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Dermatology

Other Systemic Drugs

Built from Dermatology, 5th Edition

The first 25 slides of Other Systemic Drugs
The first 25 slides, exactly as they appear. The full deck has 173 content slides.

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