atrial fibrillation
Item
Patients with atrial fibrillation, diagnosed electrocardiographically, of more than 48 hours duration in whom direct current (dc) cardioversion is planned.
boolean
C0004238 (UMLS CUI [1])
hypersensitivit angiotensin ii receptor blocker or ACE inhibitor
Item
Patients with a history of known hypersensitivity or contraindication to any angiotensin ii receptor blocker or any angiotensin-converting enzyme (ace) inhibitor.
boolean
C0020517 (UMLS CUI [1,1])
C0521942 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0003015 (UMLS CUI [2,2])
receiving medication because of heart failure
Item
Patients currently receiving an ace inhibitor or angiotensin ii antagonist because of heart failure or other strong indication.
boolean
C0018801 (UMLS CUI [1,1])
C3146298 (UMLS CUI [1,2])
C0521942 (UMLS CUI [1,3])
C0003015 (UMLS CUI [1,4])
antiarrhythmic medication
Item
Patients currently receiving any antiarrhythmic medication including sotalol. other beta-blockers will not be regarded as specific antiarrhythmic agents.
boolean
C0003195 (UMLS CUI [1])
C0037707 (UMLS CUI [2])
renal artery stenosis
Item
Significant renal artery stenosis and any medical condition in which administration of a vasodilator is contraindicated; serum creatinine > 225 micromol/l; or serum potassium > 5.5 mmol/l; or serum sodium < 128 mmol/l.
boolean
C0035067 (UMLS CUI [1])
C0021430 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
C0042402 (UMLS CUI [2,3])
C0201976 (UMLS CUI [3])
C0036743 (UMLS CUI [4,1])
C0302353 (UMLS CUI [4,2])
C0036743 (UMLS CUI [5,1])
C0523891 (UMLS CUI [5,2])
C0036743 (UMLS CUI [6,1])
C0523891 (UMLS CUI [6,2])
severe hepatic dysfunction
Item
Patients with severe hepatic dysfunction
boolean
C0086565 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
life-limiting disease or substance abuse
Item
life-limiting disease or substance abuse which may affect participation.
boolean
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
C1321605 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
C0038586 (UMLS CUI [2,3])
unwilling to participate
Item
Patients unwilling to participate
boolean
C0021430 (UMLS CUI [1])
dc cardioversion for atrial fibrillation
Item
Patients who have previously undergone dc cardioversion for atrial fibrillation within the last month.
boolean
C0542380 (UMLS CUI [1,1])
C0004238 (UMLS CUI [1,2])
thyrotoxicosis
Item
Thyrotoxicosis
boolean
C0040156 (UMLS CUI [1])
systolic blood pressure
Item
Patients with a systolic blood pressure of < 100 mm hg.
boolean
C0871470 (UMLS CUI [1])
hypertensive patients
Item
Hypertensive patients requiring intensified treatment prior to dc cardioversion
boolean
C0087111 (UMLS CUI [1,1])
C2349975 (UMLS CUI [1,2])
C0020538 (UMLS CUI [1,3])
pregnancy or lactation
Item
Pregnancy or lactation
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])