search.noResults

search.searching

dataCollection.invalidEmail
note.createNoteMessage

search.noResults

search.searching

orderForm.title

orderForm.productCode
orderForm.description
orderForm.quantity
orderForm.itemPrice
orderForm.price
orderForm.totalPrice
orderForm.deliveryDetails.billingAddress
orderForm.deliveryDetails.deliveryAddress
orderForm.noItems
infection control & hospital epidemiology july 2018, vol. 39, no. 7 original article


Effectiveness of Probiotic for Primary Prevention of Clostridium difficile Infection: A Single-Center Before-and-After Quality Improvement Intervention at a Tertiary-Care Medical Center


William E. Trick, MD;1 Stephen J. Sokalski, DO;2 Stuart Johnson, MD;3 Kristen L. Bunnell, PharmD;4 Joseph Levato, PharmD;2 Michael J. Ray, MPH;1 Robert A. Weinstein, MD1


objective. To evaluate probiotics for the primary prevention of Clostridium difficile infection (CDI) among hospital inpatients. design. A before-and-after quality improvement intervention comparing 12-month baseline and intervention periods. setting. A 694-bed teaching hospital.


intervention. Weadministered a multispecies probiotic comprising L. acidophilus (CL1285), L. casei (LBC80R), and L. rhamnosus (CLR2) to eligible antibiotic recipients within 12 hours of initial antibiotic receipt through 5 days after final dose. We excluded (1) all patients on neonatal, pediatric and oncology wards; (2) all individuals receiving perioperative prophylactic antibiotic recipients; (3) all those restricted from oral intake; and (4) those with pancreatitis, leukopenia, or posttransplant. We defined CDI by symptoms plus C. difficile toxin detection by polymerase chain reaction. Our primary outcome was hospital-onset CDI incidence on eligible hospital units, analyzed using segmented regression.


results. The study included 251 CDI episodes among 360,016 patient days during the baseline and intervention periods, and the incidence rate was 7.0 per 10,000 patient days. The incidence rate was similar during baseline and intervention periods (6.9 vs 7.0 per 10,000 patient days; P=.95). However, compared to the first 6 months of the intervention, we detected a significant decrease in CDI during the final 6 months (incidence rate ratio, 0.6; 95% confidence interval, 0.4–0.9; P=.009). Testing intensity remained stable between the baseline and intervention periods: 19% versus 20% of stools tested were C. difficile positive by PCR, respectively. From medical record reviews, only 26% of eligible patients received a probiotic per the protocol.


conclusions. Despite poor adherence to the protocol, there was a reduction in the incidence of CDI during the intervention, which was delayed ~6 months after introducing probiotic for primary prevention.


Infect Control Hosp Epidemiol 2018;39:765–770


While many proven interventions have successfully reduced certain healthcare-associated infections (HAIs),1 Clostridium difficile infection (CDI) remains common in many institutions. Strategies to reduce the risk of CDI (eg, reduced antimicrobial use and enhanced environmental cleaning)2 have been difficult to sustain across facilities. One challenge specific to controlling CDI is that the condition results in diarrhea, facilitating environmental surface contamination.3,4 In addition, C. diffi- cile spores are resistant to alcohol-based hand gel5 and most disinfectants used for room cleaning.6 To test a control strat- egy enhanced by the use of probiotics, we collaboratedwith the Illinois Department of Public Health to identify hospitals with high CDI rates as reported to the Centers for Disease Control and Prevention (CDC) that were actively engaged in infection prevention efforts (eg, hand hygiene and environmental


disinfection).We contacted these hospitals and identified a large teaching hospital with the capacity to implement a probiotic- based quality improvement intervention. Although most CDI cases can be treated with antibiotics,


primary prevention is critical for the following reasons: (1) almost 1 in 5 treated patients experiences a recurrence, and each recurrence increases the likelihood of treatment failure; (2) infected patients serve as a reservoir for ongoing trans- mission; and (3) implementation of contact isolation precau- tions can have deleterious consequences for patients.7 Also, CDI can result in severe disease, leading to colectomy and death. Because C. difficile is spread between patients,8 primary prevention reduces the risk of exposure for other patients. Some probiotic strains hold promise to interfere with colonization and/or infection with C. difficile. The appeal of


Medical Center, Oak Lawn, Illinois; 3. Loyola University Medical Center, Maywood, Illinois; 4. College of Pharmacy, University of Illinois, Chicago, Illinois. © 2018 by The Society for Healthcare Epidemiology of America. All rights reserved. 0899-823X/2018/3907-0001. DOI: 10.1017/ice.2018.76


Affiliations: 1. Department of Medicine, Cook County Health & Hospitals System, Chicago, Illinois; 2. Division of Infectious Diseases, Advocate Christ Received December 5, 2017; accepted March 4, 2018; electronically published April 26, 2018

Page 1  |  Page 2  |  Page 3  |  Page 4  |  Page 5  |  Page 6  |  Page 7  |  Page 8  |  Page 9  |  Page 10  |  Page 11  |  Page 12  |  Page 13  |  Page 14  |  Page 15  |  Page 16  |  Page 17  |  Page 18  |  Page 19  |  Page 20  |  Page 21  |  Page 22  |  Page 23  |  Page 24  |  Page 25  |  Page 26  |  Page 27  |  Page 28  |  Page 29  |  Page 30  |  Page 31  |  Page 32  |  Page 33  |  Page 34  |  Page 35  |  Page 36  |  Page 37  |  Page 38  |  Page 39  |  Page 40  |  Page 41  |  Page 42  |  Page 43  |  Page 44  |  Page 45  |  Page 46  |  Page 47  |  Page 48  |  Page 49  |  Page 50  |  Page 51  |  Page 52  |  Page 53  |  Page 54  |  Page 55  |  Page 56  |  Page 57  |  Page 58  |  Page 59  |  Page 60  |  Page 61  |  Page 62  |  Page 63  |  Page 64  |  Page 65  |  Page 66  |  Page 67  |  Page 68  |  Page 69  |  Page 70  |  Page 71  |  Page 72  |  Page 73  |  Page 74  |  Page 75  |  Page 76  |  Page 77  |  Page 78  |  Page 79  |  Page 80  |  Page 81  |  Page 82  |  Page 83  |  Page 84  |  Page 85  |  Page 86  |  Page 87  |  Page 88  |  Page 89  |  Page 90  |  Page 91  |  Page 92  |  Page 93  |  Page 94  |  Page 95  |  Page 96  |  Page 97  |  Page 98  |  Page 99  |  Page 100  |  Page 101  |  Page 102  |  Page 103  |  Page 104  |  Page 105  |  Page 106  |  Page 107  |  Page 108  |  Page 109  |  Page 110  |  Page 111  |  Page 112  |  Page 113  |  Page 114  |  Page 115  |  Page 116  |  Page 117  |  Page 118  |  Page 119  |  Page 120  |  Page 121  |  Page 122  |  Page 123  |  Page 124  |  Page 125  |  Page 126  |  Page 127  |  Page 128  |  Page 129  |  Page 130  |  Page 131  |  Page 132  |  Page 133  |  Page 134  |  Page 135  |  Page 136  |  Page 137  |  Page 138  |  Page 139  |  Page 140  |  Page 141  |  Page 142  |  Page 143  |  Page 144