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FAQ

   
What is ICUROS?

ICUROS is the The International Costs and Utilities Related to Osteoporotic Fractures Study. It is an international patient based study investigating the costs and health effects of osteoporotic fractures.

 
Why conduct ICUROS?

It is of great importance to have good estimates of costs and health effects for osteoporosis-related fractures when health economic analyses of osteoporosis are conducted. Today, the empirical data on individual costs and health effects in relation to fractures are very scarce, especially when it comes to the consequences of vertebral and wrist fractures. Previous evaluations have quite often been based on professional assumptions regarding clinical treatment praxis for each fracture. It is hence very important to evaluate the individual costs and health effects of fractures to be able to get well-founded results in cost-effectiveness studies concerning the treatment of osteoporosis.

 
Who is involved?

ICUROS is endorsed by the International Osteoporosis Foundation (IOF) and supported by a consortium of sponsors including Amgen, Novartis, Wyeth, Kyphon and Servier. The study is centrally administered by the European Health Economics (EHE).

 
What type of fractures and patients are included?

The fracture types included in ICUROS are hip, vertebral and wrist fractures. The patients are men and women over 50 years of age who suffers from an osteoporotic related fracture. The patient must also live in a private residence prior to the fracture.

 
What type of vertebral fractures will be studied?

Clinical vertebral fractures, confirmed by x-rays.

 
Why only include hip, vertebral and wrist fractures? There are other types of ostoporotic fractures!

These are the most common osteoporotic fractures, which are prevalent enough to enable a large enough sample for analysis and stable results.

 
What will be used as control group?

The patients themselves will serve as their own control by giving information on their resource use and quality of life before the fracture.

 
How do you manage patients with a cognitive impairment?

Patients who are severely cognitive impaired will not be able to participate in the study. The doctor in charge will judge whether a patient is capable of participating or not. As help, the doctor can use a Pfeiffer test, where the patient should score >3 to be eligible to participate. However, it should be noted that right after surgery, patients might score less, even though they should not be considered cognitive impaired. Therefore it is important that the doctor makes a professional judgment of the patient’s capability.

 
How are patients followed-up?

The patients will be contacted by phone at follow-ups.

 
When do patients come to the hospital?

The patients only go to the hospital when they find a reason to. The study does not inflict any extra hospital visits on the patients.

 
Will not the study itself affect resource use?

No, since all follow-ups are made by phone and since it is a naturalistic study, no extra resource use will occur due to the study.

 
Who should I contact if I want to participate?

Please send an email to: icuros@healtheconomics.se for further information

 
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