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2,379 Possible Causes for Cystic Fibrosis, Poor Outcome

  • Influenza

    Chronic lung disease (such as chronic obstructive pulmonary disease [COPD] and cystic fibrosis) Heart disease (such as congenital heart disease, congestive heart failure and[] We sought to identify certain clinical characteristics associated with a poor clinical outcome in patients acutely infected with Influenza A.[] fibrosis) Heart disease (such as congenital heart disease, congestive heart failure and coronary artery disease) Blood disorders (such as sickle cell disease) Endocrine disorders[]

  • Pseudomonas

    Pseudomonas aeruginosa is the key bacterial agent of cystic fibrosis (CF) lung infections, and the most important pathogen in progressive and severe CF lung disease.[] outcome.[] This suggests that host-microbe or microbe-microbe adaptations occur during chronic colonization, which may subsequently influence infection progression and outcome.[]

  • Bronchitis

    Abstract Aspergillus fumigatus frequently colonizes the airways of patients with cystic fibrosis (CF) and may cause various severe infections, such as bronchitis.[] The chance for recovery is poor for people with advanced chronic bronchitis.[] Cystic fibrosis patients are known to produce abundant, purulent sputum consisting mainly of DNA and cellular debris.[]

  • Pseudomonas Aeruginosa

    Cystic Fibrosis 4,49–54 ( 2005 ).[] Due to the poor outcome of Pseudomonas aeruginosa skull base osteomyelitis, prolonged outpatient parenteral antibiotic therapy administered by continuous infusion could be[] Abstract Pseudomonas aeruginosa has been amongst the top 10 'superbugs' worldwide and is causing infections with poor outcomes in both humans and animals.[]

  • Chronic Sinusitis

    Cystic fibrosis is a lethal genetic disorder whose victims currently have a median life span of approximately 30 years.[] PURPOSE OF REVIEW: Biofilms have been observed on the sinus mucosa of patients with chronic rhinosinusitis and are associated with poor clinical outcomes after surgery.[] Preoperative CT findings prior to sinus surgery may be poor predictors of surgical outcomes. [46] The goal in surgical treatment is to reestablish sinus ventilation and to[]

  • Pseudomonas Infection

    Abstract The clinical significance of the high prevalence of positive immediate skin tests in cystic fibrosis is unclear.[] While Pseudomonas infection in patients with bronchiectasis is common and linked to poor outcomes, diagnosing a persistent infection is not always straightforward.[] Abstract The discovery of the cystic fibrosis gene has provided new approaches to gene therapy and drug therapy.[]

  • Ileus

    While neonates with cystic fibrosis invariably suffer from meconium ileus, almost 21% of patients with meconium ileus do not have cystic fibrosis.[] Umpierrez, Hyperglycemia During Total Parenteral Nutrition: An important marker of poor outcome and mortality in hospitalized patients, Diabetes Care, 33, 4, (739), (2010)[] Meconium ileus is the presenting clinical manifestation of cystic fibrosis in 10 to 20% of cases. Of infants with meconium ileus, 80 to 90% have cystic fibrosis.[]

  • Vitamin D Deficiency

    Unfortunately, the prevalence of vitamin D deficiency in patients with intestinal malabsorption syndromes, including cystic fibrosis (CF), celiac disease (CD), short bowel[] The aim of this trial is to determine if vitamin D deficiency is a modifiable risk factor for poor outcome after THR/TKR.[] Fibrosis Unit, "Aghia Sophia" Children's Hospital, Athens, Greece.[]

  • Cystic Fibrosis

    Cystic fibrosis is usually recognized in infancy or early childhood.[] Progression to diabetes has been linked to poor outcomes in CF including loss of pulmonary function and increased mortality among females.[] […] overall clinical outcome.[]

  • Intestinal Obstruction

    In individuals with cystic fibrosis, mucus builds up along the intestinal tract, slowing down the emptying of food.[] outcome in individuals with SBO as the vast majority of patients subsequently diagnosed with an SBO initially present to the ED. 7 SBO: History and Physical When a patient[] Abstract The management of abdominal pain in cystic fibrosis can be complicated.[]

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