Hip Fractures Clinical Trial
Official title:
HIP Fracture Accelerated Surgical TreaTment And Care tracK (HIP ATTACK) Trial - Feasibility Pilot
There is preliminary evidence that suggests early surgical treatment of a hip fracture may improve patients' outcomes. The investigators propose to do a pilot randomized controlled trial (RCT) to assess the feasibility of a large RCT comparing accelerated surgical repair (i.e. surgery within 6 hours of a hip fracture diagnosis) versus standard care (typically surgery after 36-48 hours).
Hip fractures have devastating consequences: the 30-day mortality rate for men is 9% and for
women is 5%, and the risk of disability is substantial. Even among patients who are
community-dwelling prior to their hip fracture, 11% are bed-ridden and 16% are in a
long-term care facility after one year.
The trauma associated with a hip fracture results in pain, bleeding, and immobility. These
factors initiate inflammatory, hypercoaguable, stress, and catabolic states that can cause
medical complications, including death. Proposed mechanisms for increased mortality and
morbidity associated with delayed surgery include 1) complications related to a protracted
immobilization (e.g. venous thromboembolism, atelectasis and pneumonia, urinary tract
infections, pressure ulcers, and muscle mass loss) and 2) increased cardiovascular events.
Delay in surgery may result in protracted immobility and the associated complications, as
well as prolonged exposure to the hypercoagulable-inflammatory-sympathetic state which may
increase cardiovascular events. Observational data suggests that these mechanisms are indeed
important: delayed surgical repair is associated with increased mortality and morbidity
after a hip fracture.
A systematic review and meta-analysis of observational studies addressed the impact of
timing of surgery on the outcome after hip fracture. Five studies reported adjusted measures
for mortality. The pooled estimate, based on 721 deaths in 4,208 patients, suggested that
early surgical treatment (i.e. within the cut-off of the individual studies) of hip
fractures was associated with a significant reduction in mortality (adjusted risk ratio [RR]
0.81, 95% confidence interval [CI] 0.68-0.96).
It is possible that these observational data substantially underestimates the real potential
of early surgery. The reason is that the "early surgery" in these studies occurred within
24, 48 or 72 hours. If surgery could be uniformly undertaken within 6 hours, given the
potential benefits of earlier mobilization and minimization of the period of the
inflammatory hypercoagulable state, the benefits might be substantially greater. The
substantial impact of treatment of acute myocardial infarction (MI) or stroke within hours
adds credence to this possibility.
Despite the evidence, and the possibility that a larger effect might result from even
earlier surgery, current data supports only weak inferences. The evidence relies on
observational data and is therefore susceptible to residual confounding. The strength of
inference from current evidence does not lay a sufficient solid base to justify the
substantial system modification required to facilitate accelerated surgical access for all
hip fracture patients.
The main factors that cause surgical delay after a hip fracture are: 1) the patient presents
with comorbidities and surgery is deferred for preoperative diagnostics, risk
stratification, and medical optimization ("medical clearance") and 2) surgical operating
room and staff resources are not available because hip fractures have low priority in urgent
surgery lists ("queuing"). Both medical clearance and queuing are modifiable issues -
addressing these obstacles has the potential to substantially reduce surgical wait times.
Our ultimate goal is to undertake a large multicentre randomized controlled trial (RCT) of
accelerated surgical care (i.e., goal of surgery within 6 hours of diagnosis) versus usual
timing of surgery among elderly adults diagnosed with a hip fracture. This protocol is for a
pilot RCT that will inform the feasibility of undertaking a large RCT.
;
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor)
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