TY - JOUR
T1 - Incidence and prognosis of ventilator-associated tracheobronchitis (TAVeM)
T2 - A multicentre, prospective, observational study
AU - TAVeM study
AU - Martin-Loeches, Ignacio
AU - Povoa, Pedro
AU - Rodríguez, Alejandro
AU - Curcio, Daniel
AU - Suarez, David
AU - Mira, Jean Paul
AU - Cordero, Maria Lourdes
AU - Lepecq, Raphaël
AU - Girault, Christophe
AU - Candeias, Carlos
AU - Seguin, Philippe
AU - Paulino, Carolina
AU - Messika, Jonathan
AU - Castro, Alejandro G.
AU - Valles, Jordi
AU - Coelho, Luis
AU - Rabello, Ligia
AU - Lisboa, Thiago
AU - Collins, Daniel
AU - Torres, Antonio
AU - Salluh, Jorge
AU - Nseir, Saad
AU - Fernández, Rubén Oscar
AU - Arroyo, Jorge
AU - Gabriela, Maria
AU - Alvarez, Rodriguez
AU - Reyes, Alex Tamayo
AU - Dellera, Christian
AU - Molina, Francisco
AU - Franco, Daniel Molano
AU - Parada, Edwin Giovanny Chapeta
AU - Yepez, Estuardo Salgado
AU - Oña, Fernando Paredes
AU - Tutillo, Diego Morocho
AU - Barahona, Diego
AU - Lerma, Francisco Alvarez
AU - Álvarez, Ana Abella
AU - Gallego, Jose Manuel Allegue
AU - Morillas, Francisco José Fuentes
AU - Aguilar, Antonio Luis Ruiz
AU - Iniesta, Rafael Sanchez
AU - Almirall, Jordi
AU - Albaya, Antonio
AU - Santana, Sergio Ruiz
AU - Fernandez, Carmen
AU - Naval Potro, Miguel Angel Blasco
AU - Cortes, Pablo Vidal
AU - Jimenez, Belen
AU - Sierra, Rafael
AU - Ortiz, Maria Del Valle
N1 - Publisher Copyright:
© 2015 Elsevier Ltd.
PY - 2015/1/1
Y1 - 2015/1/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84948968565&partnerID=8YFLogxK
U2 - 10.1016/S2213-2600(15)00326-4
DO - 10.1016/S2213-2600(15)00326-4
M3 - Artículo en revista científica indexada
C2 - 26472037
AN - SCOPUS:84948968565
SN - 2213-2600
VL - 3
SP - 859
EP - 868
JO - The Lancet Respiratory Medicine
JF - The Lancet Respiratory Medicine
IS - 11
ER -