The non-immunosuppressive management of childhood nephrotic syndrome

被引:38
作者
McCaffrey, James [1 ,2 ]
Lennon, Rachel [1 ,2 ]
Webb, Nicholas J. A. [1 ,2 ]
机构
[1] Cent Manchester Univ Hosp NHS Fdn Trust, Royal Manchester Childrens Hosp, Dept Paediat Nephrol, Manchester Acad Hlth Sci Ctr, Oxford Rd, Manchester M13 9WL, Lancs, England
[2] Univ Manchester, Inst Human Dev, Fac Med & Human Sci, Manchester, Lancs, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
Idiopathic nephrotic syndrome; Infection; Vaccination; Oedema; Thrombosis; Dyslipidaemia; FOCAL SEGMENTAL GLOMERULOSCLEROSIS; PNEUMOCOCCAL CONJUGATE VACCINE; ZOSTER IMMUNE GLOBULIN; MINIMAL CHANGE DISEASE; RENAL-VEIN THROMBOSIS; BONE-MINERAL DENSITY; LONG-TERM; THROMBOEMBOLIC COMPLICATIONS; STEROID-RESISTANT; RISK-FACTORS;
D O I
10.1007/s00467-015-3241-0
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Idiopathic nephrotic syndrome (INS) is one of the most common renal diseases found in the paediatric population and is associated with significant complications, including infection and thrombosis. A high proportion of children enter sustained remission before adulthood, and therapy must therefore mitigate the childhood complications, while minimising the long-term risk to health. Here we address the main complications of INS and summarise the available evidence and guidance to aid the clinician in determining the appropriate treatment for children with INS under their care. Additionally, we highlight areas where no consensus regarding appropriate management has been reached. In this review, we detail the reasons why routine prophylactic antimicrobial and antithrombotic therapy are not warranted in INS and emphasise the conservative management of oedema. When pharmacological intervention is required for the treatment of oedema, we provide guidance to aid the clinician in determining the appropriate therapy. Additionally, we discuss obesity and growth, fracture risk, dyslipidaemia and thyroid dysfunction associated with INS. Where appropriate, we describe how recent developments in research have identified potential novel therapeutic targets.
引用
收藏
页码:1383 / 1402
页数:20
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