2/10/2017 Les programmes nationaux de Surveillance en Belgique – nsih.be Boudewijn Catry Louisa Ben Abdelhafidh Katrien Latour Barbara Legiest Marie-Laurence Lambert Els Duysburgh Theofilos Papadopoulos Karl Mertens Thaddé Mahmourian Annie Uwineza Syvlanus Fonguh Béatrice Jans Rue Juliette Wytsmanstraat 14 | 1050 Brussels | Belgium T +32 2 642 51 11 | F +32 2 642 54 10 | email: [email protected] | http://www.iph.fgov.be Objectifs de la présentation Introduction Cadre légal nsih.be Campagne HDM Surveillances Conclusions 1 2/10/2017 Point prevalence survey: PPS (photo) Surveillance continue (film) & Point Prevalence Survey: HAI - ABU Pourcentage de patients avec une HAI: 7.0% 20% 15% 10% Mean prevalence: 7% [0%-23%] 5% 0% 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 % patients w ith H A I 25% Hospital number Goossens, M WIV-ISP 2 2/10/2017 http://www.ecdc.europa.eu/en/publications/Publications/healthcareassociated-infections-antimicrobial-use-PPS.pdf Point Prevalence Survey: HAI - ABU 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% Zarb et al., 2012 Eurosurveillance 3 2/10/2017 Point Prevalence Survey: HAI - ABU On antimicrobials: 36.6% Mean antimicrobials for those on antimicrobials: 1.5 Indication for Antimicrobial N=5543 1% 13% HI :acute 4% 4% 3% 44% 15% 8% hospital-acquired :community-acquired CI LI :acquired in NH M :medical prophylaxis U :unknown reason S1:single dose S2:one day Surg S3:> 1 day 23% Goossens, M WIV-ISP Belgium 2011 PPS continued http://www.ecdc.europa.eu/en/publications/Publications/healthcareassociated-infections-antimicrobial-use-PPS.pdf 4 2/10/2017 Belgium 2011 PPS continued MRSA 0.368*11%= 4.048% Candida spp = 6% http://www.ecdc.europa.eu/en/publications/Publications/healthcare-associatedinfections-antimicrobial-use-PPS.pdf Mission To provide standardized definitions and tools for the containment of health care associated infections in hospitals and nursing homes, and to establish national reference data on incidence of nosocomial infections and antimicrobial resistance. 5 2/10/2017 Nosocomial infection (1/3) An active infection was defined as “healthcareassociated” (associated to acute care hospital stay only for the purpose of this protocol) when: The onset of the signs and symptoms had started on Day 3 of the current admission or later (where Day 1 is the day of admission) OR The signs and symptoms were present at admission or became apparent before Day 3, but the patient had been discharged from another hospital less than two days before admission Zarb et al., 2013 Eurosurveillance Nosocomial infection (2/3) OR The signs and symptoms of an active surgical site infection were present at admission or started before Day 3, and the surgical site infection occurred within 30 days of a surgical intervention (or in the case of surgery involving an implant, a deep or organ/space surgical site infection that developed within a year of the intervention), Zarb et al., 2013 Eurosurveillance 6 2/10/2017 Nosocomial infection (3/3) OR The signs and symptoms of a Clostridium difficile infection were present at admission or started before Day 3, with the patient having been discharged from an acute care hospital less than 28 days before the current admission. Zarb et al., 2013 Eurosurveillance Objectifs de la présentation Introduction Cadre légal nsih.be Campagne HDM Surveillances Conclusions 7 2/10/2017 Cadre légal (annexes) Le financement de l’infirmier en hygiène hospitalière est porté à 53 105,00 euros (°2007 indexé) par équivalent temps plein. Cette majoration est conforme au positionnement de l’infirmier au niveau du cadre intermédiaire. Cette mesure s’applique aux hôpitaux aigus, spécialisés (Sp), gériatriques (G) et psychiatriques. Par ailleurs, pour les hôpitaux généraux et pour les hôpitaux spécialisés (Sp) et gériatriques (G) comptant au moins 150 lits, un encadrement minimal est prévu pour l’équipe d’hygiène hospitalière. Ces institutions doivent employer au moins 1 infirmier en hygiène hospitalière ETP et au moins 0.5 médecin en hygiène hospitalière ETP. Le budget prévu pour les frais de fonctionnement – 10 % du budget affecté aux salaires de l’infirmier en hygiène hospitalière et du médecin en hygiène hospitalière – est maintenu. Arrêt royal 2015 8 2/10/2017 Arrêt Royal 2015 9 2/10/2017 Burden = ‘Frais des extras soins’ 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 10 2/10/2017 Objectifs de la présentation Introduction Cadre légal nsih.be Campagne HDM Surveillances Conclusions Objectifs de la présentation Introduction Cadre légal nsih.be Campagne HDM Surveillances Conclusions 11 2/10/2017 Data Collection & Analysis: WIV • Objectives • Improve HH compliance & basic requirements in institutions • Target : 100% • Methods • Measurement of compliance • Software • continuous measurements possible • reports immediately available Mobile version • Internet connection • Connect via WiFi • Designed for Internet explorer 11 browser (Safari ok) 12 2/10/2017 Report • https://nsihweb.wiv-isp.be: secured website • Password: www.nsih.be/contact – include NSIHcode ! • simple • for all measurement periods • hospital report • Online available • national report • available after national campaigns • allows comparison of hospital data with national Table1 : Hand hygiene compliance in Belgian hospitals over different campaigns (before and after campaign) Campaigns (Year) Compliance before Compliance after 1st campaign (2005) 49.6% 68.6% 2nd campaign (2006-2007) 53.2% 69.5% 3rd campaign (2008-2009) 58.0% 69.1% 4th campaign (2010-2011) 62.3% 72.9% 5th 64.1% 75.8% campaign (2013) Fonguh, S WIV-ISP 2013 13 2/10/2017 Fonguh, S WIV-ISP 2013 Fonguh, S WIV-ISP 2013 14 2/10/2017 Fongugh Sylvanus, 2013 www.nsih.be Fongugh Sylvanus, 2013 www.nsih.be 15 2/10/2017 Fongugh Sylvanus, 2013 www.nsih.be Point Prevalence Survey: HAI - ABU 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% Zarb et al., 2012 Eurosurveillance 16 2/10/2017 Taux d'observance de l'hygiène des mains selon les 5 indications 5 Indications Nombre d'opportunités observées (n) Hygiène des mains Alcool + savon (n) Taux d'observance (%) Avant contact patient 258 121 47 Après contact patient 323 210 65 Avant acte propre/invasif 96 54 56 Après contact liquide biologique + muqueuse 22 17 77 Après contact matériel et environnement du patient 128 62 48 Fonguh, S WIV-ISP 2013 Exigences de base… 17 2/10/2017 Figure 16: Pourcentage de personnes portant une bague, par catégorie professionnelle. Avant et Après campagne 2013 (N hôpitaux=83) . Fonguh, S WIV-ISP 2014 Figure 18: Pourcentage de personnes portant une montre par catégorie professionnelle. Avant et Après campagne 2013 (N hôpitaux=83) . Fonguh, S WIV-ISP 2014 18 2/10/2017 Figure 20: Pourcentage de personnes portant un bracelet par catégorie professionnelle. Avant et Après campagne 2013 (N hôpitaux=83) . Fonguh, S WIV-ISP 2014 Figure 28: Pourcentage de personnes avec vernis à ongles par catégorie professionnelle. Avant et Après campagne 2013 (N hôpitaux=83) . Fonguh, S WIV-ISP 2014 19 2/10/2017 Figure 30: Pourcentage de personnes avec des ongles artificiels par catégorie professionnelle. Avant et Après campagne 2013 (N hôpitaux=83). Fonguh, S WIV-ISP 2014 Fonguh, S WIV-ISP 2016 20 2/10/2017 Compliance in ICU Objectifs de la présentation • • • • • Introduction Cadre légal nsih.be Campagne HDM Surveillances – – – – ISO & USI SEP Clostridium difficile ABUH • Conclusions 21 2/10/2017 National surveillances of Surgical Site Infections (SSI) and Nosocomial Infections (NI) in Intensive Care Units (ICU) Ir. Karl Mertens National Programme on Healthcare-associated Infections Scientific Institute of Public Health, Brussels (BE) Rue Juliette Wytsmanstraat 14 | 1050 Brussels | Belgium T +32 2 642 51 11 | F +32 2 642 50 01 | email: [email protected] | www.wiv-isp.be 22 2/10/2017 Background: Importance Surgical Site Infections Nosocomial Infections in the ICU Impact: readmission, re-intervention Impact: extra length of stay, morbidity, mortality SSI: 3rd most frequent type of infection (14.6%) ICU: bed index with highest prevalence (25.3%) National Prevalence Study of Nosocomial Infections (KCE, 2007) • • • clear association with healthcare related procedures Varies according to surgical intervention & procedures, intervention duration, wound contamination, patient severity high rates of surgical interventions taking place • • Severe pathology of patient population, vulnerable to NI High exposure to medical (invasive) acts 1/3rd of nosocomial infections can be prevented by means of an intensive program of infection prevention and surveillance SENIC study: Am J Epidemiol 1985; 121(2):182-205 SSI & ICU surveillance: tools • • • • • • 2 protocols • follow closely ECDC (HAI-Net) protocols • describe background, inclusion of surgical interventions (SSI) / patients (ICU), case definitions, details on surveillance data to be collected, participation options Paper forms for manual data entry NSIHwin software for local follow-up: data input, data import, validation, analysis, export Individual feedback reports for the hospital Annually: national reports with aggregated indicators + submission of data to ECDC – The European Electronic Surveillance System (TESSy). http://www.nsih.be (SSI / ICU / NSIHwin webpages) : protocols, forms, national annual reports, software & manual 23 2/10/2017 SSI surveillance in a glance • • • • • Participation period: 3 months Choose >=1 group of interventions to follow from the list of NHSN (US) intervention codes and its associated ICD-9-CM procedures Recommended list of interventions (ECDC, optional) Follow-up of SSI post-intervention, default 30d, 365d in case of foreign bodies or materials Optional: • • • • post-discharge follow-up intrinsic risk variables microbial ecology antimicrobial resistance SSI surveillance: recommended interventions Code NHSN Description CBGB Pontage coronaire avec incision du thorax ainsi que périphérique (B=Both) Interventions à thorax ouvert en vue de revascularisation directe du myocarde, y compris le prélèvement du greffon veineux CBGC Pontage coronaire avec incision du thorax seule (C=Chest only) Comme ci-dessus, mais sans incision complémentaire CHOL Cholécystectomie Cholécystectomie avec ou sans geste sur la voie biliaire principale COLO Chirurgie du colon Incision, résection ou anastomose du colon; comprenant également les anastomoses entre l’intestin grêle et le colon CSEC Césarienne HPRO Prothèse de hanche Prothèse articulaire de hanche KPRO Prothèse du genou Prothèse articulaire de genou LAM Laminectomie Exploration ou décompression des racines nerveuses spinales par excision des structures vertébrales; excision ou destruction de disque intervertébral 24 2/10/2017 Data input & analysis using NSIHwin software • • • • • • Local software, MS Access based, developed by IPH Freely available Used for 3 surveillances + Hand hygiene campaigns Manual data input, Analysis using predefined reports Export to IPH (WIV-ISP) Data import using NSIHwin software • • • • In combination with NSIHwin data entry & analysis Objective: use surveillance data that is already available in electronic format XLS format Detailed manual available from http://www.nsih.be (NSIHwin webpage) 25 2/10/2017 Surveillance data: Indicators for Infection Incidence • • • • Objective: standardize Nosocomial Infection rates to make them comparable across hospitals, countries Construction of denominator Progressive standardization according to the detail of the collected denominator data: • patients • patientdays • patientdays under fixed follow-up | invasive device days • Stratified for intrinsic (case-mix) risk factors (SSI) or hospital types | expected number of infections based on intrinsic risk factor data (ICU) In its most refined case, differences in adjusted infection rates are due to • Sampling variability • Differences in sensitivity / specificity • Differences in quality of care, infection prevention, structure & process parameters. SSI surveillance: Indicators for SSI occurrence # SSIs within 30d* # interventions • Cumulative Incidence = • Cumulative Incidence within the hospital = • Incidence Density = • If available: stratification for NHSN risk index categories # SSIs in hospital within 30d* # interventions # SSIs in hospital within 30d* # post-operative hospital days * 1 year for HPRO or KPRO 26 2/10/2017 ICU surveillance: Indicators for infection occurrence Nosocomial Pneumonia, Bloodstream, Urinary Tract Infections: # Infections • Cumulative incidence = # Patients # Infections # Patientdays • Incidence density = • Device-adjusted incidence density = • If available: Patients and patientdays, Infection Incidence, device-adjusted Infections incidence, mortality rates stratified for risk factor levels • If available: Standardized Infection rate: # Observed infections / # Expected Infections # device-associated Infections # device days Individual feedback reports • • • Created and send back after reception of surveillance data Restricted to participating hospitals, contact persons for the particular surveillance within the hospital Versions: participation period, year, cumulative | single, multiple units (ICU) 27 2/10/2017 Individual feedback reports Tables showing for particular participation period, for each indicator: • hospital’s mean • the mean and relevant percentiles of the national distribution • ranking of the hospital mean within the national distribution Individual feedback reports For most relevant indicators : • • Benchmarks graphs showing graphically the national distribution + position of the hospital’s mean Evolution graphs showing the long term evolution of the hospital’s mean + relevant percentiles of the national distribution 28 2/10/2017 SSI Surveillance: results 2002-2003 Cumulative incidence of SSI: SSI Surveillance: results 2002-2003 Completeness of post-operative follow-up 29 2/10/2017 http://www.ecdc.europa.eu/en/publications/Publications/SSI-in-europe-2010-2011.pdf 30 2/10/2017 Coronary artery bypass graft (CABG) Key points • 41 725 CABG operations were reported for 2010– 2011. • The cumulative incidence of SSI was 3.5% [intercountry range: 2.8%–7.1%] in 2010–2011. • The incidence density of SSI was 1.9 [intercountry range: 0.6–5.6] in-hospital SSI per 1 000 post-operative patient-days in 2010–2011. 31 2/10/2017 ICU Surveillance: Incidence 1997-2009 Nosocomial Pneumonia / 1000 patient days: Nosocomial intubation–associated Pneumonia / 1000 intubation days Mertens, et al., J Hosp Infect 2013 32 2/10/2017 ICU Surveillance: Incidence 1997-2009 Nosocomial Bloodstream Infections / 1000 patient days Nosocomial catheter–associated Bloodstream Infections / 1000 catheter days Mertens, et al., J Hosp Infect 2013 Objectifs de la présentation • • • • • Introduction Cadre légal nsih.be Campagne HDM Surveillances – – – – ISO & USI SEP Clostridium difficile ABUH • Conclusions 33 2/10/2017 Naïma Hammami & Marie-Laurence Lambert Belgian national surveillance of bloodstream infections in the hospital (SEP) Rue Juliette Wytsmanstraat 14 | 1050 Brussels | Belgium T +32 2 642 51 11 | F +32 2 642 50 01 | email: [email protected] | www.wiv-isp.be Relevance Public Health Severity of infection 1: • • • High mortality Increase length of stay Increased health care cost Incidence hospital acquired bloodstream infections (HA-BSI): 5.9/1000 admissions and 8,2/10.000 patientdays2 Impact of preventive measures 3: • • Origin: association invasive devices ↓ 10-70% of infection rates 1. Vrijens 2010 & Vrijens 2012 2. Belgian national surveillance of nosocomial Septicemia, data 2013 77 3. Harbarth 2003, Pronovost 2006 – 2010, Umsheid 2011 34 2/10/2017 OBJECTIVES • Monitoring trends : incidence hospital-acquired bloodstream infections (HA-BSI), focus preventable infections • • Local and national level Causal micro-organisms - resistance profile • • Local and national level Hammami, et al., WIV-SIP 2014 78 METHODS: Study design Surveillance (start 1992, protocol review 2013) Study population: • Belgian hospitals (KB/AR 2007): • • Acute, chronic (if > 150 beds), Hospitalised patients with HA-BSI episode: • Excl: non HA-BSI episodes (ambulatory patients, community,etc), non hospital-Sp Study (participation) period: • • 79 minimum 1 quarter / year compulsory participation 2015 (new KB/AR June 2014) Hammami, et al., WIV-SIP 2014 35 2/10/2017 OUTCOME INDICATORS HOSPITAL Indicator Numerator Denominator Incidence HA-BSI N HA-BSI ≥ 2 d hospital Admissions & pat.days hospital Incidence ICU-BSI N HA-BSI ≥ 2 d ICU Admissions & pat.days in ICU (Admissions & pat.days ≥ 2 d in ICU) Incidence MO specific BSI (e.g. MRSA HA-BSI) →VIP2 (Flemish QI) N HA-BSI ≥ 2 d hospital, with specific MO Admissions & pat.days hospital Incidence CVC associated HA-BSI →Federal QI N CLABSI ≥ 2 d hospital Admissions & pat.days hospital (Total patients with CVC) (Total CVC days) HA-BSI: hospital acquired bloodstream infections ICU-BSI: ICU acquired bloodstream infections MO: microorganism, CVC: central venous catheter, CLABSI: central line associated 80 bloodstream infections RESULTS: national report 2000-13 Descriptive: • Increasing participation: • • Origin Top3: • • ICU (22%), geriatrics (15%), internal medicine (12%) µ-organism Top3: • 81 central vascular catheter (27%), urinary (21%), pulmonary (11%), Location Top3: • • 109 hospitalsites (>90%); E. coli (22%), coag-neg. staphylococci (13%), Staph. aureus (11%) Hammami, et al., WIV-SIP 2014 36 2/10/2017 METHODS: Data flow since 2013 Data entry : By hospitals in Web-based application (Sharepoint) (https://nsihweb.wiv-isp.be/SEP/ ) Bv. 2101 nsih code Nombre de septicémies par mois • • Data transfer: Hospital → SQL database • Feedback: Hospital ( https://nsihweb.wiv-isp.be/SEP/ ): • • individual FB, real time (scripts in SAS) National: • • • annual (closure database end of March Y+1) available on website Hammami, et al., WIV-SIP 2014 82 RESULTS: national report 2000-13(2) Overall incidence HA-BSI stable over years • 2,5 Bias; changing participation Incidence per µ-organism SEP verworven in ziekenhuis /10.000 pd 2,0 2,0 Staphylococus aureus 1,5 Esherichia coli 1,2 Klebsiella pneumoniae 1,0 1,0 1,1 Pseudomonas aeruginosa 0,6 0,5 Enterococcus faecalis 0,5 0,4 0,4 0,3 0,0 2000 83 2001 2002 2003 2004 2005 2006 2007 Jaar 2008 2009 2010 2011 2012 2013 Hammami, et al., WIV-SIP 2014 37 2/10/2017 Hammami, et al., WIV-SIP 2014 Bloodstream infections hospital wide Duysburgh E & Lambert, MLL, WIV-ISP 2016 38 2/10/2017 Micro-organisms Bloodstream infections Duysburgh E & Lambert, MLL, WIV-ISP 2016 Bloodstream infections 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%). Duysburgh E & Lambert, MLL, WIV-ISP 2016 39 2/10/2017 Objectifs de la présentation Introduction Cadre légal nsih.be Campagne HDM Surveillances • • • • ISO & USI SEP Clostridium difficile ABUH Conclusions Evolution C. difficile The peak in incidence around 2008 diminished and stabilised in 2010-2011 at an elevated level. Since then it is again showing a slight increase. In 2013, the total incidence was reported as 1.65 cases / 1000 admissions in hospitals. In the same year, the mean incidence of hospital-acquired cases (onset of symptoms > 2 days after admission in the declaring hospital) was 1.29 / 10 000 hospitals days, more than the preceding three years (data taken from hospitals participating in one complete year [two semesters] of surveillance. The proportion of cases which are community-associated has not substantially increased in recent years, as described in other countries. Neely, et al., WIV-SIP 2014 40 2/10/2017 Table 1: Epidemiological surveillance of Clostridium difficile infection (CDI): episodes of CDI in hospitalized patients in Belgian hospitals 2008-2015 Year 2008 2009 2010 2011 2012 2013 2014 2015 2 989 2 949 2 466 2 516 2 507 2 711 2 444 2 975 65% 62% 62% 63% 61% 60% 59% 60% Episodes Total episodes reported Episodes with hospital-associated (HA) CDI* (%) For episodes other than HA-CDI – Suspected origin of infection Community 56% 57% 59% 60% 63% 62% 63% 67% Declaring hospital** 18% 17% 17% 18% 16% 15% 17% 15% Other hospital 16% 14% 12% 10% 10% 10% 8% 9% Unknown/missing 10% 12% 11% 12% 12% 12% 11% 9% Yes 16% 12% 12% 11% 13% 13% 12% 15% No 68% 70% 69% 72% 67% 68% 72% 70% Unknown 16% 18% 19% 16% 20% 18% 16% 16% Recurrent episodes*** (%) *Defined as onset of diarrhoea 2 days or more after admission in the declaring hospital (onset date minus admission date >=2) **Declaring hospital : episodes with onset less than 2 days after admission subjectively thought to have their origin in the declaring hospital (e.g. readmissions within 4 weeks after discharge) ***Defined as the proportion of episodes which are recurrent, and not the incidence of recurrences in patients presenting with a new episode of CDI Valencia et al., 2016 41 2/10/2017 Table 1: Top 5 CDI ribotypes isolated within the national surveillance programme, by the number of hospitals in which they are isolated. Belgium, 2009-2015 Year N hospitals sending strains for typing (100%) 2009 104 2010 103 2011 84 2012 111 2013 103 2014 112 2015 97 35 33 11 11 34 33 26 25 32 38 20 24 45 41 35 32 42 38 39 35 6 5 38 37 25 24 29 28 28 27 13 13 42 38 28 25 41 37 27 24 18 16 46 47 41 42 35 36 30 31 N hospitals with... BR014 (UCL16) % BR078 (UCL 3) % BR020 (UCL16a,16a+) % BR002 (UCL32,32+) % BR0106 (UCL048d) % 21 22 Valencia et al., 2016 Mean incidence of hospital- associated Clostridium difficile infections per 10 000 hospital days in acute hospitals, by province. Belgium,2015 Mean incidence: sum of episodes / sum of hospital-days for all acute hospitals providing data (one or two semesters) in 2015. Categories based on quartiles of the incidence distribution. Valencia et al., 2016 42 2/10/2017 Figure 1 : Mean annual incidence of infection with Clostridium difficile (CDI) – total cases and hospital associated cases /1000 admissions, in acute care$ Belgian hospitals, 2008-2015 Episodes CDI/1000 admissions 2,50 2,00 1,50 Hospital associated episodes 1,00 Total episodes 0,50 0,00 2008 2009 2010 2011 2012 2013 2014 2015 Year * Only acute hospitals providing data for the whole year are included. $ Acute hospitals: defined on the basis of mean length of stay <14 days Valencia et al., 2016 43 2/10/2017 Table 1 : Hospital stays with an intestinal infection due to Clostridium difficile (code ICD-9_CM 008.45*), Belgium 1999-2010 1999 2000 2001 2002 2003 2004 2005 2006 2007 2008 2009 2010 2011 CDI as primary diagnostic code (no.) 415 467 423 501 723 907 959 1007 1040 1116 1148 920 866 26% 23% 23% 25% 23% 22% 23% 22% 23% 25% 24% 24% % of the total 25% CDI as secondary diagnostic code (no.) Total 1270 1356 1404 1698 2155 3086 3456 3383 3646 3633 3514 2947 2715 1685 1823 1827 2199 2878 3993 4415 4390 4686 4749 4662 3867 3581 *ICD9-CM International classification of diseases, CDI: Clostridium difficile infection Neely et al., 2014 – WIV-ISP 44 2/10/2017 C. difficile USA RESULTS: The population-based rate of CDI in older Americans was 282.9/100,000 person-years (95% confidence interval (CI)) 226.3 to 339.5) for individuals with depression and 197.1/100,000 person-years for those without depression (95% CI 168.0 to 226.1). The odds of CDI were 36% greater in persons with major depression (95% CI 1.06 to 1.74), 35% greater in individuals with depressive disorders (95% CI 1.05 to 1.73), 54% greater in those who were widowed (95% CI 1.21 to 1.95), and 25% lower in adults who did not live alone (95% CI 0.62 to 0.92). Self-reports of feeling sad or having emotional, nervous or psychiatric problems at baseline were also associated with the later development of CDI. Use of certain antidepressant medications during hospitalization was associated with altered risk of CDI. CONCLUSIONS: Adults with depression and who take specific anti-depressants seem to be more likely to develop CDI. Older adults who are widowed or who live alone are also at greater risk of CDI. Rogers, M.A.M., Greene, M.T., Young, V.B., Saint, S., Langa, K.M., Kao, J.Y., Aronoff, D.M., 2013. Depression, antidepressant medications, and risk of Clostridium difficile infection. BMC Med. 11, 121. http://dx.doi.org/10.1186/1741-7015-11-121. Conclusions Antibiotic agents are ‘invasive’, also if given orally 45 2/10/2017 Objectifs de la présentation • • • • • Introduction Cadre légal nsih.be Campagne HDM Surveillances – – – – ISO & USI SEP Clostridium difficile ABUH • Conclusions Specialities to be reported (WHO, ESAC, pubMED) ATC classification: A07A Antibiotics for gastro-intestinal use J01, P01AB Antibiotics J02, D01BA Antimycotics for systemic use J04A Tuberculostatics 46 2/10/2017 ATC Class J01C Beta-lactam antibacterials, penicillins J01D Other beta-lactam antibacterials J01M Quinolone antibacterials J01X Other antibacterials J02A Antimycotics for systemic use J01F Macrolides, lincosamides and streptogramins J01G Aminoglycoside antibacterials J04A Drugs for treatment of tuberculosis J01E Sulfonamides and trimethoprim A07A Intestinal anti-infectives P01A Agents against amoebiasis/protozoal diseases J01A3 Tetracyclines D01B Antifungals for systemic use J01B0 Amphenicols FEEDBACK Compare own use with national mean 47 2/10/2017 AUTOMATIC FEEDBACK Local follow up FEEDBACK 48 2/10/2017 Conclusions ABUH - Résultats: points faibles - dénominateur: journées d’hosp vs. admissions? Stratification: unité, type d’hôpital, taille, région? - Evolution MRSA, MRE, C.diff, … complémentaire Nécessite collecte mensuelle (rétrospective) - - Plusieurs hôpitaux l’ont déjà fait! Résultats: points forts - Suivi interne plus important que le ‘benchmarking’ Ingenbleek, A et al. WIV-ISP 2015 49 2/10/2017 Ingenbleek, A et al. WIV-ISP 2015 J01 - Non-paediatrics 15 most used products DDD/1000 bed-days 40 30 20 10 C ef az C ol ip in ro P flo ip er xa & ci n en zy in Fl h ib uc lo xa ci M lli n er op en em C ef tri ax on M ox e ifl ox ac C in ef ur ox im C lin e da m C yc la rit in hr om M yc et in ro ni da zo le A m ox ic illi n Te m oc ill C in ef ta zi di m V an e co m yc in 0 2007 2008 2009 2010 2011 2012 2013 Note: National median consumption in acute care settings. J01CR02 excluded Participation: 2007 n=55; 2008 n=96; 2009 n=98; 2010 n=97; 2011 n=97; 2012 n=93; 2013 n=83 Ingenbleek, A et al. WIV-ISP 2015 50 2/10/2017 Ingenbleek, A et al. WIV-ISP 2015 Stratified by ward: antibacterials 51 2/10/2017 Stratified by ward: antimycotics ESAC National level, all antimicrobials included HOSPITALS Year Participants Total DDD for the year DDD/1000 Nights 2008 121 7315319.20 579.734 2009 124 7273099.57 583.651 2010 120 6940067.65 585.087 2011* 106 6561559.15 581.215 2011*: The data collection for the year 2011* is on-going. 52 2/10/2017 53 2/10/2017 Conclusions Antibiotic agents are ‘invasive’, also if given orally Denominator /1000 patient days is superior unit for hospitals (not DDD/1000 inhabitants per day). 35 1,75 30 1,5 25 1,25 20 1 15 0,75 10 0,5 5 0,25 0 0 1997 1998 1999 2000 2001 2002 2003 2004 2005 2006 2007 2008 2009 2010 2011 2012 2013 2014 2015 Years DDD per 1000 inhabitants and per day DDD per 1000 inhabitants and per day Ambulant care J01 J02 Figure 2. Trends of antimicrobial (ATC group J01) and antimycotic (ATC group J02) drugs for systemic use in the ambulant care in Belgium. Reporting years 1997-2015. (DDD: defined daily dose). WIV-ISP, 2017 NSIH report Catry et al., in press 54 2/10/2017 Introduction des données par https://www.healthstat.be 1. Authentication par eID Selectionnez: ‘LOG IN’: 138 https://www.healthstat.be 1. Authentication par eID Selectionnez le certificat et introduisez votre code pin (e-ID): 139 139 55 2/10/2017 https://www.healthstat.be 2. Indiquez l’organisation/site/fusion – ensuite ‘Enregistrer’ 140 140 Ingenbleek A, Vrancken K, WIV-ISP 2016 56 2/10/2017 Objectifs de la présentation Introduction Cadre légal nsih.be Campagne HDM Surveillances • • • • ISO & USI SEP Clostridium difficile ABUH Conclusions 57 2/10/2017 Conclusions (1) Antibiotic agents are ‘invasive’, also if given orally Hand hygiene alone is insufficient to control HAI Monthly FQ consumption, expressed as DDD/1000 PD. Filled circles, pre-intervention period values; open circles, intervention period values; diamonds, post-intervention period values. Lafaurie M et al. J. Antimicrob. Chemother. 2012;67:10101015 © The Author 2012. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For Permissions, please e-mail: [email protected] 58 2/10/2017 Monthly consumption of ABHR solution. Lafaurie M et al. J. Antimicrob. Chemother. 2012;67:10101015 © The Author 2012. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For Permissions, please e-mail: [email protected] Change in monthly FQ-resistant P. aeruginosa rates, from 2002 to 2010. Lafaurie M et al. J. Antimicrob. Chemother. 2012;67:10101015 © The Author 2012. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For Permissions, please e-mail: [email protected] 59 2/10/2017 Change in monthly MRSA rates, from 2002 to 2010. Lafaurie M et al. J. Antimicrob. Chemother. 2012;67:10101015 © The Author 2012. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For Permissions, please e-mail: [email protected] Conclusions (2) Antibiotic agents are ‘invasive’, also if given orally Hand hygiene alone is insufficient to control HAI Denominator /1000 patient days is superior unit for hospitals (not DDD/1000 inhabitants per day). Hotspots: ICU/HAE-ONC & livestock 60 2/10/2017 61 2/10/2017 Figuur 1Non-pediatric antimicrobial use in the community in Daily Defined Doses per 1000 inhabitant days. Belgium 2007-2013 62 2/10/2017 Conclusions (3) Antibiotic agents are ‘invasive’, also if given orally Hand hygiene alone is insufficient to control HAI Denominator /1000 patient days is superior unit for hospitals (not DDD/1000 inhabitants per day). Hotspots: ICU/HAE-ONC & livestock Fast diagnostics (AB spectrum) and automatisation (hand hygiene & GLIMS), and qualtiy validation of National Ref Centers are needed. The detailed information is out there… Acknowledgements: The NSIH team, ECDC, BAPCOC The labs, NRCs & hospitals & nursing homes [email protected] Slides available on: www.nsih.be 63
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