Diagnostic techniques and procedures

诊断技术和程序
  • 文章类型: Journal Article
    从日本的精神病医生和妇产科医生(OB/GYN)的角度研究和比较经前期综合征(PMS)和经前期烦躁不安(PMDD)的诊断和治疗。
    在2021年12月至2022年2月之间,对日本神经精神病诊所协会的成员进行了基于网络的调查。对上述调查做出回应的262名精神科医生的数据与2021年日本妇产科学会成员进行的一项调查的409名妇产科医生的数据进行了比较。
    总的来说,79.8%的精神科医生和97.3%的OB/GYN参与了PMS/PMDD的诊断和治疗。大多数精神科医生认为PMS应由OB/GYN治疗(74.4%),PMDD应由精神科医生治疗(75.6%)。只有86.6%的精神科医生进行了模糊的医疗访谈,只有9.7%的人保持了两个周期的症状日记。精神科医生大多开选择性5-羟色胺/5-羟色胺和去甲肾上腺素再摄取抑制剂(SSRI/SNRI)连续给药(91.1%),其次是康波药物,尤其是神明丸(73.3%);只有2.8%的人选择口服避孕药,与妇产科不同,而SSRI连续(32.8%)和黄体期给药(20.6%)和Kampo药物(42.1%)是最常见的一线治疗。63.6%的精神科医生规定了生活方式指导,其次是认知行为疗法(13.8%)和症状日记观察法(11.1%),与妇产科医生的选择相似。
    许多日本精神科医生和OB/GYN并没有将PMS/PMDD诊断建立在使用特定诊断标准的前瞻性监测方法上,因此没有提供循证治疗。此外,倾向于观察到专门部门的治疗。
    UNASSIGNED: To investigate and compare the diagnoses and treatment of premenstrual syndrome (PMS) and premenstrual dysphoric disorder (PMDD) from the perspectives of psychiatrists and obstetricians/gynecologists (OB/GYNs) in Japan.
    UNASSIGNED: Between December 2021 and February 2022, a web-based survey was conducted among the members of the Japanese Association of Neuro-Psychiatric Clinics. Data from 262 psychiatrists who responded to the aforementioned survey were compared with data from 409 OB/GYNs from a survey conducted in 2021 among members of the Japanese Society of Obstetrics and Gynecology.
    UNASSIGNED: Overall, 79.8% of psychiatrists and 97.3% of OB/GYNs were involved in practicing PMS/PMDD diagnosis and treatment. Most psychiatrists believed that PMS should be treated by OB/GYNs (74.4%) and PMDD by psychiatrists (75.6%). Only vague medical interviews were conducted by 86.6% of psychiatrists, and only 9.7% maintained a two-cycle symptom diary. Psychiatrists mostly prescribed selective serotonin/serotonin and noradrenaline reuptake inhibitor (SSRI/SNRI) continuous dosing (91.1%), followed by Kampo medicines, especially Kamishoyosan (73.3%); only 2.8% chose oral contraceptive pills, unlike OB/GYNs, while SSRI continuous (32.8%) and luteal phase dosing (20.6%) and Kampo medicine (42.1%) were the most common first-line treatments. Lifestyle guidance was prescribed by 63.6% of psychiatrists, followed by cognitive behavioral therapy (13.8%) and the symptom diary observation method (11.1%), which were similar to OB/GYNs\' choices.
    UNASSIGNED: Many Japanese psychiatrists and OB/GYNs do not base PMS/PMDD diagnoses on prospective monitoring methods using specific diagnostic criteria and therefore do not provide evidence-based treatment. Moreover, a tendency of being biased toward treatments in which the department specialized was observed.
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  • 文章类型: Journal Article
    CobasEGFR突变测试v2被FDA批准为非小细胞肺癌(NSCLC)中可行的EGFR变体的定性液体活检。它产生与突变等位基因水平相关的半定量指标(SQI)值,但临床应用于NSCLC监测的决策阈值尚缺乏.我们在20名EGFR突变的NSCLC受试者中进行了长期ctDNA监测;产生了155个治疗样品。我们定义了最佳SQI间隔以预测/排除采样后12周内的进展,并进行了正交校准与深度测序和数字PCR。SQI显示出显着的诊断能力(AUC0.848,95%CI0.782-0.901)。SQI低于5(63%的样本)的净现值为93%(95%CI87-96%),而SQI高于10(25%的样品)的PPV为69%(95%CI56-80%)。CobasEGFR与测序(Kappa0.860;95%CI0.674-1.00)和数字PCR显示完美的一致性。SQI值(r:0.910,95%0.821-0.956)与突变等位基因浓度密切相关,SQI为5和10,分别对应于6-9(0.2-0.3%)和64-105(1.1-1.6%)突变等位基因拷贝/mL(VAF)。我们的SQI0/5/10双阈值分类器在88%的抽血中产生了信息性结果,具有高NPV和良好的整体临床实用性,可用于以患者为中心的转移性NSCLC监测。
    Cobas EGFR mutation Test v2 was FDA-approved as qualitative liquid biopsy for actionable EGFR variants in non-small cell lung cancer (NSCLC). It generates semiquantitative index (SQI) values that correlate with mutant allele levels, but decision thresholds for clinical use in NSCLC surveillance are lacking. We conducted long-term ctDNA monitoring in 20 subjects with EGFR-mutated NSCLC; resulting in a 155 on-treatment samples. We defined optimal SQI intervals to predict/rule-out progression within 12 weeks from sampling and performed orthogonal calibration versus deep-sequencing and digital PCR. SQI showed significant diagnostic power (AUC 0.848, 95% CI 0.782-0.901). SQI below 5 (63% of samples) had 93% (95% CI 87-96%) NPV, while SQI above 10 (25% of samples) had 69% (95% CI 56-80%) PPV. Cobas EGFR showed perfect agreement with sequencing (Kappa 0.860; 95% CI 0.674-1.00) and digital PCR. SQI values strongly (r: 0.910, 95% 0.821-0.956) correlated to mutant allele concentrations with SQI of 5 and 10 corresponding to 6-9 (0.2-0.3%) and 64-105 (1.1-1.6%) mutant allele copies/mL (VAF) respectively. Our dual-threshold classifier of SQI 0/5/10 yielded informative results in 88% of blood draws with high NPV and good overall clinical utility for patient-centric surveillance of metastatic NSCLC.
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  • 文章类型: Journal Article
    简介C反应蛋白(CRP)是一种广泛用于评估感染的实验室测试,炎症性疾病,和恶性肿瘤,在临床诊断和管理中起着至关重要的作用。尽管它很实用,CRP测量实践因医生而异,经常受到培训和临床经验的影响。本研究探讨了全科医生对临床实践中CRP测量的看法,专注于其诊断价值,相关的困境,以及对临床生长和决策的影响。方法这项定性研究采用主题分析的方法来检验Unnan市医院全科医生的看法,Unnan,日本关于CRP测量。通过有目的的抽样选择了16名普通医生,并参加了一对一的半结构化访谈。采访是用日语进行的,记录,逐字转录,并进行归纳分析以确定主题。分析涉及迭代编码和研究团队之间的广泛讨论,以确保研究结果的可靠性和有效性。结果分析中出现了三个主要主题:CRP对诊断和协作的有用性,与CRP使用相关的困境,通过重新考虑CRP的重要性和临床生长。医生强调CRP在区分炎症和非炎症性疾病中的价值,预测临床课程,促进与专家的沟通。然而,困境是由CRP水平和临床症状之间的差异引起的,各种非特定因素的影响,和训练驱动的习惯性测试,导致不必要的测试和临床技能下降。与会者认识到需要将CRP视为许多诊断工具之一,养成质疑其必要性的习惯,并反思其用于增强临床推理和专业成长。结论CRP检测是一种有价值的诊断工具。但是有效的使用需要平衡和关键的方法。CRP水平和临床症状之间的差异可能导致过度依赖实验室结果和不必要的测试。一般医生应将CRP纳入更广泛的诊断框架,结合病史,体检,和其他测试。反思CRP测量的必要性和含义可以改善临床推理和决策,最终加强患者护理和资源管理。未来的研究应该在不同的医疗保健环境中探索相似的看法,并制定策略来优化临床实践中的CRP使用。
    Introduction C-reactive protein (CRP) is a widely used laboratory test for assessing infections, inflammatory diseases, and malignancies, playing a critical role in clinical diagnosis and management. Despite its utility, CRP measurement practices vary among physicians, often influenced by training and clinical experience. This study explores general physicians\' perceptions of CRP measurement in clinical practice, focusing on its diagnostic value, associated dilemmas, and impact on clinical growth and decision-making. Methods This qualitative study employed thematic analysis to examine the perceptions of general physicians at Unnan City Hospital, Unnan, Japan regarding CRP measurement. Sixteen general physicians were selected through purposive sampling and participated in one-on-one semi-structured interviews. The interviews were conducted in Japanese, recorded, transcribed verbatim, and analyzed inductively to identify themes. The analysis involved iterative coding and extensive discussion among the research team to ensure the reliability and validity of the findings. Results Three main themes emerged from the analysis: the usefulness of CRP for diagnosis and collaboration, dilemmas associated with CRP usage, and clinical growth through reconsideration of CRP\'s importance. Physicians highlighted CRP\'s value in distinguishing inflammatory from non-inflammatory diseases, predicting clinical courses, and facilitating communication with specialists. However, dilemmas arose from discrepancies between CRP levels and clinical symptoms, the influence of various non-specific factors, and habitual testing driven by training, leading to unnecessary tests and diminished clinical skills. Participants recognized the need to view CRP as one of many diagnostic tools, cultivate a habit of questioning its necessity, and reflect on its use to enhance clinical reasoning and professional growth. Conclusions CRP measurement is a valuable diagnostic tool, but effective use requires a balanced and critical approach. Discrepancies between CRP levels and clinical symptoms can lead to over-reliance on laboratory results and unnecessary testing. General physicians should integrate CRP within a broader diagnostic framework, combining it with patient history, physical examination, and other tests. Reflecting on the necessity and implications of CRP measurements can improve clinical reasoning and decision-making, ultimately enhancing patient care and resource management. Future research should explore similar perceptions in diverse healthcare settings and develop strategies to optimize CRP use in clinical practice.
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  • 文章类型: Journal Article
    目的:为了研究使用身材矮小同源异型盒2(SHOX2)和前列腺素E2受体EP4(PTGER4)基因的甲基化状态的联合生物标志物方法的性能,与血清CYFRA21-1水平一起,用于恶性胸膜间皮瘤(MPM)与良性反应性间皮增生(RMH)的鉴别诊断。
    方法:我们分析了48例MPM组织或胸腔积液细胞块标本和42例RMH。实时定量甲基化特异性PCR用于检测SHOX2,PTGER4,ras关联域家族1亚型A的甲基化状态,septin9基因和同源异型盒基因A9基因。此外,我们采用电化学发光免疫分析法测定了9种常用于泛癌症筛查试验的血清肿瘤标志物.
    结果:受试者工作曲线表明SHOX2、PTGER4基因甲基化和血清生物标志物CYFRA21-1在鉴定MPM方面表现出良好的诊断性能,曲线下面积(AUC)分别为0.761、0.904和0.847。SHOX2、PTGER4甲基化和CYFRA21-1的组合产生0.972的AUC值。该小组在区分MPM和RMH方面的诊断敏感性和特异性分别为91.3%(42/46)和97.6%(41/42),分别。组织和细胞块标本均可用于诊断过程。此外,CYFRA21-1水平升高与不良预后相关(p<0.05).PTGER4的甲基化水平可能提示MPM的预后不良。但差异无统计学意义。
    结论:联合检测SHOX2和PTGER4甲基化以及血清CYFRA21-1水平可显著提高MPM的诊断。此外,CYFRA21-1可作为MPM的预后指标。
    OBJECTIVE: To investigate the performance of a combined biomarker approach using the methylation status of the short stature homeobox 2 (SHOX2) and prostaglandin E2 receptor EP4 (PTGER4) genes, along with the serum levels of CYFRA21-1, for differential diganosis of malignant pleural mesothelioma (MPM) from benign reactive mesothelial hyperplasia (RMH).
    METHODS: We analysed 48 MPM tissue or pleural effusion cell block specimens and 42 cases with RMH. Real-time quantitative methylation-specific PCR was used to examine the methylation status of SHOX2, PTGER4, ras association domain family 1 isoform A, septin 9 gene and homeobox gene A9 genes. Additionally, we employed electrochemiluminescence immunoassay to measure nine serum tumour markers commonly used in pan-cancer screening tests.
    RESULTS: The receiver operating curve indicated that SHOX2, PTGER4 gene methylation and serum biomarker CYFRA21-1 exhibited good diagnostic performance in identifying MPM, with area under curves (AUCs) of 0.761, 0.904 and 0.847, respectively. The combination of SHOX2, PTGER4 methylation and CYFRA21-1 yielded an AUC value of 0.972. The diagnostic sensitivity and specificity of this panel in differentiating MPM from RMH were 91.3% (42/46) and 97.6% (41/42), respectively. Both tissue and cell block specimens can be used in the diagnostic process. Furthermore, elevated CYFRA21-1 levels were associated with poor prognosis (p<0.05). Hypermethylation level of PTGER4 may indicate an unfavourable prognosis of MPM, but the difference was not statistically significant.
    CONCLUSIONS: The combined detection of SHOX2 and PTGER4 methylation alongside serum CYFRA21-1 level significantly enhances the diagnosis of MPM. Additionally, CYFRA21-1 can serve as a prognostic indicator for MPM.
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  • 文章类型: Journal Article
    背景:将COVID-19大流行的影响降至最低的策略导致诊断检测的减少。重要的是要评估这种影响的程度和持续时间,以计划持续的护理并避免大流行的长期影响。目的:我们研究了COVID-19大流行与乳腺诊断检查率之间的关系,子宫颈,和马尼托巴省的结肠直肠癌,加拿大。设计和参与者:以人口为基础,我们采用横断面研究设计,采用中断时间序列分析,包括2015年1月1日至2022年8月31日的诊断性试验.设置:曼尼托巴,加拿大。主要结果:结果包括乳房X光检查,乳腺超声,阴道镜检查,和结肠镜检查率每100,000。估计了拟合和反事实测试数量之间的累积和百分比累积差异。意思是,中位数,和按转诊类型划分的从转诊到结肠镜检查日期的第90百分位数(选择性,半紧急,紧急)已确定。结果:2020年4月,在宣布COVID-19突发公共卫生事件后,双侧乳房X线照片减少了77%,单侧乳房X线检查70%,53%的乳房超声检查,阴道镜检查率为63%,结肠镜检查75%。在温尼伯(全省最大的城市中心),选择性和半紧急结肠镜检查减少了76%和39%,分别。紧急结肠镜检查没有减少。截至2022年8月,双侧乳房X光检查估计减少了7270例(10.7%),2722(14.8%)减少乳房超声检查,减少836(3.3%)阴道镜检查,在没有COVID-19的情况下,结肠镜检查比预期少11600(13.8%)。截至2022年12月,在温尼伯,估计有6030(23.9%)的选择性结肠镜检查,减少313(2.6%)半紧急结肠镜检查,和438(27.3%)更紧急结肠镜检查。结论:在曼尼托巴省,COVID-19大流行与乳腺诊断检查的大幅减少有关,结直肠,还有宫颈癌.两年半后,双侧乳房X线照片仍有大量累积缺陷,乳腺超声检查,结肠镜检查。
    Background: Strategies to minimize the impact of the COVID-19 pandemic led to a reduction in diagnostic testing. It is important to assess the magnitude and duration of this impact to plan ongoing care and avoid long-lasting impacts of the pandemic. Objective: We examined the association between the COVID-19 pandemic and the rate of diagnostic tests for breast, cervical, and colorectal cancer in Manitoba, Canada. Design and Participants: A population-based, cross-sectional study design with an interrupted time series analysis was used that included diagnostic tests from January 1, 2015 until August 31, 2022. Setting: Manitoba, Canada. Main Outcomes: Outcomes included mammogram, breast ultrasound, colposcopy, and colonoscopy rates per 100,000. Cumulative and percent cumulative differences between the fitted and counterfactual number of tests were estimated. Mean, median, and 90th percentile number of days from referral to colonoscopy date by referral type (elective, semiurgent, urgent) were determined. Results: In April 2020, following the declaration of the COVID-19 public health emergency, bilateral mammograms decreased by 77%, unilateral mammograms by 70%, breast ultrasounds by 53%, colposcopies by 63%, and colonoscopies by 75%. In Winnipeg (the largest urban center in the province), elective and semiurgent colonoscopies decreased by 76% and 39%, respectively. There was no decrease in urgent colonoscopies. As of August 2022, there were an estimated 7270 (10.7%) fewer bilateral mammograms, 2722 (14.8%) fewer breast ultrasounds, 836 (3.3%) fewer colposcopies, and 11 600 (13.8%) fewer colonoscopies than expected in the absence of COVID-19. As of December 2022, in Winnipeg, there were an estimated 6030 (23.9%) fewer elective colonoscopies, 313 (2.6%) fewer semiurgent colonoscopies, and 438 (27.3%) more urgent colonoscopies. Conclusions: In Manitoba, the COVID-19 pandemic was associated with sizable decreases in diagnostic tests for breast, colorectal, and cervical cancer. Two and a half years later, there remained large cumulative deficits in bilateral mammograms, breast ultrasounds, and colonoscopies.
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  • 文章类型: Journal Article
    背景:对腰椎后路椎间融合术后体间植骨重建的生物学过程以及该过程是否与背痛和体间融合状态的变化有关,缺乏了解。作为常用但不可靠的融合标准的替代方案,Hounsfield单位可用于量化生物活性和骨矿物质含量的变化。然而,迄今为止进行的评估Hounsfield单位的研究没有提供足够的细节,说明如何将骨移植物分段以测量Hounsfield单位以允许复制,并且没有评估个体患者移植物随时间变化的趋势。利用9例腰椎后路椎间融合术后患者的资料,开发了一种新的Hounsfield单位测量程序,并用于探索其量化骨移植物重建过程的可用性。
    方法:我们报告了9例患者(6例男性,三个女人,平均年龄64岁,所有高加索人),均在腰椎后路椎间融合术后1年和2年进行了计算机断层扫描。总的来说,9例(78%)中有7例(手术后1-2年,Hounsfield骨移植单位增加了3-41%.随着时间的推移,这些病例的Hounsfield单位值显示出很大的个体差异,这与不同程度的背痛和体间融合状态相吻合。
    结论:本病例系列使用的Hounsfield单位测量程序可能有助于量化腰椎后路椎间融合术后患者的体间骨移植重建,并且可以用作辅助诊断措施来监测骨移植物随时间的重建。未来的研究有必要探索如何根据临床变量或体间融合状态解释植骨Hounsfield单位值和Hounsfield单位轨迹。
    BACKGROUND: There is a lack of knowledge about the biological process of intercorporal bone graft remodeling after posterior lumbar interbody fusion surgery and whether this process is associated with changes in back pain and intercorporal fusion status. As an alternative to the commonly used but unreliable fusion criteria, Hounsfield units can be used to quantify biological activity and changes in bone mineral content. However, studies assessing Hounsfield units conducted to date do not provide sufficient details about how the bone grafts were segmented to measure the Hounsfield units to allow for replication, and did not assess individual patient trends in graft changes over time. Using the data of nine patients after posterior lumbar interbody fusion, a novel Hounsfield units measurement procedure was developed and used to explore its usability to quantify the bone graft remodeling process.
    METHODS: We report a case series of nine patients (six male, three female, mean age 64 years, all Caucasian) who all had computed tomography scans performed at 1 and 2 years after posterior lumbar interbody fusion surgery. Overall, seven out of the nine (78%) cases had a 3-41% increase in their bone grafts\' Hounsfield units between 1 and 2 years after surgery. The cases showed large interindividual variability in their Hounsfield units values over time, which coincided with varying levels of back pain and intercorporal fusion status.
    CONCLUSIONS: The Hounsfield units measurement procedure used for this case series may be useful to quantify intercorporal bone graft remodeling in patients after posterior lumbar interbody fusion, and may be used as an adjunct diagnostic measure to monitor bone graft remodeling over time. Future research is warranted to explore how to interpret bone graft Hounsfield units-values and Hounsfield units trajectories in light of clinical variables or intercorporal fusion status.
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  • 文章类型: Journal Article
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  • 文章类型: Journal Article
    诊断错误会影响患者管理,由于血气分析主要是在没有实验室的情况下进行的,用户必须意识到潜在的陷阱。目的是提供用户应了解的常见问题的摘要。使用PubMed等在线数据库进行了叙述性审查,谷歌学者和已识别论文的参考列表。语言仅限于英语。错误可以预先分析,分析或分析后。样品应在15分钟内进行分析,并保持在室温下,并在改变吸入氧气和呼吸机设置后至少15-30分钟采集。准确的氧气测量。如果冷藏,塑料注射器的氧气渗透性更高。目前,分析仪运行动脉,静脉,毛细血管和骨内样本,但参考区间的变化可能不会被理解或报告。分析问题可能是由继发于药物的干扰引起的,如水杨酸盐的假高氯血症和乙二醇的高乳酸血症,或病理学,如假性低氧血症伴白细胞增多和低蛋白血症中的碱中毒。解释因结果调整而变得复杂,例如,温度(α-stat调整可能会高估体温过低的二氧化碳分压(pCO2),例如),和不适当的参考间隔,例如,在怀孕的碳酸氢盐,和pCO2范围应降低。缺乏对特定于患者和特定环境的参考间隔的理解,包括极端的年龄和海拔,将测量转换为标准条件会导致不适当的假设。对于用户来说,优化标本收集至关重要,了解分析方法,并了解参考区间何时适用于其样本类型,临床问题或患者。
    Diagnostic errors affect patient management, and as blood gas analysis is mainly performed without the laboratory, users must be aware of the potential pitfalls. The aim was to provide a summary of common issues users should be aware of.A narrative review was performed using online databases such as PubMed, Google Scholar and reference lists of identified papers. Language was limited to English.Errors can be pre-analytical, analytical or post-analytical. Samples should be analysed within 15 min and kept at room temperature and taken at least 15-30 min after changes to inspired oxygen and ventilator settings, for accurate oxygen measurement. Plastic syringes are more oxygen permeable if chilled. Currently, analysers run arterial, venous, capillary and intraosseous samples, but variations in reference intervals may not be appreciated or reported. Analytical issues can arise from interference secondary to drugs, such as spurious hyperchloraemia with salicylate and hyperlactataemia with ethylene glycol, or pathology, such as spurious hypoxaemia with leucocytosis and alkalosis in hypoalbuminaemia. Interpretation is complicated by result adjustment, for example, temperature (alpha-stat adjustment may overestimate partial pressure of carbon dioxide (pCO2) in hypothermia, for example), and inappropriate reference intervals, for example, in pregnancy bicarbonate, and pCO2 ranges should be lowered.Lack of appreciation for patient-specific and circumstance-specific reference intervals, including extremes of age and altitude, and transformation of measurements to standard conditions can lead to inappropriate assumptions. It is vitally important for users to optimise specimen collection, appreciate the analytical methods and understand when reference intervals are applicable to their specimen type, clinical question or patient.
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  • 文章类型: Journal Article
    背景:连续勃起脊柱平面(ESP)镇痛是创伤性肋骨骨折疼痛患者的常用辅助治疗方法,其成功依赖于ESP导管在放置期间保持在正确的筋膜平面内。然而,关于留置ESP导管的放置后位置的知识在很大程度上是缺乏的。我们假设穿针ESP导管的迁移是常见的,并且可以通过巧合的术后CT检测到。
    方法:在这项单中心回顾性队列研究中,对2020年1月至2022年7月期间因外伤性肋骨骨折进入外科重症监护室的成人进行了筛查.包括通过留置导管接受持续ESP镇痛并随后进行胸部CT的患者。主要结果是迁移到ESP外的导管的比例。次要结果是导管尖端与最近的横突(TP)或筋膜平面之间的距离。
    结果:筛选了160份医疗记录是否符合纳入标准,15例患者(18根导管)符合纳入标准。检查的18个导管中有16个是在ESP外发现的。此外,据报道,导管位置为肌内14根导管和皮下4根导管.导管尖端与最近的TP(或ESP)之间的中位距离为矢状23.20mm,轴向为25.05mm。
    结论:大多数ESP导管在放置后的几天内发现位于筋膜平面的浅层。导管和ESP之间的中值距离在23和25mm之间。前瞻性研究应解决导管迁移问题,并提出解决这一常见问题的解决方案。
    BACKGROUND: Continuous erector spinae plane (ESP) analgesia is a common adjuvant for patients with traumatic rib fracture pain and success relies on the ESP catheter remaining within the correct fascial plane for the duration of its placement. However, knowledge on postplacement position of indwelling ESP catheters is largely absent. We hypothesized that migration of over-the-needle ESP catheters was common and detectable with coincidental postprocedure CT.
    METHODS: In this single-center retrospective cohort study, adults admitted to the surgical intensive care unit for traumatic rib fractures between January 2020 and July 2022 were screened. Those receiving continuous ESP analgesia via indwelling catheter and undergoing subsequent chest CT were included. The primary outcome was the proportion of catheters that migrated outside the ESP. The secondary outcome was the distance between the catheter tip and the nearest transverse process (TP) or fascial plane.
    RESULTS: 160 medical records were screened for eligibility and 15 patients (18 catheters) met the inclusion criteria. 16 of 18 catheters reviewed were found outside the ESP. Furthermore, catheter position was reported as intramuscular in 14 catheters and subcutaneous in 4 catheters. The median distance between catheter tip and the nearest TP (or the ESP) was 23.20 mm sagittally and 25.05 mm axially.
    CONCLUSIONS: Most ESP catheters were found superficial to the fascial plane in the days following their placement. The median distance between the catheter and the ESP is between 23 and 25 mm. Prospective studies should address catheter migration concerns and propose solutions to this common issue.
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  • 文章类型: Journal Article
    目的:本研究旨在验证和实施一种快速筛查方法,用于检测淋病奈瑟菌中与头孢曲松耐药相关的penA-60等位基因,用于分离裂解物和临床标本DNA提取物。
    方法:淋病奈瑟菌penA实时(RT)-PCR适用于包括物种特异性pap确认靶标和市售内部对照以监测PCR抑制。使用淋病奈瑟菌阳性(n=24)和淋病奈瑟菌阴性(n=42)临床标本和分离裂解物来验证修改的测定。该小组包括七个具有由该测定靶向的penA等位基因赋予的抗性的样品和四个具有不同penA等位基因的样品。使用来自伦敦性健康诊所的54名患者的临床标本评估了使用penART-PCR进行分子监测的可行性,这些患者也有2020年淋病奈瑟菌耐药性监测计划(GRASP)中包括的淋病奈瑟菌分离株。
    结果:该测定正确地鉴定了淋病奈瑟氏球菌标本(n=7),其具有该测定靶向的penA-60/64等位基因。没有检测到pena假阴性/阳性,赋予测定的PIA目标灵敏度,特异性,正负预测值(PPV,净现值)为100%(95%CI;灵敏度;56.1-100%,特异性;93.6-100%,PPV;56.1-100%,净现值;93.6-100%)。未检测到与其他奈瑟球菌或其他泌尿生殖道病原体的交叉反应性。在78份淋病奈瑟菌阳性标本中,有73份检测到淋病奈瑟菌目标(pap),产生92.6%的灵敏度(95%CI83.0%至97.3%),100%特异性(95%CI75.9%至100%)和PPV,净现值为89.4%(95%CI为52.5%至90.9%)。在GRASP2020可行性分子监测研究的临床标本中未检测到penA-59/60/64等位基因(n=54个个体)。
    结论:实施此PCR检测用于患者管理,公共卫生和监视目的可以快速检测最广泛流行的penA等位基因赋予的淋球菌头孢曲松耐药性。
    OBJECTIVE: This study aimed to validate and implement a rapid screening assay for molecular detection of the penA-60 allele that is associated with ceftriaxone resistance in Neisseria gonorrhoeae for use on both isolate lysates and clinical specimen DNA extracts.
    METHODS: A N. gonorrhoeae penA real-time (RT)-PCR was adapted to include a species-specific pap confirmation target and a commercially available internal control to monitor for PCR inhibition.The modified assay was validated using N. gonorrhoeae-positive (n=24) and N. gonorrhoeae-negative (n=42) clinical specimens and isolate lysates. The panel included seven samples with resistance conferred by penA alleles targeted by the assay and four samples with different penA alleles. The feasibility of using the penA RT-PCR for molecular surveillance was assessed using clinical specimens from 54 individuals attending a London sexual health clinic who also had a N. gonorrhoeae isolate included in the 2020 Gonococcal Resistance to Antimicrobials Surveillance Programme (GRASP).
    RESULTS: The assay correctly identified N. gonorrhoeae specimens (n=7) with penA-60/64 alleles targeted by the assay. No penA false negatives/positives were detected, giving the penA target of the assay a sensitivity, specificity, positive and negative predicted values (PPV, NPV) of 100% (95% CIs; sensitivity; 56.1-100%, specificity; 93.6-100%, PPV; 56.1-100%, NPV; 93.6-100%).No cross-reactivity with other Neisseria species or other urogenital pathogens was detected. The N. gonorrhoeae target (pap) was detected in 73 out of 78 of the N. gonorrhoeae-positive specimens, resulting in 92.6% sensitivity (95% CI 83.0% to 97.3%), 100% specificity (95% CI 75.9% to 100%) and PPV, and a NPV of 89.4% (95% CI 52.5% to 90.9%). No penA-59/60/64 alleles were detected within the clinical specimens from the GRASP 2020 feasibility molecular surveillance study (n=54 individuals).
    CONCLUSIONS: The implementation of this PCR assay for patient management, public health and surveillance purposes enables the rapid detection of gonococcal ceftriaxone resistance conferred by the most widely circulating penA alleles.
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