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Table 3 GRADE evidence profile of RCTs for effect of BPs on periprosthetic bone loss after TKA

From: Effect of bisphosphonates on periprosthetic bone loss after total knee arthroplasty: a meta-analysis of randomized controlled trials

 

Summary of findings

Quality assessment

Time points

n (treated/control)

WMD (95%CI, g/cm2)

Limitations

Inconsistency

Indirectness

Imprecision

Others

Quality

Tibia

3 months

2 (48/50)

0.07 (0.04–0.10)

No seriousa

No seriousb

No serious

Seriousc

Strong associationd

Moderate

6 months

3 (78/80)

0.12 (0.10–0.15)

No serious

No serious

No serious

No serious

Strong associationd

High

12 months

3 (77/75)

0.12 (0.10–0.15)

No serious

Serious

No serious

No serious

None

Moderate

Femur

3 months

3 (56/61)

0.07 (0.04–0.10)

No serious

No serious

No serious

Serious

Strong association

Moderate

6 months

5 (91/97)

0.12 (0.10–0.15)

No serious

Serious

No serious

No serious

Strong association

Moderate

12 months

4 (85/86)

0.12 (0.10–0.15)

No serious

Serious

No serious

No serious

Strong association

Moderate

  1. aThe inadequate blinding and substantial loss follow-up in some trials may raise risk of bias
  2. bInconsistent report of outcomes and significant heterogeneity existed across the trials
  3. cThe number of included patients less than 150 is considered to be small and may cause imprecision
  4. dEffect size more than 0.05 is considered to be large and strengthen the evidence