Evidence generation plan for HTG10877 Technologies for diagnosing endometriosis in primary care
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6 Implementation considerations
The following considerations around implementing the evidence generation process have been identified through working with system partners.
6.1 Implementing the guidance
The committee heard that diagnosis is often delayed and access to care is unequal for certain population groups, including:
people with female reproductive organs who do not identify as women, including trans men and non-binary people
young people
women, trans men and non-binary people:
from ethnic minority backgrounds (frequent misdiagnosis or dismissal of pain, or cultural barriers to discussing menstrual health)
with learning disabilities or who have difficulties communicating their symptoms
who find transvaginal ultrasound unacceptable
who do not have access to healthcare professionals in primary care with high levels of expertise in transvaginal ultrasound.
The technologies may offer additional benefit to women, trans men or non-binary people with a needle phobia.
Reporting intervention-related adverse events (for example, worsening pain) is essential to assess any risk associated with the use of the technologies in the NHS.
6.2 Implementing data collection
The technologies are currently only available in the private healthcare sector.
It is likely that evidence generation within the NHS will cause additional resource and staffing burden. The process is most likely to succeed with dedicated research staff to reduce the burden on NHS staff.
Practical requirements, such as fasting, medication cessation, long appointment times and the need for a quiet clinical environment, may result in missed appointments and incomplete datasets.
ISBN: [to be added at publication]
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