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Telemedical Versus Conventional Emergency Care of Hypertensive Emergencies

Completed
Conditions
Hypertensive Emergency
Hypertensive Urgency
Interventions
Other: Telemedical care
Registration Number
NCT02924805
Lead Sponsor
RWTH Aachen University
Brief Summary

Comparison of telemedical prehospital emergency care and conventional on-scene physician based care of hypertensive emergencies and urgencies. The adherence to current Guidelines should be researched.

Detailed Description

Telemedically guided cases of hypertensive emergencies (april 2014 - March 2015) and urgencies are compared with a historical control group of conventional emergency medical service physician care on-scene for these scenarios. The historical control group is a time period prior to implementation of the telemedicine system and after a research project with a precursor telemedicine system. No telemedical support but only conventional on-scene EMS physician care was available (November 2013 - March 2014).

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
331
Inclusion Criteria
  • prehospital diagnosis of hypertensive emergency of hypertensive urgency
Exclusion Criteria

Prehospital diagnoses of:

  • pulmonary edema
  • aortic dissection
  • acute coronary syndrome
  • acute stroke
  • acute respiratory insufficiency

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Telemedicine groupTelemedical careCases of hypertensive emergencies and urgencies in which the prehospital emergency care was performed by on-scene paramedics, guided by a qualified physician in a teleconsultation center.
Primary Outcome Measures
NameTimeMethod
Blood pressure difference between initial contact and emergency room handover2 hours
Secondary Outcome Measures
NameTimeMethod
Difference of heart rate between initial contact and emergency room handover2 hours
Magnitude of blood pressure reduction using categories2 hours

To measure guideline adherence blood pressure (BP) reductions were evaluated with four categories: no BP reduction, reduction \<= 25%, reduction \>25-30%, reduction \> 30% (BP difference between initial contact and emergency room handover)

Trial Locations

Locations (1)

University Hospital Aachen

🇩🇪

Aachen, Germany

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