Safety and Quality > Our Work > Transvaginal Mesh > Resources for consumers, clinicians and health service organisations – transvaginal mesh

The Commission has finalised a number of resources and guidance documents to improve health care for women considering the treatment options for pelvic organ prolapse (POP), stress urinary incontinence (SUI), and complications of transvaginal mesh.

These include:

  • Consumer information resources
  • Care pathways for POP, SUI and complications of transvaginal mesh
  • Guidance for hospital credentialing of senior medical practitioners to implant and remove mesh for treatment of POP and SUI
  • Service model framework for transvaginal mesh complications and removal.

These documents were informed by detailed consideration of the peer-reviewed evidence and consultation with consumers, clinicians, relevant colleges and surgical specialty societies, state and territory health departments, the Australian Government Department of Health and the Reference Group that was convened to support this work.

These resources have taken into account recent changes to the registration of a number of transvaginal mesh devices on the Australian Register of Therapeutic Goods (ARTG) by the Therapeutic Goods Administration (TGA). While registration of transvaginal mesh products for treatment of POP has been cancelled, there is still potential for clinicians to use these devices with the necessary approvals. For this reason, the Commission has continued to produce guidance documents for POP.

Consumer information resources on treatment options for POP, SUI and complications of transvaginal mesh

These resources have been developed following extensive consultation with women affected by complications of transvaginal mesh.

The resources explain the symptoms of POP, SUI and complications of transvaginal mesh, the range of treatment options – doing nothing, non-surgical and surgical treatments – and their risks and benefits. Information is included about changes made by the TGA to remove transvaginal mesh products from the ARTG, where the sole use is the treatment of POP via transvaginal implantation, and to remove single incision mini-slings for treatment of SUI.  The resources also include advice that use of these mesh products in Australia now requires special approval.

Each resource also includes information on complications which may result from insertion of transvaginal mesh, and where to find more detail about the complications.  A list of questions which women might consider asking their doctor, prior to these procedures is also included.

Care pathways for POP, SUI and complications of transvaginal mesh

The care pathways describe clinical considerations to be made when clinicians are assessing women who have POP, SUI and transvaginal mesh complications. The pathways provide clinicians with an evidence-based approach to first line management, specialised surgical and non-surgical care and the types of medical specialists who may be involved in providing care.

The care pathways provide an opportunity for alignment with the pathways used by a number of Primary Health Networks to guide the discussions between women and their general practitioners

There are also surgical pathways for POP and SUI.  These use a traffic light approach (red, yellow, green) to identify options for surgical treatments, based on the strength of evidence and potential patient outcomes for each type of procedure:

The pathways are informed by the work of the International Collaboration on Incontinence.  The Commission acknowledges the contribution of this group in the development of the Commission’s versions of the resources.

Guidance for hospital credentialing of senior medical practitioners to implant and remove transvaginal mesh for treatment of POP and SUI

Credentialing is the process used by public and private hospitals to ensure that only suitably experienced, trained and qualified medical practitioners provide particular types of services. Credentialing is essential to ensure the safety of patient care.

Guidance has been finalised for hospital credentialing and training of senior medical practitioners who perform transvaginal mesh surgeries and mesh removal including:

The Guidance describes the experience and qualifications that senior medical practitioners need to be credentialed to implant and remove mesh for treatment of POP and SUI. It also includes recommendations on device specific training, the requirements for maintaining skills, monitoring and reporting on patient outcomes, the types of specialty supports services hospitals should have if they offer implantation and removal of transvaginal mesh and the requirement for post-operative follow-up.

The states and territories will consider the use of the Guidance in their local credentialing processes. The private health sector also undertakes credentialing processes, and the Commission will be working with the private health sector to promote the use of these Guidance documents for credentialing across private hospitals.

Service Model Framework

The Commission has completed a service model framework to support state and territories and the private sector in their planning of services for the use and removal of transvaginal mesh devices and management of mesh-related complications.  Clinical care pathways, models of care, and workforce considerations also inform the development of service models and service delivery.  The framework was developed with input from the reference group and informed by the states and territories.  A number of core components of the model of care and service delivery have been determined in consideration of the issues reported by women who have received services in relation to transvaginal mesh implantation, treatment for complications; and/or removal.  This resource also provides information from the states and territories on their services.

  • Service model framework for transvaginal mesh complications and removal (PDF 151KB) (Word 283KB)