638 research outputs found

    Exact solution of variable coefficient mixed hyperbolic partial differential problems

    Get PDF
    AbstractThis paper is concerned with the construction of exact series solution of mixed variable coefficient hyperbolic problems

    Chronic disease risk typologies among young adults in community college

    Get PDF
    Objectives: To address chronic disease risk holistically from a behavioral perspective, insights are needed to refine understanding of the covariance of key health behaviors. This study aims to identify distinct typologies of young adults based on 4 modifiable risk factors of chronic disease using a latent class analysis approach, and to describe patterns of class membership based on demographic characteristics, living arrangements, and weight. Methods: Overall, 441 young adults aged 18-35 attending community colleges in the Minnesota Twin Cities area completed a baseline questionnaire for the Choosing Healthy Options in College Environments and Settings study, a RCT. Behavioral items were used to create indicators for latent classes, and individuals were classified using maximum-probability assignment. Results: Three latent classes were identified: ‘active, binge-drinkers with a healthy dietary intake’ (13.1%); ‘non-active, moderate-smokers and non-drinkers with poor dietary intake’ (38.2%); ‘moderately active, non-smokers and non-drinkers with moderately healthy dietary intake’ (48.7%). Classes exhibited unique demographic and weight-related profiles. Conclusions: This study may contribute to the literature on health behaviors among young adults and provides evidence that there are weight and age differences among subgroups. Understanding how behaviors cluster is important for identifying groups for targeted interventions in community colleges

    Second-order corrections to neutrino two-flavor oscillation parameters in the wave packet approach

    Full text link
    We report about an analytic study involving the {\em intermediate} wave packet formalism for quantifying the physically relevant information which appear in the neutrino two-flavor conversion formula and help us to obtain more precise limits and ranges for neutrino flavor oscillation. By following the sequence of analytic approximations where we assume a strictly peaked momentum distribution and consider the second-order corrections in a power series expansion of the energy, we point out a {\em residual} time-dependent phase which, coupled with the {\em spreading/slippage} effects, can subtly modify the neutrino oscillation parameters and limits. Such second-order effects are usually ignored in the relativistic wave packet treatment, but they present an evident dependence on the propagation regime so that some small modifications to the oscillation pattern, even in the ultra-relativistic limit, can be quantified. These modifications are implemented in the confront with the neutrino oscillation parameter range (mass-squared difference \Delta m^{\2} and the mixing-angle ξ\theta) where we assume the same wave packet parameters previously noticed in the literature in a kind of {\em toy model} for some reactor experiments. Generically speaking, our analysis parallels the recent experimental purposes which concern with higher precision parameter measurements. To summarize, we show that the effectiveness of a more accurate determination of \Delta m^{\2} and ξ\theta depends on the wave packet width aa and on the averaged propagating energy flux Eˉ\bar{E} which still correspond to open variables for some classes of experiments. \Comment: 25 pages, 5 figure

    High-Intensity Interval Training for Knee Osteoarthritis: A Pilot Study

    Get PDF
    Objective: To assess the feasibility and changes in outcomes of a 12-week high-intensity interval training (HIIT) program in individuals with symptomatic knee osteoarthritis (OA). Methods: The single-arm trial included 29 participants (mean ± SD age 63 ± 7 years; 66% women; 66% obese). Measures of participant flow, adherence, and tolerability were collected. Pain, function, and balance were assessed at baseline, 6 weeks, and 12 weeks using the Western Ontario and McMaster Universities Osteoarthritis Index, 20-m fast-paced walk test, 30-second chair-stand test, stair-climb test, timed up and go test, and single leg stance. Cardiorespiratory fitness, strength, and body composition were evaluated using peak oxygen consumption (VO2peak), isometric knee extensor/flexor strength, and dual-energy x-ray absorptiometry, respectively. HIIT was completed two times/week (cycling or treadmill) and consisted of 10 repetitions of 1-minute bouts at 90% VO2peak, with 1-minute rest periods. Separate multivariable-adjusted linear mixed models were fit for each outcome with fixed effects of time, age, sex, body mass index, and random effects of baseline values to estimate mean changes and 95% confidence intervals (CIs) between baseline and 12-week assessments. Results: Recruitment aligned with the anticipated enrollment rate, adherence was 70%, and no adverse events were reported. At 12 weeks, improvements were observed for most outcomes, with notable mean changes for the 20-m fast-paced walk (−1.13 [95% CI −1.61 to −0.64] seconds), 30-second chair-stand (2.6 [1.8-3.4] stands), and VO2peak (0.14 [0.03-0.24] liters/minute). Conclusion: In this 12-week pilot study, HIIT improved multiple aspects of health in individuals with knee OA; larger studies are needed

    Recommendations For Long-term Home Oxygen Therapy In Children And Adolescents

    Get PDF
    Objective: To advise pediatricians, neonatologists, pulmonologists, pediatric pulmonologists, and other professionals in the area on the main indications and characteristics of long-term home oxygen therapy in children and adolescents. Data source: A literature search was carried out in the MEDLINE/PubMed database (1990 to 2011). Additionally, references from selected studies were included. As consistent scientific evidence does not exist for many aspects, some of the recommendations were based on clinical experience. Data synthesis: Long-term home oxygen therapy has been a growing practice in pediatric patients and is indicated in bronchopulmonary dysplasia, cystic fibrosis, bronchiolitis obliterans, interstitial lung diseases, and pulmonary hypertension, among others. The benefits are: decrease in hospitalizations, optimization of physical growth and neurological development, improvement of exercise tolerance and quality of sleep, and prevention of pulmonary hypertension/cor pulmonale. The levels of oxygen saturation indicative for oxygen therapy differ from those established for adults with chronic obstructive pulmonary disease, and vary according to age and disease. Pulse oximetry is used to evaluate oxygen saturation; arterial blood gas is unnecessary. There are three available sources of oxygen: gas cylinders, liquid oxygen, and oxygen concentrators. The flows used are usually smaller, as are the number of hours/day needed when compared to the use in adults. Some diseases show improvement and oxygen therapy discontinuation is possible. Conclusions: Long-term home oxygen therapy is increasingly common in pediatrics and has many indications. There are relevant particularities when compared to its use in adults, regarding indications, directions for use, and monitoring. Copyright © 2013 Sociedade Brasileira de Pediatria. Published by Elsevier Editora Ltda. All rights reserved.891617Doherty, D.E., Petty, T.L., Bailey, W., Carlin, B., Cassaburi, R., Christopher, K., Recommendations of the 6th long-term oxygen therapy consensus conference (2006) Respir Care., 51, pp. 519-525Mocelin, H.T., Fischer, G.B., Ranzi, L.C., Rosa, R.D., Philomena, M.R., Home oxygen therapy in children: Seven years experience (2001) J Pneumol, 27, pp. 148-152Primhak, R.A., Hicks, B., Shaw, N.J., Donaldson, G.C., Balfour-Lynn, I.M., Use of home oxygen for children in England and Wales (2011) Arch Dis Child, 96, pp. 389-392Munhoz, A.S., Adde, F.V., Nakaie, C.M., Doria Filho, U., Silva Filho, L.V., Rodrigues, J.C., Long-term home oxygen therapy in children and adolescents: Analysis of clinical use and costs of a home care program (2011) J Pediatr (Rio J), 87, pp. 13-18Continuous or nocturnal oxygen therapy in hypoxemic chronic obstructive lung disease: A clinical trial (1980) Ann Intern Med, 93, pp. 391-398. , Nocturnal Oxygen Therapy Trial GroupReport of the medical research council working party (1981) Lancet, 1, pp. 681-686. , Long term domiciliary oxygen therapy in chronic hypoxic corpulmonale complicating chronic bronchitis and emphysemaGuyatt, G.H., McKim, D.A., Austin, P., Bryan, R., Norgren, J., Weaver, B., Appropriateness of domiciliary oxygen delivery (2000) Chest, 118, pp. 1303-1308Kotecha, S., Allen, J., Oxygen therapy for infants with chronic lung disease (2002) Arch Dis Child Fetal Neonatal Ed, 87, pp. F11-F14Simonds, A.K., Home ventilation (2003) Eur Respir J Suppl, 47, pp. 38s-46sBalfour-Lynn, I.M., Primhak, R.A., Shaw, B.N., Home oxygen for children: Who, how and when? (2005) Thorax, (60), pp. 76-81MacLean, J.E., Fitzgerald, D.A., A rational approach to home oxygen use in infants and children (2006) Paediatr Respir Rev, 7, pp. 215-222Fitzgerald, D.A., Massie, R.J., Nixon, G.M., Jaffe, A., Wilson, A., Infants with chronic neonatal lung disease: Recommendations for the use of home oxygen therapy (2008) Med J Aust, 189, pp. 578-582. , Thoracic Society of Australia and New ZealandBalfour-Lynn, I.M., Field, D.J., Gringras, P., Hicks, B., Jardine, E., Jones, R.C., BTS guidelines for home oxygen in children (2009) Thorax, 64, pp. ii1-26Balfour-Lynn, I.M., Domiciliary oxygen for children (2009) Pediatr Clin North Am, 56, pp. 275-296Harrison, G., Shaw, B., Prescribing home oxygen (2007) Arch Dis Child Fetal Neonatal Ed, 92, pp. F241-F243Viegas, C.A., Adde, F.V., Paschoal, I.A., Godoy, I., MacHado, M.C., I consenso brasileiro de oxigenoterapia domiciliar prolongada/SBPT (2000) J Pneumol, 26, pp. 341-350Tin, W., Gupta, S., Optimum oxygen therapy in preterm babies (2007) Arch Dis Child Fetal Neonatal Ed, 92, pp. F143-F147McMorrow, R.C., Mythen, M.G., Pulse oximetry (2006) Curr Opin Crit Care, 12, pp. 269-271Sinex, J.E., Pulse oximetry: Principles and limitations (1999) Am J Emerg Med, 17, pp. 59-67Barker, S.J., Badal, J.J., The measurement of dyshemoglobins and total hemoglobin by pulse oximetry (2008) Curr Opin Anaesthesiol, 21, pp. 805-810Hunt, C.E., Corwin, M.J., Lister, G., Weese-Mayer, D.E., Neuman, M.R., Tinsley, L., Longitudinal assessment of hemoglobin oxygen saturation in healthy infants during the first 6 months of age (1999) J Pediatr, 135, pp. 580-586. , Collaborative Home Infant Monitoring Evaluation (CHIME) Study GroupHunt, C.E., Corwin, M.J., Weese-Mayer, D.E., Ward, S.L., Ramanathan, R., Lister, G., Longitudinal assessment of hemoglobin oxygen saturation in preterm and term infants in the first six months of life (2011) J Pediatr, 159, pp. 377-383Masters, I.B., Goes, A.M., Healy, L., O'Neil, M., Stephens, D., Harris, M.A., Age-related changes in oxygen saturation over the first year of life: A longitudinal study (1994) J Paediatr Child Health, 30, pp. 423-428Stebbens, V.A., Poets, C.F., Alexander, J.R., Arrowsmith, W.A., Southall, D.P., Oxygen saturation and breathing patterns in infancy. 1: Full term infants in the second month of life (1991) Arch Dis Child, 66, pp. 569-573Poets, C.F., Stebbens, V.A., Alexander, J.R., Arrowsmith, W.A., Salfield, S.A., Southall, D.P., Oxygen saturation and breathing patterns in infancy. 2: Preterm infants at discharge from special care (1991) Arch Dis Child, 66, pp. 574-578Richard, D., Poets, C.F., Neale, S., Stebbens, V.A., Alexander, J.R., Southall, D.P., Arterial oxygen saturation in preterm neonates without respiratory failure (1993) J Pediatr, 123, pp. 963-968Poets, C.F., Stebbens, V.A., Lang, J.A., O'Brien, L.M., Boon, A.W., Southall, D.P., Arterial oxygen saturation in healthy term neonates (1996) Eur J Pediatr, 155, pp. 219-223Meyts, I., Reempts, P.V., Boeck, K.D., Monitoring of haemoglobin oxygen saturation in healthy infants using a new generation pulse oximeter which takes motion artifacts into account (2002) Eur J Pediatr, 161, pp. 653-655Ng, A., Subhedar, N., Primhak, R.A., Shaw, N.J., Arterial oxygen saturation profiles in healthy preterm infants (1998) Arch Dis Child Fetal Neonatal Ed, 79, pp. F64-F66Poets, C.F., Stebbens, V.A., Samuels, M.P., Southall, D.P., Oxygen saturation and breathing patterns in children (1993) Pediatrics, 92, pp. 686-690Urschitz, M.S., Wolff, J., Von Einem, V., Urschitz-Duprat, P.M., Schlaud, M., Poets, C.F., Reference values for nocturnal home pulse oximetry during sleep in primary school children (2003) Chest., 123, pp. 96-101Jobe, A.H., The new bronchopulmonary dysplasia (2011) Curr Opin Pediatr, 23, pp. 167-172Chess, P.R., D'Angio, C.T., Pryhuber, G.S., Maniscalco, W.M., Pathogenesis of bronchopulmonary dysplasia (2006) Semin Perinatol, 30, pp. 171-178Coalson, J.J., Pathology of bronchopulmonary dysplasia (2006) Semin Perinatol, 30, pp. 179-184Monte, L.F., Silva Filho, L.V., Miyoshi, M.H., Rozov, T., Displasia broncopulmonar (2005) J Pediatr (Rio J), 81, pp. 99-110Bancalari, E., Claure, N., Definitions and diagnostic criteria for bronchopulmonary dysplasia (2006) Semin Perinatol, 30, pp. 164-170Ellsbury, D.L., Acarregui, M.J., McGuinness, G.A., Eastman, D.L., Klein, J.M., Controversy surrounding the use of home oxygen for premature infants with bronchopulmonary dysplasia (2004) J Perinatol, 24, pp. 36-40I: Primary outcomes (2000) Pediatrics, 105, pp. 295-310. , Supplemental Therapeutic Oxygen for Prethreshold Retinopathy of Prematurity (STOP-ROP), a randomized, controlled trialAskie, L.M., Henderson-Smart, D.J., Irwig, L., Simpson, J.M., Oxygensaturation targets and outcomes in extremely preterm infants (2003) N Engl J Med, 349, pp. 959-967Higgins, R.D., Bancalari, E., Willinger, M., Raju, T.N., Executive summary of the workshop on oxygen in neonatal therapies: Controversies and opportunities for research (2007) Pediatrics, 119, pp. 790-796Groothuis, J.R., Rosenberg, A.A., Home oxygen promotes weight gain in infants with bronchopulmonary dysplasia (1987) Am J Dis Child, 141, pp. 992-995Garcia, E.A., Mezzacappa, M.A., Pessoto, M.A., Home oxygen therapy program for infants after neonatal unit discharge: Report of a ten-year experience (2010) Rev Paul Pediatr, 28, pp. 276-282Moon, N.M., Mohay, H.A., Gray, P.H., Developmental patterns from 1 to 4 years of extremely preterm infants who required home oxygen therapy (2007) Early Hum Dev, 83, pp. 209-216Greenough, A., Alexander, J., Burgess, S., Bytham, J., Chetcuti, P.A., Hagan, J., Preschool healthcare utilization related to home oxygen status (2006) Arch Dis Child Fetal Neonatal Ed, 91, pp. F337-F341Bhandari, A., Panitch, H.B., Pulmonary outcomes in bronchopulmonary dysplasia (2006) Semin Perinatol, 30, pp. 219-226Zinman, R., Corey, M., Coates, A.L., Canny, G.J., Connolly, J., Levison, H., Nocturnal home oxygen in the treatment of hypoxemic cystic fibrosis patients (1989) J Pediatr, 114, pp. 368-377Urquhart, D.S., Montgomery, H., Jaffé, A., Assessment of hypoxia in children with cystic fibrosis (2005) Arch Dis Child, 90, pp. 1138-1143Douglass, H., Potter, H., Jarad, N., Current practice in prescription, assessment and use of oxygen therapy in cystic fibrosis: A national UK survey (2008) J Cystic Fibrosis, 7, pp. S77Elphick, H.E., Mallory, G., Oxygen therapy for cystic fibrosis (2009) Cochrane Database Syst Rev, (1), pp. CD003884Frangolias, D.D., Wilcox, P.G., Predictability of oxygen desaturation during sleep in patients with cystic fibrosis: Clinical, spirometric, and exercise parameters (2001) Chest, 119, pp. 434-441De Castro-Silva, C., De Bruin, V.M., Cavalcante, A.G., Bittencourt, L.R., De Bruin, P.F., Nocturnal hypoxia and sleep disturbances in cystic fibrosis (2009) Pediatr Pulmonol, 44, pp. 1143-1150Milross, M.A., Piper, A.J., Norman, M., Willson, G.N., Grunstein, R.R., Sullivan, C.E., Predicting sleep-disordered breathing in patients with cystic fibrosis (2001) Chest, 120, pp. 1239-1245Narang, I., Pike, S., Rosenthal, M., Balfour-Lynn, I.M., Bush, A., Threeminute step test to assess exercise capacity in children with cystic fibrosis with mild lung disease (2003) Pediatr Pulmonol, 35, pp. 108-113Fischer, G.B., Sarria, E.E., Mattiello, R., Mocelin, H.T., Castro-Rodriguez, J.A., Post infectious bronchiolitis obliterans in children (2010) Paediatr Respir Rev, 11, pp. 233-239Champs, N.S., Lasmar, L.M., Camargos, P.A., Marguet, C., Fischer, G.B., Mocelin, H.T., Post-infectious bronchiolitis obliterans in children (2011) J Pediatr (Rio J), 87, pp. 187-198Paiva, M.A., Amaral, S.M., Chronic interstitial lung diseases in children (2009) J Bras Pneumol, 35, pp. 792-803Clement, A., Nathan, N., Epaud, R., Fauroux, B., Corvol, H., Interstitial lung diseases in children (2010) Orphanet J Rare Dis, 5, p. 22Das, S., Langston, C., Fan, L.L., Interstitial lung disease in children (2011) Curr Opin Pediatr, 23, pp. 325-331Berger, S., Konduri, G.G., Pulmonary hypertension in children: The twenty-first century (2006) Pediatr Clin North Am, 53, pp. 961-987Schulze-Neick, I., Beghetti, M., Issues related to the management and therapy of paediatric pulmonary hypertension (2010) Eur Respir Rev, 19, pp. 331-339GaliÚ, N., Hoeper, M.M., Humbert, M., Torbicki, A., Vachiery, J.L., Barbera, J.A., Guidelines for the diagnosis and treatment of pulmonary hypertension: The Task Force for the Diagnosis and Treatment of Pulmonary Hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS), endorsed by the International Society of Heart and Lung Transplantation (ISHLT) (2009) Eur Heart J., 30, pp. 2493-2537Fishman, A.P., Hypoxia on the pulmonary circulation. How and where it acts (1976) Circ Res, 38, pp. 221-231Fuso, L., Baldi, F., Di Perna, A., Therapeutic strategies in pulmonary hypertension (2011) Front Pharmacol, 2, p. 21Bowyer, J.J., Busst, C.M., Denison, D.M., Shinebourne, E.A., Effect of long term oxygen treatment at home in children with pulmonary vascular disease (1986) Br Heart J, 55, pp. 385-390Sandoval, J., Aguirre, J.S., Pulido, T., Martinez-Guerra, M.L., Santos, E., Alvarado, P., Nocturnal oxygen therapy in patients with the Eisenmenger syndrome (2001) Am J Respir Crit Care Med, 164, pp. 1682-1687Darrow, D.H., Surgery for pediatric sleep apnea (2007) Otolaryngol Clin North Am, 40, pp. 855-875Kirk, V.G., O'Donnell, A.R., Continuous positive airway pressure for children: A discussion on how to maximize compliance (2006) Sleep Med Rev, 10, pp. 119-127Marcus, C.L., Carroll, J.L., Bamford, O., Pyzik, P., Loughlin, G.M., Supplemental oxygen during sleep in children with sleep-disordered breathing (1995) Am J Respir Crit Care Med, 152, pp. 1297-1301Aljadeff, G., Gozal, D., Bailey-Wahl, S.L., Burrell, B., Keens, T.G., Ward, S.L., Effects of overnight supplemental oxygen in obstructive sleep apnea in children (1996) Am J Respir Crit Care Med, 153, pp. 51-55Robert, D., Argaud, L., Clinical review: Long-term noninvasive ventilation (2007) Crit Care, 11, p. 210Benditt, J.O., Initiating noninvasive management of respiratory insufficiency in neuromuscular disease (2009) Pediatrics, 123, pp. S236-S238Seakins, M., Gibbs, W.N., Milner, P.F., Bertles, J.F., Erythrocyte Hb-S concentration. An important factor in the low oxygen affinity of blood in sickle cell anemia (1973) J Clin Invest, 52, pp. 422-432Moreira, G.A., Respiratory repercussions of sickle cell anemia (2007) J Bras Pneumol, 33, pp. 18-20Ortiz, F.O., Aldrich, T.K., Nagel, R.L., Benjamin, L.J., Accuracy of pulse oximetry in sickle cell disease (1999) Am J Respir Crit Care Med, 159, pp. 447-451Blaisdell, C.J., Goodman, S., Clark, K., Casella, J.F., Loughlin, G.M., Pulse oximetry is a poor predictor of hypoxemia in stable children with sickle cell disease (2000) Arch Pediatr Adolesc Med, 154, pp. 900-903Pianosi, P., Charge, T.D., Esseltine, D.W., Coates, A.L., Pulse oximetry in sickle cell disease (1993) Arch Dis Child, 68, pp. 735-738Uong, E.C., Boyd, J.H., Debaun, M.R., Daytime pulse oximeter measurements do not predict incidence of pain and acute chest syndrome episodes in sickle cell anemia (2006) J Pediatr, 149, pp. 707-709Hargrave, D.R., Wade, A., Evans, J.P., Hewes, D.K., Kirkham, F.J., Nocturnal oxygen saturation and painful sickle cell crises in children (2003) Blood, 101, pp. 846-848Kirkham, F.J., Hewes, D.K., Prengler, M., Wade, A., Lane, R., Evans, J.P., Nocturnal hypoxaemia and central-nervous-system events in sickle-cell disease (2001) Lancet, 357, pp. 1656-1659Milross, M.A., Piper, A.J., Dobbin, C.J., Bye, P.T., Grunstein, R.R., Sleep disordered breathing in cystic fibrosis (2004) Sleep Med Rev, 8, pp. 295-308Fauroux, B., Burgel, P.R., Boelle, P.Y., Cracowski, C., Murris-Espin, M., Nove-Josserand, R., Practice of noninvasive ventilation for cystic fibrosis: A nationwide survey in France (2008) Respir Care, 53, pp. 1482-148

    Cystic Fibrosis At A Brazilian Center Of Excellence: Clinical And Laboratory Characteristics Of 104 Patients And Their Association With Genotype And Disease Severity

    Get PDF
    Objective: To identify the clinical, laboratory and radiographic characteristics of the cystic fibrosis patients under care at Universidade Estadual de Campinas (UNICAMP) in the last decade of the twentieth century, and to investigate the association of these characteristics with genotype and severity of the disease as measured by the Shwachman score. Methods: Descriptive, retrospective and cross-sectional study of the patients assisted at UNICAMP hospital's Cystic Fibrosis Clinic from July 1990 to July 2000. Results: One hundred and four patients were studied; 53.8% male; 93.3% Caucasian; 89.4% presented with respiratory symptoms; 59.6% presented with digestive symptoms; 5.8% had meconium ileus; 4.8% had diabetes. The mean age at onset of symptoms was 3 months, and the mean age at diagnosis was 2 years and 4 months. At diagnosis, 69.9 and 56.6% of the patients had weight and height below 10th percentile, respectively; in 10.6%, sweat chloride was < 60 mEq/l. Staphylococcus aureus was found in 80.2%, Pseudomonas aeruginosa in 76.0%, and Burkholderia cepacia in 5.2%. ΔF508 homozygosis was observed in 18.75%, whereas 62.50% of the patients were ΔF508 heterozygous. A moderate/severe Shwachman score was found in 15.7%. Eighteen patients died in that period (17.3%). The mean age at death was 7 years and 8 months; median survival after diagnosis was 18 years and 4 months. Patients who have at least one ΔF508 mutation have more frequent alterations in fecal fat levels when compared to patients who do not have this mutation (p < 0.05). There were no differences in any parameter between ΔF508 homozygous and heterozygous patients. Conclusions: The clinical and laboratory characteristics of the 104 patients studied were similar to the characteristics described for patients in other countries. Exceptions are the higher age at diagnosis and lower survival. Our results support the recommendation for early diagnosis and the need for more treatment opportunities in the population of cystic fibrosis patients. Copyright © 2004 by Sociedade Brasileira de Pediatria.805371379World Health Organization and International Cystic Fibrosis (Mucoviscidosis) Association - Implementation of cystic fibrosis services in developing countries: Memorandum from a joint WHO/ICF (M)A meeting (1997) Bulletin of the World Health Organization, 75 (1), p. 10Gibson, L.E., Cooke, R.E., A test for concentration of electrolytes in sweat in cystic fibrosis of the pancreas utilizing pilocarpine by iontophoresis (1959) Pediatrics, 23, pp. 545-549Rommens, J.M., Kerem, B., Greer, W., Chang, P., Tsui, L.C., Ray, P., Rapid non radioactive detection of the major cystic fibrosis mutation (1990) Am J Hum Genet, 46, pp. 395-396(2003) 2002 Annual Data Report, , Bethesda, MarylandCamargos, P.A.M., GuimarĂŁes, M.D.C., Reis, F.J.C., Prognostic aspects of cystic fibrosis in Brazil (2000) Ann Trop Pediatr, 20, pp. 287-291(1993) Informe del Cuarto Año, p. 21. , Buenos AiresHuang, N., Schidlow, D., Szatrowski, T., Palmer, J., Laraya-Cuasay, L., Yeung, W., Clinical features, survival rate and prognostic factors in young adults with cystic fibrosis (1987) Am J Med, 2, pp. 871-879Welsh, M.J., Tsui, L.C., Boat, T.F., Beaudet, A.L., Cystic fibrosis (1995) The Metabolic and Molecular Bases of Inherited Disease. 7th Ed., pp. 3799-3876. , Scriver CR, Beaudet AL, Sly WS, Valle D. New York: McGraw-HillKerem, E., Corey, M., Kerem, B., Rommens, J.M., Markiewicz, D., Levison, H., The relationship of the most common mutation ΔF508 (1990) N Engl J Med, 323, pp. 1517-1522Borgo, G., Mastella, G., Gasparini, P., Zoranello, A., Doro, R., Pignatti, P.F., Pancreatic function and genetic ΔF508 in cystic fibrosis (1990) J Med Genet, 27, pp. 665-669Santis, G., Osborne, L., Knight, R.A., Hodson, M.E., Independent genetic determinants of pancreatic and pulmonary status in cystic fibrosis (1990) Lancet, 336, pp. 1081-1084Campbell III, P.W., Phillips III, J.A., Krishnamani, M.R., Maness, K.J., Hajinski, T.A., Cystic fibrosis: Relationship between clinical status and ΔF508 deletion (1991) J Pediatr, 118, pp. 239-241Johansen, H.K., Nir, M., Hoib, Y.N., Koch, C., Schwartz, M., Severity of cystic fibrosis in patients homozygous and heterozygous for ΔF508 mutation (1991) Lancet, 337, pp. 631-634McKone, E.F., Emerson, S.S., Edwards, K.L., Aitken, M.L., Effect of genotype on phenotype and mortality in cystic fibrosis: A retrospective cohort study (2003) Lancet, 361, pp. 1671-1676(1997) Clinical Practice Guidelines for Cystic FibrosisPark, R.W., Grand, R.J., Gastrointestinal manifestations of cystic fibrosis: A review (1981) Gastroenterology, 81, p. 1143Finkelstein, S.M., Wielinski, C.L., Elliott, G.R., Diabetes mellitus associated with cystic fibrosis (1988) J Pediatr, 112, p. 373Rosenecker, J., Eichler, I., Kuhn, L., Harms, H.K., Von De Hardt, J., Genetic determination of diabetes mellitus in Danish CF patients: Prevalence and late diabetic complications (1994) Acta Paediatr, 83, pp. 72-77Bargon, J., Rickmann, J., Jacobi, V., Straub, R., Arnemann, J., Wagner, T.O., Cystic fibrosis: Initial diagnosis in a 39 year-old patient (2000) Med Klin, 95, pp. 697-700Mitcell-Heggs, P., Mearns, M., Batten, J.C., Cystic fibrosis in adolescents and adults (1976) Quarter J Med New Series, 45, pp. 479-504MarĂłstica, P.J.C., (1995) Avaliação PneumolĂłgica de Pacientes Portadores de Fibrose CĂ­stica: Sua Relação Com Grupos GenĂ©ticos, , [tese]. Porto Alegre, Universidade Federal do Rio Grande do SulDomec Espinoza, M.P.S., (1998) Fibrose CĂ­stica Em Jovens e Adultos Do Hospital Das ClĂ­nicas Da Unicamp, , [dissertação]. Campinas, Universidade Estadual de Campinas;Tauber, E., Eichler, I., Gartner, C., Halmerbauer, G., Gotz, M., Rath, R., Improvements of lung function in cystic fibrosis (2002) Pediatr Pulmonol, 33, pp. 263-268Wang, S.S., O'Leary, L.A., Fitzsimmons, S.C., Khoury, M.J., The impact of early cystic fibrosis on pulmonary function in children (2002) J Pediatr, 141, pp. 804-810Wagener, J.S., Headley, A.A., Cystic fibrosis: Current trends in respiratory care (2003) Respir Care, 48, pp. 234-245Emerson, J., Rosenfeld, M., McNamara, S., Ramsey, B., Gibson, R.L., Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis (2002) Pediatr Pulmonol, 34, pp. 91-100Bush, A., Decisions facing the cystic fibrosis clinician at the first isolation of Pseudomonas aeruginosa (2002) Paediatr Respir Rev, 3, pp. 82-88Merelle, M.E., Nagelkerke, A.F., Lees, C.M., Dezateaux, C., Newborn screening for cystic fibrosis (2001) Cochrane Database Syst Rev, 3, pp. CD001402Farrell, P.M., Li, Z., Kosorok, M.R., Laxova, A., Green, C.G., Collins, J., Bronchopulmonary disease in children with cystic fibrosis after early or delayed diagnosis (2003) Am J Respir Crit Care Med, 168, pp. 1100-1108Lee, D.S., Rosenberg, M.A., Peterson, A., Makholm, L., Hoffman, G., Laessig, R.H., Analysis of the costs of diagnosing cystic fibrosis with a newborn screening program (2003) J Pediatr, 142, pp. 617-623Siret, D., Bretaudeau, G., Branger, B., Dabadie, A., Dagorne, M., David, V., Comparing the clinical evolution of cystic fibrosis screened neonatally to that of cystic fibrosis diagnosed from clinical symptoms: A 10-year retrospective study in a French region (Brittany) (2003) Pediatr Pulmonol, 35, pp. 342-349West, S.E., Zeng, L., Lee, B.L., Kosorok, M.R., Rock, M.J., Splaingard, M.J., Respiratory infections with Pseudomonas aeruginosa in children with cystic fibrosis: Early detection by serology and assessment of risk factors (2002) JAMA, 287, pp. 2958-2967Oliveira, M.C., Reis, F.J., Oliveira, E.A., Colosimo, E.A., Monteiro, A.P., Penna, F.J., Prognostic factors in cystic fibrosis in a single center in Brazil: A survival analysis (2002) Pediatr Pulmonol, 34, pp. 3-10Maclusky, I., Levison, H., Cystic fibrosis (1990) Kendig's Disorders of the Respiratory Tract in Children, pp. 692-729. , Chernick V, Boat TE. Philadelphia: SaundersKerem, E., Reisman, J., Corey, M., Canny, G.J., Levison, H., Prediction of mortality in patients with cystic fibrosis (1992) N Engl J Med, 326, pp. 1187-1191Bolyard, D.R., Sexuality and cystic fibrosis (2001) Am J Matern Child Nurs, 26, pp. 39-41Kulich, M., Rosenfeld, M., Goss, C.H., Wilmott, R., Improved survival among young patients with cystic fibrosis (2003) J Pediatr, 142, pp. 631-636Doull, I.J., Recent advances in cystic fibrosis (2001) Arch Dis Child, 85, pp. 62-66Reis, F.J.C., Camargos, P.A.M., Rocha, S.F., Survival analysis for cystic fibrosis in Minas Gerais State, Brazil (1998) J Trop Pediatr, 44, pp. 329-331Farrell, P.M., Kosorok, M.R., Laxova, A., Shen, G., Nutritional benefits of neonatal screening for cystic fibrosis (1997) N Engl J Med, 337, pp. 963-969Zemel, B.S., Jawad, A.F., FitzSimmons, S., Stallings, V.A., Longitudinal relationship among growth, nutritional status and pulmonary function in children with cystic fibrosis: Analysis of the Cystic Fibrosis Foundation National Patient Registry (2000) J Pediatr, 137, pp. 374-380Schechter, M.S., Shelton, B.J., Margolis, P.A., Fitzsimmons, S.C., The association of socioeconomic status with outcomes in cystic fibrosis in the United States (2001) Am J Respir Crit Care Med, 163, pp. 1331-1337O'Connor, G.T., Quinton, H.B., Kahn, R., Robichaud, P., Maddock, J., Lever, T., Case-mix adjustment for evaluation of mortality in cystic fibrosis (2002) Pediatr Pulmonol, 33, pp. 99-105Huff, D.S., Huang, N.N., Arey, J.B., Atypical cystic fibrosis of the pancreas with normal levels of sweat chloride and minimal pancreatic lesions (1979) J Pediatr, 94, p. 237Stewart, B., Zabner, J., Shuber, A.P., Welsh, M.J., Mccray Jr., P.B., Normal sweat chloride values do not exclude the diagnosis of cystic fibrosis (1995) Am J Respir Crit Care Med, 151, pp. 899-903Desmarquest, P., Feldman, N., Tamalat, A., Boule, M., Fauroux, B., Tournier, G., Genotype analysis and phenotypic manifestations of children with intermediate sweat chloride test results (2000) Chest, 118, pp. 1591-1597Lebecque, P., Leal, T., De Boeck, C., Jaspers, M., Cuppens, H., Cassiman, J., Mutations of the cystic fibrosis gene and intermediate sweat chloride levels in children (2002) Am J Respir Crit Care Med, 165, pp. 757-761Rosentein, B.J., Cuting, G.R., The diagnosis of cystic fibrosis: A consensus statement (1998) J Pediatr, 132, pp. 589-595. , Cystic Fibrosis Foundation Consensus PanelRosentein, B.J., What is a cystic fibrosis diagnosis? (1998) Clin Chest Med, 19, pp. 423-441Ratjen, F., Döring, G., Cystic fibrosis (2003) Lancet, 361, pp. 681-689Burns, J.L., Gibson, R.L., Mcnamara, S., Yim, D., Emerson, J., Rosenfeld, M., Longitudinal assessment of Pseudomonas aeruginosa in young children with cystic fibrosis (2001) J Infect Dis, 183, pp. 444-452Dornelas, E.C., Fernandes, M.I.M., GalvĂŁo, L.C., Silva, G.A., Estudo do quadro pulmonar de pacientes com fibrose cĂ­stica (2000) J Pediatr, 76, pp. 295-299. , Rio JSoni, R., Marks, G., Henry, D.A., Robison, M., Moriaty, C., Parsons, S., Effects of Burkholderia cepacia infection in the clinical course of patients with cystic fibrosis: A pilot study in a Sydney clinic (2002) Respirology, 7, pp. 241-245Jones, A.M., Dodd, M.E., Webb, A.K., Burkholderia cepacia: Current clinical issues, environmental controversies and ethical dilemmas (2001) Eur Respir J, 17, pp. 295-301Lewin, L.O., Byard, P.J., Davis, P.B., Effect of Pseudomonas cepacia colonization on survival and pulmonary function of cystic fibrosis patients (1990) J Clin Epidemiol, 43, pp. 125-131Speert, D.P., Henry, D., Vandamme, P., Corey, M., Mahenthiralingam, E., Epidemiology of Burkholderia cepacea complex in patients with cystic fibrosis, Canada (2002) Emerg Infec Dis, 8, pp. 181-187Raskin, S., Philips III, J.A., Krishnamani, M.R.S., Jones, C., Parker, R.A., Rozov, T., DNA analysis of cystic fibrosis in Brazil by direct PCR amplification from guthrie cards (1993) Am J Med Gen, 46, pp. 665-669Cystic Fibrosis Genetic Analysis Consortium - Population variation of common cystic fibrosis mutations (1994) Human Mutation, 4, pp. 167-177Guilloud-Batalie, M., De Crozes, D., Rault, G., Degioanni, A., Feingold, J., Cystic fibrosis mutations: Report from the French Registry (2000) Hum Hered, 50, pp. 142-145. , The Clinical Centers of the CFSaleh, M.C., Botelli, A., Melano De Botelli, M., Rezzonico, C.A., Argaraña, C.E., Cystic fibrosis: Frequency of delta F508 and G542X mutations in Cordoba, Argentina (1996) Medicina, 56, pp. 14-16. , B. AiresVillarreal, M.T., Chavez, M., Lezana, J.L., Cuevas, F., Carnevale, A., Codova, E., G542X mutation in Mexican cystic fibrosis patients (1996) Clin Genet, 49, pp. 54-56Henry, R.L., Mellis, C.M., Petrovic, L., Mucoid Pseudomonas aeruginosa is a marker of poor survival in cystic fibrosis (1992) Pediatr Pulmonol, 12, pp. 158-161Assis, I., Camargos, P.A.M., Reis, F.J.C., Sulmonett, N., Carneiro, A.P.S., Assessing correlations between spirometry and Shwachman-Kulczycki score in children and adolescents (2003) Pediatr Pulmonol, 36, pp. 305-309Farrell, P.M., Koscik, R.E., Sweat chloride concentrations in infants homozygous or heterozygous for ΔF508 cystic fibrosis (1996) Pediatrics, 97, pp. 524-52

    Numerical simulation of strongly nonlinear and dispersive waves using a Green-Naghdi model

    Full text link
    We investigate here the ability of a Green-Naghdi model to reproduce strongly nonlinear and dispersive wave propagation. We test in particular the behavior of the new hybrid finite-volume and finite-difference splitting approach recently developed by the authors and collaborators on the challenging benchmark of waves propagating over a submerged bar. Such a configuration requires a model with very good dispersive properties, because of the high-order harmonics generated by topography-induced nonlinear interactions. We thus depart from the aforementioned work and choose to use a new Green-Naghdi system with improved frequency dispersion characteristics. The absence of dry areas also allows us to improve the treatment of the hyperbolic part of the equations. This leads to very satisfying results for the demanding benchmarks under consideration

    Portion control tableware differentially impacts eating behaviour in women with and without overweight

    Get PDF
    Portion control tableware has been described as a potentially effective approach for weight management, however the mechanisms by which these tools work remain unknown. We explored the processes by which a portion control (calibrated) plate with visual stimuli for starch, protein and vegetable amounts modulates food intake, satiety and meal eating behaviour. Sixty-five women (34 with overweight/obesity) participated in a counterbalanced cross-over trial in the laboratory, where they self-served and ate a hot meal including rice, meatballs and vegetables, once with a calibrated plate and once with a conventional (control) plate. A subsample of 31 women provided blood samples to measure the cephalic phase response to the meal. Effects of plate type were tested through linear mixed-effect models. Meal portion sizes (mean ± SD) were smaller for the calibrated compared with the control plate (served: 296 ± 69 vs 317 ± 78 g; consumed: 287 ± 71 vs 309 ± 79 g respectively), especially consumed rice (69 ± 24 vs 88 ± 30 g) (p < 0.05 for all comparisons). The calibrated plate significantly reduced bite size (3.4 ± 1.0 vs 3.7 ± 1.0 g; p < 0.01) in all women and eating rate (32.9 ± 9.5 vs 33.7 ± 9.2 g/min; p < 0.05), in lean women. Despite this, some women compensated for the reduced intake over the 8 h following the meal. Pancreatic polypeptide and ghrelin levels increased post-prandially with the calibrated plate but changes were not robust. Plate type had no influence on insulin, glucose levels, or memory for portion size. Meal size was reduced by a portion control plate with visual stimuli for appropriate amounts of starch, protein and vegetables, potentially because of the reduced self-served portion size and the resulting reduced bite size. Sustained effects may require the continued use of the plate for long-term impact

    Incidence and progression of hand osteoarthritis in a large community-based cohort: the Johnston County Osteoarthritis Project

    Get PDF
    Objective: To describe the incidence and progression of radiographic and symptomatic hand osteoarthritis (rHOA and sxHOA) in a large community-based cohort. Design: Data were from the Johnston County OA Project (1999–2015, 12 ± 1.2 years follow-up, age 45+). Participants had bilateral hand radiographs each visit, read for Kellgren–Lawrence grade (KLG) at 30 joints. We defined rHOA as KLG ≄2 in ≄1 joint. SxHOA was defined in a hand/joint with rHOA and self-reported symptoms or tenderness on exam. Incidence was assessed in those without, while progression was assessed in those with, baseline rHOA. Proportions or medians are reported; differences by sex and race were assessed using models appropriate for dichotomous or continuous definitions, additionally adjusted for age, education, body mass index (BMI), and weight change. Results: Of 800 participants (68% women, 32% African American, mean age 60 years), 327 had baseline rHOA and were older, more often white and female, than those without rHOA (n = 473). The incidence of HOA was high, for rHOA (60%) and for sxHOA (13%). Women were more likely than men to have incident HOA, particularly for distal interphalangeal joint radiographic osteoarthritis (DIP rOA) (adjusted odds ratios (aOR) 1.60 95% confidence intervals (95% CI) [1.03, 2.49]) and sxHOA (aOR 2.98 [1.50, 5.91]). Progressive HOA was more similar by sex, although thumb base rOA progressed more frequently in women than in men (aOR 2.56 [1.44, 4.55]). Particularly HOA incidence, but also progression, was more frequent among whites compared with African Americans. Conclusion: This study provides much needed information about the natural history of HOA, a common and frequently debilitating condition, in the general population

    Epidemiological And Genetic Characteristics Associated With The Severity Of Acute Viral Bronchiolitis By Respiratory Syncytial Virus

    Get PDF
    Objective: to assess the epidemiological and genetic factors associated with severity of acute viral bronchiolitis (AVB) by respiratory syncytial virus (RSV). Data source: the key words "bronchiolitis", "risk factor", "genetics" and "respiratory syncytial virus", and all combinations among them were used to perform a search in the PubMed, SciELO, and Lilacs databases, of articles published after the year 2000 that included individuals younger than 2 years of age. Data synthesis: a total of 1,259 articles were found, and their respective summaries were read. Of these, 81 were selected, which assessed risk factors for the severity of AVB, and were read in full; the 60 most relevant studies were included. The epidemiologic factors associated with AVB severity by RSV were prematurity, passive smoking, young age, lack of breastfeeding, chronic lung disease, congenital heart disease, male gender, ethnicity, viral coinfection, low weight at admission, maternal smoking during pregnancy, atopic dermatitis, mechanical ventilation in the neonatal period, maternal history of atopy and/or asthma during pregnancy, season of birth, low socioeconomic status, Down syndrome, environmental pollution, living at an altitude > 2,500 meters above sea level, and cesarean section birth. Conversely, some children with severe AVB did not present any of these risk factors. In this regard, recent studies have verified the influence of genetic factors on the severity of AVB by RSV. Polymorphisms of the TLRs, RANTES, JUN, IFNA5, NOS2, CX3CR1, ILs, and VDR genes have been shown to be associated with more severe evolution of AVB by RSV. Conclusion: the severity of AVB by RSV is a phenomenon that depends on the varying degrees of interaction among epidemiological, environmental, and genetic variables. © 2013 Sociedade Brasileira de Pediatria. Published by Elsevier Editora Ltda. All rights reserved.896531543Chåvez-Bueno, S., Mejías, A., Welliver, R.C., Respiratory syncytial virus bronchiolitis: Current and future strategies for treatment and prophylaxis (2006) Treat Respir Med, 5, pp. 483-494Ogra, P.L., Respiratory syncytial virus: The virus, the disease and the immune response (2004) Paediatr Respir Rev, 5, pp. 119-S126Stockman, L.J., Curns, A.T., Anderson, L.J., Fischer-Langley, G., Respiratory syncytial virus-associated hospitalizations among infants and young children in the United States, 1997-2006 (2012) Pediatr Infect Dis J, 31, pp. 5-9Leader, S., Kohlhase, K., Recent trends in severe respiratory syncytial virus (RSV) among US infants, 1997 to 2000 (2003) J Pediatr, 143, pp. 127-S132Ranmuthugala, G., Brown, L., Lidbury, B.A., Respiratory syncytial virus - The unrecognised cause of health and economic burden among young children in Australia (2011) Commun Dis Intell, 35, pp. 177-184SimÔes, E.A., Carbonell-Estrany, X., Impact of severe disease caused by respiratory syncytial virus in children living in developed countries (2003) Pediatr Infect Dis J, 22, pp. 13-S18. , discussion S18-20Albernaz, E.P., Menezes, A.M., César, J.A., Victora, C.G., Barros, F.C., Halpern, R., Risk factors associated with hospitalization for bronchiolitis in the post-neonatal period (2003) Rev Saude Publica, 37, pp. 485-493Deshpande, S.A., Northern, V., The clinical and health economic burden of respiratory syncytial virus disease among children under 2 years of age in a defined geographical area (2003) Arch Dis Child, 88, pp. 1065-1069Fryzek, J.P., Martone, W.J., Groothuis, J.R., Trends in chronologic age and infant respiratory syncytial virus hospitalization: An 8-year cohort study (2011) Adv Ther, 28, pp. 195-201Sung, C.C., Chi, H., Chiu, N.C., Huang, D.T., Weng, L.C., Wang, N.Y., Viral etiology of acute lower respiratory tract infections in hospitalized young children in Northern Taiwan (2011) J Microbiol Immunol Infect, 44, pp. 184-190García, M.L., Ordobås Gabin, M., Calvo Reya, C., Gonzålez Alvarez, M., Aguilar Ruiz, J., Arregui Sierra, A., Viral infection of the lower respiratory tract in hospitalized infants: Etiology, clinical features and risk factors (2001) An Esp Pediatr, 55, pp. 101-107Riccetto, A.G., Ribeiro, J.D., Silva, M.T., Almeida, R.S., Arns, C.W., Baracat, E.C., Respiratory syncytial virus (RSV) in infants hospitalized for acute lower respiratory tract disease: Incidence and associated risks (2006) Braz J Infect Dis, 10, pp. 357-361Salomão Junior, J.B., Gardinassi, L.G., Simas, P.V., Bittar, C.O., Souza, F.P., Rahal, P., Human respiratory syncytial virus in children hospitalized for acute lower respiratory infection (2011) J Pediatr (Rio J), 87, pp. 219-224Sly, P.D., Jones, C.M., Viral co-detection in infants hospitalized with respiratory disease: Is it important to detect? (2011) J Pediatr (Rio J), 87, pp. 277-280Miller, E.K., Williams, J.V., Gebretsadik, T., Carroll, K.N., Dupont, W.D., Mohamed, Y.A., Host and viral factors associated with severity of human rhinovirus-associated infant respiratory tract illness (2011) J Allergy Clin Immunol, 127, pp. 883-891Nascimento, M.S., Souza, A.V., Ferreira, A.V., Rodrigues, J.C., Abramovici, S., Silva Filho, L.V., High rate of viral identification and coinfections in infants with acute bronchiolitis (2010) Clinics (Sao Paulo), 65, pp. 1133-1137Groothuis, J.R., Fryzek, J.P., Makari, D., Steffey, D., Martone, W.J., Respiratory syncytial virus hospitalization trends in infants with chronic lung disease of infancy, 1998-2008 (2011) Clin Epidemiol, 3, pp. 245-250Gouyon, J.B., Rozé, J.C., Guillermet-Fromentin, C., Glorieux, I., Adamon, L., Di Maio, M., Hospitalizations for respiratory syncytial virus bronchiolitis in preterm infants at < 33 weeks gestation without bronchopulmonary dysplasia: The CASTOR study (2012) Epidemiol Infect, 15, pp. 1-11Semple, M.G., Taylor-Robinson, D.C., Lane, S., Smyth, R.L., Household tobacco smoke and admission weight predict severe bronchiolitis in infants independent of deprivation: Prospective cohort study (2011) PLoS One, 6, p. 22425Koehoorn, M., Karr, C.J., Demers, P.A., Lencar, C., Tamburic, L., Brauer, M., Descriptive epidemiological features of bronchiolitis in a population-based cohort (2008) Pediatrics, 122, pp. 1196-1203Ochoa Sangrador, C., Gonzålez De Dios, J., Idoneidad y Adecuación). Consensus conference on acute bronchiolitis (VI): Prognosis of acute bronchiolitis. Review of scientific evidence (2010) An Pediatr (Barc), 72 (354), pp. e1-3634. , Grupo de Revisión del Proyecto aBREVIADo (BRonquiolitis-Estudio de VariabilidadGrimwood, K., Cohet, C., Rich, F.J., Cheng, S., Wood, C., Redshaw, N., Risk factors for respiratory syncytial virus bronchiolitis hospital admission in New Zealand (2008) Epidemiol Infect, 136, pp. 1333-1341López Guinea, A., Casado Flores, J., Martín Sobrino, M.A., Espínola Docio, B., De La Calle Cabrera, T., Serrano, A., García Teresa, M.A., Severe bronchiolitis. Epidemiology and clinical course of 284 patients (2007) An Pediatr (Barc), 67, pp. 116-122Chan, P.W., Lok, F.Y., Khatijah, S.B., Risk factors for hypoxemia and respiratory failure in respiratory syncytial virus bronchiolitis (2002) Southeast Asian J Trop Med Public Health, 33, pp. 806-810Garcia, C.G., Bhore, R., Soriano-Fallas, A., Trost, M., Chason, R., Ramilo, O., Mejias, A., Risk factors in children hospitalized with RSV bronchiolitis versus non-RSV bronchiolitis (2010) Pediatrics, 126, pp. 1453-e1460Chatzimichael, A., Tsalkidis, A., Cassimos, D., Gardikis, S., Tripsianis, G., Deftereos, S., The role of breastfeeding and passive smoking on the development of severe bronchiolitis in infants (2007) Minerva Pediatr, 59, pp. 199-206Jones, L.L., Hashim, A., McKeever, T., Cook, D.G., Britton, J., Leonardi-Bee, J., Parental and household smoking and the increased risk of bronchitis, bronchiolitis and other lower respiratory infections in infancy: Systematic review and meta-analysis (2011) Respir Res, 12, p. 5Bradley, J.P., Bacharier, L.B., Bonfiglio, J., Schechtman, K.B., Strunk, R., Storch, G., Severity of respiratory syncytial virus bronchiolitis is affected by cigarette smoke exposure and atopy (2005) Pediatrics, 115, pp. 7-e14Hervås, D., Reina, J., Yañez, A., Del Valle, J.M., Figuerola, J., Hervås, J.A., Epidemiology of hospitalization for acute bronchiolitis in children: Differences between RSV and non-RSV bronchiolitis (2012) Eur J Clin Microbiol Infect Dis, 31, pp. 1975-1981Oñoro, G., Pérez Suårez, E., Iglesias Bouzas, M.I., Serrano, A., Martínez De Azagra, A., Severe bronchiolitis. Changes in epidemiology and respiratory support (2011) An Pediatr (Barc), 74, pp. 371-376Damore, D., Mansbach, J.M., Clark, S., Ramundo, M., Camargo Jr., C.A., Prospective multicenter bronchiolitis study: Predicting intensive care unit admissions (2008) Acad Emerg Med, 15, pp. 887-894Papoff, P., Moretti, C., Cangiano, G., Bonci, E., Roggini, M., Pierangeli, A., Incidence and predisposing factors for severe disease in previously healthy term infants experiencing their first episode of bronchiolitis (2011) Acta Paediatr, 100, pp. 17-e23Vidaurreta, S.M., Marcone, D.N., Ellis, A., Ekstrom, J., Cukier, D., Videla, C., Acute viral respiratory infection in children under 5 years: Epidemiological study in two centers in Buenos Aires, Argentina (2011) Arch Argent Pediatr, 109, pp. 296-304Dornelles, C.T., Piva, J.P., Marostica, P.J., Nutritional status, breastfeeding, and evolution of infants with acute viral bronchiolitis (2007) J Health Popul Nutr, 25, pp. 336-343Al-Shehri, M.A., Sadeq, A., Quli, K., Bronchiolitis in Abha, Southwest Saudi Arabia: Viral etiology and predictors for hospital admission (2005) West Afr J Med, 24, pp. 299-304Che, D., Nicolau, J., Bergounioux, J., Perez, T., Bitar, D., Bronchiolitis among infants under 1 year of age in France: Epidemiology and factors associated with mortality (2012) Arch Pediatr, 19, pp. 700-706Fjaerli, H.O., Farstad, T., Bratlid, D., Hospitalisations for respiratory syncytial virus bronchiolitis in Akershus, Norway, 1993-2000: A population-based retrospective study (2004) BMC Pediatr, 4, p. 25Meissner, H.C., Selected populations at increased risk from respiratory syncytial virus infection (2003) Pediatr Infect Dis J, 22, pp. 40-S45Riccetto, A.G., Silva, L.H., Spilki, F.R., Morcillo, A.M., Arns, C.W., Baracat, E.C., Genotypes and clinical data of respiratory syncytial virus and metapneumovirus in Brazilian infants: A new perspective (2009) Braz J Infect Dis, 13, pp. 35-39D'Elia, C., Siqueira, M.M., Portes, S.A., Sant'Anna, C.C., Respiratory syncytial virus - Associated lower respiratory tract infections in hospitalized infants (2005) Rev Soc Bras Med Trop, 38, pp. 7-10Weigl, J.A., Puppe, W., Schmitt, H.J., Variables explaining the duration of hospitalization in children under two years of age admitted with acute airway infections: Does respiratory syncytial virus have a direct impact? (2004) Klin Padiatr, 216, pp. 7-15Brand, H.K., De Groot, R., Galama, J.M., Brouwer, M.L., Teuwen, K., Hermans, P.W., Infection with multiple viruses is not associated with increased disease severity in children with bronchiolitis (2012) Pediatr Pulmonol, 47, pp. 393-400De Paulis, M., Gilio, A.E., Ferraro, A.A., Ferronato, A.E., Do Sacramento, P.R., Botosso, V.F., Severity of viral coinfection in hospitalized infants with respiratory syncytial virus infection (2011) J Pediatr (Rio J), 87, pp. 307-313Jartti, T., Söderlund-Venermo, M., Hedman, K., Ruuskanen, O., MÀkelÀ, M.J., New molecular virus detection methods and their clinical value in lower respiratory tract infections in children (2013) Paediatr Respir Rev, 14, pp. 38-45Carroll, K.N., Gebretsadik, T., Griffin, M.R., Dupont, W.D., Mitchel, E.F., Wu, P., Maternal asthma and maternal smoking are associated with increased risk of bronchiolitis during infancy (2007) Pediatrics, 119, pp. 1104-1112Bloemers, B.L., Van Furth, A.M., Weijerman, M.E., Gemke, R.J., Broers, C.J., Van Den Ende, K., Down syndrome: A novel risk factor for respiratory syncytial virus bronchiolitis - A prospective birth-cohort study (2007) Pediatrics, 120, pp. 1076-e1081Karr, C., Lumley, T., Schreuder, A., Davis, R., Larson, T., Ritz, B., Effects of subchronic and chronic exposure to ambient air pollutants on infant bronchiolitis (2007) Am J Epidemiol, 165, pp. 553-560Choudhuri, J.A., Ogden, L.G., Ruttenber, A.J., Thomas, D.S., Todd, J.K., Simoes, E.A., Effect of altitude on hospitalizations for respiratory syncytial virus infection (2006) Pediatrics, 117, pp. 349-356Moore, H.C., De Klerk, N., Holt, P., Richmond, P.C., Lehmann, D., Hospitalisation for bronchiolitis in infants is more common after elective caesarean delivery (2012) Arch Dis Child, 97, pp. 410-414Thomsen, S.F., Stensballe, L.G., Skytthe, A., Kyvic, K.O., Backer, V., Bisgaard, H., Increased concordance of severe respiratory syncytial virus infection in identical twins (2008) Pediatrics, 121, pp. 493-496Tal, G., Mandelberg, A., Dalal, I., Cesar, K., Somekh, E., Tal, A., Association between common Toll-like receptor 4 mutations and severe respiratory syncytial virus disease (2004) J Infect Dis, 189, pp. 2057-2063Douville, R.N., Lissitsyn, Y., Hirschfeld, A.F., Becker, A.B., Kozyrskyj, A.L., Liem, J., TLR4 Asp299Gly and Thr399Ile polymorphisms: No impact on human immune responsiveness to LPS or respiratory syncytial virus (2010) PLoS One, 5, p. 12087Löfgren, J., Marttila, R., Renko, M., RÀmet, M., Hallman, M., Toll-like receptor 4 Asp299Gly polymorphism in respiratory syncytial virus epidemics (2010) Pediatr Pulmonol, 45, pp. 687-692Mandelberg, A., Tal, G., Naugolny, L., Cesar, K., Oron, A., Houri, S., Lipopolysaccharide hyporesponsiveness as a risk factor for intensive care unit hospitalization in infants with respiratory syncitial virus bronchiolitis (2006) Clin Exp Immunol, 144, pp. 48-52Puthothu, B., Forster, J., Heinzmann, A., Krueger, M., TLR-4 and CD14 polymorphisms in respiratory syncytial virus associated disease (2006) Dis Markers, 22, pp. 303-308Mailaparambil, B., Krueger, M., Heinze, J., Forster, J., Heinzmann, A., Polymorphisms of toll like receptors in the genetics of severe RSV associated diseases (2008) Dis Markers, 25, pp. 59-65Amanatidou, V., Sourvinos, G., Apostolakis, S., Neonaki, P., Tsilimigaki, A., Krambovitis, E., RANTES promoter gene polymorphisms and susceptibility to severe respiratory syncytial virus-induced bronchiolitis (2008) Pediatr Infect Dis J, 27, pp. 38-42Kresfelder, T.L., Janssen, R., Bont, L., Venter, M., Confirmation of an association between single nucleotide polymorphisms in the VDR gene with respiratory syncytial virus related disease in South African children (2011) J Med Virol, 83, pp. 1834-1840Janssen, R., Bont, L., Siezen, C.L., Hodemaekers, H.M., Ermers, M.J., Doornbos, G., Genetic susceptibility to respiratory syncytial virus bronchiolitis is predominantly associated with innate immune genes (2007) J Infect Dis, 196, pp. 826-834Amanatidou, V., Sourvinos, G., Apostolakis, S., Tsilimigaki, A., Spandidos, D.A., T280 M variation of the CX3C receptor gene is associated with increased risk for severe respiratory syncytial virus bronchiolitis (2006) Pediatr Infect Dis J, 25, pp. 410-414Ampuero, S., Luchsinger, V., Tapia, L., Palomino, M.A., Larrañaga, C.E., SP-A1, SP-A2 and SP-D gene polymorphisms in severe acute respiratory syncytial infection in Chilean infants (2011) Infect Genet Evol, 11, pp. 1368-1377Mulet, J.F., Rodríguez De Torres, B.O., Viral induced bronchiolitis and genetics (2010) An Pediatr (Barc), 73, pp. 159-16
    • 

    corecore