Director-General of Health recommends time-limited pause on the use of female pelvic surgical mesh products to treat stress urinary incontinence

Source: New Zealand Ministry of Health

The Director-General of Health, Dr Diana Sarfati, has supported, effective 23 August 2023, a time-limited pause on the use of surgical mesh for stress urinary incontinence.

The Surgical Mesh Roundtable (MRT), an oversight and monitoring group chaired by Manatū Hauora | Ministry of Health, has been investigating a pause since earlier this year, Dr Sarfati says.

Alongside this, Parliament’s Health Committee recommended in June that Manatū Hauora investigate a pause in the procedure after it considered the petition of Sally Walker, a woman who has been injured by mesh.

The MRT’s assessment is that the balance of benefit and harm from the procedure will be improved by the series of additional measures already planned, and it recommends a pause until those measures are substantively in place.

‘After considering the MRT’s assessment, I have decided to support a pause to allow the following steps to be put in place to reduce the harms linked to the procedure as much as possible,’ Dr Sarfati says.

Those steps are:  

  • providing tailored training and certification for surgeons performing the procedure;  
  • establishing a registry of all public and private patients who could benefit from it;  
  • reviewing patients and the decision to carry out the procedure at multi-disciplinary meetings, which include a range of experts from physiotherapists to surgeons; and  
  • using a structured and guided informed consent process for patients.

‘No surgery is without risks, and it’s important to remember that this particular procedure has changed the lives of many people for the better,’ Dr Sarfati says.

‘However, we recognise it has caused ongoing pain and lessened the quality of life for some people, and we therefore need to act to minimise these outcomes.  

‘We also acknowledge the process has been slow at times and that has potentially added to the frustrations of those who have suffered harm from surgical mesh.’ 

Recognising the length of time to put these measures in place has been a significant factor behind our decision to put in place this time limited pause.

Dr Sarfati says, ‘It is important to note the procedure is paused, not banned. 

‘That means there may be exceptions, and that the procedure might be carried out during the pause if a multi-disciplinary team agree there is no viable alternative. Any use would only happen after extensive consultation and review. 

‘We acknowledge that this pause may cause additional uncertainty for patients awaiting treatment, and concern for those who have recently had it. However, we need to make sure that patients are given treatment that appropriately limits the risk of harm for as many people as possible, and we believe this move will help us achieve that.’

Background

Surgical mesh is a net-like fabric or tape that can be introduced as part of surgery to help repair weakened structures in the human body. As a net-like fabric it is used in the treatment of hernias and historically was also used in the treatment of pelvic organ prolapse (POP). As a tape it is used in the treatment of stress unrinary incontinence. These tapes are frequently known as TVTs (tension-free vaginal tapes) or MUS (mid-urethral slings). Mesh for treatment of POP has not been available for some years. This pause only affects mesh tapes used for stress urinary incontinence.

Urinary incontinence is the unintentional loss of urine. Stress incontinence happens when physical movement puts pressure on your bladder, causing you to leak urine.   

The Ministry recognises that its advice has no legal weight, though it is supported by the Royal Australasian College of Surgeons and the Royal Australian and New Zealand College of Obstetricians and Gynaecologists and Medical Council of New Zealand. The recommendation to the sector would likely be considered in any review of complaints against health professionals by health regulatory agencies.  

Alternative treatments for stress urinary incontinence can include surgery without the use of mesh, and non-surgical interventions.  

The Surgical Mesh Roundtable, chaired by the Ministry of Health’s Chief Medical Officer Dr Joe Bourne, will retain oversight on the progress and will provide advice to Manatū Hauora, at the point, a pause can be lifted.

It is difficult to quantity the risks and benefits for these procedures. We know they are successful for many people, and that procedures using mesh have a good outcome for 75% of women, slightly higher than the 70% of good outcomes for women who undergo a non-mesh procedure.

The evidence around risk of harm is more complex. We know that the Health and Disability Commissioner has reported 64 complaints in the past ten years and there is also a 3.6% injury rate for procedures involving mesh based on ACC figures over the past 17 years.

While this incidence is broadly consistent with the international data it is not possible to accurately track how it has changed across those years. 

If people have recently had surgery that involves the use of mesh, the decision would have carefully been considered and was likely to have been the most appropriate option. Most patients have had successful stress urinary incontinence mesh procedures without complications. If people are not experiencing complications, there is no need to take any action.   
  
If a person becomes concerned that they have symptoms which could be related to mesh they should follow up with their medical practitioner. More information about pelvic mesh complications and the symptoms can be found on The New Zealand Female Pelvic Mesh Service. A referral to the NZ Female Pelvic Mesh Service run by Te Whatu Ora is an option to you if you are experiencing any problems that could be related to previous pelvic mesh surgery. 

Precision health: exploring opportunities and challenges to predict, prevent, diagnose, and treat health needs more precisely in Aotearoa New Zealand.

Source: New Zealand Ministry of Health

Summary

The Public Service Act 2020 requires all government departments to produce a LTIB at least once every three years. LTIBs contribute to future decision-making by improving public sector thinking around opportunities and challenges and put such opportunities into the public domain for discussion and debate. LTIBs are independent of Ministers and are not government policy.

Manatū Hauora has published its inaugural Long-term Insights Briefing – Precision health: Exploring opportunities and challenges to predict, prevent, diagnose, and treat health needs more precisely in Aotearoa New Zealand.

‘Precision health’ is an umbrella term for the use of technology and information to develop more precise ways of keeping people healthy. The briefing explores precision health opportunities and challenges through two examples: genomics and artificial intelligence. It also considers areas where changes might be needed to realise the opportunities offered by precision health and to mitigate risks over the next 10 years and beyond.

This document elevates conversations about precision health in Aotearoa New Zealand, with the insights gathered throughout the LTIB’s development providing guidance on what is most important to consider and discuss further. It is also part of a much larger conversation to understand the actions we need to take to ensure all New Zealanders live healthy lives.

Mental Health and Addiction Workforce Action Plan 2017–2021

Source: New Zealand Ministry of Health – Press Release/Statement:

Headline: Mental Health and Addiction Workforce Action Plan 2017–2021

Published online: 
23 April 2018
Cover for the Mental Health and Addiction Workforce Action Plan 2017–2021

Summary

The Mental Health and Addiction Workforce Action Plan is part of an outcomes approach. It contributes to achieving the vision of the New Zealand Health Strategy. For mental health and addiction, this means enabling people to thrive and experience wellbeing wherever they live and whatever their circumstances.

Together with the Mental Health and Wellbeing Outcome Framework and the Commissioning Framework, it will help us reshape our system to centre on people and what matters to them.

Our workforce is our most valuable resource, and achieving our vision depends on a capable and motivated workforce that works with people and their families and whānau to get the best outcomes.

This Action Plan recognises the importance of a combined effort to address the social determinants of health by working across health, justice and social sectors to ensure equitable positive outcomes for all New Zealanders.

It includes actions to develop a workforce with the right skills, knowledge, competencies and attitudes needed to design and deliver integrated and innovative responses.

The actions outlined in this action plan will support the development of the primary health care, community and specialist workforce to be well equipped, integrated, competent and capable to focus on improving health and wellbeing. It will guide decisions about investment and resourcing for the next five years and is relevant to all people working to improve outcomes for those with mental health and addiction issues.

What People Can Buy with Disability Funding: Ministry of Health Purchasing Guidelines

Source: New Zealand Ministry of Health – Press Release/Statement:

Headline: What People Can Buy with Disability Funding: Ministry of Health Purchasing Guidelines

Published online: 
17 April 2018

This document describes what government disability support funding (funding) can be used to buy. It is for people using:

  • Enhanced Individualised Funding (EIF)
  • Choice in Community Living (CiCL)
  • Enabling Good Lives (EGL) hosted personal budgets
  • Flexible Respite Budgets
  • Flexible Disability Supports (FDS).

Disabled people who can make choices about how they use their funding are more likely to buy goods and services that make their lives easier and/or better. This purchasing policy aims to give disabled people as much flexibility as possible over what they can buy with government funding.

A disability support (support) is a good or a service that helps a person overcome barriers that come with having an impairment within a disabling society.

Criteria

There are four criteria that must be met to be able to use funding to help buy a disability support.

One: It helps people live their life or makes their life better

The support should help people live a good life.

Each person has a different idea about what a good life is. The person’s goals and aspirations for a good life should be written out in a personal plan. This can be done with help from their Needs Assessment and Service Coordination (NASC) organisation or Independent Facilitator. Personal plans should include goals such as:

  • having good relationships
  • maintaining or improving skills
  • being able to do everyday activities at home or in the community
  • the person’s family/whānau being supported to continue their caring roles
  • being able to live in a home of the person’s own choice.

Two: It is a disability support

The support:

  • is only needed because the person is disabled and/or
  • costs more than would be the case if the person weren’t disabled and/or
  • is in addition to, or complements, the goods and/or services the person would need if they didn’t experience disability.

Three: It is reasonable and cost- effective

Generally, the support should be ‘reasonable’. Here it means that the support should cost about the same as (or less than) the market price for comparable things.

‘Cost-effective’ here means the best available outcome for the money spent.
 
It might cost more than another type of support but will help the person more, it will last longer or mean that less is spent on some other support now or in the future.

Four: It is not subject to a limit or exclusion

A person should explore other funding options to help get a support. Examples of other options include:

  • the Disability Allowance (from Work and Income)
  • grants, charitable donations
  • equipment funding (either by the Ministry of Education or the Ministry of Health)
  • specialist services, (eg, the Ministry of Health’s Behaviour Support Services and Child Development Services)
  • district health board funded therapies
  • transport allowances (eg, the Total Mobility transport scheme).

In some cases, people can buy a support when funding for that support has been turned down by (or on behalf of) the responsible government agency or if waiting times are too long and the proposed support is expected to:

  • achieve a person’s life goal that would not otherwise be achievable and/or
  • reduce disability support costs over time and/or
  • reduce the risk that disability support costs will increase in the future.

The funding cannot be used for:

  • paying family carers who are either a family member living with the disabled person or a parent or a spouse
  • illegal activities, gambling or alcohol
  • things that are not disability supports, such as health services provided by a hospital or income support.

Further help

For more help in understanding this policy, people can talk to their NASC organisation or their provider to work out if a support they want to buy meets the criteria.

See Ministry of Health Purchasing Guidelines Processes (docx, 221 KB) and Ministry of Health Purchasing Guidelines Notes (docx, 186 KB) for more information.

Mortality 2015 data tables

Source: New Zealand Ministry of Health – Press Release/Statement:

Headline: Mortality 2015 data tables

Published online: 
16 April 2018

These tables contain information on the underlying causes of all deaths registered in New Zealand in 2015. A ‘Quick facts’ section also includes information on rates of death by ethnicity and selected causes of mortality.

Most information is broken down by age, sex, ethnicity, district health board and statistical classification chapters, subgroups and three character codes.

These tables form part of the Mortality and Demographic Data annual series.

This data is sourced from the Mortality Collection.

Quick facts

  • There were 31,796 deaths registered in 2015, equating to an age-standardised rate of 380.1 deaths per 100,000 population.
  • Males accounted for 15,929 deaths in 2015, slightly higher than for females (15,867).
  • Māori accounted for 3,413 deaths in 2015, 10.7% of all deaths registered.
  • The leading causes of death were cancer, ischaemic heart diseases and cerebrovascular diseases. Cancer deaths made up 30.2% of all deaths, ischaemic heart diseases 15.8% and cerebrovascular diseases 7.8% in 2015.
  • For Māori, the leading causes of death in 2015 were cancer, ischaemic heart diseases and chronic lower respiratory diseases.
  • Similar to previous years, mortality rates were generally higher for males than for females. For example, males had higher mortality rates for melanoma and ischaemic heart diseases compared with females in 2015.
  • As seen in previous years, mortality rates for Māori were generally higher than for non-Māori. For example, Māori had higher mortality rates for diabetes mellitus and chronic lower respiratory diseases compared with non-Māori in 2015.
Total number of deaths and mortality rates, 2015
  Number of deaths Percentage of deaths by sex Mortality rate
Total Male Female Male Female Total Male Female
Māori 3,413 1,801 1,612 52.8 47.2 648.9 746.5 567.8
Non-Māori 28,383 14,128 14,255 49.8 50.2 354.1 411.3 303.4
Total 31,796 15,929 15,867 50.1 49.9 380.1 441.0 326.1

Note: rates per 100,000 population, age standardised to WHO World Standard Population.

Mortality: Historical summary 1948–2015

Source: New Zealand Ministry of Health – Press Release/Statement:

Headline: Mortality: Historical summary 1948–2015

Published online: 
16 April 2018

Summary

These tables present mortality data (numbers and age-standardised rates) by sex for certain causes of death for each year from 1948 to 2015. Māori and non-Māori mortality data is presented from 1996 to 2015.

The causes of death included are:

  • All cancer
  • Ischaemic heart disease
  • Cerebrovascular disease
  • Chronic lower respiratory diseases
  • Other forms of heart disease
  • Influenza and Pneumonia
  • Diabetes mellitus
  • Motor vehicle accidents
  • Intentional self-harm
  • Assault
  • All deaths.

Numbers and rates are available as:

About the data used in this edition

Data from 1948 to 1995 presented in these tables was sourced from publications in the Ministry of Health Mortality data and stats series.

Data from 1996 to 2015 was extracted from the New Zealand Mortality Collection electronic records on 13 February 2018. Rates have been re-calculated for data on deaths registered between 1996 and 2015, to reflect ongoing updates to data in the New Zealand Mortality Collection (eg, following the release of coroners’ findings) and the revision of population estimates. This has resulted in small changes to some numbers and rates from those reported in previous publications.

At the time of data extraction, there were 575,058 deaths registered from 1996 to 2015. Included in this data were 669 deaths provisionally coded (awaiting coroners’ findings) and 32 deaths awaiting coroners’ findings with no known cause.

Ethnic breakdowns of mortality data are only shown from 1996 onwards because there was a significant change in the way ethnicity was defined, and in the way ethnicity data was collected in 1995. For more information please refer to the Ministry of Health report, Mortality and Demographic Data 1996.

Mortality 2015 data tables (provisional)

Source: New Zealand Ministry of Health – Press Release/Statement:

Headline: Mortality 2015 data tables (provisional)

Published online: 
20 December 2017

These tables contain provisional information on the underlying causes of all deaths registered in New Zealand in 2015. A ‘Quick facts’ section also includes information on rates of death by ethnicity and selected causes of mortality.

Most information is broken down by age, sex, ethnicity, district health board and statistical classification chapters, subgroups and three character codes. Information for deaths from external causes has been aggregated. Further detail will be provided when the final data for 2015 is released in 2018.

These tables form part of the Mortality and Demographic Data annual series.

This data is sourced from the Mortality Collection.

Key mortality statistics – 2015
  Number of deaths Percentage of deaths by sex Mortality rate
Total Male Female Male Female Total Male Female
Māori 3,413 1,801 1,612 52.8 47.2 648.9 746.5 567.8
Non-Māori 28,383 14,128 14,255 49.8 50.2 354.1 411.3 303.4
Total 31,796 15,929 15,867 50.1 49.9 380.1 441.0 326.1

Note: rates per 100,000 population, age standardised to WHO World Standard Population.

Whāia Te Ao Mārama 2018 to 2022: The Māori Disability Action Plan

Source: New Zealand Ministry of Health – Press Release/Statement:

Headline: Whāia Te Ao Mārama 2018 to 2022: The Māori Disability Action Plan

Published online: 
04 April 2018

Summary

Whāia Te Ao Mārama is a culturally anchored approach to supporting Māori with disabilities (tāngata whaikaha) and their whānau because Māori are more likely to be disabled than the general population. Most tāngata whaikaha identify as Māori first, so access to Te Ao Māori (the Māori world) is important to them.

The previous version of the plan, Whāia Te Ao Mārama 2012 to 2017, led to changes that improved outcomes for tāngata whaikaha and their whānau. While much has been achieved between 2012 and 2017, improving outcomes for tāngata whaikaha and their whānau remains an important priority.

Whāia Te Ao Mārama:

  • supports tāngata whaikaha to achieve their aspirations and to reduce the barriers they face
  • builds on the foundation, vision and outcomes of Whāia Te Ao Mārama 2012 to 2017
  • outlines progress and changes since 2012
  • documents goals and actions for 2018 to 2022.
  • was developed in partnership with Māori disability stakeholders and with the oversight and endorsement of Te Ao Mārama: the Māori Disability Advisory Group.

Whāia Te Ao Mārama recognises that everyone must work together to achieve the vision – tāngata whaikaha pursue a good life with support. It outlines what the Ministry is committing to do from 2018 to 2022 and provides examples of actions tāngata whaikaha, whānau, health and disability providers, iwi and other organisations can take.

Where I Live; How I Live – Disability Support Services Community Residential Support Services Strategy 2018 to 2020

Source: New Zealand Ministry of Health – Press Release/Statement:

Headline: Where I Live; How I Live – Disability Support Services Community Residential Support Services Strategy 2018 to 2020

Published online: 
28 March 2018
Disability Support Services Community Residential Support Services Strategy.

Where I Live; How I Live is about optimising the independence and self-determination of disabled people. It is in line with the Enabling Good Lives (EGL) principles that support people with a disability to make decisions about the kind of life they want.

This strategy guides the Ministry’s Disability Support Services, disabled people and their families/whānau, and residential service providers, in achieving the following outcomes:

  • greater choice, control and flexibility over where and how disabled people live
  • access to information and support to enable well-considered choices about where and how disabled people choose to live and receive support
  • increasing independence and choice fostered by service providers.

The strategy also aims to improve options for disabled people whose complex support requirements present challenges for the delivery of a sustainable service.

National Booking Reporting System File Specification

Source: New Zealand Ministry of Health – Press Release/Statement:

Headline: National Booking Reporting System File Specification

Version 4.4

Published online: 
28 March 2018

The National Booking Reporting System (NBRS) File Specification defines the file format used to send information to the Ministry for inclusion in the NBRS national collection. This includes the file layout and, to a lesser extent, the business rules used for validating the data items within the file.

There are two audiences for this document:

  • Software developers designing, implementing and altering provider systems to ensure that they export information in a format suitable for loading into the national collection.
  • Business analysts verifying that all required data elements are present and specified correctly.

This document should be read in conjunction with the National Booking Reporting System Data Dictionary.