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. 2024 Dec 2;82:231. doi: 10.1186/s13690-024-01459-2

Table 2.

GRADE table reporting evidence certainty for HbA1c, TIR, TAR, TBR and PROM outcomes summarized from this umbrella review of systematic reviews evaluating the effectiveness of CGM from 2011 to 2024

CONTINUOUS GLUCOSE MONITORING IN THE MANAGEMENT OF TYPE 2 DIABETES
Population Patients with Type 2 Diabetes in a Community Setting
Intervention Continuous Glucose Monitoring
Comparator Self-Monitoring of Blood Glucose
Certainty assessment № of patients Certainty Key Message
№ of studies Study design Risk of bias Inconsistency Indirectness Imprecision Other considerations CGM SMBG

Absolute

(95% CI)

pre-post HbA1c (%) change (follow-up: mean 5.08 months)
28 randomized trials serious [a] not serious not serious not serious none 1434 1261

MD 0.42% lower

(0.60 lower to 0.24 lower)

⨁⨁⨁◯

Moderate

HbA1c reduction was significantly greater amongst type 2 diabetes patients using CGM over SMBG/UC
pre-post TIR (% day) change (follow-up: mean 5.26 months)
14 randomized trials serious [a] not serious not serious not serious none 813 639

MD 6.00% higher

(3.13 higher to 8.88 higher)

⨁⨁⨁◯

Moderate

TIR increase was significantly greater amongst type 2 diabetes patients using CGM over SMBG
pre-post TAR (% day) change (follow-up: mean 4.62 months)
11 randomized trials serious [a] not serious not serious serious none 653 460

MD 4.33% lower

(8.37 lower to 0.28 lower)

⨁⨁◯◯

Low

TAR decrease was significantly greater amongst type 2 diabetes patients using CGM over SMBG
pre-post TBR (% day) change (follow-up: mean 4.65 months)
14 randomized trials serious [a] not serious not serious serious none 723 531

MD 0.33% lower

(0.75 lower to 0.09 higher)

⨁◯◯◯

Very low

No difference in TBR changes betweem T2DM patients using CGM or SMBG/UC
pre-post PROMs change [Adherence] (follow-up: mean 4 months)
1 randomized trials serious [a] very serious [b] serious [c] serious [d] none 51 48

SMD 0.06 SD higher

(0.33 lower to 0.46 higher)

⨁◯◯◯

Very low

No significant difference in treatment adherence change between CGM or SMBG/UC
pre-post PROMs change [Distress] (follow-up: mean 6.43 months)
7 randomized trials serious [a] very serious [b] serious [c] serious [d] none 511 427

SMD 0.66 SD higher

(0.79 lower to 2.11 higher)

⨁◯◯◯

Very low

No significant difference in diabetes-related distress change between CGM or SMBG/UC
pre-post PROMs change [Empowerment] (follow-up: mean 7.67 months)
3 randomized trials serious [a] very serious [b] serious [c] serious [d] none 246 239

SMD 0.10 SD higher

(0.24 lower to 0.45 higher)

⨁◯◯◯

Very low

No significant difference in patient empowerment change between CGM or SMBG/UC
pre-post PROMs change [Patient Education] (follow-up: mean 5 months)
1 randomized trials serious [a] very serious [b] serious [c] serious [d] none 20 10

SMD 0.26 SD higher

(0.46 lower to 0.97 higher)

⨁◯◯◯

Very low

No significant difference in patient education change between CGM or SMBG/UC
pre-post PROMs change [Quality-of-Life] (follow-up: mean 6.90 months)
5 randomized trials serious [a] very serious [b] serious [c] serious [d] none 339 328

SMD 0.43 SD higher

(0.14 lower to 0.99 higher)

⨁◯◯◯

Very low

No significant difference in quality-of-life change between CGM or SMBG/UC
pre-post PROMs change [Satisfaction] (follow-up: mean 6.13 months)
8 randomized trials serious [a] very serious [b] serious [c] serious [d] none 479 385

SMD 1.32 SD higher

(0.65 lower to 3.29 higher)

⨁◯◯◯

Very low

No significant difference in treatment satisfaction change between CGM or SMBG/UC
pre-post PROMs change [Self-Management] (follow-up: mean 6.17 months)
6 randomized trials serious [a] very serious [b] serious [c] serious [d] none 290 288

SMD 0.68 SD higher

(0.37 lower to 1.73 higher)

⨁◯◯◯

Very low

No significant difference in diabetes self-management change between CGM or SMBG/UC

CGM continuous glucose monitoring, CI confidence interval, MD Mean difference, PROMs Patient-reported outcome measure, SMBG/UC Self-monitoring of blood glucose or usual care, SD Standard deviation, SMD Standardized mean difference

Explanations

aPrimary studies poorly documented, or did not carry out, proper allocation concealment, and some studies had incomplete outcome reporting

bPrimary studies assessing quality-of-life used different quality-of-life questionnaires, which led to inconsistencies in data collection and outcome measurement, even within domains. This is especially so given the content and objectives of the questionnaires deployed were significantly different (e.g. comparing the PAID and DDS), which constitutes as heterogenous exposure to experience recall and outcome measurement amongst participants

cSome primary studies used questionnaires that studied not quality-of-life, but related constructs such as diabetes-related distress

dWithin-study variance was significant, and extensive subgroup analysis was unable to identify sources of heterogeneity across studies, leading to unexplained imprecision of results