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PubblicatoCristoforo Ferrara Modificato 8 anni fa
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Uomo di 75 anni, altezza 178 cm, peso 80 Kg, pensionato, residente in casa di cura, in a.b.s., a seguito ad incidente stradale viene ricoverato in terapia intensiva. All’ingresso il quadro clinico è caratterizzato dalla presenza di un trauma toracico con fratture costali, frattura del femore sx e della mandibola. Non si rilevano lesioni di organi interni. Il paziente viene posto in coma farmacologico ed sottoposto a ventilazione meccanica. Dopo 7 giorni di ricovero, il quadro clinico si complica con la comparsa di febbre. Vengono effettuati esami di laboratorio, Xgrafia torace, esame colturale dell’aspirato tracheale e del lavaggio broncoalveolare. Si decide di iniziare una terapia antibiotica empirica.
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Esami di laboratorio e strumentali Leucocitosi neutrofila (> 20.000/mm 3 ) Indici di flogosi elevati RX torace: interessamento di tipo flogistico dei lobi inferiori polmonari bilateralmente Viene posta diagnosi di polmonite nosocomiale associata a ventilazione meccanica
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Siete d’accordo con questa diagnosi? 1) Si 2) No 3) Sono necessari altri accertamenti
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Polmonite Nosocomiale: definizione “Hospital acquired pneumonia is defined as pneumonia occurring ≥ 48 h after admission and excluding any infection that is incubating at the time of admission is not a reportable illness” (ATS, Am. J. Respir. Crit. Care Med., 1996)
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Iniziereste subito la terapia antibiotica anche in assenza di un isolamento batterico? 1) Si 2) No
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Clinical importance of delays in the initiation of appropriate antibiotic treatment for Ventilator Associated Pneumonia Iregui M., Chest, 122, 2002 Study objectives To determine the influence of initially delayed appropriate antibiotic treatment (IDAAT) on the outcomes of patients with VAP Measurements and results 107 pts received mechanical ventilation and antibiotic treatment for VAP 33 pts (30.8%) received antibiotic treatment that was delayed for 24 h after first meeting the diagnostic criteria for VAP and were classified as receiving IDAAT The mean duration of time from when pts initially met the diagnostic criteria for VAP until the administration of antibiotics was 28.6 5.8 h among pts classified as receiving IDAAT, compare to 12.5 4.2 h for all other pts 44 pts (41.1%) with VAP died during their hospitalization Increased APACHE II scores, the presence of malignancy, and the administration of IDAAT were identified as risk factors independently associated with hospital mortality by logistic regression analysis. Conclusion These data suggest that patients classified as receiving IDAAT are at greater risk for hospital mortality. Clinicians should avoid delaying tha administration of appropriate antibiotic treatment to patients with VAP in order to minimize their risk of mortality.
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Mortalità associata al ritardo della terapia antibiotica (Iregui M, Chest, 2002) p 0.001
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Independent predictors of hospital mortality using logistic regression VariablesAdjusted odds Rate 95% confidence Interval p Value IDAAT7.684.50-13.090.001 Underlying malignancy3.201.79-5.710.044 APACHE II score (1-point increments) 1.131.09-1.180.001 (Iregui M, Chest, 2002)
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Impact of BAL on the Therapy and Outcome of Ventilator Associated Pneumonia Luna C.M., Chest, 111, 1997 Study objectives To define the impact of BAL data on the selection of antibiotics and the outcomes of patients with VAP Design Prospective observation and bronchoscopy with BAL, performed within 24 h of estabilishing a clinical diagnosis of new episode of hospital-acquired VAP or progression of a prior episode of nosocomial pneumonia (NP) Patients 132 pts hospitalized for more then 72 h were mechanically ventilated and had a new or progressive lung infiltrate plus at least two the following three clinical criteria for VAP: abnormal temperature (>38 °C or <35 °C) abnormal leukocyte count (>10,000/mm 3 or <3,000/mm 3 ) purulent bronchial secretions Interventions Bronchoscopy with BAL within 24 h All patients received antibiotics: 107 prior to bronchoscopy 25 immediately after bronchoscopy Conclusions Patients with a strong clinical suspicion of VAP have a high mortality rate, regardless of whether BAL cultures confirm the clinical diagnosis of VAP When adeguate antibiotic therapy is initiated very early mortality rate is reduced compared to when this therapy is inadeguate or no therapy is given
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Influenza del trattamento antibiotico precoce sulla mortalità per polmonite nosocomiale (Luna CM, Chest, 1997) p=NS P< 0.001
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Viene iniziata terapia empirica con: Linezolid 600 mg ogni 12 h Ceftazidime 2 g ev ogni 8 ore Levofloxacina 500 mg ev ogni 12 ore
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Siete d’accordo con questa terapia? 1) Si 2) No
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Association between mortality and infection with MRSA: two meta-analyses (a: Cosgrove S.E., Clin Infect Dis 2003; b: Whitby M., Med J Aust, 2001) n=3963n=2209 ab
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Microbiology of patients with HAP Mild-moderate No risk factor Early onset Mild-moderate With risk factor Onset any time Severe With risk factor Late onset Enteric Gram negative bacilli (non pseudomonal) Aneroboes P. aeruginosa MSSA MSSA, MRSA Acinetobacter spp. S. pneumoniae Legionella MRSA P. aeruginosa (ATS, Am. J. Respir. Crit. Care Med., 1996)
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Credete sia giusto iniziare una terapia d’associazione con linezolid piuttosto che con un glicopeptide?
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Secondo voi qual è la durata ottimale della terapia antibiotica nelle HAP? 1) <10 giorni 2) 14 giorni 3) >14-21 4) Fino alla risoluzione clinico-strumentale
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Duration of Antimicrobial Therapy The treatment duration proposed by the American Thoracic Society remains imprecise (ATS, Am. J. Respir. Crit. Care Med., 1995)
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Hospital-Acquired Pneumonia in Adults: Diagnosis, Assessment of Severity, Initial Antimicrobial Therapy, and Preventative Strategies Am. J. Respir. Crit. Care Med. 1995 “long” treatment (14- 21 days): multilobar involvement malnutrition cavitation Gram-negative necrotizing pneumonia isolation of P. aeruginosa or Acinetobacter spp. “short” treatment (7-10 days): S. aureus MS or H. influenzae pneumonia
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Comparison of 8 vs 15 days of antibiotic therapy for Ventilator Associated Pneumonia in adults Chastre J., J. Am. Med. Assoc., 2003 Context The optimal duration of antimicrobial treatment for VAP is unknown Shortening the lenght of treatment may help to contain the emergence of multiresistant bacteria in ICU Objective To determine whether 8 days is as effective as 15 days of antibiotic treatment of pts with microbiologically proven VAP Intervention 197 pts were randomly assigned to receive 8 days 204 to receive 15 days therapy with an antibiotic regimen selected by the treating physician Main outcome measures Death from any cause Microbiologically documented pulmonary infection recurrence Antibiotic free days were assessed 28 days after VAP onset and analyzed on an intent to treat basis
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All patients (Chastre J., JAMA, 2003) MortalityRecurrent Infections
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Non-fermenting Gram-negative bacilli MortalityRecurrent Infections (Chastre J., JAMA, 2003)
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Onset of multiresistant pathogens in patients who developed recurrent infections p 0.04 (Chastre J., JAMA, 2003)
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Il paziente continua la stessa terapia agli stessi dosaggi e dopo 7 giorni il quadro clinico è nettamente migliorato Dopo 10 giorni il paziente è apiretico ed interrompe la ventilazione meccanica La terapia viene protratta immodificata fino alla ventesima giornata
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