Traumastem Powder in Treatment of Non-Traumatic Anterior Epistaxis in Emergency Department; a Randomized Clinical Trial
Traumastem Powder in Treatment of Non-Traumatic Anterior Epistaxis in Emergency Department; a Randomized Clinical Trial
نویسندگان: محبوب پورآقائی , سینا شفیعی , هانیه ابراهیمی بختور , فرزاد رحمانی
کلمات کلیدی: Epistaxis; Emergency Service, Hospital; Treatment Outcome; Patient Satisfaction
نشریه: 0 , 1 , 8 , 2020
| نویسنده ثبت کننده مقاله |
فرزاد رحمانی |
| مرحله جاری مقاله |
تایید نهایی |
| دانشکده/مرکز مربوطه |
تیم های تحقیقاتی دانشگاه |
| کد مقاله |
74056 |
| عنوان فارسی مقاله |
Traumastem Powder in Treatment of Non-Traumatic Anterior Epistaxis in Emergency Department; a Randomized Clinical Trial |
| عنوان لاتین مقاله |
Traumastem Powder in Treatment of Non-Traumatic Anterior Epistaxis in Emergency Department; a Randomized Clinical Trial |
| ناشر |
5 |
| آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ |
خیر |
| عنوان نشریه (خارج از لیست فوق) |
Archives of Academic Emergency Medicine |
| نوع مقاله |
Original Article |
| نحوه ایندکس شدن مقاله |
ایندکس شده سطح یک – ISI - Web of Science |
| آدرس لینک مقاله/ همایش در شبکه اینترنت |
|
| Introduction: Various studies are being conducted because of the value of finding an appropriate medication to
control bleeding in patients with epistaxis faster andmore conveniently. This study aimed to compare the effect
of Traumastem powder with routine tampons in treatment of non-traumatic epistaxis. Methods: This randomized
clinical trial enrolled patients with epistaxis presenting to the emergency departments of two hospitals
affiliated to Tabriz University of Medical sciences. Patients were divided into two groups using randomization
software (intervention group: 107 patients, control group: 96 patients). Primary outcome variables included
bleeding control time and patient satisfaction. Secondary outcome variable was recurrence of bleeding within
the first 24 hours after treatment. Visual assessment scoring system was used to assess patient satisfaction. Results:
Epistaxis was controlled in less than 5 minutes in 85 (79.4%) patients in the intervention group and 85
(88.5%) patients in the control group (P=0.058). Patient satisfaction in the intervention group was higher than
that of the control group (P<0.05). In the intervention group, 10 patients experienced recurrence of epistaxis
within 24 hours of treatment, while 9 patients in the control group experienced recurrence (P= 0.591). Conclusion:
Based on the findings, bleeding control time was similar in the two groups, but patient satisfaction was
higher in Traumastem group. It is concluded that Traumastem can conveniently control anterior epistaxis, but
it is not successful in cases with severe bleeding. |
| نام فایل |
تاریخ درج فایل |
اندازه فایل |
دانلود |
| 826-Title page-4186.pdf | 1399/07/21 | 414945 | دانلود |