Systematic Review and Meta-Analysis of Native Kidney Biopsy Complications.


Journal

Clinical journal of the American Society of Nephrology : CJASN
ISSN: 1555-905X
Titre abrégé: Clin J Am Soc Nephrol
Pays: United States
ID NLM: 101271570

Informations de publication

Date de publication:
06 11 2020
Historique:
received: 09 04 2020
accepted: 21 07 2020
pubmed: 17 10 2020
medline: 23 11 2021
entrez: 16 10 2020
Statut: ppublish

Résumé

Native kidney biopsies are commonly performed in the diagnosis of acute kidney diseases and CKD. Because of the invasive nature of the procedure, bleeding-related complications are not uncommon. The National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases-sponsored Kidney Precision Medicine Project requires that all participants undergo a kidney biopsy; therefore, the objective of this analysis was to study complication rates of native kidney biopsies performed using automated devices under kidney imaging. This is a systematic review and meta-analysis of the literature published from January 1983 to March 2018. The initial PubMed search yielded 1139 manuscripts. Using predetermined selection criteria, 87 manuscripts were included in the final analysis. A random effects meta-analysis for proportions was used to obtain combined estimates of complication rates. Freeman-Tukey double-arcsine transformations were used to stabilize variance as complications were rare. A total of 118,064 biopsies were included in this study. Patient age ranged from 30 to 79 years, and 45% of patients were women. On the basis of our meta-analysis, pain at the site of biopsy is estimated to occur in 4.3% of biopsied patients, hematomas are estimated to occur in 11%, macroscopic hematuria is estimated to occur in 3.5%, bleeding requiring blood transfusions is estimated to occur in 1.6%, and interventions to stop bleeding are estimated to occur in only 0.3%. Death attributed to native kidney biopsy was a rare event, occurring only in an estimated 0.06% of all biopsies but only 0.03% of outpatient biopsies. Complication rates were higher in hospitalized patients and in those with acute kidney disease. The reported complications varied on the basis of study type and geographic location. Although the native kidney biopsy is an invasive diagnostic procedure, the rates of bleeding complications are low. Albeit rare, death can occur postbiopsy. Complications are more frequently seen after kidney biopsies of hospitalized patients with AKI.

Sections du résumé

BACKGROUND AND OBJECTIVES
Native kidney biopsies are commonly performed in the diagnosis of acute kidney diseases and CKD. Because of the invasive nature of the procedure, bleeding-related complications are not uncommon. The National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases-sponsored Kidney Precision Medicine Project requires that all participants undergo a kidney biopsy; therefore, the objective of this analysis was to study complication rates of native kidney biopsies performed using automated devices under kidney imaging.
DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS
This is a systematic review and meta-analysis of the literature published from January 1983 to March 2018. The initial PubMed search yielded 1139 manuscripts. Using predetermined selection criteria, 87 manuscripts were included in the final analysis. A random effects meta-analysis for proportions was used to obtain combined estimates of complication rates. Freeman-Tukey double-arcsine transformations were used to stabilize variance as complications were rare.
RESULTS
A total of 118,064 biopsies were included in this study. Patient age ranged from 30 to 79 years, and 45% of patients were women. On the basis of our meta-analysis, pain at the site of biopsy is estimated to occur in 4.3% of biopsied patients, hematomas are estimated to occur in 11%, macroscopic hematuria is estimated to occur in 3.5%, bleeding requiring blood transfusions is estimated to occur in 1.6%, and interventions to stop bleeding are estimated to occur in only 0.3%. Death attributed to native kidney biopsy was a rare event, occurring only in an estimated 0.06% of all biopsies but only 0.03% of outpatient biopsies. Complication rates were higher in hospitalized patients and in those with acute kidney disease. The reported complications varied on the basis of study type and geographic location.
CONCLUSIONS
Although the native kidney biopsy is an invasive diagnostic procedure, the rates of bleeding complications are low. Albeit rare, death can occur postbiopsy. Complications are more frequently seen after kidney biopsies of hospitalized patients with AKI.

Identifiants

pubmed: 33060160
pii: 01277230-202011000-00010
doi: 10.2215/CJN.04710420
pmc: PMC7646247
doi:

Types de publication

Journal Article Meta-Analysis Research Support, N.I.H., Extramural Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1595-1602

Subventions

Organisme : NIDDK NIH HHS
ID : UH3 DK114908
Pays : United States
Organisme : NIDDK NIH HHS
ID : U2C DK114886
Pays : United States
Organisme : NIDDK NIH HHS
ID : UH3 DK114861
Pays : United States
Organisme : NIDDK NIH HHS
ID : UH3 DK114937
Pays : United States
Organisme : NIDDK NIH HHS
ID : UG3 DK114861
Pays : United States
Organisme : NIDDK NIH HHS
ID : UG3 DK114870
Pays : United States
Organisme : NIDDK NIH HHS
ID : U24 DK114886
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : ErratumIn

Informations de copyright

Copyright © 2020 by the American Society of Nephrology.

Références

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Auteurs

Emilio D Poggio (ED)

Department of Nephrology and Hypertension, Glickman Urological and Kidney Institute, Cleveland Clinic, Cleveland, Ohio.

Robyn L McClelland (RL)

Department of Biostatistics, University of Washington, Seattle, Washington.

Kristina N Blank (KN)

Department of Biostatistics, University of Washington, Seattle, Washington.

Spencer Hansen (S)

Department of Biostatistics, University of Washington, Seattle, Washington.

Shweta Bansal (S)

Division of Nephrology, Department of Medicine, University of Texas Health San Antonio, San Antonio, Texas.

Andrew S Bomback (AS)

Division of Nephrology, Department of Medicine, Vagelos College of Physicians & Surgeons, Columbia University, New York, New York.

Pietro A Canetta (PA)

Division of Nephrology, Department of Medicine, Vagelos College of Physicians & Surgeons, Columbia University, New York, New York.

Pascale Khairallah (P)

Division of Nephrology, Department of Medicine, Vagelos College of Physicians & Surgeons, Columbia University, New York, New York.

Krzysztof Kiryluk (K)

Division of Nephrology, Department of Medicine, Vagelos College of Physicians & Surgeons, Columbia University, New York, New York.

Stewart H Lecker (SH)

Division of Nephrology and Department of Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts.

Gearoid M McMahon (GM)

Division of Nephrology, Brigham and Women's Hospital, Boston, Massachusetts.

Paul M Palevsky (PM)

Renal Section, Veterans Affairs Pittsburgh Healthcare System, Pittsburgh, Pennsylvania.
Renal-Electrolyte Division, Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.

Samir Parikh (S)

Division of Nephrology, Ohio State University Wexner Medical Center, Columbus, Ohio.

Sylvia E Rosas (SE)

Kidney and Hypertension Unit, Joslin Diabetes Center, Boston, Massachusetts.
Nephrology Division, Beth Israel Deaconess Medical Center, Boston, Massachusetts.
Harvard Medical School, Boston, Massachusetts.

Katherine Tuttle (K)

Division of Nephrology, Providence Medical Research Center, Sacred Heart Medical Center, Spokane, Washington.

Miguel A Vazquez (MA)

Division of Nephrology, UT Southwestern Medical Center, Dallas, Texas.

Anitha Vijayan (A)

Division of Nephrology, Washington University in St. Louis, St. Louis, Missouri.

Brad H Rovin (BH)

Division of Nephrology, Ohio State University Wexner Medical Center, Columbus, Ohio.

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