Drugs to Tx Pulmonary HTN Flashcards

1
Q

Use of what drugs are viewed as a risk factor for pulmonary arterial HTN?

A

Fenfluramine/phentermine (“fen/phen” weight loss pills)

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2
Q

What constitutes a positive vasopressor test?

A

1) Pulmonary artery pressure falls ≥ 10 mm Hg
2) Mean pulmonary artery pressure ≤ 40 mm Hg
3) Cardiac output is unchanged or increased

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3
Q

If a patient’s vasopressor test is considered positive then what may they take to achieve sustained functional improvement and prolonged survival?

May they still take this drug if their vasopressor test was negative?

A

1) CCBs (nifedipine, diltiazem or amlodipine)

2) No, they can be potentially deleterious in non-responders

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4
Q

What drugs make up the prostanoids?

A

1) epoprostenol
2) treprostinil
3) iloprost
4) selexipag

(Prost)

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5
Q

What do prostanoids mimic the actions of?

What does this cause?

A

Mimics the actions of endogenous prostacyclins which causes:

1) Vascular relaxation
2) Suppression of vascular smooth muscle cell growth
3) Inhibition of platelet aggregation

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6
Q

Prostanoids exert their effects by?

A

Binding to GPCRs to generate cAMP

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7
Q

What clinical effects are seen with prostanoids in the treatment of PAH?

A

1) Lowers pulmonary arterial resistance
2) Decreases pulmonary arterial pressure
3) Increases exercise tolerance

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8
Q

Which prostanoid has very short half-life (~ 6 min) and must be given by continuous IV infusion with a pump that can keep the drug cold?

A

epoprostenol

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9
Q

Which prostanoid has multiple routes of administration such as subcutaneous infusion (but causes pain), qid inhalation, and extended-release oral form?

A

treprostinil

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10
Q

How does treprostinil differ from epoprostenol when both are given by continuous IV infusion?

A

1) treprostinil has a longer half life (4 hours vs 6 min)

2) Doesn’t require refrigeration

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11
Q

What serious adverse effects can be seen with both epoprostenol and treprostinil?

A

Sepsis due to chronic catheter

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12
Q

Which prostanoid is administered by inhalation 6-9 times per day?

A

iloprost

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13
Q

What adverse effect is seen with iloprost?

A

Fainting due to hypotension

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14
Q

Which prostanoid is administered orally BID?

A

selexipag

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15
Q

What common side effects are seen with all prostanoids?

A

1) Headache
2) Flushing
3) Jaw pain

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16
Q

What are the endothelin antagonists?

A

1) bosentan
2) ambrisentan
3) macitentan

(entan)

17
Q

Which endothelin antagonist nonspecifically blocks ETA and ETB endothelin receptors?

A

bosentan

18
Q

Which endothelin antagonist selectively blocks ETA endothelin receptors?

A

ambrisentan

19
Q

What clinical effects are seen with endothelin antagonists in the treatment of PAH?

A

Improves exercise tolerance and slows symptom progression

20
Q

How are the endothelin antagonists administered?

A

Orally

21
Q

What toxicities are noted with bosentan?

A

1) Hepatotoxicity

2) Teratogenesis

22
Q

What drug interaction does bosentan have causing acceleration of their metabolism?

A

1) Warfarin

2) Oral contraceptives

23
Q

How does ambrisentan differ from bosentan in terms of toxicities and drug interactions?

A

1) Does not damage liver

2) Does not accelerate metabolism of warfarin and oral contraceptives

24
Q

What toxicities are noted with ambrisentan?

A

Teratogenesis

25
Q

Which endothelin antagonist is a non-selective agent distinguished by ~18 hr half life that permits once/day dosing?

A

macitentan

26
Q

What are the Phosphodiesterase type V Inhibitors?

A

1) sildenafil
2) tadalafil

(afil)

27
Q

What is the MOA of the PDE type V inhibitors?

A

Potentiates cGMP mediated vascular relaxation

28
Q

What clinical effects are seen with PDE type V inhibitors in the treatment of PAH?

A

Improves exercise tolerance and slows symptom progression

29
Q

Which PDE type V inhibitors has the longer half life?

A

tadalafil

30
Q

The PDE type V inhibitors can cause a large drop in BP if taken with?

A

1) α-blockers for hypertension

2) Nitrates for anginal pain

31
Q

What is the guanylate cyclase sensitizer?

A

riociguat

32
Q

What is the MOA of riociguat?

A

Increased generation of cGMP

33
Q

What clinical effects are seen with riociguat in the treatment of PAH?

A

Improves exercise tolerance and slows symptom progression

34
Q

What should riociguat not be adminstered with?

A

1) Nitric oxide donors

2) PDE type V inhibitors

35
Q

What patients are classified as WHO Functional Class I?

WHO FC II?

WHO FC III?

WHO FC IV?

A

1) Pts with pulmonary HTN but without limitation of physical activity
2) Pts with pulmonary HTN which causes slight limitation of physical activity
3) Patients with pulmonary hypertension resulting in marked limitation of physical activity
4) Patients with pulmonary hypertension with inability to carry out any physical activity without symptoms

36
Q

In the Tx of naїve PAH patients with WHO FC II and WHO FC III (without rapid disease progression), what do you administer if they are able to tolerate combination therapy?

If they can’t, what are the monotherapy options given?

A

1) Ambrisentan and tadalafil

2) Either macitentan, ambrisentan, riociguat, sildenafil or tadalafil

37
Q

In the Tx of naїve PAH patients with WHO FC III (with rapid disease progression) and WHO FC IV what do you administer?

A

One of the parenteral prostanoids:

1) IV epoprostenol
2) IV treprostinil
3) SC treprostinil

38
Q

In the Tx of naїve PAH patients with WHO FC III (with rapid disease progression) and WHO FC IV what do you administer if they are unable to tolerate parenteral prostanoids?

A

1) Inhaled prostanoid
2) Oral PDE-5 inhibitor
3) Oral ET-antagonist

39
Q

What is the most common PAH drug combination?

A

Ambrisentan and tadalafil