Unveiling the enigma of acute kidney disease: predicting prognosis, exploring interventions, and embracing a multidisciplinary approach.

IF 2.9 3区 医学 Q1 UROLOGY & NEPHROLOGY
Kidney Research and Clinical Practice Pub Date : 2024-07-01 Epub Date: 2024-06-25 DOI:10.23876/j.krcp.23.289
Szu-Yu Pan, Thomas Tao-Min Huang, Zheng-Hong Jiang, Li-Chun Lin, I-Jung Tsai, Tsung-Lin Wu, Chih-Yi Hsu, Ting Wang, Hui-Chuen Chen, Yu-Feng Lin, Vin-Cent Wu
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Abstract

Acute kidney disease (AKD) is a critical transitional period between acute kidney injury and chronic kidney disease. The incidence of AKD following acute kidney injury is approximately 33.6%, and it can occur without identifiable preceding acute kidney injury. The development of AKD is associated with increased risks of chronic kidney disease, dialysis, and mortality. Biomarkers and subphenotypes are promising tools to predict prognosis in AKD. The complex clinical situations in patients with AKD necessitate a comprehensive and structured approach, termed "KAMPS" (kidney function check, advocacy, medications, pressure, sick day protocols). We introduce "MAND-MASS," an acronym devised to summarize the reconciliation of medications during episodes of acute illness, as a critical component of the sick day protocols at AKD. A multidisciplinary team care, consisting of nephrologists, pharmacists, dietitians, health educators, and nurses, is an optimal model to achieve the care bundle in KAMPS. Although the evidence for patients with AKD is still lacking, several potential pharmacological agents may improve outcomes, including but not limited to angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, mineralocorticoid receptor antagonists, sodium-glucose cotransporter 2 inhibitors, and glucagon-like peptide 1 receptor agonists. In conclusion, accurate prognosis prediction and effective treatment for AKD are critical yet unmet clinical needs. Future studies are urgently needed to improve patient care in this complex and rapidly evolving field.

揭开急性肾病之谜:预测预后、探索干预措施、采用多学科方法。
急性肾脏病(AKD)是急性肾损伤和慢性肾脏病之间的一个关键过渡期。急性肾损伤后,急性肾脏病的发病率约为 33.6%,而且可以在没有可识别的急性肾损伤之前发生。AKD 的发生与慢性肾病、透析和死亡风险的增加有关。生物标志物和亚型是预测 AKD 预后的有效工具。由于 AKD 患者的临床情况复杂,因此有必要采用一种全面、结构化的方法,即 "KAMPS"(肾功能检查、宣传、药物、压力、病假协议)。我们引入了 "MAND-MASS",这是一个缩写,用来概括急性病发作期间的药物调节,是 AKD 病假方案的重要组成部分。由肾病专家、药剂师、营养师、健康教育工作者和护士组成的多学科团队护理是实现 KAMPS 护理捆绑的最佳模式。虽然目前仍缺乏针对 AKD 患者的证据,但几种潜在的药物可改善预后,包括但不限于血管紧张素转换酶抑制剂、血管紧张素受体阻滞剂、矿物质皮质激素受体拮抗剂、钠-葡萄糖共转运体 2 抑制剂和胰高血糖素样肽 1 受体激动剂。总之,AKD 的准确预后预测和有效治疗是至关重要但尚未得到满足的临床需求。在这一复杂而快速发展的领域中,急需开展未来的研究,以改善对患者的护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.60
自引率
10.00%
发文量
77
审稿时长
10 weeks
期刊介绍: Kidney Research and Clinical Practice (formerly The Korean Journal of Nephrology; ISSN 1975-9460, launched in 1982), the official journal of the Korean Society of Nephrology, is an international, peer-reviewed journal published in English. Its ISO abbreviation is Kidney Res Clin Pract. To provide an efficient venue for dissemination of knowledge and discussion of topics related to basic renal science and clinical practice, the journal offers open access (free submission and free access) and considers articles on all aspects of clinical nephrology and hypertension as well as related molecular genetics, anatomy, pathology, physiology, pharmacology, and immunology. In particular, the journal focuses on translational renal research that helps bridging laboratory discovery with the diagnosis and treatment of human kidney disease. Topics covered include basic science with possible clinical applicability and papers on the pathophysiological basis of disease processes of the kidney. Original researches from areas of intervention nephrology or dialysis access are also welcomed. Major article types considered for publication include original research and reviews on current topics of interest. Accepted manuscripts are granted free online open-access immediately after publication, which permits its users to read, download, copy, distribute, print, search, or link to the full texts of its articles to facilitate access to a broad readership. Circulation number of print copies is 1,600.
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