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DOI: 10.1055/a-2645-1463
Single-use versus reusable endoscopes in gastroenterology: Systematic review of full and partial economic evaluations
Supported by: NIHR Health and Social Care Delivery Research Programme NIHR152311
- Abstract
- Introduction
- Methods
- Results
- Discussion
- Conclusions
- References
Abstract
Background and study aims
Future decision making on health care will need to consider broader environmental and sustainability issues. One example is adoption of single-use endoscopes instead of reusable endoscopes in gastroenterology, largely due to their perceived benefit of reducing cross-infection. Besides considerations related to technical performance, there are differences not only in the cost to healthcare but also in the impact they have on the environment. The primary aim of this systematic review was to synthesize evidence on the costs and consequences of using single-use gastrointestinal endoscopes vs. reusable ones adopting various reprocessing methods. The secondary aim was to review and discuss the way in which environmental impact is costed and reported by the studies included in this review.
Methods
We searched multiple databases and the internet to September 2024. We included and quality-assessed partial and full economic evaluations according to predetermined criteria.
Results
Seven studies (2 cost analyses and 5 cost-utility analyses [CUA]) were included. All focused on duodenoscopes for endoscopic retrograde cholangiopancreatography. Five studies compared single-use with reusable duodenoscopes whereas two studies compared different reprocessing methods for reusable duodenoscopes. The most common outcomes were infection risk (n = 6) and quality-adjusted life years (n = 5). Environmental impact was considered in only two studies. All studies stated that the per-procedure cost was higher using single-use endoscopes but three CUAs indicated that single-use endoscopes were more cost-effective. Several studies used doubtful assumptions, reducing their credibility.
Conclusions
Future economic evaluations of single-use vs. reusable endoscopes require more robust comparative evidence and should include costs and consequences beyond health, especially environmental impact.
Keywords
Endoscopy Upper GI Tract - Endoscopy Lower GI Tract - Pancreatobiliary (ERCP/PTCD) - StatisticsIntroduction
Every year, over 22 million endoscopies are undertaken in the United States [1] and approximately 1.5 million in the United Kingdom (UK) [2]. In the UK National Health Service (NHS), most endoscopes are reusable and are used at least hundreds of times after cleaning and disinfection. A recent French study reported usage for an average of 1,280 procedures over the 6-year life span of a reusable gastroscope [3].
Decontamination processes for reusable devices are essential to prevent cross-infection but require considerable resources and chemicals and, consequently, add to the carbon footprint of endoscopy practice. The NHS aims to deliver a net zero carbon emissions target by 2040 [4]. To achieve that, some practices in health care may need to change.
Disposable single-use endoscopes are being marketed on the grounds they reduce or eliminate risk of infection. Their technical performances are comparable to reusable endoscopes [5] [6]. However, if we switch to disposable endoscopes, the cost to health care and to the environment may be much greater [7] due to continuous replacement and waste generation. The primary aim of this systematic review is to synthesize evidence on the costs and consequences of using single-use gastrointestinal endoscopes compared with reusable ones in patients undergoing gastrointestinal endoscopy. The secondary aim is to review and discuss the way in which environmental impact is costed and reported by the studies included in this review. To our knowledge, this is the first systematic review of published economic evaluations of single-use vs. reusable gastrointestinal endoscopes.
Methods
This systematic review follows the reporting guidelines of Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) [8]. The protocol is registered with the international prospective register of systematic reviews (PROSPERO) database (reference number CRD42024465642). The study’s Advisory Group included gastroenterologists and health technology assessment experts.
Search strategy
We searched MEDLINE, Embase, Web of Science, Cochrane Database of Systematic Reviews and CENTRAL, HTA databases (CRD and INAHTA), NHS EED, EconPapers (RePec) and Cost-effectiveness analysis (CEA) Registry up to September 25, 2024, as well as Google Scholar, Google and the NICE, CADTH, and ICER websites. An information specialist (AB) developed search strategies following guidance in the Cochrane Handbook [9]. Searches combined controlled vocabulary terms (e.g. MeSH and EMTREE) with free text keywords and included concepts related to gastrointestinal endoscopy, single-use/disposable, multiple-use/reusable and environmental impact. No language restrictions, date limits, or study type filters were applied. The search strategy was initially developed for searches in MEDLINE (via Ovid) (Supplementary Table 1) and adapted for other databases. Reference lists of identified studies were checked. Literature search results were managed using EndNote 21 software.
Eligibility criteria
Studies were included (or excluded) based on the following criteria:
Format: only full-text articles.
Year: studies published from January 1, 2000.
Language: only studies in English.
Publication status: peer-reviewed journal articles and grey literature. Non-empirical articles (e.g., narrative reviews) were excluded.
Populations: patients undergoing gastrointestinal endoscopy; health care staff involved in the operation, cleaning, reprocessing and disposal of endoscopes.
Intervention: gastrointestinal endoscopy using single-use gastroscopes, sigmoidoscopes, duodenoscopes, colonoscopes. Cholangioscopy was excluded.
Comparator: reusable gastrointestinal endoscopes.
Outcomes: any measure of health (e.g., infections to patients/staff, adverse events [AEs]), patient reported (quality-adjusted life years (QALYs)) and environmental (e.g., carbon footprint); resource use/cost associated with the use of gastrointestinal endoscope (e.g., purchase, reprocessing, repair, treating infection, disposal of endoscopes and their environmental impact).
Study type: full economic evaluations (which consider both costs and consequences as defined by Drummond et al. [10]) and partial economic evaluations (i.e. cost studies, budget impact analyses).
Environmental effects: studies with or without considerations given to environmental effects. Studies solely focusing on environmental effects were excluded.
Country of origin: any country.
Study selection procedure
The main researcher (MZ) and NW screened titles and abstracts of identified publications against the selection criteria. If in doubt, articles were checked based on the full text. Full-text papers were reviewed by two researchers (MZ and LA) and a final decision was made with respect to the inclusion/exclusion criteria. Any disagreements over eligibility of specific studies were discussed. If disagreement persisted, input was sought from an additional reviewer (NW).
Data extraction
Characteristics and findings from the included studies were extracted by one researcher (YJ), using data extraction forms designed for this review with independent checking by another researcher (MZ). Any discrepancies were resolved by discussion or by consensus with an additional reviewer (LA). Extracted information included: 1) details of study (authors, publication year, country, data source, aims/purpose, study population, intervention/s and comparator/s); and 2) a detailed account of the economic evaluation methods and results (type of economic evaluation, model type, study perspective, time horizon, price year/currency, discount rate, outcome measures, resource use/costs, base-case results, sensitivity analyses, generalizability, source of funding, and declared conflicts of interest).
Quality assessment of included studies
The Consensus on Health Economic Criteria (CHEC) checklist [11] was used by one researcher (YJ) to quality assess included studies with independent checking by a second reviewer (MZ). Any discrepancies were resolved by discussion with an additional reviewer (LA).
The CHEC and other health economic checklists do not assess quality of clinical effectiveness studies from which inputs are obtained. Therefore, we checked key clinical assumptions used in cost-utility modelling. These were the proportion of exogenous and endogenous infections after gastrointestinal endoscopy, the proportion of gastrointestinal endoscopes that are contaminated despite standard disinfection processes, and the proportions of patients who develop clinical infection or colonization after endoscopic procedures using a contaminated endoscope.
Results
[Fig. 1] shows that 7,796 records were identified by the literature search, 4,112 were screened after removal of duplicates, 4,069 were excluded based on titles and abstracts, leaving 43 papers considered potentially relevant for full-text assessment, with a further 36 papers excluded (the most common reasons being non-eligible publication status and non-eligible intervention/comparator [Supplementary Table 2]), leaving the final set of seven papers [12] [13] [14] [15] [16] [17] [18].


Details of study context
Study contexts are presented in [Table 1]. Six studies were published between 2020 and 2023 [13] [14] [15] [16] [17] [18]. Four were from the United States [12] [13] [14] [15], and three from Europe [16] [17] [18]. In all studies, patients underwent endoscopic retrograde cholangiopancreatography (ERCP) [12] [13] [14] [15] [16] [17] [18]. Five studies [13] [15] [16] [17] [18] directly compared single-use duodenoscopes with reusable duodenoscopes whereas two studies [12] [14] focused on comparisons between reusable duodenoscopes adopting different reprocessing methods. Four studies specified manufactures (single-use scopes: Boston Scientific [15] [17], Ambu [17] [18]; and reusable scopes: Olympus [16], Pentax Medical [16]). Reprocessing methods included high-level disinfection (HLD), double HLD, culture and hold, and ethylene oxide (EtO) sterilization.
Authors/ year |
Country |
Data source |
Aims/purpose |
Study population |
Intervention |
Comparator |
CBDE, common bile duct exploration; CQ, culture and quarantine; CRE, carbapenem-resistant Enterobacteriaceae; ERCP, endoscopic retrograde cholangiopancreatography; EtO, ethylene oxide; FD, fully disposable; HLD, high-level disinfection; LC, laparoscopic cholecystectomy; MDRO, multidrug-resistant microorganism; NTAP, new technology add-on payment; PD, partially disposable; SRT, surveillance and reprocessing technique; TPT, transitional pass-through payment. |
||||||
Almario et al, 2015 [12] |
USA |
Hypothetical cohort hospitalized and published studies |
To measure cost-effectiveness of four competing strategies for CRE risk management |
A hypothetical cohort of patients hospitalized for symptomatic common bile duct stones and underwent ERCP |
Four competing strategies (see comparator) |
1. ERCP followed by US FDA-recommended reprocessing; 2. ERCP followed by “endoscope culture and hold”; 3. ERCP followed by EtO sterilization of the endoscope; and 4. stop ERCP in lieu of LC with CBDE |
Barakat et al, 2022 [13] |
USA |
Medical center and published studies |
To assess cost of 6 approaches to minimize infection, taking into account duodenoscope-transmitted infection cost |
Patients undergoing ERCP in tertiary care academic medical center and sterile processing division. Mean age of patients 60 years (range, 18–99) |
PD duodenoscope and FD duodenoscope |
Reusable duodenoscope with single HLD, double HLD, EtO sterilization, and culture and hold |
Bomman et al, 2021 [14] |
USA |
Multicenter study (includes two centers with high ERCP volumes) |
To estimate economic impacts of 3 commonly used enhanced-SRT compared to single HLD for performing ERCP |
Patients undergoing ERCP in two institutions (Virginia Mason Medical Centre, Seattle and University of California Los Angeles, CA adopted enhanced-SRT) |
Three used enhanced-SRT (Double HLD, EtO gas sterilization and CQ) for reusable duodenoscope |
Single HLD for reusable duodenoscope |
Das et al, 2022 [15] |
USA |
Simulated cohort, hospital and published studies |
To estimate cost-effectiveness of EXALT single-use duodenoscope versus current duodenoscope |
Simulated cohort undergoing ERCP. Sub analysis for ERCP for Medicare patients in both hospital outpatient for TPT; hospital inpatient for NTAP. Age: 50 (20–90) |
Single-use duodenoscope: (EXALT Model D, Boston Scientific Corp) |
Reusable duodenoscope with current reprocessing methods (Standard HLD, CQ, EtO sterilization) |
Kwakman et al, 2023 [16] |
The Netherlands, USA |
Medical center and published studies |
To investigate costs associated with two scenarios in which single-use duodenoscopes are used in patients carrying MDROs |
Two crossover scenarios, selected patients were treated with single-use duodenoscopes (ERCP) instead of regular reusable duodenoscopes, depending on MDRO carrier status. It was in the Erasmus Medical Centre: Rotterdam, US healthcare |
Single-use duodenoscope |
Reusable duodenoscope: (Pentax Medical, Dodewaard; Olympus, Zoeterwoude) |
Nicolas-Perez et al, 2024 [17] |
Spain |
Hypothetical cohort hospitalized and published studies |
To investigate cost-effectiveness of reusable duodenoscope versus a mixed option that also includes use of a single-use duodenoscope |
A hypothetical cohort of 300 patients undergoing ERCP in Hospital Universitario de Canarias |
Single-use duodenoscope: (EXALT Model D, Boston Scientific Corp: base-case; Ambu aScope Duodenum) |
Reusable duodenoscope |
Travis et al, 2020 [18] |
Denmark |
Clinical data and published studies |
To investigate expected incremental costs and patient outcomes of using a reusable duodenoscope versus single-use Ambu aScope Duodenoscope |
Patients undergone an ERCP |
Single-use duodenoscope: (Ambu aScope Duodeno) |
Reusable duodenoscope |
Economic evaluation methods and results
Details of economic evaluation methods and results are presented in [Table 2], [Table 3], and [Table 4].
Authors/ year |
Type of economic evaluation |
Model type |
Study perspective |
Time horizon |
Price year/currency |
Discount |
Authors/ year |
CRE, carbapenem-resistant Enterobacteriaceae; CUA, cost-utility analysis; DAI, duodenoscope-associated infection; ERCP, endoscopic retrograde cholangiopancreatography; MDRO, multidrug-resistant organism; QALY, quality-adjusted life year; PTC, percutaneous transhepatic cholangiography; UTI, urinary tract infection. |
|||||||
Almario et al, 2015 [12] |
Full economic evaluation (CUA) |
Decision tree model using TreeAge software |
Health care (hospital and payer) |
1 year |
2015/US$ |
N/A |
CRE sepsis had a case fatality rate of 43%. Pretest probability of CRE-infected endoscope is 1%. probability of CRE transmission after ERCP with CRE-infected endoscope is 31%. Assumption that 73% of patients with CRE develops clinical symptoms. Proportion of initial admissions complicated by cholangitis requiring PTC tube placement is estimated to be 23%. QALYs |
Barakat et al, 2022 [13] |
Full economic evaluation (CUA) |
Monte Carlo analysis model in R (used a multistate trial framework) |
Health care |
Post-ERCP lifespan of 7 years |
Not stated/US$ |
Not stated |
MDRO transmission rate after ERCP performed with MDRO-infected duodenoscope: 30%; rate of clinical symptom development in MDRO-infected patients: 50%; rate of survival after MDRO infection: 70%. QALYs lost by ERCP-transmitted infection. Environmental outcome stated |
Bomman et al, 2021 [14] |
Partial economic evaluation (cost analysis) |
N/A |
Not stated. Assumed from perspective of medical center |
1 year |
Not stated/US$ |
N/A |
N/A |
Das et al, 2022 [15] |
Full economic evaluation (CUA) |
Decision tree and Markov models |
Health care |
Lifetime Post-ERCP |
2020/US$ |
2% for both cost and benefits |
Probability of transmission of infection after exposure to contaminated duodenoscope scope with high-concern organism 0.4; probability of clinical infection requiring hospitalization after transmission of high-concern organisms associated with a contaminated duodenoscope 0.5; probability of different types of clinical infections from high-concern organisms: Pneumonia 0.3, Sepsis 0.2, UTI 0.2. QALYs |
Kwakman et al, 2023 [16] |
Partial economic evaluation (Break-even cost analysis) |
Decision tree models involving two crossover scenarios |
From perspective of a large tertiary care academic center |
Not stated |
Not stated/Euro, US$ |
Not stated |
In the analyses, they used three different DAI infection risks; a bare minimum risk of 0.01% and maximum risks of 1% and 1.5% |
Nicolas-Perez et al, 2024 [17] |
Full economic evaluation (CUA) |
Decision tree model using TreeAge software |
Spanish National Health Service |
1 year |
2023/Euro |
N/A |
Risk of infection (probabilities): Infection by MDROs 0.01, cholangitis 0.01. QALYs |
Travis et al, 2020 [18] |
Full economic evaluation (CUA) |
Decision-analytic Markov model |
Hospital |
10 years |
Not stated/US$ |
Not stated |
MDRO infection risk was estimated based on previously published literature. The reusable duodenoscope-related infection risk 1.21%. QALYs |
Authors/year |
Outcomes/resource use and costs |
Largest cost drivers |
Excluded costs |
Methods for estimating/collecting |
AER, automated endoscope reprocessor; CBDE, common bile duct exploration; CQ, culture and quarantine; ERCP, endoscopic retrograde cholangiopancreatography; EtO, ethylene oxide; FD, fully disposable; HLD, high-level disinfection; ICU, Intensive Care Unit; LC, laparoscopic cholecystectomy; PD, partially disposable; UTI, urinary tract infection. |
||||
Almario et al, 2015 [12] |
Direct healthcare costs with each ERCP reprocessing strategy (per procedure), FDA-recommended endoscope: $69, culture and hold: $400, EtO sterilization: $1044; Hospital admissions |
Admissions (e.g., PTC and LC/CBDE with major adverse event: $33,350) |
Litigation, repair, disposal |
Hospital admissions from Healthcare Cost and Utilization Project database. Physician services and procedures |
Barakat et al, 2022 [13] |
Per use cost of each approach: single reprocessing: $130.92, double reprocessing: $188.32, culture and hold: $386.67, EtO sterilization: $643.68, PD duodenoscopes: $251.28, and FD duodenoscopes: $2991.30. Environmental cost stated |
Cost of management of cholangitis was based on 2 days of intensive care unit level care and 1 day of care in a step-down unit ($375,000); FD ERCP: $2,991.30 |
Repair |
Parameters based on their tertiary care academic medical center and sterile processing division. Estimated comprehensive per use cost for each approach values from manufacturers prices |
Bomman et al, 2021 [14] |
Reprocessing cost: Single HLD: $80.47; Double HLD: $117.58; EtO gas sterilization: $296.49; Scope culturing-monitoring: $208.28. Materials: $49.59 single HLD, $74.83 double HLD, $51.28 EtO gas sterilization, $64.53 scope culturing-monitoring. Staff labor: $30.88 single HLD, $42.75 double HLD, $41.08 EtO gas sterilization, $33.95 scope culturing-monitoring. Labor: $109.82 scope culturing-monitoring, $204.13 EtO gas sterilization |
Labor: EtO gas sterilization $204.13, culturing/monitoring $109.82 |
Training, AERs, leak testers, purchase, repair, disposal |
Labor costs were categorized into 3 classes (low, mid, high): gastrointestinal tech III salary/hour. Estimated cost of capital as scope inventory/frequency of scope use per unit time, reprocessing costs required on a per-cycle basis; labor & staffing needs |
Das et al, 2022 [15] |
Standard HLD: $962; Double HLD: $977; CQ: $1,279; EtO gas sterilization: $1,561; EXALT Model D: $3,000; EXALT Model D in HIPD setting with NTAP estimated to offset $1,715 of SUD cost: $1,285; EXALT Model D in HOPD setting with TPT payment offsetting 100% of SUD cost: $0. Per use average cost of reprocessing: standard HLD: $200, double HLD: $215, CQ: $480, EtO sterilization: $1,180. Maintenance is included in reprocessing costs |
Sepsis: $50,038 Cholangitis: $40,000 Misc. infection: $38,494 UTI: $33,400 Pneumonia: $30,432 EXALT Model D: $3,000 |
Caregiving time, physician services, litigation, disposal |
Hospital costs of management of choledocholithiasis, post-ERCP contaminated scope; and infection adverse events cost: 2018 weighted national estimated inpatient diagnoses; and published literature |
Kwakman et al, 2023 [16] |
Price per ERCP procedure (reusable duodenoscopes): €180. Reusable: purchase (€39,309 per duodenoscope, €100 per ERCP procedure), reprocessing (€47 per ERCP procedure), maintenance (€2,500 (per year) per duodenoscope; €22 per ERCP procedure), surveillance culturing (€ 110 (per surveillance moment) per duodenoscope, €11 per ERCP procedure). Details of reprocessing cost was not stated |
Costs for a duodenoscope-associated infection (cholangitis) total €6,774 per infection |
Staff, specific instruments, productivity losses, disposal |
Costs of materials, staff based on estimates from their own department at the Erasmus Medical Centre.US: They performed same break-even analyses for a US scenario |
Nicolas-Perez et al, 2024 [17] |
Single-use per-procedure cost: €2,900. Reusable per procedure cost: €1,333. Reprocessing, maintenance costs for reusable included but values not stated. Environmental cost stated |
Single-use purchase: €2,900, Reusable ICU bed: €2,651 |
Not stated |
Single-use scope. Reusable scope: average cost of ERCP in hospital and literature |
Travis et al, 2020 [18] |
Single-use: total per-procedure cost: $1,999. Reusable: weighted per-procedure cost in Markov model: $1,017. Purchase per use: single use: $1,995, reusable: $722. Equipment reprocessing: AER, supplies (e.g., sponges, brushes, and detergents), labor; reprocessing: $103, Reusable: microbiological sampling, culturing: $110, repair/maintenance: $83, Single: cost for a Box: $4 |
Endoscope-related MDRO infection cost $47,181; Purchase per use: single use: $1,999 |
Loss of earning, disposal |
Per-procedure cost of reusable, cost of treating infection derived from a US multicenter micro-costing study. Infection risks, utilities, other parameters obtained from literature. Cost of single-use: Ambu |
Authors/year |
Results (ICER, e.g., incremental costs and outcomes) |
Sensitivity analyses |
Funding source |
Declared conflicts |
CBDE, common bile duct exploration; CRE, carbapenem-resistant Enterobacteriaceae; CUA, cost-utility analysis; CQ, culture and quarantine; ERCP, endoscopic retrograde cholangiopancreatography; EtO, ethylene oxide; FD, fully disposable; HLD, high-level disinfection; LC, laparoscopic cholecystectomy; PD, partially disposable; QALY, quality-adjusted life year; SUD, single-use duodenoscope. |
||||
Almario et al, 2015 [12] |
ERCP with FDA most cost-effective strategy. Both ERCP with culture and hold ($4,228,170/QALY) and ERCP with EtO sterilization ($50,572,348/QALY) strategies had unacceptable incremental costs/QALY. LC with CBDE being more costly, marginally less effective |
A number of one-way sensitivity analyses. In sensitivity analysis, ERCP with culture and hold became the most cost-effective approach when pretest probability of CRE exceeded 24% |
Not stated |
All authors do not have any relevant disclosures or conflicts of interest |
Barakat et al, 2022 [13] |
At infection transmission rates <1%, PD duodenoscopes most favorable from a CUA. FD duodenoscope minimizes potential for infection transmission and is more favorable from a CUA than use of reprocessable duodenoscopes after single or double HLD at all infection rates, EtO sterilization for infection rates >.32%, and culture and hold for infection rates >.56% |
Alternate scenarios of variation in hospital volume, QALY value, post-ERCP lifespan, environmental cost shifted cost-utility profiles. A sensitivity analysis for cost of treatment. With it, PD duodenoscope remained approach most favorable from a CUA |
Not stated |
Banerjee disclosed financial relationships: Consultant for Boston Scientific and Olympus. Other authors disclosed no financial relationships |
Bomman et al, 2021 [14] |
Compared to single HLD, double HLD increased costs by 47% ($80 vs $118). Similarly, CQ and EtO sterilization increased costs by 160% and 270 % ($80 vs $208 and $296) |
Not stated |
Not stated |
Kozarek receives research support from Boston Scientific, National Institutes of Health. Thaker is a consultant for, receives research support from Boston Scientific. Muthusamy is a consultant for, receives research support from Boston Scientific, Medtronic; a consultant for Medivators, Interpace Diagnostics; a stockholder in Capsovision; receives honoraria from Torax Medical. Ross a consultant for Boston Scientific |
Das et al, 2022 [15] |
EXALT provided highest cost-savings to the hospital versus alternative strategies by maintaining QALY gains while decreasing estimated net cost |
Sensitivity analyses were performed by varying cost estimates and clinical probabilities |
Stated "None" |
MC is an employee and stockholder of Boston Scientific Corp, which manufacturers the EXALT Model D single-use duodenoscope |
Kwakman et al, 2023 [16] |
In Dutch situation, single-use duodenoscopes needed to be priced at a maximum of € 140 to € 250 to break-even |
Sensitivity analysis of DAI costs with a 20% and 40% increase of the separate variables included in the Erasmus MC |
Not stated |
The authors declare that they have no conflict of interest |
Nicolas-Perez et al, 2024 [17] |
Considering cholangiopancreatographies with single-use and reusable duodenoscopes at a cost of €2900 and €1333 respectively, and a 10% rate of single-use duodenoscopes, the ICER is € 3,967,917/QALY: base-case |
Deterministic and probabilistic sensitivity analyses. 2- and 3-way sensitivity analysis confirmed increasing values of reusable ERCP and decreasing values of SUD-ERCP favored SUD-ERCP |
Not stated |
The authors declare that they have no conflict of interest |
Travis et al, 2020 [18] |
An additional cost of $28,525 per QALY, using an estimated cost of $1,995 per single-use duodenoscope. Thus, single-use duodenoscopes are cost-effective at a WTP threshold of $50,000 per QALY |
Deterministic, probabilistic sensitivity analyses. A one-way sensitivity analysis to check results after changing cost of infection treatment. Cost $80,000-$85,000 to make single-use dominant |
No financial support |
HST, RVR, SA, and SL are employed by Ambu A/S, Ballerup, Denmark. NBL declared no conflicts of interest |
Type of economic evaluation
There were five cost utility analyses [12] [13] [15] [17] [18] and two cost analyses [14] [16].
Type of modelling approach
Six studies employed a decision-analytic model [12] [13] [15] [16] [17] [18]. Almario et al. used a decision tree model to evaluate a cohort of patients with common bile duct (CBD) stones to measure cost-effectiveness of four strategies for carbapenem-resistant Enterobacteriaceae (CRE) risk management [12]. Barakat et al. developed a Monte Carlo analysis model to assess cost utilities of six approaches to minimizing infection transmission for all patients having ERCP [13]. Das et al. constructed a decision tree model for patients with CBD stones to project consequences of contaminated scopes, with a Markov model to simulate colonization’s, infections, and treatment of infection [15]. Kwakman et al. used decision tree models involving two crossover scenarios based on presence or absence of multidrug-resistant organism (MDRO) carriage [16]. Nicolas-Perez et al. used a decision tree model to compare two ERCP modalities in a hypothetical cohort of 300 patients (case mix not reported) undergoing ERCP [17]. Travis et al. used a decision-analytic Markov model to compare the total cost and utilities [18].
Perspective, time horizon, discount rate, and price year/currency
Six studies were from a healthcare provider perspective [12] [13] [15] [16] [17] [18]. Bomman et al. did not state their perspective but it appeared to be that of healthcare provider [14]. The time horizons ranged from 12 months [12] [14] [17] to lifetime [15]. Three studies justified their choice of horizon [12] [13] [17]. Kwakman et al. did not state their time horizon [16]. In three studies [12] [14] [17], discounting was unnecessary as the time horizons were 1 year [10]. Three studies did not state a discount rate [13] [16] [18]. Das et al. [15] reported an annual discount rate of 2% for both costs and benefits. The US Second Panel on Cost-Effectiveness in Health and Medicine recommends using a discount rate of 3% [19]. Only three studies specified their price year [12] [15] [17]. We converted currencies to 2024 British Pound Sterling (GBP) using the Bank of England exchange rates database and inflation calculator [20] [21]. When price years were not reported, we used 1 year before publication.
Outcomes consequences measures
The most common outcomes were QALYs (n = 4) [12] [13] [15] [18] and infection risk (n = 5) [12] [13] [15] [16] [18].
QALYs
Five studies reported QALYs. Almario et al. [12] used QALYs as main outcome measure based on health state utilities from the Tufts Cost-Effectiveness Analysis Registry. Utility estimates were 0.50 (0.40–0.60) for CRE-related sepsis; 0.80 (0.70–0.90) for post CRE sepsis survival; 0.89 (0.79–0.95), 0.88 (0.78–0.95), and 0.76 (0.66–0.86), respectively, for ERCP without, with minor, and with major AEs. Barakat et al. [13] simulated QALYs lost by infection but the numbers lost were not reported. Das et al. [15] derived utility values of post-ERCP health states from literature, and estimated QALYs based on a post ERCP lifetime horizon. Reported utility value for an individual in full health was 1 (0.9–1.0), utility value with long-term colonization with high-concern organisms was 0.9 (0.85–1.0), disutility value of hospitalization for clinical infection was 0.06 (-0.02 to -0.15), and disutility value of Intensive Care Unit (ICU) admission was 0.11 (-0.06 to -0.34). QALY estimates for different reprocessing methods including standard HLD, double HLD, culture and quarantine, EtO sterilization, and for single-use EXALT Model D were 21.8938, 21.8938, 21.8904, 21.9093, and 21.9265, respectively. In Nicolas-Perez et al. [17], QALYs were estimated to determine effectiveness of each approach. Utility estimates were 0.76 for cholangitis and 0.9 for without adverse outcome. Travis et al. [18] obtained utility scores through literature of 0.881 for no infection, 0.275 during infection, 0.639 during the 12 months after infection, and 0 for death. Based on a 10-year time horizon, estimated QALYs for reusable and single-use duodenoscopes were 6.58 and 6.70, respectively.
Risk of infection and adverse events
Six studies reported probabilities of ERCP-related infections using reusable endoscopes. Almario et al. [12] assumed that probability of endoscopes being contaminated by CRE was 1% (Supplementary Table 3), and that the chance of transmitting CRE following an ERCP procedure using a contaminated endoscope was 31%, and 73% of those patients with CRE would develop clinical infections. This indicated an overall infection rate of 0.2%. The case fatality rate for CRE-induced sepsis was 43%. In addition to exogenous infections caused by contaminated duodenoscopes, Almario et al. [12] also incorporated a proportion (23%) of admissions with preexisting cholangitis into their model. Barakat et al. [13] assumed a transmission rate of MDRO after ERCP using a contaminated duodenoscope of 30%, with 50% of infected patients developing clinical symptoms; the post-infection survival rate was 70%, derived from infectious disease experts and literature reviews. Das et al. [15] used published information and assumed that the duodenoscope contamination rate of high-concern organism after standard HLD was 6%, and the probability of infection from contaminated duodenoscopes was 40%, giving an overall infection rate of 2.4%. 50% of the infected patients required hospitalization, 10% to ICU. Among infections, probabilities for pneumonia, sepsis, and urinary tract infections (UTIs) were 30%, 20%, and 20%, respectively. Long-term colonization with high-concern organisms could occur. Kwakman et al. [16] used three risk levels of duodenoscope-associated infections (DAI): a minimal risk of 0.01% from reviews of Dutch DAI outbreaks, and higher risks of 1% and 1.5% from US analyses. Nicolas-Perez et al. [17] reported probabilities of infection by MDROs 0.01 and cholangitis 0.01. Travis et al. [18] estimated MDRO infection risks to be 1.21% for reusable duodenoscopes (Supplementary Table 3) and the post-infection mortality rate to be 19%.
Outcomes/resource use and costs
Resource use and costs varied according to the study purpose, case mix of patients, time horizon and the intervention and comparator.
Total/average, purchase, reprocessing, maintenance/repair costs per procedure
All studies included reprocessing costs (mainly labor, and equipment/material expenses). Six included purchase costs [12] [13] [15] [16] [17] [18]. Repair and infection costs were respectively included by four [15] [16] [17] [18] and six studies [12] [13] [15] [16] [17] [18]. All studies stated that cost per procedure was greater using single-use endoscopes. Reprocessing cost was lowest using standard HLD and was progressively more expensive in the order of using double HLD, culture and hold, and EtO sterilization (Supplementary Table 4).
Costs of ERCP-related infections
Using the Healthcare Cost and Utilization Project database, Almario et al. [12] estimated cost of hospital admission for CRE to be $32,915 (£28,215) ($28,000 (£24,002) -$38,000 (£32,574)). Barakat et al. [13], with a cohort of 800, reported a mean cost of $3125 (£2723) of cholangitis management for MDRO-infected patients who developed clinical symptoms based on 2 days of care in an ICU followed by 1 day of care in a step-down unit at their center. In their cohort of 10,000 patients, Das et al. [15] used the Premier Research database to derive treatment costs of high-concern organisms related infections of $50,038 (£49,404) for sepsis; $40,000 (£39,493) for cholangitis; $38,494 (£38,006) for infections in soft tissue, skin, and surgical site; $33,400 (£32,977) for UTI; and $30,432 (£30,046) for pneumonia. Kwakman et al. [16] calculated total treatment cost for a DAI of €6,774 (£6,452) at Erasmus Medical Centre in 2015. They also analyzed a US scenario in which DAI treatment cost was $20,119 (£18,435) based on costs from the US HCUPnet database. Nicolas-Perez et al. [17] obtained infection-related costs (hospital bed, ICU bed) from their hospital and length of hospital stay based on assumptions and published literature; however, total estimated cost for specific infection is not clear from the given data. Travis et al. [18] also used the HCUPnet database and estimated a mean cost of MDRO infection treatment of $47,181 (£46,242).
Environmental costs
Environmental impact was considered in only two studies. Barakat et al. [13] estimated environmental costs of ($35 (£31) for single reprocessing, $55 (£48) for double reprocessing, $100 (£87) for EtO sterilization, $60 (£52) for culture and hold, $80 (£70) for disposable endcap, and $150 (£131) for disposable duodenoscope) including chemicals, fumes/pollutants, and disposable solid waste. Nicolas-Perez et al. [17] estimated recycling cost of single-use and reusable duodenoscopes as €150 (£130) and €35 (£30) respectively.
Largest cost drivers and excluded costs
The largest cost drivers were managing infection for reusable scopes [12] [13] [15] [16] [17] [18] and the purchase price for disposable scopes [13] [15] [17] [18]. Some costs were excluded, most commonly disposal (n = 5) [12] [14] [15] [16] [18], repair (n = 3) [12] [13] [14], and purchase (n = 1) [14] costs. Costs due to litigation were not mentioned by any studies. Other costs excluded by some studies were: training, automated endoscope reprocessors (AERs), and leak testers [14]; caregiving time and physician services [15]; staff, productivity losses [16]; and loss of earning [18].
Sensitivity analysis undertaken
Bomman et al. did not perform any SA [14]. The six model-based studies conducted at least one SA. Almario et al. had one-way SA [12]. Barakat et al. used five SAs to explore the impact of alternative input values [13]. Das et al. used a probabilistic SA [15]. Kwakman et al. used two SA of alternative input values [16]. Nicolas-Perez et al. [17] and Travis et al. [18] had a number of deterministic/probabilistic SAs.
Synthesis of incremental costs, outcomes and cost-effectiveness evidence
Almario et al. [12] stated that ERCP with the Us Food and Drug Administration-recommended reprocessing was the most cost-effective strategy for mitigating CRE transmission risk. Barakat et al. [13] concluded that at infection rates < 1%, partially disposable (PD) duodenoscopes were most favorable. They noted that the fully disposable (FD) duodenoscope minimizes potential for infection transmission and is more favorable from a CUA than use of reusable duodenoscopes after single or double HLD at all infection rates, EtO sterilization for infection rates > 0.32%, and culture and hold for infection rates > 0.56%. Alternate scenarios of variation in hospital volume, QALY value, and post-ERCP lifespan shifted cost-utility profiles. Incorporating environmental cost reduced cost utility of FD duodenoscopes, but did not change the overall ranking of these approaches. Bomman et al. [14] indicated that compared with single HLD, adoption of double HLD increased costs of ERCP by 47%. Similarly, culture and hold and EtO sterilization increased costs by 160% and 270%, respectively. Das et al. [15] noted that device-specific reimbursement for EXALT (single-use duodenoscope) in the United States provided the greatest cost-savings to the hospital by decreasing estimated net costs of ERCP. Kwakman et al. [16] concluded that in the Netherlands, single-use duodenoscopes needed to be priced at a maximum of €140 (£133) to €250 (£238) to break even. Travis et al. [18] indicated an additional cost of $28,525 (£27,957) per QALY, using a cost of $1,999 (£1,959) per ERCP procedure using single-use duodenoscopes. They stated that single-use duodenoscopes are cost-effective at a willingness-to-pay (WTP) threshold of $50,000 (£49,005) per QALY. Nicolas-Perez et al. [17] in their base-case analysis stated that considering ERCP with single-use and reusable duodenoscopes at a cost of €2,900 (£2,518) and €1,333 (£1,157) respectively, and a 10% rate of single-use duodenoscopes, the ICER is €3,967,917 (£3,444,930)/QALY. Due to diversity of studies, meta-analysis was not feasible.
Generalizability
Das et al. [15] and Nicolas-Perez et al. [17] did not report on generalizability of their results. Almario et al. [12] noted that their findings from CBD stone patients may not be generalizable to all indications for ERCP, although they tried to generate results relevant to most settings. Barakat et al. [13] noted limitations of their model including cost and infection rate assumptions and potential lack of generalizability to lower-volume centers. Bomman et al. [14] did not include service costs, training costs, capital costs of reprocessing equipment, and other costs of maintaining the instruments and costs of enhanced surveillance and reprocessing techniques; therefore, their estimates are probably conservative compared with real life. They attributed the differences between their results and Barakat et al. [13] to variability of technique, labor, and materials costs and labor costs. Kwakman et al. [16] noted that costs for using reusable duodenoscopes differ greatly among institutions depending on ERCP volume, contracts with manufacturers, organization of reprocessing, MDRO prevalence rates, and time needed for testing MDRO carriage. Therefore, generalizability of their findings to other settings is uncertain. Travis et al. [18] noted that per-procedure cost of reusable ERCPs is highly dependent on annual volume, amount of capital equipment, and reprocessing setup.
Funding source and conflict of interest
Five studies did not state funding source [12] [13] [14] [16] [17]. Despite not declaring any financial support by two studies [15] [18], at the time of publication, several named authors were employed by the manufacturers of single-use endoscopes. Four studies reported potential conflict of interest [13] [14] [15] [18] and three studies reported none [12] [16] [17].
Quality assessment of included studies
We used the 19-item CHEC checklist [11] ([Table 5]). None of the studies fulfilled all the quality criteria although none were ranked as “worthless”. Most studies had very good reporting quality. The least well-addressed criteria were items 7 (all important/relevant costs identified?), 14 (discounted?), 18 (conflicts of interest?) and 19 (ethical and distributional issues?).
Study |
Item |
||||||||||||||||||
1 |
2 |
3 |
4 |
5 |
6 |
7 |
8 |
9 |
10 |
11 |
12 |
13 |
14 |
15 |
16 |
17 |
18 |
19 |
|
Y, yes; N, no; NA, not applicable; NC, not clear. |
|||||||||||||||||||
Almario et al, 2015 [12] |
Y |
Y |
Y |
Y |
Y |
Y |
N |
Y |
Y |
Y |
Y |
Y |
Y |
NA |
Y |
Y |
Y |
Y |
N |
Barakat et al, 2022 [13] |
Y |
Y |
Y |
Y |
Y |
Y |
Y |
Y |
Y |
Y |
Y |
NC |
NC |
N |
Y |
Y |
Y |
N |
N |
Bomman et al, 2021 [14] |
Y |
Y |
Y |
Y |
Y |
NC |
N |
Y |
Y |
NA |
NA |
NA |
NA |
NA |
N |
Y |
Y |
N |
N |
Das et al, 2022 [15] |
Y |
Y |
Y |
Y |
Y |
Y |
N |
Y |
Y |
Y |
Y |
Y |
Y |
Y |
Y |
Y |
N |
N |
Y |
Kwakman et al, 2023 [16] |
Y |
Y |
Y |
Y |
NC |
Y |
N |
Y |
Y |
NA |
NA |
NA |
NA |
N |
Y |
Y |
Y |
Y |
Y |
Nicolas-Perez et al, 2024 [17] |
Y |
Y |
Y |
Y |
Y |
Y |
N |
NC |
NC |
Y |
Y |
Y |
Y |
NA |
Y |
Y |
N |
Y |
N |
Travis et al, 2020 |
Y |
Y |
Y |
Y |
Y |
Y |
Y |
Y |
Y |
Y |
Y |
Y |
Y |
N |
Y |
Y |
Y |
N |
N |
Item 1 Is the study population clearly described? |
|||||||||||||||||||
Item 2 Are competing alternatives clearly described? |
|||||||||||||||||||
Item 3 Is a well-defined research question posed in answerable form? |
|||||||||||||||||||
Item 4 Is the economic study design appropriate to the stated objective? |
|||||||||||||||||||
Item 5 Is the chosen time horizon appropriate to include relevant costs and consequences? |
|||||||||||||||||||
Item 6 Is the actual perspective chosen appropriate? |
|||||||||||||||||||
Item 7 Are all important and relevant costs for each alternative identified? |
|||||||||||||||||||
Item 8 Are all costs measured appropriately in physical units? |
|||||||||||||||||||
Item 9 Are costs valued appropriately? |
|||||||||||||||||||
Item 10 Are all important and relevant outcomes for each alternative identified? |
|||||||||||||||||||
Item 11 Are all outcomes measured appropriately? |
|||||||||||||||||||
Item 12 Are outcomes valued appropriately? |
|||||||||||||||||||
Item 13 Is an incremental analysis of costs and outcomes of alternatives performed? |
|||||||||||||||||||
Item 14 Are all future costs and outcomes discounted appropriately? |
|||||||||||||||||||
Item 15 Are all important variables, whose values are uncertain, appropriately subjected to sensitivity analysis? |
|||||||||||||||||||
Item 16 Do the conclusions follow from the data reported? |
|||||||||||||||||||
Item 17 Does the study discuss the generalizability of the results to other settings and patient/ client groups? |
|||||||||||||||||||
Item 18 Does the article indicate that there is no potential conflict of interest of study researcher(s) and funder(s)? |
|||||||||||||||||||
Item 19 Are ethical and distributional issues discussed appropriately? |
Discussion
Our systematic review set out to assess all economic evaluations comparing single-use and reusable gastrointestinal endoscopes adopting various reprocessing strategies, although all included studies focused on duodenoscopes, where cross-infection was a particular concern. Lack of economic evaluation for other types of single-use gastrointestinal endoscopes was an important finding in its own right, because lack of cost-effectiveness evidence could serve as a precaution and a barrier to their wider adoption. Among the duodenoscope studies, per-procedure cost was higher using single-use endoscopes but three CUAs indicated that single-use endoscopes were more cost-effective. However, we have considerable reservations about the underlying clinical estimates (Supplementary Table 3).
Disutility value of hospitalization for clinical infection and disutility value of ICU admission reported by Das et al. [15] seemed very conservative. Utility scores during infection reported by Travis et al. [18] seemed very low considering that some were UTIs.
Infections after ERCP are a mixture of exogenous (organism from outside the body, for example from a contaminated endoscope) and endogenous (organism already present but moved from one part of the gastrointestinal tract into another) so assumptions of no infections should not be made for single-use endoscopes. Barakat et al. [13] and Travis et al. [18] made an assumption of no infection following ERCP with a single-use duodenoscope. However, Hutfless et al [22], reported a 3.5% infection rate following ERCP with single-use duodenoscopes. Because the CUAs assumed no infection risk with a single-use scope, this is likely to have introduced significant bias into their analysis.
There was significant variation in reported rates of scope contamination, ranging from 1%. [12] to 6% [15] [18]. Das et al. [15] cited several studies reporting 6% contamination rate. However, on review of the cited references, the authors could not find support for this assumption. However, the authors did note an FDA report from 2020 [23] reporting similar rates of scope contamination.
Almario et al. [12] assumed a transmission rate from a contaminated duodenoscope of 31% but the references they cited do not support that figure, and the cited references have a much higher ratio of infection (73%) to colonization than other studies (Supplementary Table 3). Barakat et al. [13] assumed a similar figure for transmission but that only half result in clinical infections with half only colonized. Das et al. [15] assumes 40% transmission but based on “expert opinion” and it appears that all 40% are infections not colonizations. Therefore, we have concerns about the variability of assumptions in and findings of the CUAs.
Infection costs had the most impact on cost-effectiveness calculations. In the Barakat et al study [13], the cost of cholangitis management was $3,125 (£2,723). Treatment costs in other studies ranged from €6,774 [16] (£6,452) to $50,038 [15] (£49,404). Per-procedure cost of reusable duodenoscopes is dependent on infection rates, ERCP volume, number of endoscopes and associated equipment, and reprocessing costs [18] [24] [25]. High purchase costs can be partially offset by labor, capital, and equipment/material expenses associated with different reprocessing approaches. Enhanced reprocessing methods could reduce infection risk but also increase cost of ERCP [13].
The broader impact of endoscopy on the environment and ultimately human health is receiving increasing attention [26] [27]. Le et al. [26] performed a life-cycle assessment comparing single-use and reusable duodenoscopes. Carbon emissions during manufacturing, reprocessing, and disposal of the scopes were evaluated, and emissions associated with single-use scopes were 24 to 47 times higher than reusable ones. Moreover, 90% of materials in single-use duodenoscopes are plastics, processing and accumulation of which may cause negative environmental and health impacts [17] [28] [29]. Only two of the included papers [13] [17] incorporated environmental impacts in their economic evaluations, both as costs, without providing detailed rationale or calculations. The environmental costs they identified (waste or recycling costs) did not account for the full life-cycle of endoscopes and reprocessing strategies, potentially leading to underestimation of the environmental impacts.
There are challenges in assigning monetary values to environmental impacts but efforts are being made to develop methodologies for this type of economic evaluation [30]. Hensher [31] suggested the environmental impact can be incorporated into health economic evaluation, preferably using a cost-based approach to monetarily represent AEs caused by one additional ton of CO2 equivalent emission. This approach has been used by de Preux and Rizmie [32] to internalize greenhouse gas emissions as a cost within a cost-effectiveness analysis of different modes of hemodialysis delivery in the UK NHS, using a non-traded price of carbon (nTPC) of £52 (£78) per ton, which would add 0.7% to 1.3% to total costs.
In the studies reviewed, endoscope choice was primarily driven by healthcare costs. However, there is growing interest in sustainability, which has raised valid questions about conflicting findings and necessary trade-offs between cost-effectiveness and environmental impact. As part of our broader SUMU Endo project, we are currently assessing environmental impacts, including conducting a life-cycle assessment to translate these impacts into monetary terms for integration into cost-effectiveness analyses. In our view, future decisions regarding endoscope use are likely to be influenced by both healthcare costs and environmental impacts among other patient, clinical, and service delivery considerations. Therefore, determining the appropriate weight to assign to each factor will be crucial—particularly when they point in different directions. We believe that, ultimately, the decision may come down to local policy.
Strengths and limitations of this review
We used a comprehensive search strategy of a broad range of electronic databases and grey literature. We quality assessed economic evaluations. Limitations included the shortcomings of the included studies, which are partly due to the evidence base at their timepoints. This systematic review may be affected by publication bias because unfavorable economic analysis of novel devices is less likely to reach publication. Some studies are supported by the manufacturers of single-use devices, and they may be reluctant to published unfavorable results.
Conclusions
All studies stated that cost per procedure was greater using single-use endoscopes but three CUAs argued that using single-use endoscopes was more cost-effective. We have reservations about these studies due to the lack of support for their clinical effectiveness assumptions and inputs. Importantly, costs and consequences of single-use duodenoscopes would change if environmental costs and impacts were included. To achieve sustainable healthcare/balance sustainability and cost-effectiveness, life-cycle assessments that capture environmental impacts are needed, and future economic evaluations should incorporate these broader considerations beyond health.
Conflict of Interest
The authors declare that they have no conflict of interest.
Acknowledgement
This study was funded by the NIHR Health and Social Care Delivery Research Programme. https://fundingawards.nihr.ac.uk/award/NIHR152311. We invited four manufacturers of endoscopes to comment on a draft of this review, and we thank Olympus and Boston Scientific for useful comments while absolving them from any errors in the final article. "SUMU Endo" project group: Mojtaba Ahmadinozari, Stuart Coles, Anjan Dhar, Julia Gauly, Amy Grove, Bu'Hussain Hayee, Thomas Matthews, Violet Matthews, Poonam Parmar, Shaji Sebastian, Natalie Tyldesley-Marshall
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Correspondence
Publication History
Received: 11 December 2024
Accepted after revision: 28 May 2025
Article published online:
29 July 2025
© 2025. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/).
Georg Thieme Verlag KG
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Mandana Zanganeh, Yufei Jiang, Norman Waugh, Anna Brown, Yen-Fu Chen, Ramesh P. Arasaradnam, Lazaros Andronis. Single-use versus reusable endoscopes in gastroenterology: Systematic review of full and partial economic evaluations. Endosc Int Open 2025; 13: a26451463.
DOI: 10.1055/a-2645-1463
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