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Evidence that periodontal treatment improves diabetes outcomes: a systematic review and meta‐analysis
Author(s) -
Engebretson Steven,
Kocher Thomas
Publication year - 2013
Publication title -
journal of clinical periodontology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.456
H-Index - 151
eISSN - 1600-051X
pISSN - 0303-6979
DOI - 10.1111/jcpe.12084
Subject(s) - medicine , meta analysis , randomized controlled trial , diabetes mellitus , sample size determination , random effects model , publication bias , medline , study heterogeneity , periodontitis , confidence interval , dentistry , type 2 diabetes , subgroup analysis , statistics , mathematics , political science , law , endocrinology
Context The effect of periodontal therapy on diabetes outcomes has not been established. Objective This update examines the effect of periodontal treatment on diabetes outcomes. Data sources Literature since October 2009 using MEDLINE . Study eligibility criteria Published RCT s including periodontal therapy for diabetic subjects, a metabolic outcome, an untreated control group, and follow‐up of 3 months. Data extraction Pre‐defined data fields, including study quality indicators were used. Data synthesis A search revealed 56 publications of which 9 met inclusion criteria. Mean change of HbA1c from baseline was compared across treatment groups. Pooled analysis was based on random effects models. Results A meta‐analysis indicated a mean treatment effect of −0.36% HbA1c ( CI −0.54, −0.19) compared to no treatment after periodontal therapy ( p  < 0.0001). Heterogeneity tests revealed only minimal evidence of publication bias ( I 2  = 9%). Limitations Small sample size and high risk of bias remain problematic for studies of this type. Periodontal therapy varied considerably. Conclusion The modest reduction in HbA1c observed as a result of periodontal therapy in subjects with type 2 diabetes is consistent with previous systematic reviews. Despite this finding, there is limited confidence in the conclusion due to a lack of multi‐centre trials of sufficient sample size are lacking.

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