Design: This study was designed as a single-center, single-blind, randomized controlled trial conducted at Hospital Fundación Jimenez Diaz (Madrid, Spain) from February 2020 to December 2021. It is a pilot study which has the objective of obtaining significant results in order to conduct a major research in the future with the purpose of including broadly the use of BIA in HF management. This study was approved by an institutional review committee and performed under Helsinki Declaration Guidelines. All patients provided written informed consent to participate.
Study Procedures All patients included in the study were measured weight and height at admission, and blood tests with hemogram and serum biochemistry including cardiac biomarkers such as NT-proBNP and troponin I were also ordered.
In the first 24 hours after admission an echocardiogram, a lung ultrasound (LUS) and a BIA were done in all patients. BIA was always performed by nephrologists from our hospital not involved in the patient's clinical care. BIA analysis to achieve assessments of fluid status, especially dry-weight, was performed with the portable Biomasc touch i8 (MaltronInternationl, Essex, UK). During the hospitalization period, blood parameters were measured according to standard clinical practice in all patients, with the condition of taking a blood chemistry including NT-proBNP on the day of discharge.
All patients were followed up for 90 days with a new complete blood test including NT-proBNP.
Eligible patients were randomized into two groups:
* Group I (study arm): included 24 patients who received a diuretic treatment guided by BIA. These patients were discharged when dry-weight was achieved according to BIA measurements if there was none clinical condition which justified the hospitalization.
* Group II (control arm): included 24 patients who received the standard clinical practice. In those patients, BIA parameters were not known by the physician responsible. These patients were discharged when they achieved the euvolemic state based in the criteria of their physician.
Outcomes Given the pilot nature of the study the investigators looked for a feasible, clinically meaningful, in-hospital outcome. Development of acute kidney injury (AKI) during hospitalization, defined as an increase in serum creatinine by \>0.5 mg/dL (AKIN classification stage III), was the primary outcome. Patients were followed for at least 3 months after discharge. The first secondary outcome was the percentage of patients who achieved levels of NT-proBNP levels \<1.000 pg/mL within 90 days after discharge.
Additional secondary outcomes included length of stay in hospital, NT-proBNP reduction \>30% during hospitalization, and the combined endpoint of all-cause death, rehospitalization for HF or visit to the ED (emergency department) because of congestion symptoms measured at 90 days after discharge. Patients were contacted by telephone or returned for hospital or outpatient visits.
Statistical analysis Discrete variables were summarized as counts and percentages. Continuous variables were described using median and interquartile range (IQR)and were tested for normality using the Kolmogorov-Smirnov or Shapiro-Wilk test.Baseline characteristics were compared among standard treatment vs BIA-guided treatment with the chi-square test or Fisher´s test for discrete variables, and with Student´s t test and non-parametric Mann-Whitney test for normally and non-normally distributed quantitative variables respectively. Primary and secondary outcomes were also compared between both treatment groups using a chi-square test for independence.Results of these analyses were considered exploratory to study future differences between the groups in terms of time to first adverse outcome or event-free survival. A two-sided P value of less than 0.05 was considered to be statistically significant for all analyses. All statistical analyses were performed using SPSS for Windows Version 19.0 (IBM Corp, Armonk NY).
