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347 citation(s) found for "Lynch, JE".

The effect of an automated point of care tool on diagnosis and management of childhood obesity in primary care
Gentile, Natalie, Cristiani, Valeria, Lynch, Brian , Wilson, Patrick M. , Weaver, Amy L. , Jacobson, Debra J., Chaudhry, Rajeev , Sriram, Swetha, Kumar, Seema , Lynch, Brian A, Rutten, Lila J, Rutten, Lila J. Finney

Journal of Evaluation in Clinical Practice | June 10, 2016 | Volume: 22 | Issue: 6 | Pages: 962-968

10.1111/jep.12572 | PMID 27282887 Get It

AbstractBackgroundChildhood obesity is underdiagnosed in primary care practices. Our study aimed to compare rates of documentation of diagnosis of obesity and counselling for nutrition and physical activity at an academic primary care practice prior to and following implementation of a body mass index (BMI)‐based electronic point of care clinical reminder tool.MethodsWe performed a retrospective record review of children aged 2–18 years undergoing well child visits during any of three calendar years (2009, 2011 and 2013). The electronic clinical reminder tool was implemented in September 2010. Records of children with BMI > 95th percentile were electronically searched for terms of documentation of diagnosis of obesity and nutrition and physical activity counselling. Multivariable logistic regression models were used to adjust for potential patient and provider confounders.ResultsAmong those with BMI ≥ 95th percentile, there was a statistically significant increase in documentation of diagnosis of obesity (45.5% in 2009 vs. 52.4% in 2011; P < 0.001; adjusted odds ratio 1.36; 95% CI 1.13–1.65) and in counselling for physical activity and nutrition (66.8% in 2009 vs. 75.2% in 2011; P < 0.001; adjusted odds ratio 1.33; 95% CI 1.06–1.66) following implementation of the tool. Compared with 2011, there was no statistically significant increase in documentation of obesity (50.4%) or nutrition and physical activity counselling (77.9%) in 2013.ConclusionsThe implementation of a point of care clinical reminder tool was associated with improvement in documentation of diagnosis of obesity and counselling for nutrition and physical activity. Further studies are needed to determine the impact of these automated tools on weight outcomes in children.
Tumor testing to identify lynch syndrome in two Australian colorectal cancer cohorts
Buchanan, Daniel D. , Rosty, Christophe , Eriksen, Stine V , Walsh, Michael D. , Walters, Rhiannon, Thibodeau, Stephen N. , Stewart, Jenna R., Preston, Susan , Win, Aung Ko , Ouakrim, Driss Ait , Boussioutas, Alex , Winship, Ingrid , Southey, Melissa C. , English, Dallas R. , Jenkins, Mark A. , investigators, on behalf of the Melbourne Collaborative Cohort Study and the Australasian Colorectal Cancer Family Registry Cohort, Clendenning, Mark , Flander, Louisa Beyer , Macrae, Finlay , Giles, Graham G. , Hopper, John L. , investigators, on behalf of the Melbourne Collaborative Cohort Study and the Australasian Colorectal Cancer Family Registry Cohort, Buchanan, Daniel D , Win, Aung K , Southey, Melissa C , English, Dallas R , Jenkins, Mark A , Rosty, Christophe , Winship, Ingrid M

Journal of Gastroenterology and Hepatology | June 6, 2016 | Volume: 32 | Issue: 2 | Pages: 427-438

10.1111/jgh.13468 | PMID 27273229 Get It

AbstractBackground and AimTumor testing of colorectal cancers (CRC) for mismatch repair (MMR) deficiency is an effective approach to identify carriers of germline MMR gene mutation (Lynch syndrome). The aim of this study was to identify MMR gene mutation carriers in two cohorts of population‐based CRC utilizing a combination of tumor and germline testing approaches.MethodsColorectal cancers from 813 patients diagnosed with CRC < 60 years of age from the Australasian Colorectal Cancer Family Registry (ACCFR) and from 826 patients from the Melbourne Collaborative Cohort Study (MCCS) were tested for MMR protein expression using immunohistochemistry, microsatellite instability (MSI), BRAFV600E somatic mutation, and for MLH1 methylation. MMR gene mutation testing (Sanger sequencing and Multiplex Ligation Dependent Probe Amplification) was performed on germline DNA of patients with MMR‐deficient tumors and a subset of MMR‐proficient CRCs.ResultsOf the 813 ACCFR probands, 90 probands demonstrated tumor MMR deficiency (11.1%), and 42 had a MMR gene germline mutation (5.2%). For the MCCS, MMR deficiency was identified in the tumors of 103 probands (12.5%) and seven had a germline mutation (0.8%). All the mutation carriers were diagnosed prior to 70 years of age. Probands with a MMR‐deficient CRC without MLH1 methylation and a gene mutation were considered Lynch‐like and comprised 41.1% and 25.2% of the MMR‐deficient CRCs for the ACCFR and MCCS, respectively.ConclusionsIdentification of MMR gene mutation carriers in Australian CRC‐affected patients is optimized by immunohistochemistry screening of CRC diagnosed before 70 years of age. A significant proportion of MMR‐deficient CRCs will have unknown etiology (Lynch‐like) proving problematic for clinical management.
Routine Screening Endoscopy before Bariatric Surgery: Is It Necessary?
Gómez, Victoria , Bhalla, Rajat, Florit, Paul T. Kröner, Diehl, Nancy N. , Rawal, Bhupendra, Lynch, Scott, Loeb, David S. , Lynch, Scott A., Heckman, Michael G.

Bariatric Surgical Practice and Patient Care | May 17, 2016 | Volume: 9 | Issue: 4 | Pages: 143-149

10.1089/bari.2014.0024 | PMID 25516819 Get It

Elementary School–Based Obesity Intervention Using an Educational Curriculum
Lynch, Brian , Gentile, Natalie, Maxson, Julie, Quigg, Stephanie, Swenson, L, Kaufman, Tara K. , Lynch, Brian A, Swenson, Laura, Kaufman, Tara

Journal of Primary Care & Community Health | April 28, 2016 | Volume: 7 | Issue: 4 | Pages: 265-271

10.1177/2150131916644888 | PMID 27121724 Get It

Background: Pediatric obesity is a significant public health problem with a prevalence of 16.9% among US children. School-based obesity interventions show promise for reducing adiposity in elementary age children. This pilot study evaluated the impact of the Let’s Go! 5-2-1-0 pediatric obesity intervention program in an elementary school setting. Methods: This was a cluster randomized controlled field trial comprising 8 classrooms of second- and third-grade children. The impact of implementation of a standardized 5-2-1-0 curriculum was evaluated in the classrooms by looking at health behavior (self-reported fruit and vegetable and sugar-containing beverage intake, and screen time), physical activity (steps measured by pedometer), and body mass index (BMI). Half of the classrooms were given 5-2-1-0 teaching over a 4-month period. Results: There was no statistical difference in improvement of healthy habits, BMI, or physical activity in the intervention group compared with the control group. Conclusions: The 5-2-1-0 intervention used in this study was feasible. There was no significant change in healthy habits, likely due to the small number of participants in the study. The intervention and control sites were in different classrooms and there could be factors such as teacher enthusiasm, socioeconomic factors, and individual traits affecting habits. Future studies could use pre- and post-intervention quizzes to assess healthy habits knowledge retention, involving the environments the child participates in outside of school, using research-grade pedometers or accelerometers for measuring activity data collection, and recruiting larger samples to ensure adequate statistical power.
Improved Diagnosis of Prosthetic Joint Infection by Culturing Periprosthetic Tissue Specimens in Blood Culture Bottles
Peel, Trisha , Dylla, Brenda L., Lynch, David T. , Greenwood‐Quaintance, Kerryl E. , Cheng, Allen , Mandrekar, Jayawant N. , Patel, Robin , Peel, Trisha N, Hughes, John G, Hughes, John , Patel, Robin

mBio | January 29, 2016 | Volume: 7 | Issue: 1 | Pages: No page available

10.1128/mbio.01776-15 | PMID 26733067 Get It

ABSTRACT Despite known low sensitivity, culture of periprosthetic tissue specimens on agars and in broths is routine. Culture of periprosthetic tissue samples in blood culture bottles (BCBs) is potentially more convenient, but it has been evaluated in a limited way and has not been widely adopted. The aim of this study was to compare the sensitivity and specificity of inoculation of periprosthetic tissue specimens into blood culture bottles with standard agar and thioglycolate broth culture, applying Bayesian latent class modeling (LCM) in addition to applying the Infectious Diseases Society of America (IDSA) criteria for prosthetic joint infection. This prospective cohort study was conducted over a 9-month period (August 2013 to April 2014) at the Mayo Clinic, Rochester, MN, and included all consecutive patients undergoing revision arthroplasty. Overall, 369 subjects were studied; 117 (32%) met IDSA criteria for prosthetic joint infection, and 82% had late chronic infection. Applying LCM, inoculation of tissues into BCBs was associated with a 47% improvement in sensitivity compared to the sensitivity of conventional agar and broth cultures (92.1 versus 62.6%, respectively); this magnitude of change was similar when IDSA criteria were applied (60.7 versus 44.4%, respectively; P = 0.003). The time to microorganism detection was shorter with BCBs than with standard media ( P < 0.0001), with aerobic and anaerobic BCBs yielding positive results within a median of 21 and 23 h, respectively. Results of our study demonstrate that the semiautomated method of periprosthetic tissue culture in blood culture bottles is more sensitive than and as specific as agar and thioglycolate broth cultures and yields results faster. IMPORTANCE Prosthetic joint infections are a devastating complication of arthroplasty surgery. Despite this, current microbiological techniques to detect and diagnose infections are imperfect. This study examined a new approach to diagnosing infections, through the inoculation of tissue samples from around the prosthetic joint into blood culture bottles. This study demonstrated that, compared to current laboratory practices, this new technique increased the detection of infection. These findings are important for patient care to allow timely and accurate diagnosis of infection.
Posterior Wall Pharyngectomy with Preservation of Laryngeal Function
Levine, Paul A., Salassa, John R., Lynch, Dennis J., Lenis, Armando, Verheyden, Charles N.

Otolaryngology–Head and Neck Surgery | November 25, 2015 | Volume: 97 | Issue: 1 | Pages: 79-82

10.1177/019459988709700116 | PMID 3112691 Get It

Immature myeloid progenitors promote disease progression in a mouse model of Barrett's-like metaplasia
Kong, Jianping , Sai, Hong, Crissey, Mary Ann S. , Jhala, Nirag, Ginsberg, Gregory G. , Rustgi, Anil K. , Wang, Timothy C. , Falk, Gary W. , Abrams, Julian A , Nakagawa, Hiroshi , Wang, Kenneth , Lynch, John Patrick

Oncotarget | October 25, 2015 | Volume: 6 | Issue: 32 | Pages: 32980-33005

10.18632/oncotarget.5431 | PMID 26460825 Get It

DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patients
Lorenzo‐Betancor, Oswaldo , Ogaki, Kotaro, Soto‐Ortolaza, Alexandra I., Walton, Ronald L., Strongosky, Audrey , Gerpen, Jay A. van, Uitti, Ryan J. , McLean, Pamela J. , Springer, Wolfdieter , Siuda, Joanna , Opala, Grzegorz, Krygowska‐Wajs, Anna , Barcikowska, Maria , McCarthy, A., Lynch, Timothy , Puschmann, Andreas , Rektorová, Irena , Sanotsky, Yanosh, Vilariño‐Güell, Carles , Farrer, Matthew J. , Ferman, Tanis J. , Petersen, Ronald C. , Parisi, Joseph E., Graff‐Radford, Neill R. , Ross, Owen A. , Soto‐Beasley, Alexandra I. , Labbé, Catherine , Siuda, Joanna S. , Czyźewski, K , Boeve, Bradley F. , Dickson, Dennis W. , Wszołek, Zbigniew K. , Ross, Owen A , Puschmann, Andreas , Springer, Wolfdieter , Ferman, Tanis J , Rektorova, Irena , Beasley, Alexandra I , McLean, Pamela J

European Journal of Neurology | August 17, 2015 | Volume: 22 | Issue: 9 | Pages: 1323-1325

10.1111/ene.12770 | PMID 26278106 Get It

BackgroundRecently, a novel mutation in exon 24 of DNAJC13 gene (p.Asn855Ser, rs387907571) has been reported to cause autosomal dominant Parkinson's disease (PD) in a multi‐incident Mennonite family.MethodsIn the present study the mutation containing exon of the DNAJC13 gene has been sequenced in a Caucasian series consisting of 1938 patients with clinical PD and 838 with pathologically diagnosed Lewy body disease (LBD).ResultsOur sequence analysis did not identify any coding variants in exon 24 of DNAJC13. Two previously described variants in intron 23 (rs200204728 and rs2369796) were observed.ConclusionOur results indicate that the region surrounding the DNAJC13 p.Asn855Ser substitution is highly conserved and mutations in this exon are not a common cause of PD or LBD among Caucasian populations.