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National Collaborating Centre for Methods and Tools

avril 2015 · Numéro 125

Dans ce bulletin :

Vous recevez déjà des mises à jour de PublicHealth + dans le Round-up.

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Consultez McMaster PLUS!

McMaster PLUS, une division de la McMaster Health Knowledge Refinery (http://hiru.mcmaster.ca/hiru/HIRU_McMaster_HKR.aspx), s’occupe d’articles évalués de manière critique afin de trouver ceux qui sont solides du point de méthodologique, pertinents et d’importance majeure.  Public Health+ (http://www.nccmt.ca/public_health_plus/all/1/list-fra.html) fait partie de plusieurs abonnements hebdomadaires par courriel de McMaster PLUS que vous pouvez obtenir.

Par example, vous pouvez également vous abonner à Obesity+ (http://plus.mcmaster.ca/obesity/Default.aspx?Page=1) : les meilleures données probantes actuelles sur les causes, le cours, le diagnostic, la prévention et le traitement de l’obésité et des complications métaboliques et mécaniques s’y rapportant et les aspects économiques de celles-ci.

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Quoi de neuf dans Public Health +?

Cryptococcal meningitis screening and community-based early adherence support in people with advanced HIV infection starting antiretroviral therapy in Tanzania and Zambia: an open-label, randomised controlled trial.

BACKGROUND: Mortality in people in Africa with HIV infection starting antiretroviral therapy (ART) is high, particularly in those with advanced disease. We assessed the effect of a short period of community support to supplement clinic-based services combined with serum cryptococcal antigen screening. METHODS: We did an open-label, randomised controlled trial in six urban clinics in Dar es Salaam, Tanzania, and Lusaka, Zambia. From February, 2012, we enrolled eligible individuals with HIV infection (age >/=18 years, CD4 count of <200 cells per muL, ART naive) and randomly assigned them to either the standard clinic-based care supplemented with community support or standard clinic-based care alone, stratified by country and clinic, in permuted block sizes of ten. Clinic plus community support consisted of screening for serum cryptococcal antigen combined with antifungal therapy for patients testing antigen positive, weekly home visits for the first 4 weeks on ART by lay workers to provide support, and in Tanzania alone, re-screening for tuberculosis at 6-8 weeks after ART initiation. The primary endpoint was all-cause mortality at 12 months, analysed by intention to treat. This trial is registered with the International Standard Randomised Controlled Trial Number registry, number ISCRTN 20410413. FINDINGS: Between Feb 9, 2012, and Sept 30, 2013, 1001 patients were randomly assigned to clinic plus community support and 998 to standard care. 89 (9%) of 1001 participants in the clinic plus community support group did not receive their assigned intervention, and 11 (1%) of 998 participants in the standard care group received a home visit or a cryptococcal antigen screen rather than only standard care. At 12 months, 25 (2%) of 1001 participants in the clinic plus community support group and 24 (2%) of 998 participants in the standard care group had been lost to follow-up, and were censored at their last visit for the primary analysis. At 12 months, 134 (13%) of 1001 participants in the clinic plus community support group had died compared with 180 (18%) of 998 in the standard care group. Mortality was 28% (95% CI 10-43) lower in the clinic plus community support group than in standard care group (p=0.004). INTERPRETATION: Screening and pre-emptive treatment for cryptococcal infection combined with a short initial period of adherence support after initiation of ART could substantially reduce mortality in HIV programmes in Africa. FUNDING: European and Developing Countries Clinical Trials Partnership.

The full text may be available from PubMed

Incentives to Promote Breastfeeding: A Systematic Review.

BACKGROUND AND OBJECTIVES: Few women in industrialized countries achieve the World Health Organization`s recommendation to breastfeed exclusively for 6 months. Governments are increasingly seeking new interventions to address this problem, including the use of incentives. The goal of this study was to assess the evidence regarding the effectiveness of incentive interventions, delivered within or outside of health care settings, to individuals and/or their families seeking to increase and sustain breastfeeding in the first 6 months after birth. METHODS: Searches of electronic databases, reference lists, and grey literature were conducted to identify relevant reports of published, unpublished, and ongoing studies. All study designs published in English, which met our definition of incentives and that were from a developed country, were eligible for inclusion. Abstract and full-text article review with sequential data extraction were conducted by 2 independent authors. RESULTS: Sixteen full reports were included in the review. The majority evaluated multicomponent interventions of varying frequency, intensity, and duration. Incentives involved providing access to breast pumps, gifts, vouchers, money, food packages, and help with household tasks, but little consensus in findings was revealed. The lack of high-quality, randomized controlled trials identified by this review and the multicomponent nature of the interventions prohibited meta-analysis. CONCLUSIONS: This review found that the overall effect of providing incentives for breastfeeding compared with no incentives is unclear due to study heterogeneity and the variation in study quality. Further evidence on breastfeeding incentives offered to women is required to understand the possible effects of these interventions.

The full text may be available from PubMed

The effect of tofacitinib on pneumococcal and influenza vaccine responses in rheumatoid arthritis.

OBJECTIVE: To evaluate tofacitinib`s effect upon pneumococcal and influenza vaccine immunogenicity. METHODS: We conducted two studies in patients with rheumatoid arthritis using the 23-valent pneumococcal polysaccharide vaccine (PPSV-23) and the 2011-2012 trivalent influenza vaccine. In study A, tofacitinib-naive patients were randomised to tofacitinib 10 mg twice daily or placebo, stratified by background methotrexate and vaccinated 4 weeks later. In study B, patients already receiving tofacitinib 10 mg twice daily (with or without methotrexate) were randomised into two groups: those continuing (`continuous`) or interrupting (`withdrawn`) tofacitinib for 2 weeks, and then vaccinated 1 week after randomisation. In both studies, titres were measured 35 days after vaccination. Primary endpoints were the proportion of patients achieving a satisfactory response to pneumococcus (twofold or more titre increase against six or more of 12 pneumococcal serotypes) and influenza (fourfold or more titre increase against two or more of three influenza antigens). RESULTS: In study A (N=200), fewer tofacitinib patients (45.1%) developed satisfactory pneumococcal responses versus placebo (68.4%), and pneumococcal titres were lower with tofacitinib (particularly with methotrexate). Similar proportions of tofacitinib-treated and placebo-treated patients developed satisfactory influenza responses (56.9% and 62.2%, respectively), although fewer tofacitinib patients (76.5%) developed protective influenza titres (>/=1:40 in two or more of three antigens) versus placebo (91.8%). In study B (N=183), similar proportions of continuous and withdrawn patients had satisfactory responses to PPSV-23 (75.0% and 84.6%, respectively) and influenza (66.3% and 63.7%, respectively). CONCLUSIONS: Among patients starting tofacitinib, diminished responsiveness to PPSV-23, but not influenza, was observed, particularly in those taking concomitant methotrexate. Among existing tofacitinib users, temporary drug discontinuation had limited effect upon influenza or PPSV-23 vaccine responses. TRIAL REGISTRATION NUMBERS: NCT01359150, NCT00413699.

The full text may be available from PubMed

Effectiveness of lifestyle-based weight loss interventions for adults with type 2 diabetes: a systematic review and meta-analysis.

AIMS: To provide a systematic review and meta-analysis of recent evidence on the effectiveness of lifestyle-based weight loss interventions for adults with type 2 diabetes. METHODS: A search of the literature from January 2003 to July 2013 was conducted (PubMed, Embase, CINAHL and Web of Science). The studies considered eligible were randomized controlled trials evaluating weight loss interventions (diet and physical activity, with or without behavioural strategies) of >/=12 weeks duration, compared with usual care or another comparison intervention. Ten studies were included for review. Some heterogeneity was present in the sample, therefore, random-effects models were used to calculate pooled effects. RESULTS: Intervention duration ranged from 16 weeks to 9 years, with all but one delivered via individual or group face-to-face sessions. From six studies comparing lifestyle intervention with usual care the pooled effect on weight (n = 5795) was -3.33 kg [95% confidence interval (CI) -5.06, -1.60 kg], and on glycated haemoglobin (HbA1c; n = 5784) was -0.29% (95% CI -0.61, 0.03%), with both attenuated in sensitivity analyses. The pooled within-group effect on weight (n = 3063) from all 10 lifestyle intervention groups was -5.33 kg (95% CI -7.33, -3.34 kg), also attenuated in sensitivity analyses. None of the participant or intervention characteristics examined explained the heterogeneity. Only one study assessed whether intervention effects were maintained after the end of the intervention. CONCLUSIONS: Lifestyle-based weight loss intervention trials in type 2 diabetes achieve, on average, modest reductions in weight and HbA1c levels, but results were heavily influenced by one trial. Evidence-based approaches for improving the effectiveness of lifestyle-based interventions in type 2 diabetes are needed, along with future studies reporting on maintenance and cost-effectiveness.

The full text may be available from PubMed

Webinaires à venir du Health Evidence

Programmes d’exercices basés sur la Wii afin d’améliorer l’équilibre chez les personnes âgées : quelles sont les données probantes?

11 mai 2015
de 13 h à 14 h 30 (HNE)

Joignez-vous à Maureen Dobbins, directrice scientifique de Health Evidence, pour examiner les données probantes issues de la revue systématique suivante :

Laufer Y., Dar G., et Kodesh E. (2014). Est-ce qu'un programme d'exercice basé sur Wii peut améliorer le contrôle de l'équilibre des personnes âgées fonctionnelles? Une revue systématique. http://healthevidence.org/view-article.aspx?a=28111. Clinical Interventions in Aging, 9:1803-13.

Pour vous inscrire : https://health-evidence.webex.com/health-evidence/onstage/g.php?MTID=e3ce3c5b04478c1ec5a126958d15e2fdf

Programmes axés sur les familles afin de prévenir le tabagisme chez les enfants et les adolescents : quelles sont les données probantes?

11 juin 2015
de 13 h à 14 h 30 (HNE)

Joignez-vous à Roger Thomas, Professeur, Faculté de médecine, Université de Calgary, pour un aperçu des résultats de sa dernière revue systématique Cochrane qui examine si des interventions en milieu familial peuvent influencer les enfants et les adolescents à ne pas fumer :

Thomas, R.E., Baker, P.R.A., Thomas, B.C., et Lorenzetti, D. (2015). Programmes de prévention du tabagisme chez les enfants et les adolescents axés sur la famille. http://www.healthevidence.org/view-article.aspx?a=16998. Cochrane Database of Systematic Reviews,2015(2), Art. No.: CD004493.

Pour vous inscrire : https://health-evidence.webex.com/health-evidence/onstage/g.php?MTID=e5ebf045cbf3548d3672343043864b121

Regardez les précédents webinaires en ligne : http://www.healthevidence.org/webinars.aspx

Récemment mis en ligne ! Le webinaire du 31 mars : L'amélioration des environnements nutritionnels des enfants et des jeunes par l'accès à des fruits et légumes dans les écoles et les foyers : quelles sont les données probantes? https://www.youtube.com/watch?v=PrEPKWtFTpY&feature=youtu.be

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