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Health follow-up visits of children with autism 自闭症儿童的健康随访
Pub Date : 2024-03-01 DOI: 10.51271/kmj-0136
Ayşe Esra Tapci̇, Aysu Duyan Çamurdan
Child health follow-up is the most important of basic health services and should continue at regular intervals until the age of 18 years. Physicians’ child health follow-up examinations present the best opportunity to deliver evidence-based preventive health services, such as monitoring the growth and development of the child, conducting age-appropriate screenings, providing vitamin/mineral support according to age and requirements, administering childhood vaccinations, informing the family about home accidents and nutrition, monitoring the child in terms of child neglect and abuse risks, and raising the awareness of the family in this regard. Child health follow-up should encompass not only children without any health problems but also those with mental, physical, visual, or hearing impairments, or special needs such as those with autism. Autism spectrum disorder is a neurodevelopmental disorder characterized by social and communication limitations and repetitive, restricted behaviors. The presence of a child with special needs such as autism can have social, psychological, and economic implications for family members. While there are many difficulties in caring for a healthy child, these difficulties increase exponentially in the care of a child with special needs. Professional assistance is necessary for families to address matters such as monitoring the child’s development, providing nourishment, and administering vaccinations. Children with autism constitute a group that needs to be closely followed up for vitamin-mineral deficiencies and growth retardation due to their higher risk of malnutrition. For these reasons, regular health follow-up of children with autism is essential at regular intervals.
儿童健康随访是最重要的基本保健服务,应定期持续到 18 岁。医生的儿童健康随访检查是提供循证预防性保健服务的最佳机会,如监测儿童的生长发育、进行适龄筛查、根据年龄和需求提供维生素/矿物质支持、接种儿童疫苗、告知家庭有关家庭事故和营养的信息、监测儿童被忽视和虐待的风险以及提高家庭在这方面的意识。儿童健康跟踪不仅应包括没有任何健康问题的儿童,还应包括有智力、身体、视力或听力障碍的儿童,或有自闭症等特殊需要的儿童。自闭症谱系障碍是一种神经发育障碍,其特点是社交和沟通能力受限,行为重复、受限。有自闭症等特殊需求的儿童的存在会给家庭成员带来社会、心理和经济方面的影响。照顾一个健康的孩子会遇到很多困难,而照顾一个有特殊需要的孩子,这些困难就会成倍增加。家庭需要专业人员的帮助,以解决诸如监测儿童发育、提供营养和接种疫苗等问题。由于自闭症儿童营养不良的风险较高,因此需要对他们的维生素-矿物质缺乏症和发育迟缓情况进行密切跟踪。因此,定期跟踪自闭症儿童的健康状况至关重要。
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引用次数: 0
Ultrasound-guided neuromonitoring methods in the intensive care unit 重症监护室的超声引导神经监测方法
Pub Date : 2023-12-17 DOI: 10.51271/kmj-0128
U. Demir, Ö. Taşkın, Z. Doğanay
Ultrasonography (USG) is a non-invasive, portable, bedside, reproducible, radiation-free, inexpensive, and easily accessible imaging method. It provides morphological and functional information. It allows for diagnosis, monitoring, and guiding treatment. The usage areas of USG in the ICU are broad. In interventional procedures (thoracentesis, vascular interventions, percutaneous tracheostomy), evaluation of lung pathologies (pneumothorax, pleural effusion, pulmonary edema, consolidation, A-line, B line), diaphragm evaluation, abdominal imaging (trauma, kidney, liver), diagnosis and follow-up of deep vein thrombosis and the assessment and follow-up of fluid resuscitation (IVCI) and neuromonitoring. USG-guided neuromonitoring can detect stenosis or occlusion of intracranial arteries, monitor the development of patients with vasospasm after subarachnoid hemorrhage, detect cerebral embolism, evaluate the cerebral collateral system, and determine brain death. It can also indirectly calculate intracranial pressure (ICP) and cerebral perfusion under USG guidance.
超声造影(USG)是一种无创、便携、床旁、可重复、无辐射、价格低廉且易于获取的成像方法。它可提供形态和功能信息。它可用于诊断、监测和指导治疗。USG 在重症监护室的应用领域非常广泛。在介入手术(胸腔穿刺术、血管介入术、经皮气管切开术)、肺部病变评估(气胸、胸腔积液、肺水肿、合并症、A 线、B 线)、膈肌评估、腹部成像(创伤、肾脏、肝脏)、深静脉血栓的诊断和随访以及液体复苏(IVCI)和神经监测的评估和随访中都有应用。USG 引导下的神经监测可检测颅内动脉狭窄或闭塞、监测蛛网膜下腔出血后血管痉挛患者的病情发展、检测脑栓塞、评估脑侧支系统以及判断脑死亡。它还可以在 USG 引导下间接计算颅内压(ICP)和脑灌注。
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引用次数: 0
The effect of general anesthesia applied during cesarean section on newborn bilirubin 剖腹产时全身麻醉对新生儿胆红素的影响
Pub Date : 2023-12-17 DOI: 10.51271/kmj-0124
Deniz Turan, A. Karayel
Aims: Today, delivery is often performed as normal spontaneous vaginal delivery (NSVD) and cesarean section operations. Deliveries with NSVD mostly take place in the delivery room without the need for additional anesthetic agents. General anesthesia and regional anesthesia techniques are applied in cesarean section operations. In this study; The aim of this study was to examine the effect of general anesthesia on newborn bilirubin and to compare it with the bilirubin level of babies born without general anesthesia with NSVD method.Methods: Between March 2022 and September 2022, 152 patients over the age of 18 with term pregnancy NSVD and elective cesarean section without complications were randomly included in the study. Cases diagnosed with liver and biliary tract disease, systemic liver and biliary tract effective drug use, DCOOMBS( +) and Covid (+) clinics were excluded.Results: Of the patients included in our study, 75 (49.3%) were given general anesthesia and 77 (50.7%) delivered with NSVD without general anesthesia. It was determined that the first hour bilirubin and the fourth hour bilirubin values were significantly higher (p <0.05) in the general anesthesia group compared to the group that did not receive general anesthesia. In the group that did not receive general anesthesia, the APGAR 5th min score was found to be significantly (p <0.05) higher than the general anesthesia group. APGAR 1 min value did not differ significantly (p > 0.05) between the anesthesia-free and general anesthesia groups. Neonatal weight, head circumference, and infant height did not differ significantly between the groups that did not receive general anesthesia and those who did not receive general anesthesia (p> 0.05). Conclusion: Among the groups that did not receive general anesthesia and anesthesia; Bilirubin value was found to be higher among babies born by cesarean section under general anesthesia. It seems that it is more beneficial to avoid systemic effects as much as possible and to disseminate NSVD.
目的:如今,分娩通常分为正常自然阴道分娩(NSVD)和剖腹产手术。正常自然阴道分娩大多在产房进行,不需要额外的麻醉剂。剖腹产手术则采用全身麻醉和区域麻醉技术。本研究旨在探讨全身麻醉对新生儿胆红素的影响,并将其与未使用全身麻醉的 NSVD 法新生儿的胆红素水平进行比较:2022年3月至2022年9月期间,随机纳入152例18岁以上足月妊娠NSVD和无并发症的择期剖宫产患者。排除确诊为肝胆道疾病、全身肝胆道有效药物使用、DCOOMBS(+)和Covid(+)门诊的病例:在纳入研究的患者中,75 例(49.3%)进行了全身麻醉,77 例(50.7%)在未进行全身麻醉的情况下进行了 NSVD 分娩。经测定,无麻醉组和全身麻醉组的第一小时胆红素值和第四小时胆红素值明显更高(P 0.05)。新生儿体重、头围和身高在未接受全身麻醉组和未接受全身麻醉组之间没有明显差异(P> 0.05)。结论在未接受全身麻醉组和麻醉组中,发现在全身麻醉下剖宫产的婴儿胆红素值较高。由此看来,尽可能避免全身影响和传播 NSVD 更为有益。
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引用次数: 0
Pulmonary candidiasis presenting as tumor-like shadow 表现为肿瘤样阴影的肺念珠菌病
Pub Date : 2023-12-17 DOI: 10.51271/kmj-0129
M. Babayiğit, N. Dereli, Zehra Baykal, Handan Güleç, Filiz Koç, M. Şahap, E. Horasanlı
Lung fungal infections are rare and carry a high risk of death in critically ill patients. Further investigations including radiological imaging are needed for differential diagnosis. In this article, we present a patient with a tumor-like shadow on chest X-ray and a mildly necrotic soft tissue mass of 4 cm in the first computed tomography (CT) examination of the thorax, who was therefore prediagnosed with Lung Cancer. Due to the poor general condition of the patient, his family did not accept further examinations for cancer. Approximately 40 days later, the patient was taken to the intensive care unit with the complaint of respiratory distress. The bronchial sample was negative for malignant cells and Candida Tropicalis was detected in cultures. The size of the mass decreased in CT controls after treatment with antifungal agents. We thought that the image on CT was due to Candida Tropicalis infection and regressed with antifungal treatment. In conclusion, we can conclude that pulmonary candidiasis may present with atypical radiological findings. Fungal infections should be kept in mind in the differential diagnosis of lung cancer in cases with confusing mass-like images.
肺部真菌感染十分罕见,在重症患者中死亡风险很高。鉴别诊断需要进一步检查,包括放射成像。在本文中,我们介绍了一名在胸部 X 光片上有肿瘤样阴影,并且在首次胸部计算机断层扫描(CT)检查中发现 4 厘米轻度坏死软组织肿块的患者,该患者因此被预先诊断为肺癌。由于患者全身状况不佳,其家人没有接受进一步的癌症检查。大约 40 天后,患者因呼吸困难被送入重症监护室。支气管样本中的恶性细胞呈阴性,培养液中检测到热带念珠菌。在使用抗真菌药物治疗后,CT 对照组中肿块的大小有所减小。我们认为,CT 上的图像是由于热带念珠菌感染所致,并在抗真菌治疗后消退。总之,我们可以得出结论,肺念珠菌病可能会出现不典型的影像学表现。在肺癌的鉴别诊断中,如果出现令人困惑的肿块样影像,应注意真菌感染。
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引用次数: 0
Our experiences with carotid artery endarterectomy operations 我们在颈动脉内膜切除手术方面的经验
Pub Date : 2023-12-17 DOI: 10.51271/kmj-0123
Ümit Halıcı, İ. Karal, Hüseyin Ağırbaş, Atilla Kanca, Z. Doğanay
Aims: In this retrospective study, we aimed to presentour experiences with patients undergoing carotid endarterectomy (CEA) operations.Methods: Between January 2011 and January 2021, a total of 88 patients (27 female, 61 male, mean age; 68.9 ± 8.7 and 41-88 years old) who underwent CEA were included in the study.Patients' files were reviewed.Bilateral CEA was performed in 2 of the patients. The complaints and demographic characteristics of the patients are shown in Table 1 and Table 2, respectively. Coronary artery bypass grafting (CABG) was also performed in 10 (8 of them simultaneously and 2 of them 1 month later)of the patients. In one of these simultaneously operated patients, aortic valve replacement was performed in addition to CEA and CABG. On the other hand, the operation was terminated due to the development of intraoperative sudden cardiac arrest in 2 patients.Results: Polytetrafluoroethylene patch, biological patch, Dacron patch, and great saphenous vein patch were used in 1, 1, 3,and 40 patients, respectively, while the CEA site was primarily closed in 43 patients.Characteristic features ofthe CEA operations are shown in Table 3. Also, complications of CEA surgery are shown in Table 4.In-hospital mortality was detected in 3 patients. Conclusion: The early results of our CEA operations are in line with the literature.
目的:在这项回顾性研究中,我们旨在介绍颈动脉内膜剥脱术(CEA)患者的手术经验:在 2011 年 1 月至 2021 年 1 月期间,共有 88 例患者(女性 27 例,男性 61 例,平均年龄为 68.9±8.7 岁,41-88 岁)接受了颈动脉内膜剥脱术(CEA)。患者的主诉和人口统计学特征分别见表 1 和表 2。10名患者还接受了冠状动脉旁路移植术(CABG)(其中8人同时接受手术,2人一个月后接受手术)。在这些同时接受手术的患者中,有一人在接受 CEA 和 CABG 手术的同时还接受了主动脉瓣置换术。另一方面,2 名患者因术中发生心脏骤停而终止了手术:表 3 显示了 CEA 手术的特征。CEA手术的并发症见表4。结论我们的 CEA 手术的早期结果与文献报道一致。
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引用次数: 0
Coagulation parameters and prognosis analysis in COVID-19 patients COVID-19 患者的凝血参数和预后分析
Pub Date : 2023-12-17 DOI: 10.51271/kmj-0126
Filiz Koç, M. Babayiğit
Aims: There are many factors that affect morbidity and mortality in COVID-19. Coagulopathy is thought to be one of the important mechanisms in COVID-19 mortality. In this study, it was aimed to investigate coagulation factors and their relationship with prognosis in COVID-19.Methods: Patients diagnosed with COVID-19 were retrospectively reviewed in our hospital. The patients' demographic data, laboratory data on admission to the hospital, intensive care admissions, and surveillance were recorded. Patients were divided into two groups; Group 1 is non-critical patients followed up in the clinic, Group 2 is critical patients who need treatment in the intensive care unit.Results: 403 patients followed up for COVID-19 were analyzed. It was determined that the average age of the patients in Group 1 was statistically significantly lower than those in Group 2. (1: 45.28 ± 15.31 vs. 2: 60.15 ± 15.72, respectively, p <0.001). It was observed that the rates of HT, DM, CHD, and COPD in Group 2 were statistically significantly higher than Group 1 (p <0.05). While APTT values were similar in both groups, D-Dimer values were significantly higher in Group 2. As QSOFA, SIC, DIC, and coagulation marker scores increased, the percentage of patients with death increased significantly (p <0.05). Age, HT, COPD, PT, and high fibrinogen levels were found to increase the mortality risk rates statistically (p <0.05).Conclusion: It was determined that the most important factors determining mortality in COVID-19 are COPD and HT. APTT and D-dimer values were not found to be a prognostic factor in terms of mortality. However, PT, fibrinogen, and age are poor prognostic factors and can be used to predict mortality requiring intensive care.
目的:影响 COVID-19 发病率和死亡率的因素很多。凝血功能障碍被认为是导致 COVID-19 死亡的重要机制之一。本研究旨在探讨凝血因子及其与 COVID-19 预后的关系:方法:对本院确诊的 COVID-19 患者进行回顾性研究。方法:对本院确诊的 COVID-19 患者进行回顾性研究,记录患者的人口统计学数据、入院时的实验室数据、重症监护入院情况以及监测情况。患者被分为两组:第一组是在诊所随访的非危重患者,第二组是需要在重症监护室接受治疗的危重患者:对 403 名 COVID-19 随访患者进行了分析。经统计,第一组患者的平均年龄明显低于第二组(第一组:45.28 ± 15.31,第二组:60.15 ± 15.72,P <0.001)。据观察,第 2 组的高血压、糖尿病、冠心病和慢性阻塞性肺病发病率在统计学上明显高于第 1 组(P <0.05)。虽然两组的 APTT 值相似,但第 2 组的 D-Dimer 值明显高于第 1 组。随着 QSOFA、SIC、DIC 和凝血标志物评分的增加,死亡患者的比例也明显增加(P <0.05)。经统计发现,年龄、高血压、慢性阻塞性肺病、PT 和高纤维蛋白原水平会增加死亡风险率(P <0.05):结论:COVID-19中决定死亡率的最重要因素是慢性阻塞性肺病和高血压。APTT和D-二聚体值并不是死亡率的预后因素。然而,PT、纤维蛋白原和年龄是不良预后因素,可用于预测需要重症监护的死亡率。
{"title":"Coagulation parameters and prognosis analysis in COVID-19 patients","authors":"Filiz Koç, M. Babayiğit","doi":"10.51271/kmj-0126","DOIUrl":"https://doi.org/10.51271/kmj-0126","url":null,"abstract":"Aims: There are many factors that affect morbidity and mortality in COVID-19. Coagulopathy is thought to be one of the important mechanisms in COVID-19 mortality. In this study, it was aimed to investigate coagulation factors and their relationship with prognosis in COVID-19.\u0000Methods: Patients diagnosed with COVID-19 were retrospectively reviewed in our hospital. The patients' demographic data, laboratory data on admission to the hospital, intensive care admissions, and surveillance were recorded. Patients were divided into two groups; Group 1 is non-critical patients followed up in the clinic, Group 2 is critical patients who need treatment in the intensive care unit.\u0000Results: 403 patients followed up for COVID-19 were analyzed. It was determined that the average age of the patients in Group 1 was statistically significantly lower than those in Group 2. (1: 45.28 ± 15.31 vs. 2: 60.15 ± 15.72, respectively, p <0.001). It was observed that the rates of HT, DM, CHD, and COPD in Group 2 were statistically significantly higher than Group 1 (p <0.05). While APTT values were similar in both groups, D-Dimer values were significantly higher in Group 2. As QSOFA, SIC, DIC, and coagulation marker scores increased, the percentage of patients with death increased significantly (p <0.05). Age, HT, COPD, PT, and high fibrinogen levels were found to increase the mortality risk rates statistically (p <0.05).\u0000Conclusion: It was determined that the most important factors determining mortality in COVID-19 are COPD and HT. APTT and D-dimer values were not found to be a prognostic factor in terms of mortality. However, PT, fibrinogen, and age are poor prognostic factors and can be used to predict mortality requiring intensive care.","PeriodicalId":369732,"journal":{"name":"Kastamonu Medical Journal","volume":"355 13","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138966580","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Concurrent diagnosis of Sjogren’s syndrome and polycthemia vera: a rare co-existence 同时诊断出 Sjogren's 综合征和多血症:罕见的并存现象
Pub Date : 2023-12-17 DOI: 10.51271/kmj-0130
Serkan Ünal, S. Kocaer
Primary Sjogren's Syndrome(pSS) is a chronic autoimmune disease and focal lymphocytic infiltration of the exocrine glands is the key pathological feature (1). Polycythemia vera(PV) is a chronic myeloproliferative disorder characterized by JAK-2 mutations and increased red blood cell mass(2,3). Autoimmune diseases and hematological malignancies can often be observed together. Patients with SS are at a higher risk of developing lymphoproliferative diseases mainly low-grade B-cell lymphomas and predominantly marginal zone lymphoma. Moreover, PV can rarely be presented with paraneoplastic events including small vessel vasculitis (2). However, PV and pSS co-existence had never been reported. We here want to present a case of concurrently diagnosed PV and pSS.
原发性斯约格伦综合征(pSS)是一种慢性自身免疫性疾病,外分泌腺局灶性淋巴细胞浸润是其主要病理特征(1)。多发性红细胞症(PV)是一种慢性骨髓增生性疾病,其特征是 JAK-2 基因突变和红细胞增多(2,3)。自身免疫性疾病和血液恶性肿瘤常常同时出现。SS 患者罹患淋巴增生性疾病的风险较高,主要是低级别 B 细胞淋巴瘤和边缘区淋巴瘤。此外,PV 在极少数情况下会出现副肿瘤事件,包括小血管炎(2)。然而,PV 和 pSS 同时存在的病例从未报道过。我们在此介绍一例同时确诊的 PV 和 pSS 病例。
{"title":"Concurrent diagnosis of Sjogren’s syndrome and polycthemia vera: a rare co-existence","authors":"Serkan Ünal, S. Kocaer","doi":"10.51271/kmj-0130","DOIUrl":"https://doi.org/10.51271/kmj-0130","url":null,"abstract":"Primary Sjogren's Syndrome(pSS) is a chronic autoimmune disease and focal lymphocytic infiltration of the exocrine glands is the key pathological feature (1). Polycythemia vera(PV) is a chronic myeloproliferative disorder characterized by JAK-2 mutations and increased red blood cell mass(2,3). Autoimmune diseases and hematological malignancies can often be observed together. Patients with SS are at a higher risk of developing lymphoproliferative diseases mainly low-grade B-cell lymphomas and predominantly marginal zone lymphoma. Moreover, PV can rarely be presented with paraneoplastic events including small vessel vasculitis (2). However, PV and pSS co-existence had never been reported. We here want to present a case of concurrently diagnosed PV and pSS.","PeriodicalId":369732,"journal":{"name":"Kastamonu Medical Journal","volume":"26 7","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138966197","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
ESR1 rs2234693 might be associated with TMD risk in the Turkish population, but not rs9340799 在土耳其人群中,ESR1 rs2234693 可能与 TMD 风险有关,但与 rs9340799 无关
Pub Date : 2023-12-17 DOI: 10.51271/kmj-0125
A. Nursal, S. Yıgıt, Adem Keskin, Mehmet Kemal Tümer
Aims: The gender and age distribution of temporomandibular disorder (TMD) suggest a possible role for the female hormonal axis in the pathogenesis. The goal of this study was to evaluate if estrogen receptor (ESR1) gene variants contribute to TMD susceptibility in the Turkish population.Methods: A total of 270 people, 130 of whom were TMD patients and 140 healthy controls, were included in the study. The ESR1 PvuII (rs2234693) and Xbal (rs9340799) variants were genotyped using the polymerase chain reaction based restriction fragment length polymorphism (PCR-RFLP). The results were evaluated statistically.Results: There were 110 women (81.48%) and 25 men (18.52%) in the patient group. We found there was a significant association between rs2234693 T/C, C/C genotypes and TMD (p=0.007). Also, the C allele was more prevalent in patients compared to controls (p=0.002). A statistically significant association was observed when the patients were compared with the controls according to TT versus TC+CC (p=0.002). There was no statistical significance between the patient and control groups in terms of rs9340799 genotype and allele distribution. Then we evaluated the relationship between genotype distributions and clinical characteristics. Both males and females had the highest rs2234693 T/C genotype (p=0.049). The majority of people with bruxism, bruxomania, and bruxism plus bruxoma carried the rs2234693 T/C genotype (p=0.025).Conclusion: Our results showed that ESR1 rs2234693 might be associated with TMD risk in the Turkish population, but not rs9340799.
目的:颞下颌关节紊乱症(TMD)的性别和年龄分布表明,女性荷尔蒙轴在发病机制中可能扮演着重要角色。本研究的目的是评估雌激素受体(ESR1)基因变异是否对土耳其人群的 TMD 易感性有影响:研究共纳入 270 人,其中 130 人为 TMD 患者,140 人为健康对照组。使用基于聚合酶链式反应的限制性片段长度多态性(PCR-RFLP)对 ESR1 PvuII(rs2234693)和 Xbal(rs9340799)变体进行基因分型。结果进行了统计评估:患者组中有 110 名女性(81.48%)和 25 名男性(18.52%)。我们发现 rs2234693 T/C、C/C 基因型与 TMD 有明显的关联(P=0.007)。此外,与对照组相比,C 等位基因在患者中更为普遍(p=0.002)。当根据 TT 与 TC+CC 对患者和对照组进行比较时,发现两者之间有统计学意义(p=0.002)。在 rs9340799 基因型和等位基因分布方面,患者组和对照组之间没有统计学意义。然后,我们评估了基因型分布与临床特征之间的关系。男性和女性的 rs2234693 T/C 基因型最高(P=0.049)。大多数磨牙症、磨牙躁狂症和磨牙症加磨牙瘤患者的基因型为rs2234693 T/C(P=0.025):我们的研究结果表明,在土耳其人群中,ESR1 rs2234693可能与TMD风险有关,但与rs9340799无关。
{"title":"ESR1 rs2234693 might be associated with TMD risk in the Turkish population, but not rs9340799","authors":"A. Nursal, S. Yıgıt, Adem Keskin, Mehmet Kemal Tümer","doi":"10.51271/kmj-0125","DOIUrl":"https://doi.org/10.51271/kmj-0125","url":null,"abstract":"Aims: The gender and age distribution of temporomandibular disorder (TMD) suggest a possible role for the female hormonal axis in the pathogenesis. The goal of this study was to evaluate if estrogen receptor (ESR1) gene variants contribute to TMD susceptibility in the Turkish population.\u0000Methods: A total of 270 people, 130 of whom were TMD patients and 140 healthy controls, were included in the study. The ESR1 PvuII (rs2234693) and Xbal (rs9340799) variants were genotyped using the polymerase chain reaction based restriction fragment length polymorphism (PCR-RFLP). The results were evaluated statistically.\u0000Results: There were 110 women (81.48%) and 25 men (18.52%) in the patient group. We found there was a significant association between rs2234693 T/C, C/C genotypes and TMD (p=0.007). Also, the C allele was more prevalent in patients compared to controls (p=0.002). A statistically significant association was observed when the patients were compared with the controls according to TT versus TC+CC (p=0.002). There was no statistical significance between the patient and control groups in terms of rs9340799 genotype and allele distribution. Then we evaluated the relationship between genotype distributions and clinical characteristics. Both males and females had the highest rs2234693 T/C genotype (p=0.049). The majority of people with bruxism, bruxomania, and bruxism plus bruxoma carried the rs2234693 T/C genotype (p=0.025).\u0000Conclusion: Our results showed that ESR1 rs2234693 might be associated with TMD risk in the Turkish population, but not rs9340799.\u0000","PeriodicalId":369732,"journal":{"name":"Kastamonu Medical Journal","volume":"360 17","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138966633","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
How much did the February 6 earthquakes affect a distant hospital? 2 月 6 日的地震对一家遥远的医院造成了多大影响?
Pub Date : 2023-12-17 DOI: 10.51271/kmj-0127
Miraç Koç, Fatma Mutlu Kukul Güven
Aims: In the earthquakes that took place in Kahramanmaraş on 06.02.2023, a large number of casualties and injuries were observed. Organizations and healthcare personnel providing healthcare services in the earthquake regions have significantly lost their functions and there have been disruptions in the provision of healthcare services. In this study, we analyzed the patients who applied due to being affected by the earthquake in Kastamonu, one of the provinces far from the epicenter of the earthquake.Methods: The records of 135 patients who admitted to Kastamonu Training and Research Hospital Emergency Medicine Clinic with the diagnosis of earthquake damage between 7-16 February 2023 were examined. They were divided into two groups: patients with trauma and other non-traumatic complaints. Demographic data, complaints, requested tests, final diagnoses, consultation and hospitalization status of the patients were recorded.Results: While 50 patients applied with complaints of trauma caused by the earthquake, 85 patients applied to the emergency department due to diseases other than trauma. 10 of these patients were hospitalized and the others were discharged. It was observed that soft tissue trauma was the most common diagnosis in applications for trauma reasons, and upper respiratory tract infection was the most common diagnosis for non-traumatic reasons.Conclusion: In our study, since we were a hospital far from the center of the earthquake, there were no patient applications on the first day, and since the patients arrived over the days, no problems arose during the triage and intervention stages.
目的:2023 年 2 月 6 日在卡赫拉曼马拉什(Kahramanmaraş)发生的地震造成了大量人员伤亡。在地震灾区提供医疗服务的机构和医护人员严重丧失职能,医疗服务中断。在本研究中,我们分析了远离震中的卡斯塔莫努省因受地震影响而提出申请的患者:对 2023 年 2 月 7 日至 16 日期间在卡斯塔莫努培训与研究医院急诊医学门诊就诊并诊断为地震损伤的 135 名患者的病历进行了研究。他们被分为两组:外伤患者和其他非外伤主诉患者。记录了患者的人口统计学数据、主诉、要求的检查、最终诊断、就诊和住院情况:结果:50 名患者因地震造成的外伤就诊,85 名患者因外伤以外的疾病就诊。其中 10 名患者住院治疗,其他患者出院。据观察,在因外伤而就诊的患者中,软组织外伤是最常见的诊断,而因非外伤而就诊的患者中,上呼吸道感染是最常见的诊断:在我们的研究中,由于我们是一家远离地震中心的医院,因此第一天没有病人申请,而且由于病人在几天内陆续到达,因此在分流和干预阶段没有出现问题。
{"title":"How much did the February 6 earthquakes affect a distant hospital?","authors":"Miraç Koç, Fatma Mutlu Kukul Güven","doi":"10.51271/kmj-0127","DOIUrl":"https://doi.org/10.51271/kmj-0127","url":null,"abstract":"Aims: In the earthquakes that took place in Kahramanmaraş on 06.02.2023, a large number of casualties and injuries were observed. Organizations and healthcare personnel providing healthcare services in the earthquake regions have significantly lost their functions and there have been disruptions in the provision of healthcare services. In this study, we analyzed the patients who applied due to being affected by the earthquake in Kastamonu, one of the provinces far from the epicenter of the earthquake.\u0000Methods: The records of 135 patients who admitted to Kastamonu Training and Research Hospital Emergency Medicine Clinic with the diagnosis of earthquake damage between 7-16 February 2023 were examined. They were divided into two groups: patients with trauma and other non-traumatic complaints. Demographic data, complaints, requested tests, final diagnoses, consultation and hospitalization status of the patients were recorded.\u0000Results: While 50 patients applied with complaints of trauma caused by the earthquake, 85 patients applied to the emergency department due to diseases other than trauma. 10 of these patients were hospitalized and the others were discharged. It was observed that soft tissue trauma was the most common diagnosis in applications for trauma reasons, and upper respiratory tract infection was the most common diagnosis for non-traumatic reasons.\u0000Conclusion: In our study, since we were a hospital far from the center of the earthquake, there were no patient applications on the first day, and since the patients arrived over the days, no problems arose during the triage and intervention stages.","PeriodicalId":369732,"journal":{"name":"Kastamonu Medical Journal","volume":"24 46","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138965716","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Results of stereotactic radiosurgery in the treatment of radioresistant brain metastases 立体定向放射外科治疗放射耐药脑转移瘤的结果
Pub Date : 2023-09-22 DOI: 10.51271/kmj-0112
Ela Delikgöz Soykut, Nilgun Sahin, Eylem Odabasi, Donay Aksan, Ahmet Baran, Hatice Tataroglu
Aims: The incidence of brain metastases in patients with renal cell carcinoma (RCC) and malignant melanoma (MM) with radioresistant histologies is over 50%. Stereotactic radiodiosurgery (SRS) may be beneficial in treating radioresistant histologies. The effectiveness of SRS in terms of local control and survival rates in the treatment of patients with radioresistant brain metastases was the focus of our study. Methods: A retrospective review of RCC and MM brain metastases treated with SRS between 2013 and 2020 was conducted. Local control rates, distant brain metastases free survival, and overall survival (OS) were study endpoints. Results: 55 brain metastases were detected in 29 patients, 14 of whom were MM and 15 were RCC. The median follow-up time was 13 (1-89) months. The 1-y and 3-y actuarial local control rates were 82.4% and 59%, respectively. Increased size and volume of brain metastases were associated with progressive disease (p=0.041, p=0.002). Local control rates were increased in those receiving whole brain radiotherapy (WBRT) prior to SRS (0.008). The 1-y and 3-y distant brain metastases free survival were 87.7% and 60.2%, respectively, and increased in those receiving WBRT before SRS, but not statistically significant (p=0.403). The median OS was 8 months (HR: 1.79, 95% CI: 4.48-11.51). There was no difference in OS according to whether the primary disease diagnosis was RCC or MM (p=0.482). Patients with 1-2 brain metastases had better OS than patients with 3 or more brain metastases (p=0.029). Recursive partitioning analysis (RPA) and graded prognostic assessment (GPA) prognostic risk scores were significantly related to OS (p=0.001, p<0.001). OS worsened in patients who received WBRT before SRS compared to those who did not (0.035). OS increased statistically in patients who received immunotherapy (p=0.033). Conclusion: Improvement in local control was found in patients with small tumor diameter and volume. The addition of WBRT to the SRS increased both local control and distant brain metastasis free survival. Regarding OS, multiple metastases, high RPA score, and low GPA score worsened OS. Another crucial observation is that a positive predictive effect on OS was detected in patients in whom immunotherapy was combined with SRS.
目的:具有放射耐药组织学的肾细胞癌(RCC)和恶性黑色素瘤(MM)患者脑转移的发生率超过50%。立体定向放射外科(SRS)可能有利于治疗放射耐药组织学。SRS在治疗放射耐药脑转移患者的局部控制和生存率方面的有效性是我们研究的重点。方法:回顾性分析2013年至2020年SRS治疗的RCC和MM脑转移病例。局部控制率、无远处脑转移生存和总生存(OS)是研究的终点。结果:29例患者共检出55例脑转移灶,其中MM 14例,RCC 15例。中位随访时间为13(1-89)个月。1年和3年精算局部控制率分别为82.4%和59%。脑转移灶的大小和体积增加与疾病进展相关(p=0.041, p=0.002)。在SRS之前接受全脑放疗(WBRT)的患者局部控制率增加(0.008)。1-y和3-y远端脑转移无生存率分别为87.7%和60.2%,在SRS前接受WBRT的患者生存率升高,但无统计学意义(p=0.403)。中位OS为8个月(HR: 1.79, 95% CI: 4.48-11.51)。原发疾病诊断为RCC还是MM, OS无差异(p=0.482)。1-2个脑转移患者的OS优于3个及以上脑转移患者(p=0.029)。递归划分分析(RPA)和分级预后评估(GPA)预后风险评分与OS显著相关(p=0.001, p<0.001)。与未接受SRS的患者相比,在SRS前接受WBRT的患者OS恶化(0.035)。接受免疫治疗的患者OS增加,差异有统计学意义(p=0.033)。结论:肿瘤直径、体积小的患者局部控制有所改善。在SRS中加入WBRT增加了局部控制和远端脑转移的生存。在OS方面,多发性转移、高RPA评分和低GPA评分加重了OS。另一个重要的观察结果是,免疫治疗联合SRS的患者对OS有积极的预测作用。
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Kastamonu Medical Journal
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