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. 2022 Jun 28;17(1):87. doi: 10.1007/s11657-022-01117-6

Table 5.

Current UK criteria used by the UK NSC for assessment of a screening programme. For each criterion, a decision has been made as to whether screening for hip fracture risk using the proposed programme would satisfy the criterion needs. The numbers in parentheses represent the number of responses saying yes, in part or no for each criterion (a total of 20 experts responded to the survey). The final four criteria were considered beyond the scope of this paper

Criterion Met (✓) or not met (χ)
(Yes, in part, no)
The condition • The condition should be an important health problem

(17,3,0)

• The epidemiology and natural history of the condition, including development from latent to declared disease, should be adequately understood and there should be a detectable risk factor, disease marker, latent period or early symptomatic stage

(18,2,0)

• All the cost-effective primary prevention interventions should have been implemented as far as practicable

(12,7,1)

The test • There should be a simple, safe, precise and validated screening test

(16,3,1)

• The distribution of test values in the target population should be known and a suitable cut-off level defined and agreed

(17,2,1)

• The test should be acceptable to the population

(19,1,0)

• There should be an agreed policy on the further diagnostic investigation of individuals with a positive test result and on the choices available to those individuals

(17,3,0)

The treatment • There should be an effective treatment or intervention for patients identified through early detection, with evidence of early treatment leading to better outcomes than late treatment

(16,3,1)

• There should be agreed evidence-based policies covering which individuals should be offered treatment and the appropriate treatment to be offered

(19,1,0)

• Clinical management of the condition and patient outcomes should be optimised in all healthcare providers prior to participation in a screening programme

(18,1,1)

The screening programme • There should be evidence from high-quality randomised controlled trials that the screening programme is effective in reducing mortality or morbidity. Where screening is aimed solely at providing information to allow the person being screened to make an informed choice (e.g. Down’s syndrome, cystic fibrosis carrier screening), there must be evidence from high-quality trials that the test accurately measures risk. The information that is provided about the test and its outcome must be of value and readily understood by the individual being screened

(16,3,1)

• There should be evidence that the complete screening programme (test, diagnostic procedures, treatment/intervention) is clinically, socially and ethically acceptable to health professionals and the public

(19,1,0)

• The benefit from the screening programme should outweigh the physical and psychological harm (caused by the test, diagnostic procedures and treatment)

(19,1,0)

• The opportunity cost of the screening programme (including testing, diagnosis and treatment, administration, training and quality assurance) should be economically balanced in relation to expenditure on medical care as a whole (i.e. value for money). Assessment against these criteria should have regard to evidence from cost benefit and/or cost-effectiveness analyses and have regard to the effective use of available resource

(16,4,0)

• All other options for managing the condition should have been considered (e.g. improving treatment, providing other services), to ensure that no more cost-effective intervention could be introduced or current interventions increased within the resources available

(14,4,2)

• There should be a plan for managing and monitoring the screening programme and an agreed set of quality assurance standards Beyond scope
• Adequate staffing and facilities for testing, diagnosis, treatment and programme management should be available prior to the commencement of the screening programme Beyond scope
• Evidence-based information, explaining the consequences of testing, investigation and treatment, should be made available to potential participants to assist them in making an informed choice Beyond scope
• Public pressure for widening the eligibility criteria for reducing the screening interval, and for increasing the sensitivity of the testing process, should be anticipated. Decisions about these parameters should be scientifically justifiable to the public Beyond scope