The value of post-biopsy ultrasound in predicting complications after percutaneous renal biopsy of native kidneys

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Abstract

Background. Clinically significant bleeding complications occur in >30 of patients undergoing percutaneous renal biopsy (PRB) of native kidneys and can be severe in up to 10 of patients. A noninvasive measure that would reliably predict which patients will do well with an uncomplicated post-biopsy course or which patients may be at risk of developing a clinically significant complication is in great demand.Methods. PRB of native kidneys was performed in 162 adult patients from February 2002 through February 2007 using real-time ultrasound and automated needle. Renal ultrasound (US) was performed at 1-h post-PRB to assess biopsy-related bleeding. Patients were observed for 24 h post-PRB to monitor clinically apparent biopsy-related complications. The value of the post-biopsy ultrasound in predicting complications was assessed.Results. A clinically apparent complication was observed in 26 (16) patients post-PRB (13 minor not requiring any intervention and 13 major requiring intervention). In patients with complicated courses, a haematoma at 1 h was seen in 77 (69 with minor and 87 with major complications). However, only 27 (20) of 136 patients without complications (P<0.0001) had a haematoma at 1 h. The presence of a haematoma 1-h post-PRB had a sensitivity of 77, specificity of 80, positive predictive value of 43 but a negative predictive value of 95 for predicting clinical complications.Conclusions. We find that with the use of renal ultrasound 1-h post-PRB, the absence of perinephric bleeding is predictive of an uncomplicated course while the presence of a perinephric haematoma is not reliably predictive of a clinically significant complication post-renal biopsy.

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Waldo, B., Korbet, S. M., Freimanis, M. G., & Lewis, E. J. (2009). The value of post-biopsy ultrasound in predicting complications after percutaneous renal biopsy of native kidneys. Nephrology Dialysis Transplantation, 24(8), 2433–2439. https://doi.org/10.1093/ndt/gfp073

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