Summary of findings for the main comparison. Tight glycaemic control compared with non‐tight control for preventing diabetic kidney disease (DKD) and its progression.
Tight glycaemic control compared with non‐tight control for preventing DKD and its progression | ||||||
Patient or population: patients with diabetes Intervention: tight glycaemic control Comparison: non‐tight glycaemic control | ||||||
Outcomes | Illustrative comparative risks* (95% CI) | Relative effect (95% CI) | No. of participants (studies) | Confidence of the evidence (GRADE) | Comments | |
Assumed risk | Corresponding risk | |||||
Non‐tight control | Tight control | |||||
Doubling serum creatinine 8.3 years |
39 per 1000 |
33 per 1000 (24.95 to 43.29) NNT: 167 |
RR 0.84 (0.64 to 1.11) | 26,874 (4) | ⊕⊕⊝⊝ low | Imprecision (‐1) Heterogeneity (‐1) |
ESKD 5.9 years |
3 per 1000 |
2 per 1000 (1.02 to 3.36) NNT: 1000 |
RR 0.62 (0.34 to 1.12) | 23,332 (4) | ⊕⊕⊝⊝ low | Imprecision (‐1) Heterogeneity (‐1) |
Sudden death 4.6 years |
2 per 1000 |
2 per 1000 (0.52 to 5.14) NNT: 0 |
RR 0.82 (0.26 to 2.57) | 5,913 (4) | ⊕⊝⊝⊝ very low | Study limitation (‐1) Imprecision (‐1) Heterogeneity (‐1) |
All‐cause mortality 5.6 years |
16 per 1000 |
16 per 1000 (13.76‐18.08) NNT: 0 |
RR 0.99 (0.86 to 1.13) | 29,094 (9) | ⊕⊕⊕⊝ moderate | Imprecision (‐1) |
Cardiovascular mortality 4.4 years |
9 per 1000 |
11 per 1000 (6.57 to 17.28) NNH: 500 |
RR 1.19 (0.73 to 1.92) | 23,673 (6) | ⊕⊕⊝⊝ low | Imprecision (‐1) Heterogeneity (‐1) |
Non‐fatal myocardial infarction 5.6 years |
8 per 1000 |
7 per 1000 (5.36 to 7.92) NNT: 1000 |
RR 0.82 (0.67 to 0.99) | 25,596 (5) | ⊕⊕⊕⊝ moderate | Study limitation (‐1) |
Onset microalbuminuria 5.4 years |
46 per 1000 |
39 per 1000 (35.42 to 43.24) NNT: 143 |
RR 0.85 (0.77 to 0.94) | 19,933 (4) | ⊕⊕⊕⊝ moderate | Heterogeneity (‐1) |
Progression of microalbuminuria 5.8 years |
4 per 1000 |
2 per 1000 (1.52 to 3.72) NNT: 500 |
RR 0.59 (0.38 to 0.93) | 13,266 (5) | ⊕⊕⊕⊝ moderate | Heterogeneity (‐1) |
*The basis for the assumed risk (e.g. the median control group risk across studies) is calculated from data in the meta‐analyses. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: Confidence Interval; RR: Risk Ratio; NNT: Number Needed to Treat; NNH: Number Needed to Harm. We did not downgrade for reason of publication bias as insufficient studies contributed to treatment estimates to draw meaningful conclusions | ||||||
GRADE Working Group grades of evidence High confidence: Further research is very unlikely to change our confidence in the estimate of effect. Moderate confidence: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate. Low confidence: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate. Very low confidence: We are very uncertain about the estimate. |
ESKD ‐ end‐stage kidney disease