Patient function after arthroplasty should ideally quickly improve.
It is not known which peri-operative function assessments predict
length of stay (LOS) and short-term functional recovery. The objective
of this study was to identify peri-operative functions assessments
predictive of hospital LOS and short-term function after hospital discharge
in hip or knee arthroplasty patients. In total, 108 patients were assessed peri-operatively with the
timed-up-and-go (TUG), Iowa level of assistance scale, post-operative
quality of recovery scale, readiness for hospital discharge scale,
and the Western Ontario and McMaster Osteoarthritis Index (WOMAC).
The older Americans resources and services activities of daily living
(ADL) questionnaire (OARS) was used to assess function two weeks
after discharge. Objectives
Methods
Objectives. Effective analgesia after total knee arthroplasty (TKA) improves
patient satisfaction, mobility and expedites discharge. This study
assessed whether continuous femoral nerve infusion (CFNI) was superior
to a single-shot femoral nerve block in primary TKA surgery completed
under subarachnoid blockade including morphine. Methods. We performed an adequately powered, prospective, randomised,
placebo-controlled trial comparing CFNI of 0.125% bupivacaine versus normal
saline following a single-shot femoral nerve block and subarachnoid
anaesthesia with intrathecal morphine for primary TKA. Patients
were randomised to either treatment (CFNI 0 ml to 10 ml/h 0.125%
bupivacaine) or placebo (CFNI 0 ml to 10 ml/h normal saline). Both
groups received a single-shot femoral nerve block (0.25% 20 ml bupivacaine)
prior to placement of femoral nerve catheter and subarachnoid anaesthesia with
intrathecal morphine. All patients had a standardised analgesic
protocol. The primary end point was post-operative visual analogue
scale (VAS) pain score over 72 hours post-surgery. Secondary outcomes
were morphine equivalent dose, range of movement, side effects,
and length of stay. Results. A total of 86 patients were recruited. Treatment and placebo
groups were comparable. No significant difference was found in VAS
pain scores, total morphine equivalent requirements, side effects,
range of movement, motor block, or
