Across all treatments for osteoporosis, patients prefer efficacy to dosing
When ranking osteoporosis treatment attributes by “importance,” postmenopausal women* consistently ranked drug effectiveness ahead of dosing frequency
Fracture risk reduction—consistently rated as more important than dosing frequency
- Drug effectiveness: How effective the drug is (eg, ability to reduce the risk of fractures).
- Dosing frequency: How often you take the drug (eg, daily, weekly, monthly).
- Relative to other attributes on the survey, “Drug effectiveness” ranked higher than “Dosing procedure” (90%), “Time on market” (89%), “Formulation” (81%), “Drug interactions” (71%), “Out-of-pocket costs” (67%), and “Side effects” (51%).
- Among the total sample, 73% ranked “Drug effectiveness” as either the #1, #2, or #3 attribute of treatment. Results across other assessed attributes included “Side effects” (76%), “Drug interactions” (52%), “Out-of-pocket costs” (42%), “Dosing frequency” (17%), “Formulation” (17%), “Dosing procedure” (10%), and “Time on market” (14%).
- Among the treated sample (n=421), 80% ranked “Drug effectiveness” as either the #1, #2, or #3 attribute of treatment. Results across other assessed attributes included “Side effects” (70%), “Drug interactions” (53%), “Out-of-pocket costs” (39%), “Dosing frequency” (22%), “Formulation” (17%), “Dosing procedure” (10%), and “Time on market” (9%).
The PREFER study1: an evaluation of patient preference among 8 key attributes of osteoporosis therapy
Study objective:
- To evaluate patient preference among 8 attributes of osteoporosis therapy among postmenopausal women diagnosed with or at risk of osteoporosis, regardless of whether they are currently taking therapy for osteoporosis.
Study inclusion criteria:
- Women 50 years or older identified as having a diagnosis of osteoporosis, being at risk of osteoporosis, or having a family history of osteoporosis based on their responses to the 2003 or 2004 National Health and Wellness Survey (NHWS), an Internet-based, cross-sectional survey of the healthcare attitudes, behaviors, and treatment choices of adult patients.
Study method and population:
- Data collected by invitational response to an online survey. Of the 5,634 eligible women invited to participate, 999 completed the survey (421 reported current treatment with at least one osteoporosis medication). Of these, 49% reported that they were diagnosed with osteoporosis in the NHWS, and the remaining 51% considered themselves at risk or had a family history of osteoporosis.
Study assessment:
- Participants completed a single, online survey, which asked them to rank attributes of osteoporosis therapies in order of importance and to rate the relative importance of each attribute. Patients were asked to evaluate the following product attribute: specific item in survey instrument (in the order in which the item appeared):
- Side effects: Side effects of the drug (eg, whether or not the drug can cause stomach/digestive problems)
- Out-of-pocket costs: Out-of-pocket costs of the drug (eg, how much money you have to pay for the drug yourself)
- Dosing frequency: How often you take the drug (eg, daily, weekly, monthly)
- Formulation: How you take the drug (eg, oral tablets, inhaled, injection, patch, or intravenous)
- Drug effectiveness: How effective the drug is (eg, ability to reduce the risk of fractures)
- Dosing procedure: Procedure for taking the drug (eg, what time of the day you have to take it; whether or not you have to take it with food; how long you have to wait to eat after taking it)
- Drug interaction: Whether or not the drug interacts with other drugs you take
- Time on market: How long the drug has been on the market
Important Information About FOSAMAX® (alendronate sodium) and FOSAMAX PLUS D
FOSAMAX and FOSAMAX PLUS D are contraindicated in patients with esophageal abnormalities which delay esophageal emptying (eg, stricture or achalasia) and in patients unable to stand or sit upright for at least 30 minutes. Patients at increased risk of aspiration should not receive FOSAMAX oral solution. FOSAMAX and FOSAMAX PLUS D are contraindicated in patients with hypocalcemia (see WARNINGS AND PRECAUTIONS) and in patients with hypersensitivity to any component of these products. Hypersensitivity reactions including urticaria and angioedema have been reported. FOSAMAX and FOSAMAX PLUS D, like other bisphosphonates, may cause local irritation of the upper gastrointestinal mucosa.
In postmarketing experience, severe and occasionally incapacitating bone, joint, and/or muscle pain has been reported in patients taking bisphosphonates that are approved for the prevention and treatment of osteoporosis. The time to onset of symptoms varied from one day to several months after starting the drug. Discontinue use if severe symptoms develop. Most patients had relief of symptoms after stopping treatment.
Osteonecrosis of the jaw, generally associated with tooth extraction and/or local infection, often with delayed healing, has been reported in patients taking bisphosphonates.
Reference: 1. Data available on request from Merck & Co., Inc., Professional Services-DAP, WP1-27, PO Box 4, West Point, PA 19486-0004. Please specify information package 20551433(1)-FOS.
