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CONCLUSION Although we did not find evidence that life-sustaining treatment is routinely continued until just beyond the one-year mark in heart and liver transplantation recipients, there was an unexpected increased risk of mortality in the 30 days following day 365 among lung transplant recipients. This article is protected by copyright. All rights reserved.Cervical radiculopathy is a relatively common neurological disorder, often resulting from mechanical compression of the nerve root within the neural foramen. Anterior cervical discectomy and fusion (ACDF) is a common treatment for radicular symptoms that do not resolve after conservative treatment. One mechanism by which ACDF is believed to resolve symptoms is by replacing degenerated disc tissue with bone graft to increase the neural foramen area, however in vivo evidence demonstrating this is lacking. The aim of this study was to evaluate the effects of age, pathology, and fusion on bony neural foramen area. Participants included 30 young adult controls ( less then 35 years old), 23 middle-aged controls (36 to 60 years old), and 36 cervical arthrodesis patients tested before and after ACDF surgery. Participants' cervical spines were imaged in the neutral, full flexion, and full extension positions while seated within a biplane radiography system. A validated model-based tracking technique determined three-dimensional vertebral position and orientation and automated software identified the neural foramen area in each head position. The neural foramen area decreased throughout the entire sub-axial cervical spine with age and pathology, however, no changes in neural foramen area were observed due solely to replacing degenerated disc tissue with bone graft. The neural foramen area was not associated with disc height in young adult controls, but moderate to strong associations were observed in middle-aged controls. The results provide evidence to inform the debate regarding localized versus systemic spinal degeneration and provide novel insight into the mechanism of pain relief after ACDF. © 2020 Orthopaedic Research Society. Published by Wiley Periodicals, Inc.BACKGROUND The evaluation of methods of intervention for children with developmental coordination disorder (DCD) is an ongoing process. SC144 in vivo Systematic and meta-analytical reviews play an important role in this process. Before 2015, only four reviews of this type were published on this topic. By 2019, the number had tripled, raising the question of whether the increase in quantity is accompanied by a similar increase in quality. The aim of this meta-review was to evaluate eight new review studies published during this time period with particular focus on the consistency of the inclusion criteria, the coverage of primary studies and the quality of evidence on which the conclusions were based. METHOD Methodological quality was evaluated using the Assessment of Multiple Systematic Reviews, Second Edition (AMSTAR 2). RESULTS The eight reviews differed in the inclusion criteria employed, the sources of primary evidence cited and in the quality of evidence provided. Using AMSTAR 2 terminology, the overall methodology of the reviews was judged to be acceptably high for only one. All others contained serious flaws. The conclusions drawn were not consistent. CONCLUSIONS In spite of the increase in the number of reviews on intervention for children with DCD, quality remains an issue. Persistent methodological problems mean that consumers still cannot be confident in any of the claims made for intervention effects. © 2020 John Wiley & Sons Ltd.A 76-year-old male underwent a pulmonary vein isolation (PVI) of atrial fibrillation. The first-pass encirclement did not isolate the left superior PV (LSPV). High-resolution activation mapping during LSPV pacing identified the earliest activation site (EAS) on the left atrial (LA) roof outside the PVI line. A radiofrequency application on the roof isolated the LSPV. Thereafter, an LSPV reconnection occurred. Second activation mapping during LSPV pacing identified the EAS at the bottom of the ridge outside the PVI line. Radiofrequency applications targeting the EAS eliminated the LSPV reconnection. The multiple residual connections may be associated with spared epicardial PV-LA connections. This article is protected by copyright. All rights reserved. This article is protected by copyright. All rights reserved.BACKGROUND AND AIM A risk-stratification score may be useful for colorectal cancer (CRC) screening, alongside screening colonoscopy (CS) and fecal immunochemical test (FIT). This study aimed to evaluate the effectiveness and cost-effectiveness of population-based CRC screening strategies using CS, FIT, and the Japanese CRC screening score. METHODS The effectiveness in quality-adjusted life years (QALYs), cost-effectiveness, and required number of CS procedures were evaluated for screening strategies with primary screening CS (strategy 1), FIT (strategy 2), and the risk score (strategy 3), using a simulation model analysis with two scenarios. In scenario 1, uptake rates for all tests were 60%. In scenario 2, uptake rates for FIT and a risk score were 40%, and those for screening CS and CS following a positive FIT or high risk score were 20% and 70%, respectively. RESULTS In scenario 1, strategy 1 gained the highest QALYs and required the highest cost. The incremental cost-effectiveness ratios per QALY gained for strategy 1 against the others were lower than 5 000 000 JPY. Strategy 1 required more than twice as many CS procedures as the other strategies. In scenario 2, strategy 3 had the highest QALYs and lowest cost, and strategy 1 had the lowest QALYs and highest cost. CONCLUSIONS Screening CS has the potential to be the most effective and cost-effective form of CRC screening, although it requires a large number of CS procedures. However, if non-invasive tests are preferred by recipients, other screening strategies, particularly those using the risk score, can be more effective and cost-effective. © 2020 Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd.