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Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University of Michigan

Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

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Page 1: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

Evaluation of Discharge Room Cleaning using UV Technology:

Focus on Clostridium difficile

Alison Gibson D.O.Fellow, Pediatric Infectious Diseases

University of Michigan

Page 2: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

Disclosures

• This study was funded by a $12,000 award from the Patient Safety Committee of University of Michigan Health System

• Both of the UV devices used in our study were provided to the institution by Xenex and iPT during the outcomes study, the Xenex device was then rented to complete the environmental culturing study

• I have no other conflicts of interest or relationships with industry

This is a confidential Quality Improvement and Assurance/peer review document of the University of Michigan Hospitals and Health Centers.  Unauthorized disclosure or duplication is absolutely prohibited.  This document is protected from disclosure pursuant to the provisions of MCL 333.20175; MCL 333.21515; MCL 331.531; MCL 331.533 or such other statutes that may be applicable.

Page 3: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

Objectives

• How does UV work?• What literature do we have to

support the use of UV?• Why did UofM choose to pursue UV

and how did we utilize it?• Outcomes study• Environmental culturing study• Future Directions

Page 4: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

Automated Room Disinfection

• Ultraviolet (UV)– UV-C (mercury bulbs)– PPX-UV (pulsed xenon bulbs)

• Hydrogen peroxide vapor (HPV)• Neither of these technologies replace

manual cleaning, and therefore both add additional time before room turnover

Page 5: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

Tru-D Lumalier (UV-C)

http://www.hpnonline.com/inside/2011-09/1109-CS-RoomDisinfection.html

Xenex (PPX-UV)

http://bionews-tx.com/wp-content/uploads/2013/04/xenex-device.jpg

Bioquell (HPV)

http://www.bioquell.com/en-us/markets/product-selector/bioquell-q10/

Page 6: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

UV – Science

• Breaks DNA bonds by inducing pyrimidine or thymine dimers (1,2,3,4,5)

http://mashable.com/category/dna/

Page 7: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

UV – Safety

• No health or safety concerns returning to room

• Direct prolonged light exposure can cause temporary corneal and conjunctival irritation (1,2,3,4,5)

http://www.clinicaladvisor.com/what-to-do-when-the-eyes-have-it/article/121816/

Page 8: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

UV – Utilization

• Easy to use, no room modifications• Shorter treatment time (depending on

device and room size, compared to HPV)• Expenses associated with machine and

bulb replacement• Safe with electronic room devices and

other room materials (1,2,3,4,5)

Page 9: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

UV - Efficacy

• 2-4 log10 reduction of spores

• May allow resistant organisms to develop due to sub-lethal dose

• Efficacy dependent on intensity of emitted light (old bulb vs. new bulb), exposure time, placement/obstructions, air movement

• Less effective out of direct line of sight• Less effective further from the source

(cannot use in large areas) (1,2,3,4,5)

Page 10: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

UV-C vs. PPX-UVUV-C (Ex. Tru-D Lumalier,

iPT)

• 200-280nm, Tru-D emits at 254nm

• Breaks DNA bonds but not at the ideal wavelength (265nm), so occurs more slowly

• Continuous dose at germicidal wavelength

• Longer treatment times (34-100min per cycle) (1,2,4,5)

PPX-UV (Ex. Xenex)• 200-320nm broad spectrum• More efficient (faster) because

more broad spectrum• Additional benefits of

photosplitting, photohydration, and photocrosslinking, all of which contributes to faster treatment times

• Pulse dose at broad wavelength including germicidal range

• Shorter treatment times (5-10 min per cycle) (1,2,5)

Page 11: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

Published UV DataStudy Device Cleaning

MethodCulture Method

Results

Anderson et al. (2013)6

Tru-D Lumalier

UV Rodac touch plates

1.16 log reduction in colony counts

Boyce et al. (2011)7

Tru-D Lumalier

UV Pre-inoculated plates

1.7-2.9 log reduction in colony counts

Sitzlar et al. (2013)8

Tru-D Lumalier

Routine cleaning followed by UV

Surface swabbing

Reduction in positive cultures from 57% to 35%

Levin et al. (2013)9

PPX-UV Bleach followed by UV

None Reduction in HO-CDI rate from 9.46 to 4.45/10,000 PDs

Page 12: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

Why did we choose to pursue use of a UV system?

• C. difficile rates are above the national and state averages

• Tried to implement daily bleach cleans of high-touch surfaces

• Appeal of a device less vulnerable to human error

Page 13: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

UV light trials

• Trialed two different lights [PPX-UV (Xenex) and UV-C (iPT)] on three units each and followed HO-CDI rates– Trial 1 was 5 months– Trial 2 was 10 months

Page 14: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

UV Utilization

http://bionews-tx.com/news/2014/10/08/xenex-uv-emitting-room-disinfection-robots-ready-to-tackle-ebola-and-other-contamination/

• Adjunct to bleach for discharge room cleans• 2 - 4 cycles per room, 5-10 min each plus

set up and take down• Device was operated by EVS personnel

trained by our institution• Spot cleaning of public areas/work areas

(family rooms, bathrooms, etc.)

Page 15: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

http://bionews-tx.com/wp-content/uploads/2013/04/xenex-device.jpg

http://www.infectionpreventiontechnologies.com/irsModel3200m.php

iPT (UV-C) Xenex (PPX-UV)

Page 16: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

5D 8C 8DNS Total0

5

10

15

20

25

30

Healthcare Facility Onset C. difficile Rates Dur-ing UV-C Trial

UV Trial5 mths prior to trial (p = .3360)Same time period previous year (p = .3793)

Hospital Unit

C.

diffi

cile R

ate

(C

ases/1

0,0

00 P

ati

ent-

Days)

*None of the units showed a statistically significant change in C. difficile rate, with the exception of 8DNS which showed a significantly worse rate when com -pared to the previous 5 months

Page 17: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

5B 6D 4D Total

0

5

10

15

20

25

30

35

Healthcare Facility Onset C. difficle Rates During PPX-UV Trial

UV Trial

10 mths prior to trial (p = .9576)

Same time period previous year (p = .5738)

Hospital Unit

C.

diffi

cil

e r

ate

(cases/1

0,0

00

pati

en

t-d

ays)

*no individual units reached a statisti-cally significant difference in C. diffi-cile rate

Page 18: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

UV Utilization

Page 19: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

Barriers to UV Utilization

• Prolonged room turnover time• Only can be used at discharge in

single occupant rooms• Burden of initial investment to

provide sufficient machines to cover all C.diff or contact isolation or every discharge

• Burden of training and maintaining additional EVS personnel to run the devices

Page 20: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

Why we chose to pursue this study

• No improvement in C. difficile outcomes after utilizing UV technology–Were we utilizing the device correctly?• Were enough rooms being treated?

–Was it actually decreasing environmental C. difficile burden?

– Is environmental contamination at discharge our primary issue?

Page 21: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

The Study• Our goal was to compare the effectiveness of manual

cleaning with quaternary ammonium cleaner (Virex), manual cleaning with bleach, and PPX-UV cleaning both separately and in combination

• Obtained cultures from confirmed C. difficile positive rooms at discharge and throughout the cleaning process• Bed rail• Tray table• Remote• Toilet seat• Toilet rim• Sink faucet• Light switch• Keyboard

Page 22: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

Soiled Room

Soiled Room

Culture #1 Culture #1

Bleach Clean

QA Clean

PPX-UV Clean

PPX-UV Clean

Ready for Admission

Bleach Clean

Culture #2 Culture #2

Culture #3 Culture #3

Page 23: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

Technicalities of swabbing and culturing

• Sites were swabbed using pre-moistened sterile swabs (EnviroMax Plus)

• Swabs were inoculated in enrichment broth (TCCFB) and incubated anaerobically for 24-48 hours

• Broth was plated on selective media (CCFA-HT) and incubated anaerobically for 24-48 hours

• Multiple colonies which were morphologically similar to/consistent with C.difficile were selected from each plate for PCR

• PCR was used to detect toxin genes tcdA, tcdB, cdtA/cdtB

• Representative isolates from each room were PCR ribotyped

Page 24: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

C. difficile Reduction with Bleach Followed by PPX-UV

Page 25: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

C. difficile Reduction with QA Followed By PPX-UV

Page 26: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

Conclusions

• Bleach effectively eradicated C. difficile from multiple surfaces (p = .011)

• PPX-UV light could not show an additive benefit when utilized after bleach cleaning (p = .343)

• Manual cleaning with a QA product followed by PPX-UV did reduce positive C. difficile cultures (p = .008)

• Manual cleaning with a QA product followed by PPX-UV is possibly not as effective for C. difficile eradication as bleach alone (p = .063)

Page 27: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

In the Meantime…

• Nerandzic et al. (2015):– Xenex (PPX-UV) device and Tru-D Lumalier (UV-C) device– C. diff, MRSA, and VRE from pre-inoculated plates

• Pathogen load did not impact killing, but distance from source did

• C. diff at 4ft was only 0.5 log10 reduction with PPX-UV

• UV-C was superior to PPX-UV for reduction of all 3 organisms with the same concentrations of organisms and distance from source (1 log10 for C. diff)

– Room contamination • Tested PPX-UV alone and bleach + PPX-UV• Saw statistically significant reductions in culture positivity with

PPX-UV, but not with bleach + PPX-UV, and did not assess for statistically significant difference between the two methods (10)

Page 28: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

In the Meantime…

• Ghantoji et al. (2015):– Xenex PPX-UV device– Environmental cultures were collected

before and after environmental cleaning with activated hydrogen peroxide followed by bleach (26/74 18/74)

– And with activated hydrogen peroxide followed by PPX-UV (29/70 16/70)

– No statistically significant difference in C. difficile positive cultures, z = 0.058 (11)

Page 29: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

Comparing Our Study

Study

Positive cultures pre-

bleach (%)

Positive cultures post-

bleach (%)

Gibson et al. 17/80 (21%) 1/80 (1%)

Ghantoji et al.11 26/74 (35%) 18/74 (24%)a

Nerandzic et al. 10 22/113 (19%) 9/113 (8%)b

aCultures were obtained pre- and post- combination of activated hydrogen peroxide followed by bleachbCultures were obtained pre- and post- combination of standard clean including bleach followed by PPX-UV

Page 30: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

Remaining Questions

• Is environmental contamination at discharge a primary contributor to C. difficile transmission at our institution?

• Does UV-C/PPX-UV have a place in an infection prevention program?

• What amount of bacterial environmental burden is permissible?

Page 31: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

Future Directions

When an excessive number of cases occur on a unit (5 in a rolling 4 week period), multi-pronged approach including: bleach cleaning ATP assessment contact precautions re-enforcement and

monitoring Possible utilization of hydrogen peroxide

vapor (Bioquell) Focusing on other aspects of C. difficile

prevention besides the terminal clean

Page 32: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

Thanks

• Patient Safety Committee of the University of Michigan Health System

• The Young Lab– Kavitha Santhosh– Vincent Young MD, PhD– Krishna Rao MD

• Infection Prevention– Amanda Valyko MPH, CIC– Laraine Washer MD– Terri Stillwell MD, MPH

Page 33: Evaluation of Discharge Room Cleaning using UV Technology: Focus on Clostridium difficile Alison Gibson D.O. Fellow, Pediatric Infectious Diseases University

References• 1. Barbut F. “How to eradicate Clostridium difficile from the environment.” J Hosp Infect. 2015 Jan 7. pii: S0195-

6701(15)00005-5.• 2. Otter JA, Yezli S, Perl TM, et al. “The role of ‘no-touch’ automated room disinfection systems in infection

prevention and control.” J Hosp Infect. 2013 Jan;83(1):1-13.• 3. Weber DJ, Anderson D, Rutala WA. “The role of the surface environment in healthcare-associated infections.”

Curr Opin Infect Dis. 2013 Aug;26(4):338-44.• 4. Rutala WA, Weber DJ. “Disinfectants used for environmental disinfection and new room decontamination

technology.” Am J Infect Control. 2013 May;41(5 Suppl):S36-41.• 5. Chemaly RF, Simmons S, Dale C, et al. “The role of the healthcare environment in the spread of multidrug-

resistant organisms: update on current best practices for containment.” Ther Adv Infect Dis. 2014 Jun;2(3-4):79-90.

• 6. Anderson DJ, Gergen MF, Smathers E, et al. “Decontamination of targeted pathogens from patient rooms using an automated ultraviolet-C-emitting device.” Infect Control Hosp Epidemiol. 2013 May;34(5):466-71.

• 7. Boyce JM, Havill NL, Moore BA. “Terminal decontamination of patient rooms using an automated mobile UV light unit.” Infect Control Hosp Epidemiol. 2011 Aug;32(8):737-42.

• 8. Sitzlar B, Deshpande A, Fertelli D, et al. “An environmental disinfection odyssey: evaluation of sequential interventions to improve disinfection of Clostridium difficile isolation rooms.” Infect Control Hosp Epidemiol. 2013 May;34(5):459-65.

• 9. Levin J, Riley LS, Parrish C, et al. “The effect of portable pulsed xenon ultraviolet light after terminal cleaning on hospital-associated Clostridium difficile infection in a community hospital.” Am J Infect Control. 2013 Aug;41(8):746-8.

• 10. Nerandzic MM, Thota P, Sankar T, et al. “Evaluation of a pulsed xenon ultraviolet disinfection system for reduction of healthcare-associated pathogens in hospital rooms.” Infect Control Hosp Epidemiol. 2015 Feb;36(2):192-7.

• 11. Ghantoji SS, Stibich M, Stachowiak J, et al. “Non-inferiority of pulsed xenon UV light versus bleach for reducing environmental Clostridium difficile contamination on high-touch surfaces in Clostridium difficile infection isolation rooms.” J Med Microbiol. 2015 Feb;64(Pt 2):191-4.