32 research outputs found

    Pertinence de la référence en orthopédie pédiatrique des cas suspectés de scoliose idiopathique : association avec la morbidité perçue et les itinéraires de soins des patients

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    La scoliose idiopathique de l’adolescent (SIA) est le type de dĂ©formation musculosquelettique le plus frĂ©quent dans la population pĂ©diatrique, pour une prĂ©valence d’environ 2,0%. Depuis l’arrĂȘt des programmes scolaires de dĂ©pistage de la SIA dans les annĂ©es 1980 au Canada, nous ne disposions d’aucune donnĂ©e sur l’utilisation des services de santĂ© par les patients prĂ©sentant une SIA suspectĂ©e. En l’absence de tels programmes, des changements dans les patrons d’utilisation des services spĂ©cialisĂ©s d’orthopĂ©die pĂ©diatrique sont anticipĂ©s. La thĂšse a donc pour but d’étudier la pertinence de la rĂ©fĂ©rence dans ces services des jeunes avec SIA suspectĂ©e. Elle est structurĂ©e autour de trois principaux objectifs. 1) Valider un instrument de mesure de la morbiditĂ© perçue (perception des symptĂŽmes) dans la clientĂšle d’orthopĂ©die pĂ©diatrique; 2) Étudier la relation entre la morbiditĂ© perçue par les profanes (le jeune et le parent) et la morbiditĂ© objectivĂ©e par les experts; 3) CaractĂ©riser les itinĂ©raires de soins des patients avec SIA suspectĂ©e, de façon Ă  en Ă©laborer une taxonomie et Ă  analyser les relations entre ceux-ci et la pertinence de la rĂ©fĂ©rence. En 2006-2007, une vaste enquĂȘte a Ă©tĂ© rĂ©alisĂ©e dans les cinq cliniques d’orthopĂ©die pĂ©diatrique du Sud-Ouest du QuĂ©bec : 831 patients rĂ©fĂ©rĂ©s ont Ă©tĂ© recrutĂ©s. Ils furent classĂ©s selon des critĂšres de pertinence de la rĂ©fĂ©rence (inappropriĂ©e, appropriĂ©e ou tardive) dĂ©finis en fonction de l’amplitude de la courbe rachidienne et de la maturitĂ© squelettique Ă  cette premiĂšre visite. La morbiditĂ© perçue par les profanes a Ă©tĂ© opĂ©rationnalisĂ©e par la gravitĂ©, l’urgence, les douleurs, l’impact sur l’image de soi et la santĂ© gĂ©nĂ©rale. L’ensemble des consultations mĂ©dicales et paramĂ©dicales effectuĂ©es en amont de la consultation en orthopĂ©die pĂ©diatrique a Ă©tĂ© documentĂ© par questionnaire auprĂšs des familles. En s’appuyant sur le ModĂšle comportemental de l’utilisation des services d’Andersen, les facteurs (dits de facilitation et de capacitĂ©) individuels, relatifs aux professionnels et au systĂšme ont Ă©tĂ© considĂ©rĂ©s comme variables d’ajustement dans l’étude des relations entre la morbiditĂ© perçue ou les itinĂ©raires de soins et la pertinence de la rĂ©fĂ©rence. Les principales conclusions de cette Ă©tude sont : i) Nous disposons d’instruments fidĂšles (alpha de Cronbach entre 0,79 et 0,86) et valides (validitĂ© de construit, concomitante et capacitĂ© discriminante) pour mesurer la perception de la morbiditĂ© dans la population adolescente francophone qui consulte en orthopĂ©die pĂ©diatrique; ii) Les profanes jouent un rĂŽle important dans la suspicion de la scoliose (53% des cas) et leur perception de la morbiditĂ© est directement associĂ©e Ă  la morbiditĂ© objectivĂ©e par les professionnels; iii) Le case-mix actuel en orthopĂ©die est jugĂ© non optimal en regard de la pertinence de la rĂ©fĂ©rence, les mĂ©canismes actuels entraĂźnant un nombre considĂ©rable de rĂ©fĂ©rences inappropriĂ©es (38%) et tardives (18%) en soins spĂ©cialisĂ©s d’orthopĂ©die pĂ©diatrique; iv) Il existe une grande diversitĂ© de professionnels par qui sont vus les jeunes avec SIA suspectĂ©e ainsi qu’une variabilitĂ© des parcours de soins en amont de la consultation en orthopĂ©die, et v) La continuitĂ© des soins manifestĂ©e dans les itinĂ©raires, notamment via la source rĂ©guliĂšre de soins de l’enfant, est favorable Ă  la diminution des rĂ©fĂ©rences tardives (OR=0,32 [0,17-0,59]). Les retombĂ©es de cette thĂšse se veulent des contributions Ă  l’avancement des connaissances et ouvrent sur des propositions d’initiatives de transfert des connaissances auprĂšs des professionnels de la premiĂšre ligne. De telles initiatives visent la sensibilisation Ă  cette condition de santĂ© et le soutien Ă  la prise de dĂ©cision de mĂȘme qu’une meilleure coordination des demandes de consultation pour une rĂ©fĂ©rence appropriĂ©e et en temps opportun.Adolescent Idiopathic Scoliosis (AIS) is the type of musculoskeletal deformity most frequently encountered in the pediatric population with a prevalence of approximately 2.0%. Since the Canadian school screening programs were discontinued in the 1980s, data detailing health service utilization or typical reference patterns for patients with suspected AIS are no longer available. Without such programs, changes in the utilization patterns of pediatric orthopedic specialized services are anticipated. The thesis therefore aims to study the appropriateness of referral of youths with suspected AIS. It comprises three main objectives: 1) To validate a measurement tool based on perceived morbidity (perception of the symptoms) in the orthopedic pediatric patient population, 2) To study the relationships between morbidity perceived by lay persons (the young patient and his parent), and the objective morbidity determined by medical professionals, 3) To characterize the healthcare service pathways of suspected AIS cases upstream of their first orthopedic consultation in order to define a taxonomy of the pathways and analyse their relationships with the appropriateness of referral. In 2006-2007, an extensive survey conducted in the five clinics serving southwest Quebec recruited 831 patients. They were categorized using criteria for the appropriateness of referral (inappropriate, appropriate or late) based on the amplitude of the main spinal curve and skeletal maturity at the first visit. Lay perceived morbidity was operationalized according to the seriousness, urgency, pain, self-image and general perceived health. Medical and paramedical visits upstream of the pediatric orthopedic consultation were documented with questionnaires to the families. Based on Andersen’s Health Behavior Model, the individual (facilitating and enabling), professional and systemic factors were considered as control variables in the study of associations between perceived morbidity or healthcare trajectories, and appropriateness of referral. The main conclusions of the thesis are: i) Reliable (Cronbach alpha between 0.79 and 0.86) and valid (construct, concurrent and discriminant validity) measurement tools are available to evaluate the perceived morbidity in the French-speaking adolescent population that consults in pediatric orthopedics, ii) Lay stakeholders play an important role in the suspicion of scoliosis (53% of cases) with their perceived morbidity directly related to the objective morbidity, and therefore associated to the appropriateness of referral, iii) The current orthopedic casemix is considered suboptimal with regards to the appropriateness of referral, and the actual mechanisms for reference are in fact responsible for a large number of inappropriate (38%) and late (18%) referrals to specialized pediatric orthopedic services, iv) Adolescents with suspected AIS consult with a wide range of health specialists resulting in a large variety of healthcare pathways upstream of the orthopedic consultation, and v) Continuity of healthcare services, mainly through a regular source of care for the child, is favourable to a reduction in late referrals (OR=0.32 [0.17-0.59]). This thesis is intended to contribute to the advancement of conceptual, empirical and applied knowledge leading to a series of knowledge translation initiatives targeting primary health care providers. Such initiatives have the potential to increase awareness of the condition, to support decision-making as well as to improve the coordination of consultation requests, thus promoting appropriateness and timeliness of referrals

    Screening for adolescent idiopathic scoliosis: an information statement by the scoliosis research society international task force

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    Background: Routine screening of scoliosis is a controversial subject and screening efforts vary greatly around the world. METHODS: Consensus was sought among an international group of experts (seven spine surgeons and one clinical epidemiologist) using a modified Delphi approach. The consensus achieved was based on careful analysis of a recent critical review of the literature on scoliosis screening, performed using a conceptual framework of analysis focusing on five main dimensions: technical, clinical, program, cost and treatment effectiveness. FINDINGS: A consensus was obtained in all five dimensions of analysis, resulting in 10 statements and recommendations. In summary, there is scientific evidence to support the value of scoliosis screening with respect to technical efficacy, clinical, program and treatment effectiveness, but there insufficient evidence to make a statement with respect to cost effectiveness. Scoliosis screening should be aimed at identifying suspected cases of scoliosis that will be referred for diagnostic evaluation and confirmed, or ruled out, with a clinically significant scoliosis. The scoliometer is currently the best tool available for scoliosis screening and there is moderate evidence to recommend referral with values between 5 degrees and 7 degrees. There is moderate evidence that scoliosis screening allows for detection and referral of patients at an earlier stage of the clinical course, and there is low evidence suggesting that scoliosis patients detected by screening are less likely to need surgery than those who did not have screening. There is strong evidence to support treatment by bracing. INTERPRETATION: This information statement by an expert panel supports scoliosis screening in 4 of the 5 domains studied, using a framework of analysis which includes all of the World Health Organisation criteria for a valid screening procedure.IRSC (MOP864910

    The effectiveness of scoliosis screening programs: methods for systematic review and expert panel recommendations formulation

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    Background: Literature on scoliosis screening is vast, however because of the observational nature of available data and methodological flaws, data interpretation is often complex, leading to incomplete and sometimes, somewhat misleading conclusions. The need to propose a set of methods for critical appraisal of the literature about scoliosis screening, a comprehensive summary and rating of the available evidence appeared essential. METHODS: To address these gaps, the study aims were: i) To propose a framework for the assessment of published studies on scoliosis screening effectiveness; ii) To suggest specific questions to be answered on screening effectiveness instead of trying to reach a global position for or against the programs; iii) To contextualize the knowledge through expert panel consultation and meaningful recommendations. The general methodological approach proceeds through the following steps: Elaboration of the conceptual framework; Formulation of the review questions; Identification of the criteria for the review; Selection of the studies; Critical assessment of the studies; Results synthesis; Formulation and grading of recommendations in response to the questions. This plan follows at best GRADE Group (Grades of Recommendation, Assessment, Development and Evaluation) requirements for systematic reviews, assessing quality of evidence and grading the strength of recommendations. CONCLUSIONS: In this article, the methods developed in support of this work are presented since they may be of some interest for similar reviews in scoliosis and orthopaedic fields.Canadian Institutes of Health Research (CIHR) by three means: CIHR Research Operating Grants (2004–2007, 2008–2011); Canada Graduate Scholarships Doctoral Awards (MB) and CIHR MENTOR and AnEIS Strategic training programs doctoral awards (MB)

    Clearance of defective muscle stem cells by senolytics reduces the expression of senescence-associated secretory phenotype and restores myogenesis in myotonic dystrophy type 1

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    Muscle weakness and atrophy are clinical hallmarks of myotonic dystrophy type 1 (DM1). Muscle stem cells, which contribute to skeletal muscle growth and repair, are also affected in this disease. However, the molecular mechanisms leading to this defective activity and the impact on the disease severity are still elusive. Here, we explored through an unbiased approach the molecular signature leading to myogenic cell defects in DM1. Single cell RNAseq data revealed the presence of a specific subset of DM1 myogenic cells expressing a senescence signature, characterized by the high expression of genes related to senescence-associated secretory phenotype (SASP). This profile was confirmed using different senescence markers in vitro and in situ. Accumulation of intranuclear RNA foci in senescent cells, suggest that RNA-mediated toxicity contribute to senescence induction. High expression of IL-6, a prominent SASP cytokine, in the serum of DM1 patients was identified as a biomarker correlating with muscle weakness and functional capacity limitations. Drug screening revealed that the BCL-XL inhibitor (A1155463), a senolytic drug, can specifically target senescent DM1 myoblasts to induce their apoptosis and reduce their SASP. Removal of senescent cells re-established the myogenic function of the non-senescent DM1 myoblasts, which displayed improved proliferation and differentiation capacity in vitro; and enhanced engraftment following transplantation in vivo. Altogether this study presents a well-defined senescent molecular signature in DM1 untangling part of the pathological mechanisms observed in the disease; additionally, we demonstrate the therapeutic potential of targeting these defective cells with senolytics to restore myogenesis

    Integrin/Fak/Src-mediated regulation of cell survival and anoikis in human intestinal epithelial crypt cells: selective engagement and roles of PI3-K isoform complexes

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    In human intestinal epithelial crypt (HIEC) cells, the PI3-K/Akt-1 pathway is crucial for the promotion of cell survival and suppression of anoikis. Class I PI3-K consists of a complex formed by a catalytic (C) and regulatory (R) subunit. Three R (p85α, ÎČ, and p55Îł) and four C (p110α, ÎČ, Îł and ÎŽ) isoforms are known. Herein, we analyzed the expression of PI3-K isoforms in HIEC cells and determined their roles in cell survival, as well as in the ÎČ1 integrin/Fak/Src-mediated suppression of anoikis. We report that: (1) the predominant PI3-K complexes expressed by HIEC cells are p110α/p85ÎČ and p110α/p55Îł; (2) the inhibition and/or siRNA-mediated expression silencing of p110α, but not that of p110ÎČ, Îł or ÎŽ, results in Akt-1 down-activation and consequent apoptosis; (3) the expression silencing of p85ÎČ or p55Îł, but not that of p85α, likewise induces Akt-1 down-activation and apoptosis; however, the impact of a loss of p55Îł on both Akt-1 activation and cell survival is significantly greater than that from the loss of p85ÎČ; and (4) both the p110α/p85ÎČ and p110α/p55Îł complexes are engaged by ÎČ1 integrin/Fak/Src signaling; however, the engagement of p110α/p85ÎČ is primarily Src-dependent, whereas that of p110α/p55Îł is primarily Fak-dependent (but Src-independent). Hence, HIEC cells selectively express PI3-K isoform complexes, translating into distinct roles in Akt-1 activation and cell survival, as well as in a selective engagement by Fak and/or Src within the context of ÎČ1 integrin/Fak/Src-mediated suppression of anoikis

    Global data on earthworm abundance, biomass, diversity and corresponding environmental properties

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    Publisher Copyright: © 2021, The Author(s).Earthworms are an important soil taxon as ecosystem engineers, providing a variety of crucial ecosystem functions and services. Little is known about their diversity and distribution at large spatial scales, despite the availability of considerable amounts of local-scale data. Earthworm diversity data, obtained from the primary literature or provided directly by authors, were collated with information on site locations, including coordinates, habitat cover, and soil properties. Datasets were required, at a minimum, to include abundance or biomass of earthworms at a site. Where possible, site-level species lists were included, as well as the abundance and biomass of individual species and ecological groups. This global dataset contains 10,840 sites, with 184 species, from 60 countries and all continents except Antarctica. The data were obtained from 182 published articles, published between 1973 and 2017, and 17 unpublished datasets. Amalgamating data into a single global database will assist researchers in investigating and answering a wide variety of pressing questions, for example, jointly assessing aboveground and belowground biodiversity distributions and drivers of biodiversity change.Peer reviewe
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