Rajasekeran et al. [59] |
|
KT (n = 6) and SPKT (n = 4) recipients treated with canaglifozin |
All patients treated with canaglifozin |
No urinary nor mycotic infections. No major complications
Small reductions in eGFR (−4.3 ± 12.2 mL/min/1.73 m2; P = 0.3), but no episodes of AKI
Discrete HbA1c reduction of −0.84 ± 1.2% (P = 0.07)
|
Schwaiger et al. [60] |
Prospective interventional study, n = 14
Follow-up: 4 weeks (n = 14), 12 months (n = 8)
|
KT with PTDM receiving treatment with insulin and eGFR >30 mL/min/1.73 m2
|
Four weeks on stable insulin treatment, and after a 3-day insulin wash-out, conversion to empaglifozin in monotherapy. Reinstitution of insulin if poor glycaemic control
*Concomitant antidiabetic drugs were discontinued
|
Increased FPG from 111 ± 21 to 144 ± 45 mg/dL (P = 0.005) and 2HGP from 232 ± 82 to 273 ± 116 mg/dL (P = 0.06) in 4 weeks
Decrease of body weight from 83.7 ± 7.6 to 81.6 ± 7.4 kg in 4 weeks (P = 0.03) and to 78.7 kg in 12 months (P = 0.02)
Decrease of eGFR from 55.6 ± 20.3 to 47.5 ± 15.1 mL/min/1.73 m2 (P = 0.008). Not statistically significant differences in 12 months
|
Attallah et al. [61] |
|
KT treated with empaglifozin (previous DM n = 4, PTDM n = 4) |
|
Slight initial worsening of renal function, but then stabilized (mean SCr from 88.5 to 99.5 mmol/L)
Mean decrease of HbA1c of 0.85%
Mean decrease of body weight of 2.4 kg
Two patients developed UTI
|
Halden et al. [62] |
RCT, n = 49
Follow-up: 24 weeks
|
KT recipients with diagnosis of PTDM |
Empaglifozin (n = 22) versus placebo (n = 22) |
Statistically significant reduction of HbA1c compared with placebo: median −0.2% (IQR −0.6, −0.1) versus 0.1 (−0.1, 0.4); P = 0.025
Median reduction of body weight of −2.5 kg (IQR −4.0, −0.05) compared with placebo group (P = 0.014)
No significant differences in adverse events or eGFR
|
Mahling et al. [63] |
|
|
All patients received empaglifozin |
eGFR remained stable
Slight decrease in the median of HbA1c of 0.2% (P > 0.05)
Median decrease of body weight −1.0 kg (IQR −1.9, −0.2 kg)
|