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Inter-hospital variation in the utilization of diagnostics and their proportionality in the management of adult community-acquired pneumonia
BACKGROUND: Utilization of diagnostics and biomarkers are the second largest cost drivers in the management of patients hospitalized with community-acquired pneumonia (CAP). The present study aimed to systematically assess the inter-hospital variation in these cost drivers in relation to antibiotic...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305565/ https://www.ncbi.nlm.nih.gov/pubmed/30603378 http://dx.doi.org/10.1186/s41479-018-0059-0 |
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author | Vestjens, Stefan M. T. Wittermans, Esther Spoorenberg, Simone M. C. Grutters, Jan C. van Ruitenbeek, Charlotte A. Voorn, G. Paul Bos, Willem Jan W. van de Garde, Ewoudt M. W. |
author_facet | Vestjens, Stefan M. T. Wittermans, Esther Spoorenberg, Simone M. C. Grutters, Jan C. van Ruitenbeek, Charlotte A. Voorn, G. Paul Bos, Willem Jan W. van de Garde, Ewoudt M. W. |
author_sort | Vestjens, Stefan M. T. |
collection | PubMed |
description | BACKGROUND: Utilization of diagnostics and biomarkers are the second largest cost drivers in the management of patients hospitalized with community-acquired pneumonia (CAP). The present study aimed to systematically assess the inter-hospital variation in these cost drivers in relation to antibiotic use in CAP. METHODS: Detailed resource utilization data from 300 patients who participated in a multicenter placebo-controlled trial investigating dexamethasone as adjunctive treatment for community-acquired pneumonia was grouped into 3 categories: clinical chemistry testing, radiological exams, and microbiological testing. Based on the identified top 5 items per category, average costs were calculated per category and per hospital. Antibiotic de-escalation at day 3 and secondary ICU admission were assessed as outcomes for proportionality of diagnostics use. RESULTS: The mean costs for diagnostics varied between hospitals from 350 (SD 31) to 841 (SD 37) euro per patient (p < 0.001). This difference was primarily explained by variation in costs for microbiological testing (mean 195 vs. 726 euro per patient, p < 0.001). There was no difference in number of secondary ICU admissions but there was an inverse association between the costs of microbiological testing and level of antibiotic de-escalation. De-escalation occurred most frequently in the hospital with the lowest cost for microbiological testing (48% vs. 30%; p = 0.018). The latter hospital had an automated physician alert system in place to consider a timely iv-to-oral switch of antibiotics. CONCLUSIONS: Large inter-hospital variation exists in resource utilization, mainly in microbiological diagnostics in the management of adult patients with community-acquired pneumonia. A counterintuitive inverse association between the magnitude of these costs and the amount of antibiotic de-escalation was found. Future studies about the optimal cost-effective set of microbiological testing for antimicrobial stewardship in pneumonia patients should acknowledge the interaction between testing, way of communication of results and triggered physician alert systems. TRIAL REGISTRATION: ClinicalTrials.gov NCT01743755. |
format | Online Article Text |
id | pubmed-6305565 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63055652019-01-02 Inter-hospital variation in the utilization of diagnostics and their proportionality in the management of adult community-acquired pneumonia Vestjens, Stefan M. T. Wittermans, Esther Spoorenberg, Simone M. C. Grutters, Jan C. van Ruitenbeek, Charlotte A. Voorn, G. Paul Bos, Willem Jan W. van de Garde, Ewoudt M. W. Pneumonia (Nathan) Brief Report BACKGROUND: Utilization of diagnostics and biomarkers are the second largest cost drivers in the management of patients hospitalized with community-acquired pneumonia (CAP). The present study aimed to systematically assess the inter-hospital variation in these cost drivers in relation to antibiotic use in CAP. METHODS: Detailed resource utilization data from 300 patients who participated in a multicenter placebo-controlled trial investigating dexamethasone as adjunctive treatment for community-acquired pneumonia was grouped into 3 categories: clinical chemistry testing, radiological exams, and microbiological testing. Based on the identified top 5 items per category, average costs were calculated per category and per hospital. Antibiotic de-escalation at day 3 and secondary ICU admission were assessed as outcomes for proportionality of diagnostics use. RESULTS: The mean costs for diagnostics varied between hospitals from 350 (SD 31) to 841 (SD 37) euro per patient (p < 0.001). This difference was primarily explained by variation in costs for microbiological testing (mean 195 vs. 726 euro per patient, p < 0.001). There was no difference in number of secondary ICU admissions but there was an inverse association between the costs of microbiological testing and level of antibiotic de-escalation. De-escalation occurred most frequently in the hospital with the lowest cost for microbiological testing (48% vs. 30%; p = 0.018). The latter hospital had an automated physician alert system in place to consider a timely iv-to-oral switch of antibiotics. CONCLUSIONS: Large inter-hospital variation exists in resource utilization, mainly in microbiological diagnostics in the management of adult patients with community-acquired pneumonia. A counterintuitive inverse association between the magnitude of these costs and the amount of antibiotic de-escalation was found. Future studies about the optimal cost-effective set of microbiological testing for antimicrobial stewardship in pneumonia patients should acknowledge the interaction between testing, way of communication of results and triggered physician alert systems. TRIAL REGISTRATION: ClinicalTrials.gov NCT01743755. BioMed Central 2018-12-25 /pmc/articles/PMC6305565/ /pubmed/30603378 http://dx.doi.org/10.1186/s41479-018-0059-0 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Brief Report Vestjens, Stefan M. T. Wittermans, Esther Spoorenberg, Simone M. C. Grutters, Jan C. van Ruitenbeek, Charlotte A. Voorn, G. Paul Bos, Willem Jan W. van de Garde, Ewoudt M. W. Inter-hospital variation in the utilization of diagnostics and their proportionality in the management of adult community-acquired pneumonia |
title | Inter-hospital variation in the utilization of diagnostics and their proportionality in the management of adult community-acquired pneumonia |
title_full | Inter-hospital variation in the utilization of diagnostics and their proportionality in the management of adult community-acquired pneumonia |
title_fullStr | Inter-hospital variation in the utilization of diagnostics and their proportionality in the management of adult community-acquired pneumonia |
title_full_unstemmed | Inter-hospital variation in the utilization of diagnostics and their proportionality in the management of adult community-acquired pneumonia |
title_short | Inter-hospital variation in the utilization of diagnostics and their proportionality in the management of adult community-acquired pneumonia |
title_sort | inter-hospital variation in the utilization of diagnostics and their proportionality in the management of adult community-acquired pneumonia |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305565/ https://www.ncbi.nlm.nih.gov/pubmed/30603378 http://dx.doi.org/10.1186/s41479-018-0059-0 |
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