The effect of a pre- and postoperative orthogeriatric service on cognitive function in patients with hip fracture: randomized controlled trial (Oslo Orthogeriatric Trial)

BMC Medicine - Tập 12 - Trang 1-12 - 2014
Leiv Otto Watne1,2, Anne Cathrine Torbergsen2,3, Simon Conroy4, Knut Engedal2,5, Frede Frihagen6, Geir Aasmund Hjorthaug6, Vibeke Juliebo7, Johan Raeder2,8, Ingvild Saltvedt9,10, Eva Skovlund11, Torgeir Bruun Wyller1,2
1Oslo Delirium Research Group, Department of Geriatric Medicine, Oslo University Hospital, Oslo, Norway
2University of Oslo, Institute of Clinical Medicine, Oslo, Norway
3Department of General Internal Medicine, Oslo University Hospital, Norway
4Department of Cardiovascular Sciences, University of Leicester School of Medicine, Leicester, UK
5Norwegian Centre for Ageing and Health, Vestfold Mental Health Trust, Vestfold, Norway
6Department of Orthopaedic Surgery, Oslo University Hospital, Oslo, Norway
7Department of Cardiology, Oslo University Hospital, Oslo, Norway
8Department of Anesthesiology, Oslo University Hospital, Oslo, Norway
9Department of Geriatrics, St. Olav Hospital, University Hospital of Trondheim, Trondheim, Norway
10Department of Neuroscience, Norwegian University of Science and Technology (NTNU), Trondheim, Norway
11School of Pharmacy, University of Oslo, Oslo, Norway

Tóm tắt

Delirium is a common complication in patients with hip fractures and is associated with an increased risk of subsequent dementia. The aim of this trial was to evaluate the effect of a pre- and postoperative orthogeriatric service on the prevention of delirium and longer-term cognitive decline. This was a single-center, prospective, randomized controlled trial in which patients with hip fracture were randomized to treatment in an acute geriatric ward or standard orthopedic ward. Inclusion and randomization took place in the Emergency Department at Oslo University hospital. The key intervention in the acute geriatric ward was Comprehensive Geriatric Assessment including daily interdisciplinary meetings. Primary outcome was cognitive function four months after surgery measured using a composite outcome incorporating the Clinical Dementia Rating Scale (CDR) and the 10 words learning and recalls tasks from the Consortium to Establish a Registry for Alzheimer’s Disease battery (CERAD). Secondary outcomes were pre- and postoperative delirium, delirium severity and duration, mortality and mobility (measured by the Short Physical Performance Battery (SPPB)). Patients were assessed four and twelve months after surgery by evaluators blind to allocation. A total of 329 patients were included. There was no significant difference in cognitive function four months after surgery between patients treated in the acute geriatric and the orthopedic wards (mean 54.7 versus 52.9, 95% confidence interval for the difference -5.9 to 9.5; P = 0.65). There was also no significant difference in delirium rates (49% versus 53%, P = 0.51) or four month mortality (17% versus 15%, P = 0.50) between the intervention and the control group. In a pre-planned sub-group analysis, participants living in their own home at baseline who were randomized to orthogeriatric care had better mobility four months after surgery compared with patients randomized to the orthopedic ward, measured with SPPB (median 6 versus 4, 95% confidence interval for the median difference 0 to 2; P = 0.04). Pre- and postoperative orthogeriatric care given in an acute geriatric ward was not effective in reducing delirium or long-term cognitive impairment in patients with hip fracture. The intervention had, however, a positive effect on mobility in patients not admitted from nursing homes. ClinicalTrials.gov NCT01009268 Registered November 5, 2009

Tài liệu tham khảo

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