KIDNEY BIOPSIES RECORD OF 12 YEARS OF FOLLOW-UP. REPORT AND ANALYSIS OF RELATED-COMPLICATIONS FROM A CENTER IN ARGENTINA.

https://storage.unitedwebnetwork.com/files/1099/35ade025c5f105757a54c3b762168258.pdf
KIDNEY BIOPSIES RECORD OF 12 YEARS OF FOLLOW-UP. REPORT AND ANALYSIS OF RELATED-COMPLICATIONS FROM A CENTER IN ARGENTINA.
Paulo
Gomez
Rafael Alberto Maldonado ramaldonado@gmail.com Clinica Privada Velez Sarsfield Nefrologia Cordoba
Daniela Porta danielajosefinaporta@gmail.com Clinica Privada Velez Sarsfield Nefrologia Cordoba
Luis Miguel Silvera argentina.madryn@gmail.com Clinica Privada Velez Sarsfield Nefrologia Cordoba
Rocio Escobar ro.esc12@gmail.com Clinica Privada Velez Sarsfield Nefrologia Cordoba
Carlos Idoria cidoria@gmail.com Clinica Privada Velez Sarsfield Nefrologia Cordoba
Maria Emilia Garcia Chiple emiliachiple@gmail.com Clinica Privada Velez Sarsfield Anatomia Patologica Cordoba
Eliana Mariel Pedraza empedraza@gmail.com Clinica Privada Velez Sarsfield Nefrologia Cordoba
Gabriela Sambuelli gabysamb@hotmail.com Clinica Universitaria Reina Fabiola Anatomia Patologica Cordoba
Maria Paula Dionisi dmaripau@gmail.com Clinica Privada Velez Sarsfield Nefrologia Cordoba
 
 
 
 
 
 

In terms of epidemiology, kidney biopsy is a key factor for the clinicopathological correlation of glomerular diseases. Accurate diagnosis is essential because of treatment election, and therefore contributes to the reduction of the incidence of end stage kidney disease.

Our objective was to study the epidemiological characteristics of 12 years of native kidney biopsy by indication in our center, as well as complications related to the procedure and predisposing factors.

Data were collected from renal biopsies (RB) performed retrospectively from March 31, 2011 to September 3, 2023.

Inclusion criteria: patients over 15 years. Exclusion criteria: kidney transplant patients.

Demographic, clinical, and outcome data were recorded in the RB cohort.

A descriptive analysis of the studied population was carried out, then an inferential analysis (Fisher test) of RB complications was performed to evaluate the association between the categorical variables and T- test study for continuous variables. The value of p ≤ 0.05 was assumed to be significant.

 

A descriptive analysis was carried out on the sample composed of 215 patients attending at the Nephrology division of Clinica Privada Vélez Sarsfield, Córdoba, Argentina (see table 1). The most frecuent GN were primary (47%), then  secondary GN (35.3%); the remaining unclassified  (17.7%). The frequency of different forms of biopsy-proven pathological diagnoses found are sumarized in table 2.


When analyzing complications, most of the patients undergoing renal biopsy did not present complications (89.8%), while the presence of hematoma was the most frequent (7.4%) and, in some cases, the presence of hematuria was also observed(2.8 %).

Only the variable higher albumin mean values and history of systemic lupus erythematosus (SLE) were significantly associaated with complications (p= 0.006 and p= 0.01 respectively).


VariableN
Total (%)215100
Sex (women, %)11051
Age (years, Mean ± SD)4344 ± 17
Recidence
     Córdoba (%)17280
     Other (%)4320
 Cliinical characteristics
Asymptomatic urinary
abnormalities(%)
 13  
6,2
AKI (%)
5023.3
CKD (%)83.7
Hematuria (%)157
Nephrotic proteinuria (%)9242.8
Nephritic syndrome (%) 104.7
HTN (%)8941.4
Edema (%)9041.9
Creatininemia(mg/dL), 
(Mean ± SD)
 1862.0 ± 2.0
FG (MDRD-IDMS)18654.2 ± 23.8
Proteinuria (gr/dL) , 
(Media ± DE)
1374.8 ± 12.4
Albuminemia (mg/dL),
 (Media ± DE)
742.9 ± 0.9
Complications (%)
2210.2
Hematoma(%)   
167.4
Hematuria(%)
62.8

 Table 1 – Demographic characteristics of general population.



DIAGNOSIS 
 N
%
SLE43
19
MGN
2913.4
unclassified  
2913.4
IGAN
28
13
MPGN
19
8.8
FSGS
15
6.9
RPGN94.2
ATIN
6
2.8
MCD
4
2.8
Sclerosing GN
41.8
ATN
31.4
AN20.9
DIABETES
20.9
TMA
20.9
OTHER188.4

Table 2 - The frequency of different forms of biopsy-proven pathological diagnoses (n = 215). SLE: systemic lupus erythematosus,  MGN membranous nephropathy, MPGN membranoproliferative glomerulonephritis syndrome, IgAN: IgA mesangioproliferative glomerulonephritis, RPGN rapidly progressive glomerulonephritis syndrome, ATIN: acute tubulointerstitial nephritis,MCD minimal change disease, ATN: acute tubular necrosis, AN: amiloyd nephropathy, TMA: thrombotic microangiopathy.


In this 12-year epidemiological study, the follow-up of complications observed were scarce, but significantly associated to higher mean serum albumin level and history of SLE of the population studied. This results could help to further define populations at risk for excessive bleeding.

There is a need for a Biopsy Registry in the region, and therefore this analysis also contributes to the knowledge of this worrisome epidemiological situation.

E-Poster Format Requirements
  • PDF file
  • Layout: Portrait (vertical orientation)
  • One page only (Dim A4: 210 x 297mm or PPT)
  • E-Poster can be prepared in PowerPoint (one (1) PowerPoint slide) but must be saved and submitted as PDF file.
  • File Size: Maximum file size is 2 Megabytes (2 MB)
  • No hyperlinks, animated images, animations, and slide transitions
  • Language: English
  • Include your abstract number
  • E-posters can include QR codes, tables and photos