Pulmonary artery compression by hematoma, a rare but life-threatening complication of Stanford type A aortic dissection.

Hemorrhagic extension along the pulmonary arteries should be recognized as a complication of Stanford type A aortic dissection. Radiologists and other physicians with an interest in cardiothoracic imaging should be aware of this rare but life-threatening pathology. The anatomical concept of the pathology is outlined in this text, through high-quality electrocardiogram-gated computerized tomography images.

Differential impact of lactose/lactase phenotype on colonic microflora.

BACKGROUND: The ability to digest lactose divides the world's population into two phenotypes that may be risk variability markers for several diseases. Prebiotic effects likely favour lactose maldigesters who experience lactose spilling into their colon. OBJECTIVE: To evaluate the effects of fixed-dose lactose solutions on fecal bifidobacteria and lactobacilli in digesters and maldigesters, and to determine whether the concept of a difference in ability to digest lactose is supported. METHODS: A four-week study was performed in 23 lactose maldigesters and 18 digesters. Following two weeks of dairy food withdrawal, subjects ingested 25 g of lactose twice a day for two weeks. Stool bifidobacteria and lactobacilli counts pre- and postintervention were measured as the primary outcome. For secondary outcomes, total anaerobes, Enterobacteriaceae, beta-galactosidase and N-acetyl-beta-D-glucosaminidase activity in stool, as well as breath hydrogen and symptoms following lactose challenge tests, were measured. RESULTS: Lactose maldigesters had a mean change difference (0.72 log10 colony forming unitsg stool; P=0.04) in bifidobacteria counts compared with lactose digesters. Lactobacilli counts were increased, but not significantly. Nevertheless, reduced breath hydrogen after lactose ingestion correlated with lactobacilli (r=-0.5; P<0.001). Reduced total breath hydrogen and symptom scorestogether, with a rise in fecal enzymes after intervention, were appropriate, but not significant. CONCLUSIONS: Despite failure to achieve full colonic adaptation, the present study provided evidence for a differential impact of lactose on microflora depending on genetic lactase status. A prebiotic effect was evident in lactose maldigesters but not in lactose digesters. This may play a role in modifying the mechanisms of certain disease risks related to dairy food consumption between the two phenotypes.

Lack of effect of lactose digestion status on baseline fecal micoflora.

BACKGROUND: The genetics of intestinal lactase divide the world's population into two phenotypes: the ability (a dominant trait) or inability (a recessive trait) to digest lactose. A prebiotic effect of lactose may impact the colonic flora of these phenotypes differently. OBJECTIVE: To detect and evaluate the effects of lactose on subjects divided according to their ability to digest lactose. METHODS: A total of 57 healthy maldigesters (n=30) and digesters (n=27) completed diet questionnaires, genetic and breath hydrogen testing, and quantitative stool analysis for species of bacteria. Log10 transformation of bacterial counts was compared with lactose intake in both groups using multiple regression analysis. RESULTS: There was a significant relationship between genetic and breath hydrogen tests. Daily lactose intake was marginally lower in lactose maldigesters (median [interquartile range] 12.2 g [31 g] versus 15 g [29.6 g], respectively). There was no relationship between lactose intake and breath hydrogen tests in either group. There were no differences in bacterial counts between the two groups, nor was there a relationship between bacterial counts and lactose intake in either group. CONCLUSION: The differential bacterial effects of lactose were not quantitatively detected in stool samples taken in the present study.

Isometric force parameters and trunk muscle recruitment strategies in a population with low back pain.

OBJECTIVE: This study correlates changes in trunk isometric force parameters and trunk muscle recruitment strategies in subjects with low back pain (LBP) and healthy participants. METHODS: A control group study with repeated measures was performed. Study participants included 15 control subjects and 14 patients with LBP. Participants were required to exert 50% and 75% of their maximal trunk flexion and extension. In a learning phase, feedback was provided, after which study participants were asked to perform 10 trials without any feedback. Spatiotemporal parameters of muscular activity and force production were recorded. Dependent variables included time to peak force, peak force variability, absolute error in peak force, electromyogram (EMG) burst duration for agonist muscles, and normalized integrated EMG. RESULTS: Average time to peak force was significantly longer for subjects with LBP than for healthy subjects. Subjects with LBP showed longer burst duration for all 4 muscles recorded. No group difference was noted in normalized integrated EMG. CONCLUSIONS: We suggest that the observed changes in trunk motor control and trunk muscle recruitment strategies are not only mediated by a neurophysiologic adaptation to chronic pain but also by cognitive adaptations modulated by fear of movement and fear of reinjury.