Citations

Showing 10 of 107966 citations.

Adult Ewing Sarcoma: Survival and Local Control Outcomes in 102 Patients with Localized Disease
Robinson, Steven I. , Okuno, Scott H. , Rose, Peter S. , Ahmed, Safia K. , Laack, Nadia N. , Robinson, Steven I

Mayo Clinic

Sarcoma | June 11, 2013 | Volume: 2013 | Issue: No issue available | Pages: 1-7

10.1155/2013/681425 | PMID 23840168 Get It

Objectives. To assess the clinical features and local control (LC) outcomes in adult patients with localized Ewing Sarcoma (ES).Methods. The records of 102 ES patients with localized disease ≥18 years of age seen from 1977 to 2007 were reviewed. Factors relevant to prognosis, survival, and LC were analyzed.Results.The 5-year overall survival (OS) and event-free survival (EFS) were 60% and 52%, respectively, for the entire cohort. Treatment era (1977–1992 versus 1993–2007) remained an independent prognostic factor for OS on multivariate analysis, with improved outcomes observed in the 1993–2007 era (P=0.02). The 5-year OS and EFS for the 1993–2007 era were 73% and 60%, respectively. Ifosfamide and etoposide based chemotherapy and surgery were more routinely used in the 1993–2007 era (P<0.01). The 5-year local failure rate (LFR) was 14%, with a 5-year LFR of 18% for surgery, 33% for radiation, and 0% for combined surgery and radiation in the 1993–2007 era (P=0.17).Conclusion. Modern survival outcomes for adults with localized ES are similar to multi-institutional results in children. This improvement over time is associated with treatment intensification with chemotherapy and increased use of surgery. Aggressive LC (combined surgery and radiation) may improve outcomes in poor prognosis patients.
The Science and Ethics of Withdrawing Mechanical Positive Pressure Ventilatory Support in the Terminally Ill
Rady, Mohamed Y. , Verheijde, Joseph L.

Mayo Clinic

Journal of Palliative Medicine | June 11, 2013 | Volume: 16 | Issue: 8 | Pages: 828-830

10.1089/jpm.2013.0166 | PMID 23758501 Get It

Simulation training for breast and pelvic physical examination: a systematic review and meta‐analysis
Dilaveri, CA, Szostek, JH, Wang, AT, Cook, DA

Mayo Clinic

BJOG: An International Journal of Obstetrics & Gynaecology | June 11, 2013 | Volume: 120 | Issue: 10 | Pages: 1171-1182

10.1111/1471-0528.12289 | PMID 23750657 Get It

BackgroundBreast and pelvic examinations are challenging intimate examinations. Technology‐based simulation may help to overcome these challenges.ObjectiveTo synthesise the evidence regarding the effectiveness of technology‐based simulation training for breast and pelvic examination.Search strategyOur systematic search included MEDLINE, EMBASE, CINAHL, PsychINFO, Scopus, and key journals and review articles; the date of the last search was January 2012.Selection criteriaOriginal research studies evaluating technology‐enhanced simulation of breast and pelvic examination to teach learners, compared with no intervention or with other educational activities.Data collection and analysisThe reviewers evaluated study eligibility and abstracted data on methodological quality, learners, instructional design, and outcomes, and used random‐effects models to pool weighted effect sizes.Main resultsIn total, 11 272 articles were identified for screening, and 22 studies were eligible, enrolling 2036 trainees. In eight studies comparing simulation for breast examination training with no intervention, simulation was associated with a significant improvement in skill, with a pooled effect size of 0.86 (95% CI 0.52–1.19; P < 0.001). Four studies comparing simulation training for pelvic examination with no intervention had a large and significant benefit, with a pooled effect size of 1.18 (95% CI 0.40–1.96; P = 0.003). Among breast examination simulation studies, dynamic models providing feedback were associated with improved outcomes. In pelvic examination simulation studies, the addition of a standardised patient to the simulation model and the use of an electronic model with enhanced feedback improved outcomes.Author's conclusionsIn comparison with no intervention, breast and pelvic examination simulation training is associated with moderate to large effects for skills outcomes. Enhanced feedback appears to improve learning.
Genomic Association Analysis of Common Variants Influencing Antihypertensive Response to Hydrochlorothiazide
Boerwinkle, Eric , O’Connell, Jeffrey R. , Bailey, Kent R. , Chapman, Arlene B. , McDonough, Caitrin W. , Beitelshees, Amber L. , Schwartz, Gary L. , Gums, John G. , Padmanabhan, Sandosh , Hiltunen, Timo P. , Citterio, Lorena , Donner, Kati , Hedner, Thomas, Lanzani, Chiara , Melander, Olle , Saarela, Janna , Wahlstrand, Björn, Manunta, Paolo , Kontula, Kimmo , Dominiczak, Anna F. , Johnson, Julie A. , Beitelshees, Amber L. , Turner, Stephen T. , Gong, Yan , Chapman, Arlene B. , Ripatti, Samuli , Cooper‐DeHoff, Rhonda M. , Padmanabhan, Sandosh , Dominiczak, Anna F.

Mayo Clinic

Hypertension | June 11, 2013 | Volume: 62 | Issue: 2 | Pages: 391-397

10.1161/hypertensionaha.111.00436 | PMID 23753411 Get It

To identify novel genes influencing blood pressure response to thiazide diuretic therapy for hypertension, we conducted genome-wide association meta-analyses of ≈1.1 million single-nucleotide polymorphisms in a combined sample of 424 European Americans with primary hypertension treated with hydrochlorothiazide from the Pharmacogenomic Evaluation of Antihypertensive Responses study (n=228) and the Genetic Epidemiology of Responses to Antihypertensive study (n=196). Polymorphisms associated with blood pressure response at P <10 –5 were tested for replication of the associations in independent samples of hydrochlorothiazide-treated European hypertensives. The rs16960228 polymorphism in protein kinase C, α replicated for same-direction association with diastolic blood pressure response in the Nordic Diltiazem study (n=420) and the Genetics of Drug Responsiveness in Essential Hypertension study (n=206), and the combined 4-study meta-analysis P value achieved genome-wide significance ( P =3.3×10 −8 ). Systolic or diastolic blood pressure responses were consistently greater in carriers of the rs16960228 A allele than in GG homozygotes (>4/4 mm Hg) across study samples. The rs2273359 polymorphism in the GNAS-EDN3 region also replicated for same-direction association with systolic blood pressure response in the Nordic Diltiazem study, and the combined 3-study meta-analysis P value approached genome-wide significance ( P =5.5×10 −8 ). The findings document clinically important effects of genetic variation at novel loci on blood pressure response to a thiazide diuretic, which may be a basis for individualization of antihypertensive drug therapy and identification of new drug targets.
Vascular Access Site Injury After Transfemoral Transcatheter Aortic Valve Insertion
Greason, Kevin L. , Suri, Rakesh M. , Huebner, Marianne , Reeder, Guy S., Williamson, Eric E. , Rihal, Charanjit S. , Mathew, Verghese, Nkomo, Vuyisile T. , Rihal, Charanjit S.

Mayo Clinic

Journal of Cardiac Surgery | June 11, 2013 | Volume: 28 | Issue: 4 | Pages: 348-352

10.1111/jocs.12140 | PMID 23750934 Get It

Online Problem-Solving Therapy for Executive Dysfunction After Child Traumatic Brain Injury
Kurowski, Brad G. , Wade, Shari L. , Kirkwood, Michael W. , Brown, Tanya M. , Stancin, Terry , Taylor, Hudson Gerry

Mayo Clinic

Pediatrics | June 11, 2013 | Volume: 132 | Issue: 1 | Pages: e158-e166

10.1542/peds.2012-4040 | PMID 23753094 Get It

OBJECTIVE: Executive dysfunction after traumatic brain injury (TBI) in children is common and leads to significant problems in functioning across multiple settings. The objective of this study was to evaluate the efficacy of a web-based counselor-assisted problem solving (CAPS) intervention compared with an Internet resource comparison (IRC) for treatment of executive dysfunction within 12 months after complicated mild to severe TBI in adolescents. We hypothesized that CAPS would significantly improve parent ratings of executive dysfunction compared with an IRC. METHODS: Participants included 132 adolescents aged 12 to 17 years who sustained a complicated mild to severe TBI within 1 to 6 months before study enrollment. Study design was a multisite, assessor-blinded, randomized controlled trial. Study sites included 3 tertiary pediatric hospitals and 2 tertiary general medical centers. The main outcome measure was primary caregiver Behavioral Rating Inventory of Executive Function Global Executive Composite at baseline and 6-month follow-up. Generalized linear models that controlled for baseline scores were used to compare the CAPS and IRC scores. RESULTS: In older teens, the CAPS group showed significant improvement in executive function behaviors at 6-month follow-up compared with the IRC group (F = 6.74, P = .01, Cohen’s d = 0.63). CONCLUSIONS: Findings indicate that web-based CAPS improves primary caregiver-rated executive functioning within the first 12 months after TBI in older adolescents. Future research needs to define the optimal timing after injury for delivery of CAPS and characteristics of individuals and families who are most likely to benefit from CAPS.
Posttranscriptional Regulation of PER1 Underlies the Oncogenic Function of IREα
Pluquet, Olivier , Dejeans, Nicolas, Bouchecareilh, Marion , Lhomond, Stéphanie , Pineau, Raphaël , Higa, Arisa, Delugin, Maylis, Combe, Chantal, Loriot, Sandrine, Cubel, Gaëlle, Dugot‐Senant, Nathalie, Vital, Anne, Loiseau, Hugues , Gosline, Sara J.C. , Taouji, Saı̈d , Hallett, Michael , Anderson, Keith, Rosenbaum, Jean , Saltel, Frédéric , Fernández-Zapico, Martín E. , Chevet, Éric , Loriot, Sandrine, Sarkaria, Jann N. , Wu, Wenting , Rodríguez, Fausto J. , Chevet, Eric

Mayo Clinic

Cancer Research | June 11, 2013 | Volume: 73 | Issue: 15 | Pages: 4732-4743

10.1158/0008-5472.can-12-3989 | PMID 23752693 Get It

Abstract Growing evidence supports a role for the unfolded protein response (UPR) in carcinogenesis; however, the precise molecular mechanisms underlying this phenomenon remain elusive. Herein, we identified the circadian clock PER1 mRNA as a novel substrate of the endoribonuclease activity of the UPR sensor IRE1α. Analysis of the mechanism shows that IRE1α endoribonuclease activity decreased PER1 mRNA in tumor cells without affecting PER1 gene transcription. Inhibition of IRE1α signaling using either siRNA-mediated silencing or a dominant-negative strategy prevented PER1 mRNA decay, reduced tumorigenesis, and increased survival, features that were reversed upon PER1 silencing. Clinically, patients showing reduced survival have lower levels of PER1 mRNA expression and increased splicing of XBP1, a known IRE-α substrate, thereby pointing toward an increased IRE1α activity in these patients. Hence, we describe a novel mechanism connecting the UPR and circadian clock components in tumor cells, thereby highlighting the importance of this interplay in tumor development. Cancer Res; 73(15); 4732–43. ©2013 AACR.
Mortality Risks in New-Onset Childhood Epilepsy
Berg, Anne T. , Nickels, Katherine , Geerts, Ada T., Callenbach, Petra M.C. , Arts, Willem F., Camfield, Peter, Camfield, Carol, Wirrell, Elaine , Rios, Christopher Romero , Berg, Anne T , Nickels, Katherine C

Mayo Clinic

Pediatrics | June 11, 2013 | Volume: 132 | Issue: 1 | Pages: 124-131

10.1542/peds.2012-3998 | PMID 23753097 Get It

OBJECTIVES: Estimate the causes and risk of death, specifically seizure related, in children followed from onset of epilepsy and to contrast the risk of seizure-related death with other common causes of death in the population. METHODS: Mortality experiences from 4 pediatric cohorts of newly diagnosed patients were combined. Causes of death were classified as seizure related (including sudden unexpected death [SUDEP]), natural causes, nonnatural causes, and unknown. RESULTS: Of 2239 subjects followed up for &gt;30 000 person-years, 79 died. Ten subjects with lethal neurometabolic conditions were ultimately excluded. The overall death rate (per 100 000 person-years) was 228; 743 in complicated epilepsy (with associated neurodisability or underlying brain condition) and 36 in uncomplicated epilepsy. Thirteen deaths were seizure-related (10 SUDEP, 3 other), accounting for 19% of all deaths. Seizure-related death rates were 43 overall, 122 for complicated epilepsy, and 14 for uncomplicated epilepsy. Death rates from other natural causes were 159, 561, and 9, respectively. Of 48 deaths from other natural causes, 37 were due to pneumonia or other respiratory complications. CONCLUSIONS: Most excess death in young people with epilepsy is not seizure-related. Mortality is significantly higher compared with the general population in children with complicated epilepsy but not uncomplicated epilepsy. The SUDEP rate was similar to or higher than sudden infant death syndrome rates. In uncomplicated epilepsy, sudden and seizure-related death rates were similar to or higher than rates for other common causes of death in young people (eg, accidents, suicides, homicides). Relating the risk of death in epilepsy to familiar risks may facilitate discussions of seizure-related mortality with patients and families.
Neurologic Complications Following Pediatric Renal Transplantation
KWON, C, Klein, M, Corder, Julie, Ghosh, Debabrata , Ghosh, Partha S. , Ghosh, Partha Sakha

Mayo Clinic

Journal of Child Neurology | June 10, 2013 | Volume: 29 | Issue: 6 | Pages: 793-798

10.1177/0883073813490074 | PMID 23752071 Get It

We reviewed neurologic complications after renal transplantation in children over a 20-year period. Neurologic complications were classified as early (within 3 months) and delayed (beyond 3 months). Of 115 children, 10 (8.7%) had complications. Early complications were found in 4.35% of patients: seizures in 4 (posterior reversible leukoencephalopathy syndrome due to immunosuppressant toxicity [2], sepsis/presumed meningitis [1], and indeterminate [1]) and headaches in 1. One patient with seizures received levetiracetam for 6 months and 1 with headaches received amitriptyline prophylaxis. Late complications were noted in 4.35% of patients: seizures in 3 (posterior reversible leukoencephalopathy syndrome due to hypertension [2], hypertensive encephalopathy [1]), headaches in 2, and tremors in 1. Two patients with seizures were treated with anti-epilepsy medications; 1 with migraine received cyproheptadine prophylaxis. Neurologic complications develop in children after renal transplantation. Seizures due to posterior reversible leukoencephalopathy syndrome were the commonest complication. Early detection and appropriate management of these complications is important.