Table 10 Continuous infusion femoral nerve block versus placebo/no treatment

Table 10 Continuous infusion femoral nerve block versus placebo/no treatment: study details and qualitative outcomes














































































Study


n treatment/
control


Comparison


Supplemental


analgesic


VAS scores and type of pain, where specified


Time to first analgesic request


Use of supplemental analgesic


Other important outcomes


Edwards 1992


(LoE 1)


19/18


30 ml 0.25% bupivacaine into ipsilateral femoral nerve sheath after induction of anaesthesia, followed by continuous infusion of 0.125% bupivacaine at 6 ml/h for 24 h (Fem) vs. control (Cont)


Postop: IM papaveretum (10–20 mg) every 4 h, on request


Fem superior at the time points recorded (i.e. 4 and 24 h) (p<0.01, in both cases)


__


Number of papaveretum doses required in the 1st 24 h: Fem superior (p<0.01); total papaveretum dose in the 1st 24 h: Fem superior (p<0.01)


__


Hirst 1996


(LoE 1)


11/11


Pre-op 20 ml 0.5% bupivacaine and 1:200,000 epinephrine, postop continuous infusion 0.125% bupivacaine at 6 ml/h for 48 h (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 (in the next 72 h)


__


Morphine requirements: NS during assessment period (i.e. over 1st 48 h postop)


PONV


Nausea: Fem superior at 24 and 48 h (p values not reported)


Kaloul 2004 1st arm


(LoE 1)


20/20


Continuous femoral block with 30 ml 0.5% ropivacaine and 1:200,000 epinephrine bolus, followed by infusion of 0.2% ropivacaine at 12 ml/h for 48 h (Fem) vs. control (Cont)


Postop: PCA-morphine, IV, for 48 h; additional oral analgesia: oxycodone, acetaminophen, codeine


At rest: Fem superior at 6 and 24 h (p<0.0001, in both cases), but NS at 48 h; during physical therapy: NS


__


0–48 h morphine consumption: Fem superior (p=0.0002)


__


Kaloul 2004 2nd arm


(LoE 1)


20/20


Continuous lumbar plexus block with 30 ml 0.5% ropivacaine and 1:200,000 epinephrine bolus, followed by infusion of 0.2% ropivacaine at 12 ml/h for 48 h (Lumb) vs. control (Cont)


Postop: PCA-morphine, IV, for 48 h; additional oral analgesia: oxycodone, acetaminophen, codeine


At rest: Lumb superior at 6 and 24 h (p<0.0001, in both cases), but NS at 48 h; during physical therapy: NS


__


0–48 h morphine consumption: Lumb superior (p<0.0001)


__


Ganapathy 1999


(LoE 1)


20/22/20


 


Modified continuous femoral block with 30 ml, followed by infusion at 10 ml/h for 48 h: 0.1% bupivacaine (LowBup) vs. 0.2% bupivacaine (HighBup) vs. saline (Cont)


Postop: PCA-morphine, IV


At rest and during activity: NS, except on day of surgery, when both LowBup and HighBup superior to Cont (p<0.05, in all cases)


__


Morphine consumption: HighBup superior to control (p<0.05) during first 4 h postop and from 8 am to 8 pm on day 1, but not during the night of surgery; total morphine consumption and hourly morphine use: NS


PONV


NS


Functional Outcomes


ROM: HighBup superior on day 1 only (p<0.05)


Serpell 1991


(LoE 2)


13/16


Postop lumbar plexus block with 0.3 ml/kg 0.5% bupivacaine, with additional doses at 68 h intervals (Fem) vs. control (Cont)


Postop: PCA-morphine,IV; additionally, 10 mg IM morphine and 1 g oral paracetamol was available if required


NS at the time points recorded (i.e. at 24 and 48 h)


__


0–48 h: Fem superior (p<0.05); additional analgesia (oral/IM): NS


PONV


NS


Singelyn 1998


(LoE 1)


15/15


Continuous femoral block with 37 ml 0.25% bupivacaine and 1:200,000 epinephrine, followed by infusion of 0.125% bupivacaine with0.1 ug/ml sufentanil and 1 ug/ml clonidine at 10 ml/h (Fem) vs. control (Cont)


Postop: 1 g IV paracetamol, followed by 10–20 mg IM piritramide if pain scores remained unchanged after 30 min


At rest: Fem superior at all time points (i.e. at 4, 24 and 48 h) (p<0.05, in all cases); on movement: Fem superior at 4 and 24 h (p<0.05, in both cases), but NS at 48 h


__


NS over 48 h postop


PONV


Nausea and/or vomiting: NS


Functional Outcomes


Flexion: Fem superior on day 1 (p=0.009), from day 2 to discharge (p<0.001) and at 6 weeks (p=0.03), but NS at 3 months; number of days required to obtain 90-degree flexion: Fem superior (p<0.001); number of patients discharged with <90-degree flexion: Fem superior (p=0.02); first ambulation: Fem superior (p=0.02)


Hospital stay


Length of hospital stay:


Fem superior (p<0.001)