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عضویت

جستجوی مقالات مرتبط با کلیدواژه « etiology » در نشریات گروه « پزشکی »

  • Musliha Mustary, Ansariadi, Aminuddin Syam, Shanti Riskiyani, Kadek Ayu Erika, Apik Indarty Moedjiono, Mukhlis Lubis
    Background

    Preeclampsia (PE) caused 30%-40% of maternal and newborn deaths worldwide. Despite unclear exact cause, strategies exist to mitigate less severe PE effects. This review explores PE etiology, pathophysiology, risk factors, impact, and prevention.

    Methods

    Searching Scopus, PubMed, ProQuest, Google Scholar, and Science Direct for “preeclampsia and pregnancy” and “prevention” yielded 2012–2022 articles.

    Results

    Preeclampsia features abnormal placental changes, altered immunity response, trophoblast apoptosis, and reduced uterine perfusion. Risk factors include hypertension history, nulliparity, age over 40, BMI over 35 kg/m², family history, amniotic pregnancy, and long pregnancy interval. This condition risks cardiovascular and neonatal morbidity, straining health resources. Prevention involves aspirin, vitamin D, exercise, folic acid, diet, early screening, and antenatal care.

    Conclusion

    Findings emphasize enhancing health literacy and preeclampsia education in prenatal care to mitigate PE risk among women. Further research, novel therapies, and assessing prevention strategies with accessible educational materials and multidisciplinary approaches are warranted to enhance pregnant women's health literacy and decrease PE risk.

    Keywords: Preeclampsia, Etiology, Risk Factor, Impact, Prevention
  • Harshada A. Kusane *, Vishnu A. Kangralkar

    Breast cancer is the most frequent cancer in women throughout the globe, and its management can be difficult due to its complex etiology. Treatment with chemotherapy, surgical procedures, radiation treatment, and hormone therapy are among the most frequently utilized treatments. However, complications and resistance to multiple drugs can cause challenges. This overview addresses how organic medicinal products obtained from edibles and plants can assist with treatment of Breast cancer. The article scrutinizes the ways by which natural substances may exert beneficial impact in the prevention and management of breast carcinoma as well as offers knowledge regarding the therapeutic plant, including its family, part used, kind of extraction, and molecular mechanisms in breast carcinoma. Following an exhaustive analysis of the various plants, we discovered that Peganum normata, Ammi visnaga, Camellia sinensis, Curcuma longa, and Allium sativam L. had potential anti-breast cancer activities. These data were gathered from PubMed, Scopus, and Google Scholar.

    Keywords: Chemotherapy, Conventional Medicine, Etiology
  • Zeki Sabah Musihb *
    Background

    The neonatal period, which encompasses the first 28 days of life, is characterized by increased vulnerability to significant health challenges, resulting in elevated mortality rates.

    Objectives

    This study aimed to identify the causes of mortality among neonates in the Neonatal Intensive Care Unit (NICU) at Karbala Teaching Hospital for Children in Iraq.

    Methods

    A retrospective study was conducted to extract data on the causes of neonatal mortality from medical records in the Neonatal Intensive Care Unit (NICU) at Karbala Teaching Hospital for Children, covering the years 2017 to 2022. The collected data included the neonate's gender, gestational age, time of death, medical history, and cause of death.

    Results

    The total mortality rates varied from 9.5% to 12.03% across different years. In 2017, the mortality rate was higher among full-term neonates; however, starting in 2018, the mortality rate for preterm infants significantly exceeded that of term infants. The trends in causes of mortality changed over the years. Septicemia was the leading cause of neonatal mortality in 2017 (42.1%), followed by asphyxia (19.7%) and congenital heart disease (CHD) (10.5%). By 2022, the most common causes of neonatal mortality included prematurity (21.3%), septicemia (17.5%), and CHD (16.3%).

    Conclusion

    Septicemia, CHD, and asphyxia were the primary causes of mortality in NICUs over the years. Tailored interventions are essential for developing effective healthcare strategies.

    Keywords: Etiology, Neonatal, Mortality Rate, Neonatal Intensive Care Unit
  • Sepehr Pourkhalili, Reza Soltani Shal, Abas Abolghasemi, Minoo Dianatkhah, Mojgan Gharipour
    Objectives

    Hoarding disorder is a complex condition that significantly impacts individuals' lives, characterized by excessive acquiring, difficulty discarding, clutter, distress, and impairment. This study aimed to examine the extent to which genetics and environment influence difficulty discarding, excessive acquisition, and clutter through the implementation of a classical twin study.

    Methods

    A total of 194 twins, consisting of 100 monozygotic (MZ) and 94 dizygotic (DZ) twins, participated in this study. Hoarding symptoms was assessed using the saving inventory-revised.  To estimate the heritability of hoarding symptoms, the classical univariate twin model was employed.

    Results

    Based on the univariate analysis, it was found that the heritability estimates for difficulty discarding and excessive acquisition are 0.43 and 0.52, respectively. However, the results did not provide support for the role of genetics in clutter. Instead, it was indicated that the common environment accounts for 0.54 of the variance in clutter, while the specific environment contributes 0.46 to this symptom.

    Conclusion

    The difficulty discarding and excessive acquisition have been found to be moderately heritable. On the other hand, considering the contribution of genetics and environment to clutter, the results raise doubts about the association of clutter with hoarding. The relatively low genetic influence suggests that this trait may overlap with other behaviors rather than hoarding.

    Keywords: Clutter, Difficulty Discarding, Etiology, Excessive Acquisition, Genetic, Heritability, Hoarding
  • Amin Doosti-Irani, Parvin Cheraghi, Nasrin Shirmohammadi, Bahraeh Khdemi-Monfared, Zahra Cheraghi
    Background

    Over the past decade, Iranian households have experienced a decline in dairy product consumption. This study aimed to evaluate the population-attributable risk of prevalent non-communicable diseases related to dairy product consumption.

    Methods

    This cross-sectional analytical study involved 628 adults over 18 years old in Hamadan City in 2021. Clusters were selected based on comprehensive urban health centers. The standardized Iranian version of the food frequency questionnaire was used. Participants were categorized into 3 levels of dairy product consumption: >1 serving per day, 1–2 servings per day, and ≥3 servings per day.

    Results

    The mean age of the 628 participants was 38.05 (SD: 12.5), with 42.36% being male. Cheese (54.5%), yogurt (39.7%), and milk (30.4%) were consumed most frequently. The prevalence of insufficient dairy product consumption was 48.6%, higher than that reported in previous studies. Insufficient dairy product consumption was associated with hypertension (9.3%), cardiovascular disease (5.6%), and osteoporosis (5.1%).

    Conclusion

    Individuals with lower education levels, female gender, lowest quartile of socioeconomic status, and those diagnosed with cardiovascular disease were more likely to have insufficient dairy product consumption. Insufficient dairy product consumption was associated with hypertension, cardiovascular disease, and osteoporosis.

    Keywords: Food-Processing Industry, Dairy Products, Biomedical Research, Methods, Humans, Population, Risk, Hypertension, Epidemiology, Etiology, Cross-Sectional Study, Iran
  • Hosein Zakeri, Elham Pishbin, Behrang Rezvani Kakhki, Hanie Ghashghaee, Sayyed Majid Sadrzadeh, Masumeh Sadeghi, Elnaz Vafadar Moradi *
    Objective
    Geriatric trauma refers to injuries sustained by elderly individuals, typically those aged 65 years andolder. The management of geriatric trauma in the Emergency Department requires a comprehensive approachthat takes into account the physiological changes associated with aging, as well as the increased vulnerabilityand complexity of injuries in this population.
    Methods
    This is a cross-sectional study aimed at evaluating the etiology of trauma in geriatric patients referredto the ED of level-1 an academic center. All patients with complaints of trauma are evaluated and patients over65 years enrolled in the study. Data were analyzed by SPSS 26.
    Results
    319 patients were investigated, 49.8% male and 50.2% female. The most common underlying diseasesare high blood pressure, diabetes type 2, and ischemic heart disease. The most common trauma cause wasfalling from the same level (48.9%), followed by a fall from a height (16.6%), accidents with cars (16%), andmotorcycles (9.1%). The most common injury was extremities trauma (71.5%) following head trauma (13.2%)and chest trauma (6%). The severity of injury in extremities was higher in women, and chest trauma was moresevere in men.
    Conclusion
    The fall and subsequent car accident had the highest frequency as a cause of trauma in elderlypatients admitted to our academic trauma center. Hypertension and diabetes have also been the most commonunderlying diseases. Head and neck injuries are life-threatening and critical in a larger number of patients thanother injuries, and protecting them can be effective in reducing mortality and serious injuries in elderly traumapatients.
    Keywords: Geriatrics, Etiology, Trauma Center, Fall, Emergencies
  • Manisha Kalher, Madhurima Kaushik, Haritha Vasudevan, Siddharth Narendran, Karthik Kumar Mani, Kavitha Ramakrishnan, Viji Rangarajan, Virna Mahesh Shah *
    Purpose

    To assess the incidence and clinical profile of hemifacial spasm (HFS) and the association between HFS and systemic diseases.

    Methods

    This retrospective study was carried out on 85 patients with HFS, presenting at a tertiary eye care center in South India. Demographic and clinical details were recorded for all patients. Of these, the patients who had undergone magnetic resonance imaging (MRI) of the brain were analyzed for primary and secondary HFS.

    Results

    The mean age of the patients was 56.11 ± 12.51 years. The age at onset of HFS was 54.9 ± 12.7 years. The disease duration was 9.51 ± 7.28 years. Male:female ratio was 1:1.17. The right side was involved in 31 patients (36.47%) and the left side in 54 patients (63.52%). MRI was performed in 54 (63.52%) patients and showed neurovascular conflict in 22 (40.74%) patients and space‑occupying lesions in 2 (3.70%) patients. Forty‑nine (57.64%) patients had primary HFS, while five (5.88%) patients had secondary HFS due to old facial palsy in 3 and space‑occupying lesions in two patients. Twenty (23.52%) patients received botulinum toxin A with a good response. Type of HFS had a significant association with hypertension (P = 0.046) while no significant association was present between laterality of HFS and systemic diseases (P > 0.05 each). Multivariate analysis showed a marginally significant association between type of HFS and hypertension (P = 0.057).

    Conclusions

    Primary HFS was the main type of HFS with female dominance and predilection for the left side. Hypertension had a relationship with HFS that needs to be investigated further for its causal nature.

    Keywords: Clinical Profile, Etiology, Hemifacial Spasm, Incidence, India
  • رقیه باغنده*، میلاد علی کاظمی، ارشاد همتی
    زمینه و هدف

    15 درصد از شکستگی های صورت در کودکان رخ می دهد. اگرچه ترومای فک و صورت در جمعیت کودکان بیشتراز جمعیت بزرگسال است، بروز شکستگی صورت کمتر است. اپیدمیولوژی و علت شناسی شکستگی های صورت، در هر کشور،گروه اقتصادی، فرهنگ و منطقه جغرافیایی متفاوت است.

    روش بررسی

    این مطالعه گذشته نگر مشاهده ای_توصیفی و مقطعی در بین مراجعین کودک) 1 تا 12 سال(به بخش جراحیفک، صورت و دهان بیمارستان امام خمینی اهواز)به علت تروما و شکستگی فک(با شاخص های سن، جنس، زمان، علتشکستگی، موقعیت شکستگی، نوع شکستگی:، وجود شکستگی همراه در مدت 5 سال از فروردین ماه 93 لغایت فروردینماه 98 انجام گرفت.

    یافته ها

    در این مطالعه 7 / 32 درصد نمونه مورد بررسی دختر و 3 / 67 درصد پسر بودند. بیشترین علت شکستگی فک و صورتMVA, (4 / 63 (، و falling (25 (درصد بودند. بیشترین فراوانی شکستگی فک در اثر تروما در سن 12 سالگی با 3 / 17 درصدو سنین 9 و 10 سالگی با 4 / 15 درصد بود. بیشترین میزان شکستگی فک در اثر تروما در فصل تابستان با 7 / 32 درصد بود.شایعترین نوع شکستگیها در فک پایین) 5 / 87 درصد(و بیشتر در مردان گزارش شد.

    نتیجه گیری

    نتایج نشان می دهد که شایعترین نوع شکستگیها در فک پایین و بیشتر در مردان می باشد. بیشترین میزانشکستگی هم در سنین بین 8 تا 12 سال گزارش گردید. بیشترین درصد از علت شکستگی فک به ترتیب MVA و falling وبیشترین روش هایدرمان مورد استفاده close reduction و ORIF بودند.

    کلید واژگان: شکستگی های فک, شکستگی فک پایین, علت شناسی, شیوع, کودکان
    Roghaye Baghande *, Milad Ali Kazemi, Ershad Hemati
    Background and Objectives

    Facial fractures in children are unusual injuries that make up to 15% of facial fractures. Although maxillofacial trauma is more common in children than in adults, the incidence of facial fractures is lower. Epidemiology and etiology of facial fractures vary from country to country, and depend largely on economic group, culture, and geographical area. Maxillofacial fractures are the most common type of facial fractures.

    Subjects and Methods

    This 5-year (2014-2019) retrospective observational-descriptive and cross-sectional study was performed among pediatric patients (1 to 12 years old) referring to the maxillofacial surgery department of Imam Khomeini Hospital in Ahvaz (due to trauma and jaw fracture). The indicators included age, sex, time, cause of fracture, fracture position, type of fracture, and existence of accompanying fracture.

    Results

    Based on the results obtained in this study, 32.7% of the participants were girls and 67.3% were boys. The most common causes of jaw fractures were MVA (63.4%) and falling (25%). The highest frequency of jaw fracture due to trauma (17.3%) was at the age of 12 years followed by the ages of 9 and 10 years (15.4%). The highest rate of jaw fracture due to trauma in children (1 to 12 years) was in summer (32.7%). The results of this study show that the most common type of fractures was in the mandible (87.5%) which was more reported in males. The most common treatments used were close reduction (67.3%) and ORIF (26.9%).

    Conclusion

    The results of this study show that the most common type of fractures are in the mandible and more in men. The highest rate of fractures was reported between the ages of 8 to 12 years. This study showed that the highest percentages of the cause of jaw fractures were MVA and falling, respectively. Also, the highest percentage of hydrotherapy methods used were close reduction and ORIF.

    Keywords: Jaw fractures, Mandibular Fractures, etiology, Prevalence, children
  • منصور سردارپور، آتوسا امین زاده گوهری*
    مقدمه

    سسرطان زایی حفره ی دهان، فرایندی پیچیده است، تشخیص و درمان زودهنگام ضایعات سرطانی و پیش سرطانی، مهم ترین عامل در کاهش مرگ و میر می باشد. هدف از مطالعه ی حاضر، بررسی میزان آگاهی دانشجویان دندان پزشکی سال آخر دانشگاه آزاد اسلامی واحد اصفهان (خوراسگان) در سال 1400-1401 در مورد سبب شناسی و اقدامات درمانی سرطان سلول های سنگفرشی حفره ی دهانی بود.

    مواد و روش ها

    مطالعه ی حاضر به روش توصیفی- تحلیلی و به شیوه ی سرشماری انجام شد. پرسش نامه ی محقق ساز به صورت حضوری توزیع و تکمیل گردید؛ تجزیه و تحلیل دادها در دو بخش توصیفی و استنباطی انجام شد. اطلاعات جمع آوری شده با استفاده از آزمون ناپارامتری Mann–Whitney و ضریب همبستگی Spearmanدر سطح خطای 0/05درصد مورد بررسی قرار گرفت (0/05 p value ≤).

    یافته ها

    در مطالعه ی حاضر حدود 6/60 درصد دانشجویان ترم 11 و حدود 39/4 درصد ترم 12 بودند و میانگین سنی دانشجویان 25/73 سال بود. طبق بررسی دادهای جمع آوری شده، میانگین نمره ی آگاهی 5/74 از 10 بود. تفاوت معنی داری بین میانگین آگاهی دانشجویان ترم 11 و 12 در حیطه ی سبب شناسی وجود نداشت (0/147 = p value) در حالی که بین میانگین آگاهی دانشجویان ترم 11 و 12 در حیطه ی پیش آگهی و درمان، تفاوت معنی دار وجود داشت (0/001 = p value)، همچنین تفاوت معنی داری بین میانگین آگاهی دانشجویان (در دو حیطه ی سبب شناسی و درمان) با سنین مختلف وجود نداشت (0/245 = p value و 0/425 = p value).

    نتیجه گیری

    نتایج مطالعه ی حاضر نشان داد، سطح دانش و آگاهی دانشجویان در رابطه با سرطان سلول های سنگفرشی دهان تا حد مطلوب و رضایت بخش فاصله دارد.

    کلید واژگان: دهان, کارسینوم سلول سنگفرشی, دانش, علت شناسی, درمان
    Mansour Sardarpour, Atousa Aminzadeh Gohari*
    Introduction

    Carcinogenesis of the oral cavity is a complex process and oral cancer is one of the 10 most common cancers worldwide. Oral squamous cell carcinoma accounts for 90% of oral cancers, the most important risk factors of Oral squamous cell carcinoma (OSCC) are using tobacco and drinking alcohol. Early detection of cancerous and pre-cancerous lesions and timely referral is the most important factor in reducing mortality associated with OSCC, the purpose of this study is to investigate the level of knowledge of final year dental students at Isfahan Islamic Azad University (Khorasgan) during 1400-1401 regarding the etiology, Diagnosis and treatment of oral squamous cell carcinoma.

    Materials and Methods

    The present study was carried out in a descriptive and analytical method and in a census method, and a researcher-made questionnaire was distributed among the students in person; Data analysis was done in two descriptive and inferential sections. The collected data were analyzed using the non-parametric Mann-Whitney test and the Spearman correlation coefficient at the error level of 0.05% (p value ≤ 0.05).

    Results

    In this study, about 60.6% of students were in the 11th semester and about 39.4% were in the 12th semester with average age of 25.73 years. The average awareness score was approximately average (score 5.74 out of 10). There was no significant difference between the average knowledge of the 11th and 12th semester students regarding etiology, while 12th semester students showed significantly higher knowledge in terms of prognosis and treatment compared to 11th semester students. There was no significant difference in the average knowledge between students of different ages in the fields of etiology and treatment.

    Conclusion

    The results of the present study showed that the level of knowledge and awareness among students regarding OSCC lesions is far from satisfactory.

    Keywords: Mouth, Carcinoma squamous cell, Knowledge, Prognosis, Etiology, Therapeutics
  • Morteza Pourqasemi, Roshanak Ale-Esmaiel, Tofigh Yaghubi-Kalurazi

    Lung cancer, also known as lung carcinoma, is a malignant tumor that begins in the lung. Lung cancer is caused by genetic damage to the DNA of cells in the airways and is often caused by cigarette smoking or inhalation of harmful chemicals. Damaged airway cells gain the ability to multiply unchecked, causing tumor growth. Without treatment, tumors spread throughout the lungs, damaging lung function. Eventually, the lung tumors metastasize and spread to other body parts. On the other hand, lung cancer or bronchogenic carcinoma refers to tumors originating in the lung parenchyma or within the bronchi. It ranks among the primary causes of cancer-related mortality globally. It is estimated that there is an increasing rate of new cases of lung cancer worldwide annually, with an approximately high mortality rate because of lung cancer. It is worth mentioning that lung cancer was a relatively uncommon condition at the beginning of the 20th century. Its dramatic rise in later decades is primarily attributable to the increase in smoking among both males and females. Treatments include surgery, chemotherapy, immunotherapy, radiation, and targeted drugs. This review article describes lung cancer's causes, pathophysiology, and presentation.

    Keywords: Lung cancer, Etiology, Diagnosis, Treatment
  • Shiva Didehban *, Alireza Abdollahi, Alipasha Meysamie
    Background & Objective

    The most frequent type of cancer found in the endocrine system is thyroid carcinoma. Among well-differentiated thyroid malignancies, the most commonly occurring type is identified as papillary thyroid carcinoma (PTC), which makes up 70-90% of the cases. A subtype of PTC is papillary thyroid microcarcinoma (PTMC), which includes tumors smaller than 10 mm in diameter. Due to the advancements in diagnostic techniques, the incidence of this type of cancer is on the rise. In this study, we aimed to analyze the factors worsening the PTMC prognosis.

    Methods

    In the first step, we searched various databases for the factors affecting this tumor. The relevant articles were collected and different outcomes of this tumor and its associated factors which were studied in more than one article, were classified. Finally, we conducted a meta-analysis of these outcomes and their related factors.

    Results

    In the meta-analysis, a significantly association was found between the following factors: recurrence with gender (P<0.001) lymph node metastasis (LNM) (P= 0.003), and extrathyroidal invasion (P<0.001); lymph node metastasis with extrathyroidal invasion (P<0.001), and multifocality (P<0.001); central lymph node metastasis (CLNM) with gender (P=0.001), tumor size (P<0.001), extracapsular invasion (P<0.001), lateral cervical lymph node metastasis (P<0.001), and extrathyroidal invasion (P<0.001); lymph node metastasis resulted in poor outcomes (P<0.001); and finally tumor size with BRAFV600E mutation (P<0.001).

    Conclusion

    In conclusion, it is essential to note that greater awareness and understanding of this tumor characteristics and special and separate attention to PTMC can significantly improve the society overall health.

    Keywords: Clinical manifestation, Etiology, Histopathology, meta-analysis, Papillary thyroid microcarcinoma
  • دارا صالح نیا، ناصر مسعودی*، سیف الله رضایی
    پیش زمینه و هدف

    آسیب اسفنکتر آنال یک وضعیت بالینی است که باعث بی اختیاری مدفوع می شود و می تواند کیفیت زندگی فرد را به شدت مختل کند. اسفنکتروپلاستی همپوشانی ارجاع ترین روش جراحی برای ترمیم ASI است. هدف از این مطالعه بررسی اتیولوژی و نتایج جراحی موارد آسیب کامل اسفنکتر آنال (ASI) در مرکز آموزشی درمانی امام خمینی (ره) بود.

    مواد و روش ها

    در این مطالعه توصیفی-تحلیلی جامعه مطالعه شامل در تمام موارد جراحی ASI در بخش جراحی بیمارستان امام خمینی ارومیه از ابتدای سال 1397 تا پایان سال 1400 موردبررسی قرار گرفته اند. اطلاعات مطالعه با استفاده از نرم افزار SPSS نسخه 20 و آزمون تحلیل واریانس و مربع کای مورد تجزیه وتحلیل قرار گرفت. سطح معنی داری 05/0 لحاظ شد.

    یافته ها

    درمجموع 45 بیمار مبتلا به ASI انتخاب شدند. نتایج نشان داد در بیماران با ASI بین شدت بی اختیاری مدفوع و نوع بی اختیاری مدفوع (گاز، مایع، جامد) قبل از جراحی با بعد از جراحی تفاوت معنی داری وجود داشت (001/0>P). همچنین بر اساس امتیاز Wexner، شدت بی اختیاری مدفوع[1] قبل از عمل جراحی (7/3 ± 9/16) نسبت به بعد از عمل جراحی (6/3 ± 1/4) بیشتر بود، که نشان دهنده کاهش آن بعد از عمل جراحی است (05/0>P). همچنین بر اساس امتیاز Wexner، میانگین بهبودی بی اختیاری در زنان 6/3 ± 14 و در مردان 2/4 ± 8/11 بود که ارتباط معنی داری نداشتند و درنتیجه جنسیت تاثیری در بهبود بی اختیاری نداشت (05/0<P). همچنین نتایج نشان داد، سن بیماران تاثیری بر بهبودی بی اختیاری نداشت (05/0<P). بااین حال، میزان بهبودی بی اختیاری در بیماران زایمان کرده و مبتلا به تروما از بیمارانی که جراحی کرده بودند، بیشتر بود (05/0>P).

    بحث و نتیجه گیری

    شدت بی اختیاری مدفوع بعد از عمل جراحی نسبت به قبل از عمل جراحی کاهش یافته است و میزان بهبودی بی اختیاری در بیماران زایمان و تروما از بیماران جراحی شده بیشتر بود.

    کلید واژگان: آسیب اسفنکتر آنال, عوارض, پیامد, اتیولوژی, جراحی
    Dara Salih Nia, Naser Masoudi*, Saifullah Rezaei
    Background & Aim

    Anal sphincter damage is a clinical condition that causes fecal incontinence and can severely disrupt a person's quality of life. Overlap sphincteroplasty is the most commonly referred surgical procedure for ASI repair. The aim of this study was to investigate the etiology and surgical outcomes of the patients with complete anal sphincter injury (ASI) in Imam Khomeini Medical Training Center, Urmia, Iran.

    Materials & Methods

    In this descriptive-analytical study, the study population included all cases of ASI surgery in the surgery department of Imam Khomeini Hospital in Urmia from March 2018 to March 2022 were investigated. Data has been analyzed by SPSS version 20 software using analysis of variance (ANOVA) and chi-square tests. A significance level of 0.05 was considered significant.

    Results

    A total of 45 patients with ASI were selected. The results showed that there was a significant difference between severity and type of fecal incontinence (gas, liquid, solid) before and after the surgery in the patients with ASI (P<0.001). Also, according to the Wexner score, the severity of fecal incontinence before surgery (16.9 ± 3.7) was higher than it after surgery (4.1 ± 3.6), which indicates its reduction after surgery (P>0.05). Also, according to the Wexner score, the average improvement in incontinence was 14 ± 3.6 in women and 11.8 ± 4.2 in men no significant relationship, indicating that gender had no effect on the improvement of incontinence (P>0.05). Also, the results showed that the age of the patients had no effect on the recovery of fecal incontinence (P>0.05). However, the recovery rate of fecal incontinence in trauma patients was higher than the patients who underwent surgery (P<0.05).

    Conclusion

    The severity of fecal incontinence after surgery has decreased compared to it before the surgery, and the recovery rate of incontinence in childbirth and trauma patients was higher than it in surgical patients.

    Keywords: Anal Sphincter Injury, Complications, Consequence, Etiology, Surgery
  • رومینا پیمانی، حسین زائری، سراج الدین عارف نیا*
    مقدمه

    کم کاری مادرزادی تیرویید یکی از علل مهم قابل پیشگیری عقب افتادگی ذهنی در کودکان است. با توجه به اهمیت اتیولوژی بیماری در مدیریت بهتر بیماران در سال های بعدی زندگی و بزرگسالی این مطالعه با هدف بررسی اتیولوژیک کم کاری تیرویید مادرزادی دایمی در بیماران مراجعه کننده به درمانگاه بیمارستان طالقانی گرگان انجام شد.

    روش ها

    این مطالعه مقطعی بر روی 75 پرونده کودک مبتلا به کم کاری تیرویید مادرزادی دایمی به صورت سرشماری انجام شد. تشخیص بیماری براساس یافته های اسکن تکنتیوم 99 تیرویید پس از اتمام دوره سه ساله درمان صورت پذیرفت. نتایج آزمایشگاهی، اسکن تیرویید و اطلاعات مربوط به ریسک فاکتورها از پرونده بیماران استخراج شد. اطلاعات جمع آوری شده در نرم افزار SPSS نسخه 18 با استفاده از آزمون یو من ویتنی، کروسکال والیس در سطح 05/0 تحلیل شد.

    یافته ها

    56% از نوزادان پسر و 32% متولد زمستان بودند. بیشترین تشخیص کم کاری تیرویید دایمی از نوع اکتوپیک بود. 33/37% نوزادان با کم کاری تیرویید دایمی، پره ترم متولد شده بودند. 67/6 درصد نوزادان متولد شده با کم کاری تیرویید مادرزادی دایمی دارای وزن کمتر از 2500 گرم بود و 3/41 درصد مادران سابقه ای از کم کاری تیرویید داشتند و در 7/42 درصد نوزادان دچار کم کاری تیرویید دایمی، والدین نسبت فامیلی داشتند.

    نتیجه گیری

    در مطالعه حاضر، نارس بودن نوزادان، کم کاری تیرویید مادر و ازدواج فامیلی والدین در نوزادان مبتلا به کم کاری تیرویید مادرزادی دایمی شیوع نسبتا زیادی دارد.

    کلید واژگان: کم کاری تیروئید مادرزادی دائمی, پره ترم, کم کاری دائمی, اتیولوژی
    Romina Peymani, Hosain Zaeri, Srajdin Arefni*
    Background

    Congenital hypothyroidism is one of the important preventable causes of mental restriction in children. Considering the importance of the etiology of the disease in the better management of patients in the later years of life and adulthood, this study was conducted with the aim of investigating the etiology of permanent congenital hypothyroidism in patients referred to children's clinic in Gorgan.

    Methods

    This cross-sectional study was conducted on 75 children's files with permanent congenital hypothyroidism. The diagnosis of the disease was made based on the findings of the technetium 99 thyroid scan after the completion of the three-year treatment period. Laboratory results, thyroid scan and information related to risk factors were extracted from patients' files.

    Results

    56% of newborns were boys, 32% were born in winter and 61.3% were from Persian ethnicity. The most diagnosed permanent hypothyroidism was ectopic type. 37.33% of babies with permanent congenital hypothyroidism were born preterm. 67.6% of babies born with permanent congenital hypothyroidism weighed less than 2500 grams, and 41.3% of mothers had a history of hypothyroidism and in 42.7% of infants with permanent maternal hypothyroidism, the parents had a family relationship.

    Conclusion

    In the present study, prematurity of babies as well as hypothyroidism of the mother and family marriage of the parents in babies with permanent congenital hypothyroidism have a relatively high prevalence.

    Keywords: Congenital hypothyroidism, Preterm, Permanent thyroid, Etiology
  • Nurbek Igissin, Vera Zatonskikh, Zhansaya Telmanova, Rais Tulebaev, Malcolm Moore

    Laryngeal cancer comprises 30%-40% of head and neck malignancies, and it is the most common malignancy in otolaryngology. The main risk factors for laryngeal cancer are tobacco use, excessive alcohol consumption, gastroesophageal reflex, Plummer-Vinson syndrome, exposure to heat, chemicals, and some viral infections. This literature review summarizes all known data over the past decade with an assessment of the main etiological factors related to cancer incidence, general measurement issues in the cancer epidemiology and the current state of science in relation to laryngeal cancer. The geographical distribution of laryngeal cancer also reveals some important aspects. Europe remains the most prevalent continent for this type of malignancy, whilst the epidemiologic burden in Africa remains low. Overall, there are clear differences in morbidity and mortality from laryngeal cancer between urban and rural areas, with gender inequalities. In some countries, the incidence rates are high in rural areas, and in some, such as in China, the urban population is more affected. High rates of laryngeal cancer are closely associated with both low average income and a high percentage of the population with lower-than-average education countries with higher Socio-demographic Index (SDI) have made greater improvements in the treatment of LC than countries with lower SDI. Epidemiological data on risk factors can provide valuable information for developing cancer prevention strategies.

    Keywords: Laryngeal cancer, Epidemiology, Etiology, Prevention
  • JOSE ANTONIO SANCHEZ, DANIEL IVAN JIMENEZ, CLAUDIA CARMINA GARCIA-GUERRERO
    Introduction

    The presented study aimed to characterise periapical disease in teeth with primary non-surgical root canal treatment in persistent or emergent categories and their risk association.

    Methods

    A retrospective observational study that evaluated permanent teeth with primary non-surgical root canal treatment, was conducted clinically and radiographically for over one year. The following variables were analysed: gender, age, type and location of tooth, previous diagnosis, treatment conditions, and type of coronalrestoration. The supplementary variables included the perspectives of the treatment outcome, such as Remains normal, Improvement, and Failure. Statistical analysis was performed using a univariate analysis that estimated the average and proportion for each factor according to the result of the primary non-surgical root canal treatment. The multiple correspondence analysis identified the hierarchy between active variables and their association with the results.

    Results

    A total of 232 teeth in 155 participants were analysed. A χ2 value, (P=0.023) showed that the emergent disease is associated with patients around the age of 50. The multiple correspondence analysis identified a tendency of grouping between the emergent disease and the short filling category, followed by symptomatic pulpitis as a previous diagnosis. The persistent disease was associated with errors and overfillings. An inadequate root filling and taper density adversely impacted the treatment outcome.

    Conclusions

    The length of obturation influenced the presence of failure. Short fillings were associated with emerging periapical disease. Errors and overfillings contributed to the persistent disease in the populations studied.

    Keywords: Endodontics, Etiology, Periapical Disease, Root Canal Therapy, Treatment Outcomes
  • فاطمه شهرکی، مرتضی اولادنبی*

    نوروفیبروماتوز (Neurofibromatosis: NF) یک گروه هتروژن از سندرم های مستعد تومور است که منجر به ایجاد بدخیمی در سیستم عصبی مرکزی و محیطی می شود. نوروفیبروماتوز نوع یک (NF1) به همراه نوروفیبروماتوز نوع دو (NF2) و شوآنوماتوز (SCH)، سه نوع اصلی NF هستند. NF1 به عنوان شایع ترین شکل، توسط نوروفیبروم ها و لکه های شیرقهوه (CALMs) در اوایل کودکی ظاهر می شوند. نوروفیبروماتوز نوع یک، ناشی از جهش در ژن NF1 است که نوروفیبرومین را کد می کند. همچنین جهش در NF2 و ژن SMARCB1 به ترتیب منجر به ایجاد بیماری های نوروفیبروماتوز نوع دو و شوآنوماتوز می شود. علاوه بر این، اکثر بیماران مبتلا به نوروفیبروماتوز نوع دو، شوانوم دهلیزی دارند که با مشکلات شنوایی و عدم تعادل بدن نیز همراه است. اخیرا شوآنوماتوز به عنوان یک اختلال ژنتیکی متمایز پیشنهاد می شود. زیرا علایم مشترک زیادی با نوروفیبروماتوز نوع یک و دو دارد که شوآنومای خوش خیم در اطراف اعصاب، به عنوان مشخصه این بیماری است. ممکن است NF1 و NF2 علایم خود را در کودکی نشان دهند؛ اما شوآنوماتوز اغلب در افراد سی ساله یا بالاتر تشخیص داده می شود. این مقاله مروری با استفاده از جدیدترین متون علمی براساس کلیدواژه های نوروفیبروماتوز، پاتوژنز، درمان،NF1، NF2، از پایگاه های داده های آنلاین Web of science، Google scholar و PubMed در مورد انواع نوروفیبروماتوز، مسیر مولکولی، معیارهای تشخیص، علایم بالینی، مدیریت شرایط، درمان های آتی و داروهای درحال توسعه نگارش گردید.

    کلید واژگان: نوروفیبروماتوز, سبب شناسی, درمان, NF1, NF2, SMARCB1
    Fatemeh Shahraki, Morteza Oladnabi*

    Neurofibromatosis (NF) is a heterogeneous group of tumor predisposition syndromes that lead to malignancy in the central and peripheral nervous systems. Neurofibromatosis type 1 (NF1), along with neurofibromatosis type 2 (NF2) and schwannomatosis (SCH), are the three main types of NF. As the most common form, NF1 is characterized by neurofibromas and Cafe-au-lait macules (CALMs) in early childhood. Neurofibromatosis type 1 is caused by mutations in the NF1 gene, which codes for neurofibromin, and mutations in NF2 and SMARCB1 gene lead to neurofibromatosis type 2 and schwannomatosis, respectively. In addition, most patients with neurofibromatosis type 2 have vestibular schwannoma, also associated with hearing problems and body imbalance. Recently, schwannomatosis has been proposed as a distinct genetic disorder because it shares many symptoms with neurofibromatosis types one and two, characterized by benign schwannoma around nerves. NF1 and NF2 may show symptoms in childhood, but schwannomatosis is often diagnosed in people in their thirties or older. This article reviews the latest scientific literature according to the keywords of neurofibromatosis, pathogenesis, treatment, NF1, and NF2 in Google Scholar, PubMed, and Web of Science online databases on the types of neurofibromatosis, molecular pathways, diagnostic criteria, clinical symptoms, condition management, treatments and drugs under development.

    Keywords: Neurofibromatoses, Etiology, Therapeutics, Neurofibromatosis 1, Neurofibromatosis 2
  • Abdulhakim Mussema, Getenet Beyene, Esayas Gudina, Dagninet Alelign, Tofik Mohammed, Solomon Bawore, Abdurezak Mohammed Seid, Wondwossen Tadesse, Mulatu Gashaw
    Background and Objectives

    Antibiotic resistance is a significant problem that restricts the options for treating bacterial pneumonia. This research aimed to determine the bacterial causes of pneumonia and antibiotic resistance among hospitalized patients in southwest Ethiopia.

    Materials and Methods

    We collected and analyzed 150 sputum samples from individuals with community-acquired pneumonia from April 1st to October 30th, 2019. Standard bacteriological procedures were used to identify the bacteria. Kirby Bauer's disk diffusion method was used to assess the bacteria's susceptibility patterns. Production of carbapenemase and extended-spectrum-lactamase were confirmed phenotypically. Odds ratios and the chi-square test were computed.

    Results

    On the whole, bacterial pathogens were verified in 50% of the sputum samples. The predominant bacterial isolates were Klebsiella species, followed by Pseudomonas aeruginosa, Staphylococcus aureus and Streptococcus pneumoniae. About 77.5% of isolates were multidrug resistant. Moreover, 40.5% and 10.8% of the isolates were ESBL and carbapenemase producers, respectively. Aging, tobacco smoking, previous history of pneumonia, heart disease, and chronic respiratory disease had association with sputum culture-positivity.

    Conclusion

    As a result, it is important to regularly monitor the bacterial etiologies and their patterns of resistance. Additionally, sociodemographic and clinical characteristics should all be taken into account while managing patients with pneumonia empirically in this context.

    Keywords: Pneumonia, Bacterial, Etiology, Antimicrobial drug resistance, Hospitalized, Ethiopia
  • حسین صیدخانی*، آزاده برخورداریان آباده، مسعود مامی
    مقدمه

    خونریزی گوارشی از مهم ترین بیماری های طب داخلی است که می تواند ناشی از خونریزی در هرکدام از ارگان های گوارشی باشد. بهترین روش تشخیصی برای یافتن منشاءخونریزی در بیماران مبتلا به خونریزی گوارشی اندوسکوپی و کولونوسکوپی است. از این رو مطالعه ی حاضر با هدف تعیین علل وقوع خونریزی گوارشی و شایع ترین عامل خطرGIB (خونریزی دستگاه گوارش)در استان ایلام انجام گرفت.

    مواد و روش ها

    در این مطالعه تحلیلی گذشته نگر تمام بیماران مبتلا به تظاهرات خونریزی واضح گوارشی شامل ملنا، دفع لخته، هماتوشزی و هماتمز که در طی سال های 1393 تا 1398 به بیمارستان شهید مصطفی خمینی شهر ایلام مراجعه کرده اند، مورد ارزیابی قرار گرفتند. اطلاعات دموگرافیک بیماران و سابقه وجود بیماری در آنان و همچنین شرح حال داروهای مصرفی آنان که در پرونده ی بیماران ثبت شده، در برگه ی پرسش نامه وارد شد.تجزیه وتحلیل داده ها با استفاده از روش های آمارتوصیفی و آزمون مجذورکای دو توسط نرم افزارSpss  نسخه 20 استفاده شد.

    یافته های پژوهش:

     درمطالعه حاضر650 بیمار مبتلا به تظاهرات خونریزی گوارشی با میانگین سنی 24/57سال در دامنه سنی 99-19سال مورد مطالعه قرار گرفتند. بیشترین فراوانی بیماران در گروه سنی بالاتر از 60 سالومرد بودند. بیشترین شکایت بیماران هماتمز(4/41%)،کمترین شکایت آنمی (8/1%) و شایع ترین علل خونریزی گوارشی در هر دو جنس زخم پپتیک، توده معده و واریس مری بود. بین سن و تظاهرات خونریزی گوارشی ارتباط معنی داری گزارش شد(05/0p <). تظاهرات خونریزی گوارشی شامل هماتمز، ملنا و رکتوراژی در مردان و در بیماران سیگاری شایع تر بود. مصرف الکل نیز در وقوع خونریزی گوارشی با تظاهرات هماتمز، ملنا و رکتوراژی تاثیر گذار بود.

    بحث و نتیجه گیری

    بزرگسالان بیش از جوانان با بروز واریس مری درگیر بوده و هماتمز، ملناو رکتوراژی در بیماران سیگاری از تظاهرات وقوع خونریزی گوارشی بود. الکل نیز بر وقوع خونریزی گوارش تاثیر گذار می باشد.

    کلید واژگان: خونریزی گوارشی, عوامل خطر, خونریزی, بیماری های دستگاه گوارش
    Hossein Seidkhani*, Azadeh Barkhordarian Abadeh, Masoud Mami
    Introduction

    Gastrointestinal bleeding (GIB) is one of the most important diseases in internal medicine, which can occur due to bleeding in any of the gastrointestinal organs. The best diagnostic method for identifying the source of bleeding in patients is endoscopy and colonoscopy. Therefore, this study was conducted to determine the causes and the most common risk factors for GIB in patients referring to Shahid Mustafa Khomeini Hospital in Ilam.

    Material & Methods

    In this retrospective analytical study, all patients with clear gastrointestinal bleeding symptoms, including melena, hematemesis, hematochezia, and passing clots, who referred to Shahid Mustafa Khomeini Hospital in Ilam from 2014 to 2019, were evaluated. The demographic information of the patients, their medical history, and the description of the medications they were taking, which were recorded in their medical records, were entered into the questionnaire form. Data analysis was performed using descriptive and inferential statistical methods.

    Findings

    In this study, 650 patients with an average age of 57.24 years, ranging from 19 to 99 years, were included. The majority of patients were in the older age group (above 60 years) and were male. The most common complaint among patients was hematemesis (41.4%), while anemia was the least common complaint (1.8%). The most common causes of gastrointestinal bleeding in both genders were peptic ulcer, gastric mass, and esophageal varices. There was a significant correlation between age and gastrointestinal bleeding symptoms (p < 0.05). Gastrointestinal bleeding symptoms, including hematemesis, melena, and rectorrhagia, were more common in men and in smokers. Alcohol consumption also had an impact on the occurrence of gastrointestinal bleeding with hematemesis, melena, and rectorrhagia.

    Discussion & Conclusion

    Endoscopy and colonoscopy are the best diagnostic methods for patients with gastrointestinal bleeding. Therefore, this study was conducted to determine the causes and the most common risk factors for GIB in patients referring to Shahid Mustafa Khomeini Hospital in Ilam from 2014 to 2019. The findings of this study can help improve the diagnosis and management of gastrointestinal bleeding in these patients.

    Keywords: Gastrointestinal Hemorrhage (GIB), Risk Factors, Etiology, Hemorrhage, Digestive System Diseases
  • Maryam Sadat Yazdanparast, MohammadMehdi Ghilian, Elnaz Sheikhpour*

    Osteosarcoma (OS) is the most common type of primary malignant bone tumor. The onset of OS is associated with local pain and swelling as well as joint dysfunction, occasionally. The most common location for OS is around the knee joint.  These patients often tend to receive medical attention following physical exercise and trauma. The affected population is mainly teenagers, children, and young adults with age range of 10-30 years. OS can be diagnosed via different approaches. The main serum markers for pediatric OS are insulin‑like growth factor (IGF‑1 and IGFBP‑3), anti‑ki57 antibody, tumor necrosis factor (TNF)‑β and sTNF‑R, T3, CD44, vascular endothelial growth factor, serum amyloid A, CXC chemokines, bone alkalin phosphatase, Interleukin (IL‑2, IL‑4, IL‑8), interferon gamma (IFN-γ), TNF‑α, and free polyamines. Given that there is no comprehensive review literature regarding OS management in our country, this study aimed to assess a survey on the management and approach of OS in children. In this regard, we have discussed the epidemiology, etiology, type, clinical feature, diagnosis, and OS therapy.

    Keywords: Childhood, Etiology, Malignancy, Osteosarcoma, Serum Marker
  • Ghobad Abangah, Tayebeh Rashidian, Marziyeh Parizad Nasirkandy *, Milad Azami
    Infertility is a serious health issue in the world affecting approximately 8-10% of couples worldwide. The meta-analysisstudy was performed to assess the prevalence and etiologic factors associated with infertility in Iran. We made surethat the implementation of study and reporting the results were consistent with the MOOSE and PRISMA guidelines,respectively. All stages of the research were conducted by two authors, and the disagreement at each stage of the researchwas resolved by consensus. On January 1, 2020, we started a detailed literature search on international onlinedatabases, and Iranian Online databases, as well as specialized journals, several authentic international publishers andGoogle Scholar. We reviewed the reference list of identified articles for missed articles and then searched online forthem. Data analysis was performed to estimate the prevalence using a random effects model. The lifetime infertilityprevalence was found to be 11.3% [95% confidence interval (CI): 8.6-14.7] and the current infertility was evaluated tobe 3.7% (95% CI: 3.2-4.3). The prevalence of primary infertility (based on 45 articles consisting of 51,021 samples)as well as secondary infertility (based on 13 articles consisting of 35,683 samples) in Iran were estimated to be 18.3%(95% CI: 15.4-21.6) and 2.5% (95% CI: 1.6-4.0), respectively. The prevalence of female, male, both and unexplainedcauses was estimated to be 32.0% (95% CI: 27.6-36.8), 43.3% (95% CI: 38.2-48.6), 12.5% (95% CI: 9.6-16.2) and13.6% (95% CI: 10.2-17.8), respectively. The prevalence of causes related to ovulation, uterine tubes, and endometriosisin infertile women was estimated to be 54.0% (95% CI: 45.6-62.2), 15.5% (95% CI: 11.3-21.0), 6.2% (95%CI: 3.5-10.6), and 5.4% (95% CI: 2.5-11.3), respectively. In summary, the estimate of infertility burden in Iran didnot change between 1990 and 2017 and its prevalence remains high. This research presents a unified and up-to-dateoverview regarding the burden of infertility in Iran.
    Keywords: Etiology, infertility, Iran, Prevalence
نکته
  • نتایج بر اساس تاریخ انتشار مرتب شده‌اند.
  • کلیدواژه مورد نظر شما تنها در فیلد کلیدواژگان مقالات جستجو شده‌است. به منظور حذف نتایج غیر مرتبط، جستجو تنها در مقالات مجلاتی انجام شده که با مجله ماخذ هم موضوع هستند.
  • در صورتی که می‌خواهید جستجو را در همه موضوعات و با شرایط دیگر تکرار کنید به صفحه جستجوی پیشرفته مجلات مراجعه کنید.
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