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Direct costs of carcinoid syndrome diarrhea among adults in the United States

BACKGROUND: The burden of carcinoid syndrome (CS) among patients with neuroendocrine tumors is substantial and has been shown to result in increased healthcare resource use and costs. The incremental burden of CS diarrhea (CSD) is less well understood, particularly among working age adults who make...

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Autores principales: Dasari, Arvind, Joish, Vijay N, Perez-Olle, Raul, Dharba, Samyukta, Balaji, Kavitha, Halperin, Daniel M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6931008/
https://www.ncbi.nlm.nih.gov/pubmed/31885426
http://dx.doi.org/10.3748/wjg.v25.i47.6857
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author Dasari, Arvind
Joish, Vijay N
Perez-Olle, Raul
Dharba, Samyukta
Balaji, Kavitha
Halperin, Daniel M
author_facet Dasari, Arvind
Joish, Vijay N
Perez-Olle, Raul
Dharba, Samyukta
Balaji, Kavitha
Halperin, Daniel M
author_sort Dasari, Arvind
collection PubMed
description BACKGROUND: The burden of carcinoid syndrome (CS) among patients with neuroendocrine tumors is substantial and has been shown to result in increased healthcare resource use and costs. The incremental burden of CS diarrhea (CSD) is less well understood, particularly among working age adults who make up a large proportion of the population of patients with CS. AIM: To estimate the direct medical costs of CSD to a self-insured employer in the United States. METHODS: CS patients with and without CSD were identified in the IBM(®) MarketScan(®) Database, including the Medicare Supplemental Coordination of Benefits database. Eligible patients had ≥ 1 medical claim for CS with continuous health plan enrollment for ≥ 12 mo prior to their first CS diagnosis and for ≥ 30 d after, no claims for acromegaly, and no clinical trial participation during the study period (2014-2016). Baseline demographic and clinical characteristics, including comorbidities and treatment, were analyzed using descriptive statistics. Measures of healthcare resource use and costs were compared between patients with and without CSD, including Emergency Department (ED) visits, hospital admissions and length of stay, physician office visits, outpatient services, and prescription claims, using univariate and multivariate analyses to evaluate associations of CSD with healthcare resource use and costs, controlling for baseline characteristics. RESULTS: Overall, 6855 patients with CS were identified of which 4,043 were eligible for the analysis (1352 with CSD, 2691 with CS only). Baseline demographic and clinical characteristics were similar between groups with the exception of age, underlying tumor type, and health insurance plan. Patients with CSD were older, had more comorbidities, and received more somatostatin analog therapy at baseline. Patients with CSD required greater use of healthcare resources and incurred higher costs than their peers without CSD, including hospitalizations (44% vs 25%) and ED visits (55% vs 31%). The total adjusted annual healthcare costs per patient were 50% higher (+ $23865) among those with CSD, driven by outpatient services (+ 56%), prescriptions (+ 48%), ED visits (+ 26%), physician office visits (+ 21%), and hospital admissions (+ 11%). CONCLUSION: The economic burden of CSD is greater than that of CS alone among insured working age adults in the United States, which may benefit from timely diagnosis and management.
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spelling pubmed-69310082019-12-27 Direct costs of carcinoid syndrome diarrhea among adults in the United States Dasari, Arvind Joish, Vijay N Perez-Olle, Raul Dharba, Samyukta Balaji, Kavitha Halperin, Daniel M World J Gastroenterol Observational Study BACKGROUND: The burden of carcinoid syndrome (CS) among patients with neuroendocrine tumors is substantial and has been shown to result in increased healthcare resource use and costs. The incremental burden of CS diarrhea (CSD) is less well understood, particularly among working age adults who make up a large proportion of the population of patients with CS. AIM: To estimate the direct medical costs of CSD to a self-insured employer in the United States. METHODS: CS patients with and without CSD were identified in the IBM(®) MarketScan(®) Database, including the Medicare Supplemental Coordination of Benefits database. Eligible patients had ≥ 1 medical claim for CS with continuous health plan enrollment for ≥ 12 mo prior to their first CS diagnosis and for ≥ 30 d after, no claims for acromegaly, and no clinical trial participation during the study period (2014-2016). Baseline demographic and clinical characteristics, including comorbidities and treatment, were analyzed using descriptive statistics. Measures of healthcare resource use and costs were compared between patients with and without CSD, including Emergency Department (ED) visits, hospital admissions and length of stay, physician office visits, outpatient services, and prescription claims, using univariate and multivariate analyses to evaluate associations of CSD with healthcare resource use and costs, controlling for baseline characteristics. RESULTS: Overall, 6855 patients with CS were identified of which 4,043 were eligible for the analysis (1352 with CSD, 2691 with CS only). Baseline demographic and clinical characteristics were similar between groups with the exception of age, underlying tumor type, and health insurance plan. Patients with CSD were older, had more comorbidities, and received more somatostatin analog therapy at baseline. Patients with CSD required greater use of healthcare resources and incurred higher costs than their peers without CSD, including hospitalizations (44% vs 25%) and ED visits (55% vs 31%). The total adjusted annual healthcare costs per patient were 50% higher (+ $23865) among those with CSD, driven by outpatient services (+ 56%), prescriptions (+ 48%), ED visits (+ 26%), physician office visits (+ 21%), and hospital admissions (+ 11%). CONCLUSION: The economic burden of CSD is greater than that of CS alone among insured working age adults in the United States, which may benefit from timely diagnosis and management. Baishideng Publishing Group Inc 2019-12-21 2019-12-21 /pmc/articles/PMC6931008/ /pubmed/31885426 http://dx.doi.org/10.3748/wjg.v25.i47.6857 Text en ©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Observational Study
Dasari, Arvind
Joish, Vijay N
Perez-Olle, Raul
Dharba, Samyukta
Balaji, Kavitha
Halperin, Daniel M
Direct costs of carcinoid syndrome diarrhea among adults in the United States
title Direct costs of carcinoid syndrome diarrhea among adults in the United States
title_full Direct costs of carcinoid syndrome diarrhea among adults in the United States
title_fullStr Direct costs of carcinoid syndrome diarrhea among adults in the United States
title_full_unstemmed Direct costs of carcinoid syndrome diarrhea among adults in the United States
title_short Direct costs of carcinoid syndrome diarrhea among adults in the United States
title_sort direct costs of carcinoid syndrome diarrhea among adults in the united states
topic Observational Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6931008/
https://www.ncbi.nlm.nih.gov/pubmed/31885426
http://dx.doi.org/10.3748/wjg.v25.i47.6857
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