Literature DB >> 16518642

Outcome of assisted ventilation for acute respiratory failure in cystic fibrosis.

Martijn G Slieker1, Josephus P J van Gestel, Harry G M Heijerman, Gerdien A Tramper-Stranders, Ferdinand Teding van Berkhout, Cornelis K van der Ent, Nicolaas J G Jansen.   

Abstract

OBJECTIVES: To assess outcome of assisted ventilation in cystic fibrosis (CF) patients with acute respiratory failure (ARF), to identify risk factors associated with poor outcome and to compare long-term outcome of CF children who were mechanically ventilated for ARF with unventilated CF controls.
DESIGN: Retrospective cohort study.
SETTING: Two large CF centres in the Netherlands. PATIENTS: CF patients who required assisted ventilation for ARF and unventilated CF controls.
INTERVENTIONS: None. MEASUREMENTS AND
RESULTS: Thirty-one CF patients required assisted ventilation for ARF between January 1990 and March 2005. All five children (under 2 years of age) and seven adults (27%) survived. In the total population, age was a statistically significant risk factor for poor outcome (p=0.02). In adult CF patients who required invasive mechanical ventilation, acute on chronic respiratory failure was associated with poor outcome. In children who required mechanical ventilation for ARF, lung function and CF related complications 5 years later were not significantly different compared with controls matched for age, gender and genotype.
CONCLUSIONS: CF patients younger than 2 years old, who are ventilated because of ARF, have a good prognosis and their long-term outcome seems identical to unventilated CF controls. ARF in adult CF patients still is associated with high mortality, especially among patients with acute on chronic respiratory failure.

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Year:  2006        PMID: 16518642     DOI: 10.1007/s00134-006-0085-x

Source DB:  PubMed          Journal:  Intensive Care Med        ISSN: 0342-4642            Impact factor:   17.440


  16 in total

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2.  Effect of a protective-ventilation strategy on mortality in the acute respiratory distress syndrome.

Authors:  M B Amato; C S Barbas; D M Medeiros; R B Magaldi; G P Schettino; G Lorenzi-Filho; R A Kairalla; D Deheinzelin; C Munoz; R Oliveira; T Y Takagaki; C R Carvalho
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3.  Survival effect of lung transplantation among patients with cystic fibrosis.

Authors:  T G Liou; F R Adler; B C Cahill; S C FitzSimmons; D Huang; J R Hibbs; B C Marshall
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4.  Outcomes of intensive care unit care in adults with cystic fibrosis.

Authors:  N Sood; L J Paradowski; J R Yankaskas
Journal:  Am J Respir Crit Care Med       Date:  2001-02       Impact factor: 21.405

5.  Assessment of survival benefit after lung transplantation by patient diagnosis.

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6.  Birth prevalence and survival in cystic fibrosis: a national cohort study in the Netherlands.

Authors:  Martijn G Slieker; Cuno S P M Uiterwaal; Maarten Sinaasappel; Harry G M Heijerman; Johan van der Laag; Cornelis K van der Ent
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7.  Invasive mechanical ventilation for acute respiratory failure in children with cystic fibrosis: outcome analysis and case-control study.

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8.  Non-invasive mechanical ventilation for cystic fibrosis patients--a potential bridge to transplantation.

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Journal:  Eur Respir J       Date:  1991-05       Impact factor: 16.671

9.  Assisted ventilation for patients with cystic fibrosis.

Authors:  P B Davis; P A di Sant'Agnese
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10.  Improved outcomes of patients with cystic fibrosis admitted to the intensive care unit.

Authors:  Hima Vedam; Carmel Moriarty; Paul J Torzillo; David McWilliam; Peter T P Bye
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Review 5.  Exacerbations in cystic fibrosis. 1: Epidemiology and pathogenesis.

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6.  Outcomes of Children With Cystic Fibrosis Admitted to PICUs.

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Journal:  Pediatr Crit Care Med       Date:  2020-10       Impact factor: 3.971

7.  Critical illness among adults with cystic fibrosis in Texas, 2004-2013: Patterns of ICU utilization, characteristics, and outcomes.

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Journal:  PLoS One       Date:  2017-10-24       Impact factor: 3.240

8.  Sepsis and acute respiratory distress syndrome requiring extracorporeal life support in an adolescent with mild cystic fibrosis.

Authors:  Lauren Elizabeth Faricy; Gwynne Church
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  8 in total

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