Dtsch Med Wochenschr 2009; 134(22): 1179-1184
DOI: 10.1055/s-0029-1222586
Übersicht | Review article
Hämatologie
© Georg Thieme Verlag KG Stuttgart · New York

Probleme erwachsener Sichelzellpatienten in Deutschland

Problems of adult sickle cell patients in GermanyR. Dickerhoff1 , A von Rücker2 , G. Maschmeyer3 , H. Heimpel4
  • 1Asklepios Klinik, St. Augustin
  • 2Hämatopathologie, Institut für Pathologie, Universität Bonn
  • 3Klinik für Hamatologie und Onkologie, Klinikum Ernst von Bergmann, Potsdam
  • 4Klinik für Innere Medizin III, Universitätsklinikum Ulm
Further Information

Publication History

eingereicht: 28.11.2008

akzeptiert: 30.4.2009

Publication Date:
20 May 2009 (online)

Literatur

  • 1 Ataga K I, Orringer E P. Renal abnormalities in sickle cell disease.  Am J Hematol. 2000;  63 205-211
  • 2 Bellet P S, Kalinyak K A, Shukla R. et al . Incentive spirometry to prevent acute pulmonary complications in sickle cell disease.  N Engl J Med. 1995;  333 699-703
  • 3 Charache S, Terrin M L, Moore R D. et al . Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia.  N Engl J Med. 1995;  332 1317-1322
  • 4 Dickerhoff R, von Ruecker A, Kohne E. Heterozygote Hämoglobin-S-Anlage.  Dt Ärztebl. 2000;  97 A 2717-2719
  • 5 Dickerhoff R. Milzsequestrationen bei Patienten mit Sichelzellerkrankungen.  Klin Pädiatr. 2002;  214 70-73
  • 6 Gladwin M T, Sachdev V, Jison M L. et al . Pulmonary hypertension as a risk factor for death in patients with sickle cell disease.  N Engl J Med. 2004;  350 886-895
  • 7 Hernigou P, Beaujean F. Treatment of osteonecrosis with autologous bone marrow grafting.  Clin Orthop Relat Res. 2002;  405 14-23
  • 8 van der Horst C, Seif C, Naumann C M, Jünemann K P, Martinez P ortillo FJ. Methylenblau in der Therapie des pharmakoinduzierten Priapismus.  Blickpunkt Der Mann. 2005;  1 29-32
  • 9 Kirkham F J. Therapy insight: Stroke risk and its management in patients with sickle cell disease.  Nat Clin Pract Neur. 2007;  3 264-278
  • 10 Koduri P R. Iron in sickle cell disease: A review why less is better.  Am J Hematol. 2003;  73 59-63
  • 11 Koduri P R, Nathan S. Acute splenic sequestration crisis in adults with hemoglobin S-C disease: a report of nine cases.  Ann Hematol. 2006;  85 239-243
  • 12 Koshy M, Burd L, Wallace D, Moawad A, Baron J. Prophylactic red-cell transfusions in pregnant patients with sickle cell disease.  N Engl J Med. 1988;  319 1447-1452
  • 13 Krishnamurti L. hematopoietic cell transplantation for sickle cell disease: state of the art.  Expert Opin Biol Ther. 2007;  7 1-12
  • 14 Mantadakis E, Ewalt D H, Cavender J D, Rogers Z R, Buchanan G R. Outpatient penile aspiration and epinephrine irrigation for young patients with sickle cell anemia and prolonged priapism.  Blood. 2000;  95 78-82
  • 15 Maschmeyer G, Haas A, Dickerhoff R, Kleber F X. Pulmonale Hypertonie bei Sichelzellkrankheiten – Epidemiologie, Pathogenese, Diagnostik und Therapie.  Dtsch Med Wochenschr. 2007;  132 103-107
  • 16 de Montalembert M, Maunoury C, Acar P, Brousse V, Sidi D, Lenoir G. Myocardial ischaemia in children with sickle cell disease.  Arch Dis Child. 2004;  89 359-362
  • 17 National Institutes of Health Clinical Center .Improving the results of bone marrow transplantation for patients with severe congenital anemias. http://clinicaltrials.gov/ct/show/NCT00061568:jsessionid = DF8BF. 
  • 18 National Institutes of Health Clinical Center .Evaluating the Safety and Effectiveness of Stem Cell Transplants From Unrelated Donors in Children With Sickle Cell Disease. http://clinicaltrials.gov/ct2/show/NCT00745420. 
  • 19 Nolan V G, Wyszynski D F, Farrer L A, Steinberg M H. Hemolysis-associated priapism in sickle cell disease.  Blood. 2005;  106 3264-3267
  • 20 Ohene-Frempong K, Weiner S J, Sleeper L A. et al . Cerebrovascular accidents in sickle cell disease: Rates and risk factors.  Blood. 1998;  91 288-294
  • 21 Platt O S, Brambilla D J, Rosse W F. et al . Mortality in sickle cell disease. Life expectancy and risk factors for early death.  N Engl J Med. 1994;  330 1639-1644
  • 22 Preul M C, Cendes F, Just N, Mohr G. Intracranial aneurysms and sickle cell anemia: multiplicity and propensity for the vertebrobasilar territory.  Neurosurgery. 1998;  42 971-977
  • 23 Quinn C T, Rogers Z R, Buchanan G R. Survival of children with sickle cell disease.  Blood. 2004;  103 4023-4027
  • 24 Raman S V, Simonetti O P, Cataland S P, Kraut E H. Myocardial ischemia and right ventricular dysfunction in adult patients with sickle cell disease.  Hematologica. 2006;  91 1329-1335
  • 25 Rees D C, Olujohungbe A D, Parker N E. et al . Guidelines for the management of the acute painful crisis in sickle cell disease.  Br J Haematol. 2003;  120 744-752
  • 26 Schleucher R, Gaessler M, Knobloch J. Rapid healing of a late diagnosed sickle cell leg ulcer using a new combination of treatment methods.  J Wound Care. 2007;  16 197-198
  • 27 Seiberth V. Trans-scleral diode laser photocoagulation in proliferative sickle cell retinopathy.  Ophthalmology. 1999;  106 1828-1829
  • 28 Serjeant G R. Blood transfusion in sickle cell disease: a cautionary tale.  Lancet. 2003;  361 1659-1660
  • 29 Serjeant G R, Loy L L, Crowther M. et al . Outcome of pregnancy in homozygous sickle cell disease.  Obstet Gynecol. 2004;  103 1278-1285
  • 30 Serjeant G R, Higgs D R, Hambleton I R. Elderly survivors with homozygous sickle cell disease.  N Engl J Med. 2007;  356 642-643
  • 31 Solomon L R. Treatment and prevention of pain due to vaso-occlusive crises in adults with sickle cell disease: an educational void.  Blood. 2008;  111 997-1003
  • 32 Sokol J A, baron E, Lantos G, Kazim M. orbital compression syndrome in sickle cell disease.  Ophthal Plast Reconstr Surg. 2008;  24 181-184
  • 33 Stuart M J, Setty B NY. Sickle cell acute chest syndrome: pathogenesis and rationale for treatment.  Blood. 1999;  94 1555-1560
  • 34 Styles L A, Vichinsky E P. Core decompression in avascular necrosis of the hip in sickle cell disease.  Am J Hematol. 1996;  52 103-107
  • 35 Virag R, Bachir D, Lee K, Galacteros F. Preventive treatment of priapism in sickle cell disease with oral and self-administered intracavernous injection of Etilefrine.  Urology. 1996;  47 777-781
  • 36 Ware R E, Zimmerman S A, Sylvestre P B. et al . Prevention of secondary stroke and resolution of transfusional iron overload in children with sickle cell anemia using hydroxyurea and phlebotomy.  J Pediatr. 2004;  145 346-352
  • 37 www.sicklecellsociety.org/CareBook.pdf. 
  • 38 www.haemoglobin.uni-bonn.de. 
  • 39 http://www.dgho.de/_cmsdata/_file/file_220.pdf. 

Dr. med. Roswitha Dickerhoff

Asklepios Klinik

53754 St. Augustin

Phone: 02241/2491

Fax: 02241/249272

Email: roswitha.dickerhoff@uni-bonn.de

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