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Evaluation of Entry Examination Results of Apprentices and Interns Made by Workplace Health and Safety Unit 工作场所健康安全组对学徒和实习生入职考试成绩的评估
Pub Date : 2020-01-01 DOI: 10.5222/forbes.2020.87597
Ş. Budak
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引用次数: 2
Cervical Trauma Patients with Down Syndrome, Case Report 宫颈外伤合并唐氏综合征患者病例报告
Pub Date : 2020-01-01 DOI: 10.5222/forbes.2020.98608
Erkan Güvenç, M. S. Güvenç, Burcu Demirdöven
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引用次数: 0
Protracted Febrile Myalgia Associated with Fever of Unknown Origin 长期发热性肌痛伴不明原因发热
Pub Date : 2020-01-01 DOI: 10.5222/forbes.2020.98852
Özlem Üzüm, Hayrullah Manyas, Kerem Yıldız, A. Baghirov, B. Demir
Fever of unknown origin (FUO) is considered in children as fever >38.3°C (101°F) at least once a day for 8 days and more without any apparent diagnosis. There are lots of underlying factors for fever of unknown origin and the three most common etiologic categories in children are infectious diseases, connective tissue diseases, and neoplasms. In this article, we have presented a 15-year-old girl admitted with normal physical, and biochemical examination findings except fever and an elevated acute phase reactant. She was diagnosed with protracted febrile myalgia syndrome (PFMS) when severe myalgia was added to her complaints although she denied previously experienced periodic fever, abdominal pain, arthralgia or chest pain. We presented our case to emphasize that protracted febrile myalgia syndrome, one of the atypical clinical manifestations of Familial Mediterranean fever, may be the presenting symptom of Familial Mediterranean fever as well as an underlying cause of fever of unknown origin.
不明原因发热(FUO)在儿童中被认为是发烧低于38.3°C(101°F),每天至少一次,持续8天以上,没有任何明显的诊断。病因不明的发热有许多潜在因素,儿童中最常见的三种病因是感染性疾病、结缔组织疾病和肿瘤。在这篇文章中,我们报告了一位15岁的女孩,她的身体和生化检查结果正常,除了发烧和急性期反应物升高。她被诊断为持续性发热性肌痛综合征(PFMS),当她的主诉中增加了严重的肌痛时,尽管她否认以前经历过周期性发烧、腹痛、关节痛或胸痛。我们提出我们的病例,以强调持续性发热性肌痛综合征,家族性地中海热的非典型临床表现之一,可能是家族性地中海热的表现症状,以及不明原因的发热的潜在原因。
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引用次数: 0
Obstetric and Neonatal Outcomes in Congenital Isolated Cardiac Anomalies - Single Center Experience 先天性孤立性心脏异常的产科和新生儿结局-单中心经验
Pub Date : 2020-01-01 DOI: 10.5222/forbes.2020.39974
E. Çağlıyan, S. Ozmen, S. Demir, Aslı Akdöner, S. Altunyurt, B. Deliloğlu, K. Yıldız, se Seynep Genç Hal, M. Kır
Objective: Evidence shows that rather than postnatal diagnoses, prenatal diagnoses of congenital heart diseases are correlated with better long-term results and lower mortality rates. In this retrospective study, neonatal stage results of infants with isolated cardiac anomalies, their indications for operation or intervention (if any), and the mortality rates in the first age are attempted to be demonstrated. Method: The study was conducted through the retrospective analysis of 47 patients who were diagnosed with fetal cardiac anomaly in the antenatal period, and monitored during natal and postnatal stages at the same center in the Departments of Obstetrics and Gynecology and Pediatric Cardiology of Dokuz Eylul University Hospital. Results: In our center 36 patients gave birth by cesarean section, and 11 patients by spontaneous vaginal delivery. Two low birthweight neonates were born (<2500 g), and these neonates were observed to have hypoplastic left heart and Fallot tetralogy. Thirty-nine of the 47 neonates born with isolated cardiac anomaly were operated after birth. Five patients were advised follow-ups. The remaining 3 neonates died within 48 hours after birth. Survival rate of the operated neonates was 59.5% and the general survival rate was 59.5%. Average 1, and 5-minute APGAR scores of the infants were 7.8 (3-9) and 9.0 (8-10), respectively The neonates were operated an average of 3 days after birth, and the average duration hospitalization of neonates were 12 days. Twentynine neonates needed preoperative respiratory support and 37 of them received prostaglandin E1 infusion. Follow-up was advised for 3 neonates within the first month and the first year. Five neonates needed operation during the specified period, and 2 neonates died. Conclusion: In conclusion, prenatal diagnosis of congenital heart diseases allows planning the delivery in tertiary care centers, stabilization of the infants in the preoperative period and realization of emergency intervention.
目的:有证据表明,先天性心脏病的产前诊断与较好的远期疗效和较低的死亡率相关,而不是产后诊断。在这项回顾性研究中,新生儿阶段的结果孤立的心脏异常的婴儿,其手术或干预的指征(如果有的话),并在第一年龄的死亡率试图证明。方法:回顾性分析Dokuz Eylul大学附属医院妇产科和小儿心脏科同一中心诊断为胎儿心脏异常的47例患者,并对其进行产前和产后监测。结果:本组患者剖宫产36例,顺产11例。2例低出生体重新生儿(<2500 g),观察到这些新生儿有左心发育不全和法洛四联症。47例孤立性心脏异常新生儿中有39例在出生后进行了手术。5例患者建议随访。其余3例新生儿在出生后48小时内死亡。术后新生儿生存率为59.5%,总生存率为59.5%。新生儿平均1分钟、5分钟APGAR评分分别为7.8分(3-9分)和9.0分(8-10分),新生儿平均在出生后3天手术,平均住院时间为12天。29例新生儿术前需要呼吸支持,其中37例给予前列腺素E1输注。建议对3名新生儿在第一个月和第一年进行随访。5例患儿在规定时间内需要手术,2例患儿死亡。结论:先天性心脏病的产前诊断有助于在三级保健中心计划分娩,在术前稳定婴儿并实现紧急干预。
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引用次数: 0
Impact of Reducing Irritative Symptoms in Non-Muscle Invasive Bladder Cancer During BCG Instillation: A Pilot Study 卡介苗注射对减轻非肌性浸润性膀胱癌患者刺激症状的影响:一项初步研究
Pub Date : 2020-01-01 DOI: 10.5222/forbes.2020.69775
O. Kose, Y. Akın, H. Gulmez, Erhan Ateş, S. N. Gorgel, S. Ozcan, B. Kati, Y. Yılmaz
INTRODUCTION: We evaluated use of anticholinergics, mirabegron, and combination of anticholinergics with mirabegron during Bacillus Calmette-Guérin (BCG) instillation for reducing irritative symptoms in patients with non-muscle invasive bladder cancer (NMIBC). METHODS: Prospectively recorded data of NMIBC patients receiving BCG were retrospectively evaluated between August 2015 and April 2019. Patients with low-grade T1 solitary papillary lesions <4 cm were included in the study. Validated questionnaires (OAB-V8) for irritative symptoms adapted to Turkish language, and QoL index forms were filled out by the study participants. OAB-V8 scores of ≥8 were considered as an indication to start medical treatment for irritative symptoms. Groups were formed according to daily used anticholinergic drugs and combinations as follows: Group 1, tolterodine; Group 2, solifenacin 5mg; Group 3, mirabegron, and Group 4, mirabegron with solifenacin 5 mg. RESULTS: Mean follow- up period was 20.4±6.8 months. There were 132 patients [110 men (83%) and 22 (17%) women] with irritative symptoms and NMIBC. Mean age of the study population was 59.7±12.4 years. The OAB-V8 scores and QoL indexes significantly improved with all drugs. However, in subgroup analyses, Group 4 provided the most dramatic improvement in OAB-V8 and QoL index scores (P=0.02 for both). The longest in time to micturition was recorded in Group 4 (P=0.04). Tumour recurrence was similar for groups 12 months after BCG instillation (P=0.9), however the least recurrence was observed in Group 4. DISCUSSION AND CONCLUSION: Combination of solifecacin and mirabegron can reduce irritative symptoms, improve QoL, and prolong time to micturition, during BCG instillation in selected NMIBC patients. This combination may also decrease recurrence rates in this patient population.
简介:我们评估了在卡介苗(BCG)灌注期间使用抗胆碱能药物、米拉贝龙以及抗胆碱能药物与米拉贝龙联合用于减轻非肌肉浸润性膀胱癌(NMIBC)患者的刺激症状。方法:回顾性评估2015年8月至2019年4月期间接受卡介苗治疗的NMIBC患者的前瞻性记录数据。低级别T1孤立性乳头状病变<4 cm的患者纳入研究。研究参与者填写了适用于土耳其语的刺激症状验证问卷(OAB-V8)和生活质量指数表。OAB-V8评分≥8分被视为开始治疗刺激症状的指征。按每日使用抗胆碱能药物及联合用药情况分组:1组:托特罗定;2组:索利那新5mg;第3组米拉贝隆,第4组米拉贝隆联合索利那新5mg。结果:平均随访时间为20.4±6.8个月。132例患者[男性110例(83%),女性22例(17%)]伴有刺激性症状和NMIBC。研究人群的平均年龄为59.7±12.4岁。各药物组OAB-V8评分和生活质量指标均有显著改善。然而,在亚组分析中,第4组在OAB-V8和QoL指数评分方面的改善最为显著(两者的P=0.02)。第4组排尿时间最长(P=0.04)。卡介苗注射后12个月各组肿瘤复发率相似(P=0.9),但第4组肿瘤复发率最低。讨论与结论:选定的NMIBC患者在卡介苗灌注过程中,联合使用索立维卡星和米拉贝龙可减轻刺激症状,改善生活质量,延长排尿时间。这种联合治疗也可能降低这类患者的复发率。
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引用次数: 0
Çinko Düzeylerinin Ölçümünde Matriks Seçimi 按汉语水平大小选择矩阵
Pub Date : 2020-01-01 DOI: 10.5222/forbes.2020.09709
Sema Kardeşler, Fatma Demet Arslan, İnanç Karakoyun, Banu Işbilen Başok, Ayfer Çolak
INTRODUCTION: Measurement of blood zinc levels is frequently used in the diagnosis of a few conditions such as growth retardation, immunodeficiency, infertility, neurological disorder, and acrodermatitis enteropathica. The serum matrix is the most preferred one to determine zinc levels due to the ease of analysis with other tests and cost-effectiveness of blood collection tubes used to obtain serum samples. In our study, we aimed to compare serum and plasma zinc test results for accurate and reliable zinc measurement in plain tubes with clot activator and gel and in heparin-free tubes, which specifically produced for trace element analysis. METHODS: Twenty-seven randomly selected patients were included in the study. Blood samples drawn simultaneously from patients were pipetted into tubes with clot activator and gel (SST) (SST II Advance, Vacutainer, Becton Dickinson and Company, USA) as well as into trace element tubes with sodium heparin (NH) (NH Trace Elements Sodium Heparin, Vacuette, Greiner Bio-One GmbH, Austria). After the centrifugation process, zinc levels in serum and plasma samples were analyzed by colorimetric method using an autoanalyzer. Bias between serum and plasma zinc levels was evaluated according to the allowable bias criterion based on biological variation and regression analysis performed. RESULTS: The mean and standard deviation of serum and plasma zinc levels were 49.0±11.5 μg/dL and 46.4±12.0 μg/dL, respectively, and a statistically significant difference was determined (p=0.012) in between. Besides, the bias between serum and plasma was 6.8%, which was above the allowable bias (3.3%) and considered as clinically significant. No systematic or random errors detected. DISCUSSION AND CONCLUSION: When selecting a blood collection tube for trace element analysis, the structural differences between tubes and the matrix effect should be considered carefully.
简介:血锌水平的测量经常用于诊断一些条件,如生长迟缓,免疫缺陷,不孕症,神经系统疾病,肠病性肢端皮炎。血清基质是测定锌水平的最优选方法,因为它易于与其他测试一起分析,而且用于获取血清样本的采血管具有成本效益。在我们的研究中,我们的目的是比较血清和血浆锌的检测结果,以准确可靠地测量锌在普通管与凝块激活剂和凝胶和无肝素管,专门用于微量元素分析。方法:随机选取27例患者进行研究。同时从患者身上提取的血液样本被移入含有凝块激活剂和凝胶(SST)的试管(SST II Advance, Vacutainer, Becton Dickinson and Company, USA)和含有微量元素的肝素钠(NH)的试管(NH微量元素钠肝素,Vacuette, Greiner Bio-One GmbH, Austria)。离心处理后,用自动分析仪比色法分析血清和血浆样品中的锌含量。根据基于生物变异和回归分析的允许偏倚标准评估血清和血浆锌水平之间的偏倚。结果:两组患者血清、血浆锌水平均值为49.0±11.5 μg/dL,标准差为46.4±12.0 μg/dL,差异有统计学意义(p=0.012)。此外,血清和血浆之间的偏差为6.8%,高于允许偏差(3.3%),具有临床意义。没有检测到系统或随机错误。讨论与结论:在选择用于微量元素分析的采血管时,应仔细考虑管的结构差异和基质效应。
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引用次数: 0
Computed Tomography and Magnetic Resonance Assessment of Choroid Plexus Xanthogranulomas 脉络膜丛黄色肉芽肿的计算机断层和磁共振评价
Pub Date : 2020-01-01 DOI: 10.5222/forbes.2020.58066
S. Altay
INTRODUCTION: Seventy-five adult patients with retrospectively detected incidental choroid plexus xanthogranulomas (CPX) were evaluated with non-contrast brain computed tomography (CT) and contrast-enhanced brain magnetic resonance imaging (MRI) images. In this study, we aim to determine the imaging properties of CPX with CT and MRI, to evaluate the difference between white matter and CPX with diffusion-weighted imaging (DWI) and apparent diffusion coefficient (ADC), and ensure its potential use in the follow-up and treatment of CPX patients. METHODS: In this study, lesions between 5-25 mm were evaluated. CPX and white matter ADC measurements were performed on CT and MRI images in all lesions. An independent sample t-test was used for statistics. Cases with a history of cranial operation and any malignancy were excluded due to the possibility of metastasis. RESULTS: Bilateral CPX was detected in 41 and unilateral CPX in 34 patients. On CT, bilateral CPX calcifications were observed in 21 and unilateral calcifications in 44 patients. Calcification was not observed in brain CT in 10 patients. ADC (apparent diffusion coefficients) measurement was made from the widest and non-calcific parts of all lesions. ADC measurements were between 1.33-1.69x10-3/mm2/s and the mean value was 1.48x10-3/mm2/s. In all cases, the ADC value was lower relative to the white matter. ADC value was found to be higher and closer to the white matter ADC values than cases with a homogenous appearance in CPX patients with heterogeneous internal structure. DISCUSSION AND CONCLUSION: ADC value is useful in the diagnosis of CPX. In conclusion, the follow-up of the ADC value is useful in the diagnosis and follow-up of CPX.
简介:我们对75例回顾性检测到偶发脉络膜丛黄色肉芽肿(CPX)的成年患者进行了非对比脑计算机断层扫描(CT)和增强脑磁共振成像(MRI)图像的评估。在本研究中,我们旨在通过CT和MRI确定CPX的影像学特征,通过弥散加权成像(DWI)和表观弥散系数(ADC)评估白质与CPX的差异,并确保其在CPX患者的随访和治疗中的潜在应用。方法:在本研究中,对5- 25mm之间的病变进行评估。在所有病变的CT和MRI图像上进行CPX和白质ADC测量。统计学采用独立样本t检验。有颅脑手术史及任何恶性肿瘤者因可能有转移而排除。结果:41例患者检测到双侧CPX, 34例患者检测到单侧CPX。CT表现为21例双侧CPX钙化,44例单侧CPX钙化。10例患者CT未见钙化。ADC(表观扩散系数)测量从所有病变的最宽和非钙化部分。ADC测量值在1.33-1.69x10-3/mm2/s之间,平均值为1.48x10-3/mm2/s。在所有病例中,ADC值相对于白质较低。在内部结构不均匀的CPX患者中,ADC值比外观均匀的患者更高,更接近白质ADC值。讨论与结论:ADC值对CPX的诊断有一定的价值。综上所述,ADC值的随访对CPX的诊断和随访是有价值的。
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引用次数: 0
A Rare Case of Nasopharyngeal Teratoma 鼻咽畸胎瘤1例
Pub Date : 2020-01-01 DOI: 10.5222/forbes.2020.80299
İbrahim Ömeroğlu, H. Pala
Oral teratoma is a rare congenital tumor that occurs almost exclusively in infants, and usually in newborns. The incidence of live births ranges from 1: 35.000 to 1: 200.000. There is a female dominance ratio of 6: 1. Teratomas are rare in the head and neck region and represent less than 5% of all cases. In this article, a case referred to our clinic in the second trimester of pregnancy and ultrasonographically diagnosed as teratoma is presented.
口腔畸胎瘤是一种罕见的先天性肿瘤,几乎只发生在婴儿身上,通常发生在新生儿身上。活产率为1:35 000至1:20 000。雌性优势比为6:1。畸胎瘤在头颈部非常罕见,在所有病例中所占比例不到5%。在这篇文章中,一个病例提到我们的诊所在妊娠中期和超声诊断为畸胎瘤。
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引用次数: 0
The Importance of Imaging in the Diagnosis of Rectus Femoris Pyomyositis in a 35 Day-Old-Infant 35日龄婴儿股直肌化脓性炎影像学诊断的重要性
Pub Date : 2020-01-01 DOI: 10.5222/forbes.2020.54264
N. Uraş
Pyomyositis affecting the muscles around the hip may present with characteristics similar to those bof septic arthritis, which are challenging to diagnose due to their rare and vague presentation. Herein, we present a 35-day-old –male nfant with fever, restriction of hip and right limp movement and magnetic resonance imaging finding indicating rectus femoris pyomyositis.
影响髋关节周围肌肉的化脓性肌炎可能表现出与脓毒性关节炎相似的特征,由于其罕见和模糊的表现,诊断具有挑战性。在此,我们报告了一个35天大的男性婴儿,发烧,髋关节和右侧跛行活动受限,磁共振成像显示股直肌化脓性炎。
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引用次数: 0
Benefits Of Caffeine: Birth Weigth Over 1250 g Infants With Respiratuar Distress 咖啡因的好处:出生体重超过1250克的呼吸窘迫婴儿
Pub Date : 2020-01-01 DOI: 10.5222/forbes.2020.57441
Ezgi Yangın Ergon, R. Çolak, M. Kıvılcım, M. Yıldız, S. Özdemir, F. Kulali, Ş. Çalkavur
INTRODUCTION: Prophylactic caffeine therapy, reduces the frequency of apnea in premature babies. Moreover, its effect has been well established in reducing the intermittent hypoxemia, and the need for additional ventilator support of infants with a birthweight of <1.250 g. The aim of this study is to determine the effects of prophylactic caffeine use on neonatal outcomes in preterm babies with a birthweight of >1.250 g and respiratory distress. METHODS: Sixty-eight infants with birthweight of 1.250 to 2.000 g with respiratory distress and born at 32-34 GA and intubated with the indication of respiratory distress who also needed nasal ventilation for at least 48 hours were included in this prospective randomized controlled study, starting from birth one group received prophylactic caffeine citrate at loading dose of 20 mg/kg, and maintenance dose of 5 mg/kg in addition to respiratory support, long term neurological and developmental outcomes were recorded with Bayley-II. RESULTS: There was no difference in weight or gestational age at birth between the groups. Also, the groups were smilar in respiratory states. The caffeine group, was associated with a significant reduction in intubation requirement within the first 72 hr and shorter duration of mechanical and nasal ventilation, while there was no difference between the groups in total duration of oxygen therapy, and frequency of apneic episodes (respectively p=0.03, p=0.00, p=0.02, p>0.05). Any differences were not detected in terms of prematurity morbidities (p>0.05). Any significant intergroup differences were not detected as for PDA, NEC, IVC, laser-requiring ROP, and BPD (p>0.05). While the study was continuing regarding long-term neurodevelopmental outcomes Bayley neurodevelopmental tests were applied to 15 infants in the caffeine and 18 infants in the caffeine group at 12. and 18. months, and test results were csimilar in both groups (p>0.05). DISCUSSION AND CONCLUSION: The prophylactic use of caffeine in older preterm babies with respiratory distress, have short term benefits as lesser requirement for ntubation within the first 72 hours and decreased duration of ventilatory support without any advers side effects. Therefore if symptoms of respiratory distress are seen in preterm babies with a birthweight of >1.250 g, then initiation of prophylactic treatment may be considered. Larger scale randomized kontrollü studies are needed regarding this issue.
简介:预防性咖啡因治疗,减少早产儿呼吸暂停的频率。此外,它在减少间歇性低氧血症以及出生体重为1.250 g和呼吸窘迫的婴儿对额外呼吸机支持的需求方面的作用已得到充分证实。方法:本前瞻性随机对照研究纳入68名出生体重为1.250 ~ 2.000 g、出生年龄为32-34 GA、气管插管有呼吸窘迫指征且需要至少48小时鼻通气的婴儿,从出生开始,一组在呼吸支持的基础上给予20 mg/kg负荷剂量的预防性枸橼酸咖啡因,维持剂量为5 mg/kg。用bailey - ii记录长期的神经和发育结果。结果:两组新生儿出生时体重和胎龄均无差异。此外,两组的呼吸状态相似。咖啡因组与前72小时内插管需求显著减少以及机械通气和鼻通气持续时间缩短相关,而两组在氧气治疗总持续时间和呼吸暂停发作频率方面无差异(分别p=0.03, p=0.00, p=0.02, p>0.05)。在早产发病率方面没有发现任何差异(p < 0.05)。PDA、NEC、IVC、需要激光的ROP和BPD组间差异无统计学意义(p < 0.05)。在研究长期神经发育结果的同时,贝利神经发育测试应用于15名咖啡因组的婴儿和18名12岁咖啡因组的婴儿。和18。月,两组检测结果相似(p < 0.05)。讨论与结论:在有呼吸窘迫的大龄早产儿中预防性使用咖啡因具有短期益处,因为在头72小时内对插管的需求较少,并且呼吸支持的持续时间缩短,没有任何不良副作用。因此,如果出生体重为1.250 g的早产儿出现呼吸窘迫症状,则可以考虑开始预防性治疗。关于这个问题需要更大规模的随机kontrollü研究。
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引用次数: 0
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