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1.
Int J Behav Nutr Phys Act ; 19(1): 141, 2022 12 01.
Article in English | MEDLINE | ID: mdl-36451168

ABSTRACT

BACKGROUND: Whole-of-school programs have demonstrated success in improving student physical activity levels, but few have progressed beyond efficacy testing to implementation at-scale. The purpose of our study was to evaluate the scale-up of the 'Internet-based Professional Learning to help teachers promote Activity in Youth' (iPLAY) intervention in primary schools using the RE-AIM framework. METHODS: We conducted a type 3 hybrid implementation-effectiveness study and collected data between April 2016 and June 2021, in New South Wales (NSW), Australia. RE-AIM was operationalised as: (i) Reach: Number and representativeness of students exposed to iPLAY; (ii) Effectiveness: Impact of iPLAY in a sub-sample of students (n = 5,959); (iii) Adoption: Number and representativeness of schools that received iPLAY; (iv) Implementation: Extent to which the three curricular and three non-curricular components of iPLAY were delivered as intended; (v) Maintenance: Extent to which iPLAY was sustained in schools. We conducted 43 semi-structured interviews with teachers (n = 14), leaders (n = 19), and principals (n = 10) from 18 schools (11 from urban and 7 from rural locations) to determine program maintenance. RESULTS: Reach: iPLAY reached ~ 31,000 students from a variety of socio-economic strata (35% of students were in the bottom quartile, almost half in the middle two quartiles, and 20% in the top quartile). EFFECTIVENESS: We observed small positive intervention effects for enjoyment of PE/sport (0.12 units, 95% CI: 0.05 to 0.20, d = 0.17), perceptions of need support from teachers (0.26 units, 95% CI: 0.16 to 0.53, d = 0.40), physical activity participation (0.28 units, 95% CI: 0.10 to 0.47, d = 0.14), and subjective well-being (0.82 units, 95% CI: 0.32 to 1.32, d = 0.12) at 24-months. Adoption: 115 schools received iPLAY. IMPLEMENTATION: Most schools implemented the curricular (59%) and non-curricular (55%) strategies as intended. Maintenance: Based on our qualitative data, changes in teacher practices and school culture resulting from iPLAY were sustained. CONCLUSIONS: iPLAY had extensive reach and adoption in NSW primary schools. Most of the schools implemented iPLAY as intended and effectiveness data suggest the positive effects observed in our cluster RCT were sustained when the intervention was delivered at-scale. TRIAL REGISTRATION: ACTRN12621001132831.


Subject(s)
Internet , Schools , Humans , Adolescent , Students , Data Collection , Pleasure
2.
Apoptosis ; 11(2): 277-85, 2006 Feb.
Article in English | MEDLINE | ID: mdl-16502265

ABSTRACT

Despite the efficiency of fludarabine in the induction of clinical responses in B-cell chronic lymphocytic leukemia (B-CLL) patients, resistance to this drug has been documented. The present study tested whether resistance to fludarabine is related to the expression of inhibitor of apoptosis proteins (IAPs) family members. We analyzed the expression of c-IAP1, c-IAP2 and XIAP, by immunocytochemistry, in 30 blood samples from B-CLL patients and correlated protein expression to fludarabine-induced apoptosis estimated by an annexin-V assay. Expression of c-IAP1, c-IAP2 and XIAP were found predominantly in the cytoplasm, and a wide range of staining intensities was observed among distinct samples. No correlation was found between the levels of IAPs expression and prognostic factors such as age, gender, lymphocyte doubling time, white blood cell count or previous treatment. The expression of IAPs also failed to predict the sensitivity to fludarabine-induced apoptosis. Alternative pathways of cell death may explain the independence of fludarabine-induced apoptosis from the high expression of IAPs.


Subject(s)
Antineoplastic Agents/pharmacology , Apoptosis/drug effects , Inhibitor of Apoptosis Proteins/metabolism , Leukemia, Lymphocytic, Chronic, B-Cell/drug therapy , Vidarabine/analogs & derivatives , Adult , Aged , Annexin A5/metabolism , Cells, Cultured , Cytotoxicity Tests, Immunologic , Female , Humans , Immunohistochemistry , Inhibitor of Apoptosis Proteins/genetics , Leukemia, Lymphocytic, Chronic, B-Cell/pathology , Male , Middle Aged , Vidarabine/pharmacology
3.
Arq Bras Cardiol ; 73(2): 139-48, 1999 Aug.
Article in English, Portuguese | MEDLINE | ID: mdl-10752183

ABSTRACT

OBJECTIVE: Report clinical experience in surgical treatment of atrial fibrillation (AF) by Cox-maze procedure. METHODS: 61 patients underwent surgical treatment for AF. Two had primary AF and 59 AF secondary to heart disease (2 atrial septal defects, 57 mitral). Ages ranged from 20 to 74 years (mean = 49). There were 44 females (72%). The surgical technique employed was Cox 3 without cryoablation. The patients were follow-up in specific at patient clinics and underwent periodical ECG, exercise tests, echocardiogram and Holter monitoring. RESULTS: In-hospital mortality was 4.9% and late mortality 1.6%. A temporary pacemaker was used in 28 (46%) and a definitive in 7 patients (11.4%). On hospital discharge, AF remained in 17%; 63.9% had sinus rhythm, 6.9% atrial rhythm, 1.7% junctional rhythm, and 10.3% had pacemaker rhythm. In the last evaluation, AF was present in 19.5%; (70.5% sinus rhythm, 4% atrial rhythm, 2% atrial tachycardia, and 4% pacemaker rhythm). There was no report of thromboembolic episodes. Chronotropic response was considered adequate in 19%, intermediate in 29%, and inadequate in 42%. In Holter monitoring, the mean heart rate was 82 +/- 8 bpm, with a minimum of 57 +/- 7 bpm and maximum of 126 +/- 23 bpm, with supraventricular extrasystoles in 2.3 +/- 5.5% of the total heartbeats and ventricular extrasystoles in 0.8 +/- 0.5%. In the echocardiogram, the A wave was present in the left atrium in 87.5%. CONCLUSION: Maze procedure is effective and has acceptable surgical risk. Atrial or sinus rhythms remain stable with a small but remarkable frequency of atrial and ventricular arrhythmias. Left atrial contraction is present, although attenuated, as well as the chronotropic response to exercise.


Subject(s)
Atrial Fibrillation/surgery , Adult , Aged , Atrial Fibrillation/mortality , Cardiac Surgical Procedures/methods , Chronic Disease , Electrocardiography, Ambulatory , Female , Heart Rate , Humans , Male , Middle Aged , Treatment Outcome
4.
Ars cvrandi ; 16(7): 56-70, passim, 1983.
Article in Portuguese | LILACS | ID: lil-17020
11.
AMB rev. Assoc. Med. Bras ; 27(1): 23-5, 1981.
Article in Portuguese | LILACS | ID: lil-3189

ABSTRACT

Os autores expoem sua experiencia com a hernia hiatal, baseados em 255 casos, dos quais 237 (92,9%) por deslizamento e 4 (1,6%) mistas. Nao tiveram nenhum caso de hernia exclusivamente por rolamento. A doenca foi mais frequente no homem (58,5%) do que na mulher e 79% dos pacientes tinham mais de 40 anos. Estava associada a outra patologia digestiva em 35,7% dos casos, destacando-se a colelitiase com 11,7% e a ulcera duodenal com 9,8%.Em ordem decrescente, foram assinalados os seguintes sintomas: pirose (77,4%), eructacao (59,7%), empachamento (56%), dor (54,7%), regurgitacao (45,7%), disfagia (l7%) e hemorragia digestiva (3,6%). Destacaram-se a obesidade como um fator predisponente importante, o que nao comprovaram em relacao a gravidez.Com excecao de 5 pacientes, que foram operados os demais se submeteram a tratamento clinico


Subject(s)
Hernia, Hiatal
12.
Arq Gastroenterol ; 17(2): 63-8, 1980.
Article in Portuguese | MEDLINE | ID: mdl-7011279

ABSTRACT

Fourteen gastric ulcer patients were submitted to treatment with Cimetidine. They were endoscopically controlled before the beginning of treatment and at the third and sixth week. In the first phase of the investigation, cimetidine was given in a dosage of 1.0 g/day. At the end of the 3rd week, those patients who showed a reduction of less than 50% on the size of the ulcer had the cimetidine doses increased to 1.6 g/day. The second phase started with nine patients which healed at the end of the six weeks. These patients were randomly allocated to two groups in a double blind trial involving cimetidine (600 mg/day) or placebo for 12 weeks. At the end of this period, the patients were submitted to an endoscopic control. Two patients in the placebo group had a recurrence of their ulcers. This did not happen to any of the patients taking cimetidine. Two and a half months after stopping their maintenance treatment, two patients of the cimetidine group had a recurrence of their lesions.


Subject(s)
Cimetidine/therapeutic use , Guanidines/therapeutic use , Stomach Ulcer/drug therapy , Adult , Cimetidine/administration & dosage , Clinical Trials as Topic , Double-Blind Method , Female , Gastric Acid/drug effects , Gastric Acid/metabolism , Humans , Male , Middle Aged
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