TY - JOUR
T1 - Risk management of renal biopsy: 1387 cases over 30 years in a single centre
AU - STRATTA, Piero
AU - Canavese, C
AU - Marengo, M
AU - Mesiano, P
AU - Besso, L
AU - QUAGLIA, Marco
AU - Bergamo, D
AU - MONGA, Guido
AU - Mazzucco, G
AU - Ciccone, G.
PY - 2007
Y1 - 2007
N2 - Background
Although renal biopsy is largely employed, even in old patients with systemic
diseases, few clinical studies have addressed its risk management. We aimed to obtain a
comprehensive assessment of safety/utility ratio of percutaneous renal biopsy.
Patients and methods
Retrospective review of all the 1387 patients who consecutively
underwent renal biopsy in a single centre over three decades (1973–2002) was made, with
calculation of complications, multivariate logistical analyses to evaluate risk factors of
complications, and rate of alteration of clinical hypotheses by pathological diagnosis.
Results
There were no deaths and five major complications, (0·36%). One nephrectomy
(0·07%), two surgical revisions (0·1%) and two arterial-venous fistulae (0·1%). There were
also 337 minor bleeding complications (24·2%) (16·4% gross haematuria and 7·8% clinically
relevant haematomas needing at least prolonged bed rest). Multivariate analyses
demonstrated that the risk for complications was significantly increased by systemic
autoimmune diseases with odds ratio (OR) 2·06, 95% confidence interval (CI)
=
1·40–3·01,
end-stage kidney/acute-tubular necrosis (OR 2·96, 95% CI
=
1·19–7·30), and prolonged
bleeding time test (BTT) (OR 1·87, 95% CI
=
1·17–2·83). Among the 1288 cases in which
a clinical hypothesis before renal biopsy was recorded, renal pathology changed previous
diagnoses in 423/1,288 (32·8%) of cases.
Conclusions
Risk assessment demonstrates that renal biopsy is a useful procedure with a
low incidence of serious complications. Platelet function is the only modifiable factor
significantly related to bleeding complications, suggesting the need for a more standardized
alternative to the BTT. Platelet function should be evaluated to select low-risk patients for
renal biopsy as ‘a day case procedure’, in order to build adequate risk management strategies.
AB - Background
Although renal biopsy is largely employed, even in old patients with systemic
diseases, few clinical studies have addressed its risk management. We aimed to obtain a
comprehensive assessment of safety/utility ratio of percutaneous renal biopsy.
Patients and methods
Retrospective review of all the 1387 patients who consecutively
underwent renal biopsy in a single centre over three decades (1973–2002) was made, with
calculation of complications, multivariate logistical analyses to evaluate risk factors of
complications, and rate of alteration of clinical hypotheses by pathological diagnosis.
Results
There were no deaths and five major complications, (0·36%). One nephrectomy
(0·07%), two surgical revisions (0·1%) and two arterial-venous fistulae (0·1%). There were
also 337 minor bleeding complications (24·2%) (16·4% gross haematuria and 7·8% clinically
relevant haematomas needing at least prolonged bed rest). Multivariate analyses
demonstrated that the risk for complications was significantly increased by systemic
autoimmune diseases with odds ratio (OR) 2·06, 95% confidence interval (CI)
=
1·40–3·01,
end-stage kidney/acute-tubular necrosis (OR 2·96, 95% CI
=
1·19–7·30), and prolonged
bleeding time test (BTT) (OR 1·87, 95% CI
=
1·17–2·83). Among the 1288 cases in which
a clinical hypothesis before renal biopsy was recorded, renal pathology changed previous
diagnoses in 423/1,288 (32·8%) of cases.
Conclusions
Risk assessment demonstrates that renal biopsy is a useful procedure with a
low incidence of serious complications. Platelet function is the only modifiable factor
significantly related to bleeding complications, suggesting the need for a more standardized
alternative to the BTT. Platelet function should be evaluated to select low-risk patients for
renal biopsy as ‘a day case procedure’, in order to build adequate risk management strategies.
UR - https://iris.uniupo.it/handle/11579/29899
M3 - Article
SN - 0014-2972
VL - 37
SP - 954
EP - 963
JO - European Journal of Clinical Investigation
JF - European Journal of Clinical Investigation
IS - 12
ER -