2014
DOI: 10.1016/s0140-6736(14)61335-0
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Glucagon-like peptide-1 receptor agonist and basal insulin combination treatment for the management of type 2 diabetes: a systematic review and meta-analysis

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Cited by 348 publications
(291 citation statements)
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“…As an alternative, the statement mentioned that, in selected patients, simpler (but somewhat less flexible) premixed formulations of intermediateand short/rapid-acting insulins in fixed ratios could also be considered (44). Over the past 3 years, however, the effectiveness of combining GLP-1 receptor agonists (both shorter-acting and newer weekly formulations) with basal insulin has been demonstrated, with most studies showing equal or slightly superior efficacy to the addition of prandial insulin, and with weight loss and less hypoglycemia (45)(46)(47). The available data now suggest that either a GLP-1 receptor agonist or prandial insulin could be used in this setting, with the former arguably safer, at least for short-term outcomes (45,48,49).…”
Section: Implementation Strategiesmentioning
confidence: 99%
See 1 more Smart Citation
“…As an alternative, the statement mentioned that, in selected patients, simpler (but somewhat less flexible) premixed formulations of intermediateand short/rapid-acting insulins in fixed ratios could also be considered (44). Over the past 3 years, however, the effectiveness of combining GLP-1 receptor agonists (both shorter-acting and newer weekly formulations) with basal insulin has been demonstrated, with most studies showing equal or slightly superior efficacy to the addition of prandial insulin, and with weight loss and less hypoglycemia (45)(46)(47). The available data now suggest that either a GLP-1 receptor agonist or prandial insulin could be used in this setting, with the former arguably safer, at least for short-term outcomes (45,48,49).…”
Section: Implementation Strategiesmentioning
confidence: 99%
“…Over the past 3 years, however, the effectiveness of combining GLP-1 receptor agonists (both shorter-acting and newer weekly formulations) with basal insulin has been demonstrated, with most studies showing equal or slightly superior efficacy to the addition of prandial insulin, and with weight loss and less hypoglycemia (45)(46)(47). The available data now suggest that either a GLP-1 receptor agonist or prandial insulin could be used in this setting, with the former arguably safer, at least for short-term outcomes (45,48,49). Accordingly, in those patients on basal insulin with one or more oral agents whose diabetes remains uncontrolled, the addition of a GLP-1 receptor agonist or mealtime insulin could be viewed as a logical progression of the treatment regimen, the former perhaps a more attractive option in more obese individuals or in those who may not have the capacity to handle the complexities of a multidose insulin regimen.…”
Section: Implementation Strategiesmentioning
confidence: 99%
“…GLP‐1RAs reduce food intake and promote weight loss 1 and have the additional benefit of a low risk of hypoglycaemia compared with basal insulin 2, 3. These features may be helpful in overcoming some aspects of clinical inertia with respect to intensifying therapy in patients with T2D 4.…”
Section: Introductionmentioning
confidence: 99%
“…Most of those studies have indicated equal or slightly superior efficacy to the addition of prandial insulin with accompanying weight loss and decreasing hypoglycaemia. [13,14] There are different factors that cause resistance to the initiation of insulin therapy such as beliefs and perceptions concerning diabetes and its treatment and the nature and consequences of insulin therapy. [15] This may also be due to a dislike of the healthcare centres.…”
Section: Introductionmentioning
confidence: 99%