Sickle Cell Anemia Treatment Cost In Germany

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Sickle Cell Anemia is a severe blood disorder in which red blood cells become abnormal in shape and lose their ability to supply oxygen throughout the body.

In mild cases, Sickle Cell Anemia treatment requires medication and blood transfusions.

In rare cases, it may need a bone marrow transplant.

Cost related to Sickle Cell Anemia Treatment in Germany

Listing approximate price of Sickle Cell Anemia Treatment and some related procedures. The prices may change depending upon the centers and condition of the patient.

Treatment name Cost range
Bone Marrow Transplant USD 162000 to USD 198000

List of Centers for Sickle Cell Anemia Treatment in Germany

Popular Cities in Germany for Sickle Cell Anemia Treatment are:

Leading Hospitals for Sickle Cell Anemia Treatment in Germany

Doctors for Sickle Cell Anemia Treatment in Germany

The right doctor to consult for Sickle Cell Anemia is a Hematologist who specializes in treating blood disorders.

Listing popular specialists:

Prof. Dr. Antonio Pezzutto

Prof. Dr. Antonio Pezzutto

Director, 42 years of experience

Charite University HospitalLocation

Autologous transplant for multiple myeloma Hemoglobinopathies Bone marrow transplant for thalassemias and sickle cell disease Bone marrow failure syndrome Management of clots and Bleeding problems Immunodeficiency work up

Prof. Dr. Ulrich Keller

Prof. Dr. Ulrich Keller

Director, 23 years of experience

Charite University HospitalLocation

Bone marrow failure syndrome Autologous transplant for multiple myeloma Hemoglobinopathies for thalassemias and sickle cell disease Management of clots and Bleeding problems Immunodeficiency work up

Prof. Anthony D.Ho

Prof. Anthony D.Ho

Director, 46 years of experience

University Hospital HeidelbergLocation

Bone marrow failure syndrome Autologous transplant for multiple myeloma Hemoglobinopathies for thalassemias and sickle cell disease Management of clots and Bleeding problems Immunodeficiency work up

Dr. Veit Mansmann

Dr. Veit Mansmann

Director, 22 years of experience

Vivantes Hospital GroupLocation

All forms of chemotherapy, adjuvant, remission-inducing, and palliative Radiochemotherapy Antibody Therapy Immunotherapy Targeted Therapy Cytokine Therapy Puncture of Ascites and Pleura

Dr. Christian Scholz

Dr. Christian Scholz

Director, 29 years of experience

Vivantes Hospital GroupLocation

Acute leukemia Myelodysplastic syndrome (MDS) Malignant lymphoma Multiple myeloma Metastatic breast cancer Gastrointestinal cancer (e.g. colorectal cancer) Germ cell tumor Cytology of peripheral blood, bone marrow, and effusions

Prof. Dr. Ernst Spath-Schwalbe

Prof. Dr. Ernst Spath-Schwalbe

Director, 35 years of experience

Vivantes Hospital GroupLocation

Palliative medicine Geriatric oncology Tumorcenter Berlin Autologous transplant for multiple myeloma Hemoglobinopathies for thalassemias and sickle cell disease Management of clots and Bleeding problems Immunodeficiency work up

Prof. Dr. Rainer Haas

Prof. Dr. Rainer Haas

Head of Department, 38 years of experience

University Hospital DusseldorfLocation

Bronchial carcinoma Malignant lymphoma Plasmocytoma Sarcoma Antibody Therapy Immunotherapy Targeted Therapy Cytokine Therapy Puncture of Ascites and Pleura

Prof. Dr. Florian Bassermann

Prof. Dr. Florian Bassermann

Head of Department, 18 years of experience

University Hospital Rechts der IsarLocation

Bone marrow failure syndrome Autologous transplant for multiple myeloma Hemoglobinopathies for thalassemias and sickle cell disease Management of clots and Bleeding problems Immunodeficiency work up

Prof. Dr. Andreas Mackensen

Prof. Dr. Andreas Mackensen

Head of Department, 29 years of experience

University Hospital Erlangen, ErlangenLocation

Bone marrow failure syndrome Autologous transplant for multiple myeloma Hemoglobinopathies for thalassemias and sickle cell disease Management of clots and Bleeding problems Immunodeficiency work up

Prof. Dr. Elke Jaeger

Prof. Dr. Elke Jaeger

Chief, 35 years of experience

Nordwest Hospital, FrankfurtLocation

Bronchial carcinoma Malignant lymphoma Plasmocytoma Sarcoma Antibody Therapy Immunotherapy Targeted Therapy Cytokine Therapy Puncture of Ascites and Pleura

Prof. Dr. Eckhart Weidmann

Prof. Dr. Eckhart Weidmann

Chief, 34 years of experience

Nordwest Hospital, FrankfurtLocation

Bronchial carcinoma Malignant lymphoma Plasmocytoma Sarcoma Antibody Therapy Immunotherapy Targeted Therapy Cytokine Therapy Puncture of Ascites and Pleura

Dr. Farouk Dahmash

Dr. Farouk Dahmash

Senior Consultant, 15 years of experience

Asklepios St. Georg HospitalLocation

Bone marrow failure syndrome Autologous transplant for multiple myeloma Hemoglobinopathies for thalassemias and sickle cell disease Management of clots and Bleeding problems Immunodeficiency work up

Dr. med. Christian-Friedrich Jehn

Dr. med. Christian-Friedrich Jehn

Senior Consultant, 20 years of experience

Asklepios St. Georg HospitalLocation

Bone marrow failure syndrome Hemoglobinopathies for thalassemias and sickle cell disease Management of clots and Bleeding problems Immunodeficiency work up

Dr. Peter Borchmann

Dr. Peter Borchmann

Head of Department, 27 years of experience

Location

Hodgkin’s Lymphoma, Hematopoietic Diseases Treatment

Success Rate

With improvements in diagnosis and medical care, the success rate of Sickle Cell Anemia is above 95%.

Some symptoms of Sickle Cell Anaemia may include -

  • Yellow-colored skin
  • Blood in the urine
  • Swollen hands and feet 

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Frequently Asked Questions Related to Sickle Cell Anemia Treatment

Before the Procedure (7 Questions):

Sickle cell anemia is an inherited red blood cells disorders in which the red blood cells are not healthy enough to carry oxygen through the body, red blood cells can easily move throughout the blood vessels.

can get sickle cell anemia from when you inherit sickle cell from both your parents. When both your parents are carriers of sickle cell gene then you can get sickle cell anemia.

The organs affected by sickle cell anemia are the liver, heart, kidney, gallbladder, eyes, bones and joints.  It can cause recurrent infections, symptoms of sickle cell anemia usually appear 5 months of age. Some of the symptoms of sickle cell anemia includes anemia, episodes of pain, swelling in hands and feet, fever, pale skin, frequent infections etc.

If both mother and father are carrier then child may get affected from sickle cell anemia.

Complications of sickle cell anemia includes stroke, acute chest syndrome, pulmonary hypertension, organ damage, blindness, ulcers in leg, gall bladder stone and pulmonary hypertension.

Sickle cell anemia is being diagnosed by blood test, blood test checks for the defective form of hemoglobin causes sickle cell anemia. Adults and children can also be tested or sickle cell anemia.

Sickle cell anemic avoids the episodes of pain, relieves the symptoms and prevents complication. The treatment of sickle cell anemia included medications and blood transfusion.

During the Procedure (4 Questions):

The surgical procedure of sickle cell anemia involves blood transfusion, in red blood cell transfusion red blood cells are being removed from the supply of donated blood. This increases the supply of red blood cells.

Blood transfusion takes around 90 to 120 minutes to be completed and it can even be done in smaller children who are younger than 5 years.

The process of stem cell transplant usually takes around 3 weeks to be done.

Stem cell transplant is also known as bone marrow transplant the process of stem cell transplant involves replacing the bone marrow of the affected person with the healthy bone marrow of the donor.

Post the Procedure (3 Questions):

Stem cell transplant involves long hospital stay, after getting transplant you will need to get drug for preventing rejection of the donated stem cells. In some cases, your body may reject the transplant which may result in some life-threatening complications.

If you have sickle cell anemia by seeing a genetic counselor before you trying to conceive will help you in understanding the risk of having a child with sickle cell anemia.

Red blood cells usually live for about 120 days before they need to be replaced. But sickle cells usually die in 10 to 20 days, leaving a shortage of red blood cells,.

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