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. 2020 Jan 27;20(1):17–26. doi: 10.4103/jips.jips_373_19

Table 12.

Gradepro assessment

Question: What is the incidence of neurosensory disturbance in patients with mandibular implants

Number of studies Certainty assessment Effect Certainty Importance


Study design Risk of bias Inconsistency Indirectness Imprecision Other considerations Number of events Number of individuals Rate (95% CI)
Incidence of NSD

9 Observational studies Not serious Very seriousa Not serious Seriousb Strong association dose-response gradient 105 2112 Event rate 13.50/100 person-year(s) (10.98-16.03) ⨁⨁⨁◯ Moderate Critical

Rate of recovery

7 Observational studies Not serious Very seriousc Not serious Seriousb Strong association dose-response gradient 60 95 Event rate 51.30/100 person-year(s) (31.21-71.4) ⨁⨁⨁◯ Moderate Critical

Incidence of permanent NSD

6 Observational studies Not serious Very seriousd Not serious Seriousb Strong association dose-response gradient 34 90 Event rate 18.67/100 person-year(s) (14.54-22.79) ⨁⨁⨁◯ Moderate Important

Short-term recovery rate

2 Observational studies Not serious Very seriouse Not serious Seriousb Strong association dose-response gradient 10 11 Event rate 46.96/100 person-year(s) (−10.77-104.69) ⨁⨁⨁◯ Moderate Important

Long-term recovery rate

3 Observational studies Not serious Very seriousf Not serious Seriousb Strong association dose-response gradient 26 36 Event rate 10.97/100 person-year(s) (3.51-18.43) ⨁⨁◯◯ Low Important

Risk of NSD in anterior versus posterior implants

2 Observational studies Not serious Seriousg Not serious Very seriousb Very strong association dose-response gradient 15 177 Event rate −0.02/1 person-year(s) (−0.21-0.16) ⨁⨁⨁⨁ High Critical

⨁◯The certaintly of evidence is graded as very low to high with upto four crosshairs. One crosshair representing one point to mean very low while four crosshairs represent high certainty of evidence aThe lack of overlap in the CIs of the studies included and the high estimated heterogeneity (I2=99.8%) result in a high risk of inconsistency, bSmall sample size resulting in a serious risk for imprecision, cThe lack of overlap in the CIs of the studies included and the high estimated heterogeneity (I2=99.90%) result in a high risk of inconsistency, dThe lack of CI overlap in the studies included and the high estimated heterogeneity (I2=99.77%) result in a high risk of inconsistency, eThe lack of CI overlap in the studies included and the high estimated heterogeneity (I2=98.28%) result in a high risk of inconsistency, fThe lack of CI overlap in the included studies and the high estimated heterogeneity (I2=99.77%) result in a serious risk of inconsistency, gThe lack of CI overlap in the included studies and the high estimated heterogeneity (I2=71.94%) result in a serious risk of inconsistency. NSD: Neurosensory disturbance, CIs: Confidence intervals