Age
Item
males and females over 18 years of age
boolean
C0001779 (UMLS CUI [1])
NYHA
Item
documented chf (nyha class ii-iv symptoms)
boolean
C1275491 (UMLS CUI [1])
Symptomatic obstructive respiratory disease
Item
airflow obstruction defined as patients with symptomatic obstructive respiratory disease as manifest by any of the following symptoms of wheeze, primarily attributed to airflow obstruction requirement for intermittent or regular bronchodilator therapy fev1 less than 70% predicted pre-salbutamol
boolean
C0600260 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
informed consent
Item
confirmed written informed consent.
boolean
C0021430 (UMLS CUI [1])
Indicated to receive beta blockers
Item
clinically indicated to receive β-blockade.
boolean
C0001645 (UMLS CUI [1,1])
C1444656 (UMLS CUI [1,2])
Heart block
Item
no evidence of heart block on ecg.
boolean
C0344413 (UMLS CUI [1])
Heart Failure Medication
Item
patients will be in one of the following categories:
boolean
C0013227 (UMLS CUI [1,1])
C0018801 (UMLS CUI [1,2])
currently on carvedilol, currently on toprol-xl or metoprolol tartrate, currently on bisoprolol, clinically indicated to receive beta adrenoceptor blockade
Item
currently on carvedilol, currently on toprol-xl or metoprolol tartrate, currently on bisoprolol, clinically indicated to receive β adrenoceptor blockade but not currently prescribed a β-blocker.
boolean
C0054836 (UMLS CUI [1])
C0723783 (UMLS CUI [2])
C0700548 (UMLS CUI [3])
C0053799 (UMLS CUI [4])
C0001645 (UMLS CUI [5,1])
C1444656 (UMLS CUI [5,2])
pregnant or breastfeeding, contraception
Item
women lactating, pregnant or of childbearing potential not using a reliable contraceptive method.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0700589 (UMLS CUI [3])
Investigational New Drug
Item
patients who had received an investigational new drug within the last 4 weeks.
boolean
C0013230 (UMLS CUI [1])
patients with a history of a psychological illness or condition such as to interfere with their ability to understand the requirements of the study
Item
patients with a history of a psychological illness or condition such as to interfere with the patient's ability to understand the requirements of the study.
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])
C0004936 (UMLS CUI [2,3])
laboratory parameters
Item
laboratory parameters:
boolean
C0022885 (UMLS CUI [1])
renal and liver function
Item
creatinine >0.30 mmol/l liver function tests 3x uln
boolean
C0201976 (UMLS CUI [1])
C0023901 (UMLS CUI [2])
Myocarditis
Item
recent (<12 months) myocarditis
boolean
C0027059 (UMLS CUI [1])