Patients who underwent percutaneous coronary intervention to treat coronary heart diseases.. Ischemic heart diseases
Conditions
Interventions
Intervention 1: Intervention group: The questionnaire (which includes demographic and clinical data) will be given to the respondents as the first step in the intervention phase. After putting the pat
Sponsors
College of Nursing, University of Baghdad
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Male and female adults (18 years of age and older) who volunteered to participate in the study and signed a written consent form were eligible to be included. Patients who underwent a single-catheter coronary angioplasty through the femoral artery in the groin area. The participants had to read and write. They had not taken analgesics in the last few hours and were free from any hematoma or infection on the skin surrounding the sheath site.
Exclusion criteria
Exclusion criteria: If the subjects declined to participate, they were eliminated. If patients suffer from severe visual impairment, a changed mental state, skin conditions linked to cold sensitivity (such as Raynaud's disease), sensory-motor deficiency, diabetes, neuropathy, and scar tissue from burns, wounds, or other injuries surrounding the sheath site. Patients have a two-sheath area in the femur. Individuals undergoing peripheral catheterization. Patients have a hematoma and bleeding in the surrounding area of the femur artery before sheath removal.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Relieve the pain intensity that occurs after arterial sheath removal. Timepoint: When arterial sheath removal is immediately applied, an intervention for 20 minutes is applied, and the pain intensity is measured by the Visual Analogue Scale (VAS) after that. Method of measurement: Questionnaire and Visual Analogue Scale (VAS). | — |
Secondary
| Measure | Time frame |
|---|---|
| Relieve the pain intensity that occurs after arterial sheath removal. Timepoint: When arterial sheath removal is immediately applied, an intervention for 20 minutes is applied, and the pain intensity is measured by the Visual Analogue Scale (VAS) after that. Method of measurement: Questionnaire and Visual Analogue Scale (VAS). | — |
Countries
Iraq
Contacts
Public ContactJameel Ali Al-Zuhary
College of Nursing, University of Baghdad
Outcome results
None listed