Is self-monitoring of blood glucose effective in improving glycaemic control in type 2 diabetes without insulin treatment: a meta-analysis of randomised controlled trials.

OBJECTIVE: The present study aimed to verify the effectiveness of self-monitoring of blood glucose (SMBG) in patients with non-insulin-treated type 2 diabetes (T2D).
METHODS: A comprehensive literature search was conducted in PubMed, Cochrane Library, Web of Science, ScienceDirect and ClinicalTrials.gov from their respective inception dates to 26 October 2015. Eligible randomised controlled trials (RCTs) were included according to prespecified criteria. The quality of the included RCTs was evaluated according to the Cochrane risk of bias tool, and the evidence quality of meta-analyses was assessed by the Grading of Recommendation, Assessment, Development, and Evaluation (GRADE) criteria. A meta-analysis of primary and secondary outcome measures was performed. Sensitivity and subgroup analyses were carried out to evaluate the robustness and heterogeneity of the findings. Begg's and Egger's tests were used to quantify publication biases.
RESULTS: A total of 15 RCTs, comprising 3383 patients with non-insulin-treated T2D, met the inclusion criteria. The SMBG intervention improved glycated haemoglobin (HbA1c) (mean difference -0.33; 95% CI -0.45 to -0.22; p=3.0730e-8; n=18), body mass index (BMI; -0.65; -1.18 to -0.12; p=0.0164; n=9) and total cholesterol (TC; -0.12; -0.20 to -0.04; p=0.0034; n=8) more effectively than the control in overall effect. The sensitivity analysis revealed little difference in overall effect, indicating the robustness of the results. SMBG moderated HbA1c levels better than the control in all subgroup analyses. Most of the RCTs had high risk of bias in blinding, while the overall quality of evidence for HbA1c was moderate according to the GRADE criteria. Publication bias was moderate for BMI.
CONCLUSIONS: SMBG improved HbA1c levels in the short term (≤6-month follow-up) and long term (≥12-month follow-up) in patients with T2D who were not using insulin. TRIAL REGISTRATION NUMBER: CRD42015019099. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/

This meta-analysis provides the latest evidence for the effect of self-monitoring of blood glucose (SMBG) on non-insulin-treated type 2 diabetes (T2D) to resolve the controversy among previous studies, including the latest Cochrane review. This study is clinically relevant and significant because of the following reasons:

It is the most comprehensive meta-analysis to include the latest randomised controlled trials (RCTs) and evaluates more clinical indexes (including systolic blood pressure (SBP), diastolic blood pressure (DBP), weight, body mass index (BMI), triglyceride (TG), total cholesterol (TC) and waist circumference) than previous meta-analyses.

It is the first meta-analysis to investigate the association of geographical regions (Asia and America–Europe) with the effectiveness of SMBG.

It provides a clear demonstration that SMBG is significantly effective in controlling glycated haemoglobin (HbA1c), BMI and TC levels in the short term, while a clinically significant change in the long term is only observed in patients with newly diagnosed T2D with mildly elevated HbA1c.

Introduction

In 2011, £158 million was spent on self-monitoring of blood glucose (SMBG) by the UK's National Health Service (NHS), accounting for 21% of diabetic prescription costs.1 The Centers for Disease Control and Prevention (CDC) estimated that the daily usage rate of SMBG in the USA was 63.4% among patients with diabetes,2 while the Diabetes Glycaemic Education and Monitoring (DiGEM) trial reported that the 12-month costs of SMBG were similar in both less intensive (£92) and more intensive (£84) SMBG groups.3 SMBG has been reported effective in the management of type 1 diabetes mellitus.4 5 However, there remains a lack of consensus over the effectiveness of SMBG for self-management of patients with non-insulin-treated type 2 diabetes (T2D), despite several meta-analyses having investigated the issue.6–13 Given the high costs incurred during SMBG, if the technology was found to be ineffective in the treatment of patients with T2D without insulin administration, the expenditure would be in vain. Conversely, if SMBG was proven effective, over 200 million patients with T2D living in low-income and middle-income countries could be advised to manage their disease through SMBG as a relatively low-cost health technology. Several meta-analyses7 12 13 deemed that SMBG was effective in decreasing glycated haemoglobin (HbA1c) levels in patients with T2D. Others6 8 found that the SMBG group did not fare significantly better than the control group, but varied in the length of follow-up. The latest meta-analysis was a Cochrane review published in 2012, which suggested that SMBG had a minimal effect on improving glucose control at 6 months (mean difference −0.26; 95% CI −0.39 to −0.13), but the effect disappeared after 12 months (−0.13; −0.31 to 0.04); thus, the clinical benefit was limited.6 Since then, more randomised controlled trials (RCTs)14–17 have been published, of which three14 15 17 suggested that SMBG improved diabetic control beyond the levels estimated by the last Cochrane review6 (ie, at 6 and 12 months), and one16 reported no significant differences between SMBG and usual care for changes in HbA1c levels. Regardless of the controversial results of these previous reviews and recent RCTs, the last Cochrane review is already outdated. Therefore, the present study aimed to re-estimate the effects of SMBG in patients with non-insulin-treated T2D through a meta-analysis of RCTs. Given the significant efficacy and safety differences observed among ethnic groups in the DURAbility of Basal versus Lispro mix 75/25 insulin Efficacy (DURABLE) trial,18 the present study also investigated the possible associations of ethnicity and living environment with SMBG.

Methods

The present systematic review was conducted in accordance with the protocol registered in the International prospective register of systematic reviews (PROSPERO) (registration number: CRD42015019099) and the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guidelines.19

Eligibility criteria

Included studies met the following criteria: (1) RCTs comparing SMBG with usual care (or no SMBG) in patients with non-insulin-treated T2D above 18 years of age; (2) RCTs reporting HbA1c levels; and (3) RCTs reporting fasting plasma glucose (FPG), body mass index (BMI; calculated as weight in kilograms divided by square of the height in metres), diastolic blood pressure (DBP), systolic blood pressure (SBP), high-density lipoprotein (HDL), low-density lipoprotein (LDL), triglycerides (TGs), total cholesterol (TC), waist circumference (WC) and weight (if available). The primary outcome measure in this study was HbA1c improvement and the secondary outcome measures were FPG, BMI, DBP, SBP, HDL, LDL, TG, TC, WC and weight improvement. Meeting summaries and abstracts were excluded.

Literature search and study selection

Two reviewers (HZ and YZ) searched four bibliographical databases, namely PubMed, Web of Science, ScienceDirect and Cochrane Library, from their respective inception dates to 26 October 2015. Google Scholar and ClinicalTrials.gov were adopted as additional database sources. Manual searching was used to retrieve additional records from relevant studies. The search strategies were specified according to the database used. Basic search terms included ‘self-monitoring of blood glucose’, ‘type 2 diabetes’ and ‘non-insulin’ in the title, abstract and/or keywords. The specific search strategies used were:

PubMed: ((self-monitoring of blood glucose[Title/Abstract] OR SMBG[Title/Abstract]) AND (type 2 diabetes [Title/Abstract] OR T2D [Title/Abstract])) AND ((no insulin [Title/Abstract] OR insulin [Title/Abstract]) OR non-insulin [Title/Abstract]).

Web of Science: TS=(SMBG OR self-monitoring of blood glucose) AND TS=(T2D OR type 2 diabetes) AND TS=(non-insulin OR using insulin OR no insulin).

ScienceDirect: TITLE-ABSTR-KEY ((SMBG OR self-monitoring of blood glucose) AND (T2D OR type 2 diabetes) AND (non-insulin OR using insulin OR no insulin)).

The Cochrane Library: self-monitoring of blood glucose or SMBG in Title, Abstract, Keywords AND no insulin OR non-insulin in Title, Abstract, Keywords AND type 2 diabetes OR T2D in Title, Abstract, Keywords.

Two reviewers (HZ and YZ) independently performed the literature searches and selection. The articles retrieved by one reviewer were crosschecked by the other. Disagreements were resolved by group discussion or in consultation with a third reviewer (S-wL).

Data extraction and quality assessment

Two reviewers (HZ and YZ) independently extracted data on study characteristics (such as author, publication year, sample size and intervention) and outcome measures from the eligible studies. The extracted data were crosschecked and any disagreement was resolved by discussion between the two reviewers (HZ and YZ); a third reviewer (S-wL) was consulted when necessary. The quality of the included RCTs was evaluated according to the Cochrane Risk of Bias Tool,20 and the evidence quality of meta-analyses was assessed using the Grading of Recommendation, Assessment, Development, and Evaluation (GRADE) criteria.21

Meta-analysis

Extracted data were transferred to the ‘metafor’ package22 in R software for meta-analysis with a random-effects model. Continuous outcome measures were calculated and represented as mean differences (MDs) and their 95% CIs. Heterogeneity among RCTs was evaluated with I2 statistics. p Values <0.05 were considered statistically significant.

Sensitivity and subgroup analyses

A sensitivity analysis was performed on sample size to assess the robustness of the findings. Sample size is a dominant factor that affects precision in determining overall effects. Thus, the meta-analysis was repeated after excluding studies with sample sizes of 99 or less. Subgroup analyses were performed to explain the heterogeneity in terms of geographical region, follow-up period and diabetes history, according to the characteristics of the included studies. The Mann-Whitney-Wilcoxon test was used to determine the differences across subgroups.

Adverse events analysis

Meta-analyses on the overall adverse effects in terms of ORs and their 95% CIs were performed with a random-effects model.

Publication bias and metaregression

Funnel plots were generated to visualise any possible publication bias. Begg's rank correlation test23 and Egger's regression test24 were performed to evaluate the statistical significance of the publication bias. A metaregression with a mixed-effects model employing the restricted maximum likelihood (REML) estimation was performed to examine the possible relationships between the overall effects and factors such as sample size, history of diabetes, follow-up period and publication year.

Classification tree

A classification tree was manually constructed to indicate who might benefit from SMBG. The classification tree example in online supplementary figure S3 can be interpreted as, ‘the mean starting HbA1c of tested patients was no less than 8%, then if the follow-up period of trials was short (no more than 6 months), then if the tested patients from Asia, then if the patients is newly diagnosed’. Unpaired t-tests were performed with R software for two-group comparisons.

Results

Study characteristics

A total of 1533 records were retrieved in accordance with the specified search strategies from PubMed (n=246), Web of Science (n=400), ScienceDirect (n=352), Cochrane Library (n=234), Google Scholar (n=266) and ClinicalTrials.gov (n=35). Following removal of duplicates, 683 records were screened, of which 50 were assessed for eligibility. Finally, 15 records were included after full-text assessment (see online supplementary table S1). Figure 1 shows the study selection process and the reasons for exclusion. The 15 studies14–17 25–35 meeting the inclusion criteria comprised a total of 3383 patients with non-insulin-treated T2D. Among the 15 studies, 13 studies had HbA1c as their primary outcome and the other two16 17 had HbA1c as a secondary outcome. A total of 915 25 26 29–31 33–35 of the 15 studies were two-armed trials comparing SMBG with usual care or no SMBG, while 6 studies14 16 17 27 28 32 were three-armed trials. Among the three-armed trials, three16 28 32 compared SMBG and self-monitoring of urine glucose (SMUG) with usual care, two17 27 compared less intensive SMBG and more intensive SMBG with a control group, and one14 compared fingertip SMBG and palm SMBG with a control group.

Figure 1

Flow chart of study selection. The process of study selection included literature search, abstract screening, eligibility evaluation and study inclusion for meta-analysis. RCT, randomised controlled trial; SMBG, self-monitoring of blood glucose; T2D, type 2 diabetes.

Overall effects

A meta-analysis was performed on the primary outcome measure of HbA1c and secondary outcome measures of FPG, BMI, DBP, SBP, HDL, LDL, TG, TC, WC and body weight (table 1). The SMBG group was shown to perform better for HbA1c (MD −0.33; 95% CI −0.45 to −0.22; p=3.0730e−8; n=18), BMI (−0.65; −1.18 to −0.12; p=0.0164; n=9), TC (−0.12; −0.20 to −0.04; p=0.0034; n=8) and WC (−2.22; −4.40 to −0.03; p=0.0474; n=5) compared with the control group. There were no significant differences with regard to FPG, DBP, SBP, HDL, LDL, TG and weight between the SMBG and control groups. Among the studies, significant heterogeneity was found for HbA1c (I2=63%, p=0.0002), BMI (I2=89%, p=0.0009), LDL (I2=89%, p=0.0009) and SBP (I2=65%, p=0.0100). A forest plot of HbA1c is shown in figure 2 to allow visual assessment of the heterogeneity.

Table 1

Results of overall efficacy

Outcome	Substudies (n)	Pooled sample size	Heterogeneity		Overall effect		Quality of evidence assessed by GRADE*
			I2 (%)	p Value	MD (95% CI)	p Value
HbA1c	18	3383	63	0.0002	−0.33 (−0.45 to −0.22)	3.0730e−8	⊕⊕⊕⊖ Moderate
FPG	3	1366	0	0.6739	−0.23 (−0.56 to 0.11)	0.1804	⊕⊕⊕⊕ High
BMI	9	1391	89	0.0009	−0.65 (−1.18 to −0.12)	0.0164	⊕⊕⊖⊖ Low
DBP	7	1740	59	0.0419	−0.86 (−2.21 to 0.48)	0.2083	⊕⊕⊖⊖ Low
SBP	7	1740	65	0.0100	−1.08 (−3.46 to 1.29)	0.3710	⊕⊕⊕⊖ Moderate
HDL	4	446	67	0.0175	0.04 (−0.07 to 0.14)	0.5257	⊕⊕⊕⊖ Moderate
LDL	3	384	89	0.0009	−0.13 (−0.66 to 0.39)	0.6140	⊕⊕⊕⊖ Moderate
TG	6	736	0	0.8983	0.02 (−0.15 to 0.20)	0.7990	⊕⊕⊕⊕ High
TC	8	1342	0	0.5220	−0.12 (−0.20 to −0.04)	0.0034	⊕⊕⊕⊕ High
Weight	8	1814	0	0.9838	−0.29 (−0.62 to 0.05)	0.0958	⊕⊕⊕⊖ Moderate
WC	5	513	0	0.4779	−2.22 (−4.40 to −0.03)	0.0474	⊕⊕⊕⊖ Moderate

*Grading of Recommendation, Assessment, Development, and Evaluation (GRADE).21

BMI, body mass index; DBP, diastolic blood pressure; FPG, fasting plasma glucose; HbA1c, glycated haemoglobin; HDL, high-density lipoprotein; LDL, low-density lipoprotein; MD, mean difference; SBP, systolic blood pressure; TC, total cholesterol; TG, triglyceride; WC, waist circumference.

Figure 2

Forest plot of HbA1c for overall effect, showing the mean differences between SMBG and the control with corresponding 95% CIs in the individual studies. HbA1c, glycated haemoglobin; SMBG, self-monitoring of blood glucose.

Quality of RCTs and meta-analyses

Online supplementary figures S1 and S2 show the quality of the included RCTs assessed by the Cochrane Risk of Bias Tool. Almost 50% of the RCTs did not provide adequate information about random sequence generation, allocation concealment and selective reporting. All of the included studies had high risk of bias in blinding of participants, because the participants could not be blinded to the intervention, and only four RCTs had low risk of bias in blinding of outcome assessment. Other key aspects identified among the RCTs were mostly low for risk of bias. Table 1 shows the evidence quality of the meta-analyses evaluated by the GRADE criteria. The overall quality of evidence for HbA1c was moderate, with significant heterogeneity across studies (I2=63%; p=0.0002; n=18). The quality of evidence for FPG, TG and TC was rated as high.

Sensitivity analysis

A sensitivity analysis was performed on studies with sample sizes of 100 or above to test the robustness of the overall effects. As shown in table 2, there were minor changes in the significance of SMBG for HbA1c, BMI, TC and WC, indicating the robustness of the overall effects. A forest plot of HbA1c is shown in figure 3.

Table 2

Sensitivity analysis on studies with sample sizes of 100 or above

Outcome	Substudies (n)	Pooled sample size	Heterogeneity		Overall effect
			I2 (%)	p Value	MD (95% CI)	p Value
HbA1c	11	2953	72	<0.0001	−0.29 (−0.44 to −0.14)	0.0001
FPG	2	1299	0	0.4186	−0.21 (−0.56 to 0.14)	0.2384
BMI	6	1174	97	0.0025	−0.89 (−1.88 to 0.09)	0.0757
DBP	6	1678	65	0.0269	−0.82 (−2.24 to 0.61)	0.2628
SBP	7	1740	65	0.0100	−1.08 (−3.46 to 1.29)	0.3710
HDL	3	384	79	0.0066	0.04 (−0.11 to 0.18)	0.6268
LDL	3	384	89	0.0009	−0.13 (−0.66 to 0.39)	0.6140
TG	4	607	0	0.6740	0.03 (−0.15 to 0.21)	0.7529
TC	6	1213	7	0.3190	−0.11 (−0.21 to −0.01)	0.0254
Weight	5	1641	0	0.9447	−0.28 (−0.62 to 0.07)	0.1172
WC	3	384	13	0.2934	−3.15 (−6.46 to 0.17)	0.0630

BMI, body mass index; DBP, diastolic blood pressure; FPG, fasting plasma glucose; HbA1c, glycated haemoglobin; HDL, high-density lipoprotein; LDL, low-density lipoprotein; MD, mean difference; SBP, systolic blood pressure; TC, total cholesterol; TG, triglyceride; WC, waist circumference.

Figure 3

Forest plot of HbA1c for sensitivity analysis, showing the mean differences between SMBG and the control with corresponding 95% CIs in the individual studies whose sample sizes were bigger than 99. HbA1c, glycated haemoglobin; SMBG, self-monitoring of blood glucose.

Subgroup analyses

Subgroup analyses stratified trials according to geographical regions to examine the source of heterogeneity among the RCTs. The studies were divided into two groups: one comprising study populations from Asian countries (Asia group) and the other comprising study populations from America and Europe (America–Europe group) (see online supplementary table S2). SMBG significantly improved HbA1c levels and BMI regardless of the groups. Subgroup analyses were also performed on studies with follow-up periods of 12 months or more to test the long-term effects of SMBG (see online supplementary table S3), and studies with follow-up periods of 6 months or less to test the short-term effects. SMBG moderated HbA1c levels better than the control group in the short term and long term, while both interventions were equivalent in performance for all aspects except for BMI and TC. Subgroup analyses based on history of diabetes (≥12 months or newly diagnosed) were also performed (see online supplementary table S4). The SMBG group outperformed the control group for HbA1c, BMI and TC, indicating that SMBG was effective in controlling blood glucose in the later phase of diabetes. Only two trials with three substudies were conducted in newly diagnosed patients, and these were analysed in the Cochrane review.6

Adverse events

A total of 7 of the 15 studies reported adverse events. As shown in online supplementary table S5, the most commonly reported adverse event was hypoglycaemia. The incidence of hypoglycaemia was higher in the SMBG group than in the control group, but the rate of hypoglycaemic episodes per patient was higher in the control group. A statistical analysis of adverse events was not performed because the data available from the RCT reports were insufficient in terms of quantity.

Publication bias

Funnel plots of the outcomes for HbA1c, FPG, BMI, DBP, SBP, HDL and LDL showed various levels of asymmetries across the studies, indicating possible publication bias. Begg's rank correlation test and Egger's regression test detected moderate publication bias for BMI (see online supplementary table S6). The results of the funnel plots, Egger's test and Begg's test are not presented in the main text, because they are not recommended for fewer than 10 studies based on a high risk of inaccurate interpretation.

Metaregression

SMBG performed better for HbA1c than the control under all tested conditions, and better for BMI and TC under most of the tested conditions but with heterogeneity. Therefore, a metaregression was performed to analyse the relationships between these three outcomes and the study characteristics (including sample size, publication year, history of diabetes and follow-up) and test the source of the heterogeneity. As shown in table 3, there seemed to have significant relationships between BMI and history of diabetes, and between BMI and follow-up period. There was also a statistically significant association between history of diabetes and HbA1c.

Table 3

Metaregression analysis of the relationship between outcomes and characteristics of RCTs

Outcome	Substudies (n)	Factor	Coefficient	z	p Value
HbA1c	18	Sample size	0.0004	1.0535	0.2921
		History of diabetes	0.2559	2.0006	0.0454
		Follow-up	−0.0081	−1.5508	0.1210
		Publication year	−0.0079	−0.6481	0.5169
BMI	9	Sample size	0.0034	1.1169	0.2640
		History of diabetes	1.9653	3.4234	0.0006
		Follow-up	−0.0705	−2.3762	0.0175
		Publication year	−0.1805	−1.4780	0.1394
TC	8	Sample size	−0.0001	−0.3244	0.7456
		History of Diabetes	−0.0249	−0.2167	0.8284
		Follow-up	0.0011	0.2634	0.7923
		Publication year	−0.0021	−1.2347	0.2169

BMI, body mass index; HbA1c, glycated haemoglobin; TC, total cholesterol.

Discussion

The present meta-analysis included 15 RCTs, comprising 3383 participants, to assess the effectiveness of SMBG in patients with non-insulin-treated T2D with the primary outcome of HbA1c levels. A sensitivity analysis on sample size and subgroup analyses on geographical region and SMBG history were also performed, together with assessment of the associations of ethnicity and living environment with SMBG, because significant efficacy and safety differences were previously observed among racial/ethnic groups in the DURABLE trial.18 Various clinical indices, including SBP, DBP, body weight, BMI, TG, TC and WC, were also analysed and reported for the first time in this study. A comparison of the RCTs included in this meta-analysis with those included in some previous meta-analyses is presented (see online supplementary table S7).

The results for overall effects suggested that use of SMBG by patients with non-insulin-treated T2D led to a significant reduction in HbA1c levels (MD −0.33; 95% CI −0.45 to −0.22; p=3.0730e-8; n=18), which is consistent with previous systematic reviews.7 12 13 The sensitivity analysis of studies with large sample sizes showed that SMBG could help reduce HbA1c levels in a robust manner. The subgroup analysis of geographical regions revealed that significant decreases in HbA1c levels were observed in the Asia and America–Europe groups. SMBG improved the HbA1c levels in the short term (≤6 months), but also had long-term effects (≥12-month follow-up), being different from the Cochrane review.6 Significant reductions in HbA1c levels were also found in newly diagnosed patients and patients with diabetes for more than 12 months, indicating that SMBG seemed to benefit patients with T2D regardless of diabetes duration. The quality of evidence for HbA1c was rated as moderate, which was the same as the last Cochrane review.6 The factors influencing the evidence quality mainly appeared to be small effect size and significant heterogeneity in this meta-analysis.

In addition to HbA1c, significant reductions in several clinical indices, including BMI, TC and WC, were found in various analyses, indicating that SMBG does not simply function as a monitoring tool, but forms a component of a complex intervention capable of improving overall glycaemic control. Despite BMI and TC being the only clinical indices to show significant reductions following SMBG in patients diagnosed with T2D for over 12 months, the present results suggest that SMBG may have long-term effects on the control of BMI and TC in patients with T2D. Reductions in BMI and TC were also observed in other subgroup and sensitivity analyses. The reductions ranged from −0.87 to −0.24 for BMI and from −0.12 to −0.11 mmol/L for TC, indicating that SMBG might be useful for obese patients. Although SMBG was helpful for BMI, the evidence quality for BMI was low, and moderate publication bias was also observed. Thus, more RCTs are warranted for the effect of SMBG on BMI. Any observed reductions in the remaining indices had no clinical significance, in agreement with the findings of Farmer et al.27

The above-discussed evidence indicates that SMBG helped to improve glycaemic control, but under a single specific test condition. Thus, combinations of two or more test conditions are required to address the issue of what type of patient under what kind of intervention would achieve improvement of glycaemic control by SMBG. A classification tree method was adopted to show the influence of baseline HbA1c, follow-up period, geographical region and diabetes duration on SMBG. As shown in online supplementary figure S3, SMBG improved glycaemic control regardless of baseline HbA1c, while SMBG was significantly more effective in control patients with lower HbA1c (<8%) than in those with higher HbA1c (≥8%). Among the patients with lower HbA1c, SMBG improved glycaemic control in the short term and long term, and performed better in the former. Furthermore, SMBG might have long-term effects in the improvement of glycaemic control in newly diagnosed patients with T2D with lower HbA1c. All of the evidence shown in online supplementary figure S3 indicates that SMBG has a short-term effect in T2D, and that a clinically significant change in the long term is only observed in newly diagnosed patients with T2D with lower HbA1c.

Compared with the last Cochrane review,6 there are several differences. First, RCTs involving comparisons between SMBG and SMUG (as a control) or between SMUG and usual care (SMUG as an intervention) were not included in the present study, because SMBG was preferred for perceived accuracy and usefulness,10 and SMUG was associated with renal glucose threshold, combined diseases and drugs, which would not allow us to distinguish among hypoglycaemia, normoglycaemia and mild hyperglycaemia. Second, in our analysis, SMBG was significantly better than usual care in the short term and long term, while SMBG was better in the short term in the last Cochrane review.6

There are several limitations to this meta-analysis. First, the sample sizes in some of the included studies were too small to confidently exclude a difference in response in the reduction of HbA1c and clinical indices between the SMBG and control groups, and this might be a source of heterogeneity. Second, the heterogeneities of the pooled effect sizes on HbA1c were high, and according to previous reviews8–10 and the RCTs included in this meta-analysis, the most important heterogeneities might arise through the intensity of education, intervention components coupled to SMBG and frequency of SMBG testing. Third, there were no properly collected data for a statistical analysis of adverse events and economic assessment. Fourth, potential synonyms for SMBG and diabetes were not included in the strategy, and EMBASE was not searched, which may have led to relevant papers being missed and possible publication bias. Finally, although SMBG did not achieve the 0.5% reduction in HbA1c deemed a clinically significant change,10 it significantly reduced the HbA1c level under all tested conditions. Last, the present evidence warrants further research, because some outcome measures were reported by fewer studies and the potential associations among the outcome measures remain unclear.

Conclusion

In patients with T2D who were not using insulin, SMBG improved the HbA1c level in the short term and long term.