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Download Available titles for reviews in cystic fibrosis
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Full list of priority titles for the Cochrane Cystic Fibrosis & Genetic Disorders Group Please click on the links below to go to the different areas of our scope. Coagulopathy reviews Cystic fibrosis reviews Haemoglobinopathy reviews Inborn errors of metabolism reviews Coagulopathy reviews (priority reviews are highlighted in red) Management of coagulation inhibitors for congenital deficiencies Replacement coagulation inhibitors for congenital deficiencies Surgery for chronic haemarthropathy in people with haemophilia Non-pharmacological interventions for treating heavy menstrual bleeding (menorrhagia) in women with bleeding disorders Diagnostic strategies to assess anti-factor VIII antibodies (Diagnostic test accuracy review) Return to top of document Cystic fibrosis reviews (priority reviews are highlighted in red) Complications in cystic fibrosis Lung transplant for cystic fibrosis Surgical interventions for nasal polyps in cystic fibrosis Treatment for urinary incontinence in cystic fibrosis Correcting the basic defect in cystic fibrosis/Gene therapy ? Correcting the basic defect in cystic fibrosis/Mucus clearance ? Gastrointestinal & nutrition High strength pancreatic enzyme supplements versus other enzyme formulations for cystic fibrosis Oxygen & ventilatory support Endotracheal intubation for cystic fibrosis Physiotherapy & exercise Physical therapies for postural abnormalities in people with cystic fibrosis Pulmonary infection Antibiotic therapy for chronic infection with Burkholderia cepacia complex in people with cystic fibrosis Renal-sparing antibiotic strategies for cystic fibrosis Return to top of document Haemoglobinopathy reviews (priority reviews are highlighted in red) Sickle cell disease Anticoagulants for deep vein thrombosis in people with sickle cell disease Management of opioid addiction in sickle cell disease Screening for central nervous system damage in sickle cell disease Screening for retinopathy in sickle cell disease Surgery for retinopathy in sickle cell disease Treatment for auditory impairment in sickle cell disease Treatment for cardiomyopathy in sickle cell disease Treatment for hepato-billiary complications in sickle cell disease Interventions for neuro-cognitive impairment in sickle cell disease Management of obesity in people with beta-thalassemia* and sickle cell disease Metformin for the induction of foetal haemoglobin (HbF) in people with sickle cell disease Thalassaemias* (see above) Management of fertility for people with thalassaemia major Management of pregnancy for people with thalassaemia major Treatment for endocrine abnormalities in people with thalassaemia major Management of diabetes mellitus in people with beta-thalassemia major and intermedia Return to top of document Inborn errors of metabolism reviews (priority reviews are highlighted in red) Amino acid disorders Dietary interventions for maple syrup urine disease Newborn screening for glutaric aciduria type 1 Carbamyl glutamate for neonatal hyperammonaemia caused by propionic or methylmalonic acidaemia Vigabatrin for succinic semialdehyde dehydrogenase (SSADH) deficiency Newborn screening for tyrosinaemia type 1 Glycogen storage diseases Granulocyte colony stimulating factor for glycogen storage disease type 1b (glucose-6phoshpate transferase deficiency) Lysosomal storage diseases High protein diet for Pompe's disease Docosahexanoic acid (DHA) for Zellweger spectrum disorder Others Haemo and peritoneal dialysis for managing hyperammonaemia Newborn screening for maple syrup urine disease (MSUD) Newborn screening for medium chain acyl coA dehydrogenase (MCAD) deficiency Simvastatin for Smith-Lemli-Opitz syndrome Lorenzo's oil for X-linked adrenoleukodystrophy Statins for X-linked adrenoleukodystrophy Return to top of document
