RESUMO
IMPORTANCE: Skin cancer is the most common cancer in the United States, and men experience higher rates of skin cancer than women. Despite publicized preventative measures, men are less likely than women to use sunscreen. OBJECTIVE: To assess men's motivations, behaviors, and preferred product characteristics towards daily sunscreen use. DESIGN AND SETTING: Cross-sectional online survey of 705 men, administered July– August 2019, using Survey Monkey and distributed through Amazon Mechanical Turk. PARTICIPANTS: Men ages 20–70, having completed at least High School/GED, and living in the United States were eligible. Sampling strategy ensured diversity in terms of race, ethnicity, and sexual orientation. Main Outcome(s) and Measures: Men’s sunscreen use, behaviors, and preferred skincare product characteristics. RESULTS: Final participants included 705 men. The most frequent skincare products used regularly were liquid soap/body wash (65%), bar soap (47%), and moisturizers (32%). Most men (n=612; 83%) reported not using sunscreen daily, and 38% reported using sunscreen weekly. Income was related to daily and weekly sunscreen use, as males who earned between $40-$50,000 annually used sunscreen less often compared to people who earned $100,000 annually (OR 0.54%, 95% CI −0.34% to .88%; P = .01). Age, sexual orientation, race, ethnicity, and region were not related to daily or weekly sunscreen use. Main motivators for daily sunscreen use included reducing skin cancer risk (n=575; 82%) and looking younger (n=299; 42%). CONCLUSIONS AND RELEVANCE: This survey shows lapses in evidenced-based sunscreen behaviors to reduce skin cancer among men. Campaigns to reduce skin cancer should focus on increasing men's interest in daily sunscreen use and adherence to wearing sun-protective products. J Drugs Dermatol. 2021;20(1):88-93. doi:10.36849/JDD.5470.
Assuntos
Homens/psicologia , Higiene da Pele/psicologia , Neoplasias Cutâneas/prevenção & controle , Queimadura Solar/prevenção & controle , Protetores Solares/administração & dosagem , Adulto , Idoso , Comportamento do Consumidor/estatística & dados numéricos , Estudos Transversais , Feminino , Educação em Saúde , Humanos , Masculino , Pessoa de Meia-Idade , Pele/efeitos dos fármacos , Pele/patologia , Pele/efeitos da radiação , Higiene da Pele/estatística & dados numéricos , Neoplasias Cutâneas/etiologia , Neoplasias Cutâneas/patologia , Queimadura Solar/complicações , Queimadura Solar/patologia , Inquéritos e Questionários/estatística & dados numéricos , Estados Unidos , Adulto JovemRESUMO
BACKGROUND: Despite a growing interest in nonsurgical cosmetic procedures in men, the utilization of aesthetic treatments remains comparatively low, suggesting the presence of barriers to care. OBJECTIVE: To describe barriers to cosmetic intervention for male patients from the perspective of dermatologists. MATERIALS AND METHODS: An anonymous, online survey was distributed through a listserv made available by the American Academy of Dermatology. RESULTS: Dermatologist respondents perceived a low utilization of cosmetic services in male patients (5%) and a lack of opportunity (72.3%) to provide such services. Respondents also perceived a lack of sufficient education/training (40.9%), experience (20.5%), and a lack of evidence in the field (20.5%) for dermatologists as potential barriers to cosmetic care for male patients. Presence of targeted messaging and in-office educational materials for male patients was found to be associated with increased utilization of cosmetic treatments by male patients (p = .012, p = .012, respectively). Dermatologists reported strong confidence in delivering various noninvasive cosmetic treatments to male patients. CONCLUSION: Despite dermatologists' reported confidence in performing cosmetic procedures in men, many perceive insufficient education/training and experience with this population which may create barriers to cosmetic care for male patients. Increasing educational materials and targeted messaging to male patients may decrease barriers for patients to receive desired cosmetic care.
Assuntos
Atitude do Pessoal de Saúde , Técnicas Cosméticas/estatística & dados numéricos , Dermatologistas/estatística & dados numéricos , Higiene da Pele/estatística & dados numéricos , Competência Clínica/estatística & dados numéricos , Técnicas Cosméticas/psicologia , Dermatologistas/educação , Educação Continuada , Feminino , Acessibilidade aos Serviços de Saúde , Humanos , Masculino , Aceitação pelo Paciente de Cuidados de Saúde/estatística & dados numéricos , Fatores Sexuais , Higiene da Pele/psicologia , Inquéritos e Questionários/estatística & dados numéricos , Estados UnidosRESUMO
Cultural and social constructs may influence a patient’s understanding of their acne vulgaris affecting treatment preferences and valuation. Understanding these differences can better equip healthcare professionals when providing treatment recommendations. The objective of this study was to determine how perception, treatment preferences, and treatment valuation of acne vulgaris vary across different races. This was a cross-sectional study run from June 2017–February 2018. Participants with self-identified acne completed a one-time 31 question online survey distributed through ResearchMatch (national research registry) and campus recruitment. 217 English-speaking participants with self-identified acne who were over 18 years-old attempted the survey, and 3 participants were excluded for failing to complete it. Response rate of this study was 10.5%. Compared to Whites (88%, n=126), East Asians (44%, n=12) (P<0.001) and South Asians (53%, n=16) (P=0.002) were less likely to see a healthcare professional for acne. Compared to Whites (87%, n=125), East Asians (63%, n=17) were less likely to get information from healthcare professionals (P=0.03). East Asians (93%, n=25) used the internet more frequently as a source of information about causes of acne and treatments compared to all other races (P=0.04). Race was not statistically significant as a predictor for willingness to pay (WTP). Whites (27%, n=39) preferred using prescription face washes/creams/gels, while East Asians (41%, n=11), South Asians (60%, n=18), and Blacks (37%, n=7) preferred OTC washes/creams/gels. Differences exist in perception and treatment preferences for acne between races and exploring them may enhance providers’ understanding of their patients’ preferences. Healthcare organizations and professionals may need to utilize the internet and social media to access non-White populations. J Drugs Dermatol. 2020;19(12): doi:10.36849/JDD.2020.5488.
Assuntos
Acne Vulgar/tratamento farmacológico , Fármacos Dermatológicos/administração & dosagem , Aceitação pelo Paciente de Cuidados de Saúde/psicologia , Preferência do Paciente/estatística & dados numéricos , Higiene da Pele/psicologia , Adolescente , Adulto , Idoso , Povo Asiático/estatística & dados numéricos , População Negra/estatística & dados numéricos , Comparação Transcultural , Estudos Transversais , Feminino , Humanos , Comportamento de Busca de Informação , Internet , Masculino , Pessoa de Meia-Idade , Medicamentos sem Prescrição/administração & dosagem , Aceitação pelo Paciente de Cuidados de Saúde/estatística & dados numéricos , Medicamentos sob Prescrição/administração & dosagem , Autorrelato/estatística & dados numéricos , Índice de Gravidade de Doença , Higiene da Pele/métodos , Higiene da Pele/estatística & dados numéricos , População Branca/estatística & dados numéricos , Adulto JovemRESUMO
BACKGROUND: Facial skin care (FSC) is an important routine for Japanese women. Hand motions during FSC physically affect psychological state. However, it is very difficult to evaluate hand motions during personal and complex FSC. The objective of this study was to find out objective and quantitative parameters for hand motions during facial skin care (FSC). Women who enjoy and soothe during FSC (Enjoyment group (E group), n = 20) or not (non-enjoyment group (NE group), n = 19) were recruited by an advance questionnaire. The same lotion, emulsion, and cream were provided to all subjects, and they used sequentially in the same way as the women's daily FSC. The motion of the marker on the back side of the right middle finger during FSC was tracked by a motion capture system. The heart rate variability (HRV) was also measured before and after FSC for evaluating psychological effect. RESULTS: The averaged acceleration (Avg. ACC), approximate entropy (ApEn), and power law scaling exponent (Rest γ) of the cumulative duration of slow motion from the sequential data of acceleration were evaluated. Compared to the NE group, the E group showed a lower Avg. ACC when using emulsion (p = 0.005) and cream (p = 0.007), a lower ApEn when using emulsion (p = 0.003), and a lower Rest γ (p = 0.024) when using all items, suggesting that compared to the NE group, the E group had more tender and regular motion, and sustainable slow motions, especially in the use of emulsion. In the E group, the low/high-frequency component of HRV decreased significantly after FSC, suggesting suppression of sympathetic activity (p = 0.045). NE group did not. For all subjects, ApEn and Rest γ showed significantly positive correlation with the increase in the low/high-frequency component of HRV after FSC (p < 0.01). ApEn showed significantly negative correlation with the increase in the high-frequency component of HRV after FSC (p < 0.05). Avg. ACC did not show significant correlation with them. These results suggested that the behavior of FSC influences the autonomic nerve system. CONCLUSIONS: ApEn and Rest γ are useful parameters for evaluating quality of hand motions during FSC.
Assuntos
Sistema Nervoso Autônomo/fisiologia , Face/fisiologia , Movimento/fisiologia , Descanso/psicologia , Higiene da Pele/psicologia , Adulto , Entropia , Feminino , Mãos/fisiologia , Frequência Cardíaca/fisiologia , Humanos , Japão , Pessoa de Meia-Idade , Descanso/fisiologiaRESUMO
BACKGROUND: Opportunities for meaningful engagement with the homeless can alter negative attitudes. The purpose of this study was to assess changes in attitudes towards the homeless among undergraduate nursing students participating in a service-learning foot soak experience. METHODS: This was a prospective, pretest and posttest interventional study. Student attitudes were measured through: (a) the attitudes toward homelessness inventory and (b) thematic analysis of a guided reflection on the experience. RESULTS: Mean posttest total scores (mean = 50.06; standard deviation = 7.004) were significantly (P = .001) higher from mean pretest scores (mean = 47.06; standard deviation = 5.455), indicating more positive attitudes towards the homeless (n = 47) after the clinic. Three categories of themes that reflected student experiences are as follows: (a) benefits, (b) context, and, (c) potential consequences. CONCLUSIONS: A foot soak clinic can increase students' understanding of experiences faced by homeless persons through genuine human interaction, and has benefits to community members and learners.
Assuntos
Pé , Pessoas Mal Alojadas , Higiene da Pele/enfermagem , Estudantes de Enfermagem/psicologia , Adulto , Atitude do Pessoal de Saúde , Bacharelado em Enfermagem/métodos , Feminino , Humanos , Imersão , Masculino , Aprendizagem Baseada em Problemas , Estudos Prospectivos , Higiene da Pele/psicologia , Estudantes de Enfermagem/estatística & dados numéricosRESUMO
BACKGROUND: Melanoma is a common cancer among adolescents and young adults (AYAs), yet adherence to recommended surveillance and factors related to adherence are not well understood in this population. This study assessed the prevalence and correlates of physician-conducted skin examination (PSE) and skin self-examination (SSE) among AYA-aged long-term survivors of melanoma. PROCEDURES: Melanoma cases were identified from the Los Angeles County cancer registry and surveys were then completed by 128 respondents diagnosed between the ages 0 and 24, with stage 1 melanoma or higher, at least 5 years from diagnosis, and who were between the ages 18 and 39 at the time of survey. RESULTS: Eighty-two percent of AYA melanoma survivors reported SSE within the past 6 months, while 65% reported annual PSE. Greater health care self-efficacy was positively associated with adherence to PSE, SSE, and both types of skin examinations (P < .01). Higher socioeconomic status and having a regular source of primary health care were positively associated with annual PSE and adherence to both surveillance practices (P < .05 and P < .01, respectively). Hispanic ethnicity was negatively associated with annual PSE compared to non-Hispanics (P < .01), and greater depressive symptoms were negatively associated with adherence to both skin examinations (P < .05). CONCLUSIONS: High rates of SSE were observed, but PSE adherence was lower than optimal in this sample. Interventions to improve PSE are needed for at-risk AYA survivors of melanoma, and strategies that help melanoma survivors navigate the health care system and access primary care may facilitate greater adherence.
Assuntos
Sobreviventes de Câncer/psicologia , Sobreviventes de Câncer/estatística & dados numéricos , Melanoma/prevenção & controle , Cooperação do Paciente/estatística & dados numéricos , Autoexame/estatística & dados numéricos , Higiene da Pele/estatística & dados numéricos , Neoplasias Cutâneas/prevenção & controle , Adolescente , Adulto , Criança , Pré-Escolar , Estudos Transversais , Feminino , Seguimentos , Humanos , Lactente , Recém-Nascido , Masculino , Melanoma/psicologia , Cooperação do Paciente/psicologia , Prognóstico , Autoexame/psicologia , Higiene da Pele/psicologia , Neoplasias Cutâneas/psicologia , Adulto Jovem , Melanoma Maligno CutâneoRESUMO
The objective of this study was to analyse the sun exposure habits of elite aquatics athletes, together with their sunburn history and skin examination habits, taking into account differences by sex and between sports. A cross-sectional health survey was conducted at world championship events during which elite surfers, windsurfers and Olympic sailors from 30 different countries were invited to participate. The athletes were asked to complete a self-administered questionnaire focused on sun protection habits, sun exposure and sports practices. The survey was completed by 240 athletes, 171 men (71.3%) and 69 women (28.8%), with a mean age of 22 years (SD 5.86) and skin phototypes I (6.3%), II (3.3%), III (22.0%), IV (32.5%), V (9.2%) and VI (1.7%). There were significant differences between male and female athletes in skin self-examination (p < 0.001) and in the use of sunglasses (p < 0.001). In sunburn history during the last season, there were significant differences (p < 0.001) among the three sports analysed, in both sexes. The mean rate of sunburn during the previous season was 76.7%, and 27.5% of participants reported having experienced three or more sunburns that lasted at least 1 day. This type of athlete is at high risk of sunburn and hence of future skin cancer. However, there is a general lack of awareness of this risk. This study highlights the need to inform such athletes and to raise awareness of the dangers, through educational interventions on the importance of protecting against sunburn in order to reduce the future incidence of skin cancer.
Assuntos
Atletas/psicologia , Hábitos , Conhecimentos, Atitudes e Prática em Saúde , Higiene da Pele/psicologia , Neoplasias Cutâneas/prevenção & controle , Queimadura Solar/prevenção & controle , Adolescente , Adulto , Atletas/educação , Estudos Transversais , Feminino , Humanos , Incidência , Masculino , Higiene da Pele/estatística & dados numéricos , Neoplasias Cutâneas/epidemiologia , Neoplasias Cutâneas/psicologia , Espanha/epidemiologia , Queimadura Solar/epidemiologia , Queimadura Solar/psicologia , Protetores Solares/uso terapêutico , Inquéritos e Questionários , Adulto JovemAssuntos
Dermatologia/estatística & dados numéricos , Disseminação de Informação/métodos , Comportamento de Busca de Informação , Higiene da Pele/psicologia , Rede Social , Adulto , Dermatologia/tendências , Feminino , Humanos , Masculino , Higiene da Pele/estatística & dados numéricos , Higiene da Pele/tendências , Adulto JovemRESUMO
Lymphoedema is a long-term chronic condition that results from lymphatic insufficiency and may cause skin changes, which can cause discomfort and impact patient' quality of life. The four cornerstones of lymphoedema management are exercise, lymphatic massage, compression and skin care. This article critically examines self-management in lymphoedema focusing on skin care. Patients may initially demonstrate enthusiasm to undertake the required skin care independently. However, psychosocial factors, such as financial burden and physical restraints, can affect motivation and behaviours over time. A patient's knowledge of the importance of skin care self-management should not be limited to the initial assessment, but should be continually assessed throughout their lymphoedema journey. The ongoing provision of patient-centred care may have psychological and behavioural benefits and help optimise skin care self-management.
Assuntos
Conhecimentos, Atitudes e Prática em Saúde , Linfedema/enfermagem , Autogestão/métodos , Higiene da Pele/enfermagem , Efeitos Psicossociais da Doença , Humanos , Linfedema/economia , Linfedema/psicologia , Motivação , Educação de Pacientes como Assunto , Assistência Centrada no Paciente , Autogestão/psicologia , Higiene da Pele/métodos , Higiene da Pele/psicologiaRESUMO
Background: The aims of this study were to explore, using visual art methodology, how children and adolescents perceive their lymphedema and conceptualize the barriers and enablers in self-management and to explore the role of an educational camp in promoting self-efficacy. Methods: Participants (speaking English, French, and Italian) were recruited during an educational camp for children with lymphedema. Children and adolescents used different methodologies to depict living and self-managing their condition. Younger children (aged 5-12 years) drew pictures, and all children and adolescents (aged 5-18 years) were given cameras and asked to take photographs that depicted their experience of learning self-management of their condition during the camp. Rose's critical visual methodology framework was used for analysis. Results: Analysis of the data produced five categories: Normal versus altered childhood, living with lymphedema; perceptions of lymphedema and self-care in younger children; adolescents' perception of living and managing lymphedema; learning self-efficacy; and insights into cultural differences in self-care. Conclusions: The study has shown that self-management is complex. Children and adolescents face many daily challenges and frustrations in managing their condition in addition to the normal challenges of development and growth that impact on: home life, time with friends, school activities, and relationships. Children expressed a deep longing for cure and a recognition that their lives were altered by having the condition that led to limitations in sport and wearing fashionable clothes and shoes. The importance of relationships with professionals was critical as was the experience of meeting and learning with other children through the camp experience. Attempts to simplify self-management techniques would appear to be a key priority as would a greater understanding of the self-beliefs young people have of their ability to influence and control their condition and its impact on their life.
Assuntos
Recursos Audiovisuais/provisão & distribuição , Linfedema/psicologia , Educação de Pacientes como Assunto/métodos , Qualidade de Vida/psicologia , Autocuidado/psicologia , Autogestão/psicologia , Adolescente , Criança , Pré-Escolar , Doença Crônica , Bandagens Compressivas , Gerenciamento Clínico , Ajustamento Emocional , Feminino , França , Humanos , Itália , Extremidade Inferior/patologia , Extremidade Inferior/fisiopatologia , Sistema Linfático/patologia , Sistema Linfático/fisiopatologia , Linfedema/patologia , Linfedema/fisiopatologia , Linfedema/terapia , Masculino , Massagem/métodos , Massagem/psicologia , Autoeficácia , Autogestão/educação , Higiene da Pele/métodos , Higiene da Pele/psicologia , Inquéritos e Questionários , Resultado do Tratamento , Reino Unido , Extremidade Superior/patologia , Extremidade Superior/fisiopatologiaRESUMO
Background: The aim of this study was to explore the professional experience of caring for children and adolescents with lymphedema and to explore the way in which they understand and implement self-management strategies and the influence of their own self-efficacy beliefs on this process. Methods and Results: Participants were recruited during an educational camp for children with lymphedema. Three individual semistructured focus groups were undertaken in English, French, and Italian with simultaneous translation. Data were analyzed using interpretative phenomenological analysis (IPA). Analysis of the data produced three superordinate themes: professional concepts of self-management, professional practice, and redefining the cornerstone of lymphedema care. An additional seven subthemes were as follows: readiness to self-management, professional perspectives on self-management, defining success and treatment failure, emotional burden, traditional views on complex decongestive therapy, new ways to practice, and sole practitioner versus multidisciplinary teams. Conclusions: The purpose of the study was to explore the challenges professionals face when introducing self-management to children and adolescents with lymphedema and their parents and to explore their own sense of self-efficacy in approaching this. The research allowed in-depth discussion about the ways they conceptualize self-management and faced professional challenges. The research highlighted the need to define what is considered an acceptable outcome within a complex and uncertain condition and the self-management strategies that are needed to support this.
Assuntos
Ajustamento Emocional , Linfedema/psicologia , Qualidade de Vida/psicologia , Autocuidado/psicologia , Autogestão/psicologia , Adolescente , Criança , Doença Crônica , Bandagens Compressivas , Gerenciamento Clínico , Feminino , França , Humanos , Itália , Extremidade Inferior/patologia , Extremidade Inferior/fisiopatologia , Sistema Linfático/patologia , Sistema Linfático/fisiopatologia , Linfedema/patologia , Linfedema/fisiopatologia , Linfedema/terapia , Masculino , Massagem/métodos , Massagem/psicologia , Autoeficácia , Autogestão/educação , Higiene da Pele/métodos , Higiene da Pele/psicologia , Inquéritos e Questionários , Resultado do Tratamento , Reino Unido , Extremidade Superior/patologia , Extremidade Superior/fisiopatologiaRESUMO
Background: Limited research has shown the impact lymphedema has on children and families. The aim of this study was to explore the parental experience of caring for a child or adolescent with lymphedema and the daily challenges of self-management and self-efficacy. Methods and Results: Participants were recruited during an educational camp for children with lymphedema (N = 26). Three individual semistructured focus groups were undertaken in English, French, and Italian with simultaneous translation. Data were analyzed using interpretative phenomenological analysis. Analysis identified four superordinate themes; the journey, treatment management, independence, and psychosocial impact. Ten subthemes were identified: bandaging/compression, professional support, holistic care, fear, self-efficacy, acceptance, friendship, guilt, distress, and hope. Conclusions: Parental self-management of children with lymphedema is complex and invades many aspects of life. Lack of professional agreement over what constitutes self-management leads to parental confusion and anxiety. Self-management is demanding, and parents are ambivalent to its effectiveness, but choose to persevere through fear of their child's condition deteriorating. Self-efficacy is evident in complex problem solving, despite parents believing that they are not adequately prepared for this.
Assuntos
Cuidadores/psicologia , Linfedema/psicologia , Pais/psicologia , Educação de Pacientes como Assunto/métodos , Qualidade de Vida/psicologia , Autocuidado/psicologia , Autogestão/psicologia , Adolescente , Criança , Pré-Escolar , Doença Crônica , Bandagens Compressivas , Gerenciamento Clínico , Ajustamento Emocional , Feminino , França , Humanos , Itália , Extremidade Inferior/patologia , Extremidade Inferior/fisiopatologia , Sistema Linfático/patologia , Sistema Linfático/fisiopatologia , Linfedema/patologia , Linfedema/fisiopatologia , Linfedema/terapia , Masculino , Massagem/métodos , Massagem/psicologia , Pais/educação , Autoeficácia , Autogestão/educação , Higiene da Pele/métodos , Higiene da Pele/psicologia , Inquéritos e Questionários , Resultado do Tratamento , Reino Unido , Extremidade Superior/patologia , Extremidade Superior/fisiopatologiaRESUMO
Peristomal skin complications are a common problem for persons with an ileostomy. PURPOSE: The purpose of this pilot study was to solicit user feedback and perform an initial assessment of the performance of a new barrier seal designed to decrease the risk of chemical-induced dermatitis. METHODS: Seven (7) potential participants who were at least 18 years of age, >6 months post surgery, with an end or loop ileostomy and unbroken peristomal skin, and who were capable of changing their appliance themselves or had the availability of care assistance were identified and recruited by the stoma care nurse at the University Hospital, Limerick, Ireland. At the initial visit and after 1 and 2 weeks, participants were asked to rate device comfort, security, and handling; skin condition was assessed by the research nurse using the Ostomy Skin Tool. Descriptive statistics were used to tabulate the results. RESULTS: Five (5) participants completed the study. Discoloration, erosion, and tissue overgrowth scores improved in 3 of 5 patients, and the mean Ostomy Skin Tool score decreased from 5.4 ± 2.19 at the initial assessment to 4 ± 1.87 at the week 2 visit. Comfort, handling, and security ratings increased from a median of 8 at the beginning of the study to 10 at week 2. CONCLUSION: Initial patient feedback regarding the new product was positive, and skin assessment results suggest the new seal may help improve peristomal skin condition. Larger studies with longer patient follow-up are needed to confirm the results of this pilot evaluation.
Assuntos
Ileostomia/psicologia , Satisfação do Paciente , Higiene da Pele/psicologia , Higiene da Pele/normas , Adulto , Idoso , Dermatite de Contato/etiologia , Dermatite de Contato/psicologia , Feminino , Humanos , Ileostomia/efeitos adversos , Ileostomia/métodos , Irlanda , Masculino , Pessoa de Meia-Idade , Projetos Piloto , Higiene da Pele/métodosRESUMO
Hyperkeratosis of the nipple and areola is a rare condition first described by Tauber in 1923. Less than 100 cases have been reported in the literature. Hyperkeratosis of the nipple and areola presents as hyperkeratotic, hyperpigmented plaques on the nipple and areola. It is more common in females. An 18-year-old female patient presented with hyperkeratotic, plaque-like, hard crusts on both nipples and areolas. The examining physician could successfully remove this crust using his finger. The crust had accumulated as a result of the patient's reluctance to touch or clean the breast area due to psychological issues. A crusted nipple and areola may occur as a secondary condition due to a patient's reluctance to touch or clean their breasts.
Assuntos
Higiene , Hiperpigmentação/etiologia , Ceratose/etiologia , Mamilos/fisiopatologia , Higiene da Pele/psicologia , Adolescente , Feminino , Humanos , Hiperpigmentação/fisiopatologia , Ceratose/fisiopatologia , Arábia SauditaRESUMO
Despite the availability of a range of skin care products for the prevention of incontinence-associated dermatitis (IAD), prevalence remains high. Nurses' attitude is an important determinant to take into account in quality improvement projects. This study aimed to design a psychometrically test the attitude towards the prevention of incontinence-associated dermatitis instrument (APrIAD). A prospective psychometric instrument validation study was performed in a convenience sample of 217 Belgian nurses. Construct validity and reliability (internal consistency, stability) were tested. The exploratory factor analysis demonstrated a model consisting of four factors and 14 items: (a) beliefs about the impact of IAD on patients, (b) beliefs about team responsibility to prevent IAD, (c) beliefs about personal responsibility to prevent IAD, and (d) beliefs about the effectiveness of IAD prevention products and procedures. Cronbach's α was 0.72 for factor 1, 0.65 for factor 2, 0.63 for factor 3, and 0.47 for factor 4. The intra-class correlation coefficient was 0.689 (95% confidence interval [CI] 0.477-0.825) for the total instrument, 0.591 (95% CI 0.388-0.764) for factor 1, 0.387 (95% CI 0.080-0.626) for factor 2, 0.640 (95% CI 0.406-0.795) for factor 3, and 0.768 (95% CI 0.597-0.872) for factor 4. Psychometric testing of the APrIAD demonstrated adequate validity and reliability measures.
Assuntos
Dermatite/enfermagem , Dermatite/prevenção & controle , Incontinência Fecal/enfermagem , Recursos Humanos de Enfermagem Hospitalar/psicologia , Higiene da Pele/métodos , Higiene da Pele/psicologia , Incontinência Urinária/enfermagem , Adulto , Atitude do Pessoal de Saúde , Dermatite/etiologia , Incontinência Fecal/complicações , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Psicometria , Incontinência Urinária/complicaçõesRESUMO
Atopic dermatitis (AD) is a bothersome and common skin disease affecting â¼10.7% of children in the United States. This skin condition significantly decreases quality of life in not only patients, but in their families as well. Pediatricians are often the first physicians to diagnose and manage these patients and thus are relied on by families to answer questions about this disease. AD is complex, multifactorial, and has historically had limited therapeutic options, but the landscape of this disease is now rapidly changing. Pathways contributing to the pathogenesis of this disease are continually being discovered, and new therapies for AD are being developed at an unprecedented rate. With this article, we will review the current guidelines regarding the management of AD, outline updates in the current understanding of its pathophysiology, and highlight novel developments available for the treatment of this burdensome disease.
Assuntos
Dermatite Atópica/epidemiologia , Dermatite Atópica/terapia , Qualidade de Vida , Higiene da Pele/tendências , Administração Tópica , Anticorpos Monoclonais/uso terapêutico , Anticorpos Monoclonais Humanizados , Criança , Ensaios Clínicos como Assunto/métodos , Dermatite Atópica/psicologia , Humanos , Qualidade de Vida/psicologia , Higiene da Pele/métodos , Higiene da Pele/psicologiaRESUMO
Background: Nurses are at high risk of hand dermatitis. Regular hand moisturizing can prevent dermatitis, but nurses' use of hand moisturizers is suboptimal. Aims: To establish (i) what beliefs about hand dermatitis and hand moisturizer use are associated with hand moisturizer use by nurses at home and at work and (ii) if hand moisturizer use behaviours in nurses are associated with the prevalence of hand dermatitis. Methods: We used a questionnaire to investigate nurses' knowledge, beliefs and behaviours regarding hand dermatitis and use of hand moisturizers. Results: The response rate was 55/65 (85%). Forty-two (76%) participants agreed that applying hand moisturizers reduced the risk of dermatitis, and 53 (96%) agreed that dermatitis increased the risk of skin carrying pathogenic organisms. Frequent moisturizer application was associated with beliefs that it was part of the nurse's role to apply hand creams, a belief that they had had training in the use of moisturizers and believing that patients approved of them moisturizing their hands. Conclusions: Hand moisturizer use by nurses can be improved by enhancing their beliefs that it is part of their professional role to apply hand cream regularly.
Assuntos
Dermatoses da Mão/prevenção & controle , Mãos , Enfermeiras e Enfermeiros/psicologia , Creme para a Pele/farmacologia , Adulto , Feminino , Humanos , Masculino , Higiene da Pele/métodos , Higiene da Pele/psicologia , Creme para a Pele/uso terapêutico , Inquéritos e QuestionáriosRESUMO
The most common wound care procedures (WPCs) performed on open wounds are dressing changes and wound cleansing. Dressing changes cause moderate to severe pain in 74% of patients, nearly half (36%) of whom experience severe pain (rated as 8-10 on a 10-point numeric rating scale). The purpose of this paper is to propose a model of clinically accessible factors that can be tested in order to develop a clinical tool to identify which patients are likely to experience high intensity pain during nonoperative WCPs, such as dressing changes. Although multiple factors are known to be associated with pain, the factors selected for this model were limited to those that (1) are supported based on evidence and/or pain mechanisms and (2) are readily accessible to clinicians/practitioners and can be tested as a prediction tool to be used prior to WCPs. This model may be helpful to identify those likely to experience high intensity pain during WCPs. In this way, use of aggressive pain management strategies, including specialty dressings, pharmacologic analgesics, and/or non-pharmacological strategies, such as high intensity transcutaneous electrical stimulation.
Assuntos
Analgésicos/uso terapêutico , Bandagens , Catastrofização/psicologia , Dor Crônica/psicologia , Higiene da Pele/psicologia , Estimulação Elétrica Nervosa Transcutânea/métodos , Ferimentos e Lesões/psicologia , Fatores Etários , Bandagens/efeitos adversos , Dor Crônica/complicações , Dor Crônica/terapia , Etnicidade , Feminino , Humanos , Medição da Dor , Curva ROC , Índice de Gravidade de Doença , Fatores Sexuais , Higiene da Pele/efeitos adversos , Cicatrização , Ferimentos e Lesões/complicações , Ferimentos e Lesões/terapiaRESUMO
BACKGROUND/OBJECTIVES: Children with atopic dermatitis are at increased risk of both general behaviour problems, and those specific to the condition and its treatment. This can hamper the ability of parents to carry out treatment and manage the condition effectively. To date, there is no published instrument available to assess child behaviour difficulties in the context of atopic dermatitis management. Our aim was to develop a reliable and valid instrument to assess atopic dermatitis-specific child behaviour problems, and parents' self-efficacy (confidence) for managing these behaviours. METHODS: The Eczema Behaviour Checklist (EBC) was developed as a 25-item questionnaire to measure (i) extent of behaviour problems (EBC Extent scale), and (ii) parents' self-efficacy for managing behaviour problems (EBC Confidence scale), in the context of child atopic dermatitis management. A community-based sample of 292 parents completed the EBC, measures of general behaviour difficulties, self-efficacy with atopic dermatitis management and use of dysfunctional parenting strategies. RESULTS: There was satisfactory internal consistency and construct validity for EBC Extent and Confidence scales. There was a negative correlation between atopic dermatitis-specific behaviour problems and parents' self-efficacy for dealing with behaviours (r = -.53, p < .001). Factor analyses revealed a three-factor structure for both scales: (i) treatment-related behaviours; (ii) symptom-related behaviours; and (iii) behaviours related to impact of the illness. Variation in parents' self-efficacy for managing their child's atopic dermatitis was explained by intensity of illness-specific child behaviour problems and parents' self-efficacy for dealing with the behaviours. CONCLUSIONS: The new measure of atopic dermatitis-specific child behaviour problems was a stronger predictor of parents' self-efficacy for managing their child's condition than was the measure of general child behaviour difficulties. Results provide preliminary evidence of reliability and validity of the EBC, which has potential for use in clinical and research settings, and warrant further psychometric evaluation.