RELIAFIT MALE URINARY DEVICE. Case Study

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RELIAFIT MALE URINARY DEVICE Case Study

Quality Improvement Initiative Successful in Achieving CAUTI Reduction Mary Fitzwater, RN INTRODUCTION Catheter-associated urinary tract infections (CAUTI) negatively impact patient safety. Aside from complications associated with CAUTI, such as extended hospital length of stay, patient discomfort, and urosepsis, CAUTIs are considered never events and have negative economic consequences. 1-3 Prevention of CAUTI is an important focus of infection prevention efforts nationwide. 4-6 Researchers have demonstrated a positive correlation between number of Foley catheter device days and incidence of CAUTI (r2=0.79; N= 22,134 Foley catheter device days; P<.0001). 7 This has influenced the strong emphasis that has been placed on use of Foley catheters. 8 Alternatives for urinary management are now considered, such as external collection devices (ECDs). A hospital in Albuquerque trialed a quality improvement (QI) initiative hospital-wide using ECDs on male patients who met specific inclusion criteria and a 60 day study was conducted to measure their impact on CAUTI rates and prevalence.

Methods Clinical Setting: The QI initiative was implemented in November of 2014 hospital-wide for 60 days to determine the impact of ECDs on CAUTI rates in male patients. Metrics: A 60-day comparison of CAUTI rates was made before, during, and after the QI initiative to determine the effectiveness of the intervention. Intervention: A novel male ECD for urinary management was utilized instead of an indwelling urinary catheter in patients who met the following inclusion criteria: No restraints No benign prostatic hypertrophy No neurogenic bladder Cooperative with no urinary issues Hospitalized 2 weeks or greater Education: Staff received education on appropriate application of the male ECD, and a train the trainer program was implemented to ensure staff competency and knowledge of anticipated wear time (approximately 24 hours). Change Management: The QI coordinator conducted daily evaluations to determine average wear time, ensure there were no patient skin issues, or other questions/ problems associated with the ECD interventions.

Results The QI initiative was determined to be successful, with CAUTI rates falling to 0 during the 60 days of the ECD intervention (Figure 1). The average wear time of the ECD was approximately 24 hours. Figure 1. CAUTI rate before, during, and after intervention The Foley Utilization Rate (FUR) is listed in Table 1 for all time periods. It is important to note that the average FUR during the 60-day intervention period was substantially lower compared with the average FUR during the two months before and after the intervention (32.5% lower average FUR compared with before; 30% lower average FUR compared with after). No complications or adverse events were reported as a result of the ECD intervention. Table 1. Foley utilization rate before, during, and after intervention Before: Before: Intervention: Intervention: After: After: September October November December January February 2014 2014 2014 2014 2015 2015 FUR 38% 42% 25% 29% 34% 43% Foley catheter days 556 629 363 429 499 552 Patient days 1445 1507 1441 1468 1463 1273 FUR= Foley utilization rate (Foley Days/Patient Days)

CLINICAL IMPLICATIONS Use of ECDs can successfully manage urinary incontinence in circumstances where indwelling urinary catheters are deemed inappropriate. This 60-day QI intervention resulted in a lower average FUR compared with the time periods before and after the intervention, thereby lowering patient risk for CAUTI. Ensuring appropriateness criteria are adhered to for urinary catheterization is essential for prevention of CAUTI and related complications. REFERENCES 1. Kizilbash QF, Petersen NJ, Chen GJ, Naik AD, Trautner BW. Bacteremia and mortality with urinary catheter-associated bacteriuria. Infect Control Hosp Epidemiol. 2013 Nov;34(11):1153-9. doi: 10.1086/673456. Epub 2013 Sep 23. PubMed PMID: 24113598. 2. Meddings JA, Reichert H, Rogers MA, Saint S, Stephansky J, McMahon LF. Effect of nonpayment for hospital-acquired, catheter-associated urinary tract infection: a statewide analysis. Ann Intern Med. 2012 Sep 4;157(5):305-12. doi: 10.7326/0003-4819-157-5-201209040-00003. PubMed PMID: 22944872; PubMed Central PMCID: PMC3652618. 3. Wald H, Richard A, Dickson VV, Capezuti E. Chief nursing officers perspectives on Medicare s hospital-acquired conditions non-payment policy: implications for policy design and implementation. Implement Sci. 2012 Aug 28;7:78. doi:.1186/1748-5908- 7-78. PubMed PMID: 22928995; PubMed Central PMCID: PMC3499379. 4. Saint, S et al. (2002). Enhancing the Safety of Critically Ill Patients by Reducing Urinary and Central Venous Catheter-related Infections. American Journal of Respiratory and Critical Care Medicine, 165, pp. 1475-1479. Available at: http://www.ccmpitt.com/ebm/infectious_ disease/0061.pdf. 5. Fakih MG, et.al (2014). Engaging health care workers to prevent catheter-associated urinary tract infection and avert patient harm. Am J Infect Control. Vol 42:S223-29. 6. O Grady et al. (2008). Guidelines for evaluation of new fever in critically ill adult patients: 2008 update from the American College of Critical Care Medicine and the Infectious Diseases Society of America, Crit Care Med, 36(4), pp. 1330-1349. 7. Titsworth WL, Hester J, Correia T, Reed R, Williams M, Guin P, Layon AJ, Archibald LK, Mocco J. Reduction of catheter-associated urinary tract infections among patients in a neurological intensive care unit: a single institution s success. J Neurosurg. 2012 Apr; 116(4):911-20. doi: 10.3171/2011.11.JNS11974. Epub 2012 Jan 6. PubMed PMID: 22224785. 8. American Nurses Association. (2014). Streamlined Evidence-Based RN Tool: Catheter Associated Urinary Tract Infection Prevention. Available at: http://nursingworld.org/mainmenucategories/ ThePracticeofProfessionalNursing/Improving-Your- Practice/ANA-CAUTI-Prevention-Tool/ANA-CAUTI- Prevention-Tool.pdf.

ReliaFit is an essential product in the Eloquest Healthcare portfolio. This case study does not imply approval or endorsement by Kindred Hospital of any products. RE15 04/16