ArticleBMC health services research2010
A toolkit for incorporating genetics into mainstream medical services: Learning from service development pilots in England.
Article in BMC health services research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
21 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Current Genetic Service Delivery Models for the Provision of Genetic Testing in Europe: A Systematic Review of the Literature.Frontiers in genetics · 2019Pooled it
- Patients offered genomic testing for rare disease and cancer: a real-world evaluation of impact and processes of care.European journal of human genetics : EJHG · 2026Article
- Precision Medicine in Rural Settings: Patient Perspectives on Clinician-Ordered Genetic Testing.Research square · 2026Article
- Inherited Susceptibility to Cancer: Past, Present and Future.Annals of human genetics · 2025Review
- Improved provider preparedness through an 8-part genetics and genomic education program.Genetics in medicine : official journal of the American College of Medical Genetics · 2022Article
- Pitfalls and challenges in genetic test interpretation: An exploration of genetic professionals experience with interpretation of results.Clinical genetics · 2021Article
- Mainstreaming Genetic Testing for Adult Patients With Autosomal Dominant Polycystic Kidney Disease.Canadian journal of kidney health and disease · 2021Article
- The Provision of Genetic Testing and Related Services in Quebec, Canada.Frontiers in genetics · 2020Article
- Article
- Moving into the mainstream: healthcare professionals' views of implementing treatment focussed genetic testing in breast cancer care.Familial cancer · 2019Article
- Healthcare System Priorities for Successful Integration of Genomics: An Australian Focus.Frontiers in public health · 2019Review
- Increasing nursing capacity in genomics: Overview of existing global genomics resources.Nurse education today · 2018Article
- Preparing for genomic medicine: a real world demonstration of health system change.NPJ genomic medicine · 2017Review
- Developing and assessing the utility of a You-Tube based clinical genetics video channel for families affected by inherited tumours.Familial cancer · 2016Article
- What results to disclose, when, and who decides? Healthcare professionals' views on prenatal chromosomal microarray analysis.Prenatal diagnosis · 2016Article
- Are Australasian Genetic Counselors Interested in Private Practice at the Primary Care Level of Health Service?Journal of genetic counseling · 2015Article
- A prospective cohort study assessing clinical referral management & workforce allocation within a UK regional medical genetics service.European journal of human genetics : EJHG · 2015Article
- Development of cancer genetic services in the UK: A national consultation.Genome medicine · 2015Article
- Developing a framework for implementation of genetic services: learning from examples of testing for monogenic forms of common diseases.Journal of community genetics · 2014Article
- Ten years of the national genetic diabetes nurse network: a model for the translation of genetic information into clinical care.Clinical medicine (London, England) · 2014Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
Abstract
backgroundAs advances in genetics are becoming increasingly relevant to mainstream healthcare, a major challenge is to ensure that these are integrated appropriately into mainstream medical services. In 2003, the Department of Health for England announced the availability of start-up funding for ten 'Mainstreaming Genetics' pilot services to develop models to achieve this.
methodsMultiple methods were used to explore the pilots' experiences of incorporating genetics which might inform the development of new services in the future. A workshop with project staff, an email questionnaire, interviews and a thematic analysis of pilot final reports were carried out.
resultsSeven themes relating to the integration of genetics into mainstream medical services were identified: planning services to incorporate genetics; the involvement of genetics departments; the establishment of roles incorporating genetic activities; identifying and involving stakeholders; the challenges of working across specialty boundaries; working with multiple healthcare organisations; and the importance of cultural awareness of genetic conditions. Pilots found that the planning phase often included the need to raise awareness of genetic conditions and services and that early consideration of organisational issues such as clinic location was essential. The formal involvement of genetics departments was crucial to success; benefits included provision of clinical and educational support for staff in new roles. Recruitment and retention for new roles outside usual career pathways sometimes proved difficult. Differences in specialties' working practices and working with multiple healthcare organisations also brought challenges such as the 'genetic approach' of working with families, incompatible record systems and different approaches to health professionals' autonomous practice. 'Practice points' have been collated into a Toolkit which includes resources from the pilots, including job descriptions and clinical tools. These can be customised for reuse by other services.
conclusionsHealthcare services need to translate advances in genetics into benefits for patients. Consideration of the issues presented here when incorporating genetics into mainstream medical services will help ensure that new service developments build on the body of experience gained by the pilots, to provide high quality services for patients with or at risk of genetic conditions.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.