Those found with the sickle cell trait or disease are registered and receiving treatment at government health facilities in Karnataka.
The state health department has set an ambitious target of screening 3.5 lakh people for sickle cell anaemia by 2026.
Sickle cell trait indicates that the person has inherited the sickle-cell gene mutation from one parent.
In sickle cell crisis, blood flow can be blocked, leading to severe pain in the body.
Haemoglobinopathy prevalence in KarnatakaHaemophilia: 2,706 casesThalassemia: 2,288 casesSickle cell trait: 2,004 peopleSickle cell anaemia: 192 cases
Dr Shakila N, Deputy Director, and State Nodal Officer of the State Blood Cell, pointed out that all identified cases so far have been concentrated in the first three districts among the seven. Those found with the sickle cell trait or disease are registered and receiving treatment at government health facilities in Karnataka. They have access to free blood transfusions and hydroxyurea medicines even at the primary health centre (PHC) level.
The state health department has set an ambitious target of screening 3.5 lakh people for sickle cell anaemia by 2026. However, screening for haemoglobinopathies, which are inherited blood disorders affecting haemoglobin, is currently conducted only for those with a family history or who are symptomatic.
Sickle cell trait indicates that the person has inherited the sickle-cell gene mutation from one parent. They will present with no clinical manifestation of symptoms but carry the gene. If both parents are carriers, there is a 50% chance their children will inherit the trait and a 25% chance of the children developing a sickle cell disease, note haematologists. In sickle cell crisis, blood flow can be blocked, leading to severe pain in the body.
"The lack of a premarital or prenatal screening for such disorders means that there is often retrospective testing done only if someone comes to the hospital with symptoms," said Dr Manoj Reddy, paediatric haemato-oncologist, and bone marrow transplant physician, BMJH Sankalp India Foundation.
Dr Sitalakshmi Subramanian, a haematopathologist and transfusion medicine specialist at St John's Medical College Hospital, emphasised that early detection of gene mutations, even during pregnancy, allows families to receive counselling about the potential consequences and options for preventing further transmission or accessing available treatments.
Since treatment is lifelong — or expensive in the case of a bone marrow transplant — prenatal screening and counselling are the only ways to prevent transmission of the gene mutation.
Centres at Koppal, Kalaburagi
The proposal to establish an Integrated Centre for Diagnosis and Treatment (ICDT) for Haemoglobinopathies at Koppal and Kalaburagi has been approved by the government.
“The two ICDT centres would greatly help us in screening for such blood disorders. After an expert consultation, the state will plan for a pilot project to screen for such disorders,” said a senior health department official.
Haemoglobinopathy prevalence in Karnataka
Haemophilia: 2,706 cases
Thalassemia: 2,288 cases
Sickle cell trait: 2,004 people
Sickle cell anaemia: 192 cases
