Maladie rénale chronique

maladie r é nale chronique
  • 文章类型: English Abstract
    慢性肾脏病(CKD)是一个公共卫生问题。然而,CKD患者的治疗仅限于疾病的诊断及其通过透析或肾移植的常规治疗。本文的目的是描述患有肾脏疾病的患者的具体特征,并根据其肾脏疾病的阶段确定其需求。
    Chronic kidney disease (CKD) is a public health problem. However, the management of patients with CKD is confined to the diagnosis of the disease and its conventional treatment by dialysis or renal transplantation. The aim of this article is to describe the specific characteristics of patients suffering from kidney disease and to determine their needs according to the stage of their renal disease.
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  • 文章类型: English Abstract
    慢性肾脏病(CKD)影响了近10%的世界人口,超过30%的70岁以上的人[1,2]。在法国,治疗的CKD的总体发病率稳定,但在85岁以上的人群中继续急剧上升[3]。在其高级阶段,CKD与许多与水紊乱相关的并发症有关,酸碱和磷钙平衡,以及贫血和心血管风险增加。更好地了解风险因素,改进促进肾保护的做法,治疗教育的进展和补充技术的准备将有助于降低这种风险。
    Chronic kidney disease (CKD) affects almost 10% of the world\'s population, and over 30% of people aged over 70 [1,2]. The overall incidence of treated CKD is stable in France, but continues to rise sharply in people aged over 85 [3]. In its advanced stages, CKD is associated with numerous complications linked to disturbances in water, acid-base and phosphocalcium balance, as well as anemia and increased cardiovascular risk. A better understanding of risk factors, improved practices to promote nephroprotection, and progress in therapeutic education and preparation for suppletive techniques would help reduce this risk.
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  • 文章类型: English Abstract
    神经认知障碍(NCD)在慢性肾脏病(CKD)患者中很常见。必须在早期阶段识别和表征这些疾病,以便能够提供适当的治疗。在慢性疾病如CKD中,患者参与决策是一项重大挑战,鉴于补充治疗的前景:血液透析,腹膜透析,肾移植或非透析药物治疗。许多因素与CKD患者NCD的发生发展有关,并且多种情况会影响这些患者的认知评估结果。
    Neurocognitive disorders (NCD) are common in patients with chronic kidney disease (CKD). It is essential to identify and characterize these disorders at an early stage, so as to be able to offer appropriate treatment. In a chronic disease such as CKD, the patient\'s involvement in decision-making is a major challenge, given the prospects for suppletive treatment: hemodialysis, peritoneal dialysis, kidney transplantation or non-dialytic drug therapy. Many factors are associated with the development and progression of NCD in patients with CKD, and a variety of conditions can influence the outcome of cognitive assessment in these patients.
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  • 文章类型: English Abstract
    腹膜透析仅是在患者家中进行的肾外净化技术。病人要么是自主的,或由私人护士或其家庭成员协助。患者被护理的中心的护理团队组织家访,以在他们的生活环境中与患者及其家人会面。这些访问提供了审查对协议的遵守情况并保持与患者的伙伴关系的机会。卡昂诺曼底大学肾脏疾病中心的团队分享了在这一护理领域的经验。
    Peritoneal dialysis is exclusively an extrarenal purification technique performed in the patient\'s own home. The patient is either autonomous, or assisted by a private nurse or a member of his or her family. The nursing team at the center where the patient is being cared for organizes home visits to meet the patient and his or her family in their living environment. These visits provide an opportunity to review compliance with protocols and maintain the partnership with the patient. The team at the Caen Normandy university center for kidney disease shares its experience in this area of care.
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  • 文章类型: English Abstract
    肾功能衰竭的并发症可能对血液透析患者的生活质量产生影响,这就是为什么特定的随访是由肾脏病学家组织的。高级执业护士(APN)可以与医生一起解决这个问题。SantélysBourgogneFranche-Comté协会进行的一项调查显示,专业人士赞成与APN合作,并且后续行动是由医疗和辅助医疗团队进行的,没有标准化的做法。RPN的干预可以改善不同行为者之间的协调。
    The complications of renal failure are likely to have an impact on the quality of life of hemodialysis patients, which is why specific follow-ups are organized by the nephrologist. Advanced practice nurses (APNs) could take care of this alongside physicians. A survey conducted by the Santélys Bourgogne Franche-Comté association shows that professionals are in favor of working with APNs and that follow-up is carried out by medical and paramedical teams without standardized practices. The intervention of an RPN could improve coordination between the different actors.
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  • 文章类型: English Abstract
    贫血是慢性肾脏病(CKD)的常见并发症。肾脏产生的促红细胞生成素(EPO)不足和缺铁是主要原因。补充铁和施用重组EPO是主要的治疗方式。可以口服的新铁制剂,最近已经开发了静脉内或直接通过透析液来改善功效和耐受性。在缺铁的情况下,口服柠檬酸铁可以有效地纠正贫血,此外还可以在肠腔中螯合磷酸盐。羧基麦芽糖铁允许静脉内给予较低频率的较大剂量。经由透析液直接施用的柠檬酸焦磷酸铁允许在血液透析期间补偿铁损失。HIF-脯氨酸酰-羟化酶抑制剂是一类新的红细胞生成刺激剂。口服药,它们通过稳定HIF转录因子起作用,所述HIF转录因子参与缺氧启动促红细胞生成素的产生。一些临床研究最近评估了这些新分子与重组EPO的比较。与重组EPO相比,在尚未接受透析或接受透析治疗的CKD患者中,已证明在纠正贫血方面具有非劣效性。它们诱导的循环铁调素的减少似乎大于可注射重组EPO诱导的减少。目前有关HIF-脯氨酸酰-羟化酶抑制剂安全性的报道令人放心,但需要在更大规模的长期研究中得到证实。©2022由ElsevierMassonSAS代表法国法语国家集团发布,透析et移植。
    Anemia is a common complication of chronic kidney disease (CKD). The insufficient erythropoietin (EPO) production by the kidneys and iron deficiency are the main causes. Iron supplementation and the administration of recombinant EPO are the main treatment modalities. New iron formulations that can be administered orally, intravenously or directly via the dialysate have recently been developed to improve efficacy and tolerance. Ferric citrate administered orally can effectively corrects anemia in case of iron deficiency and in addition chelate phosphate in the gut lumen. Ferric carboxymaltose allows intravenous administration of larger doses given less frequently. Ferric pyrophosphate citrate administered directly via the dialysate allows the compensation of iron losses during the hemodialysis session. HIF-prolyl-hydroxylase inhibitors are a new therapeutic class of erythropoiesis-stimulating agents. Orally administered, they act by stabilizing the HIF transcription factor involved in the initiation of erythropoietin production by hypoxia. Several clinical studies have recently evaluated these new molecules in comparison with recombinant EPO. In CKD patients not yet on dialysis or undergoing dialysis therapy non-inferiority in correcting anemia has been demonstrated compared with recombinant EPO. The decrease in circulating hepcidin they induce appears greater than that induced by injectable recombinant EPO. Presently available reports on the safety of HIF-prolyl-hydroxylase inhibitors are reassuring but need to be confirmed in longer-term studies of larger size. © 2022 Published by Elsevier Masson SAS on behalf of Société francophone de néphrologie, dialyse et transplantation.
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  • 文章类型: English Abstract
    2型钠葡萄糖协同转运蛋白(iSGLT2)的抑制剂在糖尿病患者的管理方面取得了重大进展,心力衰竭和慢性肾病(CKD)。随机对照研究表明,射血分数降低的2型糖尿病和/或心力衰竭患者的心血管风险显着降低。这些研究观察到肾病恶化的风险降低,导致CKD患者的随机对照研究:CREDENCE,DAPA-CKD和EMPA-KIDNEY.iSGLT2与终末期肾病进展缓慢相关,GFR斜率较低,白蛋白尿发生率较低。在患有蛋白尿的CKD患者中,无论是否患有糖尿病,DAPA-CKD和EMPA-KIDNEY研究已证明具有肾保护作用.对于没有蛋白尿的患者尚未发现这种作用。对于其他肾病,需要进一步的研究来证实在没有2型糖尿病和大量白蛋白尿的患者中获得的结果.因此,iSGLT2的适应症,加上适当剂量的RAS抑制剂,对于患有2型糖尿病和/或蛋白尿和/或心力衰竭的CKD患者的最佳肾保护似乎是不可否认的。除了常规的肾保护和心脏保护治疗和护理外,还必须开处方。副作用有限。然而,必须牢记有关生殖器感染和正常血糖酮症酸中毒(糖尿病患者)风险的特殊教育和监测。CKD患者的治疗库正在扩大,导致根据潜在的肾病考虑个性化护理。©2022由ElsevierMassonSAS代表法国法语国家集团发布,透析et移植。
    Inhibitors of sodium glucose co-transporter type 2 (iSGLT2) constitute a considerable advance in the management of patients with diabetes, heart failure and with chronic kidney disease (CKD). Randomized controlled studies have shown a significant reduction of cardiovascular risk in diabetic type 2 and/or heart failure with reduced ejection fraction patients. These studies observed a risk reduction of worsening nephropathy, leading to randomized controlled studies in CKD patients : CREDENCE, DAPA-CKD and EMPA-KIDNEY. iSGLT2 are associated with a slower progression toward end-stage kidney disease, a lower slope of GFR and a lower rate of albuminuria. In CKD patients with proteinuria either diabetic or not, the DAPA-CKD and the EMPA-KIDNEY studies have demonstrated a nephroprotective effect. This effect has not been found for patients without proteinuria. For the other nephropathies, further studies are required to confirm results obtained in patients without type 2 diabetes and macroalbuminuria. Therefore, the indication of iSGLT2, with appropriate dose of RAS inhibitor, seems undeniable to an optimal nephroprotection in CKD patients with type 2 diabetes and/or albuminuria and/or heart failure. They must be prescribed in addition to conventional nephroprotective and cardioprotective treatments and care. Side effects are limited. However, special education and monitoring concerning risks of genital infection and euglycemic ketoacidosis (diabetic patients) must be taken in mind. The therapeutic arsenal for CKD patients is expanding, leading to consider a personalized care according to the underlying nephropathy. © 2022 Published by Elsevier Masson SAS on behalf of Société francophone de néphrologie, dialyse et transplantation.
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  • 文章类型: Review
    慢性肾脏病相关瘙痒(CKD-aP)是CKD患者常见的并发症,尤其是透析患者。然而,CKD-aP的治疗仍然是一个挑战,因为病理生理学和研究研究规模太小.最后,有一些建议的治疗方案具有显著的临床获益.本综述将总结CKD-aP的所有可用治疗方法,并强调当前药物的临床疗效和局限性。值得注意的是,我们将重点关注阿片受体在CKD-aP和最近的Kappa阿片受体激动剂的病理生理学中的意义。©2022由ElsevierMassonSAS代表法国法语国家集团发布,透析et移植。
    Chronic Kidney Disease associated Pruritus (CKD-aP) is a well-established and frequent complication observed in patient with CKD, especially in dialysis patients. However, the management of CKD-aP remains a challenge as the pathophysiology and research studies are too small. Finally, there are a few proposed treatment options with significant clinical benefits. This general review will summarize all the available treatments for the CKD-aP and will highlight the clinical efficacy and limits of the current drugs. Notably, we will focus on the implication of the opioid receptor in the pathophysiology of the CKD-aP and the recently Kappa opioid receptor agonist. © 2022 Published by Elsevier Masson SAS on behalf of Société francophone de néphrologie, dialyse et transplantation.
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  • 文章类型: English Abstract
    缺铁在慢性肾脏病中很常见,甚至在透析阶段之前。它是非透析慢性肾脏病患者发病率和死亡率的独立因素。在慢性肾病期间,铁缺乏定义为转铁蛋白饱和度<20%和/或血清铁蛋白<100μg/L。在法国,约一半的非透析慢性肾脏病患者存在绝对铁缺乏(转铁蛋白饱和度<20%,血清铁蛋白<100μg/L)和/或功能性铁缺乏(转铁蛋白饱和度<20%,血清铁蛋白>100μg/L)。尽管如此,铁缺乏通常不调查。事实上,超过60%的肾脏科医师每年至少不评估一次铁状态.此外,铁缺乏很少治疗:只有12%的患者口服或静脉注射铁。早期发现和治疗是基本的,应该是系统的。为了帮助改善非透析慢性肾脏病患者缺铁的管理,我们提出了一种算法,该算法考虑了当前的建议和文献中的最新数据。最初的血液检查需要测量血红蛋白浓度,转铁蛋白饱和度和血清铁蛋白。转铁蛋白饱和度<20%可以诊断为铁缺乏,血清铁蛋白水平指向绝对或功能缺乏。这两个值的结合使得适应治疗成为可能,特别是在口服铁无效的炎症环境中。
    Iron deficiency is very common in chronic kidney disease, even before the dialysis stage. It is an independent factor of morbidity and mortality in patients with non-dialysis chronic kidney disease. During chronic kidney disease, iron deficiency is defined by a transferrin saturation <20% and/or a serum ferritin <100 μg/L. In France, about half of non-dialysis chronic kidney disease patients have absolute iron deficiency (transferrin saturation <20% and serum ferritin <100 μg/L) and/or functional iron deficiency (transferrin saturation <20% and serum ferritin >100 μg/L). Despite this, iron deficiency is usually not investigated. In fact, more than 60% of nephrologists do not assess iron status at least once a year. In addition, iron deficiency is rarely treated: only 12% of patients are prescribed oral or intravenous iron. Early detection and treatment are fundamental and should be systematic. In order to help improve the management of iron deficiency among non-dialysis chronic kidney disease patients, we propose an algorithm that takes into account current recommendations and the most recent data from the literature. Initial blood test requires the measurement of hemoglobin concentration, transferrin saturation and serum ferritin. A transferrin saturation <20% establishes the diagnosis of iron deficiency and the serum ferritin level points towards an absolute or functional deficiency. The combination of both values makes it possible to adapt the treatment, particularly in an inflammatory context where oral iron is not effective.
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  • 文章类型: English Abstract
    慢性肾脏病,其极端后果是透析或移植,需要高度结构化的护理途径,以精确的护理和治疗建议为标志。鉴于人口老龄化,患者数量的增加是不可避免的。肾病学家和高级实践护士之间的协同作用允许在包括咨询和处方在内的能力领域实施组织协议。
    Chronic kidney disease, the extreme consequence of which is dialysis or transplantation, requires a highly structured care pathway, marked by precise care and treatment recommendations. Given the aging of the population, the increase in the number of patients is inevitable. Synergy between nephrologists and advanced practice nurses allows the implementation of organization protocols in fields of competence including consultations and prescriptions.
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