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Impact of Selective Reporting of Antibiotic Susceptibility Test Results on Antibiotic Use in Patients with Bloodstream Infection with Streptococcus pneumoniae. 选择性报告抗生素药敏试验结果对肺炎链球菌血流感染患者使用抗生素的影响。
Pub Date : 2024-05-20 eCollection Date: 2024-01-01 DOI: 10.1159/000537770
Florian Geismann, Kathleen Brueckner, Michael Pfeifer, Bernd Salzberger, Stilla Bauernfeind, Florian Hitzenbichler, Michaela Simon, Aila Caplunik-Pratsch, Wulf Schneider-Brachert, Clemens Wiest, Thilo Hinterberger, Tamara Ruegamer, Arno Mohr

Introduction: Invasive pneumococcal disease is a major cause of morbidity and mortality in infectious diseases. Selective reporting of antibiotic susceptibility test results might lead to a tailored antibiotic therapy and could therefore be an important antibiotic stewardship program intervention. The aim of this study was to analyse whether a switch to selective reporting of antibiotic test results leads to a more focused antibiotic therapy in patients with a bloodstream infection with Streptococcus pneumoniae.

Methods: This study was performed as a retrospective cohort study at the University Hospital Regensburg, Germany. All blood cultures positive for Streptococcus pneumoniae between 2006 and 2021 were analysed. In 2014, a switch to selective reporting of antibiotic susceptibility test results omitting sensitivity results for agents not recommended was introduced.

Results: Twenty-four hours after final antibiotic susceptibility test results were available, 20.9% before (BI) versus 15.4% after implementation (AI) of selective reporting of antibiotic test results received a narrow-spectrum penicillin, while only 2.3% BI versus 5.8% AI received a narrow-spectrum penicillin from the beginning.

Conclusion: Selective reporting of antibiotic susceptibility test results without further antimicrobial stewardship interventions did not lead to a higher use of a narrow-spectrum penicillin in this study.

导言:侵袭性肺炎球菌疾病是传染病发病和死亡的主要原因。有选择性地报告抗生素药敏试验结果可能会带来有针对性的抗生素治疗,因此可能成为抗生素管理计划的一项重要干预措施。本研究旨在分析在肺炎链球菌血流感染患者中改用选择性报告抗生素检测结果是否会使抗生素治疗更有针对性:本研究是在德国雷根斯堡大学医院进行的一项回顾性队列研究。研究分析了 2006 年至 2021 年间所有肺炎链球菌阳性血培养结果。2014 年,医院开始有选择性地报告抗生素药敏试验结果,省略了不推荐使用的药物的药敏结果:在最终抗生素药敏试验结果出来 24 小时后,选择性报告抗生素试验结果之前(BI)有 20.9%的人使用了窄谱青霉素,而实施之后(AI)有 15.4%的人使用了窄谱青霉素,而从一开始就使用窄谱青霉素的 BI 只有 2.3%,AI 只有 5.8%:结论:在本研究中,选择性报告抗生素药敏试验结果而不采取进一步的抗菌药物管理干预措施并不会导致窄谱青霉素的使用率提高。
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引用次数: 0
Spontaneous Remission of Minimal Change Disease in a Colon Cancer Patient: A Case Report 一名结肠癌患者的微小病变自发缓解:病例报告
Pub Date : 2024-04-18 DOI: 10.1159/000538279
Seunghye Lee, Sehyun Jung, Hyejin Jeon, Hani Jang, Hyun-Jung Kim, T. W. Lee, Eunjin Bae, D. J. Park, Se‐Ho Chang
Abstract Introduction Minimal change disease (MCD) is most often primary but may occur secondary to other systemic diseases such as malignancy. In secondary MCD, spontaneous remission of nephrotic syndrome after the treatment of related diseases without steroid therapy is rare. Case Presentation A 78-year-old man visited the outpatient clinic with foamy urine and generalized edema that had persisted for 2 months. The patient had nephrotic syndrome. Before a kidney biopsy, he underwent several tests to determine the secondary cause of the nephrotic syndrome. The serum CEA was slightly elevated, and colon cancer was detected in the sigmoid colon. MCD was diagnosed from a kidney biopsy. He immediately underwent surgery for colon cancer. Complete remission of the MCD was achieved within 2 weeks after surgery. Conclusion Here, we report a rare case of a patient with secondary MCD who successfully achieved spontaneous remission after colon cancer surgery.
摘要 引言 肾小球疾病(MCD)多为原发性,但也可能继发于其他系统疾病,如恶性肿瘤。在继发性肾病综合征(MCD)中,治疗相关疾病后肾病综合征不使用类固醇治疗而自发缓解的情况非常罕见。病例介绍 一位 78 岁的男性患者因泡沫尿和全身水肿就诊,已持续 2 个月。患者患有肾病综合征。在进行肾活检前,他接受了多项检查,以确定肾病综合征的继发性病因。血清癌胚抗原(CEA)轻度升高,乙状结肠发现结肠癌。肾活检确诊为 MCD。他立即接受了结肠癌手术。术后两周内,MCD 完全缓解。结论 我们在此报告了一例罕见的继发性 MCD 患者在结肠癌手术后成功实现自发缓解的病例。
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引用次数: 0
Evaluation of Initial Enoxaparin Dosing and Antifactor Xa Levels in Infants Admitted to the Neonatal Intensive Care Unit 评估新生儿重症监护室收治婴儿的初始依诺肝素剂量和抗因子 Xa 水平
Pub Date : 2024-04-12 DOI: 10.1159/000537797
Rosemarie Nagy, T. Hemmelgarn, Stephen Deptola, Brianna Hemmann
Abstract Introduction Infants are at risk for thrombotic conditions due to multiple risk factors such as congenital heart defects and sepsis. According to the American College of Chest Physicians (ACCP) 2012 guidelines, enoxaparin may be given for thrombotic conditions at a dose of 1.5 mg/kg/dose every 12 h for patients less than 2 months of age and 1 mg/kg/dose every 12 h for those older than 2 months. Several studies have reported that infants typically require a higher initial dose of enoxaparin to reach therapeutic antifactor Xa levels than what is currently recommended. Methods This is a single-center retrospective case-control study of hospitalized infants less than 12 months of age who received treatment with enoxaparin while admitted to the neonatal intensive care unit (NICU) at a freestanding children’s hospital. The primary objective was the difference between the initial enoxaparin dose (mg/kg) compared to the enoxaparin dose in which the patient first achieved a therapeutic antifactor Xa level of 0.5–1.0 units/mL. Results A total of 56 infants were included in this study. The median enoxaparin dose at initiation was 1.5 mg/kg/dose, and the median enoxaparin dose at the first therapeutic antifactor Xa level was 1.9 mg/kg/dose (z = −12.7, p < 0.0001). There was no correlation between gestational age and weight with the enoxaparin dose required to reach a therapeutic antifactor Xa level. Conclusion Infants admitted to the NICU, specifically those less than 4 months of age, require higher initial enoxaparin dosing to reach therapeutic antifactor Xa levels than what is currently recommended.
摘要 引言 由于先天性心脏缺陷和败血症等多种风险因素,婴儿有血栓形成的风险。根据美国胸科医师学会(ACCP)2012 年指南,对于年龄小于 2 个月的患者,可按 1.5 毫克/千克/剂量每 12 小时给药一次;对于年龄大于 2 个月的患者,可按 1 毫克/千克/剂量每 12 小时给药一次。有几项研究报告称,与目前推荐的剂量相比,婴儿通常需要更高的依诺肝素初始剂量才能达到治疗性抗因子 Xa 水平。方法 这是一项单中心回顾性病例对照研究,研究对象是在一家独立儿童医院新生儿重症监护室(NICU)住院期间接受依诺肝素治疗的 12 个月以下的住院婴儿。首要目标是初始依诺肝素剂量(毫克/千克)与患者首次达到 0.5-1.0 单位/毫升治疗抗因子 Xa 水平的依诺肝素剂量之间的差异。结果 本研究共纳入了 56 名婴儿。开始使用时依诺肝素剂量的中位数为 1.5 毫克/千克/剂量,首次达到治疗性抗因子 Xa 水平时依诺肝素剂量的中位数为 1.9 毫克/千克/剂量(z = -12.7,p < 0.0001)。胎龄和体重与达到治疗性抗因子 Xa 水平所需的依诺肝素剂量之间没有相关性。结论 与目前推荐的剂量相比,新生儿重症监护室收治的婴儿(尤其是 4 个月以下的婴儿)需要更高的初始依诺肝素剂量才能达到治疗性抗因子 Xa 水平。
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引用次数: 0
Redefining Rare Disease Care in the Digital Age: Insights and Key Takeaways from a Digital Health Symposium Focused on Empowering Rare Disease Communities 在数字时代重新定义罕见病护理:以增强罕见病社区能力为重点的数字健康研讨会的见解和主要收获
Pub Date : 2024-04-10 DOI: 10.1159/000536274
Emily Lewis, Anuradha Dayal, Ron Li
Abstract At the Stanford-UCB Rare Disease Digital Health Symposium held in Stanford, California, on September 8, 2023, researchers, clinicians, payers, thought leaders, and rare disease caregivers and advocates discussed the current state of care delivery and future perspectives of digitally-enabled care for rare disease patient populations. Digital health aims to improve healthcare delivery through novel ways of providing access to more precise diagnosis, monitoring of disease progression, treatment, prognosis, and care management for rare disease patients. The meeting focused on highlighting challenges and unmet needs, data infrastructure and analytics, the need for targeted and effective personalized therapies, and the importance of digital care transformation. The meeting also covered the social and ethical impact of access to digitally delivered, patient-centered care, as well as views on implementation and patient autonomy and empowerment.
摘要 在 2023 年 9 月 8 日于加利福尼亚州斯坦福大学举行的斯坦福大学-加州大学伯克利分校罕见病数字健康研讨会上,研究人员、临床医生、付款人、思想领袖以及罕见病护理人员和倡导者讨论了罕见病患者群体的护理服务现状和数字化护理的未来前景。数字医疗旨在通过新颖的方式改善医疗服务,为罕见病患者提供更精确的诊断、疾病进展监测、治疗、预后和护理管理。会议重点强调了挑战和未满足的需求、数据基础设施和分析、对有针对性和有效的个性化疗法的需求,以及数字医疗转型的重要性。会议还讨论了获得以患者为中心的数字化医疗服务所带来的社会和伦理影响,以及对实施、患者自主权和赋权的看法。
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引用次数: 0
Value of Flemish Version of the Triage Risk Screening Tool in Predicting Unfavorable Outcomes after Elective Cancer Surgery: A Propensity Score-Matched Retrospective Cohort Study. 弗拉芒语版分流风险筛查工具在预测癌症择期手术后不利结局中的价值:倾向评分匹配的回顾性队列研究。
Pub Date : 2024-04-10 eCollection Date: 2024-01-01 DOI: 10.1159/000538247
Shugo Yajima, Yasukazu Nakanishi, Ryo Andy Ogasawara, Naoki Imasato, Kohei Hirose, Sao Katsumura, Madoka Kataoka, Hitoshi Masuda

Introduction: The Flemish version of the Triage Risk Screening Tool (fTRST), derived from the Triage Risk Screening Tool for assessing risk of readmission to the emergency department, is increasingly used as a simple screening tool in oncology. This study aimed to evaluate the utility of the fTRST in the context of elective surgical treatment for urologic cancer patients.

Methods: We included 886 patients who underwent major urologic cancer surgery at our institution between 2020 and 2022 and underwent preoperative screening, including fTRST. We set the fTRST cutoff at 2 and used propensity score matching and multivariate regression analysis to assess how fTRST affected two postoperative outcomes: ambulation failure and delirium.

Results: Of the 886 patients, 693 (78%) had an fTRST score <2, and 193 (22%) had an fTRST score ≥2 (high likelihood of frailty). After matching the groups by propensity scores, we compared the outcomes of 131 patients in each group. We found that the group with fTRST ≥2 had significantly higher rates of ambulation failure (15 vs. 11%, p = 0.03) and delirium (16 vs. 11%, p = 0.008) than the group with fTRST <2. Multivariate logistic regression analysis showed that fTRST score ≥2 was an independent risk factor for postoperative ambulation failure (odds ratio [OR] = 4.05, p = 0.02), along with age ≥75 years (OR = 6.62, p = 0.02), preoperative benzodiazepine medications (OR = 5.12, p = 0.01), and receiving radical cystectomy (OR = 9.30, p = 0.02). Similarly, for delirium, fTRST score ≥2 was an independent risk factor (OR = 2.88, p = 0.03), along with preoperative benzodiazepine medications (OR = 4.38, p = 0.002).

Conclusion: The fTRST might be a screening tool with great potential for identifying patients at high risk for unfavorable postoperative outcomes in elective urologic cancer surgery.

简介弗拉芒语版分诊风险筛查工具(fTRST)源自用于评估急诊科再入院风险的分诊风险筛查工具,作为一种简单的筛查工具,在肿瘤科的应用日益广泛。本研究旨在评估 fTRST 在泌尿系统癌症患者择期手术治疗中的实用性:我们纳入了 2020 年至 2022 年期间在我院接受泌尿系统癌症大手术并接受术前筛查(包括 fTRST)的 886 例患者。我们将 fTRST 临界值设定为 2,并使用倾向评分匹配和多变量回归分析来评估 fTRST 如何影响两种术后结果:行走失败和谵妄:结果:在886名患者中,693人(78%)的fTRST评分(p = 0.03)和谵妄(16 vs. 11%,p = 0.008)高于fTRST评分(p = 0.02)组,同时年龄≥75岁(OR = 6.62,p = 0.02)、术前服用苯二氮卓类药物(OR = 5.12,p = 0.01)和接受根治性膀胱切除术(OR = 9.30,p = 0.02)。同样,对于谵妄而言,fTRST评分≥2是一个独立的风险因素(OR = 2.88,p = 0.03),术前苯二氮卓类药物也是一个独立的风险因素(OR = 4.38,p = 0.002):fTRST可能是一种筛查工具,在识别泌尿系统癌症择期手术中术后不良预后的高风险患者方面具有巨大潜力。
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引用次数: 0
Salivary Cathelicidin (LL-37) in Children and Adolescents Living with HIV. 感染艾滋病毒的儿童和青少年唾液中的蜡样抗原 (LL-37)。
Pub Date : 2024-01-29 eCollection Date: 2024-01-01 DOI: 10.1159/000535596
Ana Lucia Seminario, Ashley E Karczewski, Whasun Chung, Yan Wang, Dalton Wamalwa, Sarah Benki-Nugent, Grace John-Stewart, Jennifer A Slyker, Arthur Kemoli

Introduction: Human cathelicidin LL-37 is a salivary antimicrobial peptide (AMP) with broad-spectrum activity against oral diseases, but few studies have assessed its role in children and adolescents living with HIV (CALHIV). We assessed salivary LL-37 levels and correlates in a long-term cohort of Kenyan CALHIV followed since antiretroviral therapy (ART) initiation.

Methods: Saliva was collected from 76 CALHIV who were recruited from two ongoing pediatric HIV studies in Nairobi, Kenya. Oral examinations documenting oral manifestations of HIV, dental caries, and gingivitis were completed. Additional variables included age, sex, HIV treatment (initial ART regimen) and disease parameters, caregivers' demographics, and oral pathologies were conducted. Data were statistically analyzed using the independent T test on the log-transformed LL-37.

Results: At the oral exam visit, the mean age of participants was 13.3 years (±SD = 3.4), and the median CD4 count was 954 cells/mm3. Mean salivary cathelicidin values of the cohort were 23.7 ± 21.1 ng/mL. Children with permanent dentition at time of oral examination, and children who initiated ART at ≥2 years old had higher mean LL-37 concentrations compared to those with mixed dentition and those who initiated ART <2 years old (p = 0.0042, 0.0373, respectively). LL-37 levels were not found to differ by initial type of ART regimen, CD4 count, or oral disease.

Conclusion: Further research and longitudinal studies are necessary to evaluate and improve the innate immunity of CALHIV in Kenya.

简介:人类柔毛鞘氨醇 LL-37 是一种唾液抗菌肽 (AMP),具有抗口腔疾病的广谱活性,但很少有研究评估其在儿童和青少年艾滋病病毒感染者 (CALHIV) 中的作用。我们评估了自开始抗逆转录病毒疗法(ART)以来长期跟踪的肯尼亚 CALHIV 队列中唾液 LL-37 的水平及其相关性:从肯尼亚内罗毕正在进行的两项儿科艾滋病研究中招募的 76 名 CALHIV 采集了唾液。完成了记录 HIV 口腔表现、龋齿和牙龈炎的口腔检查。其他变量包括年龄、性别、艾滋病治疗(初始抗逆转录病毒疗法方案)和疾病参数、护理人员的人口统计学特征以及口腔病理学。采用独立 T 检验对 LL-37 对数变换进行数据统计分析:口腔检查时,参与者的平均年龄为 13.3 岁(±SD = 3.4),CD4 细胞计数中位数为 954 cells/mm3。组群中唾液中猫毒素的平均值为 23.7 ± 21.1 纳克/毫升。与混合牙和开始接受抗逆转录病毒疗法的儿童相比,口腔检查时有恒牙的儿童和≥2 岁开始接受抗逆转录病毒疗法的儿童的平均 LL-37 浓度更高(分别为 p = 0.0042 和 0.0373)。LL-37水平并未因最初的抗逆转录病毒疗法类型、CD4计数或口腔疾病而有所不同:有必要开展进一步研究和纵向研究,以评估和改善肯尼亚 CALHIV 的先天免疫力。
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引用次数: 0
GLI-12 Reference Values versus Fixed 0.7 Ratio for the Detection of Airflow Obstruction in the Presence of Lung Hyperinflation. GLI-12 参考值与固定 0.7 比率用于检测肺过度充气时的气流阻塞。
Pub Date : 2024-01-23 eCollection Date: 2024-01-01 DOI: 10.1159/000535507
Lora Wahab, Christian G Cornelissen, Wolfram Windisch, Michael Dreher

Introduction: Airflow obstruction (AO) is evidenced by reduced forced expiratory volume in 1 s/forced vital capacity (FEV1/FVC) with the threshold for diagnosis often being set at <0.7. However, currently the ATS/ERS standards for interpretation of lung function tests recommend the lower limit of normal (LLN), calculated by reference equations of the Global Lung Initiative from 2012 (GLI-12), as a threshold for AO diagnosis. The present study aims to investigate phenotypes, with focus on hyperinflation, which influence AO prevalence defined by FEV1/FVC < LLN when compared to the fixed 0.7 threshold.

Methods: Data from 3,875 lung function tests (56.4% men, aged 18-95) including 3,824 body plethysmography recordings performed from July 2021 to June 2022 were analysed. The difference between both classifiers was quantified, before and after stratification by sex, age, and hyperinflation.

Results: AO diagnosis was significantly less frequent with the LLN threshold (18.2%) compared to the fixed threshold (28.0%) (p < 0.001) with discordance rate of 10.5%. In the presence of mild or moderate hyperinflation, there was substantial agreement (Cohen's kappa: 0.616, 0.718) between the classifiers compared to near perfect agreement in the presence of severe hyperinflation (Cohen's kappa: 0.896). In addition, subgroup analysis after stratification for sex, age, and hyperinflation showed significant differences between both classifiers.

Conclusion: The importance of using the LLN threshold instead of the fixed 0.7 threshold for the diagnosis of AO is highlighted. When using the fixed threshold AO, misdiagnosis was more common in the presence of mild to moderate hyperinflation.

导言:气流阻塞(AO)表现为1秒内用力呼气量/用力肺活量(FEV1/FVC)降低,诊断阈值通常设定为方法:分析了 2021 年 7 月至 2022 年 6 月期间进行的 3,875 次肺功能测试(56.4% 为男性,年龄在 18-95 岁之间)的数据,包括 3,824 次人体胸透记录。根据性别、年龄和过度充气进行分层前后,对两种分类器之间的差异进行了量化:LLN阈值的AO诊断率(18.2%)明显低于固定阈值(28.0%)(p < 0.001),不一致率为10.5%。在存在轻度或中度过度充气的情况下,分类器之间有很大的一致性(Cohen's kappa:0.616,0.718),而在存在严重过度充气的情况下,分类器之间几乎完全一致(Cohen's kappa:0.896)。此外,对性别、年龄和过度充气进行分层后进行的亚组分析表明,两种分类器之间存在显著差异:结论:使用LLN阈值而非固定的0.7阈值诊断AO的重要性得到了强调。结论:使用 LLN 临界值而非固定的 0.7 临界值诊断 AO 的重要性得到了强调。使用固定临界值诊断 AO 时,轻度至中度过度充气的误诊率更高。
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引用次数: 0
Point Cloud Registration for Measuring Shape Dependence of Soft Tissue Deformation by Digital Twins in Head and Neck Surgery 在头颈部手术中利用数字双胞胎测量软组织变形的形状依赖性的点云注册技术
Pub Date : 2024-01-09 DOI: 10.1159/000535421
Sara Monji-Azad, D. Männle, Jürgen Hesser, Jan Pohlmann, N. Rotter, Annette Affolter, Cleo-Aron Weis, Sonja Ludwig, Claudia Scherl
Introduction: A 2½ D point cloud registration method was developed to generate digital twins of different tissue shapes and resection cavities by applying a machine learning (ML) approach. This demonstrates the feasibility of quantifying soft tissue shifts. Methods: An ML model was trained using simulated surface scan data obtained from tumor resections in a pig head cadaver model. It hereby uses 438 2½ D scans of the tissue surface. Tissue shift was induced by a temperature change from 7.91 ± 4.1°C to 36.37 ± 1.28°C. Results: Digital twins were generated from various branched and compact resection cavities (RCs) and cut tissues (CT). A temperature increase induced a tissue shift with a significant volume increase of 6 mL and 2 mL in branched and compact RCs, respectively (p = 0.0443; 0.0157). The volumes of branched and compact CT were decreased by 3 and 4 mL (p < 0.001). In the warm state, RC and CT no longer fit together because of the significant tissue deformation. Although not significant, the compact RC showed a greater tissue deformation of 1 μL than the branched RC with 0.5 μL induced by the temperature change (p = 0.7874). The branched and compact CT forms responded almost equally to changes in temperature (p = 0.1461). Conclusions: The simulation experiment of induced soft tissue deformation using digital twins based on 2½ D point cloud models proved that our method helps to quantify shape-dependent tissue shifts.
简介通过应用机器学习(ML)方法,开发了一种 2½ D 点云配准方法,用于生成不同组织形状和切除腔的数字双胞胎。这证明了量化软组织移位的可行性。方法:使用从猪头尸体模型的肿瘤切除术中获得的模拟表面扫描数据训练 ML 模型。该模型使用了 438 次组织表面的 2½ D 扫描。温度从 7.91 ± 4.1°C 变化到 36.37 ± 1.28°C,诱发组织移动。结果:从不同的分支和紧凑切除腔(RC)和切口组织(CT)中生成了数字孪晶。温度升高会引起组织转移,支离和紧密 RC 的体积分别显著增加 6 mL 和 2 mL(p = 0.0443; 0.0157)。分枝型和紧密型 CT 的体积分别减少了 3 毫升和 4 毫升(p < 0.001)。在温热状态下,RC 和 CT 由于组织的显著变形而不再吻合。紧凑型 RC 的组织变形量为 1 μL,而支化型 RC 的组织变形量为 0.5 μL,虽然不明显,但温度变化引起的组织变形量更大(p = 0.7874)。分枝型和紧密型 CT 对温度变化的反应几乎相同(p = 0.1461)。得出结论:使用基于 2½ D 点云模型的数字双胞胎进行的软组织诱导变形模拟实验证明,我们的方法有助于量化与形状相关的组织变化。
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引用次数: 0
Comparison of Ultrasound-Guided Umbilical Venous Catheter Insertion with Blind Method: A Randomized Controlled Trial. 超声引导下脐带静脉导管插入与盲法的比较:随机对照试验
Pub Date : 2024-01-03 eCollection Date: 2024-01-01 DOI: 10.1159/000535096
Purbasha Mishra, Pankaj Kumar Mohanty, Tapas Kumar Som, Tanushree Sahoo, Usha Devi, Nerbadyswari Deep Bag

Introduction: Ultrasonography (USG) can be used in neonates to manipulate and place the umbilical catheter in the correct position. Although chest radiograph (CXR) is the gold standard, a noninvasive method like USG without radiation exposure may be an alternative bedside armamentarium to the clinician. The purpose of the study was to evaluate whether USG-guided umbilical venous catheter (UVC) insertion is superior to the conventional method for the successful insertion of UVC.

Method: The neonates born between 25 and 42 weeks of gestation requiring parenteral fluids and admission to neonatal intensive care unit (NICU) between September 2020 and November 2022 were randomized in two weight-based strata: ≤1,200 and >1,200 g. USG-guided UVC insertion was done in the intervention group and blind UVC insertion was done in the control group.

Results: Out of 112 enrolled neonates, 58 were in the USG-guided group and 54 in the blind group. There was no significant difference in the failure rate between the intervention and control groups (20% versus 29% [RR: 0.69, 95% CI: 0.36-1.33]). The sensitivity and specificity of USG in locating tip position were 97 and 46.8%, respectively. The mean procedure time in USG and blind groups was 8.9 and 8.3 min, respectively (p value 0.56).

Conclusion: USG does not reduce the failure rates during the insertion of umbilical catheters. However, being a safe, noninvasive procedure, it can be considered a rescue modality to CXR in NICUs equipped with portable USG for guiding UVC insertion.

导言:新生儿可使用超声波检查(USG)来操作脐导管并将其置于正确位置。虽然胸片(CXR)是金标准,但像 USG 这样无辐射的无创方法可能会成为临床医生的另一种床旁工具。本研究旨在评估 USG 引导下的脐静脉导管(UVC)插入是否优于传统方法,以成功插入 UVC:干预组在 USG 引导下插入 UVC,对照组盲插 UVC:结果:在 112 名登记的新生儿中,58 名新生儿在 USG 引导组,54 名新生儿在盲法组。干预组和对照组的失败率无明显差异(20% 对 29% [RR:0.69,95% CI:0.36-1.33])。USG 对定位尖端位置的敏感性和特异性分别为 97% 和 46.8%。USG 组和盲法组的平均手术时间分别为 8.9 分钟和 8.3 分钟(P 值为 0.56):结论:USG 并不能降低脐导管插入过程中的失败率。结论:USG 并不能降低插入脐导管时的失败率,但作为一种安全、无创的程序,在配备了便携式 USG 的新生儿重症监护室中,USG 可被视为 CXR 的一种辅助方式,用于指导 UVC 插入。
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引用次数: 0
Research Progress on the Etiology and Treatment of Premature Ovarian Insufficiency. 关于卵巢早衰病因和治疗的研究进展。
Pub Date : 2023-12-13 eCollection Date: 2023-01-01 DOI: 10.1159/000535508
Yuxian Wang, Jianqiu Jiang, Jiali Zhang, Peiyin Fan, Jian Xu

Background: Menopause in women marks the knot of reproductive life, and menopause is defined as the last menstrual period in a woman, but this is caused by the failure of the ovarian reserve. The average age of natural menopause in the general population of women has remained around 50-52 years. Premature ovarian insufficiency (POI) is a debilitating clinical syndrome that manifests as a decline in ovarian function in women under 40. This condition is a prominent cause of female infertility.

Summary: POI is a debilitating condition that not only wreaks havoc on patients' physical and mental well-being but also imposes substantial mental, psychological, and economic burdens, particularly on women. In addition to diminished fertility, individuals afflicted with POI face an elevated risk of developing debilitating conditions such as osteoporosis and cardiovascular disease. The etiologies of POI are highly heterogeneous, and it can be caused by spontaneous genetic defects or induced by autoimmune diseases, infections, and iatrogenic or environmental factors. Alarmingly, idiopathic POI, a subtype characterized by an unknown etiology, accounts for more than half of all POI cases. Currently, clinical interventions for POI primarily consist of hormone replacement therapy. Fertility preservation methods are cryopreservation of embryos, oocytes, and ovarian tissue. Immunological interventions, gene editing techniques, and stem cell-based therapies are being explored to unravel the diverse etiologies and underlying mechanisms of POI, thereby enabling the identification of optimal therapeutic interventions. These innovative approaches offer unprecedented opportunities to advance the field of reproductive medicine.

Key messages: The main aim of this paper was to offer a succinct summary of the latest research breakthroughs concerning the elucidation of the mechanisms governing the origin and management of POI.

背景:妇女绝经标志着生育期的结束,绝经是指妇女的最后一次月经,但这是由卵巢储备功能衰竭引起的。一般女性自然绝经的平均年龄保持在 50-52 岁左右。卵巢功能早衰(POI)是一种使人衰弱的临床综合征,表现为 40 岁以下女性卵巢功能衰退。摘要:早发性卵巢功能不全是一种使人衰弱的疾病,它不仅会对患者的身心健康造成严重破坏,还会给患者(尤其是女性)带来巨大的精神、心理和经济负担。除了生育能力下降之外,POI 患者还面临着罹患骨质疏松症和心血管疾病等衰弱性疾病的更高风险。POI 的病因多种多样,可由自发性遗传缺陷引起,也可由自身免疫性疾病、感染、先天性或环境因素诱发。令人担忧的是,病因不明的特发性 POI 亚型占所有 POI 病例的一半以上。目前,针对 POI 的临床干预措施主要包括激素替代疗法。生育力保存方法包括胚胎、卵母细胞和卵巢组织的冷冻保存。目前正在探索免疫学干预、基因编辑技术和干细胞疗法,以揭示 POI 的不同病因和潜在机制,从而确定最佳治疗干预措施。这些创新方法为生殖医学领域的发展提供了前所未有的机遇:本文的主要目的是简明扼要地总结有关阐明 POI 起源和管理机制的最新研究突破。
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