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Follow the links below to find systematic reviews of the evidence for the effectiveness of treatments for anaemia.
Reviewed July 2009
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| Title: |
Blood transfusions for treating acute chest syndrome in people with sickle cell disease
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| Publisher: |
John Wiley and Sons, Ltd. for The Cochrane Collaboration
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| Description: |
Sickle cell disease is an inherited blood condition affecting over 250 million people worldwide and is particularly common in Sub-Saharan Africa, South and Central America, Saudi Arabia, India and a number of Mediterranean countries. It is characterised...
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| Date: |
Oct 2009
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| Title: |
Vaccines for preventing invasive salmonella infections in people with sickle cell disease
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| Publisher: |
John Wiley and Sons, Ltd. for The Cochrane Collaboration
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| Description: |
Salmonella organisms are probably second only to pneumococcus among bacterial causes of infection in people with sickle cell disease. Infection with these bacteria can lead to complications and reduce the quality of life of people with the disease and s...
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| Date: |
Aug 2009
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| Title: |
Blood transfusion for preventing stroke in people with sickle cell disease
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| Publisher: |
John Wiley and Sons, Ltd. for The Cochrane Collaboration
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| Description: |
In sickle cell disease there are fewer red blood cells. This means less oxygen is carried to tissues and there are problems throughout the body. Sickled red blood cells can block blood vessels in the brain, leading to strokes. We aimed to compare long-t...
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| Date: |
Jun 2009
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| Title: |
Antibiotics for treating osteomyelitis in people with sickle cell disease
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| Publisher: |
John Wiley and Sons, Ltd. for The Cochrane Collaboration
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| Description: |
Sickle cell disease affects millions of people throughout the world. Osteomyelitis, a bone infection, is one of the major complications. Antibiotics are given to treat it, but there is no worldwide standard treatment. We searched for randomised controll...
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| Date: |
Apr 2009
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| Title: |
Treatment for avascular necrosis of bone in people with sickle cell disease
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| Publisher: |
John Wiley and Sons, Ltd. for The Cochrane Collaboration
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| Description: |
Many people with sickle cell disease experience bone death due to temporary or permanent loss of blood supply to parts of their bones. This can be very painful. The bones usually affected are the thigh bones at the hip joint and the arm bones at the sho...
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| Date: |
Mar 2009
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| Title: |
Erythropoiesis-stimulating agents for anaemia in chronic heart failure patients
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| Publisher: |
John Wiley and Sons, Ltd. for The Cochrane Collaboration
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| Description: |
Chronic heart failure is a disorder in which the heart is unable to pump blood and deliver oxygen adequately throughout the body. Patients with heart failure may also suffer from anaemia, a condition of reduced red blood cells and diminished ability of...
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| Date: |
Mar 2009
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| Title: |
Hematopoietic stem cell transplantation for children with sickle cell disease
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| Publisher: |
John Wiley and Sons, Ltd. for The Cochrane Collaboration
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| Description: |
Sickle cell disease is a genetic disorder mainly characterized by the presence of deformed, sickle-shaped red blood cells in the blood stream. These cells deprive tissues of blood and oxygen resulting in periodic and recurrent painful attacks. Complicat...
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| Date: |
Nov 2008
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| Title: |
Antibiotics for treating acute chest syndrome in people with sickle cell disease
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| Publisher: |
John Wiley and Sons, Ltd. for The Cochrane Collaboration
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| Description: |
Sickle cell disease affects millions of people throughout the world. Acute chest syndrome is a major cause of illness and death in people with sickle cell disease. Symptoms include fever, chest pain and a raised white blood cell count. Acute infection o...
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| Date: |
Oct 2008
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| Title: |
Inhaled nitric oxide for acute chest syndrome in people with sickle cell disease
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| Publisher: |
John Wiley and Sons, Ltd. for The Cochrane Collaboration
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| Description: |
Sickle cell disease is an inherited blood disorder affecting approximately 250 million people worldwide. Sickle-shaped red blood cells which are characteristic of sickle cell disease may block blood vessels causing pain, tissue death and even severe dam...
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| Date: |
Oct 2008
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| Title: |
Piracetam for reducing the incidence of painful sickle cell disease crises
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| Publisher: |
John Wiley and Sons, Ltd. for The Cochrane Collaboration
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| Description: |
Sickle cell disease is one of the most common genetic disorders and affects about 250 million people (5% of the world's population). It is characterised by sickle-shaped red blood cells which may block blood vessels. This can lead to pain and damage to ...
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| Date: |
Oct 2008
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| Title: |
Iron supplementation for reducing morbidity and mortality in children with HIV
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| Publisher: |
John Wiley and Sons, Ltd. for The Cochrane Collaboration
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| Description: |
Anaemia is one of the most common haematologic problem found in children with HIV/AIDS, second only to depletion of CD4/helper T lymphocytes. Anaemia in HIV-infected children can be caused by direct effects of HIV, other prevalent infections and opport...
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| Date: |
Sep 2008
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| Title: |
Pneumococcal vaccines for sickle cell disease
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| Publisher: |
John Wiley and Sons, Ltd. for The Cochrane Collaboration
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| Description: |
People with sickle cell disease are particularly prone to pneumococcal infection, which may be fatal. Children aged up to 23 months are at high risk, but usual polysaccharide pneumococcal vaccines may not work in this age group. New conjugate pneumococc...
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| Date: |
Sep 2008
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| Title: |
Treatments for priapism in boys and men with sickle cell disease
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| Publisher: |
John Wiley and Sons, Ltd. for The Cochrane Collaboration
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| Description: |
Priapism (the prolonged painful erection of the penis) is common in males with sickle cell disease (SCD). The length of time priapism lasts differs for different types and so does the medical treatment for it. Self-management approaches may be helpful. ...
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| Date: |
Sep 2008
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| Title: |
Neonatal screening for sickle cell disease
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| Publisher: |
John Wiley and Sons, Ltd. for The Cochrane Collaboration
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| Description: |
Sickle cell diseases are inherited and affect mainly people of African origin. The red blood cells are abnormally (sickle) shaped, which can lead to life-threatening complications. They are most likely to be fatal in the first few years of life since af...
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| Date: |
Aug 2008
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