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عضویت

جستجوی مقالات مرتبط با کلیدواژه « screening test » در نشریات گروه « پزشکی »

  • Aliyeh Mohamadzdeh, Minoo Fallahi *, Mahmoud Hajipour, Aliraza Amirshahi, Mohammad Kazemian
    Background
    Neonate screening is a preventative measure that can contribute to early diagnosis of treatable diseases. Hypothyroidism in neonates is among the common preventable factors leading to intellectual disability. This study aims to describe the prevalence and experience with four-step screening to diagnose congenital hypothyroidism.
    Methods
    The statistical population of this cross-sectional study included 392 preterm neonates (gestational ages less than 36 weeks and 6 days) in 2018-2019 from the health centers covered by Shahid Beheshti University of Medical Sciences (Tehran, Iran) who had been referred for screening. Neonates were screened in the first 3-6 days after birth and then on days 14, 42, and 72. In neonates with TSH serum levels of 10 mU/L, TSH-T4 was measured. Next, the physician decided on the medication based on the results.
    Results
    At the primary screening of the neonates average TSH level was 2.08 ± 2.4 mU/L. Thirty-three neonates (8.4%) indicated disrupted screening results. The secondary screening of 388 neonates (98.97%) revealed an average TSH serum level of 1.9 ± 1.96 mU/L, and 19 (5.9%) indicated TSH serum levels higher than 5 (mU/L). The third screening test was performed on 382 (97.44%) of the neonates. The average TSH level was 1.3 ± 2.4 mU/L, 340 (85.96%) indicated normal levels, and 42 (11.47%) had unfavorable results. Finally, the fourth screening test was performed on 373 (95.15%) neonates. The mean TSH level was 2.21 ± 1.9 mU/L, which revealed 24 (6.12%) unfavorable test results. The percentage of hypothyroidism in neonates was 5.6% (23 cases).  In this study, the prevalence of hypothyroidism was 4.33% (17 cases) in girls and 1.53% (6 cases) in boys.   
    Conclusion
    The results of this study revealed the high incidence rate of congenital hypothyroidism among preterm neonates. Therefore, preventing congenital hypothyroidism misdiagnosis requires a series of screening tests. Also, findings indicated that the results of screening tests for preterm neonates with prolonged GAs and higher birth weights are more accurate and reliable.
    Keywords: Hypothyroidism, neonate, Screening test}
  • Masoud Amanzadeh, Mahnaz Hamedan, Alireza Mohammadnia, Abdollah Mahdavi *

    Context: 

    The number of people with dementia is increasing dramatically. With the outbreak of the COVID-19 pandemic, digital screening tests can play a significant role in the remote and timely detection of people with dementia. This study aimed to review digital cognitive tests for dementia screening.

    Methods

    We searchedWeb of Science, ProQuest, PubMed, Scopus, and Cochrane using related terms such as “dementia,” “mobile,” “digital,” “computer,” and “cognitive assessment,” leading to the emergence of 1,348 articles. Titles, abstracts, and full texts were screened to select the relevant articles based on inclusion/exclusion criteria. Study characteristics and digital test features such as diagnostic performance and deploying platforms were extracted from selected articles. The risk of bias and reporting quality were evaluated in the included studies.

    Results

    Out of 1,348 identified articles, 32 were eligible for inclusion. We categorized digital cognitive tests into 3 groups based on deploying platforms: 1) Mobile-based screening tests (59.5%), 2) desktop-based screening tests (28%), and 3) web-based screening tests (12.5%).

    Conclusions

    Digital cognitive tests, especially mobile-based screening tests, facilitate the timely diagnosis of dementia. The development of AI-based screening tests and the use of technologies such as virtual reality and chatbots will set a bright future in the early detection of dementia.

    Keywords: Dementia, Cognitive Impairment, Digital Health, Computerized Cognitive Assessment, Screening Test}
  • Aseel Ghazi Rifat*
    Objectives

    So far, there is no concrete consensus on using uterine Doppler measurements for predicting the adverse outcomes in the early stages of pregnancy between 6-14 weeks. Hence, the current study was planned to investigate the role of uterine artery Doppler in predicting the miscarriage in early pregnancy and to evaluate whether uterine artery Doppler indices abnormality is associated with a complicated pregnancy and adverse outcomes.

    Materials and Methods

    The present cross-sectional prospective study estimated the uterine artery Doppler of right and left uterine arteries and the mean of pulsatility index (PI), resistance index (RI), and systolic/diastolic (SD) ratio was obtained for each patient. The gestational age, at which the Doppler study was performed, was 6-14 weeks for all groups. Finally, the groups of normal and threatened miscarriage were followed up for the outcome up to 20 weeks of gestation.

    Results

    There was a significant difference in the means of PI, RI, and S/D ratio among the three groups. However, PI was the only parameter which was significantly associated with the outcome of pregnancy. In addition, the cut-off value for PI was 2.64 at 91% sensitivity and 81% specificity for predicting miscarriage.

    Conclusions

    In general, uterine artery Doppler should be introduced as the routine screening test for identifying the women who could have an adverse pregnancy outcome for its effective management.

    Keywords: Uterine artery Doppler, Pregnancy outcome prediction, Screening test}
  • Revathi Panduranga Shenoy, Gagana Hanumaiah, Varashree Bolar Suryakanth*, Priyanka Shridharan
    Background

    The study aims at the comparison and correlation of serum levels of fructosamine and erythrocyte Na+/ K+ ATPase in Gestational diabetes mellitus (GDM) and Non Gestational Diabetes Mellitus (Non GDM).

    Methods

    A total of 326 samples were divided into 4 groups. Pregnant women between the age group of 20-40 years who gave samples for Oral Glucose Tolerance Test (OGTT) were included as the subjects. Anonymized and left over fasting and 2 hours’ samples were collected from biochemistry laboratory, Kasturba Hospital, Manipal.

    Results

    In the comparison of fructosamine levels in GDM and Non GDM, fructosamine was found to be significant (p value<0.001) in both fasting and 2 hours (G2) blood glucose condition. Na+/ K+ ATPase did not show any significant variation between the groups. Correlation was not significant between the parameters.

    Conclusions

    Fructosamine showed significant increase when compared between the groups, whereas significant correlation is not obtained between the parameters. Thus, the use fructosamine as a diagnosis tool becomes inconclusive. Further studies must be carried out to identify a marker which reduces the interferences observed in fructosamine and to find out the exact relationship between hyperglycaemia and Na+/ K+ ATPase activity.

    Keywords: Fructosamine, Gestational Diabetes Mellitus, Na+, K+ Atpase Enzyme Activity, Screening Test}
  • شیوا قاسمی کاکلر، معصومه سهرابی، پریا امیری، مرجان مظاهری
    مطالعات مختلفی در مورد اختلال در تحمل کربوهیدارت در طی دوران بارداری (GDM) انجام شده و در مطالعه حاضر عوامل و متغیرهای بیشتری مورد بررسی قرار گرفتند.
    مواد و روش ها
    این مطالعه مقطعی در بازه ی زمانی 14 ماهه بر روی 301 زن باردار مراجعه کننده به درمانگاه نیکخواه انجام و تمام زنان باردار در طی هفته های 24 تا 28 حاملگی تحت آزمایش OGCT قرار گرفتند.
    یافته ها
    بیشترین گروه سنی در جمعیت مورد مطالعه 20 تا 34 ساله بودند و درصد ابتلای به GDM داشتند. از پارامتر های مطالعه شده شاخص توده بدن و سابقه فامیلی دیابت با GDM ارتباط داشته و فعالیت فیزیکی روزانه، نوع آخرین زایمان، سن منارک، تحصیلات، تعداد افراد خانواده، روند تغذیه، سقط در حاملگی های قبلی، نظم پریودهای قبل از حاملگی، سن حاملگی، ویار حاملگی و تولد نوزاد کم وزن ارتباط معنی داری نداشتند. در رابطه با سابقه ی GDM در حاملگی قبلی، یک مورد داشتیم که براساس تست آماری، تخمین ریسک نتیجه ی آماری مشخص نمی توان گرفت.
    نتیجه گیری
    شیوع دیابت بارداری در مراجعین به این درمانگاه با توجه به وضعیت اجتماعی – اقتصادی پایین، بالاتر بوده و پارامترهای جدید مطالعه شده لازم است در مطالعات بیشتر، راستی آزمایی شوند.
    کلید واژگان: دیابت بارداری, عوامل خطر ساز, تست غربالگری, شیوع}
    Shiva Ghasemi kakalar, Masumeh Sohrabi, Paria Amiri, Marjan Mazahri
    Background & Aims
    Different studies had done about disorder in carbohydrate tolerance during pregnancy time and at present study more factors and divorces were considered.
    Materials & Methods
    This sectional study was accomplished in 14 mounths time output on 301 pregnant women in Nikkhah clinic and all the women were accomplished OGCT experiment.
    Results
    The most aged group had more percent in affection to GDM. In studied parameters, the index of body node and diabetes family recording had relationship with GDM and daily physical activity, kind of last confinement, age of mother, Schooling, the number of family persons, process of nutrition, feticide in last pregnancies, regulation of last periods, age of pregnancy, pregnancy tonging and birth of low-weight newborn had meaningful relationship. About relationship between GDM record and before pregnancies, there were one case that could not reach to distinctive outcomes about risk estimation.
    Conclusion
    prevalence scale of pregnancy diabetes in 301 referenced pregnant woman in Urmia Nikkhah clinic were high in low economic families and social conditions and new parameters should studied and experimented more in other considerations.
    Keywords: GDM, Risk factors, Screening test, Prevalence}
  • Jalal Bakhtiyari, Masoomeh Salmani *, Reyhaneh Noruzi, Payam Sarraf, Ebrahim Barzegar, Majid Mirmohammadkhani
    Introduction
    Speech and language therapists (SLTs) require proper tools to detect dysphagia in the early stages. One of these screening tools is the Northwestern Dysphagia Patient Check Sheet (NDPCS). However, this tool needs to be adapted, validated, and shown to be reliable for the Persian culture. The aim of the present study was to report the validity and reliability of the Persian NDPCS (P-NDPCS).
    Materials And Methods
    The NDPCS has 28 items and five sections. Beaton’s guidelines were followed in terms of the translation process. To report the content validity index (CVI) and the content validity ratio (CVR), eight SLTs experienced in swallowing disorders examined the content and face validities of the P-NDPCS in terms of the quality of translation, fluency, understandability, and the cultural context. In total, 140 patients with neurogenic and mechanical dysphagia were evaluated using the P-NDPCS. Internal consistency reliability was investigated using the Kuder–Richardson formula 20. The interclass correlation coefficient (ICC) was used for test-retest reliability.
    Results
    The P-NDPCS preserved the 28 items and the five categories of the original version. However, semantic and food adjustments were applied due to cultural differences. The scoring system was changed from safe/unsafe to yes/no for four subsections and to normal/abnormal for the oromotor section. Food requirements were also changed. The CVR and CVI were both 75%. The P-NDPCS was shown to have good content validity. The internal reliability was 0.95, indicating excellent reliability.
    Conclusion
    The equivalence between the original version of the NDPCS and the P-NDPCS was preserved. Our findings indicate that the P-NDPCSis a valid and reliable screening tool for the diagnosis of dysphagia in the early phase.
    Keywords: Dysphagia, Screening test, Validity, Reliability}
  • مجتبی بکتاشیان، مریم صدقی، منصور صالحی، فاطمه سادات میرلوحی، الهه زارعان، عاطفه باقرصاد، صادق ولیان، رسول سراییان، مجید حسین زاده *
    مقدمه
    با توجه به شیوع نسبتا زیاد سندرم داون (یک در هر 700 زایمان)، روش های گوناگون غربالگری برای شناسایی زنان باردار ابداع شده است. در صورتی که نتایج تست غربالگری مثبت باشد، تست های ژنتیک پیش از تولد توصیه می شود. مطالعه حاضر با هدف بررسی آزمایشات غربالگری و مقایسه آن با نتایج کاریوتیپ جنین انجام شد.
    روش کار
    در این مطالعه مقطعی، توصیفی و تحلیلی، نتایج تست های غربالگری و آزمایشات ژنتیک 1009 زن بارداری که در سال های 94-1393 بر اساس نتایج تست غربالگری در خطر ابتلاء به آنیوپلوئیدی بوده و به دنبال آن تست کاریوتیپ انجام داده بودند و نتایج هر دو تست در دسترس بود، مورد بررسی قرار گرفت. اطلاعاتی شامل مشخصات فردی، سابقه تولد فرزند مبتلا به سندرم داون، وجود نسبت فامیلی بین پدر و مادر، نتایج تست های غربالگری و آزمایش ژنتیک، در پرسشنامه طراحی شده تکمیل گردید. تجزیه و تحلیل داده ها با استفاده از نرم افزار آماری SPSS (نسخه 19) و آزمون های آماری انجام شد. میزان p کمتر از 05/0 معنی دار در نظر گرفته شد.
    یافته ها
    بر اساس نتایج آزمایش ژنتیک، 59 مورد (6%) از جنین های مورد مطالعه مبتلا به آنیوپلوئیدی بودند که از این تعداد 41 مورد سندرم داون داشتند. در این مطالعه بین آزمایشات غربالگری و بروز آنیوپلوئیدی ارتباط معنی داری وجود داشت (05/0>p)، ولی بین خطر نقص لوله عصبی (NTD) با آنیوپلوئیدی ارتباط معنی داری وجود نداشت (05/0p>). همچنین بین NT بیشتر از 3 میلی متر و بروز آنیوپلوئیدی ارتباط معنی داری مشاهده شد (001/0>p). در محاسبه انجام شده حساسیت تست NT جهت غربالگری آنیوپلوئیدی 47% و ویژگی تست 90% به دست آمد.
    نتیجه گیری
    آزمایشات غربالگری سلامت جنین می توانند در یافتن زنان در معرض خطر داشتن فرزند مبتلا به اختلالات کروموزومی کمک کننده باشند. مطالعات بیشتر جهت تعیین حساسیت تست های غربالگری توصیه می شود.
    کلید واژگان: آنیوپلوئیدی, تست غربالگری, سندرم داون, کاریوتایپ}
    Mojtaba Baktashian, Maryam Sedghi, Mansour Salehi, Fateme Sadat Mirlohi, Elahe Zarean, Atefe Baghersad, Sadegh Valian, Rasoul Saraian, Majid Hoseinzade *
    Introduction
    Regarding to the high prevalence of Down syndrome (1 per 700 births) different prenatal screening methods have been developed to identify high risk pregnant women. If the screening results were positive, prenatal genetic tests are recommended. This study was performed with aim to evaluate screening tests and comparison with fetal karyotype results.
    Methods
    In this cross-sectional, descriptive and analytical study, the results of screening tests and genetic tests of 1009 pregnant women who underwent aneuploidy screening test in the years2015-2016, was examined. The information includes demographic data, familial history of previous child affected with Down syndrome, consanguineous marriage was obtained and then the results of screening and genetic test were recorded in a designed questionnaire. Data were analyzed using SPSS software (version 19), P value less than 0.05 was considered significant.
    Results
    Based on the results of genetic tests, 59 cases (6%) of the studied fetuses had aneuploidy that 41 cases had Down syndrome. There was a significant relationship between screening tests and aneuploidy (P0.05). Also, significant relationship was found between NT>3mm and aneuploidy (P
    Conclusion
    Fetal screening tests can help in finding pregnant women at risk for a child with chromosomal abnormalities. Further studies are recommended to determine the sensitivity of screening tests.
    Keywords: Aneuploidy, Down syndrome, Karyotype, Screening test}
  • Mehrab Sayadi, Mohammadjavad Zibaeenezhad, Seyyed Mohammad Taghi Ayatollahi *
    Background
    Type 2 Diabetes Mellitus (T2DM) is one of the most important risk factors in cardiovascular disorders considered as a common clinical and public health problem. Early diagnosis can reduce the burden of the disease. Decision tree, as an advanced data mining method, can be used as a reliable tool to predict T2DM.
    Objectives
    This study aimed to present a simple model for predicting T2DM using decision tree modeling.
    Materials And Methods
    This analytical model-based study used a part of the cohort data obtained from a database in Healthy Heart House of Shiraz, Iran. The data included routine information, such as age, gender, Body Mass Index (BMI), family history of diabetes, and systolic and diastolic blood pressure, which were obtained from the individuals referred for gathering baseline data in Shiraz cohort study from 2014 to 2015. Diabetes diagnosis was used as binary datum. Decision tree technique and J48 algorithm were applied using the WEKA software (version 3.7.5, New Zealand). Additionally, Receiver Operator Characteristic (ROC) curve and Area Under Curve (AUC) were used for checking the goodness of fit.
    Results
    The age of the 11302 cases obtained after data preparation ranged from 18 to 89 years with the mean age of 48.1 ± 11.4 years. Additionally, 51.1% of the cases were male. In the tree structure, blood pressure and age were placed where most information was gained. In our model, however, gender was not important and was placed on the final branch of the tree. Total precision and AUC were 87% and 89%, respectively. This indicated that the model had good accuracy for distinguishing patients from normal individuals.
    Conclusions
    The results showed that T2DM could be predicted via decision tree model without laboratory tests. Thus, this model can be used in pre-clinical and public health screening programs.
    Keywords: Heart Disease, Decision Tree, Risk Factors, Screening Test}
  • Sousan Salehi, Ali Jahan, Najva Mousavi, Mazyar Hashemilar, Zohreh Razaghi, Maryam Moghadam, Salimi
    Background
    As there is no standard aphasia screening tool for Azeri language yet, the aim of this study was to develop an aphasia screening test with acceptable validity and reliability.
    Methods
    The present study was conducted in two phases. In the first phase, by literature search, the screening test was designed and to obtain validity it was peer reviewed by expert panel. After collecting experts’ ratings and comments, appropriate modifications were applied. For test-retest reliability in the second phase, edited test was administered in 32 patients with brain injuries, then the retest was performed two weeks later.
    Results
    The developed test had eight subscales including: A) picture description, B) syntax, C) linguistic reasoning, D) descriptive naming, E) perception of minimal pairs, F) comprehensive vocabulary, G) expressive vocabulary, H) verbal fluency. Each section had five questions except verbal fluency which had 3 items. Content validity ratio (CVR) according to Lawshe’s approach, was 82% for the whole test. Intraclass correlation for all subscales were more than 0.8. Cronbach’s alpha coefficient for internal reliability was 0.901.
    Conclusion
    This aphasia screening test seems to have acceptable psychometric properties. This test can probably be used in clinical setting by specialists.
    Keywords: Screening Test, Aphasia, Azeri Language, Brain Injury, Iran}
  • پیمان بهلولی، محمدرضا نهایی *، صفر فرج نیا، مجتبی ورشوچی، مرتضی قوجازاده، محمد اکبری دیباور، فیروزه صفاییان
    زمینه و هدف
    آنتی بیوتیک وانکومایسین یکی از مهمترین داروهای موجود در درمان عفونتهای ناشی از سویه های استافیلوکوکوس اورئوس مقاوم به متی سیلین (MRSA) می باشد. از آنجایی که استافیلوکوکوس اورئوس های با کاهش حساسیت به وانکومایسین در ارتباط با مورتالیتی بالایی بوده و در حال افزایش در جهان هستند، لذا بررسی شیوع این سویه ها ضروری به نظر می رسد.
    روش بررسی
    تعداد 100 ایزوله MRSA با استفاده از تستهای فنوتیپی نظیر رنگ آمیزی گرم، کاتالاز، کواگولاز، DNase، تخمیر مانیتول و آزمون مقاومت به متی سیلین مورد شناسایی قرار گرفتند. جهت تشخیص مقاومت به وانکومایسین تستهای فنوتیپی با روش دیسک دیفیوژن، تعیین MIC با روش E-test و آزمونهای غربالی در محیط کشت برین هارت اینفیوژن آگار (BHIA) حاوی وانکومایسین انجام و آزمون مولکولی PCR برای شناسائی ژنهای femB، mecA و vanA مورد استفاده قرار گرفت.
    یافته ها
    میزان مقاومت به متی سیلین 59% بود. دامنه MIC وانکومایسین بین μg/ml 0/75 تا μg/ml 4 قرار داشت. با روش E-test میزان 92% ایزوله ها حساس و 8% دارای مقاومت هتروژن به وانکومایسین بودند. ولی آزمونهای غربالی در محیط کشت BHIA حاوی μg/ml 3 و μg/ml 4 وانکومایسین بترتیب 18% مقاومت هتروژن و 4% مقاومت بینابینی به وانکومایسین را شناسایی نمود. در آزمون غربالی در BHIA محتوی μg/ml 6 وانکومایسین هیچ ایزوله ای قادر به رشد نبود. 100% ایزوله ها دارای ژنهای femB و mecA بودند ولی هیچ ایزوله ای حاوی ژن vanA نبود.
    نتیجه گیری
    آزمون E-test به تنهایی قادر به شناسایی تمامی ایزوله های با مقاومت هتروژن و بینابینی به وانکومایسین نبود. لذا استفاده از آزمونهای غربالی در کنار آزمونهای MIC الزامی است.
    کلید واژگان: استافیلوکوکوس اورئوس مقاوم به متی سیلین, وانکومایسین, E, test, آزمون غربالی, PCR}
    Peyman Bohlouli, Mohammad Reza Nahaei *, Safar Farajnia, Mojtaba Varshochi, Morteza Ghojazadeh, Mohammad Akbari Dibavar, Firoozeh Safaeeyan
    Background And Aim
    Vancomycin is one of the last drugs used by human for treatment of infections caused by Methicillin resistant Staphylococcus aureus (MRSA) isolates. Since Staphylococcus aureus with heterogeneous, intermediate and complete resistance to vancomycin are in relation to high mortality rate and are increasing in the world, so investigating the incidence of these isolates is necessary.
    Materials And Methods
    By using several phenotypic tests such as Gram stain, catalase, coagulase, DNase and mannitol fermentations and by screening resistance to methicillin, 100 MRSA isolates were identified. For identifying resistance to vancomycin, phenotypic tests with the disc diffusion method, determining MIC by E-test method and screening test in BHIA (Brain Heart Infusion Agar) containing vancomycin and molecular PCR test were carried out in order to identify femB, mecA and vanA genes.
    Results
    Resistance to methicillin was 59%. Ranges of vancomycin MICs were between 0.75 µg/ml to 4 µg/ml. By E-test method 92% of isolates were sensitive and 8% showed heterogeneous resistance to vancomycin. However, screening tests in BHIA, containing 3 μg/ml and 4 μg/ml vancomycin, detected 18% heterogeneous resistance and 4% intermediate resistance to vancomycin, respectively. In screening tests using BHIA, with 6 μg/ml vancomycin no isolate was able to grow. Although all of the isolates contained femB and mecA genes, but none of them contained vanA gene.
    Conclusion
    E-test alone was not able to identify all S.aureus isolates of heterogeneous resistance and intermediate resistance to vancomycin. As a result, the screening tests also should be used along with MIC tests.
    Keywords: Methicillin, resistant Staphylococcus aureus, Vancomycin, E, test, Screening test, PCR}
  • بررسی آزمونهای غربالگری نقص های عصبی عضلانی موثر در آسیب غیربرخوردی لیگامان صلیبی قدامی) مقاله مروری)
    هیمن محمدی*، حسن دانشمندی، محمدحسین علیزاده، علی شمس ماجلان
    مقدمه
    پارگی لیگامان صلیبی قدامی، علاوه بر هزینه درمانی زیاد، موجب از دست دادن مشارکت ورزشی، آسیب های ثانویه و مشکلات روحی ورزشکارن می گردد و پیشگیری از آن در اولویت کاری محققان قرار گرفته است. هدف از این تحقیق مروری بر آزمون های غربالگری نقص های عصبی عضلانی موثر در آسیب غیر برخوردی لیگامان صلیبی قدامی می باشد.
    روش بررسی
    جستجوی مقالات مرتبط در سایت های تخصصی PubMed Medline و Science Direct با محدوده پوشش مقالات در زمینه های «آزمون غربالگری»، «نقص عصبی عضلانی» و «آسیب غیربرخوردی ACL» در دو دهه اخیر بود.
    نتایج
    آزمون های جهش، دارای اعتبار بالایی هستند و ارتباط معنی داری بین شاخص تقارن اندام ها و گشتاور ایزوکنتیکی اکستنسور زانو وجود دارد. آزمون های تعادلی ایستا و پویا دارای روایی و پایایی بالایی بوده و نتایج این آزمون ها با آسیب ACL ارتباط دارد. هر دو آزمون اسکات جفت پا و تک پا، اعتبار بالایی داشته و جهت ارزیابی ضعف کنترل عصبی عضلانی، کنترل تنه، انعطاف پذیری پویا، قدرت ران و تعادل استفاده می شوند. آزمون تعدیل شده سیستم امتیازدهی خطای فرود جهت شناسایی الگوهای حرکتی مرتبط با افزایش خطر بروز آسیب غیربرخوردی ACL استفاده می شود. آزمون غربالگری ویدیوئی فرود پرش در صفحه فرونتال و جهت ارزیابی راستای ولگوس زانو و آزمون پرش تاک جهت شناسایی شایع ترین نقص های عصبی عضلانی مرتبط با مکانیسم های زیربنایی آسیب ACL، استفاده می شوند.
    نتیجه گیری
    آشنایی با آزمون های غربالگری معتبر و مرتبط با آسیب غیر برخوردی ACL، به محققان پیشگیری از آسیب در انتخاب آزمون مناسب، جهت شناسایی افراد دارای نقص های عصبی عضلانی ویژه و مستعد آسیب ACL کمک می نماید و پژوهشگران می توانند برنامه های تمرینات اصلاحی تخصصی تر ارائه نمایند.
    کلید واژگان: آزمون غربالگری, نقص عصبی عضلانی, آسیب غیربرخوردی لیگامان صلیبی قدامی}
    Screening tests for neuromuscular defects affecting non-contact ACL injury- A review article
    Himan Mohammadi *, Dr Hasan Daneshmandi, Dr Mohammad Hossein Alizadeh, Dr Ali Shamsimajlan
    Background And Aim
    In addition to high cost of treatment, anterior cruciate ligament tear leads to lesser participation in sports, secondary injury and mental problems. Therefore, prevention of ACL injury in athletes is a top priority in many studies. The aim of this study was to conduct a review over screening tests for neuromuscular imbalance causing non-contact ACL injuries.
    Material And Methods
    Scientific citations search engines such as PubMed, Medline, and ScienceDirect were looked for relevant articles using the following keywords: "Screening Test", "Neuromuscular Imbalance" and "Non-Contact ACL Injury" during the previous two decades.
    Results
    Hop tests have high reliability and there is a statistically significant correlation between lower extremity symmetry index of this test and isokinetic knee extensor strength. Static and dynamic balance tests have high reliability and validity and their results have correlation with ACL injury. Both double-leg squat test and single leg squat test are used to assess poor neuromuscular control of the trunk, dynamic flexibility, strength of hip, and balance. Modified Landing Error Scoring System Tests are used to identify movement patterns that increase the risk of non-contact ACL injury. In order to identify the most common neuromuscular imbalance related to ACL injuries, we used tuck jump test. Video drop-jump screening test was used to assess valgus alignment in knee.
    Conclusion
    Familiarity with reliable and valid screening tests related to non- contact ACL injuries will be of benefit to researchers specialized in ACL for prevention of injuries. They will be able to select appropriate tests to identify neuromuscular imbalance in people at risk of ACL injury. Therefore, researchers can provide more specific corrective exercise programs.
    Keywords: Screening Test, Neuromuscular Defects, Non, Contact ACL Injury}
  • Farin Soleimani, Ali Khakshour, Zohreh Abbasi, Samira Khayat, Seyede Zahra Ghaemi, Nayereh Azam Hajikhani Golchin
    Background
    Autism is a neurodevelopmental disorder that onset in the first 3 years of life and led to lifelong disability. Despite the early onset of symptoms, diagnosis of thissyndromedoes not happenuntil severalyears later, somany childrenlosethe opportunityfor earlyintervention. There arevarious toolsforscreening anddiagnosis, buttheirdesign, strengths and weaknesses aredifferent. The aim of this study was assess these tools from various aspects to provide a comprehensive view.
    Materials And Methods
    This study is a narrative literature review on screeningtoolsof autism. Comprehensive searches of the scientific literature were conducted in textbooks and 8 electronic databases (proquest, wiley, google scholar, SID, Scopus, Web of Science، Science Direct، and Medline) and Pediatric book. language restriction (Persian and English) was applied. The search strategy consisted of keywords and medical subject headings for autism and various screening tests.
    Result
    In this study, 28 screening tests were identified from 1992 to 2014. CHAT is oldest test and the most recent test is CAST The minimum age that can perform the screening is six months that related to ITC. Minimum time of testing was 5 minutes for CHAT and the maximum time was 90-120 minutes for ASIEP-3. RAADS-R test was the highest specificity and specificity (100%) and the lowest specificity was 14% in ESAT test
    Conclusion
    The results of this study indicate that any of the autism screening tools consider specific skill and various aspects of the disease, careful evaluation is need to choose proper test.
    Keywords: Autism, Child, Pervasive developmental disorder, Screening test}
نکته
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