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Dermatology

Other Systemic Drugs

Built from Dermatology, 5th Edition

What’s inside

14 sections · 173 slides

  1. 01

    Introduction and general principles

    Systemic drugs used in dermatology beyond biologics, retinoids and antimicrobials

    • What this deck covers
    • Systemic medications covered in other chapters.
    • Systemic medications covered in other chapters. (continued)
    • Four broad categories of systemic drug
    • Categories of systemic drugs used in dermatology based upon mechanism of action.
    • Systemic drug categories at a glance
    • Choosing a systemic therapy
    • Baseline screening before immunosuppression
    • Pregnancy and lactation labeling
    • REMS programs and parenteral safety

    10 slides

  2. 02

    Antimalarials

    Hydroxychloroquine and chloroquine — first-line therapy for cutaneous lupus

    • History and drug options
    • Absorption and metabolism
    • Mechanism of action
    • Typical dosing
    • Dosing for porphyria cutanea tarda
    • Ocular toxicity: overview
    • Risk factors and types of retinopathy associated with antimalarial therapy.
    • Risk factors and types of retinopathy associated with antimalarial therapy. (continued)
    • Risk factors and types of retinopathy associated with antimalarial therapy. (continued)
    • Eye screening schedule
    • Skin discoloration from antimalarials
    • Hair changes and drug rashes
    • Lichenoid drug eruption from hydroxychloroquine
    • Pustular psoriasis induced by hydroxychloroquine
    • Psoriasis flares and lab monitoring
    • Monitoring guidelines – Antimalarials
    • Monitoring guidelines – Antimalarials
    • Indications
    • Contraindications
    • Pregnancy and lactation
    • Drug interactions
    • Side effects – Antimalarials

    22 slides

  3. 03

    Apremilast

    An oral small-molecule PDE-4 inhibitor for psoriasis and psoriatic arthritis

    • Overview and pharmacokinetics
    • Apremilast and PDE-4 inhibitor mechanism of action
    • Mechanism of action
    • Dosing
    • Major side effects
    • Side effects – Apremilast
    • Plaque psoriasis response to apremilast
    • Indications and trial results
    • Contraindications, pregnancy, and interactions

    9 slides

  4. 04

    Azathioprine

    A TPMT-guided immunosuppressant for severe, treatment-resistant skin disease

    • History and absorption
    • Azathioprine metabolic pathway
    • Why TPMT activity matters
    • Dosing of azathioprine as determined by baseline thiopurine methyltransferase (TPMT) activity.
    • Mechanism of action
    • Dosing
    • Monitoring guidelines – Azathioprine
    • Major side effects: immune suppression
    • Hypersensitivity and PPP syndrome
    • Side effects – Azathioprine
    • Azathioprine hypersensitivity reaction
    • Indications
    • Contraindications, pregnancy, and interactions

    13 slides

  5. 05

    Bleomycin, clofazimine and colchicine

    Three older agents with narrow but well-defined dermatologic roles

    • Bleomycin: source and use
    • Bleomycin.
    • Bleomycin: dosing and side effects
    • Clofazimine: source and use
    • Clofazimine.
    • Clofazimine: dosing and side effects
    • Colchicine: source and use
    • Colchicine.
    • Colchicine: dosing and side effects

    9 slides

  6. 06

    Cyclophosphamide

    A DNA-alkylating agent reserved for severe vasculitis and mucosal disease

    • History and pharmacokinetics
    • Mechanism of action
    • How cyclophosphamide kills cells
    • Dosing
    • Monitoring guidelines – Cyclophosphamide
    • Major side effects
    • Side effects – Cyclophosphamide
    • Indications
    • Contraindications, pregnancy, and interactions

    9 slides

  7. 07

    Cyclosporine

    A fast-acting calcineurin inhibitor for severe psoriasis flares

    • History and formulations
    • Pharmacokinetics
    • Mechanism of action
    • How cyclosporine blocks T cell activation
    • Dosing in psoriasis
    • Monitoring kidney function
    • Monitoring guidelines – Cyclosporine
    • Major side effects
    • Long-term risk and cancer
    • Eruptive sebaceous hyperplasia with cyclosporine
    • Side effects – Cyclosporine
    • Indications
    • Contraindications, pregnancy, and interactions

    13 slides

  8. 08

    Dapsone

    A sulfone antibiotic repurposed for neutrophil-driven skin disease

    • History and pharmacokinetics
    • Metabolism
    • Mechanism of action
    • Dosing
    • Monitoring guidelines – Dapsone
    • Major side effects: dose-related
    • Dapsone hypersensitivity syndrome
    • Side effects – Dapsone
    • Indications
    • Contraindications, pregnancy, and interactions

    10 slides

  9. 09

    Hydroxyurea and leukotriene inhibitors

    A psoriasis maintenance drug and asthma drugs used off-label in skin disease

    • Hydroxyurea: overview
    • Hydroxyurea.
    • Hydroxyurea-induced skin ulceration and mucosal pigmentation
    • Hydroxyurea-associated malleolar ulcer
    • Side effects – Hydroxyurea
    • Hydroxyurea: dosing and monitoring
    • Leukotriene inhibitors: overview
    • Leukotriene inhibitors.
    • Leukotriene inhibitors: cautions

    9 slides

  10. 10

    Methotrexate

    A folic-acid-blocking antiproliferative, first used in psoriasis in the 1950s

    • History and pharmacokinetics
    • Mechanism of action
    • Two separate mechanisms
    • Dosing schedule
    • Starting and escalating the dose
    • Monitoring guidelines – Methotrexate
    • Major side effects
    • Risk factors for developing hepatic toxicity from methotrexate. Adapted from reference 33 .
    • Monitoring for liver fibrosis
    • Methods of monitoring for hepatic fibrosis.
    • Serum and imaging tests for hepatic fibrosis
    • Serum and imaging tests for hepatic fibrosis (continued)
    • Serum and imaging tests for hepatic fibrosis (continued)
    • Methotrexate hepatotoxicity monitoring algorithm
    • Side effects – Methotrexate
    • Indications
    • Contraindications
    • Counseling patients of childbearing potential
    • Methotrexate (MTX) – counseling for patients of childbearing potential.
    • Drug interactions

    20 slides

  11. 11

    Mycophenolate mofetil

    A purine-synthesis blocker that favors fast-dividing lymphocytes

    • History and pharmacokinetics
    • Mechanism of action of mycophenolic acid
    • Mechanism of action
    • Dosing
    • Monitoring guidelines – Mycophenolate mofetil
    • Major side effects
    • Side effects – Mycophenolate mofetil
    • Indications
    • Contraindications, pregnancy, and interactions

    9 slides

  12. 12

    Potassium iodide, sirolimus and tacrolimus

    An old anti-inflammatory solution and two mTOR/calcineurin-pathway drugs

    • SSKI: overview
    • Saturated solution of potassium iodide (SSKI).
    • SSKI: dosing and side effects
    • Side effects – SSKI
    • Sirolimus and tacrolimus: overview
    • Sirolimus (rapamycin; Rapamune®) and tacrolimus (Prograf®).
    • Sirolimus (rapamycin; Rapamune®) and tacrolimus (Prograf®). (continued)
    • Viral-associated trichodysplasia in a transplant recipient
    • Side effects – Tacrolimus
    • Dermatologic uses and side effects

    10 slides

  13. 13

    Thalidomide and lenalidomide

    From 1960s tragedy to tightly controlled therapy for leprosy reactions and lupus

    • History
    • REMS safety programs
    • Pharmacokinetics and comparison
    • Mechanism of action
    • Dosing
    • Monitoring guidelines – Thalidomide and lenalidomide
    • Discoid lupus erythematosus response to thalidomide
    • Clinical response in lupus
    • Major side effects: thalidomide
    • Major side effects: lenalidomide
    • Side effects – Thalidomide and lenalidomide
    • Subacute cutaneous lupus response to thalidomide
    • Extensive subacute cutaneous lupus clearance with thalidomide
    • Indications: thalidomide
    • Indications: lenalidomide
    • Contraindications and interactions
    • Pregnancy and lactation

    17 slides

  14. 14

    Summary and references

    Key numbers to remember, cross-drug indications, and the chapter's source list

    • 40–50 days
    • Matching disease to drug
    • Select cutaneous disorders that can be treated with specific systemic drugs.
    • Select cutaneous disorders that can be treated with specific systemic drugs. (continued)
    • Select cutaneous disorders that can be treated with specific systemic drugs. (continued)
    • References
    • References (continued)
    • References (continued)
    • References (continued)
    • References (continued)
    • References (continued)
    • References (continued)
    • Dermatology, 5th Edition (2-Volume Set)

    13 slides