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Optimalisatie van telefonische triage op huisartsenposten bij patiënten verdacht voor acute hart- en vaatziekten.

Optimization of telephone triage of patients suspected of having acute cardiovascular disease in out of hours primary care: the Safety First study.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON20507
Enrollment
3000
Registered
2018-06-26
Start date
2016-01-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Acute cardiovascular disease, acute coronary syndrome, transient ischemic attack, stroke. Acute hart- en vaatziekten, acuut coronair syndroom, beroerte.

Interventions

N.A.

Sponsors

Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, the Netherlands.
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: (I) Recordings of triage conversations of patients with chest discomfort suspected of having an ACS (II) Recordings of triage conversations of patients with neurological symptoms suspected of having a TIA or stroke

Exclusion criteria

Exclusion criteria: (I) No triage conversation (recordings of conversations between colleagues or about medication questions) (II) Recordings of poor quality (III) Patients younger than 18 years (IV) Patients that don’t live in the vicinity of Utrecht (V) Patients’ whose GP refuses to cooperate

Design outcomes

Primary

MeasureTime frame
The diagnostic accuracy of the NTS will be analyzed in terms of sensitivity, specificity, positive and negative predictive values of the urgency allocation (high; U1-U2, and low; U3-U5) on the outcomes ACS, and TIA/stroke.

Secondary

MeasureTime frame
In addition, a) sensitivity analyses with inclusion of other emergency cases that can result in chest discomfort such as pulmonary embolism, acute heart failure, and thoracic aortic dissection, and other emergency cases that can result in neurological symptoms such as subarachnoid hemorrhage (SAH) and epilepsy, and b) pre-specified subgroup analyses for gender and age will be performed.

Contacts

Public ContactD.C.A. Erkelens

University Medical Center Utrecht, Julius Center for Health Sciences and Primary Care, HP STR 6.131

d.c.a.erkelens@umcutrecht.nl+31 (0)88 75 69289

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)