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Articles

GIS-automated delineation of hospital service areas in Florida: from Dartmouth method to network community detection methods

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Pages 93-109 | Received 26 Mar 2021, Accepted 01 Jan 2022, Published online: 01 Feb 2022
 

ABSTRACT

Since the Dartmouth Hospital Service Areas (HSAs) were proposed three decades ago, there has been a large body of work using the unit in examining the geographic variation in health care in the U.S. for evaluating health care system performance and informing health policy. However, many studies question the replicability and reliability of the Dartmouth HSAs in meeting the challenges of an ever-changing and a diverse set of health care services. This research develops a reproducible, automated, and efficient GIS tool to implement Dartmouth method for defining HSAs. Moreover, the research adapts two popular network community detection methods to account for spatial constraints for defining HSAs that are scale flexible and optimize an important property such as maximum service flows within HSAs. A case study based on the state inpatient database in Florida from the Healthcare Cost and Utilization Project is used to evaluate the efficiency and effectiveness of the methods. The study represents a major step towards developing HSA delineation methods that are computationally efficient, adaptable for various scales (from a local region to as large as a national market) and automated without a steep learning curve for public health professionals.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Notes

1. In general, a larger number of HSAs and thus smaller HSAs on average imply that fewer hospitalization flows could be captured within HSAs, and therefore lower LI values.

2. On an Intel® Xeon® Gold 6140 CPU @ 2.30 GHz 2.29 GHz desktop with a memory of 128GB, it took 9.36 h for the 1,000 simulations of HSAs in Florida.

3. Visit https://faculty.lsu.edu/fahui/news/2021/book-gis-hsa-by-crc.php for free downloading the programmes and sample data sets.

Additional information

Funding

This work was supported by the National Cancer Institute [R21CA212687].