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Table 1 Characteristics of the 7 included studies

From: Postoperative bisphosphonate do not significantly alter the fusion rate after lumbar spinal fusion: a meta-analysis

First author

Ken Nagahama

Chao Li

Seiji Ohtori

Sang-Mok Kim

Chao-Wei Tu

Fei Chen

Qirui Ding

Publication year

2011

2012

2013

2014

2014

2016

2017

Study location

Japan

China

Japan

South Korea

China

China

China

Surgical methods

Single-level PLIF

TLIF(with 23 one level, 16 two levels, 2 three levels in BPs group, 21 one level, 19 two levels, 1 three levels in control group)

Decompression and posterolateral fusion surgery at the level of spondylolisthesis

Single-level PLIF

Lumbar interbody fusion surgery (with 23 one level, 9 two levels in BPs group, 24 one level, 8 two levels in control group)

Single-level PLIF

TLIF

Number of patients in BPs/control group

19/17

41/41

20/22

22/22

32/32

33/36

30/34

Number of male patients in BPs/control group

1/1

13/16

0/0

9

5/6

6/7

3/4

Diseases type and number of diseases in BPs/control group

Degenerative spondylolisthesis (15), isthmic spondylolisthesis (1), foraminal stenosis (3)/degenerative spondylolisthesis (14), isthmic spondylolisthesis (1), foraminal stenosis (2)

Degenerative disc disease alone (26), isthmic or degenerative spondylolisthesis (12), recurrent disc herniations (3)/degenerative disc disease alone (25), isthmic or degenerative spondylolisthesis (14), recurrent disc herniations (2)

Lumbar degenerative spondylolisthesis with spinal stenosis

-

Degenerative lumbar spondylolisthesis

Single-level degenerative spondylolisthesis and diagnosis of osteoporosis

-

Number of operative levels in BPs/control group

L3-4 (1), L4-5 (14), L5-S1 (4)/L2-3 (1), L3-4 (3), L4-5 (12), L5-S1 (1)

L2-3 (1), L3-4 (7), L4-5 (27), L5-S1 (26)/L2-3 (1), L3-4 (5), L4-5 (31), L5-S1 (25)

-

-

-

L4-5 (24), L5-S1 (9)/L4-5 (25), L5-S1 (11)

-

Mean age of patients in BPs/control group

70.2/67.4

63.63 (SE 6.36)/63.83 (SE 5.70)

75 (SD 5)/77 (SD 5.8)

64.7 (range 60–74)

70.8 (SD 6.09)/69.7 (SD 6.02)

65 (SD 8)/63 (SD 7)

64.53 (SD 6.86)/66.44 (SD 6.44)

Mean BMI of patients in BPs/control group

-

23.01 (SE 3.53)/22.76 (SE 3.54)

-

-

31 (SD 2.1)/30 (SD 1.8)

 

23.98 (SD 2.32)/24.12 (SD 2.07)

Intervention methods in BPs/control group

Alendronate sodium 35 mg per week/ alfacalcidol 1 mg per day

An infusion of ZOL (5 mg, 100 ml) or physiological saline (100 ml) was administered 3 days after the surgery.

Risedronate2.5 mg per day for 10 months/no medication

Alendronate sodium 35 mg per week/no medication

Zoledronate 5 mg IV infusion 3 d after surgery and once-yearly thereafter/no medication

Zoledronic acid infusion (5mg), or the same volume of saline after surgery.

Intravenous zoledronic acid 5 mg at 3rd–5th days after operation/no medication

Background treatment

-

Calcium (1,000 mg/day) and vitamin D (400 IU/day) orally

-

-

-

Daily 1000 mg calcium and 800 IU vitamin D

Oral calcium 600 mg and vitamin D 800 IU

Preoperative lumbar spine BMD t-score in BPs/control group

−1.9/−2.2

Less than −1.5 (7), −1.5 to −2.5 (14), no less than −2.5 (20)/less than −1.5 (9), −1.5 to −2.5 (13),no less than −2.5 (19)

-

-3.75/-3.98

−3.1 (SD 0.59)/−2.9 (SD 0.5)

BMD of lumbar spine (L1-4) 0.709 (SD 0.003)g/cm2/0.698 (SD 0.004)g/cm2

-

Preoperative mean ODI scores in BPs/control group

20.3/21.6

-

36 (SD 10)/40 (SD 10)

-

63.5 (SD 6.3)/64 (SD 5.67)

20.8 (SD 2.6)/21.9 (SD 2.6)

39.2 (SD 2.27)/38.7 (SD 2.69)

Mean follow-up duration

12 months

12 months

1 year

33.8 months

24 months

1 year

30 months

  1. PLIF posterior lumbar interbody fusion, TLIF transforaminal lumbar interbody fusion, SD standard deviation