I Sessione: Le infezioni nosocomiali: quale gestione nelle strutture residenziali assistite? Epidemiologia e prevenzione Paolo Durando Dipartimento di Scienze della Salute Scuola di Scienze Mediche e Farmaceutiche IRCCS AOU San Martino-IST, Università degli Studi di Genova Gruppo Tecnico Regionale per il Controllo delle Infezioni Correlate all’Assistenza Società Italiana Multidisciplinare per la Prevenzione delle Infezioni nelle Organizzazioni Sanitarie (SIMPIOS) – Sezione Liguria HEALTH CARE-ASSOCIATED INFECTIONS THE RESULT OF A DINAMIC INTERACTION Host Microrganisms Environment (setting, procedures, HCWs behaviour) Prevalenza di Infezioni Correlate all’Assistenza (ICA): studi italiani pubblicati fra il 2000 e oggi % 88 Ospedali 18667 Pazienti arruolati 10 Ospedali 1315 Pazienti arruolati 59 Ospedali 15 Ospedali 9467 Pazienti 2165 Pazienti arruolati arruolati 21 Ospedali 6352 Pazienti arruolati 51 Ospedali 9609 Pazienti arruolati 25 Ospedali 912 Pazienti 3176 Pazienti arruolati arruolati 1 Infection control and quality health care: current challenges and future perspectives , A/H1N1, MERS-CoV, Ebola… Pittet D, AJIC 2005 Resistance in Enterobacteriaceae: impact and ability of different β-lactamases Livermore DM, K J Intern Med 2012 Cosgrove SE et al, Arch Int Med 2002 2 MultiDrug Resistance of Gram-Negative Bacilli (MDR-GNB): an important clinical and public health issue Emergence of resistance to multiple antimicrobial agents in pathogenic GNB has become a significant public health threat, having a significant impact on morbidity, mortality (risk estimated nearly 2-3 times) and on LOS and health-related costs. The greater problem is for empirical theraphy, where growing resistance increases the risk that the antimicrobial used will prove inactive: in particular, highly-resistant Gram-negative bacteria e.g. multidrug-resistant carbapenemase-producing Klebsiella pneumoniae and Acinetobacter spp. can be resistant to all currently available antimicrobial agents or remain susceptible only to older, potentially more toxic agents like the polymyxins, leaving limited and suboptimal options for treatment. Antibiotic treatment options for multidrug-resistant GNB are often very limited and finding an appropriate drug is an increasing challenge since very few new antibiotics are expected to enter the market as the older classes lose their efficacy Testing and evaluation of antibiotic lead substances should identify epidemiologically frequent and clinically relevant resistance mechanisms, as a basis for recommended hygiene measures in patient care. Magiorakos AP et al, Clin Microbiol Infect 2012; de Kraker ME et al, J Antimicrob Chemother 2011; ECDC 2011; MMWR 2009; Roberts RR et al, Clin Infect Dis 2009; Falagas ME et al Clin Infect Dis 2008, Pitout JDD Lancet Infect Dis 2008 Antimicrobial resistance data from invasive isolates (blood and cerebrospinal fluid) reported to EARS-Net by 29 EU/EEA countries in 2012 (data referring to 2011), and on trend analyses of EARSS/EARSNet data reported by the participating countries during the period 2008 to 2011 Dramatic increase in Carbapenem-Resistant Klebsiella Pneumoniae in Italy (I) 2009 2010 2011 2012 Klebsiella pneumoniae. Percentage (%) of invasive isolates with resistance to carbapenems, by country, EU/EEA countries, 2009-2013. 2013 European Centre for Disease Prevention and Control. Antimicrobial resistance surveillance in Europe. Annual Report of the European Antimicrobial Resistance Surveillance Network (EARS-Net). 2009-2013. 3 Dramatic increase in Carbapenem-Resistant Klebsiella Pneumoniae in Italy (II) Escherichia coli: trends of invasive isolates with combined resistance (resistant to fluoroquinolones, third generation cephalosporins and aminoglycosides), by country, EU/EEA countries, 2008–2011 The rise of carbapenem resistance in Europe: just the tip of the iceberg? A trend analysis showed increasing trends for Greece, Cyprus, Hungary and Italy (p < 0.01) EARS-Net collects data on invasive bacterial isolates, which likely correspond to a fraction of the total number of infections. Increasing reports of community cases suggest that dissemination of carbapenem-resistant K. pneumoniae has penetrated into the community. Good surveillance and infection control measures are urgently needed to contain this spread. Magiorakos et al. Antimicrobial Res Infect Control 2013 4 The results highlight the emergence of carbapenemase-producing K. pneumoniae strains in different hospitals and wards and the urgent need for infection control, antibiotic stewardship programmes and utilization of a surveillance and prevention system Univariate analysis of risk factors for in-hospital mortality among 91 patients infected by carbapenem-resistant Klebsiella pneumoniae (CR-KP) Results (II) Multivariate analysis adjusted for appropriate treatment, combination therapy and infectious-source removal, showed the following as independent risk factors for mortality: Background From January 2007 to May 2010, the five ICUs of the San Martino University Hospital, Genoa, Italy, experienced sequential outbreaks of A. baumannii infection. Aims (i) to study the population structure of A. baumannii and identify the spread of epidemic clones in the San Martino hospital; (ii) to compare characterization data obtained using different molecular approaches and evaluate their utility in molecular investigation; (iii) to study the emergence of antimicrobial resistance. 5 Cases of infections caused by A. baumannii among ICUs and other wards by the most frequently found genotypes of carbapenem-resistant A. baumannii 6 Epidemic clusters of A. baumannii In ICUs, 27 (50.9%) and 26 (49.1%) patients were colonized and infected, respectively. The mean age for colonized and infected patients was 68.5 and 56.2 years, respectively. • • • • BSI: 53.8% VAP: 19.2% Complicated skin and soft tissue infections: 11.5% meningitis or urinary tract infection: 7.7% Among infected patients admitted in ICUs, the fatality rate was 33.3%. Antimicrobial susceptibility patterns of Acinetobacter baumannii isolates belonging to the most frequently found genotypes: ST4, ST118, ST95 Most A. baumannii isolates were multidrug-resistant. The majority of the strains typed were resistant to ampicillin-sulbactam, piperacillin-tazobactam, broad spectrum cephems and fluoroquinolones, but susceptible to colistin. This pattern may have contributed to the rapid and successful spread. 6 Geographical distribution of Clostridium difficile PCR ribotypes in European countries with more than five typable isolates, November, 2008 Rybotypes 018, 056, 027 are usually associated with complicated disease outcome 7 Con legge regionale n. 2/2011 è stata costituito l'IRCCS AOU San Martino – IST di Genova, a seguito dell'accorpamento dell’AOU San Martino e dell'Istituto Scientifico Tumori. Il nuovo Istituto è stato costituito dal 1° settembre 2011, a seguito del riconoscimento del carattere scientifico per la disciplina di Oncologia, con conseguente estinzione dei due pregressi enti. L'Istituto è costituito da 6 Dipartimenti ad Attività Integrata: Dipartimento di Chirurgia generale, specialistica e oncologica Dipartimento di Neuroscienze ed Organi di senso Dipartimento di Medicina Interna Generale e Specialistica Dipartimento di Emergenza ed Accettazione Dipartimento delle Terapie Oncologiche Integrate Dipartimento della Diagnostica, della patologia e delle cure ad alta complessità tecnologica Ospedale di riferimento regionale per acuti Numero di posti letto ordinari (anno 2013): circa 1200 Numero di ricoveri ordinari (anno 2013): circa 45.000 Numero di accessi totali (anno 2013): circa 90.000 Giornate di degenza (media 2011 – 2013): 473.810 HAI surveillance and control activities at I.R.C.C.S. AOU San Martino – IST Genoa, Italy Laboratory surveillance of alert microrganisms for all hospital wards Point-prevalence surveys Carbapenemase-producing Enterobacteriacee (CPE)-BSI passive surveillance CPE-Colonization Screening in patients and hospital wards at higher risk Active surveillance of environmental cleaning and decontamination procedures Active surveillance of health-care workers adherence and compliance with HAI prevention measures (i.e. hand hygiene, perioperative antimicrobial prophylaxis) Antimicrobial stewardship IRCCS Azienda Ospedaliera Universitaria San Martino ‐ IST Istituto Nazionale per la Ricerca sul Cancro Largo Rosanna Benzi, 10 16132 GENOVA SORVEGLIANZA DEI MICRORGANISMI SENTINELLA ANALISI DATI 2012-2013 Valutazione semestrale prevista nel 2014 8 FLUSSO INFORMATIVO Nel momento in cui il Laboratorio referta un esame ed inserisce i dati nel programma di Laboratorio, il dato viene rilevato dal sistema informatico “Controllo infezioni ospedaliere” che, in automatico, invia una mail alla Direzione Sanitaria e al Team ICA. Contemporaneamente il referto è leggibile presso l’U.O. di interesse su LaboWeb. L’U.O. Igiene ed Epidemiologia Ospedaliera invia, via fax, il modulo “SCHEDA DI SEGNALAZIONE DI ISOLAMENTO DI MICRORGANISMO SENTINELLA” MODAZHEP_0044 all’U.O. di pertinenza. In tale modulo è riportato: Indicazione della U.O. (Padiglione, CdC, fax) • Data, nome del paziente, microrganismo isolato, sede di isolamento • Indicazioni delle precauzioni da contatto • Consulenza infettivologo • Data e firma di chi segnala • Data e firma del ricevente. Il fax datato e firmato dal ricevente, dovrà essere inserito dal Medico di reparto nella cartella clinica del paziente. L’U.O. provvede ad attuare le misure specifiche previste dalle procedure: - LGAZHEP_0002 “RACCOMANDAZIONI PER LE MISURE DI ISOLAMENTO IN OSPEDALE” - IOAZHEP_0044 “GESTIONE E SORVEGLIANZA PAZIENTI COLONIZZATI/INFETTI DA MICRORGANISMI SENTINELLA” Primi Isolamenti dei Principali Microrganismi Alert * 608 * Trattandosi di un patogeno endemico la sorveglianza è stata sospesa a marzo 2013 9 Studio di prevalenza delle infezioni correlate all’assistenza all’interno dell’I.R.C.C.S. S. Martino – IST Gennaio - Febbraio 2014 Complessivamente sono stati inclusi nello studio 956 pazienti ricoverati in 74 reparti ospedalieri afferenti a 5 Dipartimenti ad Attività Integrata. 34,4% 63,9% Percentuale di pazienti 1,7% Anni 10 Percentuale di pazienti Percentuale di pazienti Analisi multivariata: principali ICA (overall e per singola localizzazione) e valutazione dei fattori di rischio associati Durando P et al., J Hosp Infect 2009 11 Durata della degenza (giorni) Totale IRCCS (n=956) MED (n=556) SUR (n=236) RHB (n=50) ICU (n=43) PSY (n=30) GO (n=27) PED (n=14) Media 12,9 12,1 10,3 27,9 29,0 11,8 3,2 5,9 Mediana 7 8 6 22 20 7 3 4 IQR 3-16 4 – 15,5 2 - 12 10 - 38 10 - 39 2 - 13 1-6 2–7 Range 0-139 1 - 129 0 - 139 1 - 102 2 - 103 0 - 133 0-7 0 - 17 HAI prevalence and key results (European PPS) 2011/12 IRCCS 2014 AOU San Martino Europe 2007 DIPME DIPEA DIPOE DIPCR DIPNS TOT IRCCS Italy N° of pts 314 156 120 209 157 956 14784 231459 N° of pts with HAI 40 34 27 36 11 148 938 13829 72 17,2 (12,4 – 23,0) 7,0 (3,6 – 12,2) 15,5 (13,3 – 18,0) 6,3 (5,4 – 7,4) 6,0 (5,7 – 6,3) 7,9 HAI Prevalence % (IC95%) 12,7 21,8 22,5 (9,4 – 17,0) (15,6 – 29,1) (15,4 – 31,0) 912 N° of HAIs 44 41 29 42 11 167 1068 15000 84 N° of HAIs per infected pt 1,10 1,21 1,07 1,17 1,0 1,13 1,14 1,08 1,17 N° of HAIs with microrg. (%) 26 (59,1) 20 (48,8) 6 (20,7) 22 (52,4) 7 (63,6) 81 (48,5) 652 (61,0) 8114 (54,1) 70 (83,3) Total N° of reported microrg. 35 28 8 28 7 106 841 10076 107 Totale IRCCS N. microrganismi % Microrganismi totali 106 106 Staphylococcus aureus 16 15,1 Escherichia coli 13 12,3 Staphylococci coagulasi-negativi 13 12,3 Enterococcus spp 11 10,4 Klebsiella pneumoniae 11 10,4 Pseudomonas aeruginosa 9 8,5 Candida spp 9 8,5 Clostridium difficile 7 6,6 Proteus spp 6 5,7 Enterobateriacee spp 5 4,7 Morganella spp 2 1,9 Serratia marcescens 2 MRSA: 87,5% 3GC-R: 30,8% CAR-R: 0 VRE: 18,2% 3GC-R: 90,9% CAR-R: 63,6 , CAR-R: 44,4% 1,9 Corynebacterium spp 1 0,9 Bacilli Gram Positivi non spec. 1 0,9 12 HAIs with onset during current hospitalization in ICUs IRCCS 2014 UA1D1 N HAIs TOT UA1D UA1D2 Rel % N HAIs Rel % N HAIs HAND1 Rel % TOT HAND HAND4 N HAIs Rel % N HAIs Rel % TOT ICU N HAIs Rel % N HAIs Rel % 3,6 Day of HAI onset Day 1 – 2 0 - 0 - 0 - 1 16,7 0 - 1 6,7 1 Day 3 - 4 2 18,2 0 - 2 15,4 0 - 0 - 0 - 2 7,1 Day 5 – 7 2 18,2 0 - 2 15,4 0 - 1 11,1 1 6,7 3 10,7 Day 8 - 14 1 9,1 0 - 1 7,7 2 33,3 2 22,2 4 26,6 5 17,9 Day 15 - 21 2 18,2 0 - 2 15,4 1 16,7 2 22,2 3 20 5 17,9 > Day 21 4 16,4 2 100 6 46,2 2 33,3 4 44,5 6 40 12 42,9 Patients with positive culture for carpapenem-resistant Klebsiella pneumoniae (any site, only first isolate) at I.R.C.C.S. San Martino – IST Genoa, Italy (years 2008-2013) June 2012: mandatory screening 13 Mortalità per tutte le cause a 30 giorni: analisi univariata N Pazienti/totale (%) Sopravvissuti (n=298) Deceduti (n=164) OR CI95% P-value 103/291 (35,40%) 0,99 0,67 - 1,47 0,95 8/41 (19,51%) 3/32 (9,38%) 16/56 (28,57%) 41/112 (36,61%) 67/156 (42,95%) 29/65 (44,62%) ref 0,43 1,65 2,38 3,11 3,32 0,10 - 1,76 0,63 - 4,33 1,01 - 5,64 1,35 - 7,16 1,33 - 8,29 0,24 0,31 0,05 0,008 0,01 Mortalità per 51/134 (38,06%) 1,16 tutte 0,77le - 1,77 60/149cause (40,27%)in pazienti 1,35 0,91 - 2,03 affetti 81/244 (33,20%) 0,81CRKP 0,55-1,18 da BSI da 0,46 0,14 0,27 Caratteristiche demografiche Sesso (M/F) 188/291 (64,60%) Età 40< 33/41 (80,49%) 40-49 29/32 (90,63%) 50-59 40/56 (71,43%) 60-69 71/112 (63,39%) 70-79 89/156 (57,05%) ≥80 36/65 (55,38%) Condizioni di comorbosità Mortalità per tutte le Neoplasia 83/134 (61,94%) Infezioni 89/149 (59,73%) cause in pazienti affetti Intervento chirurgico (66,80%) da BSI 163/244 da CSKP Charlson comorbidity index a 30 giorni 26,21% 0 18/22 (81,82%) 1-2 30/35 (85,71%) 3 32/37 (86,49%) 4 41/63 (65,08%) ≥5 177/305 (58,03%) Pattern di resistenza Resistenza ai carbapenemi 191/317 (60,25%) Area specialistica di insorgenza ICU 142/237 (59,92%) MED 84/138 (60,87%) RHB 18/22 (81,82%) SUR 58/69 (84,06%) a 30 giorni 4/22 (18,18%) ref39,75% 5/35 (14,29%) 0,75 0,18 - 3,16 5/37 (13,51%) 0,70 0,17 - 3,0 22/63 (34,92%) 2,41 0,73 - 8,02 128/305 (41,97%) 3,25 1,08 - 9,85 0,70 0,63 0,15 0,04 126/317 (39,75%) 1,86 1,2-2,86 0,005 95/237 (40,08%) 54/138 (39,13%) 4/22 (18,18%) 11/69 (15,94%) 3,43 3,31 1,20 ref 1,71 - 6,89 1,59 - 6,88 0,34 - 4,25 0,0005 0,001 0,78 Stimare l’incidenza delle infezioni da Clostridium difficile acquisite durante il ricovero presso l’IRCCS San Martino – IST di Genova Stimare la mortalità da tutte le cause nei 30 giorni successivi all’infezione da Clostridium difficile Descrivere le caratteristiche demografiche e cliniche dei pazienti con infezione da Clostridium difficile acquisite durante il ricovero presso l’IRCCS San Martino – IST di Genova Descrivere i fattori di rischio correlati alla mortalità da tutte le cause nei 30 giorni successivi all’infezione da Clostridium difficile Studio retrospettivo basato sulla definizione di caso del National Health Safety Network (NHSN) di Laboratory Identified Event (LabID Event): « A case of CDI is defined as a positive laboratory test result (non duplicative) for C. difficile toxin A and/or B, or a toxin-producing C. difficile organism detected by culture or other laboratory means performed on a stool sample» Incident (new case) CDI Assay: Any LabID Event from a specimen obtained >8 weeks after the most recent LabID Event (or with no previous LabID Event documented) for that patient. Recurrent CDI Assay: Any LabID Event from a specimen obtained >2 weeks and ≤8 weeks after the most recent LabID Event for that patient. 14 Sulla base delle tempistiche della diagnosi di CDI e della storia clinica del paziente, le CDI sono state ulteriormente categorizzate come prescritto dal NHSN Community-Onset (CO): CDI identified as an outpatient or an inpatient ≤3 days after admission to the facility (i.e., before or on days 1, 2, or 3 of admission). Community-Onset Healthcare Facility– Associated (CO-HCFA): Community onset Healthcare Facility–Onset (HO): CDI identified from a patient who was discharged from the facility ≤4 weeks prior to current date of stool specimen collection CDI identified >3 days after admission to the facility (i.e., on or after day 4) 3282 stool specimens tested (from April 2010 to August 2014) 450 positive specimens (13,7%) Correction for duplicate positivites and CDI recurrences 374 patients Excluded 26 community onset or community onset healthcare facility associated CDI patients 348 patients 2010A 2011 2012 2013 2014B Ai Bi Totale Test Totale positivi Nuovi casi totali (>56 giorni) Recidive (≤56; >14 giorni) Duplicati (< 14 giorni) Healthcare Facility onset HO-CDI (nuovi casi) 277 442 678 1122 813 24 (8,7%) 38 (8,6%) 82 (12,1%) 164 (14,6%) 142 (17,5%) 21 35 75 134 109 2 1 6 15 11 1 2 1 15 22 19 32 74 127 96 dati iniziano dal 1/4/2010 dati arrivano fino al 31/8/2014 Facility-Onset (HO): CDI identified > 3 days after admission to the facility (or after day 4) C Healthcare Hospital Onset – Clostridium difficile Infection (HO-CDI) incidence at I.R.C.C.S. San Martino – IST Genoa, 2010 – 2014 2010 N° 2011 Hosp. days Incide nce (x 1000 pd) N° 2012 Hosp. days Incide nce (x 1000 pd) N° 2013 Hosp. days Incide nce (x 1000 pd) N° 2014 Hosp. days Incide nce (x 1000 pd) N° Hosp. days Incide nce (x 1000 pd) 19 351450 0,05 32 485309 0,07 74 475438 0,16 127 460683 0,28 96 298006 0,32 9 187399 0,05 24 250474 0,10 54 240704 0,22 53 223616 0,24 59 152190 0,39 SUR 3 93908 0,03 1 130901 0,01 1 123733 0,01 5 117828 0,04 6 73923 0,08 ICU 3 12613 0,24 0 18521 0,00 3 16451 0,18 4 14940 0,27 1 10387 0,10 RHB 4 17669 0,23 7 33423 0,21 15 45487 0,33 65 62927 1,03 30 34347 0,87 +3 Standard Deviation +2 Standard Deviation +1 Standard Deviation giu-14 ago-14 apr-14 ott-13 dic-13 feb-14 giu-13 apr-13 ago-13 ott-12 dic-12 feb-13 giu-12 apr-12 ago-12 ott-11 dic-11 feb-12 giu-11 apr-11 ago-11 ott-10 dic-10 feb-11 giu-10 Mean apr-10 0,65 0,6 0,55 0,5 0,45 0,4 0,35 0,3 0,25 0,2 0,15 0,1 0,05 0 ago-10 per 1000 patient days Tot IRCCS MED 15 80 72,7 70 p value = 0,0005 60 50 % 40 29,4 30 18,7 17,7 20 10 0 Area medica Area chirurgica Area terapia intensiva Area riabilitativa e lungo-degenza It is not antibiotic resistance genes that kill people, it is bacteria… A steady stream of new antibiotics aimed at MDR Gram-negative bacteria would be welcome, but this alone might make a relatively modest impact on clinical outcomes. Much more effective would be innovative approaches to reducing the likelihood of colonization and subsequent infection, thereby reducing both the need to use antibiotics at all and the constant pressure leading to multiple antibiotic resistance. Such strategies are likely to be more effective in the long term than relying on a pipeline of antibiotics that will only ever have a limited lifespan. Cohen J, Antimicrob Chemother 2013 Strategie per il controllo delle infezioni Misure generali Sorveglianza Precauzioni standard Misure aggiuntive (isolamento, ecc.) Antibiotico profilassi e terapia Misure specifiche (Immunoprofilassi) Specificamente dirette contro: Infezioni del Tratto Urinario Infezioni del Sito Chirurgico Infezioni Respiratorie (es., VAPs) Sepsi (es., CR-BSIs) …… 16 Strategies to preventi HAIs in the hospital setting (I) Ongoing epidemiological and lab-based surveillance (i.e., prevalence surveys, alert-microrganism periodic reports, etc.) Health-care personnel education and direct observation on proper hand hygiene following the WHO multimodal strategy (i.e., posters in wards, leaflets for parents, alcohol-based hand rub at points of care) Strategies to preventi HAIs in the hospital setting (II) Health-care personnel education and direct observation on appropriate management of colonized/infected patients (i.e., strenghtening isolation measures, cohorting, etc.) and of invasive medical devices (i.e., adoption of care bundles for the prevention of central line infections, SSIs and VAP) Controlled use of antimicrobials (annual reporting and production of local recommendations on antimicrobial treatment and surgical prophylaxis) In neonatal units, use of human milk and involvment of parents in children’ care RECOMMENDATIONS FOR APPLICATION OF STANDARD PRECAUTIONS FOR THE CARE OF ALL PATIENTS IN ALL HEALTHCARE SETTINGS 51 Healthcare Infection Control Practices Advisory Committee (HICPAC) 17 RECOMMENDATIONS FOR APPLICATION OF STANDARD PRECAUTIONS FOR THE CARE OF ALL PATIENTS IN ALL HEALTHCARE SETTINGS Healthcare Infection Control Practices Advisory Committee (HICPAC) 52 Impatto della promozione dell’igiene delle mani Negli ultimi 30 anni, oltre 20 studi hanno dimostrato l’efficacia nel ridurre le ICPA Increase of hand hygiene compliance Year Hospital setting Follow-up Reference 1989 Adult ICU From 14% to 73% (before pt contact) HCAI rates: from 33% to 10% 6 years Conly et al 2000 Hospital-wide From 48% to 66% HCAI prevalence: from 16.9% to 9.5% 8 years Pittet et al From 43% to 80% HCAI incidence: from 15.1 to 10.7/1000 patient-days 2 years 2004 NICU 2005 Adult ICUs Reduction of HCAI rates From 23.1% to 64.5% HCAI incidence: from 47.5 to 27.9/1000 patient-days 21 months 2005 Hospital-wide From 62% to 81% Significant reduction in rotavirus infections 2007 Neonatal unit From 42% to 55% HCAI incidence: overall from 11 to 8.2 infections/1000 patient-days) and in very low birth weight neonates from 15.5 to 8.8 infections /1000 patient-days 2007 Neurosurgery NA 2008 1) 6 pilot health-care facilities 2) all public health-care facilities in Victoria (Aus) 2008 NICU Won et al Rosenthal et al 4 years Zerr et al 27 months Pessoa-Silva et al 2 years Thu et al 1) from 21% to 48% 2) from 20% to 53% MRSA bacteraemia: 1) from 0.05 to 0.02/100 patient-discharges per month; 2) from 0.03 to 0.01/100 patient-discharges per month SSI rates: from 8.3% to 3.8% 1) 2 years 2) 1 year Grayson et al NA HCAI incidence: from 4.1 to 1.2/1000 patient-days 18 months Capretti et al Compliance per l’igiene delle mani in diverse strutture sanitarie Author Year Sector Compliance Preston 1981 General Wards ICU 16% 30% Albert 1981 ICU ICU 41% 28% 1983 Hospital-wide 45% 1987 Neonatal ICU 30 1990 ICU 32 Larson Donowitz Graham Dubbert Pettinger Larson Doebbeling <40% ICU 81 1991 Surgical ICU 51 1992 1990 Neonatal Unit 29 ICU 40 Zimakoff 1993 ICU 40 Meengs 1994 1992 Emergency Room 32 Pittet 1999 Hospital-wide 48 Pittet and Boyce. Lancet Infectious Diseases 2001 18 Descending Order of Resistance to Germicidal Chemicals Activity Levels of Selected Liquid Germicides 19 20 21 2013 Early recognition of CDI Antimicrobial stewardship Hand hygiene Healthcare personnel education Implementation of Contact Precautions for CDI pts. Patient education Administrative support Environmental controls 22 Ambulatorio Prevenzione Malattie Trasmissibili, Vaccinazioni e Sperimentazioni Cliniche Dipartimento di Scienze della Salute Scuola di Scienze Mediche e Farmaceutiche Università degli Studi di Genova IRCCS AOU San Martino-IST di Genova H-030-014 Study “Efficacy, Immunogenicity, and Safety Study of Clostridium difficile Toxoid Vaccine in Subjects at Risk for C. difficile Infection” Noi operatori sanitari seguiamo le linee guida e raccomandazioni internazionali e nazionali per la prevenzione del rischio infettivo nei nostri reparti? 23 We can do better tha this! Durando P et al, AJIC 2012 “….intervention in infection control should be education-based, processbased and system-based.” “ ….only a multidsciplinary team can cope successfully with the challenges of modern infection control and epidemiology.” Pittet D. AJIC, 2005 “ Today ’ s infection control professionals should not only continue to recognize, explain, and act but also demonstrate their administrators the costeffectiveness of infection control plans !!” I.F. Semmelweis F. Nightingale 24 Società scientifiche e gruppi di lavoro sulle infezioni correlate all’assistenza Gruppo Italiano di Studio di Igiene Ospedaliera (GISIO) http://www.societaitalianaigiene.org/ Società Italiana Multidisciplinare per la Prevenzione delle Infezioni nelle Organizzazioni Sanitarie http://www.simpios.it/ GRAZIE!!! 25