TAILIEUCHUNG - Chapter 108. Hematopoietic Cell Transplantation (Part 7)

Pneumocystis jiroveci pneumonia, once seen in 5–10% of patients, can be prevented by treating patients with oral trimethoprim-sulfamethoxazole for 1 week pretransplant and resuming the treatment once patients have engrafted. The risk of infection diminishes considerably beyond 3 months after transplant unless chronic Most GVHD transplant develops, centers requiring recommend continuous continuing immunosuppression. trimethoprim-sulfamethoxazole prophylaxis while patients are receiving any immunosuppressive drugs and also recommend careful monitoring for late CMV reactivation. In addition, many centers recommend prophylaxis against varicella zoster, using acyclovir for 1 year posttransplant. Treatment Transplantation of Specific Diseases Using Hematopoietic Cell Nonmalignant Diseases: Treatment Immunodeficiency Disorders By replacing abnormal stem cells with cells from a normal donor, hematopoietic. | Chapter 108. Hematopoietic Cell Transplantation Part 7 Pneumocystis jiroveci pneumonia once seen in 5-10 of patients can be prevented by treating patients with oral trimethoprim-sulfamethoxazole for 1 week pretransplant and resuming the treatment once patients have engrafted. The risk of infection diminishes considerably beyond 3 months after transplant unless chronic GVHD develops requiring continuous immunosuppression. Most transplant centers recommend continuing trimethoprim-sulfamethoxazole prophylaxis while patients are receiving any immunosuppressive drugs and also recommend careful monitoring for late CMV reactivation. In addition many centers recommend prophylaxis against varicella zoster using acyclovir for 1 year posttransplant. Treatment of Specific Diseases Using Hematopoietic Cell Transplantation Nonmalignant Diseases Treatment Immunodeficiency Disorders By replacing abnormal stem cells with cells from a normal donor hematopoietic cell transplantation can cure patients of a variety of immunodeficiency disorders including severe combined immunodeficiency Wiskott-Aldrich syndrome and Chédiak-Higashi syndrome. The widest experience has been with severe combined immunodeficiency disease where cure rates of 90 can be expected with HLA-identical donors and success rates of 5070 have been reported using haplotype-mismatched parents as donors Table 108-3 . Table 108-3 Estimated 5-Year Survival Rates Following Transplantation Disease Allogeneic Autologous Severe combined immunodeficiency 90 N A Aplastic anemia 90 N A Thalassemia 90 N A Acute myeloid leukemia First remission 55-60 50 Second remission 40 30 Acute lymphocytic leukemia First remission 50 40 Second remission 40 30 Chronic myeloid leukemia

TỪ KHÓA LIÊN QUAN
TAILIEUCHUNG - Chia sẻ tài liệu không giới hạn
Địa chỉ : 444 Hoang Hoa Tham, Hanoi, Viet Nam
Website : tailieuchung.com
Email : tailieuchung20@gmail.com
Tailieuchung.com là thư viện tài liệu trực tuyến, nơi chia sẽ trao đổi hàng triệu tài liệu như luận văn đồ án, sách, giáo trình, đề thi.
Chúng tôi không chịu trách nhiệm liên quan đến các vấn đề bản quyền nội dung tài liệu được thành viên tự nguyện đăng tải lên, nếu phát hiện thấy tài liệu xấu hoặc tài liệu có bản quyền xin hãy email cho chúng tôi.
Đã phát hiện trình chặn quảng cáo AdBlock
Trang web này phụ thuộc vào doanh thu từ số lần hiển thị quảng cáo để tồn tại. Vui lòng tắt trình chặn quảng cáo của bạn hoặc tạm dừng tính năng chặn quảng cáo cho trang web này.