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. 2021 Apr 22;9(1):e001906. doi: 10.1136/bmjdrc-2020-001906

Table 1.

Study design, type of data source and treatment*

Type of hypoglycemia Not defined Non-severe Severe Both Nocturnal† Total
(n=14) (n=40) (n=113) (n=76) (n=41) (n=243)
Study design
 Cross-sectional 0 (0) 15 (37.5) 18 (15.9) 20 (26.3) 8 (19.5) 53 (21.8)
 Prospective cohort 5 (35.7) 14 (35.0) 38 (33.6) 42 (55.3) 31 (75.6) 99 (40.7)
 Retrospective case–control 0 (0) 0 (0) 1 (0.9) 1 (1.3) 0 (0) 2 (0.8)
 Retrospective cohort 9 (64.3) 11 (27.5) 56 (49.6) 13 (17.1) 2 (4.9) 89 (36.6)
Type of data source
 Administrative data 5 (35.7) 3 (7.5) 33 (29.2) 4 (5.3) 0 (0) 45 (18.5)
 EHR 3 (21.4) 3 (7.5) 12 (10.6) 9 (11.8) 0 (0) 27 (11.1)
 Interview 0 (0) 1 (2.5) 2 (1.8) 3 (3.9) 1 (2.4) 6 (2.5)
 Registry 2 (14.3) 5 (12.5) 19 (16.8) 2 (2.6) 0 (0) 28 (11.5)
 Study cohort 4 (28.6) 15 (37.5) 34 (30.1) 42 (55.3) 33 (80.5) 95 (39.1)
 Survey 0 (0) 13 (32.5) 13 (11.5) 16 (21.1) 7 (17.1) 42 (17.3)
Type of treatment
 Not specified 7 (50) 10 (25.0) 42 (37.2) 17 (22.4) 3 (17.6) 76 (31.3)
 Insulin 4 (28.6) 17 (42.5) 41 (36.3) 33 (43.4) 36 (87.8) 95 (39.1)
 Sulfonylurea 0 (0) 1 (2.5) 7 (6.2) 9 (11.8) 0 (0) 17 (7)
 Insulin+SU 1 (7.1) 2 (5.0) 10 (8.8) 3 (3.9) 0 (0) 16 (6.6)
 Other (TZD, DPP-4, GLP1 and SGLT-2) 1 (7.1) 6 (15.0) 8 (7.1) 7 (9.2) 0 (0) 22 (9.1)
 Insulin+other (TZD, DPP-4, GLP1 and SGLT-2) 1 (7.1) 2 (5.0) 3 (2.7) 3 (3.9) 2 (4.9) 9 (3.7)
 SU+others (TZD, DPP-4, GLP1 and SGLT-2) 0 (0) 2 (5.0) 2 (1.8) 4 (5.3) 0 (0) 8 (3.3)

*Data are presented as number (percentage) unless specified otherwise.

†Studies that reported nocturnal hypoglycemia were the same studies that evaluated severe and/or non-severe episodes and therefore were not included in the statistical analysis.

DPP-4, dipeptidyl peptidase 4 inhibitor; EHR, electronic health record; GLP1, glucagon-like peptide 1 receptor agonist; SGLT-2, sodium glucose cotransporter-2 inhibitor; SU, sulfonylurea; TZD, thiazolidinedione.