Systematic Reviews of Treatments for Anaemia

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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38 Resources Found
Results 1 to 20 displayed.
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Title:   Vaccines for preventing invasive salmonella infections in people with sickle cell disease
Publisher:   John Wiley and Sons, Ltd. for The Cochrane Collaboration
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...
Date:   Aug 2009

Title:   Erythropoietin or Darbepoetin for patients with cancer - meta-analysis based on individual patient data
Publisher:   John Wiley and Sons, Ltd. for The Cochrane Collaboration
Description:   People with cancer may develop a blood problem called anemia, due to the treatment or from the disease itself. They will have very low levels of healthy red blood cells, causing additional health problems.
Date:   Jul 2009

Title:   Oral iron supplementation for preventing or treating anaemia among children in malaria-endemic areas
Publisher:   John Wiley and Sons, Ltd. for The Cochrane Collaboration
Description:   Children commonly develop anaemia (low haemoglobin) after birth. Anaemia is associated with several ill-effects, including hindering motor development and learning skills, and it may have an adverse effect on immunity. Babies and children are therefore ...
Date:   Apr 2009

Title:   Antibiotics for treating osteomyelitis in people with sickle cell disease
Publisher:   John Wiley and Sons, Ltd. for The Cochrane Collaboration
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...
Date:   Apr 2009

Title:   Treatment for avascular necrosis of bone in people with sickle cell disease
Publisher:   John Wiley and Sons, Ltd. for The Cochrane Collaboration
Description:   There is currently insufficient evidence, in the form of randomised controlled trials, to assess the beneficial and harmful effects of specific therapies for avascular necrosis of bone in people with sickle cell disease. High quality randomised controll...
Date:   Mar 2009

Title:   Erythropoietin as an adjuvant treatment with (chemo) radiation therapy for head and neck cancer
Publisher:   John Wiley and Sons, Ltd. for The Cochrane Collaboration
Description:   Severe anaemia in cancer patients is linked with decreased tumour oxygen supply (hypoxia), which is associated with more rapid tumour progression, poor response to therapy and consequently has a negative impact on prognosis. Erythropoietin (EPO), a horm...
Date:   Feb 2009

Title:   Hematopoietic stem cell transplantation for children with sickle cell disease
Publisher:   John Wiley and Sons, Ltd. for The Cochrane Collaboration
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...
Date:   Nov 2008

Title:   Splenectomy versus conservative management for acute sequestration crises in people with sickle cell disease
Publisher:   John Wiley and Sons, Ltd. for The Cochrane Collaboration
Description:   In some people with sickle cell disease, red blood cells become trapped and destroyed in the spleen. This damages the spleen, which may become enlarged leading to splenic sequestration crises. These crises consist of abdominal pain, rapid heart rate and...
Date:   Nov 2008

Title:   Pre and peri-operative erythropoeitin for reducing allogeneic blood transfusions in colorectal cancer surgery.
Publisher:   John Wiley and Sons, Ltd. for The Cochrane Collaboration
Description:   Patients with cancer of the large bowel are often anaemic and sometimes receive transfusions which may be harmful. The medication erythropoietin can be used to increase hemoglobin levels in a variety of situations and several studies have looked at this...
Date:   Oct 2008

Title:   Antibiotics for treating acute chest syndrome in people with sickle cell disease
Publisher:   John Wiley and Sons, Ltd. for The Cochrane Collaboration
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...
Date:   Oct 2008

Title:   Prophylactic antibiotics for preventing pneumococcal infection in children with sickle cell disease
Publisher:   John Wiley and Sons, Ltd. for The Cochrane Collaboration
Description:   People with sickle cell disease (SCD) are especially prone to respiratory infections and blood poisoning. These infections are often caused by pneumococcal bacteria. Infections occur partly due to the spleen not working correctly, but also because damag...
Date:   Oct 2008

Title:   Inhaled nitric oxide for acute chest syndrome in people with sickle cell disease
Publisher:   John Wiley and Sons, Ltd. for The Cochrane Collaboration
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...
Date:   Oct 2008

Title:   Piracetam for reducing the incidence of painful sickle cell disease crises
Publisher:   John Wiley and Sons, Ltd. for The Cochrane Collaboration
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 ...
Date:   Oct 2008

Title:   Iron supplementation for reducing morbidity and mortality in children with HIV
Publisher:   John Wiley and Sons, Ltd. for The Cochrane Collaboration
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...
Date:   Sep 2008

Title:   Pneumococcal vaccines for sickle cell disease
Publisher:   John Wiley and Sons, Ltd. for The Cochrane Collaboration
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...
Date:   Sep 2008

Title:   Treatments for priapism in boys and men with sickle cell disease
Publisher:   John Wiley and Sons, Ltd. for The Cochrane Collaboration
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. ...
Date:   Sep 2008

Title:   Neonatal screening for sickle cell disease
Publisher:   John Wiley and Sons, Ltd. for The Cochrane Collaboration
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...
Date:   Aug 2008

Title:   Blood transfusion for preventing stroke in people with sickle cell disease
Publisher:   John Wiley and Sons, Ltd. for The Cochrane Collaboration
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...
Date:   Jul 2008

Title:   Inhaled bronchodilators for acute chest syndrome in people with sickle cell disease
Publisher:   John Wiley and Sons, Ltd. for The Cochrane Collaboration
Description:   Sickle cell disease is an inherited blood disorder. People with sickle cell disease often suffer from acute chest syndrome, although it is not known why. Acute chest syndrome can cause fever, coughing, chest pain and shortness of breath and can be life-...
Date:   Jul 2008

Title:   Fluid replacement therapy for acute episodes of pain in people with sickle cell disease
Publisher:   John Wiley and Sons, Ltd. for The Cochrane Collaboration
Description:   Sickle cell disease is a common genetic disorder characterised by periodic episodes of pain which usually happen again and again throughout life. These episodes occur when sickled cells obstruct blood vessels. The degree of pain may range from a mild di...
Date:   Jan 2008
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