Infection Control & Hospital Epidemiology
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Fig. 1. Transfer of a viral DNA surrogate marker from inoculated portable equipment on a medical ward to environmental surfaces on other wards or other sites in the hospital during a 3-day period. The DNA marker was inoculated onto 6 items of portable equipment on the index ward including 3 bladder scanners, an electrocardiogram machine, a portable vital signs unit, and a cardiac monitor. Observations were conducted to identify episodes when the contaminated equipment was shared by other wards or used on the index ward by personnel who subsequently moved to other areas of the hospital. Swabs were used to sample environmental surfaces, prioritizing sites observed to be contacted by personnel or equipment. (A) A contaminated cardiac monitor (1) and electrocardiogram (EKG) machine (2) were used while caring for a patient who was then transferred with the cardiac monitor attached (3) to ward 2 (4) and then without the monitor to the intensive care unit (ICU) (5 and 6), resulting in detection of DNA marker on surfaces on each ward. (B) A bladder scanner (1) was borrowed by a nurse from another ward (2) resulting in transfer to 3 patient rooms where it was used (3). (C) A physician used contaminated equipment on ward 1 (1) and DNA marker was subsequently recovered from the sleeves of the physician’s white coat that was hung in a physicians’ work room on ward 2 (2). (D) Personnel on the index ward used contaminated equipment (1) and then went to the cafeteria for break, resulting in recovery of DNA marker from a table top (2).
patients were not aware of the study. A fluorescent marker was placed on the equipment adjacent to the marker to allow an assessment of cleaning. For a 3-day period after inoculation, research personnel con-
ducted observations to identify episodes when the contaminated equipment was shared by other wards or used by personnel who subsequently moved to other areas of the hospital. If such epi- sodes were observed, cotton-tipped swabs were used to sample 5×10-cm areas of surfaces, prioritizing sites observed to be contacted by personnel or equipment. Additional swabs were collected from physician call rooms and nursing stations on other wards. To further assess the potential for ward-to-ward transmission by contaminated equipment, we inoculated mobile wound-care
carts on 3 separate days and a phlebotomy cart on 1 day. Per- sonnel using these items were observed and swabs were collected to identify sites of marker transfer.
Results
During the 3-day study, each inoculated device was observed being used at least once, but the fluorescent marker was removed from only 1 of 6 devices (17%). Two inoculated devices were used on other wards, including a cardiac monitor that moved with a transferred patient and a borrowed bladder scanner. Transfer of the DNA marker to surfaces on the other wards occurred with both episodes of equipment sharing (Fig. 1A and 1B). The DNA
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