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Department of Dermatology
Dermatology Pearls and News Flash
ACP Utah Chapter Scientific Meeting 2017
• Christopher M Hull, MD
• Department of Dermatology
• University of Utah School of Medicine
• Christopher.hull@hsc.utah.edu
Department of Dermatology
Conflict of interest
• No conflicts to disclose
• I have chosen articles of interest published in the past year
Department of Dermatology
Educational Objectives
• Review recent dermatology topics of
importance to internal medicine
• Understand current guidelines for managing
simple abscess
• Be familiar with latest treatment options for
hidradenitis suppurativa and atopic dermatitis
• Review recent information about skin cancer
prevention option for high risk patients
Department of Dermatology
Presentation of case
• A 22 year old previously healthy female
presents to clinic with a 3 day history of
erythema, edema and pain of L thigh
• Exam: fluctuance, erythema, 3 cm nodule L
thigh
Department of Dermatology
• How would you treat this patient?
• A. Incision and drainage
• B. Treat with oral antibiotics
• C. Incision and drainage followed by oral
antibiotics
• Background: recent studies have recommended
incision and drainage alone for simple abscess
– Singer et al. Systemic antibiotics after I+D of simple
abscess: meta analysis. Emerg Med J 2013
Department of Dermatology
Management of simple abscesses
• Talan et al. Trimethoporim-sulfa vs placebo for
uncomplicated skin abscess. NEJM 2016
• Randomized controlled trial of 5 US E.D.
comparing trimethoprim/sulfa to placebo in
patients undergoing I+D
• Outcome: clinical cure of abscess at day 7-14
Department of Dermatology
Results
• 45.3% cultures positive for MRSA
• Clinical cure 80.5% in T-S group compared to
73.6% in I+D only group (MITP) and 92.9% TS
vs 85.7% (PP)
• T-S superior in secondary measures:
– Lower subsequent surgical drainage
– Lower skin infections at new sites
– Lower infections in household members
– TS had more GI side effects
Department of Dermatology
Conclusions
• In settings where MRSA is prevalent, T-S
treatment resulted in a higher cure rate
among patients with a drained abscess
compared to placebo
– Differences are small but significant
– Only 1 antibiotic studied
– In both arms, the abscesses subsequently resolved
– IDSA published guidelines
Department of Dermatology
Presentation of case
• A 40 year old healthy female presents for
treatment of toe nail fungus.
• Previous treatments: Vicks vapor rub, apple
cider vinegar and topical clotrimazole without
improvement
• Past medical history: hypothyroid, acne
• Medications: thyroid replacement, tretinoin
cream
Department of Dermatology
Department of Dermatology
How would you treat this patient?
• No treatment. Medications too risky
• Oral ketoconazole
• Oral terbinafine
• Topical efinaconazole
• Topical clotrimazole
Department of Dermatology
Answer
• No treatment. Medications too risky
• Oral ketoconazole
• Oral terbinafine
• Topical efinaconazole
• Topical clotrimazole
Department of Dermatology
Evaluating the need for laboratory
testing in the treatment of
onychomycosis
• Mikailov et al. Cost effectiveness of confirmatory testing
before treatment of onychomycosis JAMA Derm 2016
• Kanzler. Reevaluating the need for laboratory testing in the
treatment of onychomycosis JAMA Derm 2016.
Department of Dermatology
Onychomycosis therapy
• Empirical treatment with terbinafine is more
cost effective than confirmatory testing with
minimal effect on patient safety
• Confirmatory testing before treatment with
efinaconazole 10% is associated with reduced
costs
Department of Dermatology
Onychomycosis treatment
• When onychomycosis is suspected. Treat w/ course of
terbinafine
– If no response, could be saprophyte or yeast (don’t
respond to terbinafine). Treat with pulse fluconazole
200mg weekly x 3-9 months
– Cost for terbinafine and fluconazole is low
– Cost of efinaconazole is high (cure rates 15%). Better to
have confirmation of onychomycosis
– Safety of oral agents is good
• Significant liver injury is uncommon and most resolve with
discontinuation of the drug
• Need to reconsider need for extensive lab testing for derm drugs
like pulse anti fungal therapy, isotretinoin, spironolactone and
others
Department of Dermatology
Presentation of case
• 24 year old male with asthma and seasonal
allergies presents to clinic with worsening
eczema
• Current treatment: triamcinolone 0.%
ointment, neosporin, loratadine and
diphenhydramine as needed
• Prior treatments: clobetasol ointment,
pimecrolimus cream, cephalexin, medrol dose
pack, prednisone
Department of Dermatology
Department of Dermatology
How would you treat this patient?
A. Prednisone taper
B. Mometasone cream BID
C. Diphenhydramine and hydrocortisone 1%
cream BID
D. Dupilumab
E. UVB Phototherapy
Department of Dermatology
Answer
A. Prednisone taper
B. Mometasone cream BID
C. Diphenhydramine and hydrocortisone 1%
cream BID
D. Dupilumab
E. UVB Phototherapy
Department of Dermatology
• New Drug for Severe Eczema is Successful in 2
New Trials
– Gina Kolata, Oct 1, 2016
– “on Saturday the results of 2 large clinical trials of
a new drug offered hope to an estimated
1.6million adult Americans with uncontrolled
moderate-severe atopic dermatitis…”
Department of Dermatology
Dupilumab for atopic dermatitis
• Simpson et al. 2 phase 3 trials of dupilumab vs
placebo in atopic dermatitis. NEJM 2016
– Dupilumab monoclonal antibody that binds and
inhibits IL-4 and IL-13 (type 2 cytokines)
– Adults with moderate-severe atopic derm
inadequately controlled on topical treatment
– 1:1:1:1 dupilumab 300mg sq weekly, 300mg sq every
other week or placebo, placebo
– Primary outcome: proportion of patients with IGA of 0
or 1 (clear, almost clear) or reduction of 2 points or
more from baseline at week 16
Department of Dermatology
Results-dupilumab
• Big study: 671 study 1, 708 study 2
• IGA 0/1: 38% dupilumab every 14 days, 37%
dupilumab weekly, 10% placebo both arms
– Significantly more patients in dupilumab arms
achieved EASI 75% reduction compared to
placebo
– Reduction in pruritus, decreased
anxiety/depression, and improved quality of life
– Injection reactions and conjunctivitis greater in
dupi arms
Department of Dermatology
How do we treat moderate-severe
atopic dermatitis?
• Skin care, emollients, bleach baths, anti itch
products, antibiotics
• Topical corticosteroids and calcineurin inhibitors
• Systemic steroids
• Phototherapy
• Immunosuppressive medications:
– Cyclosporine, methotrexate, mycophenolate,
azathioprine
• And soon, dupilumab
Department of Dermatology
Presentation of case
• 30 year old female presents to clinic with a 5
year history of recurrent draining nodules of
the bilateral axillae, inguinal folds, proximal
thighs
• Previous treatments: topical clindamycin
lotion, I+D, intralesional steroids,
trimethoprim/sulfa, doxycycline
Department of Dermatology
Department of Dermatology
Department of Dermatology
How do you treat this patient?
A. Excision of all nodules
B. Refer to another provider
C. Clindamycin lotion BID
D. Treat with adalimumab
E. Minocycline 100mg BID x 10days
Department of Dermatology
Answer
A. Excision of all nodules
B. Refer to another provider
C. Clindamycin lotion BID
D. Treat with adalimumab
E. Minocycline 100mg BID x 10days
Department of Dermatology
Adalimumab for hidradenitis
suppurativa (HS)
• Kimball et al. 2 phase 3 trials of adalimumab
for HS. NEJM 2016
– Period 1: adalimumab 40mg weekly vs placebo x
12 weeks
– Period 2: adalimumab 40mg every other week vs
adalimumab 40mg weekly x 24 weeks
• Primary end point: 50% reduction in abscess and
inflammatory nodule count and no increase in abscess
or draining fistula counts
Department of Dermatology
Adalimumab and HS: results
• Clinical response at week 12 for adalimumab
>placebo (41.8% vs 26%) and (58.9% vs 27.6%)
• Also superior for lesions, pain, Sartorius score
• SAEs were low in both period 1 and period 2
• Conclusion: treatment with adalimumab 40mg
weekly as compared to placebo resulted in
significantly higher clinical response rates in both
trials at 12 weeks. Rates of SAEs were similar in
study groups
Department of Dermatology
Hidradenitis Suppurativa Treatments by Hurley Stage
Hurley Stage I and II Topical, injectable and
intralesional
• Topical antibiotics (e.g. clindamycin 1%)
• Intralesional corticosteroids
Oral options • Oral antibiotics
• Hormonal therapies
• Metformin
Surgical and physical options • Less invasive surgical approaches
• Laser therapy
• Photodynamic therapy
Hurley Stage II and III (Includes Stage I to II
approaches)
• More invasive surgical approaches
• Systemic retinoids
• Biological treatments
All Stages • Weight loss
• Pain control
• Smoking cessation
• Zinc supplementation
• Antimicrobial wash
Also consider infliximab, anakinra
Department of Dermatology
Case example
• 28 y.o. female with a many year history of
recurrent painful oral ulcers
• Multiple ulcers present in mouth nearly every
day
– No genital ulcers
Department of Dermatology
How would you treat this patient?
A. Dexamethasone elixir swish and spit
B. Medrol dose pack
C. Valacyclovir episodically for flares
D. Silver nitrate application to lesions
E. Apremilast
F. Colchicine
Department of Dermatology
Answer
A. Dexamethasone elixir swish and spit
B. Medrol dose pack
C. Valacyclovir episodically for flares
D. Silver nitrate application to lesions
E. Apremilast
F. Colchicine
Department of Dermatology
Introduction
• Recurrent aphthous ulcers (RAU), recurrent
aphthous stomatitis (RAS)
• Most common oral ulcerative condition
• Shallow, round ulcers with a pseudomembrane
and peripheral erythema
• Size varies: 1mm to >10mm
• 5-25% of general population
• More common in females, adults <40yrs,
Caucasians
Department of Dermatology
Systemic conditions associated with
aphthous ulcers
• Behcet’s disease
• Sweet’s syndrome
• Reiter’s syndrome
• Inflammatory bowel disease
• HIV infection
• Celiac disease
• Systemic lupus erythematosis
• Cyclic neutropenia
Department of Dermatology
Diagnostic tests for aphthous ulcers
• Nutritional deficiencies:
– Iron, ferritin, folate, vitamin B1, B2, B6, B12, zinc
• CBC
• ANA
• HIV
• Total IgA, IgA tissue transglutaminase
• Mucosal biopsy (edge of lesion. Get some epithelium)
• If bullous disease suspected, studies for
immunofluorescence
• Endoscopy
Department of Dermatology
Hatemi et al. Apremilast for Behcet’s syndrome.
Phase 2 Placebo controlled Study. NEJM 2015
• 111 patients w/ Behcets received apremilast
30mg BID vs placebo x 12 weeks with an
extension phase where all received apremilast
• Primary end point: number of oral ulcers
• Mean number of oral ulcers reduced in
apremilast arm
– Also reduced pain
– Nausea, vomiting, diarrhea higher in apremilast
arm
Department of Dermatology
Topical Treatment
• Corticosteroid gels (clobetasol gel)
– Other vehicles for oral mucosa available (orabase)
– Dexamethasone elixir
• Topical anesthetics
– Viscous lidocaine, benzocaine lozenges, Magic
mouthwash
• Antimicrobial agents
– Chlorhexadine rinse
– Topical tetracyclines
• Topical sucralfate
– 5mL 4x/day
Department of Dermatology
My Treatment strategy
• For minor RAS:
– topical corticosteroid gel BID +/- topical anesthetic
agent
• For major RAS:
– Colchicine 0.6mg BID along w/ corticosteroid gel and
topical anesthetic agent
– If no response, add/switch to dapsone
– If no response, consider azathioprine, TNF inhibitor,
apremilast
– Also vitamin B12, zinc, omega 3
Department of Dermatology
High risk skin cancer patients
Department of Dermatology
Reduction of non-melanoma skin
cancer in high-risk patients
• Chen et al. Phase 3 randomized trial of
nicotinamide for skin cancer
chemoprevention. NEJM 2015
• Nicotinamide 500mg BID vs placebo in high
risk patients x 1 year
– 386 patients with at least 2 skin cancers in
previous 5 years
– Evaluated number of new skin cancers and safety
Department of Dermatology
Nicotinamide and skin cancer
• At 12 months, rate of new NMSC was lower by
23% in nicotinamide arm (both BCC and SCC)
– Number of AKs was 11% lower at 3 months, 14%
lower at 6 months and 13% lower at 12 months
– No difference if AE between groups
– Benefits dissipated when nicotinamide
discontinued
– Compliance with nicotinamide 90% (whereas
sunscreen compliance was 50%)
Department of Dermatology
Select resources
• HS-Foundation.org
• Nationaleczema.org
• UpToDate Dermatology sections
• AAD.org
– basic derm curriculum
– Clinical guidelines
Department of Dermatology
References
• Talan et al. Trimethoporim-sulfa vs placebo for uncomplicated skin
abscess. NEJM 2016
• Kimball et al. 2 phase 3 trials of adalimumab for HS. NEJM 2016
• Simpson et al. 2 phase 3 trials of dupilumab vs placebo in atopic
dermatitis. NEJM 2016
• Chen et al. Phase 3 randomized trial of nicotinamide for skin cancer
chemoprevention. NEJM 2015
• Cunningham et al. Randomized trial of calcipotriol combined with 5-
fluorouracil for skin cancer precursor immunotherapy. J Clinical
Investigation 2016
• Mikailov et al. Cost effectiveness of confirmatory testing before treatment
of onychomycosis JAMA Derm 2016
• Kanzler. Reevaluating the need for laboratory testing in the treatment of
onychomycosis JAMA Derm 2016.
• Hatemi et al. Apremilast for Behcets syndrome-phase 2 placebo controlled
study. NEJM 2015

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06. Dermatology Pearls and News Flash (Power Point Presentation) Autor Christopher M Hull, MD.pdf

  • 1. Department of Dermatology Dermatology Pearls and News Flash ACP Utah Chapter Scientific Meeting 2017 • Christopher M Hull, MD • Department of Dermatology • University of Utah School of Medicine • Christopher.hull@hsc.utah.edu
  • 2. Department of Dermatology Conflict of interest • No conflicts to disclose • I have chosen articles of interest published in the past year
  • 3. Department of Dermatology Educational Objectives • Review recent dermatology topics of importance to internal medicine • Understand current guidelines for managing simple abscess • Be familiar with latest treatment options for hidradenitis suppurativa and atopic dermatitis • Review recent information about skin cancer prevention option for high risk patients
  • 4. Department of Dermatology Presentation of case • A 22 year old previously healthy female presents to clinic with a 3 day history of erythema, edema and pain of L thigh • Exam: fluctuance, erythema, 3 cm nodule L thigh
  • 5. Department of Dermatology • How would you treat this patient? • A. Incision and drainage • B. Treat with oral antibiotics • C. Incision and drainage followed by oral antibiotics • Background: recent studies have recommended incision and drainage alone for simple abscess – Singer et al. Systemic antibiotics after I+D of simple abscess: meta analysis. Emerg Med J 2013
  • 6. Department of Dermatology Management of simple abscesses • Talan et al. Trimethoporim-sulfa vs placebo for uncomplicated skin abscess. NEJM 2016 • Randomized controlled trial of 5 US E.D. comparing trimethoprim/sulfa to placebo in patients undergoing I+D • Outcome: clinical cure of abscess at day 7-14
  • 7. Department of Dermatology Results • 45.3% cultures positive for MRSA • Clinical cure 80.5% in T-S group compared to 73.6% in I+D only group (MITP) and 92.9% TS vs 85.7% (PP) • T-S superior in secondary measures: – Lower subsequent surgical drainage – Lower skin infections at new sites – Lower infections in household members – TS had more GI side effects
  • 8. Department of Dermatology Conclusions • In settings where MRSA is prevalent, T-S treatment resulted in a higher cure rate among patients with a drained abscess compared to placebo – Differences are small but significant – Only 1 antibiotic studied – In both arms, the abscesses subsequently resolved – IDSA published guidelines
  • 9. Department of Dermatology Presentation of case • A 40 year old healthy female presents for treatment of toe nail fungus. • Previous treatments: Vicks vapor rub, apple cider vinegar and topical clotrimazole without improvement • Past medical history: hypothyroid, acne • Medications: thyroid replacement, tretinoin cream
  • 11. Department of Dermatology How would you treat this patient? • No treatment. Medications too risky • Oral ketoconazole • Oral terbinafine • Topical efinaconazole • Topical clotrimazole
  • 12. Department of Dermatology Answer • No treatment. Medications too risky • Oral ketoconazole • Oral terbinafine • Topical efinaconazole • Topical clotrimazole
  • 13. Department of Dermatology Evaluating the need for laboratory testing in the treatment of onychomycosis • Mikailov et al. Cost effectiveness of confirmatory testing before treatment of onychomycosis JAMA Derm 2016 • Kanzler. Reevaluating the need for laboratory testing in the treatment of onychomycosis JAMA Derm 2016.
  • 14. Department of Dermatology Onychomycosis therapy • Empirical treatment with terbinafine is more cost effective than confirmatory testing with minimal effect on patient safety • Confirmatory testing before treatment with efinaconazole 10% is associated with reduced costs
  • 15. Department of Dermatology Onychomycosis treatment • When onychomycosis is suspected. Treat w/ course of terbinafine – If no response, could be saprophyte or yeast (don’t respond to terbinafine). Treat with pulse fluconazole 200mg weekly x 3-9 months – Cost for terbinafine and fluconazole is low – Cost of efinaconazole is high (cure rates 15%). Better to have confirmation of onychomycosis – Safety of oral agents is good • Significant liver injury is uncommon and most resolve with discontinuation of the drug • Need to reconsider need for extensive lab testing for derm drugs like pulse anti fungal therapy, isotretinoin, spironolactone and others
  • 16. Department of Dermatology Presentation of case • 24 year old male with asthma and seasonal allergies presents to clinic with worsening eczema • Current treatment: triamcinolone 0.% ointment, neosporin, loratadine and diphenhydramine as needed • Prior treatments: clobetasol ointment, pimecrolimus cream, cephalexin, medrol dose pack, prednisone
  • 18. Department of Dermatology How would you treat this patient? A. Prednisone taper B. Mometasone cream BID C. Diphenhydramine and hydrocortisone 1% cream BID D. Dupilumab E. UVB Phototherapy
  • 19. Department of Dermatology Answer A. Prednisone taper B. Mometasone cream BID C. Diphenhydramine and hydrocortisone 1% cream BID D. Dupilumab E. UVB Phototherapy
  • 20. Department of Dermatology • New Drug for Severe Eczema is Successful in 2 New Trials – Gina Kolata, Oct 1, 2016 – “on Saturday the results of 2 large clinical trials of a new drug offered hope to an estimated 1.6million adult Americans with uncontrolled moderate-severe atopic dermatitis…”
  • 21. Department of Dermatology Dupilumab for atopic dermatitis • Simpson et al. 2 phase 3 trials of dupilumab vs placebo in atopic dermatitis. NEJM 2016 – Dupilumab monoclonal antibody that binds and inhibits IL-4 and IL-13 (type 2 cytokines) – Adults with moderate-severe atopic derm inadequately controlled on topical treatment – 1:1:1:1 dupilumab 300mg sq weekly, 300mg sq every other week or placebo, placebo – Primary outcome: proportion of patients with IGA of 0 or 1 (clear, almost clear) or reduction of 2 points or more from baseline at week 16
  • 22. Department of Dermatology Results-dupilumab • Big study: 671 study 1, 708 study 2 • IGA 0/1: 38% dupilumab every 14 days, 37% dupilumab weekly, 10% placebo both arms – Significantly more patients in dupilumab arms achieved EASI 75% reduction compared to placebo – Reduction in pruritus, decreased anxiety/depression, and improved quality of life – Injection reactions and conjunctivitis greater in dupi arms
  • 23. Department of Dermatology How do we treat moderate-severe atopic dermatitis? • Skin care, emollients, bleach baths, anti itch products, antibiotics • Topical corticosteroids and calcineurin inhibitors • Systemic steroids • Phototherapy • Immunosuppressive medications: – Cyclosporine, methotrexate, mycophenolate, azathioprine • And soon, dupilumab
  • 24. Department of Dermatology Presentation of case • 30 year old female presents to clinic with a 5 year history of recurrent draining nodules of the bilateral axillae, inguinal folds, proximal thighs • Previous treatments: topical clindamycin lotion, I+D, intralesional steroids, trimethoprim/sulfa, doxycycline
  • 27. Department of Dermatology How do you treat this patient? A. Excision of all nodules B. Refer to another provider C. Clindamycin lotion BID D. Treat with adalimumab E. Minocycline 100mg BID x 10days
  • 28. Department of Dermatology Answer A. Excision of all nodules B. Refer to another provider C. Clindamycin lotion BID D. Treat with adalimumab E. Minocycline 100mg BID x 10days
  • 29. Department of Dermatology Adalimumab for hidradenitis suppurativa (HS) • Kimball et al. 2 phase 3 trials of adalimumab for HS. NEJM 2016 – Period 1: adalimumab 40mg weekly vs placebo x 12 weeks – Period 2: adalimumab 40mg every other week vs adalimumab 40mg weekly x 24 weeks • Primary end point: 50% reduction in abscess and inflammatory nodule count and no increase in abscess or draining fistula counts
  • 30. Department of Dermatology Adalimumab and HS: results • Clinical response at week 12 for adalimumab >placebo (41.8% vs 26%) and (58.9% vs 27.6%) • Also superior for lesions, pain, Sartorius score • SAEs were low in both period 1 and period 2 • Conclusion: treatment with adalimumab 40mg weekly as compared to placebo resulted in significantly higher clinical response rates in both trials at 12 weeks. Rates of SAEs were similar in study groups
  • 31. Department of Dermatology Hidradenitis Suppurativa Treatments by Hurley Stage Hurley Stage I and II Topical, injectable and intralesional • Topical antibiotics (e.g. clindamycin 1%) • Intralesional corticosteroids Oral options • Oral antibiotics • Hormonal therapies • Metformin Surgical and physical options • Less invasive surgical approaches • Laser therapy • Photodynamic therapy Hurley Stage II and III (Includes Stage I to II approaches) • More invasive surgical approaches • Systemic retinoids • Biological treatments All Stages • Weight loss • Pain control • Smoking cessation • Zinc supplementation • Antimicrobial wash Also consider infliximab, anakinra
  • 32. Department of Dermatology Case example • 28 y.o. female with a many year history of recurrent painful oral ulcers • Multiple ulcers present in mouth nearly every day – No genital ulcers
  • 33. Department of Dermatology How would you treat this patient? A. Dexamethasone elixir swish and spit B. Medrol dose pack C. Valacyclovir episodically for flares D. Silver nitrate application to lesions E. Apremilast F. Colchicine
  • 34. Department of Dermatology Answer A. Dexamethasone elixir swish and spit B. Medrol dose pack C. Valacyclovir episodically for flares D. Silver nitrate application to lesions E. Apremilast F. Colchicine
  • 35. Department of Dermatology Introduction • Recurrent aphthous ulcers (RAU), recurrent aphthous stomatitis (RAS) • Most common oral ulcerative condition • Shallow, round ulcers with a pseudomembrane and peripheral erythema • Size varies: 1mm to >10mm • 5-25% of general population • More common in females, adults <40yrs, Caucasians
  • 36. Department of Dermatology Systemic conditions associated with aphthous ulcers • Behcet’s disease • Sweet’s syndrome • Reiter’s syndrome • Inflammatory bowel disease • HIV infection • Celiac disease • Systemic lupus erythematosis • Cyclic neutropenia
  • 37. Department of Dermatology Diagnostic tests for aphthous ulcers • Nutritional deficiencies: – Iron, ferritin, folate, vitamin B1, B2, B6, B12, zinc • CBC • ANA • HIV • Total IgA, IgA tissue transglutaminase • Mucosal biopsy (edge of lesion. Get some epithelium) • If bullous disease suspected, studies for immunofluorescence • Endoscopy
  • 38. Department of Dermatology Hatemi et al. Apremilast for Behcet’s syndrome. Phase 2 Placebo controlled Study. NEJM 2015 • 111 patients w/ Behcets received apremilast 30mg BID vs placebo x 12 weeks with an extension phase where all received apremilast • Primary end point: number of oral ulcers • Mean number of oral ulcers reduced in apremilast arm – Also reduced pain – Nausea, vomiting, diarrhea higher in apremilast arm
  • 39. Department of Dermatology Topical Treatment • Corticosteroid gels (clobetasol gel) – Other vehicles for oral mucosa available (orabase) – Dexamethasone elixir • Topical anesthetics – Viscous lidocaine, benzocaine lozenges, Magic mouthwash • Antimicrobial agents – Chlorhexadine rinse – Topical tetracyclines • Topical sucralfate – 5mL 4x/day
  • 40. Department of Dermatology My Treatment strategy • For minor RAS: – topical corticosteroid gel BID +/- topical anesthetic agent • For major RAS: – Colchicine 0.6mg BID along w/ corticosteroid gel and topical anesthetic agent – If no response, add/switch to dapsone – If no response, consider azathioprine, TNF inhibitor, apremilast – Also vitamin B12, zinc, omega 3
  • 41. Department of Dermatology High risk skin cancer patients
  • 42. Department of Dermatology Reduction of non-melanoma skin cancer in high-risk patients • Chen et al. Phase 3 randomized trial of nicotinamide for skin cancer chemoprevention. NEJM 2015 • Nicotinamide 500mg BID vs placebo in high risk patients x 1 year – 386 patients with at least 2 skin cancers in previous 5 years – Evaluated number of new skin cancers and safety
  • 43. Department of Dermatology Nicotinamide and skin cancer • At 12 months, rate of new NMSC was lower by 23% in nicotinamide arm (both BCC and SCC) – Number of AKs was 11% lower at 3 months, 14% lower at 6 months and 13% lower at 12 months – No difference if AE between groups – Benefits dissipated when nicotinamide discontinued – Compliance with nicotinamide 90% (whereas sunscreen compliance was 50%)
  • 44. Department of Dermatology Select resources • HS-Foundation.org • Nationaleczema.org • UpToDate Dermatology sections • AAD.org – basic derm curriculum – Clinical guidelines
  • 45. Department of Dermatology References • Talan et al. Trimethoporim-sulfa vs placebo for uncomplicated skin abscess. NEJM 2016 • Kimball et al. 2 phase 3 trials of adalimumab for HS. NEJM 2016 • Simpson et al. 2 phase 3 trials of dupilumab vs placebo in atopic dermatitis. NEJM 2016 • Chen et al. Phase 3 randomized trial of nicotinamide for skin cancer chemoprevention. NEJM 2015 • Cunningham et al. Randomized trial of calcipotriol combined with 5- fluorouracil for skin cancer precursor immunotherapy. J Clinical Investigation 2016 • Mikailov et al. Cost effectiveness of confirmatory testing before treatment of onychomycosis JAMA Derm 2016 • Kanzler. Reevaluating the need for laboratory testing in the treatment of onychomycosis JAMA Derm 2016. • Hatemi et al. Apremilast for Behcets syndrome-phase 2 placebo controlled study. NEJM 2015