Table 9: Single injection femoral nerve block versus placebo/no treatment/systemic analgesia: study details and qualitative outcomes
Study |
n treatment/ |
Comparison |
Supplemental analgesic |
VAS scores and type of pain, where specified |
Time to first analgesic request |
Use of supplemental analgesic |
Other important outcomes |
Hirst 1996(LoE 1) |
11/11 |
Pre-op single injection femoral nerve block with 20 ml 0.5% bupivacaine and 1:200,000 epinephrine (Fem) vs. “mock” femoral nerve blocks (Cont) |
Postop: PCA-morphine, IV |
Fem superior during passive flexion (30°) in recovery room (p<0.05); NS at other time points recorded (i.e. in the next 72 h) |
__ |
Morphine requirements: NS during assessment period (i.e. over 1st 48 h postop) |
PONVNausea: Fem superior at 24 and 48 h (p values not reported) |
29/28 |
Before induction of GA: femoral nerve block with 0.5% bupivacaine and 2% lidocaine (25 ml of LA solution injected) with 1:200,000 epinephrine (Fem) vs. 10 ml saline at site of femoral nerve (Cont) |
Postop: PCA-morphine, IV |
NS during assessment period (i.e. 1st 6 h postop) |
__ |
NS during assessment period (i.e. 1st 6 h postop) |
PONVNSComplicationsRespiratory depression: NS | |
(LoE 1) |
19/21 |
Pre-op single injection femoral nerve block with 30 ml 0.5% bupivacaine and 1:200,000 epinephrine (Fem) vs. sham femoral nerve block with 30 ml saline (Cont) |
Postop: PCA-morphine, IV; 5 mg oral oxycodone or 325 mg oral acetaminophen available every 4 h if required |
Fem superior on day of surgery (day 0), (p=0.002), but NS on days 1 and 2; average pain score (days 0–2): Fem superior (p=0.013) |
__ |
Morphine consumption: Fem superior on day 1 (p=0.003) and over the entire postop period (i.e. over days 0–3) (p=0.011) |
PONVNS Functional outcomes Degree of ambulation, ROM: NS ComplicationsSedation: Fem superior on day 1 (p=0.045), but NS on days 2 and 3; pruritus, urinary retention, dizziness: NS Hospital stayLength of hospital stay: NS |
(LoE 1) |
41/39 |
Pre-op :30 ml 0.375% bupivacaine with 5 µg/ml epinephrine into femoral sheath (Fem) vs. control (Cont) |
Background analgesia: spinal-epidural anaesthesia in both groups; postop: PCEA 0.06% bupivacaine + 10 µg/ml hydromorphone; oral analgesics (hydrocodone/acetaminophen or oxycodone/acetaminophen) on day 2 |
At rest VAS: NS; during physical therapy VAS: Fem superior on days 1 and 2 (p<0.05, in both cases); proportion patients reporting VAS score ³6 during physical therapy: Fem superior on day 1 (p=0.045) and day 2 (p=0.0062) |
__ |
PCEA–volume administered: NS |
Functional outcomesROM: Fem superior on day 2 (p<0.05), but NS on days 1 or 3; ambulation distance, independent transfer, continuous passive motion flexion, use of walker, progression to cane, stair use: NSComplicationsHospital stayLength of hospital stay: NS |
Ng 2001(LoE 1) |
12/12/12/12 |
Intra-op femoral nerve block with 30 ml 0.25% ropivacaine (LowRop) vs. femoral nerve block with 30 ml 0.5% ropivacaine (HighRop) vs. femoral nerve block with 30 ml 0.25% bupivacaine (Bup) vs. sham block with 30 ml saline (Cont) |
Postop: PCA-morphine, IV; 1g oral acetaminophen every 6 h, starting 24 h after surgery |
__ |
__ |
Cumulative morphine consumption: all treatment groups (LowRop, HighRop, Bup) superior to Cont at 1, 8, 24 and 48 h (p<0.05, in all cases); HighRop, Bup superior to Cont at 4 h (p<0.05, in both cases); NS between HighRop, LowRop and Bup |
Pain VRS pain scores (0=no pain, 3=severe pain) At rest and on movement: all treatment groups (LowRop, HighRop, Bup) superior to Cont at 1, 4 and 8 h (p<0.01, in all cases); HighRop and Bup superior to Cont at 24 h (p<0.01, in both cases) and LowRop superior to Cont at 24 h (p<0.05); all comparisons NS at 48 h at rest; HighRop and Bup superior to Cont at 48 h (p<0.01 in both cases) and LowRop superior to Cont (p<0.05) on movement at 48 h; NS between HighRop, LowRop and BupComplicationsPONV, pruritus, sedation: NS Hospital stayLength of hospital stay: NS |
(LoE 2) |
21/21 |
At first expression of pain postop: femoral block with 40 ml 0.375% bupivacaine (Bup) vs. up to 0.2 mg/kg IV piritramide, until clear decrease in pain, then 100 mg rectal diclofenac and PCA IV piritramide (0.025 mg/kg bolus, 10-min lockout) (Cont) |
Postop: femoral block or piritramide, dependent on study group |
NS during the assessment period (0–180 min) |
__ |
__ |
PONV NS |
(LoE 1) |
12/12 |
Postop femoral nerve block with 30 ml 0.25% bupivacaine with 1:400,000 epinephrine and sham sciatic nerve block (Fem) vs. sham femoral and sham sciatic injections (Cont) |
Postop: PCA-morphine, IV |
At rest: Fem superior for first 8 h post-PACU (p<0.05, in all cases); data incomplete after the 8-h measurement; NS during physical therapy |
__ |
Fem superior on days 0 and 1 (p<0.02, in both cases), but NS on days 2 or 3 |
Complications Nausea, sedation, pruritus: NS |
(LoE 1) |
15/15 |
Postop 40 ml femoral nerve injection: 0.25% bupivacaine with 1:100,000 epinephrine (Fem) vs. saline (Cont) |
Postop: PCA-morphine, IV |
Fem superior at 1 h (PACU) (p<0.01); at rest and during rehab on day 1: Fem superior (p<0.01; p<0.05, respectively), but NS on days 2 and 3 |
__ |
Morphine requirements: Fem superior in PACU (p<0.01) and on day 1 (p<0.05), but NS on days 2 and 3; total morphine consumption: Fem superior (p<0.05) |
Functional Outcomes Ambulation: Fem superior (larger proportion in Bup able to ambulate to preset distance goals) (p<0.05); distance ambulated at discharge: Fem superior (p<0.01); knee flexion: Fem superior on day 2 (p<0.05), but NS on discharge Complications Overall incidence of morphine-related side-effects (e.g. nausea): NS Hospital stay Length of hospital stay: Fem superior (p<0.05) |