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Objective: To compare the clinical characteristics, treatments, and evolution of critical patients with COVID-19 pneumonia treated in intensive care units (ICU) after one year of pandemic. Methodology: Multicenter, prospective study, which included critical COVID-19 patients in 9 ICUs in northwestern Spain. The clinical characteristics, treatments, and evolution of patients admitted to the ICU during the months of March-April 2020 (period 1) were compared with patients admitted in January-February 2021 (period 2). Results: 337 patients were included (98 in period 1 and 239 in period 2). In period 2, fewer patients required invasive mechanical ventilation (IMV) (65% vs. 84%, P < .001), using high-flow nasal cannulas (CNAF) more frequently (70% vs. 7%, P < .001), ventilation non-invasive mechanical (NIMV) (40% vs. 14%, P < .001), corticosteroids (100% vs. 96%, P = .007) and prone position in both awake (42% vs. 28%, P = .012), and intubated patients (67% vs. 54%, P = .034). The days of IMV, ICU stay and hospital stay were lower in period 2. Mortality was similar in the two periods studied (16% vs. 17%). Conclusions: After one year of pandemic, we observed that in patients admitted to the ICU, CNAF, NIMV, use of the prone position, and corticosteroids have been used more frequently, reducing the number of patients in IMV, and the length of stay in the ICU and hospital stay. Mortality was similar in the two study periods.
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A 31-year-old female presented to the clinic with a 2 year history of proptosis of the right eye. She was diagnosed with cavernous hemangioma during her initial ophthalmologic consult and was advised monitoring. However, after a considerable increase in proptosis, she underwent an excision biopsy of the right orbital mass. A diagnosis of Rosai Dorfman disease was made after the histopathology report revealed a fibrosclerotic tissue with histiocytic proliferation showing emperipolesis that is mixed with numerous small lymphocytes and plasma cells. Rosai Dorfman disease is a rare disease presenting with lymphadenopathy and sinus histiocytosis. Orbital involvement can be the principal manifestation with proptosis as the most common presentation. Resection of the orbital lesion helped in the resolution of the mild ophthalmic symptoms but since the disease has other systemic associations, a complete systemic workup should be done to monitor recurrence.
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Exoftalmia , Hemangioma Cavernoso , Histiocitosis Sinusal , Enfermedades Orbitales , Femenino , Humanos , Adulto , Histiocitosis Sinusal/diagnóstico , Histiocitosis Sinusal/cirugía , Histiocitosis Sinusal/patología , Enfermedades Orbitales/cirugía , Exoftalmia/diagnóstico , Células Plasmáticas/patología , Hemangioma Cavernoso/diagnóstico por imagen , Hemangioma Cavernoso/cirugíaRESUMEN
OBJECTIVE: To compare the clinical characteristics, treatments, and evolution of critical patients with COVID-19 pneumonia treated in Intensive Care Units (ICU) after one year of pandemic. METHODOLOGY: Multicenter, prospective study, which included critical COVID-19 patients in 9 ICUs in northwestern Spain. The clinical characteristics, treatments, and evolution of patients admitted to the ICU during the months of March-April 2020 (period 1) were compared with patients admitted in January-February 2021 (period 2). RESULTS: 337 patients were included (98 in period 1 and 239 in period 2). In period 2, fewer patients required invasive mechanical ventilation (IMV) (65% vs 84%, pâ¯<â¯0.001), using high-flow nasal cannulas (CNAF) more frequently (70% vs 7%, pâ¯<â¯0.001), ventilation non-invasive mechanical (NIMV) (40% vs 14%, pâ¯<â¯0.001), corticosteroids (100% vs 96%, pâ¯=â¯0.007) and prone position in both awake (42% vs 28%, pâ¯=â¯0.012), and intubated patients (67% vs 54%, pâ¯=â¯0.034). The days of IMV, ICU stay and hospital stay were lower in period 2. Mortality was similar in the two periods studied (16% vs 17%). CONCLUSIONS: After 1â¯year of pandemic, we observed that in patients admitted to the ICU, CNAF, NIMV, use of the prone position, and corticosteroids have been used more frequently, reducing the number of patients in IMV, and the length of stay in the ICU and hospital stay. Mortality was similar in the two study periods.
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COVID-19 , Humanos , COVID-19/epidemiología , COVID-19/terapia , Estudios Prospectivos , Pandemias , SARS-CoV-2 , Unidades de Cuidados IntensivosRESUMEN
BACKGROUND: Multiple factors affect treatment adherence in individuals with cardiovascular disease. However, information on the relationships among treatment adherence, family functioning, and self-care agency in these patients and their families is limited. PURPOSE: This study was developed to determine the relationships among treatment adherence, family functioning, self-care agency, and sociodemographic variables in patients with cardiovascular disease. Self-care agency, as defined by Orem, is the dynamic process patients use to engage in their own healthcare that involves discerning and addressing factors that allow their making decisions that improve self-care abilities. METHODS: This cross-sectional, observational-analytical study enrolled 151 adult patients with cardiovascular diseases who had undergone pharmacological and nonpharmacological treatments and 108 family members of these patients who had consented to participate. Measurements were performed using the "Questionnaire for measuring treatment adherence in patients with cardiovascular disease," the "Family Functioning Assessment Scale," and the "Self-care Agency Scale." RESULTS: Of the 151 patients, 119 (78.8%) were assessed as having a low risk of nonadherence, 60 (39.7%) as having low family functioning, and 131 (86.8%) as having high self-care agency. Treatment adherence and self-care agency showed a moderate and significant correlation ( r = .66, p < .001). Similarly, treatment adherence and family functioning showed a low but significant correlation ( r = .35, p < .001). Moreover, significant multivariate associations were found among the variables of interest. Patients with a low risk of nonadherence were found to be more likely to have a secondary or postsecondary education, not to have vision or hearing problems, and to have a contributory affiliation mode with the health system or private health insurance. In addition, participants with moderate or high levels of family functioning were less likely to be workers or to not have hearing or vision problems. Finally, significant differences were noted between patients with low self-care agency and those with high self-care agency in terms of kinship relationship with family members and affiliation mode with the health system. CONCLUSIONS/IMPLICATIONS FOR PRACTICE: The results of this research help clarify the issue of treatment adherence in patients with cardiovascular disease. Although family functioning and self-care agency were found to be low to moderately correlated with treatment adherence, relevant information regarding these variables and sociodemographic variables is presented in this study. Nurses may use these results as a reference to design nursing care plans and interventions to address the conditions of their patients more appropriately.
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Enfermedades Cardiovasculares , Autocuidado , Adulto , Enfermedades Cardiovasculares/terapia , Colombia , Estudios Transversales , Humanos , Autocuidado/métodos , Cumplimiento y Adherencia al TratamientoRESUMEN
Menkes disease (MD) is a rare X-linked recessive neurodegenerative disorder caused by mutations in the ATP7A gene, with a high mortality rate within the first 3 years of life. It typically affects males and is characterized by impaired copper distribution and malfunction of several copper-dependent enzymes. Patients develop progressive muscle hypotonia associated with neurological damage and hair shaft dysplasia - particularly pili torti. Pili torti is usually very subtle in the first 3 months of life and gradually increases during the first year. Light microscopy examination in search for pili torti requires the observation of more than 50 hair shafts. In contrast, trichoscopy with a hand-held dermatoscope allows to easily identify the hair shaft defect. We report a case of a Hispanic male infant with MD in whom we show that trichoscopy is superior to hair light microscopy in revealing pili torti.
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BACKGROUND: The justification for this consensus is the absence of local protocols on Medication-Related Osteonecrosis of the Jaws (MONJ), for prevention, evaluation, and treatment, involving physicians and dentists, leading to suspension of antiresorptive treatments, despite their benefit in the prevention of fragility fractures (40-70%). These fractures cause disability and mortality (80% and 20-30%, respectively), as opposed to the low risk associated with MONJ in osteoporotic (0.01-0.03%) and oncological patients (1.3-1.8%). PURPOSE: To provide management recommendations through algorithms that guide health professionals to prevent, diagnose, and treat MONJ in different clinical scenarios. METHOD: A technical multidisciplinary team composed of specialists with extensive experience in osteoporosis or osteonecrosis of the jaw from Fundación Santa Fé (Bogotá, Colombia) and the Asociación Colombiana de Osteoporosis y Metabolismo Mineral was selected. Three rounds were carried out: definition of questions, answers using Delphi methodology, and the discussion of questions in order to have an agreement. The whole group participated in two phases, and the developer group in the total number of rounds. A literature review was conducted to obtain academic support to design questions with clinical relevance. RESULTS AND CONCLUSIONS: The consensus group generated definitions and recommendations useful for doctors and dentists, following clinical algorithms involving four scenarios: osteoporosis patient who requires dental procedures and has not received antiresorptives, osteoporosis patient who are under treatment with antiresorptives, cancer patients, and MONJ-instituted patients. The therapeutic approach in osteoporosis and cancer patients, in invasive dental procedures, must be relied on the risk-benefit treatment.
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Osteonecrosis , Algoritmos , Conservadores de la Densidad Ósea/efectos adversos , Colombia , Denosumab , Difosfonatos , Humanos , Enfermedades Maxilomandibulares , Osteonecrosis/inducido químicamente , Osteonecrosis/terapiaRESUMEN
Positive Steps is a six month residential program in southeastern Los Angeles County. The program seeks to assist residents in recovery from chemical dependency and to prevent sexual and other risk factors which promote HIV transmission. Positive Steps serves a multicultural population of women and transgender male to female. Program participants are allowed to bring up to two children with them in residence. Motivational interviewing serves as the foundation for chemical dependency treatment and HIV transmission risk reduction. Positive Steps also provides intensive group education. Individual counseling with a licensed mental health professional is provided for HIV Positive residents. External evaluation of the program involves a comprehensive assessment at baseline, six months post-baseline, and follow up. Program outcomes include statistically significant reductions in substance use, sexual risk behaviors, and symptoms of mental distress.
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Servicios Comunitarios de Salud Mental/métodos , Infecciones por VIH/prevención & control , Promoción de la Salud/métodos , Tratamiento Domiciliario , Trastornos Relacionados con Sustancias/rehabilitación , Adulto , Consejo , Diagnóstico Dual (Psiquiatría) , Femenino , Humanos , Los Angeles/epidemiología , Masculino , Trastornos Mentales/terapia , Persona de Mediana Edad , Evaluación de Resultado en la Atención de Salud , Asunción de Riesgos , Trastornos Relacionados con Sustancias/etnología , Trastornos Relacionados con Sustancias/psicología , Resultado del Tratamiento , Adulto JovenRESUMEN
Objetivo: las personas que viven con una enfermedad crónica experimentan procesos complejos de transformación personal para adaptarse a su nueva condición de salud. El objetivo del artículo es develar el significado de vivir con VIH en personas que fueron diagnosticadas en etapa de sida. Materiales y métodos: estudio cualitativo descriptivo en el que se realizaron entrevistas en profundidad a 15 personas que viven con VIH (PVVIH) en etapa de sida, que se atienden en el sistema público de salud chileno. Resultados: del análisis de contenido emergieron seis dimensiones del significado de vivir con la enfermedad: cambios personales posteriores al diagnóstico; apoyo social y acompañamiento, resignación a la adquisición del VIH; percepción de discriminación / rechazo; revelación del diagnóstico; cuidar a otros de la adquisición del VIH. Conclusiones: los hallazgos orientan a los profesionales de la salud sobre las estrategias que se deben utilizar en la atención directa de las personas que viven con VIH con el fin de otorgar un cuidado integral considerando el apoyo para el desarrollo de estrategias de autocuidado y la revelación del diagnóstico a su núcleo cercano, para reducir los costos psicosociales asociados a la enfermedad.
Objective: Those who live with chronic disease undergo complex processes of personal transformation to adapt to their new health condition. The aim of this article is to show what it means to live with HIV for persons who have been diagnosed with AIDS. Materials and methods: This is a descriptive qualitative study based on 15 people who are living with HIV/AIDS and being treated through the Chilean public health system. Results: The content analysis showed six dimensions of what it means to live with the disease: personal changes after the diagnosis, social support and accompaniment, being resigned to having contracted HIV, perceived discrimination / rejection, disclosure of the diagnosis, and protecting others from contracting HIV. Conclusion: The findings can provide guidance to health professionals on the strategies that should be used in providing direct care to persons living with HIV. In this respect, the goal is to offer comprehensive care, taking into account support for the development of self-care strategies and disclosure of the diagnosis to the patient's family and close friends, so as to reduce the psycho-social costs of the disease.
Objetivo: as pessoas que vivem com uma doença crônica experimentam processos complexos de transformação pessoal para se adaptar a sua nova condição de saúde. O objetivo deste artigo é revelar o significado de viver com HIV em pessoas que foram diagnosticadas em etapa de Aids. Materiais e métodos: estudo qualitativo descritivo no qual se realizaram entrevistas em profundidade com 15 pessoas que vivem com o HIV (PVHIV) em etapa de Aids, que se atendem no sistema público de saúde chileno. Resultados: da análise de conteúdo emergiram seis dimensões do significado de viver com a doença: mudanças pessoais posteriores ao diagnóstico; apoio social e acompanhamento, resignação à aquisição do HIV; percepção de discriminação ou rejeição; revelação do diagnóstico; cuidar a outros sobre a aquisição do HIV. Conclusões: as descobertas orientam os profissionais da saúde sobre as estratégias que se devem utilizar no atendimento direto das pessoas que vivem com o HIV, com o objetivo de outorgar um cuidado integral que considere o apoio para o desenvolvimento de estratégias de autocuidado e a revelação do diagnóstico a seu núcleo de pessoas próximas, para reduzir os custos psicossociais associados à doença.