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. 2020 Feb;9(1):43–58. doi: 10.21037/gs.2019.11.03

Table 7. Mortality in hypercortisolism.

Type of hypercortisolism Active hypercortisolism (persistent, untreated or recurrent) Treated hypercortisolism
Patients, n SMR (95% CI)/or mortality (%) Citations Patients, n SMR (95% CI) Follow-up after treatment, years Citations
Cushing Disease 766 4.6 (2.9–7.3) van Haalen et al., 2015 (95) 766 2.5 (1.4–4.2) Range: 1.3–12.8 van Haalen et al., 2015 (95)
40 6.9 (4.3–10) Ragnarsson et al., 2019 (96) 419 1.9 (1.5–2.3) 13 Ragnarsson et al.,2019 (96)
Ectopic Cushing syndrome 11 66.7 (21.2–160.8) Ntali et al., 2013 (74) 11 83.3 (4.2–411) 12 Ntali et al., 2013(74)
Adrenal Cushing syndrome No studies reported 109 1.9 (0.9–3.1) Range: 7.4–11.2 Graversen et al., 2012 (97)
Mild autonomous cortisol secretion 431 11.5% Elhassan et al., 2019 (23) No studies reported
Endogenous Cushing syndrome of any etiology, combined 386 2.4 (0.87–8.19) Yaneva et al., 2013 (98) 386 1.7 (0.6–3.6) 7.1 Yaneva et al., 2013 (98)

Selection criteria: publication year: 2001 or after; design: retrospective, prospective studies, systematic reviews or meta-analyses; outcome: all-course mortality. SMR, standardized mortality ratio; CI, confidence interval.