<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Dondo TB</submitter><funding>British Heart Foundation</funding><funding>Medical Research Council</funding><funding>National Institute for Health Research (NIHR)</funding><pagination>e011600</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4947744</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>6(7)</volume><pubmed_abstract>&lt;h4>Objectives&lt;/h4>To investigate geographic variation in guideline-indicated treatments for non-ST-elevation myocardial infarction (NSTEMI) in the English National Health Service (NHS).&lt;h4>Design&lt;/h4>Cohort study using registry data from the Myocardial Ischaemia National Audit Project.&lt;h4>Setting&lt;/h4>All Clinical Commissioning Groups (CCGs) (n=211) in the English NHS.&lt;h4>Participants&lt;/h4>357 228 patients with NSTEMI between 1 January 2003 and 30 June 2013.&lt;h4>Main outcome measure&lt;/h4>Proportion of eligible NSTEMI who received all eligible guideline-indicated treatments (optimal care) according to the date of guideline publication.&lt;h4>Results&lt;/h4>The proportion of NSTEMI who received optimal care was low (48 257/357 228; 13.5%) and varied between CCGs (median 12.8%, IQR 0.7-18.1%). The greatest geographic variation was for aldosterone antagonists (16.7%, 0.0-40.0%) and least for use of an ECG (96.7%, 92.5-98.7%). The highest rates of care were for acute aspirin (median 92.8%, IQR 88.6-97.1%), and aspirin (90.1%, 85.1-93.3%) and statins (86.4%, 82.3-91.2%) at hospital discharge. The lowest rates were for smoking cessation advice (median 11.6%, IQR 8.7-16.6%), dietary advice (32.4%, 23.9-41.7%) and the prescription of P2Y12 inhibitors (39.7%, 32.4-46.9%). After adjustment for case mix, nearly all (99.6%) of the variation was due to between-hospital differences (median 64.7%, IQR 57.4-70.0%; between-hospital variance: 1.92, 95% CI 1.51 to 2.44; interclass correlation 0.996, 95% CI 0.976 to 0.999).&lt;h4>Conclusions&lt;/h4>Across the English NHS, the optimal use of guideline-indicated treatments for NSTEMI was low. Variation in the use of specific treatments for NSTEMI was mostly explained by between-hospital differences in care. Performance-based commissioning may increase the use of NSTEMI treatments and, therefore, reduce premature cardiovascular deaths.&lt;h4>Trial registration number&lt;/h4>NCT02436187.</pubmed_abstract><journal>BMJ open</journal><pubmed_title>Geographic variation in the treatment of non-ST-segment myocardial infarction in the English National Health Service: a cohort study.</pubmed_title><pmcid>PMC4947744</pmcid><funding_grant_id>RP-PG-0407-10314</funding_grant_id><funding_grant_id>NIHR-CTF-2014-03-03</funding_grant_id><funding_grant_id>PG/13/81/30474</funding_grant_id><funding_grant_id>05/40/04</funding_grant_id><funding_grant_id>NF-SI-0513-10130</funding_grant_id><funding_grant_id>PG/13/81/3047</funding_grant_id><funding_grant_id>MC_PC_13041</funding_grant_id><funding_grant_id>G0902393</funding_grant_id><funding_grant_id>MR/K006584/1</funding_grant_id><pubmed_authors>Hall M</pubmed_authors><pubmed_authors>Hemingway H</pubmed_authors><pubmed_authors>Bloor K</pubmed_authors><pubmed_authors>Yan AT</pubmed_authors><pubmed_authors>Alabas OA</pubmed_authors><pubmed_authors>Timmis AD</pubmed_authors><pubmed_authors>Oliver G</pubmed_authors><pubmed_authors>Deanfield JE</pubmed_authors><pubmed_authors>Gale CP</pubmed_authors><pubmed_authors>Dondo TB</pubmed_authors><pubmed_authors>Batin PD</pubmed_authors><pubmed_authors>Norman P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Geographic variation in the treatment of non-ST-segment myocardial infarction in the English National Health Service: a cohort study.</name><description>&lt;h4>Objectives&lt;/h4>To investigate geographic variation in guideline-indicated treatments for non-ST-elevation myocardial infarction (NSTEMI) in the English National Health Service (NHS).&lt;h4>Design&lt;/h4>Cohort study using registry data from the Myocardial Ischaemia National Audit Project.&lt;h4>Setting&lt;/h4>All Clinical Commissioning Groups (CCGs) (n=211) in the English NHS.&lt;h4>Participants&lt;/h4>357 228 patients with NSTEMI between 1 January 2003 and 30 June 2013.&lt;h4>Main outcome measure&lt;/h4>Proportion of eligible NSTEMI who received all eligible guideline-indicated treatments (optimal care) according to the date of guideline publication.&lt;h4>Results&lt;/h4>The proportion of NSTEMI who received optimal care was low (48 257/357 228; 13.5%) and varied between CCGs (median 12.8%, IQR 0.7-18.1%). The greatest geographic variation was for aldosterone antagonists (16.7%, 0.0-40.0%) and least for use of an ECG (96.7%, 92.5-98.7%). The highest rates of care were for acute aspirin (median 92.8%, IQR 88.6-97.1%), and aspirin (90.1%, 85.1-93.3%) and statins (86.4%, 82.3-91.2%) at hospital discharge. The lowest rates were for smoking cessation advice (median 11.6%, IQR 8.7-16.6%), dietary advice (32.4%, 23.9-41.7%) and the prescription of P2Y12 inhibitors (39.7%, 32.4-46.9%). After adjustment for case mix, nearly all (99.6%) of the variation was due to between-hospital differences (median 64.7%, IQR 57.4-70.0%; between-hospital variance: 1.92, 95% CI 1.51 to 2.44; interclass correlation 0.996, 95% CI 0.976 to 0.999).&lt;h4>Conclusions&lt;/h4>Across the English NHS, the optimal use of guideline-indicated treatments for NSTEMI was low. Variation in the use of specific treatments for NSTEMI was mostly explained by between-hospital differences in care. Performance-based commissioning may increase the use of NSTEMI treatments and, therefore, reduce premature cardiovascular deaths.&lt;h4>Trial registration number&lt;/h4>NCT02436187.</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Jul</publication><modification>2026-06-08T06:48:00.582Z</modification><creation>2026-06-08T03:14:01.06Z</creation></dates><accession>S-EPMC4947744</accession><cross_references><pubmed>27406646</pubmed><doi>10.1136/bmjopen-2016-011600</doi></cross_references></HashMap>