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1.
J Cancer Educ ; 37(5): 1296-1303, 2022 10.
Artículo en Inglés | MEDLINE | ID: mdl-33432468

RESUMEN

The patient-provider relationship is a key driver of patient satisfaction as it relates to overall healthcare experience. We surveyed patients undergoing radiation therapy to determine what they consider to be the most valued qualities in their interactions with the healthcare team. An ethics-approved 35-item patient satisfaction survey was developed in-house to gain insights on patients' perception of their relationship with the healthcare team throughout their cancer journey. There were 199 completed survey, median age 68 years, 54% women and 45% men. Almost all (95%) "agreed" or "strongly agreed" that their physicians had been sensitive and compassionate. Over 90% felt that they received adequate explanations about their treatment, and had their questions answered. The vast majority (93%) felt included in the decision-making process. Patients reported the 5 most highly rated qualities among their healthcare providers (HCPs) as knowledge, kindness, honesty, good communication, and a cheerful attitude. Overall satisfaction was high but areas for improvement were identified including being offered future appointments for further discussion, more information about clinical trials, other treatments, and community resources. Patients noted their HCPs tended to focus on the physical and emotional needs of patients, but spiritual and cultural needs were rarely addressed. Patients receiving radiotherapy reported high rates of satisfaction across many aspects of their care. These findings also reinforce the different aspects of holistic care that can be improved, and serve as a reminder to clinicians that patients perceive their role as more than just that of a medical expert.


Asunto(s)
Neoplasias , Satisfacción del Paciente , Anciano , Comunicación , Femenino , Personal de Salud/educación , Humanos , Masculino , Neoplasias/terapia , Relaciones Profesional-Paciente
2.
BMC Public Health ; 19(1): 43, 2019 Jan 09.
Artículo en Inglés | MEDLINE | ID: mdl-30626356

RESUMEN

BACKGROUND: Individuals with fetal alcohol spectrum disorder (FASD) experience a range of cognitive, affective, and physical deficits following prenatal alcohol exposure. They are thought to be overrepresented in criminal justice settings. However, limited evidence is available to inform prevalence. We sought to estimate the prevalence of FASD in a Northern Canadian correctional population. METHODS: Using an active case ascertainment approach we recruited a representative sample of 80 justice-involved adults (ages 18-40, 85% male) over an 18-month period from 2013 to 2015. Participants completed interdisciplinary clinical assessments comprising medical and psychological evaluations that adhered to the 2005 Canadian FASD Diagnostic Guidelines. RESULTS: We identified a high rate of FASD (17.5, 95% CI [9.2, 25.8%]) in this sample, and this rate could have been as high as 31.2% with confirmation of prenatal alcohol exposure. Most participants in this study presented with significant neurodevelopmental and cognitive deficits in at least two domains of functioning, irrespective of diagnosis, with only five of 80 participants (6.3%) demonstrating no cognitive impairment. CONCLUSIONS: Findings showed disproportionately high estimated FASD prevalence in this representative sample compared to general population estimates in both Canada and the U.S. (2-5%), underscoring the need for improved FASD screening and diagnosis in correctional settings, and education for clinicians working in the justice context. Strengthened health prevention and intervention efforts to support the needs of individuals with FASD outside the criminal justice context are needed.


Asunto(s)
Derecho Penal , Trastornos del Espectro Alcohólico Fetal/epidemiología , Efectos Tardíos de la Exposición Prenatal/epidemiología , Prisiones , Adolescente , Adulto , Canadá/epidemiología , Niño , Trastornos del Conocimiento/epidemiología , Trastornos del Conocimiento/etiología , Femenino , Humanos , Masculino , Embarazo , Prevalencia , Prisioneros/psicología , Adulto Joven
3.
Eye (Lond) ; 38(1): 118-126, 2024 01.
Artículo en Inglés | MEDLINE | ID: mdl-37402864

RESUMEN

BACKGROUND/OBJECTIVES: To examine prevalence of failed visual assessment at 8-10 years in children born to methadone-maintained opioid dependent (MMOD) mothers and relate this to known in utero substance exposure. SUBJECTS/METHODS: Follow up of observational cohort study of methadone-exposed and comparison children matched for birthweight, gestation and postcode of residence at birth. Participants were 144 children (98 exposed, 46 comparison). Prenatal drug exposure was previously established via comprehensive maternal and neonatal toxicology. Children were invited to attend for visual assessment and casenotes were reviewed. Presence of acuity poorer than 0.2 logMAR, strabismus, nystagmus and/or impaired stereovision constituted a 'fail'. Fail rates were compared between methadone-exposed and comparison children after adjusting for known confounding variables. RESULTS: 33 children attended in person: data were also derived from casenote review for all children. After controlling for maternal reported tobacco use, methadone-exposed children were more likely to have a visual 'fail' outcome, adjusted odds ratio 2.6, 95% CI 1.1-6.2; adjusted relative risk 1.8 (95% CI 1.1-3.4). Visual 'fail' outcome rates did not differ between methadone-exposed children who had (n = 47) or had not (n = 51) received pharmacological treatment for neonatal abstinence/opioid withdrawal syndrome (NAS/NOWS); fail rate 62% vs 53% (95% CI of difference-11-27%). CONCLUSIONS: Children born to MMOD mothers are almost twice as likely as unexposed peers to have significant visual abnormalities at primary school age. Prenatal methadone exposure should be considered in the differential diagnosis of nystagmus. Findings support visual assessment prior to school entry for children with any history of prenatal opioid exposure. TRIAL REGISTRATION: The study was prospectively registered on ClinicalTrials.gov (NCT03603301), https://clinicaltrials.gov/ct2/show/NCT03603301 .


Asunto(s)
Síndrome de Abstinencia Neonatal , Nistagmo Patológico , Complicaciones del Embarazo , Efectos Tardíos de la Exposición Prenatal , Recién Nacido , Niño , Femenino , Embarazo , Humanos , Metadona/efectos adversos , Analgésicos Opioides/efectos adversos , Efectos Tardíos de la Exposición Prenatal/inducido químicamente , Efectos Tardíos de la Exposición Prenatal/epidemiología , Efectos Tardíos de la Exposición Prenatal/diagnóstico , Estudios de Cohortes , Síndrome de Abstinencia Neonatal/epidemiología , Síndrome de Abstinencia Neonatal/tratamiento farmacológico , Complicaciones del Embarazo/tratamiento farmacológico
4.
Curr Oncol ; 27(4): e350-e353, 2020 08.
Artículo en Inglés | MEDLINE | ID: mdl-32905157

RESUMEN

Background: Humour has long been considered an important coping tool for patients with cancer, but published quantitative data about its significance are limited. The purpose of our study was to survey patients with cancer undergoing radiotherapy regarding their opinions about the use of humour in their care. Methods: An anonymous 35-item questionnaire evaluating the patient experience, including the value of humour, was developed by an interdisciplinary team of health care providers (hcps) working within the Radiation Medicine program. This anonymous, voluntary, paper-based survey for self-completion required approximately 10 minutes to finish and was administered during the fall of 2018 and the spring of 2019. Results: For the 199 patients who completed the survey [108 women, 89 men (2 respondents did not specify)], median age was 68 years. That group represents approximately 30%-35% of the patients on treatment during the study period. Almost all respondents (86%) indicated that, during their visits to the cancer centre, it was "somewhat important" or "very important" for health care providers (hcps) to use appropriate humour, and 61% of respondents indicated using humour "frequently" or "always" when dealing with their individual cancers. Most respondents (79%) said that humour decreased anxiety, and 86% indicated that laughing was considered "somewhat important" or "very important." Approximately 4% of respondents even listed "sense of humour" as being the most important quality that they looked for in their interactions with their hcps. Conclusions: Cancer patients undergoing radiotherapy clearly view humour as being important for coping and dealing with their disease, and oncology hcps should routinely consider incorporating the use of appropriate humour into the care that they provide.


Asunto(s)
Risoterapia/métodos , Risa/psicología , Neoplasias/psicología , Oncología por Radiación/métodos , Adulto , Anciano , Anciano de 80 o más Años , Comunicación , Femenino , Humanos , Masculino , Persona de Mediana Edad , Encuestas y Cuestionarios
6.
Cochrane Database Syst Rev ; (2): CD005289, 2008 Apr 16.
Artículo en Inglés | MEDLINE | ID: mdl-18425917

RESUMEN

BACKGROUND: Traditional monitoring of ovarian hyperstimulation during in vitro fertilisation (IVF) treatment has included ultrasonography plus serum estradiol concentration to ensure safe practice by reducing the incidence and severity of ovarian hyperstimulation syndrome (OHSS). The need for intensive monitoring during ovarian stimulation in IVF is controversial. It has been suggested that close monitoring is time consuming, expensive and inconvenient for the woman and simplification of IVF therapy by using ultrasound only should be considered. This systematic review assessed the effects of ovarian monitoring by ultrasound only versus ultrasound plus serum estradiol measurement on IVF outcomes and the occurrence of OHSS in women undergoing stimulated cycles in IVF and intra-cytoplasmic sperm injection (ICSI) treatment. OBJECTIVES: To quantify the effect of monitoring controlled ovarian stimulation in IVF and ICSI cycles with ultrasound plus serum estradiol concentration versus ultrasound only in terms of live birth rates, pregnancy rates and the incidence of OHSS. SEARCH STRATEGY: We searched the Menstrual Disorders and Subfertility Group Specialised Register of controlled trials, Cochrane Central Register of Controlled Trials (CENTRAL) on the latest issue of The Cochrane Library, MEDLINE (1966 to May 2007), EMBASE (1980 to May 2007), CINAHL (1982 to May 2007), the National Research Register, and web-based trial databases such as Current Controlled Trials. There was no language restriction. Additionally all references in the identified trials and background papers were checked and authors were contacted to identify relevant published and unpublished data. SELECTION CRITERIA: Only randomised controlled trials that compared monitoring with ultrasound plus serum estradiol concentration versus ultrasound only in women undergoing ovarian hyperstimulation for IVF and ICSI treatment were included. DATA COLLECTION AND ANALYSIS: Two review authors independently examined the electronic search results for relevant trials, extracted data and assessed trial quality. They resolved disagreements by discussion with two other authors. Outcomes data were pooled when appropriate and summary statistics presented when limited data did not allow meta-analysis. MAIN RESULTS: Our search strategy identified 1119 potentially eligible reports, of which two met our inclusion criteria. These involved 411 women who underwent controlled ovarian stimulation monitoring. Our primary outcome of live birth rate was not reported in either study. One trial reported clinical pregnancy rate per woman (33% versus 31%; RR 1.07, 95% CI 0.77 to 1.49), the second trial reported clinical pregnancy rate per oocyte retrieval (22% versus 25%). There was no significant difference between the ultrasound plus estradiol group and the ultrasound alone group in the mean number of oocytes retrieved (WMD -0.55, 95% CI -1.79 to 0.69) and the incidence of ovarian hyperstimulation (RR 0.73, 95% CI 0.30 to 1.78) for the two studies. AUTHORS' CONCLUSIONS: There is no evidence from randomised trials to support cycle monitoring by ultrasound plus serum estradiol as more efficacious than cycle monitoring by ultrasound only on outcomes of live birth and pregnancy rates. A large well-designed randomised controlled trial is needed that reports on live birth rates and pregnancy, with economic evaluation of the costs involved and the views of the women undergoing cycle monitoring. A randomised trial with sufficiently large sample size to test the effects of different monitoring protocols on OHSS, a rare outcome, will pose a great challenge. Until such a trial is considered feasible, cycle monitoring by transvaginal ultrasound plus serum estradiol may need to be retained as a precautionary good practice point.


Asunto(s)
Estradiol/sangre , Fertilización In Vitro , Síndrome de Hiperestimulación Ovárica/diagnóstico , Inducción de la Ovulación/métodos , Biomarcadores/sangre , Femenino , Humanos , Nacimiento Vivo , Síndrome de Hiperestimulación Ovárica/diagnóstico por imagen , Embarazo , Índice de Embarazo , Ensayos Clínicos Controlados Aleatorios como Asunto , Ultrasonografía
7.
Eur J Clin Nutr ; 71(7): 858-864, 2017 07.
Artículo en Inglés | MEDLINE | ID: mdl-28443607

RESUMEN

Despite increased evidence for the importance of lifestyle modification, physical activity and diet in diabetes prevention and management, habitual physical activity levels have declined in recent decades in China and India. Further, other risk factors for type 2 diabetes, including overweight, obesity and physical inactivity, have also worsened. Here we present evidence for the importance of physical activity and exercise in the amelioration of type 2 diabetes and propose a novel approach to address the challenge of improving lifestyle behaviors in China and India-Movement is Medicine and a P4 (predictive, preventive, personalized and participatory) approach.


Asunto(s)
Diabetes Mellitus Tipo 2/epidemiología , Diabetes Mellitus Tipo 2/prevención & control , Ejercicio Físico , Promoción de la Salud , Capacidad Cardiovascular , China/epidemiología , Dieta , Manejo de la Enfermedad , Humanos , India/epidemiología , Estilo de Vida , Obesidad/epidemiología , Obesidad/prevención & control , Sobrepeso/epidemiología , Sobrepeso/prevención & control , Factores de Riesgo
8.
Cochrane Database Syst Rev ; (3): CD004829, 2005 Jul 20.
Artículo en Inglés | MEDLINE | ID: mdl-16034953

RESUMEN

BACKGROUND: Various methods of sedation and analgesia have been used for pain relief during oocyte recovery in IVF/ICSI procedures. The choice of agents has also been influenced by quality of analgesia as well as by concern about possible detrimental effects on reproductive outcome. OBJECTIVES: To assess the efficacy of conscious sedation and analgesia versus alternative methods on pregnancy outcomes and pain relief in patients undergoing transvaginal oocyte retrieval. SEARCH STRATEGY: We searched the Specialised Register of the Menstrual Disorders and Subfertility Group, The Central Register of Controlled Trials (CENTRAL) , MEDLINE (1966 to present), EMBASE (1980 to present), CINAHL (1982 to present), the National Research Register, and Current Controlled Trials. There was no language restriction. All references in the identified trials and background papers were checked and authors contacted to identify relevant published and unpublished data. SELECTION CRITERIA: Only randomised controlled trials comparing conscious sedation and analgesia versus alternative methods for pain relief during oocyte recovery were included. DATA COLLECTION AND ANALYSIS: Two reviewers independently scanned abstracts of the reports identified by electronic searching to identify relevant papers, extracted data and assessed trial quality. Interventions were classified and analysed under broad categories/strategies of pain relief comparing conscious sedation/analgesia with alternative methods and administration protocols. MAIN RESULTS: Our search strategy identified 390 potentially eligible reports and 12 papers met our inclusion criteria. There were no significant differences in clinical pregnancy rates per woman and patient satisfaction between the methods compared. Women's perception of pain showed conflicting results. Due to considerable heterogeneity, in terms of types and dosages of sedation or analgesia used, and tools used to assess the principal outcomes of pain and satisfaction, a meta-analysis of all the studies was not attempted. Of the three trials which compared the effect of conventional medical analgesia plus paracervical block versus electro-acupuncture plus paracervical block, there was no significant difference in clinical pregnancy rates per woman in the two groups (OR 1.01; 95% CI 0.73 to 1.4). For intra-operative pain score as measured by visual analogue scale (VAS), there was a significant difference (WMD -4.95; 95% CI -7.84 to -2.07), favouring conventional medical analgesia plus paracervical block . There was also a significant difference in intra-operative pain by VAS between patient-controlled sedation and physician-administered sedation (WMD 5.98; 95% CI 1.63 to 10.33), favouring physician -administered sedation. However, as different types and dosages of sedative and analgesic agents were used in these trials, these data should be interpreted with caution. For the rest of the trials, a descriptive summary of the outcomes was presented. AUTHORS' CONCLUSIONS: There is insufficient evidence to determine the effect of different methods of pain relief when compared with conscious sedation and analgesia used during oocyte recovery. In this review, no one particular pain relief method or delivery system appeared to be better than the other. In future, greater consensus is needed to determine both the tools used to evaluate pain and the timing of pain evaluation during and after the procedure. Pain assessment using both subjective and objective measures may merit consideration. In addition, future trials should include intra- and post-operative adverse respiratory and cardiovascular events as outcomes.


Asunto(s)
Sedación Consciente , Fertilización In Vitro , Recolección de Tejidos y Órganos/métodos , Analgesia/métodos , Femenino , Humanos , Ensayos Clínicos Controlados Aleatorios como Asunto
9.
AIDS ; 7(4): 531-9, 1993 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-8099489

RESUMEN

OBJECTIVE: To establish whether various accepted and proposed AIDS definitions have clinical and biological validity: because the Centers for Disease Control and Prevention (CDC) and World Health Organization (WHO) reclassifications of AIDS are important not only for describing the epidemiology of HIV disease but also to individual patients. SETTING: Regional Infectious Diseases Unit, City Hospital, Edinburgh, Scotland, UK. PATIENTS: We analysed the disease progression of 532 HIV-seropositive individuals seen at the City Hospital, Edinburgh, up to the end of July 1991. MAIN OUTCOME MEASURES: Annual numbers of potentially reportable cases from the Edinburgh City Hospital Cohort according to three proposed AIDS case definitions based on: (1) first lymphocyte count < or = 1000 x 10(6)/l; (2) first CD4 cell count < or = 200 x 10(6)/l; or (3) first of two consecutive CD4 cell counts < or = 200 x 10(6)/l. Lifetables to death (irrespective of cause) from month of satisfying the above case definitions, and proportion of patients who satisfied each definition in their calendar year of enrollment in the cohort are reported. RESULTS: There is a threefold increase in patients in the Edinburgh City Hospital Cohort defined as having AIDS under the 1987 and the proposed 1992 CDC definitions--a substantial change for patients and epidemiologists alike. That they are describing different immunodeficiency states is clear from lifetable analysis, which reveals median survivals of 20 and 50 months under the 1987 and the proposed 1992 AIDS definitions, respectively. For epidemiological purposes, redefinitions based on the WHO proposed classification of HIV disease using either a lymphocyte count < or = 1000 x 10(6)/l or a CD4 cell count < or = 200 x 10(6)/l are broadly interchangeable. They are not equally effective for monitoring individual progression (CD4 cell count is superior). Both, for different reasons, lack biological plausibility. CONCLUSIONS: We therefore suggest that the stricter, biologically more plausible, case definition used in Scotland of two consecutive CD4 cell counts of < or = 200 x 10(6)/l [CD4(200) (x 2)] should be adopted--not as a new definition of AIDS, but as an additional important state of severe HIV-related immunodeficiency (SHRID). Median survival under the CD4(200) (x 2) case definition was 40 months in the Edinburgh cohort. We have illustrated differences in CD4(200) case ascertainment between injecting drug users and other HIV-infected patients in the Edinburgh City Hospital Cohort. We recommend that surveillance centres should ascertain date of first immunological monitoring as well as date of SHRID diagnosis in order to identify differential case ascertainment.


Asunto(s)
Síndrome de Inmunodeficiencia Adquirida/clasificación , Síndrome de Inmunodeficiencia Adquirida/sangre , Síndrome de Inmunodeficiencia Adquirida/epidemiología , Adolescente , Adulto , Linfocitos T CD4-Positivos , Centers for Disease Control and Prevention, U.S. , Femenino , Infecciones por VIH/sangre , Infecciones por VIH/clasificación , Infecciones por VIH/epidemiología , Humanos , Recuento de Leucocitos , Masculino , Persona de Mediana Edad , Escocia/epidemiología , Tasa de Supervivencia , Estados Unidos , Organización Mundial de la Salud
10.
AIDS ; 10(4): 419-30, 1996 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-8728047

RESUMEN

OBJECTIVE: To describe progression and survival of individuals infected with HIV by injecting drug use in Edinburgh. DESIGN AND METHODS: From 313 HIV-infected patients with retrospectively estimated narrow seroconversion intervals, 260 infected via injecting drug use in the years 1983-1985 were selected for the study group. MAIN OUTCOME MEASURES: The effects of gender, age, human leukocyte antigen (HLA) type and zidovudine (ZDV) treatment on progression and survival from seroconversion; Weibull estimates of the AIDS incubation distribution and the overall survival distribution; slopes of absolute CD4 lymphocyte loss (on the square root scale) and loss of CD4 percentage. RESULTS: The cumulative progression rates at 10 years were 68% to CDC stage IV and 31% to AIDS with a mortality rate of 25%. Three-year survival rates for AIDS and CDC stage IV cases were 25 and 72%, respectively. Gender and age effects on progression or overall survival were not found, although those aged over 30 years experienced poorer survival from AIDS. A strong HLA (A1, B8, DR3) association with faster progression and poorer survival was found. Median survival was estimated by Weibull distribution to be 12.6 years; median AIDS-free time was estimated to be 11.6 years. CD4 cell loss was approximately linear when transformed to the square root scale as was the decline in CD4 percentage. Only HLA effects on slopes were found: A1,B8, DR3 was significantly associated with faster loss of both absolute CD4 cells and CD4 percentage (P < 0.001) and B27 was significantly associated with slower loss of CD4 percentage (P = 0.01). CONCLUSIONS: Edinburgh IDU do not seem to progress more rapidly than other cohorts with predominantly different risk activities. Older age was associated with poorer survival from AIDS but no gender effect was found for progression or overall survival. The clearest significant association with AIDS progression, mortality and loss of CD4 cells was the phenotype HLA A1,B8,DR3. In contrast HLA B27 was associated with slower loss of CD4 cells.


Asunto(s)
Infecciones por VIH/epidemiología , Seropositividad para VIH/epidemiología , Abuso de Sustancias por Vía Intravenosa , Adulto , Factores de Edad , Antivirales/uso terapéutico , Recuento de Linfocito CD4 , Progresión de la Enfermedad , Estudios de Seguimiento , Infecciones por VIH/tratamiento farmacológico , Infecciones por VIH/inmunología , Infecciones por VIH/mortalidad , Seropositividad para VIH/inmunología , Prueba de Histocompatibilidad , Humanos , Masculino , Estadística como Asunto , Reino Unido/epidemiología , Zidovudina/uso terapéutico
11.
J Clin Endocrinol Metab ; 84(6): 1997-2001, 1999 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-10372700

RESUMEN

Menopause is associated with an increase in venous bicarbonate concentrations that is reversible with hormone replacement therapy (HRT). However, the mechanism underlying this effect is not known. To address this question, we studied the changes in acid-base indexes in the arterialized venous blood of normal postmenopausal women commencing conjugated equine estrogen (0.625 mg/day), medroxyprogesterone acetate (MPA; 5 mg/day), their combination, or placebo, in a double blind randomized controlled study over 3 months. Serum bicarbonate concentrations decreased significantly in the groups receiving either MPA or estrogen plus MPA (P = 0.008). This trend was apparent as early as 2 days and reached 2.7 and 2.3 mmol/L in the respective groups by 3 months. Similar changes were seen with partial pressure of carbon dioxide (P = 0.04); a change of -0.7 kPa occurred in the estrogen plus MPA group at 3 months. There were no changes in bicarbonate concentrations or partial pressure of carbon dioxide in those receiving estrogen alone or placebo. Accompanying changes in blood pH were apparent in the estrogen plus MPA group, where there was an upward trend at 1 week (P = 0.056) and a significant change from baseline (+0.013) at 3 months (P = 0.03). In the whole group, the changes in pH were inversely correlated with those in urinary excretion of hydroxyproline (r = -0.44; P = 0.01). We conclude that HRT using conjugated estrogens and MPA produces small, but sustained, changes in acid-base status. These may contribute to the effects of HRT and menopause on many tissues and disease processes, including the development of osteoporosis.


Asunto(s)
Alcalosis Respiratoria/inducido químicamente , Terapia de Reemplazo de Estrógeno/efectos adversos , Posmenopausia/metabolismo , Equilibrio Ácido-Base/efectos de los fármacos , Calcio/metabolismo , Calcio/orina , Método Doble Ciego , Quimioterapia Combinada , Estrógenos/efectos adversos , Estrógenos/uso terapéutico , Femenino , Humanos , Acetato de Medroxiprogesterona/efectos adversos , Acetato de Medroxiprogesterona/uso terapéutico , Persona de Mediana Edad , Congéneres de la Progesterona/efectos adversos , Congéneres de la Progesterona/uso terapéutico
12.
Am J Med ; 109(5): 362-70, 2000 Oct 01.
Artículo en Inglés | MEDLINE | ID: mdl-11020392

RESUMEN

PURPOSE: Thiazide diuretics reduce urine calcium excretion and might therefore reduce postmenopausal bone loss. In some, but not all, case-control studies, their use has been associated with a reduced incidence of hip fractures. We studied the effects of hydrochlorothiazide on bone loss in normal postmenopausal women. SUBJECTS AND METHODS: We performed a randomized, double-blind, 2-year trial of the effects of hydrochlorothiazide (50 mg per day) and placebo on bone mineral density in normal postmenopausal women. Participants were not required to have either low bone mineral density or hypertension. Bone mineral density was measured using dual-energy x-ray absorptiometry. RESULTS: One hundred eighty-five women entered the study, of whom 138 completed 2 years of follow-up. In an intention-to-treat analysis, hydrochlorothiazide produced significant benefits on bone mineral density of the total body (between-group difference at 2 years of 0.8%, 95% confidence interval [CI]: 0.3% to 1.3%, P <0.0001), legs (0.9%, 95% CI: 0.2% to 1.7%, P <0.0001), mid-forearm (1.2%, 95% CI: 0.2% to 2.2%, P = 0.02), and ultradistal forearm (1.7%, 95% CI: 0.1% to 3.2%, P = 0.04). There was no effect in the lumbar spine (0.5%, 95% CI: -0.5% to 1.6%) or femoral neck (0.2%, 95% CI: 1.3% to 1.7%). The between-group changes tended to be greatest during the first 6 months, except in the mid-forearm where there appeared to be a progressive divergence. An as-treated analysis produced similar results. Urine calcium excretion and indices of bone turnover decreased in the thiazide group, but parathyroid hormone concentrations did not differ between the groups. Treatment was tolerated well. CONCLUSIONS: Hydrochlorothiazide (50 mg per day) slows cortical bone loss in normal postmenopausal women. It may act directly on bone as well as on the renal tubule. The small size of the effect suggests that thiazides may have a role in the prevention of postmenopausal bone loss, but that they are not an appropriate monotherapy for treating osteoporosis.


Asunto(s)
Densidad Ósea/efectos de los fármacos , Calcio/metabolismo , Hidroclorotiazida/farmacología , Menopausia/metabolismo , Osteoporosis Posmenopáusica/prevención & control , Inhibidores de los Simportadores del Cloruro de Sodio/farmacología , Absorciometría de Fotón , Anciano , Diuréticos , Método Doble Ciego , Esquema de Medicación , Femenino , Cuello Femoral/metabolismo , Humanos , Hidroclorotiazida/administración & dosificación , Vértebras Lumbares/metabolismo , Persona de Mediana Edad , Osteoporosis Posmenopáusica/metabolismo , Valores de Referencia , Inhibidores de los Simportadores del Cloruro de Sodio/administración & dosificación , Factores de Tiempo , Resultado del Tratamiento
13.
QJM ; 88(7): 479-91, 1995 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-7633874

RESUMEN

We describe baseline characteristics, enrollment, progression and mortality of the Edinburgh City Hospital HIV cohort. There were 431 men and 191 (31%) women; 439 (71%) infected via injection drug use (IDU); 92 (15%) via homosexual intercourse; 84 (13%) via heterosexual intercourse and 7 from blood products. Median annual rate of CD4 cell loss was 49 (90% range: 15-146); Both homosexual men and patients aged > 40 years at enrollment lost CD4 cells significantly more quickly. In multifactorial analysis controlled for baseline CD4 count and IgA, there was no gender effect, but young patients (< 25 years) progressed significantly more slowly to AIDS (RR 0.4, p = 0.00). Homosexual men progressed significantly more quickly than IDUs, with adjusted relative risks (RR) of 2.9 (p = 0.00), 2.5 (p = 0.01) and 1.5 (p = 0.1) for progression to CDC stage IV, AIDS and death, respectively. The three-year survival rate post-AIDS was 25% (SE 4.3) and there was no gender effect on survival. There was, however, an age effect whereby individuals diagnosed with AIDS in their 40s or later showed poorer survival (RR 1.9, p = 0.04). Zidovudine treatment after an AIDS diagnosis significantly lengthened post-AIDS survival (RR 0.5, p = 0.08).


Asunto(s)
Infecciones por VIH/mortalidad , Síndrome de Inmunodeficiencia Adquirida/mortalidad , Adulto , Recuento de Linfocito CD4 , Estudios de Cohortes , Progresión de la Enfermedad , Femenino , Infecciones por VIH/diagnóstico , Infecciones por VIH/inmunología , Humanos , Masculino , Pronóstico , Escocia/epidemiología , Tasa de Supervivencia
14.
QJM ; 89(3): 177-85, 1996 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-8731561

RESUMEN

We examined how HLA types A1-B8-DR3 and B27 were related to progression of clinical disease and rate of loss of CD4 lymphocytes in the Edinburgh City Hospital cohort of HIV-positive patients, mainly injection drug users. Patients (n = 692) were prospectively followed from 1985 through March 1994. Accurately estimated seroconversion times were determined retrospectively for a subgroup of 313 (45%). Of 262 patients (39%) who were fully or partially HLA typed, 155 (50%) had known seroconversions. Of 34 patients typed positive for A1-B8-DR3, 29 progressed to CDC stage IV, 22 to AIDS and 20 died. Twelve patients were typed positive for B27; six of these progressed to CDC stage IV, one to AIDS and none died. In a proportional hazards analysis of the 313 patients with known seroconversions, A1-B8-DR3 was significantly associated with covariate-adjusted relative risks of 3.7 (95% CI 1.9-7.2), 3.1 (1.6-6.0) and 1.9 (1.1-3.2) for progression from seroconversion to death, AIDS and CDC stage IV, respectively. Events for B27 were too rare to include B27 in analyses to death and AIDS, but B27 was significantly associated with slower progression to CDC stage IV (0.3, CI 0.1-0.9). Random effects growth curve models were used to estimate individual rates of loss of square root CD4 count and loss of CD4 percentage, for 603 and 617 patients, respectively. A1-B8-DR3 was associated with rapid loss of both markers (p = 0.02 and p = 0.01, respectively); B27 was associated with slow loss of both markers (p = 0.04 and p < 0.005).


Asunto(s)
Infecciones por VIH/inmunología , Antígeno HLA-A1/análisis , Antígeno HLA-B27/análisis , Antígeno HLA-B8/análisis , Antígeno HLA-DR3/análisis , Abuso de Sustancias por Vía Intravenosa , Síndrome de Inmunodeficiencia Adquirida/inmunología , Adulto , Recuento de Linfocito CD4 , Linfocitos T CD4-Positivos/patología , Estudios de Cohortes , Progresión de la Enfermedad , Femenino , Humanos , Inmunofenotipificación , Masculino , Fenotipo , Modelos de Riesgos Proporcionales , Estudios Prospectivos , Factores de Riesgo , Escocia
15.
Int J STD AIDS ; 3(2): 96-100, 1992.
Artículo en Inglés | MEDLINE | ID: mdl-1315159

RESUMEN

By the end of March 1990 470 HIV positive patients, 77% injection drug use (IDU) related, had attended the outpatient department of the Regional Infectious Disease Unit with a cumulative loss to follow-up of only 20%. Coincident with the prescribing of oral methadone and a specific all-day IDU-related HIV medical clinic the total number of appointments increased from 28/month in May 1986 to 300/month in May 1989 (P less than 0.001) and the number of defaulted appointments decreased from a maximum of 60% (17/28) to 16% (48/294, P less than 0.001) in these months. There was a significant initial increase in the number of defaulted appointments for the infectious disease (ID) clinics from 11% (77/726) to 16% (124/797, P less than 0.01) which returned to previous levels once a specific IDU-related HIV clinic was established. There was also a significant decline in the number of new patients referred which was greater for the urinary tract infection clinics (108 to 56 per 6 months, P less than 0.0001) than for the ID clinics (119 to 88 per 6 months, P less than 0.05).


Asunto(s)
Infecciones por VIH/terapia , VIH-1 , Servicio Ambulatorio en Hospital/normas , Centros de Tratamiento de Abuso de Sustancias/normas , Abuso de Sustancias por Vía Intravenosa/complicaciones , Adolescente , Adulto , Femenino , Infecciones por VIH/epidemiología , Infecciones por VIH/etiología , Investigación sobre Servicios de Salud , Hospitales Urbanos , Humanos , Masculino , Metadona/uso terapéutico , Persona de Mediana Edad , Objetivos Organizacionales , Servicio Ambulatorio en Hospital/organización & administración , Servicio Ambulatorio en Hospital/estadística & datos numéricos , Pacientes Desistentes del Tratamiento/estadística & datos numéricos , Derivación y Consulta/estadística & datos numéricos , Estudios Retrospectivos , Escocia/epidemiología , Centros de Tratamiento de Abuso de Sustancias/organización & administración , Centros de Tratamiento de Abuso de Sustancias/estadística & datos numéricos , Abuso de Sustancias por Vía Intravenosa/tratamiento farmacológico , Abuso de Sustancias por Vía Intravenosa/epidemiología
16.
Dent Clin North Am ; 19(4): 627-41, 1975 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-1057523

RESUMEN

The most important factors involved in administering sedation and anesthesia to patients undergoing dental treatment are good preoperative evaluation, a well equipped facility with all necessary equipment not only for the safe administration of drugs but also for resolving complications that may ensue, and a team of experts capable of working together smoothly and able to deal with any emergency. This care is possible in the office situation; however, we believe it is only achieved at great expense and with the underutilization of equipment as well as personnel. It may be, therefore, that the best way to achieve this goal is for dentists and anesthesiologists to work together in the hospital environment. Hopefully, an ever increasing number of dentists will be joining the staffs of hospitals so that these objections may be achieved simply and with maximal utilization of equipment and personnel.


Asunto(s)
Anestesia Dental , Anestesiología , Servicio Odontológico Hospitalario , Grupo de Atención al Paciente , Anestesia Dental/efectos adversos , Presión Sanguínea , Enfermedades Cardiovasculares , Delirio/etiología , Urgencias Médicas/terapia , Enfermedades del Sistema Endocrino , Epilepsia , Equipos y Suministros de Hospitales , Halotano , Auscultación Cardíaca , Hepatitis , Humanos , Óxido Nitroso , Cuidados Posoperatorios , Cuidados Preoperatorios , Enfermedades Respiratorias , Inconsciencia/etiología
17.
N Z Med J ; 110(1051): 331-3, 1997 Sep 12.
Artículo en Inglés | MEDLINE | ID: mdl-9323371

RESUMEN

AIM: To review the experience in Auckland with the use of urinary catecholamine measurements in the diagnosis of phaeochromocytoma. METHODS: Review of the test results of patients with proven phaeochromocytoma and retrospective analysis of the outcome of patients with increased 24-hour urinary excretion of the catecholamines noradrenaline, adrenaline and dopamine. RESULTS: Over six years the majority (16/18) of patients with proven phaeochromocytoma had raised urinary noradrenaline excretion either alone (3/16) or with raised adrenaline and/or dopamine (13/16). One phaeochromocytoma secreted adrenaline alone, none secreted dopamine alone and one had urinary catecholamine levels that were normal. Urinary adrenaline excretion was unexpectedly elevated in two patients with extra-adrenal phaeochromocytomas. Approximately 10% of 2590 24 hour urine specimens analysed over a 14 month period had an elevation of one or more catecholamine. Forty-six patients had urinary catecholamine excretion greater than twice the upper limit of normal. This group contained five of the six phaeochromocytomas diagnosed during this period. The other patients were normal (35/46, 76%) or were lost to follow up (6/46, 13%). CONCLUSIONS: In this series most patients with phaeochromocytoma (89%) had increases in the 24-hour urinary excretion of one or more than one catecholamine which exceeded twice the upper limit of normal for our laboratory with noradrenaline being most commonly affected. Increased catecholamine excretion was often seen in patients without phaeochromocytoma.


Asunto(s)
Neoplasias de las Glándulas Suprarrenales/diagnóstico , Dopamina/orina , Epinefrina/orina , Norepinefrina/orina , Feocromocitoma/diagnóstico , Adolescente , Neoplasias de las Glándulas Suprarrenales/orina , Adulto , Anciano , Femenino , Humanos , Masculino , Persona de Mediana Edad , Feocromocitoma/orina , Estudios Retrospectivos , Resultado del Tratamiento
18.
N Z Med J ; 113(1117): 374-6, 2000 Sep 08.
Artículo en Inglés | MEDLINE | ID: mdl-11050902

RESUMEN

AIM: To describe the characteristics of children with vitamin D deficiency rickets and identify common features and predisposing factors. METHODS: A review of the clinical notes of all children less than five years of age with radiological evidence of rickets and serum 25-hydroxyvitamin D levels of less than 10 micrograms/L. Patients were identified by searching all low vitamin D levels performed at the Endocrinology laboratory at Auckland Hospital and children presenting to the Starship Childrens' Hospital with rickets in 1998. RESULTS: In 1998, there were eighteen children (ten males and eight females) with vitamin D deficient rickets. The age range was 3 to 36 months with a median of 12 months. There were twelve children of Indian ethnic origin, one Maori, one Tongan, one Western Samoan, one Ethiopian, one Moroccan and one Indonesian. All children had an elevated alkaline phosphatase level and most had very low serum 25-hydroxyvitamin D levels (< or = 5 micrograms/L), and over half were hypocalcaemic. The common presenting features were delayed walking and bowed legs, swollen wrists or ankles, hypocalcaemic seizure, incidental radiological abnormalities and failure to thrive. CONCLUSIONS: There are a significant number of children in Auckland presenting with florid clinical rickets. The majority with vitamin D deficient rickets in this survey were of Indian ethnic origin. Strategies are needed to detect children at risk of vitamin D deficiency and supplement them with vitamin D.


Asunto(s)
Raquitismo/tratamiento farmacológico , Raquitismo/epidemiología , Vitamina D/administración & dosificación , Distribución por Edad , Preescolar , Femenino , Encuestas Epidemiológicas , Humanos , Incidencia , Lactante , Masculino , Nueva Zelanda/epidemiología , Pronóstico , Raquitismo/diagnóstico , Factores de Riesgo , Población Rural , Distribución por Sexo
19.
BMJ ; 320(7248): 1502-4, 2000 Jun 03.
Artículo en Inglés | MEDLINE | ID: mdl-10834890

RESUMEN

OBJECTIVE: To assess whether a raised serum troponin T concentration would be an independent predictor of death in patients with an acute ischaemic stroke. DESIGN: Observational study. SETTING: Auckland Hospital, Auckland, New Zealand. SUBJECTS: All 181 patients with an acute ischaemic stroke admitted over nine months in 1997-8, from a total of 8057 patients admitted to the acute medical service. MAIN OUTCOME MEASURES: Blood samples for measuring troponin T concentration were collected 12-72 hours after admission; other variables previously associated with severity of stroke were also recorded and assessed as independent predictors of inpatient mortality. RESULTS: Troponin T concentration was raised (>0.1 microgram/l) in 17% (30) of patients admitted with an acute ischaemic stroke. Thirty one patients died in hospital (12/30 (40%) patients with a raised troponin T concentration v 19/151 (13%) patients with a normal concentration (relative risk 3.2 (95% confidence 1.7 to 5. 8; P=0.0025)). Of 17 possible predictors of death, assessed in a multivariate stepwise model, only a raised troponin T concentration (P=0.0002), age (P=0.0008), and an altered level of consciousness at presentation (P=0.0074) independently predicted an adverse outcome. CONCLUSIONS: Serum troponin T concentration at hospital admission is a powerful predictor of mortality in patients admitted with an acute ischaemic stroke.


Asunto(s)
Accidente Cerebrovascular/sangre , Troponina T/sangre , Enfermedad Aguda , Anciano , Biomarcadores/sangre , Femenino , Humanos , Masculino , Nueva Zelanda/epidemiología , Accidente Cerebrovascular/mortalidad , Análisis de Supervivencia
20.
Aust Fam Physician ; 30(11): 1083, 2001 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-11770486

RESUMEN

A 27 year old man presented with 24 hours of unexplained vomiting. His past health was unremarkable except for a deep vein thrombosis one year earlier. At that time his serum electrolytes were normal. The results of repeat electrolyte measurement are shown in Table 1.


Asunto(s)
Cetoacidosis Diabética/complicaciones , Cetoacidosis Diabética/diagnóstico , Vómitos/complicaciones , Desequilibrio Hidroelectrolítico/etiología , Acidosis/etiología , Adulto , Alcalosis/etiología , Bicarbonatos/sangre , Cetoacidosis Diabética/terapia , Humanos , Masculino
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