{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,1]],"date-time":"2026-04-01T13:41:33Z","timestamp":1775050893638,"version":"3.50.1"},"reference-count":26,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"3","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2020,3]]},"abstract":"<jats:sec>\n            <jats:title>Background:<\/jats:title>\n            <jats:p>Visit-to-visit office blood pressure (BP) variability (BPV) has been associated with morbidity and mortality outcomes in several cardiovascular conditions. The aim of this study was to evaluate the association between BPV and outcomes in patients with heart failure and reduced ejection fraction and the effect of eplerenone on BPV.<\/jats:p>\n          <\/jats:sec>\n          <jats:sec>\n            <jats:title>Methods and results:<\/jats:title>\n            <jats:p>We evaluated the associations between BPV, calculated as SBP coefficient of variation (SBP-CoV\u200a=\u200aSD\/mean\u200a\u00d7\u200a100%), and the primary composite endpoint of cardiovascular mortality or heart failure hospitalization (HFH), and its components, in 2549 patients from the Eplerenone in Patients with Systolic Heart Failure and Mild Symptoms trial. Lower SBP-CoV was independently associated with a higher risk of all the studied outcomes, while higher as well as lower SBP-CoV were associated with a higher risk of cardiovascular death. After a median follow-up period of 21 months the risk of the composite outcome of cardiovascular death or HFH was almost double in the lower SBP-CoV tertile as compared with the intermediate tertile [adjusted hazard ratio: 2.01, 95% confidence interval (1.62\u20132.51), <jats:italic toggle=\"yes\">P<\/jats:italic>\u200a&lt;\u200a0.001]. The relationship between SBP-CoV and outcomes was not modified by eplerenone (<jats:italic toggle=\"yes\">P<\/jats:italic> value for interaction\u200a=\u200a0.48). An interaction was detected between mean SBP and SBP-CoV for the primary outcome (<jats:italic toggle=\"yes\">P<\/jats:italic>\u200a=\u200a0.048) and for HFH (<jats:italic toggle=\"yes\">P<\/jats:italic>\u200a=\u200a0.018). The effect modification was slight, but lower SBP-CoV was associated with worse outcomes in patients with both low and high SBP, while this interaction was less clear for patients with SBP in the \u2018normal\u2019 range.<\/jats:p>\n          <\/jats:sec>\n          <jats:sec>\n            <jats:title>Conclusion:<\/jats:title>\n            <jats:p>In our patients with heart failure and reduced ejection fraction and mild symptoms, both a lower and higher SBP-CoV were associated with worse outcomes. SBP-CoV did not modify the benefit of eplerenone. Further studies are warranted to clarify the role of BPV in heart failure.<\/jats:p>\n          <\/jats:sec>\n          <jats:sec>\n            <jats:title>ClinicalTrials.gov identifier:<\/jats:title>\n            <jats:p>NCT00232180.<\/jats:p>\n          <\/jats:sec>","DOI":"10.1097\/hjh.0000000000002275","type":"journal-article","created":{"date-parts":[[2019,10,4]],"date-time":"2019-10-04T14:47:50Z","timestamp":1570200470000},"page":"420-425","source":"Crossref","is-referenced-by-count":20,"title":["Visit-to-visit blood pressure variation and outcomes in heart failure with reduced ejection fraction: findings from the Eplerenone in Patients with Systolic Heart Failure and Mild Symptoms trial"],"prefix":"10.1097","volume":"38","author":[{"given":"Luca","family":"Monzo","sequence":"first","affiliation":[{"name":"Department of Cardiovascular, Respiratory, Nephrological and Geriatric Sciences, \u2018Sapienza\u2019 University, Rome, Italy"}]},{"given":"Jo\u00e3o Pedro","family":"Ferreira","sequence":"additional","affiliation":[{"name":"Universit\u00e9 de Lorraine, INSERM, Centre d\u2019Investigations Cliniques-Plurith\u00e9matique 1433, and INSERM U1116, CHRU, F-CRIN INI-CRCT (Cardiovascular and Renal Clinical Trialists), Nancy, France"}]},{"given":"Paula","family":"Abreu","sequence":"additional","affiliation":[{"name":"Pfizer, New York, New York, USA"}]},{"given":"Annette","family":"Szumski","sequence":"additional","affiliation":[{"name":"Pfizer, New York, New York, USA"}]},{"given":"Michael","family":"B\u00f6hm","sequence":"additional","affiliation":[{"name":"Department of Cardiology, Saarland University, Homburg, Saarland, Germany"}]},{"given":"John J.V.","family":"McMurray","sequence":"additional","affiliation":[{"name":"The British Heart Foundation Cardiovascular Research Centre, University of Glasgow, Glasgow, UK"}]},{"given":"Bertram","family":"Pitt","sequence":"additional","affiliation":[{"name":"University of Michigan School of Medicine, Ann Arbor, Michigan, USA"}]},{"given":"Karl","family":"Swedberg","sequence":"additional","affiliation":[{"name":"Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden"}]},{"given":"Dirk J.","family":"van Veldhuisen","sequence":"additional","affiliation":[{"name":"University of Groningen, University Medical Center Groningen, Groningen, The Netherlands"}]},{"given":"Nicolas","family":"Girerd","sequence":"additional","affiliation":[{"name":"Universit\u00e9 de Lorraine, INSERM, Centre d\u2019Investigations Cliniques-Plurith\u00e9matique 1433, and INSERM U1116, CHRU, F-CRIN INI-CRCT (Cardiovascular and Renal Clinical Trialists), Nancy, France"}]},{"given":"John","family":"Vincent","sequence":"additional","affiliation":[{"name":"Pfizer, New York, New York, USA"}]},{"given":"Faiez","family":"Zannad","sequence":"additional","affiliation":[{"name":"Universit\u00e9 de Lorraine, INSERM, Centre d\u2019Investigations Cliniques-Plurith\u00e9matique 1433, and INSERM U1116, CHRU, F-CRIN INI-CRCT (Cardiovascular and Renal Clinical Trialists), Nancy, France"}]},{"given":"Patrick","family":"Rossignol","sequence":"additional","affiliation":[{"name":"Universit\u00e9 de Lorraine, INSERM, Centre d\u2019Investigations Cliniques-Plurith\u00e9matique 1433, and INSERM U1116, CHRU, F-CRIN INI-CRCT (Cardiovascular and Renal Clinical Trialists), Nancy, France"}]}],"member":"276","reference":[{"key":"R1-20230912","doi-asserted-by":"crossref","first-page":"965","DOI":"10.1161\/HYPERTENSIONAHA.114.03903","article-title":"Visit-to-visit variability of blood pressure and cardiovascular disease and all-cause mortality: a systematic review and meta-analysis","volume":"64","author":"Diaz","year":"2014","journal-title":"Hypertension"},{"key":"R2-20230912","doi-asserted-by":"crossref","first-page":"39","DOI":"10.1161\/HYPERTENSIONAHA.115.06960","article-title":"The association between antihypertensive medication nonadherence and visit-to-visit variability of blood pressure: findings 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