Targeted Infection Prevention (TIP) Study: Rationale and
Transcription
Targeted Infection Prevention (TIP) Study: Rationale and
Targeted Infection Prevention (TIP) Study: Rationale and Results Lona Mody, MD, M.Sc Associate Professor, Division of Geriatric & Palliative Care Medicine, University of Michigan Associate Director, GRECC VA Ann Arbor Healthcare Systems 5.8.2014 OUTLINE • Emerging and resistant pathogens – MRSA – R-GNB – VRE • Approach to preventing MDROs in Nursing Homes (NHs) • TIP Project Overview CASE STUDY Mrs. Decker, 87 yrs. old, was admitted to your facility after hospitalization for a new stroke, delirium, pneumonia and acute renal failure. Prior to her hospitalization, she had lived at home with her husband, but needed 24 hour supervision and assistance in dressing & bathing because of a history of vascular dementia. On admission to the hospital, she experienced new left sided weakness with little recovery during her three weeks of hospital stay. CASE: CONT’D While in acute care, she is found to have swallowing difficulty and was incontinent of urine. An indwelling urinary catheter was placed within the first 24 hours and a decision to place a feeding tube has also made. She developed a 3 x 3 cm stage 2 pressure ulcer. Considering her lack of progress in PT, a decision was made to place her in a NH for long-term care. She is now admitted to your NH. The questions in her case are: 1. What are the most common infections she can get? 2. What is the risk of colonization with MDRO in a resident like her? BURDEN OF INFECTIONS IN NURSING HOMES • Range widely from 1.4 to 5.2 infections/1000 resident-days – Single day, point prevalence of 5.2% to 7.6% – MI NH research consortium: • No-device: 5.7/1,000 resident-days • device: 11/1,000 resident-days • Using this more recent data – Extrapolated to the 1.5 million adults in U.S. NHs suggests 765,000 to 2.8 million infections/yr • UTIs, pneumonia, skin and soft tissue, GI infections CONSEQUENCES OF NH INFECTIONS • 150,000 – 300,000 transfers to acute care due to infections • $ 675 million in additional healthcare costs • Leading cause of mortality and morbidity • Higher antibiotic use increased MDROs IMPACT OF MULTI-DRUG RESISTANT ORGANISMS (MDROS) • MDROs: one of the greatest healthcare challenge • Responsible for – over 12,000 deaths – 3.5 billion dollars (in US) • Prevalence estimates show an increase in MDROs • New antibiotics Resistance • New antibiotics not the only solution, need effective infection prevention strategies OUTLINE • Emerging and resistant pathogens – MRSA – R-GNB – VRE • Approach to preventing MDROs in Nursing Homes (NHs) MRSA • Emerged in acute care in 1960s • Staphylococcal infections due to MRSA – 1974: 2% – 1995: 22% – 2004: 63% • Transmission MRSA: RISK FACTORS IN NHS • Impaired functional status • Indwelling devices such as urinary catheters and feeding tubes • Prior hospitalization • Urinary incontinence • Prior antimicrobial usage • Wounds and pressure ulcers MRSA: NATURAL HISTORY IN NHS • Transfers from acute care – 2-25% of new residents colonized • Persist and spread – Enclosed environment, poor functional status, presence of devices – HCW to resident and resident to resident spread – Serial studies show persistence MDRO COLONIZATION: MRSA IN NHS Location Year No. % Colonized Patients Comment St. Louis 1985 74 12 Nasal LA 1987 170 6.0-7.3 Nasal & wound Pittsburgh VA-CLC 1986 432 13 Nasal Vancouver 1989 120 34 Nasal & wound Ann Arbor (VA-CLC) 1990 120 23 Nasal & wound Ann Arbor (VA-CLC, Co NH) 2000-1 426 15 Nasal & wound MI NH Research Consortium 2004-5 200 29 - no device 52 - device Multiple anatomic sites MRSA PERSISTENCE Mody et al ICHE 2006; 27:2124 MRSA FROM ENVIRONMENTAL CULTURES MRSA NOT THE ONLY MDRO… Environmental sampling MRSA VRE R-GNB C. difficile Pagers Stethoscopes Bedrails Bed frames White coats Bed rails Sinks Blood pressure cuffs Side table Ventilator water Toilet seats Computer keyboards Adapted from: Hebert and Weber, Infection Prevention and Control in the Hospital, 2011 OUTLINE • Emerging and resistant pathogens – MRSA – R-GNB – VRE • Approach to preventing MDROs in Nursing Homes (NHs) MDRO COLONIZATION: R-GNB • Rates exceed MRSA • Frequent use of antibiotics to treat NH infections • Resistance in GNB (NH data) – E. coli: 5-41% – P. aeruginosa: 27- 67% – K. pneumoniae: 7-14% – P. mirabilis: 38-57% • • • • Bonomo R, Clin Infect Dis, 2000;31:1414-22 Viray M, Infect Control Hosp Epidemiol 2005;26:56-62 O’fallon et al, Infect Control Hosp Epidemiol 2010 Fisch J, Wang L, Mody L et al, EJCMID & J Clin Micro, 2012 RISK FACTORS FOR R-GNB • • • • • Indwelling devices Poor functional status Pressure ulcers/wounds Quinolone use Prior hospitalization QUINOLONE RESISTANCE • Frequent use to treat NH infections • Resistance in GNB – E. coli: 5-41% – P. aeruginosa: 27- 67% – K. pneumoniae: 7-14% – P. mirabilis: 38-57% • Viray M, Infect Control Hosp Epidemiol 2005;26:56-62 • Bonomo R, Clin Infect Dis, 2000;31:1414-22 • Antibiotic pressure PERSISTENT CIPR GNB COLONIZATION, BY SPECIES Number and Name of Species Present 1 2 3 ≥4 Preexisting Colonization (n=27) New Acquisition (n=19) Escherichia coli 10 3 Proteus mirabilis 2 4 Pseudomonas aeruginosa 1 0 Providencia stuartii 2 0 Morganella morganii 1 4 E. coli, P. mirabilis 7 4 E. coli, P. stuartii 0 1 P. mirabilis, P. stuartii 0 1 P. mirabilis, P. fluorescens 1 0 E. coli, P. mirabilis, M. morganii 0 1 E. coli, P. mirabilis, K. pneumoniae 1 0 1 0 Fisch J, Mody L et al. J Clin Microbiol. 2012; 50:1698-1703 -LACTAM RESISTANCE IN GNBS • GNB carry extended spectrum -lactamases (ESBLs) Outbreaks: – Massachusetts Chronic Care Facility: 1990 • 25 patients over 4 months • Ceftazidime use – Chicago: 1992 • 55 hospitalized patients with CTZ-R • 31/55 from 8 NHs with CTZ-R • Point prevalence study in 1 NH: 18/39 CTZ-R GNB Bonomo R, Clin Infect Dis, 2000;31:1414-22 FUNCTIONAL DISABILITY: R-GNB PREVALENCE 100% 24 80% % of NH residents (no device) 60% 92 83 65 CIP-S 40% 76 20% 0% 8 17 CIP-R 35 1 2 3 4 Functional Status (PSMS): Category 1: Independent to Category 4 = Dependent Dommeti P, Wang L, Mody L et al, Infect Control Hosp Epid 2011 FUNCTIONAL DISABILITY: RISK FOR MRSA/VRE CO-COLONIZATION MRSA/VRE No Co-colonizationc co-colonizationb Characteristic (n=17) (n=246) RR(95%) Age, mean years 75.9 77.9 1.0(1.0-1.1) Charlson Comorbidity score, mean 3.2 3.2 0.9(0.8-1.1) Follow-up Months, mean 6.8 6.6 1.0(0.9-1.2) Functional disability, mean 26.3 22 1.3 (1.1-1.4)*** Male, No.(%) 13 (76) 103 (42) 3.1(0.9-10.4) Wound, No.(%) 8 (53) 62 (27) 3.4(1.4-8.6)** Antibiotics, No.(%) 9 (53) 82 (33) 3.0(1.0-9.1) Hospitalization, No.(%) 6 (38) 69 (30) 1.6(0.3-9.9) Long Stayf, No.(%) 7 (41) 97 (39) 1.8(0.5-6.3) CCS=Charlson’s Comorbidity Score, PSMS=Physical Self Maintenance Score, Adjusted for repeated measures using GEE, b MRSA/VRE cocolonization modeled as the outcome for each analysis, * p<0.05, ** p<0.01, *** p<0.001 Flannery E, et al. Clin Infect Dis. 2011; 53:1215-1222 OUTLINE • Emerging and resistant pathogens – MRSA – R-GNB – VRE • Approach to preventing MDROs in Nursing Homes (NHs) VRE (VANCOMYCIN RESISTANT ENTEROCOCCI) • VRE a relatively recent discovery – But widespread, esp. in hospitals with significant mortality and morbidity • VRE accounts for ~ 30% of ICU isolates of Enterococcus in the United States – NHs – Prevalence varies from 5-20% COMMONALITY OF RISK FACTORS: MDROS • • • • • Use of indwelling devices Functional disability Presence of wounds Prior antimicrobial usage Prior hospitalization • Move from pathogen-based to risk-factor based infection prevention programs? OUTLINE • Emerging and resistant pathogens – MRSA – R-GNB – VRE • Approach to preventing MDROs in Nursing Homes (NHs) INFECTION CONTROL STRATEGIES IN NHS • Progress in NHs infection control – Guidelines from various national societies • Immense variations in practice – Do-nothing to do-everything – No controlled trials • Issues to remember – NHs are not hospitals – Rehab and socialization critical • Significant gaps in healthcare workers’ knowledge regarding device care practices • Paucity of RCTs to reduce device-associated MDRO colonization and infections Mody L et al, J Am Geriatr Soc 2007, Wang L et al, E J Clin Micro 2011, Mody L, Bradley SF, Kauffman C et al, Clin Infect Dis 2008, Mody L, Saint S, Krein S et al; J Am Geriatr Soc 2010 BACKGROUND MDROs common in NHs indwelling devices increase risk multi-anatomic site colonization with MDROs frequent device specific pattern Significant gaps in healthcare workers’ knowledge regarding device care practices Paucity of RCTs to reduce device-associated MDRO colonization and infections Mody L et al, J Am Geriatr Soc 2007, Wang L et al, E J Clin Micro 2011, Mody L, Bradley SF, Kauffman C et al, Clin Infect Dis 2008, Mody L, Saint S, Krein S et al; J Am Geriatr Soc 2010 29 TYPES OF INTERVENTIONS STUDIED • Studies conducted at single NHs have generally focused on one of four types of interventions – hand hygiene • Mody L, ICHE 2003; Schwoen S, AJIC 2011; Chami K, JAMDA 2012 – gown use and contact precaution • Trick WE, JAGS 2004 – decolonization regimens • Wendt C, ICHE 2007, Mody L , Bradley SF et al CID 2003, Kauffman CA et al 1993 – infection prevention education • Baldwin NS, J Hosp Infect 2010 • Aim to design integrated infection prevention program focused on high-risk residents TIP (TARGETED INFECTION PREVENTION PROGRAM): STUDY DESIGN Aims: To determine the effectiveness of a multimodal intervention in reducing: 1. MDRO prevalence 2. New, incident device-related infections Design: Cluster-randomized trial Facilities: 12 Nursing Homes in SE Michigan Population: Residents with indwelling urinary catheters and feeding tubes HYPOTHESES A multi-modal evidence-based Targeted Infection Program (TIP) intervention will: - reduce the burden of MDROs & - incident device-related infections in high risk NH residents with urinary catheters and/or feeding tubes TIP INTERVENTION DETAILS Intervention Group (TIP) Precautions Preemptive enhanced barrier precautions Glove and gown use for AM, PM care Control Group (Usual Care) Standard precautions as per NH policy Surveillance Active surveillance Cultures collected at baseline, D15, and then MDROs Passive surveillance monthly and reported back to the facilities every month, along with reminders of key strategies to prevent infections Infections Infections identified by study definitions and reported back to the facilities q30d, along with reminders of key strategies to prevent infections Education Hand hygiene promotion Posters, videos, Glo GermTM, pre-post cultures Interactive infection prevention modules 9 sessions for healthcare workers Infection surveillance pocket cards Provided to nurse, nurse aide, physician, and infection preventionist upon resident enrollment Half-day IP skills mini-conference Clinical cultures, hospital discharge reports, Cultures collected for outcome evaluation with no feedback Infections identified by study definitions for outcome evaluation only, no reports given to the facilities Education provided as needed (i.e., annual requirements, in response to state surveys or audits, etc.) PRIMARY OUTCOME: REDUCE MDRO BURDEN nares oropharynx device peri-anal area groin Outcome measures = patient-level colonization, device-associated infections Staphyloccocus Enterococcus aureus spp. Gram negatives wound Methicillin Vancomycin Ceftazidime, Cipro SECONDARY OUTCOME: REDUCE INFECTIONS • Device associated infections: – Indwelling CAUTIs • uretheral catheters • suprapubic catheters – Skin and soft tissue infections around feeding tube sites • Clinical infection definition – Specific infection documentation in chart followed by at least three days of systemic antibiotics STATISTICAL ANALYSES • Primary outcome: MDRO Prevalence – Mixed-effect multi-level Poisson regression model to predict the mean number of MDROs/visit as a function of intervention, including facility as a random effect and offset by the number of cultures obtained at each visit. – Excluded patients with only one visit – Controlled for baseline colonization – Log transformation with ratios based on geometric means • Secondary outcome: Device-associated infections – Cox proportional hazard model to predict time to first infection while adjusting for patient-level and facility level predictors 13 Nursing homes screened for eligibility 1 Nursing home did not participate 12 Nursing homes randomized 6 Nursing homes assigned to Intervention Cohort 6 Nursing homes assigned to Control Cohort 589 Nursing home residents assessed for eligibility 641 Nursing home residents assessed for eligibility 206 Nursing home residents not eligible: 58 Unable to reach family/guardian 74 Discharged before enrollment 41 Device was discontinued before enrollment 18 Died before enrollment 15 Other 383 Nursing home residents eligible 180 Resident/family/guardian refused 203 (53%) Nursing home residents enrolled 49 residents with baseline visit only 41 Reached end point 3 Died 2 Withdrew 2 Other 154 Residents with more than 1 follow-up visit 119 Reached end point 24 Died 9 Residents withdrew 2 Other 245 Nursing home residents not eligible: 46 Unable to reach family/guardian 112 Discharged before enrollment 67 Device was discontinued before enrollment 10 Died before enrollment 10 Other 396 Nursing home residents eligible 181 Resident/family/guardian refused 215 (54%) Nursing home residents enrolled 53 residents with baseline visit only 48 Reached end point 5 Died 0 Withdrew 0 Other 162 Residents with more than 1 follow-up visit 138 Reached end point 17 Died 4 Residents withdrew 3 Other DESCRIPTION OF NURSING HOMES Facility Beds Intervention H 136 D 156 F L A C 217 94 180 88 Mean 145·2 Control B J 120 91 G K E I 149 135 180 99 Mean 129·0 Ownership Status Star Mean Age, Mean CoRating y Morbidity Score Mean Male, % Functiona l Status Gov. Not for profit For profit For profit For profit For profit 5 2 78·4 77·4 3·1 2·6 20·2 20·9 50·0 50·0 4 3 2 1 70·9 74·1 73·7 74·6 2·7 3·2 2·8 3·4 22·5 23·3 23·9 22·6 38·6 65·0 33·3 57·9 2·8 74·4 2·8 22·0 56·3 4 5 75·9 84·7 3·4 2·6 22·8 21·5 53·3 50·0 4 3 2 1 61·1 64·7 71·4 74·8 1·9 3·5 3·2 2·9 22·6 23·8 21·1 21·4 64·7 68·4 58·5 42·9 3·2 72·5 3·0 21·6 49·1 Gov. Not for profit For profit For profit For profit For profit ENROLLED & VISITED # Enrolled 418 residents with Feeding tubes, Urinary catheters Intervention 203 Control 215 # Visits = 1830 Intervention 920 Control 910 Mean f/u: 4.5 visits Mean f/u: 4.2 visits ENHANCED BARRIER PRECAUTIONS SIGNAGE RESIDENT PRECAUTIONS This resident is taking place in a Research Study Resident Room BEFORE ENTERING RESIDENT ROOM Please wash your hands and wear gloves WHEN PROVIDING DIRECT CARE Please wear protective gowns AFTER LEAVING RESIDENT ROOM Please remove gloves and wash your hands HAND HYGIENE POSTERS (ROTATING 4-5M) HAND HYGIENE POSTERS 2 HIT THE ROAD GERMS!! Nurse Clean Hands! GERMS ! A song and dance to practice hand hygiene BASELINE CHARACTERISTICS Residents with more than 1 f/u visit Characteristic Follow-up Days, mean (SD) Intervention Group Control Group P-value 116·1 (121·1) 104·2 (123·5) 0·38 Age, mean (SD) Males, n (%) White, n (%) Co-morbidity Score, mean (SD) 74·0 (12·4) 76 (49·4) 132 (85.7) 2·8 (1·6) 72·2 (13·5) 93 (57·4) 144 (88.9) 2·9 (2·1) 0·22 0·15 .39 0·66 PSMS, mean (SD) Device Use, n (%) Urinary Catheter Feeding Tube Both 22·6 (4·1) 22·1 (4·1) 0·23 84 (54·6) 46 (29·9) 24 (15·6) 79 (48·8) 54 (33·3) 29 (17·9) 0·30 0·50 0·58 21 (13·6) 9 (5·8) 32 (20·8) 29 (17·9) 13 (8·0) 39 (24·1) 0·29 0·44 0·48 Prior History of MDRO, n (%) MRSA VRE R-GNB ACTIVE SURVEILLANCE CULTURES, BY VISIT Follow-up Visit, days 0 (baseline) 15 30 60 90 120 150 180 210 240 270 300 330 360 Total No. swabs collected (%) Intervention Control 473 (48·5) 483 (50·5) 433 (49·7) 439 (50·3) 375 (52·6) 338 (47·4) 317 (54·0) 270 (46·0) 254 (57·0) 192 (43·1) 184 (54·6) 153 (45·4) 129 (48·5) 137 (51·5) 137 (52·9) 122 (47·1) 134 (52·0) 124 (48·1) 102 (45·5) 122 (54·5) 97 (47·6) 107 (52·5) 81 (43·3) 106 (56·7) 73 (48·3) 78 (51·7) 52 (59·1) 36 (40·9) 2841 (51·2) 2707 (48·8) ACTIVE SURVEILLANCE CULTURES, BY SITE Anatomic Site Nares Oropharynx Groin Perianal Enteral feeding tube site Suprapubic catheter site Wounds Total Swabs Collected (%) Intervention Control 704 (51·1) 674 (48·9) 561 (52·0) 517 (48·0) 728 (51·7) 680 (48·3) 345 (52·1) 317 (47·9) 341 (51·0) 329 (49·1) 131 (45·5) 157 (54·5) 31 (48·4) 2841 (51·2) 33 (51·6) 2707 (48·8) MICROBIAL SURVEY FOR MDROS MRSA Nares Oropharnyx Groin Perianal Feeding Tube Site Suprapubic Catheter Site Wound VRE Nares Oropharnyx Groin Perianal Feeding Tube site Suprapubic Catheter site Wound Number of MDRO Positive Samples No. Positive Samples/No. Samples Collected (%) Intervention Control 254/3116 (8·2) 323/3072 (10·5) 70/767 (9·1) 96/755 (12·7) 34/606 (5·6) 23/576 (4·0) 50/794 (6·3) 66/762 (8·7) 24/394 (6·1) 48/380 (12·6) 35/370 (9·5) 39/374 (10·4) 32/149 (21·5) 43/177 (24·3) 9/36 (25·0) 8/48 (16·7) 122/3116 (3·9) 162/3072 (5·3) 0/767 (0·00) 3/755 (0·4) 8/606 (1·3) 12/576 (2·1) 56/794 (7·1) 71/762 (9·3) 47/394 (11·9) 52/380 (13·7) 5/370 (1·4) 4/374 (1·1) 5/149 (3·4) 15/177 (8·5) 1/36 (2·8) 5/48 (10·4) MICROBIAL SURVEY FOR MDROS (CONT’D) CTZ-R GNB Nares Oropharnyx Groin Perianal Feeding Tube Site Suprapubic Catheter Site Wound CIP-R GNB Nares Oropharnyx Groin Perianal Feeding Tube Site Suprapubic Catheter Site Wound Number of MDRO Positive Samples No. Positive Samples/No. Samples Collected (%) Intervention Control 168/3116 (5·4) 257/3072 (8·4) 1/767 (0·1) 18/755 (2·4) 10/606 (1·7) 27/576 (4·7) 61/794 (7·7) 72/762 (9·5) 52/394 (13·2) 74/380 (19·5) 9/370 (2·4) 15/374 (4·0) 26/149 (17·5) 25/177 (14·1) 9/36 (25·0) 26/48 (54·2) 609/3116 (19·5) 742/3072 (24·2) 12/767 (1·6) 31/755 (4·1) 36/606 (5·9) 57/576 (9·9) 240/794 (30·2) 294/762 (38·6) 207/394 (52·5) 207/380 (54·5) 34/370 (9·2) 65/149 (43·6) 15/36 (41·7) 42/374 (11·2) 75/177 (42·4) 36/48 (75·0) CLUSTER-LEVEL SUMMARY OF ACTIVE SURVEILLANCE CULTURES Active surveillance cultures for MDROs Facility H D F C A L Intervention E I B G J K Control First month Swabs Positive collected swabs, % 30 38 106 19 59 23 275 96 52 24 59 34 100 365 13·3 23·7 24·5 26·3 42·4 56·5 31·1 27·1 28·9 29·2 32·2 32·4 53·0 33·8 Study period Swabs Positive collected swabs, % 272 436 1283 291 391 168 2841 821 300 354 380 421 428 2707 22·4 20·0 28·9 16·5 29·9 36·9 25·8 27·8 34·3 24·1 40·5 26·6 43·7 32·8 Difference (Study period–First month), % 9·1 -3·7 4·4 -9·8 -12·5 -19·6 -5·3 0·7 5·4 -5·1 8·3 -5·8 -9·3 -1·0 MDRO PREVALENCE RATES Intervention (N=154 residents) Control (N=162 residents) Clusteradjusted Rate Ratio Cluster and covariate adjusted Rate Ratio, Algebraic Mean Cluster and co-variate adjusted Rate Ratio, Geometric Mean 0·67 0·65 0·77 No. % No. % MDRO Positive MDRO Positive isolated swabs isolated swabs All MDRO 1299 MRSA VRE 254 122 26·6 8·2 3·9 1732 323 162 32·6 10·5 5·3 (0·51– 0·88)* (0·50–0·85)* (0·62–0·94)* 0·92 0·81 0·78 (0·55–1·53) (0·55–1·18) (0·64–0·96)* 1·78 1·81 1·20 (0·68–4·67) CTZ-R CIP-R 185 738 5·4 19·5 295 952 8·4 24·2 (0·72–4·55) (0·82–1·75) 0·93 0·87 0·94 (0·50–1·72) (0·49–1·55) (0·61–1·44) 0·94 0·96 0·75 (0·61–1·46) (0·63–1·47) (0·58–0·97)* CLINICALLY-DEFINED INFECTIONS Intervention Group Control Group ClusterP-value Cluster & Padjusted Covariate-adjusted value Hazard Ratio Hazard Ratio Infections Device Infections Device-Days Days First new CAUTI 31 5,982 43 All new CAUTIs, 56 includes recurrent infections 9,413 75 Feeding tubeassociated skin & soft tissue infection 4 5,635 3 Feeding tubeassociated pneumonia 10 4,292 0·49 0·022 0·54 (0·30–0·97) 0·039 8,118 (0·27–0·90) 0·62 0·008 0·69 (0·49–0·99) 0·045 0·72 1·09 (0·22–5·45) 0·92 0·88 1·83 (0·53–6·31) 0·34 (0·43–0·88) 5,062 1·21 (0·43–3·43) 5,635 8 5,062 1·09 (0·36–3·26) EVALUATION OF IMPLEMENTATION PROCESS • Use of appropriate surveillance definitions to monitor infections – Baseline: Intervention & Control: 3/6 used NH app. surveillance def. – Study end: Intervention: 6/6; Control: 3/6 used surveillance def. • HCW knowledge scores – 300 in-services across 9 topics over 3 years – attendance ranged from 211 to 375 HCWs (38·0%–68·2% of nursing staff working that day)/topic. – Post-test knowledge scores in the intervention group were significantly higher than the control group for all education modules combined [88·7% vs. 76·5%; mean difference 12·2 (11·3–13·1); P<0·001]. EVALUATION OF IMPLEMENTATION PROCESS (CONT’D) • 472 in-room observation periods (30 mins. each) – 112 observations without any HCW entry – 366 observations with 658 opp. to observe HCW • Gown use: Higher in the intervention group than in the control group (40·5% vs. 1·8%; mean difference 38·7 (20·3–57·1); P<0·001) • In-room hand hygiene compliance: 37·3% vs. 18·2%; mean difference 19·2 (1·4–36·9); P=0·03. • No differences in participant self-reporting: – Washed in the last 24 hrs. (79·8% vs. 81·9%; P=0·84) – Overall satisfaction with care (83·3% vs. 83·9%; P=0·95) SUMMARY/DISCUSSION • Our multi-modal TIP intervention significantly reduced MDRO prevalence density and clinically-defined CAUTI rates in NH residents with indwelling devices – Reduced overall MDRO prevalence in high risk residents by 23% – Reduced clinically-defined CAUTIs by 31% DISCUSSION/LIMITATIONS • Few clusters, focused in one geographic area • Targeted one high risk group of residents- with indwelling devices • Did not evaluate the impact of our intervention on transmission to room-mates, environment, referring hospitals • Using the horizontal approach, our power calculations were based on overall prevalence of MDROs and not individual organisms • Use of clinically-defined infections DISCUSSION/STRENGTHS • Intervention components designed with the aim to integrate individual practices into routine clinical settings – We showed the beneficial effects of a predominantly organizational, healthcare-worker based intervention – Simplified intervention designed for high-risk patients rather than individual MDROs • Engaged a group of NHs in rigorous infection prevention interventions that involved facility IPs, leadership, clinical and non-clinical staff BRINGING ABOUT A CHANGE: THE CHANAKYA WAY (370-283 BCE) • ‘Sham’: reasoning, negotiations, ‘evidence-based’ • ‘Dam’: reward, ‘carrot’, ‘incentives’ • ‘Dand’: ‘stick’, discipline ‘F tags’ or ‘citations’ • ‘Bhed’: differentiating good from bad ‘star ratings’ HAND HYGIENE CONTEST! • To promote hand hygiene compliance we created a contest for the 6 intervention sites to boost rates of carrying a personal bottle of hand sanitizer • Collected 1 baseline audit and 4 follow-up audits over 4 weeks • Asked employees with direct patient care at each site if they had their hand sanitizer on them (on a clip or in pocket) • Calculated results: # Had hand sanitizer x 100 = % Compliance # Asked Mean Overall Increase from Baseline: 21% ATTRIBUTES OF A WELL RUN INFECTION PREVENTION PROGRAM Culture supportive of Infection Prevention • Infection preventionist enthusiasm, commitment, training, time spent • Director of nursing attendance at the inservices • ICP and DON relationship High hand hygiene rates to begin with High attendance at each in-service • often 3-5 sessions so that all staff may attend HAI PREVENTION ACTION PLAN: PHASE 3 • National action plan to prevent healthcare-associated infections: roadmap to elimination – Phase 3: Long-term care facilities – Priority areas: • Facilitate standardized infection reporting • Reduce catheter-associated UTIs • Enhance influenza vaccine uptake among short stay residents and healthcare workers • Standardize C. difficile surveillance processes MRS. DECKER • Two indwelling devices, functional disability & wounds – High risk for infections and new MDRO acquisition – Presence of wounds increase the risk of cocolonization with MRSA and VRE – She can have up to 3 new infections/yr. • She can continue PT, OT and Speech therapy – Potential for social isolation • Anticipate reassessment of her rehab potential and future goals of care SUMMARY • Risk factors for MDROs: – Recent hospitalization – Functional disability – Indwelling devices – Presence of wounds • Strategies: – Identify high risk groups, common infections, MDROs – QA programs to implement strategies to reduce MDROs, infections – Hand hygiene, enhanced barrier precautions, environmental cleaning, antimicrobial stewardship, staff education ACKNOWLEDGEMENTS All participating facilities, HCWs, residents Co-Investigators: Suzanne Bradley, MD (ID, Geriatrics) Andrzej Galecki, MD, Ph.d (IoG) Mohammed Kabeto, MS (IoG) Carol Kauffman, MD (ID) Sarah Krein, Ph.d (Gen Med, HSR) Lillian Min, MD, MPH (Geriatrics) Sanjay Saint, MD, M.P.H (Gen Med, HSR) Ana Montoya, MD (Geriatrics) Consultants: Tom Fitzgerald, Ph. D (GRECC AD, Ed) Russ Olmsted, (Hosp. Epidemiologist) Ruth-Anne Rye, (Infection Preventionist) Field Team: Bonnie Lansing, LPN Sara McNamara, MPH Dianna Hammer, RN Lab team: Kathy Symons Kay Cherian Evonne Koo Trainees, Mentees and Students: Kristen Gibson (SPH) Amanda Horcher (SPH) Jay Fisch, MS Linda Wang, BS VA Healthcare System Geriatric Research Clinical Care Center (GRECC, Mody), NIA-Pepper Center (Mody), NIH (K23AG028943 and R01AG032298 Mody), T Franklin Williams (Mody), AHRQ (R18HS019979 Mody), a hand sanitizer company for donating personal use bottles – approved by NIA.