2014
DOI: 10.1016/j.ahj.2014.04.008
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Rationale and design of PRIMA II: A multicenter, randomized clinical trial to study the impact of in-hospital guidance for acute decompensated heart failure treatment by a predefined NT-PRoBNP target on the reduction of readmIssion and Mortality rAtes

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Cited by 36 publications
(18 citation statements)
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“…17,18) Paulo, et al 19) enrolled 182 subjects and revealed that the admission NT-proBNP level was not an independent predictor for in-hospital mortality. However, several studies have observed a close relationship between admission NT-proBNP and HF prognosis.…”
Section: Discussionmentioning
confidence: 99%
“…17,18) Paulo, et al 19) enrolled 182 subjects and revealed that the admission NT-proBNP level was not an independent predictor for in-hospital mortality. However, several studies have observed a close relationship between admission NT-proBNP and HF prognosis.…”
Section: Discussionmentioning
confidence: 99%
“…Rationale and design of the study have been previously reported [9]. This substudy was approved by the Medical Ethics Committee of the University of Amsterdam and Academic Medical Center, The Netherlands and written informed consent was obtained from all patients.…”
Section: Original Cohortmentioning
confidence: 99%
“…Patients were randomized at the day of clinical stability, a discharge criterion requiring the presence of 3 of 4 clinical variables [9]. No attempts were made to adjust therapy using these measurements before randomization.…”
Section: Original Cohortmentioning
confidence: 99%
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“…[2][3][4] Besides, the reduction in NT-proBNP levels directly reflects blood volume response to diuretic therapy. [5][6][7] NT-proBNP in acute heart failure; hospital admission versus discharge Int J Cardiovasc Sci. 2017;30(6)469-475…”
Section: Introductionmentioning
confidence: 99%