Поиск
Закладки
Озвучить текст Озвучить книгу
Изменить режим чтения
Изменить размер шрифта
Оглавление
Для озвучивания и цитирования книги перейдите в режим постраничного просмотра.
Серповидно-клеточные нарушения

Список литературы

  1. Sickle cell disease in childhood. Standards and guidelines for clinical care. 2nd edition. 2010. 88 p.
  2. The Management of Sickle Cell Disease. National Heart, Lung, and Blood Institute (NHLBI), 2002. 206 p.
  3. Rees D.C., Williams T.N., Gladwin M.T. Sickle-cell disease // The Lancet. 2010. Vol. 376, № 9757. P. 2018–2031.
  4. Stuart M.J., Nagel R.L. Sickle-cell disease // Lancet. 2004. Vol. 364, № 9442. P. 1343–1360.
  5. Steinberg M.H. In the clinic. Sickle cell disease // Annals of internal medicine. 2011. Vol. 155, № 5.
  6. Румянцев А.Г., Токарев Ю.Н., Сметанина Н.С. Гемоглобинопатии и талассемические синдромы. М.: Практическая медицина, 2015. 448 p.
  7. Costa F.F., Conran N. Sickle cell anemia: From basic science to clinical practice // Sickle Cell Anemia: From Basic Science to Clinical Practice. Springer International Publishing, 2016. 1–435 p.
  8. Serjeant G.R. One hundred years of sickle cell disease // British Journal of Haematology. 2010. Vol. 151, № 5. P. 425–429.
  9. Malowany J.I., Butany J. Pathology of sickle cell disease // Semin. Diagn. Pathol. 2012. Vol. 29, № 1. P. 49–55.
  10. Vos T. et al. Global, regional, and national incidence, prevalence, and years lived with disability for 301 acute and chronic diseases and injuries in 188 countries, 1990-2013: A systematic analysis for the Global Burden of Disease Study 2013 // Lancet. Lancet Publishing Group, 2015. Vol. 386, № 9995. P. 743–800.
  11. Naghavi M. et al. Global, regional, and national age-sex specific all-cause and cause-specific mortality for 240 causes of death, 1990-2013: A systematic analysis for the Global Burden of Disease Study 2013 // Lancet. Lancet Publishing Group, 2015. Vol. 385, № 9963. P. 117–171.
  12. Fernandes A.P.P.C. et al. Mortality of children with sickle cell disease: a population study // J Pediatr (Rio J). 2010. Vol. 86, № 4. P. 279–284.
  13. Scheinin L., Wetli C. V. Sudden death and sickle cell trait: Medicolegal considerations and implications // Am. J. Forensic Med. Pathol. 2009. Vol. 30, № 2. P. 204–208.
  14. Platt O.S. et al. Mortality in sickle cell disease – life expectancy and risk factors for early death // N. Engl. J. Med. 1994. Vol. 330, № 23. P. 1639–1644.
  15. Wierenga K.J., Hambleton I.R., Lewis N.A. Survival estimates for patients with homozygous sickle-cell disease in Jamaica: a clinic-based population study. // Lancet (London, England). 2001. Vol. 357, № 9257. P. 680–683.
  16. Quinn C.T., Rogers Z.R., Buchanan G.R. Survival of children with sickle cell disease // Blood. 2004. Vol. 103, № 11. P. 4023–4027.
  17. Serjeant G.R., Higgs D.R., Hambleton I.R. Elderly survivors with homozygous sickle cell disease // New England Journal of Medicine. Massachussetts Medical Society, 2007. Vol. 356, № 6. P. 642–643.
  18. Yanni E. et al. Trends in Pediatric Sickle Cell Disease-Related Mortality in the United States, 1983-2002 // J. Pediatr. 2009. Vol. 154, № 4. P. 541–545.
  19. Quinn C.T. et al. Improved survival of children and adolescents with sickle cell disease // Blood. 2010. Vol. 115, № 17. P. 3447–3452.
  20. Makani J. et al. Mortality in Sickle Cell Anemia in Africa: A Prospective Cohort Study in Tanzania // PLoS One / ed. Schrijver I. 2011. Vol. 6, № 2. P. e14699.
  21. Darbari D.S. et al. Circumstances of death in adult sickle cell disease patients // Am. J. Hematol. 2006. Vol. 81, № 11. P. 858–863.
  22. Khatib R., Rabah R., Sarnaik S.A. The spleen in the sickling disorders: An update // Pediatric Radiology. 2009. Vol. 39, № 1. P. 17–22.
  23. Ohene-Frempong K. et al. Cerebrovascular accidents in sickle cell disease: Rates and risk factors // Blood. 1998. Vol. 91, № 1. P. 288–294.
  24. Leight L. et al. Hemodynamic studies in sickle cell anemia. // Circulation. 1954. Vol. 10, № 5. P. 653–662.
  25. Covitz W. et al. The heart in sickle cell anemia: The cooperative study of sickle cell disease (CSSCD) // Chest. American College of Chest Physicians, 1995. Vol. 108, № 5. P. 1214–1219.
  26. Braden D.S., Covitz W., Milner P.F. Cardiovascular function during rest and exercise in patients with sickle-cell anemia and coexisting alpha thalassemia-2 // Am. J. Hematol. 1996. Vol. 52, № 2. P. 96–102.
  27. Johnson C.S., Giorgio A.J. Arterial blood pressure in adults with sickle cell disease. // Arch. Intern. Med. 1981. Vol. 141, № 7. P. 891–893.
  28. Pegelow C.H. et al. Natural history of blood pressure in sickle cell disease: Risks for stroke and death associated with relative hypertension in sickle cell anemia // Am. J. Med. 1997. Vol. 102, № 2. P. 171–177.
  29. Martin C.R. et al. Myocardial infarction in sickle cell disease. // J. Natl. Med. Assoc. 1996. Vol. 88, № 7. P. 428–432.
  30. Romero Mestre J.C. et al. Cardiovascular autonomic dysfunction in sickle cell anemia: a possible risk factor for sudden death? // Clin. Auton. Res. 1997. Vol. 7, № 3. P. 121–125.
  31. Paul R.N. et al. Acute chest syndrome: Sickle cell disease // European Journal of Haematology. 2011. Vol. 87, № 3. P. 191–207.
  32. Howard J. et al. Guideline on the management of acute chest syndrome in sickle cell disease // Br. J. Haematol. 2015. Vol. 169, № 4. P. 492–505.
  33. Vichinsky E.P. et al. Causes and outcomes of the acute chest syndrome in sickle cell disease. National Acute Chest Syndrome Study Group.[Erratum appears in N Engl J Med 2000 Sep 14;343(11):824] // N. Engl. J. Med. 2000. Vol. 342, № 25. P. 1855–1865.
  34. Vichinsky E.P. et al. Acute chest syndrome in sickle cell disease: Clinical presentation and course // Blood. 1997. Vol. 89, № 5. P. 1787–1792.
  35. Vichinsky E. et al. Pulmonary fat embolism: a distinct cause of severe acute chest syndrome in sickle cell anemia. // Blood. 1994. Vol. 83, № 11. P. 3107–3112.
  36. Milner P.F., Brown M. Bone marrow infarction in sickle cell anemia: correlation with hematologic profiles. // Blood. 1982. Vol. 60, № 6. P. 1411–1419.
  37. Castro O. Systemic fat embolism and pulmonary hypertension in sickle cell disease. // Hematol. Oncol. Clin. North Am. 1996. Vol. 10, № 6. P. 1289–1303.
  38. Johnson C.S. et al. Liver involvement in sickle cell disease // Med. (United States). 1985. Vol. 64, № 5. P. 349–356.
  39. Walker T.M., Hambleton I.R., Serjeant G.R. Gallstones in sickle cell disease: observations from The Jamaican Cohort study. // J. Pediatr. 2000. Vol. 136, № 1. P. 80–85.
  40. Stewart West M. et al. Laboratory profile of sickle cell disease: A cross-sectional analysis // J. Clin. Epidemiol. 1992. Vol. 45, № 8. P. 893–909.
  41. Passon R.G., Howard T.A., Zimmerman S.A. The effect of UDP-glucuronosyltransferase (UGTIA) promotor polymorphisms on serum bilirubin levels and cholelithiasis in patients with sickle cell anemia // Blood. 1999. Vol. 94, № Supp. 1. P. 645a.
  42. Nzeh D.A., Adedoyin M.A. Sonographic pattern of gallbladder disease in children with sickle cell anaemia. // Pediatr. Radiol. 1989. Vol. 19, № 5. P. 290–292.
  43. Lee S.P., Maher K., Nicholls J.F. Origin and fate of biliary sludge // Gastroenterology. 1988. Vol. 94, № 1. P. 170–176.
  44. Al-Salem A.H., Qaisruddin S. The significance of biliary sludge in children with sickle cell disease // Pediatr. Surg. Int. 1998. Vol. 13, № 1. P. 14–16.
  45. Serafini A.N. et al. Diagnostic Studies in Patients With Sickle Cell Anemia and Acute Abdominal Pain // Arch. Intern. Med. 1987. Vol. 147, № 6. P. 1061–1062.
  46. Shao S.H., Orringer E.P. Sickle cell intrahepatic cholestasis: approach to a difficult problem. // Am. J. Gastroenterol. 1995. Vol. 90, № 11. P. 2048–2050.
  47. Solanki D.L., Kletter G.G., Castro O. Acute splenic sequestration crises in adults with sickle cell disease // Am. J. Med. 1986. Vol. 80, № 5. P. 985–990.
  48. Statius van Eps L.W. et al. Nature of concentrating defect in sickle-cell nephropathy. Microradioangiographic studies. // Lancet (London, England). 1970. Vol. 1, № 7644. P. 450–452.
  49. Allon M. Renal abnormalities in sickle cell disease // Archives of Internal Medicine. 1990. Vol. 150, № 3. P. 501–504.
  50. Powars D.R. et al. Chronic renal failure in sickle cell disease: Risk factors, clinical course, and mortality // Ann. Intern. Med. 1991. Vol. 115, № 8. P. 614–620.
  51. Chrouser K.L. et al. Priapism in the United States: The changing role of sickle cell disease // Am. J. Surg. 2011. Vol. 201, № 4. P. 468–474.
  52. Almeida A., Roberts I. Bone involvement in sickle cell disease // British Journal of Haematology. 2005. Vol. 129, № 4. P. 482–490.
  53. Aguilar C.M. et al. Clinical evaluation of avascular necrosis in patients with sickle cell disease: Children’s hospital oakland hip evaluation scale - A modification of the harris hip score // Arch. Phys. Med. Rehabil. 2005. Vol. 86, № 7. P. 1369–1375.
  54. Worrall V.T., Butera V. Sickle-cell dactylitis. // J. Bone Joint Surg. Am. 1976. Vol. 58, № 8. P. 1161–1163.
  55. Management of Sickle Cell Disease in Pregnancy. 2011.
  56. Mousa S.A., Qari M.H. Diagnosis and management of sickle cell disorders // Methods Mol. Biol. 2010. Vol. 663. P. 291–307.
  57. Clarke G.M., Higgins T.N. Laboratory investigation of hemoglobinopathies and thalassemias: Review and update // Clinical Chemistry. 2000. Vol. 46, № 8 II. P. 1284–1290.
  58. Garg D. et al. Studies on the hepatic and renal status of patients with sickle cell disease from western zone of Maharashtra, India // Int. J. Res. Med. Sci. Medip Academy, 2018. Vol. 6, № 4. P. 1224.
  59. Silva G.S. et al. Transcranial Doppler in adult patients with sickle cell disease // Cerebrovasc. Dis. 2006. Vol. 21, № 1–2. P. 38–41.
  60. Valadi N. et al. Transcranial Doppler ultrasonography in adults with sickle cell disease // Neurology. 2006. Vol. 67, № 4. P. 572–574.
  61. Transcranial Doppler Scanning for Children with Sickle Cell Disease Standards and Guidance Second Edition. 2016.
  62. Seibert J.J. et al. Transcranial Doppler, MRA, and MRI as a screening examination for cerebrovascular disease in patients with sickle cell anemia: An 8-year study // Pediatr. Radiol. 1998. Vol. 28, № 3. P. 138–142.
  63. Berdoukas V. et al. Tissue iron evaluation in chronically transfused children shows significant levels of iron loading at a very young age // Am. J. Hematol. 2013. Vol. 88, № 11.
  64. De Montalembert M. et al. ENERCA clinical recommendations for disease management and prevention of complications of sickle cell disease in children // American Journal of Hematology. Wiley-Liss Inc., 2011. Vol. 86, № 1. P. 72–75.
  65. Brousse V., Makani J., Rees D.C. Management of sickle cell disease in the community // BMJ (Online). BMJ Publishing Group, 2014. Vol. 348.
  66. Yawn B.P. et al. Management of sickle cell disease: summary of the 2014 evidence-based report by expert panel members // JAMA - J. Am. Med. Assoc. 2014. Vol. 312, № 10. P. 1033–1048.
  67. Amrolia P.J. et al. Therapeutic challenges in childhood sickle cell disease Part 1: current and future treatment options // Br. J. Haematol. 2003. Vol. 120, № 5. P. 725–736.
  68. Lane P.A. et al. Health supervision for children with sickle cell disease // Pediatrics. American Academy of Pediatrics, 2002. Vol. 109, № 3. P. 526–535.
  69. Rasel M., Mahboobi S.K. Transfusion Iron Overload // StatPearls. StatPearls Publishing, 2021.
  70. Elagouz M. et al. Sickle cell disease and the eye: Old and new concepts // Survey of Ophthalmology. 2010. Vol. 55, № 4. P. 359–377.
  71. Charache S. et al. Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia // N. Engl. J. Med. 1995. Vol. 332, № 20. P. 1317–1322.
  72. Steinberg M.H. et al. Effect of Hydroxyurea on Mortality and Morbidity in Adult Sickle Cell Anemia: Risks and Benefits Up to 9 Years of Treatment // J. Am. Med. Assoc. 2003. Vol. 289, № 13. P. 1645–1651.
  73. Platt O.S. Hydroxyurea for the treatment of sickle cell anemia // N. Engl. J. Med. Massachussetts Medical Society, 2008. Vol. 358, № 13. P. 1362.
  74. Shilalukey K. et al. Counseling sexually active teenagers treated with potential human teratogens // J. Adolesc. Heal. 1997. Vol. 21, № 3. P. 143–146.
  75. Diav-Citrin O. et al. Hydroxyurea use during pregnancy: a case report in sickle cell disease and review of the literature. // Am. J. Hematol. 1999. Vol. 60, № 2. P. 148–150.
  76. Byrd D.C., Pitts S.R., Alexander C.K. Hydroxyurea in two pregnant women with sickle cell anemia // Pharmacotherapy. Pharmacotherapy Publications Inc., 1999. Vol. 19, № 12. P. 1459–1462.
  77. Manchikanti A. et al. Steroid hormones for contraception in women with sickle cell disease // Cochrane Database of Systematic Reviews. John Wiley and Sons Ltd, 2007. № 2.
  78. Davis B.A. et al. Guidelines on red cell transfusion in sickle cell disease Part II: indications for transfusion // Br. J. Haematol. 2017. Vol. 176, № 2. P. 192–209.
  79. Chou S.T. Transfusion therapy for sickle cell disease: a balancing act. // Hematology / the Education Program of the American Society of Hematology. American Society of Hematology. Education Program. 2013. Vol. 2013. P. 439–446.
  80. Gyang E. et al. Effect of chronic red cell transfusion therapy on vasculopathies and silent infarcts in patients with sickle cell disease // American Journal of Hematology. 2011. Vol. 86, № 1. P. 104–106.
  81. Mirre E. et al. Feasibility and efficacy of chronic transfusion for stroke prevention in children with sickle cell disease // Eur. J. Haematol. Blackwell Publishing Ltd, 2010. Vol. 84, № 3. P. 259–265.
  82. Adams R.J. et al. Prevention of a first stroke by transfusions in children with sickle cell anemia and abnormal results on transcranial Doppler ultrasonography // N. Engl. J. Med. 1998. Vol. 339, № 1. P. 5–11.
  83. Quirolo K. How do i transfuse patients with sickle cell disease? // Transfusion. 2010. Vol. 50, № 9. P. 1881–1886.
  84. Win N. et al. Use of intravenous immunoglobulin and intravenous methylprednisolone in hyperhaemolysis syndrome in sickle cell disease // Hematology. Hematology, 2004. Vol. 9, № 5–6. P. 433–436.
  85. Федорова Д.В., Сметанина Н.С. Синдром гипергемолиза (обзор литературы) // Вопросы гематологии/онкологии и иммунопатологии в педиатрии. 2013. Vol. 12, № 4. P. 5–12.
  86. Win N. et al. Hyperhemolysis syndrome in sickle cell disease: case report (recurrent episode) and literature review // Transfusion. Transfusion, 2008. Vol. 48, № 6. P. 1231–1238.
  87. Сметанина Н.С. Современные возможности хелаторной терапии // Российский журнал детской гематологии и онкологии. 2014. Vol. 1. P. 51–59.
  88. Walters M.C. et al. Bone marrow transplantation for sickle cell disease // N. Engl. J. Med. 1996. Vol. 335, № 6. P. 369–376.
  89. Hsieh M.M. et al. Allogeneic Hematopoietic Stem-Cell Transplantation for Sickle Cell Disease // N. Engl. J. Med. 2009. Vol. 361, № 24. P. 2309–2317.
  90. Cappelli B. et al. Hemoglobinopathies (Sickle Cell Disease and Thalassemia) // The EBMT Handbook. Hematopoietic Stem Cell Transplantation and Cellular Therapies / ed. Carreras E. et al. Springer, 2019. P. 595–603.
  91. Olowoyeye A., Okwundu C.I. Gene therapy for sickle cell disease // Cochrane Database of Systematic Reviews. John Wiley and Sons Ltd, 2014. Vol. 2014, № 10.
  92. Oringanje C., Nemecek E., Oniyangi O. Hematopoietic stem cell transplantation for people with sickle cell disease // Cochrane Database of Systematic Reviews. John Wiley and Sons Ltd, 2016. Vol. 2016, № 5.
  93. Vichinsky E.P. et al. A comparison of conservative and aggressive transfusion regimens in the perioperative management of sickle cell disease // N. Engl. J. Med. N Engl J Med, 1995. Vol. 333, № 4. P. 206–214.
  94. Roberts-Harewood M., Nokes T.J.C., Taylor P.C. Adenotonsilectomy in suckle cell disease: is routine transfusion necessary? // Br. J. Haematol. 1997. Vol. 97, № Suppl. 1. P. 75.
  95. Haberkern C.M. et al. Cholecystectomy in sickle cell anemia patients: Perioperative outcome of 364 cases from the national preoperative transfusion study // Blood. 1997. Vol. 89, № 5. P. 1533–1542.
  96. Hatley R.M. et al. Laparoscopic cholecystectomy in children with sickle cell disease. // Am. Surg. 1995. Vol. 61, № 2. P. 169–171.
  97. Rogers Z.R. Management of fever in sickle cell disease [Electronic resource]. 2021. URL: https://www.uptodate.com/contents/management-of-fever-in-sickle-cell-disease (accessed: 12.08.2021).
  98. Ochocinski D. et al. Life-Threatening Infectious Complications in Sickle Cell Disease: A Concise Narrative Review // Front. Pediatr. Frontiers Media SA, 2020. Vol. 8. P. 38.
  99. 9Lionnet F. et al. Guidelines for management of adult sickle cell disease // Rev. Med. Interne. Elsevier Masson SAS, 2009. Vol. 30, № SUPPL. 3.
  100. Bundy D.G. et al. Burden of influenza-related hospitalizations among children with sickle cell disease // Pediatrics. American Academy of Pediatrics, 2010. Vol. 125, № 2. P. 234–243.
  101. Ellison A.M. et al. Pneumococcal bacteremia in a vaccinated pediatric sickle cell disease population // Pediatr. Infect. Dis. J. 2012. Vol. 31, № 5. P. 534–536.
  102. Wong W.Y., Overturf G.D., Powars D.R. Infection caused by streptococcus pneumoniae in children with sickle cell disease: Epidemiology, immunologic mechanisms, prophylaxis, and vaccination // Clin. Infect. Dis. 1992. Vol. 14, № 5. P. 1124–1136.
  103. Strouse J.J. et al. Severe pandemic H1N1 and seasonal influenza in children and young adults with sickle cell disease // Blood. 2010. Vol. 116, № 18. P. 3431–3434.
  104. Pearson H.A. Sickle Cell Anemia and Severe Infections Due to Encapsulated Bacteria // J. Infect. Dis. Oxford University Press (OUP), 1977. Vol. 136, № Supplement 1. P. S25–S30.
  105. Wong W.Y. et al. Polysaccharide encapsulated bacterial infection in sickle cell anemia: A thirty year epidemiologic experience // Am. J. Hematol. 1992. Vol. 39, № 3. P. 176–182.
  106. Slavov S.N. et al. Human parvovirus B19: General considerations and impact on patients with sickle-cell disease and thalassemia and on blood transfusions // FEMS Immunology and Medical Microbiology. 2011. Vol. 62, № 3. P. 247–262.
  107. Mccavit T.L., Gilbert M., Buchanan G.R. Prophylactic penicillin after 5 years of age in patients with sickle cell disease: A survey of sickle cell disease experts // Pediatr. Blood Cancer. 2013. Vol. 60, № 6. P. 935–939.
  108. Hirst C., Owusu-Ofori S. Prophylactic antibiotics for preventing pneumococcal infection in children with sickle cell disease // Cochrane Database of Systematic Reviews. 2009. № 4.
  109. McCavit T.L. et al. Increase in invasive streptococcus pneumoniae infections in children with sickle cell disease since pneumococcal conjugate vaccine licensure // J. Pediatr. 2011. Vol. 158, № 3. P. 505–507.
  110. Hyacinth H.I., Gee B.E., Hibbert J.M. The Role of Nutrition in Sickle Cell Disease. // Nutr. Metab. Insights. 2010. Vol. 3. P. 57–67.
  111. Claster S. et al. Nutritional deficiencies in iron overloaded patients with hemoglobinopathies // Am. J. Hematol. 2009. Vol. 84, № 6. P. 344–348.
  112. Kawchak D.A. et al. Adequacy of Dietary Intake Declines with Age in Children with Sickle Cell Disease // J. Am. Diet. Assoc. 2007. Vol. 107, № 5. P. 843–848.
  113. van der Dijs F.P. et al. Elevated homocysteine levels indicate suboptimal folate status in pediatric sickle cell patients. // Am. J. Hematol. 1998. Vol. 59, № 3. P. 192–198.
  114. Kennedy T.S. et al. Red blood cell folate and serum vitamin B12 status in children with sickle cell disease // Am. J. Pediatr. Hematol. Oncol. 2001. Vol. 23, № 3. P. 165–169.
  115. Dixit R. et al. Folate supplementation in people with sickle cell disease // Cochrane database Syst. Rev. Cochrane Database Syst Rev, 2018. Vol. 3, № 3.
  116. Soe H.H.K. et al. Vitamin D supplementation for sickle cell disease // Cochrane Database Syst. Rev. John Wiley and Sons Ltd, 2020. Vol. 2020, № 5.
  117. Ross A.C. et al. The 2011 Report on Dietary Reference Intakes for Calcium and Vitamin D from the Institute of Medicine: What Clinicians Need to Know // J. Clin. Endocrinol. Metab. The Endocrine Society, 2011. Vol. 96, № 1. P. 53.
  118. Olujohungbe A., Burnett A.L. How I manage priapism due to sickle cell disease // British Journal of Haematology. 2013. Vol. 160, № 6. P. 754–765.
  119. DeBaun M.R. et al. Associated risk factors for silent cerebral infarcts in sickle cell anemia: Low baseline hemoglobin, sex, and relative high systolic blood pressure // Blood. 2012. Vol. 119, № 16. P. 3684–3690.
  120. Roach E.S. Stroke in children // Curr. Treat. Options Neurol. 2000. Vol. 2, № 4. P. 295–303.
  121. Powars D.R. Management Of Cerebral Vasculopathy In Children With Sickle Cell Anaemia // Br. J. Haematol. 2000. Vol. 108, № 4. P. 666–678.
  122. Pavlakis S.G. et al. Neurologic complications of sickle cell disease. // Adv. Pediatr. 1989. Vol. 36. P. 247–276.
  123. Kutlar A. et al. The methylene tetrahydrofolate reductase (C677T) mutation as a potential risk factor for avascular necrosis in sickle cell disease. // Hemoglobin. 2001. Vol. 25, № 2. P. 213–217.
  124. Zimmerman S.A., Ware R.E. Inherited DNA mutations contributing to thrombotic complications in patients with sickle cell disease // Am. J. Hematol. 1998. Vol. 59, № 4. P. 267–272.
  125. Nsiri B. et al. Antiphospholipid antibodies: lupus anticoagulants, anticardiolipin and antiphospholipid isotypes in patients with sickle cell disease. // Hematol. Cell Ther. 1998. Vol. 40, № 3. P. 107–112.
  126. Roberts M.Z. et al. Effectiveness and safety of oral anticoagulants in patients with sickle cell disease and venous thromboembolism: a retrospective cohort study // J. Thromb. Thrombolysis. J Thromb Thrombolysis, 2018. Vol. 45, № 4. P. 512–515.
  127. Евтушенко С.К. Инсульты у детей как актуальная проблема в современной педиатрической ангионеврологии // Вестник Алматинского государственного института усовершенствования врачей. 2010. Vol. 1. P. 66–72.
  128. Tissue plasminogen activator for acute ischemic stroke // N. Engl. J. Med. 1995. Vol. 333, № 24. P. 1581–1588.
  129. Kahn S.R. et al. Prevention of VTE in nonsurgical patients. Antithrombotic therapy and prevention of thrombosis, 9th ed: American College of Chest Physicians evidence-based clinical practice guidelines // Chest. American College of Chest Physicians, 2012. Vol. 141, № 2 SUPPL. P. e195S-e226S.
  130. Naik R.P., Streiff M.B., Lanzkron S. Sickle cell disease and venous thromboembolism: What the anticoagulation expert needs to know // Journal of Thrombosis and Thrombolysis. 2013. Vol. 35, № 3. P. 352–358.
  131. Strouse J.J., Lanzkron S., Urrutia V. The epidemiology, evaluation and treatment of stroke in adults with sickle cell disease // Expert Rev. Hematol. Expert Rev Hematol, 2011. Vol. 4, № 6. P. 597–606.
  132. Furie K.L. et al. Guidelines for the prevention of stroke in patients with stroke or transient ischemic attack: a guideline for healthcare professionals from the american heart association/american stroke association // Stroke. Stroke, 2011. Vol. 42, № 1. P. 227–276.
  133. Brousse V. et al. Acute splenic sequestration crisis in sickle cell disease: Cohort study of 190 paediatric patients // Br. J. Haematol. Br J Haematol, 2012. Vol. 156, № 5. P. 643–648.
  134. Sickle cell acute painful episode. Management of an acute painful sickle cell episode in hospital. NICE clinical guideline. 2012. 179 p.
  135. Ballas S.K. et al. Hydroxyurea and acute painful crises in sickle cell anemia: Effects on hospital length of stay and opioid utilization during hospitalization, outpatient acute care contacts, and at home // J. Pain Symptom Manage. 2010. Vol. 40, № 6. P. 870–882.
  136. Glassberg J. Evidence-based management of sickle cell disease in the emergency department. // Emergency medicine practice. 2011. Vol. 13, № 8.
  137. Anie K.A., Green J. Psychological therapies for sickle cell disease and pain. // Cochrane database Syst. Rev. 2012. № 2. P. CD001916.
  138. Smith W.R. et al. Daily assessment of pain in adults with sickle cell disease // Ann. Intern. Med. American College of Physicians, 2008. Vol. 148, № 2. P. 94–101.
  139. Rees D.C. et al. Guidelines for the management of the acute painful crisis in sickle cell disease // British Journal of Haematology. 2003. Vol. 120, № 5. P. 744–752.
  140. Ballas S.K. Treatment of pain in adults with sickle cell disease // Am. J. Hematol. 1990. Vol. 34. P. 49.
  141. Elander J. et al. Understanding the causes of problematic pain management in sickle cell disease: Evidence that pseudoaddiction plays a more important role than genuine analgesic dependence // J. Pain Symptom Manage. Elsevier Inc., 2004. Vol. 27, № 2. P. 156–169.
  142. Solomon L.R. Treatment and prevention of pain due to vaso-occlusive crises in adults with sickle cell disease: An educational void // Blood. 2008. Vol. 111, № 3. P. 997–1003.
  143. Darbari D.S. et al. Pharmacogenetics of morphine: Potential implications in sickle cell disease // American Journal of Hematology. 2008. Vol. 83, № 3. P. 233–236.
  144. Sutton M. et al. Resolving conflicts: misconceptions and myths in the care of the patient with sickle cell disease. // Mt. Sinai J. Med. 1999. Vol. 66, № 4. P. 282–285.
  145. Tamayo-Sarver J.H. et al. Racial and Ethnic Disparities in Emergency Department Analgesic Prescription // Am. J. Public Health. American Public Health Association Inc., 2003. Vol. 93, № 12. P. 2067–2073.
  146. Geller A.K., O’Connor M.K. The sickle cell crisis: A dilemma in pain relief // Mayo Clinic Proceedings. Elsevier Ltd, 2008. Vol. 83, № 3. P. 320–323.
  147. Pletcher M.J. et al. Trends in opioid prescribing by race/ethnicity for patients seeking care in US emergency departments // JAMA - J. Am. Med. Assoc. 2008. Vol. 299, № 1. P. 70–78.
  148. Zempsky W.T. Treatment of sickle cell pain: Fostering trust and justice // JAMA - Journal of the American Medical Association. 2009. Vol. 302, № 22. P. 2479–2480.
  149. Ware M.A. et al. Day-care management of sickle cell painful crisis in Jamaica: A model applicable elsewhere? // Br. J. Haematol. 1999. Vol. 104, № 1. P. 93–96.
  150. Benjamin L.J., Swinson G.I., Nagel R.L. Sickle cell anemia day hospital: An approach for the management of uncomplicated painful crises // Blood. 2000. Vol. 95, № 4. P. 1130–1137.
  151. Wright J. et al. Day case management of sickle pain: 3 years experience in a UK sickle cell unit // Br. J. Haematol. 2004. Vol. 126, № 6. P. 878–880.
  152. Frei-Jones M.J. et al. Vaso-occlusive episodes in older children with sickle cell disease: emergency department management and pain assessment // J. Pediatr. 2008. Vol. 152. P. 281.
  153. Brookoff D., Polomano R. Treating sickle cell pain like cancer pain // Ann. Intern. Med. 1992. Vol. 116, № 5. P. 364–368.
  154. Lynch M.E. A review of the use of methadone for the treatment of chronic noncancer pain // Pain Research and Management. Hindawi Limited, 2005. Vol. 10, № 3. P. 133–144.
  155. Mangla A., Hamad H. Pure Red Cell Aplasia // StatPearls. StatPearls Publishing, 2021.
  156. Gladwin M.T., Sachdev V. Cardiovascular Abnormalities in Sickle Cell Disease // J. Am. Coll. Cardiol. NIH Public Access, 2012. Vol. 59, № 13. P. 1123–1133.
  157. Gordeuk V.R. et al. Relative systemic hypertension in patients with sickle cell disease is associated with risk of pulmonary hypertension and renal insufficiency // Am. J. Hematol. Am J Hematol, 2008. Vol. 83, № 1. P. 15–18.
  158. Dessap A.M. et al. Pulmonary hypertension and cor pulmonale during severe acute chest syndrome in sickle cell disease // Am. J. Respir. Crit. Care Med. 2008. Vol. 177, № 6. P. 646–653.
  159. Miller S.T. How I treat acute chest syndrome in children with sickle cell disease // Blood. 2011. Vol. 117, № 20. P. 5297–5305.
  160. Morris C., Vichinsky E., Styles L. Clinician assessment for acute chest syndrome in febrile patients with sickle cell disease: is it accurate enough? // Ann. Emerg. Med. 1999. Vol. 34, № 1. P. 64–69.
  161. Lee E.S.H., Chu P.C.M. Reverse sequestration in a case of sickle crisis // Postgrad. Med. J. BMJ Publishing Group, 1996. Vol. 72, № 850. P. 487–488.
  162. Pappo A., Buchanan G.R. Acute splenic sequestration in a 2-month-old infant with sickle cell anemia. // Pediatrics. 1989. Vol. 84, № 3. P. 578–579.
  163. Orringer E.P. et al. Case report: Splenic infarction and acute splenic sequestration in adults with hemoglobin SC disease // Am. J. Med. Sci. 1991. Vol. 302, № 6. P. 374–379.
  164. Rao S., Gooden S. Splenic sequestration in sickle cell disease: role of transfusion therapy. // Am. J. Pediatr. Hematol. Oncol. 1985. Vol. 7, № 3. P. 298–301.
  165. Grover R., Wethers D.L. Management of acute splenic sequestration crisis in sickle cell disease. // J. Assoc. Acad. Minor. Phys. 1990. Vol. 1, № 3. P. 67–70.
  166. Wright J.G. et al. Postsplenectomy course in homozygous sickle cell disease. // J. Pediatr. 1999. Vol. 134, № 3. P. 304–309.
  167. Baron B.W., Mick R., Baron J.M. Hematuria in sickle cell anemia - not always benign: Evidence for excess frequency of sickle cell anemia in african americans with renal cell carcinoma // Acta Haematol. 1994. Vol. 92, № 3. P. 119–122.
  168. McInnes B.K. The management of hematuria associated with sickle hemoglobinopathies. // J. Urol. 1980. Vol. 124, № 2. P. 171–174.
  169. Black W.D., Hatch F.E., Acchiardo S. Aminocaproic acid in prolonged hematuria of patients with sicklemia. // Arch. Intern. Med. 1976. Vol. 136, № 6. P. 678–681.
  170. Readett D.R.J., Morris J., Serjeant G.R. Determinants of nocturnal enuresis in homozygous sickle cell disease // Arch. Dis. Child. 1990. Vol. 65, № 6. P. 615–618.
  171. Brooks L.J., Topol H.I. Enuresis in children with sleep apnea // J. Pediatr. Mosby Inc., 2003. Vol. 142, № 5. P. 515–518.
  172. Koshy M. et al. Management of sickle cell anemia and pregnancy // J. Clin. Apher. 1991. Vol. 6, № 4. P. 230–233.
  173. Koshy M. et al. Prophylactic Red-Cell Transfusions in Pregnant Patients with Sickle Cell Disease // N. Engl. J. Med. 1988. Vol. 319, № 22. P. 1447–1452.
  174. Tuck S.M. et al. Prophylactic blood transfusion in maternal sickle cell syndromes // BJOG An Int. J. Obstet. Gynaecol. 1987. Vol. 94, № 2. P. 121–125.
  175. Morrison J.C. et al. Use of continuous flow erythrocytapheresis in pregnant patients with sickle cell disease // J. Clin. Apher. 1991. Vol. 6, № 4. P. 224–229.
  176. Christin-Maitre S., Bouchard P., Spitz I.M. Medical termination of pregnancy // New England Journal of Medicine. 2000. Vol. 342, № 13. P. 946–956.
  177. Wong D. et al. Whaley and Wong’s Nursing Care of Infants and Children, ed. 6. St. Louis, Mosby, 1999. 1153 p.

Для продолжения работы требуется Registration
На предыдущую страницу

Предыдущая страница

Следующая страница

На следующую страницу
Список литературы
На предыдущую главу Предыдущая глава
оглавление
Следующая глава На следующую главу