| Literature DB >> 30370263 |
Karin E Steinmann1, Dirk Lehnick2, Michael Buettcher1,3, Katharina Schwendener-Scholl1,4, Karin Daetwyler1,4, Matteo Fontana1,4, Davide Morgillo1,4, Katja Ganassi1,4, Kathrin O'Neill1,4, Petra Genet1,4, Susanne Burth1,4, Patrizia Savoia1,4, Ulrich Terheggen1,4, Christoph Berger5, Martin Stocker1,4.
Abstract
Background: Antimicrobial stewardship (AMS) is an important strategy of quality improvement for every hospital. Leadership is an important factor for implementation of quality improvement and AMS programs. Recent publications show successful AMS programs in children's hospitals, but successful implementation is often difficult to achieve and literature of AMS in neonatal and pediatric intensive care units (NICU/PICU) is scarce. Lack of resources and prescriber opposition are reported barriers. A leadership style focusing on empowering frontline staff to take responsibility is one approach to implement changes in health care institutions. Aim: Literature review regarding empowering leadership and AMS in health care and assessment of the impact of such a leadership style on AMS in a NICU/PICU over 3 years.Entities:
Keywords: antimicrobial stewardship; distributed leadership; empowerment; intensive care unit; leadership; pediatrics; shared leadership
Year: 2018 PMID: 30370263 PMCID: PMC6194187 DOI: 10.3389/fped.2018.00294
Source DB: PubMed Journal: Front Pediatr ISSN: 2296-2360 Impact factor: 3.418
Figure 1Flow chart illustrating selection process of literature review.
Overview of publications used in the review.
| Van Buul Laura et al. ( | 2014 | Qualitative Study | Tertiary care center, community hospitals, nursing homes and residential care facilities in Netherland | “Participatory action research in antimicrobial stewardship: a novel approach to improving antimicrobial prescribing in hospitals and long-term care facilities” | The study indicates, that the collaborative nature of the participatory action research results in greater engagement compared with top-down approaches | Improvement in antimicrobial prescription |
| Jeffs et al. ( | 2015 | Qualitative study | Intensive care units of 3 teaching hospitals in Toronto and Ontario | “A qualitative analysis of implementation of antimicrobial stewardship at 3 academic hospitals: Understanding the key influences on success” | Successful implementation of an antimicrobial stewardship program should include the following key themes: 1.Get the right people on board; 2.Build collegial relationships (formally and informally) with prescribers; 3.Establishing a track record | Successful implementation of an antimicrobial stewardship program |
| Sinkowitz-Cochran ( | 2012 | Descriptive survey based study | Medical, surgical and intensive care units of Veterans Affairs Medical Centres in the USA | “The associations between organizational culture and knowledge, attitudes, and practices in a multicentre Veterans Affairs quality improvement initiative to prevent methicillin-resistant Staphylococcus aureus” | Greater engagement of healthcare personnel is associated with having a good leadership structure and the feeling of being supported by leadership is positively associated with better MRSA prevention practices | Improvement in MRSA prevention practices leads to reduced infection rate |
| Pronovost et al. ( | 2016 | Quantitative intervention study | Intensive care units in Michigan, USA | “Sustaining Reductions in central line-associated bloodstream infections in Michigan intensive care units: a 10-year analysis” | In order to implement and sustain an improvement in antimicrobial stewardship the active involvement of hospital leaders is important | Reduction of central line-associated bloodstream infections |
| Jain et al. ( | 2006 | Quantitative intervention study | Single intensive care unit in Mississippi, USA | “Decline in ICU adverse events, nosocomial infections and cost through a quality improvement initiative focusing on teamwork and culture change” | Adverse events and nosocomial infections declined following the introduction of a changed system of care in the ICU | Reduction of nosocomial infections after intervention |
Baseline characteristics of study population on admission.
| Admissions ( | 556 | 575 | 571 |
| Patients total ( | 521 | 518 | 528 |
| Newborns < 44 weeks of gestational age (n) | 302 58.0 | 299 57.7 | 291 55.1 |
| Preterm infants < 32 weeks of gestational age ( | 63 | 76 | 82 |
| Preterm infants < 28 weeks of gestational age ( | 22 | 23 | 26 |
| CRIB II (mean ± SD) | 6.5 (±2.8) | 6.0 (±2.8) | 5.7 (±2.5) |
| PIMS II (mean ± SD) | 3.4 (±9.7) | 3.9 (±9.9) | 5.4 (±12.3) |
Annual comparison of outcomes.
| Patient days ( | 2628 | 2729 | 2518 | NA |
| Antibiotic days per 1000 patient days ( | 474.1 | 398.3 | 403.9 | |
| Antibiotic days for culture-negative situations per 1000 patient days ( | 418.2 | 358.0 | 309.4 | |
| Meropenem days per 1000 patient days ( | 53.2 | 27.4 | 25.5 | |
| Vancomycin days per 1000 patient days ( | 86.8 | 43.1 | 33.1 | |
| Ventilation days ( | 956 36.4 | 739 27.1 | 545 21.6 | |
| Suspected VAP per 1000 ventilation days ( | 26.2 | 19.0 | 9.2 | |
| Proven VAP per 1000 ventilation days ( | 3.1 | 0 | 0 | NA |
| Antibiotic days for suspected VAP per 1000 ventilation days ( | 214.4 | 150.2 | 56.9 | |
| Antibiotic days for proven VAP per 1000 ventilation days ( | 32.4 | 0 | 0 | p < 0.001 |
| Catheter days ( | 1687 64.2 | 1618 59.3 | 1197 47.5 | |
| Suspected CLABSI per 1000 catheter days ( | 10.7 | 8.7 | 6.7 | |
| Proven CLABSI per 1000 catheter days ( | 1.8 | 0.6 | 0 | |
| Antibiotic days for suspected CLABSI per 1000 catheter days ( | 70.0 | 63.7 | 33.4 | |
| Antibiotic days for proven CLABSI per 1000 catheter days ( | 17.8 | 4.3 | 0 | |
| Positive blood cultures ( | 10 | 10 | 17 | |
| Positive blood cultures within 48 h of hospitalization (= community acquired infections) | 4 | 2 | 12 | |
| Positive blood cultures after 48 h of hospitalization (= hospital acquired infections) | 6 | 8 | 5 | |
| Positive CSF cultures ( | 1 | 0 | 0 | NA |
| Antibiotic days for culture proven infections per 1000 patient days ( | 55.9 | 40.3 | 94.5 | |
| Antibiotic days for community acquired, culture proven infections per 1000 patient days ( | 14.8 | 8.4 | 71.5 | |
| Antibiotic days for hospital acquired, culture proven infections per 1000 patient days ( | 41.1 | 31.9 | 23.0 | |
| Percentage of antibiotic days for culture proven infections (%) | 11.8 | 10.1 | 23.4 | NA |
| Correct initial antibiotic use ( | 9/10 90.0 | 9/10 90.0 | 14/17 82.4 | |
| Correct streamlining ( | 7/10 70.0 | 8/10 80.0 | 12/17 70.6 | |
| Mortality all patients ( | 11 2.1 | 8 1.5 | 8 1.5 | |
| Mortality newborns < 44 weeks of gestational age ( | 10 3.3 | 6 2.0 | 5 1.7 | |
Cuzick's nonparametric test for trend;
Fisher's exact test;
Poisson regression (adjusted for number of ventilation or catheter days);
Poisson regression (adjusted for number of patient days); NA, not applicable.
Figure 2Relative annual index to 2015 (base 100%) of antibiotic days overall, meropenem and vancomycin days, and antibiotic days for hospital acquired, culture-proven infections, and culture-negative situations per 1000 patient days; not shown are antibiotic days for community acquired, culture-proven infections because development of infection is independent of the unit; *Culture-negative situations: suspected infections and prophylaxis; aCuzick's non-parametric test for trend: p < 0.001.