Reducing Procedural Waste on the Internal Medicine Wards
Alice Yu, Jessica Evans, Husein Moloo, Tim Ramsay, Salmaan Kanji, Mathilde Gaudreau-Simard

Abstract
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
- —The Ottawa Hospital Academic Medical Association (TOHAMO)
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Taxonomy
TopicsHealthcare cost, quality, practices · Patient Safety and Medication Errors · Healthcare Quality and Management
INTRODUCTION
Healthcare is a significant contributor to global greenhouse gas emissions, with waste responsible for 20% of this sector’s emissions.^1^ Numerous strategies aimed at reducing unnecessary waste generated from bedside procedures have been described.^2–4^ We aimed to develop a quality improvement intervention to reduce waste produced from bedside paracentesis and thoracentesis.
METHODS
This study was performed at The Ottawa Hospital, a tertiary academic center with over 1300 beds across two campuses. This study adhered to the Standards for Quality Improvement Reporting Excellence (SQUIRE 2.0) guidelines and received an ethics waiver from our Research Ethics Board.^5^
A baseline waste audit of bedside paracentesis and thoracentesis on the internal medicine (IM) wards was performed from January to June 2023 to establish baseline waste estimates and identify opportunities for waste reduction. Interventions were developed based on findings from the first audit, in consultation with local experts and affected parties, with a goal of reducing waste by 50%. The audit was repeated from July 2023 to February 2024 after interventions were implemented. Data was collected through direct observation and by structured reporting.
Interventions
- Development and dissemination of a minimal supplies checklist: Residents were observed to use various functionally equivalent trays that differed in waste. An evidence-based minimal supplies checklist was created to standardize supplies and minimize waste (see Table 1).^6,7^
- Optimization of the on-site procedure cart: The procedure cart was reorganized to include only the recommended supplies. Regular cart restocking was undertaken by unit administrators.
- “Just in Case” to “Just in Time”: To minimize waste from over-gathering “just in case” supplies, while ensuring standard of care, additional “just in time” supplies were instead readily accessible immediately outside of the procedure areas. Unused and uncontaminated “just in time” supplies were returned to the clean utility.
- Educational interventions: A video demonstrating implementation of the minimal supplies list was produced and distributed to internal medicine residents. Further training was communicated through weekly e-newsletters, teaching sessions, and the clinical teaching unit orientation. Table 1. Minimal Supplies ChecklistChecklist itemNumber requiredGeneral 1% or 2% lidocaine, 10 mL1 18 G blunt needle2 22G 1–1/2″ needle1 10 mL syringe1 Chlorhexidine soluprep swabs3 Sterile gloves1 Dressing tray (includes sterile fenestrated drape and gauze)1 Tegaderm dressing1A. Diagnostic paracentesis* Angiocath 14G1 IV Luer lock1 50 mL syringe1B. Thoracentesis, therapeutic paracentesis* Scalpel1 Tape roll1 Vacuum bottles 1 L† Safety needle1*Checklist “A” items produce less waste but can be used only for diagnostic paracentesis; “B” items can be used for both diagnostic and therapeutic paracentesis and thoracentesis†Number varies depending on volume removed
Outcomes and Analysis
Outcome measures included the number of wasted supplies, defined as the number of unused and discarded items gathered per procedure, as well as the per procedure waste weight. Considering that the number of fluid collection bottles used per procedure varies inherently due to patient factors, a “fixed supply waste weight metric” was calculated by subtracting the weight associated with the collection bottles from the total weight. Whitney U tests with continuity correction were used to compare differences between the number of wasted supplies and fixed supply waste weight for the pre- and post-intervention audits.
RESULTS
Pre- and post-intervention audits comprised 10 procedures each (13 paracentesis and 7 thoracentesis total). Between the two audits, there was a statistically significant difference in the primary outcomes, as shown in Table 2. The proportion of total unused and wasted supplies per audit was successfully reduced by half, from 55.9% (n = 292) to 24.2% (n = 104) for the pre- and post-intervention audits, respectively. Table 2. Pre- and Post-Intervention Median (IQR) Per Procedure Waste Audit OutcomesPre-intervention (n = 10)Post-intervention (n = 10)p-valueNumber of wasted supplies25.0 (19.0–43.8)8.5 (5.0–14.0)p = 0.002Fixed supply waste weight485.0 g (361.9–749.8)325.3 g (238.9–351.5)p = 0.012IQR* interquartile range, n number of procedures observed per audit*Generated by Mann–Whitney U test
DISCUSSION
The implementation of a minimal supplies checklist, procedure cart optimization, adoption of a “just in time” approach, and educational initiatives led to a reduction of more than 50% in wasted procedural supplies. Extrapolating from the number of thoracentesis and paracentesis that were performed by IM at our center in 2023 (n = 220), adoption of this initiative has the potential to reduce bedside procedure-associated waste by over 35 kg annually.
Limitations and Strengths
A significant limitation of this work is the lack of life cycle assessments for paracentesis and thoracentesis procedures. The absence of this evidence in the literature prevented us from calculating exact carbon savings per procedure. While a larger sample size might improve the precision of our estimates, the impact and sustainability of quality improvement initiatives are best assessed through frequent cohort assessments as opposed to designing larger scale studies. The simplicity of our methods increases the feasibility of repeated assessments over time with the possibility of expansion to other procedures, units, and institutions.
Future Directions
Further audits are planned to assess the sustainability of this initiative, with ongoing refinement of our change ideas. There is potential for this intervention to be adopted across other specialties and centers.
The reference list from the paper itself. Each links out to its DOI / PubMed record.
- 1Ogrinc G, Davies L, Goodman D, Batalden P, Davidoff F, Stevens D. SQUIRE 2.0 (Standards for Q Uality Improvement Reporting Excellence): revised publication guidelines from a detailed consensus process. BMJ Qual Saf. 2016;25(12):986–992.10.1136/bmjqs-2015-004411 PMC 525623326369893 · doi ↗ · pubmed ↗
