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Both groups were eligible to receive radiotherapy or other palliative treatment as required.
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For observational studies, only those which involved control groups without exposure to bisphosphonates and reported the proportion of patients with AF on both bisphosphonate exposed and unexposed groups were eligible because our aim is to identify the risk of AF from bisphosphonates exposure.
Looking first at eligibility for screening, the same proportions from the two groups were eligible for screening (93%).
In the predecessor program, the Medicare Physician Group Practice Demonstration, participating doctor groups were eligible for up to 80percentt of any savings they generated if they could also show improvement on 32 quality measures.
All women in the intervention and control groups were eligible to participate in the exit interviews.
After 12-months, the 'usual care' groups were eligible to receive the appropriate interventions.
Trials using a factorial design with multiple intervention groups were eligible for inclusion.
Third, families and clinicians of diverse cultural groups were eligible to participate and informed of the study.
Experimental [randomised controlled trials (RCTs) and non-randomised controlled trials] and observational studies with control groups were eligible for inclusion in this systematic review.
Men and women of all ethnic groups were eligible if they were > 16 years old with an ECOG performance status of 0 2 and any proven solid tumor for which no curative or standard treatment was available, regardless of prior therapy.
All men and women employed in these organisations for more than 6 months in any year between 1991 and 2005, and from the full spectrum of socioeconomic groups were eligible (n=151 901).
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