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      Notes from the Field: Carbapenemase-Producing Klebsiella pneumoniae in a Ventilator-Capable Skilled Nursing Facility — Maricopa County, Arizona, July–November 2018

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          Abstract

          On August 2, 2018, Maricopa County (Arizona) Department of Public Health (MCDPH) identified two isolates of carbapenemase-producing Klebsiella pneumoniae (KPC-KP), a type of carbapenemase-producing carbapenem-resistant Enterobacteriaceae (CP-CRE), from urine specimens collected on July 17 and July 23 from two residents of a ventilator-capable unit in a skilled nursing facility. CP-CRE are multidrug-resistant organisms typically isolated from persons with a health care exposure ( 1 , 2 ). Invasive CP-CRE infections are associated with a 50% case-fatality rate ( 3 ); however, only 31%–63% of asymptomatic carriers are identified with clinical cultures ( 4 , 5 ) and might serve as sources of CP-CRE transmission. Both residents at this skilled nursing facility had indwelling urinary catheters and urinary tract infections, resided in neighboring rooms, and were dependent on nursing care for their activities of daily living; one resident was mechanically ventilated. The Antibiotic Resistance Laboratory Network Mountain Region laboratory in Austin, Texas, performed pulsed-field gel electrophoresis (PFGE) on the two clinical isolates, which were found to have indistinguishable PFGE patterns, suggesting health care–associated transmission. MCDPH and the Arizona Department of Health Services (ADHS) investigated the cluster to prevent additional cases. MCDPH recommended that the ventilator-capable unit perform contact screening for KPC-KP colonization by rectal swab and culture. The skilled nursing facility had 192 resident beds, 48 (25%) of which were in the ventilator-capable unit; the average length of stay was 14 days. A case was defined as isolation of KPC-KP with a PFGE pattern indistinguishable from that of the two index patients from any specimen source collected from a resident of the ventilator-capable unit during July–November 2018. Contacts were defined as residents residing for ≥3 days in the same ventilator-capable unit as either of the two index patients. On August 13, among 42 identified contacts, six (14%) declined screening, seven (17%) had been discharged, two (5%) were deceased, and one (2%) had a recent infection with a different carbapenem-resistant organism. Among the remaining 26 (62%) residents who were screened, KPC-KP isolates were detected in five (19%) asymptomatic contacts, three of which had indistinguishable PFGE patterns from those of the two index patients. On September 6, MCDPH and ADHS conducted a site visit to the facility to observe infection control practices with emphasis on the ventilator-capable unit and recommend targeted control measures. Observations included missed opportunities for hand hygiene before and after physical contact with residents and lapses in aseptic technique during routine sterile procedures. MCDPH recommended housing residents with CP-CRE infection in the same ward or in the same room when possible; implementing contact precautions with room restriction for residents with CP-CRE infection who are mechanically ventilated, have tracheostomies, or have uncontained body fluids; requiring staff members to perform hand hygiene with alcohol-based hand sanitizer before and after physical contact with residents; increasing access to alcohol-based hand sanitizer by installing additional dispensers; and offering trainings to staff members for commonly performed sterile procedures. On November 5, contacts were rescreened to determine whether recommended control measures were successful in containing the cluster. Twenty-eight residents, none of whom had had KPC-KP isolates detected previously, were identified using the previous criteria for rescreening; nine (32%) declined and 19 (68%) consented, 10 of whom had been screened previously. All 19 (100%) rescreened cultures were negative for KPC-KP. Both index patients were treated with antibiotics for KPC-KP urinary infections, and neither died. Following this investigation, one patient had multiple urine specimens collected in which a KPC-KP isolate was identified, suggesting urinary colonization. Among 26 screened ventilator-capable unit contacts, the investigation identified three (12%) additional cases of KPC-KP colonization with an isolate that had an indistinguishable PFGE pattern from that of the two index patients, which supported health care–associated transmission. Closer adherence to CDC recommendations that could prevent health care–associated KPC-KP transmission include housing together residents with infection, improving adherence to hand hygiene, using gowns and gloves when interacting with residents who require mechanical ventilation or have tracheostomies, and implementing contact precautions for uncontained body fluids ( 6 ).

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          Outcomes of carbapenem-resistant Klebsiella pneumoniae infection and the impact of antimicrobial and adjunctive therapies.

          Carbapenem-resistant Klebsiella pneumoniae is an emerging healthcare-associated pathogen. To describe the epidemiology of and clinical outcomes associated with carbapenem-resistant K. pneumoniae infection and to identify risk factors associated with mortality among patients with this type of infection. Mount Sinai Hospital, a 1,171-bed tertiary care teaching hospital in New York City. Two matched case-control studies. In the first matched case-control study, case patients with carbapenem-resistant K. pneumoniae infection were compared with control patients with carbapenem-susceptible K. pneumoniae infection. In the second case-control study, patients who survived carbapenem-resistant K. pneumoniae infection were compared with those who did not survive, to identify risk factors associated with mortality among patients with carbapenem-resistant K. pneumoniae infection. There were 99 case patients and 99 control patients identified. Carbapenem-resistant K. pneumoniae infection was independently associated with recent organ or stem-cell transplantation (P=.008), receipt of mechanical ventilation (P=.04), longer length of stay before infection (P=.01), and exposure to cephalosporins (P=.02) and carbapenems (P<.001). Case patients were more likely than control patients to die during hospitalization (48% vs 20%; P<.001) and to die from infection (38% vs 12%; P<.001). Removal of the focus of infection (ie, debridement) was independently associated with patient survival (P=.002). The timely administration of antibiotics with in vitro activity against carbapenem-resistant K. pneumoniae was not associated with patient survival. Carbapenem-resistant K. pneumoniae infection is associated with numerous healthcare-related risk factors and with high mortality. The mortality rate associated with carbapenem-resistant K. pneumoniae infection and the limited antimicrobial options for treatment of carbapenem-resistant K. pneumoniae infection highlight the need for improved detection of carbapenem-resistant K. pneumoniae infection, identification of effective preventive measures, and development of novel agents with reliable clinical efficacy against carbapenem-resistant K. pneumoniae.
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            Epidemiology of Carbapenem-Resistant Enterobacteriaceae in 7 US Communities, 2012-2013.

            Carbapenem-resistant Enterobacteriaceae (CRE) are increasingly reported worldwide as a cause of infections with high-mortality rates. Assessment of the US epidemiology of CRE is needed to inform national prevention efforts.
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              Vital Signs: Carbapenem-Resistant Enterobacteriaceae

              Background Enterobacteriaceae are a family of bacteria that commonly cause infections in health-care settings as well as in the community. Among Enterobacteriaceae, resistance to broad-spectrum carbapenem antimicrobials has been uncommon. Over the past decade, however, carbapenem-resistant Enterobacteriaceae (CRE) have been recognized in health-care settings as a cause of difficult-to-treat infections associated with high mortality. Methods The percentage of acute-care hospitals reporting at least one CRE from health-care–associated infections (HAIs) in 2012 was estimated using data submitted to the National Healthcare Safety Network (NHSN) in 2012. The proportion of Enterobacteriaceae infections that were CRE was calculated using two surveillance systems: 1) the National Nosocomial Infection Surveillance system (NNIS) and NHSN (for 2001 and 2011, respectively) and 2) the Surveillance Network–USA (TSN) (for 2001 and 2010). Characteristics of CRE culture-positive episodes were determined using data collected as part of a population-based CRE surveillance project conducted by the Emerging Infections Program (EIP) in three states. Results In 2012, 4.6% of acute-care hospitals reported at least one CRE HAI (short-stay hospitals, 3.9%; long-term acute-care hospitals, 17.8%). The proportion of Enterobacteriaceae that were CRE increased from 1.2% in 2001 to 4.2% in 2011 in NNIS/NHSN and from 0% in 2001 to 1.4% in 2010 in TSN; most of the increase was observed in Klebsiella species (from 1.6% to 10.4% in NNIS/NHSN). In the EIP surveillance, 92% of CRE episodes occurred in patients with substantial health-care exposures. Conclusions Carbapenem resistance among common Enterobacteriaceae has increased over the past decade; most CRE are associated with health-care exposures. Implications for Public Health Interventions exist that could slow the dissemination of CRE. Health departments are well positioned to play a leading role in prevention efforts by assisting with surveillance, situational awareness, and coordinating prevention efforts.
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                Author and article information

                Journal
                MMWR Morb Mortal Wkly Rep
                MMWR Morb. Mortal. Wkly. Rep
                WR
                Morbidity and Mortality Weekly Report
                Centers for Disease Control and Prevention
                0149-2195
                1545-861X
                13 March 2020
                13 March 2020
                : 69
                : 10
                : 274-275
                Affiliations
                Epidemic Intelligence Service, CDC; Maricopa County Department of Public Health, Phoenix, Arizona; Arizona Department of Health Services; Career Epidemiology Field Officer Program, Division of State and Local Readiness, Center for Preparedness and Response, CDC.
                Author notes
                Corresponding author: Sarah E. Scott, sarah.scott@ 123456maricopa.gov , 602-359-0424.
                Article
                mm6910a5
                10.15585/mmwr.mm6910a5
                7075252
                32163379
                f7685a09-08cc-4cec-83f5-103b26824934

                All material in the MMWR Series is in the public domain and may be used and reprinted without permission; citation as to source, however, is appreciated.

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