hypermagnesemia

  • 文章类型: English Abstract
    虽然肾功能下降是氧化镁(MgO)引起高镁血症的已知危险因素,很少有研究全面调查其他影响因素。在这项研究中,研究者分析了在松山世民医院接受MgO治疗的256例住院患者发生高镁血症的危险因素.多变量分析确定血尿素氮≥22mg/dL,估计肾小球滤过率≤43.1毫升/分钟,MgO≥1000mg/d为危险因素。此外,研究人员的研究结果表明,危险因素的数量与高镁血症的发病率之间存在相关性,包括3级病例的患病率。有趣的是,低体重指数是一个潜在的危险因素,即使在没有这三个因素的患者中也是如此.这些发现强调了药剂师提倡对具有本研究中确定的危险因素的患者进行常规血清Mg水平监测的重要性。
    While decreased renal function is a known risk factor for hypermagnesemia caused by magnesium oxide (MgO), few studies have comprehensively investigated other contributing factors. In this study, the researchers analyzed the risk factors for hypermagnesemia development in 256 inpatients receiving MgO treatment at the Matsuyama Shimin Hospital. Multivariate analysis identified blood urea nitrogen ≧22 mg/dL, estimated glomerular filtration rate ≦43.1 mL/min, and MgO ≧1000 mg/d as risk factors. Additionally, the researchers\' findings suggest a correlation between the number of risk factors and the incidence of hypermagnesemia, including the prevalence of Grade 3 cases. Interestingly, low body mass index emerged as a potential risk factor even in patients without the three identified factors. These findings highlight the importance for pharmacists to advocate for routine serum Mg level monitoring in patients with the risk factors identified in this study.
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  • 文章类型: Case Reports
    高镁血症通常发生在肾功能不全的患者中。由于高镁血症的稀有性和缺乏对镁水平的常规监测,诊断高镁血症是一项挑战。此外,临床医生缺乏对这种罕见疾病的认识经常导致诊断延迟.很少有患者在血清镁水平超过7mmol/L时存活。本文介绍了肾功能正常的患者口服泻盐导致的近致命性高镁血症的案例研究。一名60岁的女性于10月出现在消化内科6,2023年,有3天的黑大便史。她于2005年接受了胃大部切除术,有稳定的肾病综合征病史。调查她出血的原因,电子胃镜和结肠镜检查定于10月2023年11月11日。摄入泻盐后30分钟,她突然失去知觉。主治医师怀疑是严重的镁中毒。她及时服用了葡萄糖酸钙,用Ambu袋通气进行气管插管,并接受早期连续性肾脏替代治疗(CRRT)。快速诊断和CRRT有助于她的血清镁水平从最初的8.71mmol/L降低到1.35mmol/L,导致与高镁血症相关的毒性症状显着改善。随后,她在消化内科管理,胃镜检查显示胃肠道吻合口溃疡出血。在包括酸抑制在内的保守治疗之后,胃保护,和止血,她的症状有所改善,她成功出院了.这项研究旨在提醒临床医生注意肾功能正常个体高镁血症的可能性。医生在给患有潜在胃肠道疾病的患者开泻盐时应谨慎行事。如有必要,可考虑替代药物治疗以降低高镁血症的风险.及时干预对于避免与高镁血症相关的危及生命的并发症至关重要。
    Hypermagnesemia commonly occurs in patients with renal dysfunction. Diagnosing hypermagnesemia represents a challenge due to its rarity and the absence of routine monitoring of magnesium levels. Furthermore, the lack of awareness among clinicians regarding this uncommon condition frequently leads to delayed diagnoses. Few patients survive with a serum magnesium level exceeding 7 mmol/L. This article presents a case study of near-fatal hypermagnesemia resulting from the oral administration of Epsom salts in a patient with normal renal function. A 60-year-old female presented to the gastroenterology department on Oct. 6, 2023, with a 3-day history of black stools. She underwent subtotal gastrectomy in 2005 and has a stable history of nephrotic syndrome. To investigate the cause of her bleeding, electronic gastroscopy and colonoscopy were scheduled for Oct. 11, 2023. She experienced a sudden loss of consciousness 30 min after the ingestion of Epsom salts. The attending physician suspected a severe magnesium poisoning. She was promptly administered calcium gluconate, underwent tracheal intubation with ambu bag ventilation, and received early continuous renal replacement therapy (CRRT). Swift diagnosis and CRRT contributed to a reduction in her serum magnesium levels from an initial 8.71 mmol/L to 1.35 mmol/L, leading to a remarkable improvement in the toxic symptoms associated with hypermagnesemia. Subsequently, she was managed in the gastroenterology department, with gastroscopy revealing bleeding from the gastrointestinal anastomotic ulcer. Following conservative treatments including acid suppression, stomach protection, and hemostasis, her symptoms improved, and she was successfully discharged. This study aims to alert clinicians to the possibility of hypermagnesemia in individuals with normal renal function. Physicians should exercise caution when prescribing Epsom salts to patients with underlying gastrointestinal conditions. If necessary, alternative drug therapies may be considered to mitigate the risk of hypermagnesemia. Timely intervention is pivotal in averting life-threatening complications linked to hypermagnesemia.
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  • 文章类型: Journal Article
    简介:镁是一种重要的细胞内阳离子,对于与能量代谢相关的320多个酶促反应至关重要,肌肉骨骼功能,和核酸合成,在人体生理中起着举足轻重的作用。本研究旨在探讨糖尿病患者血镁异常的患病率及其与血糖控制的相关性。药物使用,和糖尿病并发症。方法:在苏丹卡布斯大学医院进行了一项横断面研究,包括316名18岁或以上的糖尿病患者。数据包括人口统计,病史,药物,和生化参数。测定血清总镁浓度,镁血症定义为镁≤0.69mmol/L的低镁血症和≥1.01mmol/L的高镁血症。结果:糖尿病患者的低镁血症患病率为17.1%(95%CI:13.3-21.7%),高镁血症为4.1%(95%CI:2.4-7.0%)。女性在低镁血症组中的比例明显过高,高镁血症组高血压患病率较高,视网膜病变,白蛋白/肌酐比率增加,慢性肾脏病(CKD),肌酐水平升高,和较低的调节钙浓度。多因素logistic回归显示,女性和较高的血清调整钙是低镁血症的独立危险因素。相比之下,高血压的存在,更高水平的白蛋白/肌酐比率,5期CKD是高镁血症的独立危险因素。结论:低镁血症在糖尿病患者中很常见;然而,高镁血症与微血管并发症相关。
    Introduction: Magnesium is a vital intracellular cation crucial for over 320 enzymatic reactions related to energy metabolism, musculoskeletal function, and nucleic acid synthesis and plays a pivotal role in human physiology. This study aimed to explore the prevalence of dysmagnesemia in patients with diabetes mellitus and evaluate its correlations with glycemic control, medication use, and diabetic complications. Methods: A cross-sectional study was conducted at Sultan Qaboos University Hospital, including 316 patients aged 18 years or older with diabetes mellitus. Data included demographics, medical history, medications, and biochemical parameters. Serum total magnesium concentrations were measured, and dysmagnesemia was defined as magnesium ≤ 0.69 mmol/L for hypomagnesemia and ≥1.01 mmol/L for hypermagnesemia. Results: The prevalence of hypomagnesemia in patients with diabetes was 17.1% (95% CI: 13.3-21.7%), and hypermagnesemia was 4.1% (95% CI: 2.4-7.0%). Females were significantly overrepresented in the hypomagnesemia group, while the hypermagnesemia group showed a higher prevalence of hypertension, retinopathy, an increased albumin/creatinine ratio, chronic kidney disease (CKD), elevated creatinine levels, and a lower adjusted calcium concentration. The multinominal logistic regression exhibited that the female sex and higher serum-adjusted calcium were independent risk factors of hypomagnesemia. In contrast, the presence of hypertension, higher levels of albumin/creatinine ratio, and stage 5 CKD were independent risk factors of hypermagnesemia. Conclusions: Hypomagnesemia was common among patients with diabetes mellitus; however, hypermagnesemia was associated with microvascular complications.
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  • 文章类型: Case Reports
    高镁血症是临床上观察到的罕见电解质异常。患有这种疾病的患者会出现各种症状,取决于血清镁水平。高镁血症很少因四肢无力而并发。我们报告了一例32岁女性患者,由于高镁血症而出现双侧上下肢无力。校正血清镁水平后,四肢无力消退,病人出院后好转。这里,我们讨论了这种类型的临床表现的诊断和治疗延迟。
    Hypermagnesemia is a rare electrolyte abnormality observed in the clinical setting. Patients with this condition can present with a variety of symptoms, depending on the level of serum magnesium. Hypermagnesemia is rarely complicated by weakness of the extremities. We report the case of 32 years old female patient who presented with bilateral upper- and lower-extremity weakness due to hypermagnesemia. Following correction of the serum magnesium level, extremity weakness subsided, and the patient was discharged with improvement. Here, we discuss the delay in the diagnosis and management of this type of clinical presentation.
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  • 文章类型: Journal Article
    入院时体温过低与早产儿死亡率增加相关。给予孕妇的药物与它的发生有关。由于硫酸镁有肌肉松弛作用,我们旨在评估早产儿出生时高镁血症与入院时体温过低(腋窝温度<36.5°C)的相关性.
    我们对前瞻性队列研究数据库进行了二次分析,其中包括<34周的新生儿,没有先天性畸形。如果脐带镁水平>2.5mEq/L,则考虑高镁血症。使用孕产妇和新生儿变量来调整模型,提交给多元分层建模过程。
    我们评估了249例新生儿的中位出生体重和胎龄为1375(IQR1020-1375)g和31(IQR28-32)周,分别。高镁血症发生率为28.5%,入院低温发生率为28.9%。在单变量分析中,确定以下变量与入院低温相关:高镁血症(OR3.71;CI2.06-6.68),复苏(OR2.39;CI1.37-4.19),小至胎龄(OR1.91;CI1.03-3.53),全身麻醉(OR3.34;CI1.37-8.13),出生体重(OR0.998;CI0.998-0.999)和孕龄(OR0.806;CI0.725-0.895)。在分层回归模型中,高镁血症仍然与入院低温独立相关(OR3.20;CI1.66-6.15),以及出生体重(OR0.999;CI0.998-0.999)和气管插管(3.83;CI1.88-7.80)。
    高镁血症与入院低体温风险增加相关,气管插管和降低出生体重。
    UNASSIGNED: Hypothermia on admission is associated with increased mortality in preterm infants. Drugs administered to pregnant women is implicated in its occurrence. Since magnesium sulfate has a myorelaxant effect, we aimed evaluating the association of hypermagnesemia at birth and admission hypothermia (axillary temperature <36.5°C) in preterm infants.
    UNASSIGNED: We performed a secondary analysis of a prospective cohort study database including inborn infants <34 weeks, without congenital malformations. Hypermagnesemia was considered if the umbilical magnesium level > 2.5 mEq/L. Maternal and neonatal variables were used to adjust the model, submitted to the multivariate hierarchical modelling process.
    UNASSIGNED: We evaluated 249 newborns with median birth weight and gestational age of 1375 (IQR 1020-1375) g and 31 (IQR 28-32) weeks, respectively. Hypermagnesemia occurred in 28.5% and admission hypothermia occurred in 28.9%. In the univariate analysis, the following variables were identified as being associated with admission hypothermia: hypermagnesemia (OR 3.71; CI 2.06-6.68), resuscitation (OR 2.39; CI 1.37-4.19), small to gestational age (OR 1.91; CI1.03-3.53), general anesthesia (OR 3.34; CI 1.37-8.13), birth weight (OR 0.998; CI 0.998-0.999) and gestational age (OR 0.806; CI 0.725-0.895). In the hierarchical regression model, hypermagnesemia remained independent associated with admission hypothermia (OR 3.20; CI 1.66-6.15), as well as birth weight (OR 0.999; CI 0.998-0.999) and tracheal intubation (3.83; CI 1.88-7.80).
    UNASSIGNED: Hypermagnesemia was associated with an increased risk of admission hypothermia, as did tracheal intubation and lower birth weight.
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  • 文章类型: Journal Article
    镁在自然界中无处不在。它位于食物链的起源,占据植物叶绿素的中心。在人类中,镁对不同的分子和催化过程至关重要,包括能量转移和基因组的维持。尽管它丰富,低镁血症很常见,常常得不到诊断。尽管有流行病学数据将低镁与包括糖尿病在内的慢性疾病联系起来。临床上显着的高镁血症较少,但是演讲可能是戏剧性的。分子生物学的进展和镁障碍遗传原因的阐明增强了我们对其病理生理学的理解。治疗方法也在改变。重新利用新的药物,如钠/葡萄糖协同转运蛋白2抑制剂,提供了新的治疗选择。在这篇综述中,我们整合了这个快速发展的领域的知识,为临床医生和受训者提供了一种资源,用于处理涉及镁障碍的常见临床情况。
    Magnesium is ubiquitous in nature. It sits at the origin of the food chain, occupying the center of chlorophyl in plants. In humans, magnesium is critical to diverse molecular and catalytic processes, including energy transfer and maintenance of the genome. Despite its abundance, hypomagnesemia is common and often goes undiagnosed. This is in spite of epidemiologic data linking low magnesium with chronic diseases including diabetes mellitus. Clinically significant hypermagnesemia is encountered less frequently, but the presentation may be dramatic. Advances in molecular biology and the elucidation of the genetic causes of magnesium disorders have enhanced our understanding of their pathophysiology. Treatment approaches are also changing. The repurposing of newer medications, such as sodium/glucose cotransporter 2 inhibitors, offers new therapeutic options. In this review we integrate knowledge in this rapidly evolving field to provide clinicians and trainees with a resource for approaching common clinical scenarios involving magnesium disorders.
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  • 文章类型: Letter
    暂无摘要。
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  • 文章类型: Case Reports
    高镁血症是一种罕见但可能致命的电解质疾病,由于其不熟悉而经常被忽视。镁是通过骨骼的平衡来调节的,肠道吸收,和肾脏排泄。高镁血症通常由镁摄入过多或肾脏排泄减少引起;然而,它也发生在肾功能正常的患者中。在这里,我们报告了2例服用氢氧化镁治疗便秘的高镁血症。首例病例涉及一名82岁终末期肾病女性,因高镁血症而出现代谢性脑病,每天服用3,000毫克氢氧化镁治疗便秘。她的镁水平为9.9mg/dL。她的治疗包括停止氢氧化镁和继续血液透析,这导致了她的康复。在第二种情况下,一名50岁的女性,有脑出血和智力低下的病史,尽管肾功能正常,但仍出现高镁血症。她还服用氢氧化镁治疗便秘,镁水平为11.0mg/dL。在准备连续肾脏替代疗法(CRRT)时,她经历了心脏骤停。在实现自发循环返回后,CRRT已启动,镁含量呈下降趋势.然而,生命体征和乳酸水平没有恢复,导致死亡。这些病例强调了及时诊断和干预高镁血症的重要性,以及需要定期监测接受含镁制剂的个体的镁水平。尤其是那些肾功能受损的人.
    Hypermagnesemia is a rare but potentially fatal electrolyte disorder often overlooked because of its unfamiliarity. Magnesium is regulated through a balance of bone, intestinal absorption, and renal excretion. Hypermagnesemia typically arises from excessive magnesium intake or reduced renal excretion; however, it also occurs in patients with normal kidney function. Herein, we report two cases of hypermagnesemia in patients taking magnesium hydroxide for constipation. The first case involved an 82-year-old woman with end-stage renal disease who developed metabolic encephalopathy due to hypermagnesemia, after taking 3,000 mg of magnesium hydroxide daily for constipation. Her magnesium level was 9.9 mg/dL. Her treatment involved discontinuing magnesium hydroxide and continuing hemodialysis, which led to her recovery. In the second case, a 50-year-old woman with a history of cerebral hemorrhage and mental retardation developed hypermagnesemia despite having normal renal function. She was also taking magnesium hydroxide for constipation, and her magnesium level was 11.0 mg/dL. She experienced cardiac arrest while preparing for continuous renal replacement therapy (CRRT). After achieving return of spontaneous circulation, CRRT was initiated, and her magnesium level showed a decreasing trend. However, vital signs and lactate levels did not recover, leading to death. These cases highlight the importance of prompt diagnosis and intervention for hypermagnesemia and the need to regularly monitor magnesium levels in individuals receiving magnesium-containing preparations, especially those with impaired kidney function.
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  • 文章类型: Journal Article
    镁(Mg2+)是一种主要的细胞内阳离子,在各种酶,膜,和结构体功能。作为钙(Ca2+)拮抗剂,它是许多神经肌肉活动的必要条件。体内Mg2+浓度的不平衡导致从无症状到严重危及生命的并发症的临床表现。因此,Mg2+测量对实验室和临床各方面的贡献不容忽视.Mg2+通常被描述为被遗忘的分析物。然而,它与体内钾(K+)的密切关系,Ca2+,和磷酸盐稳态证明Mg2+失衡可能作为其他电解质紊乱的根本原因或后果共存。同时,几个预分析,分析,分析后方面可能会影响Mg2+的测量。这篇综述重点介绍了Mg2+测量的实验室和临床问题以及一些与其失衡相关的分析物紊乱。了解这一基础可以帮助临床医生和实验室专业人员进行Mg2结果解释和患者管理。
    Magnesium (Mg2+) is a predominantly intracellular cation that plays significant roles in various enzymatic, membrane, and structural body functions. As a calcium (Ca2+) antagonist, it is imperative for numerous neuromuscular activities. The imbalance of body Mg2+  concentration leads to clinical manifestations ranging from asymptomatic to severe life-threatening complications. Therefore, the contribution of Mg2+ measurement regarding various laboratory and clinical aspects cannot be ignored. Mg2+ is often described as the forgotten analyte. However, its close relationship with body potassium (K+), Ca2+, and phosphate homeostasis proves that Mg2+ imbalance could co-exist as the root cause or the consequence of other electrolyte disorders. Meanwhile, several preanalytical, analytical, and postanalytical aspects could influence Mg2+ measurement. This review highlights Mg2+ measurement\'s laboratory and clinical issues and some analyte disturbances associated with its imbalance. Understanding this basis could aid clinicians and laboratory professionals in Mg2+ result interpretation and patient management.
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  • 文章类型: Journal Article
    根据流行病学研究,便秘对预期寿命有负面影响,需要适当的治疗。根据药品和医疗器械局(PMDA),长期服用氧化镁(MgO)治疗便秘的患者,尤其是那些肾功能受损的人和老年人,高镁血症的风险很高.因此,血清镁水平,在临床实践中通常不检查,应该对这些患者进行监测。因此,预测血清Mg水平升高并预防高镁血症的发展,我们的目的是确定高镁血症的危险因素,尤其是老年人口。我们的研究包括2014年1月1日至2016年3月31日在我们医院接受MgO治疗的患者。不符合纳入标准的患者被排除并匹配以调整背景因素;最后,分析包括高镁血症组的35例患者和非高镁血症组的140例患者。多变量分析确定肌酐清除率(eCcr)≤28.2mL/min为统计学上有意义的危险因素。此外,MgO剂量≥900毫克/天被确定为临床考虑的风险因素,虽然没有统计学意义。此外,MgO剂量≥900mg/天的患者高镁血症的发生率增加至11.6%,eCcr≤28.2mL/min的为27.0%,两者都有53.1%。高镁血症可能发生在eCcr≤28.2mL/min的老年患者,服用超过900mg/天的MgO。
    According to epidemiological studies, constipation has a negative effect on life expectancy, necessitating appropriate treatment. According to the Pharmaceuticals and Medical Devices Agency (PMDA), patients who have been taking magnesium oxide (MgO) for constipation over a prolonged period, especially those with impaired renal function and older individuals, are at high risk of hypermagnesemia. Therefore, serum Mg levels, which are often not checked in clinical practice, should be monitored in these patients. Thus, to predict elevated serum Mg levels and prevent the development of hypermagnesemia, we aimed to identify the risk factors of hypermagnesemia, especially in the older population. Our study included patients who were prescribed MgO at our hospital between January 1, 2014, and March 31, 2016. Patients who did not meet the inclusion criteria were excluded and matched to adjust for background factors; finally, 35 patients in the hypermagnesemia arm and 140 patients in the non-hypermagnesemia arm were included in the analysis. Multivariate analysis identified estimated creatinine clearance (eCcr) ≤ 28.2 mL/min as a statistically significant risk factor. In addition, MgO dose ≥ 900 mg/day was identified as a risk factor for clinical consideration, although not statistically significant. Furthermore, the incidence of hypermagnesemia was shown to increase to 11.6% for those with MgO dose ≥ 900 mg/day, 27.0% for those with eCcr ≤ 28.2 mL/min, and 53.1% for those with both. Hypermagnesemia may occur in older patients with eCcr ≤ 28.2 mL/min who take more than 900 mg/day of MgO.
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