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Edi Hartoyo Alan R. Tumbelaka Infectious Disease and Tropical Pediatrics Working Group Indonesian Pediatrician Society 1
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2 1. Definitions and Criteria 2. Initial Evaluation 3. Who should receive empirical Tx? 4. Initial Empirical Antibiotics Considerations ? 5. Initial Antibiotics Recomended Choices? 6. Reassesment Afebrile and Febrile Patient 7. Duration of AntibioticTherapy When to stop? 8. Algorithm for initial management of febrile neutropenia 9. Conclusion OUTLINE
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Fever : single oral temp. > 38.3 0 C or a temp. >38.0 0 C for > 1 hr Neutropenia : neutrophil count < 500 /mm 3, or account of < 1,000 with a predicted decrease to < 500 3 Walter at al, Infect Desease Society of America. 2002; 34: 731-751 Hughes at al, Clin Infect Diss 2002; 52: 551-73
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ANC > 100 /mm3 Normal CXR Duration of neutropenia < 7 d Resolution of neutropenia <10 d No appearance of illness No comorbidity complications Malignancy in remission 4 Walter at al, Infect Desease Society of America. 2002; 34: 731-751 Hughes at al, Clin Infect Diss 2002; 52: 551-73
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Parenteral antibiotics + close monitoring Haematological malignancies Severe and prolonged neutropenia > 10 d Evidence of shock / dehydration Mucositis preventing oral hydration Complex focal infection eg CVL site infection Respiratory / gastrointestinal involvement Need for blood products Renal / hepatic insufficiency Change in mental status 5 Hughest et al, Guideline for febrile neutropenia. 2002; 34: 734-752
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Blood C/S : central line & peripheral Chest X-Ray Urine C/S Stool C/S Biopsy cultures Viral studies 6 2. INITIAL EVALUATION
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URTI Dental sepsis Mouth ulcers Skin sores Exit site of central venous catheters Anal fissures GI 7
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Gram-positive bacteria (60-70%) Staphylococcus spp : MSSA,MRSA, Enterococcus faecalis/faecium Corynebacterium spp Bacillus spp Stomatococcus mucilaginosus 8
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Gram-negative bacilli (30-40%) Escherichia coli Klebsiella spp : ESBL Pseudomonas aeruginosa Enterobacter spp Acinetobacter spp Citrobacter spp Stenotrophomonas maltophilia Anerobic Bacteria Bacteroides spp Clostridium spp Fusobacterium spp Propionibacterium spp Peptococcus spp Veillonella spp Peptostreptococcus spp 9 Del Favero at al, Clin infect Dis. 2001; 33: 1295-301 Weinstein et al, J. Clin Microbiol. 2006; 32:2103-6
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Bacterial infection Neutropenia :single most important risk factor for infection in cancer. Risk of infection increases 10-fold with declining neutrophil counts < 500/mm3 48-60% : occult infection 16-20% with neutropenia<100/mm3 have bacteremia 10 Samam MD. Commun Oncol 2006; 3 : 585-591
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Broad spectrum of bactericidal activity Local prevalence, susceptibility pattern Antibiotic toxicity : well-tolerated, allergy Host factors : severity of presentation Prior antibiotic usage Antibiotic costs Ease of administration 11
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1. Monotherapy Antipseudomonal Ceph 3 : ceftazidime Ceph 4 : cefepime Carbapenem : imipenem, meropenem 2. Combination Duo therapy without vancomycin Vancomycin plus one or two drugs 12 Lindbad et al, Scand J Infect Dis. 2005; 30: 237-43 Liat V et al, J Antimimicrobial Chem. 2004; 54:29-31 Hughest et al, Guideline for febrile neutropenia. 2002; 34: 734-752
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Aminoglycoside + Anti-pseudomonal carboxypenicillin (Piperacillin – Tazobactam + Gentamycin, Tobramycin, Amikacin or Ticarcillin-clavulanic acid + Aminoglycoside) Aminoglycoside + Anti-pseudomonal Cephalosporin Aminoglycoside + Carbapenem 13 Saman K, Commun Oncol. 2006; 3:585-591 Bucaneve et al, N Eng J Med. 2005; 353:977-987 Combination Therapy Without Vancomycin
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14 Reassess after 3-5 days Walter at al. IDSAI Guideline. 2002:34;730-51
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Persistence of fever Clinical deterioration Culture results Drug intolerance/side effects 15
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Increased bactericidal activity Potential synergistic effects Broader antibacterial spectrum Limits emergence of resistance 16
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Drug toxicities Drug interactions Potential cost increase Administration time 17
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18 Walter at al. IDSAI Guideline. 2002:34;730-51
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19 Reproduced with permission from Hughes et al. Clin Infect Dis 2002;34:730–751
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Nonbacterial infection Resistant bacteria Slow response to antibiotics Fungal sepsis Inadequate serum & tissue levels Drug fever 20 Jasic et al, Clin Infect Dis.2006; 42:597-607
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No infection identified after 3 days of Rx ANC > 500 for 2 consecutive days Afebrile > 48 hr Clinically well 21 Jasic et al, Clin Infect Dis.2006; 42:597-607
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22 Stop if no disease and condition stable Conntinue antibiotik High risk : ANC< 100/mm3, Mucousitis, unstable sign Stop when afebrile for 5- 7 days Lows risk, clinically well Stop Antibiotics 48 h after afebril ANC < 500/mm3 by day 7 DURATION OF ANTIBIOTICS THERAPY Afebrile by day 3-5 ANC≥ 500/mm3 for 2 consecutive days Persistent Fever Reassess Continue for 2 week Stop 4 – 5 days after > 500/mm3 ANC < 500/mm3ANC ≥ 500/mm3
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Terature 38.8ºC) + neutropenia (<500 neutrophils/mm 3 ) 23 Low risk High risk Oral IVVancomycin not needed Vancomycin needed Ciprofloxacin + Amoxicillin / clavulanate (adults only) Cefepime, Ceftazidime or Carbapenem Monotherapy Aminoglycoside + Antipseudomonal penicillin, Cefepime, Ceftazidime, or Carbapenem Two drugs Vancomycin + Cefepime, Ceftazidime or Carbapenem Aminoglycoside Vancomycin + Reassess after 3–5 days Reproduced with permission from Hughes et al. Clin Infect Dis 2002;34:730–751
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24 Reproduced with permission from Hughes et al. Clin Infect Dis 2002;34:730–751 Antifungal drug, with or without antibiotic change If febrile through Days 5–7 and resolution of neutropenia is not imminent Persistent fever during first 3–5 days of treatment: no aetiology Reassess patient on Days 3–5 If progressive disease or If criteria for vancomycin are met Change antibiotics If no change in patient's condition (consider stopping vancomycin) Continue initial antibiotics
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25 Guidelines Febrile Neutropenia
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Cunha, Antibiotic Essential, 2009
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Significant morbidity & mortality Choice of initial empiric therapy dependent on epidemiologic & clinical factors Monotherapy as efficacious as combination Rx Modifications upon reassessment Duration dependent on ANC 27
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Thank you for your attention edi & alan 28
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