<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Orozco-Beltran D</submitter><funding>Novo Nordisk</funding><pagination>236-43</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4832583</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>70(3)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>To investigate the effect of healthcare provider (HCP) type (primary vs. specialist) on glycaemic control and other treatment parameters.&lt;h4>Research design and methods&lt;/h4>Study of Once-Daily Levemir (SOLVE(™) ) is an international, 24-week, observational study of insulin initiation in people with type 2 diabetes.&lt;h4>Results&lt;/h4>A total of 17,374 subjects were included, comprising 4144 (23.9%) primary care subjects. Glycaemic control improved in both HCP groups from baseline to final visit [glycated haemoglobin (HbA1c) -1.2 ± 1.4% (-13.1 ± 15.3 mmol/mol) and -1.3 ± 1.6% (-14.2 ± 17.5 mmol/mol), respectively]. After adjustment for known confounders, there was no statistically significant effect of HCP group on final HbA1c [-0.04%, 95% confidence interval (CI) -0.09 to -0.01 (-0.4 mmol/mol, 95% CI -1.0-0.1 mmol/mol), p = 0.1590]. However, insulin doses at the final visit were higher in primary care patients (+0.06, 95% CI 0.06-0.07 U/kg, p &lt; 0.0001). Logistic regression demonstrated a significant effect of HCP type (primary vs. specialist care) on hypoglycaemia risk [odds ratio (OR) 0.75, 95% CI 0.64-0.87, p = 0.0002]. Primary care physicians took more time to train patients and had more frequent contact with patients than specialists (both p &lt; 0.0001).&lt;h4>Conclusions&lt;/h4>Primary care physicians and specialists achieved comparable improvements in glycaemic control following insulin initiation.</pubmed_abstract><journal>International journal of clinical practice</journal><pubmed_title>Basal insulin initiation in primary vs. specialist care: similar glycaemic control in two different patient populations.</pubmed_title><pmcid>PMC4832583</pmcid><funding_grant_id>NCT00740519</funding_grant_id><funding_grant_id>NCT00825643</funding_grant_id><pubmed_authors>Caputo S</pubmed_authors><pubmed_authors>SOLVE Study Group</pubmed_authors><pubmed_authors>Faerch L</pubmed_authors><pubmed_authors>Pan C</pubmed_authors><pubmed_authors>Svendsen AL</pubmed_authors><pubmed_authors>Orozco-Beltran D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Basal insulin initiation in primary vs. specialist care: similar glycaemic control in two different patient populations.</name><description>&lt;h4>Objective&lt;/h4>To investigate the effect of healthcare provider (HCP) type (primary vs. specialist) on glycaemic control and other treatment parameters.&lt;h4>Research design and methods&lt;/h4>Study of Once-Daily Levemir (SOLVE(™) ) is an international, 24-week, observational study of insulin initiation in people with type 2 diabetes.&lt;h4>Results&lt;/h4>A total of 17,374 subjects were included, comprising 4144 (23.9%) primary care subjects. Glycaemic control improved in both HCP groups from baseline to final visit [glycated haemoglobin (HbA1c) -1.2 ± 1.4% (-13.1 ± 15.3 mmol/mol) and -1.3 ± 1.6% (-14.2 ± 17.5 mmol/mol), respectively]. After adjustment for known confounders, there was no statistically significant effect of HCP group on final HbA1c [-0.04%, 95% confidence interval (CI) -0.09 to -0.01 (-0.4 mmol/mol, 95% CI -1.0-0.1 mmol/mol), p = 0.1590]. However, insulin doses at the final visit were higher in primary care patients (+0.06, 95% CI 0.06-0.07 U/kg, p &lt; 0.0001). Logistic regression demonstrated a significant effect of HCP type (primary vs. specialist care) on hypoglycaemia risk [odds ratio (OR) 0.75, 95% CI 0.64-0.87, p = 0.0002]. Primary care physicians took more time to train patients and had more frequent contact with patients than specialists (both p &lt; 0.0001).&lt;h4>Conclusions&lt;/h4>Primary care physicians and specialists achieved comparable improvements in glycaemic control following insulin initiation.</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Mar</publication><modification>2024-11-07T10:08:15.492Z</modification><creation>2019-03-27T02:11:36Z</creation></dates><accession>S-EPMC4832583</accession><cross_references><pubmed>26916450</pubmed><doi>10.1111/ijcp.12776</doi></cross_references></HashMap>