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2.
Rev. Hosp. Ital. B. Aires (2004) ; 40(3): 95-104, sept. 2020. ilus, tab
Article in Spanish | LILACS | ID: biblio-1128985

ABSTRACT

La relación entre inmunidad y cáncer es compleja. Las células tumorales desarrollan mecanismos de evasión a las respuestas del sistema inmunitario. Esta capacidad permite su supervivencia y crecimiento. La inmunoterapia ha transformado el tratamiento oncológico mejorando la respuesta inmunitaria contra la célula tumoral. Esta se basa en el bloqueo de los puntos de control inmunitario mediante anticuerpos monoclonales contra la molécula inhibidora CTLA-4 (antígeno 4 del linfocito T citotóxico [CTLA-4]) y la proteína 1 de muerte celular programada y su ligando (PD-1/PD-L1). Aunque los inhibidores de los puntos de control inmunitario (ICIs) son fármacos bien tolerados, tienen un perfil de efectos adversos conocido como eventos adversos inmunorrelacionados (EAI). Estos afectan varios sistemas, incluyendo las glándulas endocrinas. Los eventos adversos endocrinos más frecuentes son la disfunción tiroidea, la insuficiencia hipofisaria, la diabetes mellitus autoinmune y la insuficiencia suprarrenal primaria. El creciente conocimiento de estos efectos adversos endocrinos ha llevado a estrategias de tratamiento efectivo con el reemplazo hormonal correspondiente. El objetivo de esta revisión es reconocer la incidencia de estas nuevas endocrinopatías, la fisiopatología, su valoración clínica y el manejo terapéutico. (AU)


The relationship between immunity and cancer is complex. Tumor cells develop evasion mechanisms to the immune system responses. This ability allows their survival and progression. Immunotherapy has transformed cancer treatment by improving the immune response against tumor cells. This is achieved by blocking immune checkpoints with monoclonal antibodies against cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) and programmed cell death protein 1 and its ligand (PD-1 / PD-L1). Although the immune checkpoint inhibitors (ICIs) are well tolerated drugs, they have a profile of adverse effects known as immune-related adverse events (irAES). These involve diverse systems, including the endocrine glands. The most frequent endocrine immune-related adverse events are thyroid and pituitary dysfunction, autoimmune diabetes mellitus and primary adrenal insufficiency. The increasing knowledge of these irAES has led to effective treatment strategies with the corresponding hormonal replacement. The objective of this review is to recognize the incidence of these new endocrinopathies, the physiopathology, their clinical evaluation, and therapeutic management. (AU)


Subject(s)
Humans , Endocrine System Diseases/chemically induced , Immunotherapy/adverse effects , Thyroid Diseases/diagnosis , Thyroid Diseases/chemically induced , Thyroid Diseases/pathology , Thyroid Diseases/therapy , Thyroxine/administration & dosage , Triiodothyronine/therapeutic use , Adrenal Cortex Hormones/administration & dosage , Adrenal Insufficiency/diagnosis , Adrenal Insufficiency/chemically induced , Adrenal Insufficiency/pathology , Adrenal Insufficiency/therapy , Diabetes Mellitus, Type 1/diagnosis , Diabetes Mellitus, Type 1/chemically induced , Diabetes Mellitus, Type 1/pathology , Diabetes Mellitus, Type 1/therapy , Endocrine System Diseases/diagnosis , Endocrine System Diseases/physiopathology , Endocrine System Diseases/therapy , Hypophysitis/diagnosis , Hypophysitis/chemically induced , Hypophysitis/pathology , Hypophysitis/therapy , Glucocorticoids/administration & dosage , Insulin/therapeutic use , Methimazole/therapeutic use , Mineralocorticoids/therapeutic use , Antibodies, Monoclonal/therapeutic use , Neoplasms/immunology
3.
Rev. medica electron ; 41(4): 879-888, jul.-ago. 2019. tab
Article in Spanish | LILACS, CUMED | ID: biblio-1094095

ABSTRACT

RESUMEN Introducción: diversos autores reflejan que la morfología de la silla turca constituye un factor predisponente para algunas enfermedades. Por ejemplo, se considera que existe correlación entre la morfología de esta estructura anatómica y varias patologías; como el síndrome de la silla turca vacía, síndrome de Williams, paladar hendido, entre otras. Objetivo: describir las variaciones anatómicas de la silla turca que se observan en las radiografías laterales de cráneo del Hospital Universitario "Faustino Pérez" de la ciudad de Matanzas, en el período de enero del 2017 a enero del 2018. Materiales y métodos: el universo fue 140 radiografías laterales de cráneo, de estas 85 pertenecieron al sexo femenino y 55 al masculino. Las variables estudiadas fueron edad, sexo y variaciones anatómicas de la silla turca. Se emplearon métodos teóricos y empíricos. Resultados: se observó un predominio de la variación anatómica de la silla turca en forma de U, en ambos sexos. Seguido de la forma de J, predominando la variación en forma de U en el grupo etario de 41 a 50 años y la forma de J en los pacientes mayores de 60 años. Conclusiones: es imprescindible el conocimiento de la anatomía normal de la silla turca y de sus variaciones anatómicas, tanto para las especialidades quirúrgicas como para las no quirúrgicas. Un análisis exhaustivo de la morfología de esta estructura es necesario para establecer parámetros que excluyan determinadas patologías.


ABSTRACT Introduction: several authors declare that sella turcica morphology is a predisposing factor to several diseases. For example, it is considered that there is a correlation between the morphology of this anatomical structure and several pathologies like empty sella turcica syndrome, Williams syndrome, cleft palate and others. Objective: to describe the anatomical variants of sella turcica observed in side cranial radiographies of the University Hospital ¨Faustino Perez¨ of Matanzas, in the period January 2017-January 2018. Materials and methods: the universe was 140 side cranial radiography: 85 belonged to female patients and 55 to male patients. The studied variables were age, sex and sella turcica anatomical variables. Theoretic and empirical methods were used. Results: it was observed a predominance of the U-shaped sella turcica anatomical variant in both sexes, followed by the J-shaped one. The U-shaped form predominated in the 41-50-years-old age-group and the J-shaped form in patients elder than 60 years. Conclusions: it is essential to know sella turcica normal anatomy and its anatomical variables, both for the surgical specialties and for the non-surgical ones. It is necessary the exhaustive analysis of this structure to establish parameters excluding several pathologies.


Subject(s)
Humans , Adult , Aged , Sella Turcica/abnormalities , Sella Turcica/pathology , Sella Turcica/diagnostic imaging , Stomatognathic Diseases/diagnosis , Stomatognathic Diseases/epidemiology , Williams Syndrome/epidemiology , Williams Syndrome/diagnostic imaging , Empty Sella Syndrome/epidemiology , Empty Sella Syndrome/diagnostic imaging , Endocrine System Diseases/diagnosis , Endocrine System Diseases/epidemiology , Epidemiology, Descriptive , Causality , Anatomy, Cross-Sectional , Genetic Predisposition to Disease , Observational Study
4.
Rev. medica electron ; 41(4): 940-958, jul.-ago. 2019.
Article in Spanish | LILACS, CUMED | ID: biblio-1094100

ABSTRACT

RESUMEN El síndrome de ovario poliquístico se ha convertido en un problema de salud pública, siendo el más común de los desórdenes endocrinos en mujeres en edad reproductiva con estudios que reportan una prevalencia de hasta un 21%. El diagnóstico de esta entidad es importante debido a que representa riesgos metabólicos, cardiovasculares y afecta la capacidad reproductiva de estas pacientes. Se realizó una revisión bibliográfica de los principales artículos relacionados sobre el tema, resumiendo los aspectos fundamentales de este problema de salud.


ABSTRACT Polycystic ovary syndrome has become a public health problem, being the most common of the endocrine disorders in reproductive-age women, with studies reporting prevalence by 21 %. The diagnosis of this entity is important because it represents metabolic and cardiovascular risk, and affects the reproductive capacity of these patients. The authors carried out bibliographic review of the main articles related with the theme, summarizing the basic aspects of this health problem.


Subject(s)
Humans , Female , Polycystic Ovary Syndrome/complications , Polycystic Ovary Syndrome/etiology , Polycystic Ovary Syndrome/physiopathology , Polycystic Ovary Syndrome/diagnostic imaging , Preventive Health Services , Cardiovascular Diseases/diagnosis , Disease Management , Metabolic Syndrome/diagnosis , Endocrine System Diseases/diagnosis , Disease Prevention , Reproductive Health , Healthy Lifestyle , Genitalia/physiopathology , Insulin Resistance , Ultrasonography , Hirsutism/diagnosis , Hypertension/diagnosis , Menstruation Disturbances/diagnosis , Obesity/diagnosis
5.
Rev. cuba. endocrinol ; 27(3): 17-29, sep.-dic. 2016. ilus
Article in Spanish | LILACS | ID: biblio-830466

ABSTRACT

Introducción: en la posmenopausia se incrementa la morbilidad por afecciones endocrinas, cuya frecuencia varía en las diferentes regiones del mundo y que desconocemos en nuestro medio. Objetivo: identificar la frecuencia que en artículos originales autores cubanos hacen referencia sobre afecciones endocrinas frecuentes en la edad mediana de la mujer cubana, y reportar los artículos útiles. Métodos: estudio infométrico referido a las publicaciones de autores cubanos recuperados de las bases de datos (Lilacs, Medicc Review, Esbco, PubMed, Cochrane Library, Scielo Cuba y Cumed), repositorios de tesis, eventos médicos nacionales, relacionados con la osteoporosis posmenopausia, la diabetes mellitus tipo 2, el nódulo del tiroides, el hipo e hipertiroidismo y la tiroiditis autoinmune. Se incluyeron los artículos originales reportados entre 1995-2012, accesibles, con referencia a mujeres con edades 40-59 años, y en los que se especificara la metodología utilizada para establecer los diagnósticos de referencia. Resultados: se identificaron 7 703 trabajos que incluían al menos uno de los descriptores definidos. El 2,4 por ciento de los reportes de autores cubanos fueron útiles, y en todos se identificó una alta frecuencia de las afecciones referidas. La dificultad en el acceso virtual e impreso fue la principal causa de no utilidad de los artículos. Conclusiones: se evidencia la poca frecuencia o visibilidad de la morbilidad por afecciones endocrinas en la mujer de edad mediana(AU)


Introduction: in the postmenopausal period, morbidity from endocrine illnesses increases and their frequency varies in different parts of the world, but knowledge about this topic is limited in our country. Objective: to determine the frequency of reference to common endocrine illnesses affecting Cuban middle-aged women in original papers by Cuban authors and to report on useful articles. Methods: informative study of the publication of Cuban papers retrieved in Lilacs, Medicc Review, Esbco, PubMed, Cochrane Library, Scielo Cuba and Cumed databases, thesis repositories and national medical events, which cover postmenopausal osteoporosis, type 2 diabetes mellitus, thyroid modes, hypo and hyperthyroidism and autoimmune thyroiditis. It included accessible original papers from the 1995 to 2012 period, making reference to 40-59 years-old women and specifying the used methodology to make diagnoses. Results: there were found 7 703 papers that comprised at least one of the defined subject headings. In the group, 2.4 percent of reports by Cuban authors were useful and all identified high frequency of the above-mentioned illnesses. The extent of difficulties in having access, either digital or printed, to these articles was the main cause of classifying them as useless. Conclusions: low frequency of visibility of morbidity from endocrine illnesses in the Cuban middle-aged women was demonstrated(AU)


Subject(s)
Humans , Female , Middle Aged , Endocrine System Diseases/diagnosis , Postmenopause/metabolism , Scientific and Technical Publications , Thyroiditis, Autoimmune/diagnosis , Databases, Bibliographic/statistics & numerical data
6.
Article in English | IMSEAR | ID: sea-159392

ABSTRACT

The mouth is a unique site, due to the presence of hard and soft tissues in close approximation. It serves in various purposes of speech, mastication and digestion. It is an important entry point for many pathogens in the body. Many systemic diseases manifest in the oral cavity and mouth can show early signs or the only signs of a disease process at a site elsewhere. As the mouth is an easily accessible site, the indicators it shows of various diseases should not be overlooked. A dentist thus can frequently be exposed to such conditions and play a key role in the diagnostic procedure of various systemic diseases. Appropriate knowledge of these oral manifestations is essential for early diagnosis, treatment and referral of cases.


Subject(s)
Endocrine System Diseases/diagnosis , Gastrointestinal Diseases/diagnosis , Hematologic Diseases/diagnosis , Humans , Metabolic Diseases/diagnosis , Mouth/pathology , Nutritional and Metabolic Diseases/diagnosis , Oral Manifestations/diagnosis , Oral Manifestations/epidemiology , Oral Manifestations/etiology , Rheumatic Heart Disease/diagnosis
7.
São Paulo; s.n; 2014. [209] p. ilus, tab, graf.
Thesis in Portuguese | LILACS | ID: lil-730860

ABSTRACT

Introdução: O Hipotireoidismo congênito (HC) é uma das endocrinopatias mais frequentes em pediatria e pode causar retardo mental e do crescimento, se não for tratado precocemente. A determinação do nível do hormônio estimulador da tireoide em sangue total após o nascimento (TSHneo) constitui uma estratégia efetiva para o rastreamento de HC, embora não exista consenso em relação aos níveis considerados seguros para essa detecção. Muitos serviços utilizam os valores de corte do TSH neonatal de 10,0 e 15,0 ?UI/mL, por ensaios imunofluorimétricos. Objetivo: Analisar a capacidade de detecção dos casos de hipotireoidismo congênito por diferentes níveis de corte do TSH neonatal e os efeitos destes sobre o sistema de triagem neonatal para essa doença, em nascidos vivos avaliados pelo Programa de Triagem Neonatal (PTN) da rede pública do Estado de Mato Grosso (MT), de 01 de janeiro de 2010 a 31 de dezembro de 2012. Métodos: Estudo de coorte, de corte transversal, com coleta retrospectiva de dados obtidos a partir do banco de dados do Serviço de Referência em Triagem Neonatal do Estado de Mato Grosso, de nascidos vivos no período 01/01/2010 a 31/12/2012 e avaliados pelo PTN-MT. Estes foram divididos em dois grupos: I. Controle: Crianças com exame de triagem neonatal normal; II. Estudo: Crianças com HC. Análise estatística incluiu o uso do teste qui-quadrado ou exato de Fischer para análise das características dos recém-nascidos entre os grupos e o teste t de Student ou não paramétrico de Mann-Whitney para análise dos níveis de TSH em sangue total de ambos os grupos e, avaliação das concentrações de TSH e T4 livre no soro, em crianças com HC. Construiu-se uma curva ROC (Receiver Operating Characteristic), para a avaliação dos pontos de corte do TSHneo. O nível de significância foi p<0,05. Resultados: Entre as 111.705 crianças triadas pelo Programa, 50 tiveram o diagnóstico de HC, sob o ponto de corte do TSHneo de 5,0 ?UI/mL. A prevalência da doença foi...


Introduction: Congenital hypothyroidism (CH) is a very common pediatric endocrine disorder and can cause mental and growth retardation without early treatment. Measuring the total blood thyroid-stimulating hormone level after birth (TSHneo) is an effective screening strategy for CH, although there is not yet a consensus on the appropriate diagnostic levels. Many services use the neonatal TSH cut-off points of 10.0 and 15.0 uIU/mL per imunofluorimetric assay. Objective: The aim of the present study was to analyze the ability of various TSHneo cutoff values to detect CH and their effects on the Newborn Screening Program (NSP) of the State of Mato Grosso (MT) from January 1, 2010, to december 31, 2012. Methods: Cohort study, cross-sectional, based on retrospective data collection obtained from the database of the Reference Service for Neonatal Screening of the State of Mato Grosso, for all live births from January 1, 2010, to December 31, 2012, reviewed by NSP-MT. The infants were divided into two groups: I-Control: infants with normal newborn screening tests and II-Study: infants with CH. Statistical analysis included the chi-square or Fisher's exact test to compare the characteristics of the newborns from both groups and Student's t-test or the non-parametric Mann-Whitney test to analyse the total blood TSH level from both groups of infants and evaluate the serum TSH and free thyroxine (T4) concentrations in infants with CH. A Receiver Operating Characteristic (ROC) curve was constructed to assess the TSHneo cutoff values. The significance level was p < 0.05. Results: Using a TSHneo cutoff value 5.0 uIU/mL, 50 out of 111,705 screened infants were diagnosed with CH. The prevalence of CH was 1:2,234 live births. The state program coverage was 73.9%. For Group II, the TSHneo levels were higher than 20.0 uIU/mL in 61.4% of infants, and the serum TSH levels exceeded that level in 83.7%. The ROC curve showed that a TSHneo cutoff value of 5.03 uIU/mL had 100%...


Subject(s)
Humans , Male , Female , Infant, Newborn , Congenital Hypothyroidism , Endocrine System Diseases/diagnosis , Neonatal Screening , ROC Curve , Thyroid Hormones , Thyrotropin , Brazil/epidemiology
8.
Article in English | AIM | ID: biblio-1259384

ABSTRACT

Background: Until recently; most published research focus more on infectious diseases and malnutrition giving the impression that endocrine disorders are uncommon. Reports on endocrine disorders in children in developing countries are few compared to developed countries reflecting the different level of prevalence in the different geographical locations and or level of awareness and availability of facilities for proper diagnosis. Objective: This study aims at defining the burden of paediatric endocrine disorders in Ibadan. Subjects/Methods: A review of records of children who presented at University College Hospital; Ibadan with paediatric endocrine disorders from 2002 to 2009 was carried out. Results: During the eight-year period; a total of 110 children presented with various endocrine disorders but only 94 had complete data for this study. There were 47(50) males and 37(39.4) females; and in 10(10.6) of them; had genital ambiguity at presentation. Patients' ages ranged from 2 weeks to 15 years with a median of 3 years. Many (35) patients were malnourished with weight less than 80 of the expected weight for age and only 9 were overweight. Yearly distribution of cases showed a steady increase in number of cases from 2005. Rickets and metabolic disorders constituted 56.4 of patients; Diabetes mellitus was diagnosed in 12.8; adrenal disoders in 10.6; pubertal disorders in 5.3 and growth disorders in 4.3 of the patients. Thyroid disorders were present in 6.4; obesity in 3.2 while the least common disorder was Diabetes insipidus (1). About 58 of the children had parents in the low socioeconomic status and the management of the cases were severely hampered by lack of funds. About 60.6 of these patients were lost to follow up; during the period. Conclusions: Paediatric endocrine disorders are associated with a high incidence of malnutrition. Most patients presented with rickets which is a preventable condition


Subject(s)
Endocrine System Diseases , Endocrine System Diseases/diagnosis , Hospitals , Pediatrics , Universities
9.
Arq. bras. endocrinol. metab ; 55(8): 550-558, nov. 2011. tab
Article in English | LILACS | ID: lil-610455

ABSTRACT

Turner syndrome is a frequent chromosome disorder in clinical practice. It is characterized by short stature, gonadal dysgenesia and multisystemic involvement, responsible for a high morbidity and reduced life expectancy. The aim of the present paper is to describe the endocrinopathies and major problems at different ages, and to present suggestion for follow-up care in these patients.


A síndrome de Turner é uma doença cromossômica frequente na prática clínica. É caracterizada pela baixa estatura, disgenesia gonadal e alterações em diversos sistemas, o que leva a uma alta morbidade e diminuição da expectativa de vida. O objetivo do presente estudo é descrever as endocrinopatias e outros problemas em cada idade e apresentar uma sugestão de cuidados e segmentos dessas pacientes.


Subject(s)
Adolescent , Child , Child, Preschool , Female , Humans , Infant , Infant, Newborn , Young Adult , Endocrine System Diseases/etiology , Turner Syndrome/complications , Age Factors , Endocrine System Diseases/diagnosis , Endocrine System Diseases/therapy , Practice Guidelines as Topic , Turner Syndrome/diagnosis , Turner Syndrome/genetics , Turner Syndrome/therapy
11.
Rev. Méd. Clín. Condes ; 21(5): 733-739, sept. 2010. ilus, tab
Article in Spanish | LILACS | ID: biblio-999272

ABSTRACT

Se revisan los trastornos más comunes del sistema endocrino que se detectan en la consulta no especializada. Se hace énfasis en: a) Trastornos tiroideos tales como hipo o hipertiroidismo, nódulos de la tiroides y la importancia de la enfermedad de la tiroides durante el embarazo, b) la enfermedad adrenal en la hipertensión y el enfoque de la incidentaloma suprarrenal c) hiperparatiroidismo primario y la deficiencia de vitamina D d) Trastornos gonadal y la importancia de la detección precoz de la enfermedad hormonal, tanto en la disfunción ovárica y testicular


We review the most common disorders of the endocrine system that are detected in non-specialist consultation. Emphasis is placed on: a) thyroid disorders such as hypo-or hyperthyroidism, thyroid nodules and the importance of thyroid disease during pregnancy, b) adrenal disease in hypertension and the approach to the adrenal incidentaloma c) metabolic disorders such as primary hyperparathyroidism and vitamin Ddeficiency d) gonadal disorders and the importance of early detection of hormonal disease in both ovarian and testicular dysfunction


Subject(s)
Humans , Endocrine System Diseases/diagnosis , Thyroid Diseases/diagnosis , Vitamin D Deficiency/diagnosis , Adrenal Gland Diseases/diagnosis , Early Diagnosis , Hyperparathyroidism, Primary/diagnosis , Gonadal Disorders/diagnosis
16.
Acta méd. costarric ; 51(1): 44-48, ene. - mar. 2009.
Article in Spanish | LILACS | ID: lil-581026

ABSTRACT

En el paciente hipotiroideo la creatinina sérica puede aumentar no solo por fallo renal, sino también por miopatía en presencia de función renal normal. Se reportan 2 pacientes representativos de sendos tipos de la clasificación aquí propuesta sobre la asociación disfunción tiroidea / creatinina sérica. El primer enfermo presenta aumento de la creatinina sérica secundario a miopatía hipotiroidea con función renal normal, tipo I, esta se puede complicar con rabdomiolisis y causar insuficiencia renal aguda en hipotiroideos no diagnosticada. El otro paciente con creatina sérica alta mejoró su función renal al tratarse su hipotiroidismo, tipo 2. Ocasionalmente, este ha permanecido oculto y al ser diagnosticado y tratado, se mejora la función renal. El hipotiroidismo cursa con hipercolesterolemia y si no se valora la función tiroidea y se administran estatinas, se empeora el daño muscular del paciente. Lo mismo ha sucedido con el uso de gemfibrozil en condiciones similares. El tercer tipo de daño renal relacionado con hipotiroidismo es la proteinuria en rango de síndrome nefrótico, vinculada con suspensión de la levotiroxina. Las biopsias muestran lesiones histológicas de diversas glomerulopatías, que mejoran con la administración de levotiroxina. En pacientes con tiroiditis de Hashimoto aparecen otras glomerulopatías que responden a los glucocorticoides...


In patients with hypothyroidism is possible to find an increased serum creatinine not only due to renalfailure but to myopathy in presence of normal renal function. Two patients, each representing 1 type of a proposed classification regarding thyroid dysfunction and abnormal creatinine are presented, in order to communicate thisrelationship, until now based on isolated reports. The first individual had an increased serum creatinine withnormal renal function due to hypothyroid myopathy (type 1). Rhabdomyolysis related to this myopathy is pointed as a cause of acute renal failure. The 2nd patient had an increased serum creatinine with abnormal kidney function (type 2),which improved when he became euthyroid after levothyroxine administration. The diagnosis of hypothyroidism is often missed in patients with altered renal function, if it becomes evident and is properly treated the renal function will improve. As isknown hypothyroidism causes hypercholesterolemia, if such patient unknowingly receives statins or gemfibrozil, severe rhabdomyolysis and renal falilure may occur, as reported inthe literature. The 3d category of the classification is the occurrence of nephrotic syndrome in hypothyroid patients who discontinue T4 treatment due to thyroid cancer for further studies or by patient non adherence, developingsignificant proteinuria few months later. Kidney biopsy lesions vary from membranous glomerulopathy tomembranoproliferative glomerulonephritis. These findingswill resolve with the administration of levothiroxine, without glucocorticoids. However patients with nephrotic syndrome related to Hashimoto thyroiditis will improve withglucocorticoids.


Subject(s)
Humans , Male , Middle Aged , Creatinine , Hypercholesterolemia , Hypothyroidism , Kidney Diseases , Muscular Diseases , Polymyositis , Thyroid Hormones , Endocrine System Diseases/diagnosis
17.
J Indian Med Assoc ; 2008 Jun; 106(6): 362-4
Article in English | IMSEAR | ID: sea-99689

ABSTRACT

Pattern of endocrine changes in moderate to severely ill patients in a medical intensive care unit, correlation with the severity of illness and whether these changes can predict outcome of the critically ill patients were evaluated and studied in 80 patients admitted with acute physiology and chronic health evaluation (APACHE) II score >10 and without any pre-existing endocrinopathies or on drugs likely to affect the endocrine axis. Adrenal insufficiency was present in 45%, and mortality was higher in those with lower (<15 microg/dl) and higher (>30 microg/dl) serum cortisol. Sick euthyroid syndrome was detected in 80%, and those with low mean T3 (<0.6 ng/ml), free T4 (<0.89 ng/dl) and total T4 (<4 microg/dl) and had increased mortality. Hypotestosteronaemia was found in 92% of men and was significantly associated with severity of illness in men. Though prolactin is the first hormone to be elevated, there was no correlation between prolactin and severity of illness or mortality.


Subject(s)
APACHE , Adolescent , Adrenal Insufficiency/physiopathology , Adult , Aged , Aged, 80 and over , Critical Care , Endocrine System , Endocrine System Diseases/diagnosis , Euthyroid Sick Syndromes/physiopathology , Female , Humans , Intensive Care Units , Male , Middle Aged , Pilot Projects , Survival , Testosterone/deficiency
18.
Diagnóstico (Perú) ; 46(4): 190-192, oct.-dic. 2007. tab, ilus
Article in Spanish | LILACS, LIPECS | ID: lil-490239
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