animals) – such as nutrients and oxygen – and transports waste products away from those same cells. In vertebrates, it is composed of blo...