Adult nephrotic syndrome: Non-specific strategies for treatment

被引:21
作者
Charlesworth, John A.
Gracey, David M.
Pussell, Bruce A.
机构
[1] Prince Wales Hosp, Dept Nephrol, Sydney, NSW, Australia
[2] Univ New S Wales, Sydney, NSW, Australia
关键词
bone mineral density; hyperlipidaemia; infection; nephrotic syndrome; proteinuria; thrombo-embolism;
D O I
10.1111/j.1440-1797.2007.00890.x
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
Irrespective of aetiology, the nephrotic syndrome presents a range of potentially serious complications. These include thrombo-embolism, infection and hyperlipidaemia. Despite the prevalence of the nephrotic state among renal patients, there has been little prospective analysis of the therapeutic approach to these potentially life-threatening events even though their pathogenesis has been examined in some detail. Most of these complications are more prevalent once the albumin concentration falls below 20 g/L and it is recognized that restoration of serum albumin significantly diminishes their frequency. However, this may be difficult to achieve, especially in adults. The problems of thrombo-embolism and infection are of immediate concern but, in persistent cases, the additional issues of hyperlipidaemia and loss of bone density also require consideration for therapy. Thus, in addition to specific attempts to reduce proteinuria, it is recommended that high-risk nephrotic patients receive anticoagulation, pneumococcal vaccination and lipid lowering therapy. Strategies for the preservation of bone density should also be considered, particularly in patients who receive high-dose corticosteroids. Among a range of non-specific treatments for proteinuria, angiotensin-converting enzyme inhibitors appear best in terms of efficacy and safety. Prospective trials are required to clarify the longitudinal impact of these generic strategies on the protection of the persistently nephrotic patient.
引用
收藏
页码:45 / 50
页数:6
相关论文
共 21 条
[1]  
BELLOMO R, 1993, NEPHRON, V63, P240
[2]   EXTRARENAL COMPLICATIONS OF THE NEPHROTIC SYNDROME [J].
BERNARD, DB ;
CANZANELLO, VJ ;
PERRONE, RD ;
MADAIO, MP ;
KASSIRER, JP ;
MADIAS, NE ;
SISKIND, M ;
SALANT, D ;
LEVEY, AS .
KIDNEY INTERNATIONAL, 1988, 33 (06) :1184-1202
[3]  
BERNARD DB, 1982, NEPHROTIC SYNDROME, P85
[4]   EFFECT OF VEGETARIAN SOY DIET ON HYPERLIPEMIA IN NEPHROTIC SYNDROME [J].
DAMICO, G ;
GENTILE, MG ;
MANNA, G ;
FELLIN, G ;
CICERI, R ;
COFANO, F ;
PETRINI, C ;
LAVARDA, F ;
PEROLINI, S ;
PORRINI, M .
LANCET, 1992, 339 (8802) :1131-1134
[5]   Nephrotic syndrome: Don't forget the bones! [J].
Elder, Grahame J. .
NEPHROLOGY, 2008, 13 (01) :43-44
[6]  
Fuchshuber A, 1996, NEPHROL DIAL TRANSPL, V11, P468
[7]  
GANSEVOORT RT, 1995, NEPHROL DIAL TRANSPL, V10, P1963
[8]   DISSOCIATION BETWEEN THE COURSE OF THE HEMODYNAMIC AND ANTIPROTEINURIC EFFECTS OF ANGIOTENSIN-I CONVERTING-ENZYME INHIBITION [J].
GANSEVOORT, RT ;
DEZEEUW, D ;
DEJONG, PE .
KIDNEY INTERNATIONAL, 1993, 44 (03) :579-584
[9]   SERUM IMMUNOGLOBULINS IN NEPHROTIC SYNDROME - POSSIBLE CAUSE OF MINIMAL-CHANGE NEPHROTIC SYNDROME [J].
GIANGIACOMO, J ;
CLEARY, TG ;
COLE, BR ;
HOFFSTEN, P ;
ROBSON, AM .
NEW ENGLAND JOURNAL OF MEDICINE, 1975, 293 (01) :8-12
[10]   Are children with idiopathic nephrotic syndrome at risk for metabolic bone disease? [J].
Gulati, S ;
Godbole, M ;
Singh, U ;
Gulati, K ;
Srivastava, A .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2003, 41 (06) :1163-1169