Registry of Patients With Acute Dyspnea in the Emergency Department

NCT ID: NCT01910233

Last Updated: 2016-04-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

947 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-05-31

Study Completion Date

2015-12-31

Brief Summary

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This is a prospective registry of patients presenting with acute dyspnea to the emergency department of the city hospital in Nuremberg. There is evidence that acute dyspnea is associated with a mortality rate of 10%, however acute dyspnea is not perceived as a life-threatening condition, both in public and in health care providers. Our aim is to describe the patient collective concerning their demographics, baseline characteristics, type of referral and disposition, medical care processes and prognosis. Secondly, we want to evaluate if the subjective risk assessment of emergency department personnel matches with objective risk stratification tools and the actual outcome of the studied patients.

Detailed Description

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This is a prospective registry of patients presenting with acute dyspnea to the emergency department of the city hospital in Nuremberg during May 23th 2013 and October 31th 2013. To be included into the registry the patient has to express acute dyspnea. Minor patients are not included. The admission documents of the studied patients are accompanied by a questionnaire that has to be completed by the triage nurse and the attending physician. The questionnaire includes items like professional experience and subjective assessment of patient's prognosis. In addition the attending physician has to state if the evaluation of medical history was difficult, if previous medication is known and how likely the presence of heart failure as underlying condition is. Data of the questionnaire, the patient record and the follow up contacts are entered in a SPSS database. Finally, we measure the OPTIMIZE-HF score (Abraham et al. 2008) and the PRIDE mortality score (Baggish et al. 2007) in a retrospective manner in order to compare the subjective assessments with objective criteria.

Conditions

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Dyspnea Heart Failure COPD

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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adult patients with acute dyspnea in ED

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* expression of acute dyspnea in the emergency department

Exclusion Criteria

* age \< 18 years
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Klinikum Nürnberg

OTHER

Sponsor Role lead

Responsible Party

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Prof. Dr. Michael Christ

Prof. Dr. med. Michael Christ

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Michael Christ, Prof.

Role: PRINCIPAL_INVESTIGATOR

Klinikum Nürnberg

Locations

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Department of Emergency and Critical Care Medicine, City Hospital Nuremberg

Nuremberg, Bavaria, Germany

Site Status

Countries

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Germany

Other Identifiers

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OOB01

Identifier Type: -

Identifier Source: org_study_id

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