Author/Authors :
Efrati، نويسنده , , Ori and Bylin، نويسنده , , Irena and Segal، نويسنده , , Eran and Vilozni، نويسنده , , Daphna and Modan-Moses، نويسنده , , Dalit and Vardi، نويسنده , , Amir and Szeinberg، نويسنده , , Amir and Paret، نويسنده , , Gideon، نويسنده ,
Abstract :
Objective
mission of patients with cystic fibrosis (CF) to the intensive care unit (ICU) is controversial. Our aim was to study the long-term outcome of patients with CF who were admitted to the ICU and the effect of ventilation modality.
s
dical records of 104 admissions (1996-2006) of 48 patients with CF (age 18 ± 9 years) were reviewed. Seventeen patients were admitted with reversible conditions (group 1). Thirty-one patients were admitted for acute on chronic respiratory failure (group 2).
s
up 1, 16 of 17 patients survived up to 10 years from ICU admission. Conversely, in group 2, 23 of 31 patients (74%) died of respiratory failure. In group 2, 17 of 18 patients who were mechanically ventilated died within 90 days from admission, and 7 of 10 patients treated for prolonged periods with bi-level positive airway pressure are still alive up to 10 years after admission and transplantation.
sion
ts requiring mechanical ventilation may have a poor prognosis. The outcome of treatment with bi-level positive airway pressure is good, even in patients who had many episodes of acute respiratory failure.