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 (2019), 40, 171–177 doi:10.1017/ice.2018.319


Original Article


Molecular analysis of bacterial contamination on stethoscopes in an intensive care unit


Vincent R. Knecht1, John E. McGinniss1, Hari M. Shankar1, Erik L. Clarke2, Brendan J. Kelly3, Ize Imai1, Ayannah S. Fitzgerald1, Kyle Bittinger4,5, Frederic D. Bushman PhD2 and Ronald G. Collman1,2


1Pulmonary, Allergy and Critical Care Division, Department of Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, 2Department of Microbiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, 3Division of Infectious Diseases, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, 4Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania and 5The Children’s Hospital of Philadelphia, Philadelphia, Pennsylvania


Abstract


Background: Culture-based studies, which focus on individual organisms, have implicated stethoscopes as potential vectors of nosocomial bacterial transmission. However, the full bacterial communities that contaminate in-use stethoscopes have not been investigated. Methods: We used bacterial 16S rRNA gene deep-sequencing, analysis, and quantification to profile entire bacterial populations on stethoscopes in use in an intensive care unit (ICU), including practitioner stethoscopes, individual-use patient-room stethoscopes, and clean unused individual-use stethoscopes. Two additional sets of practitioner stethoscopes were sampled before and after cleaning using standardized or practitioner-preferred methods. Results: Bacterial contamination levels were highest on practitioner stethoscopes, followed by patient-room stethoscopes, whereas clean stethoscopes were indistinguishable from background controls. Bacterial communities on stethoscopes were complex, and community analysis by weighted UniFrac showed that physician and patient-room stethoscopes were indistinguishable and significantly different from clean stethoscopes and background controls. Genera relevant to healthcare-associated infections (HAIs) were common on practitioner stethoscopes, among which Staphylococcus was ubiquitous and had the highest relative abundance (6.8%–14% of contaminating bacterial sequences). Other HAI-related genera were also widespread although lower in abundance. Cleaning of practitioner stethoscopes resulted in a significant reduction in bacterial contamination levels, but these levels reached those of clean stethoscopes in only a few cases with either standardized or practitioner-preferred methods, and bacterial community composition did not significantly change. Conclusions: Stethoscopes used in an ICU carry bacterial DNA reflecting complex microbial communities that include nosocomially important taxa. Commonly used cleaning practices reduce contamination but are only partially successful at modifying or eliminating these communities.


(Received 1 August 2018; accepted 13 November 2018)


Stethoscopes are frequently used on multiple patients, and they have been implicated as vectors for nosocomial transfer of bacteria responsible for healthcare-associated infections (HAIs). It is well documented that practitioner stethoscopes are not routinely dis- infected,1,2 and studies based on bacterial culture show that they may be contaminated with potential pathogens including methicillin-resistant and -sensitive Staphylococcus spp, multidrug- resistant P. aeruginosa, Acinetobacter spp, Enterococcus spp, Escherichia coli, Klebsiella spp, and Streptococcus spp.3–5 Culture- based studies have also shown that thorough stethoscope decon- tamination can significantly reduce pathogen colony-forming units (CFUs),6,7 although the impact of actual practitioner practices is less clear. Culture-based studies are limited, however, because culture can only identify agents of a priori interest but not entire microbial communities that may be present.


Author for correspondence: Ronald Collman, 522 Johnson Pavilion, 3610 Hamilton Walk, Philadelphia, PA 19104. E-mail: collmanr@pennmedicine.upenn.edu


Cite this article: Knecht VR, et al. (2019). Molecular analysis of bacterial


contamination on stethoscopes in an intensive care unit. Infection Control & Hospital Epidemiology 2019, 40, 171–177. doi: 10.1017/ice.2018.319


© 2018 by The Society for Healthcare Epidemiology of America. All rights reserved. In contrast to culture, which is focused on individual bacteria


and is only semi-quantitative, emerging molecular approaches using next-generation sequencing can provide unbiased profiling of entire bacterial communities in a manner that is both com- prehensive and highly quantitative.8,9 These powerful approaches have revolutionized studies of the microbiome and of microbial ecology. Here, we used next-generation sequencing to investigate bacterial contamination on several types of stethoscopes in a medical intensive care unit (ICU), including stethoscopes carried by practitioners and used with multiple patients. We also inves- tigated the effects of cleaning protocols that are used by practi- tioners in everyday practice.


Materials and Methods Sample collection method (set A)


Stethoscope samples were collected in the medical ICU at the Hospital of the University of Pennsylvania. Stethoscope dia- phragms were swabbed for 60 seconds using a flocked swab


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  |  Page 145  |  Page 146  |  Page 147  |  Page 148  |  Page 149  |  Page 150  |  Page 151  |  Page 152  |  Page 153  |  Page 154  |  Page 155  |  Page 156