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1.
Arch. endocrinol. metab. (Online) ; 67(6): e000654, Mar.-Apr. 2023. tab
Article in English | LILACS-Express | LILACS | ID: biblio-1447274

ABSTRACT

ABSTRACT Objective: To evaluate the association between the patients' characteristics and the development of endocrine toxicity and to assess the association between endocrine-related adverse effects (ERAE) development and mortality. Subjects and methods: A retrospective observational study was conducted in 98 patients submitted to immunotherapy in our centre since its introduction in 2015 until March 2021. We excluded patients for which data regarding the corticotroph axis evaluation was missing. We used linear and logistic regression models to address our aims. Results: We observed a significant negative association between ERAE development and death (OR 0.32; p = 0.028). We detected no associations between ERAE and the following characteristics: age at immune checkpoint inhibitors (ICI) initiation, sex, diabetes mellitus, medical history, immunotherapy duration and ICI type. Conclusion: The development of an ERAE may be associated with a better overall survival rate in advanced oncologic disease, supporting the role of an unleashed immune system response to malignant cells.

2.
Article in Spanish | LILACS-Express | LILACS | ID: biblio-1527761

ABSTRACT

Introducción: Las enfermedades del tiroides son relativamente frecuentes, constituyen un importante grupo dentro de las enfermedades crónicas no transmisibles. Objetivo: Determinar la calidad de vida en pacientes con enfermedades tiroideas. Métodos: Se realizó un estudio observacional, descriptivo y transversal. El universo estuvo constituido por 210 pacientes con diagnóstico de enfermedades tiroideas, que cumplieron con los criterios de inclusión y exclusión previstos en el estudio, previo consentimiento informado y la muestra no probabilística de 198 pacientes. Se utilizaron las variables: edad, sexo, enfermedad tiroidea diagnosticada (hipertiroidismo, hipotiroidismo, bocio difuso eutiroideo) y calidad de vida (facetas según dimensiones, según la clasificación de expertos y enfermedades tiroideas y la calidad de vida integral según enfermedades tiroideas). Se utilizó el cuestionario World Health Organization Quality of Life. Resultados: Predominó el hipotiroidismo como afección tiroidea más frecuente en las féminas entre 50 a 59 años. Las manifestaciones clínicas que puntuaron las medias más bajas fueron el dolor y malestar, seguido de indicaciones médicas y sentimientos negativos; las dimensiones físicas y psicológicas puntuaron con medias bajas, al igual que el ambiente, valores considerados como deficientes. Conclusiones: Predominó una calidad de vida integral media en el mayor por ciento de los pacientes, estas enfermedades deben ser identificadas a tiempo, para evitar otras complicaciones en diferentes sistemas del organismo que pudieran comprometer la vida del paciente.


Introduction: Thyroid diseases are relatively frequent; they constitute an important group within chronic non-communicable diseases. Objective: To determine the quality of life in patients with thyroid diseases. Methods: An observational, descriptive and cross-sectional study was carried out. The universe (210 patients) with a diagnosis of thyroid diseases, who met the inclusion and exclusion criteria provided for in the study, prior informed consent, and the non-probabilistic sample (198 patients). The variables used were: age, sex, diagnosed thyroid disease (hyperthyroidism, hypothyroidism, diffuse euthyroid goiter) and quality of life (facets according to dimensions, according to expert classification and thyroid diseases and comprehensive quality of life according to diseases thyroid). The World Health Organization Quality of Life questionnaire was used. Results: Hypothyroidism predominated as the most frequent thyroid condition in women between 50 and 59 years of age. The clinical manifestations that scored the lowest average were pain and discomfort, followed by medical indications and negative feelings; the physical and psychological dimensions scored with low averages, as well as the environment, values ​​considered deficient. Conclusions: An average comprehensive quality of life prevailed in the highest percentage of patients; these diseases must be identified in time, to avoid other complications in different body systems that could compromise the patient's life.

3.
Chinese Journal of General Practitioners ; (6): 778-783, 2022.
Article in Chinese | WPRIM | ID: wpr-957904

ABSTRACT

Hyperuricemia is caused by a of purine metabolism disorder and/or reduced uric acid excretion, and the prevalence of hyperuricemia in China has increased significantly in recent years. According to the etiology, hyperuricemia can be primary or secondary. The endocrine system related diseases are one of the important causes leading to secondary hyperuricemia, which is easily missed in general practitice. This article reviews the clinical characteristics and research progress of hyperuricemia secondary to endocrine diseases.

4.
Cambios rev. méd ; 20(2): 80-88, 30 Diciembre 2021. ilus, tabs.
Article in Spanish | LILACS | ID: biblio-1368378

ABSTRACT

INTRODUCCIÓN. Los feocromocitomas son tumores que provienen de las células neuroendócrinas de la médula adrenal y producen alta secreción de catecolaminas. Generan complicaciones cardiovasculares graves que suelen asociarse con crisis hipertensivas. Es importante valorar el impacto cardiovascular de esta entidad. OBJETIVO. Realizar una revisión exhaustiva de las diversas manifestaciones de los feocromocitomas como causa de hipertensión arterial, su impacto cardiovascular, conducta diagnóstica y terapéutica. MATERIALES Y MÉTODOS. Revisión bibliográfica y análisis de 141 artículos científicos que incluyeron temas sobre el impacto cardiovascular, conducta diagnóstica y terapéutica del feocromocitoma como causa de hipertensión arterial. Se usó bases de datos: Medline, Embase, Scopus, Pubmed, Google Académico. Criterios de búsqueda en DECS, MeSH: "pheochromocytoma OR hypertension arterial AND cardiomyopathy", en inglés- español. Fueron seleccionados: 13 publicaciones de texto completo, 10 artículos retrospectivos, 2 guías de práctica clínica y 1 revisión. Se excluyeron 128 artículos científicos. RESULTADOS. Se realizó una revisión de las manifestaciones clínicas de los feocromocitomas como causa de hipertensión arterial y el impacto cardiovascular se relacionó con la producción de catecolaminas. Para el diagnóstico, la sensibilidad de la resonancia magnética es del 93-100%; la especificidad de resonancia magnética o tomografía computarizada en combinación con gammagrafía con metayodobencilguanidina con 123I es cercana al 100%. La resección del feocromocitoma tiene potencial curativo. CONCLUSIÓN. Los feocromocitomas presentan variabilidad clínica, se asocian a complicaciones cardiovasculares y cerebrovasculares graves por producción de catecolaminas. El diagnóstico oportuno y eficaz debe realizarse mediante resonancia magnética y gammagrafía en caso de alta sospecha clínica. El tratamiento quirúrgico es de elección.


INTRODUCTION. Pheochromocytomas are tumors arising from the neuroendocrine cells of the adrenal medulla and produce high secretion of catecholamines. They generate severe cardiovascular complications that are often associated with hypertensive crises. It is important to assess the cardiovascular impact of this entity. OBJECTIVE. To perform an exhaustive review of the various manifestations of pheochromocytomas as a cause of arterial hypertension, their cardiovascular impact, diagnostic and therapeutic conduct. MATERIALS AND METHODS. Bibliographic review and analysis of 141 scientific articles that included topics on the cardiovascular impact, diagnostic and therapeutic behavior of pheochromocytoma as a cause of arterial hypertension. The following databases were used: Medline, Embase, Scopus, Pubmed, Google Scholar. Search criteria in DECS, MeSH: "pheochromocytoma OR hypertension arterial AND cardiomyopathy", in English-Spanish. The following were selected: 13 full-text publications, 10 retrospective articles, 2 clinical practice guidelines, and 1 review. A total of 128 scientific articles were excluded. RESULTS. A review of the clinical manifestations of pheochromocytoma as a cause of arterial hypertension was performed and the cardiovascular impact was related to catecholamine production. For diagnosis, the sensitivity of MRI is 93-100%; the specificity of MRI or computed tomography in combination with 123I-methiodobenzylguanidine scintigraphy is close to 100%. Resection of pheochromocytoma has curative potential. CONCLUSION. Pheochromocytomas present clinical variability, are associated with severe cardiovascular and cerebrovascular complications due to catecholamine production. Timely and effective diagnosis should be made by MRI and scintigraphy in case of high clinical suspicion. Surgical treatment is the treatment of choice.


Subject(s)
Humans , Pheochromocytoma/complications , Adrenal Gland Neoplasms/complications , Hypertension/etiology , Pheochromocytoma/surgery , Pheochromocytoma/diagnosis , Catecholamines/metabolism , Adrenal Gland Neoplasms/surgery , Adrenal Gland Neoplasms/diagnosis , Heart/physiopathology , Heart Diseases/etiology
5.
Iatreia ; 34(1): 78-83, ene.-mar. 2021. tab, graf
Article in Spanish | LILACS | ID: biblio-1154361

ABSTRACT

RESUMEN El coma mixedematoso es la complicación más grave de un hipotiroidismo. Ocurre, por lo general, en mujeres ancianas con hipotiroidismo conocido sin un adecuado manejo y en presencia de un evento desencadenante. El diagnóstico es difícil y debe realizarse en forma oportuna para disminuir el riesgo de muerte. El coma es una de las presentaciones neurológicas de esta urgencia endocrinológica y no es necesario su presencia para el diagnóstico. En este reporte de caso se presentan varías manifestaciones inusuales en un paciente masculino con hipotiroidismo profundo que, al diagnóstico, debutó con coma mixedematoso con predictores de mal pronóstico durante la hospitalización, pero debido al abordaje temprano y el manejo integral, se dio una resolución satisfactoria a esta urgencia endocrinológica infrecuente.


SUMMARY Myxedema coma is the most serious complication of hypothyroidism. It usually occurs in the context of elderly women, with known hypothyroidism without proper management and in the presence of a triggering event. The diagnosis is challenging and must be made in a timely manner to prevent the development of adverse outcomes. Coma is one of the neurological manifestations of the entity, not being necessary for its diagnosis. This case report presents a constellation of unusual manifestations of a male patient with myxedema coma at the debut of severe hypothyroidism with predictors of poor prognosis during hospitalization, but due to the early approach and comprehensive management, this uncommon endocrinological emergency was satisfactorily resolved.


Subject(s)
Humans , Aged , Pericardial Effusion , Myxedema , Seizures , Coma
6.
Rev. chil. endocrinol. diabetes ; 14(3): 133-138, 2021. tab
Article in Spanish | LILACS | ID: biblio-1293389

ABSTRACT

El uso de opioides ha aumentado en forma significativa en las últimas décadas, lo que nos ha permitido conocer sus diversos efectos en el sistema endocrino. Estos efectos están sub diagnosticados, en parte porque los síntomas se confunden con los de la misma enfermedad que lleva al uso de opioides y porque no los buscamos de forma dirigida. El hipogonadismo y la insuficiencia suprarrenal son sus efectos más establecidos, sin embargo, otros efectos como los provocados en el tejido óseo requieren de especial atención. La evaluación de los ejes gonadotropo, adrenal y de la salud ósea debe tenerse en consideración en los usuarios crónicos de opioides, particularmente frente a la presencia de síntomas. La suspensión o reducción del uso de opioides es el primer tratamiento del compromiso endocrinológico.


The use of opioids has increased significantly in recent decades, which has allowed us to understand its effects on the endocrine system. These effects are underdiagnosed, the symptoms are confused with those of the same disease that leads to the use of opioids and we do not look for them in a targeted way. Hypogonadism and adrenal insufficiency are its most established effects, however, other effects such as the ones caused on bone tissue require special attention. Evaluation of gonadotropic and adrenal axes as well as bone health should be taken into consideration in chronic opioid users, particularly in the presence of symptoms. Stopping or reducing opioid use is the first treatment for endocrine compromise.


Subject(s)
Humans , Endocrine System Diseases/chemically induced , Endocrine System/drug effects , Analgesics, Opioid/adverse effects , Adrenal Insufficiency/chemically induced , Hypogonadism/chemically induced
7.
Journal of Clinical Hepatology ; (12): 2215-2219., 2021.
Article in Chinese | WPRIM | ID: wpr-886935

ABSTRACT

Nonalcoholic fatty liver disease (NAFLD) is a major cause of chronic liver diseases worldwide and covers a series of pathological manifestations from hepatic steatosis to inflammation, fibrosis, and even liver cirrhosis. NAFLD is associated with a wide range of extrahepatic diseases, including metabolic syndrome, cardiovascular disease, chronic kidney disease, endocrine diseases, obstructive sleep apnea-hypopnea syndrome, psoriasis, and skeleton-muscle diseases. The major causes of death in patients with NAFLD include cardiovascular disease, malignancies, and liver-related complications, suggesting that extrahepatic diseases associated with NAFLD should be taken seriously by clinicians. This article reviews the research advances in extrahepatic diseases associated with NAFLD, so as to provide ideas for clinical assessment and treatment.

8.
Rev. colomb. nefrol. (En línea) ; 7(1): 149-177, ene.-jun. 2020. tab, graf
Article in Spanish | LILACS, COLNAL | ID: biblio-1144383

ABSTRACT

resumen está disponible en el texto completo


Abstract In Colombia there are no guidelines for diagnosis and management of patients with short stature and for the use of recombinant human growth hormone, mainly caused by the diversity of training centers in pediatric endocrinology. In response to this situation, the Asociación Colegio Colombiana de Endocrinología Pediátrica leds the first colombian short stature expert committee in order to standardize the use of human recombinant growth hormone. This work had the participation and endorsement of a consortium of clinical experts representing the Sociedad Colombiana de Pediatría, Secretaría Distrital de Salud de Bogotá- Subred Integrada de Servicios de Salud Suroccidente, Fundación Universitaria Sanitas, Universidad de los Andes and some public and private health institutions in the country, in addition to the participation of methodological experts from the Instituto Global de Excelencia Clínica Keralty. By reviewing the literature and with the best available evidence, we proposed to unify definitions, a diagnostic algorithm, biochemical and dynamic tests with their reference parameters, a description of the considerations about growth hormone use among the indications approved by regulatory agency for medications and food in Colombia and finally a proposal for an informed consent and a medication fact sheet available for parents and patients.


Subject(s)
Humans , Male , Female , Child, Preschool , Child , Growth Hormone , Weight Loss , Colombia , Endocrinology
9.
Arch. argent. pediatr ; 118(3): e271-e277, jun. 2020.
Article in English, Spanish | LILACS, BINACIS | ID: biblio-1116919

ABSTRACT

Los problemas médicos gastrointestinales, nutricionales, metabólicos, endocrinológicos y de microbiota en los pacientes pediátricos con diagnóstico de trastorno del espectro autista (TEA) son parte de los problemas médicos concomitantes al diagnóstico. La prevalencia alcanza a más del 91 % en el caso de los problemas gastrointestinales, hasta el 89 % para los nutricionales y metabólicos, más del 50 % de disfunción tiroidea y hasta el 100 % para los relacionados con la microbiota.Es urgente actualizar la práctica médica para incluir la evaluación, testeo, diagnóstico y tratamiento de estos problemas médicos concomitantes al diagnóstico de TEA en la población pediátrica, adolescente y adulta. El tratamiento riguroso de dichos problemas genera cambios positivos en la calidad de vida y en la sintomatología bajo la cual el TEA se diagnostica en muchos casos. Debe basarse en evidencia científica de alta calidad, con control y cuidado médico adecuado


Gastrointestinal, nutritional, metabolic, endocrine, and microbiota medical problems in pediatric patients diagnosed with autism spectrum disorder (ASD) are some of the coexisting medical conditions in ASD diagnosis. Their prevalence reaches more than 91 % for gastrointestinal problems, up to 89 % for nutritional and metabolic disorders, more than 50 % for thyroid dysfunction, and up to 100 % for microbiota-related conditions.There is an urgency for medical practice to be updated and to include the assessment, testing, diagnosis, and treatment of these coexisting medical conditions in ASD diagnosis in the pediatric, adolescent, and adult population. A strict management of such conditions results in positive changes in the quality of life and symptoms based on which ASD is diagnosed many times. It should be based on high-quality scientific evidence with an adequate medical care and control


Subject(s)
Humans , Child, Preschool , Child , Adolescent , Endocrine System Diseases/metabolism , Microbiota , Autism Spectrum Disorder/microbiology , Gastrointestinal Diseases/metabolism , Concurrent Symptoms , Nutritional Status , Autism Spectrum Disorder/complications , Autism Spectrum Disorder/diet therapy , Autism Spectrum Disorder/metabolism , Gastrointestinal Diseases/complications , Gastrointestinal Diseases/diet therapy
10.
Rev. chil. pediatr ; 90(6): 598-605, dic. 2019. tab
Article in Spanish | LILACS | ID: biblio-1058190

ABSTRACT

INTRODUCCIÓN: La radioterapia, quimioterapia y la cirugía empleada en el tratamiento de los tumores cerebrales tienen efectos en el eje hipotálamo-hipofisario y pueden resultar en disfunción endocrina hasta en el 96% de los casos. PACIENTES Y MÉTODO: Estudio retrospectivo y descriptivo en pacientes diagnos ticados de meduloblastoma sometidos a tratamiento con quimio y radioterapia en los últimos 20 años en un hospital terciario. Se analizan variables edad, sexo, peso, talla, índice de masa corporal (IMC) al final del seguimiento, estadio de maduración sexual, niveles séricos de TSH y T4 libre, ACTH/cortisol e IGF-1, FSH, LH, estradiol, testosterona, perfil lipídico (colesterol total) y prueba de función dinámica de hormona de crecimiento. RESULTADOS: Muestra total de 23 pacientes. El déficit de hormona de crecimiento es la secuela más frecuente (82 %) seguido de disfunción ti roidea (44,8%) y disfunción puberal (24,1%). Solo se diagnosticó un caso de diabetes insípida y 2 casos de déficit de corticotrofina. CONCLUSIONES: El seguimiento a largo plazo de los supervivientes de meduloblastoma tratados con quimio y radioterapia revela una prevalencia muy alta de disfun ción endocrina, particularmente de deficiencia de hormona del crecimiento y de hipotiroidismo. Creemos oportuna la monitorización y el seguimiento a largo plazo de estos pacientes con el fin de garantizar un manejo terapéutico adecuado de aquellas disfunciones tratables.


INTRODUCTION: Radiation therapy, chemotherapy, and surgery used to treat brain tumors have effects on the hy pothalamic-pituitary-adrenal axis and can result in endocrine dysfunction in up to 96% of cases. PATIENTS Y METHOD: Retrospective and descriptive study in patients diagnosed with medulloblasto ma who underwent treatment with chemo and radiotherapy in the last 20 years in a tertiary hospital. The variables analyzed were age, sex, weight, height, body mass index (BMI) at the end of follow-up, sexual maturity stage, serum levels of TSH and free T4, ACTH/cortisol and IGF-1, FSH, LH, estradiol, testosterone, lipid profile (total cholesterol), and growth hormone dynamic function test. RESULTS: Total sample of 23 patients. Growth hormone deficiency is the most frequent sequelae (82%) fo llowed by thyroid dysfunction (44.8%), and disorders of puberty (24.1%). Only one case of diabetes insipidus and two cases of corticotropin deficiency were diagnosed. CONCLUSIONS: Long-term follow- up of medulloblastoma survivors treated with chemo and radiotherapy reveals a very high prevalence of endocrine dysfunction, especially growth hormone deficiency and hypothyroidism. We believe that monitoring and long-term follow-up of these patients is necessary in order to ensure adequate therapeutic management of those treatable dysfunctions.


Subject(s)
Humans , Male , Female , Child, Preschool , Child , Cerebellar Neoplasms/therapy , Chemoradiotherapy/adverse effects , Medulloblastoma/therapy , Puberty, Precocious/etiology , Thyroid Diseases/etiology , Cerebellar Neoplasms/blood , Retrospective Studies , Adrenocorticotropic Hormone/deficiency , Human Growth Hormone/deficiency , Diabetes Insipidus/etiology , Endocrine System Diseases/etiology , Overweight/etiology , Cancer Survivors , Hypogonadism/etiology , Medulloblastoma/blood
11.
Medicentro (Villa Clara) ; 23(3): 192-209, jul.-set. 2019. tab, graf
Article in Spanish | LILACS | ID: biblio-1091046

ABSTRACT

RESUMEN Introducción: la erupción de los dientes es un fenómeno biológico de interés médico y social. Este puede ser alterado por causas congénitas y adquiridas. Objetivo: caracterizar el brote dentario en individuos infanto-juveniles con enfermedades endocrinas frecuentes. Métodos: se realizó un estudio epidemiológico, descriptivo y transversal, en el Hospital Universitario Pediátrico José Luis Miranda, de Villa Clara, en el período comprendido de marzo de 2016 a abril de 2017. Se tomó una muestra intencional de 114 individuos de ambos sexos, desde tres meses a 14 años de edad, con diabetes mellitus, hipotiroidismo congénito, hipertiroidismo o hiperplasia adrenal congénita. Se aplicó un cuestionario contentivo de variables relacionadas con el tipo de enfermedad endocrina y el brote dentario, la información fue procesada mediante el paquete estadístico SPSS versión 15.0. Resultados: la muestra se caracterizó por una prevalencia del sexo masculino, del grupo de edad de 7 a 11 años. Las enfermedades endocrinas más frecuentes fueron en orden ascendente: el hipertiroidismo, el hipotiroidismo congénito y la diabetes mellitus. El brote dentario se relacionó significativamente con el tipo de enfermedad; predominó el brote dentario tardío (presente en la mayoría de los pacientes con diabetes mellitus). Conclusiones: existió una relación altamente significativa entre el tipo de enfermedad endocrina y el brote dentario.


ABSTRACT Introduction: tooth eruption is a biological phenomenon of social and medical interest. This can be altered by congenital and acquired causes. Objective: to characterize tooth eruption in infantile and juvenile individuals with common endocrine diseases. Methods: an epidemiological, descriptive and cross-sectional study was conducted at José Luis Miranda Pediatric University Hospital in Villa Clara, from March 2016 to April 2017. An intentional sample of 114 individuals of both genders, from three months to 14 years of age who suffered from diabetes mellitus, congenital hypothyroidism, hyperthyroidism or congenital adrenal hyperplasia was taken. A questionnaire containing variables related to the type of endocrine disease and tooth eruption was applied; the information was processed using the statistical package SPSS version 15.0. Results: the sample was characterized by a prevalence of male gender, from the age group of 7 to 11 years. The most frequent endocrine diseases were in ascending order: hyperthyroidism, congenital hypothyroidism and diabetes mellitus. Tooth eruption was significantly related to the type of disease; the late tooth eruption was predominant in most of patients with diabetes mellitus). Conclusions: there was a highly significant relationship between the type of endocrine disease and tooth eruption.


Subject(s)
Tooth Eruption , Endocrine System Diseases
12.
Rev. colomb. psiquiatr ; 48(1): 35-43, ene.-mar. 2019. tab, graf
Article in Spanish | LILACS, COLNAL | ID: biblio-1013958

ABSTRACT

RESUMEN La prescripción de carbonato de litio es común en la actividad psiquiátrica cotidiana. El objetivo es identificar las alteraciones endocrinas secundarias y sus bases fisiopatológicas. La revisión de la literatura se realizó en Psycinfo, EMBASE, PubMed y Scopus. Se efectuó una búsqueda computarizada de información utilizando la estrategia PICO. Las alteraciones más comunes están en riñones, tiroides, paratiroides, páncreas y vías neuroendocrinas. Los mecanismos fisiopatológicos subyacentes son diversos, y destacan la inhibición de la adenilato ciclasa tiroidea sensible a tirotropina como causa de hipotiroidismo, la expresión reducida de acuaporina 2 como causa de diabetes insípida nefrogénica, la pérdida del equilibrio iónico del calcio y la presencia de hiperparatiroidismo e hipercalcemia. En el eje hipotálamo-hipófiso-adrenal, se documenta una disminución en la producción de catecolaminas. Finalmente, se documenta la desregulación en el control de la glucemia al aumentar la resistencia a la insulina. Es necesario conocer estas eventualidades e identificarlas tempranamente a través de evaluaciones periódicas. Se propone un esquema de evaluación integral, sin que implique un algoritmo de tratamiento.


ABSTRACT The prescribing of Lithium is common in psychiatric clinical practice. The aim of this study was to identify the most common endocrine side effects associated with this drug and to clarify the pathophysiological basis. A systematic review was conducted in Psycinfo, Embase, PubMed, and Scopus. A computerised search for information was performed using a PICO (patient, intervention, comparative, outcomes) strategy. The main neuroendocrine alterations were reported in kidneys, thyroid and parathyroid glands, pancreas, and the communication pathways between the pituitary and adrenal glands. The pathophysiological mechanisms are diverse, and include the inhibition of the thyroid adenylate cyclase sensitive to the thyroid stimulant hormone (TSH) sensitive adenylate cyclase, which causes hypothyroidism. It also reduces the expression of aquaporin type 2, which is associated with nephrogenic diabetes insipidus, and the loss of the ionic balance of calcium that induces hyperparathyroidism and hypercalcaemia. Other considerations are related to alterations in the hypothalamic-pituitary-adrenal axis and a decrease in the production of catecholamines. Finally, another side-effect is the glycaemic dysregulation caused by the insulin resistance. Periodical clinical and para-clinical evaluations are necessary. The author proposes an evaluation scheme.


Subject(s)
Humans , Male , Female , Adult , Middle Aged , Lithium Carbonate , Kidney , Lithium , Parathyroid Glands , Thyroid Gland , Adrenal Glands , Diabetes Insipidus, Nephrogenic
13.
Endocrinology and Metabolism ; : 95-105, 2019.
Article in English | WPRIM | ID: wpr-763706

ABSTRACT

In the current era of effective antiretroviral therapies (ARTs), human immunodeficiency virus (HIV) infection became a chronic disorder that requires long term follow-up. Among other medical issues, these patients may develop endocrine problems, specific to HIV infection and its treatment. The purpose of this review is to give an overview of common endocrine complications associated with HIV infection, and to propose diagnostic and therapeutic strategies. HIV can affect the endocrine system at several levels. Adrenal and gonadal dysfunction, osteoporosis with increased fracture risk, dyslipidemia with increased cardiovascular risk, are some of the endocrine disorders prevalent in HIV-infected patients that may negatively influence quality of life, and increase morbidity and mortality. While ARTs have dramatically increased life expectancy in the HIV-infected population, they are not devoid of adverse effects, including endocrine dysfunction. Physicians caring for HIV-infected patients should be knowledgeable and exercise a high index of suspicion for the diagnosis of endocrine abnormalities, and in particular be aware of those that can be life threatening. Endocrine evaluation should follow the same strategies as in the general population, including prevention, early detection, and treatment.


Subject(s)
Humans , Anti-Retroviral Agents , Diabetes Mellitus , Diagnosis , Dyslipidemias , Endocrine System Diseases , Endocrine System , Follow-Up Studies , Gonads , HIV Infections , HIV , HIV-Associated Lipodystrophy Syndrome , Hyperlipidemias , Life Expectancy , Mortality , Osteoporosis , Quality of Life
14.
Saúde debate ; 42(118): 724-735, Jul.-Set. 2018. graf
Article in Portuguese | LILACS | ID: biblio-979256

ABSTRACT

RESUMO A inclusão das práticas integrativas e complementares nos serviços de saúde pública tem acontecido de forma gradual e lentificada, há cerca de 10 anos. Este estudo visa a colaborar com a ampliação do conhecimento sobre as práticas integrativas, tendo como objetivo principal apresentar os impactos do reiki e da reflexologia podal na saúde de pacientes crônicos atendidos em um centro especializado em endocrinopatias, localizado em Salvador (BA). Trata-se de um estudo observacional retrospectivo, de corte transversal, que utilizou registros em prontuários médicos. Observaram-se, a partir da análise dos dados, impactos aparentes das terapias complementares no alívio de sintomas psicológicos, emocionais e físicos, tais como ansiedade, estresse e dores no corpo.


ABSTRACT The inclusion of integrative and complementary practices in public health services has been gradual and slow, about 10 years ago. This study aims to contribute to the expansion of knowledge about integrative practices, with the main objective of presenting the impacts of reiki and foot reflexology on the health of chronic patients attended at a center specialized in endocrinopathies, located in Salvador (BA). This is a cross-sectional retrospective observational study, that used records in medical records. From the data analysis, apparent impacts of complementary therapies on the relief of psychological, emotional and physical symptoms, such as anxiety, stress and body aches, were observed.

15.
Medisur ; 15(6): 839-852, nov.-dic. 2017.
Article in Spanish | LILACS | ID: biblio-894788

ABSTRACT

La Psiconeuroinmunoendocrinología estudia la interacción entre los procesos psíquicos y los sistemas nervioso, endocrino e inmune y, de forma integradora, las interrelaciones del proceso salud-enfermedad. Diversas investigaciones muestran la estrecha relación entre el surgimiento y desarrollo de enfermedades somáticas con determinadas alteraciones psicológicas, entre ellas el estrés, la ansiedad y depresión. El objetivo de este trabajo es sistematizar los elementos teóricos que sustentan la interrelación entre la psiquis, el sistema nervioso, endocrino e inmune en el proceso salud - enfermedad y exponer las evidencias clínicas que sustentan su validez.


The Psychoneuroimmunoendocrinology studies the interaction between psychic processes and the Nervous, Endocrine and Immune systems and, in an integrative way, the health-disease process interrelationships. Several researches show the close relation between the somatic diseases emergence and development with certain psychological alterations, among them stress, anxiety and depression. This work is aimed at systematizing the theoretical elements which demonstrate the interrelation between the psyche, the Nervous System, Endocrine and Immune System in the health - illness process and to present the clinical evidences which support its validity.

16.
Annals of Pediatric Endocrinology & Metabolism ; : 164-169, 2017.
Article in English | WPRIM | ID: wpr-99771

ABSTRACT

PURPOSE: Rathke’s cleft cyst (RCC) is an asymptomatic benign lesion. With increased interest in pediatric endocrinology, the prevalence of RCCs in children is also increasing. However, the clinical relevance and proper management of RCC is not well defined in children. Therefore, we investigated the clinical manifestations and radiologic features of RCC in children and adolescents, as well as the natural progression of RCC. METHODS: We retrospectively reviewed the medical records of 91 children and adolescents with RCC diagnosed with magnetic resonance imaging (MRI) in Severance Children’s Hospital from January 2006 to December 2015. The clinical, hormonal, and imaging findings were analyzed in patient groups classified according to age. The size of each cyst was assessed in sixty patients who underwent follow-up MRI during the 2 years. RESULTS: Female patients were predominant (64 vs. 27). The common clinical features at presentation were endocrine dysfunction (59.3%), headache (23.0%), and dizziness (4.4%). Symptoms related to endocrine disorders were more frequent in younger patients. In 7 patients managed surgically, the cysts were significantly larger and more frequently located in the suprasellar region. Of 60 nonsurgical patients with a follow-up MRI performed within 2 years after the diagnosis, the RCC size increased in about 26.7% (n=16). CONCLUSION: Although 94.4% of the patients with RCC had clinical symptoms, surgery was performed in only about 7.5% of patients. RCC is associated with pituitary insufficiency, thus, baseline and follow-up endocrine function tests are required. Additionally, regular MRI follow-up is required in long-term period to monitor change in size.


Subject(s)
Adolescent , Child , Female , Humans , Central Nervous System Cysts , Diagnosis , Dizziness , Endocrine System Diseases , Endocrinology , Follow-Up Studies , Headache , Hypopituitarism , Magnetic Resonance Imaging , Medical Records , Natural History , Prevalence , Retrospective Studies
17.
Journal of Peking University(Health Sciences) ; (6): 985-989, 2017.
Article in Chinese | WPRIM | ID: wpr-664774

ABSTRACT

Objective:To describe the endocrine abnormalities in patients with POEMS syndrome in order to identify more patients with POEMS syndrome among those who have endocrine dysfunctions.Methods:We searched the inpatient medical record system of Peking University People's Hospital with "POEMS syndrome".Finally the data from 23 patients were analyzed.Epidata 3.0 was used for data entering and SPSS 19.0 was used for statistical analysis.Results:The median age of all the 23 patients was 47 years.The ratio of male to female was 1.88 ∶ 1.Polyneuropathy was the most common initial symptom which accounted for 56.5 % in the 23 patients.The median duration from the initial symptoms to diagnosis as POEMS syndrome was 30 months.Among all the departments,the number of confirmed cases was highest in the department of neurology.The median duration from the onset of initial symptoms (6 months) to the diagnosis made in neurology department was also significantly shorter than in other departments.Among all the 23 patients,100.0% of them had polyneuropathy,82.6% had organomegaly,95.7% had endocrinopathy,52.2% were M protein positive,91.3% had skin changes,45.5% had papilledema,43.5% had extravascular volume overload,43.5% had platelet elevation and 17.4% had Castleman disease.Among all the patients with endocrinopathy,the incidence of hyperprolactinemia was 60.0% which was the highest one followed by thyroid dysfunction and adrenal dysfunction.Among the patients who had endocrine system dysfunctions,most of them had two target endocrine glands involved (36.5%).Conclusion:Endocrinopathy is an important component of POEMS syndrome and it is of great importance to pay more attention to POEMS syndrome in patients with thyroid dysfunction,adrenal dysfunction,gonadal dysfunction,parathyroid dysfunction,hyperprolactinemia and glucose intolerance,especially in patients with two or more target gland dysfunctions.Symptoms and signs of polyneuropathy should be assessed carefully to reduce misdiagnosis of POEMS syndrome.Evaluation of the endocrine system should also be done in patients diagnosed with POEMS syndrome in order to treat the patients properly.

18.
Rev. Finlay ; 6(4)dic. 2016.
Article in Spanish | LILACS-Express | LILACS | ID: biblio-1507358

ABSTRACT

Fundamento: la diabetes mellitus tipo 1 es la enfermedad crónico endocrinológica más frecuente en la edad pediátrica y la segunda enfermedad crónica en la infancia después del asma bronquial, en los países desarrollados. Objetivo: identificar los aspectos epidemiológicos en el inicio de la diabetes mellitus tipo 1 en menores de 18 años en la provincia de Cienfuegos en el periodo 1997- octubre 2015. Métodos: se realizó un estudio descriptivo retrospectivo en los pacientes menores de 18 años, diagnosticados con diabetes mellitus tipo 1 en el periodo mencionado. Las variables utilizadas fueron: año y edad del inicio, sexo, color de la piel y municipio de procedencia. Los resultados se presentaron en tablas de frecuencias y porcentajes. Resultados: el porcentaje de pacientes del sexo masculino y femenino fue bastante similar con un leve predominio del masculino (53,5 %). El grupo 5-9 años presentó el mayor número de pacientes (35 casos) pero sin diferencias significativas con el de 10-14 años (34 casos). El color de piel blanca predominó con el 75,7 %. El mayor número de casos se mostraron en los meses de otoño con 30. Los municipios de mayor incidencia fueron Cienfuegos con 40 y Cumanayagua con 16 casos respectivamente. Conclusiones: se ha producido un aumento de la incidencia en los últimos años con un leve predominio del sexo masculino y el grupo de 5-9 años. Predominó la raza blanca. El mayor número del inicio ocurrió en otoño y en el municipio de Cienfuegos.


Foundation: diabetes mellitus type 1 is the most frequent chronic endocrinology disease in the pediatric age and the second chronic disease in childhood after bronchial asthma in developed countries. Objective: to identify epistemological aspects in the onset of type 1 diabetes mellitus in children under 18 years old in the Cienfuegos province from 1997 to 2015. Methods: a descriptive retrospective study was realized in patients under 18 years old diagnosed diabetic type 1 mellitus in the mentioned period. The variables used were: year and age of onset, sex, skin colour, and municipality of precedence. The results are presented in frequency tables and percentages. Results: the percentage of patients of male and female sex was quite similar with a low predominance of the male (53.5 %). The group 5-9 years old presented the highest number of patients (35 cases) but without significant differences with the group 10-14 years old (34 cases). The white skin colour predominated with 78.7 %. The highest number of cases presented during the autumn months with 30. The municipalities of higher incidence were Cienfuegos with 40 and Cumanayagua with 16 cases respectively. Conclusion: there has been an increase in the last years in the incidence with a slight predominance of the male sex and the 5-9 year old group. White race predominated. The highest number on onset occurred in autumn and in the Cienfuegos municipality.

19.
Rev. bras. ginecol. obstet ; 38(1): 9-19, jan. 2016. tab, graf
Article in Portuguese | LILACS | ID: lil-769954

ABSTRACT

Objetivo Apresentar e validar um registro eletrônico de saúde (RES) multifuncional para atendimento ambulatorial a portadoras de endocrinopatias na gestação e comparar a taxa de preenchimento de informações de saúde com o prontuário convencional. Métodos Desenvolvemos um RES denominado Ambulatório de Endocrinopatias na Gestação eletrônico (AMBEG) para registro sistematizado das informações de saúde. O AMBEG foi utilizado para atendimento obstétrico e endocrinológico de gestantes acompanhadas no ambulatório de endocrinopatias na gestação na maternidade referência em gestação de alto risco na Bahia, no período de janeiro de 2010 a dezembro de 2013. Aleatoriamente foramselecionadas 100 pacientes atendidas como AMBEG e 100 pacientes atendidas comprontuário convencional comregistro em papel e comparou-se a taxa de preenchimento de informações clínicas. Resultados Foram realizados 1461 atendimentos com o AMBEG: 253, 963 e 245 respectivamente, admissões, consultas de seguimento e puerpério. Eram portadoras de diabetes 77,2% e sendo 60,1% portadoras de diabetes pré-gestacional. O AMBEG substituiu, satisfatoriamente, o prontuário convencional. O percentual de informações clínicas registradas em ambos os prontuários foi significativamente maior no AMBEG: queixas clínicas (100 versus 87%, p < 0,01), altura uterina (89 versus 75%, p = 0,01), ganho de peso total (91 versus 40%, p < 0,01) e dados específicos sobre o diabetes (dieta, esquema de insulina, controle glicêmico e manejo de hipoglicemias) revelando diferença significativa (p < 0,01). A possibilidade de exportar dados clínicos para planilhas facilitou e agilizou a análise estatística de dados. Conclusões O AMBEG é uma ferramenta útil no atendimento clínico a mulheres portadoras de endocrinopatias na gestação. A taxa de preenchimento de informações clínicas foi superior à do prontuário convencional.


Objective To present and validate a multifunctional electronic medical record (EMR) for outpatient care to women with endocrine disorders in pregnancy and to compare health information data fill rate to conventional medical records. Methods We developed an EMR named Ambulatory of Endocrine Diseases in Pregnancy (AMBEG) for systematic registration of health information The AMBEG was used for obstetric and endocrine care in a sample of pregnant women admitted to the maternity reference in high-risk pregnancies in Bahia from January 2010 to December 2013. We randomly selected 100 patients accompanied with AMBEG and 100 patients monitored with conventional consultation and compared the health information data fill rate of the electronic consultation to that performed using conventional medical records. Results 1461 consultations were held, of which 253, 963 and 245 were first, follow-up and puerperium consultations, respectively. Most patients were pregnant women with diabetes (77.2%) and 60.1% were women with pre-gestational diabetes. The AMBEG satisfactorily replaced the conventional medical record. The percentage of registered information was significantly higher in the AMBEG: clinical symptoms (87% versus 100, p < 0.01), uterine height (89 versus 75%, p = 0.01), total weight gain (91 versus 40%, p < 0.01) and specific diabetes data (diet, insulin regimen, glycemic control and management of hypoglycemia) revealed a significant difference (p < 0.01). The ability to export data to worksheets greatly facilitated and accelerated the statistical analysis of the data. Conclusions AMBEG is a useful tool in clinical care for women with endocrine diseases during pregnancy. The fill rate of clinical information was superior to that registered in conventional medical records.


Subject(s)
Humans , Female , Pregnancy , Adult , Electronic Health Records , Pregnancy in Diabetics , Prenatal Care , Blood Glucose , Diabetes, Gestational
20.
Annals of Pediatric Endocrinology & Metabolism ; : 184-190, 2014.
Article in English | WPRIM | ID: wpr-195542

ABSTRACT

The nervous system and the endocrine system are closely interrelated and both involved intimately in maintaining homeostasis. Endocrine dysfunctions may lead to various neurologic manifestations such as headache, myopathy, and acute encephalopathy including coma. It is important to recognize the neurologic signs and symptoms caused by the endocrine disorders while managing endocrine disorders. This article provides an overview of the neurologic manifestations found in various endocrine disorders that affect pediatric patients. It is valuable to think about 'endocrine disorder' as a cause of the neurologic manifestations. Early diagnosis and treatment of hormonal imbalance can rapidly relieve the neurologic symptoms. Better understanding of the interaction between the endocrine system and the nervous system, combined with the knowledge about the pathophysiology of the neurologic manifestations presented in the endocrine disorders might allow earlier diagnosis and better treatment of the endocrine disorders.


Subject(s)
Child , Humans , Coma , Diagnosis , Early Diagnosis , Endocrine System , Endocrine System Diseases , Headache , Homeostasis , Muscular Diseases , Nervous System , Neurologic Manifestations
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