Preventing the progression of chronic kidney disease: two case reports and review of the literature

被引:3
作者
Toor, Muhammad R. [1 ]
Singla, Anjali [1 ]
Kim, Jin K. [1 ]
Sumin, Xenia [1 ]
DeVita, Maria V. [1 ]
Michelis, Michael F. [1 ]
机构
[1] Lenox Hill Hosp, New York, NY 10075 USA
关键词
Chronic kidney disease; Hypertension and chronic kidney disease; Proteinuria; Parathyroid hormone; Metabolic acidosis; Hyperuricemia; BLOOD-PRESSURE; DIABETES-MELLITUS; RENAL-FUNCTION; RISK-FACTORS; URIC-ACID; ALLOPURINOL; INHIBITION; THERAPY; PROTEINURIA; BICARBONATE;
D O I
10.1007/s11255-014-0762-6
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
A variety of therapeutic modalities are available to alter the abnormalities seen in patients with chronic kidney disease (CKD). A comprehensive plan can now be developed to slow the progression of CKD. Two clinical cases of delay in the need for renal replacement therapy are described. This delay was achieved by using recognized recommendations for optimal diabetes therapy (HbA1c target 7 %), goals for blood pressure levels, reduction of proteinuria, and the proper use of ACEI/ARB therapies. Recent recommendations include BP < 140/90 mmHg for patients < 60 years old and < 150/90 mmHg for older patients unless they have CKD or diabetes. Limits on dietary sodium and protein intake and body weight reduction will decrease proteinuria. Proper treatment for elevated serum phosphorous and parathyroid hormone levels is now appreciated as well as the benefits of therapy for dyslipidemias and anemia. Concerns regarding unfavorable outcomes with excess ESA therapy have led to hemoglobin goals in the 10-12 g/dL range. Finally, new therapeutic considerations for the treatment of acidosis and hyperuricemia are presented with data available to suggest that increasing serum bicarbonate to > 22 mmol/L is beneficial, while serum uric acid therapeutic goals are still uncertain. Also, two as yet insufficiently understood approaches to altering the course of CKD (FGF-23 level reduction and balancing gut microbiota) are noted.
引用
收藏
页码:2167 / 2174
页数:8
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