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. 2020 Sep 21;17(18):6886. doi: 10.3390/ijerph17186886

Table 1.

Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) assessment of randomised controlled trials reporting effectiveness of patient-centred medical home (PCMH) vs. standard general practitioner (GP) care on outcomes of interest.

Outcomes No of Studies Risk of Bias Inconsistency Indirectness Imprecision Publication Bias GRADE Quality of Evidence þ
Depression 31 Serious Serious Not serious Not serious Undetected Moderate
Quality of Life 21 Serious Not serious Not serious Not serious Undetected Moderate
Blood pressure 13 Serious Not serious Not serious Not serious Undetected Moderate
Glycated Hemoglobin 9 Serious Serious Not serious Not serious Undetected Low ‡¶
LDL Cholesterol 4 Serious Serious Not serious Not serious Undetected Low ‡¶
HDL Cholesterol 1 Serious - Not serious Not serious Undetected Low †‡^
Total Cholesterol 2 Serious - Not serious Not serious Undetected Low ‡^
Hospital admissions 5 Serious Not serious Not serious Not serious Undetected Moderate
Self-management (PACIC scores) 3 Serious Serious Not serious Not serious Undetected Low ‡¶
Cost-effectiveness 19 Serious Serious Not serious Not serious Undetected Low ‡¶

þ High quality: Further research is very unlikely to change our confidence in the estimate of effect; Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate; Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate; Very low quality: We are very uncertain about the estimate; LDL—Low Density Lipoprotein; HDL—High Density Lipoprotein; PACIC—Patient Assessment of Care for Chronic Conditions; Most studies did not blind participants or personnel as it was not practical. Therefore, we did not downgrade for these risks/uncertainties. However, studies not reporting blinding of outcome assessment were downgraded in quality; Significant level of heterogeneity within results (I2 between 80–90%); ^ Single study—Inconsistency not applicable; Because of the nature of the quasi-experimental designs risk of bias is unavoidable.