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1.
Actas Dermosifiliogr ; 2024 Mar 28.
Artículo en Inglés, Español | MEDLINE | ID: mdl-38554751

RESUMEN

BACKGROUND AND OBJECTIVE: Moisturizing products are widely used in conditions affecting skin hydration. However, the lack of scientific evidence leads to discrepancies and great variability in the recommendations used by different health professionals. The aim of this consensus document is to generate recommendations based on the evidence and experience of dermatologists to unify and facilitate the use of moisturizing products in the routine clinical practice. MATERIALS AND METHODS: A 49-statement questionnaire on moisturizing products was prepared and, then, arranged in 5 blocks: 1) concept; 2) characteristics, 3) frequency and quantity, 4) product use and areas of application, and 5) special populations. Twenty-two expert dermatologists in the management of patients with eczema answered to the survey using a 2-round Delphi methodology (adding an item on the 2nd round). RESULTS: Consensus was reached on 27 statements (54%), most (n=23) via agreement. The highest level of agreement was reached in the blocks on quantity, product use and areas of application (77.8%), followed by the blocks on characteristics (73%) and frequency (62.5%). Regarding the blocks on concept and special populations, the level of consensus on the items proposed was 37.5% and 10%, respectively. Consensus on the use of emollients for xeroderma (71%) was higher vs atopic dermatitis (64%) and inflamed skin (33.3%). CONCLUSIONS: Consensus recommendations can help all prescribers and improve the available evidence regarding their use.

2.
Actas Dermosifiliogr ; 2024 May 20.
Artículo en Inglés, Español | MEDLINE | ID: mdl-38777226

RESUMEN

BACKGROUND: Atopic dermatitis (AD) is one of the most prevalent skin diseases, but there are numerous knowledge gaps surrounding the impact this disease has on quality of life (QoL), mental health, and out-of-pocket expenses involved in the management of AD. The available scientific evidence on the multidimensional burden of AD is usually based on studies with measures reported by patients themselves. METHODS: In this context, the MEASURE-AD trial was developed as a cross-sectional, multicenter, multinational trial using patient- and physician-reported measures to characterize the multidimensional burden of AD in adults with moderate-to-severe AD. RESULTS: This paper presents the results of the Spanish cohort. We found that Spanish adults with moderate-to-severe AD and high EASI score (21.1-72) had a significantly increased disease burden, high severity of symptoms such as itch and sleep disturbances, impaired mental health and QoL, higher use of health care resources, and more out-of-pocket expenses than patients with low EASI scores (0-7 or 7.1-21). CONCLUSIONS: This study provides information to better understand disease burden, and identify aspects to be improved in the management of AD.

3.
Actas Dermosifiliogr ; 115(6): 539-546, 2024 Jun.
Artículo en Inglés, Español | MEDLINE | ID: mdl-38382750

RESUMEN

BACKGROUND: Psoriasis is a chronic inflammatory dermatosis whose clinical and topographic distribution requires differential diagnosis, or the possible association with allergic contact dermatitis (ACD), requiring patch testing (PT) as part of the diagnostic procedure. OBJECTIVES: To describe the epidemiological, clinical, and allergic profile of patients with a primary or secondary diagnosis of psoriasis undergoing PT and compare them with patients with a diagnosis of ACD at the end of the diagnostic process. METHODS: Cross-sectional study with data from REIDAC from 2018 through 2023 of selected patients with a diagnosis of psoriasis and/or ACD. RESULTS: A total of 11 502 patients were included, 513 of whom had been diagnosed with primary or secondary psoriasis, 3640 with ACD, and 108 with both diseases. Men were more predominant in the groups of patients with psoriasis, psoriasis+ACD, and lesions were more predominantly seen in the hands with little association with atopic factors vs the ACD group. The rate of positivity in PT to the 2022 Spanish battery of allergens was lower in the group with psoriasis only in 27% of the patients. The most common allergens found in the psoriasis group were also the most common ones found in the overall ACD population. CONCLUSIONS: Overall, 36.2% of psoriatic patients tested positive in PT to the 2022 Spanish battery of allergens, which proved that this association is not uncommon. Overall, psoriatic patients had a higher mean age, were more predominantly men, and showed more hand involvement.


Asunto(s)
Dermatitis Alérgica por Contacto , Pruebas del Parche , Psoriasis , Sistema de Registros , Humanos , Psoriasis/epidemiología , Masculino , Dermatitis Alérgica por Contacto/epidemiología , Dermatitis Alérgica por Contacto/diagnóstico , España/epidemiología , Femenino , Estudios Transversales , Persona de Mediana Edad , Adulto , Alérgenos/efectos adversos , Anciano , Adulto Joven
4.
Actas Dermosifiliogr ; 114(1): 54-59, 2023 Jan.
Artículo en Inglés, Español | MEDLINE | ID: mdl-35483422

RESUMEN

Interpreting patch test reactions is not easy. It requires experience and is characterized by high intraobserver and interobserver variability. It can sometimes be truly difficult to discern between a weak allergic reaction and an irritant reaction. A number of recent studies have investigated the dermoscopic features of patch test reactions. Homogeneous erythema is the main feature observed in patients with a positive allergic reaction, although dotted vessels, vesicles, crusts and yellow-orange areas may also provide clues. These features are somewhat similar to those observed in inflammatory conditions, such as eczema. In patients with an irritant reaction, the most common dermoscopic findings are the pore reaction pattern and perifollicular erythema. Dermoscopy could be useful for establishing a diagnosis in the case of doubtful patch test reactions.


Asunto(s)
Dermatitis Alérgica por Contacto , Eccema , Humanos , Irritantes , Dermoscopía , Dermatitis Alérgica por Contacto/diagnóstico , Dermatitis Alérgica por Contacto/etiología , Eritema , Pruebas del Parche
5.
Actas Dermosifiliogr ; 114(6): 479-487, 2023 Jun.
Artículo en Inglés, Español | MEDLINE | ID: mdl-36935039

RESUMEN

BACKGROUND: In recent years, remarkable improvements in our understanding of atopic dermatitis (AD) have revolutionized treatment perspectives, but access to reliable data from clinical practice is essential. MATERIALS AND METHOD: The Spanish Atopic Dermatitis Registry, BIOBADATOP, is a prospective, multicenter database that collects information on patients of all ages with AD requiring systemic therapy with conventional or novel drugs. We analyzed the registry to describe patient characteristics, diagnoses, treatments, and adverse events (AEs). RESULTS: We studied data entries for 258 patients who had received 347 systemic treatments for AD. Treatment was discontinued in 29.4% of cases, mostly due to a lack of effectiveness (in 10.7% of cases). A total of 132 AEs were described during follow-up. Eighty-six AEs (65%) were linked to a systemic treatment, most commonly dupilumab (39AEs) and cyclosporine (38AEs). The most common AEs were conjunctivitis (11patients), headache (6), hypertrichosis (5), and nausea (4). There was 1severe AE (acute mastoiditis) associated with cyclosporine. CONCLUSIONS: Initial findings on AEs from the Spanish BIOBADATOP registry are limited by short follow-up times precluding comparisons or calculation of crude and adjusted incidence rates. At the time of our analysis, no severe AEs had been reported for novel systemic therapies. BIOBADATOP will help answer questions on the effectiveness and safety of conventional and novel systemic therapies in AD.


Asunto(s)
Dermatitis Atópica , Humanos , Dermatitis Atópica/tratamiento farmacológico , Dermatitis Atópica/epidemiología , Estudios Prospectivos , Ciclosporina/uso terapéutico , Administración Cutánea , Sistema de Registros , Resultado del Tratamiento , Índice de Severidad de la Enfermedad
6.
J Investig Allergol Clin Immunol ; 29(6): 405-413, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-30931919

RESUMEN

The last few decades have seen a notable increase in the number of people who have a tattoo. This practice is not free from complications. Most adverse effects appear early and are temporary, although they can occasionally develop later and be permanent and serious. Recent research has generated new knowledge on the composition of inks, their degradation over time, the immune activity that is stimulated, and the various clinical disorders that can arise. This information enables better approaches to diagnosis and management when complications arise. Diagnosing allergic reactions to permanent tattoo ink can be very challenging. This review aims to identify clinical and histological clues to help practitioners differentiate allergic reactions from other complications. We discuss the yield and appropriateness of skin tests and biopsies and propose an algorithm to guide the diagnostic process.


Asunto(s)
Colorantes/efectos adversos , Dermatitis Alérgica por Contacto/diagnóstico , Tatuaje/efectos adversos , Dermatitis Alérgica por Contacto/patología , Humanos , Tinta , Pruebas del Parche , Piel/patología
10.
Allergol Immunopathol (Madr) ; 46(4): 397-412, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-29031890

RESUMEN

Atopic dermatitis (AD) is a multifaceted disease that involves a complex interplay between the skin and the immune system. The course of the disease depends strongly on the genetic background of the patient and on yet poorly-defined environmental factors. Changes in lifestyle could be behind the dramatic rise in the prevalence of AD across continents; including hygienic conditions, food, social habits, skin microbiome or exposure to a number of allergens. Although AD typically develops in childhood and disappears after a few years, in a relatively large number of patients it continues into adulthood. Adult AD can also appear de novo but it is often underdiagnosed and its treatment can be challenging. New, highly effective drugs are being developed to manage moderate and severe forms of the disease in adults. In this review, we highlight the most recent developments in diagnostic tools, current insights into the mechanistic basis of this disease, and therapeutic innovations.


Asunto(s)
Dermatitis Atópica/diagnóstico , Dermatitis Atópica/terapia , Dermatitis Atópica/etiología , Humanos
11.
J Eur Acad Dermatol Venereol ; 31(4): 664-671, 2017 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-27896884

RESUMEN

BACKGROUND: Allergic contact dermatitis caused by biocides is common and causes significant patient morbidity. OBJECTIVE: To describe the current frequency and pattern of patch test reactivity to biocide allergens included in the baseline series of most European countries. METHODS: Data collected by the European Surveillance System on Contact Allergies (ESSCA) network between 2009 and 2012 from 12 European countries were analysed. RESULTS: Methylisothiazolinone 0.2% aq. produced the highest prevalence of sensitization during the study period, with an overall prevalence of 4.5%. The mixture methylchloroisothiazolinone /methylisothiazolinone tested at 0.02% aq. followed closely, with 4.1% of positive reactions. Other preservatives with lower rates of sensitization, but still over 1%, include methyldibromo glutaronitrile (MDBGN) 0.5% pet. and iodopropynyl butylcarbamate (IPBC) 0.2% pet. Formaldehyde releasers and parabens yielded less than 1% positive reactions during the study period. Some regional differences in the prevalence of contact allergy to biocides among European countries were observed. CONCLUSIONS: Contact allergy to biocides is common throughout Europe, and regional differences could be explained by differences in exposure or characteristics of the population tested. Timely regulatory action for isothiazolinones is required. Although MDBGN is banned from cosmetics products since 2005, sensitization prevalence has not appeared to plateau. IPBC is an emerging allergen with an increasing prevalence over the last few years, and its inclusion in the European baseline series may be appropriate.


Asunto(s)
Antiinfecciosos/efectos adversos , Dermatitis Alérgica por Contacto/epidemiología , Dermatitis Alérgica por Contacto/etiología , Conservadores Farmacéuticos/efectos adversos , Adolescente , Adulto , Anciano , Carbamatos/efectos adversos , Europa (Continente)/epidemiología , Femenino , Formaldehído/efectos adversos , Humanos , Masculino , Persona de Mediana Edad , Nitrilos/efectos adversos , Prevalencia , Estudios Retrospectivos , Tiazoles/efectos adversos , Adulto Joven
12.
Allergol Immunopathol (Madr) ; 45(2): 134-144, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28029407

RESUMEN

BACKGROUND: Chronic spontaneous urticaria (CSU) is a frequent clinical entity that often presents a diagnostic and therapeutic challenge. OBJECTIVE: To explore the degree of agreement that exists among the experts caring for patients with CSU diagnosis, evaluation, and management. METHODS: An online survey was conducted to explore the opinions of experts in CSU, address controversial issues, and provide recommendations regarding its definition, natural history, diagnosis, and treatment. A modified Delphi method was used for the consensus. RESULTS: The questionnaire was answered by 68 experts (dermatologists, allergologists, and primary care physicians). A consensus was reached on 54 of the 65 items posed (96.4%). The experts concluded that CSU is a difficult-to-control disease of unpredictable evolution. Diagnostic tests should be limited and based on clinical history and should not be indiscriminate. Autoinflammatory syndromes and urticarial vasculitis must be ruled out in the differential diagnosis. A cutaneous biopsy is only recommended when wheals last more than 24h, to rule out urticarial vasculitis. The use of specific scales to assess the severity of the disease and the quality of life is recommended. In patients with severe and resistant CSU, second-generation H1-antihistamines could be used at doses up to four times the standard dose before giving second-line treatments. Omalizumab is a safe and effective treatment for CSU that is refractory to H1-antihistamines treatment. In general, diagnosis and treatment recommendations given for adults could be extrapolated to children. CONCLUSIONS: This work offers consensus recommendations that may be useful in the management of CSU.


Asunto(s)
Alergólogos/estadística & datos numéricos , Consenso , Técnica Delphi , Médicos de Atención Primaria/estadística & datos numéricos , Urticaria/epidemiología , Adulto , Niño , Preescolar , Enfermedad Crónica , Dermatólogos/estadística & datos numéricos , Diagnóstico Diferencial , Europa (Continente) , Antagonistas de los Receptores Histamínicos H1/uso terapéutico , Humanos , Omalizumab/uso terapéutico , Guías de Práctica Clínica como Asunto , Calidad de Vida , Índice de Severidad de la Enfermedad , Urticaria/diagnóstico , Urticaria/tratamiento farmacológico
13.
Actas Dermosifiliogr ; 108(4): 346-353, 2017 May.
Artículo en Inglés, Español | MEDLINE | ID: mdl-28219634

RESUMEN

INTRODUCTION: Chronic spontaneous urticaria is a prevalent and difficult-to-treat condition that has a very negative impact on patient quality of life. OBJECTIVE: To describe the epidemiological and clinical characteristics of patients presenting with chronic spontaneous urticaria and the response to treatment administered according to the EAACI/GA(2)LEN/EDF/WAO consensus guideline. MATERIAL AND METHOD: Descriptive cross-sectional study of all the patients with chronic spontaneous urticaria who consulted a skin allergy unit in the dermatology department of a tertiary hospital in Spain between July 2011 and July 2015. RESULTS: The study included 100 patients with chronic spontaneous urticaria; inducible urticaria was present in 43% of cases, and angioedema in 40%. On diagnosis, 53% of patients were taking nonsteroidal anti-inflammatory drugs. All patients were treated with second generation H1-antihistamines, but the standard dose was sufficient in only 18% of cases. Higher doses (up to 4 times the standard dose) achieved control of the urticaria in 74% of the patients studied. Higher doses of second generation H1-antihistamines were required to control the condition in patients with angioedema, and the presence of angioedema was associated with a lack of response to treatment with these drugs (OR, 6.1%; P<.001). One in 4 patients failed to respond to second generation H1-antihistamines and required treatment with omalizumab or ciclosporin to control their condition. CONCLUSIONS: Doses of H1-antihistamines higher than the standard dose are required in most cases to achieve control of chronic spontaneous urticaria. Angioedema is associated with failure to respond to treatment with antihistamines. In refractory cases, control of the condition can be achieved with omalizumab or ciclosporin. Patients with chronic spontaneous urticaria do not generally avoid the use of nonsteroidal anti-inflammatory agents.


Asunto(s)
Guías de Práctica Clínica como Asunto , Urticaria/tratamiento farmacológico , Corticoesteroides/uso terapéutico , Angioedema/complicaciones , Angioedema/tratamiento farmacológico , Antiinflamatorios no Esteroideos/uso terapéutico , Enfermedades Autoinmunes/epidemiología , Enfermedad Crónica , Comorbilidad , Estudios Transversales , Ciclosporina/uso terapéutico , Dermatología/métodos , Manejo de la Enfermedad , Quimioterapia Combinada , Hepatitis Viral Humana/epidemiología , Antagonistas de los Receptores Histamínicos H1/uso terapéutico , Humanos , Antagonistas de Leucotrieno/uso terapéutico , Omalizumab/uso terapéutico , Factores de Riesgo , Centros de Atención Terciaria , Urticaria/complicaciones , Urticaria/epidemiología
15.
Actas Dermosifiliogr ; 107(2): 107-15, 2016 Mar.
Artículo en Inglés, Español | MEDLINE | ID: mdl-26621334

RESUMEN

Corticosteroids are widely used drugs in the clinical practice, especially by topic application in dermatology. These substances may act as allergens and produce immediate and delayed hypersensitivity reactions. Allergic contact dermatitis is the most frequent presentation of corticosteroid allergy and it should be studied by patch testing in specific units. The corticosteroids included in the Spanish standard battery are good markers but not ideal. Therefore, if those makers are positive, it is useful to apply a specific battery of corticosteroids and the drugs provided by patients. Immediate reactions are relatively rare but potentially severe, and it is important to confirm the sensitization profile and to guide the use of alternative corticosteroids, because they are often necessary in several diseases. In this article we review the main concepts regarding these two types of hypersensitivity reactions in corticosteroid allergy, as well as their approach in the clinical practice.


Asunto(s)
Corticoesteroides/efectos adversos , Dermatitis Alérgica por Contacto/etiología , Hipersensibilidad Tardía/inducido químicamente , Alérgenos/efectos adversos , Humanos , Pruebas del Parche
16.
Clin Exp Allergy ; 45(4): 731-43, 2015 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-25429900

RESUMEN

In spite of being an old disease and apparently easy to diagnose, chronic spontaneous urticaria (CSU) is still perceived as an uncontrollable and difficult to manage disease. The perception of the patient is that his/her condition is not well understood and that is suffering from a disorder with hidden causes that doctors are not able to tackle. Sometimes patients go through a number of clinicians until they found some CSU expert who is familiar with the disease. It is surprising that myths and believes with no scientific support still persist. Guidelines are not widely implemented, and recent tools to assess severity are infrequently used. European and American recent guidelines do not agree in several key points related to diagnosis and treatment, which further contributes to confusion. With the aim to clarify some aspects of the CSU picture, a group of allergists and dermatologists from the Spanish Dermatology and Allergy societies developed a Frequent Asked Questions leaflet that could facilitate physicians work in daily practice and contribute to a better knowledge of common clinical scenarios related to patients with CSU.


Asunto(s)
Manejo de la Enfermedad , Urticaria/diagnóstico , Urticaria/terapia , Factores de Edad , Biomarcadores , Biopsia , Enfermedad Crónica , Diagnóstico Diferencial , Femenino , Estudios de Seguimiento , Humanos , Masculino , Embarazo , Pronóstico , Resultado del Tratamiento , Urticaria/etiología
18.
Actas Dermosifiliogr ; 106(10): 816-22, 2015 Dec.
Artículo en Inglés, Español | MEDLINE | ID: mdl-26344737

RESUMEN

INTRODUCTION: Corticosteroids can cause hypersensitivity reactions, particularly delayed-type allergic reactions. A new classification system for testing hypersensitivity to corticosteroids distributes the drugs into 3 groups according to molecular structure; patients are classified according to whether they are allergic to agents in 1 or more of the groups. We aimed to describe the clinical characteristics of corticosteroid-allergic patients treated at our clinic and apply the new classification system to them; we also compared these patients' characteristics to those of others treated at our clinic. MATERIAL AND METHODS: Retrospective study of cases of delayed-type corticosteroid hypersensitivity treated in the skin allergy clinic of a tertiary level hospital over an 11-year period. RESULTS: We reviewed the records of 2857 patients, finding 33 with at least one positive patch test result showing corticosteroid hypersensitivity. Atopic dermatitis and hand involvement were less common in our corticosteroid-allergic patients. All were allergic to a group 1 corticosteroid (most often, budesonide, the culprit in 87.9%). Testing with a specific corticosteroid series revealed that 14 (42.4%) were also allergic to corticosteroids in group 2 and/or group 3. None were allergic exclusively to group 2 or group 3 agents. Twenty-one patients were exposed to a corticosteroid cream from a group their patch test results indicated allergy to; 13 of them (61.9%) did not develop a hypersensitivity reaction. CONCLUSIONS: The Spanish standard series only contains group 1 corticosteroids. In the interest of improving allergy management, we recommend testing with a specific corticosteroid series and a patient's own creams whenever patch testing with a standard series reveals a hypersensitivity reaction to corticosteroids.


Asunto(s)
Corticoesteroides/efectos adversos , Hipersensibilidad a las Drogas/epidemiología , Hipersensibilidad Tardía/epidemiología , Corticoesteroides/química , Corticoesteroides/clasificación , Adulto , Anciano , Alergia e Inmunología , Budesonida/efectos adversos , Dermatitis Alérgica por Contacto/epidemiología , Dermatitis Alérgica por Contacto/etiología , Dermatitis Profesional/epidemiología , Dermatitis Profesional/etiología , Hipersensibilidad a las Drogas/etiología , Femenino , Dermatosis de la Mano/epidemiología , Humanos , Hipersensibilidad Tardía/inducido químicamente , Hipersensibilidad Inmediata/epidemiología , Masculino , Persona de Mediana Edad , Estructura Molecular , Servicio Ambulatorio en Hospital/estadística & datos numéricos , Pruebas del Parche , Estudios Retrospectivos , España/epidemiología , Centros de Atención Terciaria/estadística & datos numéricos
19.
Actas Dermosifiliogr ; 106(7): 533-44, 2015 Sep.
Artículo en Inglés, Español | MEDLINE | ID: mdl-26005193

RESUMEN

Management of hand eczema is complex because of the broad range of different pathogeneses, courses, and prognoses. Furthermore, the efficacy of most available treatments is not well established and the more severe forms can have a major impact on the patient's quality of life. Patient education, preventive measures, and the use of emollients are the mainstays in the management of hand eczema. High-potency topical corticosteroids are the treatment of choice, with calcineurin inhibitors used for maintenance. Phototherapy or systemic treatments are indicated in patients who do not respond to topical treatments. Switching from topical treatments should not be delayed to avoid sensitizations, time off work, and a negative impact on quality of life. Alitretinoin is the only oral treatment approved for use in chronic hand eczema.


Asunto(s)
Fármacos Dermatológicos/uso terapéutico , Eccema/tratamiento farmacológico , Dermatosis de la Mano/tratamiento farmacológico , Corticoesteroides/uso terapéutico , Alitretinoína , Inhibidores de la Calcineurina/uso terapéutico , Enfermedad Crónica , Terapia Combinada , Dermatitis por Contacto/tratamiento farmacológico , Dermatitis por Contacto/prevención & control , Dermatitis por Contacto/terapia , Manejo de la Enfermedad , Eccema/prevención & control , Eccema/terapia , Emolientes/uso terapéutico , Guantes Protectores , Dermatosis de la Mano/prevención & control , Dermatosis de la Mano/terapia , Humanos , Inmunosupresores/uso terapéutico , Enfermedades Profesionales/tratamiento farmacológico , Enfermedades Profesionales/prevención & control , Enfermedades Profesionales/terapia , Fototerapia , Guías de Práctica Clínica como Asunto , Calidad de Vida , Tretinoina/uso terapéutico
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