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TDM of antibiotics(Laboratory testing guideline in the intensive care unit)
Paul M. Tulkens, MD, PhD
Pharmacologie cellulaire et moléculaireLouvain Drug Research Institute, Université catholique de Louvain,
Brussels, Belgiumhttp://www.facm.ucl.ac.be
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Disclosures
Laboratory Medicine at the Clinical Interface, Antalya, Turkey 2
Industry support for work on investigational compounds from• Cempra Pharmaceuticals 1• GSK• Melinta Therapeutics 2• The Medicine Company 3• MerLion Pharmaceuticals• Trius Therapeutics 4• Debiopharm
Non-profit support from• the Fond de la Recherche Scientifique (F.R.S.-FNRS)• the Région Wallone• the European Union (FP7 programme)
Influenced by my participation to the • Belgian Drug Reimbursement Committee (CRM/CTG; up to 2006)• EUCAST steering committee (2008-2010) and General Assembly (current)• the Governance Body of DRIVE-AB (2014-2017)
(an EU programme aiming at (re)designing the economic framework of the discovery, development and commercialization processes for new antibiotics)
11 Oct 2018
1 merged in 2017 with and renamed as Melinta Therapeutics2 formerly RibX Pharmaceuticals; world rights holder for delafloxacin (with license to Menarini for EU and other countries)3 antibiotic portfolio acquired by Melinta Therapeutics in 2018 4 acquired by Cubist (2014), which was then acquired by Merck (2016)
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Our program
• How to define the right antibiotic ?
• The basis of the antibiotic Pharmacokinetics/Pharmacodynamics (PK/PD)
• TDM of
– aminoglycosides
– vancomycin
– fluoroquinolones
– β-lactames
– linezolid
• a few words about the techniques and the need of bedside approach
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once daily dosing: efficacy - toxicity
AUC driven TDM – continuous infusion
rational breakpoints - emergence of resistance
coping with patients' variations and susceptibility loss
minimizing toxicity
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The right antibiotic treatment ? … I always wondered…
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https://expertconsult.inkling.com/read/mandell-douglas-bennetts-infectious-diseases-8/mandell-douglas-and-bennetts/cover
Chapter 17:Principles of Anti-infective TherapyGeorge M. EliopoulosRobert C. Moellering Jr.*
"In choosing the appropriate antimicrobial agent for therapy for a given infection, a number of factors must be considered.
• First, the identity of the infecting organism must be known or, at the very least, it must be possible to arrive at a statistically reasonable guess as to its identity on the basis of clinical information.
• Second, information about the susceptibility of the infecting organism, or likely susceptibility, must be as accurate as possible.
• Finally, a series of factors specific to the patient who is being treated (and his/her disease) must be considered to arrive at the optimal choice of antimicrobial agent. "
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Here are the questions …
When choosing an antibiotic, do we know 1. for the organism
– its identity and whether it is causal or not ?
– its susceptibility to and the main key properties of the proposed antibiotic ?
2. for the patient
– the antibiotic effectiveness in the specific disease ?
– how to dose the antibiotic appropriately ?
– how to prevent / avoid patient- and drug-related side effects ?
3. for the society
– how to prevent emergence of resistance ?
– how to get "value for money" ?
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This is what we will mainly discuss
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Here are the questions …
When choosing an antibiotic, do we know 1. for the organism
– its identity and whether it is causal or not ?
– its susceptibility to and the main key properties of the proposed antibiotic ?
2. for the patient
– the antibiotic effectiveness in the specific disease ?
– how to dose the antibiotic appropriately ?
– how to prevent / avoid patient- and drug-related side effects ?
3. for the society
– how to prevent emergence of resistance ?
– how to get "value for money" ?
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But we cannot
ignore this !
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Possible answers for the organism …
When choosing an antibiotic, do we know 1. for the organism
– its susceptibility to the proposed antibiotic
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Susceptibility
• are in vitro methods predictive (and which ones to use) ?
• which interpretive criteria ?
Know the limits of your methods …
and your interpretive criteria…
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http://www.eucast.org
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Possible answers for the patient …
When choosing an antibiotic, do we know 2. for the patient
– how to dose the antibiotic appropriately ?
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Starting PK/PD with a simple in vitro microbiological comparison
• bacteria in broth• increasing
concentrations(multiples of MIC)
• measure of the change in CFUs over time
Fast and concentration-dépendant
quinolone …
Slow and time-dépendant
β-lactam …
Vogelman & Craig (1986) Jounal of Pediatrics 108:835-840
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Moving to patients: PK parameters governing the activity of antibiotics
0 6 18 2412
Con
cent
ratio
n
MIC
Time (h)
f T > MIC
f T > MICAUC24h / MIC
Cmax / MICCmax
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How to determine which PK parameter is critical ?
• If you fractionate the daily dose, you change Cmax without changing AUC24h
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Con
cent
ratio
n
MIC
Time (h)
Cmax
Cmax
AUC24h = Dose24h / ClearanceAUC24h is independent of the schedule
0 6 18 2412
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How to determine which PK parameter is critical ?
• If you increase the dose without change of schedule, you increase BOTH Cmax and AUC24h
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Con
cent
ratio
n
MIC
Time (h)
Cmax
Cmax
AUC24h = Dose24h / ClearanceAUC24h is proportional to the dose
0 6 18 2412
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antibiotic PK/PD parameter What to do ?
The 3 main patterns of antibiotic PK/PD properties(W.A. Craig, 2000; revised in 2003)
* 2d ISAP Educational Workshop, Stockholm, Sweden, 2000;revised accord. to Craig, Infect. Dis. Clin. N. Amer., 17:479-502, 2003
β-lactams time > MIC stay > MIC as needed
macrolides,oxazolidinones,vancomycin…
AUC24h / MIC give a sufficient total daily dose
quinolonesaminoglycosides
peak / MIC andAUC24h / MIC
obtain a peakand aim for a sufficient
total daily dose
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An important consideration: What should we aim for ?
ln EC50 - 2
E50%
Emax Maximal effect
Emin Minimal effect
concentration
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How to be optimal ?
If you select a β-lactam …
• cefotaxime
• neutropenic mice
• K. pneumoniae
• lung infection
100 % - Maximal effect
40 %Static dose
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Breakpoint setting…
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Aminoglycosides …
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Aminoglycosides are concentration-dependent and need to be given once-daily both for increased efficacy and possible reduction of toxicity
Nicolau et al. Antimicrob Agents Chemother. 1995;39:650-5 - PMID: 7793867
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Aminoglycosides …
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19
Aminoglycosides are concentration-dependent and need to be given once-daily both for increased efficacy and possible reduction of toxicity
After Schorderet, 1998
1. clinical efficacy is maximal if Cmax = 8 x MIC
3. Compute the desired based on MIC (if available) or breakpoint (see EUCAST documents)
4. Compute the dose (Cmax x Vd)Note: Vd = 0.2 L/kg in "nomal" patients but can be increased
to 0.3 L/kg in infected patients)
2. select the appropriate route of administration ( IV > IM )
For most patients:• gentamicin / tobramycin / netilmicin daily dose: 6 mg/kg Cmax: 16 mg/L – will cover up to an MIC of 2 mg/L
• amikacin daily dose 15 mg/kg Cmax: 32 mg/L – will cover up to an MIC of 4 mg/L
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amikacin peak
-45 to
-15
-15 to
+15
+15 t
o +45
+ 45 t
o + 75
+75 t
o + 10
5> 1
050
3
5
8
10
time (min)
no. o
f obs
erva
tions
Aminoglycoside TDM: correct sampling !!
eligible patients: 102
inclusion: 94 patients
111 treatments
vancomycin: 46
amikacin: 65 trough: 62
peak: 44
exclusions:• 2 for inability to perform
observation• 6 for limited life expectancy
Ampe et al., unpublished
Observations of a clinical pharmacist about the correct peak sampling
A large number of samples were not taken at the defined optimal
time
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Therapeutic Drug Monitoring: aminoglycosides
Nicolau et al. Experience with a once-daily aminoglycoside program administered to 2,184 adult patients. Antimicrob Agents Chemother. 1995 Mar;39(3):650-5. PubMed PMID:7793867
Single concentration measured at 8 h
• if level falls in q24h area, dosing interval is q24h
• same applies for areas q36h q48h (decr. creat. clearance).
• if near line, choose longer interval
• if above the nomogram between the 6- and 14-h time points, stop therapy and monitor for concentr. < 1 mg/L before next dose
Aminoglycosides: The "Nicolau's" nomogram with an 8h sampling time
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Once daily dosing of aminoglycosides: toxicity
When choosing an antibiotic, do we know 2. for the specific patient
– how to prevent / avoid patient- and drug-related side effects
11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 22
aminoglycosides are concentration-dependent and need to be given once-daily both for increased efficacy and possible reduction of toxicity
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Aminoglycosides: can you do better ?
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Aminoglycosides: can you do better ?
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Fluorquinolones: the first study of antibiotics PK/PD…
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Fluorquinolones: the first study of antibiotics PK/PD…
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PKP/PD of ciprofloxacin: a Japanese testimonial
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PKP/PD of ciprofloxacin: a Japanese testimonial
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PK/PD breakpoints for fluoroquinolones
Van Bambeke F, Michot JM, Van Eldere J, Tulkens PM. Quinolones in 2005: an update. Clin Microbiol Infect. 2005 Apr;11(4):256-80. PMID: 15760423
0.5-1
0.5-1
0.5-1
1-2
0.5-1
EUCAST breakpoints
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PK/PD of ciprofloxacin: a special population
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Guillot et al. Pharmacotherapy. 2010;30:1252-8 - PMID: 21114393
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PK/PD of ciprofloxacin: a special population
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Guillot et al. Pharmacotherapy. 2010;30:1252-8 - PMID: 21114393
Model 1: 10 mg/kg BID IV 1 day -- 15 mg/kg BID PO 1 day.Model 2: 10 mg/kg BID IV 1–3 days -- 15 mg/kg BID PO 1 day, or 20 mg/kg TID PO - >3 days.Model 3: 10 mg/kg IV -- 15 mg/kg BID PO
0.25 mg/L may be the max. MIC
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PK/PD of levofloxacin: limits in MICs
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PK/PD of levofloxacin: limits in MICs
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PK/PD of levofloxacin: limits in MICs
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renal function class
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PK/PD of levofloxacin: limits in MICs
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PK/PD of levofloxacin: limits in MICs
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renal function class
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PK/PD of levofloxacin: limits in MICs
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• The opportunity to define permissible doses of levofloxacin in older patients was further strengthened by the findings of two recent reviews showing that levofloxacin is the fluoroquinolone associated with the highest risk of causing tendon damage
• This may further strengthen the valuable role that a real-time therapeutic drug monitoring (TDM)-guided approach to levofloxacin dosage adjustments may have in preventing drug-related toxicity in older patients.
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Vancomycin
• Vancomycin is a AUC24h/MIC-driven antibiotic
• Vancomycin effective AUC24h/MIC should be around 400 (more than for fluoroquinolones) because of its poor tissue penetration
• Yet, most (US) guidelines suggest to only measure trough (Cmin) levels !
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Liu et al. Clin Infect Dis. 2011; ;52:e18-55 PMID:: 21208910
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Vancomycin
• Vancomycin is a AUC24h/MIC-driven antibiotic
• Vancomycin effective AUC24h/MIC should be around 400 (more than for fluoroquinolones) because of its poor tissue penetration
• Yet, most (US) guidelines suggest to only measure trough (Cmin) levels !
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Liu et al. Clin Infect Dis. 2011; ;52:e18-55 PMID:: 21208910
• Trough vancomycin concentrations are the most accurate and practical method to guide vancomycin dosing (B-II).
• For serious infections, such as bacteremia, infective endocarditis, osteomyelitis, meningitis,pneumonia, and severe SSTI (eg, necrotizing fasciitis) due to MRSA, vancomycin trough concentrations of 15–20 µg/mL are recommended (B-II).
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Vancomycin: things are moving …
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Finch et al. Antimicrob Agents Chemother. 2017;61:e01293-17 - PMID: 28923869
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Vancomycin: things are moving …
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Finch et al. Antimicrob Agents Chemother. 2017;61:e01293-17 - PMID: 28923869
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But there could be a better approach: continuous infusion
Ampe et al., International Journal of Antimicrobial Agents (2013) 41:439-446
• 54 patients (40 documented infections)• target concentration: 25-30 mg/L• loading dose: 20 mg/kg;• infusion rate: 2.5 g/day
(adapted to renal function and corrected by therapeutic drug monitoring)
patients with risk of under-
treatment
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relation between AUC24h / MIC (E-Test) and clinical efficacy (n=19)
AUIC < 450cure failure
5/9 4/9P < 0.05
AUC24h / MIC (AUIC)
CURE
CURE
FAILURE
KLI
NIS
CH
E O
UTC
OM
E (c
ure
/ fa
ilure
)
450196 (min) 2684 (max)
Results are quite clear for efficacy….
Ampe et al., International Journal of Antimicrobial Agents (2013) 41:439-446
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11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 44
But there still are huge variations in blood levels
s u c e s s iv e v a n c o m y c in s e ru m le v e ls v a lu e s in in d iv id u a l p a t ie n tsw ith > 3 d e te rm in a tio n s a f te r th e f irs t 9 6 h o f t re a tm e n t (n = 5 2 )
3 4 5 6 8 91
11
21
41
51
71
92
02
12
22
42
52
62
72
82
93
13
33
43
53
83
94
24
34
54
65
55
65
75
86
06
26
46
56
66
97
17
47
67
88
28
38
58
68
88
99
1
1 0
2 0
3 0
4 0
5 0
p a t ie n t n o .
mg
/L
Ampe et al., International Journal of Antimicrobial Agents (2013) 41:439-446
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11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 45
But there still are huge variations in blood levels
s u c e s s iv e v a n c o m y c in s e ru m le v e ls v a lu e s in in d iv id u a l p a t ie n tsw ith > 3 d e te rm in a tio n s a f te r th e f irs t 9 6 h o f t re a tm e n t (n = 5 2 )
3 4 5 6 8 91
11
21
41
51
71
92
02
12
22
42
52
62
72
82
93
13
33
43
53
83
94
24
34
54
65
55
65
75
86
06
26
46
56
66
97
17
47
67
88
28
38
58
68
88
99
1
1 0
2 0
3 0
4 0
5 0
p a t ie n t n o .
mg
/L
Ampe et al., International Journal of Antimicrobial Agents (2013) 41:439-446
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β-lactams
• β-lactams have been long considered as drugs with a very large therapeutic ratio… So, why bother about monitoring them… ?
• but two things have now appeared as critical
– the rise in MICs, creating a risk of under-treatment with the current dosages
– the huge variability of PK parameters (Vd and clearance) between patients and over time (ICU) under-treatment toxicity
11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 46
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11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 47
What is the correct target for a β-lactam ?
Delattre et al.Expert Rev Anti Infect Ther. 2017;15:677-88 - PMID: 28571493
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11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 48
What is the correct target for a β-lactam ?
Delattre et al.Expert Rev Anti Infect Ther. 2017;15:677-88 - PMID: 28571493
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11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 49
Illustration from animal data…
• cefotaxime
• neutropenic mice
• K. pneumoniae
• pulmonary infection
100 % - Maximal effect ?
40 %Static dose ?
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11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 50
What is the correct dose for your patient
40 %
Mild infections in a non-immunocompromised patient
100 % ?
Severe infection in an immunocompromised
patient
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11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 51
but maybe even more ?
Mouton JW, Vinks AA. Curr Opin Crit Care. 2007 Oct;13(5):598-606.
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But which MICs ?
11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 52
Mesaros et al. CMI (2007) 13: 560–578
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11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 53
But are all patients equal ?
But are all patients really alike
Concentration profile of a β-lactam in volunteersVd = 20 L, ka = 1.2 h-1, ke = 0.3 h-1
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11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 54
Wat is a "standard" patient ?
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11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 55
Here is the daily reality …
0.00
1.00
2.00
3.00
4.00
5.00
6.00
7.00
8.00
9.00
10.0
011
.00
12.0
013
.00
14.0
015
.00
16.0
017
.00
18.0
019
.00
20.0
021
.00
22.0
023
.00
0.20
1.20
2.20
3.20
4.20
5.20
6.20
7.20
8.20
9.20
10.20
11.20
12.20
13.20
14.20
15.20
16.20
17.20
18.20
19.20
0.95-1.00
0.90-0.95
0.85-0.90
0.80-0.85
0.75-0.80
0.70-0.75
0.65-0.70
0.60-0.65
0.55-0.60
0.50-0.55
0.45-0.50
0.40-0.45
0.35-0.40
0.30-0.35
0.25-0.30
0.20-0.25
0.15-0.20
0.10-0.15
0.05-0.10
0.00-0.05
Conc
Time
Prob
4h
10h
Concentration profiles in real patients
Mouton, Int J Antimicrob Agents april 2002
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11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 56
Today, monitoring β-lactams becomes a reality
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11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 57
β-lactam monitoring: a typical and early example
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11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 58
β-lactam monitoring: a typical and early example
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Monitoring of β-lactams in special populations (1)
11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 59
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Monitoring of β-lactams in special populations (1)
11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 60
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Monitoring of β-lactams in special populations (1)
11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 61
• In the context of critical illness, there is strong data demonstrating that standard dosing regimens for many antibiotics frequently fail to provide optimal PK/PD exposure in critically ill patients.
• Given that pharmacokinetic exposures can be very difficult-to-predict in some patients, TDM is valuable to identify these patients and guide dose optimization.
• TDM can ensure attainment of PK/PD surrogate indicators of antibiotic efficacy, and therefore potentially improve patient outcome.
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Monitoring of β-lactams in special populations (2)
11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 62
Jacobs et al. Antimicrob Agents Chemother. 2018;62:pii: e02534-17 - PMID: 29987138
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Monitoring of β-lactams in special populations (2)
11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 63
Jacobs et al. Antimicrob Agents Chemother. 2018;62:pii: e02534-17 - PMID: 29987138
Currently, we recommend, when possible, TDM-guided therapy to optimize PK/PD target attainment in critically ill patients and particularly in those at risk of ARC.
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Monitoring of β-lactams in special populations (3)
11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 64
Jung et al. Crit Care Med. 2017;45:e470-e478 - PMID: 28240688
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Monitoring of β-lactams in special populations (3)
11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 65
Jung et al. Crit Care Med. 2017;45:e470-e478 - PMID: 28240688
Piperacillin blood concentrations (median, quartiles, and individual values) over the 7-d study period for non-obese (n = 12) and severely obese (n = 11) patients. The Pseudomonas aeruginosa minimal inhibitory concentration breakpoint (16 mg/L), 4-fold the breakpoint (64 mg/L), and the potential piperacillin toxic concentration threshold (150 mg/L) are represented as dashed lines.. *Between obese and non-obese patients over time, adjusted to SOFA score.
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11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 66
Today, TDM of β-lactams may become a reality
• Therapeutic drug monitoring (TDM) is a strategy that may help to optimize dosing.
• Ideally, methods used for routine TDM should have a short turnaround time (fast run-time and fast sample preparation), a low limit of quantification and a sufficiently high upper limit of quantification.
• There is also a growing number of methods measuring free concentrations.
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What about oxazolidinones (linezolid) ?
11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 67
Cattaneo et al. Expert Opin Drug Metab Toxicol 2016;12:533-44 - PMID: 26982718
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Linezolid: huge variations in Cmin …
11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 68
Cattaneo et al. Expert Opin Drug Metab Toxicol 2016;12:533-44 - PMID: 26982718
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Linezolid: many factors affecting its pharmacokinetics…
11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 69
Cattaneo et al. Expert Opin Drug Metab Toxicol 2016;12:533-44 - PMID: 26982718
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Toxicodynamics: what drives linezolid toxicity…
11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 70
Theuretzbacher U, PK/PD of Oxazolidinones In: Fundamentals of Antimicrobial Pharmacokinetics and Pharmacodynamics, AA. Vinvk, H. Derendorf & JW Mouton eds, Springer, 2014, p 401-443
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11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 71
Where are we now ?1. know your antibiotic and its PD parameter
time-, AUC24h-, of Cmax- driven
2. look for the pertinent PK data and the recommended dosages …
3. compute the pertinent "PK/PD parameter – MIC" ratio / target that will ensure efficacy
– β-lactams: f T > MIC = 30 to 100 % of the dosing interval– aminoglycosides: Cmax = 8 x MIC– fluoroquinolones: AUC24h/MIC = 30 (min.) -125 (preferred) – vancomycin: AUC24h/MIC = 400– macrolides: AUC24h/MIC = 30– tetracyclines (incld. tigecycline): AUC24h/MIC = 7-10– linezolid: avoid Cmin > 7 mg/L (for toxicity)
4. Check your local epidemiology for MICs …
Check the drug label
and pertinent
publications… or rely on
a clinical pharmacist !
Ask your microbiologist
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Beyond the patient, answers for the Society …
When choosing an antibiotic, do we know 3. for the society
– how to prevent emergence of resistance ?
11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 72
This is probably a most difficult challenge because • resistance genes are already present in nature (resistome)• bacteria quickly adapt to new environments (mutation/selection)
Hu et al. Front Med 2017;11:161-168 - PMID: 28500429
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Answers for the Society …
When choosing an antibiotic, do we know 3. for the society
– how to prevent emergence of resistance ?
11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 73
This is probably a most difficult challenge because • resistance genes are already present in nature (resistome)• bacteria quickly adapt to new environments (mutation/selection)
Hu et al. Front Med 2017;11:161-168 - PMID: 28500429
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11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 74
MIC may increase during treatment !
meropenem (n=28)
D0 DL0.125
0.25
0.5
1
2
4
8
16
32
64
128
256
*
piperacillin-tazobactam (n=31)
D0 DL
2
4
8
16
32
64
128
256
512
1024
*
MIC
(mg/
L)
Change in MIC of antibiotics used in empiric antipseudomonal therapy (nosocomial pneumonia; intensive care units) towards the isolate identified before onset of therapy (D0) vs. the last isolate (DL) collected from the same patient and with clonal similarity with the first isolate. Differences were analyzed using both raw and log2 transformed data and found significant by both non-parametric (Wilcoxon matched pair test) and parametric (two-tailed paired t-test) analysis.
Riou et al. Int J Antimicrob Agents. 2010 Dec;36(6):513-22.
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Optimization may prevent emergence of resistance
11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 75
Tam et al. J Antimicrob Chemother 2017;72:1421-1428 - PMID: 28158470
Simulation of serum concentration levels
(hollow fibers model)
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11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 76
Tam et al. J Antimicrob Chemother 2017;72:1421-1428 - PMID: 28158470
Optimization may prevent emergence of resistance
placebo
ceftazidime0.5 g q8h
ceftazidime3 g g q8h
To prevent emergence of resistance, Cmin of β-lactams must stay > 4 x MIC (mean), which commands higher dosages…
4 x MIC
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11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 77
Avoiding the window for selection of resistance
Time after administration
MIC
MPC
conc
entra
tion
MSW
Mutation selection window
concept taken from Drlica & Zhao, Rev. Med. Microbiol. 2004, 15:73-80and Journal of Antimicrobial Chemotherapy 2008, 62:434–436
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11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 78
Avoiding the window for selection of resistance
MIC
MPC
MSW
No therapeutic effect
eradication of first mutants and efflux-mediated resistance
selection of first mutants and of efflux
Time after administration
conc
entra
tion
concept taken from Drlica & Zhao, Rev. Med. Microbiol. 2004, 15:73-80and Journal of Antimicrobial Chemotherapy 2008, 62:434–436
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11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 79
AUC24h / MIC = 125 en Cmax / MIC > 10 as parameters for efficacy and prevention of resistance of fluoroquinolones:
which MICs can you cover with standard treatments ?
Van Bambeke F, Michot JM, Van Eldere J, Tulkens PM. Quinolones in 2005: an update. Clin Microbiol Infect. 2005 Apr;11(4):256-80. PMID: 15760423
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TDM of antibiotics …
11 Oct 2018 Laboratory Medicine at the Clinical Interface, Antalya, Turkey 80
DosageSerum
concentrations
Concentration at the site of infection
Concentration in non-target organs
Therapeutic effects
Toxic effects
prevention of resistance
TDM might be the key …