Context: Poor diagnosis of haemophilia and lack of accessible prophylaxis treatment in India, despite the high global burden of disease, remains a cause of concern for experts.
UPSC Relevance:
Prelims , UPSC has been asking common disease and treatment therapies in Prelims.
PYQ:
Prelims 2021
In the context of hereditary diseases, consider the following statements:
1. Passing on mitochondrial diseases from parent to child can be prevented by mitochondrial replacement therapy either before or after in vitro fertilization of the egg.
2. A child inherits mitochondrial diseases entirely from mother and not from father.
Which of the statements given above is/are correct?
a) 1 only
b) 2 only
c) Both 1 and 2
d) Neither 1 nor 2
Prelims 2014
Consider the following diseases:
1. Diphtheria
2. Chickenpox
3. Smallpox
Which of the above diseases has/have been eradicated in India?
a) 1 and 2 only
b) 3 only
c) 1, 2 and 3
d) None
What Is Haemophilia?
- It is an inherited, rare bleeding disorder where blood doesn’t clot properly.
- Cause: A lack or deficiency of clotting factors, which are proteins essential for blood to clot, most often Factor VIII.
- Haemophilia is more common in males because it is an X-linked recessive disorder. Males have one X chromosome and one Y chromosome, so if their single X chromosome carries the gene for haemophilia, they will develop the disorder. Females are typically only carriers because they can have one normal X chromosome to compensate for the affected X chromosome.
- Types of Haemophilia
- Haemophilia A: This is the most common type, also known as classic Haemophilia. It results from a deficiency of clotting Factor VIII in the blood.
- Haemophilia B: Also called Christmas Disease (named after the first patient diagnosed with it, Stephen Christmas), this type is caused by a lack of clotting Factor IX.
- Haemophilia C: This very rare form of Haemophilia is due to a deficiency in clotting Factor XI.
- Symptoms: Excessive bleeding from small injuries and, more seriously, spontaneous internal bleeding in joints, muscles, or even the brain.
- Complications: Can cause chronic pain, permanent disability, and can be life-threatening.
- Haemophilia gained the nickname “Royal Disease” due to its widespread appearance in the royal families of Europe during the 19th and 20th centuries.
- According to a global survey conducted by the World Federation for Haemophilia, India has the second-highest load of patients with Haemophilia A in the world, and is the only developing country amongst the top five countries.
The Challenge of Diagnosis and Treatment in India
- Undiagnosed Cases: Only about 29,000 of an estimated 1-1.5 lakh patients have been diagnosed in India. Almost 80% of patients remain undiagnosed in India.
- Reasons for Low Diagnosis: Lack of awareness, limited diagnostic facilities, and socio-economic barriers.
- Impact of Undiagnosed Cases: Puts patients at risk for bleeds, leading to disability and a reduced life expectancy.
- Socio-economic Burden: Undiagnosed and untreated Haemophilia leads to school absenteeism, unemployment, and loss of productivity.
Prophylaxis: The Gold Standard of Care
- It is a regular replacement therapy of the deficient clotting factors to prevent bleeds before they occur.The ultimate goal is to achieve “zero bleeds,” allowing patients to live a more active and independent life.
- Methods: Frequent intravenous injections of clotting factors or newer non-factor products via subcutaneous injections.
- Benefits Over On-Demand Therapy:
- Prevents Joint Damage: Maintains clotting factor levels to reduce or eliminate joint bleeds, preserving mobility and limiting disability.
- Enhances Quality of Life: Patients have fewer bleeds and less pain, enabling them to attend school and work more consistently.
- Reduces Healthcare Burden: Decreases the need for urgent care and hospitalization, reducing long-term healthcare costs.
- Global vs. Indian Context:
India: On-demand therapy is still the primary treatment, though some states have begun to offer regular replacement for children.
Developed Nations: Approximately 90% of Haemophilia patients are on prophylaxis, leading to a near-normal life expectancy.
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