The data will be evaluated by using the SPSS 22.0 package program at a significance level of p<0.05 with a 95% confidence interval, and by Student-t or Mann-Whitney-U test in independent groups according to their suitability for normal distribution. No intervention will be made in the control group. A warm wet compress will be applied to the phlebitis developing area of the patients in the experimental group, three times a day for three days. The patients included in the study will be divided into experimental and control groups by the randomization method. Data will be obtained using the "Patient Information Form", "Phlebitis Follow-up Form" and "Phlebitis Care Schedule". Volunteer patients with phlebitis symptoms after drug infusion with a peripheral intravenous catheter will be included in the study. The population of the study will be the patients with phlebitis symptoms, and the sample will be 70 patients determined by G power analysis. The study will be carried out in Ordu University Training and Research Hospital oncology, hematology, palliative, infection, and obstetrics services. Therefore, this planned thesis study was designed as a randomized controlled experimental study to determine the effect of warm wet application in the care of peripheral intravenous catheter-related phlebitis. However, studies in the literature on what, how many degrees, how many times a day, and how long the warm application should be made are limited. When phlebitis symptoms are seen, the infusion is terminated, the treatment is continued from another area, the extremity is elevated, and warm application is started. Planning the care of the area where phlebitis occurs is the responsibility of the nurses. Intravenous administration of drugs with high pH and osmolarity via a peripheral intravenous catheter damages the vascular structure, causing the drug to leak out of the vessel and cause phlebitis. Phlebitis is an inflammation of the tunica intima layer of the vein. Why Should I Register and Submit Results?.
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