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Quality management of bloodstream infections today Setting standards L. Eduardo López Cortés Seville, Spain Hospital Universitario Virgen Macarena, Seville ESCMID eLibrary by author

Quality management of bloodstream infections today Setting

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Page 1: Quality management of bloodstream infections today Setting

Quality management of bloodstream infections today

Setting standards

L. Eduardo López Cortés

Seville, Spain

Hospital UniversitarioVirgen Macarena, Seville

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Conflicts of interest

None for this talk

Research grants REIPI, Instituto de Salud Carlos III, Spanish Ministry of Economy

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Overview

1. Relevancy of the issue

2. QCI in bacteremia: why are they necessary?

3. Successful examples: S. aureus, Candida spp.

4. Proposed QCI:

Blood cultures indicators

ID advice

Empirical therapy indicators

Follow-up BC

Source searching

De-escalation

Therapy duration

Clinical indicatorsESCMID eLibrary

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Population-based surveillance for all community-onset BSI

Calgary, 2000-2004

4,467 episodes Overall annual incidence of

82/100,000 people

Mortality rate of 13%

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Consequences of bacteremia

Increased patient morbidity and mortality:

Prolonged hospital stay

Excessive drug costs

Selection of resistant organisms

Rodríguez-Baño J, et al. CMI 2010; 16:1408-13ESCMID eLibrary

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Quality of care indicators (QCI)

It would be necessary to standardize their clinical management to improve prognosis and reduce associated mortality

But...There is a lack of information (almost nothing in the last 10 years…)

Why doesn´t it exist ?

Bacteremia is not a type of infection per se

Is the consequence of multiple and heterogeneous types of infections very complex task to standardize

Successful examples with impact on mortality:

S. aureus bacteremia

Candidemia

Catheter related BSI ESCMID eLibrary

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5 QCI for candidemia (nonneutropenic)

1. Follow-up BC

2. Ophthalmological evaluation to exclude endophthalmitis

3. Targeted therapy: Transition from echinocandin fluconazole

4. Removal of intravenous catheter

5. Duration of therapy: 2 weeks after documented clearance of Candida (in patients without metastatic complications)

Pappas PG, et al. CID 2009; 48:503-35ESCMID eLibrary

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Systematic review to identify evidence-based QCI for SAB management

Multicentre, before-after study Intervention: structured, written

recommendation by IDs based on those QCI

Outcomes: Adherence to QCI and mortality

López-Cortés LE, et al. CID 2013; 57:1225-33ESCMID eLibrary

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Page 9: Quality management of bloodstream infections today Setting

QCI for S. aureus bacteremia

López-Cortés LE, et al. CID 2013; 57:1225-33ESCMID eLibrary

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Proposed QCI for bacteremia

Blood culture procedure

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Blood cultures evaluation

1. Nº of BC / 100 admissions OR 100 rooms

2. Nº of (+) BC / 100 admissions OR 100 patients-days

3. Nº of BC AND (+) BC in ER / 100 ER admissions

4. Nº of contaminated BC / total BC less than 3%?

5. Nº of BC with CNS isolation / total + BC

Bacteremia work group. Unidad Clínica Intercentros Virgen Macarena y Virgen del Rocío

10-30 min.

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Proposed QCI for bacteremia

ID evaluation

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Voguel M, et al. J Infect 2016; 72(1):19-28ESCMID eLibrary

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Micro and ID evaluation

1. Number of early reported preliminary results (with management advice) by ID

consultant / 100 (+) BC

2. Nº cases with active ID consultation offered /100 BC

3. Nº of BSI classified by acquisition and source / 100 (+) BC

4. Nº of nosocomial BSI / 1,000 patient-days

Rodríguez-Baño J, et al. Expert Rev Anti Infect Ther 2010; 8:815-29. ESCMID eLibrary

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Proposed QCI for bacteremia

Empirical therapy

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Empirical therapy

A crucial decision, above all in patients with SS & septic shock

Aspects to take into account:

Severity of illness

Medical records: surgery/other procedures, endovascular and prosthetic devices, etc.

Co-morbidity

Type of acquisition associated with:

More probable etiology

More probable sources

MR risk factors

Previous microbiological isolates

Local epidemiology and more frequent susceptibilities

12 - 24 hours later: Gram stain resultESCMID eLibrary

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Antimicrob Agents Chemoth 2012; 56:472-8

***

*Multivariate logistic regression. **Propensity score. ***Propensity score + logistic regression

***

Prospective multicenter cohort including all BSI episodes (adults) 15 Spanish hospitals, 2006 - 2007. 800 BSI

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Proposed QCI for bacteremia

Follow-up blood cultures

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Follow-up BC

1. Bacteremia due to S. aureus or Candida spp. (↔ therapy duration and management)

2. Unknown source above all in Streptococcus spp. BSI

Known or suspected endocarditis

3. Presence of fever or other signs of infection > 72 h of adequate therapy

4. Known or suspected site of infection with limited antimicrobial penetration (e.g.: abscess or joint space infections)

5. Presence of prosthetic vascular grafts, intravascular lines, pacemakers, etc.

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Proposed QCI for bacteremia

Active source searching

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Acquisition & Sources

Rodríguez-Baño J, et al. Expert Rev Anti Infect Ther 2010; 8:815-29. ESCMID eLibrary

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Aetiology & sources

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Proposed QCI for bacteremia

De-escalation

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But... what is exactly to de-escalate?

Weiss E, et al. Clin Microbiol Infect 2015; 21:649.e1-10

Aim of the study: to provide a consensus definition of DE and to establish a ranking of β-lactam according to both their spectra and their ecological consequences.

28 experts from IC, ID and CM were consulted using questionnaires

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Six US hospitals during 2009 and 2010

Primary outcome: modification of antimicrobial regimen on or before the 5th day

4,119 (60%) of 6,812 inpatients received antimicrobials

12.5% of ET were escalated

21.5% were narrowed or discontinued

66,4% were unchanged

Braykov NP, et al. Lancet Infect Dis 2014; 14:1220-7ESCMID eLibrary

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De-escalation

One of the more potentially useful strategies to avoid the overuse of B-S antibiotics.

Based only on expert recommendations and few observational studies many clinicians have doubts about its safety adherence

is much lower than desired

A review of the Cochrane Library:

Silva BN, et al. Cochrane Database Syst Rev 2013ESCMID eLibrary

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Clinical trial “Simplify”

Multicenter (22 centers) Spanish phase III non-inferiority randomized clinical trial.

Inclusion criteria:Hospitalized patients with monomicrobial enterobacteriae BSI of any source

Need to maintain an IV treatment for at least 5 days

Primary outcome: Demonstrate non-inferiority of N-S vs. B-S therapy using an antipseudomonal beta-lactam

Secondary:Clinical response in short (day 5) and long-term (day 30)

Mortality until day 60

Hospital stay and recurrences

Consequences the intestinal colonization by MMRR Gram-negative bacilli

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SUSCEPTIBILITY

Ampicillin 2 g IV/6h

TMP/SMX 160/800 mg IV/8 -12h

Cefuroxime 750-1000 mg/8h

Cefotaxime 1-2g IV/8h or ceftriaxone 1 g/12-24h

Amoxicillin/clavulanic 1000/125 mg IV/8h

Ciprofloxacine 400 mg IV/12h

Ertapenem 1g/24h

Piperacillin/tazobactam 4/0.5 g IV/6-8h

Meropenem 1-2 g IV/8h

Imipenem 0.5 g IV/6h - 1g IV/6h

Aztreonam 1-2 g IV/8h

Ceftazidime 1-2 g IV/8h

Cefepime 2 g IV/8-12h.

Experimental N-S arm Control B-S anti-Pseud. arm

Clinical trial “Simplify”

Randomization in the first 24 hours of the availability ofmicro susceptibility

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Proposed QCI for bacteremia

Therapy duration

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Duration of the therapy

Adequate duration not established in most of the cases

Decision depend on: aetiology, source (controlled or not), clinical evolution, etc.

Mermel LA et al, et al. CID 2009; 49:1-45ESCMID eLibrary

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End-points

Primary end-point: To prove that a 7-day course of antimicrobial treatment is

more eficient than a 14-day course for treating EB bacteremia independtly of the

source.

Secondary end-points:

1.To prove that a 7-day course is as safe as a 14-day course in terms of:

Clinical and microbiological cure.

Adverse reactions to antibiotics and superinfections.

2.To analyze the utility of PCT as a biomarker to decide to stop antibiotics in this setting.

Optimal duration of the antimicrobial treatment for bloodstream infections produced by Enterobacteriaceae.Clinical trial "SHORTEN”

NCT02400268ESCMID eLibrary

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Principal investigator: Dafna Yahav, MD. Rabin Medical Center

Primary end-point: compare short-course antibiotic therapy (<=7 days) versus longer

treatment (>7 days) in gram-negative bacteremia.

Methods: Open Label, parallel assignment. International (Israel and Italy).

Duration of Antibiotics for the Treatment of Gram-negative Bacilli Bacteremia - a Randomized Controlled Trial

NCT01737320ESCMID eLibrary

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Proposed QCI for bacteremia

Clinical indicators

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Clinical indicators

1.Periodic evaluation of 14-day crude mortality at least:

E. coli

K. pneumoniae

S. aureus

S. pneumoniae

A. baumannii

P. aeruginosa

2.Periodic evaluation of length of stay in survivor patients

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PRO-BAC 2016

Spanish observational cohort for all bacteremia (CA, NA and HCA)

From May 2016 – May 2017

29 tertiary hospital expected 17,000 to 25,000 cases

Main outcomes:

1. Describe clinical management: empirical and targeted therapy, duration, de-escalation, sequential IV to oral, source search and management

2. Study the influence of clinical management on prognosis

3. Describe the different activities carried out by bacteremia teams

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Proposed QCI for bacteremia

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Proposed QCI

1. Evaluate how blood cultures are taken in your centre

2. Evaluate how is the ID attention in your centre

3. Adequate empirical therapy

4. Carry out follow-up blood cultures (when are indicated)

5. De-escalate based on susceptibility data

6. Adapt the antimicrobial duration

7. Periodic evaluation of 14-day crude mortality

8. Periodic evaluation of length of stay in survivor patients

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Final messages

1. QCI for bacteremia are not well described in the literature

2. Establish and follow QCI in bacteremia could help us to standardize clinical

management and improve the prognosis

3. There are some ongoing clinical trials to solve unresolved questions:

De-escalation: Simplify CT

Duration of therapy in EB BSI

4. There is an ongoing observational study (PRO-BAC) to establish QCI in

bacteremia and to describe the activities carried out by bacteremia teams

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Acknowledgements

Hospital Macarena Bacteraemia Team

Dr. Jesús Rodríguez Baño

Investigators from Hospital Universitario Virgen Macarena and REIPI

Dr. Jose Molina (PI Shorten)

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Thank you very much for your attention!!

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Page 42: Quality management of bloodstream infections today Setting

Bacteremia prevention

Essential key “better than cure”

Be alert to prevent NA and HCA bacteremia (and rest of infections) Urinary catheter

Vascular catheter

Parenteral nutrition

Others

Other ways to prevent infections:

VA pneumonia: raise the head, washed with chlorhexidine, etc

Other invasive procedures: in time and adequate prophilaxis

Pressure ulcers prevention: air mattress, early movilization…

Surgical procedures: in time and adequate prophilaxis, adequate technique

Etc.

Are they necessary TODAY?

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