Proteinuria with preserved eGFR (>60 mL/min) |
- Rule out glomerulonephritis, especially in the presence of high-grade proteinuria (>1 g/24 h) or concomitant hematuria.
- Collect 24-hour urine to determine proximal tubular dysfunction
- Consider with a nephrologist the indication of a renal biopsy.
- Consider angiotensin-converting enzyme inhibitors to decrease proteinuria.
|
Progressive tubular dysfunction |
|
Progressive eGFR decline |
- Evaluate and treat risk factors.
- Investigate the use of nephrotoxic agents.
- Collect 24-hour urine to determine proximal tubular dysfunction.
- Consider tenofovir discontinuation.
|
Chronic kidney disease with eGFR <60 mL/min |
- Consider TDF discontinuation (especially if coadministered with boosted PI).
- Adjust NRTI dose (required for all with the exception of abacavir) or maraviroc. No dose adjustment is necessary for NNRTI, PI, or integrase inhibitors).
|
End-stage kidney disease (eGFR <10 mL/min or dialysis) |
|
Kidney transplant |
- Similar indications than in the general population in ART-treated patients without overt immunosuppression (ie, CD4+ T cells <200/mm3 or AIDS).
- Similar survival rates after transplantation, although some have suggested higher incidence of acute rejection [93, 94].
- Consider switching ART to raltegravir, dolutegravir, and maraviroc-based regimens might be optimal ART choices given the narrow therapeutic index and interactions of most immunosuppressive agents and the need for dose adjustments
|