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1.
Ann Intensive Care ; 7(1): 67, 2017 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-28620893

RESUMEN

BACKGROUND: Early-onset ventilator-associated pneumonia (EO-VAP) is the leading cause of morbidity and mortality in comatose patients. However, VAP prevention bundles focus mainly on late-onset VAP and may be less effective in preventing EO-VAP in comatose patients. Systemic antibiotic administration at the time of intubation may have a role in preventing EO-VAP. Therefore, we evaluated the effectiveness of systemic antibiotic administration in VAP prevention in comatose patients through a systematic review and meta-analysis. METHODS: We searched for studies published through December 2015 that evaluated systemic antibiotic prophylaxis in comatose patients. Two authors independently selected and evaluated full-length reports of randomized clinical trials or prospective cohorts in patients aged >16 years that evaluated the impact of systemic antibiotics at the time of intubation on EO-VAP compared to placebo or no prophylaxis. The outcome variables were the incidence of EO-VAP, the duration of mechanical ventilation, ICU length of stay, and ICU mortality. RESULTS: We identified 10,988 citations, yielding 26 articles for further analysis; three studies with 267 patients were finally analyzed. Most patients (n = 135) were comatose due to head trauma. Systemic antibiotic administration was associated with decreased incidence of EO-VAP (RR 0.32; 95% CI 0.19-0.54) and shorter ICU LOS (standardized mean difference -0.32; 95% CI -0.56 to -0.08), but had no effect on mortality (RR 1.03; 95% CI 0.7-1.53) or duration of mechanical ventilation (standardized mean difference -0.16; 95% CI -0.41 to 0.08). CONCLUSIONS: Antibiotic prophylaxis in comatose patients reduced the incidence of EO-VAP and decreased the ICU stay slightly. Future trials are needed to confirm these results.

2.
Lancet Respir Med ; 3(11): 859-68, 2015 11.
Artículo en Inglés | MEDLINE | ID: mdl-26472037

RESUMEN

BACKGROUND: Ventilator-associated tracheobronchitis has been suggested as an intermediate process between tracheobronchial colonisation and ventilator-associated pneumonia in patients receiving mechanical ventilation. We aimed to establish the incidence and effect of ventilator-associated tracheobronchitis in a large, international patient cohort. METHODS: We did a multicentre, prospective, observational study in 114 intensive care units (ICU) in Spain, France, Portugal, Brazil, Argentina, Ecuador, Bolivia, and Colombia over a preplanned time of 10 months. All patients older than 18 years admitted to an ICU who received invasive mechanical ventilation for more than 48 h were eligible. We prospectively obtained data for incidence of ventilator-associated lower respiratory tract infections, defined as ventilator-associated tracheobronchitis or ventilator-associated pneumonia. We grouped patients according to the presence or absence of such infections, and obtained data for the effect of appropriate antibiotics on progression of tracheobronchitis to pneumonia. Patients were followed up until death or discharge from hospital. To account for centre effects with a binary outcome, we fitted a generalised estimating equation model with a logit link, exchangeable correlation structure, and non-robust standard errors. This trial is registered with ClinicalTrials.gov, number NCT01791530. FINDINGS: Between Sept 1, 2013, and July 31, 2014, we obtained data for 2960 eligible patients, of whom 689 (23%) developed ventilator-associated lower respiratory tract infections. The incidence of ventilator-associated tracheobronchitis and that of ventilator-associated pneumonia at baseline were similar (320 [11%; 10·2 of 1000 mechanically ventilated days] vs 369 [12%; 8·8 of 1000 mechanically ventilated days], p=0·48). Of the 320 patients with tracheobronchitis, 250 received appropriate antibiotic treatment and 70 received inappropriate antibiotics. 39 patients with tracheobronchitis progressed to pneumonia; however, the use of appropriate antibiotic therapy for tracheobronchitis was associated with significantly lower progression to pneumonia than was inappropriate treatment (19 [8%] of 250 vs 20 [29%] of 70, p<0·0001; crude odds ratio 0·21 [95% CI 0·11-0·41]). Significantly more patients with ventilator-associated pneumonia died (146 [40%] of 369) than those with tracheobronchitis (93 [29%] of 320) or absence of ventilator-associated lower respiratory tract infections (673 [30%] of 2271, p<0·0001). Median time to discharge from the ICU for survivors was significantly longer in the tracheobronchitis (21 days [IQR 15-34]) and pneumonia (22 [13-36]) groups than in the group with no ventilator-associated lower respiratory tract infections (12 [8-20]; hazard ratio 1·65 [95% CI 1·38-1·97], p<0·0001). INTERPRETATION: This large database study emphasises that ventilator-associated tracheobronchitis is a major health problem worldwide, associated with high resources consumption in all countries. Our findings also show improved outcomes with use of appropriate antibiotic treatment for both ventilator-associated tracheobronchitis and ventilator-associated pneumonia, underlining the importance of treating both infections, since inappropriate treatment of tracheobronchitis was associated with a higher risk of progression to pneumonia. FUNDING: None.


Asunto(s)
Bronquitis/epidemiología , Infección Hospitalaria/epidemiología , Unidades de Cuidados Intensivos/estadística & datos numéricos , Neumonía Asociada al Ventilador/epidemiología , Respiración Artificial/efectos adversos , Traqueítis/epidemiología , Adulto , Antibacterianos/uso terapéutico , Bronquitis/tratamiento farmacológico , Bronquitis/etiología , Infección Hospitalaria/tratamiento farmacológico , Infección Hospitalaria/etiología , Europa (Continente)/epidemiología , Femenino , Humanos , Incidencia , Tiempo de Internación , Masculino , Persona de Mediana Edad , Neumonía Asociada al Ventilador/tratamiento farmacológico , Pronóstico , Modelos de Riesgos Proporcionales , Estudios Prospectivos , América del Sur/epidemiología , Traqueítis/tratamiento farmacológico , Traqueítis/etiología , Adulto Joven
3.
Paciente crit. (Uruguay) ; 6(3): 147-51, 1993.
Artículo en Español | LILACS | ID: lil-215954

RESUMEN

El lavado broncoalveolar (BAL) es una técnica sencilla y relativamente segura que ha demostrado su utilidad en el diagnóstico de infecciones pulmonares oportunistas. La práctica de cultivos cuantitativos ha permitido incorporarla al diagnóstico etiológico de las neumonías en pacientes intubados. Un nivel de corte de 10.000 ufc/ml permite separar los microorganismos patógenoos de los contaminantes. Estudios recientes sugieren que las técnicas protegidas tienen un rendimiento que supera a las convencionales. Además el BAL permite establecer diagnósticos alternativos y, especialmente, contribuye a un diagnóstico más rápido y un tratamiento más dirigido cuando se asocia la cuantificación de bacterias intracelulares


Asunto(s)
Humanos , Lavado Broncoalveolar , Neumonía/diagnóstico , Lavado Broncoalveolar , Intubación/efectos adversos
4.
Paciente Crit ; 6(3): 147-51, 1993.
Artículo en Español | BVSNACUY | ID: bnu-5680

RESUMEN

El lavado broncoalveolar (BAL) es una técnica sencilla y relativamente segura que ha demostrado su utilidad en el diagnóstico de infecciones pulmonares oportunistas. La práctica de cultivos cuantitativos ha permitido incorporarla al diagnóstico etiológico de las neumonías en pacientes intubados. Un nivel de corte de 10.000 ufc/ml permite separar los microorganismos patógenoos de los contaminantes. Estudios recientes sugieren que las técnicas protegidas tienen un rendimiento que supera a las convencionales. Además el BAL permite establecer diagnósticos alternativos y, especialmente, contribuye a un diagnóstico más rápido y un tratamiento más dirigido cuando se asocia la cuantificación de bacterias intracelulares(AU)


Asunto(s)
Humanos , Neumonía/diagnóstico , Lavado Broncoalveolar , Intubación/efectos adversos , Lavado Broncoalveolar/métodos
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