• 文章类型: Journal Article
    目的:成人早发性糖尿病(年龄<40岁)的并发症风险增加,目前尚不清楚他们是否正在接受指南推荐的护理。我们比较了早发性和常发性糖尿病成年人的血红蛋白A1c(HbA1c)检测频率和结果,并评估了与指南一致性相关的因素。
    方法:来自艾伯塔省的人口级数据库,加拿大(约450万)被用来识别患有糖尿病的成年人。该队列在诊断时按年龄分层(<40vs.≥40年),然后随访365天进行HbA1c测试。调整后的多变量分析用于确定与指南一致性相关的临床和社会人口统计学因素。
    结果:在23,643名成年糖尿病患者中(平均年龄54.1±15.4岁;女性占42.1%),18.9%患有早发性糖尿病。早发性糖尿病与较低的测试频率相关(调整后比值比(aOR),0.80;95%CI0.70-0.90)及以上目标血糖水平与正常发作糖尿病(aOR,1.45;95%CI1.29-1.64)。与指南一致的HbA1c检测频率相关的因素是农村居住和胰岛素使用。
    结论:在我们提供免费医疗服务的全民医疗环境中,与正常发病的糖尿病患者相比,早发性糖尿病患者的HbA1c检测率较低,血糖控制处于次优状态.
    OBJECTIVE: Adults with early-onset diabetes (age < 40 years) have an increased risk of complications, and it is unclear whether they are receiving guideline recommended care. We compared the frequency and results of haemoglobin A1c (HbA1c) testing in adults with early-onset and usual-onset diabetes and assessed factors related to guideline concordance.
    METHODS: Population-level databases from Alberta, Canada (∼4.5 million) were used to identify adults with incident diabetes. The cohort was stratified by age at diagnosis (<40 vs. ≥ 40 years) and then followed for 365 days for HbA1c testing. Adjusted multivariable analyses were used to identify clinical and sociodemographic factors associated with guideline concordance.
    RESULTS: Among 23,643 adults with incident diabetes (mean age 54.1 ± 15.4 years; 42.1 % female), 18.9 % had early-onset diabetes. Early-onset diabetes was associated with lower frequency of testing (adjusted odds ratio (aOR), 0.80; 95 % CI 0.70-0.90) and above target glycaemic levels compared to usual-onset diabetes (aOR, 1.45; 95 % CI 1.29-1.64). Factors associated with guideline concordant frequency of HbA1c testing were rural residence and insulin use.
    CONCLUSIONS: In our universal care setting with premium-free health care, early-onset diabetes was associated with lower rates of HbA1c testing and sub-optimal glycaemic control compared to those with usual-onset diabetes.
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  • 文章类型: Journal Article
    背景:最近几十年揭示了有关未降睾丸AQ2(UDT)的生育力和潜在恶性肿瘤的新科学知识。因此,许多指南改变了他们关于治疗时机的建议,目标是更早的手术时间。
    方法:我们分析了新诊断的数量,并在报销的德国医院强制性年度报告中提供的预定年龄组进行了手术。信息“-2006年至2020年之间的工具。
    结果:总体而言,对124,741例病例进行分析。我们显示,第一年进行的手术每年略有增加2%,直到2011年为止主要增加,第一年和第四年之间的手术数量恒定,而在生活的5至14年之间的手术减少,直到2009年每年减少3%。
    结论:即使我们的研究结果表明指南的建议越来越适应,仍有相当多的患者接受后期治疗。需要对后者的原因和情况进行更多的研究。
    BACKGROUND: The last decades revealed new scientific knowledge regarding the fertility and potential malignancy of undescended testis AQ2(UDT). Accordingly, many guidelines changed their recommendation concerning timing of therapy, with the goal of an earlier time of surgery.
    METHODS: We analyzed the number of new diagnosis and performed surgeries in predefined age groups provided by the obligatory annual reports of German hospitals in the reimbursement.INFO\"-tool between 2006 and 2020.
    RESULTS: Overall, 124,741 cases were analyzed. We showed a slight increase in performed surgeries in the first year by 2% per year with a main increase till 2011, a constant number of surgeries between first and 4th year and a decrease of surgeries between 5 and 14th year of living with a main decrease till 2009 by 3% per year.
    CONCLUSIONS: Even if our results illustrate an increasing adaption of the guideline\'s recommendation, there is still a significant number of patients who receive later treatment. More research about the reasons and circumstances for the latter is needed.
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  • 文章类型: Journal Article
    肺癌仍然是新加坡癌症相关死亡的重要原因,在过去的20年中,被诊断为非小细胞肺癌(NSCLC)的非吸烟者比例更高。与西方国家相比,新加坡诊断的肺癌中可靶向基因组改变的患病率更高,以及精准医学时代非小细胞肺癌不断扩大的治疗前景,这两个因素都强调了高效和有效的分子谱分析的重要性。
    本文为晚期非小细胞肺癌早期生物标志物检测提供了共识建议。这些建议是由新加坡的一个多学科肺癌专家小组提出的,目的是改善患者护理和长期预后。
    这些建议解决了高级和早期设置中的注意事项,并考虑到生物标志物测试实施中的挑战以及可用数据的局限性。讨论了肿瘤组织和液体活检的生物标志物测试。
    本共识声明讨论了将分子检测纳入早期至晚期NSCLC患者临床实践的方法和挑战。并为新加坡NSCLC患者的生物标志物检测提供实用建议。
    UNASSIGNED: Lung cancer remains an important cause of cancer-related mortality in Singapore, with a greater proportion of non-smokers diagnosed with non-small cell lung cancer (NSCLC) in the past 2 decades. The higher prevalence of targetable genomic alterations in lung cancer diagnosed in Singapore compared with countries in the West, as well as the expanding therapeutic landscape for NSCLC in the era of precision medicine, are both factors that underscore the importance of efficient and effective molecular profiling.
    UNASSIGNED: This article provides consensus recommendations for biomarker testing for early-stage to advanced NSCLC. These recommendations are made from a multidisciplinary group of lung cancer experts in Singapore with the aim of improving patient care and long-term outcomes.
    UNASSIGNED: The recommendations address the considerations in both the advanced and early-stage settings, and take into account challenges in the implementation of biomarker testing as well as the limitations of available data. Biomarker testing for both tumour tissue and liquid biopsy are discussed.
    UNASSIGNED: This consensus statement discusses the approaches and challenges of integrating molecular testing into clinical practice for patients with early- to late-stage NSCLC, and provides practical recommendations for biomarker testing for NSCLC patients in Singapore.
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  • 文章类型: Journal Article
    目的:制定绝经后无出血妇女超声检查子宫内膜增厚的临床评估策略。
    方法:任何年龄的绝经后妇女。
    结果:减少无症状子宫内膜增厚妇女不必要的侵入性干预和调查,同时选择性调查有子宫内膜癌风险的妇女。
    结果:预计采用这些建议将避免绝经后妇女不必要的焦虑,疼痛,和手术并发症的风险。预计还将通过消除不必要的干预措施来降低医疗保健系统的成本。
    方法:Medline的英文文章,科克伦,和PubMed数据库,用于1995年至2022年的相关同行评审文章(例如,无症状子宫内膜厚度,子宫内膜癌,绝经后出血,经阴道超声,子宫内膜活检,宫颈狭窄,激素疗法和子宫内膜,他莫昔芬,替勃龙,芳香化酶抑制剂)。结果仅限于系统评价和荟萃分析,随机对照试验/对照临床试验,和观察性研究。
    方法:作者使用建议分级评估对证据质量和建议强度进行了评估,开发和评估(等级)方法。见附录A(表A1的定义和A2的强和条件[弱]建议的解释)。
    医生,包括妇科医生,产科医生,家庭医生,放射科医生,病理学家,和内科医生;执业护士和护士;医学学员,包括医学生,居民,和研究员;以及绝经后人群的其他医疗保健提供者。
    绝经后妇女在超声检查中经常发现子宫内膜增厚。没有出血,子宫内膜<11mm很少是一个严重问题,但应由卫生保健提供者进行评估.
    OBJECTIVE: To formulate strategies for clinical assessments for endometrial thickening on ultrasound in a postmenopausal woman without bleeding.
    METHODS: Postmenopausal women of any age.
    RESULTS: To reduce unnecessary invasive interventions and investigations in women with asymptomatic endometrial thickening while selectively investigating women at risk for endometrial cancer.
    RESULTS: It is anticipated that the adoption of these recommendations would save postmenopausal women unnecessary anxiety, pain, and risk of procedural complications. It is also expected to decrease the cost to the health care system by eliminating unnecessary interventions.
    METHODS: English language articles from Medline, Cochrane, and PubMed databases for relevant peer-reviewed articles dating from 1995 to 2022 (e.g., asymptomatic endometrial thickness, endometrial cancer, postmenopausal bleeding, transvaginal ultrasound, endometrial biopsy, cervical stenosis, hormone therapies and the endometrium, tamoxifen, tibolone, aromatase inhibitors). Results were restricted to systematic reviews and meta-analyses, randomized controlled trials/controlled clinical trials, and observational studies.
    METHODS: The authors rated the quality of evidence and strength of recommendations using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach. See Appendix A (Tables A1 for definitions and A2 for interpretations of strong and conditional [weak] recommendations).
    UNASSIGNED: Physicians, including gynaecologists, obstetricians, family physicians, radiologists, pathologists, and internists; nurse practitioners and nurses; medical trainees, including medical students, residents, and fellows; and other providers of health care of the postmenopausal population.
    UNASSIGNED: Postmenopausal women often have a thickening of the lining of the uterus found during ultrasound. Without bleeding, an endometrium <11 mm is rarely a serious problem but should be evaluated by a health care provider.
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  • 文章类型: Journal Article
    目的:为狼疮性肾炎(LN)的诊断和治疗制定第二个以证据为基础的巴西风湿病学会共识。
    方法:巴西风湿病学会LupusCommittee的两名方法学专家和20名风湿病学家参与了本指南的制定。定义了14个PICO问题,并进行了系统评价。对符合条件的随机对照试验进行了关于肾脏完全缓解的分析,部分肾脏缓解,血清肌酐,蛋白尿,血清肌酐倍增,进展为终末期肾病,肾复发,和严重不良事件(感染和死亡率)。建议评估的分级,使用开发和评估(GRADE)方法来制定这些建议。建议要求≥82%的投票成员同意,并被归类为强烈赞成,微弱地赞成,有条件的,弱反对或强烈反对特定干预。LN管理的其他方面(诊断,治疗的一般原则,合并症和难治性病例的治疗)通过文献回顾和专家意见进行了评估。
    结果:所有SLE患者均应接受肌酐和尿液分析检查以评估肾脏受累情况。肾活检被认为是诊断LN的金标准,如果不可用或该程序有禁忌症,治疗决策应基于临床和实验室参数.提出了14项建议。目标肾反应(TRR)定义为肾功能的改善或维持(治疗基线时±10%),并在3个月时24小时蛋白尿或24小时UPCR减少25%。在6个月时减少了50%,12个月时蛋白尿<0.8g/24h。应向所有SLE患者开具羟氯喹处方,除了禁忌症。糖皮质激素应以最低剂量和最短的必要时间使用。在III类或IV类(±V)中,霉酚酸酯(MMF),环磷酰胺,MMF加他克莫司(TAC),MMF加belimumab或TAC可用作诱导疗法。对于维持治疗,MMF或硫唑嘌呤(AZA)是首选,TAC或环孢菌素或来氟米特可用于不能使用MMF或AZA的患者。利妥昔单抗可用于难治性疾病。在未能实现TRR的情况下,评估依从性很重要,免疫抑制剂剂量,辅助治疗,合并症,并考虑活检/再活检。
    结论:这一共识提供了基于证据的数据来指导LN的诊断和治疗。支持巴西制定公共和补充卫生政策。
    OBJECTIVE: To develop the second evidence-based Brazilian Society of Rheumatology consensus for diagnosis and treatment of lupus nephritis (LN).
    METHODS: Two methodologists and 20 rheumatologists from Lupus Comittee of Brazilian Society of Rheumatology participate in the development of this guideline. Fourteen PICO questions were defined and a systematic review was performed. Eligible randomized controlled trials were analyzed regarding complete renal remission, partial renal remission, serum creatinine, proteinuria, serum creatinine doubling, progression to end-stage renal disease, renal relapse, and severe adverse events (infections and mortality). The Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach was used to develop these recommendations. Recommendations required ≥82% of agreement among the voting members and were classified as strongly in favor, weakly in favor, conditional, weakly against or strongly against a particular intervention. Other aspects of LN management (diagnosis, general principles of treatment, treatment of comorbidities and refractory cases) were evaluated through literature review and expert opinion.
    RESULTS: All SLE patients should undergo creatinine and urinalysis tests to assess renal involvement. Kidney biopsy is considered the gold standard for diagnosing LN but, if it is not available or there is a contraindication to the procedure, therapeutic decisions should be based on clinical and laboratory parameters. Fourteen recommendations were developed. Target Renal response (TRR) was defined as improvement or maintenance of renal function (±10% at baseline of treatment) combined with a decrease in 24-h proteinuria or 24-h UPCR of 25% at 3 months, a decrease of 50% at 6 months, and proteinuria < 0.8 g/24 h at 12 months. Hydroxychloroquine should be prescribed to all SLE patients, except in cases of contraindication. Glucocorticoids should be used at the lowest dose and for the minimal necessary period. In class III or IV (±V), mycophenolate (MMF), cyclophosphamide, MMF plus tacrolimus (TAC), MMF plus belimumab or TAC can be used as induction therapy. For maintenance therapy, MMF or azathioprine (AZA) are the first choice and TAC or cyclosporin or leflunomide can be used in patients who cannot use MMF or AZA. Rituximab can be prescribed in cases of refractory disease. In cases of failure in achieving TRR, it is important to assess adherence, immunosuppressant dosage, adjuvant therapy, comorbidities, and consider biopsy/rebiopsy.
    CONCLUSIONS: This consensus provides evidence-based data to guide LN diagnosis and treatment, supporting the development of public and supplementary health policies in Brazil.
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  • 文章类型: Editorial
    暂无摘要。
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  • 文章类型: Journal Article
    目的:家族性高胆固醇血症(FH)是一种脂蛋白代谢的遗传性疾病,可导致过早发生动脉粥样硬化性心血管疾病(ASCVD)的风险增加。尽管FH的早期诊断和治疗可显著改善心血管预后,这种疾病未被诊断和治疗。出于这些原因,意大利动脉粥样硬化研究学会(SISA)组建了一个共识小组,其任务是为FH的诊断和治疗提供指导。
    结果:我们的指南包括:i)FH的遗传复杂性概述以及与LDL代谢有关的候选基因的作用;ii)人群中FH的患病率;iii)FH诊断所采用的临床标准;iv)ASCVD的筛查和心血管成像技术的作用;v)分子诊断在建立纯合子疾病的遗传基础中的作用;vi)杂合FH的当前治疗选择。治疗策略和目标目前基于低密度脂蛋白胆固醇(LDL-C)水平,FH的预后很大程度上取决于降脂治疗降低LDL-C的程度.有或没有依泽替米贝的他汀类药物是治疗的主要支柱。添加新的药物如PCSK9抑制剂,纯合FH中的ANGPTL3抑制剂或lomitapide导致LDL-C水平的进一步降低。LDL单采术适用于对降胆固醇疗法反应不足的FH患者。
    结论:FH是常见的,可治疗的遗传性疾病和,尽管我们对这种疾病的认识有所提高,在识别和管理方面仍然存在许多挑战。
    OBJECTIVE: Familial Hypercholesterolemia (FH) is a genetic disorder of lipoprotein metabolism that causes an increased risk of premature atherosclerotic cardiovascular disease (ASCVD). Although early diagnosis and treatment of FH can significantly improve the cardiovascular prognosis, this disorder is underdiagnosed and undertreated. For these reasons the Italian Society for the Study of Atherosclerosis (SISA) assembled a Consensus Panel with the task to provide guidelines for FH diagnosis and treatment.
    RESULTS: Our guidelines include: i) an overview of the genetic complexity of FH and the role of candidate genes involved in LDL metabolism; ii) the prevalence of FH in the population; iii) the clinical criteria adopted for the diagnosis of FH; iv) the screening for ASCVD and the role of cardiovascular imaging techniques; v) the role of molecular diagnosis in establishing the genetic bases of the disorder; vi) the current therapeutic options in both heterozygous and homozygous FH. Treatment strategies and targets are currently based on low-density lipoprotein cholesterol (LDL-C) levels, as the prognosis of FH largely depends on the magnitude of LDL-C reduction achieved by lipid-lowering therapies. Statins with or without ezetimibe are the mainstay of treatment. Addition of novel medications like PCSK9 inhibitors, ANGPTL3 inhibitors or lomitapide in homozygous FH results in a further reduction of LDL-C levels. LDL apheresis is indicated in FH patients with inadequate response to cholesterol-lowering therapies.
    CONCLUSIONS: FH is a common, treatable genetic disorder and, although our understanding of this disease has improved, many challenges still remain with regard to its identification and management.
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  • 文章类型: Journal Article
    应对生存挑战需要全面、以患者为中心的方法,专注于通过改变生活方式来降低风险,识别远处复发,和优化乳腺成像。本文将讨论生存期的当前和新兴临床策略,倡导多学科和全面的方法。以这种方式,早期乳腺癌幸存者被授权以增强的知识驾驭他们的旅程,促进向癌症以外的生命过渡。
    Addressing the challenges of survivorship necessitates a comprehensive, patient-centered approach, focusing on mitigating risk through lifestyle modification, identifying distant recurrence, and optimization of breast imaging. This article will discuss the current and emerging clinical strategies for the survivorship period, advocating a multidisciplinary and comprehensive approach. In this manner, early-stage breast cancer survivors are empowered to navigate their journey with enhanced knowledge, facilitating a transition to life beyond cancer.
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  • 文章类型: Journal Article
    目的:评估英国国家健康与护理卓越研究所(NICE)指南对预防和治疗新生儿早发性感染(EOI)的影响(临床指南149(CG149),2012年发布,其2021年更新(NG195)关于极早产儿抗生素使用情况。
    方法:使用来自国家新生儿研究数据库的数据进行中断时间序列分析。
    方法:英格兰和威尔士的新生儿单位。
    方法:2010年1月1日至2022年12月31日妊娠22-31周出生并存活出院的婴儿。
    方法:CG149(2012年8月)和NG195(2021年4月)的出版物。
    方法:抗生素使用措施,按出生月汇总:抗生素使用率(AUR),接受至少一种抗生素治疗的护理天数比例;EOI治疗第1~3天和迟发性感染(LOI)治疗第3天后接受抗生素治疗≥1天的婴儿百分比;EOI和LOI治疗延长抗生素疗程≥5天的婴儿百分比.
    结果:96%的婴儿在住院期间接受了抗生素治疗。AUR在CG149的出版物上拒绝了,在NG195出版物上没有进一步影响。CG149对接受EOI或LOI≥1天抗生素的婴儿的潜在趋势没有影响,但NG195后,EOI的月度趋势开始下降(-0.20%,-0.26至-0.14)和LOI(-0.23%,-0.33至-0.12)。在CG149发表时,EOI和LOI的长期抗生素疗程的使用有所下降,而对于LOI,这种趋势在NG195之后加速了。
    结论:NICE指南的出版物与抗生素使用的减少有关;然而,新生儿抗生素暴露仍然非常高。
    OBJECTIVE: To assess the impact of publication of UK National Institute for Health and Care Excellence (NICE) guidelines on the prevention and treatment of early-onset infections (EOIs) in neonates (clinical guideline 149 (CG149), published in 2012, and its 2021 update (NG195) on antibiotic use in very preterm infants.
    METHODS: Interrupted time series analysis using data from the National Neonatal Research Database.
    METHODS: Neonatal units in England and Wales.
    METHODS: Infants born at 22-31 weeks\' gestation from 1 January 2010 to 31 December 2022 and survived to discharge.
    METHODS: Publication of CG149 (August 2012) and NG195 (April 2021).
    METHODS: Measures of antibiotic use, aggregated by month of birth: antibiotic use rate (AUR), the proportion of care days in receipt of at least one antibiotic; percentage of infants who received ≥1 day of antibiotics on days 1-3 for EOI and after day 3 for late-onset infection (LOI); percentage who received ≥1 prolonged antibiotic course ≥5 days for EOI and LOI.
    RESULTS: 96% of infants received an antibiotic during inpatient stay. AUR declined at publication of CG149, without further impact at NG195 publication. There was no impact of CG149 on the underlying trend in infants receiving ≥1 day antibiotics for EOI or LOI, but post-NG195 the monthly trend began to decline for EOI (-0.20%, -0.26 to -0.14) and LOI (-0.23%, -0.33 to -0.12). Use of prolonged antibiotic courses for EOI and LOI declined at publication of CG149 and for LOI this trend accelerated post-NG195.
    CONCLUSIONS: Publications of NICE guidance were associated with reductions in antibiotic use; however neonatal antibiotic exposure remains extremely high.
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