We propose that bisphosphonate effectiveness
may then be estimated by measuring the change in fracture incidence over time on therapy. For this study, administrative billing data were used to follow three cohorts of women aged 65 and older after starting therapy either on alendronate, risedronate, or ibandronate. Within each cohort, the baseline incidence of clinical fractures check details at the hip, vertebral, and nonvertebral sites was defined by the initial 3-month period after starting therapy. Relative to these baselines, we then compared the fracture incidence during the subsequent 12 months on therapy. Materials and methods Data source Computerized records of administrative billing provide a convenient data source for studying drug use and outcomes in large populations. Records include patient-level data of: (1) inpatient and outpatient services specified by diagnoses codes of the International Classification of Diseases, 9th Revision, Clinical Modification (ICD-9-CM);
click here (2) retail and mail-order pharmacy dispensations specified by national drug codes; and (3) demographic information including sex, age, and eligibility dates of health plan coverage. The data for this study, inclusive of January 2000–December 2007, originated from two mutually exclusive sources: Ingenix Lab/Rx (Eden Prairie, MN, USA) and Medstat MarketScan
(Ann Arbor, MI, USA). During that period, the average number of eligible enrollees was 14 million in Medstat, representing multiple health plans, Buspirone HCl and 10 million in Ingenix, representing a single health plan. Geographically, one half of this population was located in Michigan, California, Florida, Ohio, Georgia, or Texas and one half in the other 44 states. Study population The study population consisted of three cohorts—one prescribed alendronate, one prescribed risedronate, and one prescribed ibandronate. Subjects entered a cohort on the date of their initial filled EPZ015666 ic50 prescription for alendronate 70 mg/week, risedronate 35 mg/week, or ibandronate 150 mg/month during the time period of market introduction through December 2006. Market introduction was November 2000 for alendronate cohort, May 2002 for risedronate cohort, and April 2005 for ibandronate cohort. The initial bisphosphonate prescription was defined by a subject having at least 6 months of prior coverage in the data source without any other bisphosphonate use (e.g., another bisphosphonate type or dose). After 6 months without any bisphosphonate use, a subject was allowed to enter a new cohort (i.e., a subject could be in more than one cohort—1% of alendronate cohort, 4% of risedronate cohort, and 20% of ibandronate cohort was preceded by inclusion in another cohort).