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1.
Ann Am Thorac Soc ; 11(4): 546-53, 2014 May.
Artículo en Inglés | MEDLINE | ID: mdl-24640938

RESUMEN

RATIONALE: Between 10% and 57% of lung transplant (LTx) recipients develop primary graft dysfunction (PGD) within 72 hours of LTx. PGD is clinically and histologically analogous to the acute respiratory distress syndrome. In patients at risk for or with acute respiratory distress syndrome, lung-protective ventilation strategies (low tidal volume and positive end-expiratory pressure) improve outcomes. There is, however, little information available on mechanical ventilation strategies after LTx. OBJECTIVES: Our aim in this international survey was to describe the current practices of mechanical ventilation immediately after LTx. METHODS: An electronic survey was sent to the medical and surgical directors of U.S. LTx programs (n = 111) and to members of the Pulmonary Council of the International Society for Heart and Lung Transplantation (n = 470). RESULTS: A total of 149 individuals from 18 countries responded to the questionnaire. The most common modes of ventilation were pressure assist/control (37%) and volume assist/control (35%). Tidal volumes were most often determined by recipient characteristics. Donor characteristics were rarely considered (35%) and were infrequently known by the team managing the ventilator (42%). When presented with a choice of ideal tidal volumes, a majority of respondents selected 6 ml/kg recipient predicted body weight (58%), fewer selected 10 ml/kg (21%), and none selected 15 ml/kg. A majority preferred limiting the fraction of inspired oxygen rather than positive end-expiratory pressure (PEEP) (69% versus 31%, P = 0.006). The median minimum PEEP was 5 cm H2O, and the median maximum PEEP was 11.5 cm H2O. The presence of PGD increased the perceived importance of monitoring plateau pressure to adjust tidal volumes. The median plateau pressure limit perceived as a threshold triggering reduction in tidal volume was 30 cm H2O. CONCLUSIONS: Most respondents reported using lung-protective approaches to mechanical ventilation after lung transplantation. Low tidal volumes based on recipient characteristics were frequently chosen. Donor characteristics often were not considered and frequently were not known by the team managing mechanical ventilation after LTx.


Asunto(s)
Trasplante de Pulmón , Pautas de la Práctica en Medicina/estadística & datos numéricos , Disfunción Primaria del Injerto/terapia , Respiración Artificial/métodos , Lesión Pulmonar Inducida por Ventilación Mecánica/prevención & control , Adulto , Anciano , Humanos , Persona de Mediana Edad , Respiración con Presión Positiva/métodos , Encuestas y Cuestionarios , Volumen de Ventilación Pulmonar
2.
J Cyst Fibros ; 13(4): 373-7, 2014 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-24418186

RESUMEN

BACKGROUND: Disrupted HCO3(-) transport and reduced airway surface liquid (ASL) pH in cystic fibrosis (CF) may initiate airway disease. We hypothesized that ASL pH is reduced in neonates with CF. METHODS: In neonates with and without CF, we measured pH of nasal ASL. We also measured nasal pH in older children and adults. RESULTS: In neonates with CF, nasal ASL (pH5.2 ± 0.3) was more acidic than in non-CF neonates (pH6.4 ± 0.2). In contrast, nasal pH of CF children and adults was similar to values measured in people without CF. CONCLUSIONS: At an age when infection, inflammation and airway wall remodeling are minimal, neonates with CF had an acidic nasal ASL compared to babies without CF. The CF:non-CF pH difference disappeared in older individuals, perhaps because secondary manifestations of disease increase ASL pH. These results aid understanding of CF pathogenesis and suggest opportunities for therapeutic intervention and monitoring of disease.


Asunto(s)
Líquidos Corporales/química , Fibrosis Quística/metabolismo , Mucosa Nasal/metabolismo , Adolescente , Adulto , Niño , Preescolar , Fibrosis Quística/genética , Regulador de Conductancia de Transmembrana de Fibrosis Quística/genética , Regulador de Conductancia de Transmembrana de Fibrosis Quística/metabolismo , Femenino , Estudios de Seguimiento , Genotipo , Humanos , Concentración de Iones de Hidrógeno , Lactante , Recién Nacido , Masculino , Persona de Mediana Edad , Mutación , Proyectos Piloto , Estudios Retrospectivos , Adulto Joven
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