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Sickle Cell Anemia Treatment cost in India

If you're seeking affordable and effective treatment options for sickle cell anemia, India offers world-class medical facilities at affordable cost.

Average Cost

$25000

Recovery Time
3 Months


Success Rate
85%

Hospital Stay
28 Days


Treatment Type
Treatment

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Home Treatments Hematology Sickle Cell Anemia Treatment

Introduction

Are you seeking affordable, advanced options for sickle cell anemia treatment?

Sickle cell anemia is a disease you can receive from your parents through their genes. It affects your blood by causing your body to make a different type of hemoglobin.

If you have sickle cell anemia, your body doesn’t get enough oxygen, which can also make your tissues and organs not work.

No need to worry now!

Choose India for superior sickle cell anemia treatment, expertise, and high-quality care to support your recovery. Hospitals there provide advanced sickle cell anemia procedures such as acute chest syndrome, frequent pain episodes, and stroke with high success rates and experienced hematologists.

sickle cell anemia treatment cost in india

Why Sickle Cell Anemia Treatment Performed?

Sickle cell anemia treatments help manage the disease, prevent problems, and reduce pain caused by vaso-occlusive crises (VOCs). VOCs happen when sickle-shaped blood cells block blood flow, causing severe pain in the arms, legs, lower back, and belly.

There is no cure for sickle cell anemia, but treatments can help people live better with the condition. These treatments are:

  • Ease the pain with medications like pain relievers
  • Reduce complications with medications like hydroxyurea
  • Prevent infections and minimize organ damage
  • Include blood transfusions when needed.

Cost Breakdown

The total cost of sickle cell anemia treatment includes hospital charges for your stay, use of the treatment room, and nursing care.

Cost Component

Details

Estimated Cost in USD

Pre-operative Consultation & Diagnosis

Consultations, X-rays, MRI scans, CT scans, and blood tests.

1200 USD

Surgery Costs

Includes surgeon fees, hospital stays, and surgery type.

25000 USD

Allogenic stem cell transplant (match siblings).

Type of surgery, and surgeon fees.

26000 USD

Haplo identical stem cell transplant (unmatched donor).

Surgery type, and surgeon fees.

25000 USD

Rehabilitation and Follow-up

Medications, supportive devices, follow-up visits.

Types of Sickle Cell Anemia

Sickle cell anemia happens when the red blood cells in your body don’t work the way they should because of changes in a special protein called hemoglobin. Here are four main types of sickle cell anemia such as:

Hemoglobin SS Disease

  • This is the most common and severe type of sickle cell anemia and it happens when you inherit the sickle cell gene called hemoglobin S from both parents. People with this type have the most serious symptoms like pain and severe anemia.

Hemoglobin SC Disease

  • Hemoglobin SC disease is the second most common type of sickle cell anemia and it happens when you inherit one sickle cell gene (Hb S) from one parent and another gene (Hb C) from the other parent. Their symptoms are similar to Hemoglobin SS disease but are usually less severe.

Hemoglobin SB+ (Beta) Thalassemia

  • It affects the production of hemoglobin, making red blood cells smaller. If combined with a sickle cell gene (Hb S), it’s called hemoglobin S beta-thalassemia. However, their symptoms are milder than Hemoglobin SS disease.

Hemoglobin SB 0 (Beta-Zero) Thalassemia

  • This type also affects hemoglobin production, but the symptoms can be more severe. It has similarities to Hemoglobin SS disease and can cause a worse outlook.

Other Rare Types of Sickle Cell Anemia

Hemoglobin SD

  • Hemoglobin SD is a rare type of sickle cell disease that occurs when red blood cells contain hemoglobin S and D.

Symptoms include:

  • Sudden severe pain attacks
  • Jaundice

Hemoglobin SE

  • Hemoglobin SE (HbSE) sickle cell anemia is a rare inherited blood condition and it occurs when a person inherits a hemoglobin S (HbS) allele and a hemoglobin E (HbE) variant. 

Symptoms include:

  • Anemia
  • Clinical complications
  • Acute chest syndrome which may be life-threatening

Hemoglobin SO

  • Hemoglobin S is an abnormal type of hemoglobin that causes red blood cells to become rigid and sickle-shaped, which is characteristic of sickle cell anemia.

Symptoms include:

  • Anemia
  • Repeated infections 
  • Periodic episodes of pain 
  • Shortness of breath 
  • Fatigue.

Sickle Cell Trait

  • If you assume the sickle cell gene (Hb S) from just one parent, you have a sickle cell trait.
  • People with this typically don’t have symptoms and have only mild symptoms.

Factors Affecting the Cost of Sickle Cell Anemia Treatment

Diagnostic tests

  • The type of diagnostic tests such as blood tests, genetic tests, prenatal screening, and MRI can affect the overall cost of treatment.

Hospital type

  • Hospitals with advanced facilities and good infrastructure have higher fees than less accredited hospitals.

Experienced Surgeons

  • A highly experienced surgeon will charge more as compared to a less experienced surgeon this will affect the cost.

Treatment type

  • The cost of treatment can also depend upon the availability of blood and a suitable bone marrow donor which affects the cost.

Availability of blood and bone marrow

  • The cost can depend upon the availability of blood for transfusions and a suitable bone marrow donor.

Hospital infrastructure

  • Hospitals with advanced facilities and good infrastructure charge higher fees than less accredited hospitals.

Additional medications

  • Medications, surgical supplies, and nursing care are needed during the procedure. The cost of post-operative care can also add to the total treatment expense.

Country-Wise Cost Comparison of Sickle Cell Anemia Treatment

Country 

Cost Structure

India

25000 USD

United States

100000-150000 USD

Germany

76000-90000 USD

Turkey

50000-70000 USD

◾Key Takeaways

✅ Affordable Treatment Costs: India provides affordable treatment options for sickle cell anemia with highly skilled hematologists and advanced facilities, making excellent care accessible to international patients.

✅ Advanced Medical Technology: Indian hospitals are equipped with advanced technology and modern infrastructure, providing quality care comparable to international standards at a more affordable cost.

Sickle Cell Anemia Treatment cost
Treatment Name Estimated Cost
Sickle Cell Anemia Treatment25000 USD

Quality of care in Sickle Cell Anemia Treatment

  • India has some of the best hospitals for sickle cell anemia. These hospitals have special teams that provide care from diagnosis to recovery after the treatment. 
  • Indian hospitals have advanced facilities with the latest medical equipment and offer 24/7 patient support and care for each patient.
  • India has highly skilled and experienced medical professionals like hematologists who are proficient in treating sickle cell anemia treatment.
  • Indian hospitals provide a variety of treatment options for sickle cell anemia treatment such as blood transfusions, antibiotics to fight infections, and medications to manage symptoms.
  • In India, patients receive quality care at lower costs compared to other countries, making treatment available without compromising quality.
  • India is the best choice for medical care because it offers affordable treatment options, attracting patients from all over the world for surgeries and treatments.
  • Indian hospitals are experienced in caring for international patients. They offer various services to help patients manage the process, ensuring a smooth and stress-free treatment process.

Best Doctors for Sickle Cell Anemia Treatment in India

India has proficient hematologists for sickle cell anemia treatment. With personalized care and advanced techniques, they provide effective treatment for international patients.

Best Hospitals for Sickle Cell Anemia Treatment in India

Indian hospitals offer highly skilled specialists, advanced technology, and high-quality care, for accurate diagnosis, successful treatment, and supportive recovery for each patient’s requirements.

Technologies Used in India for Sickle Cell Anemia Treatment

India uses various types of technologies and treatments to control sickle cell anemia, symptoms and improve patient outcomes.

Pharmacological Treatments:

  • Hydroxyurea

Hydroxyurea is mostly used to reduce the frequency of pain episodes and the need for blood transfusions by increasing fetal hemoglobin production.

Blood Transfusion Therapies:

  • Automated Red Blood Cell Exchange (aRBCX)

This technology makes easy the replacement of sickle-shaped red blood cells with healthy ones and also reduces complications related to the disease.

Bone Marrow and Stem Cell Transplantation:

  • Matched Sibling Donor Transplants

This procedure involves replacing the patient's bone marrow with healthy stem cells from a compatible donor.

Gene Therapy:

  • CRISPR-Cas9 Technology

India is researching gene-editing techniques to fix the genetic mutations that cause sickle cell anemia and develop a permanent cure for this disease.

Diagnostic Innovations:

  • High-Performance Optical Spectroscopy (HPOS)

This technology includes portable monitors like HaemoCube and test kits such as SickleCert for enhancing early detection and diagnosis.

Preoperative Preparations for Sickle Cell Anemia Treatment

Necessary diagnostic tests

Before your treatment surgeon advises some diagnostic tests to examine the severity of the disease that are listed below:

Tests

Description

Blood tests

Check for the presence of hemoglobin S, the protein associated with sickle cell anemia. In adults, a blood sample is taken from a vein in the arm, while in children and babies, it's usually taken from a finger or heel. 

Hemoglobin electrophoresis

A blood test can determine if you have sickle cell anemia, are a carrier, or have other diseases linked to the sickle cell gene. 

Genetic tests

Can determine if you have one or two copies of the sickle cell gene. Genetic tests can help confirm a diagnosis if blood test results are unclear.

Prenatal screening

Can be performed as early as 8 to 10 weeks into a pregnancy. This test uses a sample of amniotic fluid or tissue from the placenta to look for the sickle hemoglobin gene.

MRI

Can detect changes in bone marrow that may be associated with sickle cell disease.


🟢Do’s Before Surgery

✅ You should follow your doctor’s instructions for taking any medicine they give you.

✅ Eating a healthy and balanced diet will help you stay strong and fight against infection.

✅ You must take a folic acid tablet every day and your doctor might suggest other vitamins too.

✅ Drink lots of water, because staying hydrated helps prevent sickle cell problems.

✅ If you see any side effects, you must inform your doctor. Many types of treatments are available to help with side effects.

🔴Don’ts Before Surgery

❌ Avoid smoking and also being around smoke because it makes it harder for your blood to carry oxygen.

❌ You should not be drinking alcohol can dry out your body and it makes side effects worse.

❌ Don’t take too much stress because it can cause problems, you must learn ways to relax such as deep breathing.

❌ You should stay active, but don’t push yourself too hard because too much exercise can make you lose water and feel short of breath.

Treatment Procedure of Sickle Cell Anemia Treatment

Treatment for sickle cell anemia depends on your symptoms and overall health. If you have serious complications like acute chest syndrome, frequent pain episodes, and a stroke, your doctor might recommend a stem cell transplant. This is the only cure for sickle cell anemia disease.

Blood Transfusions

  • Red blood cells from donated blood are given to a person with sickle cell disease through a vein and this adds healthy red blood cells to the body. It helps prevent complications like strokes and reduces symptoms of the disease.

Stem Cell Transplant (Bone Marrow Transplant)

  • Bone marrow, where blood cells are made from a healthy donor, replaces the person's sickle cell-affected bone marrow and this procedure can cure sickle cell disease. Generally, it is suitable for children with severe symptoms and complications. This is a high-risk procedure and can sometimes lead to death.

Stem Cell Gene Addition Therapy

  • Doctors take the person's stem cells, add a healthy gene to make normal hemoglobin, and then return the treated stem cells to the body. This procedure has been performed to cure sickle cell disease for people who don’t have a matching donor.

Gene Editing Therapy

  • The sickle cell gene in a person's stem cells is assembled to make healthy red blood cells. The treated cells are then put back into the body through an infusion and this treatment helps the body create normal red blood cells and may cure sickle cell disease.

Other treatments include antibiotics to fight infections, and medications to manage symptoms. These medications include:

Hydroxyurea (Droxia, Hydrea, Siklos, Mylocel)

  • This medicine is used for babies 6 to 9 months old, children, and adults. It helps reduce the number of serious complications and eases symptoms of anemia.

Voxelotor (Obryta)

  • This medicine helps stop red blood cells from becoming sickle-shaped. It is for children aged 4 and older.

L-glutamine therapy (Endari)

  • This treatment helps prevent sickled cells from becoming even more damaged. It is for children aged 5 and older as well as adults.

Crizanlizumab-tmca (Adakveo)

  • This medicine reduces how often you experience sudden pain called vaso-occlusive crises (VOC). It is for people aged 16 and older.

Post Treatment Care and Recovery

Hospital Stay and Recovery Time

After sickle cell anemia treatment, you will likely stay in the hospital for 28 days. However, their recovery time takes 3 months.

Success Rate of Sickle Cell Anemia Treatment in India

The success rate of sickle cell anemia is 85%. However, it depends on the type of treatment and the age of the patient. 

Possible Complications of Sickle Cell Anemia Treatment

Here are some common complications of sickle cell anemia:

Complications

Descriptions

Acute chest syndrome

In this type of sickle cell anemia is a severe lung-related complication.

Anemia

In people having sickle cell anemia, the red blood cells die early; it is called anemia.

Avascular necrosis

It happens when bone tissue dies due to sickled cells blocking blood flow to bones.

Blood clots

Sickled cells can increase the chance of blood clots forming, and these clots can sometimes be permanent.

Dactylitis

Dactylitis is a complication of sickle cell anemia in which pain and swelling in the hands and feet.

Fever

A fever may be the first sign of an infection and other severe sickle cell anemia diseases.

Infection

People who have sickle cell anemia typically have harmful infections like flu, meningitis, and pneumonia.

Kidney problems

Sickle cell anemia lowers the blood flow to the kidneys, causing kidney damage and chronic kidney disease.

Leg ulcers

Poor circulation of blood in the leg can cause painful leg ulcers.

Liver problems

If sickled cells in the liver can damage the liver and cause severe liver disease.

Organ damage

Not enough blood and oxygen reach the organs can cause organ damage.

Pain

Sometimes pain might be mild to severe and last for any length of time.

Priapism

Sickled cells in the penis leading to a continuous painful erection are called priapism.

Pulmonary hypertension

Develops high blood pressure in the lungs due to sickle cell anemia.

Sleep disorder breathing

It can cause lung problems that create sleep and breathing disorders.

Splenic sequestration

Splenic sequestration may form when sickled cells are caught in the spleen and block blood flow.

Stroke

A stroke can happen if sickled cells get stuck in a blood vessel and block blood flow to your brain.

Vision loss

Sickle cell anemia blocks blood flow in the blood vessels in the eye which can cause vision problems.


Why Choose Mejocare for Sickle Cell Anemia Treatment in India

✅ Experienced Hematologists: We connect you with proficient hematologists who have over 20 years of experience, ensuring high-quality and reliable care.

✅ JCI/NABH Accredited Hospitals: We partner with hospitals equipped with the latest technologies, including robotics, machine learning, and advanced diagnostic and therapeutic tools. These advanced facilities provide complete and personalized care.

✅ Additional Benefits: We provide quick responses, accurate cost estimates, accommodation in India, assistance with medical visas, and priority scheduling with doctors. Moreover, we make your arrival in India very easy, with airport pickup, hotel transfers, and support during your hospital stay, ensuring a smooth experience.

Conclusion

Sickle cell anemia can cause severe and sometimes it can cause permanent complications. For example, people with sickle cell anemia often need emergency medical care and are admitted to the hospital because they experience complications like acute chest syndrome (ACS) and vaso-occlusive crisis (VOC). However, treatment reduces and helps manage symptoms and increases longevity. With proper care, many people with sickle cell disease can live happy and healthy lives.

Disclaimer

The information in this article is for general purposes only and does not provide an exact cost estimate. If you need professional advice, we can help you connect with top doctors in India. Connect to Mejocare today.

Medically Reviewed By

Dr. Aryan Malhotra

QualificationsMBBS, DTMU University, Georgia,Radiation Oncology Resident at Burdwan Medical College and HospitalDr. Aryan Malhotra is a skilled and caring doctor. He is a Radiation Oncology Resident at Burdwan Medical College and Hospital. He treats people with cancer and works closely with patients during their treatment.He completed his MBBS from David Tvildiani Medical University in Georgia. He has passed the USMLE... Read More

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Frequently Asked Questions on Sickle Cell Anemia Treatment

The cost of Sickle Cell Anemia Treatment in India is 25000 USD.

The success rate of Sickle Cell Anemia in India is around 85-90%.

5 days for adults and 4 days for children.

The expected recovery period after sickle cell anemia treatment in India is 40 to 90 days.

Sickle cell disease can lead to complications due to blocked blood flow to specific organs. These complications include severe effects like stroke, acute chest syndrome, organ damage, disabilities, and sometimes premature death. Acute chest syndrome notably reduces oxygen levels in the body.

Physical therapy like gentle exercises and targeted massage by a physiotherapist can effectively manage pain and improve blood circulation, complementing medication for symptom relief.

Yes, it is necessary to have a companion.

When receiving treatment for Sickle Cell Anaemia in India, it's best to consult your specialist 2-4 weeks before any planned travel. If you've had a serious sickle cell crisis within 2 weeks of your trip, it's advisable to postpone traveling for your health's sake.

Yes, you can do your own research and choose your therapist.

You can use Paracetamol regularly to manage mild to moderate pain. Moderate pain can be managed using non-steroidal anti-inflammatory drugs (NSAIDs) like diclofenac or ibuprofen.

Yes, insurance will cover the cost of Sickle Cell Anemia Treatment in India.

To discover the top doctors or hospitals in India, you can visit our website, mejocare on the doctors' page, you can filter and find the finest doctors, while on the hospital page, you can identify the best hospitals. Additionally, you can reach out to us, and we will gladly offer you all the necessary suggestions and information you need.

Treating Sickle Cell Anaemia involves introducing new stem cells into the patient's bloodstream. It takes a few weeks for these cells to begin developing in the bone marrow, during which the child stays in the hospital.

No, there is no waiting list for Sickle Cell Anemia Treatment in India.

Before medical procedures, tests like CBC, urine analysis, Chest X-ray, ECG, and Kidney Function Tests are typically performed to evaluate different aspects of your health.

Sickle Cell Anemia treatments in India often use Propofol, a safe and swift-acting sedative. Patients are not fully unconscious but comfortably sleep through the procedure, often forgetting the experience afterward.

As soon as you're ready.

Medications like opioids commonly lead to constipation after surgery. To prevent it, avoid high-fat cheeses, processed foods, red meats, dried or dehydrated foods, full-fat dairy, and sugary treats.

It's important to monitor vital signs, tend to the wound, manage any complications, consider rehabilitation services, and attend follow-up appointments for a smooth recovery.

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