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Clinical outcomes of female external urine wicking devices as alternatives to indwelling catheters: a systematic review and meta-analysis

Published online by Cambridge University Press:  06 May 2024

Nicholas Pryor Open the ORCID record for Nicholas Pryor [Opens in a new window] ,
JiCi Wang ,
Jordan Young ,
Whitney Townsend Open the ORCID record for Whitney Townsend [Opens in a new window] ,
Jessica Ameling Open the ORCID record for Jessica Ameling [Opens in a new window] ,
James Henderson Open the ORCID record for James Henderson [Opens in a new window]  and
Jennifer Meddings Open the ORCID record for Jennifer Meddings [Opens in a new window]
Nicholas Pryor*
Affiliation:
Division of General Medicine, Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI, USA School of Public Health, University of Michigan, Ann Arbor, MI, USA
JiCi Wang
Affiliation:
University of Michigan Medical School, Ann Arbor, MI, USA
Jordan Young
Affiliation:
Michigan Surgical Quality Collaborative, University of Michigan, Ann Arbor, MI, USA
Whitney Townsend
Affiliation:
University of Michigan Taubman Health Sciences Library, Ann Arbor, MI, USA
Jessica Ameling
Affiliation:
Division of General Medicine, Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI, USA Patient Safety Enhancement Program, University of Michigan and VA Ann Arbor Healthcare System, Ann Arbor, MI, USA
James Henderson
Affiliation:
Division of General Medicine, Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI, USA University of Michigan Institute for Healthcare Policy and Innovation, Ann Arbor, MI, USA
Jennifer Meddings
Affiliation:
Division of General Medicine, Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI, USA University of Michigan Medical School, Ann Arbor, MI, USA Center for Clinical Management Research, VA Ann Arbor Healthcare System, Ann Arbor, MI, USA Division of General Pediatrics, Department of Pediatrics and Communicable Diseases, University of Michigan Medical School, Ann Arbor, MI, USA
*
Corresponding author: Nicholas Pryor; Email: [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Background:

Female patients using indwelling urinary catheters (IUCs) are disproportionately at risk for developing catheter-associated urinary tract infections (CAUTIs) compared to males. Female external urine wicking devices (FEUWDs) have emerged as potential alternatives to IUCs for incontinence management.

Objectives:

To assess the clinical risks and benefits of FEUWDs as alternatives to IUCs.

Methods:

Ovid MEDLINE, Embase, Scopus, Web of Science Core Collection, CINAHL Complete, and ClinicalTrials.gov were searched from inception to July 10, 2023. Included studies used FEUWDs as an intervention and reported measures of urinary tract infections and secondary outcomes related to incontinence management.

Results:

Of 2,580 returned records, 50 were systematically reviewed. Meta-analyses assessed rates of indwelling CAUTIs and IUC utilization. Following FEUWD implementation, IUC utilization rates decreased 14% (RR = 0.86, 95% CI = [0.76, 0.97]) and indwelling CAUTI rates nonsignificantly decreased up to 32% (IRR = 0.68, 95% CI = [0.39, 1.17]). Limited only to studies that described protocols for implementation, the incidence rate of indwelling CAUTIs decreased significantly up to 54% (IRR = 0.46, 95% CI = [0.32, 0.66]). Secondary outcomes were reported less routinely.

Conclusions:

Overall, FEUWDs nonsignificantly reduced indwelling CAUTI rates, though reductions were significant among studies describing FEUWD implementation protocols. We recommend developing standard definitions for consistent reporting of non-indwelling CAUTI complications such as FEUWD-associated UTIs, skin injuries, and mobility-related complications.

Type
Review
Information
Infection Control & Hospital Epidemiology , Volume 45 , Issue 9 , September 2024 , pp. 1121 - 1129
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Creative Commons
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This is a work of the US Government and is not subject to copyright protection within the United States. Published by Cambridge University Press on behalf of The Society for Healthcare Epidemiology of America.
This is an Open Access article, distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided that no alterations are made and the original article is properly cited. The written permission of Cambridge University Press must be obtained prior to any commercial use and/or adaptation of the article.
Copyright
© United States Department of Veterans Affairs (VA), 2024

Introduction

Catheter-associated urinary tract infections (CAUTIs) are a leading source of hospital-acquired infections and associated with complications that increase patient morbidity Reference Magill, Edwards and Bamberg1,Reference Meddings, Rogers, Krein, Fakih, Olmsted and Saint2 . Many hospital-acquired urinary tract infections develop in patients using indwelling urinary catheters (IUCs) (i.e., Foley catheters) Reference Meddings, Rogers, Krein, Fakih, Olmsted and Saint2 . IUCs disrupt innate immune defenses, causing biofilm formation on catheter surfaces and subsequent bacteriuria Reference Magill, Edwards and Bamberg1 . The risk of bacteriuria increases each day an IUC is in place, making it imperative to limit the duration of catheterization or avoid catheterization altogether Reference Hooton, Bradley and Cardenas3 .

IUC alternatives for male patients have existed for quite some time Reference Gray, Skinner and Kaler4–Reference Saint, Kaufman and Rogers6 . Yet, until recently, a viable alternative for female patients has been lacking. In 2016, a noninvasive collection device designed for female genitalia was developed and trademarked as PureWick Reference Newton, Call and Chan7 . Utilizing a soft and flexible wicking material to absorb urine, which is gently drawn away from the body using low, continuous suction, it is placed between the labia majora, with the wicking material facing the body, the top of the device aligned with the pubic bone, and the bottom tucked into the gluteal cleft Reference Uhr, Glick and Barron8–Reference Beeson and Davis10 . These devices have the potential to reduce indwelling CAUTI incidence in female patients, who are particularly susceptible to CAUTIs given the short length of the female urethra and its proximity to the perineum. Current research has examined two similar female external urine wicking devices (henceforth, FEUWDs) that differ only slightly in shape and options for securing the device to the patient: PureWick (Becton, Dickinson and Co.) and PrimaFit (Sage Products LLC) 11,12 . Here, we perform a systematic review and meta-analysis of the existing literature to assess the clinical risks and benefits of FEUWDs, hypothesizing that FEUWD use would result in reduced CAUTI rates (without increasing non-indwelling catheter-associated UTIs) due to their less invasive technology than traditional indwelling catheters. Because non-indwelling catheter-associated UTI data were insufficient, our analysis was only able to evaluate the effect of FEUWD use on CAUTI rates.

Methods

We are compliant with Meta-Analysis of Observation Studies in Epidemiology (MOOSE) reporting guidelines. This systematic review was registered in PROSPERO (ID: CRD42022340503). Protocol updates are provided in Supplement Methods 1.

Data sources and searches

The following databases were searched from inception to July 12, 2022 to identify relevant articles, trials, or meeting abstracts describing alternatives to indwelling catheters: Ovid Medline (Ovid Medline, Embase.com, Scopus, Web of Science Core Collection, CINAHL Complete, and ClinicalTrials.gov. Search updates were performed on March 24, 2023 and July 10, 2023. Each search utilized controlled vocabulary in combination with relevant keywords, and no limits were applied. Reference tracking was performed on highly relevant articles. Original search strategies were developed in Ovid Medline and translated to other databases using the Systematic Review Accelerator Polyglot tool Reference Clark, Sanders and Carter13 . Complete search terms and strategies are available in Supplement Methods 2.

Study selection

Eligibility criteria were left broad to capture all possible relevant data. Studies of female and male patients were eligible for inclusion based on reports that certain male patients (such as those with penile retraction) may use FEUWDs despite not being designed for male use. Furthermore, both randomized and non-randomized studies, published or unpublished, were eligible for inclusion, given that they implemented an appropriate intervention (i.e., FEUWD) and reported at least one outcome of interest.

Although FEUWDs are the intervention of interest, no formal definition of female external urinary device-associated UTIs (FEUWD-UTIs) currently exists (Supplement Methods 3). Because FEUWD use is hypothesized to reduce IUC use and, consequently, indwelling catheter-associated UTI (CAUTI) rates, indwelling CAUTIs are evaluated as the primary outcome. Secondary outcomes included IUC use, antibiotic use, skin breakdown, skin pressure injury, vaginal/vulvar dryness or chaffing, cost effectiveness, and mobility-related complications.

Citations were deduplicated by librarian WT using a modified version of the Bramer Endnote Deduplication Technique Reference Bramer, Giustini and de Jonge14 . Within Rayyan, each record was screened by two independent, trained investigators: NP (Records 1-1,256), JW (1–592), JY (593–1,256) Reference Ouzzani, Hammady and Fedorowicz15 . Records were selected if they made sufficient reference to the intervention and outcome(s) of interest or if reference to “external urinary catheters” was vague and needed further clarification.

Having obtained full-text records, citations were discarded if they contained no additional clarification or the wrong catheter type was identified. Records published prior to 2015 were excluded as FEUWDs were brought to market in 2016. Still, experimental use of the devices might have occurred earlier; thus, we restricted included studies to only those dated 2015 to present. At each step, discrepancies in reviewer decisions were resolved through deliberation.

Data extraction and quality assessment

Remaining records underwent dual independent review: NP (Records 1–50), JW (1–20), JY (21–50). Outcome data was collected in identical electronic data extraction forms. Two independent reviewers used the Risk of Bias in Non-Randomized Studies—of Interventions (ROBINS-I) tool to assess the methodological quality of included records, excluding abstracts, which provide limited information on methods used, and non-interventional studies (NP (Records 1–14), JA (1–3), JW (4–6), JY (7–14)) (16).

Data synthesis and analysis

Studies included in meta-analyses provided sufficient data to calculate or infer the rate ratios of CAUTIs per 1,000 patient-days (pd), CAUTIs per 1,000 device-days (dd), or IUC utilization (device-days per patient-days) from pre- to post-FEUWD implementation periods. Random-effects meta-analysis models then determined the pooled effect of FEUWD implementation on the rate of CAUTIs per 1,000 pd, CAUTIs per 1,000 dd, and IUC utilization. Although IUC use is a secondary outcome, it was frequently reported and therefore included in meta-analysis. Other secondary outcomes, although reported inconsistently, were systematically evaluated and summarized. We planned to assess publication bias using funnel plot visualization and Egger’s regression tests.

Some studies included in the meta-analyses explicitly described the use of protocols for FEUWD implementation. However, other studies either did not follow a protocol or failed to specify. Because the nature of implementation could be unclear, studies were categorized post hoc according to their overall risk of bias score (ROB), which reflects the strength of implementation protocols. Measures of heterogeneity were calculated for subgroup and overall random-effects models (Cochran’s Q, I 2, and τ2). Statistical analyses were performed using R Statistical Software, version 4.1.2 (metafor package) Reference Viechtbauer17 .

Role of the funding source

The funder had no role in any part of the design or conduct of the study.

Results

Fifty records were included for review (Supplement Fig. 1). Two randomized control trials were reviewed for eligibility: (1) a pilot in collaboration with Becton, Dickinson and Co. studying the use of PureWick to manage nocturia and nighttime falls associated with going to the bathroom and (2) a C.R. Bard-sponsored trial evaluating risk of skin injury and the urine capture rate of PureWick in incontinent women requiring diapers Reference Chughtai18,Reference Bard19 . Because these are ongoing, no results were available for consideration. Consequently, all 50 records were non-randomized intervention studies. Only 14 studies, providing sufficient methodological information and interventional in design, were evaluated for quality. Of these, 7 studies provided adequate outcomes data required for inclusion in meta-analyses. All 7 studies included in meta-analyses demonstrated a moderate or serious risk of bias overall (Supplement Fig. 2).

Table 1 summarizes the outcomes reported in each record. Most reported some measure of UTI and IUC utilization, though only two reported FEUWD-UTIs. With few exceptions, all abstracts reported decreased indwelling CAUTI incidence upon FEUWD implementation, although reporting of statistical significance, confidence intervals, and sample sizes varied. Study characteristics and outcomes of records included in meta-analyses are given in Table 2, with more detailed outcomes provided in Supplement Table 1. Of the 7 studies included in meta-analyses, studies either implemented FEUWDs amid other interventions designed to reduce IUC utilization and CAUTI rates, which could have influenced outcomes, or did not specify (Table 2). Study characteristics and outcomes of all other records are provided in Supplement Table 2. Table 3 provides a summary of secondary outcomes.

Table 1. Summary of outcomes reported in included records*

* All studies are based in the United States except for Cilluffo et al. (Italy).

UTI, urinary tract infection not associated with an indwelling urinary catheter.

CAUTI, indwelling catheter-associated urinary tract infection.

FEUWD-UTI, female external urine wicking device-associated urinary tract infection.

IUC Utilization, indwelling urinary catheter utilization.

Urine Cultures Ordered, a test ordered by a clinician to determine the presence of infectious microorganisms in urine samples.

Bacteriuria, a positive culture of bacteria in urine (with or without symptoms of UTI, treated or untreated with antibiotics).

Skin Complications, inclusive of skin dermatitis, dermatologic allergic reaction, skin breakdown, pressure injuries.

Other: LOH, length of hospitalization; ABX, antibiotic use; MRC, mobility-related complications (e.g., deep vein thrombosis, falls); UC, urine collection; CE, cost-effectiveness; CS, comfort or patient/provider satisfaction.

Table 2. Characteristics and outcomes of peer-reviewed published manuscripts included in meta-analyses

* Author indicated the use of simultaneous CAUTI reduction initiatives, such as CAUTI bundles or QI projects, but did not provide a specific explanation of included components.

† Author indicated the use of simultaneous IUC reduction initiatives but did not provide a specific explanation of included components (e.g., IUC indication restrictions, reminders, or stop orders).

‡ Incidence rate ratios were calculated using only female patient-days. Many studies did not stratify patient-days by sex and were only able to calculate rate ratios using total (male and female) patient-days.

FEUWD, female external urine wicking device; UIM, urinary management; NR, not reported; NS, not specified.

Table 3. Summary of secondary outcomes

* These studies failed to track temporal changes in IUC and FEUWD status, making it difficult to determine if outcomes were associated with IUC or FEUWD use.

† HAPIs are multifactorial and may not be associated with urinary catheter use.

Meta-analyses

Due to limited reported data, only 7 studies contributed to the pooled estimates of CAUTIs per 1,000 pd and CAUTIs per 1,000 dd, while 6 studies contributed to the pooled estimate of IUC utilization. Overall, there was no significant difference in indwelling CAUTI rates before and after FEUWD implementation (Fig. 1). That is, while CAUTIs per 1,000 pd decreased 32% following implementation of FEUWDs (IRR = 0.68, 95% CI = [0.39, 1.17], p = .1658, I 2 = 60.9%) and CAUTIs per 1,000 dd decreased 18% (IRR = 0.82, 95% CI = [0.48, 1.40], p = .4564, I 2 = 59.3%), neither reduction was significant. The pooled rate of IUC utilization indicates that IUC use decreased significantly by 14% after implementation of FEUWDs (RR = 0.86, 95% CI = [0.76, 0.97], p = .0136, I 2 = 99.0%).

Figure 1. Meta-analyses of the effect of FEUWDs on CAUTI rates and IUC utilization.

Note that Fig. 1c has a different scale to facilitate the visualization of very narrow confidence intervals.

FEUWD, female external urine wicking device; RE, random effects.

Heterogeneity across studies was high. However, according to post hoc analyses, there were significant reductions and less heterogeneity in studies with moderate ROBs. Specifically, CAUTIs per 1,000 pd decreased 54% (IRR = 0.46, 95% CI = [0.32, 0.66], p < .001, I 2 = 0.0%) and CAUTIs per 1,000 dd decreased 45% (IRR = 0.55, 95% CI = [0.38, 0.79], p = .0014, I 2 = 0.0%). In this subgroup, there was a reduction of 16% for the IUC utilization rate (RR = 0.84, 95% CI = [0.80, 0.89], p < .001, I 2 = 94.8%), though heterogeneity remained high.

Discussion

To the best of our knowledge, this is the first systematic review and meta-analysis of clinical outcomes associated with female external urine wicking devices (FEUWDs), which have the potential to supplement existing CAUTI prevention initiatives. The results of this meta-analysis suggest that rigorously protocolized implementations of FEUWDs can significantly reduce indwelling urinary catheter (IUC) utilization and indwelling CAUTI rates in hospital settings, though the inconsistent reporting of outcomes such as FEUWD-associated UTIs limits our ability to fully assess the original hypothesis. Secondary outcomes like skin injury and mobility-related complications were reported rarely and with varied or unspecified definitions.

Meta-analyses demonstrated that studies with moderate ROBs were associated with significant reductions in IUC utilization and indwelling CAUTI rates. Because these studies typically indicated the use of protocols to guide their introductions of FEUWDs, it appears that the process by which FEUWDs are implemented is an important determinant of their effect on IUC utilization and indwelling CAUTI rates. Implementation of FEUWDs may reduce CAUTIs through two paths: (1) by reducing IUC utilization (i.e., preventing the onset of the “lifecycle of the catheter”)—patients never catheterized cannot, by definition, have a CAUTI, while patients with fewer catheter-days are at lower risk of CAUTI Reference Patel, Gupta and Vaughn71 —and (2) by reducing CAUTI rates among those catheterized (CAUTI per dd) if FEUWD roll-out was part of a “bladder bundle” that optimizes CAUTI prevention practices Reference Saint, Olmsted and Fakih72 . Based on the pooled estimates, IUC utilization was reduced by 14% while CAUTI rates among those catheterized were reduced by 45%, suggesting that pathway (2) is very important. This is consistent with protocols that direct FEUWD use toward patients at higher risk of CAUTI but could also reflect bias from other efforts to reduce CAUTIs. FEUWDs also appear to be a promising means of accurate urine collection, associated with high user satisfaction, and a potential cost-cutting intervention, though the need for frequent replacement (i.e., every 8–12 hours or when soiled by blood or stool) might countervail potential savings.

Limitations

All studies included in meta-analyses demonstrated a moderate to serious risk of bias. Because several studies were conducted as QI projects rather than controlled interventions, implementation protocols varied across sites, which contributed to heterogenous effects. This also typically meant that the introduction of FEUWDs occurred alongside existing interventions to reduce CAUTIs. Studies with moderate ROBs failed to adequately account for confounding interventions, which undermined the internal validity of their findings and may be attributable to weak implementation protocols. Studies with serious ROBs demonstrated additional methodological problems. For example, both studies with serious ROBs, which shared language to describe the absence of an implementation protocol, failed to account for temporal changes to intervention status, making it difficult to ascertain which device type (FEUWD or IUC) had the effect of increasing their indwelling CAUTI and FEUWD-associated UTI rates Reference Jasperse, Hernandez-Dominguez and Deyell23,Reference Lem, Jasperse and Grigorian25 .

In the meta-analyses, confidence intervals for IUC utilization rates are exceedingly narrow because included studies treated each patient-day independently rather than nested within patients and we lack the information needed to adjust for this properly. Another limitation is that some studies calculated rates based on total (male and female) patient-days Reference Beeson, Pittman and Davis20,Reference Zavodnick, Harley and Zabriskie35 . Because interest lies in the comparison of rate ratios as opposed to rates themselves, the rate ratios for these studies can still be compared to others. However, this relies on the assumption that the fraction of female patient-days to total patient-days is relatively stable between pre- and post-intervention periods.

Although publication bias is a potential limitation (Supplement Fig. 3), the low number of studies included in meta-analyses and considerable inter-study heterogeneity make this difficult to assess Reference Sterne, Sutton and Ioannidis70 . The risk of publication bias should be reassessed when more studies are available to be included in meta-analysis.

Recommendations

Because the quality of existing data regarding the clinical outcomes of FEUWDs is limited, the results of our systematic review and meta-analysis should be interpreted judiciously. Nevertheless, we feel that it is important to share these findings to improve the quality of future research on FEUWDs, and we have identified areas for improvement to help researchers achieve this aim.

First, we recommend developing a standardized definition of female external urine wicking device-associated urinary tract infections (FEUWD-UTIs) to facilitate comparison across future studies. In addition to the joint reporting of IUC utilization and indwelling CAUTI rates, FEUWD utilization and FEUWD-UTI rates should be reported, as well as skin- and mobility-related complications associated with FEUWD use. Although some studies have reported measures of FEUWD use, they vary greatly and are often not expressed as device-days per patient-days Reference Eckert, Mattia and Patel22,Reference Jasperse, Hernandez-Dominguez and Deyell23,Reference Lem, Jasperse and Grigorian25,Reference Rearigh, Gillett and Sy27,Reference Tran, Rodrigue, Jones and Bell30,Reference Warren, Fosnacht and Tremblay32,Reference Whitaker, Colgrove, Scheutzow, Ramic, Monaco and Hill33,Reference Gentile, Jacob and Ashraf46,Reference Peters, Grote and Spera63 . It would also be useful for researchers to report IUC utilization and indwelling CAUTI rates among female patients only so that evaluations of the relationship between FEUWD and IUC use are specific to the patient population of interest.

Ultimately, more rigorously protocolized intervention studies reporting these outcomes are needed to provide sufficient data to measure the correlation between device utilization and UTI outcomes, which could corroborate the hypothesized mechanism by which FEUWDs reduce UTI rates. Ideal FEUWD implementation protocols should include: (1) standardized guidelines for FEUWD use rather than clinician discretion only, (2) consistent and standardized charting, (3) maintained attention to local hygiene as would be expected for IUCs, and (4) documentation of all potential FEUWD-associated complications.

There is also variation in the types of units in which FEUWDs are implemented, which may be an important factor in gauging FEUWD utility. We recommend that FEUWDs first be introduced in the ICU. Warren et al. (2021) recommended first implementing FEUWDs in ICUs given their observation that PureWick implementation had the greatest effect on IUC utilization and indwelling CAUTI rates in ICU patients Reference Warren, Fosnacht and Tremblay32 . Similarly, Gentile et al. (2020) observed significant reductions in IUC utilization and indwelling CAUTI rates after introduction of PureWick in ICUs only Reference Gentile, Jacob and Ashraf46 . Because ICUs tend to have the greatest number of patients using IUCs, CAUTI incidence is likely to be higher than on other hospital units. These findings suggest that where the preponderance of CAUTI is greatest, so too will be the protective effect of FEUWDs. Further research is needed to ascertain FEUWD effectiveness in environments with traditionally lower IUC use. Still, even in settings with low baseline IUC utilization, Gentile et al. (2020) found that successful FEUWD implementation can lead to further, if modest, reductions in IUC utilization and indwelling CAUTI rates Reference Gentile, Jacob and Ashraf46 .

Conclusions

FEUWDs have the potential to significantly reduce IUC utilization and indwelling CAUTI rates in hospital settings when introduced with a protocol to guide use. Although secondary outcomes of FEUWD use were reported less routinely, there is evidence that their benefit extends beyond reducing CAUTI incidence. Inconsistent implementation protocols contribute to significant heterogeneity and studies likely do not control for important confounders, limiting our understanding of the true effect of FEUWDs. Improved implementation protocols and a standardized definition of FEUWD-UTIs should help harmonize interventions and comparisons of effects across future studies.

Supplementary material

The supplementary material for this article can be found at https://doi.org/10.1017/ice.2024.73.

Financial support

This project was funded under grant number R01HS026912 from the Agency for Healthcare Research and Quality (AHRQ), U.S. Department of Health and Human Services (HHS). The authors are solely responsible for this document’s contents, findings, and conclusions, which do not necessarily represent the views of AHRQ. Jennifer Meddings is an employee of Michigan Medicine with the University of Michigan and a Federal Employee of the VA Ann Arbor Healthcare System. She reports grant funding from the AHRQ, CDC, Ralph E. Wilson Foundation, and the VA HSR&D.

Competing interests

Jennifer Meddings works as an Associate Editor for the Annals of Internal Medicine: Clinical Cases journal.

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Figure 0

Table 1. Summary of outcomes reported in included records*

Figure 1

Table 2. Characteristics and outcomes of peer-reviewed published manuscripts included in meta-analyses

Figure 2

Table 3. Summary of secondary outcomes

Figure 3

Figure 1. Meta-analyses of the effect of FEUWDs on CAUTI rates and IUC utilization.Note that Fig. 1c has a different scale to facilitate the visualization of very narrow confidence intervals.FEUWD, female external urine wicking device; RE, random effects.

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