Skip to main content
PLOS One logoLink to PLOS One
. 2022 Dec 29;17(12):e0276377. doi: 10.1371/journal.pone.0276377

Standardization of laparoscopic trays using an inventory optimization model to produce immediate cost savings and efficiency gains

Jay Toor 1,*,#, Ajay Shah 1,#, Aazad Abbas 2,#, Jin Tong Du 2,#, Erin Kennedy 1,3
Editor: Kush Raj Lohani4
PMCID: PMC9799292  PMID: 36580456

Abstract

Perioperative services comprise a large portion of hospital budgets; the procurement and processing of surgical inventories can be an area for optimization in operational inefficiency. Surgical instrument trays can be customized as procedure-specific or standardized as trays that can be used in numerous procedure types. We conducted an interventional study to determine the cost savings from standardizing laparoscopic surgery instrument trays. A single-period inventory optimization model was used to determine the configuration of a standardized laparoscopic (SL) tray and its minimal stock quantity (MSQ). Utilization of instruments on the general surgery, gynecology, and gynecological oncology trays was recorded, and daily demand for trays (mean, SD) was assessed using daily operating room (OR) case lists. Pre- and post-intervention costs were evaluated by reviewing procurement data and quantifying medical device reprocessing (MDR) and OR processes. The SL tray was trialled in the OR to test clinical safety and user satisfaction. Prior to standardization, the customized trays had a total inventory size of 391 instruments (mean instruments per tray: 17, range: 12–22). Daily demand was an MSQ of 23 trays. This corresponded to a procurement cost of $322,160 and reprocessing cost of $41,725. The SL tray (mean instruments per tray: 15, mean trays/day: 9.2 ± 3.2) had an MSQ of 17 trays/day. The total inventory decreased to 255 instruments, corresponding to a procurement cost of $266,900 with savings of $55,260 and reprocessing cost of $41,562 with savings of $163/year. After 33 trial surgeries, user satisfaction improved from 50% to 97% (p < .05). Standardization to a single SL tray using the inventory optimization model led to increased efficiency, satisfaction, and significant savings through aggregating specific service demands. The inventory optimization model could provide custom solutions for various institutions with the potential for large-scale financial savings. Thus, future work using this model at different centres will be necessary to validate these results.

Introduction

In the current healthcare environment, cost containment is more important than ever [1]. Perioperative services are often scrutinized as they comprise one-third of a hospital’s budget [2]. The procurement and processing of surgical instruments make up a significant portion of these budgets [3]. Accordingly, increasing attention is being devoted to determining how to generate cost savings via process improvements and quality improvement initiatives. For example, a recent systematic review compared costs of disposable versus reusable surgical instruments, with inconclusive results due to a lack of primary data [4].

In particular, the focus has been placed on optimizing the surgical instrument tray by removing instruments used infrequently to reduce reprocessing costs. The techniques used include Lean-style clinician review, cost analysis and mathematical modelling [512]. Larger-scale optimization studies have been published in the industrial engineering literature, although significant limitations prevent practical application in the hospital setting, including institutional barriers to cultural change [5].

One possible strategy to reduce procurement and processing costs of surgical instruments is to consider the standardization of laparoscopic trays. Unlike the trays in specialties such as orthopedic surgery that are typically quite customized to a specific surgery type, laparoscopic instruments can be used by both general surgeons and gynecologic surgeons. However, no prior studies have explored the concept of combining trays from these surgical specialties into a standardized laparoscopic tray. We hypothesize that standardization to a single tray via demand aggregation may reduce the total inventory requirement and result in fewer instrument purchasing, processing and replacement costs. Secondary outcomes include perioperative staff satisfaction.

Methods

Study design

This was a single-site interventional quality improvement study conducted at a large academic hospital in a major metropolitan city which performs over 800 general surgery (GS), gynecology (GY), and gynecological oncology (GO) procedures annually using customized specialty-specific trays.

The minimum stock quantity (MSQ) of the GS, GY, and GO trays were calculated using a single-period inventory optimization model (IOM) based on the Newsvendor problem [13].

Briefly, the Newsvendor problem determines the optimal inventory required for a given perishable item. The classic analogy for this problem is that of a newspaper vendor who needs to know how many copies of the day’s paper to stock while faced with varying demand. Since items on surgical trays need to be reprocessed after use, this model is directly applicable to this study. Accordingly, the MSQ can be modelled by the following equation:

MSQ=μ+zσ, (1)

where μ is the mean utilization of the trays, z is the service level of the trays, and σ is the standard deviation of utilization. The trays were then standardized into a single standardized laparoscopic (SL) tray, and its MSQ was calculated.

The effect of standardization was measured by determining the difference in procurement costs, tray reprocessing costs, and total reprocessing costs for the customized trays versus the SL tray. This study was performed with the assistance of the managers of the Operating Room (OR) and Medical Device Reprocessing Department (MDRD).

Optimization of SL tray

All instruments used in three customized trays were combined and standardized into a single SL tray. This was completed through a clinician review of tray contents by all users and a mathematical model based on observations of intraoperative instrument utilization. The methodology was described in detail in the literature [13]. The SL tray was presented to laparoscopic surgeons, registered nurses (RNs) and medical devices reprocessing (MDR) technicians. It was thenceforth utilized in place of the previously customized trays in all subsequent laparoscopic procedures.

Data collection

Hospital procedure data for the preceding four fiscal years (2014–2018) was retrieved. Procurement and reprocessing costs were provided by the manager of the MDRD. The number of daily GS, GY and GO procedures over this period was calculated to estimate the number of customized trays used. An observer was present in the OR during GS, GY, and GO procedures to document instrument use over a period of 3 weeks; variables collected were: procedure type, surgeon name, instruments used, pick list contents, pick list related adverse events, trayy related adverse events., and intra-operative item retrieval time. This observer was also present in the MDRD to document tray reprocessing; variables collected were: instrument name, time to decontaminate, time to assemble, total tray assembly time, and list assembly time [13].

Minimal Stock Quantity (MSQ)

The daily number of procedures during the four-year period was used to determine the MSQ requirement for customized and standardized trays. The general demand required inventory of the UL tray (MSQUL) for a set of trays T of size N may be described as follows:

MSQUL=i=1Nμi+zi=1Nσi2, (2)

where i is a tray in the set T, μi is the mean demand of each tray, and σi is the standard deviation of tray i. Simplifying for our case of GS, GY, and GO trays, we have:

MSQST=(μGS+μGY+μGO)+zσGS2+σGY2+σGO2 (3)

Since we cannot have a fraction of a surgical tray, the MSQ is always rounded up to the nearest integer to ensure there is safety stock available.

Cyclic service level assumption

The cyclic service level (CSL) is defined as the probability that a tray is available when it is needed for a procedure [14]. We chose a CSL of 99%; this infers that only 1 out of 100 procedures will not have a tray available when it is requested. This is an essential component of the equations required to calculate MSQ. Accordingly, the CSL can be modelled by the following equation:

CSL=coveragecoverage+cunderage, (4)

coverage is the overage cost (cost of having an extra tray in inventory when it is not needed) and cunderage is the underage cost (cost of not having a tray available when it is needed i.e., stockout event). In the healthcare setting, it is difficult to place a discrete financial value on a stockout event as the implications extend beyond the quantifiable loss of OR time into the domain of impact on patient care.

Cost metrics

The procurement costs for each surgical instrument were obtained from previous hospital invoices. The procurement costs for each surgical tray were calculated as the sum of the procurement costs for each instrument on the tray. The total procurement costs for each tray were calculated as the product of the procurement costs for each tray and the MSQ for each instrument. Procurement cost (Cprocurement) may be defined as the costs associated with obtaining the surgical trays. For some surgical tray T with N number of instruments, Cprocurement may be defined as:

Cprocurement=MSQi=1Nci, (5)

where ci is the procurement cost for each instrument on the surgical tray, and MSQ is the minimum stock quantity of the surgical tray.

The reprocessing costs for each instrument on the tray were determined via timed observation of instrument reprocessing. The mean reprocessing time for each instrument on each tray was calculated, and the reprocessing costs for each tray was determined as the sum of the mean reprocessing costs of all instruments on the tray. As such, the reprocessing costs (Creprocess) can be defined as:

Creprocess=treprocessW, (6)

where treprocess is reprocessing time in minutes, and W is the MDR technician wages per minute in CAD. The total reprocessing costs per year for each tray would be determined as a product of the reprocessing costs for each tray and the yearly number of procedures requiring each tray. Reprocessing costs are calculated annually. The difference in procurement and reprocessing costs between the customized trays and the SL tray were used to determine the overall cost savings obtained with the standardized tray model. The difference was calculated using a side-by-side cost comparison.

User satisfaction and safety

Pre- and post-intervention surveys were distributed to surgeons, RNs and MDR technicians comparing satisfaction between customized and standardized inventory. The questionnaire was administered at two time points: immediately before tray standardization and one month after. Respondents were asked if they were (1) satisfied or (2) dissatisfied with the inventory configuration. For surgeons, satisfaction refers to the ability to perform a given procedure without concerns regarding the availability of required instruments. For RNs and MDR technicians, satisfaction was referred to the requirements of familiarity with instrument and tray configurations. The chi-squared statistical test was used to analyse the satisfaction survey results, with significance set at p < .05.

Results

Customized trays (GS, GY, GO)

The variables used in the mathematical model are shown in Table 1. Prior to standardization, there were three procedure-specific tray types: GS, GY, and GO, with a total inventory size of 391 instruments (mean instruments per tray: 17, range: 12–22). Daily demand was calculated for GS (mean 4.6 trays/day, SD ±2.1), GY (2.8 ±2.1), and GO (1.8 ±1.2) trays, with an MSQ of 23 trays total. This corresponded to a total procurement cost of $322,160 and reprocessing cost of $41,725, as shown in Table 2. The configurations of the various trays used may be found in Table 3. The configuration of specific instruments in each customized tray can be found in the S1-S3 Tables in S1 File.

Table 1. Variables for Newsvendor formula used to determine MSQ per tray.

Tray Name Demand (Trays per day) SD of Demand (Trays per day) Cyclic Service Level (%) Z Score Raw Minimal Stock Quantity (MSQ) Rounded Minimal Stock Quantity (MSQ)
GS 4.6 2.1 99% 2.33 9.49 10
GY 2.8 2.1 99% 2.33 7.69 8
GO 1.8 1.2 99% 2.33 4.59 5
SL 9.2 3.2 99% 2.33 16.65 17

GS: general surgery, GY: gynecology, GO: gynecology oncology, SL tray: standardized laparoscopic tray.

Table 2. Costs savings breakdown per tray.

Tray Name Procurement Cost per Tray (CAD) Number of Instruments Minimal stock quantity (MSQ) Total Procurement Cost for Necessary Inventory (CAD) Reprocessing Labour Costs* /Tray (CAD) Procedures per tray Total Reprocessing Costs (CAD)
GS $12,360 22 10 $123,600 $14.46 1548 $22,415.05
GY $15,720 12 8 $125,760 $17.59 898 $15,795.82
GO $14,560 15 5 $72,800 $10.88 323 $3,514.24
SLT $15,700 15 17 $266,900 $15.01 2769 $41,562.69

GS: general surgery, GY: gynecology, GO: gynecology oncology, SL: standardized laparoscopic.

Table 3. Configuration of the various trays used in this study.

General Surgery Tray Gynecology Tray Gynecology Oncology Tray Standardized Laparoscopic Tray
Dissector (1) Rounded/bullet graspers (2) Small tip laparoscopic clinch (2) Bowel grasper ratchet (2)
Debakey flat (2) Fundus grasper (1) Hunter grasper (2) Bowel grasper non (1)
Crile (1) Needle nose grasper (1) Duckbill grasping forceps (2) Maryland dissector (2)
Horizontal clip applier (1) Maryland dissector (1) Maryland dissector (1) Rounded grasper (2)
Suction irrigator (4) Suction irrigator (1) Suction irrigator (1) Suction irrigator (1)
Bowel grasper (3) L hook (1) L hook (1) L hook (1)
Laparoscopic scissors (1) Probe (1) Laparoscopic scissors (1) Horizon clip applier (1)
L hook (1) Bipolar forceps (1) Needle driver (1) Reusable laparoscopic shears/scissors (1)
Claw forceps (1) Bowel grasper (3) Maryland dissector (1) Laparoscopic Kocher (1)
Senn retractors (2) Maryland dissector (1) Needle driver (1)
Right angle retractor (2) Needle driver (2) Bipolar forceps (1)
Maryland dissector (1)
Needle driver (2)

GS: general surgery, GY: gynecology, GO: gynecology oncology, SL: standardized laparoscopic. Numbers in brackets indicate the number of each instrument.

Standardized laparoscopic tray

An SL tray was generated, with instruments listed in the S4 Table in S1 File. The SL tray had lower daily tray and instrument requirements (mean instruments per tray: 15, mean trays/day: 9.2 ±3.2). This reduced the MSQ by approximately 26% (MSQ: 17 trays). After standardization, the total inventory decreased to 255, corresponding to a procurement cost of $266,900 (savings of $55,260) and reprocessing costs of $41,562 (savings of $163/year).

User satisfaction and safety

30 staff completed the pre- and post-intervention satisfaction questionnaire (8 surgeons, 12 RNs, and 10 MDR technicians) at 1-month pre-standardization and 1-month post-standardization, respectively. The proportion of all staff satisfied with instrument configuration was 50% with the customized inventory and 97% with the standardized inventory. The satisfaction for surgeons was not significantly different between the customized and standardized trays (χ² = 0.39, p = .53). The satisfaction of RNs and MDR technicians between the customized and standardized trays was significantly different (χ² = 17.1, p < .05). Table 4 includes results of the satisfaction survey. RNs and MDR technicians were unsatisfied with the customized trays due to redundant infrequently used instruments and missing critical instruments.

Table 4. Satisfaction survey results of customized trays vs standardized trays.

Staff Satisfied (n) Unsatisfied (n)
Customized Inventory
Surgeons 7 1
RNs and MDRs 8 14
Total 15 15
Standardized Inventory
Surgeons 8 0
RNs and MDRs 21 1
Total 29 0

Discussion

The most important finding in this study is that the conversion of customized specialty-specific trays to a single SL tray resulted in significant annual cost savings via reduced total instrument inventory and tray quantity requirements to meet daily demand. This study showed that the use of mathematical optimization is a successful strategy to realize savings in the procurement of surgical instruments in the OR setting. The practical and quality improvement aspects of implementing this intervention are described in Toor et al. [13]. As expected, reprocessing and instrument turnover costs stayed relatively unchanged as the number of procedures per year primarily dictates the reprocessing costs [15].

The financial benefits of standardization versus customization of instrument trays are well documented [13], which suggests that this mathematical model may be generalizable for laparoscopic tray standardization at other hospitals [2]. In this study, the subspecialty trays had already undergone optimization before standardization, thereby under-estimating the potential cost savings. Additionally, the minimum quantity required was for 99% quantity satisfaction, higher than the 96% currently required in hospitals, which further underestimates real-world savings. This mathematical inventory optimization process has shown promising financial and clinical satisfaction results with other specialty trays, including large Orthopaedic and ENT trays [13]. The hybrid model of mathematical and clinician-directed optimization will likely mitigate the shortcomings of using either approach alone.

During the process of tray standardization, several factors were identified that could influence the degree of cost savings from similar interventions at other institutions. These broadly fall into surgical scheduling, inventory procurement, and workflow efficiency.

Surgical schedule variability’s impact on inventory

The calculation of MSQ shown in Eq (1) reveals an important consideration when scheduling surgeries over multiple days. For example, in a scenario with a daily demand of 5 trays (SD 3), an MSQ of 12 is required to maintain a 99% service level. In contrast, reducing SD to 2 reduces MSQ to 10. Increasing the mean to 6 (SD 2) only requires an MSQ of 11. This demonstrates the disproportionately large effect of schedule variability on MSQ. A surgical schedule that reduces variability by scheduling the same number of surgeries daily will reduce SSQ and MSQ. If tray demand variability is low such as in a “smooth” surgical schedule, then the benefits of demand aggregation to an SL tray are reduced.

Volume-based procurement discounts

Procurement cost decreases can occur from bulk purchases made possible by standardization. For example, at a 15% discount, savings would increase from $55,260 to $95,295 per annum. In our case, we did not receive a direct financial discount for procurements during the study period.

The effect of standardization on the workforce

A common argument in favour of inventory standardization is the reduction in various instruments and tray types. This reduces task variety for nurses and MDR technicians, who will have only a single laparoscopic tray to be familiar with during the tasks of OR case set-up and instrument reprocessing, respectively. A decrease in task variety has long been understood to increase efficiency and decrease time spent per task [16, 17]. Increased satisfaction rates among MDR technicians and RNs support this assumption.

Limitations

The primary limitation of this study is the inability to assess all impacts of the intervention comprehensively. For example, we could not calculate the number of instruments opened in peel-packs after the intervention. The implications of this intervention at a large time scale (e.g., tray/instrument maintenance, instrument replacement) escape the scope of this study. Apart from no explicit adverse safety incidents being documented in the post-intervention period, there is no way to conclusively determine that this intervention had no negative impact on patient safety. In addition, the clinician review was conducted over a short period. It consisted of only 30 staff, which may have revealed issues such as missing instruments for all procedures and all surgeons. However, given the cost savings and high satisfaction, it is likely that patient safety was not impaired.

Furthermore, this study hinges on the ability of laparoscopic trays to be used by many specialties such as GS, GY, and GO, allowing the creation of a single SLT that can serve different specialties. The concept of standardization may be more challenging to apply to other trays, such as the Orthopedic Surgery trays, which are more differentiated for that specific surgical specialty. Thus different optimization methods will have to be considered [13]. Lastly, a normal distribution was used to approximate the probability distribution of daily demand on surgical trays. Given that our sample size was procedures per day over two years, our large sample size justifies this assumption as suggested by the Central Limit Theorem [18]. Although there are limitations to the generalized application of standardization over customization, this underscores the utmost importance of a systematic, mathematically sound approach to decision-making. The limitations above and discussions reinforce the importance of our mathematical model; it creates a custom solution for each institution’s unique circumstances with the potential for large-scale financial savings.

Conclusion

Standardizing three laparoscopic surgical trays (general surgery, gynecology, gynecological oncology) into a single standardized laparoscopic tray resulted in significant cost savings and increased satisfaction at our institution. However, as illustrated by our study, the potential cost impacts may differ between institutions, underscoring the importance of using an evidence-based business approach such as the inventory optimization model. Future work should involve multiple centers to address generalizability.

Supporting information

S1 File. Contains all the supporting tables and figures.

(DOCX)

S1 Data

(XLSX)

Acknowledgments

We thank all the surgeons, nurses, and MDR technicians who made this research possible.

Data Availability

All relevant data are within the paper and its Supporting information files.

Funding Statement

The author(s) received no specific funding for this work.

References

  • 1.Van Meter MM, Adam RA. Costs associated with instrument sterilization in gynecologic surgery. Am J Obstet Gynecol. 2016;215(5):652.e1–652.e5. [DOI] [PubMed] [Google Scholar]
  • 2.Cima RR, Brown MJ, Hebl JR, et al. Use of lean and six sigma methodology to improve operating room efficiency in a high-volume tertiary-care academic medical center. Journal of the American College of Surgeons. 2011;213(1):83–92. https://search.datacite.org/works/10.1016/j.jamcollsurg.2011.02.009 [DOI] [PubMed] [Google Scholar]
  • 3.Dyas AR, Lovell KM, Balentine CJ, et al. Reducing cost and improving operating room efficiency: Examination of surgical instrument processing. The Journal of surgical research. 2018;229:15–19. 10.1016/j.jss.2018.03.038 [DOI] [PubMed] [Google Scholar]
  • 4.Ahmadi E, Masel DT, Metcalf AY, Schuller K. Inventory management of surgical supplies and sterile instruments in hospitals: A literature review. Health Systems. 2018;8(2):134–151. https://search.datacite.org/works/10.1080/20476965.2018.1496875 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Siu J, Hill AG, MacCormick AD. Systematic review of reusable versus disposable laparoscopic instruments: costs and safety. ANZ J Surg. 2017. Jan;87(1–2):28–33. doi: 10.1111/ans.13856 [DOI] [PubMed] [Google Scholar]
  • 6.Cichos KH, Hyde ZB, Mabry SE, et al. Optimization of orthopedic surgical instrument trays: Lean principles to reduce fixed operating room expenses. The Journal of arthroplasty. 2019;34(12):2834–2840. 10.1016/j.arth.2019.07.040 [DOI] [PubMed] [Google Scholar]
  • 7.Cichos KH, Linsky PL, Wei B, Minnich DJ, Cerfolio RJ. Cost savings of standardization of thoracic surgical instruments: The process of lean. The Annals of thoracic surgery. 2017;104(6):1889–1895. 10.1016/j.athoracsur.2017.06.064 [DOI] [PubMed] [Google Scholar]
  • 8.Avansino JR, Goldin AB, Risley R, Waldhausen JHT, Sawin RS. Standardization of operative equipment reduces cost. Journal of pediatric surgery. 2013;48(9):1843–1849. https://www.clinicalkey.es/playcontent/1-s2.0-S0022346812009657 [DOI] [PubMed] [Google Scholar]
  • 9.Sethi R, Yanamadala V, Burton DC, Bess RS. Using lean process improvement to enhance safety and value in orthopaedic surgery: The case of spine surgery. J Am Acad Orthop Surg. 2017;25(11):e244–e250. doi: 10.5435/JAAOS-D-17-00030 [DOI] [PubMed] [Google Scholar]
  • 10.Farrokhi FR, Gunther M, Williams B, Blackmore CC. Application of lean methodology for improved quality and efficiency in operating room instrument availability. Journal for healthcare quality. 2015;37(5):277–286. https://search.datacite.org/works/10.1111/jhq.12053 [DOI] [PubMed] [Google Scholar]
  • 11.Dobson G, Seidmann A, Tilson V, Froix A. Configuring surgical instrument trays to reduce costs. IIE transactions on healthcare systems engineering. 2015;5(4):225–237. http://www.tandfonline.com/doi/abs/10.1080/19488300.2015.1094759. [Google Scholar]
  • 12.Wannemuehler TJ, Elghouche AN, Kokoska MS, Deig CR, Matt BH. Impact of lean on surgical instrument reduction: Less is more. The Laryngoscope. 2015;125(12):2810. doi: 10.1002/lary.25407 [DOI] [PubMed] [Google Scholar]
  • 13.Toor J, Bhangu A, Wolfstadt J, et al. Optimizing the surgical instrument tray to immediately increase efficiency and lower costs in the operating room. Canadian Journal of Surgery. 2021. Forthcoming. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Cachon G, Terwiesch C. Matching supply with demand: An introduction to operations management. 3rd ed. Pittsburg: McGraw-Hill Education; 2011. [Google Scholar]
  • 15.Toor J, Du JT, Koyle M, Abbas A, Shah A, Bassi G, et al. Inventory Optimization in the Perioperative Care Department Using Kotter’s Change Model. Jt Comm J Qual Patient Saf. 2022. Jan;48(1):5–11. doi: 10.1016/j.jcjq.2021.09.011 [DOI] [PubMed] [Google Scholar]
  • 16.Smith A. The wealth of nations. London, England: W. Strahan and T. Cadell; 1776. [Google Scholar]
  • 17.Staats BR, Gino F. Specialization and variety in repetitive tasks: Evidence from a Japanesebank. Management Science. 2012;58(6):1141–1159. https://repository.upenn.edu/fnce_papers/111/ [Google Scholar]
  • 18.Holmes A, Illowsky B, Dean S. The central limit theorem for proportions. In: Introductory business statistics. Houston, Texas: OpenStax; 2019. https://openstax.org/books/introductory-business-statistics/pages/7-3-the-central-limit-theorem-for-proportions. [Google Scholar]

Decision Letter 0

Federico Ferrari

24 Jan 2022

PONE-D-21-17028Standardization of laparoscopic trays using an inventory optimization model to produce immediate cost savings and efficiency gainsPLOS ONE

Dear Dr. Toor,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

Please submit your revised manuscript by Mar 10 2022 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

Please include the following items when submitting your revised manuscript:

  • A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'.

  • A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'.

  • An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'.

If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

If applicable, we recommend that you deposit your laboratory protocols in protocols.io to enhance the reproducibility of your results. Protocols.io assigns your protocol its own identifier (DOI) so that it can be cited independently in the future. For instructions see: https://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols. Additionally, PLOS ONE offers an option for publishing peer-reviewed Lab Protocol articles, which describe protocols hosted on protocols.io. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols.

We look forward to receiving your revised manuscript.

Kind regards,

Federico Ferrari

Academic Editor

PLOS ONE

Journal Requirements:

When submitting your revision, we need you to address these additional requirements.

1. Please ensure that your manuscript meets PLOS ONE's style requirements, including those for file naming. The PLOS ONE style templates can be found at 

https://journals.plos.org/plosone/s/file?id=wjVg/PLOSOne_formatting_sample_main_body.pdf and 

https://journals.plos.org/plosone/s/file?id=ba62/PLOSOne_formatting_sample_title_authors_affiliations.pdf

2. Please include additional information regarding the survey or questionnaire used in the study and ensure that you have provided sufficient details that others could replicate the analyses. For instance, if you developed a questionnaire as part of this study and it is not under a copyright more restrictive than CC-BY, please include a copy, in both the original language and English, as Supporting Information.

Furthermore, we have noted that ethics approval has been waived by Mount Sinai Hospital Research Ethics Board for this particular study. Please ensure that this is indicated in the manuscript text.

3. In your Data Availability statement, you have not specified where the minimal data set underlying the results described in your manuscript can be found. PLOS defines a study's minimal data set as the underlying data used to reach the conclusions drawn in the manuscript and any additional data required to replicate the reported study findings in their entirety. All PLOS journals require that the minimal data set be made fully available. For more information about our data policy, please see http://journals.plos.org/plosone/s/data-availability.

Upon re-submitting your revised manuscript, please upload your study’s minimal underlying data set as either Supporting Information files or to a stable, public repository and include the relevant URLs, DOIs, or accession numbers within your revised cover letter. For a list of acceptable repositories, please see http://journals.plos.org/plosone/s/data-availability#loc-recommended-repositories. Any potentially identifying patient information must be fully anonymized.

Important: If there are ethical or legal restrictions to sharing your data publicly, please explain these restrictions in detail. Please see our guidelines for more information on what we consider unacceptable restrictions to publicly sharing data: http://journals.plos.org/plosone/s/data-availability#loc-unacceptable-data-access-restrictions. Note that it is not acceptable for the authors to be the sole named individuals responsible for ensuring data access.

We will update your Data Availability statement to reflect the information you provide in your cover letter.

4. Please include captions for your Supporting Information files at the end of your manuscript, and update any in-text citations to match accordingly. Please see our Supporting Information guidelines for more information: http://journals.plos.org/plosone/s/supporting-information. 

5. Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript. If you need to cite a retracted article, indicate the article’s retracted status in the References list and also include a citation and full reference for the retraction notice.

[Note: HTML markup is below. Please do not edit.]

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: Yes

**********

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

Reviewer #2: Yes

**********

3. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

**********

4. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

**********

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: This article has standard language and clear thinking.This study mainly demostrated that Standardization of three laparoscopic surgical trays (GS, GY, GO) into a single SL tray resulted in 261 significant cost savings and increased satisfaction at our institution. I have 2 suggestions for this study. First,the statistical method is not very clear in this article.The statisical method using in every test should be clearly described.Next,The actual clinical application effect in different regions needs to be further analyzed by increasing the number of samples and adopting multi-center method.

Reviewer #2: This scientific paper is vell written and informed. The content of study is very interesting and useful for surgeons, RNs ann MDRs. I congratualte the author for their successful research which will play a very important role for cost control in operating room. There are some grammatical and typing errors in this manuscript.

**********

6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: Yes: kai Zhang

Reviewer #2: Yes: Tuerhongjiang Tuxun

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.]

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.

PLoS One. 2022 Dec 29;17(12):e0276377. doi: 10.1371/journal.pone.0276377.r002

Author response to Decision Letter 0


7 Apr 2022

Dear Drs. Ferrari and Chenette,

Thank you on behalf of the reviewers for your consideration of our manuscript “Standardization of laparoscopic trays using an inventory optimization model to produce immediate cost savings and efficiency gains” to be considered for publication in PLOS ONE. We have taken the time to consider the feedback from the reviewers, and we have made the following changes to the manuscript:

Reviewer #1:

“First, the statistical method is not very clear in this article” Thank you kindly for this comment. We elaborated that we used a side-by-side cost comparison (Line 149-150). We have also described our methodology in detail including equations. Having incorporated the suggestion, we are confident the readers of PLOS ONE will be able to better understand our work.

“The actual clinical application effect in different regions needs to be further analyzed by increasing the number of samples and adopting multi-center method” Thank you for this insightful comment. We included the suggestion in Line 266-267.

Reviewer #2:

“There are some grammatical and typing errors in this manuscript.” Thank you for this constructive feedback. We have reviewed the manuscript in great detail and corrected any grammar and punctuation errors (Line 50, 75).

Thank you for your time and efforts in enhancing our work.

Sincerely,

Jay Toor MD MBA

Orthopaedic Surgery Resident Physician

Department of Surgery

University of Toronto

Tel: 1-416-918-9519

Email: jaysinghtoor@gmail.com

Attachment

Submitted filename: Lap Tray Standardization Response to Reviewers.docx

Decision Letter 1

Kush Raj Lohani

6 Jul 2022

PONE-D-21-17028R1Standardization of laparoscopic trays using an inventory optimization model to produce immediate cost savings and efficiency gainsPLOS ONE

Dear Dr. Toor,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

Please submit your revised manuscript by Aug 20 2022 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

Please include the following items when submitting your revised manuscript:

  • A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'.

  • A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'.

  • An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'.

If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

If applicable, we recommend that you deposit your laboratory protocols in protocols.io to enhance the reproducibility of your results. Protocols.io assigns your protocol its own identifier (DOI) so that it can be cited independently in the future. For instructions see: https://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols. Additionally, PLOS ONE offers an option for publishing peer-reviewed Lab Protocol articles, which describe protocols hosted on protocols.io. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols.

We look forward to receiving your revised manuscript.

Kind regards,

Kush Raj Lohani, Master of Surgery

Academic Editor

PLOS ONE

[Note: HTML markup is below. Please do not edit.]

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #2: All comments have been addressed

Reviewer #3: (No Response)

**********

2. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #2: (No Response)

Reviewer #3: Partly

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #2: (No Response)

Reviewer #3: Yes

**********

4. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #2: (No Response)

Reviewer #3: Yes

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #2: (No Response)

Reviewer #3: Yes

**********

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #2: (No Response)

Reviewer #3: Thank you for inviting me to review this paper.

The manuscript reports a study that aimed to produce cost and efficiency gains by standardizing the contents of laparoscopic surgery instrument trays. Research and improvement in the delivery of sterile processing services is an important and often overlooked component of surgical safety and efficiency. While there have been a small number of similar studies this can be a useful addition to that literature.

It seems that there have been prior reviews, so it’s unfortunate, and probably frustrating for the authors, that I have a range of new comments; however, while challenging, I feel they are important and would substantially enhance the paper.

Overall, the focus on mathematical approaches belies some of the nuanced complexities of sterile processing. There are also quite a few areas where more clarification or precision is warranted (e.g. survey response rates; costs ‘per year’ or other). I also don’t feel that the operational consequences have been fully thought through. There is no discussion of how the trays were changed and the new “standard” was introduced into practice.

Looking at the tables detailing the changes, one original tray has more instruments than the final one. Does this mean that the new tray was missing critical instruments for certain procedures, or simply the older tray had legacy instruments that weren’t used (in which case this isn’t just about standardization but also optimization)? Similarly, another original tray has exactly the same number of instruments as the new tray – are these the same or are there differences? Definitely missing here is the consideration – at least a discussion point - not just of the numbers of instruments in a tray, but also the types and uses of instruments.

I think it’s really valuable work, but can’t help thinking it’s ignored many of the real-world implications that may make this appear to be more straightforward that in actually is. Addressing the wider context of the work system in the Introduction and Discussion would make this a much stronger and more relevant paper.

INTRO

The first sentence of a paper or abstract is important. Consider qualifying why surgical inventories can be a “source of inefficiency” with some reasons why and / or some effect. Of course, they can also be a source of efficiency.

The introduction is very short. There is space to expand on the learning from prior work. I’d like to see more on the reasons why there are “limitations preventing practical application.” You could also discuss a little more the methods and results of the other prior studies, especially as you haven’t addressed this in your own work. An extra sentence or 3 would be valuable for establishing how your study builds on this prior work.

The introduction doesn’t really go into the challenges or trade-offs of standardization. Including surgeon preferences, generic vs specific uses, or the trade-off between having a range of instruments to cover a broader set of preferences/procedures, which may lead to more instruments in a tray vs specialist trays with less instruments. It might not need that, but I think a little more nuanced thought about the challenges of “standardization” and what it really means would be helpful. Of course, standardization can lead to standardized inefficiency.

In moving on to the methods, I would also like to see more discussion of the background of the “Newsvendor” problem, and the modelling methods chosen. Most readers will be unfamiliar with these. This could be in the intro or methods, but I would suggest the former as that is naturually more discursive.

METHODS

How were procurement & reprocessing costs discovered?

What did the “clinical review” of the SL tray involve? How many clinicians? What did they review? Were any operational trials (ie. A clinical review might not reveal missing instruments for all procedures & all surgeons).

How might this affect scheduling? If you have different procedure-specific trays, simultaneous surgeries would not be an issue. However, instead with “one size fits all” trays you presumably need more of them, or carefully schedule procedures and reprocessing to allow appropriate sharing?

Might using “mean” demand not immediately disadvantage periods of demand above the mean? Ie. During peak times, trays might not be available if calculations are only done on “means”. I think you allude to this later, but a little more about it in the methods could be useful.

Did you study or explore the types and uses of instruments in each tray? How did you know it was acceptable to remove some and not others? Are any of your team actively involved in sterile processing, or did you conduct any site vists?

How did you make the changes? Did you do this over time or change all the trays over to the standardized ones in one go? How did you ensure that no critical instruments were missing? Some sense or narrative of how you did this would be very informative.

Where and how were timed observations of instrument reprocessing made? Did this time include decontamination, and assembly? In assembly, did you study the time taken for inspection, functional checking and missing instrument retrieval (as well as ensuring all instruments are present)?

Mean instruments per tray of 17 seems relatively low compared to some trays. Do you think this has implications for generalization of your methods/findings to other trays?

Are the calculated reprocessing costs yearly, monthly, or per procedure? Time scale would be precise here.

RESULTS

How can the GS tray have more instruments than the standardized tray? Does this mean that there were redundant instruments in the GS tray, or that 7 extra instruments were needed for any GS procedure? That would make the cost saving calculations misleading. What was the overlap in instruments between the “old” and “new” versions (i.e. which stayed the same, were added, or removed?). Maybe that’s all too much, but the numbers don’t tell us anything about how the new tray differed. That’s really important.

Presumably the “standardized” trays basically used the same instruments – so the 15 in GO wer the same 15 in SLT….so aren’t GO and SLT the same tray? If not, presumable in the SLT tray there were instruments that were needed in the GO cases (so important instruments were missing from the SLT); or that some of the instruments in the GO trays were never used (which means this is less about standardization and more about just removing unused instruments).

There was a lot of dissatisfaction with the customized trays with RNs and MDRs. Why was this?

How long after the standardization process was the survey delivered? How was it delivered (onoine,paper etc)? How many people was it sent to vs completed it (% response rate?).

I could not see any data on the reprocessing times for each instrument (as per the method).

DISCUSSION

The mathematical focus of this paper ignores many of the operational nuances that may be found in this type of approach.

“Financial benefits….well documented” – this is a very broad brush. In fact, it’s well documented that the wrong sort of standardization can lead to inefficiencies. Furthermore, standardization and patient-centered care are often in opposition.

How do you think your approach would fare with other types of trays e.g. general surgery? These trays often have >100 instruments. What about the trade-offs with

How many surgeries required extra instruments (or “peel packs?”)?

One challenge with standard trays is that surgeons who trained differently have different preferences. Did you find that this suited some surgeons more than others; that they all used similar approaches; or that the particular procedures you worked on required a standard set of instruments, with little personal or procedural variation?

The cost calculations are well discussed but I think this misses a lot of nuanced implications / discussion points.

Did you calculate the “lifespan” of the instruments? Presumably if they are being turned over faster, they will need to be replaced sooner?

Again, please state over what time period the “savings” (line 220) refer to,

Some trays have rarely used instruments that nevertheless are important to have at the right time. How/are you sure that you didn’t remove instruments like this?

How did the implementation of the new trays happen? Making change in organizations is complex, especially with surgeons who are used to doing this a certain way. Did this present challenges?

Overall, the conclusion should consider not just the mathematical calculations, but the safety, quality, and operational implications for this work. Can this approach be used on all trays or only a subset? Are the authors planning more studies in other specialties or procedures or trays?

As I’ve said, there’s no consideration (as far as I can tell) for the implications in tray assembly, routine maintenance, or replacement of instruments.

**********

7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #2: Yes: Tuerhongjiang Tuxun

Reviewer #3: No

**********

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.]

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.

Attachment

Submitted filename: comments.docx

PLoS One. 2022 Dec 29;17(12):e0276377. doi: 10.1371/journal.pone.0276377.r004

Author response to Decision Letter 1


14 Aug 2022

Dear Dr. Ferrari,

Thank you on behalf of the reviewers for your re-consideration of our manuscript “Standardization of laparoscopic trays using an inventory optimization model to produce immediate cost savings and efficiency gains” to be considered for publication in PLOS ONE. We have taken the time to consider the most recent feedback from the reviewers, and we have made the following changes to the manuscript, submitted in tracked changes and clean versions:

Overall, the focus on mathematical approaches belies some of the nuanced complexities of sterile processing. There are also quite a few areas where more clarification or precision is warranted (e.g. survey response rates; costs ‘per year’ or other). I also don’t feel that the operational consequences have been fully thought through. There is no discussion of how the trays were changed and the new “standard” was introduced into practice.

Looking at the tables detailing the changes, one original tray has more instruments than the final one. Does this mean that the new tray was missing critical instruments for certain procedures, or simply the older tray had legacy instruments that weren’t used (in which case this isn’t just about standardization but also optimization)? Similarly, another original tray has exactly the same number of instruments as the new tray – are these the same or are there differences? Definitely missing here is the consideration – at least a discussion point - not just of the numbers of instruments in a tray, but also the types and uses of instruments.

I think it’s really valuable work, but can’t help thinking it’s ignored many of the real-world implications that may make this appear to be more straightforward that in actually is. Addressing the wider context of the work system in the Introduction and Discussion would make this a much stronger and more relevant paper.

Thank you for these helpful comments. The purpose of this paper was to describe the process of developing a tray that was both mathematically and functionally optimized to serve as a standardization of three existing trays for laparoscopic surgeries. We have included citations to other publications which describe the quality improvement initiatives that were undertaken to operationalize these changes. We have also included more details as to the specific types of instruments that were removed/included, which have also been published in another paper. We thank you for your helpful review, and hope that you find our responses below satisfactory.

INTRO

The first sentence of a paper or abstract is important. Consider qualifying why surgical inventories can be a “source of inefficiency” with some reasons why and / or some effect. Of course, they can also be a source of efficiency.

Thank you for this comment. The first line of the abstract was amended to explain why this domain was chosen as a target for operational efficiency optimization. (Lines 27-28).

The introduction is very short. There is space to expand on the learning from prior work. I’d like to see more on the reasons why there are “limitations preventing practical application.” You could also discuss a little more the methods and results of the other prior studies, especially as you haven’t addressed this in your own work. An extra sentence or 3 would be valuable for establishing how your study builds on this prior work.

Thank you for this comment. Unfortunately, the literature around surgical inventory optimization is lacking, which is noted in the discussion. We have added some context by providing a comment on the barriers to practical application of optimization, and some of the other surgical inventory research. (Lines 58-60 and 65-66).

The introduction doesn’t really go into the challenges or trade-offs of standardization. Including surgeon preferences, generic vs specific uses, or the trade-off between having a range of instruments to cover a broader set of preferences/procedures, which may lead to more instruments in a tray vs specialist trays with less instruments. It might not need that, but I think a little more nuanced thought about the challenges of “standardization” and what it really means would be helpful. Of course, standardization can lead to standardized inefficiency.

Thank you for this helpful comment. While we agree that this discussion is within the scope of this paper, we have elected to carry out an analysis of this topic in the Discussion (Lines 255-260)

In moving on to the methods, I would also like to see more discussion of the background of the “Newsvendor” problem, and the modelling methods chosen. Most readers will be unfamiliar with these. This could be in the intro or methods, but I would suggest the former as that is naturually more discursive.

Thank you for this comment. We agree with your suggestion, and will include background about the Newsvendor problem in the Methods (Lines 84-87).

METHODS

How were procurement & reprocessing costs discovered? What did the “clinical review” of the SL tray involve? How many clinicians? What did they review? Were any operational trials (ie. A clinical review might not reveal missing instruments for all procedures & all surgeons).

Thank you for this comment. Procurement and reprocessing costs were provided by the manager of the MDRD, and we have clarified in Line 108-109. As described in the results section under “User satisfaction and safety”, clinician review involved pre-and post- intervention satisfaction questionnaire. A total of 30 clinicians including 8 surgeons, 12 RNs, and 10 MDR technicians completed the survey measuring their satisfaction with the traditional and standardized inventory. We agree that this clinician review may not review missing instruments for all procedures and all surgeons and have included this as a limitation.

How might this affect scheduling? If you have different procedure-specific trays, simultaneous surgeries would not be an issue. However, instead with “one size fits all” trays you presumably need more of them, or carefully schedule procedures and reprocessing to allow appropriate sharing?

Thank you for this comment. We understand the concern with scheduling. This was considered in calculating the MSQ (minimum stock quantity) which accounts for the general demand for required inventory. As shown by the results, the total stock quantity for GS+GY+GO pre-standardization was 10+8+5=23 trays, and post-standardization, 17 trays. As seen in this case, there is more SLT than any of the GS/GY/GO trays individually, however the standardization processed allowed us to decrease the number of total tray needed in stock.

Might using “mean” demand not immediately disadvantage periods of demand above the mean? Ie. During peak times, trays might not be available if calculations are only done on “means”. I think you allude to this later, but a little more about it in the methods could be useful.

Thank you for this comment. The MSQ not only takes into consideration of the mean demand but as well as the variance in the demand as shown in equation 2 (Line 122), this is essentially the upper bound the number of tray needed routinely (greater than the mean). In addition, another assumption that is made is shown in the cyclic service level assumption (Line 131), which in our study was chosen to be 99%, inferring only 1/100 procedures will not have a tray available.

Did you study or explore the types and uses of instruments in each tray? How did you know it was acceptable to remove some and not others? Are any of your team actively involved in sterile processing, or did you conduct any site vists?

Thank you for this comment. Multiple trained observers were involved in the study by being present in the OR to document instrument usage and being present in the MDRD to document the tray reprocessing process. We have included this information in Line 111. One team member who was not an author on this specific paper was the manager of the MDRD, however, authors JT and JTD conducted many site visits observing both in the OR and MDRD.

How did you make the changes? Did you do this over time or change all the trays over to the standardized ones in one go? How did you ensure that no critical instruments were missing? Some sense or narrative of how you did this would be very informative.

Thank you for this comment. The change to SLT occurred as a single event - we first collected the data from the observers and performed the analysis behind the scenes, then produced a SLT that was then used and tested. We were able to identify that there were no critical instruments missing given the positive user satisfaction. We agree that this is a limitation to ensuring that there will be no incidence of missing critical instruments in the future and have included this point in the limitations.

Where and how were timed observations of instrument reprocessing made? Did this time include decontamination, and assembly? In assembly, did you study the time taken for inspection, functional checking and missing instrument retrieval (as well as ensuring all instruments are present)?

Thank you for your comment. The timed observation of instrument reprocessing was made in the MDRD and by a trained observer. The variables collected have been added to the methods (Line 153-155). This did include the time for decontamination and assembly (including inspection and functional checking). Missing instrument retrieval was a variable collected in the OR observations.

Mean instruments per tray of 17 seems relatively low compared to some trays. Do you think this has implications for generalization of your methods/findings to other trays?

Thank you for your comment. There were 15 instruments on the SLT, which we agree is a decrease from the GS tray at 22 instruments. However, given the high user satisfaction with the SLT, it proved that if not all, at least most of the instruments that were removed from the traditional tray were not often used. In terms of the implication for generalization of our method to standardize trays - the laparoscopic tray is unique in that the majority of the instruments on the tray is used by all 3 specialties GS/GY/GO, and thus allowing us to create 1 tray. This is admittedly more difficult to do with other trays such as Orthopedics trays and we have included this as a limitation (Lines 274-277), however we do have another paper describing alternative optimization processes (Ref #13)

Are the calculated reprocessing costs yearly, monthly, or per procedure? Time scale would be precise here.

Thank you for this comment. Reprocessing costs are calculated annually. We have included that in Line 160.

RESULTS

How can the GS tray have more instruments than the standardized tray? Does this mean that there were redundant instruments in the GS tray, or that 7 extra instruments were needed for any GS procedure? That would make the cost saving calculations misleading. What was the overlap in instruments between the “old” and “new” versions (i.e. which stayed the same, were added, or removed?). Maybe that’s all too much, but the numbers don’t tell us anything about how the new tray differed. That’s really important.

Thank you for your comment. This is an excellent observation. There were unnecessary legacy instruments on the GS tray that were removed to form the SLT. A configuration of the trays used in the study can be found in Table 3 which demonstrate the overlap between the traditional GS, GY, GO trays and the SLT.

Presumably the “standardized” trays basically used the same instruments – so the 15 in GO wer the same 15 in SLT….so aren’t GO and SLT the same tray? If not, presumable in the SLT tray there were instruments that were needed in the GO cases (so important instruments were missing from the SLT); or that some of the instruments in the GO trays were never used (which means this is less about standardization and more about just removing unused instruments).

Thank you for your comment. Again, a very good observation. A step in the standardization process is identifying redundant and infrequently used instruments in the traditional trays and removing them from the trays to be put into peel packs so that they do not have to be reprocessed frequently and at the same time they are still available for use. To put it simply, there were instruments in each of the GS, GY, and GO trays that were infrequently used and thus were removed from the SLT, and the rest of the frequently used instruments were combined and thus producing the SLT. As shown in Table 3, the SLT is distinct to the GS, GY, and GO trays.

There was a lot of dissatisfaction with the customized trays with RNs and MDRs. Why was this?

Thank you for this comment. The dissatisfaction with the traditional customized trays originate from the fact that they are often redundant instruments which makes the set up and instrument selection more tedious. In addition, aside from having redundant instruments, the tray was also frequently missing critical instruments. This was added in Lines 208-210.

How long after the standardization process was the survey delivered? How was it delivered (onoine,paper etc)? How many people was it sent to vs completed it (% response rate?).

Thank you for your comment. The surveys were distributed 1 month pre- and post- standardization. We have included this in Line 202-203. This survey was given on paper and the response rate was 100%.

I could not see any data on the reprocessing times for each instrument (as per the method).

Thank you for this comment. We observed reprocessing times and found minimal variation between instruments, as documented in the paper describing our process.

DISCUSSION

The mathematical focus of this paper ignores many of the operational nuances that may be found in this type of approach.

Thank you for this comment. We have commented on the operational nuances of this intervention and cited the relevant paper in Line 219-220.

“Financial benefits….well documented” – this is a very broad brush. In fact, it’s well documented that the wrong sort of standardization can lead to inefficiencies. Furthermore, standardization and patient-centered care are often in opposition.How do you think your approach would fare with other types of trays e.g. general surgery? These trays often have >100 instruments. What about the trade-offs with

Thank you for this comment. We have described a paper with a similar process of optimizing large trays in other subspecialties in Lines 224-226 and 229-231. Although incorrect standardization can lead to inefficiency and reduced satisfaction, our hybrid model of both computational and clinical optimization describes a novel approach to operative inventory optimization that minimizes the tradeoffs.

How many surgeries required extra instruments (or “peel packs?”)?

Thank you for this insightful comment. Unfortunately, this data was not collected - we have reflected this shortcoming in the Limitations (Lines 264-265)

One challenge with standard trays is that surgeons who trained differently have different preferences. Did you find that this suited some surgeons more than others; that they all used similar approaches; or that the particular procedures you worked on required a standard set of instruments, with little personal or procedural variation? The cost calculations are well discussed but I think this misses a lot of nuanced implications / discussion points.

Thank you for this insightful comment. We have commented on this challenge at length in the quality improvement paper cited here. The present study primarily describes a quantitative and mathematical technique to standardize trays in a novel fashion.

Did you calculate the “lifespan” of the instruments? Presumably if they are being turned over faster, they will need to be replaced sooner?

Thank you for this comment. We address this question in Lines __ (Discussion) where we state that reprocessing and procurement costs were unchanged.

Again, please state over what time period the “savings” (line 220) refer to.

Thank you for this comment. We have specified the time period of savings (annual) in Line 251.

Some trays have rarely used instruments that nevertheless are important to have at the right time. How/are you sure that you didn’t remove instruments like this?

Thank you for this comment. By utilizing a hybrid model of mathematical and clinician review, we mitigated the risk of removing important instruments. Additionally, we ensured that all peel pack instruments were either in the operating room or nearby in the sterile core.

How did the implementation of the new trays happen? Making change in organizations is complex, especially with surgeons who are used to doing this a certain way. Did this present challenges? Overall, the conclusion should consider not just the mathematical calculations, but the safety, quality, and operational implications for this work. Can this approach be used on all trays or only a subset? Are the authors planning more studies in other specialties or procedures or trays? As I’ve said, there’s no consideration (as far as I can tell) for the implications in tray assembly, routine maintenance, or replacement of instruments.

Thank you for this comment. We feel that the model of standardizing the GS/GY laparoscopic tray was an ideal starting point, due to the familiarity and generalizability of the problem. We have used this approach on instrument trays in other specialties, and will continue applying quantitative strategies to address this common problem. We have expanded on some of the safety, quality, and operational implications of this work in the Discussion (Lines 217-227) and Limitations (Lines 268-276).

Thank you for your time and efforts in enhancing our work.

Sincerely,

Jay Toor MD MBA

Orthopaedic Surgery Resident Physician

Department of Surgery

University of Toronto

Tel: 1-416-918-9519

Email: jaysinghtoor@gmail.com

Attachment

Submitted filename: Lap Tray Standardization_Letter_Final.docx

Decision Letter 2

Kush Raj Lohani

6 Oct 2022

Standardization of laparoscopic trays using an inventory optimization model to produce immediate cost savings and efficiency gains

PONE-D-21-17028R2

Dear Dr. Toor,

We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication.

An invoice for payment will follow shortly after the formal acceptance. To ensure an efficient process, please log into Editorial Manager at http://www.editorialmanager.com/pone/, click the 'Update My Information' link at the top of the page, and double check that your user information is up-to-date. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org.

If your institution or institutions have a press office, please notify them about your upcoming paper to help maximize its impact. If they’ll be preparing press materials, please inform our press team as soon as possible -- no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact onepress@plos.org.

Kind regards,

Kush Raj Lohani, Master of Surgery

Academic Editor

PLOS ONE

Additional Editor Comments (optional):

"Suggestions - kindly use the full forms in conclusion for - IOM, GS, GY and GO."

I want to congratulate authors on their vision and hard work on this often overlooked topic. I am confident that this manuscript will get a proper recognition in the Surgical field. Readers will get the sense of necessity on proper planning of their instrument trays for enhancing OR efficiency and lowering the avoidable expenses.

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #2: All comments have been addressed

Reviewer #3: All comments have been addressed

**********

2. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #2: Yes

Reviewer #3: Yes

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #2: Yes

Reviewer #3: Yes

**********

4. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #2: Yes

Reviewer #3: Yes

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #2: Yes

Reviewer #3: Yes

**********

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #2: This paper is now well written and informative. All the concerns have been well answered and the manuscript was well revised.

Reviewer #3: Thank you for addressing the critique. This is much improved and now an excellent paper that I hope get a good audience.

**********

7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #2: Yes: Tuerhongjiang Tuxun

Reviewer #3: No

**********

Acceptance letter

Kush Raj Lohani

17 Nov 2022

PONE-D-21-17028R2

Standardization of laparoscopic trays using an inventory optimization model to produce immediate cost savings and efficiency gains

Dear Dr. Toor:

I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department.

If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org.

If we can help with anything else, please email us at plosone@plos.org.

Thank you for submitting your work to PLOS ONE and supporting open access.

Kind regards,

PLOS ONE Editorial Office Staff

on behalf of

Dr. Kush Raj Lohani

Academic Editor

PLOS ONE

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    S1 File. Contains all the supporting tables and figures.

    (DOCX)

    S1 Data

    (XLSX)

    Attachment

    Submitted filename: Lap Tray Standardization Response to Reviewers.docx

    Attachment

    Submitted filename: comments.docx

    Attachment

    Submitted filename: Lap Tray Standardization_Letter_Final.docx

    Data Availability Statement

    All relevant data are within the paper and its Supporting information files.


    Articles from PLOS ONE are provided here courtesy of PLOS

    RESOURCES