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1.
Arch Intern Med ; 153(22): 2588-92, 1993 Nov 22.
Artículo en Inglés | MEDLINE | ID: mdl-8239851

RESUMEN

OBJECTIVES: Practicing internists commonly provide gynecologic care, yet internists receive little formal training in ambulatory gynecology. To evaluate current residency training, we surveyed house staff perceptions of their training in gynecology. METHODS: Data were collected from house staff at five Portland, Ore, internal medicine training programs by questionnaire using a Likert scale about training in 24 gynecologic and five nongynecologic internal medicine problems. Responses were compared by level of training, institution, and gender. RESULTS: Responses were received from 195 (89%) of 221 residents. House staff reported less than adequate training in gynecology, particularly in the areas of family planning and medical complications of pregnancy, while reporting much superior training in the traditional medicine problems. CONCLUSIONS: House staff in internal medicine report little training in the diagnosis and treatment of gynecologic problems. Training in family planning may be particularly deficient. Residency programs must seek effective teaching strategies to address this deficiency.


Asunto(s)
Ginecología/educación , Medicina Interna/educación , Internado y Residencia , Atención Ambulatoria , Servicios de Planificación Familiar/educación , Femenino , Humanos , Masculino , Análisis Multivariante , Oregon , Análisis de Regresión , Factores Sexuales , Encuestas y Cuestionarios
2.
AIDS ; 11(11): 1347-52, 1997 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-9302444

RESUMEN

OBJECTIVE: Weight loss in HIV-infected patients is extremely common and is associated with increased morbidity and mortality. Decreased testosterone concentrations occur commonly in patients with HIV disease and are associated with weight loss. This study assessed the effect of testosterone therapy on HIV associated weight loss in patients with AIDS. METHODS: Forty HIV-seropositive patients with CD4+ counts of < 2 x 10(5)/l and weight loss greater than 5% of usual body weight were randomized in a double-blind manner to receive 200 mg of testosterone cypionate of placebo intramuscularly every 2 weeks for 3 months. Patients were then crossed to receive the alternate treatment for the next 3 months. Outcome variables included weight, skin fold measurement, a quality-of-life questionnaire, Karnofsky score, T-cell subset analysis, complete blood count, routine blood chemistry measurements and free testosterone concentration. RESULTS: Thirty-nine patients entered the study. Of these, 35 completed the first 3-month period (18 on placebo, 17 on testosterone) and 23 completed the whole 6 month trial. Analysis of these 23 patients did not show any significant differences between testosterone and placebo treatment. Analysis of the first 3 months only for the 35 patients who completed it did not show any significant difference between the effects of testosterone and placebo treatment on weight gain. Patients treated with testosterone reported improved overall well-being (P = 0.03) and a trend towards increased muscle strength (P = 0.08). There was no difference between the two groups in terms of side-effects or other effects on hematopoetic, liver, renal, or immune function. CONCLUSIONS: Treatment with testosterone cypionate compared with placebo did not result in significant weight gain. Testosterone supplementation did appear to produce an improved overall sense of well-being and possibly some increases in muscle strength. This randomized, double-blinded study does not confirm the results of other recent studies which show potential benefits of testosterone and its analogs when used as a treatment for weight loss in HIV-positive patients.


Asunto(s)
Síndrome de Inmunodeficiencia Adquirida/complicaciones , Síndrome de Inmunodeficiencia Adquirida/tratamiento farmacológico , Testosterona/uso terapéutico , Pérdida de Peso/efectos de los fármacos , Adolescente , Adulto , Recuento de Células Sanguíneas , Análisis Químico de la Sangre , Peso Corporal/efectos de los fármacos , Recuento de Linfocito CD4 , Estudios Cruzados , Método Doble Ciego , Humanos , Masculino , Músculos/efectos de los fármacos , Calidad de Vida , Subgrupos de Linfocitos T/inmunología , Testosterona/administración & dosificación , Testosterona/efectos adversos , Aumento de Peso
3.
AIDS ; 7(12): 1595-600, 1993 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-7904452

RESUMEN

OBJECTIVE: We measured micronutrient values in patients with the HIV wasting syndrome and in other HIV-seropositive patients to determine whether specific micronutrient deficiencies were associated with the wasting syndrome. METHODS: Serum from 47 HIV-seropositive patients was evaluated for concentrations of vitamin A, B6, B12, C, D, E, folate, the mineral zinc, carotene and glutathione. Comparisons were made between groups stratified by CD4 cell count and wasting/non-wasting status. RESULTS: Mean serum levels were significantly lower for vitamin A (P = 0.04), folate (P = 0.04) and carotene (P = 0.06) in patients with the HIV wasting syndrome than in non-wasting patients with comparable CD4 cell counts. Values of vitamins A, B6, C, D, carotene and glutathione were below the normal range in over 10% of HIV-seropositive patients in this study. CONCLUSION: Decreased micronutrient concentrations are common in HIV-infected patients and occur more frequently in patients with the wasting syndrome. Clinicians may wish to evaluate HIV-seropositive patients with wasting for individual micronutrient deficiencies, although they should note that particular deficiencies may be only part of the larger picture of malabsorption and undernutrition.


Asunto(s)
Infecciones por VIH/sangre , Infecciones por VIH/complicaciones , Oligoelementos/sangre , Pérdida de Peso , Linfocitos T CD4-Positivos , Diarrea/etiología , Femenino , Fiebre/etiología , Infecciones por VIH/metabolismo , Infecciones por VIH/patología , Humanos , Leucocitos , Masculino , Síndrome , Oligoelementos/metabolismo , Vitaminas/sangre
4.
AIDS ; 10(9): 967-73, 1996 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-8853729

RESUMEN

OBJECTIVE: Several small short-term intervention studies have suggested that beta-carotene supplementation in HIV-infected patients can increase the number of various immune cells including CD4 cells. This prospective double-blinded study was designed to investigate whether beta-carotene supplementation would result in this immuno-enhancement in a larger number of patients over a longer time period. METHODS: HIV-positive patients were randomly assigned to receive either 60 mg beta-carotene orally three times daily or a matched placebo. In addition, all patients received a multivitamin supplement. Patients were evaluated at baseline, 1 month, and 3 months for T-cell quantitative subsets, natural killer cells, HIV p24 antigen, beta-carotene levels, complete blood counts and chemistry batteries. Body weights and Karnofsky scores were evaluated at each visit. RESULTS: Seventy-two patients signed informed consent forms and entered the study. Except for serum beta-carotene concentration, there were no statistically significant differences (P < 0.05) between the treatment (60 mg beta-carotene three times daily and multivitamins) and placebo (placebo and multivitamins) groups at baseline or after either 1 or 3 months of treatment. DISCUSSION: Earlier studies suggesting that beta-carotene supplementation increased levels of immune cells in HIV-infected patients were not replicated in this study. The addition of a multivitamin supplement to both arms of this study may have masked any difference between the two groups. However, on the basis of the results of this study, we would not recommend supplementation with high doses of beta-carotene for HIV-infected patients.


Asunto(s)
Proteína p24 del Núcleo del VIH/análisis , Infecciones por VIH/tratamiento farmacológico , VIH-1/aislamiento & purificación , Subgrupos de Linfocitos T/patología , Linfocitos T/patología , beta Caroteno/administración & dosificación , Administración Oral , Método Doble Ciego , Infecciones por VIH/sangre , Infecciones por VIH/inmunología , Humanos , Recuento de Linfocitos , Estudios Prospectivos , Subgrupos de Linfocitos T/inmunología , Linfocitos T/inmunología
5.
J Acquir Immune Defic Syndr (1988) ; 7(1): 46-51, 1994 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-8263752

RESUMEN

We compared endocrine function in patients with the HIV wasting syndrome with other HIV-positive patients without wasting to determine associations between endocrine dysfunction and wasting. Sixty-six HIV-seropositive patients were evaluated by thyroid, gonadal, and adrenal function tests. Fourteen of these patients met the clinical definition of wasting. Total and free testosterone levels were significantly lower in patients with wasting compared with patients without wasting with both similar and higher mean CD4 counts. Prolactin levels were significantly higher, and cortisol levels were higher with borderline significance in patients with wasting compared with patients with similar CD4 counts without wasting. These findings suggest that endocrine function in the HIV wasting syndrome differs from that of HIV-infected patients without wasting, which may have implications about the pathogenesis and treatment of the HIV wasting syndrome.


Asunto(s)
Emaciación/metabolismo , Glándulas Endocrinas/fisiopatología , Seropositividad para VIH/metabolismo , Pérdida de Peso/fisiología , Emaciación/complicaciones , Femenino , Seropositividad para VIH/complicaciones , Humanos , Hidrocortisona/sangre , Masculino , Infección por Mycobacterium avium-intracellulare/complicaciones , Infección por Mycobacterium avium-intracellulare/metabolismo , Prolactina/sangre , Síndrome , Testosterona/sangre , Hormonas Tiroideas/sangre
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