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2.
J Am Acad Dermatol ; 70(3): 401.e1-14; quiz 415, 2014 Mar.
Article in English | MEDLINE | ID: mdl-24528911

ABSTRACT

Dermatologists are frequently faced with questions about the safety of commonly prescribed topical and systemic medications during pregnancy and lactation from women of childbearing age who are pregnant, considering pregnancy, or breastfeeding. Safety data, particularly regarding medications that are unique to dermatology, can be difficult to locate and are not consolidated in a single reference guide for clinicians. Parts I and II of this continuing medical education article provide a capsule summary of key points for the most commonly prescribed dermatologic medications to facilitate patient medication risk counseling in pregnancy. A summary table details safety classification data for 3 primary international classification systems: the US Food and Drug Administration, the Swedish Catalogue of Approved Drugs, and the Australian Drug Evaluation Committee. In addition, this table includes an alternative pregnancy classification system developed by a consortium of active members of teratology societies in the US and Europe detailed in Drugs during Pregnancy and Lactation: Treatment Options and Risk Assessment and a safety classification system developed for breastfeeding mothers detailed in Medications and Mother's Milk.


Subject(s)
Abnormalities, Drug-Induced/prevention & control , Dermatologic Agents/adverse effects , Drug-Related Side Effects and Adverse Reactions/prevention & control , Lactation/drug effects , Patient Safety , Administration, Oral , Administration, Topical , Adult , Australia , Breast Feeding , Dermatologic Agents/therapeutic use , Education, Medical, Continuing , Europe , Female , Gestational Age , Humans , Pharmaceutical Preparations , Pregnancy , Prenatal Care/methods , Risk Assessment , Skin Diseases/diagnosis , Skin Diseases/drug therapy , United States , United States Food and Drug Administration , Young Adult
3.
J Am Acad Dermatol ; 70(3): 417.e1-10; quiz 427, 2014 Mar.
Article in English | MEDLINE | ID: mdl-24528912

ABSTRACT

Dermatologists are frequently faced with questions from women who are breastfeeding about the safety of commonly prescribed topical and systemic medications during lactation. Safety data in lactation, particularly regarding medications that are unique to dermatology, are limited and can be difficult to locate. We have consolidated the available safety data in a single reference guide for clinicians. We review literature pertaining to the safety of common dermatologic therapies in lactation and offer recommendations based on the available evidence.


Subject(s)
Abnormalities, Drug-Induced/prevention & control , Dermatologic Agents/adverse effects , Drug-Related Side Effects and Adverse Reactions/prevention & control , Lactation/drug effects , Patient Safety , Skin Diseases/drug therapy , Administration, Oral , Administration, Topical , Adult , Breast Feeding , Dermatologic Agents/therapeutic use , Education, Medical, Continuing , Female , Humans , Pharmaceutical Preparations , Practice Guidelines as Topic , Pregnancy , Risk Assessment , Skin Diseases/diagnosis , United States
4.
Dermatol Ther ; 26(4): 331-6, 2013.
Article in English | MEDLINE | ID: mdl-23914890

ABSTRACT

Dermatoses of the breast during lactation can be difficult to diagnose because of their overlapping clinical appearances. It is important to properly diagnose and treat nipple dermatitis since it can be a significant source of pain when nursing. Poorly controlled nipple pain in nursing mothers is one of the primary reasons for breastfeeding to be discontinued earlier than is recommended. Therefore, it is relevant for practicing dermatologists to be aware of certain facts in a patient's history, specific physical exam findings, and the most appropriate laboratory tests used to diagnose these conditions. In addition, the therapeutic approach should be effective and safe for the mother and infant. This review article provides dermatologists with a detailed discussion on the clinical features and management of various breast dermatoses seen in lactation, including atopic dermatitis, irritant contact dermatitis, allergic contact dermatitis, psoriasis, bacterial infections, yeast infections and herpes simplex virus infections.


Subject(s)
Breast Diseases/therapy , Lactation , Skin Diseases/therapy , Dermatitis, Allergic Contact/therapy , Dermatitis, Atopic/therapy , Eczema/therapy , Female , Humans , Nipples , Pregnancy , Psoriasis/therapy , Raynaud Disease/therapy
5.
Dermatol Ther ; 26(4): 347-53, 2013.
Article in English | MEDLINE | ID: mdl-23914892

ABSTRACT

Many women of childbearing age use prescription and non-prescription medications. Therefore, patients need to be counseled regarding the potential teratogenicity of medications if they are, or could become, pregnant. In this editorial, the present authors will explain the three advantages of the evidence-based medicine system when compared with the US Food and Drug Administration system for medication risk classification in pregnancy. The present authors will also comment on medication use during lactation and provide resources on medication use during pregnancy and lactation for clinicians and their patients.


Subject(s)
Counseling , Dermatologic Agents/adverse effects , Evidence-Based Medicine , Lactation , Pregnancy Complications/drug therapy , Dermatologic Agents/classification , Female , Humans , Pregnancy , Risk
6.
Dermatol Ther ; 26(4): 337-46, 2013.
Article in English | MEDLINE | ID: mdl-23914891

ABSTRACT

Many drugs have been reported to impair semen parameters, leading to temporary or persistent infertility. Therefore, potential fathers may be concerned about the effect of medications on fertility. We searched the MEDLINE database of articles in English combining key terms including "male infertility," "spermatogenesis," "fertility," "drug effects," and "dermatology." Administration of methotrexate and finasteride has resulted in severe oligospermia and reversible infertility. Ketoconazole has had negative effects on sperm motility and testosterone production. Few individual case reports and a limited number of studies have demonstrated negative effects of tetracyclines, erythromycin, chloroquine, glucocorticoids, spironolactone, and antihistamines on fertility. It is important to counsel male patients when appropriate about the reversible negative effect on fertility when taking methotrexate and finasteride, and the adverse effect of ketoconazole. Patients may be reassured that taking oral retinoids, cyclosporine, azathioprine, and tumor necrosis factor alpha inhibitors should not affect their fertility.


Subject(s)
Dermatologic Agents/adverse effects , Infertility, Male/chemically induced , Acitretin/adverse effects , Anti-Infective Agents/adverse effects , Azathioprine/adverse effects , Cyclosporine/adverse effects , Finasteride/adverse effects , Humans , Male , Methotrexate/adverse effects , Tumor Necrosis Factor-alpha/antagonists & inhibitors
7.
Int J Dermatol ; 52(7): 775-83, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23789596

ABSTRACT

Patients with delusional infestations (DI), previously named delusions of parasitosis, have a fixed, false belief that they are infested with living or non-living pathogens. Patients have abnormal cutaneous symptoms such as itching, biting, or crawling sensations. They often demonstrate self-destructive behavior in an effort to rid the pathogens from under their skin, leading to excoriations, ulcerations, and serious secondary infections. This review article aims to provide an overview of DI including its clinical presentation, diagnosis, and treatment. Strategies on how to establish a strong therapeutic alliance with DI patients are discussed. In addition, antipsychotic medications used in the treatment of DI are described.


Subject(s)
Antipsychotic Agents/therapeutic use , Delusional Parasitosis , Physician-Patient Relations , Skin Diseases/psychology , Delusional Parasitosis/diagnosis , Delusional Parasitosis/psychology , Delusional Parasitosis/therapy , Humans , Medical History Taking , Patient Care Planning , Physical Examination , Skin Diseases/diagnosis , Trust
8.
JAMA Dermatol ; 149(3): 300-6, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23682366

ABSTRACT

OBJECTIVE: To elucidate the diagnostic criteria of Raynaud phenomenon of the nipple that will aid in recognizing and treating Raynaud phenomenon in breast feeding mothers with chronic deep nipple pain during lactation. DESIGN: Retrospective review of a patient database composed of 22 cases of breastfeeding mothers who fit the diagnostic criteria for Raynaud phenomenon of the nipple. SETTING: Menlo Dermatology Medical Group in Menlo Park, California, an academic-affiliated, private dermatologic referral center. PATIENTS: All patients diagnosed as having Raynaud phenomenon of the nipple evaluated from January 1, 2004,through December 31, 2010. MAIN OUTCOME MEASURES: The rate of failed treatment for Candida mastitis, the rate of improvement of symptoms with nifedipine use, and the overall rate of improvement of symptoms with appropriate therapy involving treatment of Raynaud phenomenon. RESULTS: Among the 22 patients with Raynaud phenomenon of the nipple, previous treatment for Candida mastitis with oral or topical antifungals was ineffective in 20(91%). Of the 12 patients who tolerated a trial of nifedipine,10 (83%) reported decreased or resolved nipple pain. All patients experienced marked improvement of symptoms with appropriate therapy involving treatment of Raynaud phenomenon. CONCLUSIONS: Most patients were treated with antifungals before presentation without resolution of nipple pain. Nifedipine appears to be an effective medication for the treatment of Raynaud phenomenon of the nipple. With appropriate management of Raynaud phenomenon,breastfeeding mothers demonstrated improvement of nipple pain. Raynaud phenomenon of the nipple should be considered in the differential diagnosis of nipple pain during lactation.


Subject(s)
Breast Diseases/diagnosis , Breast Feeding , Pain/etiology , Raynaud Disease/diagnosis , Adult , Antifungal Agents/therapeutic use , Breast Diseases/pathology , Candidiasis/diagnosis , Candidiasis/drug therapy , Databases, Factual , Female , Follow-Up Studies , Humans , Mastitis/diagnosis , Mastitis/drug therapy , Mastitis/microbiology , Middle Aged , Nipples , Raynaud Disease/pathology , Retrospective Studies , Treatment Failure
9.
J Drugs Dermatol ; 12(2): e20-4, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23377400

ABSTRACT

Progressive multifocal leukoencephalopathy (PML) is a frequently fatal demyelinating disease of the brain caused by activation of the John Cunningham virus. It typically occurs in immunocompromised patients, including transplant recipients on immunosuppressant medications, patients receiving chemotherapy for hematologic malignancies, and patients with human immunodeficiency virus. Unfortunately, there is no effective treatment for PML. By contrast, reversible progressive leukoencephalopathy syndrome (RPLS) is a generally treatable disorder that is diagnosed based on clinical symptoms (eg, altered mental status, visual abnormalities, headache, and seizures) and neuroradiographic changes (eg, cerebral edema). It is classically associated with malignant hypertension and immunosuppressive medications. Symptoms usually resolve over time, or with treatment of the underlying cause. Amid the relatively recent withdrawal of efalizumab from the US market because of its association with PML, and the added warning found on ustekinumab describing RPLS as a possible adverse effect, there has been an increasing level of concern in dermatology that biologics and other systemic medications used in the treatment of psoriasis may be related to an increased risk of specific leukoencephalopathies. In this review, we evaluate the association of prebiologics (eg, cyclosporine, methotrexate, acitretin) and biologics (eg, adalimumab, alefacept, efalizumab, etanercept, infliximab, rituximab, and ustekinumab) with the potential risk of developing PML and RPLS.


Subject(s)
Dermatologic Agents/adverse effects , Immunosuppressive Agents/adverse effects , Leukoencephalopathy, Progressive Multifocal/chemically induced , Antibodies, Monoclonal/adverse effects , Biological Therapy , Humans , Leukoencephalopathy, Progressive Multifocal/epidemiology , Psoriasis/complications , Psoriasis/drug therapy , Risk
10.
J Am Acad Dermatol ; 68(5): 817-24, 2013 May.
Article in English | MEDLINE | ID: mdl-23399460

ABSTRACT

When treating psoriasis, various topical emollients exist that can affect the penetration of ultraviolet radiation in phototherapy. Compared with normal-appearing skin with a reflectance of 4% to 5%, psoriatic skin has higher reflectance as a result of its increased air-to-corneocyte interfaces. Studies have tested the effect of emollients on light penetration by assessing psoriatic plaque clearance, differences in minimal erythema dose, and physical properties of the emollient (eg, monochromatic protection factor and absorbance). Psoriatic plaque clearance was found to improve with serous (thin liquid)-based emollients (eg, Vaseline oil [Unilever, Blackfriars, London, UK], mineral oil, and glycerol), whereas clearance decreased with salicylic acid and viscous-based emollients (eg, petrolatum). Emollients with high ultraviolet absorbance properties increased minimal erythema dose, and those with low absorbance properties decreased minimal erythema dose. Interestingly, when a liquid emollient with a refractive index close to that of normal-appearing skin was applied, there was a net increase in light absorption, or a reduction in reflection that exceeded the emollient's innate ability to absorb light.


Subject(s)
Emollients/adverse effects , Phototherapy/methods , Psoriasis/therapy , Ultraviolet Therapy/methods , Humans , Phototherapy/standards , Refractometry , Ultraviolet Therapy/standards
11.
J Dermatolog Treat ; 24(1): 34-7, 2013 Feb.
Article in English | MEDLINE | ID: mdl-22329632

ABSTRACT

As early as 1925, patients suffering from psoriasis have been effectively treated with combination crude coal tar and ultraviolet B radiation, commonly known as Goeckerman therapy. Even though the efficacy of Goeckerman therapy is as good as, if not better than, other more recently available treatment options, its use virtually disappeared after extended inpatient therapies became no longer feasible in the USA. Our clinic at the University of California San Francisco is one of the few outpatient dermatologic clinics that still offer Goeckerman therapy. We present a case report of a patient with severe generalized plaque-type psoriasis, who demonstrated dramatic improvement within 28 days of Goeckerman therapy. It is our hope that this case report serves to remind physicians that Goeckerman therapy is viable treatment option for patients with severe psoriasis, especially those with treatment-resistant psoriasis.


Subject(s)
Coal Tar/administration & dosage , Keratolytic Agents/administration & dosage , Photochemotherapy , Psoriasis/drug therapy , Ultraviolet Rays , Humans , Male , Middle Aged , San Francisco , Treatment Outcome
12.
J Dermatolog Treat ; 24(4): 261-7, 2013 Aug.
Article in English | MEDLINE | ID: mdl-22103655

ABSTRACT

Vitamin D as a topical treatment has become one of the mainstays for treatment of psoriasis vulgaris. Oral vitamin D on the other hand has for the most part become a forgotten option. But a review of the literature on oral vitamin D as a treatment for psoriasis reveals that this treatment is efficacious. The main side effect of this therapy is hypercalcemia, which appears to be easily monitored and avoidable with proper dosing and monitoring. The literature also suggests a correlation between low levels of serum vitamin D in this patient population associated with increased severity of disease involvement. In addition, oral vitamin D improves psoriatic arthropathy. Moreover, vitamin D has been proven to have many health benefits such as prevention of cancer, improved cardiovascular health among many others. Psoriatic patients as a population are at increased risk of developing adverse health complications such as cardiovascular disease, and oral vitamin D may prove to be of benefit in this population. Oral vitamin D is inexpensive and easily available. It is still a viable option and should not be forgotten as a possible treatment for psoriasis.


Subject(s)
Psoriasis/drug therapy , Vitamin D/administration & dosage , Vitamins/administration & dosage , Administration, Oral , Humans , Treatment Outcome , Vitamin D/adverse effects , Vitamin D Deficiency/diagnosis , Vitamins/adverse effects
13.
J Dermatolog Treat ; 24(2): 148-52, 2013 Apr.
Article in English | MEDLINE | ID: mdl-21888569

ABSTRACT

Recent studies have suggested that inflammatory responses may play an important role in the pathophysiology of depression. In fact, depressed individuals have been found to have higher levels of pro-inflammatory cytokines, especially tumor necrosis factor-alpha (TNF-α) and interleukin-6. This appears to be independent of any pre-existing chronic inflammatory disorders. In this article, various studies correlating increased levels of cytokines to depression are reviewed. As much as 60% of individuals with psoriasis also suffer from clinical depression. TNF-α antagonists, frequently used in the treatment of psoriasis, may be helpful in directly reducing depressive symptoms for patients with psoriasis and other chronic inflammatory conditions.


Subject(s)
Depressive Disorder/physiopathology , Interleukin-6/physiology , Psoriasis/physiopathology , Tumor Necrosis Factor-alpha/physiology , Adalimumab , Animals , Anti-Inflammatory Agents/therapeutic use , Antibodies, Monoclonal, Humanized/therapeutic use , Chronic Disease , Depressive Disorder/drug therapy , Humans , Interleukin-6/antagonists & inhibitors , Psoriasis/drug therapy , Tumor Necrosis Factor-alpha/antagonists & inhibitors
14.
J Dermatolog Treat ; 24(1): 13-24, 2013 Feb.
Article in English | MEDLINE | ID: mdl-22007699

ABSTRACT

The availability of new biologic agents for the treatment of psoriasis provides hope for improved quality of life outcomes. However, the way patients come to use biologics, the potential barriers they encounter, and their attitudes towards using these medications are still not well studied. Here, we conducted a survey of 106 psoriasis patients at an academic medical center to discern patient attitudes towards biologics. We found that most patients learn of biologics through their physician and perform follow-up research using the Internet. Most patients did not find it difficult to make the decision to start a biologic. Difficulty in obtaining biologics was associated with age less than 55 (p = 0.01), lower income level (p = 0.007), and lack of insurance (p = 0.04). Patients were found to have high satisfaction and compliance rates on biologics. Of patients who missed a dose of their biologic, this was mainly due to logistical reasons such as not having the medication or forgetting to take it, rather than being depressed or overwhelmed. Patients with lower income levels had increased cut backs in personal expenses due to co-payments (p = 0.001). Among respondents, the mean annual out-of-pocket expense for a biologic was $557.12 per year, with a range of $0-7000.


Subject(s)
Academic Medical Centers/statistics & numerical data , Dermatologic Agents/therapeutic use , Drug Utilization/statistics & numerical data , Psoriasis/drug therapy , Adolescent , Adult , Aged , Child , Female , Health Care Surveys , Humans , Internet , Male , Middle Aged , Patient Compliance , Patient Education as Topic/statistics & numerical data , Patient Satisfaction , Surveys and Questionnaires , Young Adult
15.
J Dermatolog Treat ; 24(2): 119-21, 2013 Apr.
Article in English | MEDLINE | ID: mdl-21801112

ABSTRACT

The ideal repair mechanism for overcoming barrier disruption in atopic dermatitis (AD) needs to completely eliminate microbe and allergen penetration as well as transepidermal water loss. We propose the hydrogel patch as an innovative approach to complete barrier repair. It is composed of an adhesive, thin, flexible, hydrogel layer on an impermeable urethane surface. We conducted a 6-week pilot study with 15 AD patients, who applied the hydrogel patch over one lesion for 6-8 h daily and triamcinolone (TAC) 0.1% cream twice daily to another lesion. Results after 2-week no treatment follow-up showed hydrogel patch had notable efficacy, and comparable to TAC 0.1% cream. Larger studies are needed to validate these results.


Subject(s)
Dermatitis, Atopic/therapy , Hydrogel, Polyethylene Glycol Dimethacrylate/chemistry , Occlusive Dressings , Transdermal Patch , Adolescent , Adult , Dermatitis, Atopic/drug therapy , Female , Glucocorticoids/administration & dosage , Humans , Male , Pilot Projects , Treatment Outcome , Triamcinolone Acetonide/administration & dosage
16.
Dermatol Online J ; 18(10): 15, 2012 Oct 15.
Article in English | MEDLINE | ID: mdl-23122022

ABSTRACT

Prescription and non-prescription medications are frequently used by women of childbearing age. As many as 40 to 80 percent of women receive at least one prescription drug during pregnancy. It is essential to understand the potential teratogenicity of medications and offer pregnant women appropriate counseling. Available classification references include the Swedish Catalogue of Approved Drugs, the US Food and Drug Administration, the Australian system, and the Evidence-Based Medicine system.


Subject(s)
Dermatologic Agents/classification , Dermatologic Agents/therapeutic use , Pregnancy Complications/drug therapy , Abnormalities, Drug-Induced/prevention & control , Evidence-Based Medicine , Female , Fetus/drug effects , Humans , Pregnancy , Risk Assessment , United States , United States Food and Drug Administration
17.
Int J Dermatol ; 51(10): 1149-61, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22994661

ABSTRACT

Breastfeeding is thought to be the most optimal form of infant nutrition. Nursing mothers are generally advised to continue breastfeeding until the infant is two years of age or beyond. Unfortunately, however, a majority of nursing mothers will discontinue breastfeeding much earlier than recommended. The most common reason for early discontinuation of breastfeeding is nipple pain. It is, therefore, essential that dermatologists know how to appropriately diagnose and effectively treat nipple pain associated with nipple dermatitis among nursing mothers. This review article provides a detailed discussion on the clinical features and management of various causes of nipple dermatitis during lactation, including problems with infant latch-on, congenital oral anomalies, plugged lactiferous ducts, atopic dermatitis, irritant contact dermatitis, allergic contact dermatitis, yeast infections, bacterial infections, herpes simplex virus, and Raynaud's phenomenon of the nipple.


Subject(s)
Breast Feeding/adverse effects , Dermatitis, Atopic/diagnosis , Dermatitis, Contact/diagnosis , Mothers , Nipples , Sucking Behavior/physiology , Dermatitis, Atopic/complications , Dermatitis, Atopic/microbiology , Dermatitis, Contact/complications , Dermatitis, Contact/microbiology , Dermatomycoses/complications , Dermatomycoses/diagnosis , Female , Herpes Simplex/complications , Herpes Simplex/diagnosis , Humans , Infant, Newborn , Mammary Glands, Human/physiopathology , Pain/etiology , Psoriasis/diagnosis , Raynaud Disease/complications , Raynaud Disease/diagnosis , Raynaud Disease/microbiology , Skin Diseases, Bacterial/complications , Skin Diseases, Bacterial/diagnosis
18.
J Drugs Dermatol ; 11(3): 413-4, 2012 Mar.
Article in English | MEDLINE | ID: mdl-22395596

ABSTRACT

The treatment options for psoriasis in HIV-infected individuals are limited due to the immunosuppressive nature of the therapeutic modalities and the patient's immunocompromised state. Etanercept has been shown to be safe and effective in the non-HIV psoriasis population with nearly 20 years of experience. However, there is limited data on the safety of etanercept use in the HIV patient population. The authors report a case of an HIV-infected patient with psoriasis who has remained mostly clear on continuous, uninterrupted etanercept use for over six years.


Subject(s)
HIV Infections/complications , Immunoglobulin G/therapeutic use , Immunologic Factors/therapeutic use , Psoriasis/drug therapy , Receptors, Tumor Necrosis Factor/therapeutic use , Adult , Etanercept , Humans , Immunoglobulin G/administration & dosage , Immunoglobulin G/adverse effects , Immunologic Factors/administration & dosage , Immunologic Factors/adverse effects , Male , Psoriasis/pathology , Receptors, Tumor Necrosis Factor/administration & dosage , Severity of Illness Index , Time Factors
19.
Dermatol Clin ; 30(2): 281-91, ix, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22284142

ABSTRACT

The negative impact of psoriasis on a patient's quality of life (QoL) is well documented in the literature. Patients often suffer poor self-esteem, difficulties in social interactions, and significant psychological distress. It is, therefore, critically important that a clinician evaluate the extent to which the disease impacts a patient's QoL. This chapter reviews several validated and reliable generic, dermatology-specific, and disease-specific QoL instruments useful in measuring the impact of psoriasis on patient's QoL. These QoL instruments can be especially helpful in identifying those patients who would most benefit from systemic or biologic therapy.


Subject(s)
Psoriasis/psychology , Quality of Life , Health Status , Humans , Stress, Psychological , Surveys and Questionnaires , Treatment Outcome
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