Abstract: SA-PO1094
Accuracy of Nephrologist in Identifying Kidney Disorders Prior to Kidney Biopsy
Session Information
- Pathology and Lab Medicine: Clinical
October 27, 2018 | Location: Exhibit Hall, San Diego Convention Center
Abstract Time: 10:00 AM - 12:00 PM
Category: Pathology and Lab Medicine
- 1502 Pathology and Lab Medicine: Clinical
Authors
- Bapat, Manasi, Icahn School of Medicine, Mount Sinai Hospital, NY, New York, New York, United States
- Martin, Timothy Charles, Albany Medical Center, Albany, New York, United States
- Kattamanchi, Siddhartha, Mount Sinai Medical Center, New Rochelle, New York, United States
- Tokita, Joji E., Mount Sinai School of Medicine, New York, New York, United States
- Sharma, Shuchita, Icahn School of Medicine, Mount Sinai Hospital, NY, New York, New York, United States
- Nadkarni, Girish N., Ichan School of Medicine, New York, New York, United States
- Coca, Steven G., Icahn School of Medicine at Mount Sinai, New York, New York, United States
- Mehta, Swati, Icahn school of medicine at Mount Sinai, Rensselaer, New York, United States
- Chan, Lili, Icahn School of Medicine, Mount Sinai Hospital, NY, New York, New York, United States
Background
New biomarkers have been developed for identification of kidney diseases; however the kidney biopsies remain the gold standard in diagnosis and management. Our aim was to determine the ability of nephrologist to accurately identify etiology of kidney dysfunction prior to a biopsy.
Methods
This is a retrospective cohort study of 251 patients who underwent a native kidney biopsy at Mount Sinai Hospital (MSH) and Albany Medical Center (AMC) from 2013 - 2017. Clinical indication and nephrologist diagnosis was determined by review of pre-biopsy provider notes while final diagnoses were determined by review of biopsy pathology reports.
Results
There were 251 patients who underwent kidney biopsy; mean age was 51 ± 16 years, 52% were male, 50% were inpatient, and 60% were done under ultrasound guidance. The most frequent indication for biopsy was non-nephrotic range proteinuria, 83 (33.2%) and acute kidney injury, 79 (32%). We were able to identify the nephrologist pre-biopsy diagnosis in only 93 patients. The most frequent diagnoses were diabetic nephropathy (20%), ANCA vasculitis (12%), and membranous nephropathy (8%). The post-biopsy diagnosis matched 45% of the time; the highest concordance was seen in diabetic nephropathy (32/39) and IgA nephropathy (10/11) while the lowest concordance seen in ANCA (6/21), FSGS (2/12), and minimal change (2/7). There was no consistent alternative diagnosis in the lowest concordance groups; patients who were biopsied with a presumptive diagnosis of ANCA were found to have diabetic nephropathy, HSP, and MPGN among others on pathology.
Conclusion
Nephrologists were able to accurately identify underlying etiologies nearly half the time in patients who were referred for biopsy. Given the relative safety of kidney biopsies, we should have a low threshold to refer patients for kidney biopsies.
Funding
- NIDDK Support