Drug Burden Index and Its Association With Hip Fracture Among Older Adults:A National Population-Based Study

被引:22
|
作者
Jamieson, Hamish A. [1 ,2 ]
Nishtala, Prasad S. [1 ]
Scrase, Richard [3 ,4 ]
Deely, Joanne M. [1 ]
Abey-Nesbit, Rebecca [1 ]
Hilmer, Sarah N. [5 ,7 ]
Abernethy, Darrell R. [6 ]
Berry, Sarah D. [7 ]
Mor, Vincent [8 ]
Lacey, Cameron J. [1 ,9 ]
Schluter, Philip J. [10 ,11 ]
机构
[1] Univ Otago, Dept Med, Christchurch, New Zealand
[2] Burwood Hosp, Older Persons Hlth Specialist Serv, Christchurch, New Zealand
[3] Univ Otago, Sch Pharm, Dunedin, New Zealand
[4] Canterbury Dist Hlth Board, Dept Nursing, Christchurch, New Zealand
[5] Univ Sydney, Sch Med, Kolling Inst Med Res, Cognit Decline Partnership Ctr,Ageing & Pharmacol, St Leonards, NSW, Australia
[6] US Dept Hlth & Human Serv, US FDA, Drug Safety Off Clin Pharmacol, Baltimore, MD USA
[7] Harvard Med Sch, Beth Israel Deaconess Med Ctr, Dept Med, Boston, MA 02115 USA
[8] Brown Univ, Sch Publ Hlth, Dept Hlth Serv Policy & Practice, Providence, RI 02912 USA
[9] West Coast Dist Hlth Board, Greymouth, New Zealand
[10] Univ Canterbury, Coll Educ Hlth & Human Dev, Sch Hlth Sci, Christchurch, New Zealand
[11] Univ Queensland, Primary Care Clin Unit, Sch Clin Med, Brisbane, Qld, Australia
关键词
Polypharmacy; Medications; RAI; Falls; PHYSICAL FUNCTION; RISK-FACTORS; FALLS; ANTIDEPRESSANTS; MORTALITY; PRESCRIPTIONS; POLYPHARMACY; MEDICATIONS; OUTCOMES;
D O I
10.1093/gerona/gly176
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Background: The Drug Burden Index (DBI) calculates the total sedative and anticholinergic load of prescribed medications and is associated with functional decline and hip fractures in older adults. However, it is unknown if confounding factors influence the relationship between the DBI and hip fractures. The objective of this study was to evaluate the association between the DBI and hip fractures, after correcting for mortality and multiple potential confounding factors. Methods: A competing-risks regression analysis conducted on a prospectively recruited New Zealand community-dwelling older population who had a standardized (International Resident Assessment Instrument) assessment between September 1, 2012, and October 31, 2015, the study's end date. Outcome measures were survival status and hip fracture, with time-varying DBI exposure derived from 90-day time intervals. The multivariable competing-risks regression model was adjusted for a large number of medical comorbidities and activities of daily living. Results: Among 70,553 adults assessed, 2,249 (3.2%) experienced at least one hip fracture, 20,194 (28.6%) died without experiencing a fracture, and 48,110 (68.2%) survived without a fracture. The mean follow-up time was 14.9 months (range: 1 day, 37.9 months). The overall DBI distribution was highly skewed, with median time-varying DBI exposure ranging from 0.93 (Q(1) = 0.0, Q(3) = 1.84) to 0.96 (Q(1) = 0.0, Q(3) = 1.90). DBI was significantly related to fracture incidence in unadjusted (p < .001) and adjusted (p < .001) analyses. The estimated subhazard ratio was 1.52 (95% confidence interval: 1.28-1.81) for those with DBI > 3 compared with those with DBI = 0 in the adjusted analysis. Conclusions: In this study, increasing DBI was associated with a higher likelihood of fractures after accounting for the competing risk of mortality and adjusting for confounders. The results of this unique study are important in validating the DBI as a guide for medication management and it could help reduce the risk of hip fractures in older adults.
引用
收藏
页码:1127 / 1133
页数:7
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