Experience of a systematic approach to care and prevention of fragility fractures in New Zealand.
Author
Gill, Christine EllenMitchell, Paul James
Clark, Jan
Cornish, Jillian
Fergusson, Peter
Gilchrist, Nigel
Hayman, Lynne
Hornblow, Sue
Kim, David
Mackenzie, Denise
Milsom, Stella
von Tunzelmann, Adrienne
Binns, Elizabeth
Fergusson, Kim
Fleming, Stewart
Hurring, Sarah
Lilley, Rebbecca
Miller, Caroline
Navarre, Pierre
Pettett, Andrea
Sankaran, Shankar
Seow, Min Yee
Sincock, Jenny
Ward, Nicola
Wright, Mark
Close, Jacqueline Clare Therese
Harris, Ian Andrew
Armstrong, Elizabeth
Hallen, Jamie
Hikaka, Joanna
Kerse, Ngaire
Vujnovich, Andrea
Ganda, Kirtan
Seibel, Markus Joachim
Jackson, Thomas
Kennedy, Paul
Malpas, Kirsten
Dann, Leona
Shuker, Carl
Dunne, Colleen
Wood, Philip
Magaziner, Jay
Marsh, David
Tabu, Irewin
Cooper, Cyrus
Halbout, Philippe
Javaid, Muhammad Kassim
Åkesson, Kristina
Mlotek, Anastasia Soulié
Brûlé-Champagne, Eric
Harris, Roger
Date
2022-08-02Journal
Archives of OsteoporosisPublisher
Springer NatureType
Article
Metadata
Show full item recordAbstract
This narrative review describes efforts to improve the care and prevention of fragility fractures in New Zealand from 2012 to 2022. This includes development of clinical standards and registries to benchmark provision of care, and public awareness campaigns to promote a life-course approach to bone health. Purpose: This review describes the development and implementation of a systematic approach to care and prevention for New Zealanders with fragility fractures, and those at high risk of first fracture. Progression of existing initiatives and introduction of new initiatives are proposed for the period 2022 to 2030. Methods: In 2012, Osteoporosis New Zealand developed and published a strategy with objectives relating to people who sustain hip and other fragility fractures, those at high risk of first fragility fracture or falls and all older people. The strategy also advocated formation of a national fragility fracture alliance to expedite change. Results: In 2017, a previously informal national alliance was formalised under the Live Stronger for Longer programme, which includes stakeholder organisations from relevant sectors, including government, healthcare professionals, charities and the health system. Outputs of this alliance include development of Australian and New Zealand clinical guidelines, clinical standards and quality indicators and a bi-national registry that underpins efforts to improve hip fracture care. All 22 hospitals in New Zealand that operate on hip fracture patients currently submit data to the registry. An analogous approach is ongoing to improve secondary fracture prevention for people who sustain fragility fractures at other sites through nationwide access to Fracture Liaison Services. Conclusion: Widespread participation in national registries is enabling benchmarking against clinical standards as a means to improve the care of hip and other fragility fractures in New Zealand. An ongoing quality improvement programme is focused on eliminating unwarranted variation in delivery of secondary fracture prevention.Rights/Terms
© 2022. International Osteoporosis Foundation and Bone Health and Osteoporosis Foundation.Identifier to cite or link to this item
http://hdl.handle.net/10713/19520ae974a485f413a2113503eed53cd6c53
10.1007/s11657-022-01138-1