Tomlin, A. The Mental Elf Blog. Published online: 29 September 2016
NICE recommends a range of psychological and drug treatments for PTSD such as trauma-focused cognitive behavioural therapy, but does not recommend computer-based psychotherapies. A recent systematic review and meta-analysis from the Netherlands may persuade the guideline developers to think again.
The aim of this meta-analysis was to evaluate the effectiveness of Internet-delivered Cognitive Behavioural Therapy (iCBT) compared to inactive (waitlist control or treatment-as-usual) and active other interventions in reducing PTSD symptoms.
Overall, the results show that iCBT is superior to waitlist, with a trend suggesting that iCBT is more effective than active controls (e.g. psychoeducation and supportive counselling).
iCBT compared to waitlist or treatment as usual (11 comparisons from 10 studies of 1,139 participants) found a moderate pooled effect size (g = 0.71, 95% CI 0.49 to 0.93, P < .001) with moderate heterogeneity
iCBT compared to other interventions (3 comparisons from 3 studies) found a small pooled effect size (g = 0.28, 95% CI -0.00 to 0.56, P = .05) with low heterogeneity
The effects were strongest when iCBT interventions were therapist-assisted and longer than eight sessions. This echoes what we know from other web-based psychotherapy evidence.
When comparing iCBT to waitlist, visual inspection of the funnel plot and Egger’s test (P = .34) did not indicate the presence of publication bias.
Greenhill, R. et al. Journal of Adolescent Health. Published online: 29 September 2016
Adult electronic cigarette (e-cigarette) use is increasing globally, and early studies have suggested that similar trends may be observed among the adolescent population, albeit at lower levels.
The current literature review presents data collected since 2014 from 21 cross-sectional studies and one cohort study that were all published in English. In particular, it focuses on awareness, ever use, past 30-day use, and regular use of e-cigarettes.
The article suggests that adolescents are nearing complete awareness of e-cigarettes. Furthermore, in relation to ever use and past 30-day use, higher prevalence rates continue to be reported across time, especially in the United States. Nonetheless, reported regular use of e-cigarettes remains much lower than past 30-day use, although conclusions are limited due to inconsistencies with measurement and consequent lack of cross-cultural applicability. The majority of studies do not report whether adolescents use non-nicotine e-cigarettes.
There is a current absence of longitudinal studies that explore any association between e-cigarettes and tobacco use and little qualitative data that may illuminate how and why adolescents use e-cigarettes. Through addressing these methodological limitations, future research will be able to inform health care and policy more effectively.
A PACS can be defined as a population-based accountable care model, with general practice at its core. It is organised around patients’ needs and aims to improve the physical, mental and social health and wellbeing of its local population.
However, it will also include most hospital based care, as well as primary, community, mental health and social care services. By aligning the goals and incentives of hospitals with other health and care providers, it offers the potential for a radical new approach to population health.
The integrated (PACS) Framework outlines the next steps required to set up the model – including the need to develop new contractual, funding and organisational form. It sets out three contractual options that will help make a phased transition towards a fully-fledged PACS – a single provider with a single contract for all local health and care services.
This puts clinicians in the driving seat by pooling and allocating resources to areas that will have the greatest impact on the health of their local community and creates a shared responsibility towards the most vulnerable patients.
One in seven people aged 85 or over is living permanently in a care home. The evidence suggests that many of these people are not having their needs properly assessed and addressed. As a result, they often experience unnecessary, unplanned and avoidable admissions to hospital, and sub-optimal medication.
The enhanced health care homes model lays out a clear vision for providing joined up primary, community and secondary, social care to residents of care and nursing homes, via a range of services.
Seven key components and eighteen sub-components which define the care homes model are put forward, with practical guidance explaining how organisations and providers can make the transition and implement the whole model.
These plans can help transform the way care is delivered, with staff from across health and social care organisations working together as part of multidisciplinary teams to deliver high quality and financially sustainable care.
The inquiry found that the discharge failures identified by the May 2016 PHSO report are not isolated incidents but examples of problems that patients, relatives and carers are experiencing more widely. The committee identified a need for more data to be gathered on the scale and impact of these discharge failures. It identified a lack of integration between health and social care is preventing seamless discharge processes, coordinated around the patient’s needs.
Public Health England has published a range of products which examine the deaths of people recorded with dementia between 2012 and 2014.
Figures show the number of deaths with a mention of dementia was:
6.6% of all deaths in 2001
15.8% of deaths in 2014
This is most likely due to an increase in awareness and recording of dementia.
New reports have been produced by the Dementia Intelligence Network (DIN) in collaboration with the National End of Life Care Intelligence Network (NEoLCIN) and draw on national data to see if there have been changes in dementia deaths over time, who the people dying with dementia are, where they die and the cause of their death.
The findings suggest that people who live in more deprived areas die with dementia at a younger age than those who live in more affluent areas.
There are also considerable differences between the place of death for people who have dementia and the general population. People with dementia are considerably more likely to die in hospitals and care homes and less likely to die at home or in end of life care settings such as hospices.
Read the Dementia Intelligence Network (DIN) and the National End of Life Care Intelligence Network (NEOLCIN) reports here
The Academy of Medical Sciences has published a report ‘Improving the health of the public by 2040’.
Over the coming decades, the UK population will face a wide range of complex health challenges and opportunities, many of which can only be fully addressed through strategies to secure and improve the health of the public as a whole. The report explores how to organise our research environment to generate and translate the evidence needed to underpin such strategies.
This report concludes that while public health research has provided fundamental insights into human health, there remains much we do not know about the complex array of interlinking factors that influence the health of the public, and about how to prevent and solve the many health challenges we face as a population.
Solving these challenges will require shifting towards a ‘health of the public’ approach, involving disciplines that would not usually be considered to be within the public health field. This is turn requires six key developments:
Rebalancing and enhancing the coordination of research.
Harnessing new technologies and the digital revolution.
Developing transdisciplinary research capacity.
Aligning perspectives and approaches between clinical and public health practice.
Working with all sectors of society, including policymakers, practitioners, the commercial sector and the public.
Read the full report here Read the press release here