LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 5 of total 5

Search options

  1. Article ; Online: Assessment of Resident Knowledge in Pediatric Rheumatology.

    Guglielmo-Roxby, Tiffany / Louissaint, Valerie / Ettinger, Abigail / Llanos, Adana / Cahill, Ellen / Chefitz, Dalya / Boneparth, Alexis / Amato, Indira / Moorthy, Lakshmi Nandini

    Global pediatric health

    2021  Volume 8, Page(s) 2333794X211062020

    Abstract: Pediatric Rheumatic illnesses are complex, chronic, and often multi-systemic. Our goal was to assess the efficacy of 2 standardized pediatric rheumatology lectures, administered to pediatric residents, in improving the pediatric residents' knowledge and ... ...

    Abstract Pediatric Rheumatic illnesses are complex, chronic, and often multi-systemic. Our goal was to assess the efficacy of 2 standardized pediatric rheumatology lectures, administered to pediatric residents, in improving the pediatric residents' knowledge and confidence in pediatric rheumatology. Two lectures, 1 hour each, were delivered by 2 residents and given 1 week apart to 28 pediatric residents. Pre- and post-tests assessed knowledge and residents' self-rated competence. Change in knowledge was assessed using paired
    Language English
    Publishing date 2021-12-17
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2785531-4
    ISSN 2333-794X ; 2333-794X
    ISSN (online) 2333-794X
    ISSN 2333-794X
    DOI 10.1177/2333794X211062020
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article: Poststreptococcal reactive arthritis in children: a retrospective study.

    Moorthy, Lakshmi Nandini / Gaur, Sunanda / Peterson, Margaret G / Landa, Yanetsi Flores / Tandon, Mandvi / Lehman, Thomas J

    Clinical pediatrics

    2009  Volume 48, Issue 2, Page(s) 174–182

    Abstract: The duration of treatment and appropriate guidelines for antibiotic prophylaxis for children with poststreptococcal reactive arthritis (PSRA) have not been determined. The authors performed a retrospective chart review of 40 children with PSRA and ... ...

    Abstract The duration of treatment and appropriate guidelines for antibiotic prophylaxis for children with poststreptococcal reactive arthritis (PSRA) have not been determined. The authors performed a retrospective chart review of 40 children with PSRA and examined their clinical features at initial evaluation and at 6, 12, and 24 months. At baseline, 18% (n = 7) had a finding noted on the echocardiogram. Although most patients developed cardiac findings early on in the course of their disease, 2 patients with a normal baseline echocardiogram may have developed findings after 12 months of follow-up. The mean duration of prophylaxis was 22 months. During the follow-up period, there was improvement in Physician's Global Assessment, number of patients with arthralgia, tender and swollen joints, erythrocyte sedimentation rate, anti-streptolysin O, and anti-DNAse B antibody titers. The authors conclude that marked improvement in clinical features and laboratory values was seen over time. Patients may benefit with long-term cardiac follow-up.
    MeSH term(s) Arthritis, Reactive/drug therapy ; Arthritis, Reactive/immunology ; Arthritis, Reactive/microbiology ; Child ; Cohort Studies ; Echocardiography ; Electrocardiography ; Ethnic Groups ; Female ; Heart Diseases/diagnosis ; Humans ; Male ; Retrospective Studies ; Streptococcal Infections/drug therapy
    Language English
    Publishing date 2009-03
    Publishing country United States
    Document type Journal Article
    ZDB-ID 207678-0
    ISSN 1938-2707 ; 0009-9228
    ISSN (online) 1938-2707
    ISSN 0009-9228
    DOI 10.1177/0009922808330107
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  3. Article ; Online: Efficacy of an Interinstitutional Mentoring Program Within Pediatric Rheumatology.

    Moorthy, Lakshmi Nandini / Muscal, Eyal / Riebschleger, Meredith / Klein-Gitelman, Marisa / Nigrovic, Lise E / Horon, Jeffrey R / Rouster-Stevens, Kelly / Ferguson, Polly J / Eberhard, B Anne / Brunner, Hermine I / Prahalad, Sampath / Schneider, Rayfel / Nigrovic, Peter A

    Arthritis care & research

    2015  Volume 68, Issue 5, Page(s) 645–651

    Abstract: Objective: The small size of many pediatric rheumatology programs translates into limited mentoring options for early career physicians. To address this problem, the American College of Rheumatology (ACR) and the Childhood Arthritis and Rheumatology ... ...

    Abstract Objective: The small size of many pediatric rheumatology programs translates into limited mentoring options for early career physicians. To address this problem, the American College of Rheumatology (ACR) and the Childhood Arthritis and Rheumatology Research Alliance (CARRA) developed a subspecialty-wide interinstitutional mentoring program, the ACR/CARRA Mentoring Interest Group (AMIGO). We sought to assess the impact of this program on mentoring within pediatric rheumatology.
    Methods: In a longitudinal 3-year study, participant ratings from the AMIGO pilot program were compared with those after the program was opened to general enrollment. Access to mentoring as a function of career stage was assessed by surveys of the US and Canadian pediatric rheumatologists in 2011 and 2014, before and after implementation of AMIGO.
    Results: Participants in the pilot phase (19 dyads) and the general implementation phase (112 dyads) reported comparable success in establishing mentor contact, suitability of mentor-mentee pairing, and benefit with respect to career development, scholarship, and work-life balance. Community surveys showed that AMIGO participation as mentee was high among fellows (86%) and modest among junior faculty (31%). Implementation correlated with significant gains in breadth of mentorship and in overall satisfaction with mentoring for fellows but not junior faculty.
    Conclusion: AMIGO is a career mentoring program that serves most fellows and many junior faculty in pediatric rheumatology across the US and Canada. Program evaluation data confirm that a subspecialty-wide interinstitutional mentoring program is feasible and can translate into concrete improvement in mentoring, measurable at the level of the whole professional community.
    MeSH term(s) Adult ; Canada ; Child ; Feasibility Studies ; Fellowships and Scholarships/methods ; Female ; Humans ; Interinstitutional Relations ; Longitudinal Studies ; Male ; Mentoring/methods ; Mentors/psychology ; Pediatrics/education ; Pediatrics/methods ; Physicians/psychology ; Pilot Projects ; Program Evaluation ; Rheumatology/education ; Rheumatology/methods ; Surveys and Questionnaires ; United States
    Language English
    Publishing date 2015-09-09
    Publishing country United States
    Document type Evaluation Studies ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 645059-3
    ISSN 2151-4658 ; 0893-7524 ; 2151-464X
    ISSN (online) 2151-4658
    ISSN 0893-7524 ; 2151-464X
    DOI 10.1002/acr.22732
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  4. Article ; Online: Physical function assessment tools in pediatric rheumatology.

    Moorthy, Lakshmi Nandini / Peterson, Margaret Ge / Harrison, Melanie J / Onel, Karen B / Lehman, Thomas Ja

    Pediatric rheumatology online journal

    2008  Volume 6, Page(s) 9

    Abstract: Pediatric rheumatic diseases with predominant musculoskeletal involvement such as juvenile idiopathic arthritis (JIA) and juvenile dermatomyositis(JDM) can cause considerable physical functional impairment and significantly affect the children's quality ... ...

    Abstract Pediatric rheumatic diseases with predominant musculoskeletal involvement such as juvenile idiopathic arthritis (JIA) and juvenile dermatomyositis(JDM) can cause considerable physical functional impairment and significantly affect the children's quality of life (QOL). Physical function, QOL, health-related QOL (HRQOL) and health status are personal constructs used as outcomes to estimate the impact of these diseases and often used as proxies for each other. The chronic, fluctuating nature of these diseases differs within and between patients, and complicates the measurement of these outcomes. In children, their growing needs and expectations, limited use of age-specific questionnaires, and the use of proxy respondents further influences this evaluation. This article will briefly review the different constructs inclusive of and related to physical function, and the scales used for measuring them. An understanding of these instruments will enable assessment of functional outcome in clinical studies of children with rheumatic diseases, measure the impact of the disease and treatments on their lives, and guide us in formulating appropriate interventions.
    Language English
    Publishing date 2008-06-04
    Publishing country England
    Document type Journal Article
    ZDB-ID 2279468-2
    ISSN 1546-0096 ; 1546-0096
    ISSN (online) 1546-0096
    ISSN 1546-0096
    DOI 10.1186/1546-0096-6-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  5. Article: Health related quality of life measure in systemic pediatric rheumatic diseases and its translation to different languages: an international collaboration.

    Moorthy, Lakshmi Nandini / Roy, Elizabeth / Kurra, Vamsi / Peterson, Margaret G E / Hassett, Afton L / Lehman, Thomas J A / Scott, Christiaan / El-Ghoneimy, Dalia / Saad, Shereen / El Feky, Reem / Al-Mayouf, Sulaiman / Dolezalova, Pavla / Malcova, Hana / Herlin, Troels / Nielsen, Susan / Wulffraat, Nico / van Royen, Annet / Marks, Stephen D / Belot, Alexandre /
    Brunner, Jurgen / Huemer, Christian / Foeldvari, Ivan / Horneff, Gerd / Saurenman, Traudel / Schroeder, Silke / Pratsidou-Gertsi, Polyxeni / Trachana, Maria / Uziel, Yosef / Aggarwal, Amita / Constantin, Tamas / Cimaz, Rolando / Giani, Theresa / Cantarini, Luca / Falcini, Fernanda / Manzoni, Silvia Magni / Ravelli, Angelo / Rigante, Donato / Zulian, Fracnceso / Miyamae, Takako / Yokota, Shumpei / Sato, Juliana / Magalhaes, Claudia S / Len, Claudio A / Appenzeller, Simone / Knupp, Sheila Oliveira / Rodrigues, Marta Cristine / Sztajnbok, Flavio / de Almeida, Rozana Gasparello / de Jesus, Adriana Almeida / de Arruda Campos, Lucia Maria / Silva, Clovis / Lazar, Calin / Susic, Gordana / Avcin, Tadej / Cuttica, Ruben / Burgos-Vargas, Ruben / Faugier, Enrique / Anton, Jordi / Modesto, Consuelo / Vazquez, Liza / Barillas, Lilliana / Barinstein, Laura / Sterba, Gary / Maldonado, Irama / Ozen, Seza / Kasapcopur, Ozgur / Demirkaya, Erkan / Benseler, Susa

    Pediatric rheumatology online journal

    2014  Volume 12, Page(s) 49

    Abstract: Background: Rheumatic diseases in children are associated with significant morbidity and poor health-related quality of life (HRQOL). There is no health-related quality of life (HRQOL) scale available specifically for children with less common rheumatic ...

    Abstract Background: Rheumatic diseases in children are associated with significant morbidity and poor health-related quality of life (HRQOL). There is no health-related quality of life (HRQOL) scale available specifically for children with less common rheumatic diseases. These diseases share several features with systemic lupus erythematosus (SLE) such as their chronic episodic nature, multi-systemic involvement, and the need for immunosuppressive medications. HRQOL scale developed for pediatric SLE will likely be applicable to children with systemic inflammatory diseases.
    Findings: We adapted Simple Measure of Impact of Lupus Erythematosus in Youngsters (SMILEY©) to Simple Measure of Impact of Illness in Youngsters (SMILY©-Illness) and had it reviewed by pediatric rheumatologists for its appropriateness and cultural suitability. We tested SMILY©-Illness in patients with inflammatory rheumatic diseases and then translated it into 28 languages. Nineteen children (79% female, n=15) and 17 parents participated. The mean age was 12±4 years, with median disease duration of 21 months (1-172 months). We translated SMILY©-Illness into the following 28 languages: Danish, Dutch, French (France), English (UK), German (Germany), German (Austria), German (Switzerland), Hebrew, Italian, Portuguese (Brazil), Slovene, Spanish (USA and Puerto Rico), Spanish (Spain), Spanish (Argentina), Spanish (Mexico), Spanish (Venezuela), Turkish, Afrikaans, Arabic (Saudi Arabia), Arabic (Egypt), Czech, Greek, Hindi, Hungarian, Japanese, Romanian, Serbian and Xhosa.
    Conclusion: SMILY©-Illness is a brief, easy to administer and score HRQOL scale for children with systemic rheumatic diseases. It is suitable for use across different age groups and literacy levels. SMILY©-Illness with its available translations may be used as useful adjuncts to clinical practice and research.
    MeSH term(s) Adolescent ; Antirheumatic Agents/therapeutic use ; Child ; Child, Preschool ; Feasibility Studies ; Female ; Humans ; Immunosuppressive Agents/therapeutic use ; International Cooperation ; Language ; Male ; Psychometrics ; Quality of Life/psychology ; Research Design ; Rheumatic Diseases/drug therapy ; Rheumatic Diseases/psychology ; Surveys and Questionnaires ; Translating ; Treatment Outcome
    Chemical Substances Antirheumatic Agents ; Immunosuppressive Agents
    Language English
    Publishing date 2014
    Publishing country England
    Document type Evaluation Studies ; Journal Article
    ZDB-ID 2279468-2
    ISSN 1546-0096
    ISSN 1546-0096
    DOI 10.1186/1546-0096-12-49
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

To top