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Core - Pharmacology

    Chapter 20

    Other Respiratory Disorders

    20.1 : Pulmonary Hypertension: Classification and Pathogenesis01:30

    20.1 : Pulmonary Hypertension: Classification and Pathogenesis

    Pulmonary hypertension, or PH, denotes the resting mean pulmonary arterial pressure of 25 mm Hg or higher. Pulmonary hypertension can be classified into ...

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    20.2 : Treatment for Pulmonary Arterial Hypertension: Phosphodiesterase Inhibitors01:28

    20.2 : Treatment for Pulmonary Arterial Hypertension: Phosphodiesterase Inhibitors

    Phosphodiesterase inhibitors treat pulmonary arterial hypertension or PAH by inhibiting the activity of the phosphodiesterase enzyme. Phosphodiesterase 5 ...

    129 views
    20.3 : Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists01:18

    20.3 : Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists

    Endothelin receptor antagonists or ERAs counteract the effects of endothelins, or ETs, to treat pulmonary arterial hypertension or PAH. ETs are produced ...

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    20.4 : Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists01:23

    20.4 : Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists

    Prostacyclin receptor agonists are vital in managing pulmonary arterial hypertension. They mimic prostaglandin I2  and bind to its receptor, IPR, on ...

    147 views
    20.5 : Treatment for Pulmonary Arterial Hypertension: Receptor Tyrosine Kinase Inhibitors and Calcium Channel Blockers01:26

    20.5 : Treatment for Pulmonary Arterial Hypertension: Receptor Tyrosine Kinase Inhibitors and Calcium Channel Blockers

    Receptor tyrosine kinase inhibitors or TKIs and calcium channel blockers or CCBs are used for pulmonary arterial hypertension or PAH treatment. TKIs like ...

    135 views
    20.6 : Treatment for Pulmonary Arterial Hypertension: Oxygen Therapy for Respiratory Failure01:16

    20.6 : Treatment for Pulmonary Arterial Hypertension: Oxygen Therapy for Respiratory Failure

    Oxygen therapy can enhance the quality of life of patients with pulmonary arterial hypertension or PAH who experience hypoxemia or low oxygen levels. This ...

    171 views
    20.7 : Cystic Fibrosis: Pathogenesis01:23

    20.7 : Cystic Fibrosis: Pathogenesis

    Cystic fibrosis, or CF, is an autosomal recessive disorder resulting from mutations in the cystic fibrosis transmembrane conductance regulator or CFTR ...

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    20.8 : Cystic Fibrosis: Management01:24

    20.8 : Cystic Fibrosis: Management

    Cystic fibrosis, or CF, is an autosomal genetic disorder caused by mutations in the cystic fibrosis transmembrane conductance regulator or CFTR gene. CF ...

    139 views
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