electrolyte imbalance

电解质不平衡
  • 文章类型: Case Reports
    嗜铬细胞瘤很少出现原因不明的低钾血症,虽然文献中有一些病例报道。其背后的机制可能是β-2-肾上腺素受体过度激活和胰岛素抵抗促进的细胞钾摄取增加。我们介绍了一名68岁的高血压女性患者的情况,该患者在血管CT上发现了单侧肾上腺肿块,并伴有典型的肾上腺素能过度刺激(高血压危象,头痛,和出汗)与多次心律失常发作有关,但血浆和尿儿茶酚胺水平正常。在激素分泌过多和停止抗醛固酮药物治疗的过程中,患者出现耐药性低钾血症.由于无法纠正的低钾血症,我们无法对原发性醛固酮增多症进行激素检查,并将患者转诊为腹腔镜肾上腺切除术.组织学诊断为左嗜铬细胞瘤。术后,患者出现反弹型高钾血症.在单侧肾上腺肿块和低钾血症的患者中,除了原发性醛固酮增多症和促肾上腺皮质激素依赖性皮质醇增多症,手术前,临床医生也应排除可能的嗜铬细胞瘤。
    Pheochromocytoma rarely presents with unexplained hypokalaemia, although there are some case reports in the literature. The mechanism behind this could be the increased cellular potassium uptake promoted by beta-2-adrenoreceptor hyperactivation and insulin resistance. We present the case of a 68-year-old hypertensive female patient with a unilateral adrenal mass discovered on angio-CT and typical signs of adrenergic hyperstimulation (hypertensive crisis, headache, and sweating) associated with multiple arrhythmic episodes but with normal plasma and urinary catecholamine levels. During the work-up for hormonal hypersecretion and the cessation of anti-aldosterone medication, the patient presented resistant hypokalaemia. Due to uncorrectable hypokalaemia, we were unable to perform hormonal investigations for primary hyperaldosteronism and referred the patient for laparoscopic adrenalectomy. The histological diagnosis revealed left pheochromocytoma. Postoperatively, the patient experienced rebound hyperkalaemia. In a patient with a unilateral adrenal mass and hypokalaemia, besides primary hyperaldosteronism and adrenocorticotropic hormone-independent hypercortisolism, a possible pheochromocytoma should be ruled out as well by the clinician before surgery.
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  • 文章类型: Journal Article
    新诊断的血液系统恶性肿瘤患者通常具有相当大的细胞负担,导致并发症,包括高钾血症。然而,假性高钾血症,来自体外细胞裂解,可能会在临床实践中带来挑战。尽管在成人血液系统恶性肿瘤中经常报道假性高钾血症,它在儿科患者中的发生率被低估,其在这一人群中的发病率尚不清楚。我们回顾性回顾了2011年至2022年在台中退伍军人总医院接受血液系统恶性肿瘤新诊断的儿科患者的病历。高钾血症定义为血清或血浆钾水平超过5.5mEq/L。假性高钾血症的定义为:1)在没有干预的情况下,在4小时内钾下降超过1mEq/L,或2)没有指示高钾血症的心电图变化。排除有明显红细胞溶血的病例。共纳入157例新诊断为血液系统恶性肿瘤的儿科患者,其中14人表现出高钾血症。在这14个案例中,假性高钾血症7例(4.5%)。在最初的高白细胞增多患者中,这一比率增加到21.2%。假性高钾血症与较高的初始白细胞计数和较低的血清钠水平有关。所有假性高钾血症都发生在儿科急诊科,样品是作为血浆获得的,而所有真正的高钾血症病例都是在普通病房或重症监护病房观察到的,其中样品作为血清获得。及时识别假性高钾血症对于避免新诊断的血液系统恶性肿瘤的儿科患者进行不必要的降钾干预至关重要。
    Patients with newly diagnosed hematological malignancies often present with a considerable cellular burden, leading to complications including hyperkalemia. However, pseudohyperkalemia, arising from in vitro cell lysis, can pose challenges in clinical practice. Although pseudohyperkalemia is frequently reported in adult hematological malignancies, its occurrence in pediatric patients is underreported, and its incidence in this demographic remains unclear. We retrospectively reviewed the medical records of pediatric patients who received a new diagnosis of hematological malignancies from 2011 to 2022 at Taichung Veterans General Hospital. Hyperkalemia was defined by a serum or plasma potassium level exceeding 5.5 mEq/L. Pseudohyperkalemia was defined by 1) a potassium decrease of over 1 mEq/L in within 4 h without intervention or 2) the absence of electrocardiography changes indicative of hyperkalemia. Cases with apparent red blood cell hemolysis were excluded. A total of 157 pediatric patients with a new diagnosis of hematological malignancies were included, 14 of whom exhibited hyperkalemia. Among these 14 cases, 7 cases (4.5%) were of pseudohyperkalemia. This rate increased to 21.2% in patients with initial hyperleukocytosis. Pseudohyperkalemia was associated with a higher initial white blood cell count and lower serum sodium level. All episodes of pseudohyperkalemia occurred in the pediatric emergency department, where samples were obtained as plasma, whereas all true hyperkalemia cases were observed in the ordinary ward or intensive care unit, where samples were obtained as serum. Timely recognition of pseudohyperkalemia is crucial to avoiding unnecessary potassium-lowering interventions in pediatric patients with newly diagnosed hematological malignancies.
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  • 文章类型: Journal Article
    横纹肌溶解症,由横纹肌纤维破坏引起的医疗状况,可以有许多病因,最常见的是创伤性病因,也就是说,压伤,剧烈运动,被困在瓦砾下,等等。横纹肌溶解导致许多并发症,包括急性肾损伤和不同的电解质失衡,这后来会导致心律失常甚至死亡。本系统综述和荟萃分析调查了外伤性横纹肌溶解症患者中四种重要电解质失衡的发生率。PubMed,Scopus,WebofScience,和Embase数据库使用与我们研究主题相关的关键词搜索任何与创伤性横纹肌溶解相关的文章,不包括案例研究和案例系列。从收录的文章中提取相关数据,最后,我们对它们进行了荟萃分析,以计算每种电解质失衡的汇总发生率.总的来说,32篇文章被纳入我们的研究(通过数据库和引文检查)。以下是每种电解质失衡的汇总发生率:高钾血症,31%(95CI22%-41%);低钾血症,10%(95CI4%-17%);高钠血症,3%(95CI0%-8%);低钠血症,23%(95CI7%-44%);高钙血症,0%(95CI0%-1%);低钙血症,57%(95CI:22%-88%);高磷血症,33%(95CI11%-59%);低磷酸盐血症,4%(95CI0%-16%)。根据荟萃分析,高钾血症的发生率,低钠血症,低钙血症,在诊断为外伤性横纹肌溶解症的患者中,高磷血症高于高磷血症。
    Rhabdomyolysis, a medical condition caused by the destruction of striated muscle fibers, can have many etiologies, with the most common one being traumatic etiologies, that is, crushing injuries, heavy exertion, and being trapped under rubbles, and so forth. Rhabdomyolysis causes many complications, including acute kidney injury and different electrolyte imbalances, which later can cause cardiac dysrhythmia and even death as a result. This systematic review and meta-analysis investigate the incidence of imbalances of four important electrolytes among patients diagnosed with traumatic rhabdomyolysis. PubMed, Scopus, Web of Science, and Embase databases were searched for any article related to traumatic rhabdomyolysis using keywords related to the topic of our study, excluding case studies and case series. Relevant data were extracted from the included articles, and finally, a meta-analysis was performed on them to calculate the pooled incidence of each electrolyte imbalance. Collectively, 32 articles were included in our study (through the database and citation checking). The following were the pooled incidence of each electrolyte imbalance: hyperkalemia, 31% (95%CI 22%-41%); hypokalemia, 10% (95%CI 4%-17%); hypernatremia, 3% (95%CI 0%-8%); hyponatremia, 23% (95%CI 7%-44%); hypercalcemia, 0% (95%CI 0%-1%); hypocalcemia, 57% (95%CI: 22%-88%); hyperphosphatemia, 33% (95%CI 11%-59%); hypophosphatemia, 4% (95%CI 0%-16%). According to the meta-analyses, the rate of hyperkalemia, hyponatremia, hypocalcemia, and hyperphosphatemia is higher than their counterpart in patients diagnosed with traumatic rhabdomyolysis.
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  • 文章类型: Journal Article
    背景:卒中是世界范围内死亡和长期残疾的主要原因。不同人群的发病率和危险因素各不相同。本研究旨在分析人口统计,临床,以及沙特阿拉伯人群中卒中的实验室危险因素,以增强对其行为和相关死亡率的了解。方法在这项回顾性队列研究中,我们分析了2020年1月1日至2022年11月11日在法哈德国王医疗城诊断为出血性或非出血性卒中的3586例患者的数据.我们收集了人口统计学变量的数据,既往病史,社会史,国籍,和实验室组件。使用IBMSPSSStatisticsforWindows进行统计分析,版本27.0。(Armonk,纽约:IBM公司),显著性设置为p<0.05。结果研究人群以男性为主(57.86%),年龄在51~80岁(58.8%)。很大一部分患者是沙特国民(99.6%),高血压(50.2%)和糖尿病(40.4%)是最常见的合并症。与钠和钾水平相关的实验室异常与死亡率密切相关。值得注意的是,缺血性卒中是所有年龄组中最常见的类型,除了16岁以下的出血性卒中更为普遍的患者.结论:我们的发现揭示了沙特阿拉伯人群卒中危险因素和死亡率之间的显著关联。强调高血压的影响,糖尿病,和电解质失衡。该研究强调了沙特阿拉伯有针对性的卒中预防和管理策略的必要性。与全球趋势保持一致,以减轻这种疾病的负担。
    Background Stroke is a major cause of death and long-term disability worldwide, with varying incidence and risk factors across different populations. This study aims to analyze demographic, clinical, and laboratory risk factors for stroke among the Saudi Arabian population to enhance the understanding of its behavior and associated mortality. Methods In this retrospective cohort study, we analyzed data from 3586 patients diagnosed with hemorrhagic or non-hemorrhagic stroke at King Fahad Medical City from January 1, 2020, to November 11, 2022. We collected data on demographic variables, past medical history, social history, nationality, and laboratory components. Statistical analyses were performed using IBM SPSS Statistics for Windows, Version 27.0. (Armonk, NY: IBM Corp.), with significance set at p<0.05. Results The study population was predominantly male (57.86%) and within the age group of 51 to 80 years (58.8%). A significant portion of patients were Saudi nationals (99.6%), with hypertension (50.2%) and diabetes (40.4%) being the most common comorbidities. Laboratory abnormalities related to sodium and potassium levels were strongly linked to mortality rates. Notably, ischemic stroke was the most common type across all age groups, except for patients under age 16, where hemorrhagic stroke was more prevalent. Conclusions Our findings reveal significant associations between stroke risk factors and mortality within the Saudi Arabian population, highlighting the impact of hypertension, diabetes, and electrolyte imbalances. The study underscores the need for targeted stroke prevention and management strategies in Saudi Arabia, aligning with global trends to mitigate the burden of this disease.
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  • 文章类型: Journal Article
    背景在这项研究中,研究人员通过使用唾液来解决慢性肾脏病(CKD)患者频繁静脉切开术的需求,研究了分析肌酐水平的非侵入性方法,由于反复抽血进行肌酐水平评估,这可能会损害他们的静脉。方法这是一项在三级医疗机构中对50例诊断为CKD的患者进行的横断面研究。收集血清和唾液肌酐后,我们使用Pearson相关性来评估这两个因素之间的相关性。结果患者的平均年龄为50岁,标准偏差为±15.32岁。33例(66%)患者为男性,17例(34%)为女性。大多数患者年龄在51-70岁之间,包含26(52%)的样品。血清肌酐和唾液肌酐值分别在7.26-12.00和0.45-0.98之间。中位数分别为9.72和0.75。血清和唾液肌酐水平之间存在非常弱的正线性关系;然而,两者之间无显著关联(p=0.52).尽管如此,具有统计学意义的,血清尿素和血清白蛋白之间存在中度负线性相关(r=-0.36;p=0.01)。此外,血清氯化物和血清尿素之间存在统计学上显著的弱负线性相关(r=-0.3;p=0.03)。比较血清氯化物和血清钠显示有统计学意义,中度正线性关系(r=0.4;p=0.004)。血清磷与血清肌酐呈中度正线性关系(r=0.44;p=0.001)。此外,估计的肾小球滤过率(eGFR)和血清肌酐表现出统计学显著的强负线性相关(r=-0.79;p<0.001),而eGFR和血清磷显示出统计学上显着的弱负线性相关(r=-0.30;p=0.03)。结论该研究发现唾液和血清肌酐水平之间没有显着关联。必须对更大的人群进行进一步的多中心研究,以发现血清和唾液标志物之间的潜在相关性。
    Background In this study, researchers investigated non-invasive methods for analyzing creatinine levels by using saliva to address the need for frequent phlebotomy in chronic kidney disease (CKD) patients, which can damage their veins due to repeated blood withdrawals for creatinine level assessments. Methods This is a cross-sectional study in a tertiary healthcare setting conducted on 50 patients diagnosed with CKD. After collecting serum and salivary creatinine, we used Pearson correlation to assess the correlation between the two factors. Results The mean age of the patients was 50 years with a standard deviation of ± 15.32 years. 33 (66%) patients were males and 17 (34%) were females. Most patients were in the age group of 51 - 70 years, comprising 26 (52%) of the sample. The serum creatinine and salivary creatinine values ranged between 7.26-12.00 and 0.45-0.98, respectively. The median values were 9.72 and 0.75, respectively. There was a very weak positive linear relationship between serum and salivary creatinine levels; however, there was no significant association between them (p = 0.52). Nonetheless, a statistically significant, moderately negative linear correlation exists between serum urea and serum albumin (r = -0.36; p = 0.01). Additionally, there is a statistically significant weak negative linear correlation between serum chloride and serum urea (r = -0.3; p = 0.03). Comparing serum chloride and serum sodium reveals a statistically significant, moderately positive linear relationship (r = 0.4; p = 0.004). Serum phosphorus and serum creatinine display a statistically significant moderate positive linear relationship (r = 0.44; p = 0.001). Moreover, estimated glomerular filtration rate (eGFR) and serum creatinine exhibit a statistically significant strong negative linear correlation (r = -0.79; p < 0.001), while eGFR and serum phosphorus demonstrate a statistically significant weak negative linear correlation (r = -0.30; p = 0.03). Conclusion The study found no significant association between salivary and serum creatinine levels. Further multicentric studies on a larger population must be conducted to find the potential correlation between serum and salivary markers.
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  • 文章类型: Case Reports
    质子泵抑制剂(PPIs)是治疗多种胃肠道疾病的常用药物。通过不可逆地抑制氢钾ATP酶泵,它们显著减少胃酸分泌。然而,长期服用PPI会导致严重的并发症,包括严重的低镁血症.以下病例报告介绍了难治性PPI引起的低镁血症(PPIH)的严重病例,抗连续口服和静脉补充镁,一名70岁的男性患者,由于持续的上腹痛而长期使用PPI。在10例入院时,他出现了严重的低镁血症体征和症状,比如恶心,肌肉震颤,弥漫性抽筋,弱点,神经肌肉易怒,和心电图紊乱,包括非特异性T波异常。事实上,2006年首次报道了PPIH。人们认为,过度,长期摄入PPI可以干扰瞬时受体电位的正常功能6/7(TRPM6/7),这是肠镁吸收的主要途径,导致低镁血症.PPIH的典型特征是对口服和静脉补充镁的顽固抵抗,但通常在PPI停药后消退。因此,尽管是最安全和最常用的处方药之一,当计划长期使用时,应密切监测PPI的摄入量。此外,连续随访和定期评估血清镁水平对于避免PPIH的发生和预防其潜在的有害并发症至关重要。包括危及生命的心律失常.
    Proton pump inhibitors (PPIs) are frequently used medications to treat a wide variety of gastrointestinal conditions. By irreversibly inhibiting the hydrogen-potassium ATPase pump, they remarkably reduce gastric acid secretion. However, chronic PPI intake can result in serious complications, including severe hypomagnesemia. The following case report presents a severe case of refractory PPI-induced hypomagnesemia (PPIH), resistant to continuous oral and intravenous magnesium replacement, in a 70-year-old male patient, with a long history of PPI use due to persistent epigastric pain. Upon each of the 10 admissions to the hospital, he presented with severe signs and symptoms of hypomagnesemia, such as nausea, muscle fasciculation, diffuse cramps, weakness, neuromuscular irritability, and ECG disturbances, including non-specific T-wave abnormalities. In fact, PPIH has been reported for the first time in 2006. It is believed that the excessive, chronic intake of PPIs can disturb the normal functioning of the transient receptor potential melastatin 6/7 (TRPM 6/7), which is the main pathway of active intestinal magnesium absorption, leading to hypomagnesemia. PPIH is typically characterized by stubborn resistance to oral and intravenous magnesium replenishment but usually resolves after PPI withdrawal. Hence, despite being among the safest and most commonly prescribed drugs, PPI intake should be closely monitored when prolonged usage is planned. Additionally, continuous follow-up and regular assessment of serum magnesium levels are crucial to avoid the occurrence of PPIH and to prevent its potentially deleterious complications, including life-threatening arrhythmias.
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  • 文章类型: Journal Article
    造口是胃肠道与腹部皮肤壁的人工吻合,以重新引导粪便流。粪便分流,肠减压,吻合保护是气孔的常见适应症。相对于其他外科手术,气孔发病率很高,平均比率为40%,范围为14-79%。最常见的早期并发症是造口周围皮肤刺激。相比之下,造口旁疝是最常见的晚期并发症。
    这项研究是在巴林王国的哈马德国王大学医院(KHUH)进行的。我们的研究包括接受过回肠造口术和结肠造口术的患者。纳入标准包括15岁及以上的成年患者,紧急和选择性案件,ASA评分为1-4分。排除在外的患者是那些在KHUH以外进行了造口的患者,以及那些在我们医院高压科没有跟进的患者。本研究采用回顾性研究设计。样本量为98,其中包括2018年1月至2021年2月期间与高压团队跟进的气孔患者。
    我们已经分解了造口形成的适应症。给定的图中说明了我们所有记录的并发症的细目。
    在我们的机构研究中,造口并发症的63.3%包括皮肤问题。这形成了大多数的并发症。建立造口护理单元将为患者提供持续的支持和护理,并帮助他们恢复最佳生活质量。此外,这一目标可以通过术前和术后有关手术和造口形成的教育来实现.这包括术前造口标记和定位,以及通过知识渊博的造口护理专家关于动手造口护理的指导来改善恢复。最后,患者可以通过专门的造口诊所得到帮助。
    QassimT,SaeedMF,QassimA,etal.肠梗阻-当前的实践和挑战:机构审查。欧亚J肝胃肠病2023;13(2):115-119。
    UNASSIGNED: A stoma is an artificial anastomosis of the gastrointestinal tract to the abdominal skin wall to reroute the stream of feces. Fecal diversion, bowel decompression, and anastomosis protection are common indications for stomas. Relative to other surgical operations, stomas have a high morbidity rate, with rates averaging 40% and ranging 14-79%. The most common early complication was peristomal skin irritation. In contrast, parastomal hernias were the most common late complication.
    UNASSIGNED: This research was performed at King Hamad University Hospital (KHUH) in the Kingdom of Bahrain. Our study included patients who had undergone ileostomies and colostomies. The inclusion criteria included adult patients who are 15 years and older, both emergency and elective cases, and with ASA score of 1-4. The excluded patients were those who had had their stomas performed outside of KHUH and those who were not following up in the hyperbaric department of our hospital. This study was performed using a retrospective study design. The sample size was 98 which included patients with stomas that were following up with the hyperbaric team between January 2018 and February 2021.
    UNASSIGNED: We have broken down the indications for stoma formation. The breakdown of all our documented complications are illustrated in the given figure.
    UNASSIGNED: Within our institutional study, 63.3% of stoma complications consisted of skin problems. This formed the majority of complications. Establishing a stoma care unit would offer continuous support and care to patients and help them in returning to an optimal quality of life. Additionally, this goal can be met through preoperative and postoperative education regarding surgery and stoma formation. This includes preoperative stoma marking and siting, as well as improved recovery through instruction from knowledgeable stoma care specialists regarding hands-on stoma care.Finally, patients can be assisted through specialized stoma clinics.
    UNASSIGNED: Qassim T, Saeed MF, Qassim A, et al. Intestinal Stomas-Current Practice and Challenges: An Institutional Review. Euroasian J Hepato-Gastroenterol 2023;13(2):115-119.
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  • 文章类型: Review
    CLDN10中的双等位基因致病变体引起非常罕见和独特的多发性上皮功能障碍,表现为汗症和电解质失衡(HELIX)综合征。HELIX患者常表现为热不耐受和泪液分泌减少。这里,我们报道了8例新患者(4个家庭),他们在出生后不久出现手掌和脚底的细鳞片以及与高体温相关的多汗症。外显子组测序在一个家族中的CLDN10中鉴定了一种新的纯合致病性变体(NM_006984:外显子1:c.138G>A:p。W46*)和其他三个先前报道的致病性变体的共同创始人(NM_006984:exon5:c.653del:P218Lfs*21)。这些患者的详细临床报告和对先前报道的患者的回顾进一步描述了这种极为罕见的疾病的表型。
    Biallelic pathogenic variants in CLDN10 cause the very rare and distinct multiplex epithelium dysfunction manifested by hypohidrosis and electrolyte imbalance (HELIX) syndrome. HELIX patients often present with heat intolerance and reduced tear secretion. Here, we report on eight new patients (four families) who presented soon after birth with fine scales in the palms and soles and hypohidrosis that was associated with high body temperature. Exome sequencing identified a novel homozygous pathogenic variant in CLDN10 in one family (NM_006984:exon1:c.138G>A:p.W46*) and a previously reported pathogenic founder variant in the other three (NM_006984:exon5:c.653del:P218Lfs*21). The detailed clinical reports of these patients and a review of previously reported patients further delineate the phenotype of this extremely rare disorder.
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  • 文章类型: Case Reports
    本病例系列描述了2名接受III类抗心律失常药物长期治疗的妇女,由于QTc延长因素,在导管消融治疗心房颤动的情况下,发生了扭转性尖端性多形性室性心动过速。临床医生必须在围手术期提高对QTc延长药物的警惕。(难度等级:中级。).
    This case series describes 2 women on prolonged therapy with class III antiarrhythmics who developed torsades de pointes polymorphic ventricular tachycardia in the setting of catheter ablation for atrial fibrillation as a result of QTc prolonging factors. Clinicians must exercise increased vigilance in the perioperative period in patients on QTc-prolonging medications. (Level of Difficulty: Intermediate.).
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  • 文章类型: Journal Article
    电解质异常在急性中风患者中很常见,对疾病的病程和预后有重大影响。电解质失衡,如低钠血症,低钾血症,低钙血症,低镁血症,和磷酸盐异常常见于该患者人群。发病率,根本原因,在这项综合研究中,研究了急性中风患者电解质异常的医学后果。根据我们的研究,低钠血症是最常见的电解质失衡。中风患者低钠血症的最常见原因是抗利尿激素分泌不当综合征(SIADH)。死亡率较高,住院时间更长,和较差的功能结局都与低钠血症有关。急性中风患者通常也会出现低钾血症,影响中风的严重程度和功能能力的恢复。该综述进一步强调了高钙血症的发生率和临床后果,低镁血症,低磷酸盐血症,急性中风患者的低钙血症。结果突出了早期电解质失衡检测和治疗在急性脑卒中患者中的意义。为了更好地理解治疗方法,评估它们对卒中结局的影响,并分析预后影响,需要更多的研究。
    Electrolyte abnormalities are common in acute stroke patients and have a substantial impact on the course and prognosis of the disease. Electrolyte imbalances such as hyponatremia, hypokalemia, hypocalcemia, hypomagnesemia, and phosphate abnormalities are frequently seen in this patient population. The incidence, root causes, and medical ramifications of electrolyte abnormalities in acute stroke patients are investigated in this comprehensive study. According to our research, hyponatremia is the most prevalent electrolyte imbalance. The most common reason for hyponatremia in stroke patients is the syndrome of inappropriate antidiuretic hormone secretion (SIADH). Higher mortality rates, longer hospital admissions, and less favorable functional outcomes are all linked to hyponatremia. Acute stroke patients also typically experience hypokalemia, which affects the severity of the stroke and the recovery of functional abilities. The review furthermore emphasizes the incidence and clinical consequences of hypercalcemia, hypomagnesemia, hypophosphatemia, and hypocalcemia in patients with acute stroke. The results highlight the significance of early electrolyte imbalance detection and treatment in acute stroke patients. To better comprehend therapeutic approaches, evaluate their influence on stroke outcomes, and analyze prognostic implications, more research is required.
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