به جمع مشترکان مگیران بپیوندید!

تنها با پرداخت 70 هزارتومان حق اشتراک سالانه به متن مقالات دسترسی داشته باشید و 100 مقاله را بدون هزینه دیگری دریافت کنید.

برای پرداخت حق اشتراک اگر عضو هستید وارد شوید در غیر این صورت حساب کاربری جدید ایجاد کنید

عضویت

فهرست مطالب niloufar amini

  • Bahareh Abtahi-Naeini, Reza Makhmali, Niloufar Amini, MohammadReza Maracy, Nikta Nouri, Tooba Momen
    Background

    There are limited data on severe cutaneous adverse reactions (SCARs) associated with antiepileptic medications. The current study aims to investigate the clinical and epidemiological characteristics of antiepileptic medication-induced SCARs in hospitalized children.

    Materials and Methods

    The current five-year retrospective study was conducted at Isfahan University of Medical Sciences, Iran. This study included all children with a definite diagnosis of SCARs secondary to the use of antiepileptic medications based on the world health organization (WHO) definition. In our study SCARs were categorized into three fields: Hypersensitivity syndrome, drug reaction with eosinophilia and systemic symptoms (DRESS), and Stevens-Johnson syndrome (SJS)/toxic epidermal necrolysis (TEN).

    Results

    Among 259 children with SCARs induced by antiepileptic medications, 199 (76.83%), 42 (16.22%), and 18 (6.95%) had hypersensitivity syndrome, DRESS, and SJS/TEN, respectively. Phenobarbital was the most common offending drug in all types of SCARs. The multinomial logistic regression model revealed that lymphadenopathy increased the occurrence of DRESS by 35 times compared to hypersensitivity syndrome (P < 0.001). Girls were at risk of SJS/TEN approximately 6 times more than boys (P = 0.027). Age (P = 0.021), weight (P = 0.036), and mucosal involvement (P < 0.001) affected the hospitalization duration in children with SCARs related to antiepileptic medication.

    Conclusion

    There are some similarities and differences in the clinical and epidemiological features of Iranian children suffering from antiepileptic medication-induced SCARs.

    Keywords: Adverse drug reactions, Allergy, immunology, Antiepileptic drug, Drug reaction with eosinophilia, systemic symptoms}
  • Alaleh Gheissari, Maryam Riahinejad, Mehryar Mehrkash, Alireza Merrikhi, Yahya Madihi, Ziba Farajzadegan, Behnoosh Esteki, Niloufar Amini, Minoo Saeidi, Bahareh Vard, Rasool Kermani, Roya Kelishadi, Mohammad Ali Pourmirzaiee, Amirmohammad Ghanei, Neda Azin
    Introduction

      The prevalence of congenital anomaly of kidney and urinary tract (CAKUT) and related chronic kidney disease (CKD) may be increased in countries with higher rate of consanguineous marriage. Therefore, we evaluated the prevalence of CKD by biochemical and kidney ultrasound measurements in the firstgrade pupils.

    Methods

    This cross -sectional study was carried on children aged 6 to 7 years. Urine analysis, serum creatinine, urine microalbumin to creatinine ratio and kidney ultrasound have been evaluated for participants.

    Results

    653 children were recruited to the study. Stage 1 and stage 2 systolic hypertension have been found in 6.5 and 1%, respectively. The percentage of stage 1 and stage 2 diastolic hypertension were 1.3 and 0.3%, respectively. Both weight Z-score and waist Z-score had positive correlation with systolic and diastolic blood pressure. Microalbuminuria (in 2.5%) did not have any correlation with the following factors: hypertension, body mass index, microscopic hematuria, glomerular filtration rate, kidney sonographic abnormalities or kidney parenchymal thickness and family history of kidney transplantation. GFR less than 90 mL/ min /1.73 m2 has been detected in 1.8% of the students. Only 1.7% had urine RBC more than 5 in each high-power field (hpf). Approximately 1.5% had anatomical abnormality of kidney and urinary tract (hydronephrosis or hydroureter).

    Conclusion

      Considering the higher prevalence of elevated blood pressure and microalbuminuria in Iranian children, a CKD screening program based on evaluating microalbuminuria and blood pressure measurement is needed. However, irrespective of high prevalence of consanguineous marriage in Iran, using kidney ultrasound as a screening tool has not been recommended.

    Keywords: chronic kidneydisease, diagnostic screeningprograms, children, bloodpressure, microalbuminuria}
  • Niloufar Amini, Tooba Momen *, Maryam Ghaderian, Hossein Saneian, Mohammad Hasan Emami
    Background
    The prevalence of eosinophilic esophagitis (EoE) has increased in recent decades. Recent studies have found that the prevalence of EoE in patients with celiac disease (CD) is much higher compared with the general population. In this study, the prevalence of EoE in children with CD was calculated and their clinical symptoms, endoscopic and histopathological findings were compared.
    Methods
    This was a retrospective study conducted on the data records of the patients diagnosed with celiac disease during 2012-2020, and registered at Imam Hossein Children’s Hospital and the Institute of the Celiac Association in Isfahan, Iran. Clinical findings, endoscopic reports, serological and histopathological data of the patients were recorded and analyzed.
    Results
    A total of 80 children with CD were included in the study. The mean age of the patients with CD and EoE (n=8) was 7.75± 3.99 years, and in children with CD alone (n=72), the mean age was 7.85± 3.83. The most common clinical findings were abdominal pain, anorexia, diarrhea and constipation. There were no significant differences in the symptoms of either group. The most common endoscopic view was duodenal scalloping and esophagitis; and 50% of EoE patients had a normal endoscopic view of the esophagus. With regards to serological findings, the level of TTG-IgA (U/ml) in the CD and EoE group was higher than the CD group (183.73 ± 101.54 vs. 117.07 ± 95.34 U/ml); however, no statistically significant difference was observed.
    Conclusion
    Our study found that the prevalence of EoE in children with CD appears to be higher than in previous studies.  We have also shown that the presence of EoE cannot be detected solely based on clinical and even endoscopic results.  Therefore, an esophageal biopsy is recommended in celiac patients.
    Keywords: Eosinophilic esophagitis, Celiac disease, upper gastrointestinal tract, Epidemiology, Children}
  • طوبی مومن، نیلوفر امینی*، سحر حسینی

    مقدمه:

      کهیر مزمن، یک اختلال التهابی پوستی است که حداقل شش هفته از مدت بیماری گذشته باشد. امروزه، نقش ویتامین D در بیماری های التهابی از جمله کهیر بسیار مورد توجه است. هدف از انجام این مطالعه، بررسی ارتباط ویتامین D و کهیر مزمن بود.

    روش ها

    در این مطالعه ی مقطعی، 40 بیمار مبتلا به کهیر مزمن و 40 فرد سالم با دامنه ی سنی 60-18 سال از بین مراجعه کنندگان به کلینیک سرپایی بیمارستان الزهرای (س) اصفهان در سال های 97-1396 تحت مطالعه قرار گرفتند. در کلیه ی این افراد، سطح ویتامین D با روش High-performance liquid chromatography (HPLC) اندازه گیری شد. سطح 25-هیدروکسی ویتامین D به میزان کمتر از 20 نانوگرم/میلی لیتر به عنوان کمبود (Deficiency) و سطح 30-20 نانوگرم/میلی لیتر به عنوان ناکافی (Insufficiency) در نظر گرفته شد. داده ها با روش های آماری مناسب مورد واکاوی قرار گرفتند.

    یافته ها

    میزان متوسط ویتامین D سرم در گروه مورد 6/21 و در گروه شاهد 8/30 نانوگرم/میلی لیتر بود. در گروه بیماران، 5/42 درصد و در گروه شاهد 5/22 درصد سطح ویتامین D کمتر از 20 نانوگرم/میلی لیتر و همچنین در گروه مورد 5/42 درصد و در گروه شاهد 0/25درصد سطح ویتامین D بین 30-20 نانوگرم/میلی لیتر داشتند. بنابراین، شیوع کمبود و سطح ناکافی ویتامین D در بیماران 0/85 درصد و در گروه شاهد 5/47 درصد بود.

    نتیجه گیری

    این مطالعه نشان می دهد که شیوع کمبود ویتامین D در مبتلایان به کهیر مزمن نسبت به افراد سالم بیشتر است، اما یافتن رابطه ی علت و معلولی بین کهیر مزمن و ویتامین D نیازمند مطالعات وسیع تری می باشد.

    کلید واژگان: ویتامین D, کهیر مزمن, کمبود}
    Tooba Momen, Niloufar Amini*, Sahar Hosseini
    Background

    Urticaria is an inflammatory skin disorder lasting for six weeks or longer. Nowadays, the role of vitamin D in inflammatory disease such as urticaria is a matter of great interest. The aim of this study was to investigate the relationship between vitamin D and chronic urticaria.

    Methods

    In this cross-sectional study, 40 patients with chronic urticaria and 40 healthy individuals aged 18 to 60 years were studied during the years 2017-2018 in Alzahra hospital, Isfahan, Iran. In all cases, vitamin D levels were measured using high-performance liquid chromatography (HPLC) method. Levels of 25-hydroxyvitamin D less than 20 ng/ml were considered as deficiency and levels of 20-30 ng/ml were considered as insufficiency. Data were analyzed with appropriate statistical tests.

    Findings

    The mean serum vitamin D level was 21.6 ng/ml in the patients group and 30.8 ng/ml in the control group. In the patient group 42.5%, and in the control group 22.5%, had vitamin D level of less than 20 ng/ml, and in the patient group 42.5%, and in the control group 25%, had vitamin D level of between 20-30 ng/ml. Therefore, the prevalence of vitamin D deficiency and insufficiency in patients and in the control group was 85% and 47.5%, respectively.

    Conclusion

    This study shows that vitamin D deficiency is more common in people with chronic urticaria than in normal population. However, finding a cause-and-effect relationship between chronic urticaria and vitamin D requires more extensive studies.

    Keywords: Vitamin D, Chronic urticaria, Deficiency}
بدانید!
  • در این صفحه نام مورد نظر در اسامی نویسندگان مقالات جستجو می‌شود. ممکن است نتایج شامل مطالب نویسندگان هم نام و حتی در رشته‌های مختلف باشد.
  • همه مقالات ترجمه فارسی یا انگلیسی ندارند پس ممکن است مقالاتی باشند که نام نویسنده مورد نظر شما به صورت معادل فارسی یا انگلیسی آن درج شده باشد. در صفحه جستجوی پیشرفته می‌توانید همزمان نام فارسی و انگلیسی نویسنده را درج نمایید.
  • در صورتی که می‌خواهید جستجو را با شرایط متفاوت تکرار کنید به صفحه جستجوی پیشرفته مطالب نشریات مراجعه کنید.
درخواست پشتیبانی - گزارش اشکال