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As part of the response to the Health and Sport Committee Governance Report of July 2018, I asked Healthcare Improvement Scotland (HIS) to carry out a review of its role and approach to the adverse events process.

As a first step, HIS has been working to establish a baseline to determine where there is uniformity and divergence in the way that NHS Boards approach significant adverse event reporting and to gain a greater understanding of the contributing factors to this variation. The baseline report has involved detailed engagement with individual NHS Boards and I understand that it will be published in the next few weeks.

I have been clear that health and social care providers throughout Scotland must use learning from all reporting systems to support a culture of openness and learning. I have asked HIS to look further than the existing National Adverse Events Framework, which while essential, is only part of the solution to developing a reporting and learning system which drives continuously improving services and outcomes for patients, carers and staff.

I have instructed my officials to work closely with HIS, NHS Education for Scotland and other stakeholders to ensure that now that the baseline review is concluded, actions can be identified and implemented, as quickly as possible.

The Scottish Government believes clinical research should be rigorous, be of high quality, and should be considered by relevant professional groups. The research in question is considered by the clinical community in NHS Scotland to be of a reasonable quality.

The manufacturer of Essure, the device that was used in the hysteroscopic sterilisation procedure, voluntarily withdrew it from the European market in 2017. Information on withdrawal can be found on the Medicines and Healthcare products Regulatory Agency’s website here and advice given by the manufacturer to healthcare professionals and patients can be viewed here .

No Health Board in Scotland presently offers any form of hysteroscopic sterilisation.

The next phase of funding under the Waiting Times Improvement Plan was announced on 28 April. An additional investment of £70 million will be allocated to NHS Boards to target long waits during the financial year 2019-20.

An announcement will be made later this month which will provide detail around the allocation of funding and which specialities it covers.

Mental health is priority for the Scottish Government and it is committed to improving the provision of perinatal mental health services. Women who experience post-traumatic stress disorder (PTSD) following childbirth are currently able to access support from their midwife, GP, health visitor, from psychological services in primary care and, in some areas, from specialist perinatal mental health services.

The 'Delivering Effective Services' report from the national Perinatal Mental Health Managed Clinical Network sets out a range of recommendations which will improve access to care for postnatal women with PTSD. These include increasing the provision of psychological therapies at primary care level, developing maternity and neonatal psychological interventions services based in maternity units, which will include midwives with additional specialist skills in detecting and managing mental health problems, and the roll-out of specialist community perinatal mental health teams across Scotland.

The Scottish Government has supported these recommendations by committing £50 million over the next four years to perinatal and infant mental health. The recently established Perinatal and Infant Mental Health Programme Board will drive forward this improvement at pace and ensure the delivery of improved perinatal mental health services.

During 2018-19, £27,000 was made available under the Waiting Times Improvement Plan for Chronic pain services.

I also refer the member to the answer to question S5W-24078 on 18 July 2019. All answers to written parliamentary questions are available on the Parliament's website, the search facility for which can be found at http://www.parliament.scot/parliamentarybusiness/28877.aspx .

The Scottish Government provides secretariat support to the Task and Finish Group. The Group is chaired by a consultant physician in respiratory and general internal medicine.

The cost for the secretariat is met within existing resources.

I refer the member to the answer to question S5W-20583 on 20 December 2018. All answers to written parliamentary questions are available on the Parliament's website, the search facility for which can be found at http://www.parliament.scot/parliamentarybusiness/28877.aspx . .

Third sector groups are engaged in the development of the Respiratory Care Action Plan including Chest, Heart & Stroke Scotland and the British Lung Foundation. We are also engaging with respiratory experts, such as consultant clinicians, physiotherapists, specialist respiratory nurses, anaesthetists and representatives from the Scottish Ambulance Service.

The Scottish Health Survey provides annual estimates of smoking prevalence at national level.

The Scottish Surveys Core Questions provides annual smoking prevalence data for health boards, local authorities and smaller subgroups of the population.

The Quality and Outcomes Framework (QOF) ended 1 April 2016. Removing the link between achievement and payment by dismantling QOF did not remove or reduce the obligation on general practitioners to treat patients in a clinically appropriate way and practices still maintain their disease registers.

The Scottish Access Collaborative Programme recently published a report setting out recommendations to sustainably improve chronic pain patient pathways and outcomes that will be taken forward with NHS Boards and Health and Social Care Partnerships. Based on the recommendations set out in the report, the Scottish Government are developing a quality improvement approach which will be developed in partnership with the Modern Outpatient Programme. Workshop participants will be involved to develop Driver Diagrams, aligned to the Scottish Pain model, before the end of July 2019.

Third sector colleagues are taking forward the establishment of a Chronic Pain Patient Reference Group, and a scoping meeting is being scheduled for August 2019. The Chronic Pain report will be distributed more widely across the chronic pain community and wider stakeholders over the coming weeks and it is anticipated that further connection events and learning opportunities will take place following the summer break to share good practice and to co-produce the implementation plan and progress actions.