25
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Development, Validation and Deployment of a Real Time 30 Day Hospital Readmission Risk Assessment Tool in the Maine Healthcare Information Exchange

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Objectives

          Identifying patients at risk of a 30-day readmission can help providers design interventions, and provide targeted care to improve clinical effectiveness. This study developed a risk model to predict a 30-day inpatient hospital readmission for patients in Maine, across all payers, all diseases and all demographic groups.

          Methods

          Our objective was to develop a model to determine the risk for inpatient hospital readmission within 30 days post discharge. All patients within the Maine Health Information Exchange (HIE) system were included. The model was retrospectively developed on inpatient encounters between January 1, 2012 to December 31, 2012 from 24 randomly chosen hospitals, and then prospectively validated on inpatient encounters from January 1, 2013 to December 31, 2013 using all HIE patients.

          Results

          A risk assessment tool partitioned the entire HIE population into subgroups that corresponded to probability of hospital readmission as determined by a corresponding positive predictive value (PPV). An overall model c-statistic of 0.72 was achieved. The total 30-day readmission rates in low (score of 0–30), intermediate (score of 30–70) and high (score of 70–100) risk groupings were 8.67%, 24.10% and 74.10%, respectively. A time to event analysis revealed the higher risk groups readmitted to a hospital earlier than the lower risk groups. Six high-risk patient subgroup patterns were revealed through unsupervised clustering. Our model was successfully integrated into the statewide HIE to identify patient readmission risk upon admission and daily during hospitalization or for 30 days subsequently, providing daily risk score updates.

          Conclusions

          The risk model was validated as an effective tool for predicting 30-day readmissions for patients across all payer, disease and demographic groups within the Maine HIE. Exposing the key clinical, demographic and utilization profiles driving each patient’s risk of readmission score may be useful to providers in developing individualized post discharge care plans.

          Related collections

          Most cited references16

          • Record: found
          • Abstract: found
          • Article: not found

          Potentially avoidable 30-day hospital readmissions in medical patients: derivation and validation of a prediction model.

          Because effective interventions to reduce hospital readmissions are often expensive to implement, a score to predict potentially avoidable readmissions may help target the patients most likely to benefit. To derive and internally validate a prediction model for potentially avoidable 30-day hospital readmissions in medical patients using administrative and clinical data readily available prior to discharge. Retrospective cohort study. Academic medical center in Boston, Massachusetts. All patient discharges from any medical services between July 1, 2009, and June 30, 2010. Potentially avoidable 30-day readmissions to 3 hospitals of the Partners HealthCare network were identified using a validated computerized algorithm based on administrative data (SQLape). A simple score was developed using multivariable logistic regression, with two-thirds of the sample randomly selected as the derivation cohort and one-third as the validation cohort. Among 10 731 eligible discharges, 2398 discharges (22.3%) were followed by a 30-day readmission, of which 879 (8.5% of all discharges) were identified as potentially avoidable. The prediction score identified 7 independent factors, referred to as the HOSPITAL score: h emoglobin at discharge, discharge from an o ncology service, s odium level at discharge, p rocedure during the index admission, i ndex t ype of admission, number of a dmissions during the last 12 months, and l ength of stay. In the validation set, 26.7% of the patients were classified as high risk, with an estimated potentially avoidable readmission risk of 18.0% (observed, 18.2%). The HOSPITAL score had fair discriminatory power (C statistic, 0.71) and had good calibration. This simple prediction model identifies before discharge the risk of potentially avoidable 30-day readmission in medical patients. This score has potential to easily identify patients who may need more intensive transitional care interventions.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Patterns of hospital performance in acute myocardial infarction and heart failure 30-day mortality and readmission.

            In 2009, the Centers for Medicare & Medicaid Services is publicly reporting hospital-level risk-standardized 30-day mortality and readmission rates after acute myocardial infarction (AMI) and heart failure (HF). We provide patterns of hospital performance, based on these measures. We calculated the 30-day mortality and readmission rates for all Medicare fee-for-service beneficiaries ages 65 years or older with a primary diagnosis of AMI or HF, discharged between July 2005 and June 2008. We compared weighted risk-standardized mortality and readmission rates across Hospital Referral Regions and hospital structural characteristics. The median 30-day mortality rate was 16.6% for AMI (range, 10.9% to 24.9%; 25th to 75th percentile, 15.8% to 17.4%; 10th to 90th percentile, 14.7% to 18.4%) and 11.1% for HF (range, 6.6% to 19.8%; 25th to 75th percentile, 10.3% to 12.0%; 10th to 90th percentile, 9.4% to 13.1%). The median 30-day readmission rate was 19.9% for AMI (range, 15.3% to 29.4%; 25th to 75th percentile, 19.5% to 20.4%; 10th to 90th percentile, 18.8% to 21.1%) and 24.4% for HF (range, 15.9% to 34.4%; 25th to 75th percentile, 23.4% to 25.6%; 10th to 90th percentile, 22.3% to 27.0%). We observed geographic differences in performance across the country. Although there were some differences in average performance by hospital characteristics, there were high and low hospital performers among all types of hospitals. In a recent 3-year period, 30-day risk-standardized mortality rates for AMI and HF varied among hospitals and across the country. The readmission rates were particularly high.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Hospital Readmission in General Medicine Patients: A Prediction Model

              Background Previous studies of hospital readmission have focused on specific conditions or populations and generated complex prediction models. Objective To identify predictors of early hospital readmission in a diverse patient population and derive and validate a simple model for identifying patients at high readmission risk. Design Prospective observational cohort study. Patients Participants encompassed 10,946 patients discharged home from general medicine services at six academic medical centers and were randomly divided into derivation (n = 7,287) and validation (n = 3,659) cohorts. Measurements We identified readmissions from administrative data and 30-day post-discharge telephone follow-up. Patient-level factors were grouped into four categories: sociodemographic factors, social support, health condition, and healthcare utilization. We performed logistic regression analysis to identify significant predictors of unplanned readmission within 30 days of discharge and developed a scoring system for estimating readmission risk. Results Approximately 17.5% of patients were readmitted in each cohort. Among patients in the derivation cohort, seven factors emerged as significant predictors of early readmission: insurance status, marital status, having a regular physician, Charlson comorbidity index, SF12 physical component score, ≥1 admission(s) within the last year, and current length of stay >2 days. A cumulative risk score of ≥25 points identified 5% of patients with a readmission risk of approximately 30% in each cohort. Model discrimination was fair with a c-statistic of 0.65 and 0.61 for the derivation and validation cohorts, respectively. Conclusions Select patient characteristics easily available shortly after admission can be used to identify a subset of patients at elevated risk of early readmission. This information may guide the efficient use of interventions to prevent readmission.
                Bookmark

                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                8 October 2015
                2015
                : 10
                : 10
                : e0140271
                Affiliations
                [1 ]HBI Solutions Inc., Palo Alto, California, United States of America
                [2 ]Departments of Surgery, Stanford University, Stanford, California, United States of America
                [3 ]Departments of Pediatrics, Stanford University, Stanford, California, United States of America
                [4 ]Shanghai Children's Hospital, Shanghai Jiao Tong University, Shanghai, China
                [5 ]HealthInfoNet, Portland, Maine, United States of America
                D'or Institute of Research and Education, BRAZIL
                Author notes

                Competing Interests: The authors have the following interests: KGS, EW and XBL are co-founders and equity holders of HBI Solutions, Inc., which is currently developing predictive analytics solutions for healthcare organizations. BJ, CZ, ZH, CF, DD, FS and EW are employed by HBI Solutions, Inc. From the Departments of Pediatrics, Surgery, and Statistics, Stanford University School of Medicine, Stanford, California, AYS, KGS, and XBL conducted this research as part of a personal outside consulting arrangement with HBI Solutions, Inc. The research and research results are not, in any way, associated with Stanford University. There are no patents, further products in development or marketed products to declare. This does not alter the authors' adherence to all the PLOS ONE policies on sharing data and materials, as detailed online in the guide for authors.

                Conceived and designed the experiments: AYS FS KGS EW XBL. Analyzed the data: SH Yue Wang BJ CZ MH LZ JL ZH CF DD Yicheng Wang. Wrote the paper: SH Yue Wang BJ CZ MH LZ JL ZH CF DD Yicheng Wang AYS FS KGS EW XBL DSC STA TR. Coordinated and supervised data acquisition: DSC STA TR.

                Article
                PONE-D-15-13798
                10.1371/journal.pone.0140271
                4598005
                26448562
                4e86ed27-4646-4b0a-b3df-0dea02e0118f
                Copyright @ 2015

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited

                History
                : 30 March 2015
                : 23 September 2015
                Page count
                Figures: 4, Tables: 2, Pages: 15
                Funding
                The authors received no specific funding for this work. HBI Solutions, Inc. (HBI) is a private commercial company, and several authors are employed by HBI. HBI provided funding in the form of salaries to the authors employed by HBI: BJ, CZ, ZH, CF, DD, FS and EW. HBI did not provide any funding or support outside of the salary support for the study, and HBI did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of manuscript. The specific roles of these authors are articulated in the ‘author contributions’ section.
                Categories
                Research Article
                Custom metadata
                The work was performed under a business arrangement between HealthInfoNet ( http://www.hinfonet.org), the operators of the Maine Health Information Exchange and HBI Solutions, Inc. (HBI) located in California. By business arrangement we mean HBI is a contracted vendor to HealthInfoNet (HIN), and HBI is under contract to deploy its proprietary applications and risk models on the HIN data for use by HIN members. HIN is a steward of the data on behalf of its members which includes health systems, hospitals, medical groups and federally qualified health centers. The data is owned by the HIN members, not HIN. HIN is responsible for security and access to its members' data and has established data service agreements (DSAs) restricting unnecessary exposure of information. HIN and its board (comprised from a cross section of its members) authorized the use of the de-identified data for this research, as the published research helps promote the value of the HIE and value to Maine residents. HBI receives revenue for providing this service, which is performed remotely. HBI does not own or have access to the data outside of providing services to HIN. HIN manages and controls the data within its technology infrastructure. The research was conducted on HIN technology infrastructure, and the researchers accessed the de-identified data via secure remote methods. All data analysis and modeling for this manuscript was performed on HIN servers and data was accessed via secure connections controlled by HIN. Access to the data used in the study requires secure connection to HIN servers and should be requested directly to HIN. Researchers may contact Phil Prefenno at pprofenno@ 123456hinfonet.org , (207) 541–4115 to request data. Data will be available upon request to all interested researchers. HIN agrees to provide access to the de-identified data on a per request basis to interested researchers. Future researchers will access the data through exact the same process as the authors of the manuscript.

                Uncategorized
                Uncategorized

                Comments

                Comment on this article