RESUMO
OBJECTIVE: The authors discuss obstacles and incentives associated with successful community-based public-academic liaison activities and illustrate their conclusions by describing their public-academic liaison program, which received the American College of Psychiatrists' first annual Award for Creativity in Psychiatric Education. METHOD: The first 8 years of a state/university collaboration are described in which the parties involved first developed a variety of innovative services designed to fill specific gaps in the public service delivery system and subsequently integrated academic research and training components. RESULTS: The carefully planned and monitored process resulted in the exponential growth of interest in public sector work, the realization of the university's primary goals of developing high quality training and research sites, a substantial increase in the number of graduates accepting positions in the public sector, several projects funded by the National Institute of Mental Health, and two national awards. CONCLUSIONS: These collaborations illustrate the highly complementary relationship of public-academic liaison activities and their potential capacity to improve access to services, substantially improve the quality of these services, generate extramural support for services research, and increase the number of well-trained professionals in the public sector.
Assuntos
Centros Médicos Acadêmicos/organização & administração , Centros Comunitários de Saúde Mental/organização & administração , Psiquiatria/educação , Setor Público/organização & administração , Atitude do Pessoal de Saúde , Escolha da Profissão , Serviços Contratados , Pesquisa sobre Serviços de Saúde , Humanos , Relações Interinstitucionais , Internato e Residência/organização & administração , Motivação , Ensino , Recursos HumanosRESUMO
OBJECTIVE: The authors' goal was to assess dexamethasone for the treatment of depression. METHOD: Thirty-seven outpatients (11 men and 26 women) meeting DSM-III-R criteria for major depressive disorder were randomly assigned to receive either placebo or 4 mg/day of oral dexamethasone for 4 days. Baseline Hamilton depression scale scores were compared with scores obtained 14 days after the first dose of study medication. Data were analyzed by using two-sample t tests, chi-square methods, and Fisher's exact test. RESULTS: Seven (37%) of the 19 patients given dexamethasone but only one (6%) of the 18 patients given placebo responded positively. No adverse events or side effects were reported, and all patients who entered the study completed it. CONCLUSIONS: A brief course of oral dexamethasone (4 days) was significantly more effective than placebo within 14 days for the treatment of depression in a randomized, double-blind study of depressed outpatients.
Assuntos
Transtorno Depressivo/tratamento farmacológico , Dexametasona/uso terapêutico , Administração Oral , Adolescente , Adulto , Idoso , Assistência Ambulatorial , Transtorno Depressivo/psicologia , Dexametasona/administração & dosagem , Método Duplo-Cego , Esquema de Medicação , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Placebos , Escalas de Graduação PsiquiátricaRESUMO
Nephrosis was induced in Sprague-Dawley rats in two separate studies by injections of aminonucleoside with sacrifice of animals on days 20 and 54, respectively. Experimental animals in both studies showed the typical findings of nephrosis, i.e., hypoalbuminemia, hypercholesterolemia, and proteinuria. Biochemical findings included hypozincemia and hyperzincuria. A significant correlation between hypozincemia and hypoalbuminemia was noted in the short-term study. Proteinuria occurred on the 10th day in the short-term study and the 15th day in the long-term study and increased quantitatively over the remaining days. The hyperzincuria and proteinuria correlated significantly in the long-term study. Measurements of tissue zinc revealed no change in testes and kidney in the short-term study. Kidney and muscle zinc were increased, testicular zinc was unchanged and femur zinc was decreased in the long-term study. Our conclusions are that in the aminonucleoside induced nephrosis of the rat: 1) hypozincemia occurs probably as a result of hypoalbuminemia, 2) the hyperzincuria is likely due to proteinuria and 3) zinc deficiency is not observed in nephrotic rats who receive ample zinc in their diet and who are observed up to 6 weeks.
Assuntos
Nefrose/metabolismo , Puromicina Aminonucleosídeo , Puromicina/análogos & derivados , Zinco/metabolismo , Animais , Proteínas Sanguíneas/metabolismo , Nitrogênio da Ureia Sanguínea , Peso Corporal , Osso e Ossos/metabolismo , Hipercolesterolemia/complicações , Rim/metabolismo , Masculino , Músculos/metabolismo , Nefrose/induzido quimicamente , Nefrose/complicações , Proteinúria/complicações , Ratos , Albumina Sérica/metabolismo , Testículo/metabolismo , Zinco/deficiênciaRESUMO
This study describes the seated blood pressure distributions of 6,622 predominantly white schoolchildren in Muscatine, Iowa. Subjects with seated pressures equal to or greater than the 95th percentile for age and sex or 140 mm Hg systolic or 90 mm Hg diastolic were examined on repeated occasions. Approximately 13% of subjects were found to have blood pressures at these levels when first examined, but less than 1% were found to have persistent blood pressure elevations. Of 41 subjects found to have persistent blood pressure elevations, 23 were obese with relative weights in excess of 120%. Of the 18 lean subjects, 5 had secondary hypertension and 13 were considered to have essential hypertension. Mass screening of school-age children identifies many children with transient elevation of blood pressure and few with fixed high blood pressures. Children's blood pressures should be assessed during their continuing care where pressures can be measured over a period of time to identify those with fixed blood pressure elevations.
Assuntos
Pressão Sanguínea , Hipertensão/epidemiologia , Adolescente , Peso Corporal , Criança , Pré-Escolar , Feminino , Humanos , Iowa , Masculino , Programas de RastreamentoRESUMO
We report on a 13-yr-old boy with acrodysostosis, a review of 30 cases in the literature, and metacarpophalangeal pattern profile (MCPP) analysis. The prominent manifestations (present in greater than 75% of cases) of this condition include nasal and maxillary hypoplasia, peripheral dysostosis, first ray hyperplasia of the foot, acromesomelic brachymelia, decreased interpedicular distance, advanced skeletal maturation and mental retardation. Results of chromosome studies have been normal. An autosomal dominant inheritance pattern was reported in two families. Maternal and paternal ages were 2 and 3 yr, respectively, above the average age of the general parent population, which suggests that advanced parental age may be a factor in the cause of this condition. A characteristically abnormal MCPP was found in our patient and in 16 additional cases studied from the literature. A mean MCPP was developed for the syndrome. MCPP analysis may be useful as a diagnostic tool in patients suspected to have acrodysostosis.
Assuntos
Disostoses/patologia , Metacarpo/anormalidades , Adolescente , Disostoses/genética , Deformidades Congênitas do Pé , Deformidades Congênitas da Mão , Humanos , Masculino , SíndromeRESUMO
A prospective study was conducted to examine the usefulness of screening tests for pyuria in combination with culture in the diagnosis of urinary tract infection (UTI) in outpatients. Midstream urine specimens were collected from 340 patients seen in the emergency treatment center (ETC) and were examined for pyuria using the chamber count method and the Leukocyte Esterase Dipstick test (LE; Bio Dynamics, Indianapolis, IN). All specimens were cultured quantitatively using both 0.01 ml and 0.001 ml calibrated bacteriologic loops. A total of 100 UTIs, defined by combined clinical and laboratory critera, were identified. Sixty-four (64%) infections were identified by culture using the standard interpretive breakpoint of greater than or equal to 10(5) CFU/ml and an additional 36 (36%) were detected using the low-count interpretive breakpoint of greater than or equal to 10(3) CFU/ml. We found pyuria detection by either the chamber count method or the LE test to be extremely useful in directing subsequent culture efforts. By using either of the tests for pyuria to determine the significance of low-count bacteriuria (10(3) - less than 10(5) CFU/ml) we were able to achieve maximum sensitivity (92%-99%) and specificity (99.2-99.6%) for the diagnosis of UTI while minimizing the number of specimens in which low numbers of organisms must be evaluated.
Assuntos
Piúria/diagnóstico , Infecções Urinárias/diagnóstico , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Bacteriúria/diagnóstico , Criança , Pré-Escolar , Esterases/urina , Feminino , Humanos , Contagem de Leucócitos , Masculino , Pessoa de Meia-Idade , Valor Preditivo dos Testes , Estudos ProspectivosRESUMO
Multiple endocrine neoplasia type II (MEN-II) syndrome is an autosomal dominant condition characterized by medullary carcinoma of the thyroid, pheochromocytoma, and parathyroid adenoma. A cytogenetic investigation was conducted on 13 MEN-II syndrome patients from four unrelated kindreds and 13 age-matched control subjects for chromosome instability and the chromosome 20 deletion reported in MEN-II syndrome. A significant increase (p less than 0.05) was found in the total number of chromatid and chromosome aberrations in MEN-II cells (12.3%) compared with control cells (6.9%) grown at 96 hours in mitomycin C (20 ng/ml, final concentration). The major difference between the two groups was in chromatid, and not chromosome, aberrations. There was no difference between MEN-II and control individuals in fragile site expression, the number of sister chromatid exchanges or cell kinetics. A blind analysis of high-resolution G-banded chromosomes was performed on blood specimens from 13 MEN-II and seven control individuals. Twelve of 13 MEN-II patients and one of seven control subjects were scored as having a 20p12.2 deletion (chi 2 = 12.6; p less than 0.001). Additional research is needed to determine if this cytogenetic finding is due to a chromosome deletion, inversion, or polymorphism.
Assuntos
Aberrações Cromossômicas , Neoplasia Endócrina Múltipla/genética , Adulto , Células Cultivadas , Bandeamento Cromossômico , Feminino , Ácido Fólico/farmacologia , Humanos , Cariotipagem , Linfócitos/ultraestrutura , Masculino , Pessoa de Meia-Idade , Mitomicina , Mitomicinas/farmacologia , Troca de Cromátide IrmãAssuntos
Transplante de Rim , Uremia/cirurgia , Adolescente , Cadáver , Criança , Pré-Escolar , Feminino , Glomerulonefrite/complicações , Transtornos do Crescimento/complicações , Humanos , Rim/anormalidades , Neoplasias Renais/cirurgia , Masculino , Cuidados Pós-Operatórios , Complicações Pós-Operatórias , Pielonefrite/complicações , Transplante Homólogo , Uremia/etiologia , Tumor de Wilms/cirurgiaAssuntos
Distúrbio Mineral e Ósseo na Doença Renal Crônica/fisiopatologia , Hiperparatireoidismo Secundário/fisiopatologia , Glândulas Paratireoides/fisiopatologia , Uremia/fisiopatologia , Adolescente , Adulto , Cálcio/administração & dosagem , Cálcio/uso terapêutico , Criança , Pré-Escolar , Distúrbio Mineral e Ósseo na Doença Renal Crônica/tratamento farmacológico , Creatinina/sangue , Humanos , Hiperparatireoidismo Secundário/tratamento farmacológico , Lactente , Infusões Parenterais , Radioisótopos do Iodo , Túbulos Renais/fisiopatologia , Magnésio/sangue , Hormônio Paratireóideo/sangue , Fósforo/sangue , RadioimunoensaioRESUMO
Hypertension is an important accelerator of the atherosclerotic process. Detection in childhood may be important although longitudinal data are lacking of the prognosis of blood pressure measurement in childhood through adult life. The blood pressure of children should be measured. In populations where salt intake is high, values for blood pressure increase with age. Populations who eat small quantities of salt are relatively free from hypertension. There is an epidemiological argument for limiting salt intake in children. There are few data to indicate the level of blood pressure in children which should be treated. Children's blood pressures are labile and elevated levels are sustained only in a small minority. In these secondary causes, advice should be sought. In subjects with extreme persistent hypertension drug therapy should be considered; in subjects with values of blood pressure not so extremely raised surveillance should be maintained to prevent the development of sustained hypertension.