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Day 2 ENT Flashback

Total questions: 15

Worksheet time: 10mins

Name
Class
Date
1.

Which of the following statement is TRUE about the rationale of targeted 200mg BD dosage of sacubitril/valsartan?

a)

To deliver similar exposure as Valsartan (Diovan) 80mg BD

b)

To ensure a 24-hour neprilysin enzyme inhibition

c)

To deliver a maximal 80% neprilysin enzyme inhibition

d)

To achieve a higher mean daily dose than doses used in Val-HeFT

2.

Which of the following is/are recommended by the 2017 updated ACC/AHA/HFSA guideline for the Management of Chronic Heart Failure (HF)?

I. ACE inhibitor

II. Diuretics

III. ARNI

IV. SGLT2

a)

I & II

b)

I & III

c)

I, II & III

d)

All of the above

3.

Which of the following biomarker was increased in HF patients treated on sacubitril/valsartan?

a)

BNP & cGMP

b)

NT-proBNP & troponin

c)

BNP & troponin

d)

NT-proBNP & troponin

4.

Compared to enalapril, sacubitril/Valsartan resulted in greater reduction in all cause mortality. Its NNT was ____?

a)

16

b)

21

c)

31

d)

36

5.

How many percentages of patients in PARADIGM-HF were Asian

a)

15%

b)

18%

c)

19%

d)

21%

6.

In PARADIGM-HF, as compared to enalapril, sacubitril/valsartan was more effective in reducing

a)

RRR of death from CV causes by 21%

b)

RRR of first HF hospitalization by 21%

c)

RRR of sudden cardiac death by 16%

d)

RRR of all-cause death by 20%

7.

Initiation of sacubitril/valsartan in-hospital led significantly greater reduction in NT-proBNP versus enalapril with _____ of relative risk reduction after 8 weeks of follow up

a)

26%

b)

27%

c)

28%

d)

29%

8.

Patients that are currently on ACE inhibitor are required to stop the drug for 36 hours before starting of Sacubitril/valsartan due to

a)

Hypotension

b)

Hyperkalaemia

c)

Cough

d)

Angioedema

9.

The following are the contraindications for sacubitril/valsartan EXPECT

a)

End-stage renal disease

b)

Concomitant used with Aliskiren

c)

History of angioedema

d)

Second and third trimester pregnancy

10.

How many percentages of patients in PIONEER-HF trial were ACEi/ARB-naive?

a)

52%

b)

53%

c)

54%

d)

55%

11.

Treatment with sacubitril/valsartan should not be initiated in patients with serum potassium level

a)

>5.2 mmol/L

b)

>5.4 mmol/L

c)

≥5.2 mmol/L

d)

≥5.4 mmol/L

12.

Sacubitril is rapidly converted into its active metabolite, Sacubitrilat in

a)

Kidney

b)

Heart

c)

Vascular

d)

Liver

13.

Which of the following statement is TRUE about the safety events based on the PARADIGM-HF trail?

a)

Number of incidence of cough between patients on sacubitril/valsartan and enalapril were similar

b)

Fewer patients on sacubitril/valsartan discontinued the study drug due to any adverse event as compared to enalapril

c)

Significant higher number of patients were required to discontinue enalapril than sacubitril/valsartan due to hyperkalemia

d)

Incidence of angioedema was numerically lower in patients on sacubitril/valsartan versus enalpril

14.

How many percentages of patients in PARADIGM-HF trial were on diuretics and beta blockers at baseline?

a)

90%, 83%

b)

90%, 60%

c)

80%, 93%

d)

80%, 60%

15.

In PARADIGM-HF trial, how many percentages of the patients were in respective NYHA class?

a)

A

b)

B

c)

C

d)

D