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Mayo Clinic

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USE OF AUTOGENOUS VEIN OR SYNTHETIC GRAFTS
Hakaim, Albert G., Oldenburg, W. Andrew

Dialysis Access | June 15, 2010 | Volume: No volume available | Issue: No issue available | Pages: 181-210

10.1142/9781848161726_0009 Get It

Reply to I.D. Nagtegaal et al
Gunderson, Leonard L., Jessup, J. Milburn , Sargent, Daniel J. , Greene, Frederick L. , Stewart, Andrew K., Compton, Carolyn A., Sobin, Leslie H., Compton, Carolyn C. , Compton, Carolyn A., Sargent, Daniel J

Journal of Clinical Oncology | June 15, 2010 | Volume: 28 | Issue: 23 | Pages: e399-e400

10.1200/jco.2010.28.7250 Get It

Reply to T.A. James et al
Boughey, Judy C. , Goetz, Matthew P. , Degnim, Amy C.

Journal of Clinical Oncology | June 15, 2010 | Volume: 28 | Issue: 21 | Pages: e365-e365

10.1200/jco.2010.28.3309 Get It

Successful Nonsurgical Treatment of Pneumomediastinum, Pneumothorax, Pneumoperitoneum, Pneumoretroperitoneum, and Subcutaneous Emphysema following ERCP
Fujii, Larissa L., Lau, A. , Fleischer, David E., Harrison, M. Edwyn

Gastroenterology Research and Practice | June 14, 2010 | Volume: 2010 | Issue: No issue available | Pages: 1-7

10.1155/2010/289135 | PMID 20631834 Get It

Complications related to endoscopic retrograde cholangiopancreatography (ERCP) include pancreatitis, hemorrhage, cholangitis, and perforation. ERCP-related perforation is uncommon, but mortality rates are high. Diagnosis requires a high clinical suspicion for early detection to allow optimal management of the perforation and a better prognosis. Treatment depends on the location and mechanism and increasingly involves nonoperative management. We report a case of successful nonsurgical treatment of a patient with extensive air involving the peritoneum, retroperitoneum, thorax, mediastinum, and subcutaneous tissues following an ERCP perforation.
Nucleoside/nucleobase transport and metabolism by microvascular endothelial cells isolated from ENT1−/−mice
Bone, Derek B.J. , Coe, Imogen R. , Hammond, James R. , Choi, Doo‐Sup

American Journal of Physiology-Heart and Circulatory Physiology | June 12, 2010 | Volume: 299 | Issue: 3 | Pages: H847-H856

10.1152/ajpheart.00018.2010 | PMID 20543083 Get It

Nucleoside and nucleobase uptake is integral to mammalian cell function, and its disruption has significant effects on the cardiovasculature. The predominant transporters in this regard are the equilibrative nucleoside transporter subtypes 1 (ENT1) and 2 (ENT2). To examine the role of ENT1 in more detail, we have assessed the mechanisms by which microvascular endothelial cells (MVECs) from ENT1−/−mice transport and metabolize nucleosides and nucleobases. Wild-type murine MVECs express mainly the ENT1 subtype with only trace levels of ENT2. These cells also have a Na+-independent equilibrative nucleobase transport mechanism for hypoxanthine (ENBT1). In the ENT1−/−cells, there is no change in ENT2 or ENBT1, resulting in a very low level of nucleoside uptake in these cells, but a high capacity for nucleobase accumulation. Whereas there were no significant changes in nucleoside transporter subtype expression, there was a dramatic increase in adenosine deaminase and adenosine A2areceptors (both transcript and protein) in the ENT1−/−tissues compared with WT. These changes in adenosine deaminase and A2areceptors likely reflect adaptive cellular mechanisms in response to reduced adenosine flux across the membranes of ENT1−/−cells. Our study also revealed that mouse MVECs have a nucleoside/nucleobase transport profile that is more similar to human MVECs than to rat MVECs. Thus mouse MVECs from transgenic animals may prove to be a useful preclinical model for studies of the effects of purine metabolite modifiers on vascular function.
Subcoracoid Bursitis as an Unusual Cause of Painful Anterior Shoulder Snapping in a Weight Lifter
Thompson, Jeffrey M., Collins, Mark S., Dahm, Diane L., Finnoff, Jonathan T.

The American Journal of Sports Medicine | June 11, 2010 | Volume: 38 | Issue: 8 | Pages: 1687-1692

10.1177/0363546510369546 | PMID 20543147 Get It

Exercise Hemodynamics Enhance Diagnosis of Early Heart Failure With Preserved Ejection Fraction
Sorajja, Paul , Redfield, Margaret M. , Borlaug, Barry A. , Nishimura, Rick A. , Sorajja, Paul , Lam, Carolyn S.P.

Circulation: Heart Failure | June 11, 2010 | Volume: 3 | Issue: 5 | Pages: 588-595

10.1161/circheartfailure.109.930701 | PMID 20543134 Get It

Background— When advanced, heart failure with preserved ejection fraction (HFpEF) is readily apparent. However, diagnosis of earlier disease may be challenging because exertional dyspnea is not specific for heart failure, and biomarkers and hemodynamic indicators of volume overload may be absent at rest. Methods and Results— Patients with exertional dyspnea and ejection fraction >50% were referred for hemodynamic catheterization. Those with no significant coronary disease, normal brain natriuretic peptide assay, and normal resting hemodynamics (mean pulmonary artery pressure <25 mm Hg and pulmonary capillary wedge pressure [PCWP] <15 mm Hg) (n=55) underwent exercise study. The exercise PCWP was used to classify patients as having HFpEF (PCWP ≥25 mm Hg) (n=32) or noncardiac dyspnea (PCWP <25 mm Hg) (n=23). At rest, patients with HFpEF had higher resting pulmonary artery pressure and PCWP, although all values fell within normal limits. Exercise-induced elevation in PCWP in HFpEF was confirmed by greater increases in left ventricular end-diastolic pressure and was associated with blunted increases in heart rate, systemic vasodilation, and cardiac output. Exercise-induced pulmonary hypertension was present in 88% of patients with HFpEF and was related principally to elevated PCWP, as pulmonary vascular resistances dropped similarly in both groups. Exercise PCWP and pulmonary artery systolic pressure were highly correlated. An exercise pulmonary artery systolic pressure ≥45 mm Hg identified HFpEF with 96% sensitivity and 95% specificity. Conclusions— Euvolemic patients with exertional dyspnea, normal brain natriuretic peptide, and normal cardiac filling pressures at rest may have markedly abnormal hemodynamic responses during exercise, suggesting that chronic symptoms are related to heart failure. Earlier and more accurate diagnosis using exercise hemodynamics may allow better targeting of interventions to treat and prevent HFpEF progression.
The transwall gradient across the mouse colonic circular muscle layer is carbon monoxide dependent
Sha, L., Farrugia, Gianrico , Szurszewski, Joseph H., Sha, Lei , Sha, L., Linden, David R.

The FASEB Journal | June 11, 2010 | Volume: 24 | Issue: 10 | Pages: 3840-3849

10.1096/fj.10-156232 | PMID 20543114 Get It

ABSTRACT Gastric and small intestinal circular smooth muscle layers have a transwall resting membrane potential (RMP) gradient that is dependent on release of carbon monoxide (CO) from interstitial cells of Cajal (ICCs). Our aim was to determine whether a RMP gradient exists in the mouse colon and whether the gradient is CO dependent. Microelectrodes were used to record RMPs from muscle cells at different depths of the circular muscle layer from wild‐type and heme oxygenase‐2‐knockout (HO‐2‐KO) mice. A transwall RMP gradient was present in wild‐type mice. The CO scavenger oxyhemoglobin (20 µM) and the heme oxygenase inhibitor chromium mesoporphyrin IX (CrMP, 5 µM) abolished the transwall gradient. The gradient was absent in HO‐2‐KO mice. Tetrodotoxin (1 µM) caused a significant depolarization in circular smooth muscle cells throughout the circular muscle layer and abolished the transwall gradient. Removal of the submucosal neurons abolished the gradient. The majority of submucosal neurons contained HO‐2 immunoreactivity (HO‐2‐IR), while ICCs did not. These data show for the first time that a transwall gradient exists across the circular smooth muscle layer of the mouse colon, that the gradient is due to CO, and that the source of CO is the submucosal neurons.—Sha, L., Farrugia, G., Linden, D. R., Szurszewski, J. H. The transwall gradient across the mouse colonic circular muscle layer is carbon monoxide dependent. FASEB J. 24, 3840–3849 (2010). www.fasebj.org
Brief Multiple Behavior Health Interventions for Older Adolescents
Werch, Chudley E., Bian, Hui , Moore, Michele , Ames, Steven C. , DiClemente, Carlo C. , Thombs, Dennis L., Pokorny, Steven B.

American Journal of Health Promotion | June 11, 2010 | Volume: 23 | Issue: 2 | Pages: 92-96

10.4278/ajhp.07040533 | PMID 19004157 Get It

Purpose. This study examined whether brief intervention strategies founded on the Behavior-Image Model and addressing positive images of college and career success could be potentially efficacious in impacting multiple health habits of high-risk adolescents transitioning into adulthood. Design. Participants were stratified by grade level and drug use and individually randomized to one of the three Plan for Success interventions, with baseline and 1 month postintervention data collections. Setting. A large, relatively diverse suburban school in northeast Florida. Subjects. A total of 375 11th and 12th grade students participated during the spring semester 2006. Intervention. Three interventions studied included: (1) Goal Survey, (2) Goal Survey plus Contract, or (3) Goal Survey plus Consult. Measures. Outcome measures included multiple health risk, health promotion, and personal development behaviors, as well as image and belief measures. Analysis. Repeated-measures MANOVAs and ANOVAs were used to examine intervention effects. Results. MANOVAs were significant for alcohol use, F (4,328) = 6.33, p = .001; marijuana use, F (4,317) = 3.72, p = .01; exercise, F (3,299) = 4.28, p = .01; college preparation, F (2,327) = 6.26, p = .001; and career preparation, F (2,329) = 6.17, p = .001, with most behaviors improving over time, whereas group-by-time interaction effects were found for nutrition habits, F (6,652) = 2.60, p = .02; and career preparation, F (4,658) = 3.26, p = .01, favoring the consultation. Conclusion. Brief interventions founded on the Behavior-Image Model may have potential to improve selected health and personal development habits among older adolescents.
Discovery of the Wonder Drug: From Cows to Cortisone
Saenger, Amy K.

Clinical Chemistry | June 11, 2010 | Volume: 56 | Issue: 8 | Pages: 1349-1350

10.1373/clinchem.2010.149120 | PMID 20538878 Get It