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Care infections in Belgium: a overview OCTOBRE 2017 Dr. Boudewijn Catry Rue Juliette Wytsmanstraat 14 | 1050 Brussels | Belgium T +32 2 642 57 62 | email: [email protected]

Care infections in Belgium: a overview - beMedTech€¦ · Care infections in Belgium: a overview ... total burden of all other 32 communicable diseases included in the BCoDE 2009

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Care infections in Belgium: a overview

OCTOBRE 2017

Dr. Boudewijn Catry

Rue Juliette Wytsmanstraat 14 | 1050 Brussels | Belgium

T +32 2 642 57 62 | email: [email protected]

Mission NSIH.be

For the containment of healthcare-associated infections in hospitals

and nursing homes we provide :

- standardized definitions and tools,

- national reference data on incidence of nosocomial infections and

antimicrobial resistance,

- outbreak support in collaboration with competent authorities.

Point prevalence survey: PPS (photo)

Surveillance (film)

&

ECDC PPS

▪ ECDC PPS 2011-2012▪ ECDC PPS 2017-2018

HALT-3

www.ecdc.europa.eu

▪ HALT-1: May-September 2010▪ HALT-2: April-May 2013▪ HALT-3: 2016-2017

Point Prevalence Survey: Hai - ABU

Zarb et al., 2012 Eurosurveillance

N pts (a) Prevalence%

(95%CI) (b)

N HAI (c) Relative

% HAI (d)

Pneumonia & other LRTI 392 2.0% (1.8-2.2) 394 25.7%

Surgical site infections (e) 290 1.5% (1.3-1.6) 290 18.9%

Urinary tract infections 263 1.3% (1.2-1.5) 264 17.2%

Bloodstream infections (BSI)(f) 216 1.1% (0.9-1.2) 217 14.2%

Gastro-intestinal system

infections

118 0.6% (0.5-0.7) 119 7.8%

Skin and soft tissue infections 59 0.3% (0.2-0.4) 59 3.9%

Bone and joint infections 38 0.2% (0.1-0.3) 39 2.5%

Eye, Ear, Nose or Mouth infection 47 0.2% (0.2-0.3) 47 3.1%

Systemic infections(f) 40 0.2% (0.1-0.3) 40 2.6%

Belgian : 7.1 % European : 6.0 % (country range 2.3%-10.8%)

Point Prevalence Survey: HAI - ABU

Pourcentage de patients avec une HAI: 7.0%

0%

5%

10%

15%

20%

25%

11

13

15

20

38

59

58

34

27

63

49

30

50 2

62

14

51

61

40

37 7

48

55

41

16

18

17

46

33

24

57

21

12

36

56

19

39

43

60 5

53

22

42 4

29

45

23

28

32

44

52

35 6

54 8

47 3 1

26

31 9

25

10

Hospital number

% p

ati

en

ts w

ith

HA

I

Mean prevalence: 7% [0%-23%]

Goossens, M WIV-ISP

Burden = ‘Extra cost in

morbidity and mortality’

PLOS Medicine, 2016

We estimated that 2,609,911 new cases of HAI occur every year in the European Union

and European Economic Area (EU/EEA). The cumulative burden of the six HAIs was estimated

at 501 DALYs per 100,000 general population each year in EU/EEA. HAP and HA

primary BSI were associated with the highest burden and represented more than 60% of

the total burden, with 169 and 145 DALYs per 100,000 total population, respectively. HA

UTI, SSI, HA CDI, and HA primary BSI ranked as the third to sixth syndromes in terms of

burden of disease. HAP and HA primary BSI were associated with the highest burden

because of their high severity. The cumulative burden of the six HAIs was higher than the

total burden of all other 32 communicable diseases included in the BCoDE 2009±2013

study. The main limitations of the study are the variability in the parameter estimates, in particular

the disease models' case fatalities, and the use of the Rhame and Sudderth formula

for estimating incident number of cases from prevalence data.

PLOS Medicine | DOI:10.1371/journal.pmed.1002150 October 18, 2016

Extra cost MDRO

(hospital ES, 2005-2012)A total of 571 admissions with bacteremia matched the inclusion criteria and 82,022 wereincluded in the control group. The mean cost was € 25,891 for admissions with bacteremiaand € 6,750 for those without bacteremia

HALT-3: Results 2016

Prevalence evolutions

2016 2013 2010

BE BE EU BE EU

Prevalence of residents with at least one antimicrobial (%) 5.4 5.1 4.4 4.3 4.3

Prevalence of residents with at least one HAI (%) 3.5 3.6 3.4 2.7 2.4

Conclusion on ‘Pictures’

▪ HAI prevalence (%) in Belgium• Hospitals: 7.1• LTCFs: 3.5

▪ Estimated number of patients per year with an HAI in Belgium• Hospital: 111 276• LTCFs: 170 090

▪ No decline of HAI occurrence in healthcare facilities▪ Challenge for LTCFs

• Limited resources for infection prevention and control• Home-like facilities

Point prevalence survey: PPS (photo)

Surveillance (film)

&

Royal Decree 2015

Surveillances

&

FEEDBACK

MRSA

Campagnes

IndicateursUSI & ISO

Septicémies

C. difficile

Gram -

ABU

Rectangle = mandatory

Surveillances

&

FEEDBACK

MRSA

Campagnes

IndicateursUSI & ISO

Septicémies

C. difficile

Gram -

ABU

Rectangle = mandatory

VRE

Methicillin resistant S. aureus in

hospitals: 1994-20140

10

20

30

n-M

RS

A/1

000

am

iss

ions

199

4

199

5

199

6

199

7

199

8

199

9

200

0

200

1

200

2

200

3

200

4

200

5

200

6

200

7

200

8

200

9

201

0

201

1

201

2

201

3

201

4

(WIV-ISP Jans, 2015)

Mobile version NSIHweb

Internet connection

Connect via WiFi

Designed for Internet explorer 11

browser (Safari ok)

Quality indicators

Compliance in ICU

Reference : Fonguh et al., 2016

https://link.springer.com/content/pdf/10.1186%2Fs13690-016-0159-3.pdf

Participation/Number of opportunities

± 79%Campaigns Number of opportunities

Before campaign After campaign

2004-2005 73 663 72 705

2006-2007 88 480 84 883

2008-2009 107 653 109 826

2010-2011 89 583 79369

2012-2013 123 204 115 599

2014-2015 117 411 104 186

2016-2017 123 484

Preliminary results PreCampaign 2017

2016-2017 Hand hygiene compliance

stratified by type of contact

NSIH, in prep

Compliance HDM ‘14-’15

77% 32337 30814

36867 36074

17535 17550

9324 8955

21793 20862

117856 0,772103 114255 0,768019

Fonguh, S

WIV-ISP 2016

Campaigns are succesfull

- Ever increasing participation rate

- Increase of HH compliance at short and long term

- Alcohol rub is widely used

- Compliance increases

To be improved:

- HH compliance before & after contact

- More data entry out of campaign

Ongoing: Seventh campaign – patient survey

Quote: Svetlan Taneva, ICU Management & Practice, Spring 2017

“Asking indivudals to be more vigilant is essentially

aksing them to compensate for deficiencies in the

system”.

MULTIDRUG RESISTANT (MDR) ORGANISMS

Micro-organism Example of Resistance

MRSA Staphylococcus aureus Methicilline

ESBL+ Enterobacteriaceae (E.coli / Klebsiella / …)

3de gen. cefalosporins

CPE Enterobacteriaceae Carbapenems

VRE Enterococcus faecalis/faecium Vancomycin

MDR Pseudomonas/Acinetobacter Several classes

CDIF Clostridium difficile Intrinsic (Anaerobic)

Courtesy: Latour & Jans, WIV 2015

MRSA & ESBL in Belgian hospitals

Description BSI episodes, 2016

Total 10,106 BSI of which 7,627 HA-BSI

HA-BSI

o 21% intensive care unit (ICU)-associated BSI

o 40% HA-BSI associated directly (central line - CL)

or indirectly (urinary catheter or endotracheal tube)

with invasive devices

33 Description BSI episodes, 2016

Microorganism specific HA-BSI

incidence

Incidence MO34Duysburgh et al., 2017

Duysburgh E & Lambert, MLL, WIV-ISP 2016

Figure 10: Variation hospital associated bloodstream infections between hospitals, Belgium 2015

HA-BSI, hospital associated bloodstream infection; SD, standard deviation – The funnel plots gives a visual

identification of outliers; above or below 2SD (95%) and 3 SD (99.7%).

Bloodstream infections

• Competent authorities

Outbreak

Surveillance & notification

• experts

Outbreak support

Reference

lab

WIV

ISP

37Remark: For confidentiality reasons, the locations of the bullets representing

individual hospitals do not correspond to the real location of the hospitals in the

province.

Entérobactéries productrices de carbapénémases (CPE) à partir de prélèvementscliniques: par type de carbapénémase et par province:

2012 - 2014

CPE en MRS (2015):

1 seul porteur (OXA-

48)

dans une MRS

Vlaanderen:

OXA-48 = 95% de tous

les CPE

Wallonie:

KPC = 49%

OXA-48=

39%

Bruxelles:

OXA-48:

64%

KPC: 18%

NDM: 10%

VIM: 6%

Les Pays-Bas

600-620 lits

Experts indépendents

Klebsiella OXA-48

Mortalité:

3 confirmés + 10 probables

Coûts

9-10 million €

Average Length of stay &

admissions, Maasstadt, NL

33 labos

283 souches

10 épidémies54 labos,

552 souches

22 épidémies

35 labos

218 souches

2014 2015

2016-Q1Centre National de

Référence:

nombre d’isolats reçus entre

1/1/2014 et 30/04/2016

Enkele gegevensEnterobacteriaceae

Enterobacteriaceae

Enterobacteriaceae

Enterobacteriaceae

Conclusions OST

Moves & fusions often implicated

Mortalité & mortalité & stress (cohorte)

underestimated

Cost ~ 0,5 – 9 million euro per year

- Speed of declaration

(>50% cost: personnel)

- Strain & type ABR

- Support from direction = budget & structure

- Soft skills & priorisation

Antimicrobial consumption is weak point and

contaminates everything (endoscope, ....) :

Sources & Solutions : ‘ENDOGENEOUS’

Incidence of Clostridium difficile infections in

acute care hospitals, Belgium 2008-2016

44* Hospital associated CDI: onset of symptoms 2 days or more after admission in the declaring

hospital *Acute care hospitals: average length of stay <14 days,

0,00

0,50

1,00

1,50

2,00

2,50

2008 2009 2010 2011 2012 2013 2014 2015 2016

N/1

000

ad

mis

sio

ns

Total

Hospital-associated

https://youtu.be/84VmUgQpzgE

AbstractRapid antimicrobial susceptibility testing (AST) is urgently needed for informing treatment decisions and

preventing the spread of antimicrobial resistance resulting from the misuse and overuse of antibiotics. To

date, no phenotypic AST exists that can be performed within a single patient visit (30 min) directly from

clinical samples. We show that AST results can be obtained by using digital nucleic acid quantification to

measure the phenotypic response of Escherichia coli present within clinical urine samples exposed to an

antibiotic for 15 min. We performed this rapid AST using our ultrafast (~7 min) digital real-time loop-

mediated isothermal amplification (dLAMP) assay [area under the curve (AUC), 0.96] and compared the

results to a commercial (~2 hours) digital polymerase chain reaction assay (AUC, 0.98). The rapid dLAMP

assay can be used with SlipChip microfluidic devices to determine the phenotypic antibiotic susceptibility of

E. coli directly from clinical urine samples in less than 30 min. With further development for additional

pathogens, antibiotics, and sample types, rapid digital AST (dAST) could enable rapid clinical decision-

making, improve management of infectious diseases, and facilitate antimicrobial stewardship.

Rapid pathogen-specific phenotypic antibiotic susceptibility testing using digital LAMP quantification in

clinical samples

Science Translational Medicine 04 Oct 2017:

Vol. 9, Issue 410, eaal3693

DOI: 10.1126/scitranslmed.aal3693

https://www.healthstat.be

Figuur 1Non-pediatric antimicrobial use in the community in Daily Defined Doses per 1000 inhabitant days. Belgium 2007-2013

https://www.youtube.com/watch?v=plVk4NVIUh8

Conclusion overall

Source = endogenous

a.o. the GUT

Outbreak support team

also enables

endogenous solutions,

provided collaboration

between all partners

Partners:

-Competent authorities

-General direction

-Medical staff: AB

-Nursing: HH

-Technical/Infrastructure:

automatisation…

-PATIENT & relatives

Thanks to:

theNSIH team*, ECDC, EMA, EFSA, BAPCOC

The labs, NRCs & healthcare settings

[email protected]

www.nsih.be

*Eline Vandael, Karl Mertens, Thomas Struyf, Naima Benhammadi, Els Duysburgh, Laure Mortgat, Theofilos Papadopoulos, Barbara Legiest, Louisa Ben Abdelhafidh, Annie Uwineza, Hélène De Pauw, Katrien Latour.