16 research outputs found
Effects of antiplatelet therapy on stroke risk by brain imaging features of intracerebral haemorrhage and cerebral small vessel diseases: subgroup analyses of the RESTART randomised, open-label trial
Background
Findings from the RESTART trial suggest that starting antiplatelet therapy might reduce the risk of recurrent symptomatic intracerebral haemorrhage compared with avoiding antiplatelet therapy. Brain imaging features of intracerebral haemorrhage and cerebral small vessel diseases (such as cerebral microbleeds) are associated with greater risks of recurrent intracerebral haemorrhage. We did subgroup analyses of the RESTART trial to explore whether these brain imaging features modify the effects of antiplatelet therapy
Effects of antiplatelet therapy on stroke risk by brain imaging features of intracerebral haemorrhage and cerebral small vessel diseases:Subgroup analyses of the RESTART randomised, open-label trial
BACKGROUND: Findings from the RESTART trial suggest that starting antiplatelet therapy might reduce the risk of recurrent symptomatic intracerebral haemorrhage compared with avoiding antiplatelet therapy. Brain imaging features of intracerebral haemorrhage and cerebral small vessel diseases (such as cerebral microbleeds) are associated with greater risks of recurrent intracerebral haemorrhage. We did subgroup analyses of the RESTART trial to explore whether these brain imaging features modify the effects of antiplatelet therapy. METHODS: RESTART was a prospective, randomised, open-label, blinded-endpoint, parallel-group trial at 122 hospitals in the UK that assessed whether starting antiplatelet therapy might reduce the risk of recurrent symptomatic intracerebral haemorrhage compared with avoiding antiplatelet therapy. For this prespecified subgroup analysis, consultant neuroradiologists masked to treatment allocation reviewed brain CT or MRI scans performed before randomisation to confirm participant eligibility and rate features of the intracerebral haemorrhage and surrounding brain. We followed participants for primary (recurrent symptomatic intracerebral haemorrhage) and secondary (ischaemic stroke) outcomes for up to 5 years (reported elsewhere). For this report, we analysed eligible participants with intracerebral haemorrhage according to their treatment allocation in primary subgroup analyses of cerebral microbleeds on MRI and in exploratory subgroup analyses of other features on CT or MRI. The trial is registered with the ISRCTN registry, number ISRCTN71907627. FINDINGS: Between May 22, 2013, and May 31, 2018, 537 participants were enrolled, of whom 525 (98%) had intracerebral haemorrhage: 507 (97%) were diagnosed on CT (252 assigned to start antiplatelet therapy and 255 assigned to avoid antiplatelet therapy, of whom one withdrew and was not analysed) and 254 (48%) underwent the required brain MRI protocol (122 in the start antiplatelet therapy group and 132 in the avoid antiplatelet therapy group). There were no clinically or statistically significant hazards of antiplatelet therapy on recurrent intracerebral haemorrhage in primary subgroup analyses of cerebral microbleed presence (2 or more) versus absence (0 or 1) (adjusted hazard ratio [HR] 0·30 [95% CI 0·08-1·13] vs 0·77 [0·13-4·61]; pinteraction=0·41), cerebral microbleed number 0-1 versus 2-4 versus 5 or more (HR 0·77 [0·13-4·62] vs 0·32 [0·03-3·66] vs 0·33 [0·07-1·60]; pinteraction=0·75), or cerebral microbleed strictly lobar versus other location (HR 0·52 [0·004-6·79] vs 0·37 [0·09-1·28]; pinteraction=0·85). There was no evidence of heterogeneity in the effects of antiplatelet therapy in any exploratory subgroup analyses (all pinteraction>0·05). INTERPRETATION: Our findings exclude all but a very modest harmful effect of antiplatelet therapy on recurrent intracerebral haemorrhage in the presence of cerebral microbleeds. Further randomised trials are needed to replicate these findings and investigate them with greater precision. FUNDING: British Heart Foundation
A CASE STUDY ON REGRESSION TEST AUTOMATION FOR DATA WAREHOUSE QUALITY ASSURANCE
ABSTRACT: In current trend, every software development, enhancement, or maintenance project includes some quality assurance activities. Quality assurance attempts defects prevention by concentrating on the process of producing the rather than working on the defect detection after the product is built. Regression testing means rerunning test cases from existing test suites to build confidence that software changes have no unintended side-effects. Data warehouse obtains the data from a number of operational data source systems which can be relational tables or ERP package, etc. The data from these sources are converted and loaded into data warehouse in suitable form, this process is called Extraction, Transformation and Loading (ETL). In addition to the target database, there will be another data base to store the metadata, called the metadata repository. This data base contains data about data-description of source data, target data and how the source data has been transformed into target data. In data warehouse migration or enhancement projects, data quality checking process includes ensuring all expected data is loaded, data is transformed correctly according to design specifications, comparing record counts between source data loaded to the warehouse and rejected records, validating correct processing of ETL-generated fields such as surrogate keys. The quality check process also involves validating the data types in the warehouse are as specified in the design and/or the data model. In our work, have automated regression testing for ETL activities, which will saves effort and resource while being more accurate and less prone to any issues. Author experimented around 338 Regression test cases, manual testing is taking around 800 hrs so with RTA it will take around 88 hrs which is a reduction of 84%. This paper explains the process of automating the regression suite for data quality testing in data warehouse systems
Prophylactic and therapeutic potential of tender coconut water intervention on antioxidant status in electron beam irradiated Swiss albino mice
656-661Ionizing radiation induces oxidative stress due to free radicals production. The in vitro study has shown that tender coconut water (TCW) of West Coast tall variety exhibits potent antioxidant property. Here, we attempted to evaluate the potency of TCW in reducing radiation induced oxidative stress in the mice model. The LD50/30 dose of electron beam radiation (EBR) for Swiss albino mice was assessed and was found to be 9.33Gy. Therefore, a sublethal dose of 6Gy was selected for further intervention studies to assess the levels of antioxidants. To evaluate the effective dose, the mice were irradiated with a lethal dose of 10Gy with the oral intervention of 50, 100 and 200 µL of TCW/20 g body wt. of mice. Findings of the study suggest that 100 µL/20 g body wt. was found to be effective in decreasing the mortality of irradiated mice. Further, intervention with TCW significantly increased the antioxidant levels compared to that of radiation control group. The results suggest that TCW exhibits radioprotective activity by potentiating the antioxidant levels in mice exposed to a sublethal dose of whole body EBR
Clinicopathologic Characteristics, Treatment, and Outcomes of Post-transplant Lymphoproliferative Disorders: A Single-institution Experience Using 2017 WHO Diagnostic Criteria
The World Health Organization Classification of Tumours of Haematopoietic and Lymphoid Tissues (WHO 2017) included updated criteria for diagnosis and classification of post-transplant lymphoproliferative disorders (PTLDs). This study evaluated the clinicopathologic spectrum using WHO 2017 criteria and adult PTLD patients’ outcomes over 30 years between 1987 and 2017 at Mayo Clinic (Rochester, MN). Patients were retrospectively reviewed for clinical features, outcomes, and diagnostic pathology material and classified based on WHO 2017 criteria. A total of 227 patients were diagnosed with PTLD, with a median time from transplant to PTLD of 45 months. PTLD occurred >1 year after transplant in 149 (66%) patients. Monomorphic PTLD was the most common subtype (173, 76%), with diffuse large B cell lymphoma as the commonest morphology (n = 137). Epstein-Barr virus was positive in 61% of total cases and 90% of PTLD that developed within 1 year from transplant. The median event-free survival (EFS) and overall survival for the entire cohort were 21 months (95% confidence interval [CI]: 9–35) and 82 months (95% CI: 39–115), respectively. The EFS or overall survival was not impacted by Epstein-Barr virus status but differed based on WHO subtypes and year of diagnosis. Management changed over time with increased use of rituximab or chemotherapy + immunosuppression reduction as initial therapy. When compared to the matched general population and de novo diffuse large B cell lymphoma, patients not achieving EFS 24 status (no progression/treatment or death within 24 mo of diagnosis) had a worse standardized mortality ratio 16.75 (95% CI: 13.91–20) versus SMR 1.72 (95% CI: 1.26–2.28) in those who achieved EFS24. Cause of death was mostly attributed to non-lymphoma–related causes in those achieving EFS 24
Hypoglycemia and Glycemic Control in Older Adults With Type 1 Diabetes: Baseline Results From the WISDM Study
BACKGROUND: Knowledge regarding the burden and predictors of hypoglycemia among older adults with type 1 diabetes (T1D) is limited.
METHODS: We analyzed baseline data from the Wireless Innovations for Seniors with Diabetes Mellitus (WISDM) study, which enrolled participants at 22 sites in the United States. Eligibility included clinical diagnosis of T1D, age \u3e/=60 years, no real-time continuous glucose monitoring (CGM) use in prior three months, and HbA1c \u3c10.0%. Blinded CGM data from 203 participants with at least 240 hours were included in the analyses.
RESULTS: Median age of the cohort was 68 years (52% female, 93% non-Hispanic white, and 53% used insulin pumps). Mean HbA1c was 7.5%. Median time spent in the glucose range \u3c70 mg/dL was 5.0% (72 min/day) and \u3c54 mg/dL was 1.6% (24 min/day). Among all factors analyzed, only reduced hypoglycemia awareness was associated with greater time spent \u3c54 mg/dL (median time of 2.7% vs 1.3% [39 vs 19 minutes per day] for reduced awareness vs aware/uncertain, respectively, P = .03). Participants spent a mean 56% of total time in target glucose range of 70-180 mg/dL and 37% of time above 180 mg/dL.
CONCLUSIONS: Over half of older T1D participants spent at least an hour a day with glucose levels/dL. Those with reduced hypoglycemia awareness spent over twice as much time than those without in a serious hypoglycemia range (glucose levels/dL). Interventions to reduce exposure to clinically significant hypoglycemia and increase time in range are urgently needed in this age group