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Background Bleeding among populations undergoing percutaneous coronary intervention or coronary artery bypass grafting and among conservatively managed patients with acute coronary syndrome exposed to different dual antiplatelet therapy and triple therapy (i.e. dual antiplatelet therapy plus an anticoagulant) has not been previously quantified. Objectives The objectives were to estimate hazard ratios for bleeding for different antiplatelet and triple therapy regimens, estimate resources and the associated costs of treating bleeding events, and to extend existing economic models of the cost-effectiveness of dual antiplatelet therapy. Design The study was designed as three retrospective population-based cohort studies emulating target randomised controlled trials. Setting The study was set in primary and secondary care in England from 2010 to 2017. Participants Participants were patients aged ≥ 18 years undergoing coronary artery bypass grafting or emergency percutaneous coronary intervention (for acute coronary syndrome), or conservatively managed patients with acute coronary syndrome. Data sources Data were sourced from linked Clinical Practice Research Datalink and Hospital Episode Statistics. Interventions Coronary artery bypass grafting and conservatively managed acute coronary syndrome: aspirin (reference) compared with aspirin and clopidogrel. Percutaneous coronary intervention: aspirin and clopidogrel (reference) compared with aspirin and prasugrel (ST elevation myocardial infarction only) or aspirin and ticagrelor. Main outcome measures Primary outcome: any bleeding events up to 12 months after the index event. Secondary outcomes: major or minor bleeding, all-cause and cardiovascular mortality, mortality from bleeding, myocardial infarction, stroke, additional coronary intervention and major adverse cardiovascular events. Results The incidence of any bleeding was 5% among coronary artery bypass graft patients, 10% among conservatively managed acute coronary syndrome patients and 9% among emergency percutaneous coronary intervention patients, compared with 18% among patients prescribed triple therapy. Among coronary artery bypass grafting and conservatively managed acute coronary syndrome patients, dual antiplatelet therapy, compared with aspirin, increased the hazards of any bleeding (coronary artery bypass grafting: hazard ratio 1.43, 95% confidence interval 1.21 to 1.69; conservatively-managed acute coronary syndrome: hazard ratio 1.72, 95% confidence interval 1.15 to 2.57) and major adverse cardiovascular events (coronary artery bypass grafting: hazard ratio 2.06, 95% confidence interval 1.23 to 3.46; conservatively-managed acute coronary syndrome: hazard ratio 1.57, 95% confidence interval 1.38 to 1.78). Among emergency percutaneous coronary intervention patients, dual antiplatelet therapy with ticagrelor, compared with dual antiplatelet therapy with clopidogrel, increased the hazard of any bleeding (hazard ratio 1.47, 95% confidence interval 1.19 to 1.82), but did not reduce the incidence of major adverse cardiovascular events (hazard ratio 1.06, 95% confidence interval 0.89 to 1.27). Among ST elevation myocardial infarction percutaneous coronary intervention patients, dual antiplatelet therapy with prasugrel, compared with dual antiplatelet therapy with clopidogrel, increased the hazard of any bleeding (hazard ratio 1.48, 95% confidence interval 1.02 to 2.12), but did not reduce the incidence of major adverse cardiovascular events (hazard ratio 1.10, 95% confidence interval 0.80 to 1.51). Health-care costs in the first year did not differ between dual antiplatelet therapy with clopidogrel and aspirin monotherapy among either coronary artery bypass grafting patients (mean difference £94, 95% confidence interval –£155 to £763) or conservatively managed acute coronary syndrome patients (mean difference £610, 95% confidence interval –£626 to £1516), but among emergency percutaneous coronary intervention patients were higher for those receiving dual antiplatelet therapy with ticagrelor than for those receiving dual antiplatelet therapy with clopidogrel, although for only patients on concurrent proton pump inhibitors (mean difference £1145, 95% confidence interval £269 to £2195). Conclusions This study suggests that more potent dual antiplatelet therapy may increase the risk of bleeding without reducing the incidence of major adverse cardiovascular events. These results should be carefully considered by clinicians and decision-makers alongside randomised controlled trial evidence when making recommendations about dual antiplatelet therapy. Limitations The estimates for bleeding and major adverse cardiovascular events may be biased from unmeasured confounding and the exclusion of an eligible subgroup of patients who could not be assigned an intervention. Because of these limitations, a formal cost-effectiveness analysis could not be conducted. Future work Future work should explore the feasibility of using other UK data sets of routinely collected data, less susceptible to bias, to estimate the benefit and harm of antiplatelet interventions. Trial registration This trial is registered as ISRCTN76607611. Funding This project was funded by the National Institute for Health and Care Research (NIHR) Health Technology Assessment programme and will be published in full in Health Technology Assessment; Vol. 27, No. 8. See the NIHR Journals Library website for further project information. Plain language summary People who have a heart attack are treated with a stent to open up the blocked artery that caused the heart attack, with surgery to bypass the blocked artery or with medication only. Whatever the treatment, they are prescribed one or more antiplatelet drugs, either aspirin only or aspirin and an additional antiplatelet (clopidogrel, prasugrel or ticagrelor), for 12 months after the heart attack. Antiplatelets are given to prevent another heart attack, but increase the risk of bleeding. We used a large general practice database and a database describing patients’ attendances and admissions to hospital to determine how many people bleed with different antiplatelet combinations. We found that, overall, up to 1 in 10 people taking antiplatelets (rising to 2 in 10 if also taking an anticoagulant such as warfarin or dabigatran) reported a bleed. Among patients treated with surgery or medication only, we compared aspirin only (which is a less potent therapy) with aspirin and clopidogrel (a more potent therapy). Among patients treated with stents, we compared aspirin and clopidogrel (less potent therapy) with aspirin and prasugrel or ticagrelor (more potent therapy). In all three populations, the more potent therapy increased the risk of bleeding by about one and a half times, but this was not offset by a reduced risk of having a subsequent heart attack. This may be explained by low adherence to the medication: between one-third and almost half of all patients did not adhere to their regimen, and non-adherence was generally higher among patients taking a more potent therapy. It may also be explained by bias inherent in the study, for example if the groups prescribed different antiplatelet regimens had different risks of having another heart attack. Nevertheless, the results show that doctors should be cautious about prescribing more potent antiplatelet therapy because it may increase serious bleeds without necessarily reducing the number of heart attacks. Scientific summary Background Dual antiplatelet therapy (DAPT), a combination of aspirin and clopidogrel, prasugrel or ticagrelor, is recommended for up to 12 months for secondary prevention of ischaemic events (heart attack and stroke) among people undergoing coronary interventions [coronary artery bypass grafting (CABG) and percutaneous coronary intervention (PCI)] and people with acute coronary syndrome (ACS) who are medically managed. Randomised controlled trials (RCTs) in these populations suggest that DAPT increases the risk of bleeding compared with aspirin monotherapy, and that more potent DAPT (with prasugrel and ticagrelor) increases the risk of bleeding compared with less potent DAPT (with clopidogrel). Adding an anticoagulant to DAPT (e.g. for the management of atrial fibrillation), known as triple therapy (TT), increases risk further. ‘Real-world’ bleeding among populations exposed to different DAPT and TT regimens has not been previously quantified. The economic impact of bleeding events is poorly characterised, in particular for minor bleeding, as is their impact on health-related quality of life (HRQoL). Objectives 1.Estimate rates of major and minor bleeding events with different DAPT (and TT) exposures among CABG, PCI and conservatively treated ACS patients. 2.Estimate hazard ratios (HRs) for bleeding for different antiplatelet regimens: for the PCI cohort, we compared aspirin and clopidogrel (AC) with aspirin and prasugrel (AP) or aspirin and ticagrelor (AT); for the CABG and ACS no-procedure cohorts, we compared aspirin with AC. 3.Review the literature to estimate the deterioration in utility (quality-adjusted life-years) of patients who have minor or major bleeding events. 4.Revise/extend existing economic models of the cost-effectiveness of different DAPT regimens to include estimates of the incidence of minor and major bleeding events and associated impacts on utility in the general population. 5.Estimate the resources required and associated costs incurred of treating major and minor events of the alternative DAPT (TT) exposures in the three specified patient populations. 6.Understand patients’ perspectives of DAPT, and the factors that influence responses to nuisance bleeding focusing on adherence and information-seeking (this objective was identified through the patient and public involvement work after the start of the ADAPTT study). Methods Objectives 1 and 2 We conducted a study to identify confounders systematically by performing a systematic review of RCTs and cohort studies; conducting semistructured interviews with six cardiac surgeons, six cardiologists and five general practitioners (GPs); and conducting a survey of 79 cardiologists and 31 cardiac surgeons. We used linked Clinical Practice Research Datalink (CPRD) and Hospital Episode Statistics (HES) data to assemble populations (CABG, PCI and conservatively managed ACS patients) eligible for three ‘target trials’. Inclusion criteria for the target trial were as follows: ≥ 18 years of age, ≥ 1 year of data in CPRD before the index event, no prescription for DAPT or anticoagulants in the preceding 3 months and a prescription for aspirin or DAPT within 2 months of discharge after the index event. The primary outcome was any bleeding event (CPRD or HES data) up to 12 months after the index event. We described rates of bleeding among patients prescribed different DAPT regimens and TT. We estimated adjusted HRs for time to first bleed comparing DAPT with AC (reference) versus aspirin monotherapy for CABG and conservatively managed ACS patient, and, in the emergency PCI population, DAPT with prasugrel versus DAPT with clopidogrel for ST-elevation myocardial infarction (STEMI) patients only and DAPT with ticagrelor versus DAPT with clopidogrel for all the emergency PCI population. We prespecified five sensitivity analyses and conducted three: sensitivity analysis 1 – multiple imputation for eligible patients for whom we had no data to assign an intervention; sensitivity analysis 3 – restricted to patients at low risk of bleeding; and sensitivity analysis 4 – repeating primary outcome analysis without censoring of any CPRD or HES bleed events at transfer-out or last collection date. The transfer-out or last collection date reflect the date that a patient leaves the general practice or the date that the last capture from CPRD was made. Objective 3 A systematic review was conducted of primary research and decision-analytic modelling studies reporting utility decrements for bleeds related to DAPT through a search of MEDLINE, PubMed and references of included studies. A health elicitation study was undertaken, comprising 21 participants (PCI, CABG and conservatively managed ACS) who completed an elicitation exercise involving vignettes describing minor and major bleeds and the EuroQol-5 Dimensions, three-level version (EQ-5D-3L), and the EuroQol-5 Dimensions, five-level version (EQ-5D-5L). Utility decrements were derived using linear regression, and were compared with existing estimates. Objective 4 No formal cost-effectiveness evaluation was undertaken. Objective 5 Data on health-care use were derived from the linked CPRD–HES data set. The total health-care costs associated with the different antiplatelet regimens in the three target trials were measured at 1, 2 and 3 years after the start of follow-up. We used inverse probability of treatment weighting to adjust for the same confounders identified for the main ADAPTT analysis. The total health-care costs at 1, 2 and 3 years of follow-up were estimated by fitting weighted generalised linear models with gamma distribution and log-link. Objective 6 Two focus groups were conducted with patients at the early stages of treatment (0–3 months, nine participants), and two with patients coming to the end of treatment (9–12 months, 12 participants), to explore their experiences with DAPT. Recordings were transcribed verbatim, anonymised and analysed using framework analysis. Research findings Objectives 1 and 2 Confounders study A total of 70 potential confounders were identified by systematic review, clinician interviews and surveys; of these, 34 (49%) were classified as true confounders (factors that influence both the assigned intervention and the outcome), of which 31 (91%) were identified by systematic review and three (9%) by clinician interview, and 31 (91%) were confirmed by the survey. The clinician interviews identified hard-to-measure factors not identified in the review (drug potency, resistance to antiplatelet medication and clinician concerns about adherence). Data that would enable the characterisation of risk, including presentation risk and procedural risk factors, were unavailable for 17 of the 34 confounders (50%). The ADAPTT study A proportion of eligible participants were excluded from each target trial because they could not be assigned an intervention at baseline (17%, 40% and 9% of the CABG, conservatively managed ACS and emergency PCI patients, respectively). The incidence of any bleeding was 5%, 10% and 9% in CABG patients, conservatively managed ACS patients and emergency PCI patients, respectively; the corresponding rates of minor bleeding were 4%, 7% and 7%, respectively. Compared with aspirin monotherapy, DAPT was associated with an increase in the hazards of any bleeding and of major adverse cardiovascular events (MACEs) among CABG [HR 1.72, 95% confidence interval (CI) 1.15 to 2.57, and HR 2.06, 95% CI 1.23 to 3.46, respectively] and conservatively managed ACS patients (HR 1.43, 95% CI 1.21 to 1.69, and HR 1.57, 95% CI 1.38 to 1.78, respectively). Among emergency PCI patients, compared with less potent DAPT (with clopidogrel), more potent DAPT with ticagrelor (ACS and STEMI patients only) or prasugrel (STEMI patients only) increased the hazard of bleeding (HR 1.47, 95% CI 1.19 to 1.82; HR 1.47, 95% CI 1.08 to 2.00; and HR 1.77, 95% CI 1.21 to 2.58, respectively), but there was no association with MACEs (HR 1.06, 95% CI 0.89 to 1.27; HR 1.21, 95% CI 0.94 to 1.56; and HR 1.10, 95% CI 0.80 to 1.51, respectively). Sensitivity analyses using multiple imputation to impute for the intervention assigned at baseline did not materially change these results. Non-adherence to the treatment assigned at baseline was generally higher in the CABG and conservatively-managed ACS target trials (affecting up to 46% and 44% of patients, respectively) than in the in emergency PCI (affecting up to 33% of patients). Triple therapy The median duration of TT was 3.5 months. The incidence of any bleeding among patients prescribed TT was 18%. There was no difference in the incidence of any bleeding, or of major bleeding or minor bleeding, between patients on TT with warfarin and patients on TT with a non-vitamin K oral anticoagulant (NOAC). However, mortality from bleeding was higher among patients on TT with a NOAC than among patients on TT with warfarin (2% vs. 0%), as was the incidence of stroke (4% vs. 0%). Objective 3 Twelve eligible studies were included for review. Reported utility decrements ranged from –0.002 to –0.03 for minor bleeds and –0.007 to –0.05 for major bleeds. Data sources used to estimate the decrements lacked relevance to our population group, and few studies adequately reported details of their measurement and valuation approaches. Our patient health elicitation study elicited utility decrements that overlapped existing estimates, ranging from –0.000848 to –0.00828 for minor bleeds and from –0.0187 to –0.0621 for major bleeds. However, the magnitude of difference depended on the instrument (EQ-5D-5L or EQ-5D-3L), estimation method and valuation approach applied. Objective 5 The mean total health-care cost in the year prior to the index event was much higher for CABG patients (£13,601) than for conservatively managed ACS (£3528) or emergency PCI patients (£3625). For CABG patients, mean costs were similar between different antiplatelet regimens (£13,623 for aspirin monotherapy and £13,537 for DAPT with clopidogrel). For conservatively managed ACS, patients on DAPT with clopidogrel had a lower mean total health-care cost in the year prior to the index date than patients on aspirin monotherapy (£3317 vs. £3857, respectively). Among emergency PCI patients, those initiated on DAPT with clopidogrel had a higher mean total health-care cost in the year prior to the index event (£4492) than those initiated on DAPT with prasugrel (STEMI patients only) (£1660) or ticagrelor (£2829). Among the CABG population, there was no difference in mean cumulative health-care costs between initiation of DAPT with clopidogrel and initiation of aspirin monotherapy; the mean difference at 1, 2 and 3 years was £94 (95% CI –£555 to £763), £236 (95% CI –£831 to £1223) and £113 (95% CI –£1318 to £1102), respectively. Among the conservatively managed ACS population, the mean cumulative health-care costs were estimated to be slightly higher if all patients were treated with DAPT with clopidogrel than if all were treated with aspirin monotherapy; the mean difference at 1, 2 and 3 years was £610 (95% CI –£626 to £1516), £1118 (95% CI –£226 to £2206) and £1225 (95% CI –£426 to £2423), respectively, although there was considerable overlap between CIs. For emergency PCI patients, the estimated cumulative health-care costs were comparable under the different antiplatelet regimens among patients not receiving concurrent proton pump inhibitor (PPI) prescriptions, but were higher for patients receiving DAPT with ticagrelor than for patients receiving DAPT with clopidogrel. At 1 year, for example, the predicted mean difference in health-care costs if all patients received DAPT with ticagrelor rather than DAPT with clopidogrel was £72 (95% CI –£532 to £762) among those not receiving concurrent PPI therapy and £1145 (95% CI £269 to £2195) among those receiving concurrent PPI therapy. Among STEMI patients receiving concurrent PPI therapy, DAPT with prasugrel was associated with higher costs than DAPT with clopidogrel or DAPT with ticagrelor. Objective 6 Participants would adhere to DAPT when they believed that DAPT was important to ACS outcomes. Those who had experienced nuisance bleeding reported symptoms to be mild and manageable and did not report the bleed to their GP. Adherence was influenced by participants’ and their families’ understanding of the risks and benefits of DAPT, and their ability to manage symptoms. Factors influencing knowledge about DAPT included access to medication counselling; processing of and engaging with information communicated during medication counselling; and access to timely, relevant and expert information and advice after discharge from hospital. Conclusions There is underascertainment of minor/nuisance bleeding in the CPRD, probably as a result of under-reporting of nuisance bleeding by patients to their GPs. In three retrospective population-based cohort studies emulating target trials, there was an increased risk of bleeding among patients receiving DAPT compared with those receiving aspirin monotherapy (CABG and conservatively managed ACS patients) and among patients receiving more potent DAPT than among those receiving less potent DAPT (emergency PCI patients), but not the expected decrease in MACEs. We identified several potential biases that may have influenced the results of the ADAPTT study as a result of imperfect emulation of the defined target trials: (1) selection bias – we excluded a subgroup of the eligible population because they could not be assigned an intervention; (2) confounding – we had no data for half of the confounders identified, including procedure-related characteristics and disease complexity, and evidence from clinician interviews and surveys that clinicians balance bleeding and ischaemic risk when prescribing DAPT to their patients; and (3) non-adherence to DAPT, which was substantial, and generally higher in the stronger antiplatelet treatment groups. Medication knowledge and understanding, and confidence in dealing with symptoms facilitate positive attitudes towards adherence to DAPT, but may be hindered by opportunities to access relevant, timely and appropriate medication counselling. Although we derived relevant utility decrements for the included population using a patient elicitation exercise, based on standardised definitions of minor and major bleeding events, using a validated HRQoL instrument and valued using general population tariffs, we could not conduct a formal cost-effectiveness analysis given the uncertainty around the estimates for bleeding. Nevertheless, the results using routinely collected data need to be carefully considered by clinicians and decision-makers, given that the increased risk of bleeding we observed with more potent DAPT was not offset by a reduced risk of cardiovascular events and that several recent large meta-analyses of RCTs have also failed to show a conclusive benefit of more potent antiplatelet therapy on cardiovascular events. Future work Future research should explore the feasibility of using other UK data sets of routinely collected data, less susceptible to bias, to estimate the benefit and harm of antiplatelet interventions. Research is needed to develop guidance for identifying confounders and how confounders should be organised into confounding domains to facilitate consistent implementation of the Risk Of Bias In Non-randomized Studies – of Interventions (ROBINS-I) tool. The principle of designing an observational study to emulate a RCT by first defining a target trial appears to be a robust approach, highlighting where the emulation succeeds or fails. Nevertheless, further research is required to validate instances in which an emulation is considered to have been successful, ideally prospectively (i.e. using observational data to emulate ongoing RCTs before their data are analysed and the results are known).We recommend that our utility decrements are used in future cost-effectiveness analyses of DAPT in a UK setting, particularly for minor bleeding events for which existing evidence is limited. In addition, we recommend that future research focuses on quantifying the value of information from reducing the uncertainty of our estimated utility decrements. This research would demonstrate whether or not conducting a larger, more robust study to collect additional information on the HRQoL impact of minor and major bleeds for patients taking DAPT would be an efficient use of resources. The qualitative study with patients highlighted that medication knowledge and understanding, and confidence in dealing with symptoms, facilitate positive attitudes towards adherence to DAPT, but that, currently, there are limited opportunities for patients to access relevant, timely and appropriate DAPT medication counselling. Future qualitative research should focus on developing an intervention to support service users taking DAPT. Trial registration This trial is registered as ISRCTN76607611. Funding This project was funded by the National Institute for Health and Care Research (NIHR) Health Technology Assessment programme and will be published in full in Health Technology Assessment; Vol. 27, No. 8. See the NIHR Journals Library website for further project information.

Worldwide trends to delay childbearing have increased parental ages at birth. Older parental age may harm offspring health, but mechanisms remain unclear. Alterations in offspring DNA methylation (DNAm) patterns could play a role as aging has been associated with methylation changes in gametes of older individuals. We meta-analyzed epigenome-wide associations of parental age with offspring blood DNAm of over 9500 newborns and 2000 children (5-10 years old) from the Pregnancy and Childhood Epigenetics consortium. In newborns, we identified 33 CpG sites in 13 loci with DNAm associated with maternal age (PFDR

Maternal educational attainment (MEA) shapes offspring health through multiple potential pathways. Differential DNA methylation may provide a mechanistic understanding of these long-term associations. We aimed to quantify the associations of MEA with offspring DNA methylation levels at birth, in childhood and in adolescence. Using 37 studies from high-income countries, we performed meta-analysis of epigenome-wide association studies (EWAS) to quantify the associations of completed years of MEA at the time of pregnancy with offspring DNA methylation levels at birth (n = 9 881), in childhood (n = 2 017), and adolescence (n = 2 740), adjusting for relevant covariates. MEA was found to be associated with DNA methylation at 473 cytosine-phosphate-guanine sites at birth, one in childhood, and four in adolescence. We observed enrichment for findings from previous EWAS on maternal folate, vitamin-B12 concentrations, maternal smoking, and pre-pregnancy BMI. The associations were directionally consistent with MEA being inversely associated with behaviours including smoking and BMI. Our findings form a bridge between socio-economic factors and biology and highlight potential pathways underlying effects of maternal education. The results broaden our understanding of bio-social associations linked to differential DNA methylation in multiple early stages of life. The data generated also offers an important resource to help a more precise understanding of the social determinants of health.

Abstract Gene drives are a promising means of malaria control with the potential to cause sustained reductions in transmission. In real environments, however, their impacts will depend on local ecological and epidemiological factors. We develop a data-driven model to investigate the impacts of gene drives that causes vector population suppression. We simulate gene drive releases in sixteen ~ 12,000 km2 areas of west Africa that span variation in vector ecology and malaria prevalence, and estimate reductions in vector abundance, malaria prevalence and clinical cases. Average reductions in vector abundance ranged from 71.6–98.4% across areas, while impacts on malaria depended strongly on which vector species were targeted. When other new interventions including RTS,S vaccination and pyrethroid-PBO bednets were in place, at least 60% more clinical cases were averted when gene drives were added, demonstrating the benefits of integrated interventions. Our results show that different strategies for gene drive implementation may be required across different African settings.

Abstract Members of the leucine rich repeat (LRR) and PDZ domain (LAP) protein family are essential for animal development and histogenesis. Densin-180, encoded by LRRC7, is the only LAP protein selectively expressed in neurons. Densin-180 is a postsynaptic scaffold at glutamatergic synapses, linking cytoskeletal elements with signalling proteins such as the α-subunit of Ca2+/calmodulin-dependent protein kinase II. We have previously observed an association between high impact variants in LRRC7 and Intellectual Disability; also three individual cases with variants in LRRC7 had been described. We identify here 33 individuals (one of them previously described) with a dominant neurodevelopmental disorder due to heterozygous missense or loss-of-function variants in LRRC7. The clinical spectrum involves intellectual disability, autism, ADHD, aggression and, in several cases, hyperphagia-associated obesity. A PDZ domain variant interferes with synaptic targeting of Densin-180 in primary cultured neurons. Using in vitro systems (two hybrid, BioID, coimmunoprecipitation of tagged proteins from 293T cells) we identified new candidate interaction partners for the LRR domain, including protein phosphatase 1 (PP1), and observed that variants in the LRR reduced binding to these proteins. We conclude that LRRC7 encodes a major determinant of intellectual development and behaviour.

Abstract We describe the following shared data from N = 103 healthy adults who completed a broad set of cognitive tasks, surveys, and neuroimaging measurements to examine the construct of self-regulation. The neuroimaging acquisition involved task-based fMRI, resting state fMRI, and structural MRI. Each subject completed the following ten tasks in the scanner across two 90-minute scanning sessions: attention network test (ANT), cued task switching, Columbia card task, dot pattern expectancy (DPX), delay discounting, simple and motor selective stop signal, Stroop, a towers task, and a set of survey questions. The dataset is shared openly through the OpenNeuro project, and the dataset is formatted according to the Brain Imaging Data Structure (BIDS) standard.

One Health is a transdisciplinary approach used to address complex concerns related to human, animal, plant, and ecosystem health. One Health frameworks and operational tools are available to support countries and communities, particularly for the prevention and control of zoonotic diseases and antimicrobial resistance and the protection of food safety. However, One Health has yet to be implemented in a manner that fully considers the complexities and interconnectedness of the diverse influences that have impacts at a larger system level. This lack of consideration can undermine the sustainability of any positive outcomes. To ensure the One Health approach can function effectively within the new global context of converging and escalating health, social, economic, and ecological crises, it must evolve and expand in three overlapping dimensions: (1) Scope: the partners, knowledge, and knowledge systems included, (2) Approach: the techniques, methodologies, and scholarship considered, and (3) Worldview inclusivity: the interweaving of other worldviews together with the mainstream scientific worldview that currently predominates. Diverse partners and knowledge from outside the mainstream health and scientific sectors, including Indigenous peoples and representatives of local communities, and traditionally generated knowledge, must be included. These systems of knowledge can then be braided together with mainstream science to comprise a holistic framework for decision-making. Scholarship and methodologies being applied in other fields and contexts to solve complex challenges and manage uncertainty, such as collaborative governance, social-ecologic systems theory, and complexity science, must be recognized and incorporated. The spectrum of considered worldviews must also expand to authentically integrate the expanded scope and approach into action and sustainable impact. By increasing community and social engagement and by recognizing and entwining different worldviews, the plurality of disciplines, and traditional and scientific ways of knowing to address community concerns in the contexts in which they exist, we can ensure that One Health remains effective and true to its paradigm in our rapidly changing and complex world.

Background Stroke or transient ischaemic attack patients are at increased risk of secondary vascular events. Antiplatelet medications, most commonly clopidogrel, are prescribed to reduce this risk. Factors including CYP2C19 genetic variants can hinder clopidogrel metabolism. Laboratory-based or point-of-care tests can detect these variants, enabling targeted treatment. Objective To assess the effectiveness of genetic testing to identify clopidogrel resistance in people with ischaemic stroke or transient ischaemic attack. Specific objectives: Do people tested for clopidogrel resistance, and treated accordingly, have a reduced risk of secondary vascular events? Do people with loss-of-function alleles associated with clopidogrel resistance have a reduced risk of secondary vascular events if treated with alternative interventions compared to clopidogrel? Do people with loss-of-function alleles associated with clopidogrel resistance have an increased risk of secondary vascular events when treated with clopidogrel? What is the accuracy of point-of-care tests for detecting variants associated with clopidogrel resistance? What is the technical performance and cost of CYP2C19 genetic tests? Is genetic testing for clopidogrel resistance cost-effective compared with no testing? Design Systematic review and economic model. Results Objective 1: Two studies assessed secondary vascular events in patients tested for loss-of-function alleles and treated accordingly. They found a reduced risk, but confidence intervals were wide (hazard ratio 0.50, 95% confidence interval 0.09 to 2.74 and hazard ratio 0.53, 95% confidence interval 0.24 to 1.18). Objective 2: Seven randomised controlled trials compared clopidogrel with alternative treatment in people with genetic variants. Ticagrelor was associated with a lower risk of secondary vascular events than clopidogrel (summary hazard ratio 0.76, 95% confidence interval 0.65 to 0.90; two studies). Objective 3: Twenty-five studies compared outcomes in people with and without genetic variants treated with clopidogrel. People with genetic variants were at an increased risk of secondary vascular events (hazard ratio 1.72, 95% confidence interval 1.43 to 2.08; 18 studies). There was no difference in bleeding risk (hazard ratio 0.98, 95% confidence interval 0.68 to 1.40; five studies). Objective 4: Eleven studies evaluated Genomadix Cube accuracy; no studies evaluated Genedrive. Summary sensitivity and specificity against laboratory reference standards were both 100% (95% confidence interval 94% to 100% and 99% to 100%). Objective 5: Seventeen studies evaluated technical performance of point-of-care tests. Test failure rate ranged from 0.4% to 19% for Genomadix Cube. A survey of 8/10 genomic laboratory hubs revealed variation in preferred technologies for testing, and cost per test ranging from £15 to £250. Most laboratories expected test failure rate to be

BackgroundIn recent years, several autistic1 children and youth have shown interest in Holland Bloorview Kids Rehabilitation Hospital’s clinical brain computer interface (BCI) program. Existing literature about BCI use among autistic individuals has focused solely on cognitive skill development and remediation of challenging behaviors. To date, the benefits of recreational BCI programming with autistic children and youth have not been documented.PurposeThis case report summarizes the experiences of an autistic male adolescent with co-occurring attention deficit hyperactivity disorder using a BCI for recreation and considers possible benefits with this novel user population.MethodsA single retrospective chart review was completed with parental guardian’s consent.FindingsThe participant demonstrated enjoyment in BCI sessions and requested continued opportunities to engage in BCI programming. This enjoyment correlated with improved Canadian Occupational Performance Measure (COPM) scores in BCI programming, outperforming scores from other recreational programs. Additionally, clinicians observed changes in social communication efforts and self-advocacy in this first autistic participant.ConclusionThe use of brain computer interfaces in recreational programming provides a novel opportunity for engagement for autistic children and youth that may also support skill development.

Previous research has shown a strong positive association between right-handed gesturing and vocabulary development. However, the causal nature of this relationship remains unclear. In the current study, we tested whether gesturing with the right hand enhances linguistic processing in the left hemisphere, which is contralateral to the right hand. We manipulated the gesture hand children used in pointing tasks to test whether it would affect their performance. In either a linguistic task (verb learning) or a non-linguistic control task (memory), 131 typically developing right-handed 3-year-olds were encouraged to use either their right hand or left hand to respond. While encouraging children to use a specific hand to indicate their responses had no effect on memory performance, encouraging children to use the right hand to respond, compared to the left hand, significantly improved their verb learning performance. This study is the first to show that manipulating the hand with which children are encouraged to gesture gives them a linguistic advantage. Language lateralization in healthy right-handed children typically involves a dominant left hemisphere. Producing right-handed gestures may therefore lead to increased activation in the left hemisphere which may, in turn, facilitate forming and accessing lexical representations. It is important to note that this study manipulated gesture handedness among right-handers and does therefore not support the practice of encouraging children to become right-handed in manual activities.

Building on an exercise that identified potential harms from simulated investigational releases of a population suppression gene drive for malaria vector control, a series of online workshops identified nine recommendations to advance future environmental risk assessment of gene drive applications.

Introduction At least 10% of hospital admissions in high-income countries, including Australia, are associated with patient safety incidents, which contribute to patient harm (‘adverse events’). When a patient is seriously harmed, an investigation or review is undertaken to reduce the risk of further incidents occurring. Despite 20 years of investigations into adverse events in healthcare, few evaluations provide evidence of their quality and effectiveness in reducing preventable harm.This study aims to develop consistent, informed and robust best practice guidance, at state and national levels, that will improve the response, learning and health system improvements arising from adverse events.Methods and analysis The setting will be healthcare organisations in Australian public health systems in the states of New South Wales, Queensland, Victoria and the Australian Capital Territory. We will apply a multistage mixed-methods research design with evaluation and in-situ feasibility testing. This will include literature reviews (stage 1), an assessment of the quality of 300 adverse event investigation reports from participating hospitals (stage 2), and a policy/procedure document review from participating hospitals (stage 3) as well as focus groups and interviews on perspectives and experiences of investigations with healthcare staff and consumers (stage 4). After triangulating results from stages 1–4, we will then codesign tools and guidance for the conduct of investigations with staff and consumers (stage 5) and conduct feasibility testing on the guidance (stage 6). Participants will include healthcare safety systems policymakers and staff (n=120–255) who commission, undertake or review investigations and consumers (n=20–32) who have been impacted by adverse events.Ethics and dissemination Ethics approval has been granted by the Northern Sydney Local Health District Human Research Ethics Committee (2023/ETH02007 and 2023/ETH02341).The research findings will be incorporated into best practice guidance, published in international and national journals and disseminated through conferences.