Research Article

Enhanced Recovery after an Innovative Percutaneous Endoscopic Transforaminal Lumbar Interbody Fusion for the Treatment of Lumbar Spinal Stenosis: A Prospective Observational Study

Table 4

Interventions and outcomes of included studies.

Study no.Surgical techniqueResection of articular processOperation time (minutes)Blood loss (ml)Spinal decompressionInternal fixation methodFusion rateComplications

1Endo-LIFNo174 (117–251)57.6 (30–100)NoBilateral PS59.6%8 patients RSE, 2 patients RN, and 2 patients PSC
2PE-TLIFNo60 ± 30NoneNoBilateral PS77%8 patients RPP and 13 patients AMC
3FE-MIS-TLIFYes133.9 ± 16.1(OS)
241.3 ± 36.5 (TS)
221.8 ± 98.5 (100–550)YesBilateral PS92.9%2 patients PNC
4pTLIFYes120 ± 30 (A or B)
240 ± 120 (C)
NoneNoBilateral PSNone3 patients TD and 2 patients SIP
5E-MIS-TLIFYes113.5 ± 6.3(105–120)65 ± 38 (30–190)YesBilateral PSNoneNo complications
6PTLIFNo77 (62–100)NoneNoBilateral PS88.9%1 patient PNC, 1 patient nonunion, and 1 patient revision
7UBEYes16585.5 ± 19.41YesBilateral PSNone2 patients dura tear and 3 patients postoperative hematoma
8Endo-TLIFYes174 (130–235)95 (50–200)YesBilateral PS100%2 patients transient nerve root paresthesia
9FELIFYesNoneNoneYesBilateral PSNoneNone
10BE-TLIFYes169 ± 1074 ± 9YesBilateral PSNone1 patient L5 paralysis and 1 patient dura tear
11PELIFYes167.5 ± 30.9 (135–220)70.0 ± 24.5 (50–100)YesBilateral PSNoneNo complication
12PE-TLIFYes285117.1 (30–300)YesBilateral PS100%1 patient disc ruptured and 1 patient temporary knee tendon hyperreflexia
13Endoscopic MIS-TLIFNo1 level: 84.5 ± 21.7
2 levels: 128.1 ± 48.6
1 level: 65.4 ± 76.6
2 levels: 74.7 ± 33.6
YesBilateral PS100%4 patients convert to general anesthesia, 2 patients cage migration, 1 patient osteomyelitis, and 1 patient endplate fracture
14ULIFYes158NoneYesBilateral PS25.9%(PF)
74.1%(DF)
3 patients dural tear, 1 patient hematoma, and 1 patient infection
15Endo-LIFYes184.3 ± 70.6
191.1 ± 32.4
38.5 ± 19.5
214.6 ± 61.6
YesSpinous process laminar screw95%EG: 3 patients low back pain, CG: 1 patient cerebrospinal fluid leakage, and 1 patient incision infection
16MIS-TLIFYes180.49 ± 35.19
164.02 ± 51.91
182.00 ± 106.19
191.30 ± 93.37
YesBilateral PSNoneEG: No complication and
CG: 1 patient hematoma
17PELIFYes213.8 ± 31.7 (185–324)25.0 ± 12.6 (15–50)YesBilateral PS100%2 patients symptom was not relieved or even aggravated,
1 patient disc mass remnant, 1 patient misplacement of L5 pedicle screw, and 1 patient asymptomatic cage subsidence
18pTLIFYesNoneNoneNoBilateral PSNone12 patients transitory and ipsilateral dysesthesia,
2 patients transitory and ipsilateral muscle weakness, and
3 patients sacroiliac joint pain
19PELIFYes109.4 (73–160)NoneNoBilateral PS100%1 patient paresthesia in both legs and
1 patient left knee pain
20Endo-TLIFYesNoneNoneYesBilateral PS100%No complication

CG: control group; VAS: visual analogue scale; RMDQ: Roland–Morris Disability Questionnaire; EG: experiment group; ETD: endoscopic transforaminal decompression; LIF: lumbar interbody fusion; PPSI: percutaneous pedicle screw implantation; RSE: residual discomfort on extension; RN: residual numbness; PSC: pedicle screw-related complications; PE-TLIF: percutaneous endoscopic transforaminal lumbar interbody fusion; RPP: radicular pain with paresthesias; TS: two segments; AMC: asymptomatic migration of the cages: ODI: Oswestry Disability Index; OS: one segment; FE-MIS-TLIF: full-endoscopic minimally invasive transforaminal lumbar interbody fusion; PNC: postoperative neurological complications; PTLIF: percutaneous transforaminal lumbar interbody fusion; TD: transitory dysesthesia; SIP: sacroiliac pain; SF-36: 36-item short form health survey; UBE: unilateral biportal endoscopic technique; DT: dural tear; PEH: postoperative epidural hematoma; BE: biportal endoscopic; PF: probable fusion; DF: definite fusion.