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. 2018 Aug 14;20(12):2711–2723. doi: 10.1111/dom.13468

Table 2.

Incidence rates and NNTB/NNTH of the different CV outcomes (exposure to SGLT2‐Is), including risk of amputations

Study MACE All‐cause mortality HHF BKAs
Incidence ratea NNTB Incidence ratea NNTB Incidence ratea NNTB Incidence ratea NNTH
UK cohort (dapagliflozin vs. non‐SGLT2‐Is)16 1.338b NC 0.527b 259 / / / /
Swedish cohort (dapagliflozin only vs. insulin)17 1.68 95 0.98 66 / / / /
US cohort (canagliflozin vs. DPP4‐Is)15 0.99 2523 0.07 5889 0.89 535 / /
EASEL (SGLT2‐Is vs. non‐SGLT2‐Is)14 2.31 55 1.29 62 0.51 158 0.17 743
CVD‐REAL (SGLT2‐Is vs. non‐SGLT2‐Is)10 0.89 166 0.52 211 0.36 681 / /
CVD‐REAL Nordic (SGLT2‐Is vs. non‐SGLT2‐is)11 1.64 206 1.05 76 0.98 220 / /
CVD‐REAL Nordic (dapagliflozin vs. DDP4‐Is)12 1.86 187 1.03 108 0.99 169 / /
CVD‐REAL 2 (SGLT2‐Is vs. non‐SGLT2‐Is)13 1.91 151 0.80 173 1.23 333 / /
OBSERVE‐4D (canagliflozin vs. select non‐SGLT2‐Is)24 / / / / 1.18 58 0.45 NC
OBSERVE‐4D (SGLT2‐Is vs. select non‐SGLT2‐Is)24 / / / / 0.96 104 0.42 NC

BKAs, atraumatic below‐knee lower extremity amputations; DPP4‐Is, dipeptidyl peptidase‐4 inhibitors; NNTB, number needed to treat to benefit; NNTH, number needed to treat to harm.

/: not available.

NC: not calculated because no statistically significant difference emerged between exposed and unexposed group.

a

Data expressed × 100 person‐years.

b

Data for low‐risk population (see Table 1 for the definition of MACE, which in this case was defined as incident cardiovascular disease).