Management of proteinuria in the transplanted patient
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem, přehledy
- MeSH
- antagonisté receptorů pro angiotenzin terapeutické užití MeSH
- antihypertenziva terapeutické užití MeSH
- časové faktory MeSH
- chronické selhání ledvin diagnóza etiologie chirurgie MeSH
- fokálně segmentální glomeruloskleróza komplikace diagnóza MeSH
- hypertenze komplikace diagnóza farmakoterapie MeSH
- imunosupresiva škodlivé účinky MeSH
- inhibitory ACE terapeutické užití MeSH
- lidé MeSH
- přežívání štěpu MeSH
- proteinurie diagnóza etiologie patofyziologie terapie MeSH
- recidiva MeSH
- rejekce štěpu diagnóza etiologie terapie MeSH
- renin-angiotensin systém účinky léků MeSH
- rizikové faktory MeSH
- TOR serin-threoninkinasy antagonisté a inhibitory MeSH
- transplantace ledvin škodlivé účinky MeSH
- věkové faktory MeSH
- výsledek terapie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- přehledy MeSH
- Názvy látek
- antagonisté receptorů pro angiotenzin MeSH
- antihypertenziva MeSH
- imunosupresiva MeSH
- inhibitory ACE MeSH
- MTOR protein, human MeSH Prohlížeč
- TOR serin-threoninkinasy MeSH
Proteinuria is a relatively frequent complication in children after renal transplantation (40-80 %). It is usually mild and non-nephrotic in nature and predominantly tubular in origin. The major causes of post-transplant proteinuria are recurrence of primary glomerulonephritis [mostly focal segmental glomerulosclerosis (FSGS)], rejection (acute and chronic), mTOR inhibitors or hypertension. Proteinuria is a risk factor for graft loss and patient death in adults, and even a mild proteinuria (0.1-0.2 g/day) is associated with impaired graft and patient survival. In children, proteinuria seems to be associated with graft but not patient survival. Proteinuria (protein/creatinine ratio) should be assessed regularly in all children. In children with prior chronic kidney disease due to idiopathic FSGS, proteinuria should be assessed daily during the first month after transplantation to enable early diagnosis of recurrence. The cause of proteinuria should be identified, and graft biopsy should be considered in children with unexplained proteinuria, especially with new onset proteinuria or deterioration of previously mild proteinuria. Treatment must be primarily targeted at the cause of proteinuria, and in normotensive children symptomatic antiproteinuric therapy with angiotensin-converting enzyme inhibitors/angiotensin II receptor antagonists should also be initiated. Other antihypertensive drugs should be used to achieve target blood pressure of <75th percentile. Target proteinuria should be <20 mg/mmol creatinine.
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