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Radiographic Imaging in Autosomal Dominant Polycystic Kidney Disease: A Claims Analysis

BACKGROUND: Progression of autosomal dominant polycystic kidney disease (ADPKD) is highly variable, with some patients progressing rapidly to end-stage renal disease (ESRD). Abdominal imaging is an important modality for verifying diagnosis in patients at risk for rapidly progressing ADPKD, targetin...

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Autores principales: Sanon Aigbogun, Myrlene, Stellhorn, Robert A, Pao, Christina S, Seliger, Stephen L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112873/
https://www.ncbi.nlm.nih.gov/pubmed/33994802
http://dx.doi.org/10.2147/IJNRD.S300331
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author Sanon Aigbogun, Myrlene
Stellhorn, Robert A
Pao, Christina S
Seliger, Stephen L
author_facet Sanon Aigbogun, Myrlene
Stellhorn, Robert A
Pao, Christina S
Seliger, Stephen L
author_sort Sanon Aigbogun, Myrlene
collection PubMed
description BACKGROUND: Progression of autosomal dominant polycystic kidney disease (ADPKD) is highly variable, with some patients progressing rapidly to end-stage renal disease (ESRD). Abdominal imaging is an important modality for verifying diagnosis in patients at risk for rapidly progressing ADPKD, targeting them for early treatment that could slow onset of ESRD. Published literature is limited on the real-world abdominal imaging utilization patterns in ADPKD. METHODS: A retrospective healthcare administrative claims analysis examining abdominal imaging scans occurring from January 1, 2014, through June 30, 2017, was conducted using the IBM MarketScan(®) commercial and Medicare supplemental databases. Patients in the United States who were at least 18 years old and had at least 1 inpatient claim or 2 outpatient claims (with different dates of service) with an ADPKD diagnosis code, as defined by the International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM codes 753.12 [polycystic kidney, unspecified type] and 753.13 [polycystic kidney, autosomal dominant] and/or Tenth Revision (ICD-10-CM codes Q61.2 [polycystic kidney, adult type] and Q61.3 [polycystic kidney, unspecified]) were included. RESULTS: Of the 4637 patients with ADPKD (mean age, 51.2 years [SD = 15.52]), 59% had ≥1 abdominal imaging scan. Of these patients, 46% had ≥1 computed tomography (CT) scan, 25% had ≥1 ultrasound, 10% had ≥1 magnetic resonance imaging scan. Among the 1754 patients (38%) with chronic kidney disease (CKD) stage information, CT imaging was more frequent in later stages (31% stage 1 versus 68% stage 5). The proportion of patients undergoing at least 1 CT or MRI scan increased with disease severity (37% in stage 1, 42% in stage 2, 48% in stage 3, 56% in stage 4, and 71% in stage 5). CONCLUSION: Results of this analysis support the need for further investigation into abdominal imaging utilization in managing patients with ADPKD. Future research could clarify barriers and increase access to imaging, which has the potential to inform risk stratification, help patients delay dialysis or transplantation associated with ESRD, and help health systems avoid the costs associated with ESRD.
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spelling pubmed-81128732021-05-13 Radiographic Imaging in Autosomal Dominant Polycystic Kidney Disease: A Claims Analysis Sanon Aigbogun, Myrlene Stellhorn, Robert A Pao, Christina S Seliger, Stephen L Int J Nephrol Renovasc Dis Original Research BACKGROUND: Progression of autosomal dominant polycystic kidney disease (ADPKD) is highly variable, with some patients progressing rapidly to end-stage renal disease (ESRD). Abdominal imaging is an important modality for verifying diagnosis in patients at risk for rapidly progressing ADPKD, targeting them for early treatment that could slow onset of ESRD. Published literature is limited on the real-world abdominal imaging utilization patterns in ADPKD. METHODS: A retrospective healthcare administrative claims analysis examining abdominal imaging scans occurring from January 1, 2014, through June 30, 2017, was conducted using the IBM MarketScan(®) commercial and Medicare supplemental databases. Patients in the United States who were at least 18 years old and had at least 1 inpatient claim or 2 outpatient claims (with different dates of service) with an ADPKD diagnosis code, as defined by the International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM codes 753.12 [polycystic kidney, unspecified type] and 753.13 [polycystic kidney, autosomal dominant] and/or Tenth Revision (ICD-10-CM codes Q61.2 [polycystic kidney, adult type] and Q61.3 [polycystic kidney, unspecified]) were included. RESULTS: Of the 4637 patients with ADPKD (mean age, 51.2 years [SD = 15.52]), 59% had ≥1 abdominal imaging scan. Of these patients, 46% had ≥1 computed tomography (CT) scan, 25% had ≥1 ultrasound, 10% had ≥1 magnetic resonance imaging scan. Among the 1754 patients (38%) with chronic kidney disease (CKD) stage information, CT imaging was more frequent in later stages (31% stage 1 versus 68% stage 5). The proportion of patients undergoing at least 1 CT or MRI scan increased with disease severity (37% in stage 1, 42% in stage 2, 48% in stage 3, 56% in stage 4, and 71% in stage 5). CONCLUSION: Results of this analysis support the need for further investigation into abdominal imaging utilization in managing patients with ADPKD. Future research could clarify barriers and increase access to imaging, which has the potential to inform risk stratification, help patients delay dialysis or transplantation associated with ESRD, and help health systems avoid the costs associated with ESRD. Dove 2021-05-07 /pmc/articles/PMC8112873/ /pubmed/33994802 http://dx.doi.org/10.2147/IJNRD.S300331 Text en © 2021 Sanon Aigbogun et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Sanon Aigbogun, Myrlene
Stellhorn, Robert A
Pao, Christina S
Seliger, Stephen L
Radiographic Imaging in Autosomal Dominant Polycystic Kidney Disease: A Claims Analysis
title Radiographic Imaging in Autosomal Dominant Polycystic Kidney Disease: A Claims Analysis
title_full Radiographic Imaging in Autosomal Dominant Polycystic Kidney Disease: A Claims Analysis
title_fullStr Radiographic Imaging in Autosomal Dominant Polycystic Kidney Disease: A Claims Analysis
title_full_unstemmed Radiographic Imaging in Autosomal Dominant Polycystic Kidney Disease: A Claims Analysis
title_short Radiographic Imaging in Autosomal Dominant Polycystic Kidney Disease: A Claims Analysis
title_sort radiographic imaging in autosomal dominant polycystic kidney disease: a claims analysis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112873/
https://www.ncbi.nlm.nih.gov/pubmed/33994802
http://dx.doi.org/10.2147/IJNRD.S300331
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