Ignite Creation Date:
2024-05-06 @ 6:07 PM
Last Modification Date:
2024-10-26 @ 2:42 PM
Study NCT ID:
NCT05553821
Status:
COMPLETED
Last Update Posted:
2022-09-23
First Post:
2022-04-14
Brief Title:
Effect of Cold Pressure in the Prevention of Hematoma and Ecchymosis
Sponsor:
Eskisehir Osmangazi University
Organization:
Eskisehir Osmangazi University
Study Overview
Official Title:
Evaluation of the Effect of Cold Pressure Application in the Prevention of Hematoma and Ecchymosis After Percutan Coronary Intervention
Status:
COMPLETED
Status Verified Date:
2022-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Coronary Artery Disease CAD is the most common cardiovascular system disease According to the World Health Organization data CAD ranks first among the top 10 causes of death According to the 2014 data of the Turkish Statistical Institute TUIK deaths due to circulatory system diseases are in the first place with 404 and 396 of this is ischemic heart diseases The prevalence of CAD in Turkey is 12 in women and 14 in men The diagnosis of CAD is largely made on non-invasive tests Coronary angiography CAG is recommended for definitive diagnosis and detection of coronary stenosis CAG is defined as the manual delivery of contrast material through a catheter sent to the coronary arteries under fluoroscopy and recording the resulting image on a CD With special catheters advanced through a plastic sheath called a sheath placed in the access tract contrast agents are administered separately to the left main coronary LDA and right main coronary arteries RCA and images of the coronary arteries are taken in multiple positions
Complications related to diagnostic and therapeutic CAG are rare but vary according to the patients condition operators experience and the type of procedure The most common vascular complications are bleeding hematoma ecchymosis pseudoaneurysm retroperitoneal hemorrhage arteriovenous fistula Preventing complications before they develop is actually shown as the most successful treatment For this reason it is recommended to use a small-diameter catheter during CAG to enter the main femoral artery carefully to interrupt anticoagulant treatment before the procedure to apply manual compression to the area for at least 20 minutes after the procedure and to use percutaneous closure devices which is another method After the procedure pressure is applied with a sandbag manual compression and a pneumatic compression device In the sandbag method a 3-45 kg sandbag is placed after the bleeding is controlled by manual pressure on the femoral region where the intervention is made During this period the patients movements are restricted and he is asked to lie flat on his back In the use of the pneumatic compression device a pneumatic compression device closepad with a transparent window and balloon incision is placed to maintain the compression on the femoral artery after a short period of manual compression However it is not preferred because of the risk of embolism and high cost
In addition to pressure applications local cold application is effective in preventing perivascular complications Cold application controls bleeding by reducing capillary blood flow and capillary permeability by vasoconstriction of arterioles In addition it reduces the flow rate of the blood and increases its viscosity thereby making it coagulate It controls bleeding by blood coagulation reduced capillary permeability and metabolic requirements This situation reduces the development of ecchymosis and hematoma Considering this information cold application can be preferred for the prevention of hematoma and ecchymosis which are the most common complications after CAG because it is practical inexpensive and comfort-enhancing The number of studies in the literature in which cold application and pressure application are used together is limited Based on this information the current study was planned to evaluate the effectiveness of cold pressure application for the prevention of hematoma and ecchymosis in the CAG intervention area The hypotheses of the research H0 Cold pressure application has no effect on the prevention of hematoma and ecchymosis in the CAG intervention area
H1 Cold pressure application has an effect on the prevention of hematoma and ecchymosis in the CAG intervention area
Complications related to diagnostic and therapeutic CAG are rare but vary according to the patients condition operators experience and the type of procedure The most common vascular complications are bleeding hematoma ecchymosis pseudoaneurysm retroperitoneal hemorrhage arteriovenous fistula Preventing complications before they develop is actually shown as the most successful treatment For this reason it is recommended to use a small-diameter catheter during CAG to enter the main femoral artery carefully to interrupt anticoagulant treatment before the procedure to apply manual compression to the area for at least 20 minutes after the procedure and to use percutaneous closure devices which is another method After the procedure pressure is applied with a sandbag manual compression and a pneumatic compression device In the sandbag method a 3-45 kg sandbag is placed after the bleeding is controlled by manual pressure on the femoral region where the intervention is made During this period the patients movements are restricted and he is asked to lie flat on his back In the use of the pneumatic compression device a pneumatic compression device closepad with a transparent window and balloon incision is placed to maintain the compression on the femoral artery after a short period of manual compression However it is not preferred because of the risk of embolism and high cost
In addition to pressure applications local cold application is effective in preventing perivascular complications Cold application controls bleeding by reducing capillary blood flow and capillary permeability by vasoconstriction of arterioles In addition it reduces the flow rate of the blood and increases its viscosity thereby making it coagulate It controls bleeding by blood coagulation reduced capillary permeability and metabolic requirements This situation reduces the development of ecchymosis and hematoma Considering this information cold application can be preferred for the prevention of hematoma and ecchymosis which are the most common complications after CAG because it is practical inexpensive and comfort-enhancing The number of studies in the literature in which cold application and pressure application are used together is limited Based on this information the current study was planned to evaluate the effectiveness of cold pressure application for the prevention of hematoma and ecchymosis in the CAG intervention area The hypotheses of the research H0 Cold pressure application has no effect on the prevention of hematoma and ecchymosis in the CAG intervention area
H1 Cold pressure application has an effect on the prevention of hematoma and ecchymosis in the CAG intervention area
Detailed Description:
MATERIALS AND METHODS Purpose and type of research This study was planned as a randomized controlled intervention study to evaluate the effect of local cold pressure application on the prevention of hematoma and ecchymosis in patients undergoing CAG via the femoral artery
Dependent independent and control variables of the study
Dependent variables The dependent variable of this study is the development of bleeding hematoma and ecchymosis pain after CAG
Independent variables Application of cold pressure applied to patients Control variables Patients age gender type of procedure blood pressure thrombocyte Pt Ptz INR values heparin dose administered during CAG 60 IUkg Place and time of research The research will be carried out in Eskişehir City Hospital Cardiology and Coronary Intensive Care 12 services between Nowember 01 2021 and June 01 2022
Eskişehir City Hospital Cardiology Service It started to serve in October 2018 In the 24-bed cardiology service patients with diagnoses such as heart failure rhythm disorder and chest pain are generally hospitalized The number of physicians is 10 The number of nurses is 11
Eskişehir City Hospital Coronary ICU 1 Service It started to serve in October 2019 In the 8-bed Coronary Intensive Care 1 Service patients with diagnoses such as heart failure arrhythmia chest pain are generally hospitalized The number of physicians is 10 The number of nurses is 10
Eskişehir City Hospital Coronary ICU and 2 Service It started to serve in November 2018 In the 10-bed cardiology service patients with diagnoses such as heart failure arrhythmia chest pain are generally hospitalized The number of physicians is 10 The number of nurses is 15
The standard CAG procedure treatment and follow-up process applied to all patients in Eskişehir City Hospital Cardiology and Coronary Intensive Care 12 services are as follows Standard monitoring and care
It is questioned whether the patient has antiplatelet and anticoagulant use
The patient who comes to the Angio laboratory is monitored by the nurse Vital signs are recorded At the same time the patient is connected to a defibrillator and defibrillation is provided in case of fatal rhythm
Under local anesthesia an incision is made in the intervention area by the physician sheath is advanced to the femoral artery and the coronary arteries are visualized by means of radiopaque material
When occlusion or stenosis in the coronary arteries is seen by the physician balloon andor stent operation is performed During these procedures clarification is provided by using drugs such as heparin perliganit clotinab Sheat extraction is done at the time prescribed by the physician
If the coronary arteries are seen as open sheath is removed and the patient is brought to the service or intensive care unit
After sheat extraction manual compression is done for a minimum of 15 minutes
Rolled gauze with a diameter of 5 cm is placed on the intervention area
A sandbag is placed on the patients intervention area and immobilized The sandbag is kept in the intervention area for 4 hours
The patient whose CAG procedure is completed is taken to the bed in the ICU or the ward by the nurse his vital signs are evaluated an EKG is taken and the rhythm is followed
The intervention area is checked hourly by the nurse in terms of vascular complications pulse temperature color change
The time of sheat extraction and sandbag removal vascular complications in the intervention area and vital signs are recorded by the nurse
The treatment ordered by the doctor is applied The universe and sample of the research The population of the study is the patients who were followed up after CAG in Eskişehir City Hospital Cardiology Service and Coronary Intensive Care 12 Services The sample is the patients who meet the sample selection criteria within the specified population Sample selection criteria
over 18 years old
Conscious
Patients who underwent CAG for the first time andor did not undergo CAG in the last 1 year it is stated that the recovery period in the femoral intervention area after CAG is completed in 3 months 54 Based on this information in the study patients who had CAG before had at least 1 year from CAG criteria have been determined
Platelet values within normal limits
Patients treated with 10000 units or less of heparin during angiography Exclusion criteria from the study
Patients who do not agree to participate in the study andor want to exit the study while continuing the research
Those who developed vascular complications in the region before sheat extraction
Those who routinely use anticoagulant drugs
Those receiving antithrombotic drug clotinab treatment
Those with peripheral vascular disease In determining the number of samples in the study the sample number was calculated as 210 units 105 units in the SBG group and 105 units in the NBG based on the results of the study conducted by Güleser 201155 Data collection method The patients who meet the sampling criteria within the scope of the study will be informed verbally and in writing by the researcher before the CAG procedure and the Voluntary Consent Form prepared by the researcher will be signed Appendix-1 The Individual Identification Form will be filled in by using face-to-face interview technique for all patients Within the scope of the study the randomization of the patients who meet the sample selection criteria will be made by an expert independent of the research using the random numbers method obtained on the computer into two groups cold pressure group SBG and normal pressure group NBG The specialist will deliver the registration order and the group numbers of the patients in a sealed envelope to the researcher who performed the application
Procedure In addition to the standard treatment follow-up and care applied for CAG in Eskişehir City Hospital Cardiology and Coronary Intensive Care services the steps to be applied for SBG and NBG patients during the research are as follows Cold pressure application The following procedures will be applied to the patients in the cold pressure application group
The temperature of the cold sandbag to be applied to SBG patients will be kept at 18-20 C For this a sandbag will be placed in the freezer of the refrigerator in the clinic at least 2 hours in advance
The surface temperature measurement of the cold sandbag taken out of the freezer will be checked with the surface mode of the thermometer and processed into the KAG follow-up form In the preliminary application made by us regarding this process the temperature of the sandbag remaining in the freezer for 2 hours and then removed is 181 C in the 0th minute 10 193 C per minute It was determined that it was 195 C in the 20th minute
Cold pressure will be applied for 20 minutes by placing a cold sandbag on the patients intervention area 5657
After 20 minutes a cold ice pack will be removed and a room temperature sand bag will be placed The sandbag at room temperature will be kept in the intervention area for 3 hours and 40 minutes
Normal pressure application The following steps will be applied to the patients in the normal pressure application group
The sandbag to be used for NBG patients will be kept at room temperature and the surface temperature measurement of the sandbag will be evaluated with the surface mode of the thermometer The detected heat will be recorded on the KAG tracking form
Pressure will be applied to the intervention area of the patients by placing a sand bag at room temperature for 4 hours
During the study the treatment plan determined by the doctor will be applied to both groups of patients as specified and no changes will be made in the treatment plan Pressure will be applied to both groups of patients for 4 hours and cold pressure will be applied only to SBG patients for the first 20 minutes The CAG intervention area of all groups will be monitored and recorded for 24 hours with the CAG follow-up form According to the CAG follow-up form in both groups of patients
Vital sign monitoring every 15 minutes for the first hour
Bleeding hematoma ecchymosis pain in the intervention area will be monitored every hour and every 6 hours for the first 6 hours
Data collection tools Patient identification form Appendix-2 In the form developed by the researchers according to the literature there are 13 questions including sociodemographic and disease characteristics 58
CAG follow-up form Appendix-3 In the form developed by the researchers according to the literature there are 12 questions regarding the CAG procedure and post-CAG follow-up peripheral pulse follow-up peripheral temperature and color change follow-up bleeding ecchymosis hematoma and pain 59
Sandbag A sandbag with a height of 23 cm a width of 14 cm and a weight of 5 kg will be used
Surface heat meter It will be measured with the surface mode of Merk brand thermometer
Roll bandage 5 cm diameter roll gauze will be used Patch It will be used as 10 cm wide and 35 cm long Analysis of data The data obtained from the patient identification form and CAG follow-up form will be analyzed and reported by a biostatistician independent of the research Parametric and non-parametric tests will be used in the analysis
Research endpoint The study is planned to be completed with a total of 210 patients with at least 105 in each group When this planned number is reached the research will end and will take approximately one year
Ethical approval of the research Before starting the research written permission will be obtained from the Eskişehir Osmangazi University Clinical Research Ethics Committee and from the Eskişehir City Hospital where the research will be conducted Written informed consent will be obtained from patients who want to participate in the study
Dependent independent and control variables of the study
Dependent variables The dependent variable of this study is the development of bleeding hematoma and ecchymosis pain after CAG
Independent variables Application of cold pressure applied to patients Control variables Patients age gender type of procedure blood pressure thrombocyte Pt Ptz INR values heparin dose administered during CAG 60 IUkg Place and time of research The research will be carried out in Eskişehir City Hospital Cardiology and Coronary Intensive Care 12 services between Nowember 01 2021 and June 01 2022
Eskişehir City Hospital Cardiology Service It started to serve in October 2018 In the 24-bed cardiology service patients with diagnoses such as heart failure rhythm disorder and chest pain are generally hospitalized The number of physicians is 10 The number of nurses is 11
Eskişehir City Hospital Coronary ICU 1 Service It started to serve in October 2019 In the 8-bed Coronary Intensive Care 1 Service patients with diagnoses such as heart failure arrhythmia chest pain are generally hospitalized The number of physicians is 10 The number of nurses is 10
Eskişehir City Hospital Coronary ICU and 2 Service It started to serve in November 2018 In the 10-bed cardiology service patients with diagnoses such as heart failure arrhythmia chest pain are generally hospitalized The number of physicians is 10 The number of nurses is 15
The standard CAG procedure treatment and follow-up process applied to all patients in Eskişehir City Hospital Cardiology and Coronary Intensive Care 12 services are as follows Standard monitoring and care
It is questioned whether the patient has antiplatelet and anticoagulant use
The patient who comes to the Angio laboratory is monitored by the nurse Vital signs are recorded At the same time the patient is connected to a defibrillator and defibrillation is provided in case of fatal rhythm
Under local anesthesia an incision is made in the intervention area by the physician sheath is advanced to the femoral artery and the coronary arteries are visualized by means of radiopaque material
When occlusion or stenosis in the coronary arteries is seen by the physician balloon andor stent operation is performed During these procedures clarification is provided by using drugs such as heparin perliganit clotinab Sheat extraction is done at the time prescribed by the physician
If the coronary arteries are seen as open sheath is removed and the patient is brought to the service or intensive care unit
After sheat extraction manual compression is done for a minimum of 15 minutes
Rolled gauze with a diameter of 5 cm is placed on the intervention area
A sandbag is placed on the patients intervention area and immobilized The sandbag is kept in the intervention area for 4 hours
The patient whose CAG procedure is completed is taken to the bed in the ICU or the ward by the nurse his vital signs are evaluated an EKG is taken and the rhythm is followed
The intervention area is checked hourly by the nurse in terms of vascular complications pulse temperature color change
The time of sheat extraction and sandbag removal vascular complications in the intervention area and vital signs are recorded by the nurse
The treatment ordered by the doctor is applied The universe and sample of the research The population of the study is the patients who were followed up after CAG in Eskişehir City Hospital Cardiology Service and Coronary Intensive Care 12 Services The sample is the patients who meet the sample selection criteria within the specified population Sample selection criteria
over 18 years old
Conscious
Patients who underwent CAG for the first time andor did not undergo CAG in the last 1 year it is stated that the recovery period in the femoral intervention area after CAG is completed in 3 months 54 Based on this information in the study patients who had CAG before had at least 1 year from CAG criteria have been determined
Platelet values within normal limits
Patients treated with 10000 units or less of heparin during angiography Exclusion criteria from the study
Patients who do not agree to participate in the study andor want to exit the study while continuing the research
Those who developed vascular complications in the region before sheat extraction
Those who routinely use anticoagulant drugs
Those receiving antithrombotic drug clotinab treatment
Those with peripheral vascular disease In determining the number of samples in the study the sample number was calculated as 210 units 105 units in the SBG group and 105 units in the NBG based on the results of the study conducted by Güleser 201155 Data collection method The patients who meet the sampling criteria within the scope of the study will be informed verbally and in writing by the researcher before the CAG procedure and the Voluntary Consent Form prepared by the researcher will be signed Appendix-1 The Individual Identification Form will be filled in by using face-to-face interview technique for all patients Within the scope of the study the randomization of the patients who meet the sample selection criteria will be made by an expert independent of the research using the random numbers method obtained on the computer into two groups cold pressure group SBG and normal pressure group NBG The specialist will deliver the registration order and the group numbers of the patients in a sealed envelope to the researcher who performed the application
Procedure In addition to the standard treatment follow-up and care applied for CAG in Eskişehir City Hospital Cardiology and Coronary Intensive Care services the steps to be applied for SBG and NBG patients during the research are as follows Cold pressure application The following procedures will be applied to the patients in the cold pressure application group
The temperature of the cold sandbag to be applied to SBG patients will be kept at 18-20 C For this a sandbag will be placed in the freezer of the refrigerator in the clinic at least 2 hours in advance
The surface temperature measurement of the cold sandbag taken out of the freezer will be checked with the surface mode of the thermometer and processed into the KAG follow-up form In the preliminary application made by us regarding this process the temperature of the sandbag remaining in the freezer for 2 hours and then removed is 181 C in the 0th minute 10 193 C per minute It was determined that it was 195 C in the 20th minute
Cold pressure will be applied for 20 minutes by placing a cold sandbag on the patients intervention area 5657
After 20 minutes a cold ice pack will be removed and a room temperature sand bag will be placed The sandbag at room temperature will be kept in the intervention area for 3 hours and 40 minutes
Normal pressure application The following steps will be applied to the patients in the normal pressure application group
The sandbag to be used for NBG patients will be kept at room temperature and the surface temperature measurement of the sandbag will be evaluated with the surface mode of the thermometer The detected heat will be recorded on the KAG tracking form
Pressure will be applied to the intervention area of the patients by placing a sand bag at room temperature for 4 hours
During the study the treatment plan determined by the doctor will be applied to both groups of patients as specified and no changes will be made in the treatment plan Pressure will be applied to both groups of patients for 4 hours and cold pressure will be applied only to SBG patients for the first 20 minutes The CAG intervention area of all groups will be monitored and recorded for 24 hours with the CAG follow-up form According to the CAG follow-up form in both groups of patients
Vital sign monitoring every 15 minutes for the first hour
Bleeding hematoma ecchymosis pain in the intervention area will be monitored every hour and every 6 hours for the first 6 hours
Data collection tools Patient identification form Appendix-2 In the form developed by the researchers according to the literature there are 13 questions including sociodemographic and disease characteristics 58
CAG follow-up form Appendix-3 In the form developed by the researchers according to the literature there are 12 questions regarding the CAG procedure and post-CAG follow-up peripheral pulse follow-up peripheral temperature and color change follow-up bleeding ecchymosis hematoma and pain 59
Sandbag A sandbag with a height of 23 cm a width of 14 cm and a weight of 5 kg will be used
Surface heat meter It will be measured with the surface mode of Merk brand thermometer
Roll bandage 5 cm diameter roll gauze will be used Patch It will be used as 10 cm wide and 35 cm long Analysis of data The data obtained from the patient identification form and CAG follow-up form will be analyzed and reported by a biostatistician independent of the research Parametric and non-parametric tests will be used in the analysis
Research endpoint The study is planned to be completed with a total of 210 patients with at least 105 in each group When this planned number is reached the research will end and will take approximately one year
Ethical approval of the research Before starting the research written permission will be obtained from the Eskişehir Osmangazi University Clinical Research Ethics Committee and from the Eskişehir City Hospital where the research will be conducted Written informed consent will be obtained from patients who want to participate in the study
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None