BMJ 2004;329:1134-1137 (13 November), doi:10.1136/bmj.329.7475.1134
Primary care
Iranian national thalassaemia screening programme
Ashraf Samavat, head1,
Bernadette Modell, emeritus professor of community genetics2
1 Genetics Office, Disease Management Centre, Ministry of Health and Medical Education, Tehran, Iran,
2 University College London Centre for Health Informatics and Multiprofessional Education, London N19 5LW
Correspondence to: B Modell b.modell@pcps.ucl.ac.uk
Iran's experience shows that genetic screening can be successful in lower resource countries and also provides some lessons for high resource nations
| The first 150 words of the full text of this article appear below. |
Introduction
Progress in controlling communicable diseases increases the
relative importance of non-communicable diseases, including
genetic disorders.
1 In Iran, the development of primary health
care over the past 20 years has greatly reduced infant mortality
and crude birth rate. Accordingly, in 1991 prevention of non-communicable
diseases was added to the primary healthcare programme, and
a department for the control of non-communicable disease, including
a genetics office, was established within the Ministry of Health
and Medical Education.

Thalassaemia, which is an important
health problem in Iran,
2 was chosen to test the feasibility
of preventing non-communicable disease in primary care. We describe
how the programme has been implemented.
Primary healthcare infrastructure in Iran
Iran has a five level primary healthcare network covering the
entire population of 60 million, in 28 provinces (figure).
3 Responsibility for health and medical education are merged throughout
the system. Each medical university has a vice chancellor responsible
for primary health care. There were
. . . [Full text of this article]
Design of thalassaemia prevention programme
Results of screening programme
Effect of evaluation on development of programme
Financial aspects
Problems and further development
Lessons from the Iranian experience
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Advantages of genetic screening in primary care

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