Blood Glucose

血糖
  • 文章类型: Case Reports
    强调小儿1型糖尿病的持续性糖尿和低血糖需要进一步评估。早晨低血糖是钠葡萄糖转运蛋白2(SGLT2)抑制剂在5岁以下儿童中的限制性副作用。充当SGLT2抑制剂的SLC5A2突变可导致年幼儿童中糖化血红蛋白的可接受范围和较低的所需胰岛素剂量。
    Highlights A persistent glycosuria alongside hypoglycemia in pediatric type 1 diabetes mellitus needs further evaluation. Morning hypoglycemia is a limiting side effect of sodium glucose transporter 2 (SGLT2) inhibitors in children younger than 5 years old. SLC5A2 mutation functioning as a SGLT2 inhibitor can result in acceptable range of glycated hemoglobin in younger children and lower required doses of insulin.
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  • 文章类型: Journal Article
    背景:糖尿病患病率不断上升,由于其多方面的并发症,对全球医疗保健系统构成了紧迫的挑战。作为回应,连续葡萄糖监测(CGM)系统的出现,为日常糖尿病管理提供技术解决方案,提供了重要的机会。然而,广泛采用面临几个障碍,与设备的技术配置和患者的心理维度有关。因此,本研究旨在应用和测试一个理论模型,该模型研究了使用连续葡萄糖监测系统的意图。
    方法:建立研究模型,揭示心理因素的影响,从CGM系统持续采用的技术接受模型(TAM)中得出的功能组件和合理结构。为了确保结果的可比性,我们从使用DexcomONEDexcom(圣地亚哥,CA)首次至少一个月。采用结构方程建模(SEM)技术,评估了构建体之间的假设关系.
    结果:分析证实理性因素与使用意向呈正相关。主观规范,作为医生的影响,与感知有用性呈正相关。趋势箭头,尽管与感知有用性负相关,与感知的易用性呈正相关,加强其对感知有用性的中介作用。在心理因素中,对CGM技术的信任与使用意图呈正相关。健康素养与使用意向呈负相关。
    结论:这些发现有助于理论和管理理解,提供建议,以加强像DexcomONE这样的CGM系统的采用。
    BACKGROUND: The escalating prevalence of diabetes, with its multifaceted complications, poses a pressing challenge for healthcare systems globally. In response, the advent of continuous glucose monitoring (CGM) systems, offering technological solutions for daily diabetes management, presents significant opportunities. However, the widespread adoption faces several barriers, linked both to the technological configuration of the devices and to the psychological dimension of patients. Therefore, this study aims to apply and test a theoretical model that investigates the antecedents of the intention to use Continuous Glucose Monitoring systems.
    METHODS: The research model was built to unveil the impacts of psychological factors, functional components and rational constructs derived from the Technology Acceptance Model (TAM) on CGM systems sustained adoption. To ensure the comparability of results, we have collected data from people who had used Dexcom ONE Dexcom (San Diego, CA) for the first time for at least one month. Employing Structural Equation Modelling (SEM) techniques, the hypothesized relationships among constructs were assessed.
    RESULTS: The analyses confirmed the positive correlation of rational factors to the Intention to Use. Subjective Norm, intended as the physicians\' influence, is positively correlated with the Perceived Usefulness. Trend Arrows, albeit being negatively correlated with Perceived Usefulness, have a positive correlation on Perceived Ease Of Use, reinforcing its mediating effect towards Perceived Usefulness. Among psychological factors, Trust in the CGM technology positively correlates with Intention to Use. Health Literacy is negatively correlated to the Intention to Use.
    CONCLUSIONS: These findings contribute to theoretical and managerial understanding, providing recommendations to enhance the adoption of CGM systems like Dexcom ONE.
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  • 文章类型: Case Reports
    背景:糖化血红蛋白是用于评估长期血糖控制的众所周知的标志物。然而,糖化血红蛋白测量的准确性可能会受到血红蛋白变体的影响,这使得糖化血红蛋白值在血糖控制方面的测定和解释不仅困难而且具有误导性。在这里,我们介绍了首例来自尼泊尔的2型糖尿病患者的血红蛋白E,偶然诊断是因为虚假的糖化血红蛋白水平。
    方法:一名45岁的印度裔蒙古族女性,有约9年的2型糖尿病病史,但随访时间不是很好,她被转诊到我们的机构,以检测空腹血浆和餐后血糖水平以及糖化血红蛋白。发现空腹和餐后血糖很高。通过两种不同的高效液相色谱(HPLC)方法获得的一致的极低糖化血红蛋白迫使我们致电患者以获取详细的临床病史和过去进行的调查记录。该患者是已知的2型糖尿病病例约9年,并不定期进行随访。大约4年前,她带着疲劳去了一家医疗机构,严重的头痛,腹部疼痛,不适,头晕了几个月,在那里她被证明有高血糖。她被转诊到加德满都的一家三级医院,其中她被处方二甲双胍500毫克,每日一次(OD)。由于她的血红蛋白A1c异常报告,然后,她被送往国家公共卫生实验室进行重复调查。她的血液和尿液检查已发送。全血细胞计数结果显示红细胞和白细胞计数高,较低的平均红细胞体积,和较高的红细胞分布宽度变异系数。其他参数,包括血清电解质,肾功能试验,肝功能检查,和尿常规检查,在正常范围内。外周血涂片显示微细胞低色素红细胞和一些靶细胞。血红蛋白电泳显示血红蛋白E的百分比非常高,血红蛋白A2的百分比非常低,血红蛋白A和血红蛋白F的比例正常。建议进行家庭筛查。
    结论:临床医生应该意识到通过离子交换高效液相色谱法评估血红蛋白E和其他血红蛋白变体患者糖化血红蛋白的局限性。如果临床印象与糖化血红蛋白检测结果不符,糖化血红蛋白值应该用基于不同原理的第二种方法来确定,和血糖状态应该通过替代调查来确认,优选不受血红蛋白变体存在影响的那些(例如,硼酸酯亲和层析,果糖胺试验,糖化白蛋白试验,口服葡萄糖耐量试验,连续血糖监测,等。).一致甚至可疑的结果也应该引起对血红蛋白变异的怀疑,这应该通过进一步的评估和调查来确认。
    BACKGROUND: Glycated hemoglobin is a well-known marker for evaluating long-term glycemic control. However, the accuracy of glycated hemoglobin measurement can be affected by the presence of hemoglobin variants, which makes the determination and interpretation of glycated hemoglobin values in terms of glycemic control not only difficult but also misleading. Here we present the first ever case of a patient with type 2 diabetes with hemoglobin E from Nepal, diagnosed incidentally because of spurious glycated hemoglobin levels.
    METHODS: A 45-year-old Hindu Mongolian female with a history of type 2 diabetes for around 9 years but not very compliant with follow-ups was referred to our facility for plasma fasting and postprandial blood glucose levels and glycated hemoglobin. Fasting and postprandial blood sugars were found to be high. A consistent very low glycated hemoglobin by two different high-performance liquid chromatography (HPLC) methods compelled us to call the patient for a detailed clinical history and for the records of investigations done in the past. The patient has been a known case of type 2 diabetes for around 9 years and presented irregularly for follow-up visits. Around 4 years ago, she presented to a healthcare facility with fatigue, severe headaches, pain in the abdomen, discomfort, and dizziness for a couple of months, where she was shown to have high blood glucose. She was referred to a tertiary-level hospital in Kathmandu, where she was prescribed metformin 500 mg once daily (OD). Due to her abnormal hemoglobin A1c reports, she was then sent to the National Public Health Laboratory for repeat investigations. Her blood and urine investigations were sent. Complete blood count findings revealed high red blood cell and white blood cell counts, a low mean corpuscular volume, and a high red cell distribution width-coefficient of variation. Other parameters, including serum electrolytes, renal function tests, liver function tests, and urine routine examinations, were within normal limits. A peripheral blood smear revealed microcytic hypochromic red cells with some target cells. Hemoglobin electrophoresis showed a very high percentage of hemoglobin E, a very low percentage of hemoglobin A2, and normal proportions of hemoglobin A and hemoglobin F. A diagnosis of homozygous hemoglobin E was made, and family screening was advised.
    CONCLUSIONS: Clinicians should be aware of the limitations of glycated hemoglobin estimation by ion exchange high-performance liquid chromatography in patients with hemoglobin E and other hemoglobin variants. If the clinical impression and glycated hemoglobin test results do not match, glycated hemoglobin values should be determined with a second method based on a different principle, and glycemic status should be confirmed through alternative investigations, preferably those that are not influenced by the presence of hemoglobin variants (for example, boronate affinity chromatography, fructosamine test, glycated albumin test, the oral glucose tolerance test, continuous glucose monitoring, etc.). Consistent or even doubtful results should also raise the suspicion of a hemoglobin variant, which should be confirmed through further evaluation and investigations.
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  • 文章类型: Journal Article
    背景:关于性别确认激素疗法(GAHT)如何影响中国跨性别女性的体脂修饰的研究不足。目前尚不清楚激素治疗是否会影响该人群的肥胖患病率和血脂水平。目前的研究旨在评估GAHT和治疗持续时间如何影响中国跨性别女性体内脂肪的变化和再分配。
    方法:本研究包括40名未接受GAHT的女性和59名接受GAHT的女性。身体脂肪,血脂,并测量血糖水平。GAHT主要是一种药物(雌激素和抗雄激素)治疗。该研究还根据GAHT的持续时间对参与者进行了分层,以评估其对体内脂肪分布的影响。GAHT的持续时间在一年内,一到两年,两到三年,或超过三年。
    结果:收到GAHT后,全身脂肪增加了19.65%,体内脂肪的百分比增加了17.63%。手臂,矫正腿,和腿部区域的脂肪含量显着增加(+24.02%,+50.69%,和+41.47%,分别)和百分比(+25.19%,+34.90%,和+30.39%,分别)。总内脏脂肪含量降低(-37.49%)。根据体重指数≥28或总脂肪百分比≥25%或30%的诊断标准,发生肥胖的机会没有显著变化.血糖水平显著增加(+12.31%)。总胆固醇水平(-10.45%)显着下降。接受GAHT一到两年的人的脂肪变化与未接受GAHT的人有很大不同。
    结论:收到GAHT后,中国跨性别女性的全身脂肪和区域脂肪增加,身体脂肪分布从男性变成女性,尤其是头两年。然而,无论是人体总脂肪百分比的增加还是内脏脂肪含量的减少,都不会带来肥胖发生率的显著变化,甘油三酯或低密度脂蛋白胆固醇也没有。
    BACKGROUND: There is insufficient research on how gender-affirming hormone therapy (GAHT) affects body fat modifications in transwomen from China. It is unclear whether hormone therapy affects the prevalence of obesity and blood lipid levels within this population. The current research aimed to assess how GAHT and treatment duration had an impact on the change in and redistribution of body fat in Chinese transwomen.
    METHODS: This study included 40 transwomen who had not received GAHT and 59 who had. Body fat, blood lipid, and blood glucose levels were measured. GAHT is mainly a pharmacologic (estrogen and anti-androgen) treatment. The study also stratified participants based on the duration of GAHT to assess its impact on body fat distribution. The duration of GAHT was within one year, one to two years, two to three years, or more than three years.
    RESULTS: After receiving GAHT, total body fat increased by 19.65%, and the percentage of body fat increased by 17.63%. The arm, corrected leg, and leg regions showed significant increases in fat content (+ 24.02%, + 50.69%, and + 41.47%, respectively) and percentage (+ 25.19%, + 34.90%, and + 30.39%, respectively). The total visceral fat content decreased (-37.49%). Based on the diagnostic standards for a body mass index ≥ 28 or total body fat percentage ≥ 25% or 30%, the chance of developing obesity did not change significantly. Blood glucose levels significantly increased (+ 12.31%). Total cholesterol levels (-10.45%) decreased significantly. Fat changes in those who received GAHT for one to two years were significantly different from those who did not receive GAHT.
    CONCLUSIONS: After receiving GAHT, total body fat and regional fat increased in Chinese transwomen, and the body fat distribution changed from masculine to feminine, especially during the first two years. However, neither the increase in total body fat percentage nor the decrease in visceral fat content didn\'t bring about significant changes in the incidence of obesity, nor did triglycerides or low-density lipoprotein-cholesterol.
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  • 文章类型: Journal Article
    糖尿病仍然是一个关键的全球健康问题,需要紧急关注。闭环护理的当代临床方法,专门为胰岛素依赖患者量身定制,旨在精确监测血糖水平,同时降低因胰岛素剂量错误而导致的高血糖和低血糖的风险。本研究旨在通过评估和比较不同控制器的性能来解决这一威胁生命的问题,以实现更快的稳定和收敛速度,减少稳态误差。特别是在涉及进餐中断的情况下。该方法涉及血浆血糖水平的检测,通过控制架构将精确的胰岛素剂量输送到致动器,以及随后基于所述控制信号向患者施用所计算的胰岛素剂量。使用来自Bergman最小模型的动力学和质量平衡方程对葡萄糖-胰岛素动力学进行建模。仿真结果表明,该PID控制器具有优越的性能,维持血糖浓度在首选阈值~98.8%的时间,标准偏差为2.50。其次是RST,成功率为98.5%,标准差为5.00,SPC的成功率为58%,标准差为2.99,SFC的成功率为55%,标准差为10.08,最后LCFB的成功率为10%,标准差为64.55。
    Diabetes remains a critical global health concern that necessitates urgent attention. The contemporary clinical approach to closed-loop care, specifically tailored for insulin-dependent patients, aims to precisely monitor blood glucose levels while mitigating the risks of hyperglycaemia and hypoglycaemia due to erroneous insulin dosing. This study seeks to address this life-threatening issue by assessing and comparing the performance of different controllers to achieve quicker settling and convergence rates with reduced steady-state errors, particularly in scenarios involving meal interruptions. The methodology involves the detection of plasma blood glucose levels, delivery of precise insulin doses to the actuator through a control architecture, and subsequent administration of the calculated insulin dosage to patients based on the control signal. Glucose-insulin dynamics were modelled using kinetics and mass balance equations from the Bergman minimal model. The simulation results revealed that the PID controller exhibited superior performance, maintaining blood glucose concentration around the preferred threshold ∼98.8% of the time, with a standard deviation of 2.50. This was followed by RST with a success rate of 98.5% and standard deviation of 5.00, SPC with a success rate of 58% and standard deviation of 2.99, SFC with a success rate of 55% and standard deviation of 10.08, and finally LCFB with a rate of 10% and significantly higher standard deviation of 64.55.
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  • 文章类型: Journal Article
    背景:甘油三酯-葡萄糖指数(TyG)与缺血性卒中的预后之间的相关性已得到很好的确定。这项研究旨在评估TyG指数对患有脑出血(ICH)的危重病人的临床结局的影响。
    方法:从重症监护医学信息集市(MIMIC-IV)和eICU合作研究数据库(eICU-CRD)中回顾性检索诊断为ICH的患者。各种统计方法,包括约束三次样条(RCS)回归,多变量逻辑回归,亚组分析,和敏感性分析,用于检查TyG指数与ICH主要结局之间的关系。
    结果:共分析了来自MIMIC-IV的791例患者和来自eICU-CRD的1,113例患者。在MIMIC-IV中,住院和ICU死亡率分别为14%和10%,分别,而在eICU-CRD中,分别为16%和8%。RCS回归结果显示,在两个数据库的整个研究人群中,TyG指数与住院和ICU死亡风险之间存在一致的线性关系。Logistic回归分析显示,在两个数据库中,TyG指数与ICH患者住院和ICU死亡的可能性之间存在显著正相关。亚组和敏感性分析进一步揭示了患者年龄和TyG指数与ICH患者院内和ICU死亡率之间的交互作用。值得注意的是,对于60岁以上的病人,与MIMIC-IV和eICU-CRD数据库中的总体研究人群相比,TyG指数与院内死亡和ICU死亡风险之间的关联更为显著,提示老年(60岁以上)和TyG指数对ICH患者的院内和ICU死亡率有协同作用。
    结论:本研究在诊断为ICH的60岁以上患者中,建立了TyG指数与院内死亡和ICU死亡风险之间的正相关关系。这表明TyG指数有望作为该患者人群风险分层的指标。
    BACKGROUND: The correlation between the triglyceride-glucose index (TyG) and the prognosis of ischemic stroke has been well established. This study aims to assess the influence of the TyG index on the clinical outcomes of critically ill individuals suffering from intracerebral hemorrhage (ICH).
    METHODS: Patients diagnosed with ICH were retrospectively retrieved from the Medical Information Mart for Intensive Care (MIMIC-IV) and the eICU Collaborative Research Database (eICU-CRD). Various statistical methods, including restricted cubic spline (RCS) regression, multivariable logistic regression, subgroup analysis, and sensitivity analysis, were employed to examine the relationship between the TyG index and the primary outcomes of ICH.
    RESULTS: A total of 791 patients from MIMIC-IV and 1,113 ones from eICU-CRD were analyzed. In MIMIC-IV, the in-hospital and ICU mortality rates were 14% and 10%, respectively, while in eICU-CRD, they were 16% and 8%. Results of the RCS regression revealed a consistent linear relationship between the TyG index and the risk of in-hospital and ICU mortality across the entire study population of both databases. Logistic regression analysis revealed a significant positive association between the TyG index and the likelihood of in-hospital and ICU death among ICH patients in both databases. Subgroup and sensitivity analysis further revealed an interaction between patients\' age and the TyG index in relation to in-hospital and ICU mortality among ICH patients. Notably, for patients over 60 years old, the association between the TyG index and the risk of in-hospital and ICU mortality was more pronounced compared to the overall study population in both MIMIC-IV and eICU-CRD databases, suggesting a synergistic effect between old age (over 60 years) and the TyG index on the in-hospital and ICU mortality of patients with ICH.
    CONCLUSIONS: This study established a positive correlation between the TyG index and the risk of in-hospital and ICU mortality in patients over 60 years who diagnosed with ICH, suggesting that the TyG index holds promise as an indicator for risk stratification in this patient population.
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  • 文章类型: Journal Article
    UNASSIGNED: Type 2 diabetes mellitus is a highly prevalent disease and is associated with increased morbidity and mortality. Due to the low percentage of adequate glycemic control, new strategies for the treatment of type 2 diabetes mellitus have been sought, including sodium-glucose cotransporter type 2 inhibitorss.
    UNASSIGNED: To describe the evolution of patients with type 2 diabetes mellitus with insulin requirements treated with empagliflozin at the Peñaflor Hospital. The primary objective was to evaluate the efficacy of the medication regarding glycosylated hemoglobin A1c (HbA1c). The secondary objectives were: 1) achievement of HbA1c equal to or less than 7.5% according to survival analysis. 2) Change in glomerular filtration rate and urinary albumin excretion post treatment.
    UNASSIGNED: Review of clinical records of all patients treated with empagliflozin from November 2019 to June 2023. Average follow-up of 19 (16.3 to 40) months. To compare HbA1c values according to follow-up ranges, the paired T test or Wilcoxon test was used.
    UNASSIGNED: We included 58 patients, 15 men and 43 women (74.1%), with an average age of 58.5 ± 9.2 years, ranging from 35 to 75 years. Baseline HbA1c of 10.3 ± 1.6% and 8.98% ± 2.2 in a follow-up of 18 to 24 months post-treatment, resulted in a decrease of 1.27% (p = 0.002; confidence interval 95%: 0.5 to 2.03). The most common adverse effect was urinary tract infection.
    UNASSIGNED: Patients with type 2 diabetes mellitus with insulin requirements treated with empagliflozin at the Peñaflor Hospital achieved better glycemic control with few adverse effects.
    UNASSIGNED: La diabetes mellitus tipo 2 es una enfermedad de alta prevalencia y está asociada a mayor morbimortalidad. Debido al bajo porcentaje de compensación, se han buscado nuevas estrategias de tratamiento farmacológico, como los inhibidores del cotransportador sodio-glucosa tipo 2.
    UNASSIGNED: Describir la evolución de pacientes diabéticos tipo 2 insulino-requirentes tratados con empagliflozina en el Hospital Peñaflor, ubicado en el sector poniente de la Región Metropolitana, Chile. El objetivo primario fue evaluar la eficacia del medicamento respecto a hemoglobina glicosilada A1c. Los objetivos secundarios fueron registrar el logro de hemoglobina glicosilada A1c igual o menor a 7,5% según análisis de supervivencia. Luego, consignar el cambio en la velocidad de filtración glomerular y en la excreción urinaria de albúmina post tratamiento.
    UNASSIGNED: Revisión de ficha clínica de todos los pacientes tratados con empagliflozina desde noviembre de 2019 a junio de 2023. Media de seguimiento de 19 (de 16,3 a 40) meses. Para comparación entre valores de hemoglobina glicosilada A1c según rangos de seguimiento, se utilizó prueba T de Student de términos pareados o prueba de Wilcoxon.
    UNASSIGNED: Se estudió a 58 pacientes, 15 hombres y 43 mujeres (74,1%). Edad 58,5 ± 9,2 años, rango de 35 a 75 años. Hemoglobina glicosilada A1c basal de 10,3 ± 1,6% y 8,98% ± 2,2 en un rango de seguimiento de 18 a 24 meses post tratamiento, resultando en un descenso de 1,27% (p = 0,002; intervalo de confianza 95%: 0,5 a 2,03). El efecto adverso más frecuente fue infección del tracto urinario.
    UNASSIGNED: Los pacientes diabéticos tipo 2 insulino-requirentes tratados con empagliflozina en el Hospital Peñaflor lograron un mejor control glicémico con pocos efectos adversos.
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  • 文章类型: Journal Article
    目标:健康不平等会受到人口统计学因素的影响,例如种族和民族,精通英语,和生物性别。差异可能表现为测试的差异可能性,其与解决异常发现的干预可能性直接相关。我们的回顾性观察研究评估了重症监护病房(ICU)中葡萄糖测量值变化的存在。
    方法:使用MIMIC-IV数据库(2008-2019年),一个单一的中心,波士顿(美国)的学术转诊医院,我们确定了符合脓毒症-3标准的成年患者.排除标准为糖尿病酮症酸中毒,ICU住院时间少于1天,和未知的种族或种族。我们进行了逻辑回归分析,以评估第1天葡萄糖测量的差异可能性。拟合负二项回归以评估随后的葡萄糖读数的频率。对相关临床混杂因素进行了分析调整,跨越三个差异代理轴:种族和种族,性别,和英语水平。
    结果:我们研究了24,927名患者,其中19.5%代表种族和少数民族,42.4%是女性,9.8%的人英语水平有限。在ICU中第1天的葡萄糖测量没有发现显着差异。无论分析轴如何,这种模式都是一致的,即种族和民族,性别,或英语水平。相反,随后的测量频率揭示了潜在的差异。具体来说,男性(发病率比(IRR)1.06,95%置信区间(CI)1.01--1.21),自称为西班牙裔的患者(IRR1.11,95%CI1.01--1.21),或黑色(内部收益率1.06,95%CI1.01---1.12),精通英语的患者(IRR1.08,95%CI1.01--1.15)有更高的机会随后的血糖读数。
    结论:我们发现脓毒症患者的ICU血糖测量存在差异,尽管幅度很小。疾病监测的变化是数据偏差的来源,在对健康数据进行建模时可能会导致虚假的相关性。
    OBJECTIVE: Health inequities can be influenced by demographic factors such as race and ethnicity, proficiency in English, and biological sex. Disparities may manifest as differential likelihood of testing which correlates directly with the likelihood of an intervention to address an abnormal finding. Our retrospective observational study evaluated the presence of variation in glucose measurements in the Intensive Care Unit (ICU).
    METHODS: Using the MIMIC-IV database (2008-2019), a single-center, academic referral hospital in Boston (USA), we identified adult patients meeting sepsis-3 criteria. Exclusion criteria were diabetic ketoacidosis, ICU length of stay under 1 day, and unknown race or ethnicity. We performed a logistic regression analysis to assess differential likelihoods of glucose measurements on day 1. A negative binomial regression was fitted to assess the frequency of subsequent glucose readings. Analyses were adjusted for relevant clinical confounders, and performed across three disparity proxy axes: race and ethnicity, sex, and English proficiency.
    RESULTS: We studied 24,927 patients, of which 19.5% represented racial and ethnic minority groups, 42.4% were female, and 9.8% had limited English proficiency. No significant differences were found for glucose measurement on day 1 in the ICU. This pattern was consistent irrespective of the axis of analysis, i.e. race and ethnicity, sex, or English proficiency. Conversely, subsequent measurement frequency revealed potential disparities. Specifically, males (incidence rate ratio (IRR) 1.06, 95% confidence interval (CI) 1.01 - 1.21), patients who identify themselves as Hispanic (IRR 1.11, 95% CI 1.01 - 1.21), or Black (IRR 1.06, 95% CI 1.01 - 1.12), and patients being English proficient (IRR 1.08, 95% CI 1.01 - 1.15) had higher chances of subsequent glucose readings.
    CONCLUSIONS: We found disparities in ICU glucose measurements among patients with sepsis, albeit the magnitude was small. Variation in disease monitoring is a source of data bias that may lead to spurious correlations when modeling health data.
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  • 文章类型: Case Reports
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  • 文章类型: Case Reports
    年轻人的成熟型糖尿病(MODY)是一组单基因疾病。它的特点是主要继承,非胰岛素依赖型糖尿病。MODY比较少见,在30岁以下被诊断的人群中,高达3.5%。特定类型最常用磺酰脲治疗,特别是那些被确定为HNF4A-MODY和HNF1A-MODY的。HNF1B-MODY是另一种最常用于胰岛素治疗的类型,但缺乏明确的精确治疗。我们介绍一个18岁的孩子,诊断为HNF1B-MODY的非肥胖女性患者。她表现出完全的基因缺失,肾囊肿,和低镁血症.她的治疗计划包括长效和短效胰岛素,尽管她经常遇到低血糖和高血糖。塞马鲁肽,GLP-1RA,每周给药超过4个月。使用Dexcom的连续葡萄糖监测系统连续跟踪患者的葡萄糖水平。数据表明她的病情有了显着改善:时间范围(TIR)从70%增加到88%,有些日子达到100%,以及低血糖发作的频率,由时间低于范围值表示,从5%下降到1%。时间高于范围的值也从25%下降到10%,HbA1c水平从7%下降到5.6%。在司马鲁肽治疗期间,我们停止了她的胰岛素治疗.此外,她的体重指数(BMI)从24.1降至20.1kg/m2.然而,由于恶心等副作用,司马鲁肽治疗在4个月后停止,呕吐,食欲下降。其他促成因素包括考试压力和COVID-19感染,这迫使人们转回胰岛素。她最后一次记录的HbA1c水平在独家胰岛素治疗下上升到7.1%,BMI增加到24.9kg/m2。总之,司马鲁肽可能替代胰岛素改善血糖变异性,TIR,HNF1B-MODY患者的HbA1c。然而,需要更广泛的研究来确认其长期安全性和有效性.
    Maturity-onset diabetes of the young (MODY) is a grouping of monogenic disorders. It is characterized by dominantly inherited, non-insulin-dependent diabetes. MODY is relatively rare, encompassing up to 3.5% in those diagnosed under 30 years of age. Specific types are most commonly treated with sulfonylurea, particularly those identified as HNF4A-MODY and HNF1A-MODY. HNF1B-MODY is another type that is most frequently managed with insulin therapy but lacks a defined precision treatment. We present an 18-year-old, non-obese female patient diagnosed with HNF1B-MODY. She displays complete gene deletion, a renal cyst, and hypomagnesemia. Her treatment plan includes both long- and short-acting insulin, though she frequently encountered hypoglycemia and hyperglycemia. Semaglutide, a GLP-1RA, was administered weekly over 4 months. The patient\'s glucose level was continuously tracked using Dexcom\'s Continuous Glucose Monitoring system. The data suggested a notable improvement in her condition: time-in-range (TIR) increased from 70% to 88%, with some days achieving 100%, and the frequency of hypoglycemic episodes, indicated by time-below-range values, fell from 5% to 1%. The time-above-range values also dropped from 25% to 10%, and her HbA1c levels declined from 7% to 5.6%. During the semaglutide therapy, we were able to discontinue her insulin treatment. Additionally, her body mass index (BMI) was reduced from 24.1 to 20.1 kg/m2. However, the semaglutide treatment was halted after 4 months due to side effects such as nausea, vomiting, and reduced appetite. Other contributing factors included exam stress and a COVID-19 infection, which forced a switch back to insulin. Her last recorded HbA1c level under exclusive insulin therapy rose to 7.1%, and her BMI increased to 24.9 kg/m2. In conclusion, semaglutide could potentially replace insulin to improve glucose variability, TIR, and HbA1c in patients with HNF1B-MODY. However, more extensive studies are required to confirm its long-term safety and efficacy.
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