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Preventive Medicine 2018

Journal of Preventive Medicine

ISSN: 2572-5483

Page 79

July 16-17, 2018

London, UK

9

th

Edition of International Conference on

Preventive Medicine

& Public Health

Background:

Globally, thalassemia is the most common

hereditary hemoglobinopathy, affecting equally males

and females and occurred in 4.4/10,000 live births. In the

developing world, the majority of patients die before the age

of 20 years. In Iraq, there is a little data on epidemiology and

burden of thalassemia. The objectives of this study were to

identify the epidemiological characteristics of thalassemia

patients in Iraq, estimate its incidence, prevalence, and identify

their trends during 2010-2015.

Methods:

A retrospective review of all patients’ records for

2010-2015 that retrieved through visiting the accessible 16 (of

the 19) thalassemia centers in Iraq. Corresponding population

data of Iraq provinces obtained from Ministry of Planning. We

calculated annual incidence and prevalence for all provinces.

Results:

Thalassemia

represented

75%

of

all

hemoglobinopathies in Iraq in 2015, with a prevalence of

36/100,000 population, and incidence of 34/100,000 livebirths.

The prevalence of thalassemia increased from 32/100,000

population in 2010 to 36/100,000 population in 2015, while

the incidence decreased from 63/100,000 livebirths in

2010 to 34/100,000 livebirths in 2015. β-thalassemia major

represented 67% of all types of thalassemia. The highest

prevalence of thalassemia was registered in Basra province

(74/100,000 population). Male, female ratio was 1.1:1. Most

of the patients were in the age group 6–15 years (42%) and

only 9.5% aged ≥30 years. Around 75% of patients were of

consanguineous parents. Among 10,740 patients aged 6+

years (school age), 13% (1,401) did not attend schools. About

28% (3705) of all patients aged >18years; 18% (648) of them

were married, 8% (310) attended college, and 17% (628) were

employed.

Conclusion:

In spite of the decreasing incidence, hundreds

of new children with thalassemia are born every year. Health

education, carrier screening and premarital screening remain

the best preventive measures that can enhance health, social

and economic benefits.

kamalabdrazaq@yahoo.com

Epidemiological profile of thalassemia-Iraq, 2015

Kamal A Kadhim, Kadhim H Baldawi

and

Faris Lami

University of Baghdad, Iraq

J Prev Med 2018, Volume 3

DOI: 10.21767/2572-5483-C1-003