Access BNP Clinical Enrollment Study

Prior treatment

• Active participation in a clinical study that may interfere with participation in this study (e.g., investigational drug study)

Other illness

• Impairment in individual's capacity to give informed consent
• Dyspnea clearly not secondary to heart failure (e.g., primary lung disease or chest trauma).

Age

• Individuals less than 22 years old

Other

• On dialysis
• On nesiritide infusion
• Subject clinical/medical history access is not available to Sponsor, delegates, and FDA or other regulatory agencies upon request.
• Reason(s) determined by the Principal Investigator that would place the individual at increased risk or preclude the individual from fully complying with or completing the study.

• Ability to provide informed consent
• Adult greater than or equal to 22 years old, any gender, race, ethnicity
• Presenting with clinical suspicion of new onset heart failure or worsening symptoms suggestive of decompensated or exacerbated heart failure
• Ability to fulfill study data collection requirements (including responding to questions for the NYHA evaluation)