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Reducing waste: a guidelines-based approach to reducing inappropriate vitamin D and TSH testing in the inpatient rehabilitation setting
  1. Emma A Bateman1,
  2. Alan Gob2,
  3. Ian Chin-Yee3,
  4. Heather M MacKenzie1
  1. 1Physical Medicine & Rehabilitation, Western University, London, Ontario, Canada
  2. 2Medicine, London Health Sciences Centre, London, Ontario, Canada
  3. 3Pathology and Laboratory Medicine, London Health Sciences Centre, London, Ontario, Canada
  1. Correspondence to Emma A Bateman; eabateman{at}gmail.com

Abstract

Background Laboratory overutilisation increases healthcare costs, and can lead to overdiagnosis, overtreatment and negative health outcomes. Discipline-specific guidelines do not support routine testing for Vitamin D and thyroid-stimulating hormone (TSH) in the inpatient rehabilitation setting, yet 94% of patients had Vitamin D and TSH tests on admission to inpatient rehabilitation at our institution. Our objective was to reduce Vitamin D and TSH testing by 25% on admission to inpatient Stroke, Spinal Cord Injury, Acquired Brain Injury and Amputee Rehabilitation units.

Methods A fishbone framework for root cause analysis revealed potential causes underlying overutilisation of Vitamin D and TSH testing. A series of Plan-Do-Study-Act (PDSA) cycles were introduced to target remediable factors, starting with an academic detailing intervention with key stakeholders that reviewed applicable clinical guidelines for each patient care discipline and the rationale for reducing admission testing. Simultaneously, computerised clinical decision support (CCDS) limited Vitamin D testing to specific criteria. Audit and feedback were used in a subsequent PDSA cycle. Frequency of Vitamin D and TSH testing on admission was the primary outcome measure. The number of electronic admission order caresets containing automatic Vitamin D and/or TSH orders before and after the interventions was the process measure. Rate of Vitamin D supplementation and changes in thyroid-related medication were the balancing measures.

Results After implementation, 2.9% of patients had admission Vitamin D testing (97% relative reduction) and 53% of patients had admission TSH testing (43% relative reduction). Admission order caresets with prepopulated Vitamin D and TSH orders decreased from 100% (n=6) to 0%. The interventions were successful; similar to previous literature, CCDS was more effective than education and audit and feedback interventions alone. The interventions represent >$9000 annualised savings.

  • quality improvement
  • evidence-based medicine
  • decision support, computerised
  • clinical practice guidelines

This is an open access article 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, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.

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Footnotes

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  • Contributors All authors fulfill the authorship recommendations outlined by the ICMJE. This project was undertaken as part of a quality improvement curriculum through the Schulich School of Medicine & Dentistry and London Health Sciences Centre. EAB and HMM collaboratively identified areas of potential knowledge translation and quality improvement applicable to inpatient rehabilitation at Parkwood Institute, St. Joseph’s Healthcare London, performed root cause analysis and designed Plan-Do-Study-Act (PDSA) cycles targeting underlying causes of laboratory overutilisation to be targeted by this project. EAB was responsible for data collection and analysis, and preparation of this manuscript. All authors contributed to PDSA cycle design, analysis and interpretation of the data. AG and ICY provided feedback and expertise in quality improvement and laboratory utilisation, respectively, throughout the project. EAB drafted the manuscript, to which all authors contributed revisions. All authors reviewed, provided feedback and approved of the content of the manuscript.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Patient consent for publication Not required.

  • Ethics approval Institutional review board approval was not sought as this study met criteria for exemption based on the Tri-Council Policy Statement, Article 1.1 stating that quality assurance studies should be exempt from review.

  • Provenance and peer review Not commissioned; externally peer reviewed.