ID
12469
Beschrijving
Clinical decision units (CDUs) improve resource utilization and are a recommended care option by the American College of Cardiology / American Heart Association, but are underutilized in non-low risk chest pain patients due to weaknesses of traditional cardiac testing. Cardiac magnetic resonance imaging (CMR) is sensitive and specific for ischemia, can simultaneously assess cardiac function and myocardial perfusion, and could revolutionize the diagnostic process for intermediate risk patients with chest pain. The primary objective of this trial is to measure the efficiency and safety of a combined CDU-CMR care pathway compared to inpatient care among patients with non-low risk acute chest pain. https://clinicaltrials.gov/ct2/show/NCT01035047
Link
https://clinicaltrials.gov/ct2/show/NCT01035047
Trefwoorden
Versies (2)
- 28-07-15 28-07-15 -
- 21-11-15 21-11-15 -
Geüploaded op
21 november 2015
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY 4.0
Model Commentaren :
Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.
Itemgroep Commentaren voor :
Item Commentaren voor :
U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.
Eligibility Chest Pain Diagnostic Acute Coronary Syndrome NCT01035047
Eligibility Criteria
- StudyEvent: ODM
Beschrijving
Exclusion criteria
Beschrijving
Elevated cardiac biomarkers
Datatype
boolean
Alias
- UMLS CUI-1
- C0741921
Beschrijving
New ST-segment elevation on any electrocardiogram (>/= 1 mV)
Datatype
boolean
Alias
- UMLS CUI-1
- C0520886
Beschrijving
New ST-segment depression on any electrocardiogram (>/= 2 mV)
Datatype
boolean
Alias
- UMLS CUI-1
- C0520887
Beschrijving
Known inducible cardiac ischemia without subsequent revascularization
Datatype
boolean
Alias
- UMLS CUI-1
- C0151744
Beschrijving
Unable to lie flat
Datatype
boolean
Alias
- UMLS CUI [1]
- C1717946
Beschrijving
Symptomatic hypotension at the time of enrollment (systolic < 90 mm Hg)
Datatype
boolean
Alias
- UMLS CUI-1
- C0020649
Beschrijving
Contra-indications to MRI (examples: Pacemaker, defibrillator, cerebral aneurysm clips, metallic ocular foreign body, implanted devices, severe claustrophobia)
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0024485
- UMLS CUI [1,2]
- C0522473
Beschrijving
Terminal diagnosis with life expectancy less than 3 months
Datatype
boolean
Alias
- UMLS CUI-1
- C0679247
Beschrijving
Currently Pregnant
Datatype
boolean
Alias
- UMLS CUI-1
- C0549206
Beschrijving
Creatinine clearance < 45 ml/min at the time of enrollment or clinical concern for acute kidney injury
Datatype
boolean
Alias
- UMLS CUI-1
- C0373595
Beschrijving
Chronic liver disease with a creatinine clearance of <60 ml/min at the time of enrollment
Datatype
boolean
Alias
- UMLS CUI-1
- C0085605
Beschrijving
Hepato-renal syndrome
Datatype
boolean
Alias
- UMLS CUI-1
- C0019212
Beschrijving
History of liver transplant
Datatype
boolean
Alias
- UMLS CUI-1
- C0023911
Beschrijving
History of heart transplant
Datatype
boolean
Alias
- UMLS CUI-1
- C0018823
Beschrijving
History of kidney transplant
Datatype
boolean
Alias
- UMLS CUI-1
- C0022671
Beschrijving
Confirmed angioplasty
Datatype
boolean
Alias
- UMLS CUI-1
- C0190211
Beschrijving
Confirmed stent placement within the last 6 months
Datatype
boolean
Alias
- UMLS CUI-1
- C3272316
Beschrijving
Confirmed coronary artery bypass grafting (CABG) within the last 6 months
Datatype
boolean
Alias
- UMLS CUI-1
- C0010055
Similar models
Eligibility Criteria
- StudyEvent: ODM
C0522473 (UMLS CUI [1,2])