Hospitalized elderlies after angiography. Intraoperative and postprocedural complications and disorders of circulatory system, not elsewhere classified
Conditions
Interventions
Intervention 1: Intervention group: before angiography, the emotional freedom technique will be explained to the patients of the intervention group and they will be taught how to perform the interv
Sponsors
Shiraz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
60 Years to 90 Years
Inclusion criteria
Inclusion criteria: Elderly Patients between 60 to 90 years old Elderly patients admitted to the cardiac care units and candidate for non-emergency angiography People who want to participate in research and fill out the informed consent form People who are fully aware and able to communicate People who have not undergone other invasive procedures such as esophageal echocardiography before angiography. Elderlies who have only angiography and do not have right heart catheterization People undergoing coronary angiography for the first time
Exclusion criteria
Exclusion criteria: Having positive history of sleep disorders and taking medication before hospitalization based on the initial patient assessment form. Having known cognitive and psychological disorders at the time of the study based on the initial patient assessment form. Taking sedatives and analgesics before (8 hours before) and after angiography The need for cardiopulmonary resuscitation during angiography. Having visual impairment that prevents the selection of the correct position in the pain assessment tool (based on the initial patient assessment form). Having active hemorrhage with hemodynamic disorders that resulted in blood transfusion during and after angiography. Dangerous rhythm disorder immediately after catheterization. Having low back pain on admission. Addiction to drug, sedatives and alcohol drinks.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The quality of sleep. Timepoint: The beginning of the study (before the intervention) and the day after the intervention. Method of measurement: The St. Mary's Hospital Sleep Questionnaire (SMHS).;Low Back Pain. Timepoint: Patients' low back pain is measured before and after the three times intervention . The intervention will be performed once immediately after the patient enters the ward, once an hour later and the third stage will be performed at 8 pm on the same night. Patients in the control group at the same times set for the intervention group, the level of pain will be measured and recorded in two time intervals with an interval of 15 minutes. Method of measurement: Visual scale for pain intensity.;Blood Pressure. Timepoint: Patients' blood pressure is measured before and after the three times intervention. The intervention will be performed once immediately after the patient enters the ward, once an hour later and the third time will be performed at 8 pm on the same night. ?In the control group at the same times set for the intervention group, blood pressure will be measured and recorded in two time intervals with an interval of 15 minutes. Method of measurement: Digital model amron 3 blood pressure monitor. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFatemeh Shirazi
Shiraz University of Medical Sciences
Outcome results
None listed