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  • 1
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 2005
    In:  Faraday Discussions Vol. 130 ( 2005), p. 89-
    In: Faraday Discussions, Royal Society of Chemistry (RSC), Vol. 130 ( 2005), p. 89-
    Type of Medium: Online Resource
    ISSN: 1359-6640 , 1364-5498
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2005
    detail.hit.zdb_id: 1472891-6
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  • 2
    Online Resource
    Online Resource
    American Speech Language Hearing Association ; 2011
    In:  Journal of Speech, Language, and Hearing Research Vol. 54, No. 1 ( 2011-02)
    In: Journal of Speech, Language, and Hearing Research, American Speech Language Hearing Association, Vol. 54, No. 1 ( 2011-02)
    Abstract: Two Web-based surveys (Surveys I and II) were used to assess perceptions of faculty and students in Communication Sciences and Disorders (CSD) regarding the responsible conduct of research (RCR). Method Survey questions addressed 9 RCR domains thought important to the responsible conduct of research: (a) human subjects protections; (b) research involving animals; (c) publication practices and responsible authorship; (d) mentor/trainee responsibilities; (e) collaborative science; (f) peer review; (g) data acquisition, management, sharing, and ownership; (h) conflicts of interest; and (i) research misconduct. Respondents rated each of 37 topics for importance and for sufficiency of instructional coverage. Results Respondents to Survey I were 137 faculty members from 68 (26%) of the 261 graduate programs in CSD. By comparison, 237 students from 39 (15%) programs responded to Survey II. Data about the importance and sufficiency of coverage of each of the 37 items were transformed into z scores to reveal relative ratings among the 37 topics. Data presentations were grouped for topics in each of the 9 RCR domains. Ratings indicated the relatively high importance assigned among the 37 topics by CSD faculty and students. Sufficiency of coverage of those same topics received lower ratings. Conclusions The results of these surveys support the notion that students in CSD perceive that they are receiving information about RCR. The data pertaining to sufficiency of coverage provide a basis for improving instruction in this important aspect of research education.
    Type of Medium: Online Resource
    ISSN: 1092-4388 , 1558-9102
    Language: English
    Publisher: American Speech Language Hearing Association
    Publication Date: 2011
    detail.hit.zdb_id: 2070420-3
    SSG: 5,2
    SSG: 7,11
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  • 3
    In: Blood, American Society of Hematology, Vol. 120, No. 21 ( 2012-11-16), p. 1605-1605
    Abstract: Abstract 1605 Introduction: Overweight and obesity have been associated with an increased risk of several malignancies. There is mounting evidence that a higher body mass index (BMI) increases the risk of developing non-Hodgkin lymphoma. However, the role of BMI on the incidence of diffuse large B-cell lymphoma (DLBCL) has not been extensively studied. The primary aim of our study is to evaluate the association between BMI and incidence of DLBCL using a meta-analysis of epidemiological studies. Secondary aims are to evaluate such association according to sex and geographical region. Methods: A MEDLINE search through December 2010 was undertaken using (obesity OR “body mass index” OR BMI OR overweight) AND (lymphoma). Only epidemiological studies reporting on the incidence of DLBCL were included. Cross-sectional studies were excluded. Meta-analyses were performed for DLBCL in general, and according to sex and geographical region. The outcome was calculated as odds ratio (OR). Overweight was defined as BMI 25–29.9 kg/m2 and obesity as BMI 30 kg/m2, according to the WHO/CDC criteria. The random effects model (REM) was used to calculate the combined outcome. Heterogeneity was assessed by the I2 statistic. Publication bias was assessed by the trim-and-fill analysis. Meta-regression analyses were performed to evaluate the linear association between BMI as a continuous variable and DLBCL. Literature search and data gathering were performed independently by at least 2 of the investigators. All graphs and calculations were obtained using Comprehensive Meta-Analysis version 2 (Biostat, Englewood, NJ). Results: Our search rendered 13 studies; five case-control studies accounted for 4,399 cases and 22,298 controls, and eight prospective cohort studies accounted for 1,787 cases identified in a cohort of over 1.6 million individuals. Overweight individuals had an OR 1.14 (95% CI 1.04–1.25; p=0.01) of developing DLBCL. The OR of was significant DLBCL in overweight women (OR 1.23, 95% CI 1.07–1.42; p=0.004) but not in men (OR 1.12, 95% CI 0.78–1.60; p=0.55). Odds remained significant for American (OR 1.13, 95% CI 1.02–1.25; p=0.01) and Asian (OR 1.29, 95% CI 1.11– 1.51; p 〈 0.01), but not for European individuals (OR 1.08, 95% CI 0.84–1.38; p=0.56). For obese individuals, the OR of DLBCL was 1.27 (95% CI 1.14–1.41; p 〈 0.01). Obese women had an increased OR 1.24 (95% CI 1.06–1.46; p 〈 0.01) but not men (OR 1.23, 95% CI 0.61–2.46; p=0.57). Odds remained significant in American (OR 1.32, 95% CI 1.18–1.48; p 〈 0.01) and Asian (OR 1.35, 95% CI 1.08–1.68; p=0.01), but not in European population (OR 1.12, 95% CI 0.83– 1.51; p=0.46). Meta-regression analyses showed a relative OR of 1.014 per kg/m2 of BMI with a significant linear association with DLBCL incidence (p 〈 0.01). No linear association was found in women (p=0.76) but there was a trend for men (p=0.07). A linear association was seen in American (p=0.01), there was a trend in Asian (p=0.06) but no association was identified in European individuals (p=0.46). Conclusions: Based on this meta-analysis, an increased BMI is associated with a higher incidence of DLBCL. Such association appears stronger in women and in American and Asian populations. Disclosures: No relevant conflicts of interest to declare.
    Type of Medium: Online Resource
    ISSN: 0006-4971 , 1528-0020
    RVK:
    RVK:
    Language: English
    Publisher: American Society of Hematology
    Publication Date: 2012
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    detail.hit.zdb_id: 80069-7
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  • 4
    In: Thrombosis Research, Elsevier BV, Vol. 134, No. 1 ( 2014-07), p. 90-92
    Type of Medium: Online Resource
    ISSN: 0049-3848
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2014
    detail.hit.zdb_id: 1500780-7
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  • 5
    Online Resource
    Online Resource
    Informa UK Limited ; 2012
    In:  Expert Opinion on Investigational Drugs Vol. 21, No. 3 ( 2012-03), p. 355-361
    In: Expert Opinion on Investigational Drugs, Informa UK Limited, Vol. 21, No. 3 ( 2012-03), p. 355-361
    Type of Medium: Online Resource
    ISSN: 1354-3784 , 1744-7658
    Language: English
    Publisher: Informa UK Limited
    Publication Date: 2012
    detail.hit.zdb_id: 2030114-5
    SSG: 15,3
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  • 6
    In: Clinical Lymphoma Myeloma and Leukemia, Elsevier BV, Vol. 14, No. 2 ( 2014-04), p. 122-130
    Type of Medium: Online Resource
    ISSN: 2152-2650
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2014
    detail.hit.zdb_id: 2540998-0
    detail.hit.zdb_id: 2193618-3
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  • 7
    In: Blood, American Society of Hematology, Vol. 120, No. 21 ( 2012-11-16), p. 3336-3336
    Abstract: Abstract 3336 Introduction: Heparin Induced thrombocytopenia (HIT) is a clinicopathological entity in which thrombocytopenia occurs in temporal relation to the initiation of heparin therapy. The diagnosis is made using clinical criteria and a scoring system (4T) can be applied to assess the probability of the diagnosis. A variety of sensitive tests are available but the most widely applied is an enzyme immunoassay (EIA), which detects and semi-quantifies antibodies of any class to the heparin-PF4 complex. The role of testing is largely supplementary, but recently focus has been placed on the epidemic of HIT overdiagnosis due to overreliance on laboratory tests irrespective of the clinical scenario. A newer EIA can measure the pathogenic IgG antibody only. This study examines the number of patients started on direct thrombin inhibitor (DTI) therapy for a presumptive diagnosis of HIT prior to the implementation of the IgG antibody and after its introduction at one large academic tertiary care center. Methods: All patients placed on the DTIs argatroban and lepirudin between October 2006-May 2009 in the pre IgG subtype antibody period and May 2009-February 2012 in the post IgG subtype period for a presumptive diagnosis of HIT were identified. Demographic data including age, sex, and primary service were recorded. All HIT antibody (Ab) immunoglobulin class EIA and IgG specific EIA optical density were recorded, as available. 4T criteria and rates of thrombosis were assessed retrospectively. Incidence of WHO Grade III (requiring transfusion) or IV (life threatening) bleeding was documented. Chi Square, Mann Whitney U, and Fisher's exact tests were used as appropriate for statistical analysis. Results: 89 patients pre availability of the IgG EIA assay and 100 patients post availability of the IgG EIA assay met inclusion criteria and were evaluated. Groups were matched in terms of sex and 4T pretest probability distribution as well as rates of thrombosis. Patients post IgG EIA availability were older and had lower mean total HIT Ab optical densities. Post IgG EIA patients were treated with DTI therapy 5 days less, which was statistically significant. The incidence of Grade III and IV bleeding episodes, however, was statistically similar between groups. In the pre IgG EIA group, 7 bleeds (4 Grade III, 3 Grade IV) occurred in patients with low pretest probability for HIT based on 4T criteria. In the post IgG EIA group, 8 bleeds (5 Grade III, 3 Grade IV) occurred in patients with low pretest probability for HIT based on 4T criteria. Conclusion: Implementation of the IgG HIT EIA resulted in a decrease in the number of days on a DTI without an observed change in serious bleeding events, indicating that such bleeding occurs early after initiation of DTI therapy. Further, patients pre and post availability of the IgG EIA were started on DTI therapy despite a low pretest clinical risk for HIT. The use of a test with a shorter turn-around time to exclude HIT or more rigorous enforcement of clinical guidelines will be required to minimize misdiagnosis and avoid therapy related morbidity. Disclosures: No relevant conflicts of interest to declare.
    Type of Medium: Online Resource
    ISSN: 0006-4971 , 1528-0020
    RVK:
    RVK:
    Language: English
    Publisher: American Society of Hematology
    Publication Date: 2012
    detail.hit.zdb_id: 1468538-3
    detail.hit.zdb_id: 80069-7
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  • 8
    In: Journal of Speech, Language, and Hearing Research, American Speech Language Hearing Association, Vol. 54, No. 1 ( 2011-02)
    Abstract: The purpose of this 2-part study was to determine the importance of specific topics relating to publication ethics and adequacy of the American Speech-Language-Hearing Association’s (ASHA’s) policies regarding these topics. Method A 56-item Web-based survey was sent to (a) ASHA journal editors, associate editors, and members of the Publications Board (Group 1); (b) authors, reviewers, and members of ASHA’s Board of Ethics (Group 2); and (c) a random sample of the ASHA membership, characterized as journal readers (Group 3). The survey contained 4 questions related to ethical principles associated with the publication of research: (a) In regard to scientific integrity in research publications in general, how important is the issue of [topic]? (b) Should ASHA publication policies address this issue? (c) Do ASHA policies address this issue? (d) If yes, how adequately do ASHA policies address this issue? A second study evaluated the contents of ASHA’s publication policy documents in regard to their coverage of the survey topics. Results Results indicated many of the topics deemed most important by all groups were included in ASHA’s publication policy documents; other topics, although included, were not adequately addressed. Conclusions ASHA needs a single, unifying publication policy document, and increased education of all groups in the realm of ethics in the publication process is indicated.
    Type of Medium: Online Resource
    ISSN: 1092-4388 , 1558-9102
    Language: English
    Publisher: American Speech Language Hearing Association
    Publication Date: 2011
    detail.hit.zdb_id: 2070420-3
    SSG: 5,2
    SSG: 7,11
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  • 9
    In: Blood, American Society of Hematology, Vol. 118, No. 21 ( 2011-11-18), p. 5198-5198
    Abstract: Abstract 5198 Introduction: Lymphoma is a common hematologic malignancy, etiology of which remains largely unclear. Obesity and overweight have been associated with an increased risk of developing lymphoma; however, with conflicting results. The main objective of this meta-analysis is to evaluate the potential relationship that overweight and obesity may have in the development of lymphoma in adults. A secondary objective was to evaluate the risk of separate lymphoma subtypes, such as Hodgkin lymphoma (HL), and non-Hodgkin lymphoma (NHL) and the most common NHL subtypes – diffuse large B-cell lymphoma (DLBCL) and follicular lymphoma (FL) – in overweight and obese individuals. Methods: A MEDLINE search from January 1950 to December 2010 was undertaken using: (obesity OR “body mass index” OR BMI OR overweight) AND (leukemia OR lymphoma OR myeloma). Only prospective cohort studies reporting on the incidence of lymphoma were included. Retrospective case-control and cross-sectional studies were excluded. Meta-analyses were performed for HL, NHL and NHL subtypes. The outcome was calculated as relative risk (RR). Overweight was defined as body mass index (BMI) 25–29.9 kg/m2 and obesity as BMI ≥30 kg/m2, according to the WHO criteria. The quality of the studies was determined by the Newcastle-Ottawa scale (NOS). The random effects model was used to calculate the combined outcome. Heterogeneity was assessed by the I2 statistic. Publication bias was assessed by the trim-and-fill analysis. Meta-regression analyses were performed to evaluate the association between BMI, as a continuous variable, and the incidence of HL and NHL in general and NHL subtypes. Literature search, data gathering and study quality assessment were performed independently by at least two of the investigators. All graphs and calculations were obtained using Comprehensive Meta-Analysis version 2 (Biostat, Englewood, NJ). Results: From 758 returns, 22 prospective cohort studies evaluating the association between obesity and lymphoma were identified. All the studies were of high quality (NOS 〉 7 points). For NHL, the overall RR was 1.06 (95% CI 1.02–1.10; p=0.001). For overweight and obese patients, the RR were 1.04 (95% CI 1.01–1.07; p=0.02) and 1.11 (95% CI 1.06–1.16; p 〈 0.001), respectively. Meta-regression showed a linear association between BMI and incidence of NHL (p 〈 0.001). For DLBCL, the overall RR was 1.14 (95% CI 1.01–1.29; p=0.03). Overweight and obese patients had a RR of 1.08 (95% CI 0.96–1.22; p=0.22) and 1.24 (95% CI 1.08–1.44; p=0.003), respectively. Meta-regression showed a trend towards a significant association between BMI and incidence of DLBCL (p=0.1). For FL, the overall RR was 1.11 (95% CI 0.99–1.25; p=0.08). Overweight and obese patients had a RR of 1.10 (95% CI 0.94–1.28; p=0.25) and 1.15 (95% CI 0.97–1.36; p=0.11), respectively. Meta-regression showed no association between BMI and incidence of FL (p=0.78). For HL, the overall RR was 1.10 (95% CI 0.97–1.26; p=0.15). Overweight and obese patients had a RR of 0.91 (95% CI 0.80–1.03; p=0.13) and 1.23 (95% CI 1.05–1.44; p=0.009), respectively. Meta-regression showed a statistically significant linear relationship between BMI and incidence of HL (p=0.009). Conclusions: Obesity was associated with a mild increased risk of developing HL (23%), NHL in general (11%) and DLBCL (24%), but there was no association with FL. There was a statistically significant linear association between BMI and HL as well as for NHL in general, but only a trend towards an association with DLBCL. Disclosures: Castillo: GlaxoSmithKline: Research Funding; Millennium Pharmaceuticals: Research Funding.
    Type of Medium: Online Resource
    ISSN: 0006-4971 , 1528-0020
    RVK:
    RVK:
    Language: English
    Publisher: American Society of Hematology
    Publication Date: 2011
    detail.hit.zdb_id: 1468538-3
    detail.hit.zdb_id: 80069-7
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  • 10
    In: Blood, American Society of Hematology, Vol. 118, No. 21 ( 2011-11-18), p. 3588-3588
    Abstract: Abstract 3588 Introduction: Leukemia is a common hematologic malignancy for which the etiology remains largely unclear. The epidemiological data regarding the link between overweight and obesity, as defined by body mass index (BMI), and the risk of developing leukemia has revealed conflicting results. The main objective of this meta-analysis is to evaluate the potential relationship that overweight and obesity may have in the development of leukemia in adults. A secondary objective was to evaluate the risk of separate leukemia subtypes such as acute myeloid leukemia (AML), acute lymphoblastic leukemia (ALL), chronic myeloid leukemia (CML) and chronic lymphocytic leukemia (CLL). Methods: A MEDLINE search from January 1950 to December 2010 was undertaken using: (obesity OR “body mass index” OR BMI OR overweight) AND (leukemia OR lymphoma OR myeloma). Only prospective cohort studies reporting on the incidence of leukemia were included. Retrospective case-control and cross-sectional studies were excluded. Meta-analyses were performed for leukemia in general and leukemia subtypes. The outcome was calculated as relative risk (RR). Overweight was defined as BMI 25–29.9 kg/m2 and obesity as BMI ≥30 kg/m2, according to the WHO criteria. The quality of the studies was determined by the Newcastle-Ottawa scale (NOS). The random effects model (REM) was used to calculate the combined outcome. Heterogeneity was assessed by the I2 statistic. Publication bias was assessed by the trim-and-fill analysis. Meta-regression analyses were performed to evaluate the association between BMI, as a continuous variable, and the incidence of leukemia in general as well as BMI and leukemia subtypes. Literature search, data gathering and quality assessment were performed independently by at least 2 of the investigators. All graphs and calculations were obtained using Comprehensive Meta-Analysis version 2 (Biostat, Englewood, NJ). Results: From 758 returns, 19 prospective cohort studies evaluating the association between incidence of leukemia and BMI were identified. All the studies were of high quality (NOS 〉 7 points). When pooling all studies, the RR was 1.14 (95% CI 1.07–1.22; p 〈 0.001). Overweight patients had a RR of 1.11 (95% CI 1.06–1.17; p 〈 0.001), and obese patients had a RR of 1.19 (95% CI 1.09–1.31; p 〈 0.001). Meta-regression showed linear association between BMI and leukemia (p 〈 0.001). For AML, the overall RR was 1.24 (95% 1.10–1.41; p=0.001). Overweight patients had RR of 1.08 (95% CI 0.97–1.20; p=0.18). Obese patients had RR of 1.38 (95% CI 1.15–1.67; p=0.001; Figure). Meta-regression showed a statistically significant linear association between BMI and incidence of AML (p 〈 0.001). For ALL, the overall RR was 1.48 (95% CI 1.20–1.80; p 〈 0.001). Overweight patients had RR of 1.36 (95% CI 1.06–1.76; p=0.02). Obese patients had RR of 1.62 (95% CI 1.13–2.32; p=0.009). Meta-regression showed no association between BMI and incidence of ALL (p=0.25). For CML, the RR was 1.20 (95% CI 1.02–1.41; p=0.03). Overweight and obese patients had RR of 1.05 (95% CI 0.74–1.49; p=0.79) and 1.27 (95% CI 1.10–1.46; p=0.001), respectively. Meta-regression showed no association between BMI and CML (p=0.15). For CLL, the overall RR was 1.13 (95% CI 1.07–1.19; p 〈 0.001). Overweight and obese patients had RR of 1.09 (95% CI 1.03–1.16; p=0.003) and 1.17 (95% CI 1.09–1.25; p 〈 0.001). Meta-regression showed a trend towards a linear association between BMI and incidence of CLL (p=0.06). Conclusions: Obesity, but not overweight, is associated with a mild-to-moderate increased risk of leukemia in general (19%) and for all leukemia subtypes (AML 38%, ALL 62%, CML 27% and CLL 17%). Additionally, meta-regression analyses showed a statistically significant linear association between increasing BMI and general incidence of leukemia in addition to incidence of AML. Disclosures: No relevant conflicts of interest to declare.
    Type of Medium: Online Resource
    ISSN: 0006-4971 , 1528-0020
    RVK:
    RVK:
    Language: English
    Publisher: American Society of Hematology
    Publication Date: 2011
    detail.hit.zdb_id: 1468538-3
    detail.hit.zdb_id: 80069-7
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