TY - JOUR
T1 - Minimally invasive versus open transforaminal lumbar interbody fusion for treatment of degenerative lumbar disease
T2 - systematic review and meta-analysis
AU - Phan, Kevin
AU - Rao, Prashanth J.
AU - Kam, Andrew C.
AU - Mobbs, Ralph J.
PY - 2015/5/7
Y1 - 2015/5/7
N2 - Purpose: While open TLIF (O-TLIF) remains the mainstay approach, minimally invasive TLIF (MI-TLIF) may offer potential advantages of reduced trauma to paraspinal muscles, minimized perioperative blood loss, quicker recovery and reduced risk of infection at surgical sites. This meta-analysis was conducted to provide an updated assessment of the relative benefits and risks of MI-TLIF versus O-TLIF. Methods: Electronic searches were performed using six databases from their inception to December 2014. Relevant studies comparing MI-TLIF and O-TLIF were included. Data were extracted and analysed according to predefined clinical end points. Results: There was no significant difference in operation time noted between MI-TLIF and O-TLIF cohorts. The median intraoperative blood loss for MI-TLIF was significantly lower than O-TLIF (median: 177 vs 461 mL; (weighted mean difference) WMD, −256.23; 95 % CI −351.35, −161.1; P < 0.00001). Infection rates were significantly lower in the minimally invasive cohort (1.2 vs 4.6 %; relative risk (RR), 0.27; 95 %, 0.14, 0.53; I2 = 0 %; P = 0.0001). VAS back pain scores were significantly lower in the MI-TLIF group compared to O-TLIF (WMD, −0.41; 95 % CI −0.76, −0.06; I2 = 96 %; P < 0.00001). Postoperative ODI scores were also significantly lower in the minimally invasive cohort (WMD, −2.21; 95 % CI −4.26, −0.15; I2 = 93 %; P = 0.04). Conclusions: In summary, the present systematic review and meta-analysis demonstrated that MI-TLIF appears to be a safe and efficacious approach compared to O-TLIF. MI-TLIF is associated with lower blood loss and infection rates in patients, albeit at the risk of higher radiation exposure for the surgical team. The long-term relative merits require further validation in prospective, randomized studies.
AB - Purpose: While open TLIF (O-TLIF) remains the mainstay approach, minimally invasive TLIF (MI-TLIF) may offer potential advantages of reduced trauma to paraspinal muscles, minimized perioperative blood loss, quicker recovery and reduced risk of infection at surgical sites. This meta-analysis was conducted to provide an updated assessment of the relative benefits and risks of MI-TLIF versus O-TLIF. Methods: Electronic searches were performed using six databases from their inception to December 2014. Relevant studies comparing MI-TLIF and O-TLIF were included. Data were extracted and analysed according to predefined clinical end points. Results: There was no significant difference in operation time noted between MI-TLIF and O-TLIF cohorts. The median intraoperative blood loss for MI-TLIF was significantly lower than O-TLIF (median: 177 vs 461 mL; (weighted mean difference) WMD, −256.23; 95 % CI −351.35, −161.1; P < 0.00001). Infection rates were significantly lower in the minimally invasive cohort (1.2 vs 4.6 %; relative risk (RR), 0.27; 95 %, 0.14, 0.53; I2 = 0 %; P = 0.0001). VAS back pain scores were significantly lower in the MI-TLIF group compared to O-TLIF (WMD, −0.41; 95 % CI −0.76, −0.06; I2 = 96 %; P < 0.00001). Postoperative ODI scores were also significantly lower in the minimally invasive cohort (WMD, −2.21; 95 % CI −4.26, −0.15; I2 = 93 %; P = 0.04). Conclusions: In summary, the present systematic review and meta-analysis demonstrated that MI-TLIF appears to be a safe and efficacious approach compared to O-TLIF. MI-TLIF is associated with lower blood loss and infection rates in patients, albeit at the risk of higher radiation exposure for the surgical team. The long-term relative merits require further validation in prospective, randomized studies.
KW - Degenerative
KW - Lumbar
KW - Minimally invasive
KW - Spine
KW - TLIF
KW - Transforaminal lumbar interbody fusion
UR - http://www.scopus.com/inward/record.url?scp=84939955544&partnerID=8YFLogxK
U2 - 10.1007/s00586-015-3903-4
DO - 10.1007/s00586-015-3903-4
M3 - Article
C2 - 25813010
AN - SCOPUS:84939955544
VL - 24
SP - 1017
EP - 1030
JO - European Spine Journal
JF - European Spine Journal
SN - 0940-6719
IS - 5
ER -