Literature DB >> 35700207

Cost-effectiveness analysis of bundled innovative devices versus standard approach in the prevention of unscheduled peripheral venous catheters removal due to complications in France.

Franck Maunoury1,2, Bertrand Drugeon3, Matthieu Boisson4,5, Nicolas Marjanovic3, Raphael Couvreur3,4, Olivier Mimoz3,4,6, Jeremy Guenezan3,4,6.   

Abstract

The objective of the study was to perform a cost-effectiveness analysis of bundled devices (BDs) versus standard devices (SDs) for the prevention of unscheduled peripheral venous catheter (PVC) removal due to complication from a French investigator-initiated, open-label, single center, randomized-controlled, two-by-two factorial trial (CLEAN-3 study). A 14-day time non homogeneous semi-markovian model was performed to be fitted to longitudinal individual patient data from CLEAN-3 database. This model includes five health states and eight transitional events; a base case scenario, two scenario analyses and bootstrap sensitivity analyses were performed. The cost-effectiveness criterion was the cost per patient with unscheduled PVC removal avoided. 989 adult (age≥18 years) patients were analyzed to compare the BDs group (494 patients), and the SDs group (495 patients). The assessed intervention was a combination of closed integrated catheters, positive displacement needleless-connectors, disinfecting caps, and single-use prefilled flush syringes compared with the use of open catheters and three-way stopcocks for treatment administration. For the base case scenario, an unscheduled 1st PVC removal before discharge was significantly more frequent in the SDs group (235 patients (47.5%) in the SDs group and 172 patients (34.8%) in the BDs group, p = 0.00006). After adjustment for 1st catheter time, the number of patients with unscheduled PVC removal per day was of 16 (95%CI: 15; 18) patients (out of 100) in the BDs group and of 26 (95%CI: 24; 28) patients (out of 100) in the SDs group. The mean cost per patient (adjusted on catheter-time) was of €144 (95%CI: €135-€154) for patients in the SDs group versus €102 (95%CI: €95-€109) for patients in the BDs group; the mean saving per patient was of €42 (95%CI: €32-€54). As a consequence, the assessed BDs strategy was less costly and more effective than the SDs strategy. Trail registration: CLEAN-3 study is registered with ClinicalTrials.gov, NCT03757143.

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Year:  2022        PMID: 35700207      PMCID: PMC9197036          DOI: 10.1371/journal.pone.0269750

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.752


Introduction

Short-term peripheral venous catheters (PVCs) are the most commonly used invasive medical devices in hospitals, with about 2 billion sold annually worldwide [1]. Unfortunately, peripheral venous catheters (PVC) often fail before the end of treatment due to complications occurrence, including catheter occlusion, skin infiltration (diffusion), phlebitis, catheter dislodgement, and bloodstream or local infections [2]. These complications lead to interruption of treatment, which can be detrimental to patients. Catheter replacement causes pain and induces additional costs [3]. Additionally, bloodstream infections prolong hospitalization and increase treatment costs and mortality [4]. CLEAN-3 clinical study [5], an investigator-initiated, open-label, single center, randomized, two-by-two factorial, superiority trial was performed in 2019 at Poitiers University Hospital, France. Adult patients, visiting the emergency department (ED), with an indication for hospitalization in a medical ward and a PVC for a predicted duration of at least 48 hours were included in the study. Patients were monitored daily for catheter-related complications for up to 48 hours after catheter removal, or earlier if discharged from hospital. The CLEAN-3 study compares two different approaches to peripheral vascular access. The first one consisted of a bundle of new devices including closed integrated catheters, positive displacement needleless-connectors, disinfecting caps, and single-use prefilled flush syringes. The second was simply a conventional peripheral venous catheter to which the infusion line with a three-way stop cock was directly connected. CLEAN-3 study [5] showed that the use of the bundle, versus a standard approach, made it possible to (1) reduce the frequency of occurrence of a complication requiring catheter replacement (phlebitis, diffusion, occlusion, local infection, dislodgement) and (2) delay the time of occurrence of these complications. The material of bundle strategy is slightly more expensive (for insertion and per day of use). The standard strategy requires more frequent and earlier removal of a defective catheter and its replacement, which generates an additional expense. Treatment of complications leading to catheter replacement have their own additional costs. The question is whether the extra cost generated by the bundle (at catheter insertion, at each daily use of the venous line and at catheter removal) is offset by the savings generated by (1) less frequent and delayed replacement of the venous line, and (2) less frequent treatment of complications leading to catheter removal. CLEAN-3 clinical study [5] also confirmed the superiority of 2% chlorhexidine (CHG)– 70% isopropanol over 5% povidone iodine (PVI)– 69% ethanol in reducing both catheter colonization and local infection. This result suggests the use of 2% CHG plus alcohol as the preferred antiseptic for short-term PVC insertion and care. The results for comparison between the two antiseptics were not affected by the type of devices, nor were the results for comparison between standard and innovative devices affected by the type of antiseptic. Moreover, CLEAN-3 clinical study showed that length of stay in hospital were not affected by the choice of antiseptic agent or type of device. As a consequence, two devices groups (combining CHG and PVI solutions) were considered in the cost-effectiveness study: a bundle of innovative devices (BDs), and standard devices (SDs). The objective of the present study was to perform a cost-effectiveness analysis (CEA) of these devices strategies in the prevention of PVC unscheduled removal due to complications in France, from modeling techniques based on the CLEAN-3 database. To support the choice of the best devices strategy from a conventional hospital medical care perspective, a decision-analytic model was performed.

Methods

Study design

Statistical analysis of observed data from CLEAN-3 database was achieved. The adopted modeling approach complies with the guidelines of French National Authority for Health (Haute Autorité de Santé –HAS) [6]. The 14-day ICU-time non-homogeneous semi-Markovian model structure was based on observed data from the CLEAN-3 study. Modeling and data analyses were performed using Rstudio software (version 1.1.453 – © 2009–2018 RStudio, Inc.). RStudio is an Integrated Development Environment for R (R Core Team (2022). R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. URL https://www.R-project.org/.).

Data collection

Data of the cost-effectiveness study were from the CLEAN-3 [5] database delivered by the University Hospital of Poitiers (France). Patients were recruited at the ED before being admitted to the medical wards. The main objective of the clinical study was to hypothesize that skin preparation with 2% chlorhexidine plus 70% isopropanol (chlorhexidine plus alcohol) was more effective than a skin preparation with 5% povidone iodine plus 69% ethanol (povidone iodine plus alcohol) in preventing PVC-related infectious complications. The second assumption testing was to consider that use of closed integrated catheters, positive displacement needleless-connectors, disinfecting caps, and single-use prefilled flush syringes in combination extended the time elapsed between catheter placement and catheter failure compared with the use of open catheters and three-way stopcocks for treatment administration.

Study population

During the CLEAN-3 study, consecutive adults (age ≥18 years) visiting the ED of the Poitiers University Hospital and requiring a PVC for a predictable duration of at least 48 hours before being admitted to medical wards were enrolled. The investigators obtained written informed consent before study inclusion from competent patients and at competence recovery from incompetent patients, according to French law. The study was approved by the French Southwest and Overseas Ethics Committee and the French Drug Safety Agency. The study population included 989 patients after exclusion of 6 patients with failed catheter placement and 5 with withdrawal of consent; 494 patients were randomly assigned to the bundle of innovative devices (BDs) group and 495 patients to the standard devices (SDs) group. Overall, 407 patients (41%) had unscheduled catheter removal for "dislodgement", "diffusion", "local infection", "occlusion" and "phlebitis" complications including 195 men (48%), and 101 patients (25%) had no previous history. Their mean age was 76 years. Two of them died (0.5%) during the study period. 235 patients (47.5%) were from the SDs group and 172 (34.8%) from the BDs group. With respect to qualitative variables, patients in the BDs group were more likely to have past history of heart failure (p = 0.02580) or to be receiving anti-coagulant therapy (p = 0.01858) than patients of the SDs group. For all quantitative variables tested, there was no difference between the BDs and the SDs groups. The duration of hospitalization was comparable between the BDs group and the SDs group, with durations of 10.4 and 9.3 days, respectively (p = 0.19020). For comparison, the same statistics were calculated for the population of patients without unscheduled PVC removal (n = 582). Reasons for PVC removal for this group were PVC not useful, scheduled PVC change, suspected infection without identification of an actual complication, or death. Among these patients, with respect to the qualitative variables, there were differences between the two study groups for the absence of past history (34% in the BDs group vs. 44% in the SDs group; p = 0. 01688), history of COPD (13% in the BDs group vs. 6% in the SDs group; p = 0.00779), history of diabetes (20% in the BDs group vs. 14% in the SDs group; p = 0.03765) and history of chronic renal failure (7.5% in the BDs group vs. 3.5% in the SDs group; p = 0.04672). Patients in the BDs group thus appear to be more severe on these variables than those in the SDs group. For all quantitative variables tested, there was no difference between the two study groups except for average age significantly higher in the BDs group (70 years) than in the SDs group (66 years); the catheterization and hospitalization times were not different between the two groups.

Endpoints

The final health outcome of the cost-effectiveness analysis, adjusted on the 1st catheter-time, was the number of patients with unscheduled PVC removal avoided (per 100 patients) and the cost-effectiveness criterion was the cost per patient with unscheduled PVC removal avoided resulting from BDs devices use, instead of SDs devices.

Modeling and statistical analysis

Markov models simulate the trajectory of patients among distinct health states over time [7-9]. The main assumption of state-transition Markov models is that the next health state depends only on the present state and not on the sequence of events that preceded it. For an expected goodness of fit to CLEAN-3 data, a multi-state semi-markovian model in continuous time was performed. This type of modeling can take into account iterative occurrences for each health state (e.g., Markov state). This modeling is very close to the daily realities that can be observed through the hospital stay (changes in daily health status, costs of care, etc.). Within this model, transition probabilities between states are time dependent and well suited to individual patient data (IPD) from CLEAN-3 database. This type of modeling is suited to the context of hospital settings where progression of the patient cannot be considered as a long-term condition. Five health states (Markov states) and 8 transitional events were considered (Table 1) in our cost-effectiveness model. Transitional event is defined as an event that occurs during a cycle and which generates a transition from one model status to another. The follow-up of the patients was related to the first catheter (2 days after its removal, except in the case of death or discharge from hospital in the meantime). In case of a complication justifying the replacement of the catheter, the same device (2nd PVC) was put in place but the follow-up of the patient was stopped, the instructions being to follow the same protocol. The fate of the 2nd catheter (and any subsequent ones) was therefore unknown. The hospital length of stay (LOS) limited to 28 days was recorded.
Table 1

Health states defined from the CLEAN-3 clinical study.

Health States / EventsDefinition
Markov state 1: No Event / 1st PVCInsertion of a first catheter, no event diagnosed
Transitional event 1.1: Scheduled PVC removal / No PVC newScheduled removal of the 1st catheter / No insertion of a 2nd catheter
Transitional event 1.2: Useless PVC / No PVC new1st catheter removal because of its useless / No insertion of a 2nd catheter
Transitional event 1.3: PVC with suspected infection / No PVC new1st catheter removal because of suspected infection / No insertion of a 2nd catheter
Markov state 2: No Event / No PVCNo catheter in place, no event diagnosed
Transitional event 1.4: PVC dislodgement / PVC newUnscheduled removal of the 1st catheter due to dislodgement / Insertion of a 2nd catheter
Transitional event 1.5: PVC with phlebitis / PVC newUnscheduled removal of the 1st catheter due to phlebitis / Insertion of a 2nd catheter
Transitional event 1.6: PVC with diffusion / PVC newUnscheduled removal of the 1st catheter due to diffusion / Insertion of a 2nd catheter
Transitional event 1.7: PVC with local infection / PVC newUnscheduled removal of the 1st catheter due to local infection / Insertion of a 2nd catheter
Transitional event 1.8: PVC with occlusion / PVC newUnscheduled removal of the 1st catheter due to occlusion / Insertion of a 2nd catheter
Markov state 3: No Event / 2nd PVC2nd catheter in place, no event diagnosed
Markov state 4: DischargePatient leaves the hospital alive
Markov state 5: DeathPatient dies during the hospital stay

PVC: Peripheral Venous Catheter.

PVC: Peripheral Venous Catheter. The type of modeling is a multi-state semi-markovian model in continuous time (transition probabilities are time dependent and fitted to observational IPD from CLEAN-3 database suited to the hospital perspective). For base case scenario, time horizon was of 0–14 days, e.g., the maximum observed duration of catheterization (hospital length of stay: 0–28 days). The Markov Cycle length was the estimated mean sojourn time in each transient health state, for a given set of covariate values (from observational data in CLEAN-3 database). The number of Markov cycles depends on time horizon. The time horizon was based on the maximum catheter duration observed in each group (SDs group: 336 hours, e.g., 14 days; BDs group: 216 hours, e.g., 9 days) for accounting all types of patients (alive, discharged, or dead). As time horizon observed in CLEAN-3 database was not identical for each group, and for getting a common comparative basis for suited cost-effectiveness analyses, we set the time horizon to 14 days (for base case analysis; all events and catheters were considered from CLEAN-3 database). A scenario analysis considered a time horizon of 2–14 days (subgroup analysis considering patients with a catheter duration of more than 24 hours, or less than 24 hours but with unscheduled catheter removal due to a complication). The statistical unit of the study is the hospitalized patient within a time horizon of 14 days (including patients discharged alive from the hospital, alive but still in the hospital, or deceased during the hospital stay). Data was censored beyond 14 days as it corresponds to the maximum duration of catheterization observed in CLEAN-3 study. The estimated transition probability matrix is based on individual patient data from CLEAN-3 database. This analysis can be considered as a non-homogeneous Semi-Markov Chain (NH-SMC) analysis which takes into account time dependency of state transition, duration in each health state, and individual path of states through time. The observed transitions among health states are shown on the Markov diagram (Fig 1). In order to be as close as possible to observable realities, we have presented the cost-effectiveness results from the matrix of transition probabilities observed by the model (e.g., ’prevalence.msm’ algorithm [10]), and not from the matrix of transition probabilities estimated by the model. This approach is taken by the function prevalence.msm, which constructs a table of observed and expected numbers and percentages of individuals in each state at a set of times.
Fig 1

Observed model structure from CLEAN-3 database (BDs strategy, SDs strategy)–Markov diagram.

BDs: Bundle of devices, SDs: Standard devices, PVC: Peripheral Venous Catheter.

Observed model structure from CLEAN-3 database (BDs strategy, SDs strategy)–Markov diagram.

BDs: Bundle of devices, SDs: Standard devices, PVC: Peripheral Venous Catheter. Instead of parametric Monte Carlo simulation, the msm package [10] allows to quantify uncertainty with nonparametric bootstrap methods for probabilistic sensitivity analysis and 95% confidence intervals (CI) calculations. To populate the model, data are specified as a series of observations, grouped by patient and sorted by increasing observational time from the patient entry in ED. At minimum there should be a data frame with variables indicating: The time of the observation, The observed state of the process, The subject identification number (ID). Then all the observations are assumed to be from the same subject. The subject ID does not need to be numeric, but data must be grouped by subject, and observations must be ordered by time within subjects. Figure below shows how a non-homogeneous semi-Markov model can work (Fig 2).
Fig 2

Evolution of a multi-state model.

As an example case study within the msm package, the process is observed, for instance, on four occasions (source: msm package [10]).

Evolution of a multi-state model.

As an example case study within the msm package, the process is observed, for instance, on four occasions (source: msm package [10]). The cost of an event is independent from the outcome (survival or death or discharge): Statistical unit is the “global” patient. “Global” patient indicates a patient who could, during the hospital stay, be alive in the hospital, be alive and discharged of the hospital, or be died; The estimated cost per event at the University Hospital of Poitiers is estimated for each compared intervention; Discharge and Death Markov states are considered as absorbing states, e.g., patients cannot move from these states. As a consequence, an absorbing state is frequently valued at zero cost, except here considering the step of catheter removal before discharge or death, if a catheter is in place. As no data were available regarding 2nd catheter follow-up (date of removal), we considered the mean duration of the 2nd catheter was the difference in days between the censured time horizon (14 days) and the date of second catheter placement.

Base case input parameters for the cost analysis

The base case analysis of the cost-effectiveness study has to be the most conservative case as possible, and the most representative case of real life, taking into account current hospital settings in France, and according to clinical experts, literature and RCTs. The patients’ characteristics in the CLEAN-3 database were used for modeling (frequency and type of complications leading to catheter replacement, time of occurrence of complications, according to the two study groups). The average cost of catheter insertion, replacement and removal, the average cost of each day of use of the venous line (excluding the cost of treatments administered) and the average cost of treating complications were estimated from the cost of necessary material and nursing time. As the antiseptic cost was slightly different between the "chlorhexidine" and "povidone-iodine" solution, an average cost weighted for the number of patients included in CLEAN-3 study was used. Resources and unit costs were estimated following observations on practices at the University Hospital of Poitiers. Detailed resources use, nursing time, and unit costs are reported in the S1 File. For each patient group, the mean cost per patient was partly based on the mean number of catheters per patient (Table 2) and input parameters considered in the cost analysis (Table 3).
Table 2

Number of catheters per patient—Statistical unit: The global patient with catheterization (alive, discharge or dead).

Total PatientsSDs groupBDs group
Number of patients989495 (50.1%)494 (49.9%)
Number of catheters1,39730 (52.3%)666 (47.7%)
Number of catheters per patient1.401.501.30

SDs: Standard devices; BDs: Bundle of innovative devices.

Table 3

Input parameters considered in the cost analysis–For 1 patient-catheter (Euro 2022).

SDs group*BDs group*
Unit cost: Placement initial catheter8.209.74
Unit cost: Initial catheter removal or replacement2.322.26
Unit cost: Placement second catheter8.459.98
Total cost: Treatment for Dislodgement5.495.49
Total cost: Treatment for Phlebitis12.2712.27
Total cost: Treatment for Diffusion4.094.09
Total cost: Treatment for Local infection12.2712.27
Total cost: Treatment for Occlusion3.673.67
Unit cost for 24 hours: Daily use of catheter12.3113.27

SDs: Standard devices; BDs: Bundle of innovative devices.

*Source: University Hospital of Poitiers.

SDs: Standard devices; BDs: Bundle of innovative devices. SDs: Standard devices; BDs: Bundle of innovative devices. *Source: University Hospital of Poitiers.

Cost items for Markov states and transitional events

Cost items for Markov states and transitional events are shown in Table 4.
Table 4

Costs items for Markov states and transitional events.

Main costsSource/Data Provider1. No Events*/1st PVC1.1 E11.2 E21.3 E32. No Events*/No PVC1.4 E41.5 E51.6 E61.7 E71.8 E83. No Events*/2nd PVC4. Discharge5. Death
Unit cost: Placement initial catheterCHU PoitiersX
Unit cost: Initial catheter removalUHPXXXXXXXX
Unit cost: Placement second catheterUHPXXXXX
Unit cost: Second catheter removalUHPXX
Total cost: Treatment for DislodgementUHPX
Total cost: Treatment for PhlebitisUHPX
Total cost: Treatment for DiffusionUHPX
Total cost: Treatment for local infectionUHPX
Total cost: Treatment for OcclusionUHPX
Unit cost for 24h: Daily use of catheterUHPXX**

UHP: University Hospital of Poitiers; PVC: Peripheral venous catheter.

*Transitional events: E1 scheduled PVC removal; E2 useless PVC; E3 suspected infection (without event); E4 Dislodgement; E5 phlebitis; E6 diffusion; E7 local infection; E8 occlusion.

**As no data were available regarding 2nd catheter follow-up (date of removal), we considered the mean duration of the 2nd catheter was the difference in days between the censured time horizon (14 days) and the date of second catheter placement.

UHP: University Hospital of Poitiers; PVC: Peripheral venous catheter. *Transitional events: E1 scheduled PVC removal; E2 useless PVC; E3 suspected infection (without event); E4 Dislodgement; E5 phlebitis; E6 diffusion; E7 local infection; E8 occlusion. **As no data were available regarding 2nd catheter follow-up (date of removal), we considered the mean duration of the 2nd catheter was the difference in days between the censured time horizon (14 days) and the date of second catheter placement.

Costs per Markov states and transitional events (base case scenario)

Costs per Markov states and transitional events are shown in Table 5.
Table 5

Costs per Markov states and transitional events (Euro 2022).

Markov State Event(1)Costs for 1 catheter SDs groupCosts for 1 catheter BDs groupCosts for 1 patient SDs groupCosts for 1 patient BDs group
1. No Events*/ 1st PVC8.20+12.31 = 20.51 (1er jour) 12.31n**(>J2)9.74+13.27 = 23.01 (1er jour) 13.27n**(>J2)20.51x1.5 a (1er jour) = 30.76 12.31 x1.5a = 18.47 (>J2)23.01x1.3 b (1er jour) = 29.91 13.27 x1.3b = 17.25 (>J2)
1.1 E12.322.263.472.94
1.2 E22.322.263.472.94
1.3 E32.322.263.472.94
2. No Events*/ No PVC0.000.000.000.00
1.4 E426.77–8.20–2.32 = 16.2529.73–9.74–2.26 = 17.7324.3823.05
1.5 E533.55–8.20–2.32 = 23.0336.51–9.74–2.26 = 24.5134.5531.86
1.6 E625.37–8.20–2.32 = 14.8528.33–9.74–2.26 = 16.3322.2821.23
1.7 E733.55–8.20–2.32 = 23.0336.51–9.74–2.26 = 24.5134.5531.86
1.8 E824.95–8.20–2.32 = 14.4327.90–9.74–2.26 = 15.9121.6420.68
3. No Events*/ 2nd PVC12.31x n days***13.27x n days***12.31x n days x1.513.27x n days x1.3
4. Discharge2.32****2.26****3.47****2.94****
5. Death2.32****2.26****3.47****2.94****

(1) From CLEAN-3 database.

PVC: Peripheral venous catheter.

* Events: E1, scheduled PVC removal; E2, useless PVC; E3, suspected infection; E4, Dislodgement; E5, phlebitis; E6, diffusion; E7, local infection; E8, occlusion.

** Unit cost for daily use of catheter x Number of catheter-days.

*** As no data were available regarding 2nd catheter follow-up (date of ablation), we considered the mean duration of the 2nd catheter was the difference in days between the censured time horizon (14 days) and the date of second catheter placement.

**** Absorbing states are generally valued at zero cost, except here if we consider the step of removing the catheter before discharge or death, for a patient in state 1 (1st PVC) or state 3 (2nd PVC).

a Number of catheters per patient in SDs group (control group).

b Number of catheters per patient in BDs group (experimental group).

(1) From CLEAN-3 database. PVC: Peripheral venous catheter. * Events: E1, scheduled PVC removal; E2, useless PVC; E3, suspected infection; E4, Dislodgement; E5, phlebitis; E6, diffusion; E7, local infection; E8, occlusion. ** Unit cost for daily use of catheter x Number of catheter-days. *** As no data were available regarding 2nd catheter follow-up (date of ablation), we considered the mean duration of the 2nd catheter was the difference in days between the censured time horizon (14 days) and the date of second catheter placement. **** Absorbing states are generally valued at zero cost, except here if we consider the step of removing the catheter before discharge or death, for a patient in state 1 (1st PVC) or state 3 (2nd PVC). a Number of catheters per patient in SDs group (control group). b Number of catheters per patient in BDs group (experimental group).

Potential additional hospital length of stay due to studied complications

We can estimate the additional LOS due to studied complications based on observational data from CLEAN-3 database through the following calculation: Mean hospital LOS in patients with complications–Mean hospital LOS in patients without complications. A preliminary analysis showed that a mean difference in hospital LOS was of nearly +4 days. This original result will be studied by the University Hospital of Poitiers (UHP). Indeed, considering the studied complications could not clinically induce such an increase in LOS, UHP clinical experts and biostatisticians wish to study if other explanations could be found, as patient characteristics for instance. Therefore, the working group validated the idea for evaluating the intrinsic effect of bundled catheters by considering only the costs related to catheters and studied complications (insertion, duration of use, removal, treatment of studied complications, replacement).

Designing optimal cost-effectiveness model from observed CLEAN-3 individual patient data

Influence of catheter strategy on prevention of unscheduled PVC removal due to complications

As a reminder, among the patients with unscheduled PVC removal due to complications, there were 235 patients (47.5%) in the SDs group and 172 patients (34.8%) in the BDs group. The difference in not-adjusted on 1st catheter-time proportion was statistically significant (p = 0.00006). The result of the Fisher’s exact test also indicates that the mean odds-ratio (OR) was of 1.69 (95%CI: 1.30; 2.20). Patients in the SDs group have between 1.3 and 2.2 times the risk of having an unscheduled catheter removal. Patients in the BDs group are therefore more protected on this criterion. We performed a logistic regression of the probability of being in the unscheduled PVC removal state as a function of the device group exposure. Based on this logistic model, the SDs group (p = 0.00006; 95%CI OR: 1.31; 2.18) was a statistically significant variable to explain unscheduled PVC removal. The duration of hospitalization was comparable between the BDs group and the SDs group, with durations of 10.4 and 9.3 days, respectively (p = 0.1902).

Influence of duration of 1st catheter exposure on unscheduled PVC removal due to complications

The above results did not consider the duration of 1st catheter exposure in each group. Among the patients with unscheduled PVC removal due to complications, only the quantitative variable "Duration of 1st catheterization in days” was statistically different between the two groups (Wilcoxon rank sum test with continuity correction: p = 0.004), with a longer duration of 1st catheterization on average in the BDs group (2.12 versus 1.82 days). As a consequence, for taking into account the difference in 1st catheter-time between the two groups, we performed a comparison per one 1st PVC-day. The number of patients with unscheduled PVC removal per one 1st PVC-day was of 16 patients (out of 100) in the BDs group and of 26 patients (out of 100) in the SDs group. A nonparametric bootstrap comparison has been carried out; the percentile method estimated a 95%CI of [0.15; 0.18], e.g., between 15 and 18 patients out of 100 in the BDs group and [0.24–0.28], e.g., between 24 and 28 patients out of 100 in the SDs group. This bootstrap sensitivity analysis estimated a mean difference in number of patients of -0.10 (95%CI: [-0.12; -0.07]), e.g., the BDs strategy prevented in mean 10 (95%CI: [7; 12]) patients (out of 100) per one 1st PVC-day with unscheduled 1st PVC removal due to complications.

Influence of devices group on the proportion of patients discharged from the hospital (absorbing state) before the end of the study

Without adjustment for catheter time, the proportion of patients, with or without unscheduled PVC removal, discharged from the hospital before the end of the study was comparable (Fisher’s Exact Test: p = 1) between the BDs (152 patients, 30.8%) and SDs groups (153 patients, 30.9%). With adjustment for catheter time, the proportion of patients discharged from hospital (per 1000 patient-hours of catheter) was comparable between the BDs (95%CI: [2.9; 6.6]) and SDs (95%CI: [3.8; 7.5]) groups. For patients with unscheduled PVC removal, after adjustment for catheter time, the proportion of patients discharged from the hospital (per 1000 patient-hours of catheter) were comparable between the BDs (95%CI: [0;1.2]) and SDs (95%CI: [0; 1.8]) groups. For patients without unscheduled PVC removal, after adjustment for catheter time, the proportions of patients discharged from the hospital (per 1000 patient-hours of catheter) were comparable between the BDs (95%CI: [2.4; 6.1]) and SDs (95%CI: [2.7; 6.5]) groups. This result validates the approach of not considering the cost of the hospital stay in our cost-effectiveness study, but rather focusing on the costs of unscheduled catheter removals, catheter replacements and treating complications.

Influence of devices group on the proportion of patients in death state (absorbing state)

Without adjustment for catheter time, the proportion of deceased patients was comparable (Fisher’s Exact Test: p = 0.4206) between the BDs (8 patients, 1.6%) and SDs groups (5 patients, 1%). After adjustment for catheter time, the proportion of deceased patients (per 1000 patient-hours of catheter) were comparable between the BDs (95%CI: [0; 1.05]) and SDs (95%CI: [0; 0.96]) groups.

Final design of the cost-effectiveness model based on the above “influence” observed results

These results above were dependent on the devices group and the duration of catheter exposure. The analysis of the CLEAN-3 IPD showed that all unscheduled PVC removal events occurred through a maximum time horizon of 14 days, so we decided to calculate the intrinsic cost-effectiveness results for a 14-day time horizon in medical wards, taking into account all observed events due to 1st catheter complications in each devices group. Accordingly, the NH-SMC model was performed on this basis, taking into account a 14-day time horizon in hospital including ED visit (for base case analysis), and making assumption that all patients were catheterized during this common time period for each of the two devices groups. Also, we performed a Non-Homogeneous Semi-Markov Chain (NH-SMC) analysis on “Global” patient sample (considering observed results, as opposed to simulated results).

Scenario analyses

Scenario analysis 1

A Non-Homogeneous Semi-Markov Chain analysis (observed results) on “Global” patient sample. Time of observation was of 2–14 1st PVC-days (considering catheterized patients with catheter duration more than 24 hours or less than 24 hours with a studied complication). This scenario allows the exclusion of catheters inserted for a short foreseeable period of time, for which the benefit of the bundle on the prevention of complications is low according to the results of CLEAN 3 [5].

Scenario analysis 2

A NH-SMC analysis (observed results) on “Global” patient sample: Time of observation was of 0–14 1st PVC-days without PVC complication costs. This scenario removes the cost of complications for which management is not standardized between hospitals, potentially favoring the bundle group.

Sensitivity analyses

The estimated transition probability matrix of the NH-SMC model was based on individual patient data from CLEAN-3 study [5]. This analysis can be considered as a non-homogeneous Semi-Markov Chain Monte Carlo modeling which takes into account time dependency of state transition, duration in each state, and individual path of states through time. Instead of parametric Monte Carlo simulation, the msm package [10] allows to quantify uncertainty with nonparametric bootstrap methods. Nonparametric bootstrap 95% confidence intervals (95%CI) were estimated for the transition probability matrix between health states, and the mean cost per patient for a 14-day time horizon in hospital (including ED visit). The bootstrap method that has been adopted was that of the boot.ci algorithm from the boot package [11-13]. This function generates 5 different types of equi-tailed two-sided nonparametric confidence intervals. These are the first order normal approximation, the basic bootstrap interval, the studentized bootstrap interval, the bootstrap percentile interval, and the adjusted bootstrap percentile (BCa) interval. We used the bootstrap percentile interval (perc) method.

Results

The observed “global” patient (alive, discharge or dead) from CLEAN-3 IPD: Base case scenario

Effectiveness: Distribution of patients through health states and transitional events (observed Markov cycle: Each 1.4 days, a patient can change his/her health status) and duration in each non absorbing health state

The NH-SMC modeling estimated that patients change health states, or remain in the same health state, every 1.4 days. This Markov cycle is thus close to the observable realities of the Clean-3 database. After 1.4 days of 1st catheterization, 58% of patients were still in health state 1 (no event, 1st PVC) in BDs group, compared to 51% in SDs group. After 2.8 days of 1st catheterization, 27% of the patients were still in health state 1 (no event, 1st PVC in place) in BDs group, against 19% in SDs group. After 4.2 days of 1st catheterization, 11% of patients were still in health state 1 (no event, 1st PVC) in BDs group, compared to 6% in SDs group. The number of patients in health state 3 (no event, 2nd PVC in place), e.g., the Markov state that receives transitional events as dislodgement, phlebitis, diffusion, local infection or occlusion (the 1st PVC-related complications studied), was higher in the SDs group than in the BDs group (24% in the SDs group after 1.4 days of 1st catheterization, compared to 15% in the BDs group; 45% at 4.2 days compared to 30%). The mean duration in health state 1 (no event, 1st PVC in place) was lower (1.82 days versus 2.12 days; p = 0.004) in SDs group compared with BDs group. The mean duration in health state 3 (no event, 2nd PVC in place; 7.79 versus 7.77 days) and in health state 2 (no event, no PVC in place) (3.59 versus 3.85 days) were comparable between patients in SDs and BDs groups, respectively.

Cost-effectiveness results per patient

The adjustment coefficient for 1st catheter time in days per patient, for health state 1 (no event, 1st PVC in place) was of 1.1618 (2.1226 / 1.8269). The cost-effectiveness results for the observed “global” patient (not simulated), for each of the two compared groups and for a 14-day time horizon in hospital are shown in Table 6.
Table 6

Cost-effectiveness results per patient from observed data (CLEAN-3 database)–Observed global patient–Hospital-time Horizon: 14 days—Base case scenario.

StrategySDs Standard devices (Reference strategy)BDs Bundled devices (Assessed strategy)
Mean cost per patient, adjusted on catheter-time (nonparametric bootstrap 95%CI)€144.24 (€134.8; €154.2)€102.11 (€95.4; €108.9)
Effectiveness: Number of patients with unscheduled 1st PVC removal (%)235/495 (47.47%)172/494 (34.82%)
Difference in Cost per patient (95%CI)€-42.13 (€-53.61; €-32.01)
Difference in Effectiveness-12.65 patients / 100
ICER / DominanceDominate SDs (less costly, more effective)

CI: Confidence interval; PVC: Peripheral Venous Catheter; ICER: Incremental Cost-Effectiveness Ratio = Difference in Cost / Difference in Effectiveness.

CI: Confidence interval; PVC: Peripheral Venous Catheter; ICER: Incremental Cost-Effectiveness Ratio = Difference in Cost / Difference in Effectiveness. The 95% confidence intervals for cost per patient did not overlap; the saving per patient was statistically significant at 0.05 level (between €32 and €54), preventing 12.65 patients (out of 100) with unscheduled PVC removal.

Cost-effectiveness results per patient-PVC-day

The cost-effectiveness results for the observed “global” patient (not simulated), per patient-PVC-day, for each of the two compared groups and for a 14-day time horizon in hospital are shown in Table 7.
Table 7

Cost-effectiveness results per patient-PVC-day from observed data (CLEAN-3 database)–Observed global patient–Hospital-time Horizon: 14 days–Base case scenario.

StrategySDs Standard devices (Reference strategy)BDs Bundled devices (Assessed strategy)
Mean cost per patient-1st PVC-day (95%CI)€78.95 (€71.15; €87.86)€48.10 (€43.85; €52.44)
Effectiveness: Number of patients with unscheduled PVC removal, per PVC-day (95%CI)0.2598 (0.2399; 0.2810)0.1640 (0.1524; 0.1766)
Difference in Cost per patient-PVC-day (95%CI)€-30.85 (€-39.64; €-22.41)
Difference in Effectiveness per patient-PVC-day (95%CI)-0.0958 (-0.1191; -0.0713)
ICER / DominanceDominate SDs strategy (less costly, more effective)

CI: Confidence interval; PVC: Peripheral Venous Catheter; ICER: Incremental Cost-Effectiveness Ratio = Difference in Cost / Difference in Effectiveness.

CI: Confidence interval; PVC: Peripheral Venous Catheter; ICER: Incremental Cost-Effectiveness Ratio = Difference in Cost / Difference in Effectiveness. The 95% confidence intervals show that the saving per patient-PVC-day was estimated between €22 and €40, preventing 9.58 patients (out of 100) with unscheduled PVC removal per 1st PVC-day. As a consequence, BDs strategy is less costly and more effective than SDs strategy.

Scenario analysis 1: A non-homogeneous Semi-Markov Chain analysis on observed “Global” patient sample. Time of observation was of 2–14 1st PVC-days (considering catheterized patients with catheter duration more than 24 hours or less than 24 hours with a studied complication)

Cost-effectiveness results per patient. The cost-effectiveness results for the observed “global” patient (not simulated), for each of the two compared groups are shown in Table 8.
Table 8

Cost-effectiveness results per patient from observed data (CLEAN-3 database)–Observed global patient–Scenario analysis 1.

StrategySDs Standard devices (Reference strategy)BDs Bundled devices (Assessed strategy)
Mean cost per patient, adjusted on catheter-time (nonparametric bootstrap 95%CI)€169.42 (€160; €179)€117.87 (€110; €126)
Effectiveness: Number of patients with unscheduled PVC removal (%)235/495 (47.47%)172/494 (34.82%)
Difference in Cost per patient (95%CI)€-51.55 (€-64.57; €-40.15)
Difference in Effectiveness-12.65 patients / 100
ICER / DominanceDominate SDs (less costly, more effective)

CI: Confidence interval; PVC: Peripheral Venous Catheter; ICER: Incremental Cost-Effectiveness Ratio = Difference in Cost / Difference in Effectiveness.

CI: Confidence interval; PVC: Peripheral Venous Catheter; ICER: Incremental Cost-Effectiveness Ratio = Difference in Cost / Difference in Effectiveness. The 95% confidence intervals for cost per patient did not overlap; the saving per patient was statistically significant at 0.05 level (between €40 and €65), preventing 12.65 patients (out of 100) with unscheduled PVC removal. Cost-effectiveness results per patient-PVC-day. The cost-effectiveness results for the observed “global” patient (not simulated), per patient-PVC-day, for each of the two compared groups are shown in Table 9.
Table 9

Cost-effectiveness results per patient-PVC-day from observed data (CLEAN-3 database)–Observed global patient–Scenario analysis 1.

StrategySDs Standard devices (Reference strategy)BDs Bundled devices (Assessed strategy)
Mean cost per patient-1st PVC-day (95%CI)€78.98 (€71.12; €87.68)€47.32 (€42.96; €52.25)
Effectiveness: Number of patients with unscheduled PVC removal, per PVC-day (95%CI)0.27 (0.25; 0.29)0.17 (0.16; 0.18)
Difference in Cost per patient-PVC-day (95%CI)€-31.39 (€-41.16; €-23.27)
Difference in Effectiveness per patient-PVC-day (95%CI)-0.10 (-0.13; -0.08)
ICER / DominanceDominate SDs strategy (less costly, more effective)

CI: Confidence interval; PVC: Peripheral Venous Catheter; ICER: Incremental Cost-Effectiveness Ratio = Difference in Cost / Difference in Effectiveness.

CI: Confidence interval; PVC: Peripheral Venous Catheter; ICER: Incremental Cost-Effectiveness Ratio = Difference in Cost / Difference in Effectiveness. The 95% confidence intervals show that the saving per patient-PVC-day was estimated between €23 and €41, preventing 10.27 patients (out of 100) with unscheduled PVC removal per 1st PVC-day. As a consequence, BDs strategy is less costly and more effective than SDs strategy.

Scenario analysis 2: A NH-SMC analysis on observed “Global” patient sample: Time of observation was of 0–14 1st PVC-days without 1st PVC complication costs

Cost-effectiveness results per patient. The cost-effectiveness results for the observed “global” patient (not simulated), for each of the two compared groups are shown in Table 10.
Table 10

Cost-effectiveness results per patient from observed data (CLEAN-3 database)–Observed global patient–Scenario analysis 2.

StrategySDs Standard devices (Reference strategy)BDs Bundled devices (Assessed strategy)
Mean cost per patient, adjusted on catheter-time (nonparametric bootstrap 95%CI)€131.12 (€123.60; €139.30)€94.19 (€88.60; €100.21)
Effectiveness: Number of patients with unscheduled PVC removal (%)235/495 (47.5%)172/494 (34.8%)
Difference in Cost per patient (95%CI)€-36.93 (€-47.8; €-27.9)
Difference in Effectiveness-12.65 patients / 100
ICER / DominanceDominate SDs (less costly, more effective)

CI: Confidence interval; PVC: Peripheral Venous Catheter; ICER: Incremental Cost-Effectiveness Ratio = Difference in Cost / Difference in Effectiveness.

CI: Confidence interval; PVC: Peripheral Venous Catheter; ICER: Incremental Cost-Effectiveness Ratio = Difference in Cost / Difference in Effectiveness. The 95% confidence intervals for cost per patient did not overlap; the saving per patient was statistically significant at 0.05 level (between €28 and €48), preventing 12.65 patients (out of 100) with unscheduled PVC removal. As a consequence, BDs strategy is less costly and more effective than SDs strategy. Cost-effectiveness results per patient-PVC-day. The cost-effectiveness results for the observed “global” patient (not simulated), per patient-PVC-day, for each of the two compared groups are shown in Table 11.
Table 11

Cost-effectiveness results per patient-PVC-day from observed data (CLEAN-3 database)–Observed global patient–Scenario analysis 2.

StrategySDs Standard devices(Reference strategy)BDs Bundled devices (Assessed strategy)
Mean cost per patient-1st PVC-day (95%CI)€71.77 (€65.65; €79.66)€44.37 (€40.52; €48.14)
Effectiveness: Number of patients with unscheduled PVC removal, per PVC-day (95%CI)0.26 (0.24; 0.28)0.16 (0.15; 0.18)
Difference in Cost per patient-PVC-day (95%CI)€-27.40 (€-36.44; €-20.19)
Difference in Effectiveness per patient-PVC-day (95%CI)-0.10 (-0.12; -0.07)
ICER / DominanceDominate SDs strategy (less costly, more effective)

CI: Confidence interval; PVC: Peripheral Venous Catheter; ICER: Incremental Cost-Effectiveness Ratio = Difference in Cost / Difference in Effectiveness.

CI: Confidence interval; PVC: Peripheral Venous Catheter; ICER: Incremental Cost-Effectiveness Ratio = Difference in Cost / Difference in Effectiveness. The 95% confidence intervals show that the saving per patient-PVC-day was estimated between €20 and €36, preventing 9.58 patients (out of 100) with unscheduled PVC removal per 1st PVC-day. As a consequence, BDs strategy is less costly and more effective than SDs strategy.

Sensitivity analyses for base case scenario and scenario analyses

From the NH-SMC model, the bootstrap 95%CI lower and upper bounds of the three cost-effectiveness analyses were shown in Tables 6–11. For each of the base case scenario and scenario analysis, from a cost-effectiveness point of view, the BDs strategy statistically dominates the SDs strategy for the observed “global” patient because of the non-overlapping nature of 95%CI regarding the cost-effectiveness criteria. Indeed, the results of the probabilistic sensitivity analysis are illustrated on the cost-effectiveness (CE) plane (Fig 3), which describes the difference in number of unscheduled PVC removal per patient-1st PVC-day and the difference in cost per patient-1st PVC-day between the BDs strategy and the SDs strategy from 1,000 bootstrap replicates in each group. All the points of the CE plane (e.g., incremental cost-effectiveness ratios) from the simulations consistently confirmed that the BDs strategy is more effective and less costly than the SDs strategy.
Fig 3

Probabilistic sensitivity analysis: Cost-effectiveness plane for the base case analysis.

PVC: Peripheral Venous Catheter.

Probabilistic sensitivity analysis: Cost-effectiveness plane for the base case analysis.

PVC: Peripheral Venous Catheter.

Discussion

Regardless of the scenario analysis performed, the health technology evaluated passed the cost-effectiveness test. Indeed, after adjustment for 1st catheter time and regarding results per patient for the base case scenario, the BDs strategy avoided 10 (95%CI: 7; 12) patients (out of 100) with unscheduled first catheter removal and the average cost saving induced by the BDs strategy was estimated at €42 (95%CI: €32; €54) per patient. Regarding the cost results per day of first catheter, the average costs per first catheter day were of €79 (95%CI: €71; €88) in the SDs group and of €48 (95%CI: €44; €52) in the BDs group. The average cost saving induced by the BDs strategy was estimated at €31 (95%CI: €22; €40) per patient-day of first catheter. For the first scenario analysis (time of observation of 2–14 1st PVC-days, considering catheterized patients with catheter duration more than 24 hours or less than 24 hours with a studied complication), the BDs strategy avoided 10 (95%CI: 8; 13) patients (out of 100) with unscheduled first catheter removal and the average cost saving induced by the BDs strategy was estimated at €51 (95%CI: €40; €65) per patient. Regarding the cost results per day of first catheter, the average costs per first catheter day were of €79 (95%CI: €71; €88) in the SDs group and of €47 (95%CI: €43; €52) in the BDs group. The average cost saving induced by the BDs strategy was estimated at €31 (95%CI: €23; €41) per patient-day of first catheter. For the second scenario analysis (time of observation of 0–14 1st PVC-days, without considering 1st PVC-related complications costs), the BDs strategy avoided 10 (95%CI: 7; 12) patients (out of 100) with unscheduled first catheter removal and the average costs per patient were respectively €131 (95%CI: €124; €139) in the SDs comparator group and €94 (95%CI: €89; €100) in the BDs group. The average cost saving induced by the BDs strategy was estimated at €37 (95%CI: €28; €48) per patient. Regarding the cost results per day of first catheter, the average costs per first catheter day were of €72 (95%CI: €66; €80) in the SDs group and €44 (95%CI: €41; €48) in the BDs group. The average cost saving induced by the BDs strategy was estimated at €27 (95%CI: €20; €36) per patient-day of first catheter. In Clean 3, 407 patients (41%) required an unscheduled PVC removal before discharge. Insertion of a second catheter in connection with unscheduled removal of the first catheter was more frequent (p = 6.058e-5) in the standard approach group (235 patients [47.5%]) than the bundled approach group (172 patients [34.8%]). We note that the mean catheter-time was different between the two groups; they were longer in the group of patients with bundled approach. The results of statistical tests indicate that it was necessary to adjust the comparisons between the two devices groups on 1st catheter-time. After adjusting for 1st catheter-time, the rates of patients discharged from hospital (per 1000 patient-hours of catheter), before the end of the study and not having had an unscheduled catheter removal, were statistically comparable between the bundled approach and the standard approach groups (95% confidence intervals overlapped). We conclude that the "hospital discharge" condition has not influenced the differential cost-effectiveness outcome between patients in the bundled approach group and those in the standard approach group. This result validates the approach of not considering the cost of the hospital stay in our cost-effectiveness study, but rather focusing on the costs of complications and unscheduled catheter removals. Similarly, the rates of patient deaths (per 1000 patient-hours of catheter time) were comparable between the bundled approach and the standard approach groups. The non-homogeneous multi-state semi-markovian model (NH-SMC) in continuous time is a suitable mathematical tool to be fitted to longitudinal data based on individual patient data (IPD) available in CLEAN-3 database (Poitiers University Hospital). The literature in this field frequently offers examples based on static decision tree models, used for both cost-effectiveness or cost-benefit studies [14-16], except for the latest Maunoury et al. paper on this topic [17]. The feature of the current modeling relates to the fact that it is based on real-life individual patient data, and not on published mean values from the literature. The time-dependence addressed here (e.g., evolution of the risk of developing a PVC-complication with increased catheterization time) corroborates that the non-homogeneous modeling approach is suitable considering the nature of the available data and the medical wards settings. The rationale of the sensitivity analysis for scenario 1 (Hospital-Time Horizon: 2–14 days for all patients and 0–1 day for patients with complications) was to assess the intrinsic effect of the health technology studied by allowing it time to act beyond the first 24 hours of catheter placement, as reported in the manuscript of CLEAN3 [5]. The rationale of the sensitivity analysis for scenario 2 (not taking into account the costs of complications leading to unscheduled PVC removal for the first catheter) was to evaluate the economic impact of the technology studied by considering only the costs linked to the use of catheters, without considering the other events that the patient may experience during the studied time horizon in medical wards. Few studies have investigated costs associated with PVC insertion, daily maintenance, and catheter removal. These costs vary according to the organization of care, the type of device used, the year the study was conducted. They should include the cost of waste disposal, which is rarely the case. In addition, due to inflation, these costs need to be adjusted to allow for comparison between studies conducted at different times. In the Netherlands, the average costs for catheter insertion were estimated to be €11.67 in 2019, but varied significantly with the number of cannulation attempts, from €9.32 for patients with a successful first attempt to €65.34 when five attempts were required [18]. In Australia, the average cost in 2016 was €6.39 (€6.75 at 2019 costs, the year CLEAN-3 was performed) [19]. Costs of up to about €30 for the first attempt have been reported by others [20]. Through a series of observations of caregiver practices in our hospital, we estimated similar costs (€8.20 with the standard approach and €9.74 with the bundle approach). The cost of catheter removal was estimated at €1.92 (€1.95 at 2019 costs) in an Australian study [19], a value close to our study estimate (€2.32 with the standard approach and €2.26 with the bundled approach). Catheter failure is a frequent event, occurring in 41% of CLEAN-3 patients, a figure close to the average of 45% observed in previous randomized trials [2]. Catheter failure increases costs because of the need to change the catheter and to handle the complication. Here again, few data are available in the literature concerning the cost of changing catheters or treating complications. Indeed, there is no protocol for the management of these complications applied universally. We therefore estimated them on the basis of series of observations in our hospital. Average costs to handle one episode of diffusion (€4.09 vs [€0.12-€19.41]), occlusion (€3.67 vs [€0.25-€14.03]) and phlebitis (€12.27 vs [€0.04-€14.49]) were in the range of values reported in China [21]. This NH-SMC model has some limitations. First, it was built on a single clinical study because it was the only RCT available with this particular product. Second, the cost-effectiveness analysis was based on a scenario specific to French medical wards, with their own protocol to treat complications. As a consequence, the NH-SMC model cannot be directly transposed to other settings or other countries with different settings. This transposition would require local individual data on time-dependent probabilities of transition among health states at the daily level. Further studies involving other countries are needed to generalize our results and therefore our findings do not necessarily predict similar cost effectiveness of bundle of the studied devices in other countries or in specific patients’ subgroups. Nevertheless, our results show that 1) globally our costs for PVC insertion, daily use and ablation are in the low range of the literature data and 2) excluding the costs of complications which could be a questionable point (cf. Scenario analysis 2), the BDs strategy keep a significant benefit. This study also has the non-technical limitation of being sponsored by industry (the BD Company). However, an external research organization (Statesia) was hired by the University Hospital of Poitiers to handle independently the development of the cost-effectiveness model and the data analysis to remove any possible bias. Non-BD authors have worked for the preparation of the manuscript, with the final version being approved by all non-BD authors prior to submission.

Conclusion

According to the sensitivity analysis (nonparametric bootstrap 95% confidence intervals) which addresses the level of uncertainty of the mean results, and the results highlighted in this study, the bundled devices (BDs) passed the test for cost-effectiveness within a conservative scenario defined through the base case scenario. The BDs strategy is significantly more effective to prevent PVC-complications and, as a consequence, unscheduled PVC-removal, when compared to the standard devices approach (SDs), with significant savings for the hospital. As a consequence, from a cost-effectiveness point of view, we can recommend the routine use of these bundled devices for patients in medical wards.

Detailed resources and costs of the cost-effectiveness study.

CHG: Chlorhexidine Gluconate gel; PVI: povidone iodine-alcohol solution; PVC: Peripheral Venous Catheter. (XLSX) Click here for additional data file. 27 Apr 2022
PONE-D-22-07543
Cost-effectiveness analysis of bundled innovative devices versus standard approach in the prevention of unscheduled peripheral venous catheters removal due to complications in France
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(Please upload your review as an attachment if it exceeds 20,000 characters) Reviewer #1: The authors aimed to perform a cost-effectiveness analysis of bundled devices (BDs) versus standard devices (SDs) for the prevention of unscheduled peripheral venous catheter (PVC) removal due to complication from a French investigator-initiated, open-label, single center, randomized-controlled, two-by-two factorial trial (CLEAN-3 study). The study is very interesting but I think that in the discussion section the role of biofilm should be discussed. For this purpose please cite and comment the following work: doi: 10.2174/1574887114666191018144739. Reviewer #2: The article is interesting and well-written. Moreover, the statistical analysis il well-conducted. I have only the following minor comments: 1. In cost-effectiveness (CE) analysis (CEA), the CE plane is an important tool. It aims to clearly illustrate differences in costs and effects between different strategies (in your case, bundled devices, BDs, versus standard devices, SDs). The authors should add the CE plane of their analysis. 2. More details could be given about the estimated transition matrix. 3. An important component to any CE analysis is to assess whether the model is appropriate for the phenomena being examined, which is the purpose of model validation. In fact, very careful attention must be paid to the verification of a fundamental assumption which is the Markov property. Please discuss this aspect and perform model validation. 4. Line 91 - instead of “Statistical analyzes of observed” perhaps it is better to write “Statistical analysis of observed”. 5. Line 94 - The sentence about RStudio should be improved. To be more precise: “RStudio is an Integrated Development Environment for R, a programming language for statistical computing and graphics.” 6. Line 115: revise “by by”. 7. Always use the same number of decimals; see, just as an example, the p-values in the text. 8. Line 367: revise “Sensitivity analyzes”. ********** 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: No Reviewer #2: 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.
4 May 2022 Response to PLOS One review PLOS ONE Decision: PLOS ONE 27 avr. 2022 16:54 À Franck Maunoury PONE-D-22-07543 Cost-effectiveness analysis of bundled innovative devices versus standard approach in the prevention of unscheduled peripheral venous catheters removal due to complications in France PLOS ONE Dear Dr. Maunoury, 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. The reviewers have commented on your above paper. They have suggested that this manuscript be revised according to the reviewers suggestions and resubmitted. Provided you address the changes recommended, the manuscript will be accepted for publication Please submit your revised manuscript by Jun 11 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, Prof. Raffaele Serra, M.D., Ph.D Academic Editor PLOS ONE Response to PLOS One review –May 4 2022 Dear Prof. Raffaele Serra, On behalf of my co-authors, I would like to thank you and the reviewers for your constructive feedback on our manuscript number PONE-D-22-07543. Please find enclosed our rebuttal letter in response to each point brought up by the academic editor and the reviewers. We look forward to hearing from you in due time regarding our submission and to respond to any further questions and comments you may have. Sincerely yours, Dr. Franck Maunoury Response to comments from Academic Editor, PLOS One (Prof. Raffaele Serra) 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 Response: We have ensured that our manuscript meets the PLOS ONE’s style requirements. 2. Thank you for stating the following in the Competing Interests section: "OM received funding for congress attendance, and research funding from Becton Dickinson. MB received personal fees from Becton Dickinson. All other investigators and authors declare no competing interests." Response: "OM & JG received personal fees from Becton Dickinson, funding for congress attendance, and research funding from Becton Dickinson. MB received personal fees from Becton Dickinson. All other investigators and authors declare no competing interests." Please confirm that this does not alter your adherence to all PLOS ONE policies on sharing data and materials, by including the following statement: "This does not alter our adherence to PLOS ONE policies on sharing data and materials.” (as detailed online in our guide for authors http://journals.plos.org/plosone/s/competing-interests). If there are restrictions on sharing of data and/or materials, please state these. Please note that we cannot proceed with consideration of your article until this information has been declared. Response: “This does not alter our adherence to PLOS ONE policies on sharing data and materials.” Please include your updated Competing Interests statement in your cover letter; we will change the online submission form on your behalf. Response: Done. The updated Competing Interests statement is in our cover letter. 3. 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. Response: We reviewed the reference list; it is complete and correct. Additional Editor Comments: The manuscript is interesting. There are only minor revision in order to have the manuscript ready for publication. [Note: HTML markup is below. Please do not edit.] Response to 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: Partly Response: See our responses to Reviewer #1 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: The authors aimed to perform a cost-effectiveness analysis of bundled devices (BDs) versus standard devices (SDs) for the prevention of unscheduled peripheral venous catheter (PVC) removal due to complication from a French investigator-initiated, open-label, single center, randomized-controlled, two-by-two factorial trial (CLEAN-3 study). The study is very interesting but I think that in the discussion section the role of biofilm should be discussed. For this purpose please cite and comment the following work: doi: 10.2174/1574887114666191018144739. Response: Thank you very much for your general appreciation of our work and for this comment. In our study, we were mainly interested in non-infectious complications leading to catheter failure and replacement. Biofilm is an essential element leading to catheter-related infections. The role of biofilm in non-infectious catheter complications is less well documented. Therefore, we are not sure how to include this reference in our article. But we remain at the disposal of the reviewer if necessary. Reviewer #2: The article is interesting and well-written. Moreover, the statistical analysis il well-conducted. I have only the following minor comments: 1. In cost-effectiveness (CE) analysis (CEA), the CE plane is an important tool. It aims to clearly illustrate differences in costs and effects between different strategies (in your case, bundled devices, BDs, versus standard devices, SDs). The authors should add the CE plane of their analysis. Response: Thank you for your suggestion. The CE plane (Fig 3) has been added in the revised manuscript. 2. More details could be given about the estimated transition matrix. Response: The estimated transition probability matrix is based on individual patient data from CLEAN-3 database. This analysis is considered as a non-homogeneous Semi-Markov Chain (NH-SMC) analysis which takes into account time dependency of health state transition, duration in each health state, and individual path of health states through time. The observed transitions among health states are shown on the Markov diagram (Fig 1). The multi-state Markov model is a useful way of describing a process in which an individual moves through a series of states in continuous time. The msm package for R [ ] allows a general multi-state model to be fitted to longitudinal data. Data often consist of observations of the process at arbitrary times, so that the exact times when the state changes are unobserved. Kalbfleisch and Lawless[ ] and later Kay [ ] described a general method for evaluating the likelihood for a general multi-state model in continuous time, applicable to any form of transition matrix. The available information is the observed state at a set of times. The next state to which the individual moves, and the time of the change, are governed by a set of transition intensities qrs(t; z(t)) for each pair of states r and s. The intensities may also depend on the time of the process t, or more generally a set of individual-specific or time-varying explanatory variables z(t). The intensity represents the instantaneous risk of moving from state r to state s: qrs(t, z(t)) = lim P (S(t + δt) = s|S(t) = r)/δt (1) δt→0 The intensities form a matrix Q whose rows sum to zero, so that the diagonal entries are defined by qrr = − ∑s≠r qrs. To fit a multi-state model to data, we estimate this transition intensity matrix. Models whose intensities change with time are called time-inhomogeneous. We concentrate on Markov models here. The Markov assumption is that future evolution only depends on the current state. That is, qrs(t; z(t);Ft) is independent of Ft, the observation history Ft of the process up to the time preceding t. See Cox and Miller[ ] for a thorough introduction to the theory of continuous-time Markov chains. In a time-homogeneous continuous-time Markov model, a single period of occupancy (or sojourn time) in state r has an exponential distribution, with rate given by -qrr, (or mean -1/qrr). The remaining elements of the rth row of Q are proportional to the probabilities governing the next state after r to which the individual makes a transition. The probability that the individual’s next move from state r is to state s is -qrs/qrr. Transition probability matrix: The likelihood is calculated from the transition probability matrix P(t). For a time-homogeneous process, the (r; s) entry of P(t), prs(t), is the probability of being in state s at a time t+u in the future, given the state at time u is r. It does not say anything about the time of transition from r to s, indeed the process may have entered other states between times u and t+u. P(t) can be calculated by taking the matrix exponential of the scaled transition intensity matrix (Cox and Miller [iv]). P (t) = Exp(tQ) (2) In order to be as close as possible to observable realities, we have presented the cost-effectiveness results from the matrix of transition probabilities observed by the model (e.g., 'prevalence.msm' algorithm), and not from the matrix of transition probabilities estimated by the model. This approach is taken by the function prevalence.msm, which constructs a table of observed and expected numbers and percentages of individuals in each state at a set of times (see detailed response to #comment 3 below). 3. An important component to any CE analysis is to assess whether the model is appropriate for the phenomena being examined, which is the purpose of model validation. In fact, very careful attention must be paid to the verification of a fundamental assumption which is the Markov property. Please discuss this aspect and perform model validation. Response: To compare the relative fit of two nested models, it is easy to compare their likelihoods. However it is not always easy to determine how well a fitted multistate model describes an irregularly-observed process. Ideally we would like to compare observed data with fitted or expected data under the model. If there were times at which all individuals were observed then the fit of the expected numbers in each state or prevalences can be assessed directly at those times. Otherwise, some approximations are necessary. We could assume that an individual’s state at an arbitrary time t was the same as the state at their previous observation time. This might be fairly accurate if observation times are close together. This approach is taken by the function prevalence.msm, which constructs a table of observed and expected numbers and percentages of individuals in each state at a set of times. A set of expected counts can be produced if the process begins at a common time for all individuals. Suppose at this time, each individual is in state 0. Then given n(t) individuals are under observation at time t, the expected number of individuals in state r at time t is n(t)P(t)0,r. If the covariates on which P(t) depends vary between individuals, then this can be averaged over the covariates observed in the data. Comparing the observed and expected percentages in each state, we could see that the predicted number of individuals who die is under or over-estimated by the model. Such discrepancies could have many causes. One possibility is that the transition rates vary with the time since the beginning of the process; the age of the patient, or some other omitted covariate, so that the Markov model is non-homogeneous. This could be accounted for by modeling the intensity as a function of age, for example, such as a piecewise-constant function. The pci argument to msm can be used to automatically construct models with transition intensities which are piecewise-constant in time. In this example, the hazard of death may increase with age, so that the model underestimates the number of deaths when forecasting far into the future. Another cause of poor model fit may sometimes be the failure of the Markov assumption. That is, the transition intensities may depend on the time spent in the current state (a semi-Markov process) or other characteristics of the process history. Accounting for the process history is difficult as the process is only observed through a series of snapshots. Semi-Markov models can be fitted to this type of data using phase-type distributions. Since version 1.4.1 the phase.states option to msm can be used to define some phase-type models. As we wrote in the #comment 2 response, in order to be as close as possible to observable realities, we have presented the cost-effectiveness results from the matrix of transition probabilities observed by the model (e.g., 'prevalence.msm' algorithm), and not from the matrix of transition probabilities estimated by the model. As a consequence, the model (e.g., observed numbers and percentages of individuals in each state at a set of times) is implicitly appropriate for the phenomena being examined, which is indeed the demonstration of model validation. The Markov property has been discussed previously and implicitly handled by our non-homogeneous semi-Markov multi-state model (see explanations above). 4. Line 91 - instead of “Statistical analyzes of observed” perhaps it is better to write “Statistical analysis of observed”. Response: Done. 5. Line 94 - The sentence about RStudio should be improved. To be more precise: “RStudio is an Integrated Development Environment for R, a programming language for statistical computing and graphics.” Response: Done. 6. Line 115: revise “by by”. Response: Done. 7. Always use the same number of decimals; see, just as an example, the p-values in the text. Response: Done. We settled 2 decimals (if adapted), except for percentages (1 decimal), and for p-values which can be equal, for instance, to 0.01 or 0.00001 (we settled 5 decimals for the p-values considering all possible values, except for values equal to 0.001). 8. Line 367: revise “Sensitivity analyzes”. Response: Done. ________________________________________ 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: No Reviewer #2: 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. [i] Christopher Jackson. Multi-state modelling with R: the msm package. Journal of Statistical Software (2011) 38(8):1-29. [ii] J.D. Kalbfleisch and J.F. Lawless. The analysis of panel data under a Markov assumption. Journal of the American Statistical Association, 80(392):863–871, 1985. [iii] R.~Kay. A Markov model for analysing cancer markers and disease states in survival studies. Biometrics, 42:855–865, 1986. [iv] D.~R. Cox and H.~D. Miller. The Theory of Stochastic Processes. Chapman and Hall, London, 1965. Submitted filename: Response to Reviewers.docx Click here for additional data file. 27 May 2022 Cost-effectiveness analysis of bundled innovative devices versus standard approach in the prevention of unscheduled peripheral venous catheters removal due to complications in France PONE-D-22-07543R1 Dear Dr. Maunoury, 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, Prof. Raffaele Serra, M.D., Ph.D Academic Editor PLOS ONE Additional Editor Comments (optional): amended manuscript is acceptable Reviewers' comments: 2 Jun 2022 PONE-D-22-07543R1 Cost-effectiveness analysis of bundled innovative devices versus standard approach in the prevention of unscheduled peripheral venous catheters removal due to complications in France Dear Dr. Maunoury: 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 Prof. Raffaele Serra Academic Editor PLOS ONE
  13 in total

Review 1.  Accepted but unacceptable: peripheral IV catheter failure.

Authors:  Robert E Helm; Jeffrey D Klausner; John D Klemperer; Lori M Flint; Emily Huang
Journal:  J Infus Nurs       Date:  2015 May-Jun

2.  Cost-effectiveness analysis of clinically indicated versus routine replacement of peripheral intravenous catheters.

Authors:  Haitham W Tuffaha; Claire M Rickard; Joan Webster; Nicole Marsh; Louisa Gordon; Marianne Wallis; Paul A Scuffham
Journal:  Appl Health Econ Health Policy       Date:  2014-02       Impact factor: 2.561

3.  Economic impact of use of chlorhexidine-impregnated sponge dressing for prevention of central line-associated infections in the United States.

Authors:  Xin Ye; Marcia Rupnow; Philippe Bastide; Antoine Lafuma; Liza Ovington; William R Jarvis
Journal:  Am J Infect Control       Date:  2011-06-08       Impact factor: 2.918

4.  The Markov process in medical prognosis.

Authors:  J R Beck; S G Pauker
Journal:  Med Decis Making       Date:  1983       Impact factor: 2.583

5.  Dressings and securements for the prevention of peripheral intravenous catheter failure in adults (SAVE): a pragmatic, randomised controlled, superiority trial.

Authors:  Claire M Rickard; Nicole Marsh; Joan Webster; Naomi Runnegar; Emily Larsen; Matthew R McGrail; Fiona Fullerton; Emilie Bettington; Jennifer A Whitty; Md Abu Choudhury; Haitham Tuffaha; Amanda Corley; David J McMillan; John F Fraser; Andrea P Marshall; E Geoffrey Playford
Journal:  Lancet       Date:  2018-07-26       Impact factor: 79.321

6.  Incidence, risk factors and medical cost of peripheral intravenous catheter-related complications in hospitalised adult patients.

Authors:  Congcong Liu; Lin Chen; Dong Kong; Fangfang Lyu; Linlin Luan; Lijuan Yang
Journal:  J Vasc Access       Date:  2020-12-10       Impact factor: 2.283

7.  Cost-benefit analysis of chlorhexidine gluconate dressing in the prevention of catheter-related bloodstream infections.

Authors:  Albert G Crawford; Joseph P Fuhr; Bhaskar Rao
Journal:  Infect Control Hosp Epidemiol       Date:  2004-08       Impact factor: 3.254

8.  Chlorhexidine plus alcohol versus povidone iodine plus alcohol, combined or not with innovative devices, for prevention of short-term peripheral venous catheter infection and failure (CLEAN 3 study): an investigator-initiated, open-label, single centre, randomised-controlled, two-by-two factorial trial.

Authors:  Jérémy Guenezan; Nicolas Marjanovic; Bertrand Drugeon; Rodérick O Neill; Evelyne Liuu; France Roblot; Paola Palazzo; Vanessa Bironneau; Frederique Prevost; Julie Paul; Maxime Pichon; Matthieu Boisson; Denis Frasca; Olivier Mimoz
Journal:  Lancet Infect Dis       Date:  2021-02-01       Impact factor: 25.071

9.  Cost-utilization of peripheral intravenous cannulation in hospitalized adults: An observational study.

Authors:  Fredericus Hj van Loon; Tina Leggett; Arthur Ra Bouwman; Angelique Tm Dierick-van Daele
Journal:  J Vasc Access       Date:  2020-01-23       Impact factor: 2.283

10.  Increased Clinical and Economic Burden Associated With Peripheral Intravenous Catheter-Related Complications: Analysis of a US Hospital Discharge Database.

Authors:  Sangtaeck Lim; Gaurav Gangoli; Erica Adams; Robert Hyde; Michael S Broder; Eunice Chang; Sheila R Reddy; Marian H Tarbox; Tanya Bentley; Liza Ovington; Walt Danker
Journal:  Inquiry       Date:  2019 Jan-Dec       Impact factor: 1.730

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