Biomarker tests to help diagnose preterm labour in women with intact membranes: Diagnostics consultation
The National Institute for Health and Care Excellence (NICE) is producing guidance on using biomarker tests (Actim Partus, PartoSure and the Rapid fFN 10Q Cassette Kit) in the NHS in England. The diagnostics advisory committee has considered the evidence base and the views of clinical and patient experts.
The advisory committee is interested in receiving comments on the following:
- Has all of the relevant evidence been taken into account?
- Are the summaries of clinical and cost effectiveness reasonable interpretations of the evidence?
- Are the provisional recommendations sound, and a suitable basis for guidance to the NHS?
NICE is committed to promoting equality of opportunity, eliminating unlawful discrimination and fostering good relations between people with particular protected characteristics and others. Please let us know if you think that the preliminary recommendations may need changing in order to meet these aims. In particular, please tell us if the preliminary recommendations:
- could have a different effect on people protected by the equality legislation than on the wider population, for example by making it more difficult in practice for a specific group to access the technology
- could have any adverse effect on people with a particular disability or disabilities.
Please provide any relevant information or data you have regarding such effects and how they could be avoided or reduced.
Note that this document is not NICE's final guidance on biomarker tests (Actim Partus, PartoSure and the Rapid fFN 10Q Cassette Kit). The recommendations in section 1 may change after consultation.
After consultation, the committee will meet again to consider the evidence, this document and comments from the consultation. After considering these comments, the committee will prepare its final recommendations, which will be the basis for NICE’s guidance on the use of the technology in the NHS in England.
For further details, see the Diagnostics Assessment Programme manual.
Closing date for comments: 3 April 2018
This page was last updated: 09 March 2018