Resource description framework triples entity formations using statistical language model

A method in formatting unstructured sentences from the source corpus to a specificknowledge representation such as RDF is needed. A method for RDF entity formations from aparagraph of text using statistical language model based on N-gram is introduced. Theimplementation of RDF entity formation is applied on natural language query for informationretrieval of the Islamic knowledge. 300 concepts from the English translation of Holy Quranwith 350 relationships are used as a knowledge base. We evaluate our approach on collectionof queries from the Islamic Research Foundation website with a total, 82 queries and comparethe performance against previous method used in FREyA. The result shown the proposedmethod improved 17.07% on the accuracy of the natural language formulation analysis, whichtested on search strategy. It shows the increment on recall and precision with 7% and 3%.Keywords: semantic web; N-gram; ontology; statistical mode

In vitro assessment of the potency of some Newcastle disease vaccine brands in Ibadan, Nigeria

Background: Newcastle disease (ND) is a very common and economically important disease of poultry. There is no drug for treatment of the disease during an outbreak in poultry flocks, and prevention by vaccination is one of the recommended control measures. However, post vaccination outbreaks have been observed on many occasions in chicken flocks and one of the causes has been attributed to possible failure of vaccine to confer immunity. This study was designed to evaluate the potency of ND vaccines available in Ibadan, Nigeria. Methodology: Haemagglutination (HA) technique and elution phenomenon were employed to evaluate the potency of ND vaccines randomly selected in Ibadan. A total of 45 vaccines comprising 9 brands and 5 different strains were selected for potency test. The vaccine brands included ‘Vireo 116’ (n=10), ‘ABIC’ (n=5), ‘Biovac’(n=9), ‘Nobilis’(n=3), ‘NVRI’(n=12), ‘R2B’ (n=2), ‘BAL-ND’ (n=2), ‘Forte dodge’(n=1) and ‘Jovac’ (n=1), while the vaccine strains in the brands included Lasota, B1, Clone, Komarov, Hitcher, and an unknown strain. Results: Thirty-five of the 45 (77.8%) ND vaccines tested had more than 4 HA titer (>64) and were therefore regarded as potent. All the 15 (100%) ND Lasota vaccine strain, 7 out of 10 (70%) ND Komarov strain, 4 out of 5 (80%) ND clone and 5 out of 8 (62.5%) ND B1 strains were potent. None of the ND brand ‘R2B’ vaccine as well as Hitchner strain from ‘Nobilis’ brand was potent, but all 5, 2, 1 and 1 vaccines tested from brands ‘ABIC’, ‘BAL-ND’, ‘Fort dodge’ and ‘Jovac’ respectively were potent. Similarly, 9 of 10, 6 of 9, 2 of 3 and 9 of 12 vaccine strains tested from brands ‘Vireo 116’, ‘Biovac’, ‘Nobilis’ and ‘NVRI’ were respectively potent Conclusion: The occurrence of ND vaccines that are not potent in this study may be contributing to post vaccination failure. It is advisable to subject vaccines to potency test before use. Key words: in vitro, assessment, potency, Newcastle disease, vaccine brands, vaccine strains   French Title; Évaluation in vitro de la puissance de certaines marques de vaccins contre la maladie de Newcastle à Ibadan, Nigéria Contexte: La maladie de Newcastle (ND) est une maladie très courante et économiquement importante des volailles. Il n'existe aucun médicament pour le traitement de la maladie lors d'une épidémie dans des troupeaux de volailles, et la prévention par vaccination est l'une des mesures de contrôle recommandées. Cependant, des flambées post-vaccination ont été observées à de nombreuses reprises dans des troupeaux de poulets et l'une des causes a été attribuée à un éventuel échec du vaccin à conférer l'immunité. Cette étude a été conçue pour évaluer la puissance des vaccins contre la MN disponibles à Ibadan, au Nigéria. Méthodologie: La technique d'hémagglutination (HA) et le phénomène d'élution ont été utilisés pour évaluer la puissance des vaccins contre la MN sélectionnés au hasard à Ibadan. Un total de 45 vaccins comprenant 9 marques et 5 souches différentes ont été sélectionnés pour le test d'activité. Les marques de vaccins comprenaient 'Vireo 116' (n=10), 'ABIC' (n=5), 'Biovac' (n=9), 'Nobilis' (n=3), 'NVRI' (n=12), 'R2B' (n=2), 'BAL-ND' (n=2), 'Forte dodge' (n=1) et 'Jovac' (n=1), tandis que les souches vaccinales des marques comprenaient Lasota, B1, Clone, Komarov, Hitcher et une souche inconnue. Résultats: Trente-cinq des 45 vaccins contre la MN testés (77,8%) avaient plus de 4 titres en HA (>64) et étaient donc considérés comme puissants. Toutes les 15 (100%) souches de vaccin ND Lasota, 7 souches sur 10 (70%) ND Komarov, 4 sur 5 (80%) clones ND et 5 sur 8 (62,5%) souches ND B1 étaient puissantes. Aucun des vaccins ’R2B’ de marque ND ni la souche Hitchner de la marque ’Nobilis’ n'étaient puissants, mais tous les vaccins 5, 2, 1 et 1 testés des marques ‘ABIC’, ‘BAL-ND’, ‘Fort dodge’ et ‘Jovac’ respectivement était puissant. De même, 9 des 10, 6 des 9, 2 des 3 et 9 des 12 souches vaccinales testées des marques ’Vireo 116’, ‘Biovac’, ‘Nobilis’ et ‘NVRI’ étaient respectivement puissantes Conclusion: La présence de vaccins contre la MN qui ne sont pas puissants dans cette étude peut contribuer à l'échec post-vaccinal. Il est conseillé de soumettre les vaccins à un test de puissance avant utilisation. Mots-clés: in vitro, évaluation, puissance, maladie de Newcastle, marques de vaccin, souches vaccinale

Risk profiles and one-year outcomes of patients with newly diagnosed atrial fibrillation in India: Insights from the GARFIELD-AF Registry.

BACKGROUND: The Global Anticoagulant Registry in the FIELD-Atrial Fibrillation (GARFIELD-AF) is an ongoing prospective noninterventional registry, which is providing important information on the baseline characteristics, treatment patterns, and 1-year outcomes in patients with newly diagnosed non-valvular atrial fibrillation (NVAF). This report describes data from Indian patients recruited in this registry. METHODS AND RESULTS: A total of 52,014 patients with newly diagnosed AF were enrolled globally; of these, 1388 patients were recruited from 26 sites within India (2012-2016). In India, the mean age was 65.8 years at diagnosis of NVAF. Hypertension was the most prevalent risk factor for AF, present in 68.5% of patients from India and in 76.3% of patients globally (P < 0.001). Diabetes and coronary artery disease (CAD) were prevalent in 36.2% and 28.1% of patients as compared with global prevalence of 22.2% and 21.6%, respectively (P < 0.001 for both). Antiplatelet therapy was the most common antithrombotic treatment in India. With increasing stroke risk, however, patients were more likely to receive oral anticoagulant therapy [mainly vitamin K antagonist (VKA)], but average international normalized ratio (INR) was lower among Indian patients [median INR value 1.6 (interquartile range {IQR}: 1.3-2.3) versus 2.3 (IQR 1.8-2.8) (P < 0.001)]. Compared with other countries, patients from India had markedly higher rates of all-cause mortality [7.68 per 100 person-years (95% confidence interval 6.32-9.35) vs 4.34 (4.16-4.53), P < 0.0001], while rates of stroke/systemic embolism and major bleeding were lower after 1 year of follow-up. CONCLUSION: Compared to previously published registries from India, the GARFIELD-AF registry describes clinical profiles and outcomes in Indian patients with AF of a different etiology. The registry data show that compared to the rest of the world, Indian AF patients are younger in age and have more diabetes and CAD. Patients with a higher stroke risk are more likely to receive anticoagulation therapy with VKA but are underdosed compared with the global average in the GARFIELD-AF. CLINICAL TRIAL REGISTRATION-URL: http://www.clinicaltrials.gov. Unique identifier: NCT01090362

Tocilizumab in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial

Background: In this study, we aimed to evaluate the effects of tocilizumab in adult patients admitted to hospital with COVID-19 with both hypoxia and systemic inflammation. Methods: This randomised, controlled, open-label, platform trial (Randomised Evaluation of COVID-19 Therapy [RECOVERY]), is assessing several possible treatments in patients hospitalised with COVID-19 in the UK. Those trial participants with hypoxia (oxygen saturation &lt;92% on air or requiring oxygen therapy) and evidence of systemic inflammation (C-reactive protein ≥75 mg/L) were eligible for random assignment in a 1:1 ratio to usual standard of care alone versus usual standard of care plus tocilizumab at a dose of 400 mg–800 mg (depending on weight) given intravenously. A second dose could be given 12–24 h later if the patient's condition had not improved. The primary outcome was 28-day mortality, assessed in the intention-to-treat population. The trial is registered with ISRCTN (50189673) and ClinicalTrials.gov (NCT04381936). Findings: Between April 23, 2020, and Jan 24, 2021, 4116 adults of 21 550 patients enrolled into the RECOVERY trial were included in the assessment of tocilizumab, including 3385 (82%) patients receiving systemic corticosteroids. Overall, 621 (31%) of the 2022 patients allocated tocilizumab and 729 (35%) of the 2094 patients allocated to usual care died within 28 days (rate ratio 0·85; 95% CI 0·76–0·94; p=0·0028). Consistent results were seen in all prespecified subgroups of patients, including those receiving systemic corticosteroids. Patients allocated to tocilizumab were more likely to be discharged from hospital within 28 days (57% vs 50%; rate ratio 1·22; 1·12–1·33; p&lt;0·0001). Among those not receiving invasive mechanical ventilation at baseline, patients allocated tocilizumab were less likely to reach the composite endpoint of invasive mechanical ventilation or death (35% vs 42%; risk ratio 0·84; 95% CI 0·77–0·92; p&lt;0·0001). Interpretation: In hospitalised COVID-19 patients with hypoxia and systemic inflammation, tocilizumab improved survival and other clinical outcomes. These benefits were seen regardless of the amount of respiratory support and were additional to the benefits of systemic corticosteroids. Funding: UK Research and Innovation (Medical Research Council) and National Institute of Health Research

Convalescent plasma in patients admitted to hospital with COVID-19 (RECOVERY): a randomised controlled, open-label, platform trial

Background: Many patients with COVID-19 have been treated with plasma containing anti-SARS-CoV-2 antibodies. We aimed to evaluate the safety and efficacy of convalescent plasma therapy in patients admitted to hospital with COVID-19. Methods: This randomised, controlled, open-label, platform trial (Randomised Evaluation of COVID-19 Therapy [RECOVERY]) is assessing several possible treatments in patients hospitalised with COVID-19 in the UK. The trial is underway at 177 NHS hospitals from across the UK. Eligible and consenting patients were randomly assigned (1:1) to receive either usual care alone (usual care group) or usual care plus high-titre convalescent plasma (convalescent plasma group). The primary outcome was 28-day mortality, analysed on an intention-to-treat basis. The trial is registered with ISRCTN, 50189673, and ClinicalTrials.gov, NCT04381936. Findings: Between May 28, 2020, and Jan 15, 2021, 11558 (71%) of 16287 patients enrolled in RECOVERY were eligible to receive convalescent plasma and were assigned to either the convalescent plasma group or the usual care group. There was no significant difference in 28-day mortality between the two groups: 1399 (24%) of 5795 patients in the convalescent plasma group and 1408 (24%) of 5763 patients in the usual care group died within 28 days (rate ratio 1·00, 95% CI 0·93–1·07; p=0·95). The 28-day mortality rate ratio was similar in all prespecified subgroups of patients, including in those patients without detectable SARS-CoV-2 antibodies at randomisation. Allocation to convalescent plasma had no significant effect on the proportion of patients discharged from hospital within 28 days (3832 [66%] patients in the convalescent plasma group vs 3822 [66%] patients in the usual care group; rate ratio 0·99, 95% CI 0·94–1·03; p=0·57). Among those not on invasive mechanical ventilation at randomisation, there was no significant difference in the proportion of patients meeting the composite endpoint of progression to invasive mechanical ventilation or death (1568 [29%] of 5493 patients in the convalescent plasma group vs 1568 [29%] of 5448 patients in the usual care group; rate ratio 0·99, 95% CI 0·93–1·05; p=0·79). Interpretation: In patients hospitalised with COVID-19, high-titre convalescent plasma did not improve survival or other prespecified clinical outcomes. Funding: UK Research and Innovation (Medical Research Council) and National Institute of Health Research

Endemic fluorosis among 14-year-old Yemeni adolescents: an exploratory survey

Objective: To assess the extent of fluorosis in a representative sample of 14-year-old Yemeni adolescents. Methods: A random sample of 2,400 14-year-old Yemeni adolescents, equally distributed by gender, zone and locations, participated in the study. Fluorosis was identified using photographs for measuring Dean's Fluorosis Index. Water samples were taken and analysed for fluoride concentration using the ion selective electrode method at the Oral Biology laboratory, University of Malaya. Results: Fluorosis was found to be present in 30.8% of all subjects examined. Slightly more males (32.3%) than females (29.3%) were observed to have varying degrees of fluorosis. There were more cases with fluorosis among children in rural areas(31.9%) than urban children(29.7%). Adolescents in the south(46.9%) or east(49%) Yemen were found to have almost two times or more children with fluorosis than all other zones(North 15.2%, Central 20%, West 22.9%), the differences were significant at p=0.0001. Fluoride concentration in natural drinking water in the study locations was found to be between 0.5 - 3.8ppmF. Conclusion: Findings found fluorosis to be significant among Yemeni adolescents