Masalah pada Tata Laksana Anemia Aplastik Didapat
Sari
Anemia aplastik adalah kegagalan sumsum tulang baik secara fisiologis maupun anatomis.
Penyakit ini ditandai oleh penurunan atau tidak ada faktor pembentuk sel darah dalam
sumsum tulang, pansitopenia darah perifer, tanpa disertai hepatosplenomegali atau
limfadenopati. Penanganan anemia aplastik masih merupakan masalah yang penting karena
patofisiologi penyakit ini masih belum pasti. Tata laksana anemia aplastik terdiri dari tata
laksana suportif terhadap keadaan yang disebabkan oleh pansitopenia seperti anemia, infeksi
dan perdarahan, serta tata laksana serta pengobatan yang bertujuan untuk mengganti sel
induk yang gagal dalam memproduksi sel-sel darah dan menekan proses imunologis yang
terjadi. Tata laksana kuratif terdiri dan transplantasi sumsum tulang dan penggunaan
obat-obat imunosupresan. Namun demikian tata laksana anemia aplastik baik yang bersifat
suportif maupun kuratif, dapat menimbulkan masalah-masalah yang mempengaruhi
prognosis pasien. Prognosis pasien anemia aplastik umumnya buruk, sekitar dua pertiga
pasien meninggal setelah 6 bulan diagnosis ditegakkan sebagai anemia aplastik.
Kata Kunci
Teks Lengkap:
PDFReferensi
Young NS. Acquired aplastic anemia. Ann Intern Med
;136. h. 534-46
Young NS, Barrett AJ. The treatment of severe acquired
aplastic anemia. Blood 1995;85:3367-77.
Young NS, Maciejewski J. The pathofisiology of acquired
aplastic anemia. N engl J Med 1997;336:1365-72.
Alter BP, Young NS. The bone marrow failure syndromes.
Dalam: Nathan DG, Oski FA, penyunting.
Hematology of infancy and childhood. Edisi ke-4. Philadelphia:
Saunders, 1993. h. 216-37.
Lanzkowsky P. Bone marrow failure. Manual of pediatric
hematology and oncology. Edisi ke-2. New york:
Churchill Livingstone, 1995. h. 89-96.
Gordon Smith EC. Epidemiology and aetiology of aplastic
anemia. Disampaikan pada kongres Intemasional
society of haematology Asian Pasifik, Bangkok, 25-29
Oktober, 1999.
Young NS. Acquired aplastic anemia. JAMA 1999;
:271-8.
Issaragrisil S. Aplastic anemia: Epidemiology. Disampaikan
pada kongres Internasional society of haematology
Asian Pasifik. Bangkok, 24-28 Oktober, 1999.
Lipton JM. The hematopoetic garden: how does it grow?
J pediatr 1998;132:565-7.
Sloand S, Kim S, Tidsale J, dkk. Intracelluler interferong
in circulating and marrow T cells detected by flow
cytometry and the response to immunosuppressive
therapy in patients with aplastic anemia. Blood 2002;
:1185-91.
Shadduck RK. Aplastic anemia. Dalam : Beutler E,
Lietcman MA, Coller BS, dkk, penyunting. Wiliams
hematology. Edisi ke-5. New York:McGraw Hill, 1995.
h. 238-51.
Young NS. Aplastic anemia. Dalam: Brain MC, Carbone
PP. Kelton JG, Schiler JH, penyunting. Current therapy
in hematology-oncology. Edisi ke-5. St. Lois: Mosby,
h. 129-34.
Munthe BG. Diagnostik dan penanggulangan anemia
aplastik. Dalam: Pendidikan tambahan berkala
Ilmu Kesehatan Anak. FKUI-RSCM Jakarta 1991.
h. 33-40.
Gatot D. Penatalaksanaan transfusi pada anak. Dalam:
Update emergencies pediatrics. Jakarta : Balai Pustaka
FKUI 2002. h. 28-47.
Fonseca R, Tefferi A. Practical aspect of diagnosis and
management of aplastic anemia. Am J Med Sci 1997;
:129-34.
Speck B, Nissen C, Tichelli A, Gratwohl A. aplastic anemia:
treatment. Disampaikan pada kongres Internasional
Society of Haematology, Singapore, 25-29 Agustus, 1996.
Bakhshi S. Aplastic anemia. E-medicine journal; 2002.
Didapat dari: www.emedicine.com. Di akses tanggal 12
Pebruari 2003.
Paquete RL, Tebyani N, Frane M, dkk. Long-term outcome
of aplastic anemia in adults treated with
antithymocyte globulin: Comparison with bone marrow
transplantation. Blood 1995;85:283-90.
Marsh J, Schrezenmeier H, Marin P. Prospective randomized
study comparing cyclosponine alone versus the
combination of antithymocite globulin and cyclosporine
for treatment of patients with nonsevere aplastic anemia:
A report from the European blood and marrow
transplantation (EBMT) severe aplastic anemia working
party. Blood 1999;93:2191-5.
Brodsky RA, Sensenbrenner LL, smith BD, Dorr D, Seaman
DJ, Lee SM. Durable treatment-free remission after
high-dose cyclophosphamid therapy for previously untreated
severe aplastic anemia. Ann intern Med. 2001;87:477-83.
Broadsky RA, Sensenbrenner LL, Jones RI. Complete
remission in severe aplastic anemia high-dose cyclophospamid
without bone marrow transplantation. Blood
;87:491-4.
Scopes J, Daly S, Atkinson R. Aplastic anemia: evidence
for dysfunctional bone marrow progenitor cells and the
corrective effect of Granulocyte colony stimulating factor
in vitro. Blood 1996;87:3179-85.
Frickhofen N, Kaltwasser JP, Schrezenmeier H, Ragha
Vaghar A, Vogt HG, Herrmann F. Treatment of aplastic
anemia with antilymphocyte globulin and methylprednisolone
with or without cyclosporine. N engl J Med
;324:1298-303.
Bacigalupo N, kaltwasser JP, Corda G, Arcese W, Carotenuto
W, Gallamini W. Antilymphocyte globulin, cyclosporin and
granulocyte colony stimulating factors in patients with acquired
aplastic anemia. Blood 1995;324:1298-303
Rosenfeld S, Follmann D, Nunez O. Antythymocyte
globulin and cyclosporine for severe aplastic anemia association
between hematologic response and long-term
outcome. JAMA 2003;289:1130-5.
Rosenfeld SJ, Kimball J, Vining D. Intensive immunosupression
with antithymocyte globulin and Cyclosporin
as treatment for severe acquired aplastic anemia. Blood
;85:3058-65.
Passweg JR, Socie G, Hinterberger W. Bone marrow
transplantation for severe aplastic anemia: has outcome
improved?. Blood 1997;90:858-64.
Deeg HJ, Leisenring W, Rainer S, Nimms D, Flower M,
Sandrers J. Long-term outcome after marrow transplantation
for severe aplastic anemia. Blood 1998;91:3637-45.
Socie G, Stone JV, Wingard JR. long-term survival and
late deaths after allogeneic bone marrow transplantation.
N engl J Med 1991;341:14-21.
Gluckmann E, Rocha V, Boyer-Chammard A. Outcome
of cord-blood transplantation from related and unrelated
donors. N engl J Med 1997; 337:373-81.
Min CK, Kim DW, Lee JW, Han CW, Min WS, Kim
CC. Hematopoetic stem cell transplantation og high risk
adult patient with severe anemia aplastic; reduction of
graft failure by enhanching stem cell dose. Haematologica
;86:303-10.
Socie G, Henry-Amar M, Bacigalupo A, Hows J,
Tichelli A, Ljungman P. malignant tumors occurring
after treatment of aplastic anemia. N engl J Med 1993;
:1152-7.
DOI: http://dx.doi.org/10.14238/sp7.1.2005.26-33
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