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PIB Summary- 3rd January, 2024 | Current Affairs & Hindu Analysis: Daily, Weekly & Monthly - UPSC PDF Download

Sickle Cell Anaemia

Context
A significant milestone has been crossed by the Health Ministry. More than 1 crore people have been screened for Sickle Cell Disease under the National Sickle Cell Anaemia Elimination Mission.

Sickle Cell Anaemia

  • Haemoglobin which is tasked with carrying oxygen to all parts of the body, has four protein subunits — two alpha and two beta.
  • In some people, mutations in the gene that creates the beta subunits impact the shape of the blood cell and distorts it to look like a sickle.
  • A round red blood cell can move easily through blood vessels because of its shape but sickle red blood cells end up slowing, and even blocking, the blood flow.
  • Moreover, sickle cells die early, resulting in a shortage of red blood cells that deprive the body of oxygen.
  • These obstructions and shortages may cause chronic anaemia, pain, fatigue, acute chest syndrome, stroke, and a host of other serious health complications.
  • Without treatment, quality of life is compromised and severe cases can become fatal in the initial years of life.

Symptoms
The symptoms of sickle cell anaemia can vary from person to person, but common symptoms include:

  • Painful episodes (sickle cell crisis)
  • Anaemia
  • Fatigue and weakness
  • Shortness of breath
  • Delays in growth and development
  • Joint pain
  • frequent infections

Treatment
Currently, there is no cure for sickle cell anaemia, but treatments are available to manage the symptoms and prevent complications.

  • Pain management
  • Blood transfusions
  • Antibiotics to prevent infections
  • Hydoxyurea, a medication to reduce the frequency of sickle cell crises
  • Stem cell transplantation in some cases

Indian Government Initiatives to reduce Sickle Cell Anaemia

  • The Indian Council of Medical Research and the National Rural Health Mission in different States are undertaking outreach programmes for better management and control of the disease.
  • The Ministry of Tribal Affairs launched a portal wherein people can register themselves if they have the disease or the trait, in order to collate all information related to SCA among tribal groups.
  • In the Budget, the Union Health Minister said the government plans to distribute “special cards” across tribal areas to people below the age of 40.
    • The cards will be divided into different categories based on the screening results.
    • The mission will receive funding under the National Health Mission.

National Sickle Cell Anaemia Elimination Mission:

  • The mission aims to tackle the significant health challenges associated with sickle cell disease (SCD), with a particular focus on the tribal population.
  • It represents a crucial milestone in the Government’s ongoing efforts to eliminate SCD as a public health issue by 2047.

Objectives of the Mission:


Provision of Affordable and Accessible Care:

  • Ensure that all SCD patients have access to affordable and easily accessible healthcare services.
  • Improve the availability and affordability of SCD treatments and medications.

Quality of Care:

  • Enhance the quality of care provided to SCD patients.
  • Implement measures to ensure that healthcare facilities meet the required standards for SCD management.

Prevalence Reduction:

  • Implement strategies to reduce the prevalence of SCD in the population.
  • Focus on early detection and prevention methods to minimize the number of new SCD cases.

Health Promotion:

  • Raise awareness about SCD through health promotion campaigns.
  • Provide pre-marital genetic counseling to educate individuals about the risks associated with SCD.

Prevention:

  • Conduct universal screening programs to identify SCD cases at an early stage.
  • Emphasize the importance of early detection and prompt intervention to prevent complications.

Holistic Management & Continuum of Care:

  • Develop a comprehensive management approach for individuals with SCD.
  • Establish coordinated care across primary, secondary, and tertiary healthcare levels.
  • Ensure adequate treatment facilities at tertiary healthcare institutions.

Patient Support System:

  • Establish a robust support system for SCD patients.
  • Provide guidance, counseling, and emotional support to patients and their families.

Community Adoption:

  • Encourage community involvement in SCD prevention and care.
  • Promote the adoption of preventive measures and support systems within local communities.

Coverage Targets:

  • The mission aims to reach a total of 7 crore people.
  • Provide screening, counseling, and care services for individuals with SCD within a three-and-a-half-year timeframe.

Desert Cyclone 2024

Context
The Joint Military Exercise ‘Desert Cyclone 2024’ between India and UAE will be held from January 2 to January 15 in Rajasthan.

Joint Military Exercise “Desert Cyclone 2024”

  • Inaugural edition of a joint military exercise between India and the United Arab Emirates (UAE), focused on enhancing interoperability and sharing best practices in Urban Operations.
  • Aims to mark a significant milestone in the strategic partnership between India and the UAE.

India-UAE Relations

  • Diplomatic relations established in 1972; UAE opened its Embassy in Delhi in 1972, and India opened its Embassy in Abu Dhabi in 1973.
  • First-ever India-UAE Joint Air Forces exercise took place in September 2008.
  • Regular participation of India in the biennial International Defence Exhibition (IDEX) in Abu Dhabi.
  • Earlier this year, Indian Navy ships, INS Visakhapatnam, and INS Trikand, participated in the bilateral exercise ‘Zayed Talwar’ to enhance interoperability and synergy between the two navies.
The document PIB Summary- 3rd January, 2024 | Current Affairs & Hindu Analysis: Daily, Weekly & Monthly - UPSC is a part of the UPSC Course Current Affairs & Hindu Analysis: Daily, Weekly & Monthly.
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FAQs on PIB Summary- 3rd January, 2024 - Current Affairs & Hindu Analysis: Daily, Weekly & Monthly - UPSC

1. What is sickle cell anaemia?
Ans. Sickle cell anaemia is a genetic blood disorder characterized by abnormal red blood cells that are shaped like a crescent or sickle. These abnormal cells can cause blockages in blood vessels, leading to various complications and symptoms.
2. How is sickle cell anaemia inherited?
Ans. Sickle cell anaemia is inherited in an autosomal recessive pattern, meaning that both parents must pass on a copy of the abnormal gene for a child to develop the condition. If only one parent carries the gene, the child will have the sickle cell trait but not the full-blown disease.
3. What are the symptoms of sickle cell anaemia?
Ans. The symptoms of sickle cell anaemia can vary from person to person, but common symptoms include chronic fatigue, episodes of severe pain known as "crises," frequent infections, delayed growth, and vision problems. These symptoms are caused by the abnormal red blood cells and their effect on the body.
4. How is sickle cell anaemia diagnosed?
Ans. Sickle cell anaemia can be diagnosed through various methods, including blood tests, genetic testing, and prenatal testing. Blood tests can determine the presence of abnormal haemoglobin, while genetic testing can identify specific gene mutations. Prenatal testing can be done during pregnancy to determine if the fetus has inherited the condition.
5. Can sickle cell anaemia be cured?
Ans. Currently, there is no cure for sickle cell anaemia. Treatment focuses on managing symptoms, preventing complications, and improving the quality of life for individuals with the condition. This may include pain management, blood transfusions, medication, and regular medical monitoring. Ongoing research is being conducted to find potential curative treatments, such as gene therapy.
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