| Literature DB >> 28322345 |
Kai O Hensel1, Rhea van den Bruck2, Ingo Klare3, Michael Heldmann1, Beniam Ghebremedhin4, Andreas C Jenke5.
Abstract
In the course of a hospital management takeover, a microbial outbreak took place in a tertiary neonatal intensive care unit (NICU). Here, we characterize the outbreak and its management. About 4 months prior to takeover, there was a sharp increase in positive isolates for MSSA and multidrug-resistant organisms (MDROs). Simultaneously, the nursing staff sick leave rate increased dramatically which directly correlated with the number of infection/colonization per week (r2 = 0.95, p = 0.02). During the following months we observed several peaks in positive isolates of methicillin-sensitive staphylococcus aureus (MSSA), MDROs and subsequently a vancomycin-resistant enterococcus (VRE) outbreak. Interventional outbreak management measures were only successful after substantial recruitment of additional nursing staff. None of the VRE, but 44% (n = 4) of MDRO and 32% (n = 23) of MSSA colonized infants developed symptomatic infections (p = 0.02). Among the latter, 35% suffered from serious consequences such as osteomyelitis. The most important risk factors for colonization-to-infection progression were low gestational age and birth weight. Nursing staff fluctuation poses a substantial risk for both bacterial colonization and infection in neonates. Comprehensive outbreak management measures are only successful if adequate nursing staff is available. Non resistant strains account for most neonatal infections - possibly due to their limited perception as being harmful.Entities:
Mesh:
Year: 2017 PMID: 28322345 PMCID: PMC5359565 DOI: 10.1038/srep45014
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379
Figure 12015 Outbreak and hygienic outbreak control intervention characteristics.
Top: Pathogen colonization and infection rate in patients admitted to the NICU; Middle: Available nursing staff, 100% = estimated minimal requirement for adequate patient care according to GNPI guidelines; Bottom: Time-course of applied interventional outbreak management measures.
Epidemiological characteristic of MSSA, MDRO and VRE colonized patients.
| VRE total (n = 10) | MDRO (n = 9) | MSSA (n = 71) | p-value | |
|---|---|---|---|---|
| Gestational age (weeks) | 30.4 (28.2–32.7) | 26.0 (23.8–28.2) | 32.6 (31.5–33.7) | 0.12 |
| Birth weight (gramm) | 1500 (1094–1900) | 785 (559–1012) | 2040 (1820–2261) | |
| Age of the mother (years) | 30.8 (27.2–34.4) | 26.8 (22.3–31.3) | 30.3 (29.0–31.7) | |
| SGA | 10% | 33% | 12% | 0.26 |
| Male gender | 50% | 100% | 60% | 0.36 |
| Singeltons (%) | 60% | 67% | 72% | 0.58 |
| progression to infection | 0% | 44% | 32% |
Figure 2Correlation analysis between nursing staff coverage and incidence of pathogenic infections/colonizations per week.
Time periods were categorized depending on nursing staff coverage and correlated with the number of infections and colonizations per week by linear regression analysis.
Figure 3Cluster analysis of VRE isolates based on SmaI-macrorestriction patterns resolved in PFGE.
12 vanA-positive E. faecium isolates of NICU patients hospitalized at the neonatology department of the HELIOS University Clinic Wuppertal were positive for the virulence genes esp and hyl. The dendrogram was evaluated using Dice coefficient and UPMGA clustering (BioNumercis software). The VRE isolates showed identical or highly related banding patterns (>95% identity agreement).
Risk factors for progression from MSSA colonization to infection (p-values refer to the comparison of MSSA infection versus colonization).
| MSSA total (n = 71) | MSSA infection (n = 23) | MSSA colonization (n = 48) | p-value | |
|---|---|---|---|---|
| Gestational age (weeks) | 32.6 (31.5–33.7) | 30.4 (28.6–32.2) | 34.0 (32.8–35.3) | |
| Birth weight (gramm) | 2040 (1820–2261) | 1632 (1277–1986) | 2260 (1961–2560) | |
| Age of the mother (years) | 30.3 (29.0–31.7) | 31.2 (28.9–33.4) | 29.9 (28.2–31.7) | 0.56 |
| SGA | 12% | 12% | 12% | 0.64 |
| Male gender | 60% | 36% | 70% | |
| Singeltons (%) | 72% | 64% | 75% | 0.29 |
| prenatal steroids (<1500 g) | 79% | 75% | 82% | 0.69 |
| prenatal antibiotics (<1500 g) | 48% | 25% | 71% |
Epidemiological risk factors for systemic MSSA infection.
| Local infection (n = 17) | Systemic infection (n = 8) | p-value | |
|---|---|---|---|
| Gestational age (weeks) | 32.0 (30.6–34.9) | 28.0 (24.0–32.0) | |
| Birth weight (gramm) | 1932 (1507–2358) | 1183 (560–1806) | |
| Age of the mother (yrs) | 31.2 (28.2–34.2) | 31.4 (27.2–35.1) | 1.0 |
| SGA | 6% | 33% | 0.11 |
| Male gender | 33% | 56% | 0.41 |
| Singeltons (%) | 44% | 11% | 0.19 |
| prenatal antibiotics (<1500 g) | 56% | 13% | |
| prenatal steroids (<1500 g) | 25% | 75% |