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ICAAC 2014: Abstract and 
Poster Selection 
Marta Mora Rillo 
José Ramón Paño-Pardo 
Infectious Diseases and Clinical Microbiology Unit 
Division of Internal Medicine 
Hospital Universitario La Paz-IDIPAZ 
Madrid, Spain 
October 1st, 2014 www.proantibioticos.com
Outline 
• ICAAC 2014 Facts and Figures (JR) 
• ICAAC Keynote and other “classical” sessions (MM) 
• Most relevant sessions and abstracts by topic 
- CPE 
- Other bacteria/Mechanisms of resistance/Virus 
- New antimicrobials 
- PK/PD 
- Clinical infectious diseases (syndromes) 
- Clinical infectious diseases (hosts) 
- Advances in Micro diagnostic 
- Antimicrobial Stewardhip 
- Infection Control
ICAAC 2014 Facts and Figures 
Q: What does ICAAC stand for? 
A: Interscience Conference on 
Antimicrobial Agents and 
Chemotherapy
ICAAC 2014 Facts and Figures 
ICAAC is the main ASM* conference: 
• ASM + 40.000 members: on the largest (if not the largest) 
scientific societies 
• Multidisciplinary: Microbiologist, Infectious Diseases specialists, 
PharmD and pharmacologists, biologists…. 
• Attendees 
2014 ≈ 6,000 
2013: 5400 (126 españoles) 
Classically: +10,000 
ICAAC is losing appeal as compared w/ its 
previously back-to-back competitors: 
ECCMID y IDSA 
*ASM: American Society for Microbiology
ICAAC 2014 Facts and Figures 
• Medical Conference (especially ID) business model is coming to an 
end 
- Regulatory limitations to the relationship healthcare industry and 
healthcare professionals… 
- Antibiotics are not the most profitable drugs 
• but some are still trying to kill a goose that lays gooden eggs 
- High registration price (6 hours pre-ICAAC course: $470) 
- Slides/video library not included (as opposed to ECCMID) 
- Unacceptably bad IT experience (wifi connection)
Saturday, Sept 6th
Sunday, Sept 7th
• Antibiotic prophylaxis 
– Timing 
– Dosage 
• Cefazoline: >80kg 2gr; >120kg 3gr. 
• Vancomicine 15mg/kg 
• Gentamicine 5mg/kg 
– Re-dosign 
– MRSA risk: Vanco+Cefazoline 
• Chlorhexidine vs iodine povidone
Figure 1. Compliance with the bundle and its individual components in repeated measurements from June 2009 
through October 2011. 
van der Slegt J, van der Laan L, Veen EJ, Hendriks Y, et al. (2013) Implementation of a Bundle of Care to Reduce Surgical Site Infections in 
Patients Undergoing Vascular Surgery. PLoS ONE 8(8): e71566. doi:10.1371/journal.pone.0071566 
http://www.plosone.org/article/info:doi/10.1371/journal.pone.0071566
Annual changes in the surgical site infection (SSI) rate and 
bundle compliance and the 95% confidence interval. 
Continuous variables in relation to the occurrence 
of surgical site infections (SSI) after vascular surgery. 
van der Slegt J, van der Laan L, Veen EJ, Hendriks Y, et al. (2013) Implementation of a Bundle of Care to Reduce Surgical Site Infections in 
Patients Undergoing Vascular Surgery. PLoS ONE 8(8): e71566. doi:10.1371/journal.pone.0071566 
http://www.plosone.org/article/info:doi/10.1371/journal.pone.0071566
• Bundles 
• Dr Widmer: (ahead of pub) Mycobacterium 
chimaera outbrake associated to cooler/heating 
devices
V 
I 
H 
H 
I 
G 
H 
L 
I 
G 
H 
T 
S
Monday, Sept 8th
Tuesday, Sept 9th
Poster Sessions
CPE: Epidemiology (i) 
C-779. Carbapenemases-Producing Enterobacteriaceae in 2013: 
Increasing Prevalence of Multiple Carbapenemases in Single 
Isolates and Expansion of OXA-48-Producers and a new KPC-Variant. 
M Castanheira. Iowa, USA [Poster] 
C-800. Enterobacteriaceae producing ESBLs, AmpCs and 
carbapenemases emerging among outpatients, Italy. F Luzzaro, 
Florence, IT 
• Consecutive 3rd generation cephalosporin-resistant strains 
EC/KP/PM) in 12 Italian hospitals
CPE: Epidemiology (ii) 
C-070. Dynamics of the KPC Transposon: Tn4401 in a Single US 
Hospital, 2007-2012. N. Stoesser. Oxford & NIH 
K-1033. Predictors of Carbapenem-resistant 
Enterobacteriaceae (CRE) Acquisition Following In-hospital 
Exposure to Newly Diagnosed CRE Patients. M Schechner. 
Tel-Aviv, IL 
• Case-control study of patients newly screened for CPE (CPE contacts) 
• Case: CPE +ve; Control: CPE -ve 
• 72/841 (8%): CPE +ve 
• Multivariate analysis: a) Known MDRO.carrier (OR 4.8) b) Mech Vent 
(3.2)…more important than vicinity (shared room)
CPE: Antimicrobial Susceptibility Testing (iii) 
D-855. Inoculum Effect of Imipenem, Meropenem and Doripenem 
against Klebsielle pneumoniae Producing an OXA-48 
Carbapenemase with or without Extended-Spectrum Beta-lactamase. 
L Caillon. Nantes, FR. [Poster]
CPE: Antimicrobial Susceptibility Testing (iv) 
D-878. Study of Antimicrobial Combinations Against Carbapenem- 
Resistant Klebsiella pneumoniae (CR-Kp): Role of Double- 
Carbapenem Regimen. A Oliva. Rome, IT 
• Good correlation between in vitro ERT-MER sinergy (Time-Kill) 
and clinical therapy with 2-carbapenem 
D-883. Comparison of Etest® and Checkerboard Method for 
Determination of Antimicrobial Synergy against Colistin- 
ResistantKlebsiella pneumoniae Isolates. M. Herold. Nancy, FR 
[Poster]
CPE: BSI (v) 
K-346. Clinical and Economic Impact of a Formal Intervention Program 
Targeting Carbapenem-Resistant Klebsiella 
pneumoniae (CRKP) Bacteremia. BA Potoski, Pittsburgh, PA 
• Formal intervention program using decision support software to 
allow real-time recommendations for CRKP infections 
• Before (83)-after (9) study: 30-day mortality, LOS, 90-day readmission 
• Mortality: 34/75 (45%); LOS: 34 vs 14.5; Median cost: $395K vs $127K 
L-398. Mortality of patients with Carbapenem Resistant Klesbiella 
Pneumoniae (CRKp) Bacteremia. Y Fraenkel-Wande. Jerusalem, IL 
• Retrospective case (68 CP-KP)-control study (136 (ESBL-KP) 
• Mortality CP-KP 65% vs ESBL-KP 40%; p=0.0008
CPE: infection control (vi) 
K-1031. Reduction in Carbapenem-Resistant Klebsiella 
pneumoniae at a New York City Academic Medical Center Following a 
Multifactorial Intervention. W Huang, NY 
• Hand hygiene, enhanced cleaning and antimicrobial stewardship
Clinical Infectious Diseases: syndromes (i) 
L-1075. Maternal And Neonatal Consequences Of (un)treated 
Asymptomatic Bacteriuria In Pregnancy, The Asb Trial. SE Geerlngs. 
Amsterdam (NL) & Adelaide (AUS) 
• RCT: nitrofurantoin 200mg (41 pt) vs placebo (49%) in pregant 
women with asymptomatic bacteriuria. 159 pt refused 
• Primary outcomes: Pieloneprhytis and pre-term (<34w) birth: 
Pyelonephritis: 2.5% (nitro) vs 2.3% (placebo) vs 1.9% (no Asb) 
Preterm birth: 5% (nitro) vs 6.8% (placebo) vs 5.7% (no Asb) 
L-1068. Comparison of Methicillin-Susceptible and Methicillin- 
Resistant Staphylococcus Aureus Bacteriuria. L Saidel-Odes. Ver- 
Sheeva, IL [Poster] 
• Predictable differences between MRSA & MSSA (HO, Foley…) 
• Concomitant BSI: MRSA (18%) vs MSSA (14%)
Clinical Infectious Diseases: syndromes (ii) 
K-1712. Surgical Care And Prognosis Of Patients With Staphyloccoccal 
Prosthetic Vascular Graft Infection (pvgi). E. Senneville. Tourcoing, FR 
• Surgery performed in 78 patients (85): MSSA 46; MRSA 19; MRSE 18 
A) Autograft (vein): 12 
B) Prosthetic conduit: 10 
C) Allograft: 30 
D) Ablation w/o replacement: 5 
E) Debridement and retention: 30 
ABX: IV x 6w + PO x 6w* 
*except E: supression 
• Median follow-up: 15 months 
A) Death 25 (PVGI-related 12 pts 
B) Failure 10 
K-1714. Microbiology Of Prosthesis Vascular Graft Infections (pvgi): 
Causative Organisms, Resistance Patterns And Implications For The 
Prevention And Management. D. Sousa. Coruña, Spain
Clinical Infectious Diseases: syndromes (iii) 
L-415. Prospective Evaluation of the Incidence of Haematogenous 
Prosthetic Joint Infections (H-PJI) following Bloodstream Infections 
(BSI) E. Senneville, Torcoing, FR 
• 77 patients (8: already infected): 0/69; 6 months F/U 25 pts 
K-1717. Is Preoperative Joint Fluid Aspiration (PJA) Useful for the 
Diagnosis of Periprosthetic Joint Infection (PJI)?. E Bonnet. Lyon. FR 
• PPV 90%; NPV: 47% 
K-1709. Risk Factors for Multi-Drug Resistant Organisms (MDRO) in 
Prosthetic Joint Infections (PJIs) N Benito. REIPI, Spain
Clinical Infectious Diseases: syndromes (iv) 
K-1718. Minocycline as Long Term Suppressive Therapy for Orthopedic 
Infections. Y Hanada. Rochester, MN 
• 291 patients were included, with a mean suppression of 1394.8 days (d) 
• Relapse on LTMS occurred in 35 of 291 patients (12%) 
• Median time to first relapse was 327 d 
K-1708. F-18 FDG PET/CT As A Decision Support For Discontinuation Of 
Long-term Antimicrobial Therapy In Patients With Post-operative 
Spinal Implant Infection With High-risk Of Relapse. A Bouaziz. Lyon. FR 
• 14 patients (12 postsurgical: 8 acute; 2 vertebroplasty) 
• Mostly MSSA 
• ABX x 6 months. If negative PET-CT scan: discontinue ABX if not, 
repeat PET-CT scan each 6-months
PK/PD: S. aureus 
MSSA bacteremia: Cefazolin or Anti-Staph penicillins? 
L-402. Comparison of Treatment Outcomes and Safety with Nafcillin 
or Cefazolin for the Management of MSSA Bacteremia. MA Miller, 
Aurora, Colorado 
L-405. Evaluation of Treatment Outcomes of Cefazolin (CEZ) versus 
Oxacillin (OXA) for Methicillin-Sensitive Staphylococcus aureus (MSSA) 
Bloodstream Infections (BSI): A Multicenter Observational Study. SN 
Nevrekar. Chicago (Rush) 
Cefazolin does NOT have higher rates of treatment failure in 
MSSA BSI but LESS drug-related adverse eventes (nephrotoxicity)
PK/PD: S. aureus (ii) 
L-404. Empirical combination of vancomycin and a β-lactam Improves 
Early Outcomes for S. aureus bacteremia (SAB) N Musallam, LA, Ca
PK/PD (iii) 
b-lactams + vancomycin: increased nephrotoxicity? 
K-372. Comparative Risk of Acute Kidney Injury in Patients Receiving 
Vancomycin Monotherapy or Vancomycin and Beta-Lactam 
Combination Therapy. J Justo. Columbia, SC,USA [Poster] 
K-375. Acute Kidney Injury Associated With Beta-lactam 
Antimicrobials . K. Klinker. Gainsville. Florida [Poster]
PK/PD (iv) 
Vancomycin dosing: initial pushing 
A-1315. Evaluation of the Relationship Between the Initial Vancomycin 
Exposure Profile and Emergence of Heteroresistance to Vancomycin 
(hVISA) among Patients with MRSA Bloodstream Infections (BSIs) Who 
Received Vancomycin (VAN) TP Lodise, Albany, NY 
A-720. Effect of First Dose of Vancomycin in Critically Ill Patients 
Requiring Continuous Venovenous Hemofiltration (CVVH) on 
Achievement of Adequate 24 hour Vancomycin Trough Concentration. 
H Lin. Mass Gen 
Vancomycin: initial dosing is likely to be relevant
PK/PD (v) 
Vancomycin generics: are all created equal? 
A-1322. Comparison Of In Vivo Efficacy Of Innovator And Generic 
Vancomycin Products In A Neutropenic Mouse Thigh Infection Model 
HC Yang. Korea 
A-1323. Some Generics Of Vancomycin Prescribed In The United 
States Fail In Vivo Despite Pharmaceutical Equivalence (pe) And 
Bioequivalence (be) Demonstrated By The Fda. M Agudelo. 
Antioquia. Colombia [Poster]
PK/PD: Enterococcus (vi) 
K-379. Identification of Risk Factors Associated with the Development 
of Daptomycin Nonsusceptible Staphylococcus aureus. B. Bastian. 
Chicago (Rush). [Poster] 
E-230. Efficacy of Daptomycin (DAP) Monotherapy at a Dose of 10 mg/kg 
or Combined with Ampicillin (AMP) in the Treatment of Experimental 
Endocarditis (EE) in Rabbits Infected by Strains of Enterococcus 
faecalis with High-Level Aminoglycoside Resistance (HLAR). JM Miró. Clinic 
A-1326. Dual Beta-Lactam Activity against Enterococcus faecalis in a 
High Inoculum In Vitro Pharmacodynamic (IVPD) Bacteremic Model. LB 
Rice, Providence
PK/PD: Enterococcus (vii) 
A-1326. Dual Beta-Lactam Activity against Enterococcus faecalis in a 
High Inoculum In Vitro Pharmacodynamic (IVPD) Bacteremic Model. LB 
Rice, Providence 
• No regrowth with ampicillin + cefepime
PK/PD: b-lactam dosing (vii) 
A-711. Optimal Dosing of Continous Administration of Piperacillin- 
Tazobactam in Septic Obese and Non Obese Critically Ill patients M, 
Mahul, Bourdeaux, FR 
• 16g/2g Pip/Tazo continuous Infusion muy be insufficient for 25% of 
critically ill patients (MIC 64) 
A-713. Population Pharmacokinetics and Monte Carlo Dosing 
Simulations of Meropenem during the Early Phase of Severe Sepsis 
and Septic Shock in Critically Ill Patients in an ICU S Thengyai, 
Thailand
PK/PD: b-lactam dosing (vii) 
PTA (t>40%MIC): 1h/4h 
PTA (t>80%MIC): 1h/4h
Clinical Infectious Diseases: hosts* 
*immunecompromised 
Viral infections 
T-468. Astrovirus HMO-C: an Emerging Neurotropic Pathogen in 
Immunocompromised Patients. J. R. Lockwood, London,UK [Poster] 
• High throughput DNA sequencing technologies (deep sequencing of the 
transcriptome) on biopsy material taken from a child’s brain to evaluate a 
case of encepahlitis of unknown cause
T-466. Immune Monitoring with the T-SPOT®.CMV assay of Allogeneic 
Hematopoietic Cell Transplant (allo-HCT) Recipients: A Proof of Concept in the 
Clinical Setting L. Nesher, E. MD Anderson Cancer Ctr., Houston, USA
T-464. The Impact of IL28b Polymorphism in Allogeneic Hematopoietic Cell Transplant 
(allo-HCT) Recipients on Interferon (IFN γ) Production and CMV Reactivation. L. Nesher, 
E. MD Anderson Cancer Ctr., Houston, TX
T-467. Functional Monitoring of Cell-Mediated Immune Response Predicts the 
Occurrence of Cytomegalovirus (CMV) Disease in Kidney Transplant (KT) 
Recipients. M. A. Pérez-Jacoiste Hosp. 12 de Octubre, Spain. [Poster]
T-467. Functional Monitoring of Cell-Mediated Immune Response Predicts the 
Occurrence of Cytomegalovirus (CMV) Disease in Kidney Transplant (KT) 
Recipients. M. A. Pérez-Jacoiste Hosp. 12 de Octubre
T-467. Functional Monitoring of Cell-Mediated Immune Response Predicts the 
Occurrence of Cytomegalovirus (CMV) Disease in Kidney Transplant (KT) 
Recipients. M. A. Pérez-Jacoiste Hosp. 12 de Octubre
Clinical Infectious Diseases: hosts* 
K-1656. Bloodstream Infections in Hematological Patients and the Role of 
Multi-Drug-Resistant Strains. A. Fernandez-Cruz, HGUGM 
• 193 consecutive episodes in 129 pts: 62% neutropenia 
• GP 62% vs GN 32% vs anaerobes 2% vs yeasts 4% 
• Inappropriate Rx> if: GP (catheter) & Pseudomonas (17): 76% carba-R 
*immunecompromised 
Bacterial infections 
K-1040. Fecal Colonization with ESBL-Escherichia coli as Risk Factor for 
Bloodstream Infection and Related Complications in Patients with 
Severe Neutropenia. P. Cornejo-Juárez. México 
• Prospective cohort study (N=126): ESBLEC (col) vs non-ESBLEC 
• ESBLEC-BSI. a) ESBLEC (col): 17 EC-BSI: 14 ESBLEC (83%) 
b) Non-ESBLEC: 22 EC-BSI: 5 ESBLEC (23%)
Clinical Infectious Diseases: hosts* 
Fungal infections 
M-1083. Epidemiology of Invasive Aspergillosis and Resistance Patterns 
of Aspergillus spp. in Germany - Interim Analysis of a Multicenter 
Observational Study. MJ Vehreschild, Germany 
• Multicenter prospective registry: 780 AML/189 ALL: IFI: 6.1% (AML) and 6.9% ALL 
• 50% IFI in patients on AF prophylaxis 
• 30-day mortality: 9% 
M-1758. Mycoses Study Group-06: A Registry of 50 cases of 
Phaeohyphomycosis. S. G. Revankar (Multicenter) 
• Alternaria (9) > Scedosporium (prolificans) (7) > Exophiala (5) > 
Cladophialophora (4) > Curvularia (3) > Ochroconis (3) > Phialophora (3) 
• Immunecompromise: 76% (mainly SOT/HSCT) 
• Clinical syndromes: Skin (13); Pulmonary (8); CNS (6); Bone-Joint (4) 
• Mortality (F/U 1-36 mths): 28%
Clinical Infectious Diseases: hosts* 
Fungal infections (ii) 
T-475. Invasive Fusariosis in the Voriconazole Era: Single Center 12- 
year Experience. JM Stemple J. Boston 
M-1766. Malignant External Otitis Due To Aspergillus Spp, Our Seven 
Years' Experience. Marchionni. Paris, FR 
• 12 patients: 100% diabetics; 50% North-African 
• 10/12: A. flavus 
• Median delay: 240 days
Clinical Infectious Diseases: hosts* 
Fungal infections (iii) 
M-1765. Diagnostics for Invasive Pulmonary Aspergillosis in 
Bronchoalveolar Lavage Fluid of Patients with Underlying 
Pulmonary Diseases: Comparison of Aspergillus Lateral Flow Device, 
Galactomannan-Antigen-Test, Beta-D-Glucan-Tests and 
Conventional Culture. J Prattes (Austria/UK) 
M-1776. The Combination of Candida albicans Germ Tube Antibody 
(CAGTA) AND β-D-Glucan (BDG) May Be Useful to Stop Empiric 
Antifungal Therapy in ICU Patients with Suspected Candidasis N 
Martinez-Jimenez, HGUGM 
M-1085. Investigating Aspergillus PCR-negative Tissue Biopsy 
Samples from immunocompromised Patients using DNA Microarray 
Technology improves Diagnosis of Invasive Fungal Infections (IFI) B. 
Spiess (Germany)
Fungal infections (iv) 
M-1755. A Cost and Resource Utilization Analysis of Micafungin- 
Bridging for Hemato-Oncological High-Risk Patients Undergoing 
Allogenic Stem Cell Transplantation (aSCT) O Cornely, Cologne 
• Retrospective pharmacoeconomic evaluation (direct costs) of 106 patients with 
Posaconazole (POS) as compared with 106 patients with POS-MIC bridging** 
• €60,300 vs €58,100 (p=0.570) ** Micafungin (MIC) while intolerance to POS 
A-703. Posaconazole Serum Concentrations of the Delayed-Release 
Tablets Compared to the Oral Suspension T Jancel. NIH 
• Extended released tablets (300mg QD) achieve higher serum levels than oral 
suspension (200mg TID): 
M-1759. Clinical Experience Using Posaconazole (pos) Extended Release 
Tablet (tab) For The Prevention Of Invasive Fungal Infections In Hematological 
Cancer Patients (pt): Does One Size Fit All? MH Micelli, U of Michigan
Fungal infections (iii): isavuconazole 
M-1757. A Phase 3 Randomized, Double-Blind, Non-Inferiority Trial 
Evaluating Isavuconazole Vs. Voriconazole for the Primary Treatment of 
Invasive Mold Infection (SECURE): Outcomes in Subset of Patients with 
Hematologic Malignancies (HM) K Marr (Multicenter) [Poster] 
• Phase 3, multi-center, randomized, double-blind, non-inferiority trial: ISA vs 
VRC for the primary treatment of IMIs caused by Aspergillus spp. and other FF 
• 516 ITT patients: 433 with underlying hematological malingancy (217 
*immunecompromised 
proven/probable infections) 
• Efficacy: Non inferiority of ISA vs VRC: a) 42-day all-cause mortality (22% vs 
24%) b) Overall treatment response (39% vs 34%) 
• Safety: Less drug related adverse events (ISA): 40 vs 60%
Fungal infections (iv): isavuconazole (ii) 
M-1756. A Phase 3 Randomized, Double-Blind, Non-Inferiority Trial 
Evaluating Isavuconazole (ISA) vs. Voriconazole (VRC) for the Primary 
Treatment of Invasive Fungal Disease (IFD) Caused by Aspergillus spp. or 
other Filamentous Fungi (SECURE): Outcomes by Malignancy Status A 
Ullmann (Mulicenter) [Poster] 
M-1761. Outcomes by Minimum Inhibitory Concentrations from 
Isavuconazole Phase 3 Trial of Invasive Aspergillosis (SECURE). D Andes. 
(Multicenter) [Poster] 
M-1760. Outcomes in Patients with Invasive Mold Disease Caused 
by Fusarium or Scedosporium spp. Treated with Isavuconazole: Experience 
from the VITAL and SECURE Trials O Cornely (Multicenter) [Poster] 
*immunecompromised
Fungal infections (iv): isavuconazole (ii) 
A-699. Killing of Selected Antifungal Drugs Is Inhibited by Pulmonary 
Surfactant in Vitro P. Matzneller, Austria
Antimicrobial Stewardship 
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ICAAC 2014: Selection of sessions and abstracts

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  • 2. ICAAC 2014: Abstract and Poster Selection Marta Mora Rillo José Ramón Paño-Pardo Infectious Diseases and Clinical Microbiology Unit Division of Internal Medicine Hospital Universitario La Paz-IDIPAZ Madrid, Spain October 1st, 2014 www.proantibioticos.com
  • 3. Outline • ICAAC 2014 Facts and Figures (JR) • ICAAC Keynote and other “classical” sessions (MM) • Most relevant sessions and abstracts by topic - CPE - Other bacteria/Mechanisms of resistance/Virus - New antimicrobials - PK/PD - Clinical infectious diseases (syndromes) - Clinical infectious diseases (hosts) - Advances in Micro diagnostic - Antimicrobial Stewardhip - Infection Control
  • 4. ICAAC 2014 Facts and Figures Q: What does ICAAC stand for? A: Interscience Conference on Antimicrobial Agents and Chemotherapy
  • 5. ICAAC 2014 Facts and Figures ICAAC is the main ASM* conference: • ASM + 40.000 members: on the largest (if not the largest) scientific societies • Multidisciplinary: Microbiologist, Infectious Diseases specialists, PharmD and pharmacologists, biologists…. • Attendees 2014 ≈ 6,000 2013: 5400 (126 españoles) Classically: +10,000 ICAAC is losing appeal as compared w/ its previously back-to-back competitors: ECCMID y IDSA *ASM: American Society for Microbiology
  • 6. ICAAC 2014 Facts and Figures • Medical Conference (especially ID) business model is coming to an end - Regulatory limitations to the relationship healthcare industry and healthcare professionals… - Antibiotics are not the most profitable drugs • but some are still trying to kill a goose that lays gooden eggs - High registration price (6 hours pre-ICAAC course: $470) - Slides/video library not included (as opposed to ECCMID) - Unacceptably bad IT experience (wifi connection)
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  • 18. • Antibiotic prophylaxis – Timing – Dosage • Cefazoline: >80kg 2gr; >120kg 3gr. • Vancomicine 15mg/kg • Gentamicine 5mg/kg – Re-dosign – MRSA risk: Vanco+Cefazoline • Chlorhexidine vs iodine povidone
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  • 20. Figure 1. Compliance with the bundle and its individual components in repeated measurements from June 2009 through October 2011. van der Slegt J, van der Laan L, Veen EJ, Hendriks Y, et al. (2013) Implementation of a Bundle of Care to Reduce Surgical Site Infections in Patients Undergoing Vascular Surgery. PLoS ONE 8(8): e71566. doi:10.1371/journal.pone.0071566 http://www.plosone.org/article/info:doi/10.1371/journal.pone.0071566
  • 21. Annual changes in the surgical site infection (SSI) rate and bundle compliance and the 95% confidence interval. Continuous variables in relation to the occurrence of surgical site infections (SSI) after vascular surgery. van der Slegt J, van der Laan L, Veen EJ, Hendriks Y, et al. (2013) Implementation of a Bundle of Care to Reduce Surgical Site Infections in Patients Undergoing Vascular Surgery. PLoS ONE 8(8): e71566. doi:10.1371/journal.pone.0071566 http://www.plosone.org/article/info:doi/10.1371/journal.pone.0071566
  • 22. • Bundles • Dr Widmer: (ahead of pub) Mycobacterium chimaera outbrake associated to cooler/heating devices
  • 23. V I H H I G H L I G H T S
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  • 32. CPE: Epidemiology (i) C-779. Carbapenemases-Producing Enterobacteriaceae in 2013: Increasing Prevalence of Multiple Carbapenemases in Single Isolates and Expansion of OXA-48-Producers and a new KPC-Variant. M Castanheira. Iowa, USA [Poster] C-800. Enterobacteriaceae producing ESBLs, AmpCs and carbapenemases emerging among outpatients, Italy. F Luzzaro, Florence, IT • Consecutive 3rd generation cephalosporin-resistant strains EC/KP/PM) in 12 Italian hospitals
  • 33. CPE: Epidemiology (ii) C-070. Dynamics of the KPC Transposon: Tn4401 in a Single US Hospital, 2007-2012. N. Stoesser. Oxford & NIH K-1033. Predictors of Carbapenem-resistant Enterobacteriaceae (CRE) Acquisition Following In-hospital Exposure to Newly Diagnosed CRE Patients. M Schechner. Tel-Aviv, IL • Case-control study of patients newly screened for CPE (CPE contacts) • Case: CPE +ve; Control: CPE -ve • 72/841 (8%): CPE +ve • Multivariate analysis: a) Known MDRO.carrier (OR 4.8) b) Mech Vent (3.2)…more important than vicinity (shared room)
  • 34. CPE: Antimicrobial Susceptibility Testing (iii) D-855. Inoculum Effect of Imipenem, Meropenem and Doripenem against Klebsielle pneumoniae Producing an OXA-48 Carbapenemase with or without Extended-Spectrum Beta-lactamase. L Caillon. Nantes, FR. [Poster]
  • 35. CPE: Antimicrobial Susceptibility Testing (iv) D-878. Study of Antimicrobial Combinations Against Carbapenem- Resistant Klebsiella pneumoniae (CR-Kp): Role of Double- Carbapenem Regimen. A Oliva. Rome, IT • Good correlation between in vitro ERT-MER sinergy (Time-Kill) and clinical therapy with 2-carbapenem D-883. Comparison of Etest® and Checkerboard Method for Determination of Antimicrobial Synergy against Colistin- ResistantKlebsiella pneumoniae Isolates. M. Herold. Nancy, FR [Poster]
  • 36. CPE: BSI (v) K-346. Clinical and Economic Impact of a Formal Intervention Program Targeting Carbapenem-Resistant Klebsiella pneumoniae (CRKP) Bacteremia. BA Potoski, Pittsburgh, PA • Formal intervention program using decision support software to allow real-time recommendations for CRKP infections • Before (83)-after (9) study: 30-day mortality, LOS, 90-day readmission • Mortality: 34/75 (45%); LOS: 34 vs 14.5; Median cost: $395K vs $127K L-398. Mortality of patients with Carbapenem Resistant Klesbiella Pneumoniae (CRKp) Bacteremia. Y Fraenkel-Wande. Jerusalem, IL • Retrospective case (68 CP-KP)-control study (136 (ESBL-KP) • Mortality CP-KP 65% vs ESBL-KP 40%; p=0.0008
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  • 38. CPE: infection control (vi) K-1031. Reduction in Carbapenem-Resistant Klebsiella pneumoniae at a New York City Academic Medical Center Following a Multifactorial Intervention. W Huang, NY • Hand hygiene, enhanced cleaning and antimicrobial stewardship
  • 39. Clinical Infectious Diseases: syndromes (i) L-1075. Maternal And Neonatal Consequences Of (un)treated Asymptomatic Bacteriuria In Pregnancy, The Asb Trial. SE Geerlngs. Amsterdam (NL) & Adelaide (AUS) • RCT: nitrofurantoin 200mg (41 pt) vs placebo (49%) in pregant women with asymptomatic bacteriuria. 159 pt refused • Primary outcomes: Pieloneprhytis and pre-term (<34w) birth: Pyelonephritis: 2.5% (nitro) vs 2.3% (placebo) vs 1.9% (no Asb) Preterm birth: 5% (nitro) vs 6.8% (placebo) vs 5.7% (no Asb) L-1068. Comparison of Methicillin-Susceptible and Methicillin- Resistant Staphylococcus Aureus Bacteriuria. L Saidel-Odes. Ver- Sheeva, IL [Poster] • Predictable differences between MRSA & MSSA (HO, Foley…) • Concomitant BSI: MRSA (18%) vs MSSA (14%)
  • 40. Clinical Infectious Diseases: syndromes (ii) K-1712. Surgical Care And Prognosis Of Patients With Staphyloccoccal Prosthetic Vascular Graft Infection (pvgi). E. Senneville. Tourcoing, FR • Surgery performed in 78 patients (85): MSSA 46; MRSA 19; MRSE 18 A) Autograft (vein): 12 B) Prosthetic conduit: 10 C) Allograft: 30 D) Ablation w/o replacement: 5 E) Debridement and retention: 30 ABX: IV x 6w + PO x 6w* *except E: supression • Median follow-up: 15 months A) Death 25 (PVGI-related 12 pts B) Failure 10 K-1714. Microbiology Of Prosthesis Vascular Graft Infections (pvgi): Causative Organisms, Resistance Patterns And Implications For The Prevention And Management. D. Sousa. Coruña, Spain
  • 41. Clinical Infectious Diseases: syndromes (iii) L-415. Prospective Evaluation of the Incidence of Haematogenous Prosthetic Joint Infections (H-PJI) following Bloodstream Infections (BSI) E. Senneville, Torcoing, FR • 77 patients (8: already infected): 0/69; 6 months F/U 25 pts K-1717. Is Preoperative Joint Fluid Aspiration (PJA) Useful for the Diagnosis of Periprosthetic Joint Infection (PJI)?. E Bonnet. Lyon. FR • PPV 90%; NPV: 47% K-1709. Risk Factors for Multi-Drug Resistant Organisms (MDRO) in Prosthetic Joint Infections (PJIs) N Benito. REIPI, Spain
  • 42. Clinical Infectious Diseases: syndromes (iv) K-1718. Minocycline as Long Term Suppressive Therapy for Orthopedic Infections. Y Hanada. Rochester, MN • 291 patients were included, with a mean suppression of 1394.8 days (d) • Relapse on LTMS occurred in 35 of 291 patients (12%) • Median time to first relapse was 327 d K-1708. F-18 FDG PET/CT As A Decision Support For Discontinuation Of Long-term Antimicrobial Therapy In Patients With Post-operative Spinal Implant Infection With High-risk Of Relapse. A Bouaziz. Lyon. FR • 14 patients (12 postsurgical: 8 acute; 2 vertebroplasty) • Mostly MSSA • ABX x 6 months. If negative PET-CT scan: discontinue ABX if not, repeat PET-CT scan each 6-months
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  • 44. PK/PD: S. aureus MSSA bacteremia: Cefazolin or Anti-Staph penicillins? L-402. Comparison of Treatment Outcomes and Safety with Nafcillin or Cefazolin for the Management of MSSA Bacteremia. MA Miller, Aurora, Colorado L-405. Evaluation of Treatment Outcomes of Cefazolin (CEZ) versus Oxacillin (OXA) for Methicillin-Sensitive Staphylococcus aureus (MSSA) Bloodstream Infections (BSI): A Multicenter Observational Study. SN Nevrekar. Chicago (Rush) Cefazolin does NOT have higher rates of treatment failure in MSSA BSI but LESS drug-related adverse eventes (nephrotoxicity)
  • 45. PK/PD: S. aureus (ii) L-404. Empirical combination of vancomycin and a β-lactam Improves Early Outcomes for S. aureus bacteremia (SAB) N Musallam, LA, Ca
  • 46. PK/PD (iii) b-lactams + vancomycin: increased nephrotoxicity? K-372. Comparative Risk of Acute Kidney Injury in Patients Receiving Vancomycin Monotherapy or Vancomycin and Beta-Lactam Combination Therapy. J Justo. Columbia, SC,USA [Poster] K-375. Acute Kidney Injury Associated With Beta-lactam Antimicrobials . K. Klinker. Gainsville. Florida [Poster]
  • 47. PK/PD (iv) Vancomycin dosing: initial pushing A-1315. Evaluation of the Relationship Between the Initial Vancomycin Exposure Profile and Emergence of Heteroresistance to Vancomycin (hVISA) among Patients with MRSA Bloodstream Infections (BSIs) Who Received Vancomycin (VAN) TP Lodise, Albany, NY A-720. Effect of First Dose of Vancomycin in Critically Ill Patients Requiring Continuous Venovenous Hemofiltration (CVVH) on Achievement of Adequate 24 hour Vancomycin Trough Concentration. H Lin. Mass Gen Vancomycin: initial dosing is likely to be relevant
  • 48. PK/PD (v) Vancomycin generics: are all created equal? A-1322. Comparison Of In Vivo Efficacy Of Innovator And Generic Vancomycin Products In A Neutropenic Mouse Thigh Infection Model HC Yang. Korea A-1323. Some Generics Of Vancomycin Prescribed In The United States Fail In Vivo Despite Pharmaceutical Equivalence (pe) And Bioequivalence (be) Demonstrated By The Fda. M Agudelo. Antioquia. Colombia [Poster]
  • 49. PK/PD: Enterococcus (vi) K-379. Identification of Risk Factors Associated with the Development of Daptomycin Nonsusceptible Staphylococcus aureus. B. Bastian. Chicago (Rush). [Poster] E-230. Efficacy of Daptomycin (DAP) Monotherapy at a Dose of 10 mg/kg or Combined with Ampicillin (AMP) in the Treatment of Experimental Endocarditis (EE) in Rabbits Infected by Strains of Enterococcus faecalis with High-Level Aminoglycoside Resistance (HLAR). JM Miró. Clinic A-1326. Dual Beta-Lactam Activity against Enterococcus faecalis in a High Inoculum In Vitro Pharmacodynamic (IVPD) Bacteremic Model. LB Rice, Providence
  • 50. PK/PD: Enterococcus (vii) A-1326. Dual Beta-Lactam Activity against Enterococcus faecalis in a High Inoculum In Vitro Pharmacodynamic (IVPD) Bacteremic Model. LB Rice, Providence • No regrowth with ampicillin + cefepime
  • 51. PK/PD: b-lactam dosing (vii) A-711. Optimal Dosing of Continous Administration of Piperacillin- Tazobactam in Septic Obese and Non Obese Critically Ill patients M, Mahul, Bourdeaux, FR • 16g/2g Pip/Tazo continuous Infusion muy be insufficient for 25% of critically ill patients (MIC 64) A-713. Population Pharmacokinetics and Monte Carlo Dosing Simulations of Meropenem during the Early Phase of Severe Sepsis and Septic Shock in Critically Ill Patients in an ICU S Thengyai, Thailand
  • 52. PK/PD: b-lactam dosing (vii) PTA (t>40%MIC): 1h/4h PTA (t>80%MIC): 1h/4h
  • 53. Clinical Infectious Diseases: hosts* *immunecompromised Viral infections T-468. Astrovirus HMO-C: an Emerging Neurotropic Pathogen in Immunocompromised Patients. J. R. Lockwood, London,UK [Poster] • High throughput DNA sequencing technologies (deep sequencing of the transcriptome) on biopsy material taken from a child’s brain to evaluate a case of encepahlitis of unknown cause
  • 54. T-466. Immune Monitoring with the T-SPOT®.CMV assay of Allogeneic Hematopoietic Cell Transplant (allo-HCT) Recipients: A Proof of Concept in the Clinical Setting L. Nesher, E. MD Anderson Cancer Ctr., Houston, USA
  • 55. T-464. The Impact of IL28b Polymorphism in Allogeneic Hematopoietic Cell Transplant (allo-HCT) Recipients on Interferon (IFN γ) Production and CMV Reactivation. L. Nesher, E. MD Anderson Cancer Ctr., Houston, TX
  • 56. T-467. Functional Monitoring of Cell-Mediated Immune Response Predicts the Occurrence of Cytomegalovirus (CMV) Disease in Kidney Transplant (KT) Recipients. M. A. Pérez-Jacoiste Hosp. 12 de Octubre, Spain. [Poster]
  • 57. T-467. Functional Monitoring of Cell-Mediated Immune Response Predicts the Occurrence of Cytomegalovirus (CMV) Disease in Kidney Transplant (KT) Recipients. M. A. Pérez-Jacoiste Hosp. 12 de Octubre
  • 58. T-467. Functional Monitoring of Cell-Mediated Immune Response Predicts the Occurrence of Cytomegalovirus (CMV) Disease in Kidney Transplant (KT) Recipients. M. A. Pérez-Jacoiste Hosp. 12 de Octubre
  • 59. Clinical Infectious Diseases: hosts* K-1656. Bloodstream Infections in Hematological Patients and the Role of Multi-Drug-Resistant Strains. A. Fernandez-Cruz, HGUGM • 193 consecutive episodes in 129 pts: 62% neutropenia • GP 62% vs GN 32% vs anaerobes 2% vs yeasts 4% • Inappropriate Rx> if: GP (catheter) & Pseudomonas (17): 76% carba-R *immunecompromised Bacterial infections K-1040. Fecal Colonization with ESBL-Escherichia coli as Risk Factor for Bloodstream Infection and Related Complications in Patients with Severe Neutropenia. P. Cornejo-Juárez. México • Prospective cohort study (N=126): ESBLEC (col) vs non-ESBLEC • ESBLEC-BSI. a) ESBLEC (col): 17 EC-BSI: 14 ESBLEC (83%) b) Non-ESBLEC: 22 EC-BSI: 5 ESBLEC (23%)
  • 60. Clinical Infectious Diseases: hosts* Fungal infections M-1083. Epidemiology of Invasive Aspergillosis and Resistance Patterns of Aspergillus spp. in Germany - Interim Analysis of a Multicenter Observational Study. MJ Vehreschild, Germany • Multicenter prospective registry: 780 AML/189 ALL: IFI: 6.1% (AML) and 6.9% ALL • 50% IFI in patients on AF prophylaxis • 30-day mortality: 9% M-1758. Mycoses Study Group-06: A Registry of 50 cases of Phaeohyphomycosis. S. G. Revankar (Multicenter) • Alternaria (9) > Scedosporium (prolificans) (7) > Exophiala (5) > Cladophialophora (4) > Curvularia (3) > Ochroconis (3) > Phialophora (3) • Immunecompromise: 76% (mainly SOT/HSCT) • Clinical syndromes: Skin (13); Pulmonary (8); CNS (6); Bone-Joint (4) • Mortality (F/U 1-36 mths): 28%
  • 61. Clinical Infectious Diseases: hosts* Fungal infections (ii) T-475. Invasive Fusariosis in the Voriconazole Era: Single Center 12- year Experience. JM Stemple J. Boston M-1766. Malignant External Otitis Due To Aspergillus Spp, Our Seven Years' Experience. Marchionni. Paris, FR • 12 patients: 100% diabetics; 50% North-African • 10/12: A. flavus • Median delay: 240 days
  • 62. Clinical Infectious Diseases: hosts* Fungal infections (iii) M-1765. Diagnostics for Invasive Pulmonary Aspergillosis in Bronchoalveolar Lavage Fluid of Patients with Underlying Pulmonary Diseases: Comparison of Aspergillus Lateral Flow Device, Galactomannan-Antigen-Test, Beta-D-Glucan-Tests and Conventional Culture. J Prattes (Austria/UK) M-1776. The Combination of Candida albicans Germ Tube Antibody (CAGTA) AND β-D-Glucan (BDG) May Be Useful to Stop Empiric Antifungal Therapy in ICU Patients with Suspected Candidasis N Martinez-Jimenez, HGUGM M-1085. Investigating Aspergillus PCR-negative Tissue Biopsy Samples from immunocompromised Patients using DNA Microarray Technology improves Diagnosis of Invasive Fungal Infections (IFI) B. Spiess (Germany)
  • 63. Fungal infections (iv) M-1755. A Cost and Resource Utilization Analysis of Micafungin- Bridging for Hemato-Oncological High-Risk Patients Undergoing Allogenic Stem Cell Transplantation (aSCT) O Cornely, Cologne • Retrospective pharmacoeconomic evaluation (direct costs) of 106 patients with Posaconazole (POS) as compared with 106 patients with POS-MIC bridging** • €60,300 vs €58,100 (p=0.570) ** Micafungin (MIC) while intolerance to POS A-703. Posaconazole Serum Concentrations of the Delayed-Release Tablets Compared to the Oral Suspension T Jancel. NIH • Extended released tablets (300mg QD) achieve higher serum levels than oral suspension (200mg TID): M-1759. Clinical Experience Using Posaconazole (pos) Extended Release Tablet (tab) For The Prevention Of Invasive Fungal Infections In Hematological Cancer Patients (pt): Does One Size Fit All? MH Micelli, U of Michigan
  • 64. Fungal infections (iii): isavuconazole M-1757. A Phase 3 Randomized, Double-Blind, Non-Inferiority Trial Evaluating Isavuconazole Vs. Voriconazole for the Primary Treatment of Invasive Mold Infection (SECURE): Outcomes in Subset of Patients with Hematologic Malignancies (HM) K Marr (Multicenter) [Poster] • Phase 3, multi-center, randomized, double-blind, non-inferiority trial: ISA vs VRC for the primary treatment of IMIs caused by Aspergillus spp. and other FF • 516 ITT patients: 433 with underlying hematological malingancy (217 *immunecompromised proven/probable infections) • Efficacy: Non inferiority of ISA vs VRC: a) 42-day all-cause mortality (22% vs 24%) b) Overall treatment response (39% vs 34%) • Safety: Less drug related adverse events (ISA): 40 vs 60%
  • 65. Fungal infections (iv): isavuconazole (ii) M-1756. A Phase 3 Randomized, Double-Blind, Non-Inferiority Trial Evaluating Isavuconazole (ISA) vs. Voriconazole (VRC) for the Primary Treatment of Invasive Fungal Disease (IFD) Caused by Aspergillus spp. or other Filamentous Fungi (SECURE): Outcomes by Malignancy Status A Ullmann (Mulicenter) [Poster] M-1761. Outcomes by Minimum Inhibitory Concentrations from Isavuconazole Phase 3 Trial of Invasive Aspergillosis (SECURE). D Andes. (Multicenter) [Poster] M-1760. Outcomes in Patients with Invasive Mold Disease Caused by Fusarium or Scedosporium spp. Treated with Isavuconazole: Experience from the VITAL and SECURE Trials O Cornely (Multicenter) [Poster] *immunecompromised
  • 66. Fungal infections (iv): isavuconazole (ii) A-699. Killing of Selected Antifungal Drugs Is Inhibited by Pulmonary Surfactant in Vitro P. Matzneller, Austria

Editor's Notes

  1. ICAAC Keynote and other specific sessions (MM): ID Fellows, Keynote session (la cuelgan el 15, poner el link), literature review y ID quizz (contar un poco de qué iban)
  2. ICAAC Keynote and other specific sessions (MM): ID Fellows, Keynote session (la cuelgan el 15, poner el link), literature review y ID quizz (contar un poco de qué iban)