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Immunohistochemical investigation of the effects of different doses of some endocrine-disrupting chemicals on receptorinteracting serine/threonine-protein kinase 1 (RIPK1) levels in the testis 不同剂量内分泌干扰物对睾丸受体相互作用丝氨酸/苏氨酸蛋白激酶1 (RIPK1)水平影响的免疫组化研究
Pub Date : 2023-09-22 DOI: 10.51271/kmj-0119
Kıymet Kübra Tüfekci
Aims: The reproductive toxicity of endocrine-disrupting chemicals (EDCs) is well known, but the underlying mechanism remains unclear. Receptor-interacting serine/threonine protein kinase 1 (RIPK1) mainly mediates cell death and inflammation. It is crucial to both necroptosis and apoptosis. Therefore, in this study, we aimed to investigate the changes in RIPK1 expression levels immunohistochemically in the adverse mechanism of EDCs on spermatogenic cells. Methods: Forty-two Wistar Albino male rats (10 weeks old, 250±50 g) were assigned into seven groups. Bisphenol A (BPA), 4-Nonylphenol (NP), and their mixtures at low 25 mg/kg doses and high 100 mg/kg doses were used. The control group received corn oil via gastric tube. At the end of the 21 days of the experimental protocol, the testis tissues were extracted and immersed in Bouin's solution. Five µm sections were taken from the tissue and stained immunohistochemically with an anti-RIPK1 antibody. Histo (H)-score was calculated by determining the intensity of immunoreactivity in the sections. Results: The results showed that the mixed dose group and all high-dose group round spermatids had excessive RIPK1 immunoreactivities compared to the control group and individually low-dose group of both (p<0.01). This result might be responsible for poor sperm quality, motility disruptions, or other reproductive consequences. Conclusion: In conclusion, RIPK1 overactivation may be essential in pathophysiological conditions caused by EDC exposure at high doses and their mixture. Further studies are now needed to evaluate RIPK1 overactivation in testis tissues.
目的:内分泌干扰物(EDCs)的生殖毒性众所周知,但其潜在的机制尚不清楚。受体相互作用丝氨酸/苏氨酸蛋白激酶1 (RIPK1)主要介导细胞死亡和炎症。它对坏死下垂和细胞凋亡都至关重要。因此,在本研究中,我们旨在通过免疫组化的方法探讨EDCs对生精细胞的不良作用机制中RIPK1表达水平的变化。方法:10周龄Wistar Albino雄性大鼠42只,体重250±50 g,随机分为7组。采用双酚A (BPA)、4-壬基酚(NP)及其混合物,低剂量25 mg/kg,高剂量100 mg/kg。对照组经胃管灌胃玉米油。在实验方案的第21天结束时,提取睾丸组织并浸泡在Bouin溶液中。从组织中取5µm切片,用抗ripk1抗体免疫组织化学染色。通过测定切片的免疫反应性强度来计算Histo (H)-score。结果:结果显示,与对照组和单独低剂量组相比,混合剂量组和各高剂量组圆形精子的RIPK1免疫反应性均较高(p<0.01)。这一结果可能导致精子质量差、运动障碍或其他生殖后果。结论:综上所述,RIPK1过度激活可能是EDC高剂量及其混合暴露引起的病理生理条件所必需的。现在需要进一步的研究来评估RIPK1在睾丸组织中的过度激活。
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引用次数: 0
Characteristics and endoscopic ultrasound findings of gastrointestinal lesions: single-center experience 胃肠道病变的特点和内镜超声表现:单中心经验
Pub Date : 2023-09-22 DOI: 10.51271/kmj-0118
İdris Kurt, Doğan Albayrak, Osman Kula, Ali Rıza Soylu
Aims: We aimed to present the characteristics, indications, endoscopic ultrasonography procedure details, diagnoses and complication rate of patients who underwent endosonpgraphy in a single center. Methods: Forty six patients admitted to Trakya Unversity Faculty of Medicine and underwent EUS (±FNA) procedure between January 2021 and May 2022 were included in the study. Patients files were analysed retrospectively. Demographic characteristics, presence and types of comorbidity, presence and types of malignancy in the family, use of antithrombotic drugs, laboratory data, details of eus procedure, pathology results, adverse events were recorded. The data obtained in the study were analyzed using Statistical Package for Social Science for Windows 26 package program. Results: A total of 46 patients were included in the study. 46% (n=21) were women. The median age was 64 (28-87). Antithrombotic use was present in 25% of the patients. Comorbidities were present in 84% of patients. The indications for EUS were predominantly pancreatic lesions (n=31). Aspirations were performed in addition to ultrasonographic examination in 78% (n=36) of the patients. 19 G (Gauge) needles were used in 30 and 25 G needles were used in 6 patients. Biopsy stations were stomach (n=31), duodenum (n=4), esophagus (n=1). Median long axis of the lesions was 34 (7-173) mm and the short axis was 26 (1-76) mm. 42% of the biopsied pancreatic lesions were cystic and 58% were solid. The CA19-9 level in solid lesions was statistically significantly higher than cystic (1512 /28 U/ml; p= 0.008). CA19-9 level was found mean 2061±3295 U/ml in patients with adenocarcinoma (n=8), 71±106 U/ml in cystic neoplasm and 152±338 in benign disorders (p=0.026). Cut-off value predicting adenocarsinoma with %87,5 spesifity and %87,5 sensitivity in our cohort was 174 U/ml (( AUC 0.85 ( 0.63-1)). Spesifity and sensitivity of the level 40 ( nearest level to universaly detected upper limit: 37 U/mL) was %62,5 and %87,5 respectively. Comparing malignant and benign lesions of pancreas overall, no statistical significance was found of CA19-9 level in predicting the diagnosis of tumor (p=0.15). Of the patients who underwent biopsy, 61% were malignant and 39% were benign. Malignant diagnoses were: adenocarsinoma, cystic neoplasm, gastrointestinal stromal tumor, neuroendocrine tumor, mesenchymal tumor, lumphoma, metastasis. Benign diagnoses were: otoimmune pancreatitis, normal cyst, chronic pancreatitis, pseudocyst, walled-off necrosis, polyp, no lesion. Post-procedure complications were not observed in any of the patients. Conclusion: The availability of endoscopic ultrasonography is expanding nowadays. Endoscopy ultrasonography is a precise, advantageous, and risk-free technique when performed by trained personnel.
目的:介绍单中心超声内镜检查患者的特点、适应证、超声内镜检查程序、诊断及并发症发生率。方法:研究纳入了2021年1月至2022年5月期间在Trakya大学医学院接受EUS(±FNA)手术的46例患者。回顾性分析患者档案。记录人口统计学特征、合并症的存在和类型、家庭中恶性肿瘤的存在和类型、抗血栓药物的使用、实验室数据、eus手术的细节、病理结果、不良事件。使用Statistical Package for Social Science for Windows 26软件包程序对研究所得数据进行分析。结果:共纳入46例患者。46% (n=21)为女性。中位年龄为64岁(28-87岁)。25%的患者使用抗血栓药物。84%的患者存在合并症。EUS的适应症主要是胰腺病变(n=31)。78% (n=36)的患者在超声检查的同时进行了穿刺检查。30例使用19g (Gauge)针,6例使用25g针。活检部位为胃(31例)、十二指肠(4例)、食道(1例)。胰腺中位长轴34 (7-173)mm,短轴26 (1-76)mm。42%的活检胰腺病变为囊性,58%为实性。实性病变CA19-9水平显著高于囊性病变(1512 /28 U/ml;p = 0.008)。腺癌患者CA19-9水平平均为2061±3295 U/ml (n=8),囊性肿瘤患者为71±106 U/ml,良性疾病患者为152±338 U/ml (p=0.026)。在我们的队列中,预测腺癌的特异性和敏感性分别为% 87.5和% 87.5的临界值为174 U/ml (AUC 0.85(0.63-1))。40级(最接近普遍检测上限37 U/mL)的特异性和敏感性分别为% 62.5%和% 87.5%。总体比较胰腺良恶性病变,CA19-9水平对肿瘤诊断的预测意义无统计学意义(p=0.15)。在接受活检的患者中,61%为恶性,39%为良性。恶性诊断:腺癌、囊性肿瘤、胃肠道间质瘤、神经内分泌瘤、间质瘤、肿块、转移瘤。良性诊断:耳免疫性胰腺炎,正常囊肿,慢性胰腺炎,假性囊肿,壁闭塞性坏死,息肉,无病变。所有患者均未出现术后并发症。结论:超声内镜检查的应用范围不断扩大。内窥镜超声检查是一种精确、有利和无风险的技术,当由训练有素的人员执行时。
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引用次数: 0
Assessing characteristics, treatment approaches, and outcomes of spontaneous intracerebral hemorrhage patients in intensive care: a retrospective study 重症监护自发性脑出血患者的特征、治疗方法和预后评估:一项回顾性研究
Pub Date : 2023-09-22 DOI: 10.51271/kmj-0113
Serpil Ekin, Asiye Demirel, İlkay Ceylan, Şermin Eminoğlu, Şeyda Efsun Özgünay
Aims: Spontaneous intracerebral hemorrhage (SIH) is a common cerebrovascular disease associated with high mortality and poor clinical outcomes. This study aimed to investigate the fundamental characteristics of patients with SIH, their treatment practices, and early results to provide a comprehensive overview. Methods: Patient records from 2017 to 2021 were reviewed following approval from the ethics committee of our hospital. Demographic data, surgical and medical treatments applied in the intensive care unit (ICU), and immediate clinical outcome data of patients meeting the study criteria were recorded and analyzed. Results: A total of 153 patients were included in this study. The mortality rate in SIH patients was identified as 53.59%. The mean age value of those who died was found to be higher. In these patients, "fainting" as the initial symptom was found to be more common, while "Focal Neurological Deficits" were less common. A lower median Glasgow Coma Scale (GCS) and higher Acute Physiology and Chronic Health Evaluation II (APACHE II) scores were also observed. It was noted that the fresh frozen plasma (FFP) usage rate was higher, whereas the usage rate of oral antihypertensives was lower in those who died. It was determined that 33.33 of patients, 33.33% were transferred to a service (neurology or neurosurgery), 11.76% received palliative care, and 1.31% received home care. Conclusion: The mortality rate of patients with SIH is extremely high, and treatment in intensive care should be conducted according to current guidelines. More comprehensive studies are needed to standardize the appropriate treatment approaches. Alongside suitable treatment strategies to reduce mortality, identifying and supporting surviving patients' long-term treatment and rehabilitation needs are of great significance.
目的:自发性脑出血(SIH)是一种常见的脑血管疾病,死亡率高,临床预后差。本研究旨在探讨SIH患者的基本特征,他们的治疗实践和早期结果,以提供一个全面的概述。方法:经我院伦理委员会批准,对2017 - 2021年患者病历进行审查。记录和分析符合研究标准的患者的人口统计数据、在重症监护病房(ICU)应用的外科和药物治疗以及即时临床结果数据。结果:本研究共纳入153例患者。SIH患者的死亡率为53.59%。研究发现,死亡人群的平均年龄值更高。在这些患者中,“昏厥”作为初始症状更为常见,而“局灶性神经功能缺损”则不太常见。格拉斯哥昏迷评分(GCS)中位数较低,急性生理和慢性健康评估II (APACHE II)评分较高。我们注意到,在死亡人群中,新鲜冷冻血浆(FFP)使用率较高,而口服抗高血压药物的使用率较低。33.33%的患者转院(神经内科或神经外科),11.76%的患者接受姑息治疗,1.31%的患者接受家庭护理。结论:SIH患者死亡率极高,重症监护治疗应按现行指南进行。需要更全面的研究来规范适当的治疗方法。除了适当的治疗策略以降低死亡率外,确定并支持存活患者的长期治疗和康复需求也具有重要意义。
{"title":"Assessing characteristics, treatment approaches, and outcomes of spontaneous intracerebral hemorrhage patients in intensive care: a retrospective study","authors":"Serpil Ekin, Asiye Demirel, İlkay Ceylan, Şermin Eminoğlu, Şeyda Efsun Özgünay","doi":"10.51271/kmj-0113","DOIUrl":"https://doi.org/10.51271/kmj-0113","url":null,"abstract":"Aims: Spontaneous intracerebral hemorrhage (SIH) is a common cerebrovascular disease associated with high mortality and poor clinical outcomes. This study aimed to investigate the fundamental characteristics of patients with SIH, their treatment practices, and early results to provide a comprehensive overview. Methods: Patient records from 2017 to 2021 were reviewed following approval from the ethics committee of our hospital. Demographic data, surgical and medical treatments applied in the intensive care unit (ICU), and immediate clinical outcome data of patients meeting the study criteria were recorded and analyzed. Results: A total of 153 patients were included in this study. The mortality rate in SIH patients was identified as 53.59%. The mean age value of those who died was found to be higher. In these patients, \"fainting\" as the initial symptom was found to be more common, while \"Focal Neurological Deficits\" were less common. A lower median Glasgow Coma Scale (GCS) and higher Acute Physiology and Chronic Health Evaluation II (APACHE II) scores were also observed. It was noted that the fresh frozen plasma (FFP) usage rate was higher, whereas the usage rate of oral antihypertensives was lower in those who died. It was determined that 33.33 of patients, 33.33% were transferred to a service (neurology or neurosurgery), 11.76% received palliative care, and 1.31% received home care. Conclusion: The mortality rate of patients with SIH is extremely high, and treatment in intensive care should be conducted according to current guidelines. More comprehensive studies are needed to standardize the appropriate treatment approaches. Alongside suitable treatment strategies to reduce mortality, identifying and supporting surviving patients' long-term treatment and rehabilitation needs are of great significance.","PeriodicalId":369732,"journal":{"name":"Kastamonu Medical Journal","volume":"89 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136100334","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
Evaluation of the methylation status of the MB-COMT, APC2, NR3C1, and DRD2 genes in Turkish patients with microtia 土耳其小个子症患者MB-COMT、APC2、NR3C1和DRD2基因甲基化状态的评估
Pub Date : 2023-09-22 DOI: 10.51271/kmj-0121
Sacide Pehlivan, Ayşe Feyda Nursal, Yasemin Oyacı, Mustafa Pehlivan, Mehmet Bekerecioğlu
Aims: Microtia is defined as a congenital malformation of the middle and external ears. DNA methylation is the major epigenetic modification of genomic DNA that is regulated in the early embryonic stage. In this study, we analyzed the methylation status of the MB-COMT, APC2, NR3C1, and DRD2 genes in patients with microtia. Methods: The blood samples were taken from microtia patients and healthy controls. Genomic DNA was isolated using a commercial kit. The methylation status of the MB-COMT, APC2, NR3C1, and DRD2 genes was analyzed using the methylation-specific polymerase chain reaction (MS-PCR) method. The results were evaluated statistically. Results: The DRD2 methylation status was found to be associated with microtia (p?0.001). We found that the DRD2 gene was partially methylated in all patients with microtia. There was no significant difference between the methylation status of the MB-COMT, APC2, and NR3C1 genes and microtia. Conclusion: To our knowledge, this is the first study in our country to evaluate the relationship between the methylation of these genes and the risk of microtia. Our results demonstrate the presence of epigenetic changes in the DRD2 gene during microtia development. Methylation may have contributed to the pathogenesis of microtia as it affects gene expression. Studies with larger sample sizes and in different ethnic groups are needed to further investigate the role of these genes in microtia.
目的:小耳症是一种先天性的中耳和外耳畸形。DNA甲基化是基因组DNA的主要表观遗传修饰,在胚胎早期受到调控。在这项研究中,我们分析了MB-COMT、APC2、NR3C1和DRD2基因在小个子症患者中的甲基化状态。方法:采集小耳病患者和健康对照者的血液标本。使用商用试剂盒分离基因组DNA。采用甲基化特异性聚合酶链反应(MS-PCR)方法分析MB-COMT、APC2、NR3C1和DRD2基因的甲基化状态。对结果进行统计学评价。结果:发现DRD2甲基化状态与小个子症相关(p?0.001)。我们发现DRD2基因在所有的小个子症患者中都部分甲基化。MB-COMT、APC2和NR3C1基因的甲基化状态与小儿科之间无显著差异。结论:据我们所知,这是我国首次评估这些基因甲基化与小体病风险之间关系的研究。我们的研究结果表明,在小个子发育过程中,DRD2基因存在表观遗传变化。甲基化可能是影响基因表达的原因之一。需要在更大的样本量和不同的种族群体中进行研究,以进一步研究这些基因在小个子症中的作用。
{"title":"Evaluation of the methylation status of the MB-COMT, APC2, NR3C1, and DRD2 genes in Turkish patients with microtia","authors":"Sacide Pehlivan, Ayşe Feyda Nursal, Yasemin Oyacı, Mustafa Pehlivan, Mehmet Bekerecioğlu","doi":"10.51271/kmj-0121","DOIUrl":"https://doi.org/10.51271/kmj-0121","url":null,"abstract":"Aims: Microtia is defined as a congenital malformation of the middle and external ears. DNA methylation is the major epigenetic modification of genomic DNA that is regulated in the early embryonic stage. In this study, we analyzed the methylation status of the MB-COMT, APC2, NR3C1, and DRD2 genes in patients with microtia. Methods: The blood samples were taken from microtia patients and healthy controls. Genomic DNA was isolated using a commercial kit. The methylation status of the MB-COMT, APC2, NR3C1, and DRD2 genes was analyzed using the methylation-specific polymerase chain reaction (MS-PCR) method. The results were evaluated statistically. Results: The DRD2 methylation status was found to be associated with microtia (p?0.001). We found that the DRD2 gene was partially methylated in all patients with microtia. There was no significant difference between the methylation status of the MB-COMT, APC2, and NR3C1 genes and microtia. Conclusion: To our knowledge, this is the first study in our country to evaluate the relationship between the methylation of these genes and the risk of microtia. Our results demonstrate the presence of epigenetic changes in the DRD2 gene during microtia development. Methylation may have contributed to the pathogenesis of microtia as it affects gene expression. Studies with larger sample sizes and in different ethnic groups are needed to further investigate the role of these genes in microtia.","PeriodicalId":369732,"journal":{"name":"Kastamonu Medical Journal","volume":"91 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136100173","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
The assessment of patient-controlled analgesia with tramadol in adult tonsillectomy 曲马多在成人扁桃体切除术中的自控镇痛效果评价
Pub Date : 2023-09-22 DOI: 10.51271/kmj-0120
Asude Ünal, Mehmet Eser Sancaktar, Ayşe Çeçen, Murat Ünal
Aims: To investigate the effects of patient-controlled analgesia with tramadol (PCA-T) applicated in the postoperative inpatient period for adult tonsillectomies (TT). Methods: The records of adult TTies were retrospectively scanned. The indications, surgical technique, postoperative complaints, length of stay (LOS) and re-admissions have been recorded in both groups treated with PCA-T and conventional analgesics during inpatient period. The data was analyzed with SPSS Statistics 23 program. Results: Totally 242 patients (n=242) met the inclusion criteria with a mean age of 28.47±8.44 years. PCA-T (n = 70) was mostly preferred in patients with the indications of tonsillar hypertrophy (TH) and recurrent tonsillitis (RH) + TH indications (p<0.05). In patients operated with a Plasma blade (PB), the PCA-T application rate (50.9%) was significantly higher than those operated with bipolar radiofrequency clamp (BRC) (22.1%) or cold dissection (CD) (23.0%) (p<0,001). No significant effects of PCA-T were observed on postoperative complications, LOS, and re-admission rates (p>0.05). Conclusions: Although PCA-T is more preferred for the adult TTies with an indication of TH and TTies performed with PB, it does not provide an advantage over conventional analgesic methods.
目的:探讨曲马多自控镇痛(PCA-T)在成人扁桃体切除术(TT)术后住院期的应用效果。方法:对成人TTies病历进行回顾性扫描。记录两组患者在住院期间分别使用PCA-T和常规镇痛药治疗的适应证、手术技术、术后主诉、住院时间(LOS)和再入院情况。采用SPSS统计软件23对数据进行分析。结果:242例患者(n=242)符合纳入标准,平均年龄28.47±8.44岁。在扁桃体肥大(TH)指征和复发性扁桃体炎(RH) + TH指征的患者中,PCA-T (n = 70)更受青睐(p < 0.05)。在等离子刀片(PB)手术的患者中,PCA-T的应用率(50.9%)明显高于双极射频钳(BRC)(22.1%)或冷剥离(CD) (23.0%) (p< 001)。PCA-T对术后并发症、LOS和再入院率无显著影响(p>0.05)。结论:尽管PCA-T更适用于有TH指证的成人TTies和有PB的TTies,但它并不比传统的镇痛方法有优势。
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引用次数: 0
A modified anal eversion technique for colorectal anastomosis in laparoscopic rectal cancer surgery 改良肛门外翻技术在腹腔镜直肠癌手术中的结肠吻合术
Pub Date : 2023-09-22 DOI: 10.51271/kmj-0115
Mehmet Aslan, Oktay Karaköse
Aims: This study presents a modified colorectal anastomosis method that consists of multi-task use of a circular stapler and anal eversion to perform a safer anastomosis. We aimed to describe the anorectal eversion and anastomosis techniques in detail and compare the results of the modified technique with those of the standard laparoscopic surgical technique. Methods: This retrospective study was conducted with fifty-five patients who underwent laparoscopic TME for middle and distal rectal cancer between 2016-2022. The patients were divided into two groups: those who underwent standard laparoscopic transabdominal surgery and those who underwent anorectal eversion (Modified ASET Method). The baseline features of the patients and the distribution of surgical outcomes between the two groups were statistically compared. Results: The Modified ASET group consisted of twenty-one patients. The morbidity rate associated with this procedure was 14.2%. CRM was positive in 9.5% of patients, and a safe distal surgical margin was achieved in all patients. The local recurrence rate is 4.7%. No statistically significant difference was observed between the Modified ASET and standard TME groups in terms of oncological outcomes (p = 0.828). Conclusion: Anorectal stump eversion and extra-abdominal transection-based modified colorectal anastomosis are reliable approaches that provide satisfactory surgical outcomes.
目的:本研究提出了一种改良的结肠直肠吻合术,该方法由环形吻合器和肛门外翻的多任务使用组成,以实现更安全的吻合。我们的目的是详细描述肛门直肠外翻和吻合技术,并比较改进技术与标准腹腔镜手术技术的结果。方法:对2016-2022年间55例接受腹腔镜下直肠癌中、远端TME治疗的患者进行回顾性研究。患者被分为两组:接受标准腹腔镜经腹手术的患者和接受肛肠外翻(改良ASET方法)的患者。比较两组患者的基线特征及手术结果的分布。结果:改良ASET组共21例。与此手术相关的发病率为14.2%。9.5%的患者CRM阳性,所有患者均获得了安全的远端手术切缘。局部复发率为4.7%。改良ASET组与标准TME组在肿瘤预后方面无统计学差异(p = 0.828)。结论:肛肠残端外翻和腹外横断为基础的改良结直肠吻合术是一种可靠的手术方法,可提供满意的手术效果。
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引用次数: 0
Barriers to end-of-life decisions and care objectives in intensive care units 临终决定和重症监护病房护理目标的障碍
Pub Date : 2023-09-22 DOI: 10.51271/kmj-0111
Ahmet Sari, Osman Ekinci
Aims: Technological advancements have played a crucial role in the advanced development of organ support systems in intensive care units (ICUs). While the utilization of support systems enhances patient discharge rates, it also extends the ICU stay of patients with terminal comorbidities who have no chance of survival. This elongation of the dying process, which is the inevitable outcome, results in a suspension of life in a sense. Hence, the effective implementation of end-of-life decisions and care stands as one of the crucial steps in the intensive care process. The objective of this study is to identify barriers to end-of-life decision-making and care in intensive care settings. Its aim is to facilitate a comprehensive, suitable, and peaceful experience for patients at the end of life and their families by making the necessary arrangements. Methods: This survey study involved physicians and nurses evaluating the prepared questionnaire questions concerning the challenges encountered in intensive care settings. Results: The most important barriers to making end-of-life decisions in intensive care were; among clinician-related factors, concern about legal liability for withholding life-sustaining treatments was 98 (79.7%), among institutional and ICU-related factors, the lack of regulated protocols and standards for end-of-life decisions and care was 96 (78%), among family-related factors, unrealistic expectations of patients and/or families about the prognosis or effectiveness of ICU treatment was 83 (67.5%), and disagreements among family members about end-of-life decisions was 80 (65%).Regarding end-of-life care, the admission of patients to the intensive care unit who would not benefit from treatments in the intensive care unit was rated as 110 (89.4%) and the absence of palliative care services to which a dying patient could be transferred was rated as 108 (87.8%). Conclusion: Providing unavailing treatments to patients who will not benefit from intensive care interventions results in a decline in quality of life, increased distress among family members, and burnout among intensive care staff. Therefore, end-of-life decisions and care should be effectively implemented in intensive care units. Ensuring adequate training, fostering effective communication between clinicians and families, and maximizing collaboration and communication with the ICU team and other medical departments can facilitate prompt and effective decision-making regarding end-of-life care.
目的:技术进步在重症监护病房(icu)器官支持系统的先进发展中发挥了至关重要的作用。支持系统的使用在提高患者出院率的同时,也延长了无生存机会的晚期合并症患者的ICU住院时间。这种死亡过程的延长是不可避免的结果,在某种意义上导致了生命的暂停。因此,有效地实施临终决定和护理是重症监护过程中的关键步骤之一。本研究的目的是确定在重症监护环境中临终决策和护理的障碍。其目的是通过作出必要的安排,为临终病人及其家属提供全面、合适和平静的体验。方法:本调查研究让医生和护士对准备的关于重症监护环境中遇到的挑战的问卷进行评估。结果:在重症监护中做出临终决定的最重要障碍是;在临床相关因素中,98人(79.7%)担心停止生命维持治疗的法律责任;在制度和ICU相关因素中,96人(78%)缺乏规范的临终决定和护理方案和标准;在家庭相关因素中,83人(67.5%)对患者和/或家属对ICU治疗的预后或有效性抱有不切实际的期望;在家庭成员中,80人(65%)对临终决定存在分歧。在临终关怀方面,无法从重症监护病房治疗中获益的患者入住重症监护病房的评分为110分(89.4%),而缺乏临终患者可以转到的姑息治疗服务的评分为108分(87.8%)。结论:对无法从重症监护干预中获益的患者进行无效治疗,会导致患者的生活质量下降,家属的痛苦增加,重症监护人员的倦怠。因此,临终决定和护理应在重症监护病房有效实施。确保充分的培训,促进临床医生和家属之间的有效沟通,并最大限度地与ICU团队和其他医疗部门合作和沟通,可以促进有关临终关怀的及时有效决策。
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引用次数: 0
Can immature granulocyte (IG), an inflammatory marker, be used in the differential diagnosis of epilepsy and non-epileptic psychogenic seizure? 未成熟粒细胞(IG),一种炎症标志物,能否用于癫痫和非癫痫性心因性癫痫的鉴别诊断?
Pub Date : 2023-09-22 DOI: 10.51271/kmj-0117
Mehmet Akif Bildirici, Idris Kocatürk
Aims: Differential diagnosis of epilepsy and psychogenic non-epileptic seizures (PNES) is a great challenge. Intense neuronal activity during epileptic seizures can cause neuroinflammation. Immature granulocyte (IG) is a new inflammatory marker analyzed in hemogram. This study investigated the role of IG in differentiating epilepsy from PNES. Methods: In this retrospective study, patients who applied to the emergency department for the first time with seizures and were diagnosed with epilepsy/PNES (clinical evaluation and electroencephalography) after included the seizure by the neurology clinical follow-up. Of the 84 patients, 54 had epilepsy, and 30 had PNES. Hemogram analyses were performed within 2 hours of the onset of the seizure. Results: The IG count was 0.03 x109/L (0.02-0.06) and 0.03 x109/L (0.02-0.05) in the epilepsy and PNES groups, respectively. The two groups had no statistically significant difference (p=0.291). Only serum C-reactive protein (CRP) levels significantly differed between the two groups (p=0.031). The ROC curve analysis for the CRP test yielded a serum CRP value of 2.35 mg/L, with a sensitivity of 0.57 and a specificity of 0.73, as the optimal cut-off value for distinguishing epilepsy from PNES. The ROC analysis for the AUC yielded an estimate of 0.64 (95% confidence interval: 0.52-0.77). Conclusion: In conclusion, only CRP was useful in differentiating epilepsy from PNES in the study. However, the IG count did not help to separate the two seizures. Therefore, these findings should be confirmed by further prospective studies with large samples assessing the IG count. This study evaluating the IG count, a new inflammatory marker, will contribute to the literature.
目的:癫痫与心因性非癫痫发作(PNES)的鉴别诊断是一个巨大的挑战。癫痫发作时强烈的神经活动可引起神经炎症。未成熟粒细胞(IG)是血象中发现的一种新的炎症标志物。本研究探讨IG在癫痫与PNES鉴别中的作用。方法:回顾性研究首次就诊于急诊科并经临床评价及脑电图诊断为癫痫/PNES(临床评价及脑电图)的患者,通过神经病学临床随访纳入癫痫发作。84例患者中,54例患有癫痫,30例患有PNES。在癫痫发作后2小时内进行血象分析。结果:癫痫组和PNES组IG计数分别为0.03 × 109/L(0.02 ~ 0.06)和0.03 × 109/L(0.02 ~ 0.05)。两组比较差异无统计学意义(p=0.291)。只有血清c反应蛋白(CRP)水平在两组之间有显著差异(p=0.031)。CRP检测的ROC曲线分析结果显示,血清CRP值为2.35 mg/L,敏感性为0.57,特异性为0.73,是区分癫痫与PNES的最佳临界值。AUC的ROC分析估计为0.64(95%可信区间:0.52-0.77)。结论:在本研究中,仅CRP可用于癫痫与PNES的鉴别。然而,IG计数并没有帮助区分这两次缉获。因此,这些发现应该通过进一步的大样本前瞻性研究来评估IG计数。本研究评估IG计数这一新的炎症标志物,将有助于文献。
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引用次数: 0
The impact of COVID-19 on postoperative outcomes of emergency general surgery operations 新型冠状病毒肺炎对急诊普外科手术后疗效的影响
Pub Date : 2023-09-22 DOI: 10.51271/kmj-0116
Bora Barut, Yusuf Murat Bag
Aims: During the pandemic due to Coronavirus disease 2019 (COVID-19) many elective operations were postponed, while emergency surgical operations inevitably continued. Emergency general surgery procedures are known to have worse outcomes compared to elective ones. Besides, it is conceivable that COVID-19 itself may worsen surgical outcomes due to it may cause respiratory distress and multi-organ dysfunction. We aimed to present patients’ data who underwent surgery due to trauma and emergency general surgery diseases during the COVID-19 pandemic and the effect of COVID-19 on surgical outcomes in this study. Methods: Two hundred and thirty-five patients who underwent surgery due to trauma or emergency between March 2020 and January 2021 were enrolled. Two groups were created according to the COVID-19 status as positive (n=16) and negative (n=219). The demographics, clinical, laboratory, and perioperative data were analyzed and compared between these groups. Results: The median age of the patients was 51 (18-97) years, and 144 (61.2%) of them were male. The most common diagnosis was acute appendicitis (n= 121, 51.5%) followed by ileus. Subgroup comparisons showed that the COVID-19 (+) group had more patients with comorbidity and had higher C-reactive protein values, these differences were significant (p= 0.049, p= 0.001, respectively). Open surgery was performed significantly more in the COVID-19 (+) group (p= 0.037). Serious postoperative complications and mortality were seen more in the COVID-19 (+) group, but the differences were not significant. Patients with COVID-19 had significantly longer hospital stay (p= 0.007). Conclusion: COVID-19 positivity was found to have a negative impact on postoperative surgical outcomes in terms of emergency operations. It is not clear whether this negativity is due to the COVID-19 disease itself or the worse characteristics of patients with COVID-19.
目的:在2019冠状病毒病(COVID-19)大流行期间,许多选择性手术被推迟,而紧急手术不可避免地继续进行。众所周知,与选择性手术相比,紧急普通外科手术的结果更差。此外,COVID-19本身可能会导致呼吸窘迫和多器官功能障碍,从而恶化手术效果。我们的目的是在本研究中提供COVID-19大流行期间因创伤和急诊普外科疾病接受手术的患者数据以及COVID-19对手术结果的影响。方法:纳入2020年3月至2021年1月期间因创伤或急诊接受手术的235例患者。根据COVID-19状态分为阳性(n=16)和阴性(n=219)两组。对两组的人口统计学、临床、实验室和围手术期数据进行分析和比较。结果:患者中位年龄51岁(18 ~ 97岁),男性144例(61.2%)。最常见的诊断是急性阑尾炎(n= 121, 51.5%),其次是肠梗阻。亚组比较显示,COVID-19(+)组合并症患者较多,c反应蛋白值较高,差异均有统计学意义(p= 0.049, p= 0.001)。COVID-19(+)组开放手术次数明显增加(p= 0.037)。COVID-19(+)组术后严重并发症和死亡率较高,但差异无统计学意义。COVID-19患者住院时间明显延长(p= 0.007)。结论:在急诊手术中发现COVID-19阳性对术后手术效果有负面影响。目前尚不清楚这种消极情绪是由于COVID-19疾病本身还是由于COVID-19患者的较差特征。
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引用次数: 0
A case of occupational hypersensitivity pneumonia in a welder 焊工职业性过敏性肺炎1例
Pub Date : 2023-09-22 DOI: 10.51271/kmj-0122
Başak Güven, İlke Karabağ, Ahmet Uğur Demir
A 35-year-old male patient with a history of pigeon feeding was reported to have hypersensitivity pneumonia on thorax high-resolution computed tomography, which was taken after complaints of shortness of breath, fever, and weight loss. Firstly, hypersensitivity pneumonia due to pigeon feeding was considered a diagnosis. The patient's contact with the pigeon was cut off. His clinic improved with oral corticosteroid therapy. His symptoms recurred after oral corticosteroid therapy was discontinued. In the professional anamnesis taken, it was learned that he had been doing welding work for 14 years and his complaints increased on the days he worked. After other causes were excluded with the differential diagnosis, the case was diagnosed with hypersensitivity pneumonia due to metal dust contact. The rarity of occupational hypersensitivity pneumonia cases in welding workers makes it important to report individual cases and exposures. Occupational history can be skipped in hypersensitivity pneumonia patients, as it is often thought to be caused by contact with organic factors such as pigeon breeding. The importance of work history anamnesis is highlighted in the diagnosis of rare diseases such as occupational hypersensitivity pneumonia.
一名35岁男性患者,有喂鸽史,在主诉呼吸短促、发热和体重减轻后,胸部高分辨率计算机断层扫描报告为过敏性肺炎。首先,饲鸽引起的超敏性肺炎被认为是一种诊断。病人与鸽子的接触被切断了。口服皮质类固醇治疗改善了他的病情。停止口服皮质类固醇治疗后症状复发。在进行的专业回顾中了解到,他从事焊接工作已经14年了,他的抱怨随着工作天数的增加而增加。经鉴别诊断排除其他原因后,诊断为金属粉尘接触致超敏性肺炎。焊接工人职业性超敏性肺炎病例的罕见性使得报告个体病例和暴露情况非常重要。超敏性肺炎患者可以跳过职业史,因为它通常被认为是由接触有机因素引起的,如养鸽。在诊断罕见疾病(如职业性超敏性肺炎)时,工作经历记忆的重要性得到了强调。
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引用次数: 0
期刊
Kastamonu Medical Journal
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