Identification of Patient Phenotypes Associated With Elevated Aldosterone Levels

NCT01614860 | Completed

• 2 other identifiers: KL2-2012NWAHFKL2RR025740
• Study Type: observational
• Target: 90
• Locations: 1 country
• Sites: 1

Brief Summary

Post-discharge mortality and re-hospitalization for acute heart failure (AHF) affects 15% and 30% of patients respectively, within 90 days. With over 1 million annual hospitalizations and a financial cost exceeding 20 billion dollars, AHF is a major public health burden. Yet no AHF therapy to date definitively reduces morbidity and mortality, and in stark contrast to heart attack patients, highly rated evidence in guidelines do not exist. Although AHF is a syndrome and not one disease, typical treatment of patients hospitalized with AHF suggests otherwise. Despite substantial differences among AHF patients, therapy is largely uniform; patients receive medicine to help get rid of excess volume and little else. Although decades of empirical use support the symptomatic benefits of traditional therapies, outcomes remain extremely poor. As opposed to the "one-size-fits-all" approach used unsuccessfully to date in clinical trials, identification of specific AHF patient sub-groups is critical, so that tailored therapies can be developed and tested. Preliminary data suggests that the neurohormone aldosterone may be detrimental in AHF patients. Furthermore, this hormone level appears to rise during hospitalization. The investigators therefore propose to identify specific AHF patient phenotypes associated with high serum aldosterone levels to subsequently address the hypothesis that early aldosterone blockade continued throughout hospitalization will decrease re-hospitalization and mortality. Specifically, the investigators hypothesize that AHF patients with elevated serum aldosterone levels have a distinct phenotype compared to those with lower or normal aldosterone levels. Specifically, they will be older, have a lower systolic blood pressure, lower EF, worse renal function, higher BNP, and previous hospitalization for HF.

Conditions

Acute Heart Failure

Keywords

Aldosterone; Echocardiography; Neurohormones

Outcome Measures

Primary Outcomes (1)

• There is no prespecified primary outcome as this is an exploratory study

  2 years

Secondary Outcomes (1)

• There is no secondary outcome as this is an exploratory study

  2 years

Other Outcomes (1)

• To prospectively examine the baseline and dynamic phenotype of AHFS patients in relation to aldosterone levels on initial presentation.

  two years

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Probability Sample

Study Population

Patients who present to the Emergency Department (ED) with signs and symptoms of AHF

You may qualify if:

• Male or female ≥ 18 years of age
• AHF is the primary working diagnosis for ER management and treatment Have received or will receive IV diuretic therapy
• Enrolled within 12 hours of initial diuretic dose order

You may not qualify if:

• Serum Cr ≥ 2.5mg/dL (males) or 2.0mg/dL (females), or eGFR \< 20 ml/min/1.73m2
• Serum potassium ≥ 5.5 mEq/L
• Transplant recipients of any kind
• Fever \> 101.0
• Severe lung disease (required home O2 or daily oral steroids)
• Acute coronary syndrome within last 30 days
• Major surgery within last 30 days
• Known hypertrophic obstructive cardiomyopathy, pericardial constriction, or hemodynamically significant valvular disease
• Life expectancy less than 12 months for any reason
• Current treatment for any malignancy of any kind
• Cardiogenic shock and/or requiring IV inotropic therapy
• Pregnant or recently pregnant within last 90 days
• Known intolerance to aldosterone antagonist
• Inability to give appropriate written consent

Sponsors & Collaborators

• Northwestern University: lead
• National Center for Research Resources (NCRR): collaborator

Study Sites (1)

Northwestern Memorial Hospital

Chicago, Illinois, 60611, United States

Location

Biospecimen

Retention: SAMPLES WITHOUT DNA

Plasma storage for potential future studies with existing or novel biomarkers.

Study Officials

• Peter S Pang, MD

  Northwestern University

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Associate Professor of Emergency Medicine

Study Record Dates

• First Submitted: June 6, 2012
• First Posted: June 8, 2012
• Study Start: May 1, 2012
• Primary Completion: June 1, 2014
• Study Completion: June 1, 2014
• Last Updated: September 9, 2014

Record last verified: 2014-09

Locations

US (1)