Dermatología en Costa Rica

Saturday, November 28, 2020

Effectiveness and Safety of Risankizumab in Psoriasis Journal of the European Academy of Dermatology and Venereology: JEADV


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Abstract 

Risankizumab is a humanized IgG monoclonal antibody that binds with high affinity and specificity to the p19 subunit and selectively inhibits IL-23, critical for psoriatic inflammation. In phase-3 trials (UltIMMa-1, UltIMMa-2 and IMMvent) risankizumab demonstrated early and sustained efficacy at 12-week dosing in patients with moderate-to-severe psoriasis.1,2 To date, limited real-life data are available on its effectiveness and safety.3

Journal of the European Academy of Dermatology and Venereology: JEADV
A Multicenter Study on Effectiveness and Safety of Risankizumab in Psoriasis: An Italian 16-Week Real-Life Experience During the COVID-19 Pandemic
J Eur Acad Dermatol Venereol 2020 Oct 20;[EPub Ahead of Print], K Hansel, A Zangrilli, L Bianchi, K Peris, A Chiricozzi, A Offidani, F Diotallevi, MC Fargnoli, M Esposito, P Amerio, G Gualdi, L Bianchi, L Stingeni 


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Diagnosis, Clinical Features, and Management of Patients With Granulomatous Cheilitis JAMA Dermatology


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Abstract 

Granulomatous cheilitis (GC) is a rare disorder characterized by noncaseating granulomatous inflammation of the lips in the absence of systemic disease, eg, Crohn disease (CD) or sarcoidosis.1 A subtype of orofacial granulomatosis, the term GC was proposed in 1985 by Wiesenfeld and colleagues to encompass the spectrum of idiopathic, noncaseating granulomatous diseases of the face and mouth.2 When GC is found with lingua plicata (fissured tongue) and facial palsy, it is referred to as Melkersson-Rosenthal syndrome. Granulomatous cheilitis can have a chronic disfiguring course that is exceedingly difficult to manage.3



JAMA Dermatology
Diagnosis, Clinical Features, and Management of Patients With Granulomatous Cheilitis
JAMA Dermatol 2020 Nov 11;[EPub Ahead of Print], JS Durgin, O Rodriguez, T Sollecito, T Tanaka, JC English, BE Shields, M Rosenbach 

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Tuesday, November 24, 2020

Urea al 5 % en un alcohol en gel reduce riesgo de dermatitis de contacto

Ethanol-Based Disinfectants Containing Urea May Reduce Soap Sensitivity

Dermatitis

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Abstract


BACKGROUND

The use of disinfectants is crucial to preventing the spread of nosocomial infections in health care workers. As many as 25 applications of hand disinfectants is a realistic default value during a working day. However, alcohol-based hand disinfectants may weaken skin barrier function and induce dryness and eczema, which decrease their acceptance.

OBJECTIVE

To evaluate the effect of ethanol-containing disinfectants with 5% urea on skin barrier function and on sensitivity to an irritant soap (sodium lauryl sulfate [SLS]).

METHODS

Twenty healthy volunteers treated one of their forearms twice daily for 17 days with an ethanol-containing gel with 5% urea. Two types of gels with urea were tested. Treatment was randomized to left or right forearm, and the contralateral forearm served as untreated control. Transepidermal water loss, skin capacitance (dryness), and sensitivity to SLS were evaluated.

RESULTS

Twice-daily application of the urea-containing ethanol gels lowered transepidermal water loss, prevented dryness, and reduced sensitivity to SLS compared with the untreated control skin.

CONCLUSIONS

Improved barrier function using this ethanol gel with urea may have relevance in daily disinfectant procedures.


Dermatitis
Ethanol-Based Disinfectants Containing Urea May Reduce Soap Sensitivity
Dermatitis 2020 Sep 01;31(5)328-332, M Lodén 

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Monday, November 23, 2020

Successful Treatment With Oral Hydroxychloroquine of Seborrhoeic Dermatitis in a Patient With AIDS Clinical and Experimental Dermatology

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Abstract 

Seborrhoeic dermatitis (SD) is a common chronic inflammatory dermatosis characterized by erythematous patches with yellowish scales, which frequently occurs on the face, scalp and chest. The prevalence of SD is 1%–3% in the general population, but is much higher (30%–83%) in patients with AIDS, and in this immunocompromised population, the disease is generally much more severe.1Currently, topical corticosteroids or antifungals are recommended for SD; however, the therapeutic efficiency is unsatisfactory in patients with AIDS, presenting a huge clinical challenge. We report a case of SD in a patient with AIDS, which responded well to treatment with oral hydroxychloroquine (HCQ).


Clinical and Experimental Dermatology
Successful Treatment With Oral Hydroxychloroquine of Seborrhoeic Dermatitis in a Patient With AIDS
Clin Exp Dermatol 2020 Oct 06;[EPub Ahead of Print], YB Hu, XZ Song 

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Effect of Dapsone on HbA1c Levels Clinical and Experimental Dermatology


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Abstract 

We would like to highlight an important clinical lesson regarding a drug‐related side effect of dapsone use.

Clinical and Experimental Dermatology
HbA1c Levels: Falsely Low in a Patient Taking Dapsone
Clin Exp Dermatol 2020 Jun 23;[EPub Ahead of Print], IR Spring, C Ilangaratne, S Walsh 


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Sunday, November 22, 2020

Alkyl phenolic compounds implicated in FAA

Exposure to these chemicals can occur occupationally during their production or with exposure to domestic and industrial detergents, specialty paints, pesticides, cosmetics and hair dyes, among others (Lassen et al., 2013), but also as a consequence of non-occupational exposures, such as diet and water intake, use of personal care and household cleaning products. 
De: https://doi.org/10.1016/j.envint.2018.12.007

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Friday, November 20, 2020

Mojar y aplicar

Soak-and-smear' AD protocol backed by evidence

The most effective initial step for clearing atopic dermatitis in infants and young children involves daily bathing, followed by immediate application of a moisturizer, topical steroid, or both, according to an expert speaking at the virtual annual Coastal Dermatology Symposium.

"If they are really severe, you can do it twice-daily, but there are several studies that show there is not a huge benefit of twice-daily over once-daily," said Eric Simpson, MD, professor of dermatology, Oregon Health & Science University, Portland.

He called this technique "soak-and-smear." The "smear" is performed immediately after the bath when the skin is still damp, he said. When clearing is the goal, and the child has moderate to severe atopic dermatitis (AD), 0.1% triamcinolone or a similar medium potency topical steroid can be applied, and after clearing, the steroid can be switched for a moisturizer, according to Dr. Simpson.

Rather than restricting application to areas of greatest skin involvement, "put it all over," he advised.

The clearing regimen should be continued "for a couple of more days" after the lesions have resolved, with a return visit in about a week to confirm clearing and reinforce the next steps for keeping patients clear, he added.

The next steps depend on severity. According to Dr. Simpson, severity is defined less by the extent of skin involvement at the baseline examination than the speed at which symptoms return.

For those with only mild symptoms after an extended period of clearing, moisturizer might be sufficient to prevent a significant relapse. For children with a more rapid relapse, it will be necessary to reintroduce topical steroid either every day, every other day, or twice per week.

Whether with moisturizer or with topical steroids, the soak-and-smear technique has now been validated in a recently published crossover randomized trial.

In the trial, children aged 6 months to 11 years, with moderate to severe AD, were randomized to a twice-daily bath, called the "wet method," versus a twice-weekly bath, called the "dry method." Both groups received a cleanser and moisturizer along with a low-potency topical steroid as needed.

After 2 weeks, the 40 evaluable patients were crossed over to the opposite bathing technique. The wet, or soak-and-smear approach, was associated with a highly significant reduction in the primary endpoint of SCORing Atopic Dermatitis (SCORAD) index, compared with the dry method (95% confidence interval, 14.9-27.6; P less than .0001). In a secondary analysis, this translated into a 30% relative reduction in favor of the wet method.

In addition, there was improvement in a caregiver assessment of the Atopic Dermatitis Quickscore (ADQ). These data show that "twice-daily baths with topical steroids and moisturizer can help in more moderate to severe population," said Dr. Simpson, who noted that he has participated in open-label studies with the same soak-and-smear technique that have produced similar results.

Once children are clear, Dr. Simpson recommends a maintenance strategy individualized for severity. In many cases, this will involve moisturizers applied after the bath, supplemented intermittently, such as once or twice per week, with topical steroids. However, if parents find themselves resorting to daily steroids to maintain control, "that's when you incorporate the TCIs [topical calcineurin inhibitors]."

TCIs "can help you stay at twice-per-week topical steroids," Dr. Simpson said at the meeting, jointly presented by the University of Louisville and Global Academy for Medical Education.

TCIs also help patients avoid steroid withdrawal, a particularly common phenomenon when topical steroids are applied repeatedly to the face. He recommended a proactive approach. By applying TCIs to areas where skin lesions frequently recur, such as the eyelids, flares can often be prevented.

Repeated applications of TCIs "is perfectly safe and effective, and there are many studies that show proactive treatment is very effective and can prevent you from having to use too much topical steroids" or move to a systemic steroid, Dr. Simpson said.

These steps have been highly effective for sustained control even in challenging cases of AD, but he emphasized the importance of explaining the rationale to parents and eliciting their adherence to these treatment steps. Writing out the instructions will reduce confusion and help parents keep their children clear, he added.

Lawrence F. Eichenfield, MD, professor of pediatrics and dermatology at the University of California, San Diego, agreed that this recently published crossover trial has been helpful in counseling parents about how to manage AD in their children.

"Many times, pediatricians tell parents to avoid bathing because they feel that bathing will dry out the skin," he said. The crossover study, by showing better control of AD with frequent bathing, dispels that notion, although he is not convinced that bathing at this frequency is necessary.

"I have not advised anyone to do twice-daily bathing, with rare exceptions, on the basis on this study, but, basically, I think that whether people do daily bathing or every other day bathing, it is pretty reasonable that bathing might help as long as they are applying moisturizer immediately afterward," he said.

Dr. Simpson reports financial relationships with AbbVie, Celgene Dermira, Genentech, GlaxoSmithKline, Incyte, Lilly, Medimmune, Pfizer, Regeneron/Sanofi, and Tioga.

This publication and Global Academy for Medical Education are owned by the same parent company.


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Time to Relapse After Tildrakizumab Withdrawal in Patients With Moderate-to-Severe Psoriasis Who Were Responders at Week 28

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Abstract 


BACKGROUND

As treatment interruptions occur during psoriasis management in clinical practice, it is important to know the duration of clinical response after treatment withdrawal.

OBJECTIVES

To report time to and predictors of relapse in patients who were tildrakizumab 100 and 200 mg responders (≥75% improvement in Psoriasis Area and Severity Index, PASI 75) at week 28 re-randomized to placebo from reSURFACE 1 trial.

METHODS

Post hoc analysis of adult patients with moderate-to-severe plaque psoriasis from a 64-week phase 3 trial. Relapse was primarily defined as loss of PASI 75 response. Both relapses defined as loss of PASI 90 and loss of absolute PASI < 2 response were included as sensitivity analyses. PASI 75, PASI 90 and PASI < 2 responders re-randomized to placebo at week 28 and followed up until week 64 were included. The Kaplan-Meier (KM) estimates of the 64-week relapse rate were calculated. The log-rank test to compare KM curves from responders to tildrakizumab 100 and 200 mg was used. Independent predictors of relapse were explored.

RESULTS

Median time to loss of PASI 75/PASI 90/PASI < 2 response from week 28 was 142/111/112 days with tildrakizumab 100 mg and 172/140/113 days with tildrakizumab 200 mg, respectively (all not significant). Around 20% of patients did not relapse (either maintained a PASI 75 response or were lost to follow-up) during the 36-week period. Increase in body mass index (BMI) (hazard ratio, HR [95% confidence interval, CI] for loss of PASI 75 response: 1.0345 [1.0112-1.0582]) and increase in disease duration (HR [95% CI]: 1.0151 [1.0028-1.0275] for loss of PASI 75 response) were associated with an increased risk of relapse, regardless of the relapse definition.

CONCLUSIONS

When treatment is interrupted, tildrakizumab provides durable maintenance of efficacy with a median time to loss of PASI 75 response of 5-6 months, irrespective of the dose. Interventions on modifiable risk factors for relapse, such as BMI, may improve personalized long-term psoriasis management.


Journal of the European Academy of Dermatology and Venereology: JEADV

Time to Relapse After Tildrakizumab Withdrawal in Patients With Moderate-to-Severe Psoriasis Who Were Responders at Week 28: Post Hoc Analysis Through 64 Weeks From reSURFACE 1 Trial

J Eur Acad Dermatol Venereol 2020 Sep 26;[EPub Ahead of Print], RB Warren, JM Carrascosa, E Fumero, A Schoenenberger, MG Lebwohl, JC Szepietowski, K Reich 




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Oral and Palmoplantar Findings in Patients With COVID-19


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Abstract 

Coronavirus disease 2019 (COVID‐19) has been associated with several cutaneous manifestations.1-3 A temporary field hospital was implemented during the pandemic peak in Madrid, Spain, to attend patients with COVID‐19 who had mild‐to‐moderate pneumonia. A team of dermatologists working as medical volunteers performed a cross‐sectional study between 10 and 25 April 2020 to evaluate cutaneous findings of such patients.

The British Journal of Dermatology
Prevalence of Mucocutaneous Manifestations in 666 Patients With COVID-19 in a Field Hospital in Spain: Oral and Palmoplantar Findings
Br J Dermatol 2020 Sep 24;[EPub Ahead of Print], A Nuno-Gonzalez, P Martin-Carrillo, K Magaletsky, MD Martin Rios, C Herranz Mañas, J Artigas Almazan, G García Casasola, E Perez Castro, A Gallego Arenas, A Mayor Ibarguren, M Feito Rodríguez, B Lozano Masdemont, M Beato, E Ruiz Bravo, P Oliver, MD Montero Vega, P Herranz Pinto 


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Acne recurrence risk factors

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Abstract 

Oral isotretinoin has been used for decades to treat moderate to severe recalcitrant nodulocystic acne.One way to evaluate the effectiveness of treatments is to measure relapse rates after treatment completion. Prior studies have found factors such as cumulative dose, male gender, young age, severity, and treatment duration to be associated with acne recurrence after isotretinoin.2-5 We sought to further investigate factors associated with relapse after isotretinoin.

Journal of the American Academy of Dermatology
Analysis of Factors Associated With Relapse in Patients on Their Second Course of Isotretinoin for Acne Vulgaris
J Am Acad Dermatol 2020 Oct 20;[EPub Ahead of Print], PT Tran, HS Berman, E Leavitt, M Hogeling, CE Cheng

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Head and Neck Dermatitis, A Subtype of Atopic Dermatitis Induced by Malassezia Spp | PracticeUpdate




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Abstract 

BACKGROUND AND OBJECTIVES

Head and neck dermatitis (HND) is a clinical variant of atopic dermatitis (AD), presenting in adolescence or adulthood and characterized by involvement of the head, neck, and superior part of the trunk. The role of Malassezia spp has been advocated in the pathogenesis of HND, and antifungal agents represent the treatment of choice.

METHODS

A retrospective single-center study was performed to define the clinical features and treatment response of HND among adolescent and adult patients.

RESULTS

Thirty-one patients were identified, 17 with "adolescent-onset" and 14 with "adult-onset" HND. Adolescent-onset HND positively correlated with a past history of AD and presented with exclusive head and neck involvement (P < .05). Adult-onset HND was associated with concomitant widespread atopic eczema, involving the flexural areas of the upper and lower limbs, trunk, nipples, or hands (P < .05). A positive response to itraconazole in combination with topical treatments was observed in both groups.

CONCLUSIONS

This study delineates two HND clinical phenotypes: adolescent vs adult onset. Different characteristics were observed in terms of relationship to AD and eczema localization. A history of AD in childhood and presentation with exclusive involvement of head and neck regions was observed predominantly in the adolescent-onset form, while adult-onset HND often occurred in association with diffuse dermatitis and a past history of AD was less frequent than in the adolescent group. The study is limited by the single-center retrospective nature, which may lead to diagnostic and selection biases, and the small cohort of patients.


Pediatric Dermatology

Head and Neck Dermatitis, A Subtype of Atopic Dermatitis Induced by Malassezia Spp: Clinical Aspects and Treatment Outcomes in Adolescent and Adult Patients

Pediatr Dermatol 2020 Nov 06;[EPub Ahead of Print], A Guglielmo, A Sechi, A Patrizi, C Gurioli, I Neri 



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Friday, November 13, 2020

RecoSMA Erbium Yag en tx Psoriasis

Original Paper

Treatment of psoriatic skin lesions with a new Er:Yag laser technology: A case series study

First published: 24 February 2020

Abstract

Erbium: YAG (Er:YAG) laser with RecoSMA technology. This laser emits thousands of microbeams of energy causing superficial epidermal ablation and a separation of dermal fibers due to a mechanical‐acoustic and resonance effect. The aim of this study is to evaluate the clinical efficacy of Erbium: YAG (Er:YAG) laser with RecoSMA in the treatment of stable psoriasis vulgaris lesions. A questionnaire completed by 112 patients enrolled in the study. Photographs taken before each session, the analysis of the dynamics index PASI and histological studies were analyzed to visually monitor the clinical progress. The analyses were carried out with the help of computer software. The results after treatment of average number of sessions per course showed the complete clinical remission of the skin lesions in over 87% of the patients treated. The Er:YAG laser and RecoSMA have demonstrated the high effectiveness of the laser method of treating skin manifestations of the disease and improving the quality of life of patients.

Crio vs vacuna MMR en verrugas multiples

Original Paper

Intralesional injection of measles, mumps, and rubella vaccine versus cryotherapy in treatment of warts: A randomized controlled trial

First published: 07 February 2020

Abstract

Cutaneous warts are benign hyperkeratotic papillomas resulting from infection by human papillomavirus (HPV). Cryotherapy is a known method for warts treatment. Immunotherapy stimulates HPV recognition by the immune system; this helps resolution of warts. To determine the efficacy of intralesional immunotherapy with measles, mumps, and rubella (MMR) vaccine versus cryotherapy in the treatment of patients with multiple common and plantar warts. Forty‐eight patients with multiple common and plantar warts were divided into two groups: to undergo either intralesional injection of MMR vaccine (Group A), or cryotherapy (Group B). Forty patients completed the study. In the MMR group, 70% of the patients showed complete response, 5% partial response, and 25% showed no response to treatment. In the CRYO group, 45% of the patients showed complete response, 35% partial response, and 20% showed no response to treatment. The complete response was higher in the MMR group (70%) as compared to the CRYO group (45%), but the difference between the two groups was not statistically significant. Meanwhile, the partial response was significantly higher in the CRYO group. Intralesional MMR injection was a safe and effective treatment for multiple common and plantar warts as compared to cryotherapy.

Different antibodies

Children Produce Different Antibodies in Response to SARS-CoV-2

Children and adults produce different types and amounts of antibodies in response to infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), according to a study published in Nature Immunology.

The differences in antibodies suggest the course of the infection and immune response is distinct in children and most children easily clear the virus from their bodies.

"Our study provides an in-depth examination of SARS-CoV-2 antibodies in kids, revealing a stark contrast with adults," said Donna Farber, PhD, Columbia University Irving Medical Center, New York, New York.

"In kids, the infectious course is much shorter and probably not as disseminated as in adults," added Matteo Porotto, PhD, Columbia University. "Kids may clear this virus more efficiently than adults and they may not need a strong antibody immune response to get rid of it."

Among the 47 children in the study, 16 were treated at Columbia University Irving Medical Center for multisystem inflammatory syndrome (MIS-C) and 31 children of similar ages had tested positive for the virus after visiting the medical centre for the treatment of other conditions. Half of the children without MIS-C had no coronavirus disease 2019 (COVID-19) symptoms. The 32 adults in the study ranged from severely affected patients admitted to the hospital to those with milder disease who recovered at home.

Both groups of children produced the same antibody profile, which differed from that of adults. Compared with adults, children produced fewer antibodies against the virus's spike protein, and the children's antibodies had the least neutralising activity, while all adults, including young adults in their 20s, produced neutralising antibodies. The sickest adults had the most neutralising activity.

In contrast to adults, children also produced very few antibodies against a viral protein that is only visible to the immune system after the virus infects human cells.

"Because children clear the natural virus rapidly, they do not have a widespread infection and they do not need a strong antibody response," said Dr. Porotto.

"Even though children don't produce neutralising antibodies in response to a natural infection with SARS-CoV-2, vaccines are designed to generate a protective immune response in the absence of an infection," said Dr. Farber. "Children respond very well to vaccines, and I think they will develop good neutralizing antibody responses to a SARS-CoV-2 vaccine, and they'll probably be better protected than the adults."

Reference: https://www.nature.com/articles/s41590-020-00826-9

SOURCE: Columbia University Irving Medical Center

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