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PRognostic hEModynamIc profiling in the acUte ill eMergency department patient: PREMIUM registry

PRognostic hEModynamIc profiling in the acUte ill eMergency department patient: PREMIUM registry - PREMIUM registry

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON38388
Enrollment
200
Registered
2011-02-18
Start date
2011-04-27
Completion date
Unknown
Last updated
2024-11-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

Vrije Universiteit Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: General: 18 years of age or older Able to provide informed consent No initiated therapy since arrival to the ED Must be enrolled within 2 hours of arrival to the ED Acute CHF Recurrent or worsening (within 3 days) shortness of breath as the primary presenting ED complaint Initial treating ED physician impression that the worsening dyspnea is most likely caused by decompensated CHF Known history of physician diagnosed CHF BNP level will be ordered by the treating physician as part of the patient*s work up Acute stroke syndrome: Onset of abnormal neurological symptoms consistent with possible stroke, within the prior 24 hours, as the primary ED complaint Initial treating ED physician impression that the abnormal neurological symptoms/signs are most likely caused by an acute stroke syndrome Non contrast head CT will be ordered by the treating physician as part of the patient*s work up Acute Systemic Infection: Any combinations of acute (within 3 days) symptoms and signs that the treating ED physician, after initial history and physical examination, attributes to a systemic infection Blood cultures and/or a blood lactate will be ordered by the treating physician as part of the patient*s work up

Exclusion criteria

Exclusion criteria: ESRD requiring hemo or peritoneal dialysis Suspected pregnancy Not able to be followed up in 30 days Patients with *comfort only* DNR status Patients with known STEMI Excessive agitation Transferred from another treating facility Known aortic valve disease, aortic insufficiency or aortic stenosis On continuous IV home infusions (such as milrinone, primacor) Known Left Ventricular Assist device (LVAD) Known prior enrollment in this study In current therapeutic Investigational study

Design outcomes

Primary

MeasureTime frame
.

Secondary

MeasureTime frame
.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)